ID,SMILES,Name,HOMO,LUMO,Voc (V),Jsc (mA cm^2),FF,PCE(%),ref
1,CCCCCC(CC1=NC2=C(C(F)=C(C(C3=CC=C(S3)C4=CC5=C(C(C6=CC(F)=C(S6)CC(CCCC)CC)=C7C=CSC7=C5C8=CC(F)=C(S8)CC(CCCC)CC)S4)=C2N=C1CC(CCCCC)CC)F)C9=CC=CS9)CC,PBQ5,5.55,2.91,0.844,26.02,70.81,15.55,"C. Zhu, L. Meng, J. Zhang, S. Qin, W. Lai, B. Qiu, J. Yuan, Y. Wan, W. Huang, Y. Li, A Quinoxaline-Based D¨CA Copolymer Donor Achieving 17.62% Efficiency of Organic Solar Cells. Advanced Materials. 33, 2100474 (2021)."
2,CCCCC(CC1=C(C=C(S1)C2=NC3=C(C(F)=C(C(C4=CC=CS4)=C3N=C2C5=CC(F)=C(S5)CC(CCC)CC)F)C6=CC=C(S6)C7=CC8=C(C(C9=CC(F)=C(S9)CC(CCCC)CC)=C%10C=CSC%10=C8C%11=CC(F)=C(S%11)CC(CCCC)CC)S7)F)CC,PBQ6,5.64,3.18,0.851,26.58,77.91,17.62,"C. Zhu, L. Meng, J. Zhang, S. Qin, W. Lai, B. Qiu, J. Yuan, Y. Wan, W. Huang, Y. Li, A Quinoxaline-Based D¨CA Copolymer Donor Achieving 17.62% Efficiency of Organic Solar Cells. Advanced Materials. 33, 2100474 (2021)."
3,CCCCCCCCCCC1=C(SC(C2=C3SC4=C(C3=C(C5=C2C6=C(S5)C=CS6)C7=CC(CCCCCCCCCC)=C(S7)CCCCCCCCCC)SC(C8=C(C=C(S8)C9=C(C(F)=CC%10=NSN=C%109)F)CC(CCCC)CC)=C4)=C1)CCCCCCCCCC,PDTBDT-SBTEH,5.24,3.55,0.82,13.76,63.5,7.16,"P. Gong, P. Guo, Y. Wang, L. Yan, Z. Liang, M. Ding, J. Tong, J. Li, Y. Xia, Ultrafast Kinetics Investigation of a Fluorinated-Benzothiadiazole Polymer with an Increased Excited State Transition Dipole Moment Applied in Organic Solar Cells. ACS Appl. Energy Mater. 4, 9627¨C9638 (2021)."
4,CCCCCCCCCCC1=C(SC(C2=C3SC4=C(C3=C(C5=C2C6=C(S5)C=CS6)C7=CC(CCCCCCCCCC)=C(S7)CCCCCCCCCC)SC(C8=C(C=C(S8)C9=C(C(F)=CC%10=NSN=C%109)F)CC(CCCC)CC)=C4)=C1)CCCCCCCCCC,PDTBDT-SFBTEH,5.43,3.67,0.94,13.81,66.3,8.61,"P. Gong, P. Guo, Y. Wang, L. Yan, Z. Liang, M. Ding, J. Tong, J. Li, Y. Xia, Ultrafast Kinetics Investigation of a Fluorinated-Benzothiadiazole Polymer with an Increased Excited State Transition Dipole Moment Applied in Organic Solar Cells. ACS Appl. Energy Mater. 4, 9627¨C9638 (2021)."
5,CCCCC(CC1=CC=C(S1)C2=C3C=C(SC3=C(C4=C2SC=C4)C5=CC=C(S5)CC(CCCC)CC)C6=C(C(Cl)=CS6)Cl)CC,PBDTT1Cl,-5.47,-3.48,0.87,27.7,71.35,17.1,"H. Wang, H. Lu, Y.-N. Chen, G. Ran, A. Zhang, D. Li, N. Yu, Z. Zhang, Y. Liu, X. Xu, W. Zhang, Q. Bao, Z. Tang, Z. Bo, Chlorination Enabling a Low-Cost Benzodithiophene-Based Wide-Bandgap Donor Polymer with an Efficiency of over 17%. Advanced Materials. n/a, 2105483."
6,CCCCC(CC1=CC=C(S1)C2=C3C=C(SC3=C(C4=C2SC=C4)C5=CC=C(S5)CC(CCCC)CC)C6=C(C(Cl)=CS6)Cl)CC,PBDTT2Cl,-5.6,-3.49,0.9,21.86,58.6,11.47,"H. Wang, H. Lu, Y.-N. Chen, G. Ran, A. Zhang, D. Li, N. Yu, Z. Zhang, Y. Liu, X. Xu, W. Zhang, Q. Bao, Z. Tang, Z. Bo, Chlorination Enabling a Low-Cost Benzodithiophene-Based Wide-Bandgap Donor Polymer with an Efficiency of over 17%. Advanced Materials. n/a, 2105483."
7,CCCCCCC(CC1=C2C(C3=C(SC(C4=CC=C(S4)C5=CC6=C(C7=C(C(C8=CC(F)=C(S8)SCC(CCCC)CC)=C6S5)C=C(S7)C)C9=CC(F)=C(S9)SCC(CCCC)CC)=C3C(C2=C(S1)CC(CCCCCC)CCCC)=O)C%10=CC=CS%10)=O)CCCC,PBSF-A12,-5.52,-3.65,0.92,17.5,68.2,10.9,"K. Wang, W. Li, X. Guo, Q. Zhu, Q. Fan, Q. Guo, W. Ma, M. Zhang, Optimizing the Alkyl Side-Chain Design of a Wide Band-Gap Polymer Donor for Attaining Nonfullerene Organic Solar Cells with High Efficiency Using a Nonhalogenated Solvent. Chem. Mater. 33, 5981¨C5990 (2021)."
8,CCCCCCC(CSC1=C(C=C(S1)C2=C3C=C(SC3=C(C4=C2SC=C4)C5=CC(F)=C(S5)SCC(CCCCCC)CCCC)C6=CC=C(S6)C7=C8C(C9=C(SC(CC(CCCC)CC)=C9C(C8=C(S7)C%10=CC=CS%10)=O)CC(CCCC)CC)=O)F)CCCC,PBSF-D12,-5.5,-3.59,0.92,20.5,70.8,13.4,"K. Wang, W. Li, X. Guo, Q. Zhu, Q. Fan, Q. Guo, W. Ma, M. Zhang, Optimizing the Alkyl Side-Chain Design of a Wide Band-Gap Polymer Donor for Attaining Nonfullerene Organic Solar Cells with High Efficiency Using a Nonhalogenated Solvent. Chem. Mater. 33, 5981¨C5990 (2021)."
9,CCCCCCCCC(CN1B(C2=C(C3=CC4=C(C5=C(B(N4CC(CCCCCCCC)CCCCCC)C6=CC=CC=C6)C=CS5)C=C31)SC(C7=CC=C(S7)C8=C9C(C%10=C(SC(CC(CCCC)CC)=C%10C(C9=C(S8)C%11=CC=CS%11)=O)CC(CCCC)CC)=O)=C2)C%12=CC=CC=C%12)CCCCCC,PBNT-BDD,,,0.88,25.2,72,16.1,"S. Pang, Z. Wang, X. Yuan, L. Pan, W. Deng, H. Tang, H. Wu, S. Chen, C. Duan, F. Huang, Y. Cao, A Facile Synthesized Polymer Featuring B-N Covalent Bond and Small Singlet-Triplet Gap for High-Performance Organic Solar Cells. Angewandte Chemie International Edition. 60, 8813¨C8817 (2021)."
10,CCCCCCCCC(CN1C(C2=C(C3=C(C1=O)C=C(S3)C4=CC5=C(C6=C(C7=C(C(C8=CC=C(S8)CC(CCCC)CC)=C6S5)C9=C(S7)C=CS9)C%10=CC=C(S%10)CC(CCCC)CC)S4)SC=C2)=O)CCCCCC,PDTBDT,-5.67,-3.28,0.895,17.18,53.5,8.22,"Y. Tang, L. Xie, D. Qiu, C. Yang, Y. Liu, Y. Shi, Z. Huang, J. Zhang, J. Hu, K. Lu, Z. Wei, Optimizing the energy levels and crystallinity of 2,2¡ä-bithiophene-3,3¡ä-dicarboximide-based polymer donors for high-performance non-fullerene organic solar cells. J. Mater. Chem. C. 9, 7575¨C7582 (2021)."
11,CCCCCCCCC1=CSC(C2=CC3=C(S2)C2=C(C=C(C4=CC(CCCCCCCC)=C(C5=CC6=C(S5)C5=C(C7=CC=C(CC(CC)CCCC)S7)C7=C(C8=C(C=CS8)S7)C(C7=CC=C(CC(CC)CCCC)S7)=C5S6)S4)S2)C(=O)N(CC(CCCCCC)CCCCCCCC)C3=O)=C1,PDTBDT-T,-5.4,-3.21,0.78,24.21,65.81,12.71,"Y. Tang, L. Xie, D. Qiu, C. Yang, Y. Liu, Y. Shi, Z. Huang, J. Zhang, J. Hu, K. Lu, Z. Wei, Optimizing the energy levels and crystallinity of 2,2¡ä-bithiophene-3,3¡ä-dicarboximide-based polymer donors for high-performance non-fullerene organic solar cells. J. Mater. Chem. C. 9, 7575¨C7582 (2021)."
12,CCCCCCCCC1=CSC(C2=CC3=C(S2)C2=C(C=C(C4=CC(CCCCCCCC)=C(C5=CC6=C(S5)C5=C(C7=CC(Cl)=C(CC(CC)CCCC)S7)C7=C(C8=C(C=CS8)S7)C(C7=CC(Cl)=C(CC(CC)CCCC)S7)=C5S6)S4)S2)C(=O)N(CC(CCCCCC)CCCCCCCC)C3=O)=C1,PDTBDT-T-Cl,-5.58,-3.26,0.86,24.46,71.65,15.63,"Y. Tang, L. Xie, D. Qiu, C. Yang, Y. Liu, Y. Shi, Z. Huang, J. Zhang, J. Hu, K. Lu, Z. Wei, Optimizing the energy levels and crystallinity of 2,2¡ä-bithiophene-3,3¡ä-dicarboximide-based polymer donors for high-performance non-fullerene organic solar cells. J. Mater. Chem. C. 9, 7575¨C7582 (2021)."
13,CCCCCCC(COC(C1=C(SC=C1)/C=C/C2=C(C=C(S2)C3=CC=C(S3)C4=C5C(C6=C(SC(CC(CCCC)CC)=C6C(C5=C(S4)C7=CC=CS7)=O)CC(CCCC)CC)=O)C(OCC(CCCCCC)CCCC)=O)=O)CCCC,PV2TC-BDD,-5.5,-3.74,0.87,18.83,69.97,11.5,"Z. Liu, X. Chen, S. Huang, H. Guo, F. Wu, J. Wang, J. Liu, X. Huang, L. Chen, Y. Chen, Novel efficient accptor1-acceptor2 type copolymer donors: Vinyl induced planar geometry and high performance organic solar cells. Chemical Engineering Journal. 419, 129532 (2021)."
14,CCCCCCCCC(CCCCCC)CN1N=C2C(=N1)C(C1=CC=C(C3=CC(C(=O)OCC(CCCC)CCCCCC)=C(/C=C/C4=C(C(=O)OCC(CCCC)CCCCCC)C=CS4)S3)S1)=C(F)C(F)=C2C1=CC=C(C)S1,PV2TC-FTAZ,-5.35,-3.56,0.71,20.49,58.57,8.56,"Z. Liu, X. Chen, S. Huang, H. Guo, F. Wu, J. Wang, J. Liu, X. Huang, L. Chen, Y. Chen, Novel efficient accptor1-acceptor2 type copolymer donors: Vinyl induced planar geometry and high performance organic solar cells. Chemical Engineering Journal. 419, 129532 (2021)."
15,CCCCCCC(CC1=CC2=C(C(C3=CC=C(S3)C4=CC5=C(C6=C(C(C7=CC(Cl)=C(S7)CC(CCCC)CC)=C5S4)C=CS6)C8=CC(Cl)=C(S8)CC(CCCC)CC)=C9C=C(SC9=C2C%10=CC=CS%10)CC(CCCCCC)CCCC)S1)CCCC,PvBDT-Cl,-4.4,-2.24,0.9,15.04,57.3,7.76,"M. Zhang, X. Xu, L. Yu, Q. Peng, Efficient wide-band-gap copolymer donors for organic solar cells with perpendicularly placed benzodithiophene units. Journal of Power Sources. 499, 229961 (2021)."
16,CCCCCCC(CC1=CC2=C(C(C3=CC=C(S3)C4=CC5=C(C6=C(C(C7=CC(F)=C(S7)CC(CCCC)CC)=C5S4)C=CS6)C8=CC(F)=C(S8)CC(CCCC)CC)=C9C=C(SC9=C2C%10=CC=CS%10)CC(CCCCCC)CCCC)S1)CCCC,PvBDT-F,-4.34,-2.16,0.86,13.87,49.2,5.89,"M. Zhang, X. Xu, L. Yu, Q. Peng, Efficient wide-band-gap copolymer donors for organic solar cells with perpendicularly placed benzodithiophene units. Journal of Power Sources. 499, 229961 (2021)."
17,CCCCCCCCC1=CSC(C2=C(C=C(S2)C3=CC(CCCCCCCC)=C(S3)C4=CC5=C(C6=C(C(C7=CC(F)=C(S7)C(CCCC)CC)=C5S4)C=CS6)C8=CC(F)=C(S8)C(CCCC)CC)C#N)=C1,PBCT-2F,-5.58,-3.66,0.85,27.2,74.3,17.1,"X. Yuan, Y. Zhao, T. Zhan, J. Oh, J. Zhou, J. Li, X. Wang, Z. Wang, S. Pang, P. Cai, C. Yang, Z. He, Z. Xie, C. Duan, F. Huang, Y. Cao, A donor polymer based on 3-cyanothiophene with superior batch-to-batch reproducibility for high-efficiency organic solar cells. Energy Environ. Sci. 14, 5530¨C5540 (2021)."
18,CCCCCCC(CC1=CSC(C2=CC3=C(C4=C(C5=NSN=C53)C=C(S4)C6=CC(CC(CCCCCC)CCCC)=C(S6)C7=CC8=C(C9=C(C(C%10=CC(F)=C(N%10)CC(CCCC)CC)=C8S7)C=CS9)C%11=CC(F)=C(S%11)CC(CCCC)CC)S2)=C1)CCCC,D18,-5.44,-3.47,0.85,25.81,78.61,17.21,"A. Zeng, X. Ma, M. Pan, Y. Chen, R. Ma, H. Zhao, J. Zhang, H. K. Kim, A. Shang, S. Luo, I. C. Angunawela, Y. Chang, Z. Qi, H. Sun, J. Y. L. Lai, H. Ade, W. Ma, F. Zhang, H. Yan, A Chlorinated Donor Polymer Achieving High-Performance Organic Solar Cells with a Wide Range of Polymer Molecular Weight. Advanced Functional Materials. 31, 2102413 (2021)."
19,CCCCCCC(CC1=CSC(C2=CC3=C(C4=C(C5=NSN=C53)C=C(S4)C6=CC(CC(CCCCCC)CCCC)=C(S6)C7=CC8=C(C9=C(C(C%10=CC(Cl)=C(N%10)CC(CCCC)CC)=C8S7)C=CS9)C%11=CC(Cl)=C(S%11)CC(CCCC)CC)S2)=C1)CCCC,D18-Cl,-5.46,-3.49,0.87,26.83,76.97,17.97,"A. Zeng, X. Ma, M. Pan, Y. Chen, R. Ma, H. Zhao, J. Zhang, H. K. Kim, A. Shang, S. Luo, I. C. Angunawela, Y. Chang, Z. Qi, H. Sun, J. Y. L. Lai, H. Ade, W. Ma, F. Zhang, H. Yan, A Chlorinated Donor Polymer Achieving High-Performance Organic Solar Cells with a Wide Range of Polymer Molecular Weight. Advanced Functional Materials. 31, 2102413 (2021)."
20,CCCCCCCCC(CN1N=C2C(C(C3=CC=C(S3)C4=CC5=C(C(C6=CC(Cl)=C(S6)CC(CCCC)CC)=C7C=CSC7=C5C8=CC(Cl)=C(S8)CC(CCCC)CC)S4)=C(C(O)=C2C9=CC=CS9)O)=N1)CCCCCC,J52-CL,-5.46,-3.58,1.21,11.36,62.86,8.64,"T. Dai, P. Lei, B. Zhang, A. Tang, Y. Geng, Q. Zeng, E. Zhou, Fabrication of High VOC Organic Solar Cells with a Non-Halogenated Solvent and the Effect of Substituted Groups for ¡°Same-A-Strategy¡± Material Combinations. ACS Appl. Mater. Interfaces. 13, 21556¨C21564 (2021)."
21,CCCCCCCCC(CN1N=C2C(C3=CC=CS3)=CC=C(C2=N1)C4=CC=C(S4)C5=CC6=C(C(C7=CC(Cl)=C(S7)CC(CCCC)CC)=C8C=CSC8=C6C9=CC(Cl)=C(S9)CC(CCCC)CC)S5)CCCCCC,PE31,-5.35,-3.54,1.11,13.68,66.4,10.08,"T. Dai, P. Lei, B. Zhang, A. Tang, Y. Geng, Q. Zeng, E. Zhou, Fabrication of High VOC Organic Solar Cells with a Non-Halogenated Solvent and the Effect of Substituted Groups for ¡°Same-A-Strategy¡± Material Combinations. ACS Appl. Mater. Interfaces. 13, 21556¨C21564 (2021)."
22,CCCCCCCCC(CN1N=C2C(C(C3=CC=C(S3)C4=CC5=C(C(C6=CC(Cl)=C(S6)CC(CCCC)CC)=C7C=CSC7=C5C8=CC(Cl)=C(S8)CC(CCCC)CC)S4)=C(C(OC)=C2C9=CC=CS9)OC)=N1)CCCCCC,PE32,-5.22,-3.3,1.1,11.65,57.73,7.4,"T. Dai, P. Lei, B. Zhang, A. Tang, Y. Geng, Q. Zeng, E. Zhou, Fabrication of High VOC Organic Solar Cells with a Non-Halogenated Solvent and the Effect of Substituted Groups for ¡°Same-A-Strategy¡± Material Combinations. ACS Appl. Mater. Interfaces. 13, 21556¨C21564 (2021)."
23,CCCCCCCCC(CN1N=C2C(C(C3=CC=C(S3)C4=CC5=C(C(C6=CC(Cl)=C(S6)CC(CCCC)CC)=C7C=CSC7=C5C8=CC(Cl)=C(S8)CC(CCCC)CC)S4)=C(C(O)=C2C9=CC=CS9)O)=N1)CCCCCC,PE33,-5.42,-3.55,1.16,12.68,61.13,8.99,"T. Dai, P. Lei, B. Zhang, A. Tang, Y. Geng, Q. Zeng, E. Zhou, Fabrication of High VOC Organic Solar Cells with a Non-Halogenated Solvent and the Effect of Substituted Groups for ¡°Same-A-Strategy¡± Material Combinations. ACS Appl. Mater. Interfaces. 13, 21556¨C21564 (2021)."
24,CCCCC(CC1=C(C=C(S1)C2=C3C=C(SC3=C(C4=C2SC=C4)C5=CC(F)=C(S5)C(CCCC)CC)C6=C(C=C(S6)C7=C8C(C9=C(SC(C(CCCC)CC)=C9C(C8=C(S7)C%10=CC(F)=CS%10)=O)C(CCCC)CC)=O)F)F)CC,PM6F,-5.66,-3.88,0.9,16.1,67,9.7,"Q. Guo, J. Lin, X. Dong, L. Zhu, X. Guo, F. Liu, M. Zhang, Optimized molecular aggregation via incorporating fluorinated unit in the polymer donor for 17.3% efficiency organic solar cells. Chemical Engineering Journal, 134117 (2021)."
25,CCCCCCCCCCC(COC(C1=C(N=CC(C2=CC=CS2)=N1)C3=CC=C(S3)C4=CC5=C(C(C6=CC(F)=C(S6)CC(CCCC)CC)=C7C=CSC7=C5C8=CC(F)=C(S8)CC(CCC)CC)S4)=O)CCCCCCCC,PFBCPZ,-5.6,-3.52,0.92,21.2,78.5,15.3,"J. Wu, Q. Fan, M. Xiong, Q. Wang, K. Chen, H. Liu, M. Gao, L. Ye, X. Guo, J. Fang, Q. Guo, W. Su, Z. Ma, Z. Tang, E. Wang, H. Ade, M. Zhang, Carboxylate substituted pyrazine: A simple and low-cost building block for novel wide bandgap polymer donor enables 15.3% efficiency in organic solar cells. Nano Energy. 82, 105679 (2021)."
26,CCCCCCCCC1=CSC2=C1SC(C3=C4C(N(C(C4=C(S3)C5=CC6=C(C(CCCCCCCC)=C(S6)C7=CC8=C(C9=C(C(C%10=CC(Cl)=C(S%10)CC(CCCC)CC)=C8S7)C=CS9)C%11=CC(Cl)=C(S%11)CC(CCCC)CC)S5)=O)CC(CCCCCCCC)CCCCCC)=O)=C2,PClBDT-8ttTPD,-5.46,-3.57,0.84,24.99,72,15.05,"J.-W. Ha, C. E. Song, H. S. Kim, D. H. Ryu, W. S. Shin, D.-H. Hwang, Highly Efficient and Photostable Ternary Organic Solar Cells Enabled by the Combination of Non-Fullerene and Fullerene Acceptors with Thienopyrrolodione-based Polymer Donors. ACS Appl. Mater. Interfaces. 12, 51699¨C51708 (2020)."
27,CCCCCCCCC1=CSC2=C1SC(C3=C4C(N(C(C4=C(S3)C5=CC6=C(C(CCCCCCCC)=C(S6)C7=CC8=C(C9=C(C(C%10=CC(F)=C(S%10)CC(CCCC)CC)=C8S7)C=CS9)C%11=CC(F)=C(S%11)CC(CCCC)CC)S5)=O)CC(CCCCCCCC)CCCCCC)=O)=C2,PFBDT-8ttTPD,-5.33,-3.43,0.89,19.91,72,12.81,"J.-W. Ha, C. E. Song, H. S. Kim, D. H. Ryu, W. S. Shin, D.-H. Hwang, Highly Efficient and Photostable Ternary Organic Solar Cells Enabled by the Combination of Non-Fullerene and Fullerene Acceptors with Thienopyrrolodione-based Polymer Donors. ACS Appl. Mater. Interfaces. 12, 51699¨C51708 (2020)."
28,CCCCC(SC1=C(C=C(S1)C2=C3C=C(SC3=C(C4=C2SC=C4)C5=CC(F)=C(S5)SC(CCCC)CC)C6=CC=C(S6)C7=C8C(C9=C(SC(C(CCCC)CC)=C9C(C8=C(S7)C%10=CC=CS%10)=O)C(CCCC)CC)=O)F)CC,PBDB-T-SF,-5.4,-3.6,0.88,20.5,71.9,13.1,"W. Zhao, S. Li, H. Yao, S. Zhang, Y. Zhang, B. Yang, J. Hou, Molecular Optimization Enables over 13% Efficiency in Organic Solar Cells. J. Am. Chem. Soc. 139, 7148¨C7151 (2017)."
29,CCCCCCCCC(CC1=CSC(C2=CC(CC(CCCCCCCC)CCCCCC)=C(S2)C3=CC(F)=C(S3)C4=C(C=CS4)F)=C1)CCCCCC,P4T2F-HD,-5.35,-3.43,0.73,21.63,73.6,11.62,"J. Xiao, X. Jia, C. Duan, F. Huang, H.-L. Yip, Y. Cao, Surpassing 13% Efficiency for Polythiophene Organic Solar Cells Processed from Nonhalogenated Solvent. Advanced Materials. 33, 2008158 (2021)."
30,CCCCCCCCC(COC1=NC2=C(C(C3=CC=CS3)=C(C(F)=C2C)F)N=C1C)CCCCCC,PTQ11,-5.52,-2.76,0.88,24.79,74.8,16.32,"C. Sun, S. Qin, R. Wang, S. Chen, F. Pan, B. Qiu, Z. Shang, L. Meng, C. Zhang, M. Xiao, C. Yang, Y. Li, High Efficiency Polymer Solar Cells with Efficient Hole Transfer at Zero Highest Occupied Molecular Orbital Offset between Methylated Polymer Donor and Brominated Acceptor. J. Am. Chem. Soc. 142, 1465¨C1474 (2020)."
31,CCCCCCCCC(COC1=NC2=C(C(C3=CC=C(S3)C4=CC5=C(C6=C(C(C7=CC(F)=C(S7)CC(CCCC)CC)=C5S4)C=CS6)C8=CC(F)=C(S8)CC(CCCC)CC)=C(C(F)=C2C9=CC=CS9)F)N=C1)CCCCCC,PBQ510,-5.47,-2.89,0.85,25.77,74.6,16.34,"C. Sun, F. Pan, B. Qiu, S. Qin, S. Chen, Z. Shang, L. Meng, C. Yang, Y. Li, D¨CA Copolymer Donor Based on Bithienyl Benzodithiophene D-Unit and Monoalkoxy Bifluoroquinoxaline A-Unit for High-Performance Polymer Solar Cells. Chem. Mater. 32, 3254¨C3261 (2020)."
32,CCCCCCCCOC1=CC=CC(C2=NC3=C(C(C4=CC=C(S4)C5=CC6=C(C7=C(C(C8=CC(F)=C(S8)CC(CCCC)CC)=C6S5)C=CS7)C9=CC(F)=C(S9)CC(CCCC)CC)=C(C(F)=C3C%10=CC=CS%10)F)N=C2C%11=CC=CC(OCCCCCCCC)=C%11)=C1,PBQ7,-5.38,-3.14,0.81,25.83,64.3,13.45,"C. Sun, F. Pan, B. Qiu, S. Qin, S. Chen, Z. Shang, L. Meng, C. Yang, Y. Li, D¨CA Copolymer Donor Based on Bithienyl Benzodithiophene D-Unit and Monoalkoxy Bifluoroquinoxaline A-Unit for High-Performance Polymer Solar Cells. Chem. Mater. 32, 3254¨C3261 (2020)."
33,CCCCCCCC1=C(C2=C(C(C3=C(SC(C4=CC=C(S4)C5=CC6=C(C7=C(C(C8=CC(F)=C(S8)CC(CCCC)CC)=C6S5)C=CS7)C9=CC(F)=C(S9)CC(CCCC)CC)=C3C2=O)C%10=CC=CS%10)=O)S1)CC(CCCC)CC,PBTT-F,-5.48,-3.68,0.83,23.9,75.8,15.1,"P. Chao, H. Chen, Y. Zhu, H. Lai, D. Mo, N. Zheng, X. Chang, H. Meng, F. He, A Benzo[1,2-b:4,5-c¡ä]Dithiophene-4,8-Dione-Based Polymer Donor Achieving an Efficiency Over 16%. Advanced Materials. 32, 1907059 (2020)."
34,CCCCCCCCCCC(CCCCC)OC1=C2C=CSC2=C(C3=CC=C(C4=CC=C(OC(CC)CCCC)C=C4)C=C3)C5=C1SC(C6=CC=C(C7=C8C(C9=C(C=C(SCC(CC)CCCC)C(SCC(CC)CCCC)=C9)C(C8=C(C%10=CC=CS%10)S7)=O)=O)S6)=C5,PBNS,-5.37,-3.63,0.865,12.4,70.83,7.58,"Q. Wang, X. Gao, X. Jing, Y. Li, K. Zhang, F. Li, R. Yang, L. Yu, M. Sun, Naphtho[2,3-c]thiophene-4,9-dione based polymers for efficient fullerene solar cells. Polymer. 212, 123184 (2021)."
35,CCCCCCCCC1=CSC2=C1SC(C3=C4C(N(C(C4=C(S3)C5=CC6=C(C(CCCCCCCC)=C(S6)C7=CC8=C(C9=C(C(C%10=CC(Cl)=C(S%10)C(CCCC)CC)=C8S7)C=CS9)C%11=CC(Cl)=C(S%11)C(CCCC)CC)S5)=O)CC(CCCCCCCC)CCCCCC)=O)=C2,PBDT-Cl,-5.53,-3.64,0.85,25.69,71,15.63,"J. S. Park, G.-U. Kim, D. Lee, S. Lee, B. Ma, S. Cho, B. J. Kim, Importance of Optimal Crystallinity and Hole Mobility of BDT-Based Polymer Donor for Simultaneous Enhancements of Voc, Jsc, and FF in Efficient Nonfullerene Organic Solar Cells. Advanced Functional Materials. 30, 2005787 (2020)."
36,CCCCCCCCC1=CSC2=C1SC(C3=C4C(N(C(C4=C(S3)C5=CC6=C(C(CCCCCCCC)=C(S6)C7=CC8=C(C9=C(C(C%10=CC(F)=C(S%10)C(CCCC)CC)=C8S7)C=CS9)C%11=CC(Cl)=C(S%11)C(CCCC)CC)S5)=O)CC(CCCCCCCC)CCCCCC)=O)=C2,PBDT-F,-5.51,-3.64,0.83,25.36,68,14.86,"J. S. Park, G.-U. Kim, D. Lee, S. Lee, B. Ma, S. Cho, B. J. Kim, Importance of Optimal Crystallinity and Hole Mobility of BDT-Based Polymer Donor for Simultaneous Enhancements of Voc, Jsc, and FF in Efficient Nonfullerene Organic Solar Cells. Advanced Functional Materials. 30, 2005787 (2020)."
37,CCCCCCCCC1=CSC2=C1SC(C3=C4C(N(C(C4=C(S3)C5=CC6=C(C(CCCCCCCC)=C(S6)C7=CC8=C(C9=C(C(C%10=CC=C(S%10)C(CCCC)CC)=C8S7)C=CS9)C%11=CC=C(S%11)C(CCCC)CC)S5)=O)CC(CCCCCCCC)CCCCCC)=O)=C2,PBDT-H,-5.35,-3.48,0.74,24.91,63,11.58,"J. S. Park, G.-U. Kim, D. Lee, S. Lee, B. Ma, S. Cho, B. J. Kim, Importance of Optimal Crystallinity and Hole Mobility of BDT-Based Polymer Donor for Simultaneous Enhancements of Voc, Jsc, and FF in Efficient Nonfullerene Organic Solar Cells. Advanced Functional Materials. 30, 2005787 (2020)."
38,CCCCC(SC1=CC=C(S1)C2=C3C=C(SC3=C(C4=C2SC=C4)C5=CC=C(S5)SC(CCCC)CC)C6=CC=C(S6)C7=C8C(C9=C(SC(C(CCCC)CC)=C9C(C8=C(S7)C%10=CC=CS%10)=O)C(CCCC)CC)=O)CC,PBDT-ST,-5.43,-3.54,0.915,22.56,69.5,14.35,"X. Xu, K. Feng, Y. W. Lee, H. Y. Woo, G. Zhang, Q. Peng, Subtle Polymer Donor and Molecular Acceptor Design Enable Efficient Polymer Solar Cells with a Very Small Energy Loss. Advanced Functional Materials. 30, 1907570 (2020)."
39,CCCCC(CC)C1=C2C(=O)C3=C(C4=CC=CS4)SC(C4=CC=C(C5=CC6=CC7=C(C=C8C=CSC8=C7C7=CC=C(SC(=O)CCC)S7)C(C7=CC=C(SC(=O)CCC)S7)=C6S5)S4)=C3C(=O)C2=C(C(CC)CCCC)S1,PNDT-ST,-5.47,-3.57,0.896,22.67,67.5,13.72,"X. Xu, K. Feng, Y. W. Lee, H. Y. Woo, G. Zhang, Q. Peng, Subtle Polymer Donor and Molecular Acceptor Design Enable Efficient Polymer Solar Cells with a Very Small Energy Loss. Advanced Functional Materials. 30, 1907570 (2020)."
40,CCCC/C(CC)=C/C1=CC=C(S1)C2=C3SC(C4=C(C(C(OC)=O)=CS4)F)=CC3=C(C5=C2C=CS5)C6=CC=C(S6)CC(CCCC)CC,P1,-5.6,-3.65,1.01,17.89,63.05,11.39,"Y. Tang, H. Sun, Z. Wu, Y. Zhang, G. Zhang, M. Su, X. Zhou, X. Wu, W. Sun, X. Zhang, B. Liu, W. Chen, Q. Liao, H. Y. Woo, X. Guo, A New Wide Bandgap Donor Polymer for Efficient Nonfullerene Organic Solar Cells with a Large Open-Circuit Voltage. Advanced Science. 6, 1901773 (2019)."
41,[H]C1=CC=C(C2=C(N=C(C3=CC=C(OCC(CC)CCCC)C=C3)C(C4=CC=C(OCC(CC)CCCC)C=C4)=N5)C5=C(C6=CC=C(C7=CC(C(CCCCCCCC)(CCCCCCCC)C8=C9C=CC([H])=C8)=C9C=C7)S6)S2)S1,APFO-Green 5,,,0.58,3.67,0.47,1,"Tvingstedt K, Inganas O. Electrode grids for ITO-free organic photovoltaic devices. Advanced Materials 19, 2893-2897 (2007)."
42,O=C(OCCOCOCCOC(O[H])=O)COC1=CC=CC(N(C2=CC=CC=C2)C3=CC=C(C4=CC=C(N(C5=CC=CC=C5)C6=CC=CC([H])=C6)C=C4)C=C3)=C1,PTPD,,,----,0.33,----,0.47,"Vaddiraju S, Mathai M, Kymakis E, Papadimitrakopoulos F. Radical salt-doped hole transporters in organic photovoltaic devices. Chemistry of Materials 19, 4049-4055 (2007)."
43,Cl[Al](N1/C(C2=C(C=CC=C2)/C1=N/3)=N\4)N5C(/N=C6N=C3C7=C\6C=CC=C7)=C8C(C=CC=C8)=C5/N=C9C%10=C(C=CC=C%10)C4=N/9,ClAlP,,,0.68,6.2,0.5,2.15,"Bailey-Salzman RF, Rand BP, Forrest SR. Near-infrared sensitive small molecule organic photovoltaic cells based on chloroaluminum phthalocyanine. Applied Physics Letters 91,  (2007)."
44,O=S(CCCCCOCCC1=C([H])SC([H])=C1)[O-].[Na+],PTEBS:Na+,,,0.68,0.98,0.54,0.44,"Yang J, Garcia A, Nguyen T-Q. Organic solar cells from water-soluble poly(thiophene)/fullerene heterojunction. Applied Physics Letters 90,  (2007)."
45,CCCCCCC(S1)=CC=C1C(S2)=CC=C2C(S3)=CC=C3[Si](C4=CC=C(C5=CC=C(C6=CC=C(CCCCCC)S6)S5)S4)(C7=CC=C(C8=CC=C(C9=CC=C(CCCCCC)S9)S8)S7)C%10=CC=C(C%11=CC=C(C%12=CC=C(CCCCCC)S%12)S%11)S%10,1,,,0.66,0.36,0.46,0.2,"Roquet S, de Bettignies R, Leriche P, Cravino A, Roncali J. Three-dimensional tetra(oligothienyl)silanes as donor material for organic solar cells. Journal of Materials Chemistry 16, 3040-3045 (2006)."
46,CCCCCSC(S1)=CC=C1C(S2)=CC=C2C(S3)=CC=C3[Si](C4=CC=C(C5=CC=C(C6=CC=C(SCCCCC)S6)S5)S4)(C7=CC=C(C8=CC=C(C9=CC=C(SCCCCC)S9)S8)S7)C%10=CC=C(C%11=CC=C(C%12=CC=C(SCCCCC)S%12)S%11)S%10,2,,,0.85,1.13,0.24,0.29,"Roquet S, de Bettignies R, Leriche P, Cravino A, Roncali J. Three-dimensional tetra(oligothienyl)silanes as donor material for organic solar cells. Journal of Materials Chemistry 16, 3040-3045 (2006)."
47,CCC(C1=N/2)=C(CC)C2=C\C3=C(CC)C(CC)=C4N3[Pt]N5/C(C(CC)=C(CC)/C5=C/1)=C\C(C(CC)=C/6CC)=NC6=C/4,PtOEP,,,0.66,5.6,0.57,2.1,"Shao Y, Yang Y. Efficient organic heterojunction photovoltaic cells based on triplet materials. Advanced Materials 17, 2841-+ (2005)."
48,[H]N(C1=CC=C(/C=C/C2=CC(OCCCCCC)=C(/C=C/C3=CC=C([H])C=C3)C=C2OCCCCCC)CC1)C4=CC=CC=C4,PPAV-HH-PPV,,,0.62,6.13,0.5,1.9,"Nakamura J, Yokoe C, Murata K, Takahashi K. Efficient organic solar cells by penetration of conjugated polymers into perylene pigments. Journal of Applied Physics 96, 6878-6883 (2004)."
49,[H][Si]([H])(C)C1=CC=CC=C1,PMPS,,,0.37,0.02,0.31,0.33,"Lee JH, Seoul C, Park JK, Youk JH. Fullerene/poly(methylphenylsilane) (PMPS) organic photovoltaic cells. Synthetic Metals 145, 11-14 (2004)."
50,[H]C1=CC(CCCCCC)=C([H])S1,PAT6,,,0.41,5.2,0.43,0.91,"Fujii A, Shirakawa T, Umeda T, Mizukami H, Hashimoto Y, Yoshino K. Interpenetrating interface in organic photovoltaic cells with heterojunction of poly(3-hexylthiophene) and C-60. Japanese Journal of Applied Physics Part 1-Regular Papers Short Notes & Review Papers 43, 5573-5576 (2004)."
51,[H]C1=CC(CCCCCCCCCCCC)=C([H])S1,PAT12,,,0.8,0.005,0.37,2.23,"Feng W, Fujii A, Lee S, Wu H, Yoshino K. Broad spectral sensitization of organic photovoltaic heterojunction device by perylene and C-60. Journal of Applied Physics 88, 7120-7123 (2000)."
52,CN1C(/C(C2=CC=C(Cl)C=C2)=C3N=C(/C(C4=CC=C(Cl)C=C4)=C(C=C/5)\N([H])C5=C6\C7=CC=CN=C7)C=C\3)=CC=C1/C(C8=CC=C(Cl)C=C8)=C9C=CC6=N/9.[H+],H2pyp3p(Cl),,,0.47,----,0.32,0.82,"Takahashi K, Kuraya N, Yamaguchi T, Komura T, Murata K. Three-layer organic solar cell with high-power conversion efficiency of 3.5%. Solar Energy Materials and Solar Cells 61, 403-416 (2000)."
53,CN1C(/C(C2=CC=CC=C2)=C3N=C(/C(C4=CC=CC=C4)=C(C=C/5)\N([H])C5=C6\C7=CC=CC=C7)C=C\3)=CC=C1/C(C8=CC=CC=C8)=C9C=CC6=N/9.[H+],H2tpp,,,0.48,----,0.38,1.32,"Takahashi K, Kuraya N, Yamaguchi T, Komura T, Murata K. Three-layer organic solar cell with high-power conversion efficiency of 3.5%. Solar Energy Materials and Solar Cells 61, 403-416 (2000)."
54,CN1C(/C(C2=CC=C(Cl)C=C2)=C3N=C(/C(C4=CC=C(Cl)C=C4)=C(C=C/5)\N([H])C5=C6\C7=CC=C(Cl)C=C7)C=C\3)=CC=C1/C(C8=CC=C(Cl)C=C8)=C9C=CC6=N/9.[H+],H2tpp(Cl),,,0.46,----,0.29,0.44,"Takahashi K, Kuraya N, Yamaguchi T, Komura T, Murata K. Three-layer organic solar cell with high-power conversion efficiency of 3.5%. Solar Energy Materials and Solar Cells 61, 403-416 (2000)."
55,CN1C(/C(C2=CC=C(OC)C=C2)=C3N=C(/C(C4=CC=C(OC)C=C4)=C(C=C/5)\N([H])C5=C6\C7=CC=C(OC)C=C7)C=C\3)=CC=C1/C(C8=CC=C(OC)C=C8)=C9C=CC6=N/9.[H+],H2tpp(OMe),,,0.47,----,0.4,2.79,"Takahashi K, Kuraya N, Yamaguchi T, Komura T, Murata K. Three-layer organic solar cell with high-power conversion efficiency of 3.5%. Solar Energy Materials and Solar Cells 61, 403-416 (2000)."
56,CN1C(/C(C2=CC=CC=C2)=C3N=C(/C(C4=CC=CC=C4)=C(C=C/5)\N([Zn])C5=C6\C7=CC=CC=C7)C=C\3)=CC=C1/C(C8=CC=CC=C8)=C9C=CC6=N/9,Zntpp,,,0.24,----,0.35,0.51,"Takahashi K, Kuraya N, Yamaguchi T, Komura T, Murata K. Three-layer organic solar cell with high-power conversion efficiency of 3.5%. Solar Energy Materials and Solar Cells 61, 403-416 (2000)."
57,CN1C(/C(C2=CC=C(Cl)C=C2)=C3N=C(/C(C4=CC=C(Cl)C=C4)=C(C=C/5)\N([Zn])C5=C6\C7=CC=C(Cl)C=C7)C=C\3)=CC=C1/C(C8=CC=C(Cl)C=C8)=C9C=CC6=N/9,Zntpp(Cl),,,0.28,----,0.27,0.2,"Takahashi K, Kuraya N, Yamaguchi T, Komura T, Murata K. Three-layer organic solar cell with high-power conversion efficiency of 3.5%. Solar Energy Materials and Solar Cells 61, 403-416 (2000)."
58,CN1C(/C(C2=CC=C(OC)C=C2)=C3N=C(/C(C4=CC=C(OC)C=C4)=C(C=C/5)\N([Zn])C5=C6\C7=CC=C(OC)C=C7)C=C\3)=CC=C1/C(C8=CC=C(OC)C=C8)=C9C=CC6=N/9,Zntpp(OMe)2,,,0.33,----,0.34,1.15,"Takahashi K, Kuraya N, Yamaguchi T, Komura T, Murata K. Three-layer organic solar cell with high-power conversion efficiency of 3.5%. Solar Energy Materials and Solar Cells 61, 403-416 (2000)."
59,[O-]C1=C(C2=CC=C(N(CC)CC)C=C2O)C(C1C3C(O)=CC(N(CC)CC)C=C3)=O,OHSq,,,---,---,---,0.2,"Merritt VY, Hovel HJ. ORGANIC SOLAR-CELLS OF HYDROXY SQUARYLIUM. Applied Physics Letters 29, 414-415 (1976)."
60,[H]C1=C(CCCCCC)C=C(C2=CC=C(C3=CC(CCCCCC)=C(C(S4)=CC5=C4C(C6=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S6)=C7C=C([H])SC7=C5C8=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S8)S3)C9=NSN=C92)S1,PBDT-DTBT,,,0.94,5.12,0.3,1.42,"Ma W, Tumbleston JR, Wang M, Gann E, Huang F, Ade H. Domain Purity, Miscibility, and Molecular Orientation at Donor/Acceptor Interfaces in High Performance Organic Solar Cells: Paths to Further Improvement. Advanced Energy Materials 3, 864-872 (2013)."
61,CCCCC(CC)CC(C1=C2C=CC3=C1C=CC4=C3C(CC(CC)CCCC)(CC(CC)CCCC)C5=C4SC(C6=CC=C([H])C7=NSN=C67)=C5)(CC(CC)CCCC)C8=C2SC([H])=C8,PDTNBT,,,0.87,6.59,0.5,2.89,"Ma Y, Zheng Q, Yin Z, Cai D, Chen S-C, Tang C. Ladder-Type Dithienonaphthalene-Based Donor-Acceptor Copolymers for Organic Solar Cells. Macromolecules 46, 4813-4821 (2013)."
62,CCCCC(CC)CC(C1=C2C=CC3=C1C=CC4=C3C(CC(CC)CCCC)(CC(CC)CCCC)C5=C4SC(C6=CC=C(C7=C(OCCCCCC)C(OCCCCCC)=C(C8=CC=C([H])S8)C9=NSN=C97)S6)=C5)(CC(CC)CCCC)C%10=C2SC([H])=C%10,PDTNTBT,,,0.82,10.01,0.59,4.82,"Ma Y, Zheng Q, Yin Z, Cai D, Chen S-C, Tang C. Ladder-Type Dithienonaphthalene-Based Donor-Acceptor Copolymers for Organic Solar Cells. Macromolecules 46, 4813-4821 (2013)."
63,CCCCC(CC)CC(C1=C2C=CC3=C1C=CC4=C3C(CC(CC)CCCC)(CC(CC)CCCC)C5=C4SC(C6=CC=C(C7=C8C(C(N7CC(CC)CCCC)=O)=C(C9=CC=C([H])S9)N(CC(CC)CCCC)C8=O)S6)=C5)(CC(CC)CCCC)C%10=C2SC([H])=C%10,PDTNTDPP,,,0.75,3.8,0.56,1.6,"Ma Y, Zheng Q, Yin Z, Cai D, Chen S-C, Tang C. Ladder-Type Dithienonaphthalene-Based Donor-Acceptor Copolymers for Organic Solar Cells. Macromolecules 46, 4813-4821 (2013)."
64,CCCCCCC(CCCCCC)N1C2=C(C=CC([H])=C2)C3=C1C=C(C4=CC=C(C5=C(CCCCCC)N=C(C6=NC(CCCCCC)=C(C7=CC=C([H])S7)S6)S5)S4)C=C3,P1,,,0.53,1.93,35,0.36,"Patra D, Sahu D, Padhy H, Kekuda D, Chu C-W, Lin H-C. Synthesis and Applications of 2,7-Carbazole-Based Conjugated Main-Chain Copolymers Containing Electron Deficient Bithiazole Units for Organic Solar Cells. Journal of Polymer Science Part a-Polymer Chemistry 48, 5479-5489 (2010)."
65,CCCCCCC(CCCCCC)N1C2=C(C=CC([H])=C2)C3=C1C=C(C4=CC=C(C5=CC=C(C6=C(CCCCCC)N=C(C7=NC(CCCCCC)=C(C8=CC=C(C9=CC=C([H])S9)S8)S7)S6)S5)S4)C=C3,P3,,,0.62,2.52,37,0.57,"Patra D, Sahu D, Padhy H, Kekuda D, Chu C-W, Lin H-C. Synthesis and Applications of 2,7-Carbazole-Based Conjugated Main-Chain Copolymers Containing Electron Deficient Bithiazole Units for Organic Solar Cells. Journal of Polymer Science Part a-Polymer Chemistry 48, 5479-5489 (2010)."
66,CCCCCCC(CCCCCC)N1C2=C(C=CC([H])=C2)C3=C1C=C(C4=CC=C(C5=CC=C(C6=CC=C(C7=C(CCCCCC)N=C(C8=NC(CCCCCC)=C(C9=CC=C(C%10=CC=C(C%11=CC=C([H])S%11)S%10)S9)S8)S7)S6)S5)S4)C=C3,P4,,,0.6,4.83,35,1.01,"Patra D, Sahu D, Padhy H, Kekuda D, Chu C-W, Lin H-C. Synthesis and Applications of 2,7-Carbazole-Based Conjugated Main-Chain Copolymers Containing Electron Deficient Bithiazole Units for Organic Solar Cells. Journal of Polymer Science Part a-Polymer Chemistry 48, 5479-5489 (2010)."
67,[H]/C=C(C#N)/C1=C(OCCCCCCCCCCCC)C=C(/C(C#N)=C/C2=CC(CCCCCCCC)=C(C3=CC=C(C4=C(CCCCCCCC)C=C([H])S4)S3)S2)C(OCCCCCCCCCCCC)=C1,CNPPV©\3T,,,0.3,2.88,34.7,0.3,"Wang F, Liu Y, Wan X, Zhou J, Long G, Chen Y. Synthesis of New Conjugated CNPPV Derivatives Containing Different Lengths of Oligothiophene Units for Organic Solar Cells. Macromolecular Chemistry and Physics 211, 2503-2509 (2010)."
68,[H]/C=C(C#N)/C1=C(OCCCCCCCCCCCC)C=C(/C(C#N)=C/C2=CC(CCCCCCCC)=C(C3=CC(CCCCCCCC)=C(C4=CC=C(C5=C(CCCCCCCC)C=C(C6=C(CCCCCCCC)C=C([H])S6)S5)S4)S3)S2)C(OCCCCCCCCCCCC)=C1,CNPPV©\5T,,,0.58,2.48,34.1,0.49,"Wang F, Liu Y, Wan X, Zhou J, Long G, Chen Y. Synthesis of New Conjugated CNPPV Derivatives Containing Different Lengths of Oligothiophene Units for Organic Solar Cells. Macromolecular Chemistry and Physics 211, 2503-2509 (2010)."
69,[H]/C=C(C#N)/C1=C(OCCCCCCCCCCCC)C=C(/C(C#N)=C/C2=CC(CCCCCCCC)=C(C3=CC(CCCCCCCC)=C(C4=CC(CCCCCCCC)=C(C5=CC=C(C6=C(CCCCCCCC)C=C(C7=C(CCCCCCCC)C=C(C8=C(CCCCCCCC)C=C([H])S8)S7)S6)S5)S4)S3)S2)C(OCCCCCCCCCCCC)=C1,CNPPV©\7T,,,0.66,5.68,43.2,1.62,"Wang F, Liu Y, Wan X, Zhou J, Long G, Chen Y. Synthesis of New Conjugated CNPPV Derivatives Containing Different Lengths of Oligothiophene Units for Organic Solar Cells. Macromolecular Chemistry and Physics 211, 2503-2509 (2010)."
70,CCCCC(CC)CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC=C(CCCCCCCCCCC[Si](C)(O[Si](C)(CCCCCCCCCCCC5=CC=C(C6=CC=C(C7=CC=C(C8=CC=C(CC(CC)CCCC)S8)S7)S6)S5)C)C)S4)S3)S2)S1,D1,,,0.68,3.2,40,0.9,"Troshin PA, et al. Quaterthiophene-based multipods as promising materials for solution-processible organic solar cells and field effect transistors. Solar Energy Materials and Solar Cells 94, 2064-2072 (2010)."
71,CCCCC(CC)CC1=CC=C(C(S2)=CC=C2C3=CC=C(C4=CC=C(CCCCCCCCCCC[Si](C)(O[Si](C)(CCC[Si](CCC[Si](C)(C)O[Si](C)(C)CCCCCCCCCCCC5=CC=C(S5)C6=CC=C(C7=CC=C(C8=CC=C(S8)CC(CC)CCCC)S7)S6)(CCC[Si](C)(C)O[Si](C)(C)CCCCCCCCCCCC9=CC=C(S9)C%10=CC=C(C%11=CC=C(C%12=CC=C(S%12)CC(CC)CCCC)S%11)S%10)CCC[Si](C)(C)O[Si](C)(CCCCCCCCCCCC%13=CC=C(S%13)C%14=CC=C(S%14)C%15=CC=C(C%16=CC=C(S%16)CC(CC)CCCC)S%15)C)C)C)S4)S3)S1,D2,,,0.6,1.3,35,0.27,"Troshin PA, et al. Quaterthiophene-based multipods as promising materials for solution-processible organic solar cells and field effect transistors. Solar Energy Materials and Solar Cells 94, 2064-2072 (2010)."
72,CCCCCCC1=CC=C(C(S2)=CC=C2C3=CC=C(C4=CC=C(CCCCCCCCCCC[Si](C)(O[Si](C)(CCC[Si](CCC[Si](C)(C)O[Si](C)(C)CCCCCCCCCCCC5=CC=C(S5)C6=CC=C(C7=CC=C(C8=CC=C(S8)CCCCCC)S7)S6)(CCC[Si](C)(C)O[Si](C)(C)CCCCCCCCCCCC9=CC=C(S9)C%10=CC=C(C%11=CC=C(C%12=CC=C(S%12)CCCCCC)S%11)S%10)CCC[Si](C)(C)O[Si](C)(CCCCCCCCCCCC%13=CC=C(S%13)C%14=CC=C(S%14)C%15=CC=C(C%16=CC=C(S%16)CCCCCC)S%15)C)C)C)S4)S3)S1,D3,,,0.36,0.45,29,0.05,"Troshin PA, et al. Quaterthiophene-based multipods as promising materials for solution-processible organic solar cells and field effect transistors. Solar Energy Materials and Solar Cells 94, 2064-2072 (2010)."
73,C1(C=CC=C2)=C2C3=N/C1=N\C4=C5C(C=CC=C5)=C6N4[Zn]N7/C(C8=C(C=CC=C8)/C7=N/3)=N\C(C9=C/%10C=CC=C9)=NC%10=N/6,ZnPc,,,0.6,10.5,58,3.7,"Kim I, Haverinen HM, Li J, Jabbour GE. Enhanced power conversion efficiency of p-i-n type organic solar cells by employing a p-layer of palladium phthalocyanine. Applied Physics Letters 97,  (2010)."
74,[H]C1=CC(CCCCCCCCCCCC)=C(S1)C(S2)=CC=C2/C=C/C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC=C([H])C6=NSN=C65)S4)S3,PETVTBT,,,0.54,5.29,35,1,"Lim B, et al. Synthesis of an alternating thienylenevinylene-benzothiadiazole copolymer with high hole mobility for use in organic solar cells. Organic Electronics 11, 1772-1778 (2010)."
75,[H]C#CC(S1)=CC2=C1C3=C(C=C(C#CC4=C5N=C(C6=CC=CC=C6)C(C7=CC=CC=C7)=NC5=C([H])S4)S3)C2(CCCCCCCCCCCC)CCCCCCCCCCCC,P1,,,0.82,4.11,40,1.34,"Ashraf RS, Gilot J, Janssen RAJ. Fused ring thiophene-based poly(heteroarylene ethynylene)s for organic solar cells. Solar Energy Materials and Solar Cells 94, 1759-1766 (2010)."
76,[H]C#CC(S1)=CC2=C1C3=C(C=C(C#CC4=C5N=C(C6=CC=CC=C6)C(C7=CC=CC=C7)=NC5=C([H])S4)S3)N2C(CCCCCCCCCCCC)CCCCCCCCCCCC,P2,,,0.74,5.87,40,1.74,"Ashraf RS, Gilot J, Janssen RAJ. Fused ring thiophene-based poly(heteroarylene ethynylene)s for organic solar cells. Solar Energy Materials and Solar Cells 94, 1759-1766 (2010)."
77,[H]C#CC(S1)=CC2=C1C3=C(C=C(C#CC4=CC=C([H])C5=NSN=C45)S3)N2C(CCCCCCCCCCCC)CCCCCCCCCCCC,P3,,,0.72,4.97,39,1.4,"Ashraf RS, Gilot J, Janssen RAJ. Fused ring thiophene-based poly(heteroarylene ethynylene)s for organic solar cells. Solar Energy Materials and Solar Cells 94, 1759-1766 (2010)."
78,CCCCCCCCC1=CSC(C(C2=NSN=C23)=CC=C3C(S4)=CC(CCCCCCCC)=C4C(C=C5)=CC=C5OC6=CC7=C(/N=C8C9=C(C=C(OC%10=CC=C(C%11=C(CCCCCCCC)C=C(C%12=CC=C(C%13=CC(CCCCCCCC)=CS%13)C%14=NSN=C%14%12)S%11)C=C%10)C=C9)C%15=N/8)N([Zn]%16)C(/[Zn]=C%17N=C(/N=C(C%18=C/%19C=CC(OC%20=CC=C(C%21=C(CCCCCCCC)C=C(C%22=CC=C(C%23=CC(CCCCCCCC)=CS%23)C%24=NSN=C%24%22)S%21)C=C%20)=C%18)\N%16C%19=N/%15)C%25=C\%17C=C(OC%26=CC=C(C%27=C(CCCCCCCC)C=C(C%28=CC=C(C%29=CC(CCCCCCCC)=CS%29)C%30=NSN=C%30%28)S%27)C=C%26)C=C%25)=C7C=C6)=C1,ZnPc-TDA,,,0.68,2.26,28,0.42,"Liang F, et al. Donor-acceptor conjugates-functionalized zinc phthalocyanine: Towards broad absorption and application in organic solar cells. Solar Energy Materials and Solar Cells 94, 1803-1808 (2010)."
79,[H]C1=CC(CCCCCC)=C(C(S2)=CC3=C2C=C(C4=C(CCCCCC)C=C(C5=CC(C(CCCC)(CCCC)C6=C7C=CC([H])=C6)=C7C=C5)S4)S3)S1,P1,,,0.87,4.8,34.6,1.5,"Cha H, et al. Thermally stable amorphous polymeric semiconductors containing fluorene and thiophene for use in organic photovoltaic cells. Organic Electronics 11, 1534-1542 (2010)."
80,[H]C1=C(CCCCCC)C=C(C(S2)=CC3=C2C=C(C4=CC(CCCCCC)=C(C5=CC(C(CCCC)(CCCC)C6=C7C=CC([H])=C6)=C7C=C5)S4)S3)S1,P2,,,0.95,5,39.6,1.8,"Cha H, et al. Thermally stable amorphous polymeric semiconductors containing fluorene and thiophene for use in organic photovoltaic cells. Organic Electronics 11, 1534-1542 (2010)."
81,[H]C#CC1=CC2=C(C(SC(C#C[Pt]([PH](CCCC)(CCCC)CCCC)([H])[PH](CCCC)(CCCC)CCCC)=C3)=C3C2=O)S1,P1,,,0.72,1.28,31,0.32,"Wang X-Z, et al. Very-Low-Bandgap Metallopolyynes of Platinum with a Cyclopentadithiophenone Ring for Organic Solar Cells Absorbing Down to the Near-Infrared Spectral Region. Macromolecular Rapid Communications 31, 861-867 (2010)."
82,[H]C#CC1=C(CCCCCC)C=C(C2=CC3=C(C(SC(C4=CC(CCCCCC)=C(C#C[Pt]([PH](CCCC)(CCCC)CCCC)([H])[PH](CCCC)(CCCC)CCCC)S4)=C5)=C5C3=O)S2)S1,P2,,,0.68,2.88,33,0.63,"Wang X-Z, et al. Very-Low-Bandgap Metallopolyynes of Platinum with a Cyclopentadithiophenone Ring for Organic Solar Cells Absorbing Down to the Near-Infrared Spectral Region. Macromolecular Rapid Communications 31, 861-867 (2010)."
83,[H]/C=C/C1=CC(OC)=C([H])C=C1OCCC(C)CCCC(C)C,MDMO©\PPV,,,0.86,4.72,53.7,2.17,"Hains AW, Liu J, Martinson ABF, Irwin MD, Marks TJ. Anode Interfacial Tuning via Electron-Blocking/Hole-Transport Layers and Indium Tin Oxide Surface Treatment in Bulk-Heterojunction Organic Photovoltaic Cells. Advanced Functional Materials 20, 595-606 (2010)."
84,[H]C1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C4=C(CCCCCCCCCCCC)C=C([H])S4)[Se]3)[Se]2)S1,PDT2Se2,,,0.69,4.3,46,1.36,"Chung DS, et al. Effects of selenophene substitution on the mobility and photovoltaic efficiency of polyquaterthiophene-based organic solar cells. Organic Electronics 11, 899-904 (2010)."
85,[H]C1=CC(/C=C/C2=CC=C(N(CCCCCC)C3=C4C=CC=C3)C4=C2)=C(C5=CC=C([H])S5)S1,P1,,,0.57,1.72,30,0.29,"Li W, Han Y, Chen Y, Li C, Li B, Bo Z. Polythiophenes with Carbazole Side Chains: Design, Synthesis and Their Application in Organic Solar Cells. Macromolecular Chemistry and Physics 211, 948-955 (2010)."
86,CCCCCCN(C1=C2C=CC=C1)C(C2=C3)=CC=C3/C=C/C4=C(C5=CC=C(C6=CC(CCCCCC)=C(C7=CC=C([H])S7)S6)S5)SC(C8=CC=C(C9=C(/C=C/C%10=CC=C(N(CCCCCC)C%11=C%12C=CC=C%11)C%12=C%10)C=C(C%13=CC=C(C%14=C(/C=C/C%15=CC=C(N(CCCCCC)C%16=C%17C=CC=C%16)C%17=C%15)C=C(C%18=CC=C(C%19=C(/C=C/C%20=CC=C(N(CCCCCC)C%21=C%22C=CC=C%21)C%22=C%20)C=C(C%23=CC=C(C%24=C(/C=C/C%25=CC=C(N(CCCCCC)C%26=C%27C=CC=C%26)C%27=C%25)C=C([H])S%24)S%23)S%19)S%18)S%14)S%13)S9)S8)=C4,P2,,,0.46,2.87,42,0.56,"Li W, Han Y, Chen Y, Li C, Li B, Bo Z. Polythiophenes with Carbazole Side Chains: Design, Synthesis and Their Application in Organic Solar Cells. Macromolecular Chemistry and Physics 211, 948-955 (2010)."
87,CCCCCCN(C1=C2C=CC=C1)C(C2=C3)=CC=C3/C=C/C4=C(C5=CC=C(C6=CC(CCCCCC)=C(C7=CC=C(C8=CC(CCCCCC)=C(C9=CC=C(C%10=CC(CCCCCC)=C(C%11=CC=C(C%12=CC(CCCCCC)=C(C%13=CC=C([H])S%13)S%12)S%11)S%10)S9)S8)S7)S6)S5)SC(C%14=CC=C(C%15=C(/C=C/C%16=CC=C(N(CCCCCC)C%17=C%18C=CC=C%17)C%18=C%16)C=C(C%19=CC=C(C%20=C(/C=C/C%21=CC=C(N(CCCCCC)C%22=C%23C=CC=C%22)C%23=C%21)C=C(C%24=CC=C(C%25=C(/C=C/C%26=CC=C(N(CCCCCC)C%27=C%28C=CC=C%27)C%28=C%26)C=C(C%29=CC=C(C%30=C(/C=C/C%31=CC=C(N(CCCCCC)C%32=C%33C=CC=C%32)C%33=C%31)C=C([H])S%30)S%29)S%25)S%24)S%20)S%19)S%15)S%14)=C4,P3,,,0.49,5.19,34,0.86,"Li W, Han Y, Chen Y, Li C, Li B, Bo Z. Polythiophenes with Carbazole Side Chains: Design, Synthesis and Their Application in Organic Solar Cells. Macromolecular Chemistry and Physics 211, 948-955 (2010)."
88,[H]C1=CC(/C=C/C2=CC=C(N(CCCCCC)C3=C4C=CC=C3)C4=C2)=C(C5=CC=C(C6=CC(CCCCCC)=C(C7=CC=C(C8=CC(CCCCCC)=C(C9=CC=C(C%10=CC(CCCCCC)=C(C%11=CC=C([H])S%11)S%10)S9)S8)S7)S6)S5)S1,P4,,,0.53,3.56,37,0.7,"Li W, Han Y, Chen Y, Li C, Li B, Bo Z. Polythiophenes with Carbazole Side Chains: Design, Synthesis and Their Application in Organic Solar Cells. Macromolecular Chemistry and Physics 211, 948-955 (2010)."
89,[H]C1=CC(CCCCCC)=C(C2=CC=C([H])S2)S1,P5,,,0.54,2.37,44,0.56,"Li W, Han Y, Chen Y, Li C, Li B, Bo Z. Polythiophenes with Carbazole Side Chains: Design, Synthesis and Their Application in Organic Solar Cells. Macromolecular Chemistry and Physics 211, 948-955 (2010)."
90,[H]C1=CC=C(C(C=CC(C2=CC=C(C3=CC=C(C4=CC=C([H])S4)C5=NSN=C53)S2)=C6)=C6C7(CCCCCCCCCC)CCCCCCCCCC)C7=C1,PF10TBT,,,1.92,3.49,61,4.5,"Moet DJD, de Bruyn P, Blom PWM. High work function transparent middle electrode for organic tandem solar cells. Applied Physics Letters 96,  (2010)."
91,[H]C1=CC=C(C2=C(C3=CC=C(CCCCCCCC)C=C3)C=C([H])S2)S1,PTOPT,,,0.9,1.6,20,0.3,"Gebremichael B, Tessema G. Hole transport parameters in a PTOPT based organic solar cell. Canadian Journal of Physics 88, 253-256 (2010)."
92,BrC1=C(CCCCCC)C=C([H])S1,P3HT-Br,,,0.59,9.89,55,3.2,"Kim JS, Lee Y, Lee JH, Park JH, Kim JK, Cho K. High-Efficiency Organic Solar Cells Based on End-Functional-Group-Modified Poly(3-hexylthiophene). Advanced Materials 22, 1355-+ (2010)."
93,[H]C1=CC(CCCCCC)=C(C2=CC=C(OC(C(F)(F)C(F)(F)C(F)(F)F)=O)C=C2)S1,P3HT-CF3,,,0.6,10.89,69,4.5,"Kim JS, Lee Y, Lee JH, Park JH, Kim JK, Cho K. High-Efficiency Organic Solar Cells Based on End-Functional-Group-Modified Poly(3-hexylthiophene). Advanced Materials 22, 1355-+ (2010)."
94,[H]C1=CC(CCCCCC)=C(C2=CC=C(CC)C=C2)S1,P3HT-CH3,,,0.6,10.69,51,4,"Kim JS, Lee Y, Lee JH, Park JH, Kim JK, Cho K. High-Efficiency Organic Solar Cells Based on End-Functional-Group-Modified Poly(3-hexylthiophene). Advanced Materials 22, 1355-+ (2010)."
95,[H]C1=CC(CCCCCC)=C(C2=CC=C(O)C=C2)S1,P3HT-OH,,,0.58,7.65,46,2.1,"Kim JS, Lee Y, Lee JH, Park JH, Kim JK, Cho K. High-Efficiency Organic Solar Cells Based on End-Functional-Group-Modified Poly(3-hexylthiophene). Advanced Materials 22, 1355-+ (2010)."
96,C1(C=CC=C2)=C2C3=N/C1=N\C4=C5C(C=CC=C5)=C6N4[Fe]N7/C(C8=C(C=CC=C8)/C7=N/3)=N\C(C9=C/%10C=CC=C9)=NC%10=N/6,FePc,,,0.16,-1.06,42,0.07,"Bruder I, et al. What determines the performance of metal phthalocyanines (MPc, M = Zn, Cu, Ni, Fe) in organic heterojunction solar cells? A combined experimental and theoretical investigation. Organic Electronics 11, 377-387 (2010)."
97,C1(C=CC=C2)=C2C3=N/C1=N\C4=C5C(C=CC=C5)=C6N4[Ni]N7/C(C8=C(C=CC=C8)/C7=N/3)=N\C(C9=C/%10C=CC=C9)=NC%10=N/6,NiPc,,,0.44,-2.67,55,0.64,"Bruder I, et al. What determines the performance of metal phthalocyanines (MPc, M = Zn, Cu, Ni, Fe) in organic heterojunction solar cells? A combined experimental and theoretical investigation. Organic Electronics 11, 377-387 (2010)."
98,[H]C1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C4=C(CCCCCCCCCCCC)C=C([H])S4)S3)S2)S1,PBTBS,,,0.46,0.17,32,0.34,"Fen Q, et al. Photovoltaic characterization of poly(2,5-bis(3-dodecylthiophen-2-yl)-2 ',2 ''-biselenophene) for organic solar cells. Solar Energy Materials and Solar Cells 94, 442-445 (2010)."
99,[H]C1=CC2=C3C(C(SC(CC(CCCCCC)CCCCCCCC)=C4)=C4C5=C3SC(CC(CCCCCC)CCCCCCCC)=C5)=C6C(SC(C7=CC=C([H])C8=NSN=C78)=C6)=C2S1,PQTN©\BT,,,0.72,5.69,50.3,2.06,"Xiao S, Stuart AC, Liu S, Zhou H, You W. Conjugated Polymer Based on Polycyclic Aromatics for Bulk Heterojunction Organic Solar Cells: A Case Study of Quadrathienonaphthalene Polymers with 2% Efficiency. Advanced Functional Materials 20, 635-643 (2010)."
100,CCCCCCCCC1(CCCCCCCC)C2=C(C3=C1C=C([H])C=C3)C=CC(C4=CC=C(C5=CC=C([H])S5)S4)=C2,F8T2,,,0.67,9.55,53,3.4,"Kekuda D, Huang J-H, Ho K-C, Chu C-W. Modulation of Donor-Acceptor Interface through Thermal Treatment for Efficient Bilayer Organic Solar Cells. Journal of Physical Chemistry C 114, 2764-2768 (2010)."
101,[H]C1=CC=C2C(SC(C=C(/C=C/[H])C=C3)=C3N2C4=CC=C(OCCCCCCCCCCCC)C=C4)=C1,P1,,,0.59,1.89,30,0.33,"Son S-K, et al. Synthesis and Properties of Phenothiazylene Vinylene-Based Polymers: New Organic Semiconductors for Field-Effect Transistors and Solar Cells. Journal of Polymer Science Part a-Polymer Chemistry 48, 635-646 (2010)."
102,[H]C1=CC=C2C(SC(C=C(/C=C/C3=CC=C(/C=C/[H])C=C3)C=C4)=C4N2C5=CC=C(OCCCCCCCCCCCC)C=C5)=C1,P2,,,0.61,1.57,29,0.28,"Son S-K, et al. Synthesis and Properties of Phenothiazylene Vinylene-Based Polymers: New Organic Semiconductors for Field-Effect Transistors and Solar Cells. Journal of Polymer Science Part a-Polymer Chemistry 48, 635-646 (2010)."
103,[H]C1=CC=C2C(SC(C=C(/C=C/C3=CC=C(/C=C/[H])S3)C=C4)=C4N2C5=CC=C(OCCCCCCCCCCCC)C=C5)=C1,P3,,,0.42,5.17,35,0.76,"Son S-K, et al. Synthesis and Properties of Phenothiazylene Vinylene-Based Polymers: New Organic Semiconductors for Field-Effect Transistors and Solar Cells. Journal of Polymer Science Part a-Polymer Chemistry 48, 635-646 (2010)."
104,C1(C(C2=C(C=CC=C3)C3=CC4=C2C=CC=C4)=CC=C5)=C5C6=N/C1=N\C7=C8C(C(C9=C(C=CC=C%10)C%10=CC%11=C9C=CC=C%11)=CC=C8)=C%12N7[Zn]N%13/C(C%14=C(C(C%15=C(C=CC=C%16)C%16=CC%17=C%15C=CC=C%17)=CC=C%14)/C%13=N/6)=N\C(C%18=C/%19C=CC=C%18C%20=C(C=CC=C%21)C%21=CC%22=C%20C=CC=C%22)=NC%19=N/%12,A-ZnPc,,,0.79,-0.03,22,5*10-3,"Bruder I, et al. Theoretical and experimental investigation on the influence of the molecular polarizability of novel zinc phthalocyanine derivatives on the open circuit voltage of organic hetero-junction solar cells. Solar Energy Materials and Solar Cells 94, 310-316 (2010)."
105,C1(C(C2=CC=CC3=C2C=CC=C3)=CC=C4)=C4C5=N/C1=N\C6=C7C(C(C8=CC=CC9=C8C=CC=C9)=CC=C7)=C%10N6[Zn]N%11/C(C%12=C(C(C%13=CC=CC%14=C%13C=CC=C%14)=CC=C%12)/C%11=N/5)=N\C(C%15=C/%16C=CC=C%15C%17=CC=CC%18=C%17C=CC=C%18)=NC%16=N/%10,N-ZnPc,,,0.76,-3.24,60,1.48,"Bruder I, et al. Theoretical and experimental investigation on the influence of the molecular polarizability of novel zinc phthalocyanine derivatives on the open circuit voltage of organic hetero-junction solar cells. Solar Energy Materials and Solar Cells 94, 310-316 (2010)."
106,C1(C(C2=CC=CC=C2)=CC=C3)=C3C4=N/C1=C\C5=C6C(C(C7=CC=CC=C7)=CC=C6)=C8N5[Zn]N9/C(C%10=C(C(C%11=CC=CC=C%11)=CC=C%10)/C9=C/4)=C\C(C%12=C/%13C=CC=C%12C%14=CC=CC=C%14)=NC%13=C/8,Ph-ZnPc,,,0.68,-4.19,64,1.82,"Bruder I, et al. Theoretical and experimental investigation on the influence of the molecular polarizability of novel zinc phthalocyanine derivatives on the open circuit voltage of organic hetero-junction solar cells. Solar Energy Materials and Solar Cells 94, 310-316 (2010)."
107,CC(C)[Si](C(C)C)(C(C)C)C#CC1=C(C=CC(C2=CC=C(C3=CC=CS3)S2)=C4)C4=C(C#C[Si](C(C)C)(C(C)C)C(C)C)C5=CC=C(C6=CC=C(C7=CC=CS7)S6)C=C51,TIPSAntBT,,,0.78,4.55,40.3,1.4,"Chung DS, et al. Solution-Processed Organic Photovoltaic Cells with Anthracene Derivatives. Chemsuschem 3, 742-748 (2010)."
108,CC(C)[Si](C(C)C)(C(C)C)C#CC1=C(C=CC(C2=CC(C=CC=C3)=C3C=C2)=C4)C4=C(C#C[Si](C(C)C)(C(C)C)C(C)C)C5=CC=C(C6=CC(C=CC=C7)=C7C=C6)C=C51,TIPSAntNa,,,0.97,0.4,36.6,0.14,"Chung DS, et al. Solution-Processed Organic Photovoltaic Cells with Anthracene Derivatives. Chemsuschem 3, 742-748 (2010)."
109,[H]C(S1)=CC=C1C(S2)=C(CCCCCCCCCCCC)C=C2C(S3)=CC(CCCCCCCCCCCC)=C3C(S4)=CC=C4C5=CC6=C(C#C[Si](C(C)C)(C(C)C)C(C)C)C7=CC=C([H])C=C7C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C6C=C5,PAT4,,,0.65,-5.3,50.9,1.75,"Park J-H, et al. New anthracene-thiophene-based copolymers that absorb across the entire UV-vis spectrum for application in organic solar cells. Chemical Communications 46, 1863-1865 (2010)."
110,[H]/C=C/C1=C(OCCCCCCCCCCCC)C=C(/C=C/C2=C(CCCCCCCCCCCC)C=C(C3=CC=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C([H])S5)S4)S3)S2)C(OCCCCCCCCCCCC)=C1,PPVQT-C8,,,0.67,6.69,62,2.8,"Park JH, et al. Enhanced device performance of organic solar cells via reduction of the crystallinity in the donor polymer. Journal of Materials Chemistry 20, 5860-5865 (2010)."
111,[H]C(C=C1)=CC2=C1C(C=C3)=C(C2(CC(CC)CCCC)CC(CC)CCCC)C=C3C(S4)=CC=C4C5=C(N=C(C6=CC=CC=C6)C(C7=CC=CC=C7)=N8)C8=C(C9=CC=C([H])S9)C=C5,N-P17,,,0.99,7.35,49,3.6,"Kitazawa D, Watanabe N, Yamamoto S, Tsukamoto J. Quinoxaline-Based Donor Polymers for Organic Solar Cells. Journal of Photopolymer Science and Technology 23, 293-296 (2010)."
112,[H]C(C=C1)=CC2=C1C(C=C3)=C(C2(CCCCCC)CCCCCC)C=C3C(S4)=CC=C4C5=C(N=C(C6=CC=CC=C6)C(C7=CC=CC=C7)=N8)C8=C(C9=CC=C([H])S9)C=C5,N-P18,,,0.95,8.4,43,3.4,"Kitazawa D, Watanabe N, Yamamoto S, Tsukamoto J. Quinoxaline-Based Donor Polymers for Organic Solar Cells. Journal of Photopolymer Science and Technology 23, 293-296 (2010)."
113,[H]C(C=C1)=CC2=C1C(C=C3)=C(C2(CCCCCCCCCCCC)CCCCCCCCCCCC)C=C3C(S4)=CC=C4C5=C(N=C(C6=CC=CC=C6)C(C7=CC=CC=C7)=N8)C8=C(C9=CC=C([H])S9)C=C5,N-P19,,,0.99,4.9,54,2.63,"Kitazawa D, Watanabe N, Yamamoto S, Tsukamoto J. Quinoxaline-Based Donor Polymers for Organic Solar Cells. Journal of Photopolymer Science and Technology 23, 293-296 (2010)."
114,[H]C(S1)=CC2=C1C=C(S2)C3=C4C(C(N3CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C5=CC6=C(C=C(C7=CC(C(OCCCCCCCCCCCC)=C(SC([H])=C8)C8=C9OCCCCCCCCCCCC)=C9S7)S6)S5)N(CC(CCCCCCCC)CCCCCCCCCC)C4=O,PTTDPP-BDT,,,0.63,9.01,60,3.36,"Zhang Y, et al. Spectral response tuning using an optical spacer in broad-band organic solar cells. Applied Physics Letters 102,  (2013)."
115,CC(O[C@@H]1C[C@@](C)(O)C(C(C)(C)C1)=C=C/C(C)=C/C=C/C(C)=C/C=C/C=C(C)/C=C/C=C(C)/CC[C@]23C(C)C[C@H](O)C[C@@]2(C)O3)=O,fucoxanthin,,,0.7,0.7,28,0.14,"Wang X-F, et al. Natural Photosynthetic Carotenoids for Solution-Processed Organic Bulk-Heterojunction Solar Cells. Journal of Physical Chemistry C 117, 804-811 (2013)."
116,FC1=CC(N2N=C3C(C(C4=CC=C([H])S4)=C(N=C(C5=CC(OC)=CC=C5)C(C6=CC=CC(OC)=C6)=N7)C7=C3C8=CC=C(C9=CC=C(C(C=CC([H])=C%10)=C%10C%11(CCCCCCCC)CCCCCCCC)C%11=C9)S8)=N2)=CC(F)=C1OCC(CCCCCCCC)CCCCCCCCCC,PTQF,,,0.7,4.65,52.45,1.71,"Baran D, et al. Introducing a New Triazoloquinoxaline-Based Fluorene Copolymer for Organic Photovoltaics: Synthesis, Characterization, and Photovoltaic Properties. Journal of Polymer Science Part a-Polymer Chemistry 51, 987-992 (2013)."
117,[H]C1=C(C(N(CCCCCCCC)C2=O)=O)C2=C(C3=CC4=C(C(OCC(CC)CCCC)=C(C=C([H])S5)C5=C4OCC(CC)CCCC)S3)S1,PBDTTPD,,,0.7,-14.3,53.5,5.5,"Kim HP, Yusoff ARbM, Jang J. Organic solar cells using a reduced graphene oxide anode buffer layer. Solar Energy Materials and Solar Cells 110, 87-93 (2013)."
118,[H]C1=CC(CCCCCCCCCCCC)=C(C2=CC(CCCCCCCCCCCC)=C(C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C5=C(CCCCCCCCCCCC)C=C([H])[Se]5)[Se]4)[Se]3)[Se]2)[Se]1,P5Se,,,0.75,6.72,35,1.75,"Lee W-H, Lee S-K, Shin W-S, Moon S-J, Lee S-H, Kang I-N. Synthesis and characterization of a pentaselenophene-based donor-acceptor copolymer for use in organic photovoltaic cells. Solar Energy Materials and Solar Cells 110, 140-146 (2013)."
119,[H]C1=CC(CCCCCCCCCCCC)=C(C2=CC(CCCCCCCCCCCC)=C(C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C5=C(CCCCCCCCCCCC)C=C(C6=CC=C(C7=C8C(C(N7CC(CC)CCCC)=O)=C(C9=CC=C([H])S9)N(CC(CC)CCCC)C8=O)S6)[Se]5)[Se]4)[Se]3)[Se]2)[Se]1,P5SeDTDPP,,,0.44,10.67,51,2.4,"Lee W-H, Lee S-K, Shin W-S, Moon S-J, Lee S-H, Kang I-N. Synthesis and characterization of a pentaselenophene-based donor-acceptor copolymer for use in organic photovoltaic cells. Solar Energy Materials and Solar Cells 110, 140-146 (2013)."
120,Cl[Sn](N1/C(C2=C(C=C(C=CC=C3)C3=C2)/C1=N/4)=N\5)(Cl)N6C(/N=C7N=C4C8=C\7C=C(C=CC=C9)C9=C8)=C%10C(C=C(C=CC=C%11)C%11=C%10)=C6/N=C%12C%13=C(C=C(C=CC=C%14)C%14=C%13)C5=N/%12,SnNcCl2,,,0.38,9,53,1.2,"Pandey R, Kerner RA, Menke SM, Holst J, Josyula KVB, Holmes RJ. Tin naphthalocyanine complexes for infrared absorption in organic photovoltaic cells. Organic Electronics 14, 804-808 (2013)."
121,C1(C=CC=C2)=C2C3=N/C1=N\C4=C5C(C=CC=C5)=C6N4[Sn]N7/C(C8=C(C=CC=C8)/C7=N/3)=N\C(C9=C/%10C=CC=C9)=NC%10=N/6,SnPc,,,0.25,9,50,0.8,"Pandey R, Kerner RA, Menke SM, Holst J, Josyula KVB, Holmes RJ. Tin naphthalocyanine complexes for infrared absorption in organic photovoltaic cells. Organic Electronics 14, 804-808 (2013)."
122,[H]C1=C(CCCCCC)C=C(C2=C(CCCCCC)C=C(C3=C(CCCCCC)C=C(C4=C(CCCCCC)C=C([H])S4)S3)S2)S1,RR-P3HT,,,0.58,12.7,60,4.2,"Singh S, Vardeny ZV. Ultrafast Transient Spectroscopy of Polymer/Fullerene Blends for Organic Photovoltaic Applications. Materials 6, 897-910 (2013)."
123,[H]C(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=CC=C([H])S3)S4)C4=C2OCC(CC)CCCC,PABDT-T,,,0.68,7.24,39,2.03,"Byun Y-S, Kim J-H, Park JB, Kang I-N, Jin S-H, Hwang D-H. Full donor-type conjugated polymers consisting of alkoxy- or alkylselenophene-substituted benzodithiophene and thiophene units for organic photovoltaic devices. Synthetic Metals 168, 23-30 (2013)."
124,[H]C(S1)=CC2=C1C(C3=CC=C(CCCCCCCCCCCC)[Se]3)=C(C=C(C4=CC=C([H])S4)S5)C5=C2C6=CC=C(CCCCCCCCCCCC)[Se]6,PSeBDT-T,,,0.72,7.73,46,2.73,"Byun Y-S, Kim J-H, Park JB, Kang I-N, Jin S-H, Hwang D-H. Full donor-type conjugated polymers consisting of alkoxy- or alkylselenophene-substituted benzodithiophene and thiophene units for organic photovoltaic devices. Synthetic Metals 168, 23-30 (2013)."
125,[H]C1=CC(CCCCCCCCCCOC2=CC=C(OCCC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(C(F)(F)F)F)C=C2)=C([H])S1,PFAT,,,0.56,9.3,56,2.9,"Yao K, Chen L, Chen X, Chen Y. Self-Organized Hole Transport Layers Based on Polythiophene Diblock Copolymers for Inverted Organic Solar Cells with High Efficiency. Chemistry of Materials 25, 897-904 (2013)."
126,[H]C1=C(CCCCCCCCCCOC2=CC=C(OCCC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(C(F)(F)F)F)C=C2)C=C(S1)C3=C(CCCCCC)C=C(C4=C(CCCCCC)C=C(C5=C(CCCCCC)C=C([H])S5)S4)S3,PFT-3HT,,,0.6,11.3,64.9,4.4,"Yao K, Chen L, Chen X, Chen Y. Self-Organized Hole Transport Layers Based on Polythiophene Diblock Copolymers for Inverted Organic Solar Cells with High Efficiency. Chemistry of Materials 25, 897-904 (2013)."
127,[H]C1=C(CCCCCCCCCCOC2=CC=C(OCCC(F)(F)C(F)(F)C(F)(F)C(F)(F)C(F)(C(F)(F)F)F)C=C2)C=C(S1)C3=C(CCCCCC)C=C(C4=C(CCCCCC)C=C(C5=C(CCCCCC)C=C(C6=CC=C(C7=CC=C(C8=CC=C([H])S8)S7)S6)S5)S4)S3,PFT-6HT,,,0.59,10.4,66,4.1,"Yao K, Chen L, Chen X, Chen Y. Self-Organized Hole Transport Layers Based on Polythiophene Diblock Copolymers for Inverted Organic Solar Cells with High Efficiency. Chemistry of Materials 25, 897-904 (2013)."
128,[H]C(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C(OCCCCCCCC)C(OCCCCCCCC)=C([H])C4=N[Se]N=C43)S5)C5=C2OCC(CC)CCCC,PBDT-BSe,,,0.76,7.01,46,2.45,"Shin SA, Park JB, Kim J-H, Hwang D-H. Synthesis and characterization of 2,1,3-benzoselenadiazole-based conjugated polymers for organic photovoltaic cells. Synthetic Metals 172, 54-62 (2013)."
129,[H]C(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CSC([H])=C5)C6=N[Se]N=C64)S3)S7)C7=C2OCC(CC)CCCC,PBDT-DTBSe,,,0.7,9.37,48,3.13,"Shin SA, Park JB, Kim J-H, Hwang D-H. Synthesis and characterization of 2,1,3-benzoselenadiazole-based conjugated polymers for organic photovoltaic cells. Synthetic Metals 172, 54-62 (2013)."
130,[H]C(S1)=CC2=C1C(C3=CC=C(CCCCCCCC)S3)=C(C=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C([H])C5=N[Se]N=C54)S6)C6=C2C7=CC=C(CCCCCCCC)S7,PBDTT-BSe,,,0.77,11.03,42,3.57,"Shin SA, Park JB, Kim J-H, Hwang D-H. Synthesis and characterization of 2,1,3-benzoselenadiazole-based conjugated polymers for organic photovoltaic cells. Synthetic Metals 172, 54-62 (2013)."
131,[H]C(S1)=CC2=C1C(C3=CC=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CSC([H])=C6)C7=N[Se]N=C75)S4)S8)C8=C2C9=CC=C(CCCCCCCC)S9,PBDTT-DTBSe,,,0.67,10.23,46,3.18,"Shin SA, Park JB, Kim J-H, Hwang D-H. Synthesis and characterization of 2,1,3-benzoselenadiazole-based conjugated polymers for organic photovoltaic cells. Synthetic Metals 172, 54-62 (2013)."
132,CC1(C)C2=C(C=CC=C2)N(CC)/C1=C\C=C\C3=[N+](CC)C4=CC=CC=C4C3(C)C.FP(F)(F)(F)F.[F-],Cy3-P,,,0.88,6.2,67.8,3.7,"Berner E, et al. Influence of crystalline titanium oxide layer smoothness on the performance of inverted organic bilayer solar cells. Applied Physics Letters 102,  (2013)."
133,O=C1C(C2=C(C3=CC=C(C4=CC(CCCCCC)=C(C5=CC=C([H])S5)S4)S3)N1CC(CCCCCC)CCCCCCCC)=C(C6=CC=C(C7=CC(CCCCCC)=C([H])S7)S6)N(CC(CCCCCC)CCCCCCCC)C2=O,DPP860,,,0.554,12.8,66,4.7,"Ripolles-Sanchis T, et al. Molecular Electronic Coupling Controls Charge Recombination Kinetics in Organic Solar Cells of Low Bandgap Diketopyrrolopyrrole, Carbazole, and Thiophene Polymers. Journal of Physical Chemistry C 117, 8719-8726 (2013)."
134,CCCCCCCCOC1=CC([H])=C(OCCCCCCCCCCCCCCCCC)C=C1C#CC2=C3C=CC=CC3=C(C#CC4=CC(OCCCCCCCC)=C(/C=C/C5=CC(OCCCCCCCC)=C(/C=C/[H])C=C5OCCCCCCCCCCCCCCCCC)C=C4OCCCCCCCCCCCCCCCCC)C6=CC=CC=C26,AnEPVstat,,,0.822,8.86,59,4.3,"Aazou S, et al. Organic Bulk Heterojunction Solar Cells Based on P3HT and Anthracene-Containing PPE-PPV: Fabrication, Characterization and Modeling. Journal of Optoelectronics and Advanced Materials 15, 395-404 (2013)."
135,[O-]C(/C(C1=O)=C2C(O)=C/C(C=C\2O)=[N+](CCCC(C)C)/CCCC(C)C)=C1C3=C(O)C=C(N(CCCC(C)C)CCCC(C)C)C=C3O,DiPSQ(OH)2,,,0.55,5.7,51.9,1.54,"Spencer SD, et al. The effect of controllable thin film crystal growth on the aggregation of a novel high panchromaticity squaraine viable for organic solar cells. Solar Energy Materials and Solar Cells 112, 202-208 (2013)."
136,[H]C1=CC2=C(C#C[Si](C(C)C)(C(C)C)C(C)C)C(SC(C3=CC=C(C4=CC=C(C5=CC=C([H])S5)C6=C4N=C(C7=CC=C(OCCCCCCCC)C=C7)C(C8=CC=C(OCCCCCCCC)C=C8)=N6)S3)=C9)=C9C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C2S1,PTIPSBDT- DTQX,,,0.79,4.67,42,1.56,"Kim J-H, et al. High Open Circuit Voltage Solution-Processed Tandem Organic Photovoltaic Cells Employing a Bottom Cell Using a New Medium Band Gap Semiconducting Polymer. Chemistry of Materials 25, 2722-2732 (2013)."
137,[H]C1=CC2=C(C#C[Si](C(C)C)(C(C)C)C(C)C)C(SC(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C([H])S5)C6=C4N=C(C7=CC=C(OCCCCCCCC)C=C7)C(C8=CC=C(OCCCCCCCC)C=C8)=N6)S3)=C9)=C9C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C2S1,PTIPSBDT-DFDTQX,,,0.91,10.61,62,6.08,"Kim J-H, et al. High Open Circuit Voltage Solution-Processed Tandem Organic Photovoltaic Cells Employing a Bottom Cell Using a New Medium Band Gap Semiconducting Polymer. Chemistry of Materials 25, 2722-2732 (2013)."
138,C12=CC3=C(C=C(C4=CC=CC=C4)[Se]3)C=C1C=C5C(C=C(C6=CC=CC=C6)[Se]5)=C2,6b,,,0.46,3.03,59,0.83,"Nakano M, Mori H, Shinamura S, Takimiya K. Naphtho[2,3-b:6,7-b¡ä]dichalcogenophenes: Syntheses, Characterizations, and Chalcogene Atom Effects on Organic Field-Effect Transistor and Organic Photovoltaic Devices. Chemistry of Materials 24, 190-198 (2012)."
139,[H]C1=CC2=C(OCC(CCCC)CCCCCC)C3=C(C=C(C4=C5C(SC(C(OCC(CCCC)CCCCCC)=O)=C5)=C(C6=C(SC(C(OCC(CCCC)CCCCCC)=O)=C7)C7=C([H])S6)S4)S3)C(OCC(CCCC)CCCCCC)=C2S1,PBB3,,,0.63,6.37,51,2.04,"Carsten B, et al. Examining the effect of the dipole moment on charge separation in donor-acceptor polymers for organic photovoltaic applications. Journal of the American Chemical Society 133, 20468-20475 (2011)."
140,CC1=C(O[Pt]OC2=C(C)C=C(C)C3=CC=CN=C23)C4=NC=CC=C4C(C)=C1,Pt(Me2q)2,,,0.42,14.8,38,2.4,"Low KH, Xu ZX, Xiang HF, Chui SS, Roy VA, Che CM. Bis(5,7-dimethyl-8-hydroxyquinolinato)platinum(II) complex for efficient organic heterojunction solar cells. Chemistry, an Asian journal 6, 3223-3229 (2011)."
141,C12=CC=CN=C1C(O[Pt]OC3=CC=CC4=CC=CN=C34)=CC=C2,Ptq2,,,0.25,2.3,30,0.17,"Low KH, Xu ZX, Xiang HF, Chui SS, Roy VA, Che CM. Bis(5,7-dimethyl-8-hydroxyquinolinato)platinum(II) complex for efficient organic heterojunction solar cells. Chemistry, an Asian journal 6, 3223-3229 (2011)."
142,CCCCC(C=C(/C([H])=C(C#N)\C#N)S1)=C1C2=CC(CCCC)=C(S2)C3=CC=C(C4=CC=C(C5=C(CCCC)C=C(C6=C(CCCC)C=C(/C([H])=C(C#N)\C#N)S6)S5)S4)S3,DCV6T-Bu,,,0.81,4,67,2,"Levichkova M, et al. Dicyanovinyl sexithiophene as donor material in organic planar heterojunction solar cells: Morphological, optical, and electrical properties. Organic Electronics 12, 2243-2252 (2011)."
143,O=[Ti]12(N3C4=C(C=CC=C5)C5=C3N=C(C6=C7C=CC=C6)N2C7=N8)N9C(C(C=CC=C%10)=C%10C9=N4)=NC%11=C%12C(C=CC=C%12)=C8N1%11,TiOPc,,,0.74,4.2,38,1.2,"Obata N, Sato Y, Nakamura E, Matsuo Y. Small-Molecule-Based Organic Photovoltaic Devices Covering Visible and Near-Infrared Absorption through Phase Transition of Titanylphthalocyanine Induced by Solvent Exposure. Japanese Journal of Applied Physics 50, 121603 (2011)."
144,[H]C1=CC=C2C(C=CC(C3=CC=C(C4=CC=C(C5=CC=C6C(C=CC(N(C7=CC=C(CCCCCCCCCCCC)C=C7)[H])=C6)=C5)S4)S3)=C2)=C1,TSP-T11,,,0.75,8.03,37,2.22,"Yasuda T, Suzuki T, Takahashi M, Han L. Air-stable triarylamine-based amorphous polymer as donor material for bulk-heterojunction organic solar cells. Solar Energy Materials and Solar Cells 95, 3509-3515 (2011)."
145,[O-]C(/C1=C2[N+](CCCCCC)=C(/C=N/N(C3=CC=CC=C3)C4=CC=CC=C4)C=C\2)=C(C5=CC=C(/C=N/N(C6=CC=CC=C6)C7=CC=CC=C7)N5CCCCCC)C1=O,SQ,,,0.6,7.84,39,1.79,"Peh RJ, Lu Y, Zhao F, Lee C-LK, Kwan WL. Vacuum-free processed transparent inverted organic solar cells with spray-coated PEDOT:PSS anode. Solar Energy Materials and Solar Cells 95, 3579-3584 (2011)."
146,[H]=CC1=CC(C2=C(N3CC(CC)CCCC)C=CC(/C=C/C4=C(C5=CC=C(C6=CC=C(/C=C(C(O)=O)/C#N)S6)S5)C=C([H])S4)=C2)=C3C=C1,RCP©\1,,,0.77,4.14,32,1.04,"Chang DWK, Seo-Jin; Kim, Jin Young. Multifunctional Conjugated Polymers with Main-Chain Donors and Side-Chain Acceptors for Dye Sensitized Solar Cells (DSSCs) and Organic Photovoltaic Cells (OPVs) MACROMOLECULAR RAPID COMMUNICATIONS 32, 1809-1814 (2011)."
147,CCCCCCCC[Si]1(CCCCCCCC)C2=C(SC(C3=CC(CCCCCCCC)=C(C4=CC=C(C5=C(CCCCCCCC)C=C(/C=C(C#N)/C(OCCCCCCCC)=O)S5)S4)S3)=C2)C6=C1C=C(C7=CC(CCCCCCCC)=C(C8=CC=C(C9=C(CCCCCCCC)C=C(/C=C(C#N)/C(OCCCCCCCC)=O)S9)S8)S7)S6,DCAO3TSi,,,0.8,11.51,64,5.84,"Zhou J, et al. A Planar Small Molecule with Dithienosilole Core for High Efficiency Solution-Processed Organic Photovoltaic Cells. Chemistry of Materials 23, 4666-4668 (2011)."
148,F[B-]([N+]1=C(C2=CC=CC=C2)C(C=CC=C3)=C3C1=N4)(F)N5C4=C(C=CC=C6)C6=C5C7=CC=CC=C7,Ph2-benz-bodipy,,,0.81,5.8,53,2.3,"Meiss J, Holzmueller F, Gresser R, Leo K, Riede M. Near-infrared absorbing semitransparent organic solar cells. Applied Physics Letters 99, 193307 (2011)."
149,O=C(C1=CC2=C3N4[Cu](N5C6=NC4=C2C=C1)(N7C(C(C=C(C(O)=O)C=C8)=C8C7=N9)=NC5C%10=C6C=C(C(O)=O)C=C%10)N%11C9C(C=C(C(O)=O)C=C%12)=C%12C%11=N3)O,CuTcPc,,,0.54,0.825,32.3,0.14,"Zhang T, et al. Soluble Copper Phthalocyanine Applied for Organic Solar Cells. Journal of Nanoscience and Nanotechnology 11, 9641-9644 (2011)."
150,CCCCC1=C(SC(C2=CC=C(/C=C(C#N)\C#N)S2)=C1CCCC)C3=CC=C(C4=C(CCCC)C(CCCC)=C(C5=CC=C(/C=C(C#N)\C#N)S5)S4)[Se]3,1,,,0.99,5.5,48,3.09,"Haid S, Mishra A, Uhrich C, Pfeiffer M, B?uerle P. Dicyanovinylene-Substituted Selenophene¨CThiophene Co-oligomers for Small-Molecule Organic Solar Cells. Chemistry of Materials 23, 4435-4444 (2011)."
151,CCCCC1=C(SC(C2=CC=C(/C=C(C#N)\C#N)[Se]2)=C1CCCC)C3=CC=C(C4=C(CCCC)C(CCCC)=C(C5=CC=C(/C=C(C#N)\C#N)[Se]5)S4)S3,2,,,1,7,39,2.93,"Haid S, Mishra A, Uhrich C, Pfeiffer M, B?uerle P. Dicyanovinylene-Substituted Selenophene¨CThiophene Co-oligomers for Small-Molecule Organic Solar Cells. Chemistry of Materials 23, 4435-4444 (2011)."
152,CCCCC1=C(SC(C2=CC=C(/C=C(C#N)\C#N)[Se]2)=C1CCCC)C3=CC=C(C4=C(CCCC)C(CCCC)=C(C5=CC=C(/C=C(C#N)\C#N)[Se]5)S4)[Se]3,3,,,0.95,5.4,46,2.53,"Haid S, Mishra A, Uhrich C, Pfeiffer M, B?uerle P. Dicyanovinylene-Substituted Selenophene¨CThiophene Co-oligomers for Small-Molecule Organic Solar Cells. Chemistry of Materials 23, 4435-4444 (2011)."
153,[H]C1=C(SCCCC)C=C(C2=CC(SCCCC)=C(C3=CC=C(C(C=CC([H])=C4)=C4C5(CCCCCCCC)CCCCCCCC)C5=C3)S2)S1,P1,,,0.715,0.9,35,0.23,"Parenti F, et al. (Alkylsulfanyl)bithiophene-alt-Fluorene: ¦Ð-Conjugated Polymers for Organic Solar Cells. European Journal of Organic Chemistry 2011, 5659-5667 (2011)."
154,[H]C1=C(SCCCCCCCC)C=C(C2=CC(SCCCCCCCC)=C(C3=CC=C(C(C=CC([H])=C4)=C4C5(CCCCCCCC)CCCCCCCC)C5=C3)S2)S1,P2,,,0.715,0.5,35,0.13,"Parenti F, et al. (Alkylsulfanyl)bithiophene-alt-Fluorene: ¦Ð-Conjugated Polymers for Organic Solar Cells. European Journal of Organic Chemistry 2011, 5659-5667 (2011)."
155,[H]C1=CC(SCCCCCCCC)=C(C2=C(SCCCCCCCC)C=C(C3=CC=C(C(C=CC([H])=C4)=C4C5(CCCCCCCC)CCCCCCCC)C5=C3)S2)S1,P3,,,0.73,1.2,46,0.4,"Parenti F, et al. (Alkylsulfanyl)bithiophene-alt-Fluorene: ¦Ð-Conjugated Polymers for Organic Solar Cells. European Journal of Organic Chemistry 2011, 5659-5667 (2011)."
156,OC1=CC(N(C2=CC=CC3=C2C=CC=C3)C4=CC=CC=C4)=CC(O)=C1C5C([O-])C(C6=C(O)C=C(N(C7=CC=CC8=C7C=CC=C8)C9=CC=CC=C9)C=C6O)C5[O-],1-NPSQ,,,0.9,10,64,5.7,"Wei G, et al. Arylamine-based squaraine donors for use in organic solar cells. Nano letters 11, 4261-4264 (2011)."
157,CCCCCCCC[Si]1(CCCCCCCC)C(C=C(C2=CC=C(/C=C(C#N)/C#N)C3=NSN=C23)S4)=C4C5=C1C=C(C6=CC=C(/C=C(C#N)/C#N)C7=NSN=C76)S5,BDCDTS,,,0.43,0.73,24,0.07,"Lin L-Y, Lu C-W, Huang W-C, Chen Y-H, Lin H-W, Wong K-T. New AADAA-type electron donors for small molecule organic solar cells. Organic letters 13, 4962-4965 (2011)."
158,FC1=CC=CC2=C1C3=N/C2=N\C4=C5C(C=CC=C5F)=C6N4[Zn]N7/C(C(C=CC=C8F)C8/C7=N/C(C9=C/%10C(F)=CC=C9)=NC%10=N/6)=N\3,F4-ZnPc,,,0.66,8.3,64,3.9,"Riede M, et al. Efficient Organic Tandem Solar Cells based on Small Molecules. Advanced Functional Materials 21, 3019-3028 (2011)."
159,Cl[Al]1N2/C(C(C=CC=C3)=C3/C2=N/C(C4=CC=CC=C4/5)=NC5=N/6)=N\C7=N/C(C8=CC=CC=C87)=N\C9=C%10C(C=CC=C%10)=C6N19,AlPcCl,,,0.59,3,43,0.76,"Kaji T, et al. Co-evaporant induced crystalline donor: acceptor blends in organic solar cells. Advanced materials 23, 3320-3325 (2011)."
160,N12/C(C(C=CC=C3)=C3/C2=N/C(C4=CC=CC=C4/5)=NC5=N/6)=N\C7=N/C(C8=CC=CC=C87)=N\C9=C%10C(C=CC=C%10)=C6N9[Pb]1,PbPc,,,0.28,4.9,50,0.68,"Kaji T, et al. Co-evaporant induced crystalline donor: acceptor blends in organic solar cells. Advanced materials 23, 3320-3325 (2011)."
161,CC[P-](CC)(CC)[Pt](C1=CC=CC=C1)([P-](CC)(CC)CC)C#CC2=CC=C(S2)C(C=C3)=CC=C3N(C4=CC=C(C5=CC=C(C#C[Pt]([P-](CC)(CC)CC)([P-](CC)(CC)CC)C6=CC=CC=C6)S5)C=C4)C7=CC=C(C8=CC=C(C#C[Pt]([P-](CC)(CC)CC)([P-](CC)(CC)CC)C9=CC=CC=C9)S8)C=C7,M2,,,0.65,2.35,27,0.41,"Wang Q, et al. Platinum-acetylide polymers with higher dimensionality for organic solar cells. Chemistry, an Asian journal 6, 1766-1777 (2011)."
162,CC1=CC=C(N(C2=CC=C(C3=CC=C(C#C[H])S3)C=C2)C4=CC=C(C5=CC=C(C#C[Pt]([P-](CCCC)(CCCC)CCCC)([P-](CCCC)(CCCC)CCCC)[H])S5)C=C4)C=C1,P1,,,0.74,3.1,38,0.88,"Wang Q, et al. Platinum-acetylide polymers with higher dimensionality for organic solar cells. Chemistry, an Asian journal 6, 1766-1777 (2011)."
163,[H][Pt]([P-](CCCC)(CCCC)CCCC)([P-](CCCC)(CCCC)CCCC)C#CC1=CC=C(S1)C(C=C2)=CC=C2N(C3=CC=C(C4=CC=C(C#C[Pt]([P-](CCCC)(CCCC)CCCC)([P-](CCCC)(CCCC)CCCC)[H])S4)C=C3)C5=CC=C(C6=CC=C(C#C[Pt]([P-](CCCC)(CCCC)CCCC)([P-](CCCC)(CCCC)CCCC)C)S6)C=C5,P2,,,0.77,5.1,43,1.67,"Wang Q, et al. Platinum-acetylide polymers with higher dimensionality for organic solar cells. Chemistry, an Asian journal 6, 1766-1777 (2011)."
164,CCC1(CC)C(C=C(C2=CC=C(C#C[Pt]([P-](CCCC)(CCCC)CCCC)([P-](CCCC)(CCCC)CCCC)[H])S2)C=C3)=C3C4=CC=C(C=C41)N(C5=CC=C(C6=C7C=C(C8=CC=C(C#C[Pt]([P-](CCCC)(CCCC)CCCC)([P-](CCCC)(CCCC)CCCC)C)S8)C=C6)C(C7(CC)CC)=C5)C9=CC=C(C%10=C%11C=C(C%12=CC=C(C#C[Pt]([P-](CCCC)(CCCC)CCCC)([P-](CCCC)(CCCC)CCCC)[H])S%12)C=C%10)C(C%11(CC)CC)=C9,P3,,,0.82,5.88,56,2.24,"Wang Q, et al. Platinum-acetylide polymers with higher dimensionality for organic solar cells. Chemistry, an Asian journal 6, 1766-1777 (2011)."
165,[H]C(S1)=CC=C1C2=C3C4=C(C(N(CC(CC)CCCC)C3=O)=O)C=C(C5=CC=C(C6=CC(C7(CCCCCCCC)CCCCCCCC)=C(C8=C7C=C(C9=CC=C(C%10=CC=C(C%11=CC=C(C%12=CC(C%13(CCCCCCCC)CCCCCCCC)=C(C%14=C%13C=C([H])C=C%14)C=C%12)S%11)C%15=NSN=C%15%10)S9)C=C8)C=C6)S5)C%16C4C(C(N(CC(CC)CCCC)C%16=O)=O)=C2,PFTBTN,,,0.74,1.73,31,0.4,"Piyakulawat P, Keawprajak A, Wlosnewski J, Forster M, Asawapirom U. Low band gap copolymer containing naphthalene-1,4,5,8-tetracarboxylic bisimide: Synthesis, properties and organic solar cell applications. Synthetic Metals 161, 1238-1244 (2011)."
166,[H]C1=CC([Si]2(CC(CC)CCCC)CC(CC)CCCC)=C(S1)C3=C2C=C(C4=CC=C([H])C5=NSN=C45)S3,PSBTBT,,,0.558,15,58,5.5,"Colsmann A, Puetz A, Bauer A, Hanisch J, Ahlswede E, Lemmer U. Efficient Semi-Transparent Organic Solar Cells with Good Transparency Color Perception and Rendering Properties. Advanced Energy Materials 1, 599-603 (2011)."
167,[H]C1=CC(CCCCCCOC)=C(C2=C(CCCCCCOC)C=C([H])S2)S1,PDim1,,,0.35,0.0213,30.3,0.002,"Lanzi M, Paganin L, Caretti D, Setti L, Errani F. Synthesis of new methoxy-functionalized polythiophenes for charge transport in organic solar cells. Reactive and Functional Polymers 71, 745-755 (2011)."
168,[H]C1=CC(CCCCCCOC)=C(C2=CC=C([H])S2)S1,PDim2,,,0.55,0.865,31,0.15,"Lanzi M, Paganin L, Caretti D, Setti L, Errani F. Synthesis of new methoxy-functionalized polythiophenes for charge transport in organic solar cells. Reactive and Functional Polymers 71, 745-755 (2011)."
169,[H]C1=CC(CCCCCCOC)=C(C2=CC=C(C3=C(CCCCCCOC)C=C([H])S3)S2)S1,PTrim,,,0.33,0.14,29.8,0.014,"Lanzi M, Paganin L, Caretti D, Setti L, Errani F. Synthesis of new methoxy-functionalized polythiophenes for charge transport in organic solar cells. Reactive and Functional Polymers 71, 745-755 (2011)."
170,[H]C(S1)=CC2=C1C(SC(C3=C(C(N(CCCCCCCC)C4=O)=O)C4=C([H])S3)=C5)=C5C2(CC(CC)CCCC)CC(CC)CCCC,PCPDTTPD,,,0.87,8.7,43,3.15,"MacNeill CM, Peterson ED, Noftle RE, Carroll DL, Coffin RC. A cyclopentadithiophene/thienopyrroledione-based donor¨Cacceptor copolymer for organic solar cells. Synthetic Metals 161, 1137-1140 (2011)."
171,[H]C1=CC=C(S1)C(N(CC(CCCCCCCC)CCCCCCCCCC)C2=O)=C3C2=C(C4=CC=C(C5=CC(C=CC([H])=C6)=C6C=C5)S4)N(CC(CCCCCCCCCC)CCCCCCCC)C3=O,PDPP¨CTNT,,,0.76,11.8,52,4.7,"Sonar P, et al. High mobility organic thin film transistor and efficient photovoltaic devices using versatile donor¨Cacceptor polymer semiconductor by molecular design. Energy & Environmental Science 4, 2288 (2011)."
172,[H]C1=CC2=C(C(SC(C3=C(OCCCCCC)C(OCCCCCC)=C([H])C4=NON=C43)=C5)=C5[Si]2(CCCCCCC)CCCCCCC)S1,P1,,,0.7,9.56,55,3.7,"Caputo BJ, Welch GC, Kamkar DA, Henson ZB, Nguyen TQ, Bazan GC. A dithienosilole-benzooxadiazole donor-acceptor copolymer for utility in organic solar cells. Small 7, 1422-1426 (2011)."
173,[H]C(C[H])C1=CC=C(/C(C#N)=C/C2=CC=C(N(C3=CC=CC=C3)C4=CC=CC=C4)C=C2)C=C1,3,,,0.49,0.91,28,0.13,"Gupta A, et al. Band-gap tuning of pendant polymers for organic light-emitting devices and photovoltaic applications. Synthetic Metals 161, 856-863 (2011)."
174,[H]C(C[H])C1=CC=C(/C(C#N)=N/C2=CC=C(N(C3=CC=C(C)C=C3)C4=CC=C(C)C=C4)C=C2)C=C1,4,,,0.63,1.57,29,0.29,"Gupta A, et al. Band-gap tuning of pendant polymers for organic light-emitting devices and photovoltaic applications. Synthetic Metals 161, 856-863 (2011)."
175,[H]C1=C(CC(CC)CCCC)C=C(C2=NN=C(C3=CC(CC(CC)CCCC)=C(C4=CC(C5(CC(CC)CCCC)CC(CC)CCCC)=C(C6=C5C=C([H])S6)S4)S3)N=N2)S1,P1,,,0.78,4.73,30.2,1.11,"Li Z, et al. Alternating Copolymers of Dithienyl-s-Tetrazine and Cyclopentadithiophene for Organic Photovoltaic Applications. Chemistry of Materials 23, 1977-1984 (2011)."
176,[H]C1=C(CC(CC)CCCC)C=C(C2=NN=C(C3=CC(CC(CC)CCCC)=C(C4=CC(C5(CCCCCC)CCCCCC)=C(C6=C5C=C([H])S6)S4)S3)N=N2)S1,P2,,,0.74,11.1,47.7,3.89,"Li Z, et al. Alternating Copolymers of Dithienyl-s-Tetrazine and Cyclopentadithiophene for Organic Photovoltaic Applications. Chemistry of Materials 23, 1977-1984 (2011)."
177,[H]C1=C(CCCCCC)C=C(C2=NN=C(C3=CC(CCCCCC)=C(C4=CC(C5(CC(CC)CCCC)CC(CC)CCCC)=C(C6=C5C=C([H])S6)S4)S3)N=N2)S1,P3,,,0.81,9.44,38.4,2.93,"Li Z, et al. Alternating Copolymers of Dithienyl-s-Tetrazine and Cyclopentadithiophene for Organic Photovoltaic Applications. Chemistry of Materials 23, 1977-1984 (2011)."
178,[H]C1=C(CCCCCC)C=C(C2=NN=C(C3=CC(CCCCCC)=C(C4=CC(C5(CCCCCC)CCCCCC)=C(C6=C5C=C([H])S6)S4)S3)N=N2)S1,P4,,,0.75,12.5,59,5.53,"Li Z, et al. Alternating Copolymers of Dithienyl-s-Tetrazine and Cyclopentadithiophene for Organic Photovoltaic Applications. Chemistry of Materials 23, 1977-1984 (2011)."
179,[H]C1=C(C)C=C(C2=NN=C(C3=CC(C)=C(C4=CC(C5(CC(CC)CCCC)CC(CC)CCCC)=C(C6=C5C=C([H])S6)S4)S3)N=N2)S1,P5,,,0.6,9.08,37.1,2.02,"Li Z, et al. Alternating Copolymers of Dithienyl-s-Tetrazine and Cyclopentadithiophene for Organic Photovoltaic Applications. Chemistry of Materials 23, 1977-1984 (2011)."
180,O=S(C1C=CC2=C3N([Cu]N4/C(C(C=CC(S(=O)(O[Na])=O)=C5)=C5/C4=N/C(C6=C/7C(S(=O)(O[Na])=O)=CC=C6)=NC7=N/3)=N\C8=N/C(C9=C8C=C(S(=O)(O[Na])=O)C=C9)=N\%10)C%10C2=C1)(O[Na])=O,TSCuPc,,,0.52,1.47,41,0.32,"Schumann S, Hatton RA, Jones TS. Organic Photovoltaic Devices Based on Water-Soluble Copper Phthalocyanine. The Journal of Physical Chemistry C 115, 4916-4921 (2011)."
181,[H]C1=CC(SC(C2=C3C(C(N2CC(CCCCCCCCCC)CCCCCCCC)=O)=C(C4=CC(SC(C5=CC=C([H])S5)=C6)=C6S4)N(CC(CCCCCCCCCC)CCCCCCCC)C3=O)=C7)=C7S1,P1,,,0.58,15,61,5.4,"Bronstein H, et al. Thieno[3,2-b]thiophene-diketopyrrolopyrrole-containing polymers for high-performance organic field-effect transistors and organic photovoltaic devices. Journal of the American Chemical Society 133, 3272-3275 (2011)."
182,[H]C1=CC(SC(C2=C3C(C(N2CC(CCCCCCCCCC)CCCCCCCC)=O)=C(C4=CC(SC([H])=C5)=C5S4)N(CC(CCCCCCCCCC)CCCCCCCC)C3=O)=C6)=C6S1,P2,,,0.57,8.9,59,3,"Bronstein H, et al. Thieno[3,2-b]thiophene-diketopyrrolopyrrole-containing polymers for high-performance organic field-effect transistors and organic photovoltaic devices. Journal of the American Chemical Society 133, 3272-3275 (2011)."
183,[H]C1=C(OCCCCCCCC)C=C(/C(C#N)=C/C2=CC3=C(C=C([H])S3)S2)C(OCCCCCCCC)=C1,CN-PVTT,,,0.61,0.09,21,0.01,"Kim BG, Jeong EJ, Park HJ, Bilby D, Guo LJ, Kim J. Effect of polymer aggregation on the open circuit voltage in organic photovoltaic cells: aggregation-induced conjugated polymer gel and its application for preventing open circuit voltage drop. ACS applied materials & interfaces 3, 674-680 (2011)."
184,[H]C1=C(OCCCCCCCC)C=C(/C=C/C2=CC3=C(C=C([H])S3)S2)C(OCCCCCCCC)=C1,PVTT,,,0.57,5.55,55,1.76,"Kim BG, Jeong EJ, Park HJ, Bilby D, Guo LJ, Kim J. Effect of polymer aggregation on the open circuit voltage in organic photovoltaic cells: aggregation-induced conjugated polymer gel and its application for preventing open circuit voltage drop. ACS applied materials & interfaces 3, 674-680 (2011)."
185,[H]C1=C(SC(C(CCCCCCC)=O)=C2)C2=C(C(S3)=CC4=C3C(CCC(CCCC)CCCCC)=C(C=C([H])S5)C5=C4CCC(CCCC)CCCCC)S1,P1,,,0.78,9.8,63,4.8,"Wakim S, et al. New low band gap thieno[3,4-b]thiophene-based polymers with deep HOMO levels for organic solar cells. Journal of Materials Chemistry 21, 10920 (2011)."
186,[H]C1=C(SC(C(CCCCCCC)=O)=C2F)C2=C(C(S3)=CC4=C3C(CCC(CCCC)CCCCC)=C(C=C([H])S5)C5=C4CCC(CCCC)CCCCC)S1,P2,,,0.86,7.3,62,3.9,"Wakim S, et al. New low band gap thieno[3,4-b]thiophene-based polymers with deep HOMO levels for organic solar cells. Journal of Materials Chemistry 21, 10920 (2011)."
187,[H]C1=CCC(S1)C(N(CC(CCCCCC)CCCC)C2=O)=C3C2=C(C4=CC=C(C5=CC=C(C6=C(CCCCCCCCCCCCCCC)C7=C(C(SC(C8=CC=C([H])S8)=C9CCCCCCCCCCCCCCC)=C9S7)S6)S5)S4)N(CC(CCCCCC)CCCC)C3=O,PDPP¨CT¨CDTT,,,0.584,12.76,67.3,5.02,"Li J, Ong KH, Lim SL, Ng GM, Tan HS, Chen ZK. A random copolymer based on dithienothiophene and diketopyrrolopyrrole units for high performance organic solar cells. Chemical communications 47, 9480-9482 (2011)."
188,N#C/C(C#N)=C\C1=CC([Si]2(C3=CC=CC=C3)C4=CC=CC=C4)=C(S1)C5=C2C=C(C6=CC=C(N(C7=CC=CC=C7)C8=CC=CC=C8)C=C6)S5,TPDCDTS,,,0.83,9.53,48,3.82,"Lin HW, et al. A new donor-acceptor molecule with uniaxial anisotropy for efficient vacuum-deposited organic solar cells. Chemical communications 47, 7872-7874 (2011)."
189,O=C(C1N2C=CC=C1)O[Ir]32N(C=C4)C(C5=C3C=CC=C5)C6=C4C=CC=C6,1,,,0.46,2.32,42,0.45,"Lee W, Kwon T-H, Kwon J, Kim J-y, Lee C, Hong J-I. Effect of main ligands on organic photovoltaic performance of Ir(iii) complexes. New Journal of Chemistry 35, 2557 (2011)."
190,O=C(C1N2C=CC=C1)O[Ir]32N(C=C4)C(C5=C3C=C(N(C6=CC=CC=C6)C7=CC=CC=C7)C=C5)C8=C4C=CC=C8,2,,,0.44,2.65,43,0.5,"Lee W, Kwon T-H, Kwon J, Kim J-y, Lee C, Hong J-I. Effect of main ligands on organic photovoltaic performance of Ir(iii) complexes. New Journal of Chemistry 35, 2557 (2011)."
191,O=C(C1N2C=CC=C1)O[Ir]32N(C=C4)C(C5=C3C=C6C7=C5C=CC8=CC=CC(C=C6)=C87)C9=C4C=CC=C9,3,,,0.45,2.17,34,0.34,"Lee W, Kwon T-H, Kwon J, Kim J-y, Lee C, Hong J-I. Effect of main ligands on organic photovoltaic performance of Ir(iii) complexes. New Journal of Chemistry 35, 2557 (2011)."
192,C1([Si](C2=CC=CC=C2)(C3=CC=CC=C3)C4=CC=CC=C4)=CC=C([Si](C5=CC=CC=C5)(C6=CC=CC=C6)C7=CC=CC=C7)C=C1,UGH2,,,,,,4.4,"Menke SM, Luhman WA, Holmes RJ. Tailored exciton diffusion in organic photovoltaic cells for enhanced power conversion efficiency. Nat. Mater. 12, 152-157 (2013)."
193,CCCCCCCCOC(C(OCCCCCCCC)=C1)=CC(C1=C(C2=CC=C(C3=CC(C(CCCCCCCCC)(CCCCCCCCC)C4=C5C=CC([H])=C4)=C5C=C3)S2)C=C6)=C6C7=CC=C([H])S7,P1,,,0.89,4.9,60,2.8,"Mangold H, Howard IA, Janietz S, Laquai F. Controlled energy shuttling in terpolymers enabling independent optimization of absorption and transport properties in organic solar cell materials. Appl. Phys. Lett. 101,  (2012)."
194,[H]C1=CC=C(C(N2CC(CC)CCCC)=C3C(C2=O)=C(C(O4)=CC=C4C5=CC6=C(OCC(CC)CCCC)C7=C(C=C([H])S7)C(OCC(CC)CCCC)=C6S5)N(CC(CC)CCCC)C3=O)O1,PBDT-FDP,,,0.69,9.2,53,3.35,"Yuan J, et al. Design of benzodithiophene-diketopyrrolopyrrole based donor-acceptor copolymers for efficient organic field effect transistors and polymer solar cells. J. Mater. Chem. 22, 22734-22742 (2012)."
195,[H]C1=CC=C(C(N2CC(CC)CCCC)=C3C(C2=O)=C(C(O4)=CC=C4C5=CC6=C(C7=CC=C(CC(CC)CCCC)S7)C8=C(C=C([H])S8)C(C9=CC=C(C(CC)CCCC)S9)=C6S5)N(CC(CC)CCCC)C3=O)O1,PBDT-T-FDP,,,0.73,15.22,60,5.54,"Yuan J, et al. Design of benzodithiophene-diketopyrrolopyrrole based donor-acceptor copolymers for efficient organic field effect transistors and polymer solar cells. J. Mater. Chem. 22, 22734-22742 (2012)."
196,[H]C1=CC=C(C(N2CC(CC)CCCC)=C3C(C2=O)=C(C(S4)=CC=C4C5=CC6=C(C7=CC=C(CC(CC)CCCC)S7)C8=C(C=C([H])S8)C(C9=CC=C(C(CC)CCCC)S9)=C6S5)N(CC(CC)CCCC)C3=O)S1,PBDT-T-TDP,,,0.68,9.8,59,3.91,"Yuan J, et al. Design of benzodithiophene-diketopyrrolopyrrole based donor-acceptor copolymers for efficient organic field effect transistors and polymer solar cells. J. Mater. Chem. 22, 22734-22742 (2012)."
197,O=C1/C(C2=CC=C(C3=CC(CCCCCCCC)=C([H])S3)C=C2N1CC(CCCCCC)CCCCCCCC)=C4C(N(CC(CCCCCC)CCCCCCCC)C5=C/4C=CC(C6=CC(CCCCCCCC)=C(C7=CC=C([H])S7)S6)=C5)=O,P3TI,,,0.69,14,64,6.18,"Tang Z, et al. Semi-Transparent Tandem Organic Solar Cells with 90% Internal Quantum Efficiency. Adv. Energy Mater. 2, 1467-1476 (2012)."
198,O=C(OCCCCCCCC)/C([N+]#[C-])=C/C1=CC(CCCCCCCC)=C(C(S2)=CC=C2C3=C(CCCCCCCC)C=C(C4=CC5=C(OCC(CC)CCCC)C6=C(C=C(C7=CC(CCCCCCCC)=C(C8=CC=C(C9=C(CCCCCCCC)C=C(/C=C([N+]#[C-])/C(OCCCCCCCC)=O)S9)S8)S7)S6)C(OCC(CC)CCCC)=C5S4)S3)S1,DCAO3TBDT,,,0.95,8,60,4.56,"Zhou J, et al. Small Molecules Based on Benzo 1,2-b:4,5-b ' dithiophene Unit for High-Performance Solution-Processed Organic Solar Cells. J. Am. Chem. Soc. 134, 16345-16351 (2012)."
199,[C-]#[N+]/C(C#N)=C\C1=CC=C(C([Se]2)=CC=C2C([Se]3)=CC=C3C4=CC=C(/C=C([N+]#[C-])\C#N)[Se]4)[Se]1,DCV4S,,,0.95,4.8,53,2.4,"Haid S, Mishra A, Weil M, Uhrich C, Pfeiffer M, Baeuerle P. Synthesis and Structure-Property Correlations of Dicyanovinyl-Substituted Oligoselenophenes and their Application in Organic Solar Cells. Adv. Funct. Mater. 22, 4322-4333 (2012)."
200,[C-]#[N+]/C(C#N)=C\C1=CC=C(C([Se]2)=CC=C2C([Se]3)=CC=C3C([Se]4)=CC=C4C5=CC=C(/C=C([N+]#[C-])\C#N)[Se]5)[Se]1,DCV5S,,,0.91,7.1,53,3.4,"Haid S, Mishra A, Weil M, Uhrich C, Pfeiffer M, Baeuerle P. Synthesis and Structure-Property Correlations of Dicyanovinyl-Substituted Oligoselenophenes and their Application in Organic Solar Cells. Adv. Funct. Mater. 22, 4322-4333 (2012)."
201,CCCCCCC1=C(/C=C([N+]#[C-])/C#N)SC2=C1SC(/C=C/C(C=C3)=CC=C3N(C4=CC=C(/C=C/C5=C(CCCCCC)C6=C(C(CCCCCC)=C(/C=C([N+]#[C-])/C#N)S6)S5)C=C4)C7=CC=C(/C=C/C8=C(CCCCCC)C9=C(C(CCCCCC)=C(/C=C([N+]#[C-])/[N+]#[C-])S9)S8)C=C7)=C2CCCCCC,S(TPA¨CDHT¨CDCN),,,0.96,6.8,43.5,2.87,"Deng D, Shen S, Zhang J, He C, Zhang Z, Li Y. Solution-processable star-shaped photovoltaic organic molecule with triphenylamine core and thieno 3,2-b thiophene-dicyanovinyl arms. Org. Electron. 13, 2546-2552 (2012)."
202,C=C1C(SC(C)C1)=C.[H]C(S2)=CC(C2=C3)=CC4=C3C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C=C(C5=C(CCCCCCCCCCCC)C=C(C6=CC(CCCCCCCCCCCC)=C([H])S6)S5)S7)C7=C8)C8=C4C#C[Si](C(C)C)(C(C)C)C(C)C,PTADT2,,,0.77,1.7,42,0.55,"Kong H, Park SH, Cho NS, Cho S, Shim H-K. Anthradithiophene-thiophene copolymers with broad UV-vis absorption for organic solar cells and field-effect transistors. Journal of Polymer Science Part a-Polymer Chemistry 50, 4119-4126 (2012)."
203,C=C1C(SC(C)C1)=C.[H]C(S2)=CC(C2=C3)=CC4=C3C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C=C(C5=CC=C(C6=C(CCCCCCCCCCCC)C=C(C7=CC(CCCCCCCCCCCC)=C(C8=CC=C([H])S8)S7)S6)S5)S9)C9=C%10)C%10=C4C#C[Si](C(C)C)(C(C)C)C(C)C,PTADT4,,,0.7,4.4,42,1.3,"Kong H, Park SH, Cho NS, Cho S, Shim H-K. Anthradithiophene-thiophene copolymers with broad UV-vis absorption for organic solar cells and field-effect transistors. Journal of Polymer Science Part a-Polymer Chemistry 50, 4119-4126 (2012)."
204,[H]C(S1)=CC(C1=C2OCC(CCCC)CCCCCC)=C(OCC(CCCC)CCCCCC)C3=C2C=C(C(S4)=CC5=C4C(C6=NSN=C67)=C(N5CC(CC)CCCC)C8=C7C9=C(N8CC(CC)CCCC)C=C([H])S9)S3,PBIT1,,,0.646,4.96,61.4,1.96,"Carsten B, et al. Mediating Solar Cell Performance by Controlling the Internal Dipole Change in Organic Photovoltaic Polymers. Macromolecules 45, 6390-6395 (2012)."
205,[H]C1=CC(N(CC(CC)CCCC)C2=C3C4=NSN=C4C5=C2N(CC(CC)CCCC)C6=C5SC(C7=C(C(F)=C(C(OCC(CC)CCCC)=O)S8)C8=C([H])S7)=C6)=C3S1,PBIT3,,,0.421,4.24,26.4,0.47,"Carsten B, et al. Mediating Solar Cell Performance by Controlling the Internal Dipole Change in Organic Photovoltaic Polymers. Macromolecules 45, 6390-6395 (2012)."
206,[H]C(S1)=CC(C1=C2OCC(CCCC)CCCCCC)=C(OCC(CCCC)CCCCCC)C3=C2C=C(C(S4)=CN=C4C5=C(C(N6CC(CC)CCCC)=O)C(C(N5CC(CC)CCCC)=O)=C6C7=NC=C([H])S7)S3,PBTZ1,,,0.839,7.27,56.7,3.46,"Carsten B, et al. Mediating Solar Cell Performance by Controlling the Internal Dipole Change in Organic Photovoltaic Polymers. Macromolecules 45, 6390-6395 (2012)."
207,[H]C1=CN=C(C2=C3C(C(N2CC(CC)CCCC)=O)=C(C4=NC=C(C5=C6C(CC(CC(CCCC)CCCCCC)=C6)=C([H])S5)S4)N(CC(CC)CCCC)C3=O)S1,PBTZ2,,,0.559,2.01,25.9,0.29,"Carsten B, et al. Mediating Solar Cell Performance by Controlling the Internal Dipole Change in Organic Photovoltaic Polymers. Macromolecules 45, 6390-6395 (2012)."
208,OC1=C(C2C([O-])C(C3=C(O)C=C(C=C3O)N(C4=CC=CC=C4)C5=CC=CC=C5)C2[O-])C(O)=CC(N(C6=CC=CC=C6)C7=CC=CC=C7)=C1,DPSQ,,,0.96,7,71,4.8,"Zimmerman JD, et al. Independent Control of Bulk and Interfacial Morphologies of Small Molecular Weight Organic Heterojunction Solar Cells. Nano Lett. 12, 4366-4371 (2012)."
209,FC1=C(C(S2)=CC3=C2C(SC(C(C4=NSN=C45)=C(F)C=C5C6=CC=C(C7=CC=C(CCCCCC)S7)S6)=C8)=C8[Si]3(CC(CC)CCCC)CC(CC)CCCC)C9=NSN=C9C(C%10=CC=C(C%11=CC=C(CCCCCC)S%11)S%10)=C1,p©\DTS(PTTh2)2,,,0.82,10.8,65,5.8,"van der Poll TS, Love JA, Thuc-Quyen N, Bazan GC. Non-Basic High-Performance Molecules for Solution-Processed Organic Solar Cells. Adv. Mater. 24, 3646-3649 (2012)."
210,CCCCC(CC)CN1C(/C=C(C#N)/C2=CC=C([N+]([O-])=O)C=C2)=CC=C1N=NC3=CC(C(C=C(N=NC4=CC=C(/C=C(C#N)/C5=CC=C([N+]([O-])=O)C=C5)N4CC(CC)CCCC)C=C6)=C6N7CCCCCC)=C7C=C3,C,,,0.86,7,52,3.13,"Sharma GD, Mikroyannidis JA, Sharma SS, Thomas KRJ. Bulk heterojunction organic photovoltaic devices based on small molecules featuring pyrrole and carbazole and 2-(4-nitrophenyl)acrylonitrile acceptor segments as donor and fullerene derivatives as acceptor. Dyes and Pigments 94, 320-329 (2012)."
211,CCCCCCN1C(/C=C(C#N)/C2=CC=C([N+]([O-])=O)C=C2)=CC=C1N=NC3=CC=C(N=NC4=CC=C(/C=C(C#N)/C5=CC=C([N+]([O-])=O)C=C5)N4CCCCCC)C=C3,P,,,0.94,5.36,0.48,2.41,"Sharma GD, Mikroyannidis JA, Sharma SS, Thomas KRJ. Bulk heterojunction organic photovoltaic devices based on small molecules featuring pyrrole and carbazole and 2-(4-nitrophenyl)acrylonitrile acceptor segments as donor and fullerene derivatives as acceptor. Dyes and Pigments 94, 320-329 (2012)."
212,O=C(C1=CC2=C([H])SC(C3=CC4=C(OCC(CC)CCCC)C5=C(C=C([H])S5)C(OCC(CC)CCCC)=C4S3)=C2C=C1C(OCC)=O)OCC,PBDT©\DEAITN,,,0.64,5.9,33,1.25,"Long G, et al. Isothianaphthene-Based Conjugated Polymers for Organic Photovoltaic Cells. Macromol. Chem. Phys. 213, 1596-1603 (2012)."
213,O=C(C1=CC2=C([H])SC(C3=CC4=C(OCC(CC)CCCC)C5=C(C=C([H])S5)C(OCC(CC)CCCC)=C4S3)=C2C=C1C(OCCCCCCCC)=O)OCCCCCCCC,PBDT©\DOAITN,,,0.78,4.65,33,1.2,"Long G, et al. Isothianaphthene-Based Conjugated Polymers for Organic Photovoltaic Cells. Macromol. Chem. Phys. 213, 1596-1603 (2012)."
214,CC1=C(C2=CC=C(C3=CC=C(C4=CC=C(C5=C(C)C(C)=C(/C=C(C#N)\[N+]#[C-])S5)S4)S3)S2)SC(/C=C([N+]#[C-])\C#N)=C1C,1,,,0.91,9.6,63,4.8,"Fitzner R, et al. Correlation of pi-Conjugated Oligomer Structure with Film Morphology and Organic Solar Cell Performance. J. Am. Chem. Soc. 134, 11064-11067 (2012)."
215,CC1=C(C2=CC=C(/C=C([N+]#[C-])\C#N)S2)SC(C3=CC=C(C4=C(C)C(C)=C(C5=CC=C(/C=C(C#N)\[N+]#[C-])S5)S4)S3)=C1C,2,,,0.95,9.4,62,4.8,"Fitzner R, et al. Correlation of pi-Conjugated Oligomer Structure with Film Morphology and Organic Solar Cell Performance. J. Am. Chem. Soc. 134, 11064-11067 (2012)."
216,CC1=C(C2=CC=C(C3=CC=C(/C=C(C#N)\[N+]#[C-])S3)S2)SC(C4=CC=C(C5=CC=C(/C=C([N+]#[C-])\C#N)S5)S4)=C1C,3,,,0.95,11.5,63,6.9,"Fitzner R, et al. Correlation of pi-Conjugated Oligomer Structure with Film Morphology and Organic Solar Cell Performance. J. Am. Chem. Soc. 134, 11064-11067 (2012)."
217,CC1(C)C2=C(C=CC=C2)C3=CC=C(N(C4=CC=C(C(C=CC=C5)=C5C6(C)C)C6=C4)C7=CC=C(C=C(C8=CC=C([N+]([O-])=O)S8)S9)C9=C7)C=C31,1,,,0.75,8.54,33,2.14,"Kim J, Cho N, Ko HM, Kim C, Lee JK, Ko J. Push-pull organic semiconductors comprising of bis-dimethylfluorenyl amino benzo b thiophene donor and various acceptors for solution processed small molecule organic solar cells. Sol. Energy Mater. Sol. Cells 102, 159-166 (2012)."
218,CC1=C(CCCCCC)C=C(C2=CC=C(/C(C3=CC=C(/C(C4=CC=C(C5=CC(CCCCCC)=C(C)S5)C=C4)=C6N=C7C=C\6)N3[Zn]N8/C(C=C/C8=C7\C9=CC=C(C%10=CC(CCCCCC)=C(C)S%10)C=C9)=C%11/C%12=CC=C(C%13=CC(CCCCCC)=C(C)S%13)C=C%12)=C%14C=CC%11=N\%14)C=C2)S1,TTP1,,,0.688,2.143,,0.45,"Cho EH, Chae SH, Kim K, Lee SJ, Joo J. Photovoltaic characteristics of organic solar cells using Zn-porphyrin derivatives with controlled pi-conjugation structures. Synth. Met. 162, 813-819 (2012)."
219,CC1=C(CCCCCC)C=C(C2=CC=C(C3=CC=C(/C(C4=CC=C5N4[Zn]N6/C(C=C/C6=C7\C8=CC=C(C9=CC=C(C%10=CC(CCCCCC)=C(C)S%10)S9)C=C8)=C(C%11=CC=C(C%12=CC=C(C%13=CC(CCCCCC)=C(C)S%13)S%12)C=C%11)\C(C=C/%14)=NC%14=C5\C%15=CC=C(C%16=CC=C(C%17=CC(CCCCCC)=C(C)S%17)S%16)C=C%15)=C%18N=C7C=C/%18)C=C3)S2)S1,TTP2,,,0.664,1.951,,0.36,"Cho EH, Chae SH, Kim K, Lee SJ, Joo J. Photovoltaic characteristics of organic solar cells using Zn-porphyrin derivatives with controlled pi-conjugation structures. Synth. Met. 162, 813-819 (2012)."
220,CC1=C(CCCCCC)C=C(C2=CC=C(C3=CC=C(C4=CC=C(/C(C5=CC=C(/C(C6=CC=C(C7=CC=C(C8=CC=C(C9=CC(CCCCCC)=C(C)S9)S8)S7)C=C6)=C%10N=C%11C=C\%10)N5[Zn]N%12/C(C=C/C%12=C%11\C%13=CC=C(C%14=CC=C(C%15=CC=C(C%16=CC(CCCCCC)=C(C)S%16)S%15)S%14)C=C%13)=C%17/C%18=CC=C(C%19=CC=C(C%20=CC=C(C%21=CC(CCCCCC)=C(C)S%21)S%20)S%19)C=C%18)=C%22C=CC%17=N\%22)C=C4)S3)S2)S1,TTP3,,,0.653,1.847,,0.32,"Cho EH, Chae SH, Kim K, Lee SJ, Joo J. Photovoltaic characteristics of organic solar cells using Zn-porphyrin derivatives with controlled pi-conjugation structures. Synth. Met. 162, 813-819 (2012)."
221,CC1=C(CCCCCC)C=C(C2=CC=C(C#C/C(C3=N/C(C=C3)=C4/C5=CC=CC=C5)=C(C=C/6)/N7C6=C(C8=CC=CC=C8)/C(C=C/9)=NC9=C(C#CC%10=CC=C(C%11=CC(CCCCCC)=C(C)S%11)S%10)/C%12=CC=C4N%12[Zn]7)S2)S1,TTP4,,,0.556,5.287,,1,"Cho EH, Chae SH, Kim K, Lee SJ, Joo J. Photovoltaic characteristics of organic solar cells using Zn-porphyrin derivatives with controlled pi-conjugation structures. Synth. Met. 162, 813-819 (2012)."
222,CC1=C(CCCCCC)C=C(C2=CC=C(C#C/C(C3=N/C(C=C3)=C4/C5=C(OCCCCCC)C=CC=C5OCCCCCC)=C(C=C/6)/N7C6=C(C8=C(OCCCCCC)C=CC=C8OCCCCCC)/C(C=C/9)=NC9=C(C#CC%10=CC=C(C%11=CC(CCCCCC)=C(C)S%11)S%10)/C%12=CC=C4N%12[Zn]7)S2)S1,TTP5,,,0.621,4.129,,0.76,"Cho EH, Chae SH, Kim K, Lee SJ, Joo J. Photovoltaic characteristics of organic solar cells using Zn-porphyrin derivatives with controlled pi-conjugation structures. Synth. Met. 162, 813-819 (2012)."
223,CC1(C)C2=C(C3=C1C=CC=C3)C=CC(N(C4=CC(C(C)(C)C5=C6C=CC=C5)=C6C=C4)C7=CC=C(C8=CC=C(C9=CC=C([N+]([O-])=O)S9)S8)C=C7)=C2,1,,,0.83,8.19,40,2.7,"Cho N, Kim J, Song K, Lee JK, Ko J. Synthesis and characterization of push-pull organic semiconductors with various acceptors for solution-processed small molecule organic solar cells. Tetrahedron 68, 4029-4036 (2012)."
224,CC1(C)C2=C(C3=C1C=CC=C3)C=CC(N(C4=CC(C(C)(C)C5=C6C=CC=C5)=C6C=C4)C7=CC=C(C8=CC=C(C9=CC=C(/C=C/C%10=C([N+]#[C-])/C(OC%10(C)C)=C(C#N)\[N+]#[C-])S9)S8)C=C7)=C2,3,,,0.8,6.26,33,1.68,"Cho N, Kim J, Song K, Lee JK, Ko J. Synthesis and characterization of push-pull organic semiconductors with various acceptors for solution-processed small molecule organic solar cells. Tetrahedron 68, 4029-4036 (2012)."
225,[H]C(S1)=CC=C1C(C2=NSN=C23)=CC=C3C(S4)=CC=C4C(C=C5)=CC6=C5C(C=CC([H])=C7)=C7N6C8=CC=C(/N=C(C9=CC=C(OCC(CC)CCCC)C=C9)\C%10=CC=C(OCC(CC)CCCC)C=C%10)C=C8,PImCDTBT,,,0.46,2.12,26,0.25,"Kimoto A, Tajima Y. Donor-Acceptor-Type Low Bandgap Polymer Carrying Phenylazomethine Moiety as a Metal-Collecting Pendant Unit: Open-Circuit Voltage Modulation of Solution-Processed Organic Photovoltaic Devices Induced by Metal Complexation. Acs Macro Letters 1, 667-671 (2012)."
226,[H]C1=C(CCCCCCCCCCCC)C=C(C2=CC=C(C3=CC(CCCCCCCCCCCC)=C(C4=CC=C([H])[Se]4)[Se]3)C5C2N=C(C6=CC=C(OCCCCCCCC)C=C6)C(C7=CC=C(OCCCCCCCC)C=C7)=N5)[Se]1,PQSS,,,0.4,4.5,58,1.07,"Lee W-H, et al. Synthesis and characterization of diselenenoquinoxaline-based donor-acceptor polymers for organic photovoltaic cells. Synth. Met. 162, 873-880 (2012)."
227,[H]C1=C(CCCCCCCCCCCC)C=C(C2=CC=C(C3=CC(CCCCCCCCCCCC)=C(C4=CC=C([H])S4)[Se]3)C5C2N=C(C6=CC=C(OCCCCCCCC)C=C6)C(C7=CC=C(OCCCCCCCC)C=C7)=N5)[Se]1,PQST,,,0.46,2.09,46,0.45,"Lee W-H, et al. Synthesis and characterization of diselenenoquinoxaline-based donor-acceptor polymers for organic photovoltaic cells. Synth. Met. 162, 873-880 (2012)."
228,[H]C1=CC=C(C2=CC=C([H])C3=NN(CCCCCCCCCCCC)N=C32)C4=NSN=C14,P1,,,0.45,0.92,36,0.15,"Karakus M, Apaydin DH, Yildiz DE, Toppare L, Cirpan A. Benzotriazole and benzothiadiazole containing conjugated copolymers for organic solar cell applications. Polymer 53, 1198-1202 (2012)."
229,[H]C1=CC=C(C2=CC=C(C3=CC=C(C4=CC=C([H])S4)C5=NN(CCCCCCCCCCCC)N=C53)S2)C6=NSN=C16,P2,,,0.45,3.48,33,0.45,"Karakus M, Apaydin DH, Yildiz DE, Toppare L, Cirpan A. Benzotriazole and benzothiadiazole containing conjugated copolymers for organic solar cell applications. Polymer 53, 1198-1202 (2012)."
230,[H]C1=CC=C(C2=C(CCCCCC)C=C(C3=CC=C(C4=CC(CCCCCC)=C([H])S4)C5=NN(CCCCCCCCCCCC)N=C53)S2)C6=NSN=C16,P3,,,0.37,0.96,28,0.1,"Karakus M, Apaydin DH, Yildiz DE, Toppare L, Cirpan A. Benzotriazole and benzothiadiazole containing conjugated copolymers for organic solar cell applications. Polymer 53, 1198-1202 (2012)."
231,C[Lr]1(C)C(C=CC=C2)=C2C3N1C4=CC=CC=C4N3C5=CC=CC=C5,(pbi)2Ir(acac),,,0.81,4.64,44,1.65,"Wang N, Yu J, Zheng Y, Guan Z, Jiang Y. Organic Photovoltaic Cells Based on a Medium-Bandgap Phosphorescent Material and C-60. J. Phys. Chem. C 116, 5887-5891 (2012)."
232,[H]C1=CC(CCC(C)CCCC(C)C)=C(C2=CC=C(C3=C(CCC(C)CCCC(C)C)C=C(C4=CC=C(C5=C6C(C(N5CC(CC)CCCC)=O)=C(C7=CC=C([H])S7)N(CC(CC)CCCC)C6=O)S4)S3)S2)S1,P3TDTDPP,,,0.54,10.65,56,3.18,"Lee W-H, et al. Synthesis and Characterization of New Selenophene-Based Donor-Acceptor Low-Bandgap Polymers for Organic Photovoltaic Cells. Macromolecules 45, 1303-1312 (2012)."
233,[H]C1=CC=C(C2=CC=C(C3=CC=C(C4=CC(CCC(C)CCCC(C)C)=C(C5=CC=C(C6=C(CCC(C)CCCC(C)C)C=C([H])S6)S5)S4)S3)C7=C2N=C(C8=CC=C(OCCC(C)CCCC(C)C)C=C8)C(C9=CC=C(OCCC(C)CCCC(C)C)C=C9)=N7)S1,P3TDTQ,,,0.67,1.82,46,0.56,"Lee W-H, et al. Synthesis and Characterization of New Selenophene-Based Donor-Acceptor Low-Bandgap Polymers for Organic Photovoltaic Cells. Macromolecules 45, 1303-1312 (2012)."
234,[H]C1=CC2=C(OC(CCCCC)CCCCC)C3=C(C=C(C4=CC=C([H])C5=NON=C54)S3)C(OC(CCCCC)CCCCC)=C2S1,P1,,,0.98,11.74,45.5,5.24,"Nie W, et al. High efficiency organic solar cells with spray coated active layers comprised of a low band gap conjugated polymer. Appl. Phys. Lett. 100,  (2012)."
235,[H]C1=CC2=C(C=C1)N(C3=CC=C(OC)C=C3)C4=C(C=C(/C=C/C(C=C5)=CC6=C5N(C7=CC=C(OC)C=C7)C(C=CC(C8=C(CCCCCC)C=C(C9=CC=C(C%10=CC(CCCCCC)=C([H])S%10)C%11=NSN=C%119)S8)=C%12)=C%12S6)C=C4)S2,P1,,,0.68,4.27,41.2,1.18,"Seo Y-H, et al. Side-chain effects on phenothiazine-based donor-acceptor copolymer properties in organic photovoltaic devices. Journal of Polymer Science Part a-Polymer Chemistry 50, 649-658 (2012)."
236,[H]C1=CC2=C(C=C1)N(C3=CC=C(OCCCCCCCCCCCC)C=C3)C4=C(C=C(/C=C/C(C=C5)=CC6=C5N(C7=CC=C(OCCCCCCCCCCCC)C=C7)C(C=CC(C8=CC=C(C9=CC=C(C%10=CC=C([H])S%10)C%11=NSN=C%119)S8)=C%12)=C%12S6)C=C4)S2,P2,,,0.7,6.79,39.1,1.86,"Seo Y-H, et al. Side-chain effects on phenothiazine-based donor-acceptor copolymer properties in organic photovoltaic devices. Journal of Polymer Science Part a-Polymer Chemistry 50, 649-658 (2012)."
237,O=C(OC)C1=C([H])SC(C2=CC3=C(OCC(CC)CCCC)C4=C(C=C([H])S4)C(OCC(CC)CCCC)=C3S2)=C1,PBDT©\3MT,,,0.86,10.5,50,4.52,"Cho MJ, Seo J, Kim KH, Choi DH, Prasad PN. Enhanced Performance of Organic Photovoltaic Cells Fabricated with a Methyl Thiophene-3-Carboxylate-Containing Alternating Conjugated Copolymer. Macromol. Rapid Commun. 33, 146-151 (2012)."
238,[H]C1=CC(CCCCCCCCCCCC)=C(C([Se]2)=C(CCCCCCCCCCCC)C=C2C3=CC(CCCCCCCCCCCC)=C(C([Se]4)=CC=C4C5=CC=C(C6=C(CCCCCCCCCCCC)C=C([H])[Se]6)[Se]5)[Se]3)[Se]1,HHP6S,,,0.79,3.33,30,0.77,"Lee W-H, et al. Synthesis and characterization of new selenophene-based conjugated polymers for organic photovoltaic cells. Journal of Polymer Science Part a-Polymer Chemistry 50, 551-561 (2012)."
239,[H]C1=CC=C(C([Se]2)=CC=C2C3=CC(CCCCCCCCCCCC)=C(C([Se]4)=CC=C4C5=CC=C(C6=C(CCCCCCCCCCCC)C=C([H])[Se]6)[Se]5)[Se]3)[Se]1,P6S,,,0.7,4.57,33,1.06,"Lee W-H, et al. Synthesis and characterization of new selenophene-based conjugated polymers for organic photovoltaic cells. Journal of Polymer Science Part a-Polymer Chemistry 50, 551-561 (2012)."
240,[H]C1=C(CCCCCCCCCCCC)C=C(C([Se]2)=CC(CCCCCCCCCCCC)=C2C3=CC(CCCCCCCCCCCC)=C(C([Se]4)=CC=C4C5=CC=C(C6=C(CCCCCCCCCCCC)C=C([H])[Se]6)[Se]5)[Se]3)[Se]1,TTP6S,,,0.71,5.72,41,1.67,"Lee W-H, et al. Synthesis and characterization of new selenophene-based conjugated polymers for organic photovoltaic cells. Journal of Polymer Science Part a-Polymer Chemistry 50, 551-561 (2012)."
241,FC1=C(C(CCCCCCC)=O)SC2=C(C(S3)=CC4=C3C(OCC(CC)CCCC)=C(C=C([H])S5)C5=C4OCC(CC)CCCC)SC([H])=C21,PBDTTT-CF,,,0.75,3.17,57,1.35,"Komura T, Santhakumar K, Kumar P, Shin P-K, Kojima K, Ochiai S. Evaluation of the characteristics of the organic thin film solar cell fabricated by poly 4,8-bis(2-ethylhexyloxy)-benzo 1,2-b:4,5-' b dithiophene-2,6-diyl-alt-(4-octanoyl-5-fluoro-thieno 3,4-b thiophene-2-carboxylate)-2,6-diyl / 6,6 -phenyl-C-71-butyric acid methyl ester. In: Organic Photovoltaics Xiii (ed^(eds Kafafi ZH, Brabec CJ, Lane PA) (2012)."
242,O=C(C1=C2C(/C=C/C3=CC=C(/C=C(C4=CC=C([N+]([O-])=O)C=C4)\C#N)C=C3)=CC=C1/C=C/C5=CC=C(/C=C(C6=CC=C([N+]([O-])=O)C=C6)\C#N)C=C5)N(C7CCCCC7)C2=O,SM,,,0.84,8.8,56,4.14,"Sharma GD, Mikroyannidis JA, Kurchania R, Thomas KRJ. Organic bulk heterojunction solar cells based on solution processable small molecules (A-pi-A) featuring 2-(4-nitrophenyl) acrylonitrile acceptors and phthalimide-based pi-linkers. Journal of Materials Chemistry 22, 13986-13995 (2012)."
243,[H]C(C=C1)=CC2=C1C(C=CC(C3=CC=C(C4=CC=C(C5=CC=C([H])S5)C6=NSN=C64)S3)=C7)=C7N2C(CCCCCCCC)CCCCCCCC,PCz3TB,,,0.66,4.52,41,1.22,"Lim E, Lee KK, Lee S. Synthesis and Characterization of Carbazole-Thiophene-based Conjugated Polymers for Organic Photovoltaic Cells. Mol. Cryst. Liq. Cryst. 551, 130-137 (2011)."
244,[H]C(S1)=CC=C1C(S2)=CC=C2C3=CC4=C(C=C3)C5=C(C=C([H])C=C5)N4C(CCCCCCCC)CCCCCCCC,PCzT2,,,0.74,3.47,38,0.97,"Lim E, Lee KK, Lee S. Synthesis and Characterization of Carbazole-Thiophene-based Conjugated Polymers for Organic Photovoltaic Cells. Mol. Cryst. Liq. Cryst. 551, 130-137 (2011)."
245,[H]C(C=C1)=CC2=C1C(C=CC(C3=CC(CCCCCC)=C(C4=CC=C(C5=CC=C(C6=C(CCCCCC)C=C([H])S6)S5)S4)S3)=C7)=C7N2C(CCCCCCCC)CCCCCCCC,PCzT4,,,0.66,2.04,40,0.4,"Lim E, Lee KK, Lee S. Synthesis and Characterization of Carbazole-Thiophene-based Conjugated Polymers for Organic Photovoltaic Cells. Mol. Cryst. Liq. Cryst. 551, 130-137 (2011)."
246,CCCCCCOC1=CC(C=NCCC[Si](C)(O[Si](C)(C)O[Si](C)(C)CCCC)C)=C(OCCCCCC)C=C1C=CC2=C(OCCCCCC)C=C(C=CC3=C(OCCCCCC)C=C(C=N[H])C(OCCCCCC)=C3)C(OCCCCCC)=C2,PAZ1,,,0.75,0.01636,75,0.9,"Palewicz M, Iwan A, Sibinski M, Sikora A, Mazurek B. Organic photovoltaic devices based on polyazomethine and fullerene. In: Emrs-C: Materials Devices and Economics Issues for Tomorrow's Photovoltaics (ed^(eds Cavallini A, Estreicher S, Kveder V, Sekiguchi T) (2011)."
247,N#C/C([N+]#[C-])=C1C=C(/C=C/C(C=C2)=CC=C2/C=C/C(C=C3)=CC=C3N(C4=CC=CC=C4)C5=CC=CC=C5)OC(/C=C/C(C=C6)=CC=C6/C=C/C(C=C7)=CC=C7N(C8=CC=CC=C8)C9=CC=CC=C9)=C\1,TPA¨CDCM¨CTPA,,,0.71,5.07,38,1.4,"Zhang J, Wu G, He C, Deng D, Li Y. Triphenylamine-containing D-A-D molecules with (dicyanomethylene)pyran as an acceptor unit for bulk-heterojunction organic solar cells. J. Mater. Chem. 21, 3768-3774 (2011)."
248,CCCCCCC1=C(/C=C/C2=CC=C(N(C3=CC=CC=C3)C4=CC=CC=C4)C=C2)SC(/C=C/C5=C/C(C=C(/C=C/C6=CC(CCCCCC)=C(/C=C/C7=CC=C(N(C8=CC=CC=C8)C9=CC=CC=C9)C=C7)S6)O5)=C(C#N)\[N+]#[C-])=C1,TPA¨CHTV¨CPM,,,0.78,6.78,39,2.1,"Zhang J, Wu G, He C, Deng D, Li Y. Triphenylamine-containing D-A-D molecules with (dicyanomethylene)pyran as an acceptor unit for bulk-heterojunction organic solar cells. J. Mater. Chem. 21, 3768-3774 (2011)."
249,N#C/C([N+]#[C-])=C1C=C(/C=C/C2=CC=C(/C=C/C3=CC=C(N(C4=CC=CC=C4)C5=CC=CC=C5)C=C3)S2)OC(/C=C/C6=CC=C(/C=C/C7=CC=C(N(C8=CC=CC=C8)C9=CC=CC=C9)C=C7)S6)=C/1,TPA¨CTV¨CPM,,,0.79,5.94,44,2.06,"Zhang J, Wu G, He C, Deng D, Li Y. Triphenylamine-containing D-A-D molecules with (dicyanomethylene)pyran as an acceptor unit for bulk-heterojunction organic solar cells. J. Mater. Chem. 21, 3768-3774 (2011)."
250,[H]C1=CC=C(C2=CC=C(C3=CC=C(C4=CC(C(CCCCCCCC)(CCCCCCCC)C5=C6C=CC([H])=C5)=C6C=C4)S3)C7=NSN=C72)S1,CP-I,,,0.95,9.7,44,3.7,"Troshin PA, et al. Material solubility and molecular compatibility effects in the design of fullerene/polymer composites for organic bulk heterojunction solar cells. Journal of Materials Chemistry 22, 18433-18441 (2012)."
251,[H]C1=CC=C(C2=CC=C(C3=CC=C(C4=CC(C5(CCCCCCCC)CCCCCCCC)=C(C6=C5C=C([H])S6)S4)S3)C7=NSN=C72)S1,CP-II,,,0.55,10.7,36,2.12,"Troshin PA, et al. Material solubility and molecular compatibility effects in the design of fullerene/polymer composites for organic bulk heterojunction solar cells. Journal of Materials Chemistry 22, 18433-18441 (2012)."
252,[H]C1=C(CCCC)C=C(C2=C(CCCC)C=C([H])S2)S1,P3BT,,,0.6,8.7,41,2.2,"Troshin PA, et al. Material solubility and molecular compatibility effects in the design of fullerene/polymer composites for organic bulk heterojunction solar cells. Journal of Materials Chemistry 22, 18433-18441 (2012)."
253,[H]C1=C(CCCCCCCCCCCC)C=C(C2=C(CCCCCCCCCCCC)C=C([H])S2)S1,P3DDT,,,0.62,4.4,38,1,"Troshin PA, et al. Material solubility and molecular compatibility effects in the design of fullerene/polymer composites for organic bulk heterojunction solar cells. Journal of Materials Chemistry 22, 18433-18441 (2012)."
254,[H]C1=C(CCCCCCCCCC)C=C(C2=C(CCCCCCCCCC)C=C([H])S2)S1,P3DT,,,0.65,7.9,38,1.9,"Troshin PA, et al. Material solubility and molecular compatibility effects in the design of fullerene/polymer composites for organic bulk heterojunction solar cells. Journal of Materials Chemistry 22, 18433-18441 (2012)."
255,[H]C1=C(CCCCCCC)C=C(C2=C(CCCCCCC)C=C([H])S2)S1,P3HepT,,,0.63,9.1,49,2.8,"Troshin PA, et al. Material solubility and molecular compatibility effects in the design of fullerene/polymer composites for organic bulk heterojunction solar cells. Journal of Materials Chemistry 22, 18433-18441 (2012)."
256,[H]C1=C(CCCCCCCC)C=C(C2=C(CCCCCCCC)C=C([H])S2)S1,P3OT,,,0.65,8.6,44,2.4,"Troshin PA, et al. Material solubility and molecular compatibility effects in the design of fullerene/polymer composites for organic bulk heterojunction solar cells. Journal of Materials Chemistry 22, 18433-18441 (2012)."
257,[H]C1=C(CCCCC)C=C(C2=C(CCCCC)C=C([H])S2)S1,P3PT,,,0.62,10.6,53,3.5,"Troshin PA, et al. Material solubility and molecular compatibility effects in the design of fullerene/polymer composites for organic bulk heterojunction solar cells. Journal of Materials Chemistry 22, 18433-18441 (2012)."
258,[H]C1=CC=C(C2=CC=C(C3=CC=C(C4=CC(C(CC(CC)CCCC)(CC(CC)CCCC)C5=C6C=CC([H])=C5)=C6C=C4)S3)C7=NSN=C72)S1,APFO-3,,,0.96,4.49,40.5,1.75,"Neophytou M, et al. 2-(2,3,4,5,6-Pentafluorophenyl)-1H-benzo d imidazole, a fluorine-rich building block for the preparation of conjugated polymer donors for organic solar cell applications. Polymer Chemistry 3, 2236-2243 (2012)."
259,FC1=C(F)C(F)=C(F)C(F)=C1C2=NC3=C(C4=CC=C([H])S4)C=CC(C5=CC=C(C6=CC(C(CC(CC)CCCC)(CC(CC)CCCC)C7=C8C=CC([H])=C7)=C8C=C6)S5)=C3N2,PFTPFBZT,,,0.49,1.25,38.8,0.24,"Neophytou M, et al. 2-(2,3,4,5,6-Pentafluorophenyl)-1H-benzo d imidazole, a fluorine-rich building block for the preparation of conjugated polymer donors for organic solar cell applications. Polymer Chemistry 3, 2236-2243 (2012)."
260,CCCCCCCCOC1=CC=C(C2=NC3=C(C4=CC=C(C5=CC(CCCCCCCCCCCCCCCC)=C(C6=CC(C7S6)=CC=C8C7C=CC9=C8SC(C%10=C(CCCCCCCCCCCCCCCC)C=C([H])S%10)=C9)S5)S4)C=CC(C%11=CC=C([H])S%11)=C3N=C2C%12=CC=C(OCCCCCCCC)C=C%12)C=C1,PTNDTT-QX,,,0.69,4.52,46,1.44,"Dutta P, Park H, Lee W-H, Kim K, Kang IN, Lee S-H. Naphtho 1,2-b:5,6-b ' dithiophene-based conjugated polymer as a new electron donor for bulk heterojunction organic solar cells. Polymer Chemistry 3, 601-604 (2012)."
261,O=C1N(CC(CCCCCCCC)CCCCCCCCCC)C(C2OC([H])=CC2)=C3C1=C(C4=CC=C(C5=CC=C6C=C7C=CC([H])=CC7=CC6=C5)O4)N(CC(CCCCCCCC)CCCCCCCCCC)C3=O,PDPP-FAF,,,0.69,7.8,45,2.5,"Sonar P, Singh SP, Williams EL, Li Y, Soh MS, Dodabalapur A. Furan containing diketopyrrolopyrrole copolymers: synthesis, characterization, organic field effect transistor performance and photovoltaic properties. Journal of Materials Chemistry 22, 4425-4435 (2012)."
262,O=C1N(CC(CCCCCCCC)CCCCCCCCCC)C(C2=CC=C([H])O2)=C3C1=C(C4=CC=C(C5=CC=C6C=C([H])C=CC6=C5)O4)N(CC(CCCCCCCC)CCCCCCCCCC)C3=O,PDPP-FNF,,,0.71,8.6,42,2.6,"Sonar P, Singh SP, Williams EL, Li Y, Soh MS, Dodabalapur A. Furan containing diketopyrrolopyrrole copolymers: synthesis, characterization, organic field effect transistor performance and photovoltaic properties. Journal of Materials Chemistry 22, 4425-4435 (2012)."
263,O=C1N(CC(CCCCCCCC)CCCCCCCCCC)C(C2=CC=C([H])O2)=C3C1=C(C4=CC=C(C5=CC=C([H])C=C5)O4)N(CC(CCCCCCCC)CCCCCCCCCC)C3=O,PDPP-FPF,,,0.56,3.6,37,0.78,"Sonar P, Singh SP, Williams EL, Li Y, Soh MS, Dodabalapur A. Furan containing diketopyrrolopyrrole copolymers: synthesis, characterization, organic field effect transistor performance and photovoltaic properties. Journal of Materials Chemistry 22, 4425-4435 (2012)."
264,CC([Si](C#CC1=C2C=C(C3=CC=C(C4=CC=C(C5=CC=C(N(C6=CC(C(C)(C)C7=C8C=CC=C7)=C8C=C6)C9=CC(C(C)(C)C%10=C%11C=CC=C%10)=C%11C=C9)C=C5)S4)S3)C=CC2=C(C#C[Si](C(C)C)(C(C)C)C(C)C)C%12=CC(C%13=CC=C(C%14=CC=C(C%15=CC=C(N(C%16=CC(C(C)(C)C%17=C%18C=CC=C%17)=C%18C=C%16)C%19=CC(C(C)(C)C%20=C%21C=CC=C%20)=C%21C=C%19)C=C%15)S%14)S%13)=CC=C1%12)(C(C)C)C(C)C)C,TIPSAntBT¨CbisDMFA,,,0.85,8.58,41,2.96,"Choi H, Ko HM, Cho N, Song K, Lee JK, Ko J. Electron-Rich Anthracene Semiconductors Containing Triarylamine for Solution-Processed Small-Molecule Organic Solar Cells. ChemSusChem 5, 2045-2052 (2012)."
265,CC([Si](C#CC1=C2C=C(C3=CC=C(C4=CC=C(C5=CC=C(C=C5)N(C6=CC=CC=C6)C7=CC=CC=C7)S4)S3)C=CC2=C(C#C[Si](C(C)C)(C(C)C)C(C)C)C8=CC(C9=CC=C(C%10=CC=C(C%11=CC=C(C=C%11)N(C%12=CC=CC=C%12)C%13=CC=CC=C%13)S%10)S9)=CC=C18)(C(C)C)C(C)C)C,TIPSAntBT¨CTPA,,,0.72,6.07,40,1.97,"Choi H, Ko HM, Cho N, Song K, Lee JK, Ko J. Electron-Rich Anthracene Semiconductors Containing Triarylamine for Solution-Processed Small-Molecule Organic Solar Cells. ChemSusChem 5, 2045-2052 (2012)."
266,CCCCCCCCOC1=C([H])C=C(OCCCCCCCC)C(C#CC2=C3C=CC=CC3=C(C#CC4=CC(OCCCCCCCC)=C(CCC5=CC(OCC(CC)CCCC)=C(/C=C/[H])C=C5OCC(CC)CCCC)C=C4OCCCCCCCC)C6=CC=CC=C26)=C1,P1,,,0.774,8.3,61,3.9,"Troshin PA, et al. Material structure-composite morphology-photovoltaic performance relationship for organic bulk heterojunction solar cells. Chem. Commun. 48, 9477-9479 (2012)."
267,[H]C1=CC(C2=CC=C(CCCCCCCCCC)S2)=C(C3=CC=C(C4=CC=C(C5=C(C6=CC=C(CCCCCCCCCC)S6)C=C([H])S5)S4)S3)S1,PDTQT,,,0.91,9.9,35,3.2,"Cha H, et al. A side chain-modified quaterthiophene derivative for enhancing the performance of organic solar cell devices. Journal of Materials Chemistry 22, 15141-15145 (2012)."
268,[H]C1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C4=C(CCCCCCCCCCCC)C=C([H])S4)S3)S2)S1,PQT-C12,,,0.55,7.7,36,1.5,"Cha H, et al. A side chain-modified quaterthiophene derivative for enhancing the performance of organic solar cell devices. Journal of Materials Chemistry 22, 15141-15145 (2012)."
269,O=C1N(CC(CCCCCCCC)CCCCCCCCCC)C(C2=CC=C(C3=CC4=C(C=C(CCCCCCCCCC)S5)C5=C(C=C([H])S6)C6=C4S3)S2)=C7C1=C(C8=CC=C([H])S8)N(CC(CCCCCCCC)CCCCCCCCCC)C7=O,BTT-DPP,,,0.71,6.3,60,2.68,"Nielsen CB, et al. Random benzotrithiophene-based donor-acceptor copolymers for efficient organic photovoltaic devices. Chem. Commun. 48, 5832-5834 (2012)."
270,[H]C1=CC=C(C2=C(CCCCCCCCCCCC)C([Ge]3(CCCC)CCCC)=C(C4=C3C(CCCCCCCCCCCC)=C([H])S4)S2)C5=NSN=C51,BuGeBT,,,0.9,3.71,45,1.5,"Kim JS, Fei Z, James DT, Heeney M, Kim J-S. A comparison between dithienosilole and dithienogermole donor-acceptor type co-polymers for organic bulk heterojunction photovoltaic devices. Journal of Materials Chemistry 22, 9975-9982 (2012)."
271,[H]C1=CC=C(C2=C(CCCCCCCCCCCC)C([Si]3(CCCC)CCCC)=C(C4=C3C(CCCCCCCCCCCC)=C([H])S4)S2)C5=NSN=C51,BuSiBT,,,0.81,2.03,36,0.59,"Kim JS, Fei Z, James DT, Heeney M, Kim J-S. A comparison between dithienosilole and dithienogermole donor-acceptor type co-polymers for organic bulk heterojunction photovoltaic devices. Journal of Materials Chemistry 22, 9975-9982 (2012)."
272,[H]C1=CC=C(C2=C(CCCCCCCCCCCC)C([Ge]3(C)C)=C(C4=C3C(CCCCCCCCCCCC)=C([H])S4)S2)C5=NSN=C51,MeGeBT,,,0.94,6.11,46,2.66,"Kim JS, Fei Z, James DT, Heeney M, Kim J-S. A comparison between dithienosilole and dithienogermole donor-acceptor type co-polymers for organic bulk heterojunction photovoltaic devices. Journal of Materials Chemistry 22, 9975-9982 (2012)."
273,[H]C1=CC=C(C2=C(CCCCCCCCCCCC)C([Si]3(C)C)=C(C4=C3C(CCCCCCCCCCCC)=C([H])S4)S2)C5=NSN=C51,MeSiBT,,,0.94,4.29,45,1.84,"Kim JS, Fei Z, James DT, Heeney M, Kim J-S. A comparison between dithienosilole and dithienogermole donor-acceptor type co-polymers for organic bulk heterojunction photovoltaic devices. Journal of Materials Chemistry 22, 9975-9982 (2012)."
274,C1(/C2=N/3)=C(C=CC=C1)/C4=N/C5=N/C(C6=C5C=CC=C6)=N\C(N7[Pb]N42)=C8C=CC=CC8=C7/N=C9C%10=C(C=CC=C%10)C3=N/9,CuI (0.5)¨CPbPc (30),,,0.46,8.85,63,2.58,"Shim H-S, et al. Enhancement of near-infrared absorption with high fill factor in lead phthalocyanine-based organic solar cells. Journal of Materials Chemistry 22, 9077-9081 (2012)."
275,[H]C1=CC=C(C2=NSN=C21)C(S3)=CC4=C3C5=C([Ge]4(CC(CC)CCCC)CC(CC)CCCC)C=C(C([Ge]6(CC(CC)CCCC)CC(CC)CCCC)=C5)C7=C6C=C([H])S7,PGeTPTBT,,,0.86,10.1,58,5.02,"Fei Z, et al. Germaindacenodithiophene based low band gap polymers for organic solar cells. Chem. Commun. 48, 2955-2957 (2012)."
276,CCCCCCCCCCC(CCCCCCCC)CN(C1=C2SC(C3=CC4=C(C=C([H])S4)S3)=N1)C5=C2SC([H])=N5,PTzBT,,,0.61,9.4,53,3,"Xia R, Al-Hashimi M, Tsoi WC, Heeney M, Bradley DDC, Nelson J. Fused pyrrolo 3,2-d:4,5-d ' bisthiazole-containing polymers for using in high-performance organic bulk heterojunction solar cells. Sol. Energy Mater. Sol. Cells 96, 112-116 (2012)."
277,CCCCCCCCCCC(CCCCCCCC)CN(C1=C2SC(C3=CC=C([H])[Se]3)=N1)C4=C2SC([H])=N4,PTzSe,,,0.63,4.7,60,1.7,"Xia R, Al-Hashimi M, Tsoi WC, Heeney M, Bradley DDC, Nelson J. Fused pyrrolo 3,2-d:4,5-d ' bisthiazole-containing polymers for using in high-performance organic bulk heterojunction solar cells. Sol. Energy Mater. Sol. Cells 96, 112-116 (2012)."
278,CCCCCCCCCCC(CCCCCCCC)CN(C1=C2SC(C3=CC=C([H])S3)=N1)C4=C2SC([H])=N4,PTzT,,,0.64,2.8,44,0.8,"Xia R, Al-Hashimi M, Tsoi WC, Heeney M, Bradley DDC, Nelson J. Fused pyrrolo 3,2-d:4,5-d ' bisthiazole-containing polymers for using in high-performance organic bulk heterojunction solar cells. Sol. Energy Mater. Sol. Cells 96, 112-116 (2012)."
279,CCCCCCCCCCC(CCCCCCCC)CN(C1=C2SC(C3=CC=C(C4=CC=C([H])S4)S3)=N1)C5=C2SC([H])=N5,PTzTT,,,0.66,6,51,2,"Xia R, Al-Hashimi M, Tsoi WC, Heeney M, Bradley DDC, Nelson J. Fused pyrrolo 3,2-d:4,5-d ' bisthiazole-containing polymers for using in high-performance organic bulk heterojunction solar cells. Sol. Energy Mater. Sol. Cells 96, 112-116 (2012)."
280,[H]C1=CC=C(C2=CC=C(C3=CC=C(C(S4)=CC(C4=C5C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C#C[Si](C(C)C)(C(C)C)C(C)C)C6=C5C=C([H])S6)S3)C7=NN(C(CCCCCCCC)CCCCCCCC)N=C72)S1,PTIPSBDT- DTBTz,,,0.8,12.69,55,5.53,"Kim J-H, et al. High-Crystalline Medium-Band-Gap Polymers Consisting of Benzodithiophene and Benzotriazole Derivatives for Organic Photovoltaic Cells. ACS Appl. Mater. Interfaces 5, 12820-12831 (2013)."
281,CC([Si](C#CC1=C(C=CC=C2)C2=C3C4=C5C(C=C3)=C(C#C[Si](C(C)C)(C(C)C)C(C)C)C6=CC=CC=C6C5=CC=C41)(C(C)C)C(C)C)C,TIPS©\DBC,,,0.64,4.88,51,1.58,"Scholes FH, et al. Intraphase Microstructure-Understanding the Impact on Organic Solar Cell Performance. Adv. Funct. Mater. 23, 5655-5662 (2013)."
282,Cl[In]1N2C3=C4C=CC=CC4=C2/N=C5C6=C(C=CC=C6)C(/N=C7C8=C(C=CC=C8)/C(N/71)=N/C9=N/C(C%10=C9C=CC=C%10)=N\3)=N/5,InClPc,,,0.62,7.05,45,2,"Abe Y, Yokoyama T, Matsuo Y. Low-LUMO 56 pi-electron fullerene acceptors bearing electron-withdrawing cyano groups for small-molecule organic solar cells. Org. Electron. 14, 3306-3311 (2013)."
283,CCCCCCCCC1=C(C2=CC=C(C3=CC=C(C4=CC=C([H])S4)S3)S2)SC(C5=CC=C([H])S5)=C1CCCCCCCC,PBTOT,,,0.68,8.9,51.9,3.2,"Jeon CW, et al. Synthesis and characterization of poly(dialkylterthiophene-bithiophene) and poly(dialkylterthiophene-thienothiophene) for organic thin film transistors and organic photovoltaic cells. Synth. Met. 185, 159-166 (2013)."
284,CCCCCCCCC1=C(C2=CC=C(C3=CC4=C(S3)C=C([H])S4)S2)SC(C5=CC=C([H])S5)=C1CCCCCCCC,PTTOT,,,1,0.1,83.4,0.096,"Jeon CW, et al. Synthesis and characterization of poly(dialkylterthiophene-bithiophene) and poly(dialkylterthiophene-thienothiophene) for organic thin film transistors and organic photovoltaic cells. Synth. Met. 185, 159-166 (2013)."
285,O=C1N(CC(CCCCCC)CCCCCCCC)C(C2=CC=C(C3=CC(CCCCCC)=C(C4=CC=C([H])S4)S3)S2)=C5C1=C(C6=CC=C(C7=C(CCCCCC)C=C([H])S7)S6)N(CC(CCCCCC)CCCCCCCC)C5=O,pDPP5T-2,,,0.56,15.92,64,5.71,"Li N, et al. Towards 15% energy conversion efficiency: a systematic study of the solution-processed organic tandem solar cells based on commercially available materials. Energy & Environmental Science 6, 3407-3413 (2013)."
286,[H]C1=C(CCCCCC)N=C(C2=C(CCCCCC)C=C(C3=C(CCCCCC)C=C([H])S3)S2)S1,PTTTz,,,0.94,7.5,64,4.5,"Bronstein H, et al. Isostructural, Deeper Highest Occupied Molecular Orbital Analogues of Poly(3-hexylthiophene) for High-Open Circuit Voltage Organic Solar Cells. Chem. Mater. 25, 4239-4249 (2013)."
287,[H]C1=C(CCCCCC)N=C(C2=C(CCCCCC)C=C([H])S2)S1,PTTz,,,0.8,6.7,65,3.5,"Bronstein H, et al. Isostructural, Deeper Highest Occupied Molecular Orbital Analogues of Poly(3-hexylthiophene) for High-Open Circuit Voltage Organic Solar Cells. Chem. Mater. 25, 4239-4249 (2013)."
288,CC1=CC(CCCCCC)=C(C)S1,P3HT,,,0.75,11.94,54,4.8,"Xu M-F, et al. Aqueous Solution-Processed GeO2: An Anode Interfacial Layer for High Performance and Air-Stable Organic Solar Cells. ACS Appl. Mater. Interfaces 5, 10866-10873 (2013)."
289,[H]C1=C(CCCCCC)C=C(C2=CC=C(C3=CC(CCCCCC)=C(C4=CC5=C(C=C(C6(CCCCCCCCCCCCCCC)OCC(CCCC)(CCCC)CO6)S7)C7=C(C=C([H])S8)C8=C5S4)S3)C9=NSN=C92)S1,BTT-DTBT-Bu,,,0.77,6.91,0.37,1.97,"Nielsen CB, Ashraf RS, Rossbauer S, Anthopoulos T, McCulloch I. Post-Polymerization Ketalization for Improved Organic Photovoltaic Materials. Macromolecules 46, 7727-7732 (2013)."
290,[H]C1=C(CCCCCC)C=C(C2=CC=C(C3=CC(CCCCCC)=C(C4=CC5=C(C=C(C6(CCCCCCCCCCCCCCC)OCC(C)(C)CO6)S7)C7=C(C=C([H])S8)C8=C5S4)S3)C9=NSN=C92)S1,BTT-DTBT-Me,,,0.71,4.76,48,1.63,"Nielsen CB, Ashraf RS, Rossbauer S, Anthopoulos T, McCulloch I. Post-Polymerization Ketalization for Improved Organic Photovoltaic Materials. Macromolecules 46, 7727-7732 (2013)."
291,CCCCCCCCC1(CCCCCCCC)C2=C(C3=C1C=C([H])S3)SC(C4=CC(C5(F)F)=C(C6=C5C=C([H])S6)S4)=C2,P1,,,0.55,5.27,43,1.24,"Drozdov FV, et al. Novel Cyclopentadithiophene-Based D-A Copolymers for Organic Photovoltaic Cell Applications. Macromol. Chem. Phys. 214, 2144-2156 (2013)."
292,[H]C1=CC2=C(C3=C(C2(F)F)C=C(C4=CC(C5(CC(CC)CCCC)CC(CC)CCCC)=C(C6=C5C=C([H])S6)S4)S3)S1,P2,,,0.516,2.1,37,0.41,"Drozdov FV, et al. Novel Cyclopentadithiophene-Based D-A Copolymers for Organic Photovoltaic Cell Applications. Macromol. Chem. Phys. 214, 2144-2156 (2013)."
293,[H]C1=CC2=C(C3=C(C2(F)F)C=C(C4=CC([Si]5(CCCCCCCC)CCCCCCCC)=C(C6=C5C=C([H])S6)S4)S3)S1,P3,,,0.72,2.57,39,0.73,"Drozdov FV, et al. Novel Cyclopentadithiophene-Based D-A Copolymers for Organic Photovoltaic Cell Applications. Macromol. Chem. Phys. 214, 2144-2156 (2013)."
294,[H]C1=CC2=C(C3=C(C2(F)F)C=C(C4=CC([Si]5(CC(CC)CCCC)CC(CC)CCCC)=C(C6=C5C=C([H])S6)S4)S3)S1,P4,,,0.62,8.51,45,2.4,"Drozdov FV, et al. Novel Cyclopentadithiophene-Based D-A Copolymers for Organic Photovoltaic Cell Applications. Macromol. Chem. Phys. 214, 2144-2156 (2013)."
295,CCCCC(CC)C(C1=CC2=C(C(S3)=CC(C3=C4C5=CC=C(CC(CC)CCCC)S5)=C(C6=CC=C(CC(CC)CCCC)S6)C7=C4C=C([H])S7)SC([H])=C2S1)=O,PBDTTT©\C©\T,,,0.85,8.86,54.1,4.03,"Zhang X, et al. A Potential Perylene Diimide Dimer-Based Acceptor Material for Highly Efficient Solution-Processed Non-Fullerene Organic Solar Cells with 4.03% Efficiency. Adv. Mater. 25, 5791-+ (2013)."
296,CCCCCCC(S1)=CC=C1C2=C(C3=CC4=C(C5=CC(C(C6=CC=C(CCCCCC)C=C6)(C7=CC=C(CCCCCC)C=C7)C8=C9SC(C%10=C(C%11=CC=C(CCCCCC)S%11)C=C(C%12=CC=C([H])C%13=NSN=C%13%12)S%10)=C8)=C9C=C5C4(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15)S3)SC([H])=C2,PIDTHT©\BT,,,0.933,9.1,52.7,4.5,"Chen C-P, Hsu H-L. Increasing the Open-Circuit Voltage in High-Performance Organic Photovoltaic Devices through Conformational Twisting of an Indacenodithiophene-Based Conjugated Polymer. Macromol. Rapid Commun. 34, 1623-1628 (2013)."
297,Cl[In]1N2C3=C4C=CC=CC4=C2/N=C5C6=C(C=CC=C6)C(/N=C7C8=C(C=CC=C8)/C(N/71)=N/C9=N/C(C%10=C9C=CC=C%10)=N\3)=N/5,ClInPc,,,1.07,8.43,40,3.62,"Sutty S, Williams G, Aziz H. Role of the donor material and the donor-acceptor mixing ratio in increasing the efficiency of Schottky junction organic solar cells. Org. Electron. 14, 2392-2400 (2013)."
298,[H]C1=C2N=C3C=CC4=CC=CC=C4C3=NC2=C(C(S5)=CC(C5=C6OCC(CC)CCCC)=C(OCC(CC)CCCC)C7=C6C=C([H])S7)C=C1,PBDT©\BPz,,,0.72,7.74,37,2.04,"Kim J-H, et al. New quinoxaline derivatives as accepting units in donor-acceptor type low-band gap polymers for organic photovoltaic cells. Journal of Polymer Science Part a-Polymer Chemistry 51, 4136-4149 (2013)."
299,[H]C1=C2N=C3C=C(N4C5=C(C6=C4C=CC=C6)C=CC=C5)C7=CC=CC=C7C3=NC2=C(C(S8)=CC(C8=C9OCC(CC)CCCC)=C(OCC(CC)CCCC)C%10=C9C=C([H])S%10)C=C1,PBDT©\CBPz,,,0.78,9.68,51,3.87,"Kim J-H, et al. New quinoxaline derivatives as accepting units in donor-acceptor type low-band gap polymers for organic photovoltaic cells. Journal of Polymer Science Part a-Polymer Chemistry 51, 4136-4149 (2013)."
300,[H]C1=C2C(N=C3C4=CC=CC=C4C5=CC=CC=C5C3=N2)=C(C(S6)=CC(C6=C7OCC(CC)CCCC)=C(OCC(CC)CCCC)C8=C7C=C([H])S8)C=C1,PBDT©\DBPz,,,0.7,7.63,37,2.01,"Kim J-H, et al. New quinoxaline derivatives as accepting units in donor-acceptor type low-band gap polymers for organic photovoltaic cells. Journal of Polymer Science Part a-Polymer Chemistry 51, 4136-4149 (2013)."
301,[H]C1=C2N=CC=NC2=C(C(S3)=CC(C3=C4OCC(CC)CCCC)=C(OCC(CC)CCCC)C5=C4C=C([H])S5)C=C1,PBDT©\Qx,,,0.65,6.3,37,1.54,"Kim J-H, et al. New quinoxaline derivatives as accepting units in donor-acceptor type low-band gap polymers for organic photovoltaic cells. Journal of Polymer Science Part a-Polymer Chemistry 51, 4136-4149 (2013)."
302,O=C(C1=C(F)C2=C([H])SC(C(S3)=CC(C3=C4OCC(CC)CCCC)=C(OCC(CC)CCCC)C5=C4C=C([H])S5)=C2S1)OCC(CC)CCCC,PTB7,,,0.71,18.07,68.1,8.74,"Zhang D, et al. Plasmonic Electrically Functionalized TiO2 for High-Performance Organic Solar Cells. Adv. Funct. Mater. 23, 4255-4261 (2013)."
303,O=C1C2=C(C3=NC4=C([H])C(OCCCCCCCC)=C(OCCCCCCCC)C(C5=CC=C([H])S5)=C4N=C31)C=CC=C2,P1,,,0.77,2.49,40,0.78,"Chen J, et al. D-A Conjugated Polymers Based on Tetracyclic Acceptor Units: Synthesis and Application in Organic Solar Cells. Macromol. Chem. Phys. 214, 2054-2060 (2013)."
304,O=C1C2=C(C3=NC4=C([H])C(OCCCCCCCC)=C(OCCCCCCCC)C(C5=CC([Si]6(CC(CC)CCCC)CC(CC)CCCC)=C(C7=C6C=C([H])S7)S5)=C4N=C31)C=CC=C2,P2,,,0.65,1.32,41,0.41,"Chen J, et al. D-A Conjugated Polymers Based on Tetracyclic Acceptor Units: Synthesis and Application in Organic Solar Cells. Macromol. Chem. Phys. 214, 2054-2060 (2013)."
305,O=C1C2=C(C3=NC4=C([H])C(OCCCCCCCC)=C(OCCCCCCCC)C(C5=CC(CCCCCC)=C(C6=CC([Si]7(CC(CC)CCCC)CC(CC)CCCC)=C(C8=C7C=C([H])S8)S6)S5)=C4N=C31)C=CC=C2,P3,,,0.46,7.18,58,1.93,"Chen J, et al. D-A Conjugated Polymers Based on Tetracyclic Acceptor Units: Synthesis and Application in Organic Solar Cells. Macromol. Chem. Phys. 214, 2054-2060 (2013)."
306,[H]C1=CC2=C(C=C(C=C(C3=CC=C([H])C4=NN(C(CCCCCCCC)CCCCCCCC)N=C43)S5)C5=C2)S1,PBDT-BTz,,,0.83,6.61,58,3.17,"Kim J-H, Kim HU, Lee J-K, Park M-J, Hyun MH, Hwang D-H. Semiconducting copolymers comprising benzodithiophene and benzotriazole derivatives for organic photovoltaic cells. Synth. Met. 179, 18-26 (2013)."
307,CC([Si](C#CC1=C2C(C=C(C3=CC=C([H])C4=NN(C(CCCCCCCC)CCCCCCCC)N=C43)S2)=C(C#C[Si](C(C)C)(C(C)C)C(C)C)C5=C1C=C([H])S5)(C(C)C)C(C)C)C,PTIPSBDT-BTz,,,0.86,10.48,46,4.16,"Kim J-H, Kim HU, Lee J-K, Park M-J, Hyun MH, Hwang D-H. Semiconducting copolymers comprising benzodithiophene and benzotriazole derivatives for organic photovoltaic cells. Synth. Met. 179, 18-26 (2013)."
308,CCCCCCCCOC1=C(C2=CC=CS2)C3=N[Se]N=C3C(C4=CC=C(C5=CC=C(N(C6=CC=C(C7=CC=C(C8=C(OCCCCCCCC)C(OCCCCCCCC)=C(C9=CC=CS9)C%10=N[Se]N=C%108)S7)C=C6)C%11=CC=C(C%12=CC=C(C%13=C(OCCCCCCCC)C(OCCCCCCCC)=C(C%14=CC=CS%14)C%15=N[Se]N=C%15%13)S%12)C=C%11)C=C5)S4)=C1OCCCCCCCC,M1,,,0.91,4.54,37.2,1.54,"Guo X, Xiao L, Tang W, Liu B, Cui R, Zou Y. Synthesis and characterization of a new solution-processable star-shaped small molecule based on 5,6-bis(n-octyloxy)-2,1,3-benzoselenadiazole for organic solar cells. Journal of Materials Science 48, 5833-5839 (2013)."
309,O=C1N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C(C2=CC3=C(C=C([H])S3)S2)=C4C1=C(C5=CC6=C(C=C(C7=CC=C([H])S7)S6)S5)N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C4=O,P1,,,0.62,12.6,53,4.1,"Meager I, et al. Alkyl Chain Extension as a Route to Novel Thieno 3,2-b thiophene Flanked Diketopyrrolopyrrole Polymers for Use in Organic Solar Cells and Field Effect Transistors. Macromolecules 46, 5961-5967 (2013)."
310,O=C1N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C(C(S2)=CC3=C2C=C(C4=CC5=C(C=C([H])S5)S4)S3)=C6C1=C(C7=CC8=C(C=C([H])S8)S7)N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C6=O,P2,,,0.48,15.7,50,3.8,"Meager I, et al. Alkyl Chain Extension as a Route to Novel Thieno 3,2-b thiophene Flanked Diketopyrrolopyrrole Polymers for Use in Organic Solar Cells and Field Effect Transistors. Macromolecules 46, 5961-5967 (2013)."
311,O=C1N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C(C2=CC3=C(C=C(C4=CC=C([H])C5=NSN=C54)S3)S2)=C6C1=C(C7=CC8=C(C=C([H])S8)S7)N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C6=O,P3,,,0.68,2.9,55,1.1,"Meager I, et al. Alkyl Chain Extension as a Route to Novel Thieno 3,2-b thiophene Flanked Diketopyrrolopyrrole Polymers for Use in Organic Solar Cells and Field Effect Transistors. Macromolecules 46, 5961-5967 (2013)."
312,O=C1N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C(C2=CC3=C(C=C([H])S3)S2)=C4C1=C(C5=CC6=C(C=C(C7=CC=C([H])C=C7)S6)S5)N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C4=O,P4,,,0.61,11.7,57,4,"Meager I, et al. Alkyl Chain Extension as a Route to Novel Thieno 3,2-b thiophene Flanked Diketopyrrolopyrrole Polymers for Use in Organic Solar Cells and Field Effect Transistors. Macromolecules 46, 5961-5967 (2013)."
313,C1(C=CC=C2)=C2C3=N/C1=N\C4=C5C(C=CC=C5)=C6N4[Cu]N7/C(C8=C(C=CC=C8)/C7=N/3)=N\C(C9=C/%10C=CC=C9)=NC%10=N/6,CuPc,,,0.49,17.82,40,3.51,"Chou D-W, Chen K-L, Huang C-J, Tsao Y-J, Chen W-R, Meen T-H. Efficient small-molecule organic solar cells incorporating a doped buffer layer. Thin Solid Films 536, 235-239 (2013)."
314,[H]C(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=CC(N4C5=CC6=C(C7=C5C=CC=C7)N=C8C=CC=CC8=N6)=C(C9=C4C=C([H])C=C9)C=C3)S%10)C%10=C2OCC(CC)CCCC,PBDT©\CBP,,,0.77,6.88,39,2.08,"Kim J-H, et al. New low band-gap semiconducting polymers consisting of 5-(9H-carbazol-9-yl)benzo a phenazine as a new acceptor unit for organic photovoltaic cells. Journal of Polymer Science Part a-Polymer Chemistry 51, 2354-2365 (2013)."
315,[H]C(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=CC(N4C(CCCCCCCC)CCCCCCCC)=C(C5=C4C=C([H])C=C5)C=C3)S6)C6=C2OCC(CC)CCCC,PBDT©\CBZ,,,0.71,1.3,29,0.26,"Kim J-H, et al. New low band-gap semiconducting polymers consisting of 5-(9H-carbazol-9-yl)benzo a phenazine as a new acceptor unit for organic photovoltaic cells. Journal of Polymer Science Part a-Polymer Chemistry 51, 2354-2365 (2013)."
316,[H]C(S1)=CC2=C1C(C3=CC=C(CCCCCCCC)S3)=C(C=C(C4=CC(N5C6=CC7=C(C8=C6C=CC=C8)N=C9C=CC=CC9=N7)=C(C%10=C5C=C([H])C=C%10)C=C4)S%11)C%11=C2C%12=CC=C(CCCCCCCC)S%12,PBDTT©\CBP,,,0.71,4.05,30,0.9,"Kim J-H, et al. New low band-gap semiconducting polymers consisting of 5-(9H-carbazol-9-yl)benzo a phenazine as a new acceptor unit for organic photovoltaic cells. Journal of Polymer Science Part a-Polymer Chemistry 51, 2354-2365 (2013)."
317,CCCCCCCCC(CCCCCCCC)N1C2=CC([H])=CC=C2C3=C1C=C(C4=CC=C(C5=CC=C(C6=CC=C([H])S6)C7=NSN=C75)S4)C=C3,"P(2,7C-DTBT)",,,0.91,12.6,40,4.6,"Cha H, Lee GY, Fu Y, Kim YJ, Park CE, Park T. Simultaneously Grasping and Self-Organizing Photoactive Polymers for Highly Reproducible Organic Solar Cells with Improved Efficiency. Adv. Energy Mater. 3, 1018-1024 (2013)."
318,[H]C1=CC=C(C(S2)=CC=C2C(C3=NSN=C34)=C(OCCCCCCCC)C(OCCCCCCCC)=C4C5=CC=C(C(S6)=CC=C6C(C=C7)=CC8=C7C9=C(C8(CCCCCCCC)CCCCCCCC)C=C([H])C=C9)S5)S1,PFDT2BT©\8,,,0.92,10.44,64.5,6.2,"Watters DC, Yi H, Pearson AJ, Kingsley J, Iraqi A, Lidzey D. Fluorene-Based Co-polymer with High Hole Mobility and Device Performance in Bulk Heterojunction Organic Solar Cells. Macromol. Rapid Commun. 34, 1157-1162 (2013)."
319,[H]C1=C(C(N(CCCCCCC)C2=O)=O)C2=C(S1)C(S3)=CC(C3=C4C5=CC=C(CC(CC)CCCC)S5)=C(C6=CC=C(CC(CC)CCCC)S6)C7=C4C=C([H])S7,PTBDT©\TPD,,,0.94,9.27,63,5.44,"Kim JH, Kim HS, Park JB, Kang IN, Hwang DH. Thieno 3,2-b thiophene-Substituted Benzodithiophene in Donor-Acceptor Type Semiconducting Copolymers: A Feasible Approach to Improve Performances of Organic Photovoltaic Cells. Journal of Polymer Science Part a-Polymer Chemistry 52, 3608-3616 (2014)."
320,[H]C1=C(C(N(CCCCCCC)C2=O)=O)C2=C(S1)C(S3)=CC(C3=C4C5=CC(SC(CC(CC)CCCC)=C6)=C6S5)=C(C7=CC(SC(CC(CC)CCCC)=C8)=C8S7)C9=C4C=C([H])S9,PTTBDT©\TPD,,,0.91,10.69,62,6.03,"Kim JH, Kim HS, Park JB, Kang IN, Hwang DH. Thieno 3,2-b thiophene-Substituted Benzodithiophene in Donor-Acceptor Type Semiconducting Copolymers: A Feasible Approach to Improve Performances of Organic Photovoltaic Cells. Journal of Polymer Science Part a-Polymer Chemistry 52, 3608-3616 (2014)."
321,[H]C1=CC2=C(S1)C(S3)=C([Si]2(CCCCCC)CCCCCC)C=C3C(C=C4)=CC=C4N(C5=CC=C(/C=C(C#N)/C6=CC=C(/C=C(C#N)/C#N)S6)C=C5)C7=CC=C(C8=CC9=C(S8)C(S%10)=C([Si]9(CCCCCC)CCCCCC)C=C%10C%11=CC(CCCCCC)=C(C%12=CC=C(C%13=C(CCCCCC)C=C([H])S%13)C%14=NSN=C%12%14)S%11)C=C7,BT-SI-TPA,,,0.85,3.5,0.74,0.33,"Nayak A, Sreekanth PSR, Sahu SK, Sahu D. Structural Tuning of Low Band Gap Intermolecular Push/Pull Side-chain Polymers for Organic Photovoltaic Applications. Chinese Journal of Polymer Science 35, 1073-1085 (2017)."
322,[H]C1=CC(C(C2=CC=C(CC(CC)CCCC)S2)=C(SC(C3=CC=C(/C(C#N)=C/C4=CC(OCC(CCCCCC)CCCCCCCC)=C(/C=C(C5=CC=C([H])S5)\C#N)C=C4OCC(CCCCCC)CCCCCCCC)S3)=C6)C6=C7C8=CC=C(CC(CC)CCCC)S8)=C7S1,PBDCS,,,0.94,14.3,0.65,8.75,"Park JM, et al. A stereoregular beta-dicyanodistyrylbenzene (beta-DCS)-based conjugated polymer for high-performance organic solar cells with small energy loss and high quantum efficiency. Journal of Materials Chemistry A 5, 16681-16688 (2017)."
323,CCC(CCCC)CC(S1)=CC=C1C2=C3C(C=C(C4=CC=C([H])C5=C4N=C(C6=CC=C(OCCCCCCCC)C=C6)C(C7=CC=C(OCCCCCCCC)C=C7)=N5)S3)=C(C8=CC=C(CC(CCCC)CC)S8)C9=C2C=C([H])S9,P1,,,0.68,7.38,0.41,2.05,"Badgujar S, Oh S, Ahn T, Lee SK. Synthesis and Characterization of Benzo 1,2-b:4,5-b ' Dithiophene-Based Copolymer for Organic Photovoltaic Cells. Journal of Nanoscience and Nanotechnology 17, 5852-5855 (2017)."
324,CCC(CCCC)CC(S1)=CC=C1C2=C3C(C=C(C4=C5N=C(C6=CC=C(OCCCCCCCC)C=C6)C(C7=CC=C(OCCCCCCCC)C=C7)=NC5=C([H])S4)S3)=C(C8=CC=C(CC(CCCC)CC)S8)C9=C2C=C([H])S9,P2,,,0.43,7.61,0.45,1.46,"Badgujar S, Oh S, Ahn T, Lee SK. Synthesis and Characterization of Benzo 1,2-b:4,5-b ' Dithiophene-Based Copolymer for Organic Photovoltaic Cells. Journal of Nanoscience and Nanotechnology 17, 5852-5855 (2017)."
325,CCC(CCCC)CC1=CC=C(S1)C2=C(C=C([H])S3)C3=C(C4=CC=C(CC(CCCC)CC)S4)C5=C2SC(C6=C7C(C(F)=C(C(OCC(CCCC)CC)=O)S7)=C([H])S6)=C5,PBDTT-FTTE,,,0.78,11.4,52,4.6,"Nickel F, et al. Mechanically robust, ITO-free, 4.8% efficient, all-solution processed organic solar cells on flexible PET foil. Solar Energy Materials and Solar Cells 130, 317-321 (2014)."
326,CCCCC(CC)COC1=C2C(C=C(C3=C(CC(CC)CCCC)C=C(C4=C(F)C(F)=C(C5=C(CC(CC)CCCC)C=C([H])S5)C6=NSN=C64)S3)S2)=C(OCC(CC)CCCC)C7=C1C=C([H])S7,PBDT2FBT©\2EHO,,,0.86,15.44,61.6,8.18,"Lee J, et al. Donor-Acceptor Alternating Copolymer Nanowires for Highly Efficient Organic Solar Cells. Advanced Materials 26, 6706-6714 (2014)."
327,CCCCCCC(C=C1)=CC=C1C(C2=C3SC4=C2SC(C5=C(F)C(F)=C([H])C6=NSN=C65)=C4)(C7=CC=C(CCCCCC)C=C7)C(C3=C8)=CC9=C8C(C%10=CC=C(CCCCCC)C=C%10)(C%11=CC=C(CCCCCC)C=C%11)C%12=C9SC%13=C%12SC([H])=C%13,PIDTT©\DFQT,,,0.91,14.38,0.62,8.12,"Zuo L, et al. Microcavity-Enhanced Light-Trapping for Highly Efficient Organic Parallel Tandem Solar Cells. Advanced Materials 26, 6778-6784 (2014)."
328,CC1=CC2=C3N4[Cu]N5/C(C(C=C(C)C=C6)=C6/C5=N/C(C7=C/8C=CC(C)=C7)=NC8=N/3)=N\C9=N/C(C%10=C9C=CC(C)=C%10)=N\C4=C2C=C1,CuMePc,,,0.533,9.85,63.8,3.35,"Qu D, Guo R, Yue S, Wu Y, Yan P, Cheng G. Planar heterojunction organic photovoltaic cells based on tetramethyl substituted copper(II) phthalocyanine treated with thermal annealing. Journal of Physics D-Applied Physics 47,  (2014)."
329,[H]C1=CC2=C(C(SC(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C([H])S3)=C5)=C5[Si]2(CC(CC)CCCC)CC(CC)CCCC)S1,PDTSTPD,,,0.849,6.9,38.7,2.3,"Park BM, Chang HJ. Properties of Bulk Heterojunction Organic Solar Cells with LiF Buffer Layer at Various Concentrations of Active Layer. Molecular Crystals and Liquid Crystals 602, 177-184 (2014)."
330,CCCCCCC1=CC=C(C2=CC=C(C3=CC=C(C4=CN=C(C5=CSC6=C5[Si](CCCCCC)(CCCCCC)C7=C6SC(C8=CC9=C(N%10C%11=C(C%12(C)C)C=C(C(S%13)=CC%14=C%13C%15=C(C(C%16=NC=C(C%17=CC=C(C%18=CC=C(C%19=CC=C(CCCCCC)S%19)S%18)S%17)C%20=NSN=C%20%16)=CS%15)[Si]%14(CCCCCC)CCCCCC)C=C%11C(C)(C)C%21=C%10C(C9(C)C)=CC(C(S%22)=CC%23=C%22C%24=C(C(C%25=NC=C(C%26=CC=C(C%27=CC=C(C%28=CC=C(CCCCCC)S%28)S%27)S%26)C%29=NSN=C%29%25)=CS%24)[Si]%23(CCCCCC)CCCCCC)=C%21)C%12=C8)=C7)C%30=NSN=C4%30)S3)S2)S1,DMM-TPA[DTS-PyBTTh3]3,,,0.78,12.84,0.58,5.81,"Lim K, Lee SY, Song K, Sharma GD, Ko J. Synthesis and properties of low bandgap star molecules TPA- DTS-PyBTTh3 (3) and DMM-TPA DTS-PyBTTh3 (3) for solution-processed bulk heterojunction organic solar cells. Journal of Materials Chemistry C 2, 8412-8422 (2014)."
331,CCCCCCC1=CC=C(C2=CC=C(C3=CC=C(C4=CN=C(C5=CSC6=C5[Si](CCCCCC)(CCCCCC)C7=C6SC(C8=CC=C(N(C9=CC=C(C(S%10)=CC%11=C%10C%12=C(C(C%13=NC=C(C%14=CC=C(C%15=CC=C(C%16=CC=C(CCCCCC)S%16)S%15)S%14)C%17=NSN=C%17%13)=CS%12)[Si]%11(CCCCCC)CCCCCC)C=C9)C%18=CC=C(C(S%19)=CC%20=C%19C%21=C(C(C%22=NC=C(C%23=CC=C(C%24=CC=C(C%25=CC=C(CCCCCC)S%25)S%24)S%23)C%26=NSN=C%26%22)=CS%21)[Si]%20(CCCCCC)CCCCCC)C=C%18)C=C8)=C7)C%27=NSN=C4%27)S3)S2)S1,TPA-[DTS-PyBTTh3]3,,,0.7,10.66,0.52,3.88,"Lim K, Lee SY, Song K, Sharma GD, Ko J. Synthesis and properties of low bandgap star molecules TPA- DTS-PyBTTh3 (3) and DMM-TPA DTS-PyBTTh3 (3) for solution-processed bulk heterojunction organic solar cells. Journal of Materials Chemistry C 2, 8412-8422 (2014)."
332,O=C(C1=C(C2=CC=C(C3=CC=CS3)S2)SC(C(S4)=CC5=C4C6=C(C=C(C7=C(C(N8CCCCCC)=O)C(C8=O)=C(C9=CC=C(C%10=CC=CS%10)S9)S7)S6)[Si](CC(CC)CCCC)5CC(CC)CCCC)=C1%11)N(CCCCCC)C%11=O,DTS(HexTPD2T)2,,,0.94,11.8,0.54,6,"Choi YS, Shin TJ, Jo WH. Small Molecules Based on Thieno 3,4-c pyrrole-4,6-dione for High Open-Circuit Voltage (V-OC) Organic Photovoltaics: Effect of Different Positions of Alkyl Substitution on Molecular Packing and Photovoltaic Performance. Acs Applied Materials & Interfaces 6, 20035-20042 (2014)."
333,O=C(C1=C(C2=CC=C(C3=CC=C(CCCCCC)S3)S2)SC(C(S4)=CC5=C4C6=C(C=C(C7=C(C(N8C)=O)C(C8=O)=C(C9=CC=C(C%10=CC=C(CCCCCC)S%10)S9)S7)S6)[Si](CC(CC)CCCC)5CC(CC)CCCC)=C1%11)N(C)C%11=O,DTS(MeTPD2THex)2,,,0.93,6.4,0.52,3.1,"Choi YS, Shin TJ, Jo WH. Small Molecules Based on Thieno 3,4-c pyrrole-4,6-dione for High Open-Circuit Voltage (V-OC) Organic Photovoltaics: Effect of Different Positions of Alkyl Substitution on Molecular Packing and Photovoltaic Performance. Acs Applied Materials & Interfaces 6, 20035-20042 (2014)."
334,C/C(C1=CC=C(C2=CC=C(C3=CC([Si]4(CCCCCCCC)CCCCCCCC)=C(C5=C4C=C(C6=CC=C(C7=CC=C(/C(C)=C(C#N)/C#N)S7)S6)S5)S3)S2)S1)=C(C#N)\C#N,DTS(Oct)2-(2T-DCV-Me)2,,,0.85,10.2,0.63,5.44,"Luponosov YN, Min J, Ameri T, Brabec CJ, Ponomarenko SA. A new dithienosilole-based oligothiophene with methyldicyanovinyl groups for high performance solution-processed organic solar cells. Organic Electronics 15, 3800-3804 (2014)."
335,O=C1C(C2=C(O)C=C(N(CCCCCC)CCCCCC)C=C2O)=C([O-])/C1=C(C(O)=C/3)\C(O)=CC3=[N+](CCCCCC)\CCCCCC,SQ2,,,0.88,5.48,31,1.5,"Bruck S, et al. Structure-property relationship of anilino-squaraines in organic solar cells. Physical chemistry chemical physics : PCCP 16, 1067-1077 (2014)."
336,O=C1C(C2=C(O)C=C(N(C(C)CC)CCC)C=C2O)=C([O-])/C1=C(C(O)=C/3)\C(O)=CC3=[N+](CCC)\C(C)CC,SQ3,,,0.76,7.75,32,1.85,"Bruck S, et al. Structure-property relationship of anilino-squaraines in organic solar cells. Physical chemistry chemical physics : PCCP 16, 1067-1077 (2014)."
337,[H]C(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(SC(C(OCCOCCOCCOC)=O)=C5)=C([H])S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7,PBDTT-TT-TEO,,,0.727,11.63,48.1,4.1,"Chen L, Tian S, Chen Y. Enhanced performance for organic bulk heterojunction solar cells by cooperative assembly of ter (ethylene oxide) pendants. Polymer Chemistry 5, 4480-4487 (2014)."
338,[H]C(S1)=CC2=C1C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=CC=C(C4=C5C(C(N4CC(CCCCCCCCCC)CCCCCCCC)=O)=C(C6=CC=C([H])S6)N(CC(CCCCCCCCCC)CCCCCCCC)C5=O)S3)S7)C7=C2C#C[Si](C(C)C)(C(C)C)C(C)C,PTIPSBDT:DPP,,,0.76,16.21,65,8,"Kim J-H, Lee M, Yang H, Hwang D-H. A high molecular weight triisopropylsilylethynyl (TIPS)-benzodithiophene and diketopyrrolopyrrole-based copolymer for high performance organic photovoltaic cells. Journal of Materials Chemistry A 2, 6348 (2014)."
339,O=C(N1CCC(CCCCCCCC)CCCCCCCCCC)C2=C(C3=CC4=C(S3)C(CCCCCC)=C(C5=CC6=C(C7=CC=C(CCC(CCCC)CC)S7)C8=C(C=C([H])S8)C(C9=CC=C(CCC(CCCC)CC)S9)=C6S5)S4)SC(C%10=CC(SC([H])=C%11CCCCCC)=C%11S%10)=C2C1=O,PBDTT¨CttTPD,,,0.84,11.05,73,6.81,"Kim J-H, et al. Effect of ¦Ð-conjugated bridges of TPD-based medium bandgap conjugated copolymers for efficient tandem organic photovoltaic cells. Energy Environ. Sci. 7, 4118-4131 (2014)."
340,CC(C1=CC=C(C2=C3C(C=C(C4=CC(C5=C(C(N6CCCCCCCC)=O)C(C6=O)=C(C7=CC=CS7)S5)=CS4)S3)=C(C8=CC=C(C(CCCCCC)C)[Se]8)C9=C2C=C(C%10=CC(C%11=C(C(N%12CCCCCCCC)=O)C(C%12=O)=C(C%13=CC=CS%13)S%11)=CS%10)S9)[Se]1)CCCCCC,BDTSe-TTPD,,,0.9,10.5,46.3,4.37,"Kim YJ, et al. A high-performance solution-processed small molecule: alkylselenophene-substituted benzodithiophene organic solar cell. J. Mater. Chem. C 2, 4937-4946 (2014)."
341,FC1=C(C2=CC=C([H])S2)C3=NSN=C3C(C4=CC=C(C5=CC([Si]6(CCCCCCCC)CCCCCCCC)=C(C7=C6C=C([H])C=C7)C=C5)S4)=C1F,PDOSiF-DTDFBT,,,0.73,8.55,0.65,4.03,"Li G, et al. 5,6-Difluorobenzothiadiazole and silafluorene based conjugated polymers for organic photovoltaic cells. J. Mater. Chem. C 2, 5116-5123 (2014)."
342,[H]C1=C(CCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CCCCCCCC)=C(C4=CC([Si]5(CCCCCCCC)CCCCCCCC)=C(C6=C5C=C([H])C=C6)C=C4)S3)C7=NSN=C27)S1,PSiF-D(OT)DFBT,,,0.96,3.75,61,2.19,"Li G, et al. 5,6-Difluorobenzothiadiazole and silafluorene based conjugated polymers for organic photovoltaic cells. J. Mater. Chem. C 2, 5116-5123 (2014)."
343,FC1=C(C2=CC(CCCCCCCC)=C(C3=CC=C([H])S3)S2)C4=NSN=C4C(C5=CC(CCCCCCCC)=C(C6=CC=C(C7=CC([Si]8(CCCCCCCC)CCCCCCCC)=C(C9=C8C=C([H])C=C9)C=C7)S6)S5)=C1F,PSiF-TTDFBT,,,0.7,5.34,65,2.39,"Li G, et al. 5,6-Difluorobenzothiadiazole and silafluorene based conjugated polymers for organic photovoltaic cells. J. Mater. Chem. C 2, 5116-5123 (2014)."
344,O=C1C(C2=C(C3=CC=C(C4=CC=C(C5=CC=C(C6=CC=C(OCCCCCCCCCCCCO[H])C=C6)S5)S4)S3)N1CC(CCCCCCCCCC)CCCCCCCC)=C(C7=CC=C(C8=CC=C(C9=CC=C(C%10=CC=C(OCCCCCCCCCCCOC(NCCCCCCNC([H])=O)=O)C=C%10)S9)S8)S7)N(CC(CCCCCCCCCC)CCCCCCCC)C2=O,PU1,,,0.68,1.92,57,0.75,"Li HJ, Wang JT, Mei CY, Li WS. A new class of organic photovoltaic materials: poly(rod-coil) polymers having alternative conjugated and non-conjugated segments. Chemical communications 50, 7720-7722 (2014)."
345,O=C1C(C2=C(C3=CC=C(C4=CC=C(C5=CC=C(C6=CC=C(OCCCCCCCCCCCCO[H])C=C6)S5)S4)S3)N1CC(CCCCCCCCCC)CCCCCCCC)=C(C7=CC=C(C8=CC=C(C9=CC=C(C%10=CC=C(OCCCCCCCCCCCOC(NC%11=CC=C(NC([H])=O)C=C%11)=O)C=C%10)S9)S8)S7)N(CC(CCCCCCCCCC)CCCCCCCC)C2=O,PU2,,,0.8,2.09,58.8,0.98,"Li HJ, Wang JT, Mei CY, Li WS. A new class of organic photovoltaic materials: poly(rod-coil) polymers having alternative conjugated and non-conjugated segments. Chemical communications 50, 7720-7722 (2014)."
346,O=C1C(C2=C(C3=CC=C(C4=CC=C(C5=CC=C(C6=CC=C(OCCCCCCCCCCCCO[H])C=C6)S5)S4)S3)N1CC(CCCCCCCCCC)CCCCCCCC)=C(C7=CC=C(C8=CC=C(C9=CC=C(C%10=CC=C(OCCCCCCCCCCCOC(NC%11=CC=CC(NC([H])=O)=C%11)=O)C=C%10)S9)S8)S7)N(CC(CCCCCCCCCC)CCCCCCCC)C2=O,PU3,,,0.77,1.67,55.1,0.71,"Li HJ, Wang JT, Mei CY, Li WS. A new class of organic photovoltaic materials: poly(rod-coil) polymers having alternative conjugated and non-conjugated segments. Chemical communications 50, 7720-7722 (2014)."
347,O=C1C(C2=C(C3=CC=C(C4=CC=C(C5=CC=C(C6=CC=C(OCCCCCCCCCCCCO[H])C=C6)S5)S4)S3)N1CC(CCCCCCCCCC)CCCCCCCC)=C(C7=CC=C(C8=CC=C(C9=CC=C(C%10=CC=C(OCCCCCCCCCCCOC(NC%11=CC=C(CC%12=CC=C(NC([H])=O)C=C%12)C=C%11)=O)C=C%10)S9)S8)S7)N(CC(CCCCCCCCCC)CCCCCCCC)C2=O,PU4,,,0.78,1.99,53,0.82,"Li HJ, Wang JT, Mei CY, Li WS. A new class of organic photovoltaic materials: poly(rod-coil) polymers having alternative conjugated and non-conjugated segments. Chemical communications 50, 7720-7722 (2014)."
348,O=C(C1=C2C(N(C(CCCC)CCCCCC)C3=O)=CC(C4=CC=C(C5=CC6=C(S5)C(OC(CCCCCC)CCCC)=C7C(SC([H])=C7)=C6OC(CCCC)CCCCCC)S4)=C1)N(C(CCCC)CCCCCC)C8=C2C3=CC(C9=CC=C([H])S9)=C8,Pa,,,0.78,7.32,60.9,3.47,"Liu M, et al. Three pyrido [2, 3, 4, 5-lmn] phenanthridine derivatives and their large band gap copolymers for organic solar cells. J. Mater. Chem. A 2, 321-325 (2014)."
349,OC1N(C(CCCC)CCCCCC)C2=CC(C3=CC=C(C4=CC5=C(S4)C(OC(CCCCCC)CCCC)=C6C(SC([H])=C6)=C5OC(CCCCCC)CCCC)S3)=CC7=C2C8=C(NC7OC(CCCCCC)CCCC)C=C(C9=CC=C([H])S9)C=C81,Pb,,,0.66,1.51,,0.46,"Liu M, et al. Three pyrido [2, 3, 4, 5-lmn] phenanthridine derivatives and their large band gap copolymers for organic solar cells. J. Mater. Chem. A 2, 321-325 (2014)."
350,[H]C1=CC=C(C2=CC(NC(OC(CCCCCC)CCCC)C3=C4C(NC5OC(CCCCCC)CCCC)=CC(C6=CC=C(C7=CC8=C(S7)C(OC(CCCCCC)CCCC)=C9C(SC([H])=C9)=C8OC(CCCCCC)CCCC)S6)=C3)=C4C5=C2)S1,Pc,,,0.66,5.46,59.6,2.15,"Liu M, et al. Three pyrido [2, 3, 4, 5-lmn] phenanthridine derivatives and their large band gap copolymers for organic solar cells. J. Mater. Chem. A 2, 321-325 (2014)."
351,[H]C1=CC2=C(C=C1)C3=C(C=C(C4=CC=C(C5=CC=C(C6=C(OCCCCCCCC)C(OCCCCCCCC)=C(C7=CC=C(C8=CC=C([H])S8)S7)C9=NSN=C69)S5)S4)C=C3)N2C(CCCCCCCC)CCCCCCCC,PCDT2BT-8,,,0.88,8.7,52,3.9,"Pearson AJ, et al. Impact of dithienyl or thienothiophene units on the optoelectronic and photovoltaic properties of benzo[1,2,5]thiadiazole based donor¨Cacceptor copolymers for organic solar cell devices. RSC Adv. 4, 43142-43149 (2014)."
352,[H]C1=CC2=C(C=C1)C3=C(C=C(C4=CC5=C(C=C(C6=C(OCCCCCCCC)C(OCCCCCCCC)=C(C(S7)=CC8=C7C=C([H])S8)C9=NSN=C69)S5)S4)C=C3)N2C(CCCCCCCC)CCCCCCCC,PCDTTBT-8,,,0.9,9.6,47,4.1,"Pearson AJ, et al. Impact of dithienyl or thienothiophene units on the optoelectronic and photovoltaic properties of benzo[1,2,5]thiadiazole based donor¨Cacceptor copolymers for organic solar cell devices. RSC Adv. 4, 43142-43149 (2014)."
353,[H]C1=CC2=C(C=C1)C3=C(C=C(C4=CC5=C(C=C(C6=C(OCCCCCCCC)C(OCCCCCCCC)=C(C(S7)=CC8=C7C=C([H])S8)C9=NSN=C69)S5)S4)C=C3)C2C(CCCCCCCC)CCCCCCCC,PFDT2BT-8,,,0.91,10.3,62,5.8,"Pearson AJ, et al. Impact of dithienyl or thienothiophene units on the optoelectronic and photovoltaic properties of benzo[1,2,5]thiadiazole based donor¨Cacceptor copolymers for organic solar cell devices. RSC Adv. 4, 43142-43149 (2014)."
354,[H]C1=CC2=C(C=C1)C3=C(C=C(C4=CC5=C(C=C(C6=C(OCCCCCCCC)C(OCCCCCCCC)=C(C(S7)=CC8=C7C=C([H])S8)C9=NSN=C69)S5)S4)C=C3)C2C(CCCCCCCC)CCCCCCCC,PFDTTBT-8,,,0.93,9.5,46,4.1,"Pearson AJ, et al. Impact of dithienyl or thienothiophene units on the optoelectronic and photovoltaic properties of benzo[1,2,5]thiadiazole based donor¨Cacceptor copolymers for organic solar cell devices. RSC Adv. 4, 43142-43149 (2014)."
355,CCCCN(C1=CC=CC=C1)C2=CC(O)=C(C3C([O-])C(C3[O-])C4=C(O)C=C(N(CCCC)C5=CC=CC=C5)C=C4O)C(O)=C2,SQ-BP,,,0.98,11.01,45,4.86,"Sasabe H, Igrashi T, Sasaki Y, Chen G, Hong Z, Kido J. Soluble squaraine derivatives for 4.9% efficient organic photovoltaic cells. RSC Adv. 4, 42804-42807 (2014)."
356,OC1=CC(N(CCCCCCCCCCCC)C2=CC=CC=C2)=CC(O)=C1C3C([O-])C(C3[O-])C4=C(O)C=C(N(CCCCCCCCCCCC)C5=CC=CC=C5)C=C4O,SQ-DP,,,0.96,5.72,36,1.97,"Sasabe H, Igrashi T, Sasaki Y, Chen G, Hong Z, Kido J. Soluble squaraine derivatives for 4.9% efficient organic photovoltaic cells. RSC Adv. 4, 42804-42807 (2014)."
357,CC1=CC(C)=C(C2=C3C=CC4=C(C5=CC=C(NC6=NC(NC7=CC=C(C8=C9C=CC%10=C(C%11=CC=CC=C%11)C(N%12%13)C=CC%12=C(C%14=CC=CC=C%14)C%15=CC=C%16N%15[Zn]%13(N%17C(C=CC%178)=C%16C%18=CC=CC=C%18)N9%10)C=C7)=NC(N%19CCCCC%19)=N6)C=C5)C(N%20%21)C=CC%20=C(C%22=C(C)C=C(C)C=C%22C)C%23=CC=C%24N%23[Zn]%21(N%25C(C=CC%252)=C%24C%26=CC=C(C(O)=O)C=C%26)N34)C(C)=C1,P-tNp-P',,,0.94,8.52,52,4.16,"Sharma GD, Zervaki GE, Angaridis P, Coutsolelos AG. New solution processed bulk-heterojunction organic solar cells based on a triazine-bridged porphyrin dyad as electron donor. RSC Adv. 4, 50819-50827 (2014)."
358,CC(C)(C)C(O1)C=C(C(C)(C)C)O[Ir]21N3C=C(C4=CC=C(OC)C=C4)C=CC3C5=C2C6=C(S5)C=CC=C6,R1,,,0.77,4.3,35,1.2,"Zhen H, et al. Solution-processed bulk-heterojunction organic solar cells employing Ir complexes as electron donors. Journal of Materials Chemistry A 2, 12390 (2014)."
359,CC(C)(C)C(O1)C=C(C(C)(C)C)O[Ir]21N3C=C(C4=CC=C(N(C5=CC=CC=C5)C6=CC=CC=C6)C=C4)C=CC3C7=C2C8=C(S7)C=CC=C8,R2,,,0.74,6.52,42,2,"Zhen H, et al. Solution-processed bulk-heterojunction organic solar cells employing Ir complexes as electron donors. Journal of Materials Chemistry A 2, 12390 (2014)."
360,O=C1C(C2=C(C3=CC=C(C4=CC=C(C(C=CC([H])=C5)=C5[Si]6(CCCCCCCC)CCCCCCCC)C6=C4)S3)N1CCCCCCCC)=C(C7=CC=C([H])S7)N(CCCCCCCC)C2=O,PDPPDBSi,,,0.71,11.3,51.6,4.13,"Shin W, Park JH, Lim GE, Sylvianti N, Ahn B-H, Kim JH. A conjugated low band gap diketopyrrolopyrrole and dibenzosilole-based polymer for organic solar cell. Synthetic Metals 210, 201-207 (2015)."
361,NC1=CC=C(C2=CC=C(C3=CC=C(C4=CC=C(C5=CC([n+]([o-])[o-])=C(C#N)C([n+]([o-])[o-])=C5)S4)S3)S2)C=C1,"C2,5B4TA",,,2.04,5.58,69.57,5.25,"Zamora PP, Bieger K, Vasquez D. Effect of Nitro Groups on Electrochemical and Photovoltaic Behavior of Tris-thiophenes used in Organic Solar Cells. INTERNATIONAL JOURNAL OF ELECTROCHEMICAL SCIENCE 10, 10321-10335 (2015)."
362,NC1=CC=C(C2=CC=C(C3=CC=C(C4=CC=C(C5=CC([n+]([o-])[o-])=C(C#N)C=C5)S4)S3)S2)C=C1,C2B4TA,,,0.545,2.83,68.22,1.05,"Zamora PP, Bieger K, Vasquez D. Effect of Nitro Groups on Electrochemical and Photovoltaic Behavior of Tris-thiophenes used in Organic Solar Cells. INTERNATIONAL JOURNAL OF ELECTROCHEMICAL SCIENCE 10, 10321-10335 (2015)."
363,[H]C1=CC=C2C(N(C(CCCCCCCC)CCCCCCCC)C3=C2C=CC(C4=CC(C(CCCCCC)C)=C(C5=CC=C(C6=CC=C(C7=CC=C(C8=CC=C(C9=CC=C(C%10=C(C(CCCCCC)C)C=C([H])S%10)S9)C%11=NSN=C8%11)S7)C%12=NSN=C6%12)S5)S4)=C3)=C1,P2,,,0.757,13.3,58,6,"Akkuratov AV, et al. Design of (X-DADAD)nType Copolymers for Efficient Bulk Heterojunction Organic Solar Cells. Macromolecules 48, 2013-2021 (2015)."
364,[H]C1=CC=C(/C=C/[H])C2=NN(CCCCCC)N=C12,pBTzV12,,,0.68,9.8,42.9,2.87,"Akpinar H, et al. Poly((2-alkylbenzo[1,2,3]triazole-4,7-diyl)vinylene)s for organic solar cells. Journal of Polymer Science Part B: Polymer Physics 53, 1539-1545 (2015)."
365,[H]C1=CC=C(/C=C/[H])C2=NN(C(CCCC)CCCCC)N=C12,pBTzV20,,,0.66,4.6,45.8,1.4,"Akpinar H, et al. Poly((2-alkylbenzo[1,2,3]triazole-4,7-diyl)vinylene)s for organic solar cells. Journal of Polymer Science Part B: Polymer Physics 53, 1539-1545 (2015)."
366,CCCCCCC1=C(SC(/C=C(C#N)\C#N)=C1CCCCCC)C#CC2=C(N34)C=CC3=C(C5=C(C)C=C(C)C=C5C)C(N67)C=CC6=C(C#CC8=C(CCCCCC)C(CCCCCC)=C(/C=C(C#N)\C#N)S8)C9=CC=C%10N9[Zn]74N%11C(C=CC%112)=C%10C%12=C(C)C=C(C)C=C%12C,1a,,,0.86,5.67,28.1,1.36,"Arrechea S, Molina-Ontoria A, Aljarilla A, de la Cruz P, Langa F, Echegoyen L. New acceptor¨C¦Ð-porphyrin¨C¦Ð-acceptor systems for solution-processed small molecule organic solar cells. Dyes and Pigments 121, 109-117 (2015)."
367,CC1=CC(C)=CC(C)=C1C2=C(C=C3)N4C3=C(C#CC5=C(CCCCCC)C(CCCCCC)=C(/C=C/C6=C(CCCCCC)C(CCCCCC)=C(/C=C(C#N)/C#N)S6)S5)C(C=C7)N8C7=C(C9=C(C)C=C(C)C=C9C)C%10=CC=C%11N%10[Zn]48N%12C2C=CC%12=C%11C#CC%13=C(CCCCCC)C(CCCCCC)=C(/C=C/C%14=C(CCCCCC)C(CCCCCC)=C(/C=C(C#N)\C#N)S%14)S%13,1b,,,0.82,10.83,35.7,3.16,"Arrechea S, Molina-Ontoria A, Aljarilla A, de la Cruz P, Langa F, Echegoyen L. New acceptor¨C¦Ð-porphyrin¨C¦Ð-acceptor systems for solution-processed small molecule organic solar cells. Dyes and Pigments 121, 109-117 (2015)."
368,CC(CCCCCC)C1=CC=C(C2=CC3=C(C4=CC=C([H])S4)C5=C(C=C(C6=CC=C(C(CCCCCC)C)S6)S5)C(C7=CC=C(C8=C(C=C(C(C(CCCC)CC)=O)S9)C9=C([H])S8)S7)=C3S2)S1,P1,,,0.82,13.66,50.81,5.65,"Chakravarthi N, et al. Synthesis, Characterization, and Photovoltaic Properties of 4,8-Dithienylbenzo[1,2-b:4,5-b¡ä]dithiophene-Based Donor¨CAcceptor Polymers with New Polymerization and 2D Conjugation Extension Pathways: A Potential Donor Building Block for High Performance and Stable Inverted Organic Solar Cells. Macromolecules 48, 2454-2465 (2015)."
369,CC(CCCCCC)C1=CC=C(C2=CC3=C(C4=CC=C([H])S4)C5=C(C=C(C6=CC=C(C(CCCCCC)C)S6)S5)C(C7=CC=C(C8=C(C=C(C(OCC(CC)CCCC)=O)S9)C9=C([H])S8)S7)=C3S2)S1,P2,,,0.81,11.36,49.19,4.53,"Chakravarthi N, et al. Synthesis, Characterization, and Photovoltaic Properties of 4,8-Dithienylbenzo[1,2-b:4,5-b¡ä]dithiophene-Based Donor¨CAcceptor Polymers with New Polymerization and 2D Conjugation Extension Pathways: A Potential Donor Building Block for High Performance and Stable Inverted Organic Solar Cells. Macromolecules 48, 2454-2465 (2015)."
370,CC(CCCCCC)C1=CC=C(C2=CC3=C(C4=CC=C([H])S4)C5=C(C=C(C6=CC=C(C(CCCCCC)C)S6)S5)C(C7=CC=C(C8=CC=C(C(N(C(CCCCCCCCCC)CCCCC)C9=O)=C%10C9=C(C%11=CC=C([H])S%11)N(C(CCCCCCCCCC)CCCCC)C%10=O)S8)S7)=C3S2)S1,P3,,,0.83,13.02,54.05,5.88,"Chakravarthi N, et al. Synthesis, Characterization, and Photovoltaic Properties of 4,8-Dithienylbenzo[1,2-b:4,5-b¡ä]dithiophene-Based Donor¨CAcceptor Polymers with New Polymerization and 2D Conjugation Extension Pathways: A Potential Donor Building Block for High Performance and Stable Inverted Organic Solar Cells. Macromolecules 48, 2454-2465 (2015)."
371,FC1=C(C2=CC3=C(C#C[Si](C(C)C)(C(C)C)C(C)C)C4=C(C=C(C5=C(F)C=C(C6=CC=C(C7=CC=C(CCCCCC)S7)S6)C8=NSN=C85)S4)C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C3S2)C9=NSN=C9C(C%10=CC=C(C%11=CC=C(CCCCCC)S%11)S%10)=C1,2,,,0.94,10.44,58,5.69,"Do K, Cho N, Siddiqui SA, Singh SP, Sharma GD, Ko J. New D-A-D-A-D push¨Cpull organic semiconductors with different benzo[1,2-b:4, 5-b¡ä] dithiophene cores for solution processed bulk heterojunction solar cells. Dyes and Pigments 120, 126-135 (2015)."
372,CC(CCCCCC)C1=CC=C(C2=C(C=C(C3=CC=C(C4=C5C(C(C6=C(C(CCCCCC)C)SC(C(CCCCCC)C)=C6C5=O)=O)=C(C7=CC=C([H])S7)S4)S3)O8)C8=C(C9=CC=C(C(CCCCCC)C)C=C9)C%10=C2OC([H])=C%10)C=C1,PBDF-T1,,,0.92,13.28,77.4,9.43,"Huo L, et al. Organic Solar Cells Based on a 2D Benzo[1,2-b:4,5-b']difuran-Conjugated Polymer with High-Power Conversion Efficiency. Adv Mater 27, 6969-6975 (2015)."
373,O=C1C(C2=C(C3=CC=C([H])S3)N1CC(CCCCCCCCCC)CCCCCCCC)=C(C4=CC=C(C5=CC6=C(C7=C(C=C([H])S7)S6)S5)S4)N(CC(CCCCCCCCCC)CCCCCCCC)C2=O,PDTDP,,,0.67,10.8,62,4.45,"Kim I-B, et al. D¨CA copolymer with high ambipolar mobilities based on dithienothiophene and diketopyrrolopyrrole for polymer solar cells and organic field-effect transistors. Organic Electronics 26, 251-259 (2015)."
374,[H]C1=CC=C(C2=C(F)C(F)=C([H])C3=C2N=C(C4=CC=C(OCCCCCCCC)C=C4)C(C5=CC=C(OCCCCCCCC)C=C5)=N3)[Se]1,PSe-DFQX,,,0.78,11.71,57,5.14,"Kim J-H, Song CE, Shin WS, Kim B, Kang I-N, Hwang D-H. Modulation of optical and electronic properties of quinoxailine-based conjugated polymers for organic photovoltaic cells. Journal of Polymer Science Part A: Polymer Chemistry 53, 1904-1914 (2015)."
375,[H]C1=CC=C(C2=CC=C([H])C3=C2N=C(C4=CC=C(OCCCCCCCC)C=C4)C(C5=CC=C(OCCCCCCCC)C=C5)=N3)[Se]1,PSe-QX,,,0.64,7.17,52,2.37,"Kim J-H, Song CE, Shin WS, Kim B, Kang I-N, Hwang D-H. Modulation of optical and electronic properties of quinoxailine-based conjugated polymers for organic photovoltaic cells. Journal of Polymer Science Part A: Polymer Chemistry 53, 1904-1914 (2015)."
376,[H]C1=CC=C(C2=C(F)C(F)=C([H])C3=C2N=C(C4=CC=C(OCCCCCCCC)C=C4)C(C5=CC=C(OCCCCCCCC)C=C5)=N3)S1,PT-DFQX,,,0.78,9.68,51,3.87,"Kim J-H, Song CE, Shin WS, Kim B, Kang I-N, Hwang D-H. Modulation of optical and electronic properties of quinoxailine-based conjugated polymers for organic photovoltaic cells. Journal of Polymer Science Part A: Polymer Chemistry 53, 1904-1914 (2015)."
377,[H]C1=CC=C(C2=CC=C([H])C3=C2N=C(C4=CC=C(OCCCCCCCC)C=C4)C(C5=CC=C(OCCCCCCCC)C=C5)=N3)S1,PT-QX,,,0.69,4.72,47,1.53,"Kim J-H, Song CE, Shin WS, Kim B, Kang I-N, Hwang D-H. Modulation of optical and electronic properties of quinoxailine-based conjugated polymers for organic photovoltaic cells. Journal of Polymer Science Part A: Polymer Chemistry 53, 1904-1914 (2015)."
378,CC(CCCCCC)OC1=C2C(C=C(C3=C(C(CCCCCCCC)CCC)C=C(C4=C(F)C(F)=C(C5=CC(C(CCCCCCCC)CCC)=C([H])S5)C6=NCN=C46)S3)S2)=C(OC(CCCCCC)C)C7=C1C=C([H])S7,PBDT,,,0.86,7.35,65.8,4.15,"Lee J, Ko H, Song E, Kim HG, Cho K. Naphthodithiophene-Based Conjugated Polymer with Linear, Planar Backbone Conformation and Strong Intermolecular Packing for Efficient Organic Solar Cells. ACS Appl Mater Interfaces 7, 21159-21169 (2015)."
379,CCCC(CCCCCCCC)C1=C(C2=CC3=CC(OC(CCCCCC)C)=C(C4=C(C=C([H])S4)C=C5OC(C)CCCCCC)C5=C3S2)SC(C6=C(F)C(F)=C(C7=CC(C(CCCCCCCC)CCC)=C([H])S7)C8=NCN=C68)=C1,PNDT,,,0.84,11.92,63.5,6.35,"Lee J, Ko H, Song E, Kim HG, Cho K. Naphthodithiophene-Based Conjugated Polymer with Linear, Planar Backbone Conformation and Strong Intermolecular Packing for Efficient Organic Solar Cells. ACS Appl Mater Interfaces 7, 21159-21169 (2015)."
380,[H]C1=CC=C(C2=CC=C(C3=CC(OC(CCCCCCCCCC)CCCCC)=C(C4=CC=C([H])S4)C=C3OC(CCCCCCCCCC)CCCCC)S2)C5=NSN=C15,P5,,,0.74,9.59,51,3.6,"Livi F, Zawacka NK, Angmo D, J?rgensen M, Krebs FC, Bundgaard E. Influence of Side Chain Position on the Electrical Properties of Organic Solar Cells Based on Dithienylbenzothiadiazole-alt-phenylene Conjugated Polymers. Macromolecules 48, 3481-3492 (2015)."
381,[H]C1=C(F)C(F)=C(C2=CC=C(C3=CC(OC(CCCCCCCCCC)CCCCC)=C(C4=CC=C([H])S4)C=C3OC(CCCCCCCCCC)CCCCC)S2)C5=NSN=C15,P7,,,0.72,5.61,55,2.2,"Livi F, Zawacka NK, Angmo D, J?rgensen M, Krebs FC, Bundgaard E. Influence of Side Chain Position on the Electrical Properties of Organic Solar Cells Based on Dithienylbenzothiadiazole-alt-phenylene Conjugated Polymers. Macromolecules 48, 3481-3492 (2015)."
382,[H]C1=CC=C(C(C=C2OC(CCCCCCCCCC)CCCCC)=C(OC(CCCCCCCCCC)CCCCC)C=C2C3=CC=C(C4=C(CCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CCCCCC)=C([H])S6)C7=NSN=C57)S4)S3)S1,P8,,,0.63,5.13,37,1.2,"Livi F, Zawacka NK, Angmo D, J?rgensen M, Krebs FC, Bundgaard E. Influence of Side Chain Position on the Electrical Properties of Organic Solar Cells Based on Dithienylbenzothiadiazole-alt-phenylene Conjugated Polymers. Macromolecules 48, 3481-3492 (2015)."
383,CCCCCCCCC1=C(C2=CC=C(C3=C(CCCCCCCC)C=C(/C=C(S4)/C(N(CC)C4=S)=O)S3)S2)SC(C5=CC6=C(C=C5)C7=C(C=C(C8=CC(CCCCCCCC)=C(C9=CC=C(C%10=C(CCCCCCCC)C=C(/C=C(S%11)/C(N(CC)C%11=S)=O)S%10)S9)S8)C=C7)[Si]6(CC(CC)CCCC)CC(CC)CCCC)=C1,DR3TDTS,,,0.82,13.67,69,7.8,"Ni W, et al. Dithienosilole-Based Small-Molecule Organic Solar Cells with an Efficiency over 8%: Investigation of the Relationship between the Molecular Structure and Photovoltaic Performance. Chemistry of Materials 27, 6077-6084 (2015)."
384,CCCCCCCCC(CCCCCCCCCC)CN1C(C2=CC=C([H])S2)=C3C(N(CC(CCCCCCCCCC)CCCCCCCC)C(C4=CC=C(C5=CC=C6C(C=CC([H])=C6)=C5)S4)=C3C1=O)=O,PDPP-TNT,,,0.79,8.9,54.6,3.8,"Srivastava SB, Sonar P, Singh SP. Charge transport studies in donor-acceptor block copolymer PDPP-TNT and PC71BM based inverted organic photovoltaic devices processed in room conditions. AIP Advances 5, 077177 (2015)."
385,CC1=C(CC)C2=N/C1=C\C3=C(CC)C(C)=C(/C=C([C@H]4C)\N=C(C(CC5)=C(C5=C/6C)NC6=C/2)C4CCC(OC)=O)N3,1a,,,0.6,3.25,34,0.68,"Tamiaki H, Tanaka T, Wang X-F. Photophysical properties of synthetic monomer, dimer, trimer, and tetramer of chlorophyll derivatives and their application to organic solar cells. Journal of Photochemistry and Photobiology A: Chemistry 313, 19-26 (2015)."
386,CC1=C(CC)C2=N/C1=C\C3=C(C(C)=O)C(C)=C(/C=C([C@H]4C)\N=C(C(CC5)=C(C5=C/6C)NC6=C/2)C4CCC(OC)=O)N3,1b,,,0.7,4.47,35,1.17,"Tamiaki H, Tanaka T, Wang X-F. Photophysical properties of synthetic monomer, dimer, trimer, and tetramer of chlorophyll derivatives and their application to organic solar cells. Journal of Photochemistry and Photobiology A: Chemistry 313, 19-26 (2015)."
387,CC1=C(CC)C2=N/C1=C\C3=C(CC)C(C)=C(/C=C([C@H]4C)\N=C(C(CC5=O)=C(C5=C/6C)NC6=C/2)C4CCC(OC)=O)N3,1c,,,0.76,5.76,34,1.49,"Tamiaki H, Tanaka T, Wang X-F. Photophysical properties of synthetic monomer, dimer, trimer, and tetramer of chlorophyll derivatives and their application to organic solar cells. Journal of Photochemistry and Photobiology A: Chemistry 313, 19-26 (2015)."
388,CC1=C(CC)C2=N/C1=C\C3=C(C(C)=O)C(C)=C(/C=C([C@H]4C)\N=C(C(CC5=O)=C(C5=C/6C)NC6=C/2)C4CCC(OC)=O)N3,1d,,,0.84,5.53,34,1.52,"Tamiaki H, Tanaka T, Wang X-F. Photophysical properties of synthetic monomer, dimer, trimer, and tetramer of chlorophyll derivatives and their application to organic solar cells. Journal of Photochemistry and Photobiology A: Chemistry 313, 19-26 (2015)."
389,CCCCCCC(CCCC)CC1=CC=C(C2=CC=C(C3=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C([H])S6)C7=C5N=C(C8=CC=CC(OCCCCCCCC)=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N7)S4)S%10)C%10=C(C%11=CC=C(C%12=CC=C(CC(CCCC)CCCCCC)S%12)S%11)C%13=C3SC([H])=C%13)S2)S1,FQ-BDT-4TR,,,0.85,7.5,46,2.9,"Tessarolo M, et al. Predicting thermal stability of organic solar cells through an easy and fast capacitance measurement. Solar Energy Materials and Solar Cells 141, 240-247 (2015)."
390,O=C(N1CC(CCCCCCCCCCCC)CCCCCCCCCC)/C(C2=C1C=C(C3=CC(CCCCCCCC)=C([H])S3)C=C2)=C(C(N4CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)\C5=C4C=C(C6=CC(CCCCCCCC)=C(C7=CC8=C(C=C([H])S8)S7)S6)C=C5,PTT-MIM,,,0.76,8.8,50,3.4,"Tessarolo M, et al. Predicting thermal stability of organic solar cells through an easy and fast capacitance measurement. Solar Energy Materials and Solar Cells 141, 240-247 (2015)."
391,S=C(S/1)N(C2=CC=CC=C2OC)C(C1=C\C=C\C3=CC=CC=C3[N+]([O-])=O)=O,TH-2,,,0.41,3.52,34,0.49,"Toumi AL, et al. Optimum Compromise Between Optical Absorption And Electrical Property Of the Planar Multi-Heterojunction Organic Solar Cells Based with New Thiazol Derivative, the (2-Thioxo-3-N-(2-Methoxyphenyl) Thiazolidin-4-One), as Electron Donor. Surface Review and Letters 22, 1550025 (2015)."
392,CCCCCCC1=C([H])SC(C2=CC=C(C3=C4C(C(C3CC(CCCCCCCC)CCCCCC)=O)=C(C5=CC=C(C6=CC(CCCCCC)=C(C7=CC=C([H])S7)S6)S5)C(CC(CCCCCCCC)CCCCCC)C4=O)S2)=C1,PDPP5T,,,0.57,15.5,65,5.7,"van Franeker JJ, Kouijzer S, Lou X, Turbiez M, Wienk MM, Janssen RAJ. Depositing Fullerenes in Swollen Polymer Layers via Sequential Processing of Organic Solar Cells. Advanced Energy Materials 5, 1500464 (2015)."
393,COC1C=CC2=C(C3=CC=C(OCCOCCOCCOC)C=C3)C(N4[B](F)(F)N21)=CC=C4C5=CC6=C(C7=CC=C(CC(CC)CC)S7)C8=C(C=C(C9=CC=C%10N9[B](F)(F)N%11C(C=CC%11OC)=C%10C%12=CC=C(OCCOCCOCCOC)C=C%12)S8)C(C%13=CC=C(CC(CC)CC)S%13)=C6S5,BDTT-BODIPY,,,0.97,10.55,46.5,4.75,"Xiao L, et al. A-D-A Type Small Molecules Based on Boron Dipyrromethene for Solution-Processed Organic Solar Cells. Chemistry, an Asian journal 10, 1513-1518 (2015)."
394,COC1=[N]2C(C=C1)=C(C3=CC=C(OCCOCCOCCOC)C=C3)C4=CC=C(C5=CC(C6(CCCCCCCC)CCCCCCCC)=C(C(C6=C7)=CC=C7C8=CC=C9N8[B](F)(F)[N]%10=C(OC)C=CC%10=C9C%11=CC=C(OCCOCCOCCOC)C=C%11)C=C5)N4[B]2(F)F,FL-BODIPY,,,0.99,3.49,43.49,1.51,"Xiao L, et al. A-D-A Type Small Molecules Based on Boron Dipyrromethene for Solution-Processed Organic Solar Cells. Chemistry, an Asian journal 10, 1513-1518 (2015)."
395,CCC(CCCC)CN(C1=O)C(C2=CC(C3=C4C(OCCO4)=C(C5=CC=C(C6=CC=C([H])C=C6C7(CCCCCCCC)CCCCCCCC)C7=C5)S3)=C8C(N(CC(CCCC)CC)C(C9=C8C2=C1C(C%10=C(OCCO%11)C%11=C([H])S%10)=C9)=O)=O)=O,PEDOTNDIF,,,0.75,8.7,36,2.33,"Yasuda T, Kuwabara J, Han L, Kanbara T. Improved power conversion efficiency of bulk-heterojunction organic photovoltaic cells using neat C70 as an effective acceptor for an amorphous ¦Ð-conjugated polymer. Organic Electronics 25, 99-104 (2015)."
396,[H]C1=CC2=C(C3=CC(CCCCCCCC)=C(CCCCCCCC)S3)C4=C(C=C(C5=C(F)C(F)=C([H])C6=NSN=C65)S4)C(C7=CC(CCCCCCCC)=C(CCCCCCCC)S7)=C2S1,P-BDTdFBT,,,0.98,11.32,63,7.09,"Yuan L, et al. Oligomeric Donor Material for High-Efficiency Organic Solar Cells: Breaking Down a Polymer. Adv Mater 27, 4229-4233 (2015)."
397,C1(C2=CC=C(C(C3=CC=CN3[Ni]4)=C5N4CC=C5)S2)=CC=C(C(C=C6)=CC=C6N(C7=CC=CC=C7)C8=CC=CC=C8)C9=NSN=C19,8,,,0.59,1.04,25,0.15,"Zou L, Guan S, Li L, Zhao L. Dipyrrin-based complexes for solution-processed organic solar cells. Chemical Research in Chinese Universities 31, 801-808 (2015)."
398,C1(C2=CC=C(C(C3=CC=CN3[Zn]4)=C5N4CC=C5)S2)=CC=C(C(C=C6)=CC=C6N(C7=CC=CC=C7)C8=CC=CC=C8)C9=NSN=C19,9,,,0.41,1.13,25,0.12,"Zou L, Guan S, Li L, Zhao L. Dipyrrin-based complexes for solution-processed organic solar cells. Chemical Research in Chinese Universities 31, 801-808 (2015)."
399,C1(C2=CC=C(C(C3=CC=CN3[Pd]4)=C5N4CC=C5)S2)=CC=C(C(C=C6)=CC=C6N(C7=CC=CC=C7)C8=CC=CC=C8)C9=NSN=C19,10,,,0.47,0.75,24,0.085,"Zou L, Guan S, Li L, Zhao L. Dipyrrin-based complexes for solution-processed organic solar cells. Chemical Research in Chinese Universities 31, 801-808 (2015)."
400,F[B]1(F)N(CC=C2)C2=C(C3=CC=CN31)C4=CC=C(C5=CC=C(C(C=C6)=CC=C6N(C7=CC=CC=C7)C8=CC=CC=C8)C9=NSN=C59)S4,11,,,0.81,3.03,24,0.58,"Zou L, Guan S, Li L, Zhao L. Dipyrrin-based complexes for solution-processed organic solar cells. Chemical Research in Chinese Universities 31, 801-808 (2015)."
401,CCCCCCCC1=C(C2=CC(CCCCCCC)=C(C3=CC(CCCCCCC)=C(C4=CC=C(C5=C(CCCCCCC)C=C(C6=C(CCCCCCC)C=C(C7=C(CCCCCCC)C=C(/C=C8C(N(CC)/C(S/8)=C(C#N)/C#N)=O)S7)S6)S5)[Se]4)S3)S2)SC(/C=C9C(N(CC)/C(S/9)=C(C#N)/C#N)=O)=C1,DRCN7T-Se,,,0.913,13.06,69.6,8.3,"Zuo Y, et al. A small molecule with selenophene as the central block for high performance solution-processed organic solar cells. Organic Electronics 19, 98-104 (2015)."
402,CCCCCCC(C=C1)=CC=C1C(C(C=C([H])[Se]2)=C2C3=C4)(C5=CC=C(CCCCCC)C=C5)C3=CC6=C4C(C7=CC=C(CCCCCC)C=C7)(C8=CC=C(CCCCCC)C=C8)C9=C6[Se]C(C%10=CC=C([H])C%11=C%10N=C%12C(C(C=CC=C%13)=C%13C%14=C%12C=CC=C%14)=N%11)=C9,PIDSe-PhanQ,,,0.75,9.16,57,3.93,"Sulas DB, Yao K, Intemann JJ. Open-Circuit Voltage Losses in Selenium-Substituted Organic Photovoltaic Devices from Increased Density of Charge-Transfer States. Chemistry of Materials 27, 6583-6591 (2015)."
403,CCCCCCC(C=C1)=CC=C1C(C(C=C([H])[Se]2)=C2C3=C4)(C5=CC=C(CCCCCC)C=C5)C3=CC6=C4C(C7=CC=C(CCCCCC)C=C7)(C8=CC=C(CCCCCC)C=C8)C9=C6[Se]C(C%10=CC=C([H])C%11=C%10N=C(C%12=CC=CC=C%12)C(C%13=CC=CC=C%13)=N%11)=C9,PIDSe-PhQ,,,0.75,11.04,59,4.89,"Sulas DB, Yao K, Intemann JJ. Open-Circuit Voltage Losses in Selenium-Substituted Organic Photovoltaic Devices from Increased Density of Charge-Transfer States. Chemistry of Materials 27, 6583-6591 (2015)."
404,CCCCCCC(C=C1)=CC=C1C(C(C=C([H])S2)=C2C3=C4)(C5=CC=C(CCCCCC)C=C5)C3=CC6=C4C(C7=CC=C(CCCCCC)C=C7)(C8=CC=C(CCCCCC)C=C8)C9=C6SC(C%10=CC=C([H])C%11=C%10N=C(C%12=CC=CC=C%12)C(C%13=CC=CC=C%13)=N%11)=C9,PIDT-PhQ,,,0.87,10.86,62,5.91,"Sulas DB, Yao K, Intemann JJ. Open-Circuit Voltage Losses in Selenium-Substituted Organic Photovoltaic Devices from Increased Density of Charge-Transfer States. Chemistry of Materials 27, 6583-6591 (2015)."
405,[H]C(S1)=CC2=C1N(CC(CCCC)CC)C3=C2C4=NSN=C4C5=C3N(CC(CCCC)CC)C(S6)=C5C=C6C7=CC(C8(CCCCCCCC)CCCCCCCC)=C(C=C7)C9=C8C=C([H])C=C9,PFDTPBT,,,0.79,5.49,48,2.08,"Kim HS, Park JB, Kim J-H, Hwang D-H. Donor¨CAcceptor-Type Semiconducting Polymers Consisting of Benzothiadiazole Derivatives as Electron-Acceptor Units for Organic Photovoltaic Cells. J. Nanosci. Nanotechnol. 15, 8876-8880 (2015)."
406,[H]C1=CC(N2CC(CCCC)CC)=C(C=C1)C3=C2C(N4CC(CCCC)CC)=C(C5=NSN=C35)C6=C4C=C(C=C6)C7=CC(C8(CCCCCCCC)CCCCCCCC)=C(C=C7)C9=C8C=C([H])C=C9,PFICTh,,,0.68,1.36,37,0.34,"Kim HS, Park JB, Kim J-H, Hwang D-H. Donor¨CAcceptor-Type Semiconducting Polymers Consisting of Benzothiadiazole Derivatives as Electron-Acceptor Units for Organic Photovoltaic Cells. J. Nanosci. Nanotechnol. 15, 8876-8880 (2015)."
407,CCCCCCC(C=C(C1=C(CCCCCC)C=C(/C=C(CCCCCC)\C#N)S1)S2)=C2C(S3)=CC4=C3C(S5)=C([Si]4(CCCCCC)CCCCCC)C=C5C(S6)=CC=C6C(C=C7)=CC=C7N(C8=CC=CC=C8)C9=CC=CC=C9,1,,,0.79,5.57,38,1.67,"Paek S, Lee JK, Ko J. Synthesis and photovoltaic characteristics of push¨Cpull organic semiconductors containing an electron-rich dithienosilole bridge for solution-processed small-molecule organic solar cells. Solar Energy Materials and Solar Cells 120, 209-217 (2014)."
408,CCCCCCC(C=C(C1=C(CCCCCC)C=C(/C=C(C#N)\C#N)S1)S2)=C2C(S3)=CC4=C3C(S5)=C([Si]4(CCCCCC)CCCCCC)C=C5C(S6)=CC=C6C(C=C7)=CC=C7N(C8=CC=CC=C8)C9=CC=CC=C9,2,,,0.8,6.46,37,1.92,"Paek S, Lee JK, Ko J. Synthesis and photovoltaic characteristics of push¨Cpull organic semiconductors containing an electron-rich dithienosilole bridge for solution-processed small-molecule organic solar cells. Solar Energy Materials and Solar Cells 120, 209-217 (2014)."
409,CCCCCCC(C=C(C1=C(CCCCCC)C=C(/C=C(CCCCCC)\C#N)S1)S2)=C2C(S3)=CC4=C3C(S5)=C([Si]4(CCCCCC)CCCCCC)C=C5C(S6)=CC=C6C(C=C7)=CC=C7N(C8=CC9=C(C(C)(C)C%10=C9C=CC=C%10)C=C8)C%11=CC(C(C)(C)C%12=C%13C=CC=C%12)=C%13C=C%11,3,,,0.81,6.22,40,2.02,"Paek S, Lee JK, Ko J. Synthesis and photovoltaic characteristics of push¨Cpull organic semiconductors containing an electron-rich dithienosilole bridge for solution-processed small-molecule organic solar cells. Solar Energy Materials and Solar Cells 120, 209-217 (2014)."
410,CCCCCCC(C=C(C1=C(CCCCCC)C=C(/C=C(C#N)\C#N)S1)S2)=C2C(S3)=CC4=C3C(S5)=C([Si]4(CCCCCC)CCCCCC)C=C5C(S6)=CC=C6C(C=C7)=CC=C7N(C8=CC9=C(C(C)(C)C%10=C9C=CC=C%10)C=C8)C%11=CC(C(C)(C)C%12=C%13C=CC=C%12)=C%13C=C%11,4,,,0.81,7.31,40,2.34,"Paek S, Lee JK, Ko J. Synthesis and photovoltaic characteristics of push¨Cpull organic semiconductors containing an electron-rich dithienosilole bridge for solution-processed small-molecule organic solar cells. Solar Energy Materials and Solar Cells 120, 209-217 (2014)."
411,CC(C)[Si](C(C)C)(C(C)C)C1=CC2=C(C3=CC4=C(C5=N/C4=N\C6=C7C=C(C8=C9C=C([Si](C(C)C)(C(C)C)C(C)C)S8)C(C%10=C9C=C([Si](C(C)C)(C(C)C)C(C)C)S%10)=CC7=C%11/N=C(C%12=C%13C=C(C%14=C%15C=C([Si](C(C)C)(C(C)C)C(C)C)S%14)C(C%16=C%15C=C([Si](C(C)C)(C(C)C)C(C)C)S%16)=C%12)\N=C%13/N=C(C%17=C/%18C=C(C%19=C%20C=C([Si](C(C)C)(C(C)C)C(C)C)S%19)C(C%21=C%20C=C([Si](C(C)C)(C(C)C)C(C)C)S%21)=C%17)\N(C%18=N/5)[Zn]N6%11)C=C3C%22=C2C=C([Si](C(C)C)(C(C)C)C(C)C)S%22)S1,6,,,0.7,1.7,51,0.6,"Yan X, et al. Synthesis of an octathienyl-fused phthalocyanine as a donor material for organic solar cells. Dyes and Pigments 114, 124-128 (2015)."
412,O=C(N1CCCCCCCC)C2=C(C3=CC(CCCCCC)=C([H])S3)SC(C4=CC(CCCCCC)=C(C5=CC6=C(C(C7=CC=C(CC(CC)CCCC)S7)=C(C=C([H])S8)C8=C6C9=CC=C(CC(CC)CCCC)S9)S5)S4)=C2C1=O,PBDTTPD©\HT,,,0.99,11.8,58,6.85,"Zhang Y, et al. Synergistic Effect of Polymer and Small Molecules for High©\Performance Ternary Organic Solar Cells. Advanced materials 27, 1071-1076 (2015)."
413,CCCCC(CC)COC1=C(C=C([H])S2)C2=C(OCC(CC)CCCC)C3=C1SC(C4=C5C(C=C(C(C(CC)CCCC)=O)S5)=C([H])S4)=C3,PBDTTT-C,,,0.72,15.5,62,6.9,"Zusan A, Gieseking B, Zerson M, Dyakonov V, Magerle R, Deibel C. The effect of diiodooctane on the charge carrier generation in organic solar cells based on the copolymer PBDTTT-C. Scientific reports 5,  (2015)."
414,O=C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C1=O)C(C1=C(C2=CC=C([H])S2)C3=NSN=C34)=C4C5=CC=C(C6=CC(C(C=C(CCCCCCCCCCCCCCCC)S7)=C7C8=C9SC([H])=C8)=C9S6)S5,BBTI-1,,,0.8,16.45,63,8.3,"Nielsen CB, et al. 2, 1, 3©\Benzothiadiazole©\5, 6©\Dicarboxylic Imide¨CA Versatile Building Block for Additive©\and Annealing©\Free Processing of Organic Solar Cells with Efficiencies Exceeding 8%. Adv. Mater. 27, 948-953 (2015)."
415,O=C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C1=O)C(C1=C(C2=CC=C([H])S2)C3=NSN=C34)=C4C5=CC=C(C6=CC(C(C=C(C(CCCCCCCCC)CCCCCCCCC)S7)=C7C8=C9SC([H])=C8)=C9S6)S5,BBTI-2,,,0.81,11,67,6,"Nielsen CB, et al. 2, 1, 3©\Benzothiadiazole©\5, 6©\Dicarboxylic Imide¨CA Versatile Building Block for Additive©\and Annealing©\Free Processing of Organic Solar Cells with Efficiencies Exceeding 8%. Adv. Mater. 27, 948-953 (2015)."
416,CCCCCCC(C=C(C1=C(CCCCCC)C=C(/C=C2C(N(CC)C(N(CC)C/2=O)=S)=O)S1)S3)=C3C#C[Pt]([Pt](CCCC)(CCCC)CCCC)(C#CC4=C(CCCCCC)C=C(C5=C(CCCCCC)C=C(/C=C6C(N(CC)C(N(CC)C\6=O)=S)=O)S5)S4)[Pt](CCCC)(CCCC)CCCC,S-1,,,0.91,3.61,28,0.88,"Cui C, Zhang Y, Choy WC, Li H, Wong W-Y. Metallated conjugation in small-sized-molecular donors for solution-processed organic solar cells. Science China Chemistry 58, 347-356 (2015)."
417,CCCCCCC1=C(C2=CC=C(S2)C#C[Pt]([Pt](CCCC)(CCCC)CCCC)(C#CC3=CC=C(C4=C(CCCCCC)C=C(C5=C(CCCCCC)C=C(/C=C6C(N(CC)C(N(CC)C\6=O)=S)=O)S5)S4)S3)[Pt](CCCC)(CCCC)CCCC)SC(C7=C(CCCCCC)C=C(/C=C8C(N(CC)C(N(CC)C/8=O)=S)=O)S7)=C1,S-2,,,0.93,5.89,29,1.59,"Cui C, Zhang Y, Choy WC, Li H, Wong W-Y. Metallated conjugation in small-sized-molecular donors for solution-processed organic solar cells. Science China Chemistry 58, 347-356 (2015)."
418,CCCCCCC(C=C(C1=C(CCCCCC)C=C(/C=C(C#N)/C#N)S1)S2)=C2C#C[Pt]([Pt](CCCC)(CCCC)CCCC)(C#CC3=C(CCCCCC)C=C(C4=C(CCCCCC)C=C(/C=C(C#N)/C#N)S4)S3)[Pt](CCCC)(CCCC)CCCC,S-3,,,0.6,1.22,34,0.17,"Cui C, Zhang Y, Choy WC, Li H, Wong W-Y. Metallated conjugation in small-sized-molecular donors for solution-processed organic solar cells. Science China Chemistry 58, 347-356 (2015)."
419,CCCCCCC1=C(C2=CC=C(S2)C#C[Pt]([Pt](CCCC)(CCCC)CCCC)(C#CC3=CC=C(C4=C(CCCCCC)C=C(C5=C(CCCCCC)C=C(/C=C(C#N)/C#N)S5)S4)S3)[Pt](CCCC)(CCCC)CCCC)SC(C6=C(CCCCCC)C=C(/C=C(C#N)/C#N)S6)=C1,S-4,,,0.92,4.88,33,1.56,"Cui C, Zhang Y, Choy WC, Li H, Wong W-Y. Metallated conjugation in small-sized-molecular donors for solution-processed organic solar cells. Science China Chemistry 58, 347-356 (2015)."
420,O=C(N1CCCC(CCCCCCCCCC)CCCCCCCC)C(C2=C1C3=CC4=C(C=C(C5=CC=C([H])[Se]5)S4)S3)=C(C6=CC7=C(C=C([H])S7)S6)N(CCCC(CCCCCCCCCC)CCCCCCCC)C2=O,C3-DPPTT-Se,,,0.56,21.5,63,7.6,"Ashraf RS, et al. Chalcogenophene comonomer comparison in small band gap diketopyrrolopyrrole-based conjugated polymers for high-performing field-effect transistors and organic solar cells. Journal of the American Chemical Society 137, 1314-1321 (2015)."
421,O=C(N1CCCC(CCCCCCCCCC)CCCCCCCC)C(C2=C1C3=CC4=C(C=C(C5=CC=C([H])S5)S4)S3)=C(C6=CC7=C(C=C([H])S7)S6)N(CCCC(CCCCCCCCCC)CCCCCCCC)C2=O,C3-DPPTT-T,,,0.57,23.5,66,8.8,"Ashraf RS, et al. Chalcogenophene comonomer comparison in small band gap diketopyrrolopyrrole-based conjugated polymers for high-performing field-effect transistors and organic solar cells. Journal of the American Chemical Society 137, 1314-1321 (2015)."
422,[H]C(S1)=CC2=C1C(C3=CC=C(CC)S3)=C(C=C(C4=C5C(SC(C(C(CC)CCCC)=O)=C5)=C([H])S4)S6)C6=C2C7=CC=C(CC)S7,PBDTTT-C-T,,,0.84,12.83,56,6.08,"Zhang X, Zhan C, Yao J. Non-fullerene organic solar cells with 6.1% efficiency through fine-tuning parameters of the film-forming process. Chemistry of Materials 27, 166-173 (2014)."
423,O=C(N(CC(CCCCCC)CCCCCCCC)C1=C2SC([H])=C1)C3=C2C=C4C(N(CC(CCCCCC)CCCCCCCC)C(C=C(C5=CC(SC([H])=C6)=C6S5)S7)=C7C4=C3)=O,P1,,,0.8,11.6,59,5.5,"Kroon R, et al. Comparison of selenophene and thienothiophene incorporation into pentacyclic lactam-based conjugated polymers for organic solar cells. Polymer Chemistry 6, 7402-7409 (2015)."
424,O=C(N(CC(CCCCCC)CCCCCCCC)C1=C2SC([H])=C1)C3=C2C=C4C(N(CC(CCCCCC)CCCCCCCC)C(C=C(C5=CC=C([H])[Se]5)S6)=C6C4=C3)=O,P2,,,0.84,11.9,0.7,7.1,"Kroon R, et al. Comparison of selenophene and thienothiophene incorporation into pentacyclic lactam-based conjugated polymers for organic solar cells. Polymer Chemistry 6, 7402-7409 (2015)."
425,OC1=CC(N2CCC3=C2C=CC(C#N)=C3)=CC(O)=C1C(C4=O)=C([O-])C4=CC5=[N+](CCCC)C6=C(C(C=CC=C7)=C7C=C6)C5(C)C,ASQ-5-CN,,,0.85,12.4,58,6.11,"Yang D, et al. Cyano-substitution on the end-capping group: facile access toward asymmetrical squaraine showing strong dipole¨Cdipole interactions as a high performance small molecular organic solar cells material. J. Mater. Chem. A 3, 17704-17712 (2015)."
426,CCCCCCCCC(CCCCCCCC)N1C2=C(C(OCCCCCCCC)=CC([H])=C2)C3=C1C=C(C4=CC=C(C5=CC=C(C6=CC=C([H])S6)C7=NSN=C75)S4)C=C3,PCOC8-TBT,,,0.83,9.87,48,3.96,"Shibasaki K, Yasuda T, Yamamoto Y, Kijima M. Monosubstitution at the 4-position of 2, 7-carbazolylene expands the structural design and fundamental properties of D-¦Ð-A copolymers for organic photovoltaic cells. Polymer Chemistry 6, 5921-5930 (2015)."
427,CCCCCCCCC(CCCCCCCC)N1C2=C(C(OCCCCCCCC)=CC([H])=C2)C3=C1C=C(C4=CC=C(C5=C(F)C=C(C6=CC=C([H])S6)C7=NSN=C75)S4)C=C3,PCOC8-TBTF1,,,0.65,14.44,48,4.5,"Shibasaki K, Yasuda T, Yamamoto Y, Kijima M. Monosubstitution at the 4-position of 2, 7-carbazolylene expands the structural design and fundamental properties of D-¦Ð-A copolymers for organic photovoltaic cells. Polymer Chemistry 6, 5921-5930 (2015)."
428,[H]C(S1)=C(CC(CCCC)CCCCCC)C=C1C2=C3C(N=S=N3)=C(C4=CC(CC(CCCC)CCCCCC)=C(C5=CC(C(CCCCCCCC)(CCCCCCCC)C6=C7C=CC([H])=C6)=C7C=C5)S4)C8=NSN=C28,PBBT-FT,,,0.51,0.35,33,0.06,"Wang Y, Klein MF, Hiyoshi J, Kawauchi S, Wong WW, Michinobu T. Bulk-Heterojunction organic solar cells based on benzobisthiadiazole semiconducting polymers. Journal of Photopolymer Science and Technology 28, 385-391 (2015)."
429,[H]C(S1)=C(CC(CCCC)CCCCCC)C=C1C2=C3C(N=S=N3)=C(C4=CC(CC(CCCC)CCCCCC)=C(C5=CC=C(C6=CC(C(CCCCCCCC)(CCCCCCCC)C7=C8C=CC(C9=CC=C([H])S9)=C7)=C8C=C6)S5)S4)C%10=NSN=C2%10,PBBT-T-FT,,,0.63,0.78,41,0.2,"Wang Y, Klein MF, Hiyoshi J, Kawauchi S, Wong WW, Michinobu T. Bulk-Heterojunction organic solar cells based on benzobisthiadiazole semiconducting polymers. Journal of Photopolymer Science and Technology 28, 385-391 (2015)."
430,[H]C(S1)=C(CC(CCCC)CCCCCC)C=C1C2=C3C(N=S=N3)=C(C4=CC(CC(CCCC)CCCCCC)=C(C5=CN=C(C6=CC(C(CCCCCCCC)(CCCCCCCC)C7=C8C=CC(C9=NC=C([H])S9)=C7)=C8C=C6)S5)S4)C%10=NSN=C2%10,PBBT-Tz-FT,,,0.57,0.46,40,0.11,"Wang Y, Klein MF, Hiyoshi J, Kawauchi S, Wong WW, Michinobu T. Bulk-Heterojunction organic solar cells based on benzobisthiadiazole semiconducting polymers. Journal of Photopolymer Science and Technology 28, 385-391 (2015)."
431,CCCCCCCCCCCCN1N=C2C(C3=CC=C(C4=CC5=C(C(OCC(CC)CCCC)=C(C=C([H])S6)C6=C5OCC(CC)CCCC)S4)S3)=CC=C(C7=CC=C([H])S7)C2=N1,PTBTBDT,,,0.72,5.45,54,2.12,"Istanbulluoglu C, et al. Synthesis of a benzotriazole bearing alternating copolymer for organic photovoltaic applications. New Journal of Chemistry 39, 6623-6630 (2015)."
432,CCCCC(CC)C[Si]1(CC(CC)CCCC)C(C=C(C2=CC(N(CCCC)C(/C3=C4C(C=CC(C5=CC=C(C6=CC=C(CCCCCC)S6)S5)=C7)=C7N(CCCC)C\4=O)=O)=C3C=C2)S8)=C8C9=C1C=C(C%10=CC=C(/C(C(N%11CCCC)=O)=C%12C(N(CCCC)C%13=C\%12C=CC(C%14=CC=C(C%15=CC=C(CCCCCC)S%15)S%14)=C%13)=O)C%11=C%10)S9,DTS(IIThThHEX)2,,,0.69,11.3,0.41,3.19,"Areephong J, San Juan RR, Payne A-J, Welch GC. A narrow band gap isoindigo based molecular donor for solution processed organic solar cells. New Journal of Chemistry 39, 5075-5079 (2015)."
433,[H]C1=CC2=C(C3=CC(CCCCCC)=C(CC(CC)CCCC)S3)C4=C(C=C(C5=C(F)C(F)=C([H])C6=NSN=C65)S4)C(C7=CC(CCCCCC)=C(CC(CC)CCCC)S7)=C2S1,P1,,,0.89,9.9,45,4.1,"Xiao Z, et al. Effect of molecular weight on the properties and organic solar cell device performance of a donor¨Cacceptor conjugated polymer. Polymer Chemistry 6, 2312-2318 (2015)."
434,N#C/C(C1=CC=C([N+]([O-])=O)C=C1)=C/C(C=C2)=CC=C2N(C3=CC=CC=C3)C(C=C4)=CC=C4/C=C/C5=CC=C(C6=CC(CCCCCCCCCCCC)=C(C7=CC=C(N(C8=CC=CC=C8)C9=CC=CC=C9)C=C7)S6)C%10=NSN=C%105,SM3,,,0.85,5.22,33,1.46,"Jia T, Peng Z, Li Q, Xie Y, Hou Q, Hou L. Synthesis of triphenylamine-based molecules with cyan terminals and their application for organic solar cells. Synthetic Metals 199, 14-20 (2015)."
435,N#C/C(C1=CC=C([N+]([O-])=O)C=C1)=C\C(C=C2)=CC=C2N(C3=CC=CC=C3)C(C=C4)=CC=C4/C=C/C5=CC=C(C6=CC7=C(C(OCC(CC)CCCC)=C(C=C(C8=CC=C(/C=C/C9=CC=C(N(C%10=CC=CC=C%10)C%11=CC=C(/C=C(C#N)/C%12=CC=C([N+]([O-])=O)C=C%12)C=C%11)C=C9)C%13=NSN=C8%13)S%14)C%14=C7OCC(CC)CCCC)S6)C%15=NSN=C%155,SM4,,,0.78,4.89,33,1.27,"Jia T, Peng Z, Li Q, Xie Y, Hou Q, Hou L. Synthesis of triphenylamine-based molecules with cyan terminals and their application for organic solar cells. Synthetic Metals 199, 14-20 (2015)."
436,[H]=CC1=C(OCCCCCCCC)C=C(/C=C/C2=CC=C(C=[H])S2)C(OCCCCCCCC)=C1,PPVTV,,,,8,61,3.5,"Lim KG, Park JM, Mangold H, Laquai F, Choi TL, Lee TW. Bimolecular Crystals with an Intercalated Structure Improve Poly (p©\phenylenevinylene)©\Based Organic Photovoltaic Cells. ChemSusChem 8, 337-344 (2015)."
437,[O-]c1c(C2=C(O)C=C(N(CC(C)C)CC(C)C)C=C2O)c([O-])c1C3=C(O)C=C(N(CC(C)C)CC(C)C)C=C3O,DIB-SQ,,,0.77,2.76,51.3,1.08,"Wang Y, Zhao X, Zhan X. Layer by layer solution processed organic solar cells based on a small molecule donor and a polymer acceptor. Journal of Materials Chemistry C 3, 447-452 (2015)."
438,FC(C=C(C1=CC=C(C2=CC=C(CCCCCC)S2)S1)C3=NSN=C34)=C4C5=CC6=C(S5)C7=C(C=C(C8=C(F)C=C(C9=CC=C(C%10=CC=C(CCCCCC)S%10)S9)C%11=NSN=C%118)S7)[Si]6(CC(CC)CCCC)CC(CC)CCCC,DTS(FBTTh2)2,,,0.77,13.1,68,6.8,"Vangerven T, et al. Elucidating Batch-to-Batch Variation Caused by Homocoupled Side Products in Solution-Processable Organic Solar Cells. Chemistry of Materials 28, 9088-9098 (2016)."
439,FC(C=C(C1=CC=C(C2=CC=C(CCCCCC)S2)S1)C3=NSN=C34)=C4C5=CC6=C(S5)C7=C(C=C(C(S8)=CC9=C8C(SC(C%10=C(F)C=C(C%11=CC=C(C%12=CC=C(CCCCCC)S%12)S%11)C%13=NSN=C%13%10)=C%14)=C%14[Si]9(CC(CC)CCCC)CC(CC)CCCC)S7)[Si]6(CC(CC)CCCC)CC(CC)CCCC,DTS(FBTTh2)2-homo,,,0.64,11.3,61,4.5,"Vangerven T, et al. Elucidating Batch-to-Batch Variation Caused by Homocoupled Side Products in Solution-Processable Organic Solar Cells. Chemistry of Materials 28, 9088-9098 (2016)."
440,CCCCC(CC)C[Si]1(CC(CC)CCCC)C2=C(SC(C3=CC=C(C4=CC=C(C5=CC=C(CCCCCC)S5)S4)C6=C3CC(C7=CC(OCCCCCCCC)=CC=C7)C(C8=CC=CC(OCCCCCCCC)=C8)C6)=C2)C9=C1C=C(C%10=C(CC(C%11=CC=CC(OCCCCCCCC)=C%11)C(C%12=CC(OCCCCCCCC)=CC=C%12)C%13)C%13=C(C%14=CC=C(C%15=CC=C(CCCCCC)S%15)S%14)C=C%10)S9,DTS(QxHT2)2,,,0.98,12.46,64,7.81,"Keshtov M, et al. Synthesis and photophysical properties of semiconductor molecules D 1-AD 2-AD 1-type structure based on derivatives of quinoxaline and dithienosilole for organics solar cells. Organic Electronics 39, 361-370 (2016)."
441,FC1=C(C2=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C3=CC=C(C4=CC=C([H])S4)S3)S2)C5=NSN=C5C(C6=CC(CC(CCCCCCCC)CCCCCCCCCC)=C([H])S6)=C1F,PffBT4T©\2OD,,,0.77,18.8,70,10.1,"Czolk J, Landerer D, Koppitz M, Nass D, Colsmann A. Highly Efficient, Mechanically Flexible, Semi©\Transparent Organic Solar Cells Doctor Bladed from Non©\Halogenated Solvents. Advanced Materials Technologies 1,  (2016)."
442,CCCCCCCCSC(S1)=CC=C1C2=C3C(SC([H])=C3)=C(C4=CC=C(SCCCCCCCC)S4)C5=C2SC(C6=C(CCCCCCCC)C(SC(C7=C(F)C(F)=C(C8=CC(SC([H])=C9CCCCCCCC)=C9S8)C%10=NSN=C7%10)=C%11)=C%11S6)=C5,PBDTTS©\TTffBT,,,0.92,10.89,65,6.51,"Lee W, Jung JW. High©\Performance Non©\Fullerene Organic Solar Cells Based on a Pair of Medium Band Gap Polymer Donor and Perylene Bisimide Derivative Acceptor. Macromolecular Chemistry and Physics 217, 2647-2653 (2016)."
443,CCCCCCCCCCC(CCCCCCCC)/C(C1=CC=C(/C(C#CC2=CC(CCCCCC)=C(C3=CC=C(C4=C(CCCCCC)C=C(/C=C5C(N(CC)/C(S/5)=C(C#N)\C#N)=O)S4)S3)S2)=C6N=C7C=C\6)N1[Zn]N8/C(C=C/C8=C7\C(CCCCCCCC)CCCCCCCCCC)=C9/C#CC%10=CC(CCCCCC)=C(C%11=CC=C(C%12=C(CCCCCC)C=C(/C=C%13C(N(CC)/C(S/%13)=C(C#N)/C#N)=O)S%12)S%11)S%10)=C%14C=CC9=N\%14,PTTCNR,,,0.82,14.3,70,8.21,"Xiao L, et al. New Terthiophene-Conjugated Porphyrin Donors for Highly Efficient Organic Solar Cells. ACS applied materials & interfaces 8, 30176-30183 (2016)."
444,CCCCCCCCCCC(CCCCCCCC)/C(C1=CC=C(/C(C#CC2=CC(CCCCCC)=C(C3=CC=C(C4=C(CCCCCC)C=C(/C=C5C(N(CC)C(S/5)=S)=O)S4)S3)S2)=C6N=C7C=C\6)N1[Zn]N8/C(C=C/C8=C7\C(CCCCCCCC)CCCCCCCCCC)=C9/C#CC%10=CC(CCCCCC)=C(C%11=CC=C(C%12=C(CCCCCC)C=C(/C=C%13C(N(CC)C(S/%13)=S)=O)S%12)S%11)S%10)=C%14C=CC9=N\%14,PTTR,,,0.8,14.93,64,7.66,"Xiao L, et al. New Terthiophene-Conjugated Porphyrin Donors for Highly Efficient Organic Solar Cells. ACS applied materials & interfaces 8, 30176-30183 (2016)."
445,CC(C=C(C)C=C1C)=C1/C(C2=CC=C(/C(C#CC3=C(CCCCCC)C(CCCCCC)=C(/C=C4C(N(CC)C(S/4)=S)=O)S3)=C5N=C6C=C\5)N2[Zn]N7/C(C=C/C7=C6\C8=C(C)C=C(C)C=C8C)=C9/C#CC%10=C(CCCCCC)C(CCCCCC)=C(/C=C%11C(N(CC)C(S/%11)=S)=O)S%10)=C%12C=CC9=N\%12,1a,,,0.85,11.36,31,3.01,"Montcada NF, et al. High photo-current in solution processed organic solar cells based on a porphyrin core A-¦Ð-D-¦Ð-A as electron donor material. Organic Electronics 38, 330-336 (2016)."
446,CC(C=C(C)C=C1C)=C1/C(C2=CC=C(/C(C#CC3=C(CCCCCC)C(CCCCCC)=C(/C=C/C4=C(CCCCCC)C(CCCCCC)=C(/C=C5SC(N(CC)C\5=O)=S)S4)S3)=C6N=C7C=C\6)N2[Zn]N8/C(C=C/C8=C7\C9=C(C)C=C(C)C=C9C)=C%10/C#CC%11=C(CCCCCC)C(CCCCCC)=C(/C=C/C%12=C(CCCCCC)C(CCCCCC)=C(/C=C%13SC(N(CC)C\%13=O)=S)S%12)S%11)=C%14C=CC%10=N\%14,1b,,,0.8,13.2,40,4.24,"Montcada NF, et al. High photo-current in solution processed organic solar cells based on a porphyrin core A-¦Ð-D-¦Ð-A as electron donor material. Organic Electronics 38, 330-336 (2016)."
447,FC1=C(C2=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C([H])S2)C3=NN(CCC)N=C3C(C4=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(C5=CC=C(C6=C(F)C=C(C7=CC=C([H])S7)C(F)=C6)S5)S4)=C1F,PTFB-P,,,0.92,12.8,65,7.6,"Li Z, et al. Donor polymer design enables efficient non-fullerene organic solar cells. Nature communications 7, 13094 (2016)."
448,[H]C(S1)=CC2=C1C(C3=CC=C(SCCCCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C([H])S6)C7=NN(CC(CCCCCCCC)CCCCC)N=C75)S4)S8)C8=C2C9=CC=C(SCCCCCCCCCCCC)S9,J61,,,0.91,18.31,71,11.11,"Yang Y, et al. Side-chain isomerization on an n-type organic semiconductor ITIC acceptor makes 11.77% high efficiency polymer solar cells. Journal of the American Chemical Society 138, 15011-15018 (2016)."
449,CCCCCCOC1=C(C2=C(C=C3)N4C3=C(C#CC5=C(CCCCCC)C(CCCCCC)=C(/C=C/C6=C(CCCCCC)C(CCCCCC)=C(/C=C7C(N(CC)C(S/7)=S)=O)S6)S5)C(C=C8)N9C8=C(C%10=C(OCCCCCC)C=CC=C%10OCCCCCC)C%11=CC=C%12N%11[Zn]49N%13C2C=CC%13=C%12C#CC%14=C(CCCCCC)C(CCCCCC)=C(/C=C/C%15=C(CCCCCC)C(CCCCCC)=C(/C=C%16C(N(CC)C(S/%16)=S)=O)S%15)S%14)C(OCCCCCC)=CC=C1,1a,,,0.93,10.67,0.54,5.14,"Arrechea S, Aljarilla A, de la Cruz P, Palomares E, Sharma GD, Langa F. Efficiency improvement using bis(trifluoromethane) sulfonamide lithium salt as a chemical additive in porphyrin based organic solar cells. Nanoscale 8, 17953-17962 (2016)."
450,CCCCCCOC1=C(C2=C(C=C3)N4C3=C(C#CC5=C(CCCCCC)C(CCCCCC)=C(/C=C/C6=C(CCCCCC)C(CCCCCC)=C(/C=C(C#N)/C#N)S6)S5)C(C=C7)N8C7=C(C9=C(OCCCCCC)C=CC=C9OCCCCCC)C%10=CC=C%11N%10[Zn]48N%12C2C=CC%12=C%11C#CC%13=C(CCCCCC)C(CCCCCC)=C(/C=C/C%14=C(CCCCCC)C(CCCCCC)=C(/C=C(C#N)/C#N)S%14)S%13)C(OCCCCCC)=CC=C1,1b,,,0.88,13.34,0.65,7.63,"Arrechea S, Aljarilla A, de la Cruz P, Palomares E, Sharma GD, Langa F. Efficiency improvement using bis(trifluoromethane) sulfonamide lithium salt as a chemical additive in porphyrin based organic solar cells. Nanoscale 8, 17953-17962 (2016)."
451,CCCCCCCC[Si]1(CCCCCCCC)C(C=C(C2=CC=C(C3=CC=C(C)C4=NSN=C34)S2)C=C5)=C5C6=C1C=C(C7=CC=C(C8=CC=C(C)C9=NSN=C89)S7)C=C6,SiF-BT,,,0.9,29.8,0.53,2.06,"Mamoshina P, Vieira A, Putin E, Zhavoronkov A. Applications of Deep Learning in Biomedicine. Mol Pharm 13, 1445-1454 (2016)."
452,FC(C(F)=C(C1=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(C2=CC=C(C3=C(F)C(F)=C(C4=CC=C([H])S4)C=C3)S2)S1)C5=N6)=C(C7=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C([H])S7)C5=NN6CCC,PTFB-O,,,0.92,17.1,0.67,10.5,"Li Z, et al. Donor polymer design enables efficient non-fullerene organic solar cells. Nature Communications 7,  (2016)."
453,CCCCCCCCC(CCCCCC)CC1=CC=C(C2=C3C(SC([H])=C3)=C(C4=CC=C(CC(CCCCCC)CCCCCCCC)S4)C5=C2SC(C6=CC=C(C7=CC=C(C8=CC=C([H])S8)C9=NN(CCCCCCCC)N=C79)S6)=C5)S1,J50,,,0.71,12.93,0.53,4.8,"Gao L, et al. High-Efficiency Nonfullerene Polymer Solar Cells with Medium Bandgap Polymer Donor and Narrow Bandgap Organic Semiconductor Acceptor. Advanced Materials 28, 8288-8295 (2016)."
454,CCCCCCCCC(CCCCCC)CC1=CC=C(C2=C3C(SC([H])=C3)=C(C4=CC=C(CC(CCCCCC)CCCCCCCC)S4)C5=C2SC(C6=CC=C(C7=C(F)C(F)=C(C8=CC=C([H])S8)C9=NN(CCCCCCCC)N=C79)S6)=C5)S1,J51,,,0.82,16.47,0.69,9.26,"Gao L, et al. High-Efficiency Nonfullerene Polymer Solar Cells with Medium Bandgap Polymer Donor and Narrow Bandgap Organic Semiconductor Acceptor. Advanced Materials 28, 8288-8295 (2016)."
455,CCCCCCC1=C(C2=CC(C(OCCCCCC)=O)=C([H])S2)SC([H])=C1,P3HT50-co-3HET50,,,0.736,9.11,0.535,3.59,"Gobalasingham NS, Noh S, Howard JB, Thompson BC. Influence of Surface Energy on Organic Alloy Formation in Ternary Blend Solar Cells Based on Two Donor Polymers. Acs Applied Materials & Interfaces 8, 27931-27941 (2016)."
456,CCCCCCC1=C(C2=CC(CC(CC)CCCC)=C([H])S2)SC([H])=C1,P3HT75-co-EHT25,,,0.68,7.04,0.516,2.47,"Gobalasingham NS, Noh S, Howard JB, Thompson BC. Influence of Surface Energy on Organic Alloy Formation in Ternary Blend Solar Cells Based on Two Donor Polymers. Acs Applied Materials & Interfaces 8, 27931-27941 (2016)."
457,CCCCCC1=C(C2=CC=C(C3=CC=C(C4=C5C(C(N4CC(CC)CCCC)=O)=C(C6=CC=C([H])S6)N(CC(CC)CCCC)C5=O)S3)S2)SC([H])=C1,P3HTT-DPP-10%,,,0.608,12.86,0.631,4.93,"Gobalasingham NS, Noh S, Howard JB, Thompson BC. Influence of Surface Energy on Organic Alloy Formation in Ternary Blend Solar Cells Based on Two Donor Polymers. Acs Applied Materials & Interfaces 8, 27931-27941 (2016)."
458,CCCCCCCCCCC(S1)=C(CCCCCCCCCC)C=C1C2=C3C(SC(C4=CC=C(/C(C#N)=C/C5=CC=C([H])S5)S4)=C3)=C(C6=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S6)C7=C2SC([H])=C7,P(BDT©\TCNT),,,0.78,9.06,0.58,4.1,"Lee YS, et al. Dithieno 2,3-d:2',3'-d' benzo 1,2-b:4,5-b' dithiophene (DTBDAT)-based copolymers for high-performance organic solar cells. Journal of Polymer Science Part a-Polymer Chemistry 54, 3182-3192 (2016)."
459,CCCCCCCCCCC(S1)=C(CCCCCCCCCC)C=C1C2=C3C(SC4=C3SC([H])=C4)=C(C5=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S5)C6=C2SC7=C6SC(C8=CC=C(/C(C#N)=C/C9=CC=C([H])S9)S8)=C7,P(DTBDAT©\TCNT),,,0.77,12.2,0.62,5.83,"Lee YS, et al. Dithieno 2,3-d:2',3'-d' benzo 1,2-b:4,5-b' dithiophene (DTBDAT)-based copolymers for high-performance organic solar cells. Journal of Polymer Science Part a-Polymer Chemistry 54, 3182-3192 (2016)."
460,CCCCCCCCCC(CCCCCC)CSC1=CC=C(C2=C3C(SC(C4=C(CC(CC)CCCC)C=C(C5=CC=C(C6=CC(CC(CC)CCCC)=C([H])S6)C7=NSN=C57)S4)=C3)=C(C8=CC=C(SCC(CCCCCC)CCCCCCCCC)C=C8)C9=C2SC([H])=C9)C=C1,P1,,,0.85,4.22,0.41,1.48,"Fan M, et al. Benzodithiophene-Based Polymers Containing Alkylthiophenyl Side Chains with Lowered HOMO Energy Levels for Organic Solar Cells. Asian Journal of Organic Chemistry 5, 1273-1279 (2016)."
461,CCCCCCCCCC(CCCCCC)CSC1=CC=C(C2=C3C(SC(C4=CC=C(C5=CC=C(C6=CC=C([H])S6)C7C5N=C(C8=CC=CC(OCCCCCCCC)=C8)C(C9=CC=CC=C9OCCCCCCCC)=N7)S4)=C3)=C(C%10=CC=C(SCC(CCCCCC)CCCCCCCCC)C=C%10)C%11=C2SC([H])=C%11)C=C1,P2,,,0.81,7.72,0.688,4.28,"Fan M, et al. Benzodithiophene-Based Polymers Containing Alkylthiophenyl Side Chains with Lowered HOMO Energy Levels for Organic Solar Cells. Asian Journal of Organic Chemistry 5, 1273-1279 (2016)."
462,CCCCCCCCCC(CCCCCC)CSC1=CC=C(C2=C3C(SC(C4=CC=C(C(N(CC(CC)CCCC)C5=O)=C6C5=C(C7=CC=C([H])S7)N(CC(CC)CCCC)C6=O)S4)=C3)=C(C8=CC=C(SCC(CCCCCC)CCCCCCCCC)C=C8)C9=C2SC([H])=C9)C=C1,P3,,,0.74,4.55,0.562,1.9,"Fan M, et al. Benzodithiophene-Based Polymers Containing Alkylthiophenyl Side Chains with Lowered HOMO Energy Levels for Organic Solar Cells. Asian Journal of Organic Chemistry 5, 1273-1279 (2016)."
463,CC(S1)=CC=C1C2=C(C=CC=C3)C3=C4N=C5N([B@]6(C7=CC=CC=C7C8=C6C=CC=C8)N42)C(C9=CC=C(C)S9)=C%10C=CC=CC5%10,2c,,,0.61,8.5,0.51,2.6,"Lorenz-Rothe M, et al. From Fluorine to FluoreneA Route to Thermally Stable aza-BODIPYs for Organic Solar Cell Application. Advanced Electronic Materials 2,  (2016)."
464,CCCCCCC(CCCC)COC1=C(SC(C2=CC=C(C3=CC=C(C4=CC=C([H])S4)C5=C3N=C(C6=CC=C(CCCCCCCC)S6)C(C7=CC=C(CCCCCCCC)S7)=N5)S2)=C8)C8=C(OCC(CCCC)CCCCCC)C9=C1C=C([H])S9,PBDT-TDTQx,,,0.8,5.67,0.5,2.26,"Kim M-J, Kim J-H, Ahn JJ, Hwang D-H. Photovoltaic properties of a new quinoxaline-based copolymer with Thieno 3,2-b thiophene side chain for organic photovoltaic cell applications. Dyes and Pigments 133, 324-332 (2016)."
465,CCCCCCC(CCCC)COC1=C(SC(C2=CC=C(C3=CC=C(C4=CC=C([H])S4)C5=C3N=C(C6=CC(SC(CCCCCCCC)=C7)=C7S6)C(C8=CC(SC(CCCCCCCC)=C9)=C9S8)=N5)S2)=C%10)C%10=C(OCC(CCCC)CCCCCC)C%11=C1C=C([H])S%11,PBDT-TTDTQx,,,0.78,8.5,0.51,3.42,"Kim M-J, Kim J-H, Ahn JJ, Hwang D-H. Photovoltaic properties of a new quinoxaline-based copolymer with Thieno 3,2-b thiophene side chain for organic photovoltaic cell applications. Dyes and Pigments 133, 324-332 (2016)."
466,[H]C1=CC=C(C2=C3C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C7=C(OCCCCCCCC)C(OCCCCCCCC)=C(C8=CC=C([H])S8)C9=NON=C79)S6)C%10=NON=C5%10)S4)C=C2)C(N3C(CCCCCCCC)CCCCCCCC)=C1,P1,,,0.845,7.2,0.42,2.5,"Klimovich IV, et al. Solubilized 5,6-bis(octyloxy)benzoxadiazole as a versatile acceptor block for designing novel (-X-DADAD-)(n) and (-X-DADADAD-)(n) electron donor copolymers for bulk heterojunction organic solar cells. Solar Energy Materials and Solar Cells 155, 378-386 (2016)."
467,[H]C1=CC=C(C2=C3C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C7=C(OCCCCCCCC)C(OCCCCCCCC)=C(C8=CC=C(C9=C(OCCCCCCCC)C(OCCCCCCCC)=C(C%10=CC=C([H])S%10)C%11=NON=C9%11)S8)C%12=NON=C7%12)S6)C%13=NON=C5%13)S4)C=C2)C(N3C(CCCCCCCC)CCCCCCCC)=C1,P2,,,0.902,5.6,0.49,2.5,"Klimovich IV, et al. Solubilized 5,6-bis(octyloxy)benzoxadiazole as a versatile acceptor block for designing novel (-X-DADAD-)(n) and (-X-DADADAD-)(n) electron donor copolymers for bulk heterojunction organic solar cells. Solar Energy Materials and Solar Cells 155, 378-386 (2016)."
468,CCCCCCCCOC1=C(C2=CC=C(C3=CC=C([H])S3)S2)C4=NON=C4C(C5=CC=C(C6=C(OCCCCCCCC)C(OCCCCCCCC)=C(C7=CC=C(C8=CC=C(C9=CC%10=C(C%11=CC=C([H])C=C%11N%10C(CCCCCCCC)CCCCCCCC)C=C9)S8)S7)C%12=NON=C6%12)S5)=C1OCCCCCCCC,P3,,,0.862,10.8,0.59,5.5,"Klimovich IV, et al. Solubilized 5,6-bis(octyloxy)benzoxadiazole as a versatile acceptor block for designing novel (-X-DADAD-)(n) and (-X-DADADAD-)(n) electron donor copolymers for bulk heterojunction organic solar cells. Solar Energy Materials and Solar Cells 155, 378-386 (2016)."
469,O=C1N(CC(CCCCCCCC)CCCCCC)C(C2=CC(CCCCCCCCCC)=C([H])S2)=C3C1=C(C4=CC(CCCCCCCCCC)=C(C5=CC=C([H])S5)S4)N(CC(CCCCCCCC)CCCCCC)C3=O,P(T-DPP),,,0.62,5.5,0.544,1.84,"Lo CK, Reynolds JR. Structural and morphological effects of alkyl side chains on flanking thiophenes of diketopyrrolopyrrole polymers for organic photovoltaic devices. Polymer 99, 741-747 (2016)."
470,O=C1N(CC(CCCCCCCC)CCCCCC)C(C2=CC(CCCCCCCCCC)=C([H])S2)=C3C1=C(C4=CC(CCCCCCCCCC)=C(C5=CC(SC([H])=C6)=C6S5)S4)N(CC(CCCCCCCC)CCCCCC)C3=O,P(TT-DPP),,,0.61,10.45,0.465,3,"Lo CK, Reynolds JR. Structural and morphological effects of alkyl side chains on flanking thiophenes of diketopyrrolopyrrole polymers for organic photovoltaic devices. Polymer 99, 741-747 (2016)."
471,CCCCC(CC)CSC1=CC=C(S1)C2=C3C(SC(C4=CC=C(C5=C(C(C6=C(CC(CC)CCCC)[Se]C(CC(CC)CCCC)=C6C7=O)=O)C7=C(C8=CC=C([H])S8)S5)S4)=C3)=C(C9=CC=C(SCC(CC)CCCC)S9)C%10=C2SC([H])=C%10,PBDTS-Se,,,0.909,12.8,0.688,8.01,"Liu T, et al. High-Performance Non-Fullerene Organic Solar Cells Based on a Selenium-Containing Polymer Donor and a Twisted Perylene Bisimide Acceptor. Advanced Science 3,  (2016)."
472,CCCCC(CC)COC1=C(SC(C2=C3C(F)=C(C(OCCCCCCOCC4=CC(Cl)=C(Cl)C=C4)=O)SC3=C([H])S2)=C5)C5=C(OCC(CC)CCCC)C6=C1C=C([H])S6,PTB7-DCB,,,0.77,11.66,0.47,4.22,"Jo JW, Kim Y, Ko MJ, Son HJ. Development of intrinsically fullerene-compatible polymers: Strategy for developing high performance organic solar cells using a non-halogenated solvent. Dyes and Pigments 132, 103-109 (2016)."
473,FC1=C(C(OCCCCCCOCC2=CC(Cl)=C(Cl)C=C2)=O)SC3=C([H])SC(C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C([H])S8)=C13,PTB7-Th-DCB,,,0.82,15.11,0.49,6.07,"Jo JW, Kim Y, Ko MJ, Son HJ. Development of intrinsically fullerene-compatible polymers: Strategy for developing high performance organic solar cells using a non-halogenated solvent. Dyes and Pigments 132, 103-109 (2016)."
474,FC1=C(C2=CC([Si]3(CC(CC)CCCC)CC(CC)CCCC)=C(C4=C3C=C(C5=C(F)C=C(C6=CC=C(C7=CC=C(C(N(CCCCCC)C8=O)=O)C8=C7)S6)C9=NSN=C59)S4)S2)C%10=NSN=C%10C(C%11=CC=C(C%12=CC=C(C(N(CCCCCC)C%13=O)=O)C%13=C%12)S%11)=C1,DTS(FBT-Th-Pht-Hex)2,,,0.734,1.12,0.29,0.24,"San Juan RR, Payne A-J, Welch GC, Eftaiha AaF. Development of low band gap molecular donors with phthalimide terminal groups for use in solution processed organic solar cells. Dyes and Pigments 132, 369-377 (2016)."
475,FC1=C(C2=CC([Si]3(CC(CC)CCCC)CC(CC)CCCC)=C(C4=C3C=C(C5=C(F)C=C(C6=CC=C(C7=CC=C(C(N(CCCCCCCC)C8=O)=O)C8=C7)S6)C9=NSN=C59)S4)S2)C%10=NSN=C%10C(C%11=CC=C(C%12=CC=C(C(N(CCCCCCCC)C%13=O)=O)C%13=C%12)S%11)=C1,DTS(FBT-Th-Pht-Oct)2,,,0.867,1.7,0.47,0.7,"San Juan RR, Payne A-J, Welch GC, Eftaiha AaF. Development of low band gap molecular donors with phthalimide terminal groups for use in solution processed organic solar cells. Dyes and Pigments 132, 369-377 (2016)."
476,FC1=C(C2=CC=C(C3=CC=C(CCCCCC)S3)S2)C4=NN(CCCCCC)N=C4C(C5=CC([Si]6(CC(CC)CCCC)CC(CC)CCCC)=C(C7=C6C=C(C8=CC(F)=C(C9=CC=C(C%10=CC=C(CCCCCC)S%10)S9)C%11=NN(CCCCCC)N=C8%11)S7)S5)=C1.CC,K2,,,0.83,11.68,0.62,6.01,"Keshtov ML, et al. Design, synthesis and photophysical properties of D1-A-D2-A-D1-type small molecules based on fluorobenzotriazole acceptor and dithienosilole core donor for solution processed organic solar cells. Dyes and Pigments 132, 387-397 (2016)."
477,CCCCCCN1N=C2C(C3=CC=C(C4=CC=C(CCCCCC)S4)S3)=CC(F)=C(C5=CC([Si]6(CC(CC)CCCC)CC(CC)CCCC)=C(C7=C6C=C(C8=C(F)C=C(C9=CC=C(C%10=CC=C(CCCCCC)S%10)S9)C%11=NN(CCCCCC)N=C8%11)S7)S5)C2=N1.CC,K3,,,0.8,10.24,0.58,4.75,"Keshtov ML, et al. Design, synthesis and photophysical properties of D1-A-D2-A-D1-type small molecules based on fluorobenzotriazole acceptor and dithienosilole core donor for solution processed organic solar cells. Dyes and Pigments 132, 387-397 (2016)."
478,O=C1N(CC(CCCCCCCCCC)CCCCCCCC)C(C2=NC=C([H])C=C2)=C3C1=C(C4=NC=C(C5=CC=C(C6=CC=C([H])S6)S5)C=C4)N(CC(CCCCCCCC)CCCCCCCCCC)C3=O,PDPP2Py2T,,,0.977,11.34,0.644,7.13,"Hendriks KH, Wijpkema ASG, van Franeker JJ, Wienk MM, Janssen RAJ. Dichotomous Role of Exciting the Donor or the Acceptor on Charge Generation in Organic Solar Cells. Journal of the American Chemical Society 138, 10026-10031 (2016)."
479,O=C1N(CC(CCCCCCCC)CCCCCC)C(C2=NC=C(C3=CC(CCCCCC)=C([H])S3)C=C2)=C4C1=C(C5=NC=C(C6=CC(CCCCCC)=C(C7=CC=C([H])S7)S6)C=C5)N(CC(CCCCCC)CCCCCCCC)C4=O,PDPP2Py3T,,,0.855,11.1,0.629,5.97,"Hendriks KH, Wijpkema ASG, van Franeker JJ, Wienk MM, Janssen RAJ. Dichotomous Role of Exciting the Donor or the Acceptor on Charge Generation in Organic Solar Cells. Journal of the American Chemical Society 138, 10026-10031 (2016)."
480,O=C1N(CC(CCCCCCCC)CCCCCC)C(C2=NC=C([H])C=C2)=C3C1=C(C4=NC=C(C5=CC(N6CC(CC)CCCC)=C(C7=C6C=C([H])S7)S5)C=C4)N(CC(CCCCCC)CCCCCCCC)C3=O,PDPP2PyDTP,,,0.711,12.61,0.56,5.02,"Hendriks KH, Wijpkema ASG, van Franeker JJ, Wienk MM, Janssen RAJ. Dichotomous Role of Exciting the Donor or the Acceptor on Charge Generation in Organic Solar Cells. Journal of the American Chemical Society 138, 10026-10031 (2016)."
481,O=C1N(CC(CCCCCCCC)CCCCCC)C(C2=NC=C([H])C=C2)=C3C1=C(C4=NC=C(C5=CC=C([H])S5)C=C4)N(CC(CCCCCC)CCCCCCCC)C3=O,PDPP2PyT,,,1,7.48,0.616,4.61,"Hendriks KH, Wijpkema ASG, van Franeker JJ, Wienk MM, Janssen RAJ. Dichotomous Role of Exciting the Donor or the Acceptor on Charge Generation in Organic Solar Cells. Journal of the American Chemical Society 138, 10026-10031 (2016)."
482,FC1=C(C2=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(S2)C(S3)=CC(C3=C4)=CC5=C4C=C([H])S5)C6=NSN=C6C(C7=CC(CC(CCCCCCCC)CCCCCCCCCC)=C([H])S7)=C1F,PBDT-DTFFBT,,,0.85,14.38,0.742,9.13,"Chen W, et al. Unsubstituted Benzodithiophene-Based Conjugated Polymers for High-Performance Organic Field-Effect Transistors and Organic Solar Cells. Acs Applied Materials & Interfaces 8, 19665-19671 (2016)."
483,[H]C1=CC=C(S1)C2=CC=C(C3=CC=C(S3)C4=CC5=C(C6=C([Ge]5(CC(CCCCCCCC)CCCCCCCCCC)CC(CCCCCCCC)CCCCCCCCCC)C=C([H])S6)S4)C7=NSN=C27,P(Ge-DTBT),,,0.66,7.95,0.68,3.51,"Casey A, et al. Effect of Systematically Tuning Conjugated Donor Polymer Lowest Unoccupied Molecular Orbital Levels via Cyano Substitution on Organic Photovoltaic Device Performance. Chemistry of Materials 28, 5110-5120 (2016)."
484,[H]C1=CC=C(S1)C2=C(C#N)C(C#N)=C(C3=CC=C(S3)C4=CC5=C(C6=C([Ge]5(CC(CCCCCCCC)CCCCCCCCCC)CC(CCCCCCCC)CCCCCCCCCC)C=C([H])S6)S4)C7=NSN=C27,P(Ge-DTDCNBT),,,0.68,2.99,0.36,0.63,"Casey A, et al. Effect of Systematically Tuning Conjugated Donor Polymer Lowest Unoccupied Molecular Orbital Levels via Cyano Substitution on Organic Photovoltaic Device Performance. Chemistry of Materials 28, 5110-5120 (2016)."
485,CCCCCCCCOC1=CC=CC(C2=NC3=C(C4=CC=C(C5=CC=C(CCCCCC)S5)S4)C=CC(C6=CC7=C(C(SC(C8=C(N=C(C9=CC=CC(OCCCCCCCC)=C9)C(C%10=CC(OCCCCCCCC)=CC=C%10)=N%11)C%11=C(C%12=CC=C(C%13=CC=C(CCCCCC)S%13)S%12)C=C8)=C%14)C%14[Si]7(C(CC)CCCCC)C(CC)CCCCC)S6)=C3N=C2C%15=CC=CC(OCCCCCCCC)=C%15)=C1,DTS(FCT2)2,,,0.76,2.69,0.29,0.59,"Keshtov ML, Kuklin SA, Buzin MI, Godowsky DY, Khokhlov AR. Synthesis and photophysical properties of semiconductor molecules of D-1-A-D-2-A-D-1 structure on the basis of quinoxaline and dithienosilole derivatives for organic solar cells. Doklady Physical Chemistry 469, 106-110 (2016)."
486,FC1=C(C2=CC(C(OCC(CCCCCCCCCC)CCCCCCCC)=O)=C(S2)C3=CC(CC(CCCCCCC)CCCCCC)=C([H])S3)C4=NSN=C4C(C5=CC(C(OCC(CCCCCCCCCC)CCCCCCCC)=O)=C(C6=C(CC(CCCCCCC)CCCCCC)C=C(C7=CC=C(C8=C(F)C(F)=C(C9=CC=C([H])S9)C%10=NSN=C8%10)S7)S6)S5)=C1F,P3TEA,,,1.11,13.27,0.643,9.5,"Liu J, et al. Fast charge separation in a non-fullerene organic solar cell with a small driving force. Nature Energy 1,  (2016)."
487,CCCCCCCCSC1=CC=C(S1)C2=C(SC(C3=C4SC(C(OCC(CC)CCCCC)=O)=C(F)C4=C([H])S3)=C5)C5=C(C6=CC=C(SCCCCCCCC)S6)C7=C2C=C([H])S7,PBDT-TS1,,,0.714,14.82,0.5457,5.81,"Liang N, et al. Perylene Diimide Trimers Based Bulk Heterojunction Organic Solar Cells with Efficiency over 7%. Advanced Energy Materials 6,  (2016)."
488,CCCCCCCCSC1=CC=C(S1)C2=C(SC([H])=C3)C3=C(C4=CC=C(SCCCCCCCC)S4)C5=C2C=C(C6=C(SCCCCCCCC)C=C(C7=CC(SCCCCCCCC)=C([H])S7)S6)S5,P1,,,0.747,5.5,0.366,1.49,"Parenti F, et al. Polymers for Application in Organic Solar Cells: Bithiophene Can Work Better than Thienothiophene When Coupled to Benzodithiophene. Journal of Polymer Science Part a-Polymer Chemistry 54, 1603-1614 (2016)."
489,CCCCCCCCSC1=CC=C(S1)C2=C(SC(C3=C4SC(C(OCCCCCCCC)=O)=CC4=C([H])S3)=C5)C5=C(C6=CC=C(SCCCCCCCC)S6)C7=C2C=C([H])S7,P2,,,0.642,3.2,0.289,0.59,"Parenti F, et al. Polymers for Application in Organic Solar Cells: Bithiophene Can Work Better than Thienothiophene When Coupled to Benzodithiophene. Journal of Polymer Science Part a-Polymer Chemistry 54, 1603-1614 (2016)."
490,O=C1N(CC(CCCCCCCC)CCCCCCCCCC)C(C2=CC=C(C3=CC(N=C(OCCCCCCCC)C4=C5C=CC([H])=C4)=C5C=C3)S2)=C6C1=C(C7=CC=C([H])S7)N(CC(CCCCCCCC)CCCCCCCCCC)C6=O,P1,,,0.82,8.16,0.57,3.8,"Guerette M, et al. New Processable Phenanthridinone-Based Polymers for Organic Solar Cell Applications. Advanced Energy Materials 6,  (2016)."
491,O=C1N(CC(CCCCCCCC)CCCCCCCCCC)C(C2=CC=C(C3=CC(N(CCCCCCCC)C(C4=C5C=CC([H])=C4)=O)=C5C=C3)S2)=C6C1=C(C7=CC=C([H])S7)N(CC(CCCCCCCC)CCCCCCCCCC)C6=O,P2,,,0.86,8.22,0.51,3.6,"Guerette M, et al. New Processable Phenanthridinone-Based Polymers for Organic Solar Cell Applications. Advanced Energy Materials 6,  (2016)."
492,O=C1N(CC(CCCCCCCC)CCCCCCCCCC)C(C2=CC=C(C3=CC(N=C(OCCCCCCCC)C4=C5C=CC(C6=CC=C(S6)C7=C8C(C(N7CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C9=CC=C(C%10=CC(N(CCCCCCCC)C(C%11=C%12C=CC([H])=C%11)=O)=C%12C=C%10)S9)N(CC(CCCCCCCC)CCCCCCCCCC)C8=O)=C4)=C5C=C3)S2)=C%13C1=C(C%14=CC=C([H])S%14)N(CC(CCCCCCCC)CCCCCCCCCC)C%13=O,P3,,,0.85,11.06,0.65,6.3,"Guerette M, et al. New Processable Phenanthridinone-Based Polymers for Organic Solar Cell Applications. Advanced Energy Materials 6,  (2016)."
493,O=C1N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C(C2=CC=C([H])S2)=C3C1=C(C4=CC=C(C5=CC=C(C6=CC=C([H])S6)S5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O,PTDPP2T,,,0.63,14.89,0.7,6.58,"Lee JW, Choi YS, Ahn H, Jo WH. Ternary Blend Composed of Two Organic Donors and One Acceptor for Active Layer of High-Performance Organic Solar Cells. Acs Applied Materials & Interfaces 8, 10961-10967 (2016)."
494,CC1(C)C(C=C(C([O-])=C2C3=C(O)C=C(N4C(CCC5)C5C6=C4C=CC=C6)C=C3O)C2=O)=[N+](CCCC)C7=CC=CC=C71,USQ-11,,,0.86,10.34,0.48,4.27,"Yang D, et al. Two different donor subunits substituted unsymmetrical squaraines for solution-processed small molecule organic solar cells. Organic Electronics 32, 179-186 (2016)."
495,O=C1C(C2=C(O)C=C(N3C(CCC4)C4C5=C3C=CC=C5)C=C2O)=C([O-])C1=CC6=[N+](CCCC)C7=CC=CC=C7S6,USQ-12,,,0.72,9.34,0.45,3.03,"Yang D, et al. Two different donor subunits substituted unsymmetrical squaraines for solution-processed small molecule organic solar cells. Organic Electronics 32, 179-186 (2016)."
496,CCCCCCCCC(CCCCCCCC)N1C2=CC([H])=CC=C2C3=C1C=C(C4=CC(CC(CC)CCCC)=C(C5=CC=C(C6=CC=C(C7=CC=C(C8=C(CC(CC)CCCC)C=C([H])S8)C9=NSN=C79)S6)C%10=NSN=C5%10)S4)C=C3,P3,,,0.8,3.3,0.33,0.9,"Akkuratov AV, Susarova DK, Mukhacheva OA, Troshin PA. Design of highly soluble PCDTBTBT-type conjugated polymers for organic solar cells. Mendeleev Communications 26, 248-250 (2016)."
497,CCCCCCCCC(CCCCCCCC)N1C2=CC([H])=CC=C2C3=C1C=C(C4=C(CC(CC)CCCC)C=C(C5=CC=C(C6=CC=C(C7=CC=C(C8=CC(CC(CC)CCCC)=C([H])S8)C9=NSN=C79)S6)C%10=NSN=C5%10)S4)C=C3,P4,,,0.701,4.7,0.36,1.2,"Akkuratov AV, Susarova DK, Mukhacheva OA, Troshin PA. Design of highly soluble PCDTBTBT-type conjugated polymers for organic solar cells. Mendeleev Communications 26, 248-250 (2016)."
498,CCCCCCCCC(CCCCCCCC)N1C2=CC([H])=CC=C2C3=C1C=C(C4=CC=C(C5=CC=C(C6=CC=C(C7=CC=C(C8=CC=C([H])S8)C9=NSN=C79)S6)C%10=NSN=C5%10)S4)C=C3,PCDTBTBT,,,0.706,4.5,0.3,0.9,"Akkuratov AV, Susarova DK, Mukhacheva OA, Troshin PA. Design of highly soluble PCDTBTBT-type conjugated polymers for organic solar cells. Mendeleev Communications 26, 248-250 (2016)."
499,CCCCC(CC)C[Si]1(CC(CC)CCCC)C2=C(SC(C3=C(F)C=C(C4=CC=C(C5=CC=C(CCCCCC)S5)S4)C6=NSN=C36)=C2)C7=C1C=C(C8=C(F)C=C(C9=CC=C(C%10=CC=C(CCCCCC)S%10)S9)C%11=NSN=C8%11)S7,p-DTS(FBTTh2)2,,,0.74,17.8,0.52,6.83,"Kim IK, Jo JH, Yun J-H. Morphology-Controlled High-Efficiency Small Molecule Organic Solar Cells without Additive Solvent Treatment. Nanomaterials (Basel, Switzerland) 6,  (2016)."
500,FC1=C(C2=CC([Si](CC(CC)CCCC)(CC(CC)CCCC)C3=C4SC(C5=C6C(SC(C(C7=CC=C(OC)C=C7)=O)=C6)=C(C(S8)=CC([Si]9(CC(CC)CCCC)CC(CC)CCCC)=C8C%10=C9C=C(S%10)C%11=C(F)C=C(C%12=CC=C(C%13=CC=C(CCCCCC)S%13)S%12)C%14=NSN=C%11%14)S5)=C3)=C4S2)C%15=NSN=C%15C(C%16=CC=C(C%17=CC=C(CCCCCC)S%17)S%16)=C1,oligo-1a,,,0.56,7.16,0.47,1.88,"Wada Y, et al. Synthesis of Thieno 3,4-b thiophene-Based Donor Molecules with Phenyl Ester Pendants for Organic Solar Cells: Control of Photovoltaic Properties via Single Substituent Replacement. Chemistryselect 1, 703-709 (2016)."
501,FC1=C(C2=CC([Si](CC(CC)CCCC)(CC(CC)CCCC)C3=C4SC(C5=C6C(SC(C(C7=CC=CC=C7)=O)=C6)=C(C(S8)=CC([Si]9(CC(CC)CCCC)CC(CC)CCCC)=C8C%10=C9C=C(S%10)C%11=C(F)C=C(C%12=CC=C(C%13=CC=C(CCCCCC)S%13)S%12)C%14=NSN=C%11%14)S5)=C3)=C4S2)C%15=NSN=C%15C(C%16=CC=C(C%17=CC=C(CCCCCC)S%17)S%16)=C1,oligo-1b,,,0.56,7,0.56,2.19,"Wada Y, et al. Synthesis of Thieno 3,4-b thiophene-Based Donor Molecules with Phenyl Ester Pendants for Organic Solar Cells: Control of Photovoltaic Properties via Single Substituent Replacement. Chemistryselect 1, 703-709 (2016)."
502,FC1=C(C2=CC([Si](CC(CC)CCCC)(CC(CC)CCCC)C3=C4SC(C5=C6C(SC(C(C7=CC=C(F)C=C7)=O)=C6)=C(C(S8)=CC([Si]9(CC(CC)CCCC)CC(CC)CCCC)=C8C%10=C9C=C(S%10)C%11=C(F)C=C(C%12=CC=C(C%13=CC=C(CCCCCC)S%13)S%12)C%14=NSN=C%11%14)S5)=C3)=C4S2)C%15=NSN=C%15C(C%16=CC=C(C%17=CC=C(CCCCCC)S%17)S%16)=C1,oligo-1c,,,0.58,6.07,0.5,1.75,"Wada Y, et al. Synthesis of Thieno 3,4-b thiophene-Based Donor Molecules with Phenyl Ester Pendants for Organic Solar Cells: Control of Photovoltaic Properties via Single Substituent Replacement. Chemistryselect 1, 703-709 (2016)."
503,FC1=C(C2=CC([Si](CC(CC)CCCC)(CC(CC)CCCC)C3=C4SC(C5=C6C(SC(C(C7=CC=C(C(F)(F)F)C=C7)=O)=C6)=C(C(S8)=CC([Si]9(CC(CC)CCCC)CC(CC)CCCC)=C8C%10=C9C=C(S%10)C%11=C(F)C=C(C%12=CC=C(C%13=CC=C(CCCCCC)S%13)S%12)C%14=NSN=C%11%14)S5)=C3)=C4S2)C%15=NSN=C%15C(C%16=CC=C(C%17=CC=C(CCCCCC)S%17)S%16)=C1,oligo-1d,,,0.6,8.17,0.53,2.58,"Wada Y, et al. Synthesis of Thieno 3,4-b thiophene-Based Donor Molecules with Phenyl Ester Pendants for Organic Solar Cells: Control of Photovoltaic Properties via Single Substituent Replacement. Chemistryselect 1, 703-709 (2016)."
504,FC1=C(C2=CC=C(C3=CC(C(CC(CC)CCCC)(C4=C5C=C(C(CC(CC)CCCC)(CC(CC)CCCC)C6=C7SC(C8=CC=C(C9=C(F)C(F)=C(C%10=CC=C(C%11=CC=C(CCCCCC)S%11)S%10)C%12=NSN=C9%12)[Se]8)=C6)C7=C4)CC(CC)CCCC)=C5S3)[Se]2)C%13=NSN=C%13C(C%14=CC=C(C%15=CC=C(CCCCCC)S%15)S%14)=C1F,BIT4FSe,,,0.87,13.4,0.72,8.41,"Wang J-L, et al. Difluorobenzothiadiazole-Based Small-Molecule Organic Solar Cells with 8.7% Efficiency by Tuning of pi-Conjugated Spacers and Solvent Vapor Annealing. Advanced Functional Materials 26, 1803-1812 (2016)."
505,CCCCCCC(CCCC)COC1=C(SC(C(S2)=C(CCCCCCCCCC)C3=C2C=C(C4=C5C(C(N(CC(CCCCCC)CCCCCCCC)C5=O)=O)=C(C6=CC(SC([H])=C7CCCCCCCCCC)=C7S6)S4)S3)=C8)C8=C(OCC(CCCC)CCCCCC)C9=C1C=C([H])S9,PBDT©\10ttTPD,,,0.84,11.45,0.73,7.14,"Kim J-H, et al. Optimization and Analysis of Conjugated Polymer Side Chains for High-Performance Organic Photovoltaic Cells. Advanced Functional Materials 26, 1517-1525 (2016)."
506,CCCCCCC(CCCC)COC1=C(SC(C(S2)=C(CCCCCC)C3=C2C=C(C4=C5C(C(N(CC(CCCCCC)CCCCCCCC)C5=O)=O)=C(C6=CC(SC([H])=C7CCCCCC)=C7S6)S4)S3)=C8)C8=C(OCC(CCCC)CCCCCC)C9=C1C=C([H])S9,PBDT©\6ttTPD,,,0.79,10.07,0.55,4.39,"Kim J-H, et al. Optimization and Analysis of Conjugated Polymer Side Chains for High-Performance Organic Photovoltaic Cells. Advanced Functional Materials 26, 1517-1525 (2016)."
507,CCCCCCC(CCCC)COC1=C(SC(C(S2)=C(CCCCCCCC)C3=C2C=C(C4=C5C(C(N(CC(CCCCCC)CCCCCCCC)C5=O)=O)=C(C6=CC(SC([H])=C7CCCCCCCC)=C7S6)S4)S3)=C8)C8=C(OCC(CCCC)CCCCCC)C9=C1C=C([H])S9,PBDT©\8ttTPD,,,0.83,15.04,0.61,7.57,"Kim J-H, et al. Optimization and Analysis of Conjugated Polymer Side Chains for High-Performance Organic Photovoltaic Cells. Advanced Functional Materials 26, 1517-1525 (2016)."
508,[H]C(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C4C(SC(C(S5)=C(CCCCCCCCCC)C6=C5C=C(C7=C8C(C(N(CC(CCCCCC)CCCCCCCC)C8=O)=O)=C(C9=CC(SC([H])=C%10CCCCCCCCCC)=C%10S9)S7)S6)=C4)=C2C%11=CC=C(CC(CCCC)CCCCCC)S%11,PBDTT©\10ttTPD,,,0.81,12.53,0.71,7,"Kim J-H, et al. Optimization and Analysis of Conjugated Polymer Side Chains for High-Performance Organic Photovoltaic Cells. Advanced Functional Materials 26, 1517-1525 (2016)."
509,[H]C(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C4C(SC(C(S5)=C(CCCCCC)C6=C5C=C(C7=C8C(C(N(CC(CCCCCC)CCCCCCCC)C8=O)=O)=C(C9=CC(SC([H])=C%10CCCCCC)=C%10S9)S7)S6)=C4)=C2C%11=CC=C(CC(CCCC)CCCCCC)S%11,PBDTT©\6ttTPD,,,0.83,15.76,0.63,8.23,"Kim J-H, et al. Optimization and Analysis of Conjugated Polymer Side Chains for High-Performance Organic Photovoltaic Cells. Advanced Functional Materials 26, 1517-1525 (2016)."
510,[H]C(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C4C(SC(C(S5)=C(CCCCCCCC)C6=C5C=C(C7=C8C(C(N(CC(CCCCCC)CCCCCCCC)C8=O)=O)=C(C9=CC(SC([H])=C%10CCCCCCCC)=C%10S9)S7)S6)=C4)=C2C%11=CC=C(CC(CCCC)CCCCCC)S%11,PBDTT©\8ttTPD,,,0.83,16.29,0.64,8.67,"Kim J-H, et al. Optimization and Analysis of Conjugated Polymer Side Chains for High-Performance Organic Photovoltaic Cells. Advanced Functional Materials 26, 1517-1525 (2016)."
511,CCCCCCCCOC(C=C1)=CC=C1/C(C2=CC=C(/C(C#CC3=CC=C(C4=C5C(C(N4CC(CC)CCCC)=O)=C(C6=CC=CO6)N(CC(CC)CCCC)C5=O)O3)=C7N=C8C=C\7)N2[Zn]N9/C(C=C/C9=C8\C%10=CC=C(OCCCCCCCC)C=C%10)=C%11/C#CC%12=CC=C(C%13=C%14C(C(N%13CC(CC)CCCC)=O)=C(C%15=CC=CO%15)N(CC(CC)CCCC)C%14=O)O%12)=C%16C=CC%11=N\%16,PorODPP,,,0.81,10.52,0.5001,4.26,"Liang T, et al. Porphyrin small molecules containing furan- and selenophene-substituted diketopyrrolopyrrole for bulk heterojunction organic solar cells. Organic Electronics 29, 127-134 (2016)."
512,CCCCCCCCOC(C=C1)=CC=C1/C(C2=CC=C(/C(C#CC3=CC=C(C4=C5C(C(N4CC(CC)CCCC)=O)=C(C6=CC=C[Se]6)N(CC(CC)CCCC)C5=O)[Se]3)=C7N=C8C=C\7)N2[Zn]N9/C(C=C/C9=C8\C%10=CC=C(OCCCCCCCC)C=C%10)=C%11/C#CC%12=CC=C(C%13=C%14C(C(N%13CC(CC)CCCC)=O)=C(C%15=CC=C[Se]%15)N(CC(CC)CCCC)C%14=O)[Se]%12)=C%16C=CC%11=N\%16,PorSeDPP,,,0.71,14.93,0.5471,5.81,"Liang T, et al. Porphyrin small molecules containing furan- and selenophene-substituted diketopyrrolopyrrole for bulk heterojunction organic solar cells. Organic Electronics 29, 127-134 (2016)."
513,CCCCCCCCC1=CC=C(S1)C2=NC3=C(N=C2C4=CC=C(CCCCCCCC)S4)C(C5=CC=C([H])S5)=C(F)C=C3[H],FTTQ,,,0.74,6.31,0.569,2.59,"Gao B, Meng J, Yin X, He Y, Que W. Fluorine substituted thienyl-quinoxaline copolymer to reduce the highest occupied molecular orbit level and increase open-circuit voltage for organic solar cells. Materials Express 6, 19-27 (2016)."
514,FC1=C(C2=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(C3=CC=C(C4=CC=C([H])S4)S3)S2)C5=NSN=C5C(C6=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C([H])S6)=C1F,P4T2FBT,,,0.93,11.03,0.511,5.11,"Lee J, Singh R, Sin DH, Kim HG, Song KC, Cho K. A Nonfullerene Small Molecule Acceptor with 3D Interlocking Geometry Enabling Efficient Organic Solar Cells. Advanced Materials 28, 69-+ (2016)."
515,FC1=C(C2=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(C3=CC=C(/C=C/C4=CC=C([H])S4)S3)S2)C5=NSN=C5C(C6=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C([H])S6)=C1F,PV4T2FBT,,,0.9,12.02,0.542,5.82,"Lee J, Singh R, Sin DH, Kim HG, Song KC, Cho K. A Nonfullerene Small Molecule Acceptor with 3D Interlocking Geometry Enabling Efficient Organic Solar Cells. Advanced Materials 28, 69-+ (2016)."
516,CCCCC(CC)C[Si]1(CC(CC)CCCC)C2=C(SC(C3=CC=C(C4=CC=C(C5=CC=C(CCCCCC)S5)S4)C6=NSN=C36)=C2)C7=C1C=C(C8=CC=C(C9=CC=C(C%10=CC=C(CCCCCC)S%10)S9)C%11=NSN=C8%11)S7,0F,,,0.76,4.55,0.34,1.16,"Yun JH, et al. Enhancement of charge transport properties of small molecule semiconductors by controlling fluorine substitution and effects on photovoltaic properties of organic solar cells and perovskite solar cells. Chemical Science 7, 6649-6661 (2016)."
517,CCCCC(CC)C[Si]1(CC(CC)CCCC)C2=C(SC(C3=C(F)C=C(C4=CC=C(C5=CC=C(CCCCCC)S5)S4)C6=NSN=C36)=C2)C7=C1C=C(C8=CC=C(C9=CC=C(C%10=CC=C(CCCCCC)S%10)S9)C%11=NSN=C8%11)S7,1F,,,0.7,8.23,0.53,3.02,"Yun JH, et al. Enhancement of charge transport properties of small molecule semiconductors by controlling fluorine substitution and effects on photovoltaic properties of organic solar cells and perovskite solar cells. Chemical Science 7, 6649-6661 (2016)."
518,CCCCC(CC)C[Si]1(CC(CC)CCCC)C2=C(SC(C3=C(F)C=C(C4=CC=C(C5=CC=C(CCCCCC)S5)S4)C6=NSN=C36)=C2)C7=C1C=C(C8=C(F)C=C(C9=CC=C(C%10=CC=C(CCCCCC)S%10)S9)C%11=NSN=C8%11)S7,2F,,,0.81,14.96,0.66,7.98,"Yun JH, et al. Enhancement of charge transport properties of small molecule semiconductors by controlling fluorine substitution and effects on photovoltaic properties of organic solar cells and perovskite solar cells. Chemical Science 7, 6649-6661 (2016)."
519,CCCCC(CC)C[Si]1(CC(CC)CCCC)C2=C(SC(C3=C(F)C=C(C4=CC=C(C5=CC=C(CCCCCC)S5)S4)C6=NSN=C36)=C2)C7=C1C=C(C8=C(F)C(F)=C(C9=CC=C(C%10=CC=C(CCCCCC)S%10)S9)C%11=NSN=C8%11)S7,3F,,,0.78,13.42,0.62,6.59,"Yun JH, et al. Enhancement of charge transport properties of small molecule semiconductors by controlling fluorine substitution and effects on photovoltaic properties of organic solar cells and perovskite solar cells. Chemical Science 7, 6649-6661 (2016)."
520,CCCCC(CC)C[Si]1(CC(CC)CCCC)C2=C(SC(C3=C(F)C(F)=C(C4=CC=C(C5=CC=C(CCCCCC)S5)S4)C6=NSN=C36)=C2)C7=C1C=C(C8=C(F)C(F)=C(C9=CC=C(C%10=CC=C(CCCCCC)S%10)S9)C%11=NSN=C8%11)S7,4F,,,0.86,11.56,0.69,6.86,"Yun JH, et al. Enhancement of charge transport properties of small molecule semiconductors by controlling fluorine substitution and effects on photovoltaic properties of organic solar cells and perovskite solar cells. Chemical Science 7, 6649-6661 (2016)."
521,CCCCCCC1=CC=C(S1)/C(C2=N/C(C=C2)=C3/C#CC4=C(CCCCCC)C(CCCCCC)=C(/C=C5C(N(CC)C(S/5)=S)=O)S4)=C(C=C/6)/N7C6=C(C#CC8=C(CCCCCC)C(CCCCCC)=C(/C=C9C(N(CC)C(S/9)=S)=O)S8)/C(C=C/%10)=NC%10=C(C%11=CC=C(CCCCCC)S%11)/C%12=CC=C3N%12[Zn]7,1a,,,0.99,10.74,0.62,6.59,"Moran G, et al. CuSCN as selective contact in solution-processed small-molecule organic solar cells leads to over 7% efficient porphyrin-based device. Journal of Materials Chemistry A 4, 11009-11022 (2016)."
522,CCCCCCC1=CC=C(S1)/C(C2=N/C(C=C2)=C3/C#CC4=C(CCCCCC)C(CCCCCC)=C(/C=C/C5=C(CCCCCC)C(CCCCCC)=C(/C=C6C(N(CC)C(S/6)=S)=O)S5)S4)=C(C=C/7)/N8C7=C(C#CC9=C(CCCCCC)C(CCCCCC)=C(/C=C/C%10=C(CCCCCC)C(CCCCCC)=C(/C=C%11C(N(CC)C(S/%11)=S)=O)S%10)S9)/C(C=C/%12)=NC%12=C(C%13=CC=C(CCCCCC)S%13)/C%14=CC=C3N%14[Zn]8,1b,,,0.94,11.67,0.66,7.24,"Moran G, et al. CuSCN as selective contact in solution-processed small-molecule organic solar cells leads to over 7% efficient porphyrin-based device. Journal of Materials Chemistry A 4, 11009-11022 (2016)."
523,CC1(C)C(C=C2C([O-])=C(C3=C(O)C=C(N4C(CCC5)C5C6=C4C=CC=C6)C=C3O)C2=O)=[N+](CCCC)C7=CC=C(C8=CC(C(S8)=C9C%10=CC=C(CC(CC)CCCC)S%10)=C(C%11=CC=C(CC(CC)CCCC)S%11)C%12=C9C=C(C%13=CC=CC=C%13)S%12)C=C71,BDT-SQ,,,0.86,12.87,0.52,5.75,"Yang D, et al. An effective pi-extended squaraine for solution-processed organic solar cells with high efficiency. Journal of Materials Chemistry A 4, 18931-18941 (2016)."
524,CC1(C)C(C=C2C([O-])=C(C3=C(O)C=C(N4C(CCC5)C5C6=C4C=CC=C6)C=C3O)C2=O)=[N+](CCCC)C7=CC=C(C8=CC(C(S8)=C9C%10=CC=C(CC(CC)CCCC)S%10)=C(C%11=CC=C(CC(CC)CCCC)S%11)C%12=C9C=C(C%13=CC=C([N+](CCCC)=C(C=C%14C([O-])=C(C%15=C(O)C=C(N%16C(CCC%17)C%17C%18=C%16C=CC=C%18)C=C%15O)C%14=O)C%19(C)C)C%19=C%13)S%12)C=C71,D-BDT-SQ,,,0.83,14.89,0.6,7.41,"Yang D, et al. An effective pi-extended squaraine for solution-processed organic solar cells with high efficiency. Journal of Materials Chemistry A 4, 18931-18941 (2016)."
525,CC1(C)C(C=C2C([O-])=C(C3=C(O)C=C(N4C(CCC5)C5C6=C4C=CC=C6)C=C3O)C2=O)=[N+](CCCC)C7=CC=CC=C71,S-SQ,,,0.79,13.45,0.52,5.52,"Yang D, et al. An effective pi-extended squaraine for solution-processed organic solar cells with high efficiency. Journal of Materials Chemistry A 4, 18931-18941 (2016)."
526,CCCCCCCCC1(CCCCCCCC)C2=CC(C3=CC=C(S3)C4=C(SC(C5=CC=C(C6=C7C(C(N6CC(CC)CCCC)=O)=C(C8=CC=C([H])S8)N(CC(CC)CCCC)C7=O)S5)=C9)C9=C(C%10=CC=C(C%11=CC%12=C(C%13=CC=CC=C%13C%12(CCCCCCCC)CCCCCCCC)C=C%11)S%10)C%14=C4C=C([H])S%14)=CC=C2C%15=C1C=CC=C%15,P1,,,0.77,5.39,0.4311,1.78,"Kim T, Chakravarthi N, Kumarasamy G, Jin S-H. Synthesis, characterization and photovoltaic properties of low band gap donor-acceptor polymers containing benzodithiophene donor unit with fluorenylthiophene as 2D-conjugated side for organic solar cell application. Molecular Crystals and Liquid Crystals 635, 45-56 (2016)."
527,[H]C(S1)=CC2=C1C(C3=CC=C(C4=CC5=C(C6=CC=CC=C6C5(CC(CC)CCCC)CC(CC)CCCC)C=C4)S3)=C7C(SC(C8=CC=C(C9=C%10C(C(N9CC(CC)CCCC)=O)=C(C%11=CC=C([H])S%11)N(CC(CC)CCCC)C%10=O)S8)=C7)=C2C%12=CC=C(C%13=CC=C(C%14=C%15C=CC=C%14)C(C%15(CC(CC)CCCC)CC(CC)CCCC)=C%13)S%12,P2,,,0.73,4.96,0.329,1.2,"Kim T, Chakravarthi N, Kumarasamy G, Jin S-H. Synthesis, characterization and photovoltaic properties of low band gap donor-acceptor polymers containing benzodithiophene donor unit with fluorenylthiophene as 2D-conjugated side for organic solar cell application. Molecular Crystals and Liquid Crystals 635, 45-56 (2016)."
528,CCCCC(CC)CC1=CC=C(S1)C2=C(SC(C3=C4C(C(N(CCCCCCCCC)C4=O)=O)=C(C5=C(CCCCCC)C(CCCCCC)=C(C6=C7C(C(N(CCCCCCCCC)C7=O)=O)=C([H])S6)S5)S3)=C8)C8=C(C9=CC=C(CC(CC)CCCC)S9)C%10=C2C=C([H])S%10,PH,,,1,14.32,0.52,7.59,"Xia B, et al. A conformational locking strategy in linked-acceptor type polymers for organic solar cells. Polymer Chemistry 7, 1323-1329 (2016)."
529,CCCCC(CC)CC1=CC=C(S1)C2=C(SC(C3=C4C(C(N(CCCCCCCCC)C4=O)=O)=C(C5=C(OC)C(OC)=C(C6=C7C(C(N(CCCCCCCCC)C7=O)=O)=C([H])S6)S5)S3)=C8)C8=C(C9=CC=C(CC(CC)CCCC)S9)C%10=C2C=C([H])S%10,POM,,,0.97,7.55,0.438,3.3,"Xia B, et al. A conformational locking strategy in linked-acceptor type polymers for organic solar cells. Polymer Chemistry 7, 1323-1329 (2016)."
530,CCCCC(CC)CC1=CC=C(S1)C2=C(SC(C3=C4C(C(N(CCCCCCCCC)C4=O)=O)=C(C5=C(OCCCCC)C(OCCCCC)=C(C6=C7C(C(N(CCCCCCCCC)C7=O)=O)=C([H])S6)S5)S3)=C8)C8=C(C9=CC=C(CC(CC)CCCC)S9)C%10=C2C=C([H])S%10,POP,,,0.97,14.48,0.567,8.18,"Xia B, et al. A conformational locking strategy in linked-acceptor type polymers for organic solar cells. Polymer Chemistry 7, 1323-1329 (2016)."
531,O=C(C1=C(SC([H])=C12)C3=CC=C(S3)C4=CC(CC(CC)CCCC)=C(S4)C(S5)=NC6=C5N=C(S6)C7=C(CC(CC)CCCC)C=C(S7)C8=CC=C([H])S8)C9=C(CC(CC)CCCC)SC(CC(CC)CCCC)=C9C2=O,PtDAA,,,0.859,12.87,0.73,8.1,"Fan B, et al. High-performance conjugated terpolymer-based organic bulk heterojunction solar cells. Journal of Materials Chemistry A 4, 13930-13937 (2016)."
532,O=C(C1=C(SC([H])=C12)C3=CC=C(S3)C4=CC(CC(CC)CCCC)=C(S4)C(S5)=CC6=C5C=C(S6)C7=C(CC(CC)CCCC)C=C(S7)C8=CC=C([H])S8)C9=C(CC(CC)CCCC)SC(CC(CC)CCCC)=C9C2=O,PtDDA,,,0.7,8.69,0.55,3.4,"Fan B, et al. High-performance conjugated terpolymer-based organic bulk heterojunction solar cells. Journal of Materials Chemistry A 4, 13930-13937 (2016)."
533,CC(S1)=CC=C1C(N2CC(CCCCCCCCCC)CCCCCCCCCCCC)=C3C(C2=O)=C(C4=CC=C(C5=CC=C(C(S6)=CC=C6C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C7=O)=C(C7=C(C8=CC=C(C9=CC([H])=CC(C)=C9)S8)N%10CC(CCCCCCCCCC)CCCCCCCCCCCC)C%10=O)C=C5)S4)N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C3=O,DT-PDPPTPT,,,0.79,12.5,0.64,6.3,"Heintges GHL, van Franeker JJ, Wienk MM, Janssen RAJ. The effect of branching in a semiconducting polymer on the efficiency of organic photovoltaic cells. Chem. Commun. 52, 92-95 (2016)."
534,O=C(OCC(CC)CCCC)C1=CC2=C([H])SC(C3=CC=C(C4=C(SC(C(OCC(CC)CCCC)=O)=C5)C5=C(C6=CC(C(OCC(CC)CCCC)=C(SC([H])=C7)C7=C8OCC(CC)CCCC)=C8S6)S4)C9=NSN=C93)=C2S1,PBTTBT,,,1.85,7.4,0.54,0.46,"Kim H, et al. Donor acceptor polymers with a regioregularly incorporated thieno 3,4-b thiophene segment as a pi-bridge for organic photovoltaic devices. Synth. Met. 211, 75-83 (2016)."
535,[H]C(C=C1)=CC2=C1C(C=C3)=C(C2(CCCCCC)CCCCCC)C=C3C4=CC=C(C5=CC=C(C6=CC=C([H])S6)C7=NSN=C57)S4,PFDTBT,,,0.92,6.55,0.37,2.23,"Kim H, et al. Donor acceptor polymers with a regioregularly incorporated thieno 3,4-b thiophene segment as a pi-bridge for organic photovoltaic devices. Synth. Met. 211, 75-83 (2016)."
536,O=C(OCC(CC)CCCC)C1=CC2=C([H])SC(C3=CC=C(C4=C(SC(C(OCC(CC)CCCC)=O)=C5)C5=C(C6=CC(C7(CCCCCC)CCCCCC)=C(C8=C7C=C([H])C=C8)C=C6)S4)C9=NSN=C93)=C2S1,PFTTBT,,,0.78,7.06,0.44,2.46,"Kim H, et al. Donor acceptor polymers with a regioregularly incorporated thieno 3,4-b thiophene segment as a pi-bridge for organic photovoltaic devices. Synth. Met. 211, 75-83 (2016)."
537,CCN1C(/C(SC1=S)=C/C2=CC(OCCCCCC)=C(C3=C(C=C4)N(C4C(C5CC(OCCCCCCCCCCCC)CC(OCCCCCCCCCCCC)C5)=C(C=C6)N7C6=C(C8=C(OCCCCCC)C=C(C(OCCCCCC)=C8)/C=C(S9)/C(N(CC)C9=S)=O)C%10C=C%11)[Zn]7(N%10C%11=C%12C%13CC(OCCCCCCCCCCCC)CC(OCCCCCCCCCCCC)C%13)N%14C%12=CC=C%143)C=C2OCCCCCC)=O,4a,,,3.21,7.2,0.9,0.48,"Wang HD, et al. Structural engineering of porphyrin-based small molecules as donors for efficient organic solar cells. Chem. Sci. 7, 4301-4307 (2016)."
538,CCN1C(/C(SC1=S)=C/C2=CC(OCCCCCC)=C(C3=C(C=C4)N(C4C(C5CCC(OCCCCCCCCCCCC)CC5)=C(C=C6)N7C6=C(C8=C(OCCCCCC)C=C(C(OCCCCCC)=C8)/C=C(S9)/C(N(CC)C9=S)=O)C%10C=C%11)[Zn]7(N%10C%11=C%12C%13CCC(OCCCCCCCCCCC)CC%13)N%14C%12=CC=C%143)C=C2OCCCCCC)=O,4b,,,5.07,10.14,0.9,0.56,"Wang HD, et al. Structural engineering of porphyrin-based small molecules as donors for efficient organic solar cells. Chem. Sci. 7, 4301-4307 (2016)."
539,CC1N(C=C2C(CCCCCCCC)CCCCCC)[Zn]34N5C2=CC=C5C(C6=C(OCCCCCC)C=C(C(OCCCCCC)=C6)/C=C(S7)/C(N(CC)C7=S)=O)=C(C=C8)N3C8C(C(CCCCCC)CCCCCCCC)=C(C=C9)N4C9=C1C%10=C(OCCCCCC)C=C(C(OCCCCCC)=C%10)/C=C(S%11)/C(N(CC)C%11=S)=O,4c,,,7.7,13.32,0.91,0.64,"Wang HD, et al. Structural engineering of porphyrin-based small molecules as donors for efficient organic solar cells. Chem. Sci. 7, 4301-4307 (2016)."
540,CCCCC(CC)C[Si]1(CC(CC)CCCC)C2=C(SC(C3=CC=C([H])C4=NSN=C43)=C2)C5=C1C=C([H])S5,Si-PCPDTBT,,,0.6,18.76,0.55,6.18,"Wang J, et al. Efficient ternary organic photovoltaic cells with better trade-off photon harvesting and phase separation by doping DIB-SQ. J. Mater. Chem. C 4, 7809-7816 (2016)."
541,[H]C(S1)=CC=C1C2=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C(C3=CC=C(C4=CC5=C(C6=CC=C([H])C=C6N5CCCCCCCC)C=C4)S3)C7=NSN=C27,P1,,,1.87,4.1,1.06,0.43,"Zhang JC, et al. A nonfullerene acceptor for wide band gap polymer based organic solar cells. Chem. Commun. 52, 469-472 (2016)."
542,[H]C(S1)=CC=C1C2=C(OCC(CCCCCC)CCCCCCCC)C(F)=C(C3=CC=C(C4=CC5=C(C6=CC=C([H])C=C6N5CC(CC)CCCC)C=C4)S3)C7=NSN=C27,P2,,,1.07,6.29,0.55,3.71,"Zhang JC, et al. A nonfullerene acceptor for wide band gap polymer based organic solar cells. Chem. Commun. 52, 469-472 (2016)."
543,[H]C1=CC(CC(CCCC)CC)=C(S1)C(S2)=CC=C2C3=CC=C(C4=NON=C43)C5=CC=C(S5)C6=CC=C(C7=CC=C(C8=C(CC(CC)CCCC)C=C(C9=CC=C%10C(N(C(CCCCCCCCCCC)CCCCCCCCCCC)C%11=C%10C=CC([H])=C%11)=C9)S8)S7)C%12=NON=C%126,P1,,,0.77,10.6,0.57,4.6,"Akkuratov AV, Prudnov FA, Inasaridze LN, Troshin PA. Synthesis of the (X-DADAD)(n)-type conjugated polymers with 2,1,3-benzoxadiazole acceptor blocks and their application in organic solar cells. Tetrahedron Lett. 58, 97-100 (2017)."
544,[H]C1=CC(CC(CCCCCCCC)CCCCCC)=C(S1)C(S2)=CC=C2C3=CC=C(C4=NON=C43)C5=CC=C(S5)C6=CC=C(C7=CC=C(C8=C(CC(CCCCCC)CCCCCCCC)C=C(C9=CC=C%10C(N(C(CCCCCCCCCCC)CCCCCCCCCCC)C%11=C%10C=CC([H])=C%11)=C9)S8)S7)C%12=NON=C%126,P2,,,1.8,4.2,0.8,0.54,"Akkuratov AV, Prudnov FA, Inasaridze LN, Troshin PA. Synthesis of the (X-DADAD)(n)-type conjugated polymers with 2,1,3-benzoxadiazole acceptor blocks and their application in organic solar cells. Tetrahedron Lett. 58, 97-100 (2017)."
545,CC1=CC(C)=CC(C)=C1/C(C2=CC=C3N2[Zn]N4/C(C=C/C4=C(C5=C(C)C=C(C)C=C5C)/C6=N/C(C=C6)=C3/C#CC7=CC(C(CCCCCC)(CCCCCC)C8=C9SC(/C=C%10C(N(CC)C(S/%10)=S)=O)=C8)=C9S7)=C%11/C#CC%12=CC%13=C(C(SC(/C=C%14SC(N(CC)C\%14=O)=S)=C%15)=C%15C%13(CCCCCC)CCCCCC)S%12)=C%16C=CC%11=N\%16,SA1,,,0.85,13.38,59,6.71,"Arrechea S, Aljarilla A, de la Cruz P, Singh MK, Sharma GD, Langa F. New cyclopentadithiophene (CDT) linked porphyrin donors with different end-capping acceptors for efficient small molecule organic solar cells. J. Mater. Chem. C 5, 4742-4751 (2017)."
546,CC1=CC(C)=CC(C)=C1/C(C2=CC=C3N2[Zn]N4/C(C=C/C4=C(C5=C(C)C=C(C)C=C5C)/C6=N/C(C=C6)=C3/C#CC7=CC(C(CCCCCC)(CCCCCC)C8=C9SC(/C=C(C#N)/C#N)=C8)=C9S7)=C%10/C#CC%11=CC%12=C(C(SC(/C=C(C#N)\C#N)=C%13)=C%13C%12(CCCCCC)CCCCCC)S%11)=C%14C=CC%10=N\%14,SA2,,,0.91,13.84,63,7.93,"Arrechea S, Aljarilla A, de la Cruz P, Singh MK, Sharma GD, Langa F. New cyclopentadithiophene (CDT) linked porphyrin donors with different end-capping acceptors for efficient small molecule organic solar cells. J. Mater. Chem. C 5, 4742-4751 (2017)."
547,CCCCCCCCCCOC1=C(C2=CC=C(/C=C/C3=CC=C([H])S3)S2)C=CC4=C1C=CC([H])=C4OCCCCCCCCCC,PBTDN,,,0.74,18.1,0.41,5.4,"Cha H, Park CE, Kwon SK, An TK. Ternary blends to achieve well-developed nanoscale morphology in organic bulk heterojunction solar cells. Org. Electron. 45, 263-272 (2017)."
548,[H]C1=CC=C(C2=CC=C(C3=CC=C([H])S3)S2)C4=C1N=C(C5=CC(OCC(CCCCCC)CCCCCCCC)=CC=C5)C(C6=CC=CC(OCC(CCCCCC)CCCCCCCC)=C6)=N4,PQxBT,,,2.38,8.83,0.6,0.45,"Choi S, Park GE, Lee DH, Godumala M, Cho MJ, Choi DH. Quinoxaline-Based D-A Conjugated Polymers for Organic Solar Cells: Probing the Effect of Quinoxaline Side Chains and Fluorine Substitution on the Power Conversion Efficiency. J. Polym. Sci. Pol. Chem. 55, 1209-1218 (2017)."
549,[H]C1=CC=C(C2=CC(F)=C(C3=C(F)C=C([H])S3)S2)C4=C1N=C(C5=CC(OCC(CCCCCC)CCCCCCCC)=CC=C5)C(C6=CC=CC(OCC(CCCCCC)CCCCCCCC)=C6)=N4,PQxFBT,,,2.93,9.45,0.62,0.5,"Choi S, Park GE, Lee DH, Godumala M, Cho MJ, Choi DH. Quinoxaline-Based D-A Conjugated Polymers for Organic Solar Cells: Probing the Effect of Quinoxaline Side Chains and Fluorine Substitution on the Power Conversion Efficiency. J. Polym. Sci. Pol. Chem. 55, 1209-1218 (2017)."
550,[H]C1=CC=C(C2=CC=C(C3=CC=C([H])S3)S2)C4=C1N=C(C5=CC=C(CC(CCCCCC)CCCCCCCC)S5)C(C6=CC=C(CC(CCCCCC)CCCCCCCC)S6)=N4,TQxBT,,,0.6,10.15,0.61,3.71,"Choi S, Park GE, Lee DH, Godumala M, Cho MJ, Choi DH. Quinoxaline-Based D-A Conjugated Polymers for Organic Solar Cells: Probing the Effect of Quinoxaline Side Chains and Fluorine Substitution on the Power Conversion Efficiency. J. Polym. Sci. Pol. Chem. 55, 1209-1218 (2017)."
551,[H]C1=CC=C(C2=CC(F)=C(C3=C(F)C=C([H])S3)S2)C4=C1N=C(C5=CC=C(CC(CCCCCC)CCCCCCCC)S5)C(C6=CC=C(CC(CCCCCC)CCCCCCCC)S6)=N4,TQxFBT,,,0.62,11.02,0.61,4.18,"Choi S, Park GE, Lee DH, Godumala M, Cho MJ, Choi DH. Quinoxaline-Based D-A Conjugated Polymers for Organic Solar Cells: Probing the Effect of Quinoxaline Side Chains and Fluorine Substitution on the Power Conversion Efficiency. J. Polym. Sci. Pol. Chem. 55, 1209-1218 (2017)."
552,[H]C(S1)=CC=C1C2=C(F)C(F)=C(C3=CC=C(C4=CC5=C(C6=CC(SCCCCCCCC)=C(SCCCC)S6)C7=C(C=C([H])S7)C(C8=CC(SCCCCCCCC)=C(SCCCC)S8)=C5S4)S3)C9=NSN=C92,PBDTT-DS1-BTff,,,2.38,7.46,0.93,0.34,"Deng P, et al. Effect of bisalkylthio side chains onbenzo 1,2-b:4,5-b ' dithiophene-based polymers for organic solar cells. Dyes Pigment. 138, 47-55 (2017)."
553,[H]C(S1)=CC=C1C2=C(F)C(F)=C(C3=CC=C(C4=CC5=C(C6=CC(SCCCCCCCC)=C(SCCCCCC)S6)C7=C(C=C([H])S7)C(C8=CC(SCCCCCCCC)=C(SCCCCCC)S8)=C5S4)S3)C9=NSN=C92,PBDTT-DS2-BTff,,,5.82,11.06,0.92,0.57,"Deng P, et al. Effect of bisalkylthio side chains onbenzo 1,2-b:4,5-b ' dithiophene-based polymers for organic solar cells. Dyes Pigment. 138, 47-55 (2017)."
554,[H]C(S1)=CC=C1C2=C(F)C(F)=C(C3=CC=C(C4=CC5=C(C6=CC(SCCCCCC)=C(SCCCCCC)S6)C7=C(C=C([H])S7)C(C8=CC(SCCCCCC)=C(SCCCCCC)S8)=C5S4)S3)C9=NSN=C92,PBDTT-DS3-BTff,,,4.15,9.95,0.91,0.46,"Deng P, et al. Effect of bisalkylthio side chains onbenzo 1,2-b:4,5-b ' dithiophene-based polymers for organic solar cells. Dyes Pigment. 138, 47-55 (2017)."
555,[H]C(S1)=CC=C1C2=C(F)C(F)=C(C3=CC=C(C4=CC5=C(C6=CC(SCCCCCCCC)=C(SCCCCCCCC)S6)C7=C(C=C([H])S7)C(C8=CC(SCCCCCCCC)=C(SCCCCCCCC)S8)=C5S4)S3)C9=NSN=C92,PBDTT-DS4-BTff,,,5,10.15,0.93,0.52,"Deng P, et al. Effect of bisalkylthio side chains onbenzo 1,2-b:4,5-b ' dithiophene-based polymers for organic solar cells. Dyes Pigment. 138, 47-55 (2017)."
556,[H]C1=NC=C(C2=NSN=C21)C3=CC([Si](CCCCCCCCCCCC)(CCCCCCCCCCCC)C4=C5SC([H])=C4)=C5S3,ODTSDTPT,,,0.79,3.62,0.67,0.33,"El-Moussawi Z, et al. Development of Dithienosilole-Pyridalthiadiazole-Based Copolymer as an Electron Donor in Organic Photovoltaic Cells. IEEE Transactions on Nanotechnology 16, 574-581 (2017)."
557,[H]C(S1)=CC2=C1C(S3)=C([Si]2(CCCCCCCCCCCC)CCCCCCCCCCCC)C=C3C4=C(CCCCCC)C=C(C5=CN=C(C6=CC(CCCCCC)=C([H])S6)C7=NSN=C57)S4,PDTSDTPT,,,0.69,4.56,38,1.18,"El-Moussawi Z, et al. Development of Dithienosilole-Pyridalthiadiazole-Based Copolymer as an Electron Donor in Organic Photovoltaic Cells. IEEE Transactions on Nanotechnology 16, 574-581 (2017)."
558,[H]C1=CC=C(S1)C2=C(N=C(C3=CC=CC=C3)C(C4=CC=CC=C4)=N5)C5=C(C6=CC=C(C7=CC8=C(OCC(CCCC)CC)C9=C(C=C([H])S9)C(OCC(CCCC)CC)=C8S7)S6)C%10=NN(CCCCCCCCCCCC)N=C%102,PTQBDT,,,2,8.07,0.45,0.55,"Hacioglu SO, et al. A triazoloquinoxaline and benzodithiophene bearing low band gap copolymer for electrochromic and organic photovoltaic applications. Synth. Met. 228, 111-119 (2017)."
559,[H]C1=CC=C(S1)C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC5=C(C(C6=CC=C(SCC(CCCC)CC)C=C6)=C(C=C([H])S7)C7=C5C8=CC=C(SCC(CCCC)CC)C=C8)O4)S3)C9=NSN=C29,TBFPS-BT,,,0.69,11.93,0.8,6.55,"He DJ, Qiu LX, Yuan J, Zhang ZG, Li YF, Zou YP. An asymmetrical thieno 2,3-f benzofuran (TBF)-based conjugated polymer for organic solar cells with high fill factor. Polymer 114, 348-354 (2017)."
560,[H]C(S1)=C(CC(CC)CCCC)C=C1C(N(CCCCCCCCCCCC)C2=O)=C3C2=C(C4=CC(CC(CCCC)CC)=C(C5=CC=C([H])S5)S4)N(CCCCCCCCCCCC)C3=O,D-PDPP3T-EH,,,0.57,15.2,0.63,5.4,"Heintges GHL, Leenaers PJ, Janssen RAJ. The effect of side-chain substitution and hot processing on diketopyrrolopyrrole-based polymers for organic solar cells. J. Mater. Chem. A 5, 13748-13756 (2017)."
561,[H]C(S1)=C(CC(CC)CCCC)C=C1C(N(CCCCCCCCCCCC)C2=O)=C3C2=C(C4=CC(CC(CCCC)CC)=C(C5=CC=C(C6=CC=C([H])S6)S5)S4)N(CCCCCCCCCCCC)C3=O,D-PDPP4T-EH,,,0.59,10.1,0.57,3.4,"Heintges GHL, Leenaers PJ, Janssen RAJ. The effect of side-chain substitution and hot processing on diketopyrrolopyrrole-based polymers for organic solar cells. J. Mater. Chem. A 5, 13748-13756 (2017)."
562,[H]C(S1)=C(CC(CCCCCC)CCCCCCCC)C=C1C(N(CCCCCCCCCCCC)C2=O)=C3C2=C(C4=CC(CC(CCCCCCCC)CCCCCC)=C(C5=CC=C(C6=CC=C([H])S6)S5)S4)N(CCCCCCCCCCCC)C3=O,D-PDPP4T-HD,,,0.6,15.8,0.67,6.3,"Heintges GHL, Leenaers PJ, Janssen RAJ. The effect of side-chain substitution and hot processing on diketopyrrolopyrrole-based polymers for organic solar cells. J. Mater. Chem. A 5, 13748-13756 (2017)."
563,[H]C(S1)=C(CC(CC)CCCC)C=C1C(N(CC(CCCC)CC)C2=O)=C3C2=C(C4=CC(CC(CCCC)CC)=C(C5=CC=C(C6=CC=C([H])S6)S5)S4)N(CC(CC)CCCC)C3=O,EH-PDPP4T-EH,,,0.71,14.9,0.58,6.1,"Heintges GHL, Leenaers PJ, Janssen RAJ. The effect of side-chain substitution and hot processing on diketopyrrolopyrrole-based polymers for organic solar cells. J. Mater. Chem. A 5, 13748-13756 (2017)."
564,O=C1C2=C(C3=CC=C(C4=CC=C([H])S4)S3)N(CC(CCCCCCCC)CCCCCC)C(C2=C(C5=CC=C(C6=CC=C(C7=CC=C([H])S7)S6)S5)N1CC(CCCCCCCC)CCCCCC)=O,PDPP4T,,,3.9,8,0.78,0.63,"Jiang XD, et al. Non-fullerene organic solar cells based on diketopyrrolopyrrole polymers as electron donors and ITIC as an electron acceptor. Phys. Chem. Chem. Phys. 19, 8069-8075 (2017)."
565,O=C1C2=C(C3=CC=C(C4=CC=C([H])S4)S3)N(CC(CCCCCCCC)CCCCCC)C(C2=C(C5=CC=C(C6=CC(CCCCCC)=C(C7=CC=C(C8=CC=C(C9=C(CCCCCC)C=C([H])S9)S8)S7)S6)S5)N1CC(CCCCCCCC)CCCCCC)=O,PDPP6T,,,3.8,9.3,0.68,0.6,"Jiang XD, et al. Non-fullerene organic solar cells based on diketopyrrolopyrrole polymers as electron donors and ITIC as an electron acceptor. Phys. Chem. Chem. Phys. 19, 8069-8075 (2017)."
566,FC(C(F)=C(CC(CC)CCCC)S1)=C1C2=C3C(SC(C4=C(CCCCCCCC)C(SC(C5=C(C(N(CC(CCCCCC)CCCCCCCC)C6=O)=O)C6=C(C7=CC8=C(C(CCCCCCCC)=C([H])S8)S7)S5)=C9)=C9S4)=C3)=C(C%10=C(F)C(F)=C(CC(CC)CCCC)S%10)C%11=C2SC([H])=C%11,PBDTT(FF)©\ttTPD,,,7.45,12.49,0.98,0.61,"Kim J, Park JB, Lee WH, Kim JH, Hwang DH, Kang IN. High-performance fluorine-containing BDT-based copolymer for organic solar cells with a high open circuit voltage. J. Polym. Sci. Pol. Chem. 55, 2506-2512 (2017)."
567,CCCCCCCCCCC(CCCCCCCCCCCC)CC1=C(C2=CC(F)=C(C3=C(F)C=C([H])S3)S2)SC(C4=CC(C5=NSN=C5C(C6=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C([H])S6)=C7)=C7C8=NSN=C84)=C1,P4TNTz-2F,,,10.6,19.4,0.81,0.65,"Lee J, et al. Highly crystalline low-bandgap polymer nanowires towards high-performance thick-film organic solar cells exceeding 10% power conversion efficiency. Energy Environ. Sci. 10, 247-257 (2017)."
568,[H]C1=CC2=C(S1)C(C3=CC=C(CC(CC)CCCC)S3)=C4C(SC(C5=CC=C(C6=C7C(C(C8=C(CC(CC)CCCC)SC(CC(CC)CCCC)=C8C7=O)=O)=C(C9=CC=C([H])S9)S6)S5)=C4)=C2C%10=CC=C(CC(CC)CCCC)S%10,PBDB-T,,,0.9,16.81,0.74,11.21,"Li S, Zhang Z, Shi M, Li C-Z, Chen H. Molecular electron acceptors for efficient fullerene-free organic solar cells. Physical Chemistry Chemical Physics 19, 3440-3458 (2017)."
569,[H]C(S1)=C(CC(CCCCCCCC)CCCCCCCCCC)C=C1C2=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C3=CC=C(C4=CC=C(C5=CC=C([H])S5)C6=NSN=C64)S3)S2,POD2T-DTBT,,,5.83,11.56,0.724,0.689,"Lim S-L, et al. Efficient, large area organic photovoltaic modules with active layers processed with non-halogenated solvents in air. Organic Electronics 43, 55-63 (2017)."
570,[H]C1=C(OCC(CCCCCC)CCCC)C(OCC(CCCCCC)CCCC)=C(C2=CC(SC3=C4SC([H])=C3)=C4S2)C5=NSN=C51,PDTT-BOBT,,,0.99,8.61,0.44,3.76,"McAfee SM, et al. A non-fullerene acceptor with a diagnostic morphological handle for streamlined screening of donor materials in organic solar cells. J. Mater. Chem. A 5, 16907-16913 (2017)."
571,[H]C1=C(CC(CC)CCCC)CC(S1)C2=C(C(C(C3=C(CC(CC)CCCC)SC(CC(CC)CCCC)=C34)=O)=C(C5=CC(CC(CC)CCCC)=C(C6=CC(F)=C(C7=C(F)C=C([H])S7)S6)S5)S2)C4=O,PBDD4T-2F,,,0.9,13.67,0.75,9.23,"Qin Y, et al. Achieving 12.8% Efficiency by Simultaneously Improving Open©\Circuit Voltage and Short©\Circuit Current Density in Tandem Organic Solar Cells. Adv. Mater. 29, 1606340 (2017)."
572,[H]C(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C=C(C(OCC(CC)CCCC)=O)S5)=C([H])S4)S6)C6=C2C7=CC=C(CC(CC)CCCC)S7,PBDTTT-E-T,,,8.98,17.37,0.81,0.64,"Qin Y, et al. Achieving 12.8% Efficiency by Simultaneously Improving Open©\Circuit Voltage and Short©\Circuit Current Density in Tandem Organic Solar Cells. Adv. Mater. 29, 1606340 (2017)."
573,CCC(CCCC)COC1=C(C=C(C2=CC=C(C3=C4C(C(C5=C(CC(CC)CCCC)SC(CC(CC)CCCC)=C5C4=O)=O)=C(C6=CC=C([H])S6)S3)S2)S7)C7=C(OCC(CCCC)CC)C8=C1OC([H])=C8,TBFO-BDD,,,3.21,8.52,0.81,0.46,"Qiu LX, Yuan J, He DJ, Zhang ZG, Li YF, Zou YP. Two new medium bandgap asymmetric copolymers based on thieno 2,3-f benzofuran for efficient organic solar cells. Dyes Pigment. 140, 337-345 (2017)."
574,CCC(CCCC)COC(C=C1)=CC=C1C2=C(C=C(C3=CC=C(C4=C5C(C(C6=C(CC(CC)CCCC)SC(CC(CC)CCCC)=C6C5=O)=O)=C(C7=CC=C([H])S7)S4)S3)S8)C8=C(C9=CC=C(OCC(CCCC)CC)C=C9)C%10=C2OC([H])=C%10,TBFPO-BDD,,,0.62,12.81,0.82,6.58,"Qiu LX, Yuan J, He DJ, Zhang ZG, Li YF, Zou YP. Two new medium bandgap asymmetric copolymers based on thieno 2,3-f benzofuran for efficient organic solar cells. Dyes Pigment. 140, 337-345 (2017)."
575,CCCCC(CCCCCC)CC1=C(C2=NC(SC(C3=C(CC(CCCC)CCCCCC)C=C([H])S3)=N4)=C4S2)SC(C5=NC(OCC(CCCCCC)CCCCCCCC)=C(C6=NC(SC(C7=C(OCC(CCCCCC)CCCCCCCC)N=C([H])S7)=N8)=C8S6)S5)=C1,PTzTTz-BOoHD,,,0.84,11.2,0.84,6.2,"Saitoa M, Osaka I. Synthesis and Characterization of an Alkoxythiazole-thiazolothiazole Semiconducting Polymer for Organic Solar Cells. Electrochemistry 85, 266-271 (2017)."
576,[H]C1=CC=C(S1)C(C2=NSN=C23)=C(F)C(F)=C3C4=CC=C(C5=CC6=C(C(C(OCC(CCCCCCCC)CCCCCCCC)=CC([H])=C7)=C7N6C(CCCCCCCC)CCCCCCCC)C=C5)S4,P1,,,0.92,10.9,0.47,4.7,"Shibasaki K, Yasuda T, Yamamoto Y, Kijima M. Dual substitution at 4, 9-positions of carbazole in donor-¦Ð-acceptor copolymer enhances performance of bulk-heterojunction organic solar cells. Polymer 108, 305-312 (2017)."
577,[H]C1=CC=C(S1)C(C2=NSN=C23)=C(F)C(F)=C3C4=CC=C(C5=CC6=C(C(C(OCC(CCCCCC)CCCCCCCC)=CC([H])=C7)=C7N6C(CCCCCCCCCC)CCCCCCCCCC)C=C5)S4,P2,,,5.2,12.33,0.75,0.57,"Shibasaki K, Yasuda T, Yamamoto Y, Kijima M. Dual substitution at 4, 9-positions of carbazole in donor-¦Ð-acceptor copolymer enhances performance of bulk-heterojunction organic solar cells. Polymer 108, 305-312 (2017)."
578,[H]C1=CC=C(S1)C(C2=NSN=C23)=C(F)C(F)=C3C4=CC=C(C5=CC6=C(C(C(OCCCCCCCCC)=CC([H])=C7)=C7N6C(CCCCCCCCCCCC)CCCCCCCCCCCC)C=C5)S4,P3,,,2.1,7.16,0.55,0.55,"Shibasaki K, Yasuda T, Yamamoto Y, Kijima M. Dual substitution at 4, 9-positions of carbazole in donor-¦Ð-acceptor copolymer enhances performance of bulk-heterojunction organic solar cells. Polymer 108, 305-312 (2017)."
579,O=C1C(C(C(N2CC(CC)CCCC)=O)=C(C3=CC=CS3)N1CC(CC)CCCC)=C2C(S4)=CC=C4C5=CC6=C(C7=CC=C(/C=C/C8=CC=C(CC(CC)CCCC)[Se]8)[Se]7)C(SC(C9=CC=C(C%10=C%11C(C(N%10CC(CC)CCCC)=O)=C(C%12=CC=CS%12)N(CC(CC)CCCC)C%11=O)S9)=C%13)=C%13C(C%14=CC=C(/C=C/C%15=CC=C(CC(CC)CCCC)[Se]%15)[Se]%14)=C6S5,SeBDT©\DPP,,,0.79,10.98,0.58,5.04,"Shin Y, Song CE, Lee W-H, Lee SK, Shin WS, Kang I-N. Synthesis and Characterization of a Soluble A-D-A Molecule Containing a 2D Conjugated Selenophene-Based Side Group for Organic Solar Cells. Macromol. Rapid Commun. 38,  (2017)."
580,CCCCC(CC)CC1(CC(CC)CCCC)C2=CC(C3=C4C=C(S3)C(S5)=CC=C5C6=C(F)C(F)=C(C7=CC=C(C8=CC9=C(C%10=C(C9(CC(CC)CCCC)CC(CC)CCCC)C=C(C%11=C%12C=C(C%13=CC=C(C%14=C(F)C(F)=C(C%15=CC=C(C%16=CC=C(CCCCCC)S%16)S%15)C%17=NSN=C%14%17)[Se]%13)S%11)C(C%12(CC(CC)CCCC)CC(CC)CCCC)=C%10)S8)S7)C%18=NSN=C6%18)=C(C4(CC(CC)CCCC)CC(CC)CCCC)C=C2C%19=C1C=C(C%20=CC=C(C%21=C(F)C(F)=C(C%22=CC=C(C%23=CC=C(CCCCCC)S%23)S%22)C%24=NSN=C%21%24)[Se]%20)S%19,Se6FTh,,,0.87,14.3,0.72,8.95,"Wang JL, et al. Donor End-Capped Hexafluorinated Oligomers for Organic Solar Cells with 9.3% Efficiency by Engineering the Position of pi-Bridge and Sequence of Two-Step Annealing. Chem. Mat. 29, 1036-1046 (2017)."
581,CCCCC(CC)CC1(CC(CC)CCCC)C2=CC(C3=C4C=C(S3)C([Se]5)=CC=C5C6=C(F)C(F)=C(C7=CC=C(C8=CC9=C(C%10=C(C9(CC(CC)CCCC)CC(CC)CCCC)C=C(C%11=C%12C=C(C%13=CC=C(C%14=C(F)C(F)=C(C%15=CC=C(C%16=CC=C(CCCCCC)S%16)S%15)C%17=NSN=C%14%17)S%13)S%11)C(C%12(CC(CC)CCCC)CC(CC)CCCC)=C%10)S8)[Se]7)C%18=NSN=C6%18)=C(C4(CC(CC)CCCC)CC(CC)CCCC)C=C2C%19=C1C=C(C%20=CC=C(C%21=C(F)C(F)=C(C%22=CC=C(C%23=CC=C(CCCCCC)S%23)S%22)C%24=NSN=C%21%24)S%20)S%19,Th6FSe,,,0.87,11.78,0.67,6.84,"Wang JL, et al. Donor End-Capped Hexafluorinated Oligomers for Organic Solar Cells with 9.3% Efficiency by Engineering the Position of pi-Bridge and Sequence of Two-Step Annealing. Chem. Mat. 29, 1036-1046 (2017)."
582,[H]C1=CC2=C(S1)C(C3=CC=C(C#C[Si](C(C)C)(C(C)C)C(C)C)S3)=C4C(SC(C5=CC=C(C6=CC=C(C7=CC=C([H])S7)C8=C6N=C(C9=CC(OCCCCCCCC)=CC=C9)C(C%10=CC=CC(OCCCCCCCC)=C%10)=N8)S5)=C4)=C2C%11=CC=C(C#C[Si](C(C)C)(C(C)C)C(C)C)S%11,PBDTSi-Qx,,,4.38,9.47,0.91,0.51,"Wang L, Liu H, Huai Z, Yang S. Wide Bandgap and Highly Conjugated Copolymers Incorporating 2-(Triisopropylsilylethynyl)thiophene Substituted Benzodithiophene for Efficient Nonfullerene Organic Solar Cells. ACS applied materials & interfaces,  (2017)."
583,[H]C1=CC2=C(S1)C(C3=CC=C(C#C[Si](C(C)C)(C(C)C)C(C)C)S3)=C4C(SC(C5=CC=C(C6=C(F)C(F)=C(C7=CC=C([H])S7)C8=NN(CC(CCCCCCCC)CCCCCC)N=C68)S5)=C4)=C2C9=CC=C(C#C[Si](C(C)C)(C(C)C)C(C)C)S9,PBDTSi-TA,,,7.51,14.09,0.96,0.55,"Wang L, Liu H, Huai Z, Yang S. Wide Bandgap and Highly Conjugated Copolymers Incorporating 2-(Triisopropylsilylethynyl)thiophene Substituted Benzodithiophene for Efficient Nonfullerene Organic Solar Cells. ACS applied materials & interfaces,  (2017)."
584,[H]C1=CC=C(C2=C(C3=O)C(C(C4=C(CC(CC)CCCC)SC(CC(CC)CCCC)=C43)=O)=C(C5=CC=C(C6=CC=C(C7=C8C(C(N7CC(CCCCCC)CCCCCCCC)=O)=C(C9=CC=C([H])S9)N(CC(CCCCCC)CCCCCCCC)C8=O)S6)S5)S2)S1,P266,,,9.18,18.11,0.72,0.704,"Zhang H, et al. Low band-gap conjugated polymer based on diketopyrrolopyrrole units and its application in organic photovoltaic cells. J. Mater. Chem. A 5, 10416-10423 (2017)."
585,FC1=C(C(S2)=CC3=C2C4=C(C=C(C5=C(F)C=C(C6=CC=C(C7=CC=C(CCCCCC)S7)S6)C8=NSN=C85)S4)[Si]3(CC(CCCC)CC)CC(CC)CCCC)C9=NSN=C9C(C%10=CC=C(C%11=CC=C(CCCCCC)S%11)S%10)=C1,p©\DTS(FBTTH2)2,,,0.74,21.67,0.67,10.78,"Zhang JQ, et al. Enhancing Performance of Large-Area Organic Solar Cells with Thick Film via Ternary Strategy. Small 13, 8 (2017)."
586,FC1=CC(C2=C3C(C=C(S3)C4=CC=C(S4)C5=C(C(OCCCCCCCCCCCC)=C(C6=NSN=C56)C7=CC=C(S7)[H])OCCCCCCCCCCCC)=C(C8=C2C=C(S8)[H])C9=CC(F)=C(C(F)=C9)CC(CCCC)CC)=CC(F)=C1CC(CCCC)CC,PTFBDT©\BZS,,,0.905,17.3,70.8,11.03,"Lin Y, et al. Mapping Polymer Donors toward High-Efficiency Fullerene Free Organic Solar Cells. Advanced Materials 29,  (2017)."
587,[H]C1=C(CCOCCOC)C=C([H])S1,PDHT,,,0.56,5,32,0.9,"Bricaud Q, Cravino A, Leriche P, Roncali J. Poly(thiophenes) derivatized with oligo(oxyethylene) chains as donor materials for organic solar cells. Solar Energy Materials and Solar Cells 93, 1624-1629 (2009)."
588,[H]C#CC1=C2C(OCCO2)=C(C3=CC=C(C4=C5C(OCCO5)=C(C#C[Pt]([P-](CCCC)(CCCC)CCCC)([P-](CCCC)(CCCC)CCCC)[H])S4)C6=NSN=C63)S1,p-PtBTD-EDOT,,,0.5,4.56,35,0.78,"Mei J, et al. Low-Band-Gap Platinum Acetylide Polymers as Active Materials for Organic Solar Cells. Acs Applied Materials & Interfaces 1, 150-161 (2009)."
589,[H]C#CC1=CC=C(C2=CC=C(C3=CC=C(C#C[Pt]([P-](CCCC)(CCCC)CCCC)([P-](CCCC)(CCCC)CCCC)[H])S3)C4=NSN=C42)S1,p-PtBTD-Th,,,0.54,7.17,36,1.39,"Mei J, et al. Low-Band-Gap Platinum Acetylide Polymers as Active Materials for Organic Solar Cells. Acs Applied Materials & Interfaces 1, 150-161 (2009)."
590,[H][Pt]([P-](CCCC)(CCCC)CCCC)([P-](CCCC)(CCCC)CCCC)C#CC1=CC=C(C#C[H])C1,p-PtTh,,,0.64,0.99,43,0.27,"Mei J, et al. Low-Band-Gap Platinum Acetylide Polymers as Active Materials for Organic Solar Cells. Acs Applied Materials & Interfaces 1, 150-161 (2009)."
591,[H]C1=CC(CCCCCCCC)=C(C2=CC(CCCCCCCC)=C(C3=CC=C(C4=CC=C(C5=C(CCCCCCCC)C=C(C6=C(CCCCCCCC)C=C(C7=CC=C([H])C8=NSN=C78)S6)S5)S4)S3)S2)S1,PTh6BTD,,,0.51,5.34,51,1.39,"Liang F, Lu J, Ding J, Movileanu R, Tao Y. Design and Synthesis of Alternating Regioregular Oligothiophenes/Benzothiadiazole Copolymers for Organic Solar Cells. Macromolecules 42, 6107-6114 (2009)."
592,[H]C1=CC=C(C2=NSN=C21)C(S3)=CC(CCCCCCCC)=C3C4=CC(CCCCCCCC)=C(S4)C(S5)=CC(CCCCCCCC)=C5C6=CC=C(S6)C(S7)=CC=C7C8=C(CCCCCCCC)C=C(S8)C9=C(CCCCCCCC)C=C(C%10=C(CCCCCCCC)C=C([H])S%10)S9,PTh8BTD,,,0.68,5.2,59,1.73,"Liang F, Lu J, Ding J, Movileanu R, Tao Y. Design and Synthesis of Alternating Regioregular Oligothiophenes/Benzothiadiazole Copolymers for Organic Solar Cells. Macromolecules 42, 6107-6114 (2009)."
593,CCCCC(CC)CC1(CC(CC)CCCC)C2=C(SC(C3=C(CCCCCC)N=C(C4=NC(CCCCCC)=C([H])S4)S3)=C2)C5=C1C=C([H])S5,P1,,,0.73,6.34,53,2.45,"Li K-C, et al. Tunable Novel Cyclopentadithiophene-Based Copolymers Containing Various Numbers of Bithiazole and Thienyl Units for Organic Photovoltaic Cell Applications. Macromolecules 42, 3681-3693 (2009)."
594,CCCCC(CC)CC1(CC(CC)CCCC)C2=C(SC(C3=C(CCCCCC)N=C(C4=NC(CCCCCC)=C(C5=C(CCCCCC)N=C(C6=NC(CCCCCC)=C([H])S6)S5)S4)S3)=C2)C7=C1C=C([H])S7,P2,,,0.777,5.26,51.9,2.12,"Li K-C, et al. Tunable Novel Cyclopentadithiophene-Based Copolymers Containing Various Numbers of Bithiazole and Thienyl Units for Organic Photovoltaic Cell Applications. Macromolecules 42, 3681-3693 (2009)."
595,CCCCC(CC)CC1(CC(CC)CCCC)C2=C(SC(C3=C(CCCCCC)N=C(C4=NC(CCCCCC)=C(C5=C(CCCCCC)N=C(C6=NC(CCCCCC)=C(C7=C(CCCCCC)N=C(C8=NC(CCCCCC)=C([H])S8)S7)S6)S5)S4)S3)=C2)C9=C1C=C([H])S9,P3,,,0.822,4.43,49.3,1.78,"Li K-C, et al. Tunable Novel Cyclopentadithiophene-Based Copolymers Containing Various Numbers of Bithiazole and Thienyl Units for Organic Photovoltaic Cell Applications. Macromolecules 42, 3681-3693 (2009)."
596,CCCCC(CC)CC1(CC(CC)CCCC)C2=C(SC(C3=CC=C(C4=C(CCCCCC)N=C(C(S5)=NC(CCCCCC)=C5C(S6)=CC=C6[H])S4)S3)=C2)C7=C1C=C([H])S7,P4,,,0.683,7.7,53,2.79,"Li K-C, et al. Tunable Novel Cyclopentadithiophene-Based Copolymers Containing Various Numbers of Bithiazole and Thienyl Units for Organic Photovoltaic Cell Applications. Macromolecules 42, 3681-3693 (2009)."
597,CCCCC(CC)CC1(CC(CC)CCCC)C2=C(SC(C3=CC=C(S3)C4=CC=C(C5=C(CCCCCC)N=C(C(S6)=NC(CCCCCC)=C6C(S7)=CC=C7C8=CC=C([H])S8)S5)S4)=C2)C9=C1C=C([H])S9,P5,,,0.729,3.03,36.1,0.8,"Li K-C, et al. Tunable Novel Cyclopentadithiophene-Based Copolymers Containing Various Numbers of Bithiazole and Thienyl Units for Organic Photovoltaic Cell Applications. Macromolecules 42, 3681-3693 (2009)."
598,CCCCC(CC)CC1(CC(CC)CCCC)C2=C(SC(C3=CC=C(/C(C#N)=C/C4=C(CCCCCC)N=C(C5=NC(CCCCCC)=C(/C=C(C#N)/C6=CC=C([H])C=C6)S5)S4)C=C3)=C2)C7=C1C=C([H])S7,P6,,,0.63,2.68,32,0.54,"Li K-C, et al. Tunable Novel Cyclopentadithiophene-Based Copolymers Containing Various Numbers of Bithiazole and Thienyl Units for Organic Photovoltaic Cell Applications. Macromolecules 42, 3681-3693 (2009)."
599,CCCCCCC1=CC2=C(C3=CC(CCCCCC)=C(C4=CC(CCCCCC)=C(C5=CC(CCCCCC)=C(C6=CC(CCCCCC)=C(C7=CC(CCCCCC)=C(C8=CC(CCCCCC)=C(C9=CC(CCCCCC)=C(C%10=CC(CCCCCC)=C([H])S%10)S9)S8)S7)S6)S5)S4)S3)SC(C%11=CC(CCCCCC)=C(C%12=CC(CCCCCC)=C(C%13=CC(CCCCC)=C(C%14=CC(CCCCCC)=C(C%15=CC(CCCCCC)=C(C%16=CC(CCCCCC)=C(C%17=CC(CCCCCC)=C(C%18=CC(CCCCCC)=C([H])S%18)S%17)S%16)S%15)S%14)S%13)S%12)S%11)=C2S1,MF,,,0.54,7.42,36,1.46,"Liang Y, et al. Regioregular Oligomer and Polymer Containing Thieno 3,4-b thiophene Moiety for Efficient Organic Solar Cells. Macromolecules 42, 1091-1098 (2009)."
600,CCCCCCC1=CC2=C(C3=CC(CCCCCC)=C(C4=CC(CCCCCC)=C(C5=CC(CCCCCC)=C(C6=CC(CCCCCC)=C(C7=CC(CCCCCC)=C(C8=CC(CCCCCC)=C(C9=CC(CCCCCC)=C(C%10=CC(CCCCCC)=C([H])S%10)S9)S8)S7)S6)S5)S4)S3)SC(C%11=CC(CCCCCC)=C(C%12=CC(CCCCCC)=C(C%13=CC(CCCCC)=C(C%14=CC(CCCCCC)=C(C%15=CC(CCCCCC)=C(C%16=CC(CCCCCC)=C(C%17=CC(CCCCCC)=C(C%18=CC(CCCCCC)=C(C%19=CC=C([H])S%19)S%18)S%17)S%16)S%15)S%14)S%13)S%12)S%11)=C2S1,PF,,,0.59,10.22,40,2.38,"Liang Y, et al. Regioregular Oligomer and Polymer Containing Thieno 3,4-b thiophene Moiety for Efficient Organic Solar Cells. Macromolecules 42, 1091-1098 (2009)."
601,FC1=C(F)C(F)=C(F)C2=C3N([Cu]N4/C5=N\C6=N/C(C7=C6C(F)=C(F)C(F)=C7F)=N\3)C(/N=C8N=C(/N=C4/C9=C5C(F)=C(F)C(F)=C9F)C%10=C\8C(F)=C(F)C(F)=C%10F)=C21,F16CuPc,,,0.78,2.89,37,0.83,"Yu B, Zhu F, Wang H, Li G, Yan D. All-organic tunnel junctions as connecting units in tandem organic solar cell. Journal of Applied Physics 104,  (2008)."
602,Cl[Sn]1(Cl)N2C(/N=C3N=C4C5=C\3C=CC=C5)=C(C=CC=C6)C6=C2/N=C7C(C=CC=C8)=C8C(/N=C(C9=C/%10C=CC=C9)\N1C%10=N/4)=N/7,SnCl2Pc,,,0.88,2.85,55,1.38,"Yu B, Zhu F, Wang H, Li G, Yan D. All-organic tunnel junctions as connecting units in tandem organic solar cell. Journal of Applied Physics 104,  (2008)."
603,CC(C)[Si](C(C)C)(C(C)C)C#CC1=C2C(C=C(C=C(OC(CC)(CC)O3)C3=C4)C4=C2)=C(C#C[Si](C(C)C)(C(C)C)C(C)C)C5=CC6=CC7=C(OC(CC)(CC)O7)C=C6C=C51,EtTP-5,,,0.69,1.68,29,0.34,"Palilis LC, Lane PA, Kushto GP, Purushothaman B, Anthony JE, Kafafi ZH. Organic photovoltaic cells with high open circuit voltages based on pentacene derivatives. Organic Electronics 9, 747-752 (2008)."
604,CC(C)[Si](C(C)C)(C(C)C)C#CC1=C2C(C=C(C=CC=C3)C3=C2)=C(C#C[Si](C(C)C)(C(C)C)C(C)C)C4=CC5=CC=CC=C5C=C41,TIPS,,,0.9,1.42,33,0.42,"Palilis LC, Lane PA, Kushto GP, Purushothaman B, Anthony JE, Kafafi ZH. Organic photovoltaic cells with high open circuit voltages based on pentacene derivatives. Organic Electronics 9, 747-752 (2008)."
605,CC(C)[Si](C(C)C)(C(C)C)C#CC1=C2C(C=C(C=C(OCO3)C3=C4)C4=C2)=C(C#C[Si](C(C)C)(C(C)C)C(C)C)C5=CC6=CC7=C(OCO7)C=C6C=C51,TP-5,,,0.57,2.32,37,0.5,"Palilis LC, Lane PA, Kushto GP, Purushothaman B, Anthony JE, Kafafi ZH. Organic photovoltaic cells with high open circuit voltages based on pentacene derivatives. Organic Electronics 9, 747-752 (2008)."
606,[H]C1=C(CCCCCC)C(CCCCCC)=C(/C=C/[H])S1,Dihexyl-PTV,,,0.58,1.93,54,0.61,"Girotto C, et al. Bulk heterojunction organic solar cells based on soluble poly(thienylene vinylene) derivatives. Organic Electronics 9, 740-746 (2008)."
607,[H]C1=CC(CCCCCCCCCCCC)=C(/C=C/[H])S1,Dodecyl-PTV,,,0.35,1.03,31,0.17,"Girotto C, et al. Bulk heterojunction organic solar cells based on soluble poly(thienylene vinylene) derivatives. Organic Electronics 9, 740-746 (2008)."
608,[H]C1=CC(CCCCCC)=C(/C=C/[H])S1,Hexyl-PTV,,,0.52,0.98,30,0.15,"Girotto C, et al. Bulk heterojunction organic solar cells based on soluble poly(thienylene vinylene) derivatives. Organic Electronics 9, 740-746 (2008)."
609,CCCCCCCCC1=C(C2=CC(CCCCCCCC)=C([H])S2)SC(C3=CC=C(C4=CC(CCCCCCCC)=C(C5=CC(CCCCCCCC)=C(S5)C6=CC7=C(C(C=C(N(CC(CCCCCCCC)CCCCCC)C8=C9C=CC([H])=C8)C9=C%10)=C%10N7CC(CCCCCCCC)CCCCCC)C=C6)S4)C%11=NSN=C%113)=C1,L(TPA-BT),,,0.69,9.17,57,3.6,"Lu J, Liang F, Drolet N, Ding J, Tao Y, Movileanu R. Crystalline low band-gap alternating indolocarbazole and benzothiadiazole-cored oligothiophene copolymer for organic solar cell applications. Chemical Communications, 5315-5317 (2008)."
610,CCCCCCC1(CCCCCC)C2=C(C=CC([H])=C2)C3=C1C=C(C4=CC=C(/C(C#N)=C/C5=CC=C(N(CCCCCC)C(C=CC(C6=CC=C([H])S6)=C7)=C7S8)C8=C5)S4)C=C3,P10,,,0.27,2.21,27,0.16,"Li K-C, Hsu Y-C, Lin J-TS, Yang C-C, Wei K-H, Lin H-C. Novel narrow-band-gap conjugated copolymers containing phenothiazine-arylcyanovinyl units for organic photovoltaic cell applications. Journal of Polymer Science Part a-Polymer Chemistry 46, 4285-4304 (2008)."
611,CCCCCCC1(CCCCCC)C2=C(C=CC([H])=C2)C3=C1C=C(C4=CC=C(/C(C#N)=C/C5=CC=C(N(CCCCCC)C(C=CC(C6=CC=C(/C=C(C7=CC=C([H])C=C7)\C#N)S6)=C8)=C8S9)C9=C5)C=C4)C=C3,P12,,,0.53,1.3,26,0.18,"Li K-C, Hsu Y-C, Lin J-TS, Yang C-C, Wei K-H, Lin H-C. Novel narrow-band-gap conjugated copolymers containing phenothiazine-arylcyanovinyl units for organic photovoltaic cell applications. Journal of Polymer Science Part a-Polymer Chemistry 46, 4285-4304 (2008)."
612,CCCCCCC1(CCCCCC)C2=C(C=CC([H])=C2)C3=C1C=C(C4=CC=C(/C(C#N)=C/C5=CC=C(N(CCCCCC)C(C=CC(C6=CC=C([H])S6)=C7)=C7S8)C8=C5)C=C4)C=C3,P2,,,0.52,1.46,22,0.17,"Li K-C, Hsu Y-C, Lin J-TS, Yang C-C, Wei K-H, Lin H-C. Novel narrow-band-gap conjugated copolymers containing phenothiazine-arylcyanovinyl units for organic photovoltaic cell applications. Journal of Polymer Science Part a-Polymer Chemistry 46, 4285-4304 (2008)."
613,CCCCCCC1(CCCCCC)C2=C(C=CC([H])=C2)C3=C1C=C(C4=CC=C(/C(C#N)=C/C5=CC=C(N(CCCCCC)C(C=CC(/C=C(C6=CC=C([H])C=C6)\C#N)=C7)=C7S8)C8=C5)C=C4)C=C3,P8,,,0.43,1.86,27,0.22,"Li K-C, Hsu Y-C, Lin J-TS, Yang C-C, Wei K-H, Lin H-C. Novel narrow-band-gap conjugated copolymers containing phenothiazine-arylcyanovinyl units for organic photovoltaic cell applications. Journal of Polymer Science Part a-Polymer Chemistry 46, 4285-4304 (2008)."
614,CCCCCCC1(CCCCCC)C2=C(C=CC([H])=C2)C3=C1C=C(C4=CC=C(/C(C#N)=C/C5=CC=C(N(CCCCCC)C(C=CC(C6=CC=C(/C=C(C7=CC=C([H])S7)\C#N)S6)=C8)=C8S9)C9=C5)S4)C=C3,TPBi,,,0.64,2.7,29,0.51,"Li K-C, Hsu Y-C, Lin J-TS, Yang C-C, Wei K-H, Lin H-C. Novel narrow-band-gap conjugated copolymers containing phenothiazine-arylcyanovinyl units for organic photovoltaic cell applications. Journal of Polymer Science Part a-Polymer Chemistry 46, 4285-4304 (2008)."
615,[H]C(S1)=C(CCCCCC)C=C1C2=CC(CCCCCC)=C(C3=CC=C([H])S3)S2,1,,,0.53,0.43,24,0.11,"Zhao C, Chen X, Zhang Y, Ng M-K. 4,9-dihydro-s-indaceno 1,2-b : 5,6-b' dithiophene-4,9-dione functionalized copolymers for organic photovoltaic devices. Journal of Polymer Science Part a-Polymer Chemistry 46, 2680-2688 (2008)."
616,[H]C1=CC2=C(OCC(CCCC)CC)C3=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C([H])O6)C7=NN(CC(CCCCCCCCCC)CCCCCCCC)N=C57)O4)S3)C(OCC(CCCC)CC)=C2S1,P2,,,0.74,6.31,64,2.98,"Unlu NA, Hacioglu SO, Hizalan G, Yildiz DE, Toppare L, Cirpan A. Benzodithiophene and Benzotriazole Bearing Conjugated Polymers for Electrochromic and Organic Solar Cell Applications. Journal of The Electrochemical Society 164, G71-G76 (2017)."
617,O=C(N(CC(CCCCCCCCCC)CCCCCCCC)C(C1=CC(SC(C2=C(CCCCCCCCCCCC)C=C([H])S2)=C3)=C3S1)=C45)C4=C(C6=CC(SC(C7=C(CCCCCCCCCCCC)C=C([H])S7)=C8)=C8S6)N(CC(CCCCCCCCCC)CCCCCCCC)C5=O,DPP2TT2Ta,,,0.54,7.2,64.7,2.5,"Chochos CL, et al. Effects of alkyl side chains positioning and presence of fused aromatic units in the backbone of low-bandgap diketopyrrolopyrrole copolymers on the optoelectronic properties of organic solar cells. Journal of Polymer Science Part A: Polymer Chemistry 56, 138-146 (2018)."
618,O=C(N(CC(CCCCCCCCCC)CCCCCCCC)C(C1=CC(SC(C2=CC(CCCCCCCCCCCC)=C([H])S2)=C3)=C3S1)=C45)C4=C(C6=CC(SC(C7=CC(CCCCCCCCCCCC)=C([H])S7)=C8)=C8S6)N(CC(CCCCCCCCCC)CCCCCCCC)C5=O,DPP2TT2Tb,,,0.61,5.3,42.4,1.4,"Chochos CL, et al. Effects of alkyl side chains positioning and presence of fused aromatic units in the backbone of low-bandgap diketopyrrolopyrrole copolymers on the optoelectronic properties of organic solar cells. Journal of Polymer Science Part A: Polymer Chemistry 56, 138-146 (2018)."
619,[H]C1=CC=C(S1)C(S2)=CC=C2C3=C4C(C(N3CC(CCCCCCCCCC)CCCCCCCC)=O)=C(C5=CC=C(C6=CC=C([H])S6)S5)N(CC(CCCCCCCCCC)CCCCCCCC)C4=O,DPP4T,,,0.66,9.2,65.5,4,"Chochos CL, et al. Effects of alkyl side chains positioning and presence of fused aromatic units in the backbone of low-bandgap diketopyrrolopyrrole copolymers on the optoelectronic properties of organic solar cells. Journal of Polymer Science Part A: Polymer Chemistry 56, 138-146 (2018)."
620,[H]C1=CC(CCCCCCCCCCCC)=C(S1)C(S2)=CC=C2C3=C4C(C(N3CC(CCCCCCCCCC)CCCCCCCC)=O)=C(C5=CC=C(C6=C(CCCCCCCCCCCC)C=C([H])S6)S5)N(CC(CCCCCCCCCC)CCCCCCCC)C4=O,DPP4Ta,,,0.61,3.1,52.8,1,"Chochos CL, et al. Effects of alkyl side chains positioning and presence of fused aromatic units in the backbone of low-bandgap diketopyrrolopyrrole copolymers on the optoelectronic properties of organic solar cells. Journal of Polymer Science Part A: Polymer Chemistry 56, 138-146 (2018)."
621,[H]C1=C(CCCCCCCCCCCC)C=C(S1)C(S2)=CC=C2C3=C4C(C(N3CC(CCCCCCCCCC)CCCCCCCC)=O)=C(C5=CC=C(C6=CC(CCCCCCCCCCCC)=C([H])S6)S5)N(CC(CCCCCCCCCC)CCCCCCCC)C4=O,DPP4Tb,,,0.74,2.5,56.7,1.1,"Chochos CL, et al. Effects of alkyl side chains positioning and presence of fused aromatic units in the backbone of low-bandgap diketopyrrolopyrrole copolymers on the optoelectronic properties of organic solar cells. Journal of Polymer Science Part A: Polymer Chemistry 56, 138-146 (2018)."
622,[H]C(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C(S4)=CC5=C4C(C6=CC=C(CC(CC)CCCC)S6)=C(C=C(C(S7)=CC8=C7C(C9=CC=C(CC(CC)CCCC)S9)=C(C=C(C(S%10)=CC%11=C%10C(C%12=CC=C(CC(CC)CCCC)S%12)=C(C=C(C%13=CC=C(C(N(CC(CCCCCC)CCCC)C%14=O)=C%15C%14=C(C%16=CC=C([H])S%16)N(CC(CCCCCC)CCCC)C%15=O)S%13)S%17)C%17=C%11C%18=CC=C(CC(CC)CCCC)S%18)S%19)C%19=C8C%20=CC=C(CC(CC)CCCC)S%20)S%21)C%21=C5C%22=CC=C(CC(CC)CCCC)S%22)S%23)C%23=C2C%24=CC=C(CC(CC)CCCC)S%24,PR1,,,0.75,15.06,44,5.04,"Howard JB, Thompson BC. Design of Random and Semi-Random Conjugated Polymers for Organic Solar Cells. Macromolecular Chemistry and Physics 218, 1700255 (2017)."
623,[H]C(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C(S4)=CC5=C4C(C6=CC=C(CC(CC)CCCC)S6)=C(C=C(C7=CC=C(C(N(CC(CCCCCC)CCCC)C8=O)=C9C8=C(C%10=CC=C([H])S%10)N(CC(CCCCCC)CCCC)C9=O)S7)S%11)C%11=C5C%12=CC=C(CC(CC)CCCC)S%12)S%13)C%13=C2C%14=CC=C(CC(CC)CCCC)S%14,PR2,,,0.74,14.84,51,5.63,"Howard JB, Thompson BC. Design of Random and Semi-Random Conjugated Polymers for Organic Solar Cells. Macromolecular Chemistry and Physics 218, 1700255 (2017)."
624,[H]C(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCC)CCCC)C5=O)=C6C5=C(C7=CC=C([H])S7)N(CC(CCCCCC)CCCC)C6=O)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9,PR3,,,0.71,6.41,53,2.42,"Howard JB, Thompson BC. Design of Random and Semi-Random Conjugated Polymers for Organic Solar Cells. Macromolecular Chemistry and Physics 218, 1700255 (2017)."
625,[H]C(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCC)CCCC)C5=O)=C6C5=C(C7=CC=C(C8=CC=C(C(N(CC(CCCCCC)CCCC)C9=O)=C%10C9=C(C%11=CC=C([H])S%11)N(CC(CCCCCC)CCCC)C%10=O)S8)S7)N(CC(CCCCCC)CCCC)C6=O)S4)S%12)C%12=C2C%13=CC=C(CC(CC)CCCC)S%13,PR4,,,0.7,5.1,0.46,1.64,"Howard JB, Thompson BC. Design of Random and Semi-Random Conjugated Polymers for Organic Solar Cells. Macromolecular Chemistry and Physics 218, 1700255 (2017)."
626,[H]C(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCC)CCCC)C5=O)=C6C5=C(C7=CC=C(C8=CC=C(C(N(CC(CCCCCC)CCCC)C9=O)=C%10C9=C(C%11=CC=C(C%12=CC=C(C(N(CC(CCCCCC)CCCC)C%13=O)=C%14C%13=C(C%15=CC=C(C%16=CC=C(C(N(CC(CCCCCC)CCCC)C%17=O)=C%18C%17=C(C%19=CC=C([H])S%19)N(CC(CCCCCC)CCCC)C%18=O)S%16)S%15)N(CC(CCCCCC)CCCC)C%14=O)S%12)S%11)N(CC(CCCCCC)CCCC)C%10=O)S8)S7)N(CC(CCCCCC)CCCC)C6=O)S4)S%20)C%20=C2C%21=CC=C(CC(CC)CCCC)S%21,PR5,,,0.68,2.98,40,0.79,"Howard JB, Thompson BC. Design of Random and Semi-Random Conjugated Polymers for Organic Solar Cells. Macromolecular Chemistry and Physics 218, 1700255 (2017)."
627,[H]C1=CC([Si](CC(CC)CCCC)(CC(CC)CCCC)C2=C3SC(C4=C5C(C(C(C=C(CCCC)C(CCCC)=C6)=C6C5=O)=O)=C([H])S4)=C2)=C3S1,DTS-C4,,,0.91,10.1,47,4.28,"Ie Y, Aso Y. Development of donor¨Cacceptor copolymers based on dioxocycloalkene-annelated thiophenes as acceptor units for organic photovoltaic materials. Polymer Journal 49, 13-22 (2016)."
628,[H]C1=CC([Si](CC(CC)CCCC)(CC(CC)CCCC)C2=C3SC(C4=C5C(C(C(C=C(CCCCCC)C(CCCCCC)=C6)=C6C5=O)=O)=C([H])S4)=C2)=C3S1,DTS-C6,,,0.86,14.39,64,7.85,"Ie Y, Aso Y. Development of donor¨Cacceptor copolymers based on dioxocycloalkene-annelated thiophenes as acceptor units for organic photovoltaic materials. Polymer Journal 49, 13-22 (2016)."
629,[H]C1=CC([Si](CC(CC)CCCC)(CC(CC)CCCC)C2=C3SC(C4=C5C(C(C(C=C(CCCCCCCC)C(CCCCCCCC)=C6)=C6C5=O)=O)=C([H])S4)=C2)=C3S1,DTS-C8,,,0.88,5,53,2.35,"Ie Y, Aso Y. Development of donor¨Cacceptor copolymers based on dioxocycloalkene-annelated thiophenes as acceptor units for organic photovoltaic materials. Polymer Journal 49, 13-22 (2016)."
630,[H]C1=CC([Si](CC(CC)CCCC)(CC(CC)CCCC)C2=C3SC(C4=C5C(C(C(C=C(CC(CC)CCCC)C(CC(CC)CCCC)=C6)=C6C5=O)=O)=C([H])S4)=C2)=C3S1,DTS-CEH,,,0.94,9.46,58,5.15,"Ie Y, Aso Y. Development of donor¨Cacceptor copolymers based on dioxocycloalkene-annelated thiophenes as acceptor units for organic photovoltaic materials. Polymer Journal 49, 13-22 (2016)."
631,[H]C1=CC2=C(C(SC(C3=C4C(C(C(CCCCCC)(CCCCCC)C4=O)=O)=C([H])S3)=C5)=C5[Si]2(CC(CC)CCCC)CC(CC)CCCC)S1,DTS-Ch,,,0.95,5.83,26,1.44,"Ie Y, Aso Y. Development of donor¨Cacceptor copolymers based on dioxocycloalkene-annelated thiophenes as acceptor units for organic photovoltaic materials. Polymer Journal 49, 13-22 (2016)."
632,[H]C1=CC2=C(C(SC(C3=C4C(C(/C(C4=O)=C(CCCCCC)\CCCCCC)=O)=C([H])S3)=C5)=C5[Si]2(CC(CC)CCCC)CC(CC)CCCC)S1,DTS-Chy,,,0.85,3.91,41,1.36,"Ie Y, Aso Y. Development of donor¨Cacceptor copolymers based on dioxocycloalkene-annelated thiophenes as acceptor units for organic photovoltaic materials. Polymer Journal 49, 13-22 (2016)."
633,[H]C1=CC2=C(C(SC(C3=C(CCCCCCCCCCCC)C=C(C4=C5C(C(C(F)(F)C5=O)=O)=C(C6=CC(CCCCCCCCCCCC)=C([H])S6)S4)S3)=C7)=C7[Si]2(CC(CC)CCCC)CC(CC)CCCC)S1,DTS-D-C,,,0.88,1.9,46,0.77,"Ie Y, Aso Y. Development of donor¨Cacceptor copolymers based on dioxocycloalkene-annelated thiophenes as acceptor units for organic photovoltaic materials. Polymer Journal 49, 13-22 (2016)."
634,[H]C1=CC([Si](CC(CC)CCCC)(CC(CC)CCCC)C2=C3SC(C4=C5C(C(C6=C(CCCCCC)SC(CCCCCC)=C6C5=O)=O)=C([H])S4)=C2)=C3S1,DTS-T6,,,0.98,6.01,46,2.7,"Ie Y, Aso Y. Development of donor¨Cacceptor copolymers based on dioxocycloalkene-annelated thiophenes as acceptor units for organic photovoltaic materials. Polymer Journal 49, 13-22 (2016)."
635,O=C1C(CCCCCC)(CCCCCC)C(C2=C([H])SC(C(S3)=CC=C3C4=CC([Si]5(CC(CC)CCCC)CC(CC)CCCC)=C(S4)C6=C5C=C(C7=CC=C([H])S7)S6)=C21)=O,DTS-T-Ch,,,0.8,10.1,64,5.17,"Ie Y, Aso Y. Development of donor¨Cacceptor copolymers based on dioxocycloalkene-annelated thiophenes as acceptor units for organic photovoltaic materials. Polymer Journal 49, 13-22 (2016)."
636,O=C(C1=C(SC([H])=C1C/2=O)C(S3)=CC=C3C4=CC([Si]5(CC(CC)CCCC)CC(CC)CCCC)=C(S4)C6=C5C=C(C7=CC=C([H])S7)S6)C2=C(CCCCCC)\CCCCCC,DTS-T-Chy,,,0.68,9.1,61,3.79,"Ie Y, Aso Y. Development of donor¨Cacceptor copolymers based on dioxocycloalkene-annelated thiophenes as acceptor units for organic photovoltaic materials. Polymer Journal 49, 13-22 (2016)."
637,[H]C1=CC=C(S1)C(N(CC(CC)CCCC)C2=O)=C3C2=C(C4=CC=C(C5=CC=C(C(C=CC([H])=C6)=C6C78C(C=CC=C9)=C9C%10=C8C=CC=C%10)C7=C5)S4)N(CC(CC)CCCC)C3=O,PDPPSBF,,,0.87,11.51,41,4.13,"Josse P, et al. Direct (Hetero)Arylation Polymerization of a Spirobifluorene and a Dithienyl-Diketopyrrolopyrrole Derivative: New Donor Polymers for Organic Solar Cells. Molecules 23,  (2018)."
638,[H]C(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=CC=C(C4=C5C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C5=O)=O)=C(C6=CC=C([H])S6)S4)S3)S7)C7=C2OCC(CCCC)CC,PBDT-OR,,,0.84,6.35,60,3.21,"Kim J, et al. Synthesis and characterization of highly conjugated side-group-substituted benzo[1,2-b"
639,[H]C(S1)=CC2=C1C(C3=CC=C(/C=C/C4=CC=C(/C=C/C5=CC=C(CC(CCCCCC)CCCCCCCC)S5)S4)S3)=C(C=C(C6=CC=C(C7=C8C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C8=O)=O)=C(C9=CC=C([H])S9)S7)S6)S%10)C%10=C2C%11=CC=C(/C=C/C%12=CC=C(/C=C/C%13=CC=C(CC(CCCCCC)CCCCCCCC)S%13)S%12)S%11,PBDT-TTV,,,0.85,10,56,4.76,"Kim J, et al. Synthesis and characterization of highly conjugated side-group-substituted benzo[1,2-b"
640,[H]C1=CC=C(S1)C(S2)=CC3=C2C(SC(C4=CC(C(N(CC(CCCCCCCC)CCCCCCCCCC)C5=C6SC([H])=C5)=O)=C6S4)=C7)=C7C(N3CC(CCCCCCCC)CCCCCCCCCC)=O,PThBDT,,,0.99,14.24,73.1,10.31,"Li H, et al. Temperature-dependent Schottky barrier in high-performance organic solar cells. Sci Rep 7, 40134 (2017)."
641,[H]C(S1)=CC=C1C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC(C(OCC(CC)CCCC)=C(OCC(CC)CCCC)C5=C6SC([H])=C5)=C6S4)S3)C7=NSN=C27,PBDP-BT,,,0.88,8.5,57.7,4.3,"Nam SJ, Jeon SJ, Han YW, Moon DK. Effect of non-covalent interactions on molecular stacking and photovoltaic properties in organic photovoltaics. Journal of Industrial and Engineering Chemistry 63, 191-200 (2018)."
642,[H]C(S1)=CC=C1C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC(C(OCC(CC)CCCC)=C(OCC(CC)CCCC)C5=C6SC([H])=C5)=C6S4)S3)C7=C2N=C(C(SC=C8)=C8C9=C%10SC=C9)C%10=N7,"PBDP-DTPhz,Dn",,,0.86,9.7,56.4,4.7,"Nam SJ, Jeon SJ, Han YW, Moon DK. Effect of non-covalent interactions on molecular stacking and photovoltaic properties in organic photovoltaics. Journal of Industrial and Engineering Chemistry 63, 191-200 (2018)."
643,[H]C(S1)=CC=C1C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC(C(OCC(CC)CCCC)=C(OCC(CC)CCCC)C5=C6SC([H])=C5)=C6S4)S3)C7=C2N=C(C(C=CS8)=C8C9=C%10C=CS9)C%10=N7,"PBDP-DTPhz,Up",,,0.9,9.7,54.7,4.8,"Nam SJ, Jeon SJ, Han YW, Moon DK. Effect of non-covalent interactions on molecular stacking and photovoltaic properties in organic photovoltaics. Journal of Industrial and Engineering Chemistry 63, 191-200 (2018)."
644,CCCC(CC)CN1C2=C(C=C(/C=C(C#N)/C3=CC=C([N+]([O-])=O)C=C3)C=C2)C4=C1C=CC(/C=C(C#N)/C5=CC=C([N+]([O-])=O)C=C5)=C4,NBCS,,,0.75,4.35,30.07,0.98,"Sathiyan G, Siva G, Prakash J, Swart HC, Sakthivel P. Design and chemical engineering of carbazole-based donor small molecules for organic solar cell applications. Journal of Materials Science: Materials in Electronics 29, 14842-14851 (2018)."
645,CCCCCN1C2=C(C=C(/C=C(C#N)/C3=CC=C([N+]([O-])=O)C=C3)C=C2)C4=C1C=CC(/C=C(C#N)/C5=CC=C([N+]([O-])=O)C=C5)=C4,NHCS,,,0.77,3.9,29.76,0.9,"Sathiyan G, Siva G, Prakash J, Swart HC, Sakthivel P. Design and chemical engineering of carbazole-based donor small molecules for organic solar cell applications. Journal of Materials Science: Materials in Electronics 29, 14842-14851 (2018)."
646,[H]C(S1)=C(CC(CCCCCCCC)CCCCCCCCCC)C=C1C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C4=CC=C(C5=CC=C([H])S5)S4)S3)C6=NSN=C62,PffBT4T-2OD,,,0.784,20.12,61.2,11.33,"Xu C, et al. Realizing 11.3% efficiency in PffBT4T-2OD fullerene organic solar cells via superior charge extraction at interfaces. Applied Physics A 124,  (2018)."
647,CC1=CC=C([Se]1)/C=C/C([Se]2)=CC=C2C3=C4C(C=C(C5=CC=C(C(N(C)C6=O)=C7C6=C(C8=CC=CS8)N(C)C7=O)S5)S4)=C(C9=CC=C(/C=C/C%10=CC=C(C)[Se]%10)[Se]9)C%11=C3C=C(C%12=CC=C(C(N(C)C%13=O)=C%14C%13=C(C%15=CC=CS%15)N(C)C%14=O)S%12)S%11,SeBDT-DPP,,,0.79,10.98,58,5.04,"Shin Y, Song CE, Lee WH, Lee SK, Shin WS, Kang IN. Synthesis and Characterization of a Soluble A-D-A Molecule Containing a 2D Conjugated Selenophene-Based Side Group for Organic Solar Cells. Macromol Rapid Commun 38,  (2017)."
648,[H]C(S1)=CC=C1C2=C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C3=O)=O)C3=C(N2CCCCCCCC)C4=CC=C(C5=CC=C([H])S5)S4,P(T-TPPDT),,,0.907,11.13,52.7,5.32,"Tamilavan V, et al. Thiophene and thieno[3,2-b]thiophene ¦Ð-bridged pyrrolo[3,4-c]pyrrole-1,3-dione-based wide band-gap polymers for fullerene and non-fullerene organic solar cells. Organic Electronics 63, 78-85 (2018)."
649,[H]C(S1)=CC=C1C2=C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C3=O)=O)C3=C(N2CCCCCCCC)C4=CC=C(C5=CC6=C(C=C([H])S6)S5)S4,P(Tt-TPPDT),,,0.874,13.4,54.2,6.35,"Tamilavan V, et al. Thiophene and thieno[3,2-b]thiophene ¦Ð-bridged pyrrolo[3,4-c]pyrrole-1,3-dione-based wide band-gap polymers for fullerene and non-fullerene organic solar cells. Organic Electronics 63, 78-85 (2018)."
650,[H]C(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(C(CCCCCCCCC)=O)C(C(CCCCCCCCC)=O)=C(C6=CC=C([H])S6)N5CCCCCCCCCCCC)S4)S7)C7=C2C8=CC=C(CC(CC)CCCC)S8,P(BDTT-TPTK),,,0.72,1.87,32,0.43,"Tamilavan V, et al. Effects of inserting keto-functionalized side-chains instead of imide-functionalized side-chain on the pyrrole backbone of 2,5-bis(2-thienyl)pyrrole-based polymers for organic solar cells. Journal of Photochemistry and Photobiology A: Chemistry 371, 387-394 (2019)."
651,[H]C(S1)=CC=C1C2=C(C(CCCCCCCCC)=O)C(C(CCCCCCCCC)=O)=C(N2CCCCCCCCCCCC)C(S3)=CC=C3C4=CC=C(C(N(CCCCCCCC)C5=O)=C6C5=C(C7=CC=C([H])S7)N(CCCCCCCC)C6=O)S4,P(DKPP-TPTK),,,0.73,2.73,32,0.63,"Tamilavan V, et al. Effects of inserting keto-functionalized side-chains instead of imide-functionalized side-chain on the pyrrole backbone of 2,5-bis(2-thienyl)pyrrole-based polymers for organic solar cells. Journal of Photochemistry and Photobiology A: Chemistry 371, 387-394 (2019)."
652,[H]C(S1)=CC=C1C2=C(C(CCCCCCCCC)=O)C(C(CCCCCCCCC)=O)=C(N2CCCCCCCCCCCC)C(S3)=CC=C3C4=CC=C(C5=CC=C(C6=CC=C([H])S6)C7=NSN=C57)S4,P(DTBT-TPTK),,,0.74,3.29,32,0.79,"Tamilavan V, et al. Effects of inserting keto-functionalized side-chains instead of imide-functionalized side-chain on the pyrrole backbone of 2,5-bis(2-thienyl)pyrrole-based polymers for organic solar cells. Journal of Photochemistry and Photobiology A: Chemistry 371, 387-394 (2019)."
653,O=C(N1CC(CC)CCCC)C(C2=C1C3=CC=C(S3)C#C/C(C4=CC=C5N4[Zn]N6/C(C=C/C6=C7\C8=CC=C(CC(CC)CCCC)S8)=C(C#CC9=CC=C(C%10=C%11C(C(N%10CC(CC)CCCC)=O)=C(C%12=CC=CS%12)N(CC(CC)CCCC)C%11=O)S9)\C(C=C/%13)=NC%13=C5\C%14=CC=C(CC(CC)CCCC)S%14)=C%15N=C7C=C/%15)=C(C%16=CC=CS%16)N(CC(CC)CCCC)C2=O,DPPEZnP-TEH,,,0.8,12.4,57.26,5.68,"Tan W-Y, et al. Enhancing Performances of Solution-Processed Inverted Ternary Small-Molecule Organic Solar Cells: Manipulating the Host-Guest Donors and Acceptor Interaction. Solar RRL 1, 1600003 (2017)."
654,[H]C(S1)=C(CC(CCCC)CCCCCC)C=C1C2=CC3=C(C4=NN(CCCCCCCC)N=C42)C=C(C5=CC(CC(CCCC)CCCCCC)=C(C6=CC(F)=C(C7=C(F)C=C([H])S7)S6)S5)C8=NN(CCCCCCCC)N=C83,PDTF-TZNT,,,0.8,17.33,72.5,10.05,"Tang D, et al. Naphthobistriazole-based wide bandgap donor polymers for efficient non-fullerene organic solar cells: Significant fine-tuning absorption and energy level by backbone fluorination. Nano Energy 53, 258-269 (2018)."
655,[H]C(S1)=C(CC(CCCC)CCCCCC)C=C1C2=CC3=C(C4=NN(CCCCCCCC)N=C42)C=C(C5=CC(CC(CCCC)CCCCCC)=C(C6=CC=C(C7=CC=C([H])S7)S6)S5)C8=NN(CCCCCCCC)N=C83,PDTH-TZNT,,,0.75,10.15,58.1,4.42,"Tang D, et al. Naphthobistriazole-based wide bandgap donor polymers for efficient non-fullerene organic solar cells: Significant fine-tuning absorption and energy level by backbone fluorination. Nano Energy 53, 258-269 (2018)."
656,[O-]C1=C(/C(/C1=C/C2=[N+](CCCC)C(C=CC=C3)=C3S2)=C(C#N)/C#N)C4=CC=C(N(CCCC)CCCC)C=C4,diCN-USQ-1,,,0.61,6.51,37,1.49,"Wu J, et al. Central dicyanomethylene-substituted unsymmetrical squaraines and their application in organic solar cells. J. Mater. Chem. A 6, 5797-5806 (2018)."
657,[O-]C1=C(/C(/C1=C/C2=[N+](CCCC)C(C=CC=C3)=C3S2)=C(C#N)/C#N)C4=C(O)C=C(N(CCCC)CCCC)C=C4,diCN-USQ-2,,,0.65,7.75,38,1.91,"Wu J, et al. Central dicyanomethylene-substituted unsymmetrical squaraines and their application in organic solar cells. J. Mater. Chem. A 6, 5797-5806 (2018)."
658,[O-]C1=C(/C(/C1=C/C2=[N+](CCCC)C(C(C=CC=C3)=C3C=C4)=C4C2(C)C)=C(C#N)/C#N)C5=C(O)C=C(N6C(CCC7)C7C8=C6C=CC=C8)C=C5,diCN-USQ-3,,,0.87,10.89,49,4.58,"Wu J, et al. Central dicyanomethylene-substituted unsymmetrical squaraines and their application in organic solar cells. J. Mater. Chem. A 6, 5797-5806 (2018)."
659,FC1=C(C2=CC(CCCCCCCC)=C(C3=CC4=C(C(C#C[Si](C)(C)C)=C(C=C(C5=C(CCCCCCCC)C=C(C6=C(F)C=C(C7=CC=C(C8=CC=C(CC(CCCCCCCC)CCCCCCCCCC)S8)S7)C9=NSN=C96)S5)S%10)C%10=C4C#C[Si](C(C)C)(C(C)C)C(C)C)S3)S2)C%11=NSN=C%11C(C%12=CC=C(C%13=CC=C(CC(CCCCCCCCCC)CCCCCCCC)S%13)S%12)=C1,BDTTIPS,,,0.88,7.68,59.06,3.99,"Xie R, et al. Diethynylbenzo[1,2-b"
660,FC1=C(C2=CC(CCCCCCCC)=C(C3=CC4=C(C(C#C[H])=C(C=C(C5=C(CCCCCCCC)C=C(C6=C(F)C=C(C7=CC=C(C8=CC=C(CC(CCCCCCCC)CCCCCCCCCC)S8)S7)C9=NSN=C96)S5)S%10)C%10=C4C#CC%11=CC=C(C%12=C%13C(C(N%12CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C%14=CC=C([H])S%14)N(CC(CCCCCCCC)CCCCCCCCCC)C%13=O)S%11)S3)S2)C%15=NSN=C%15C(C%16=CC=C(C%17=CC=C(CC(CCCCCCCCCC)CCCCCCCC)S%17)S%16)=C1,PBDTE-DPP,,,0.754,2.14,50.27,0.81,"Xie R, et al. Diethynylbenzo[1,2-b"
661,FC1=C(C2=CC(CCCCCCCC)=C(C3=CC4=C(C(C#C[H])=C(C=C(C5=C(CCCCCCCC)C=C(C6=C(F)C=C(C7=CC=C(C8=CC=C(CC(CCCCCCCC)CCCCCCCCCC)S8)S7)C9=NSN=C96)S5)S%10)C%10=C4C#CC%11=C(F)C(F)=C([H])C%12=NSN=C%12%11)S3)S2)C%13=NSN=C%13C(C%14=CC=C(C%15=CC=C(CC(CCCCCCCCCC)CCCCCCCC)S%15)S%14)=C1,PBDTE-FBT,,,0.85,3.1,62.26,1.64,"Xie R, et al. Diethynylbenzo[1,2-b"
662,FC1=C(C2=CC(CCCCCCCC)=C(C3=CC4=C(C(C#C[H])=C(C=C(C5=C(CCCCCCCC)C=C(C6=C(F)C=C(C7=CC=C(C8=CC=C(CC(CCCCCCCC)CCCCCCCCCC)S8)S7)C9=NSN=C96)S5)S%10)C%10=C4C#CC%11=CC=C([H])C%11)S3)S2)C%12=NSN=C%12C(C%13=CC=C(C%14=CC=C(CC(CCCCCCCCCC)CCCCCCCC)S%14)S%13)=C1,PBDTE-Th,,,0.809,3.67,47.41,1.41,"Xie R, et al. Diethynylbenzo[1,2-b"
663,[H]C(S1)=CC2=C1C(C3=CC(F)=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C6C(C(C7=C(CC(CC)CCCC)SC(CC(CC)CCCC)=C7C6=O)=O)=C(C8=CC=C([H])S8)S5)S4)S9)C9=C2C%10=CC(F)=C(CC(CC)CCCC)S%10,PBDB-TF,,,0.87,20.73,80.79,14.57,"Zheng Z, et al. A Highly Efficient Non-Fullerene Organic Solar Cell with a Fill Factor over 0.80 Enabled by a Fine-Tuned Hole-Transporting Layer. Adv. Mater., e1801801 (2018)."
664,[H]C(S1)=CC2=C1C(C3=CC(Cl)=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C6C(C(C7=C(CC(CC)CCCC)SC(CC(CC)CCCC)=C7C6=O)=O)=C(C8=CC=C([H])S8)S5)S4)S9)C9=C2C%10=CC(Cl)=C(CC(CC)CCCC)S%10,PBDB-TCI,,,0.86,21.1,75,13.7,"Yu R, et al. Design and application of volatilizable solid additives in non-fullerene organic solar cells. Nat. Commun. 9, 4645 (2018)."
665,[H]C(S1)=CC2=C1C(C3=CC(F)=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C([H])S6)C7=NN(CC(CCCCCC)CCCCCCCC)N=C75)S4)S8)C8=C2C9=CC(F)=C(CC(CC)CCCC)S9,PBTA-TF,,,0.94,19,77,12.4,"Yu R, et al. Design and application of volatilizable solid additives in non-fullerene organic solar cells. Nat. Commun. 9, 4645 (2018)."
666,[H]C(S1)=CC=C1C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C([H])S3)C4=NSN=C42,P11,,,0.72,12.98,50.18,4.71,"Zhang G, et al. An Open-Circuit Voltage and Power Conversion Efficiency Study of Fullerene Ternary Organic Solar Cells Based on Oligomer/Oligomer and Oligomer/Polymer. Macromol Rapid Commun 38,  (2017)."
667,[H]C1=CC2=C(S1)C(C3=CC(F)=C(CC(CC)CCCC)S3)=C4C(SC(C5=CC=C(S5)C6=C7C(C(C8=C(CC(CC)CCCC)SC(CC(CC)CCCC)=C8C7=O)=O)=C(C9=CC=C([H])S9)S6)=C4)=C2C%10=CC(F)=C(CC(CC)CCCC)S%10,PBDB-T-2F,,,0.842,22.03,76.4,14.18,"Zhang H, et al. Over 14% Efficiency in Organic Solar Cells Enabled by Chlorinated Nonfullerene Small-Molecule Acceptors. Adv. Mater. 30, e1800613 (2018)."
668,[H]C1=CC(SC(C2=C3C(C(N2CC(CCCCCCCC)CCCCCCCC)=O)=C(C4=CC(SC(C5=CC=C([H])S5)=C6)=C6S4)N(CC(CCCCCCCC)CCCCCCCC)C3=O)=C7)=C7S1,PDPPTT-T-TT,,,0.53,17.9,49,4.7,"Cao B, et al. Understanding the Effects of a High Surface Area Nanostructured Indium Tin Oxide Electrode on Organic Solar Cell Performance. ACS Appl Mater Interfaces 9, 38706-38715 (2017)."
669,FC1=C(CC(CCCC)CC)SC(C2=C(C=C([H])S3)C3=C(C4=CC(F)=C(CC(CC)CCCC)S4)C5=C2SC(C6=CC(C(OCC(CCCCCC)CCCC)=O)=C(C7=CC8=C(C=C(C9=C(C(OCC(CCCCCC)CCCC)=O)C=C([H])S9)S8)S7)S6)=C5)=C1,2TC-TT -BDTFT,,,1.06,15.25,59.31,9.65,"Chen J, et al. Backbone Conformation Tuning of Carboxylate-Functionalized Wide Band Gap Polymers for Efficient Non-Fullerene Organic Solar Cells. Macromolecules 52, 341-353 (2018)."
670,FC1=C(CC(CCCC)CC)SC(C2=C(C=C([H])S3)C3=C(C4=CC(F)=C(CC(CC)CCCC)S4)C5=C2SC(C6=CC=C(C7=C(C(OCC(CCCCCC)CCCC)=O)C8=C(C(C(OCC(CCCC)CCCCCC)=O)=C(C9=CC=C([H])S9)S8)S7)S6)=C5)=C1,2T-TTC -BDTFT,,,0.97,16.57,69.37,11.15,"Chen J, et al. Backbone Conformation Tuning of Carboxylate-Functionalized Wide Band Gap Polymers for Efficient Non-Fullerene Organic Solar Cells. Macromolecules 52, 341-353 (2018)."
671,[H]C1=CC2=C(S1)C(C3=CC=C(CCCCCCCC)S3)=C4C(SC(C5=CC=C(C6=C(OCCCCCCCC)C(OCCCCCCCC)=C(C7=CC=C([H])S7)C8=NON=C68)S5)=C4)=C2C9=CC=C(CCCCCCCC)S9,PBDTTBO-C8,,,0.71,13.33,59.3,6.2,"Chiou GC, et al. Fluorene Conjugated Polymer/Nickel Oxide Nanocomposite Hole Transport Layer Enhances the Efficiency of Organic Photovoltaic Devices. ACS Appl Mater Interfaces 9, 2232-2239 (2017)."
672,[H]C1=CC2=C(S1)C(C3=CC=C(SCC(CCCC)CCCCCC)S3)=C4C(SC(C5=CC=C(C6=C7C(C(C8=C(CC(CC)CCCC)SC(CC(CC)CCCC)=C8C7=O)=O)=C(C9=CC=C(C%10=CC%11=C(S%10)C(C%12=CC=C(SCC(CC)CCCC)S%12)=C%13C(SC(C%14=CC=C(C%15=C%16C(C(C%17=C(CC(CC)CCCC)SC(CC(CC)CCCC)=C%17C%16=O)=O)=C(C%18=CC=C([H])S%18)S%15)S%14)=C%13)=C%11C%19=CC=C(SCC(CC)CCCC)S%19)S9)S6)S5)=C4)=C2C%20=CC=C(SCC(CCCC)CCCCCC)S%20,PB55,,,0.93,17,74.8,12.1,"Huo L, et al. Subtle Side-Chain Engineering of Random Terpolymers for High-Performance Organic Solar Cells. Chem. Mater. 30, 3294-3300 (2018)."
673,[H]C1=CC=C(S1)C(C2=NSN=C23)=C(F)C(F)=C3C4=CC=C(C5=CC(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C6=C7N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C8=C6C=CC([H])=C8)=C7C=C5)S4,PDHIT2FT,,,0.89,17.6,52.9,8.28,"Hwang J, et al. Indolo[3,2-b]indole-Containing Donor¨CAcceptor Copolymers for High-Efficiency Organic Solar Cells. Chem. Mater. 29, 2135-2140 (2017)."
674,[H]C1=CC=C(S1)C(C2=NSN=C23)=C(F)C=C3C4=CC=C(C5=CC(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C6=C7N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C8=C6C=CC([H])=C8)=C7C=C5)S4,PDHITFT,,,0.89,18.4,53.4,8.84,"Hwang J, et al. Indolo[3,2-b]indole-Containing Donor¨CAcceptor Copolymers for High-Efficiency Organic Solar Cells. Chem. Mater. 29, 2135-2140 (2017)."
675,[H]C1=CC=C(S1)C(C2=NSN=C23)=CC=C3C4=CC=C(C5=CC(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C6=C7N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C8=C6C=CC([H])=C8)=C7C=C5)S4,PDHITHT,,,0.89,16.1,52.3,7.49,"Hwang J, et al. Indolo[3,2-b]indole-Containing Donor¨CAcceptor Copolymers for High-Efficiency Organic Solar Cells. Chem. Mater. 29, 2135-2140 (2017)."
676,FC(C(F)=C(C1=CC(CC(CCCCCC)CCCCCCCC)=C(C2=CC(C(OCC(CCCCCC)CCCCCCCC)=O)=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C([H])S5)C6=NSN=C64)S3)S2)S1)C7=NSN=C78)=C8C9=CC(CC(CCCCCC)CCCCCCCC)=C(C%10=CC(C(OCC(CCCCCC)CCCCCCCC)=O)=C([H])S%10)S9,P3TAE,,,1.2,10.47,65,8.1,"Liu J, et al. Carboxylate substitution position influencing polymer properties and enabling non-fullerene organic solar cells with high open circuit voltage and low voltage loss. J. Mater. Chem. A 6, 16874-16881 (2018)."
677,[H]C(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C(C(OCC)=O)C=C([H])S4)S5)C5=C2C6=CC=C(CC(CC)CCCC)S6,ran-PThE,,,0.891,15.96,58.9,8.38,"Liu Y, et al. Enhancing the Performance of Non-Fullerene Organic Solar Cells Using Regioregular Wide-Bandgap Polymers. Macromolecules 51, 8646-8651 (2018)."
678,CCCCC(CC)CC(S1)=CC=C1C2=C3C(C=C(C4=C(C(OCC)=O)C=C(C5=CC6=C(C(C7=CC=C(CC(CCCC)CC)S7)=C(C=C([H])S8)C8=C6C9=CC=C(CC(CC)CCCC)S9)S5)S4)S3)=C(C%10=CC=C(CC(CC)CCCC)S%10)C%11=C2C=C(C%12=C(C(OCC)=O)C=C([H])S%12)S%11,reg-PThE,,,0.917,18.04,67.7,11.21,"Liu Y, et al. Enhancing the Performance of Non-Fullerene Organic Solar Cells Using Regioregular Wide-Bandgap Polymers. Macromolecules 51, 8646-8651 (2018)."
679,[H]/C(C(S1)=CC=C1C(S2)=CC3=C2C(OCC(CC)CCCC)=C(C=C(C4=CC=C(/C([H])=C5C(C6=CC=CC=C6)=NOC/5=O)S4)S7)C7=C3OCC(CCCC)CC)=C8C(C9=CC=CC=C9)=NOC\8=O,BDT-HTOX,,,0.88,3.26,27.9,0.8,"Sylvianti N, et al. New A-D-A type small molecules based on benzodithiophene derivative for organic solar cells. Molecular Crystals and Liquid Crystals 660, 66-71 (2018)."
680,[H]C(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC(CCCCCCCCCCCC)=C([H])S4)S3)S5)C5=C2OCC(CC)CCCC,PBDTDT-O,,,0.85,1.86,34.01,0.54,"Zhang K, Qin Y, Li F, Yu L, Sun M. Two-Dimensional BDT-Based Wide Band Gap Polymer Donor for Efficient Non-Fullerene Organic Solar Cells. The Journal of Physical Chemistry C 121, 19634-19641 (2017)."
681,[H]C(S1)=CC2=C1C(C3=CC(SC(CC(CC)CCCC)=C4)=C4S3)=C(C=C(C5=C(CCCCCCCCCCCC)C=C(C6=CC(CCCCCCCCCCCC)=C([H])S6)S5)S7)C7=C2C8=CC(SC(CC(CC)CCCC)=C9)=C9S8,PBDTDT-TT,,,0.82,16.17,63.4,8.43,"Zhang K, Qin Y, Li F, Yu L, Sun M. Two-Dimensional BDT-Based Wide Band Gap Polymer Donor for Efficient Non-Fullerene Organic Solar Cells. The Journal of Physical Chemistry C 121, 19634-19641 (2017)."
682,CCCCCCC(S1)=CC=C1C2=CC=C(S2)C3=CN=C(C4=NSN=C43)C5=CC([Si]6(CC(CC)CCCC)CC(CC)CCCC)=C(S5)C7=C6C=C(S7)C8=NC9=C(S8)C(C%10=CC=C(CC(CC)CCCC)S%10)=C%11C(SC(C%12=CC([Si](CC(CC)CCCC)(CC(CC)CCCC)C%13=C%14SC(C%15=NC=C(C%16=CC=C(C%17=CC=C(CCCCCC)S%17)S%16)C%18=NSN=C%18%15)=C%13)=C%14S%12)=N%11)=C9C%19=CC=C(CC(CC)CCCCC)S%19,BBTz-X,,,0.84,12.27,69.5,7.2,"Zhang S, et al. Intermediate-Sized Conjugated Donor Molecules for Organic Solar Cells: Comparison of Benzodithiophene and Benzobisthiazole-Based Cores. Chem. Mater. 29, 7880-7887 (2017)."
683,CCCCCCC(S1)=CC=C1C2=CC=C(S2)C3=CN=C(C4=NSN=C43)C5=CC([Si]6(CC(CC)CCCC)CC(CC)CCCC)=C(S5)C7=C6C=C(S7)C8=CC9=C(S8)C(C%10=CC=C(CC(CC)CCCC)S%10)=C%11C(SC(C%12=CC([Si](CC(CC)CCCC)(CC(CC)CCCC)C%13=C%14SC(C%15=NC=C(C%16=CC=C(C%17=CC=C(CCCCCC)S%17)S%16)C%18=NSN=C%18%15)=C%13)=C%14S%12)=C%11)=C9C%19=CC=C(CC(CC)CCCCC)S%19,BDT-X,,,0.78,13.71,73.04,7.74,"Zhang S, et al. Intermediate-Sized Conjugated Donor Molecules for Organic Solar Cells: Comparison of Benzodithiophene and Benzobisthiazole-Based Cores. Chem. Mater. 29, 7880-7887 (2017)."
684,CCCCCCC(S1)=CC=C1C2=CC=C(S2)C3=CN=C(C4=NSN=C43)C5=CC([Si]6(CC(CC)CCCC)CC(CC)CCCC)=C(S5)C7=C6C=C(S7)C8=CC=C(C9=CC([Si](CC(CC)CCCC)(CC(CC)CCCC)C%10=C%11SC(C%12=CC=C(C%13=CC([Si](CC(CC)CCCC)(CC(CC)CCCC)C%14=C%15SC(C%16=NC=C(C%17=CC=C(C%18=CC=C(CCCCCC)S%18)S%17)C%19=NSN=C%19%16)=C%14)=C%15S%13)C%20=NSN=C%20%12)=C%10)=C%11S9)C%21=NSN=C%218,X2,,,0.66,15.41,69,7.01,"Zhang S, et al. Intermediate-Sized Conjugated Donor Molecules for Organic Solar Cells: Comparison of Benzodithiophene and Benzobisthiazole-Based Cores. Chem. Mater. 29, 7880-7887 (2017)."
685,[H]C1=CC2=C(OCCCCCCCC)C3=C(C=C(C4=C(C)N(B(F)F)C(/C(C5=CC=C(OCCCCCCCC)C=C5)=C6N=C(C)C([H])=C\6C)=C4C)S3)C(OCCCCCCCC)=C2S1,BDH1,,,0.63,9.92,59.1,3.69,"He A, Qin Y, Dai W, Luo X. Novel D-A type dyes based on BODIPY for solution processed organic polymer solar cells. Dyes and Pigments 162, 671-679 (2019)."
686,[H]C(C=C1)=CC2=C1C(C=CC(C3=CC=C(C4=C5C(C(N4CC(CCCCCCCCCC)CCCCCCCC)=O)=C(C6=CC=C(C(C=C7)=CC8=C7C(C=CC(C9=CC=C(C%10=C%11C(C(N%10CC(CCCCCCCCCC)CCCCCCCC)=O)=C(C%12=CC=C([H])S%12)N(CC(CCCCCCCCCC)CCCCCCCC)C%11=O)S9)=C%13)=C%13N=C8OCCCCCCCC)S6)N(CC(CCCCCCCCCC)CCCCCCCC)C5=O)S3)=C%14)=C%14N(CCCCCCCC)C2=O,PDPPPTD,,,0.87,12.55,67.83,7.41,"Li P, et al. Air-Processed, Stable Organic Solar Cells with High Power Conversion Efficiency of 7.41. Small 15, e1804671 (2019)."
687,[H]C1=CC2=C(S1)C(C3=CC(SCCCCCC)=CC(F)=C3)=C4C(SC(C5=CC=C(C6=C(F)C(OCC(CCCC)CC)=C(C7=CC=C([H])S7)C8=NSN=C86)S5)=C4)=C2C9=CC(SCCCCCC)=CC(F)=C9,POF,,,0.86,14.9,57,7.28,"Gong X, et al. Influence of polymer side chains on the photovoltaic performance of non-fullerene organic solar cells. Journal of Materials Chemistry C 5, 937-942 (2017)."
688,[H]C1=CC2=C(S1)C(C3=CC(SCCCCCC)=CC(F)=C3)=C4C(SC(C5=CC=C(C6=C(F)C(SCC(CCCC)CC)=C(C7=CC=C([H])S7)C8=NSN=C86)S5)=C4)=C2C9=CC(SCCCCCC)=CC(F)=C9,PSF,,,0.96,5.6,29,1.55,"Gong X, et al. Influence of polymer side chains on the photovoltaic performance of non-fullerene organic solar cells. Journal of Materials Chemistry C 5, 937-942 (2017)."
689,FC1=C(C2=NSN=C2C(C3=CC=C(C4=CC=C(CCCCCC)S4)S3)=C1)C(S5)=CC6=C5C(SC(C7=C(F)C=C(C8=CC=C(C9=CC=C(CCCCCC)S9)S8)C%10=NSN=C%107)=C%11)=C%11[Si]6(CC(CC)CCCC)CC(CC)CCCC,p-DTS-(FBTTH2)2,,,0.79,11.86,69,6.5,"Xu G, et al. n-Type conjugated electrolytes cathode interlayer with thickness-insensitivity for highly efficient organic solar cells. Journal of Materials Chemistry A 5, 13807-13816 (2017)."
690,FC1=C([H])C2=NN(CCCCCC)N=C2C(C3=CC4=C(C(SC(C5=CC(F)=C(C6=CC7=C(C(SC([H])=C8)=C8[Si]7(CCCCCCCC)CCCCCCCC)S6)C9=NN(CCCCCC)N=C59)=C%10)=C%10[Si]4(CCCCCCCC)CCCCCCCC)S3)=C1,P,,,0.9,13.78,58,7.19,"Patil Y, Misra R, Keshtov ML, Sharma GD. Small molecule carbazole-based diketopyrrolopyrroles with tetracyanobutadiene acceptor unit as a non-fullerene acceptor for bulk heterojunction organic solar cells. Journal of Materials Chemistry A 5, 3311-3319 (2017)."
691,[H]C1=C(C(N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C2=O)=O)C2=C(C3=C4C(C(N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C4=O)=O)=C(C5=CC=C(C6=CC=C(C7=CC=C([H])S7)C8=NSN=C68)S5)S3)S1,P1,,,1.02,9.48,66.83,6.46,"Qiao X, Wu Q, Wu H, Zhang J, Li H. Bithienopyrroledione-Based Copolymers, Versatile Semiconductors for Balanced Ambipolar Thin-Film Transistors and Organic Solar Cells withVoc> 1 V. Advanced Functional Materials 27, 1604286 (2017)."
692,[H]C1=C(C(N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C2=O)=O)C2=C(C3=C4C(C(N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C4=O)=O)=C(C5=CC=C(C6=C(F)C(F)=C(C7=CC=C([H])S7)C8=NSN=C68)S5)S3)S1,P2,,,0.96,2.55,63.6,1.56,"Qiao X, Wu Q, Wu H, Zhang J, Li H. Bithienopyrroledione-Based Copolymers, Versatile Semiconductors for Balanced Ambipolar Thin-Film Transistors and Organic Solar Cells withVoc> 1 V. Advanced Functional Materials 27, 1604286 (2017)."
693,CC(C(C1=CC=C(/C=C2SC(SCCCCCC)=C(SCCCCCC)S/2)O1)=C3C)=C4N3[B-](F)(F)[N+]5=C(C)C(C6=CC=C(/C=C7SC(SCCCCCC)=C(SCCCCCC)S\7)O6)=C(C)C5=C4C8=CC=C(OC)C=C8,BODIPY-DTF,,,0.768,13.79,66.5,7.2,"Srinivasa Rao R, Bagui A, Hanumantha Rao G, Gupta V, Singh SP. Achieving the highest efficiency using a BODIPY core decorated with dithiafulvalene wings for small molecule based solution-processed organic solar cells. Chem Commun (Camb) 53, 6953-6956 (2017)."
694,OC1=C(C2=C([O-])/C(C2=O)=C\C3=[N+](CCCCCC)C(C=CC(C4=CC(SC5=C6C(C7=CC=C(CCCCCC)C=C7)(C8=CC=C(CCCCCC)C=C8)C9=C5C=C(C(C%10=CC=C(CCCCCC)C=C%10)(C%11=CC=C(CCCCCC)C=C%11)C%12=C%13SC%14=C%12SC(C%15=CC=C([N+](CCCCCC)=C(/C=C%16C([O-])=C(C%17=C(O)C=C(N%18C(CCC%19)C%19C%20=C%18C=CC(C#N)=C%20)C=C%17O)C\%16=O)C%21(C)C)C%21=C%15)=C%14)C%13=C9)=C6S4)=C%22)=C%22C3(C)C)C(O)=CC(N%23C%24C(CCC%24)C%25=C%23C=CC([N+]#[C-])=C%25)=C1,D-IDTT-SQ,,,0.93,14.03,54,7.05,"Yang D, Sasabe H, Sano T, Kido J. Low-Band-Gap Small Molecule for Efficient Organic Solar Cells with a Low Energy Loss below 0.6 eV and a High Open-Circuit Voltage of over 0.9 V. ACS Energy Letters 2, 2021-2025 (2017)."
695,O=C1N(CC(CC)CCCC)C(C2=C(C3=CC(OCCCCCCC)=C(C4=C(CCCCCCCC)C=C([H])S4)S3)C5=NSN=C5C([H])=C21)=O,P1,,,0.69,11.11,54.15,4.15,"Yu J, et al. 2,1,3-Benzothiadiazole-5,6-dicarboxylicimide-Based Polymer Semiconductors for Organic Thin-Film Transistors and Polymer Solar Cells. ACS Appl Mater Interfaces 9, 42167-42178 (2017)."
696,O=C1N(CC(CC)CCCC)C(C2=C(C3=CC(OCCCCCCCC)=C(C4=C(OCCCCCCCC)C=C([H])S4)S3)C5=NSN=C5C([H])=C21)=O,P2,,,0.5,7.69,55.17,2.1,"Yu J, et al. 2,1,3-Benzothiadiazole-5,6-dicarboxylicimide-Based Polymer Semiconductors for Organic Thin-Film Transistors and Polymer Solar Cells. ACS Appl Mater Interfaces 9, 42167-42178 (2017)."
697,O=C1N(CC(CC)CCCC)C(C2=C(C3=NC(OCCCCCCCC)=C(C4=C(OCCCCCCCC)N=C([H])S4)S3)C5=NSN=C5C([H])=C21)=O,P3,,,0.52,0.5,44.48,0.12,"Yu J, et al. 2,1,3-Benzothiadiazole-5,6-dicarboxylicimide-Based Polymer Semiconductors for Organic Thin-Film Transistors and Polymer Solar Cells. ACS Appl Mater Interfaces 9, 42167-42178 (2017)."
698,FC(C(F)=C(C1=CC=C([H])S1)C2=NN(CC(CCCCCC)CCCCCCCC)N=C23)=C3C4=CC=C(S4)C5=CC6=C(C7=CC=C(CC(CC)CCCC)S7)C8=C(C=C([H])S8)C(C9=CC=C(CC(CC)CCCC)S9)=C6S5,J52,,,0.847,19.7,66.8,11.1,"Yu R, et al. Two Well-Miscible Acceptors Work as One for Efficient Fullerene-Free Organic Solar Cells. Adv Mater 29,  (2017)."
699,[H]C1=CC=C(S1)C(C2=C3N=C(C4=CC=CC(CCCCCCCCC)=C4)C(C5=CC(CCCCCCCCC)=CC=C5)=N2)=CC=C3C6=CC=C(S6)C7=CC8=C(C9=CC=C(CC(CCCC)CC)S9)C%10=C(C=C([H])S%10)C(C%11=CC=C(CC(CC)CCCC)S%11)=C8S7,PBQ-0F,,,0.69,16.16,59.91,6.68,"Zheng Z, et al. Efficient Charge Transfer and Fine-Tuned Energy Level Alignment in a THF-Processed Fullerene-Free Organic Solar Cell with 11.3% Efficiency. Adv Mater 29,  (2017)."
700,[H]C1=CC=C(S1)C(C2=C3N=C(C4=CC=CC(CCCCCCCCC)=C4)C(C5=CC(CCCCCCCCC)=CC=C5)=N2)=C(F)C(F)=C3C6=CC=C(S6)C7=CC8=C(C9=CC(F)=C(CC(CCCC)CC)S9)C%10=C(C=C([H])S%10)C(C%11=CC(F)=C(CC(CC)CCCC)S%11)=C8S7,PBQ-4F,,,0.95,17.87,66.8,11.34,"Zheng Z, et al. Efficient Charge Transfer and Fine-Tuned Energy Level Alignment in a THF-Processed Fullerene-Free Organic Solar Cell with 11.3% Efficiency. Adv Mater 29,  (2017)."
701,[H]C1=CC=C(S1)C(C2=C3N=C(C4=CC=CC(CCCCCCCCC)=C4)C(C5=CC(CCCCCCCCC)=CC=C5)=N2)=C(F)C(F)=C3C6=CC=C(S6)C7=CC8=C(C9=CC=C(CC(CCCC)CC)S9)C%10=C(C=C([H])S%10)C(C%11=CC=C(CC(CC)CCCC)S%11)=C8S7,PBQ-OF,,,0.83,17.16,8.9,8.9,"Zheng Z, et al. Efficient Charge Transfer and Fine-Tuned Energy Level Alignment in a THF-Processed Fullerene-Free Organic Solar Cell with 11.3% Efficiency. Adv Mater 29,  (2017)."
702,[H]/C=C/C(C(OCCCCCCCC)=C1)=CC(OCCCCCCCC)=C1/C=C/C(C(OCCCCCCCC)=C2)=CC(OCCCCCCCC)=C2C(C3=C4C=CC=C3)=C5C(C=CC=C5)=C4C6=CC(OCCCCCCCC)=C([H])C=C6OCCCCCCCC,AnE-PVstat,,,0.83,7.951,53,3.48,"Alam S, et al. Organic solar cells based on anthracene-containing PPE¨CPPVs and non-fullerene acceptors. Chemical Papers 72, 1769-1778 (2018)."
703,[H]C(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC(C(OCC(CCCC)CCCCCC)=O)=C(C5=CC=C([H])S5)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7,PBDT-2TC,,,0.903,16.87,61.46,9.36,"An Y, et al. Nonhalogen Solvent-Processed Asymmetric Wide-Bandgap Polymers for Nonfullerene Organic Solar Cells with Over 10% Efficiency. Advanced Functional Materials 28, 1706517 (2018)."
704,[H]C(S1)=CC2=C1C(C3=CC=C(SC(CCCC)CC)S3)=C(C=C(C4=CC(C(OCC(CCCC)CCCCCC)=O)=C(C5=CC=C([H])S5)S4)S6)C6=C2C7=CC=C(SC(CCCC)CC)S7,PBDT-S-2TC,,,0.919,17.32,60.05,9.55,"An Y, et al. Nonhalogen Solvent-Processed Asymmetric Wide-Bandgap Polymers for Nonfullerene Organic Solar Cells with Over 10% Efficiency. Advanced Functional Materials 28, 1706517 (2018)."
705,S=C(N(CC)C/1=O)SC1=C\C2=CC(CCCCCCCC)=C(C3=CC=C(C4=C(CCCCCCCC)C=C(C5=CC6=C(C(C7=CC=C([Si](CCC)(CCC)CCC)S7)=C(C=C(C8=CC(CCCCCCCC)=C(C9=CC=C(C%10=C(CCCCCCCC)C=C(/C=C%11SC(N(CC)C/%11=O)=S)S%10)S9)S8)S%12)C%12=C6C%13=CC=C([Si](CCC)(CCC)CCC)S%13)S5)S4)S3)S2,H21,,,0.895,13,65.58,7.62,"Bin H, et al. High-Efficiency All-Small-Molecule Organic Solar Cells Based on an Organic Molecule Donor with Alkylsilyl-Thienyl Conjugated Side Chains. Adv Mater 30, e1706361 (2018)."
706,CCC(CCCC)COC(/C(C#N)=C/C1=CC(CCCCCCCC)=C(C2=CC=C(C3=C(CCCCCCCC)C=C(C4=CC5=C(C(C6=CC=C([Si](CCC)(CCC)CCC)S6)=C(C=C(C7=CC(CCCCCCCC)=C(C8=CC=C(C9=C(CCCCCCCC)C=C(/C=C(C(OC(CCCC)CC)=O)/C#N)S9)S8)S7)S%10)C%10=C5C%11=CC=C([Si](CCC)(CCC)CCC)S%11)S4)S3)S2)S1)=O,H22,,,0.942,15.38,71.15,10.29,"Bin H, et al. High-Efficiency All-Small-Molecule Organic Solar Cells Based on an Organic Molecule Donor with Alkylsilyl-Thienyl Conjugated Side Chains. Adv Mater 30, e1706361 (2018)."
707,FC(C(F)=C([H])C1=NN(CCCCCCCC)N=C12)=C2C3=CC(C=C(C(C=C(C=C([H])S4)C4=C5)=C5N6C(CCCCCCCC)CCCCCCCC)C6=C7)=C7S3,PBi,,,0.74,3.79,45.5,1.28,"Chung CL, et al. S,N-Heteroacene-Based Copolymers for Highly Efficient Organic Field Effect Transistors and Organic Solar Cells: Critical Impact of Aromatic Subunits in the Ladder pi-System. ACS Appl Mater Interfaces 10, 6471-6483 (2018)."
708,FC(C(F)=C([H])C1=NN(CCCCCCCC)N=C12)=C2C3=CC(S4)=C(C=C3)C5=C4C6=C(N5C(CCCCCCCC)CCCCCCCC)C7=CC=C([H])C=C7S6,PBo,,,0.91,5,43.1,1.96,"Chung CL, et al. S,N-Heteroacene-Based Copolymers for Highly Efficient Organic Field Effect Transistors and Organic Solar Cells: Critical Impact of Aromatic Subunits in the Ladder pi-System. ACS Appl Mater Interfaces 10, 6471-6483 (2018)."
709,FC(C(F)=C([H])C1=NN(CCCCCCCC)N=C12)=C2C3=CC(SC4=C5N(C(CCCCCCCC)CCCCCCCC)C6=C4SC7=C6SC([H])=C7)=C5S3,PT,,,0.63,14.28,67.1,6.04,"Chung CL, et al. S,N-Heteroacene-Based Copolymers for Highly Efficient Organic Field Effect Transistors and Organic Solar Cells: Critical Impact of Aromatic Subunits in the Ladder pi-System. ACS Appl Mater Interfaces 10, 6471-6483 (2018)."
710,O=C1N(CC(CCCC)CC)C(C2=CC=C(C#C/C(C3=CC=C(/C(C4=CC=C(OCCCCCCCC)C=C4)=C5N=C6C=C\5)N3[Zn]N7/C(C=C/C7=C6\C#CC8=CC=C(C(N(CC(CC)CCCC)C9=O)=C%10C9=C(C%11=CC=CS%11)N(CC(CCCC)CC)C%10=O)S8)=C%12/C%13=CC=C(OCCCCCCCC)C=C%13)=C%14C=CC%12=N\%14)S2)=C%15C1=C(C%16=CC=CS%16)N(CC(CC)CCCC)C%15=O,1,,,0.71,15.46,56,6.13,"Hadmojo WT, et al. Near-Infrared Harvesting Fullerene-Free All-Small-Molecule Organic Solar Cells Based on Porphyrin Donors. ACS Sustainable Chemistry & Engineering 6, 5306-5313 (2018)."
711,O=C1N(CC(CCCC)CC)C(C2=CC=C(C#C/C(C3=CC=C(/C(C4=CC=C(OCC(CCCC)CC)C=C4)=C5N=C6C=C\5)N3[Zn]N7/C(C=C/C7=C6\C#CC8=CC=C(C(N(CC(CC)CCCC)C9=O)=C%10C9=C(C%11=CC=CS%11)N(CC(CCCC)CC)C%10=O)S8)=C%12/C%13=CC=C(OCC(CC)CCCC)C=C%13)=C%14C=CC%12=N\%14)S2)=C%15C1=C(C%16=CC=CS%16)N(CC(CC)CCCC)C%15=O,2,,,0.71,14.03,53,5.21,"Hadmojo WT, et al. Near-Infrared Harvesting Fullerene-Free All-Small-Molecule Organic Solar Cells Based on Porphyrin Donors. ACS Sustainable Chemistry & Engineering 6, 5306-5313 (2018)."
712,O=C1N(CC(CCCC)CC)C(C2=CC=C(C#C/C(C3=CC=C(/C(C4=CC=C(CC(CCCC)CC)S4)=C5N=C6C=C\5)N3[Zn]N7/C(C=C/C7=C6\C#CC8=CC=C(C(N(CC(CC)CCCC)C9=O)=C%10C9=C(C%11=CC=CS%11)N(CC(CCCC)CC)C%10=O)S8)=C%12/C%13=CC=C(CC(CCCC)CC)S%13)=C%14C=CC%12=N\%14)S2)=C%15C1=C(C%16=CC=CS%16)N(CC(CC)CCCC)C%15=O,3,,,0.71,11.46,51,4.08,"Hadmojo WT, et al. Near-Infrared Harvesting Fullerene-Free All-Small-Molecule Organic Solar Cells Based on Porphyrin Donors. ACS Sustainable Chemistry & Engineering 6, 5306-5313 (2018)."
713,CCC(CCCC)CC1=CC=C(S1)/C(C2=N/C(C=C2)=C3/C#CC4=CC=C(C(N(CC(CCCC)CC)C5=O)=C6C5=C(C7=CC=CS7)N(CC(CCCC)CC)C6=O)S4)=C(C=C/8)/N9C8=C(C#C/C(C%10=CC=C%11N%10[Zn]N%12/C(C=C/C%12=C%13\C%14=CC=C(CC(CCCC)CC)S%14)=C(C#CC%15=CC=C(C%16=C%17C(C(N%16CC(CCCC)CC)=O)=C(C%18=CC=CS%18)N(CC(CC)CCCC)C%17=O)S%15)\C(C=C/%19)=NC%19=C%11\C%20=CC=C(CC(CCCC)CC)S%20)=C%21N=C%13C=C/%21)/C(C=C/%22)=NC%22=C(C%23=CC=C(CC(CCCC)CC)S%23)/C%24=CC=C3N%24[Zn]9,ZnP2-DPP,,,0.65,19.65,66.15,8.45,"Lai T, et al. Dimeric Porphyrin Small Molecules for Efficient Organic Solar Cells with High Photoelectron Response in the Near-Infrared Region. ACS Appl Mater Interfaces 10, 668-675 (2018)."
714,FC1=C(CC(CCCC)CC)SC(C2=C(C=C(C3=CC=C(C4=C5C(C(C6=C(CC(CC)CCCC)SC(CC(CCCC)CC)=C6C5=O)=O)=C(C7=CC=C([H])S7)S4)S3)S8)C8=C(C9=CC(F)=C(CC(CCCC)CC)S9)C%10=C2SC([H])=C%10)=C1,PM6,,,0.78,22.92,75,13.32,"Wang J-L, Liu K-K, Hong L, Ge G-Y, Zhang C, Hou J. Selenopheno[3,2-b]thiophene-Based Narrow-Bandgap Nonfullerene Acceptor Enabling 13.3% Efficiency for Organic Solar Cells with Thickness-Insensitive Feature. ACS Energy Letters 3, 2967-2976 (2018)."
715,[H]C1=CC(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C2=C(C#C[Si](C(C)C)(C(C)C)C(C)C)C=C(C3=CC=C(C4=C5C(C(C6=C(CC(CC)CCCC)SC(CC(CC)CCCC)=C6C5=O)=O)=C(C7=CC=C([H])S7)S4)S3)S2)S1,PT4Si-BDD,,,1.009,8.98,53.8,4.88,"Wang L, et al. Incorporating Trialkylsilylethynyl-Substituted Head-to-Head Bithiophene Unit into Copolymers for Efficient Non-Fullerene Organic Solar Cells. ACS Appl Mater Interfaces 10, 7271-7280 (2018)."
716,[H]C1=CC(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C2=C(C#C[Si](C(C)C)(C(C)C)C(C)C)C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C([H])S5)C6=NN(CC(CCCCCCCC)CCCCCC)N=C64)S3)S2)S1,PT4Si-FTAZ,,,0.922,11.2,65.9,6.79,"Wang L, et al. Incorporating Trialkylsilylethynyl-Substituted Head-to-Head Bithiophene Unit into Copolymers for Efficient Non-Fullerene Organic Solar Cells. ACS Appl Mater Interfaces 10, 7271-7280 (2018)."
717,[H]C(S1)=CC2=C1C(C3=CC=C(SCC(CCCCCC)CCCC)S3)=C(C=C(C4=C(CCCCCCCC)C=C(C5=NN=C(C6=CC(CCCCCCCC)=C([H])S6)S5)S4)S7)C7=C2C8=CC=C(SCC(CCCCCC)CCCC)S8,PBDTS-TDZ,,,1.1,17.78,65.4,12.8,"Xu X, Yu T, Bi Z, Ma W, Li Y, Peng Q. Realizing Over 13% Efficiency in Green-Solvent-Processed Nonfullerene Organic Solar Cells Enabled by 1,3,4-Thiadiazole-Based Wide-Bandgap Copolymers. Adv Mater 30,  (2018)."
718,[H]C(S1)=CC2=C1C(C3=CC=C(CC(CCCCCC)CCCC)S3)=C(C=C(C4=C(CCCCCCCC)C=C(C5=NN=C(C6=CC(CCCCCCCC)=C([H])S6)S5)S4)S7)C7=C2C8=CC=C(CC(CCCCCC)CCCC)S8,PBDT-TDZ,,,1.01,17.15,67.7,11.72,"Xu X, Yu T, Bi Z, Ma W, Li Y, Peng Q. Realizing Over 13% Efficiency in Green-Solvent-Processed Nonfullerene Organic Solar Cells Enabled by 1,3,4-Thiadiazole-Based Wide-Bandgap Copolymers. Adv Mater 30,  (2018)."
719,[H]C1=C(F)C(F)=C(C2=CC=C(C3=CC=C(C4=CC=C([H])S4)C=C3)S2)C5=C1N=C(C6=CC=C(OCCCCCCCC)C(OCCCCCCCC)=C6)C(C7=CC(OCCCCCCCC)=C(OCCCCCCCC)C=C7)=N5,P1,,,0.86,8.53,66.22,4.86,"Yang J, et al. Quinoxaline-Based Wide Band Gap Polymers for Efficient Nonfullerene Organic Solar Cells with Large Open-Circuit Voltages. ACS Appl Mater Interfaces 10, 23235-23246 (2018)."
720,[H]C1=C(F)C(F)=C(C2=CC=C(C3=CC=C(C4=CC=C([H])S4)C=C3F)S2)C5=C1N=C(C6=CC=C(OCCCCCCCC)C(OCCCCCCCC)=C6)C(C7=CC(OCCCCCCCC)=C(OCCCCCCCC)C=C7)=N5,P2,,,0.91,13.15,64.84,7.75,"Yang J, et al. Quinoxaline-Based Wide Band Gap Polymers for Efficient Nonfullerene Organic Solar Cells with Large Open-Circuit Voltages. ACS Appl Mater Interfaces 10, 23235-23246 (2018)."
721,[H]C1=C(F)C(F)=C(C2=CC=C(C3=CC(F)=C(C4=CC=C([H])S4)C=C3F)S2)C5=C1N=C(C6=CC=C(OCCCCCCCC)C(OCCCCCCCC)=C6)C(C7=CC(OCCCCCCCC)=C(OCCCCCCCC)C=C7)=N5,P3,,,1,15.99,60.89,9.7,"Yang J, et al. Quinoxaline-Based Wide Band Gap Polymers for Efficient Nonfullerene Organic Solar Cells with Large Open-Circuit Voltages. ACS Appl Mater Interfaces 10, 23235-23246 (2018)."
722,[H]C1=C(F)C(F)=C(C2=CC=C(C3=C(F)C(F)=C(C4=CC=C([H])S4)C(F)=C3F)S2)C5=C1N=C(C6=CC=C(OCCCCCCCC)C(OCCCCCCCC)=C6)C(C7=CC(OCCCCCCCC)=C(OCCCCCCCC)C=C7)=N5,P4,,,1.06,4.82,57.43,2.93,"Yang J, et al. Quinoxaline-Based Wide Band Gap Polymers for Efficient Nonfullerene Organic Solar Cells with Large Open-Circuit Voltages. ACS Appl Mater Interfaces 10, 23235-23246 (2018)."
723,O=C1C(C2=C(C3=CC=C(C#C/C(C4=CC=C5N4[Zn]N6/C(C=C/C6=C7\C8=CC(SC(CCCCCC)=C9)=C9S8)=C(C%10=CC(SC(CCCCCC)=C%11)=C%11S%10)\C(C=C/%12)=NC%12=C5\C%13=CC(SC(CCCCCC)=C%14)=C%14S%13)=C%15N=C7C=C/%15)S3)N1CC(CC)CCCC)=C(C%16=CC=C(C#C/C(C%17=CC=C%18N%17[Zn]N%19/C(C=C/C%19=C%20\C%21=CC(SC(CCCCCC)=C%22)=C%22S%21)=C(C%23=CC(SC(CCCCCC)=C%24)=C%24S%23)\C(C=C/%25)=NC%25=C%18\C%26=CC(SC(CCCCCC)=C%27)=C%27S%26)=C%28N=C%20C=C/%28)S%16)N(CC(CC)CCCC)C2=O,VC4,,,0.91,13.83,64,8.05,"Cuesta V, Singhal R, de la Cruz P, Sharma GD, Langa F. Near-IR Absorbing D-A-D Zn-Porphyrin-Based Small-Molecule Donors for Organic Solar Cells with Low-Voltage Loss. ACS Appl Mater Interfaces 11, 7216-7225 (2019)."
724,O=C1C(C2=C(C3=CC=C(C#C/C(C4=CC=C5N4[Zn]N6/C(C=C/C6=C7\C8=C(OCCCCCCCCCCCC)C=CC=C8OCCCCCCCCCCCC)=C(C9=C(OCCCCCCCCCCCC)C=CC=C9OCCCCCCCCCCCC)\C(C=C/%10)=NC%10=C5\C%11=C(OCCCCCCCCCCCC)C=CC=C%11OCCCCCCCCCCCC)=C%12N=C7C=C/%12)S3)N1CC(CC)CCCC)=C(C%13=CC=C(C#C/C(C%14=CC=C%15N%14[Zn]N%16/C(C=C/C%16=C%17\C%18=C(OCCCCCCCCCCCC)C=CC=C%18OCCCCCCCCCCCC)=C(C%19=C(OCCCCCCCCCCCC)C=CC=C%19OCCCCCCCCCCCC)\C(C=C/%20)=NC%20=C%15\C%21=C(OCCCCCCCCCCCC)C=CC=C%21OCCCCCCCCCCCC)=C%22N=C%17C=C/%22)S%13)N(CC(CC)CCCC)C2=O,VC5,,,0.79,16.98,66.3,8.89,"Cuesta V, Singhal R, de la Cruz P, Sharma GD, Langa F. Near-IR Absorbing D-A-D Zn-Porphyrin-Based Small-Molecule Donors for Organic Solar Cells with Low-Voltage Loss. ACS Appl Mater Interfaces 11, 7216-7225 (2019)."
725,O=C1C2=C(C3=CC=C(C#C/C(C(C=C/4)=NC4=C5\C6=CC=C(CC(CCCCCC)CCCC)S6)=C7C=C/C8=C(C9=CC=C(CC(CCCCCC)CCCC)S9)/C%10=N/C(C=C%10)=C(C#CC%11=C(OCCCCCC)C(/C=C%12SC(N(CC)C\%12=O)=S)=CC(OCCCCCC)=C%11)\C%13=CC=C5N%13[Zn]N\78)S3)N(CC(CCCC)CCCCCC)C(C2=C(C%14=CC=C(C#C/C(C%15=CC=C%16N%15[Zn]N%17/C(C=C/C%17=C%18\C%19=CC=C(CC(CCCCCC)CCCC)S%19)=C(C#CC%20=C(OCCCCCC)C=C(/C=C%21C(N(CC)C(S/%21)=S)=O)C(OCCCCCC)=C%20)\C(C=C/%22)=NC%22=C%16\C%23=CC=C(CC(CCCCCC)CCCC)S%23)=C%24N=C%18C=C/%24)S%14)N1CC(CCCC)CCCCCC)=O.CC,DPP-2TP,,,0.76,15.54,68.7,8,"Piradi V, et al. Panchromatic Ternary Organic Solar Cells with Porphyrin Dimers and Absorption-Complementary Benzodithiophene-based Small Molecules. ACS Appl Mater Interfaces 11, 6283-6291 (2019)."
726,O=C1C2=C(C3=CC=C(C#C/C(C(C=C/4)=NC4=C5\C6=CC=C(SCC(CCCC)CCCCCC)S6)=C7C=C/C8=C(C9=CC=C(SCC(CCCC)CCCCCC)S9)/C%10=N/C(C=C%10)=C(C#CC%11=C(OCCCCCC)C(/C=C%12SC(N(CC)C\%12=O)=S)=CC(OCCCCCC)=C%11)\C%13=CC=C5N%13[Zn]N\78)S3)N(CC(CCCC)CCCCCC)C(C2=C(C%14=CC=C(C#C/C(C%15=CC=C%16N%15[Zn]N%17/C(C=C/C%17=C%18\C%19=CC=C(SCC(CCCC)CCCCCC)S%19)=C(C#CC%20=C(OCCCCCC)C=C(/C=C%21C(N(CC)C(S/%21)=S)=O)C(OCCCCCC)=C%20)\C(C=C/%22)=NC%22=C%16\C%23=CC=C(SCC(CCCC)CCCCCC)S%23)=C%24N=C%18C=C/%24)S%14)N1CC(CCCC)CCCCCC)=O,DPP-2TTP,,,0.82,17.78,76.5,11.01,"Piradi V, et al. Panchromatic Ternary Organic Solar Cells with Porphyrin Dimers and Absorption-Complementary Benzodithiophene-based Small Molecules. ACS Appl Mater Interfaces 11, 6283-6291 (2019)."
727,CCCCC(CC)CC(S1)=CC=C1C2=C3C(SC(C4=C5C(C(F)=C(C(OCC(CC)CCCC)=O)S5)=C([H])S4)=C3)=C(C6=CC=C(CC(CC)CCCC)S6)C7=C2SC([H])=C7,PCE10,,,0.79,17.29,69,9.4,"Yan H, Tang Y, Meng X, Xiao T, Lu G, Ma W. Achieving High Doping Concentration by Dopant Vapor Deposition in Organic Solar Cells. ACS Appl Mater Interfaces 11, 4178-4184 (2019)."
728,[H]C1=CC=C(S1)C2=C(C#N)C(C#N)=C(C3=CC=C(C4=CC5=C(C(C6=CC=C(CC(CC)CCCC)S6)=C(C=C([H])S7)C7=C5C8=CC=C(CC(CC)CCCC)S8)S4)S3)C9=NN(CC(CCCC)CCCCCC)N=C92,P1,,,0.93,5.73,30,1.58,"Casey A, et al. Cyano substituted benzotriazole based polymers for use in organic solar cells. Journal of Materials Chemistry A 5, 6465-6470 (2017)."
729,[H]C1=CC=C(S1)C2=C(C#N)C(C#N)=C(C3=CC=C(C4=CC5=C(C(C6=CC=C(CC(CCCC)CCCCCC)S6)=C(C=C([H])S7)C7=C5C8=CC=C(CC(CCCC)CCCCCC)S8)S4)S3)C9=NN(CC(CCCC)CCCCCC)N=C92,P2,,,0.95,11.25,57,6.12,"Casey A, et al. Cyano substituted benzotriazole based polymers for use in organic solar cells. Journal of Materials Chemistry A 5, 6465-6470 (2017)."
730,[H]C1=CC2=C(S1)C(C3=CC=C(CC(CC)CCCC)S3)=C4C(SC(C5=CC=C(C6=C7C(C(C8=C(CC(CC)CCCC)SC(CC(CC)CCCC)=C8C7=O)=O)=C(C9=CC=C([H])S9)S6)S5)=C4)=C2C%10=CC=C(CC(CC)CCCC)S%10,BDDT,,,0.96,8.78,65,5.8,"Ding G, Tang A, Chen F, Tajima K, Xiao B, Zhou E. Inside-fused perylenediimide dimers with planar structures for high-performance fullerene-free organic solar cells. RSC Advances 7, 13749-13753 (2017)."
731,[H]C1=CC2=C(C3=CC=C(CC(CC)CCCC)S3)C4=C(C=C(C5=CC=C(C6=NN=C(C7=CC=C([H])S7)C8=C6C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C8=O)=O)S5)S4)C(C9=CC=C(CC(CC)CCCC)S9)=C2S1,PDD-BDT,,,0.86,8,66,4.5,"Knall AC, et al. Synthesis of a conjugated pyrrolopyridazinedione-benzodithiophene (PPD-BDT) copolymer and its application in organic and hybrid solar cells. Monatsh Chem 148, 855-862 (2017)."
732,O=C(N1CC(CC)CCCC)C(C2=C1C(S3)=CC=C3C#C/C(C(C=C/4)=NC4=C5\C#CC6=CC=CC=C6)=C7C=C/C8=C(C#CC9=CC=CC=C9)/C%10=N/C(C=C%10)=C(C#CC%11=CC=C(C%12=C%13C(C(N%12CC(CC)CCCC)=O)=C(C%14=CC=CS%14)N(CC(CC)CCCC)C%13=O)S%11)\C%15=CC=C5N%15[Mg]N\78)=C(C%16=CC=CS%16)N(CC(CC)CCCC)C2=O,2a,,,0.74,13.27,49,4.85,"Ogumi K, Nakagawa T, Okada H, Sakai R, Wang H, Matsuo Y. Substituent effects in magnesium tetraethynylporphyrin with two diketopyrrolopyrrole units for bulk heterojunction organic solar cells. Journal of Materials Chemistry A 5, 23067-23077 (2017)."
733,O=C(N1CC(CC)CCCC)C(C2=C1C(S3)=CC=C3C#C/C(C(C=C/4)=NC4=C5\C#CC6=CC=C(CCCCCC)C=C6)=C7C=C/C8=C(C#CC9=CC=C(CCCCCC)C=C9)/C%10=N/C(C=C%10)=C(C#CC%11=CC=C(C%12=C%13C(C(N%12CC(CC)CCCC)=O)=C(C%14=CC=CS%14)N(CC(CC)CCCC)C%13=O)S%11)\C%15=CC=C5N%15[Mg]N\78)=C(C%16=CC=CS%16)N(CC(CC)CCCC)C2=O,2b,,,0.69,14.8,56,5.73,"Ogumi K, Nakagawa T, Okada H, Sakai R, Wang H, Matsuo Y. Substituent effects in magnesium tetraethynylporphyrin with two diketopyrrolopyrrole units for bulk heterojunction organic solar cells. Journal of Materials Chemistry A 5, 23067-23077 (2017)."
734,O=C(N1CC(CC)CCCC)C(C2=C1C(S3)=CC=C3C#C/C(C(C=C/4)=NC4=C5\C#CC6=CC=C(C(F)(F)F)C=C6)=C7C=C/C8=C(C#CC9=CC=C(C(F)(F)F)C=C9)/C%10=N/C(C=C%10)=C(C#CC%11=CC=C(C%12=C%13C(C(N%12CC(CC)CCCC)=O)=C(C%14=CC=CS%14)N(CC(CC)CCCC)C%13=O)S%11)\C%15=CC=C5N%15[Mg]N\78)=C(C%16=CC=CS%16)N(CC(CC)CCCC)C2=O,2c,,,0.79,4.61,45,1.65,"Ogumi K, Nakagawa T, Okada H, Sakai R, Wang H, Matsuo Y. Substituent effects in magnesium tetraethynylporphyrin with two diketopyrrolopyrrole units for bulk heterojunction organic solar cells. Journal of Materials Chemistry A 5, 23067-23077 (2017)."
735,O=C(N1CC(CC)CCCC)C(C2=C1C(S3)=CC=C3C#C/C(C(C=C/4)=NC4=C5\C#CC6=CC=C(N(C)C)C=C6)=C7C=C/C8=C(C#CC9=CC=C(N(C)C)C=C9)/C%10=N/C(C=C%10)=C(C#CC%11=CC=C(C%12=C%13C(C(N%12CC(CC)CCCC)=O)=C(C%14=CC=CS%14)N(CC(CC)CCCC)C%13=O)S%11)\C%15=CC=C5N%15[Mg]N\78)=C(C%16=CC=CS%16)N(CC(CC)CCCC)C2=O,2d,,,0.53,12.63,46,3.06,"Ogumi K, Nakagawa T, Okada H, Sakai R, Wang H, Matsuo Y. Substituent effects in magnesium tetraethynylporphyrin with two diketopyrrolopyrrole units for bulk heterojunction organic solar cells. Journal of Materials Chemistry A 5, 23067-23077 (2017)."
736,O=C(C1=C(C2=CC=C([H])S2)SC(C3=CC=C(C4=CC=C(C5=C6C(C(N5CC(CCCCCC)CCCCCCCC)=O)=C(C7=CC=C([H])S7)N(CC(CCCCCC)CCCCCCCC)C6=O)S4)S3)=C18)C9=C(CC(CC)CCCC)SC(CC(CC)CCCC)=C9C8=O,P266,,,0.72,18.11,70.4,9.18,"Zhang H, et al. Low band-gap conjugated polymer based on diketopyrrolopyrrole units and its application in organic photovoltaic cells. Journal of Materials Chemistry A 5, 10416-10423 (2017)."
737,CCCCC(CC)CC1=CC=C(S1)C2=C3C(SC(C4=C5C(C(F)=C(C(OCC(CC)CCCC)=O)S5)=C(C6=CC7=C(S6)C(C8=CC=C(CC(CC)CCCC)S8)=C9C(SC(C%10=C%11C(C(F)=C(C(OCC(CC)CCCC)=O)S%11)=C([H])S%10)=C9)=C7C%12=CC=C(CC(CC)CCCC)S%12)S4)=C3)=C(C%13=CC=C(CC(CC)CCCC)S%13)C%14=C2SC([H])=C%14,P1,,,0.83,13.17,60,6.72,"Zhong H, et al. A regioregular conjugated polymer for high performance thick-film organic solar cells without processing additive. Journal of Materials Chemistry A 5, 10517-10525 (2017)."
738,CCCCC(CC)CC1=CC=C(S1)C2=C3C(SC(C4=C5C(SC(C(OCC(CC)CCCC)=O)=C5F)=C(C6=CC7=C(S6)C(C8=CC=C(CC(CC)CCCC)S8)=C9C(SC(C%10=C%11C(C(F)=C(C(OCC(CC)CCCC)=O)S%11)=C([H])S%10)=C9)=C7C%12=CC=C(CC(CC)CCCC)S%12)S4)=C3)=C(C%13=CC=C(CC(CC)CCCC)S%13)C%14=C2SC([H])=C%14,P2,,,0.85,17,65,9.66,"Zhong H, et al. A regioregular conjugated polymer for high performance thick-film organic solar cells without processing additive. Journal of Materials Chemistry A 5, 10517-10525 (2017)."
739,[H]C1=CC2=C(S1)C(C3=CC=C(CC(CC)CCCC)S3)=C4C(SC(C5=C6C(C(F)=C(C(OCC(CC)CCCC)=O)S6)=C([H])S5)=C4)=C2C7=CC=C(CC(CC)CCCC)S7,P3,,,0.82,16.06,66,9.03,"Zhong H, et al. A regioregular conjugated polymer for high performance thick-film organic solar cells without processing additive. Journal of Materials Chemistry A 5, 10517-10525 (2017)."
740,O=C1C2=C(C=CC=C2)C(/C1=C/C(S3)=CC4=C3C(CCCCCC)=C(S4)C(S5)=CC6=C5C(SC(C7=C(CCCCCC)C(SC(/C=C8C(C(C=CC=C9)=C9C\8=O)=O)=C%10)=C%10S7)=C%11)=C%11[Si]6(CCCCCCCC)CCCCCCCC)=O,DINTTDTS,,,0.79,8.98,39.5,2.79,"Chen X, et al. Dithienosilole-based small molecule donors for efficient all-small-molecule organic solar cells. Dyes and Pigments 158, 445-450 (2018)."
741,CC1(C)C(C=C2C([O-])=C(C3=C(O)C=C(N4CCC5=C4C=CC=C5)C=C3O)C2=O)=[N+](CCCC)C6=C1C7=C(C=C6)C=CC=C7,ASQ-5,,,0.81,11.03,48,4.29,"Chen Y, et al. Synthesis of 3H-Benzo[e]indoline and Its Application to Small-Molecule Organic Solar Cells. Chemistry 24, 8747-8750 (2018)."
742,CC1(C)C(C=C2C([O-])=C(C3=C(O)C=C(N4CCC5=C4C=CC6=C5C=CC=C6)C=C3O)C2=O)=[N+](CCCC)C7=C1C8=C(C=C7)C=CC=C8,USQ-BI,,,0.73,15.64,47,5.35,"Chen Y, et al. Synthesis of 3H-Benzo[e]indoline and Its Application to Small-Molecule Organic Solar Cells. Chemistry 24, 8747-8750 (2018)."
743,[H]C1=CC2=C(C(C3=CC=C(CC(CC)CCCC)[Se]3)=C(C=C(C4=C(CCCCCCCC)C5=C(C=C(C6=C(F)C(F)=C(C7=CC(SC([H])=C8CCCCCCCC)=C8S7)C(C(N9CC(CCCC)CCCCCC)=O)=C6C9=O)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)[Se]%11)S1,PBDT-TTffIDD,,,1.02,6.95,57.8,4.1,"Hwang H, Ko H, Park S, Suranagi SR, Sin DH, Cho K. Fluorine-functionalization of an isoindoline-1,3-dione-based conjugated polymer for organic solar cells. Organic Electronics 59, 247-252 (2018)."
744,[H]C1=CC2=C(C(C3=CC=C(CC(CC)CCCC)[Se]3)=C(C=C(C4=C(CCCCCCCC)C5=C(C=C(C6=CC=C(C7=CC(SC([H])=C8CCCCCCCC)=C8S7)C(C(N9CC(CCCC)CCCCCC)=O)=C6C9=O)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)[Se]%11)S1,PBDT-TTIDD,,,0.92,7.02,58.7,3.8,"Hwang H, Ko H, Park S, Suranagi SR, Sin DH, Cho K. Fluorine-functionalization of an isoindoline-1,3-dione-based conjugated polymer for organic solar cells. Organic Electronics 59, 247-252 (2018)."
745,[H]C1=CC(C(C2=CC(F)=C(SCC(CC)CCCC)S2)=C(SC(C3=CC=C(C4=C5C(C(C6=C(CC(CC)CCCC)SC(CC(CC)CCCC)=C6C5=O)=O)=C(C7=CC=C([H])S7)S4)S3)=C8)C8=C9C%10=CC(F)=C(SCC(CC)CCCC)S%10)=C9S1,PBDB-T-SF,,,0.851,22.35,74.3,14.1,"Kan B, et al. A chlorinated low-bandgap small-molecule acceptor for organic solar cells with 14.1% efficiency and low energy loss. Science China Chemistry 61, 1307-1313 (2018)."
746,[H]C(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CCCCCC)C=C3)=C(C=C(C4=CC=C(C5=C6C(C(C7=C(CC(CC)CCCC)SC(CC(CC)CCCC)=C7C6=O)=O)=C(C8=CC=C([H])S8)S5)S4)S9)C9=C2C%10=CC=C(CC(CCCC)CCCCCC)C=C%10,PBT1-C,,,0.94,17,78,12.5,"Liu T, et al. Optimized Fibril Network Morphology by Precise Side-Chain Engineering to Achieve High-Performance Bulk-Heterojunction Organic Solar Cells. Adv Mater 30, e1707353 (2018)."
747,[H]C(S1)=CC2=C1C(C3=CC=C(OCC(CCCC)CCCCCC)C=C3)=C(C=C(C4=CC=C(C5=C6C(C(C7=C(CC(CC)CCCC)SC(CC(CC)CCCC)=C7C6=O)=O)=C(C8=CC=C([H])S8)S5)S4)S9)C9=C2C%10=CC=C(OCC(CCCC)CCCCCC)C=C%10,PBT1-O,,,0.91,12.6,64,7.3,"Liu T, et al. Optimized Fibril Network Morphology by Precise Side-Chain Engineering to Achieve High-Performance Bulk-Heterojunction Organic Solar Cells. Adv Mater 30, e1707353 (2018)."
748,[H]C(S1)=CC2=C1C(C3=CC=C(SCC(CCCC)CCCCCC)C=C3)=C(C=C(C4=CC=C(C5=C6C(C(C7=C(CC(CC)CCCC)SC(CC(CC)CCCC)=C7C6=O)=O)=C(C8=CC=C([H])S8)S5)S4)S9)C9=C2C%10=CC=C(SCC(CCCC)CCCCCC)C=C%10,PBT1-S,,,0.94,15.2,66.7,9.5,"Liu T, et al. Optimized Fibril Network Morphology by Precise Side-Chain Engineering to Achieve High-Performance Bulk-Heterojunction Organic Solar Cells. Adv Mater 30, e1707353 (2018)."
749,[H]C1=CC=C(C2=CC=C(C(N(CCCCCCCCCCCCCCCCCC)C3=O)=C4C3=C(C5=CC=C([H])O5)N(CCCCCCCCCCCCCCCCCC)C4=O)O2)[Se]1,FDPPSe,,,0.64,16,60.4,6.16,"Oklem G, Song X, Toppare L, Baran D, Gunbas G. A new NIR absorbing DPP-based polymer for thick organic solar cells. Journal of Materials Chemistry C 6, 2957-2961 (2018)."
750,CCCCCCCCCCCCC(S1)=CC=C1C2=C3C(C=C(C4=C(CCCCCCCC)C=C(C5=CC=C(C6=CC(CCCCCCCC)=C([H])S6)C7=NSN=C75)S4)S3)=C(C8=CC=C(CCCCCCCCCCCC)S8)C9=C2C=C([H])S9,PT-BT,,,0.79,7.7,45,2.7,"Sun J, Jin F, Zhao H, Yuan J, Ma W. Enhanced Charge Transfer, Transport and Photovoltaic Efficiency in All-Polymer Organic Solar Cells by Polymer Backbone Fluorination. Chinese Journal of Chemistry 36, 280-286 (2018)."
751,CCCCCCCCCCCCC(S1)=CC=C1C2=C3C(C=C(C4=C(CCCCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CCCCCCCC)=C([H])S6)C7=NSN=C75)S4)S3)=C(C8=CC=C(CCCCCCCCCCCC)S8)C9=C2C=C([H])S9,PT-BT2F,,,0.79,8.6,50,3.4,"Sun J, Jin F, Zhao H, Yuan J, Ma W. Enhanced Charge Transfer, Transport and Photovoltaic Efficiency in All-Polymer Organic Solar Cells by Polymer Backbone Fluorination. Chinese Journal of Chemistry 36, 280-286 (2018)."
752,[H]C(S1)=CC2=C1C(C3=CC=C(C4=CC=C(CC(CCCCCCCC)CCCCCCCCCC)S4)S3)=C(C=C(C5=C(CCCCCCCCCCCC)C=C(C6=C(Cl)C=C(C7=CC(CCCCCCCCCCCC)=C([H])S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC=C(C%11=CC=C(CC(CCCCCCCC)CCCCCCCCCC)S%11)S%10,PBBCl1-T2,,,0.87,8.44,49.49,3.64,"Yang Z, et al. The integrated adjustment of chlorine substitution and two-dimensional side chain of low band gap polymers in organic solar cells. Polymer Chemistry 9, 940-947 (2018)."
753,[H]C(S1)=CC2=C1C(C3=CC=C(C4=CC=C(C5=CC=C(CC(CCCCCCCC)CCCCCCCCCC)S5)S4)S3)=C(C=C(C6=C(CCCCCCCCCCCC)C=C(C7=C(Cl)C=C(C8=CC(CCCCCCCCCCCC)=C([H])S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC=C(C%12=CC=C(C%13=CC=C(CC(CCCCCCC)CCCCCCCCCC)S%13)S%12)S%11,PBBCl1-T3,,,0.73,13.75,68.59,6.87,"Yang Z, et al. The integrated adjustment of chlorine substitution and two-dimensional side chain of low band gap polymers in organic solar cells. Polymer Chemistry 9, 940-947 (2018)."
754,[H]C(S1)=CC2=C1C(C3=CC=C(C4=CC=C(C5=CC=C(CC(CCCCCCCC)CCCCCCCCCC)S5)S4)S3)=C(C=C(C6=C(CCCCCCCCCCCC)C=C(C7=C(Cl)C(Cl)=C(C8=CC(CCCCCCCCCCCC)=C([H])S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC=C(C%12=CC=C(C%13=CC=C(CC(CCCCCCC)CCCCCCCCCC)S%13)S%12)S%11,PBBCl2-T3,,,0.84,9.9,63.94,5.33,"Yang Z, et al. The integrated adjustment of chlorine substitution and two-dimensional side chain of low band gap polymers in organic solar cells. Polymer Chemistry 9, 940-947 (2018)."
755,[H]C(S1)=CC2=C1C(C3=CC=C(C4=CC=C(CC(CCCCCCCC)CCCCCCCCCC)S4)S3)=C(C=C(C5=C(CCCCCCCCCCCC)C=C(C6=C(F)C=C(C7=CC(CCCCCCCCCCCC)=C([H])S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC=C(C%11=CC=C(CC(CCCCCCCC)CCCCCCCCCC)S%11)S%10,PBBF1-T2,,,0.81,9.48,45.37,3.49,"Yang Z, et al. The integrated adjustment of chlorine substitution and two-dimensional side chain of low band gap polymers in organic solar cells. Polymer Chemistry 9, 940-947 (2018)."
756,[H]C(S1)=CC2=C1C(C3=CC=C(C4=CC=C(C5=CC=C(CC(CCCCCCCC)CCCCCCCCCC)S5)S4)S3)=C(C=C(C6=C(CCCCCCCCCCCC)C=C(C7=C(F)C=C(C8=CC(CCCCCCCCCCCC)=C([H])S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC=C(C%12=CC=C(C%13=CC=C(CC(CCCCCCC)CCCCCCCCCC)S%13)S%12)S%11,PBBF1-T3,,,0.73,12.74,66.94,6.21,"Yang Z, et al. The integrated adjustment of chlorine substitution and two-dimensional side chain of low band gap polymers in organic solar cells. Polymer Chemistry 9, 940-947 (2018)."
757,[H]C1=CC=C(/C(C(N2CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C3C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C4=C\3C=CC(C5=CC(F)=C(C6=C(F)C=C([H])S6)S5)=C4)=O)C2=C1,PiI2fT,,,1.06,12.58,66,8.8,"Jung EH, Ahn H, Jo WH, Jo JW, Jung JW. Isoindigo-based conjugated polymer for high-performance organic solar cell with a high VOC of 1.06?V as processed from non-halogenated solvent. Dyes and Pigments 161, 113-118 (2019)."
758,[H]C1=CC=C(/C(C(N2CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C3C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C4=C\3C=CC(C5=CC=C(C6=CC=C([H])S6)S5)=C4)=O)C2=C1,PiI2T,,,0.89,9.21,60,4.92,"Jung EH, Ahn H, Jo WH, Jo JW, Jung JW. Isoindigo-based conjugated polymer for high-performance organic solar cell with a high VOC of 1.06?V as processed from non-halogenated solvent. Dyes and Pigments 161, 113-118 (2019)."
759,[H]C1=C(F)C(F)=C(C2=CC=C([H])S2)C3=C1N=C(OCC(CCCCCC)CCCCCCCC)C=N3,PTQ10,,,0.94,15.99,67.96,10.42,"Li S, et al. Highly Efficient Fullerene-Free Organic Solar Cells Operate at Near Zero Highest Occupied Molecular Orbital Offsets. J Am Chem Soc 141, 3073-3082 (2019)."
760,FC1=C(C2=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C3=CC=C([H])S3)S2)C4=NSN=C4C(C5=CC(CCC(CCCCCCCC)CCCCCCCCC)=C(C6=CC=C([H])S6)S5)=C1F,PCE-10,,,0.77,16.15,47.8,6.29,"Zhou Y, et al. Poly(sodium 4-styrenseulfonate)-modified monolayer graphene for anode applications of organic photovoltaic cells. Applied Physics Letters 111, 113302 (2017)."
761,[H]C1=CC2=C(S1)C(C3=CC=C(SCC(CC)CCCC)S3)=C4C(SC(C5=CC(C(OCCCCCCCC)=O)=C(C6=CC=C(C7=C(C(OCCCCCCCC)=O)C=C([H])S7)S6)S5)=C4)=C2C8=CC=C(SCC(CC)CCCC)S8,PB3T,,,0.98,17.2,68,11.5,"Kang Q, Yang B, Xu Y, Xu B, Hou J. Printable MoOx Anode Interlayers for Organic Solar Cells. Adv Mater 30, e1801718 (2018)."
762,[H]C(S1)=CC=C1C2=C(OC(COCCOCCOCCO)COCCOCCOCCO)C=C(C3=CC=C(C4=C(F)C(F)=C([H])C5=NSN=C45)S3)C(OC(COCCOCCOCCO)COCCOCCOCCO)=C2,PPDT2FBT-A,,,0.76,5.08,53,2.05,"Lee C, et al. Efficient and Air-Stable Aqueous-Processed Organic Solar Cells and Transistors: Impact of Water Addition on Processability and Thin-Film Morphologies of Electroactive Materials. Advanced Energy Materials 8, 1802674 (2018)."
763,[H]C1=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(C4=CC=C(C5=CC=C(C6=CC=C([H])S6)S5)S4)S3)C7=NN(CCC)N=C72)S1,PT5T,,,0.813,1.39,32.7,0.37,"Liu J, et al. A Donor Polymer Based on a Difluorinated Pentathiophene Unit Enabling Enhanced Performance for Nonfullerene Organic Solar Cells. Small Methods 2, 1700415 (2018)."
764,[H]C1=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C([H])S6)S5)S4)S3)C7=NN(CCC)N=C72)S1,PT5T-2F,,,0.822,16.64,70.8,9.69,"Liu J, et al. A Donor Polymer Based on a Difluorinated Pentathiophene Unit Enabling Enhanced Performance for Nonfullerene Organic Solar Cells. Small Methods 2, 1700415 (2018)."
765,[H]C(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C(CCCCCCCC)C4=C(C=C(C5=NC(SC(C(S6)=CC7=C6C(CCCCCCCC)=C([H])S7)=N8)=C8S5)S4)S3)S9)C9=C2OCC(CCCCCC)CCCCCCCC,PBDT-ttTZ,,,0.79,10.15,64.8,5.21,"Park J, Park JB, Ha J-W, Park HJ, Kang I-N, Hwang D-H. Efficient organic photovoltaic cells based on thiazolothiazole and benzodithiophene copolymers with ¦Ð-conjugated bridges. Journal of Polymer Science Part A: Polymer Chemistry 56, 1978-1988 (2018)."
766,[H]C(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=NC(SC(C6=CC(CC(CC)CCCC)=C([H])S6)=N7)=C7S5)S4)S8)C8=C2C9=CC=C(CC(CCCC)CCCCCC)S9,PTZ1,,,0.96,17.5,68.8,11.6,"Su W, et al. Significant enhancement of the photovoltaic performance of organic small molecule acceptors via side-chain engineering. Journal of Materials Chemistry A 6, 7988-7996 (2018)."
767,CC(C=C1C)=CC(C)=[C@@]1/[C@](C2=CC=C(/C(C#CC3=C(CCCCCC)C(CCCCCC)=C(/C=C/C4=C(CCCCCC)C(CCCCCC)=C(/C=C5C(N(CC)/C(S/5)=C(C#N)\C#N)=O)S4)S3)=C6N=C7C=C\6)N2[Zn]N8/C(C=C/C8=C7\C9=C(C)C=C(C)C=C9C)=C%10/C#CC%11=C(CCCCCC)C(CCCCCC)=C(/C=C/C%12=C(CCCCCC)C(CCCCCC)=C(/C=C%13C(N(CC)/C(S/%13)=C(C#N)\C#N)=O)S%12)S%11)=C%14C=CC%10=N\%14,MV72,,,0.92,11.25,39,4.03,"Vartanian M, de la Cruz P, Biswas S, Sharma GD, Langa F. Panchromatic ternary organic solar cells with 9.44% efficiency incorporating porphyrin-based donors. Nanoscale 10, 12100-12108 (2018)."
768,FC1=C(C2=CC(CC(CCCCCC)CCCCCCCC)=C(C3=CC(CC(CCCCCC)CCCCCCC)=C([H])S3)S2)C4=NSN=C4C(C5=CC(CC(CCCCCC)CCCCCCCC)=C(C6=CC(CC(CCCCCC)CCCCCCC)=C(C7=CC=C(C8=C(F)C(F)=C(C9=CC=C([H])S9)C%10=NSN=C%108)S7)S6)S5)=C1F,P3TA,,,1.02,10.9,48.8,5.44,"Yang G, et al. Understanding the influence of carboxylate substitution on the property of high-performance donor polymers in non-fullerene organic solar cells. Materials Chemistry Frontiers 2, 1360-1365 (2018)."
769,FC1=C(C2=CC(CC(CCCCCCCC)CCCCCCCCCC)=C([H])S2)C3=NSN=C3C(C4=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C5=CC=C(C6=CC=C([H])S6)S5)S4)=C1F,P4TA,,,0.96,8.6,39.8,3.29,"Yang G, et al. Understanding the influence of carboxylate substitution on the property of high-performance donor polymers in non-fullerene organic solar cells. Materials Chemistry Frontiers 2, 1360-1365 (2018)."
770,FC1=C(C2=CC(C(OCC(CCCCCCCC)CCCCCCCCCC)=O)=C([H])S2)C3=NSN=C3C(C4=CC(C(OCC(CCCCCCCC)CCCCCCCCCC)=O)=C(C5=CC=C(C6=CC=C([H])S6)S5)S4)=C1F,P4TE,,,1.06,9.27,54.1,5.34,"Yang G, et al. Understanding the influence of carboxylate substitution on the property of high-performance donor polymers in non-fullerene organic solar cells. Materials Chemistry Frontiers 2, 1360-1365 (2018)."
771,O=C1N(CCCCCCCCCC)C2=C(SC([H])=C2)C3=C1C=C([H])S3,BFD,,,0.72,7.37,42,2.25,"Zhao Y, et al. Regulating the optoelectronic properties of small molecule donors with multiple alternative electron-donor and acceptor units for organic solar cells. Journal of Materials Chemistry A 6, 8101-8108 (2018)."
772,[H]C1=CC(C(C2=CC=C(CCCCCC)C=C2)(C3=CC=C(CCCCCC)C=C3)C4=C5C=C6C(C(SC([H])=C7)=C7C6(C8=CC=C(CCCCCC)C=C8)C9=CC=C(CCCCCC)C=C9)=C4)=C5S1,IDTFD,,,0.82,13.13,52,5.58,"Zhao Y, et al. Regulating the optoelectronic properties of small molecule donors with multiple alternative electron-donor and acceptor units for organic solar cells. Journal of Materials Chemistry A 6, 8101-8108 (2018)."
773,CCCCCCC(C=C1)=CC=C1C(C2=C3C=C4C(C(SC5=C6SC([H])=C5)=C6C4(C7=CC=C(CCCCCC)C=C7)C8=CC=C(CCCCCC)C=C8)=C2)(C9=CC=C(CCCCCC)C=C9)C%10=C3SC%11=C%10SC([H])=C%11,IDTTFD,,,0.86,14.08,58,7.06,"Zhao Y, et al. Regulating the optoelectronic properties of small molecule donors with multiple alternative electron-donor and acceptor units for organic solar cells. Journal of Materials Chemistry A 6, 8101-8108 (2018)."
774,[H]C1=CC=C([H])S1,TFD,,,0.76,10.96,46,3.81,"Zhao Y, et al. Regulating the optoelectronic properties of small molecule donors with multiple alternative electron-donor and acceptor units for organic solar cells. Journal of Materials Chemistry A 6, 8101-8108 (2018)."
775,[H]C(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=CC=C(C4=C(N=C(C5=CC(OCCCCCCCC)=CC=C5)C(C6=CC=CC(OCCCCCCCC)=C6)=N7)C7=C(C8=CC=C([H])S8)C(F)=C4F)S3)S9)C9=C2OCC(CC)CCCC,BDT-A-TQT,,,0.704,11.3,69,5.5,"Zimmermann D, et al. Synthesis of D-¦Ð"
776,[H]C(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(N=C(C6=CC(OCCCCCCCC)=CC=C6)C(C7=CC=CC(OCCCCCCCC)=C7)=N8)C8=C(C9=CC=C([H])S9)C(F)=C5F)S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11,BDT-B-TQT,,,0.784,12.9,70,7.1,"Zimmermann D, et al. Synthesis of D-¦Ð"
777,[H]C1=C2C(C3=CC=C2)=C4C5=C6C3=CC=CC6=C(C7=CC=C(C8=C(C(N(CCCCCCCC)C9=O)=O)C9=C(C%10=CC=C([H])S%10)S8)S7)C=C5N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C4=C1,PP-TPD,,,0.78,8.71,46,3.12,"Jang W, et al. Interface engineering on phenanthrocarbazole/thienopyrroledione-based conjugated polymer for efficient organic photovoltaic devices with ideal nano-morphology and improved charge carrier dynamics. Dyes and Pigments 145, 29-36 (2017)."
778,O=C1N(CC(CCCCCCCC)CCCCCCCCCC)C(C2=C(C3=CC(CCCCCCCC)=C([H])S3)SC(C4=CC(CCCCCCCC)=C(C5=CC6=C(C(C7=CC=C(CC(CC)CCCC)S7)=C(C=C([H])S8)C8=C6C9=CC=C(CC(CCCC)CCC)S9)S5)S4)=C21)=O,PC8TPD,,,0.9,8.57,55.2,4.26,"Kim J, Lee W-H, Park JB, Hwang D-H, Kang I-N. Synthesis and characterization of the fluorinated thieno[3,4-c]pyrrole-4,6-dione-based donor-acceptor polymers for organic solar cells. Dyes and Pigments 160, 403-409 (2019)."
779,O=C1N(CC(CCCCCCCC)CCCCCCCCCC)C(C2=C(C3=CC(CCCCCCCC)=C([H])S3)SC(C4=C(F)C(CCCCCCCC)=C(C5=CC6=C(C(C7=CC=C(CC(CC)CCCC)S7)=C(C=C([H])S8)C8=C6C9=CC=C(CC(CCCC)CCC)S9)S5)S4)=C21)=O,PC8TPD-F,,,0.95,10.19,70.2,6.8,"Kim J, Lee W-H, Park JB, Hwang D-H, Kang I-N. Synthesis and characterization of the fluorinated thieno[3,4-c]pyrrole-4,6-dione-based donor-acceptor polymers for organic solar cells. Dyes and Pigments 160, 403-409 (2019)."
780,[H]C1=CC=C(C(N(CC(CC)CCCC)C2=O)=C3C2=C(C4=CC=C(C5=CC=C([H])S5)O4)N(CC(CC)CCCC)C3=O)O1,PDPP2FT,,,0.73,7.52,58,3.2,"Cowart JS, et al. Donor-fullerene dyads for energy cascade organic solar cells. Inorganica Chimica Acta 468, 192-202 (2017)."
781,[H]C1=CC(OC(CCCCCCCC)CCCCCCCC)=C2C(N(C(CCCCCCCC)CCCCCCCC)C3=C2C=CC(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C([H])S6)C7=NSN=C75)S4)=C3)=C1,P1,,,0.92,10.9,47,5,"Shibasaki K, Yasuda T, Yamamoto Y, Kijima M. Dual substitution at 4,9-positions of carbazole in donor-¦Ð-acceptor copolymer enhances performance of bulk-heterojunction organic solar cells. Polymer 108, 305-312 (2017)."
782,[H]C1=CC(OCC(CCCCCCCC)CCCCCCCC)=C2C(N(C(CCCCCCCCCC)CCCCCCCCCC)C3=C2C=CC(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C([H])S6)C7=NSN=C75)S4)=C3)=C1,P2,,,0.75,12.33,57,5.46,"Shibasaki K, Yasuda T, Yamamoto Y, Kijima M. Dual substitution at 4,9-positions of carbazole in donor-¦Ð-acceptor copolymer enhances performance of bulk-heterojunction organic solar cells. Polymer 108, 305-312 (2017)."
783,[H]C1=CC(OCCCCCCCC)=C2C(N(C(CCCCCCCCCCCC)CCCCCCCCCCCC)C3=C2C=CC(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C([H])S6)C7=NSN=C75)S4)=C3)=C1,P3,,,0.55,7.16,55,2.26,"Shibasaki K, Yasuda T, Yamamoto Y, Kijima M. Dual substitution at 4,9-positions of carbazole in donor-¦Ð-acceptor copolymer enhances performance of bulk-heterojunction organic solar cells. Polymer 108, 305-312 (2017)."
784,[H]C1=CC=C2C(N(C(CCCCCCCC)CCCCCCCC)C3=C2C=CC(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C([H])S6)C7=NSN=C75)S4)=C3)=C1,PCDT2FBT,,,0.88,6.94,34,2.07,"Shibasaki K, Yasuda T, Yamamoto Y, Kijima M. Dual substitution at 4,9-positions of carbazole in donor-¦Ð-acceptor copolymer enhances performance of bulk-heterojunction organic solar cells. Polymer 108, 305-312 (2017)."
785,[H]C1=CC2=C(S1)C(OCC(CC)CCCC)=C3C(SC(C4=CC=C(C5=CC(C(OCC(CC)CCCC)=C(SC(C6=C7C(C(N(CC(CC)CCCC)C7=O)=O)=C([H])C6)=C8)C8=C9OCC(CC)CCCC)=C9S5)C%10=NN(CC(CCCCCCCC)CCCCCCCCCC)N=C%104)=C3)=C2OCC(CC)CCCC,P1,,,0.84,4.75,64,2.55,"Azeri ?, et al. Efficient benzodithiophene and thienopyrroledione containing random polymers as components for organic solar cells. Polymer 133, 60-67 (2017)."
786,[H]C1=CC2=C(S1)C(OCC(CC)CCCC)=C3C(SC(C4=CC=C(C5=CC(C(OCC(CC)CCCC)=C(SC(C6=C7C(C(N(CC(CC)CCCC)C7=O)=O)=C([H])C6)=C8)C8=C9OCC(CC)CCCC)=C9S5)C%10=NSN=C%104)=C3)=C2OCC(CC)CCCC,P2,,,0.8,14.02,52,5.83,"Azeri ?, et al. Efficient benzodithiophene and thienopyrroledione containing random polymers as components for organic solar cells. Polymer 133, 60-67 (2017)."
787,O=C(C(/C1=C(C#N)/C#N)=C\C2=CC(CC(CCCC)CC)=C(C3=CC4=C(C(SC(C(S5)=C(CC(CCCC)CC)C=C5/C=C(/C6=C(C#N)\C#N)C(C7=C6C=CC=C7)=O)=C8)=C8[Si]4(CCCCCCCC)CCCCCCCC)S3)S2)C9=C1C=CC=C9,DINCNDTS,,,0.857,1.82,37.3,0.58,"Chen X, et al. Impact of end-capped groups on the properties of dithienosilole-based small molecules for solution-processed organic solar cells. Dyes and Pigments 147, 183-189 (2017)."
788,O=C(C1=C(C/2=O)C=CC=C1)C2=C\C3=CC(CC(CCCC)CC)=C(C4=CC5=C(C(SC(C(S6)=C(CC(CCCC)CC)C=C6/C=C(C7=O)\C(C8=C7C=CC=C8)=O)=C9)=C9[Si]5(CCCCCCCC)CCCCCCCC)S4)S3,DINDTS,,,0.799,13.5,61.2,6.6,"Chen X, et al. Impact of end-capped groups on the properties of dithienosilole-based small molecules for solution-processed organic solar cells. Dyes and Pigments 147, 183-189 (2017)."
789,CCCCC(CC)CSC(S1)=CC=C1C2=C3C(SC(C4=CC=C(C5=C6C(C(C7=C(CC(CCCCCC)CCCC)SC(CC(CCCC)CCCCCC)=C7C6=O)=O)=C(C8=CC=C([H])S8)S5)S4)=C3)=C(C9=CC=C(SCC(CC)CCCC)S9)C%10=C2SC([H])=C%10,PBT1-EH,,,0.932,13.35,71,8.664,"Xie D, et al. A new small molecule acceptor based on indaceno[2,1-b:6,5-b¡¯]dithiophene and thiophene-fused ending group for fullerene-free organic solar cells. Dyes and Pigments 148, 263-269 (2018)."
790,O=C(C(C1=CC=C(C2=CC(CCCCCC)=C(C3=C(CCCCCC)C=C([H])S3)S2)S1)=C4C5=C6C=CC=C5)N7C8=C4N6C(C(C9=CC=C(C%10=CC(CCCCCC)=C(C%11=C(CCCCCC)C=C(C%12=CC(N(CC(CCCCCCCCCC)CCCCCCCC)C%13=C%14SC([H])=C%13)=C%14S%12)S%11)S%10)S9)=C8C%15=C7C=CC=C%15)=O,P1,,,0.64,5.37,36,1.24,"Brebels J, et al. Low bandgap polymers based on bay-annulated indigo for organic photovoltaics: Enhanced sustainability in material design and solar cell fabrication. Organic Electronics 50, 264-272 (2017)."
791,O=C(C(C1=CC=C(C2=CC(CCCCCC)=C(C3=C(CCCCCC)C=C([H])S3)S2)S1)=C4C5=C6C=CC=C5)N7C8=C4N6C(C(C9=CC=C(C%10=CC(CCCCCC)=C(C%11=C(CCCCCC)C=C(C%12=CC(N(CC(CCCCCCCC)CCCCCC)C%13=C%14SC([H])=C%13)=C%14S%12)S%11)S%10)S9)=C8C%15=C7C=CC=C%15)=O,P2,,,0.82,6.67,44,2.41,"Brebels J, et al. Low bandgap polymers based on bay-annulated indigo for organic photovoltaics: Enhanced sustainability in material design and solar cell fabrication. Organic Electronics 50, 264-272 (2017)."
792,O=C(C(C1=CC=C(C2=CC(CCCCCC)=C(C3=C(CCCCCC)C=C([H])S3)S2)S1)=C4C5=C6C=CC=C5)N7C8=C4N6C(C(C9=CC=C(C%10=CC(CCCCCC)=C(C%11=C(CCCCCC)C=C(C%12=CC(N(C(C(CCCCCC)CCCC)=O)C%13=C%14SC([H])=C%13)=C%14S%12)S%11)S%10)S9)=C8C%15=C7C=CC=C%15)=O,P3,,,0.8,6.83,41,2.22,"Brebels J, et al. Low bandgap polymers based on bay-annulated indigo for organic photovoltaics: Enhanced sustainability in material design and solar cell fabrication. Organic Electronics 50, 264-272 (2017)."
793,N#CC(C1=NSN=C12)=CC=C2C3=CC4=C(C5=C([Si]4(CCCCCCCC)CCCCCCCC)C=C(C6=CC=C(C#N)C7=NSN=C67)S5)S3,BCNDTS,,,1.01,8.26,47,3.92,"Chen K-W, et al. Fluorination effects of A-D-A-type small molecules on physical property and the performance of organic solar cell. Organic Electronics 52, 342-349 (2018)."
794,CCCCCCC(OC1=C2SC([H])=C1)(CCCCCC)C3=C2C=C(C(CCCCCC)(CCCCCC)OC4=C5SC(C6=C7C(C(N(CCCCCCCC)C7=O)=O)=C([H])S6)=C4)C5=C3,PCO5PD,,,0.88,11.03,66.9,6.48,"Xiao Z, et al. A carbon-oxygen-bridged ladder-type building block for efficient donor and acceptor materials used in organic solar cells. Science Bulletin 62, 1331-1336 (2017)."
795,CCCCCCC(OC1=C2SC([H])=C1)(CCCCCC)C3=C2C=C(C(C4=C5SC(C6=C7C(C(N(CCCCCCCC)C7=O)=O)=C([H])S6)=C4)(CCCCCC)CCCCCC)C5=C3,PIDTTPD,,,0.9,10.12,45.8,4.15,"Xiao Z, et al. A carbon-oxygen-bridged ladder-type building block for efficient donor and acceptor materials used in organic solar cells. Science Bulletin 62, 1331-1336 (2017)."
796,[H]C(S1)=CC2=C1C(C3=CC(CCCCCCCC)=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(N=C(C6=CC(OCCCCCCCC)=CC=C6)C(C7=CC=CC(OCCCCCCCC)=C7)=N8)C8=C(C9=CC=C([H])S9)C=C5F)S4)S%10)C%10=C2C%11=CC(CCCCCCCC)=C(CCCCCCCC)S%11,PBDTTFTQ-DO,,,0.9,10.66,75.55,7.25,"Xiao B, et al. High efficiency organic solar cells based on amorphous electron-donating polymer and modified fullerene acceptor. Nano Energy 39, 478-488 (2017)."
797,CCC(CCCC)CC(S1)=CC=C1C2=C3C(C=C(C4=C5C(C(F)=C(C(OCC(CCCC)CC)=O)S5)=C(C(S6)=CC7=C6C(C8=CC=C(CC(CC)CCC)S8)=C(C=C(C9=C%10C(SC(C(OCC(CCCC)CC)=O)=C%10F)=C([H])S9)S%11)C%11=C7C%12=CC=C(CC(CC)CCCC)S%12)S4)S3)=C(C%13=CC=C(CC(CC)CCC)S%13)C%14=C2C=C([H])S%14,   r-PTB7-Th,,,0.83,17.91,74.1,11.17,"Yu J, et al. Boosting performance of inverted organic solar cells by using a planar coronene based electron-transporting layer. Nano Energy 39, 454-460 (2017)."
798,CCCCC(CC)CC(S1)=CC=C1C2=C3C(C=C(C4=C5C(C(F)=C(C(OCC(CC)CCCC)=O)S5)=C([H])S4)S3)=C(C6=CC=C(CC(CCCC)CC)S6)C7=C2C=C([H])S7,PTB7-Th,,,0.669,27.73,73,13.54,"Gao HH, et al. A New Nonfullerene Acceptor with Near Infrared Absorption for High Performance Ternary-Blend Organic Solar Cells with Efficiency over 13. Adv Sci (Weinh) 5, 1800307 (2018)."
799,CC1=CC(CCCCCCCCCCCCCC)=C(C2=CC3=C(S2)C=C(C4=C(CCCCCCCCCCCCCC)C=C(C)S4)S3)S1,PBTTT-C14,5.1,3.1,0.53,9.37,0.48,2.34,"Parmer, J. E.; Mayer, A. C.; Hardin, B. E.; Scully, S. R.; McGehee, M. D.; Heeney, M.; McCulloch, I. Organic Bulk Heterojunction Solar Cells Using poly(2,5-bis(3-Tetradecyllthiophen-2-ylthieno[3,2,-b] Thiophene. Appl. Phys. Lett. 2008, 92, 113309/1-3. "
800,O=C(C1=C2C(C3=C(C=C(C4=CC=C(C)S4)S5)C5=C26)=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C3=O)=O)C7=C1C=C(C)S7)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C6=O,PNDTI-T,5.8,4,0.56,4.8,0.46,1.23,"Nakano, K.; Nakano, M.; Xiao, B.; Zhou, E.; Suzuki, K.; Osaka, I.; Takimiya, K.; Tajima, K. Naphthodithiophene Diimide-Based Copolymers: Ambipolar Semiconductors in Field-Effect Transistors and Electron Acceptors with Near-Infrared Response in Polymer Blend Solar Cells. Macromolecules 2016, 49, 1752¨C1760. "
801,O=C(C1=C2C(C3=C(C=C(C4=CC5=C(C=C(C)S5)S4)S6)C6=C27)=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C3=O)=O)C8=C1C=C(C)S8)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C7=O,PNDTI-TT,5.7,4.1,0.62,6.4,0.5,2.07,"Nakano, K.; Nakano, M.; Xiao, B.; Zhou, E.; Suzuki, K.; Osaka, I.; Takimiya, K.; Tajima, K. Naphthodithiophene Diimide-Based Copolymers: Ambipolar Semiconductors in Field-Effect Transistors and Electron Acceptors with Near-Infrared Response in Polymer Blend Solar Cells. Macromolecules 2016, 49, 1752¨C1760. "
802,O=C(C1=C2C(C3=C(C=C(C4=CC5=C(C(SC(C)=C6)=C6S5)S4)S7)C7=C28)=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C3=O)=O)C9=C1C=C(C)S9)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C8=O,PNDTI-DTT,5.6,4,0.66,9.6,0.51,3.28,"Nakano, K.; Nakano, M.; Xiao, B.; Zhou, E.; Suzuki, K.; Osaka, I.; Takimiya, K.; Tajima, K. Naphthodithiophene Diimide-Based Copolymers: Ambipolar Semiconductors in Field-Effect Transistors and Electron Acceptors with Near-Infrared Response in Polymer Blend Solar Cells. Macromolecules 2016, 49, 1752¨C1760. "
803,O=C(C1=C2C(C3=C(C=C(C4=CC=C(C5=CC=C(C)S5)S4)S6)C6=C27)=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C3=O)=O)C8=C1C=C(C)S8)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C7=O,PNDTI-BT,5.6,4.1,0.66,8.1,0.49,2.6,"Nakano, K.; Nakano, M.; Xiao, B.; Zhou, E.; Suzuki, K.; Osaka, I.; Takimiya, K.; Tajima, K. Naphthodithiophene Diimide-Based Copolymers: Ambipolar Semiconductors in Field-Effect Transistors and Electron Acceptors with Near-Infrared Response in Polymer Blend Solar Cells. Macromolecules 2016, 49, 1752¨C1760. "
804,CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7,PBDTT-TT,5.3,3.17,0.77,14.99,0.639,7.42,"Cui, C.; Wong, W.-Y.; Li, Y. Improvement of Open-Circuit Voltage and Photovoltaic Properties of 2D-Conjugated Polymers by Alkylthio Substitution. Energy Environ. Sci. 2014, 7, 2276¨C2284. "
805,CC(S1)=CC2=C1C(C3=CC=C(OCC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(OCC(CCCC)CC)S7,PBDTT-O-TT,5.18,3.15,0.73,15.17,0.644,7.1,"Cui, C.; Wong, W.-Y.; Li, Y. Improvement of Open-Circuit Voltage and Photovoltaic Properties of 2D-Conjugated Polymers by Alkylthio Substitution. Energy Environ. Sci. 2014, 7, 2276¨C2284. "
806,CC(S1)=CC2=C1C(C3=CC=C(SCC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7,PBDTT-S-TT,5.41,3.27,0.84,15.32,0.655,8.42,"Cui, C.; Wong, W.-Y.; Li, Y. Improvement of Open-Circuit Voltage and Photovoltaic Properties of 2D-Conjugated Polymers by Alkylthio Substitution. Energy Environ. Sci. 2014, 7, 2276¨C2284. "
807,CC(S1)=CC2=C1C(C3=CC=C(SCCCCCCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCCCCCCCC)S7,PBDT-TS1,5.33,3.52,0.8,17.37,0.661,9.48,"Ye, L.; Zhang, S.; Zhao, W.; Yao, H.; Hou, J. Highly Efficient 2D-Conjugated Benzodithiophene-Based Photovoltaic Polymer with Linear Alkylthio Side Chain. Chem. Mater. 2014, 26, 3603¨C3605. "
808,CC1=CC=C(C2=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C3=CC=C(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC=C(C)S5)S4)C6=NSN=C63)S2)S1,PBTz4T,5.07,3.53,0.74,5.6,0.63,2.6,"Osaka, I.; Shimawaki, M.; Mori, H.; Doi, I.; Miyazaki, E.; Koganezawa, T.; Takimiya, K. Synthesis, Characterization, and Transistor and Solar Cell Applications of a Naphthobisthiadiazole-Based Semiconducting Polymer. J. Am. Chem. Soc. 2012, 134, 3498¨C3507. "
809,CC(S1)=C(CC(CCCCCCCC)CCCCCC)C=C1C2=CC(C3=NSN=C34)=C(C5=NSN=C52)C=C4C6=CC(CC(CCCCCC)CCCCCCCC)=C(S6)C7=CC8=C(C9=CC(CCCCCCCCCCCC)=C(C=C(C)S%10)C%10=C9C=C8CCCCCCCCCCCC)S7,PNNT12HD,5.22,3.54,0.82,15.6,0.64,8.2,"Osaka, I.; Kakara, T.; Takemura, N.; Koganezawa, T.; Takimiya, K. Naphthodithiophene-Naphthobisthiadiazole Copolymers for Solar Cells: Alkylation Drives the Polymer Backbone Flat and Promotes Efficiency. J. Am. Chem. Soc. 2013, 135, 8834¨C8837. "
810,CC(S1)=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C1C2=CC(C3=NSN=C34)=C(C5=NSN=C52)C=C4C6=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(S6)C7=CC8=C(C9=CC(CCCCCCCCCCCC)=C(C=C(C)S%10)C%10=C9C=C8CCCCCCCCCCCC)S7,PNNT12DT,5.22,3.54,0.86,7.3,0.65,4.1,"Osaka, I.; Kakara, T.; Takemura, N.; Koganezawa, T.; Takimiya, K. Naphthodithiophene-Naphthobisthiadiazole Copolymers for Solar Cells: Alkylation Drives the Polymer Backbone Flat and Promotes Efficiency. J. Am. Chem. Soc. 2013, 135, 8834¨C8837. "
811,CC(S1)=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C1C2=CC(C3=NSN=C34)=C(C5=NSN=C52)C=C4C6=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(S6)C7=CC8=C(C9=CC=C(C=C(C)S%10)C%10=C9C=C8)S7,PNNTDT,5.25,3.54,0.83,12.3,0.54,5.5,"Osaka, I.; Kakara, T.; Takemura, N.; Koganezawa, T.; Takimiya, K. Naphthodithiophene-Naphthobisthiadiazole Copolymers for Solar Cells: Alkylation Drives the Polymer Backbone Flat and Promotes Efficiency. J. Am. Chem. Soc. 2013, 135, 8834¨C8837. "
812,CC1=CC2=CC=C(C(C=C3)=C2S1)C4=C3C=C(S4)C5=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C6=CC=C(C7=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C)S7)C8=NSN=C68)S5,PNDT3BTz-DT,5.15,3.45,0.7,8.4,0.64,3.8,"Osaka, I.; Abe, T.; Shimawaki, M.; Koganezawa, T.; Takimiya, K.Naphthodithiophene-Based Donor-Acceptor Polymers: Versatile Semiconductors for OFETs and OPVs. ACS Macro Lett. 2012, 1, 437¨C440. "
813,CC1=CC2=CC=C(C(C=C3)=C2S1)C4=C3C=C(S4)C5=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C6=CC(C7=NSN=C7C(C8=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C)S8)=C9)=C9C%10=NSN=C6%10)S5,PNDT3NTz-DT,5.25,3.65,0.83,11.3,0.52,4.9,"Osaka, I.; Abe, T.; Shimawaki, M.; Koganezawa, T.; Takimiya, K.Naphthodithiophene-Based Donor-Acceptor Polymers: Versatile Semiconductors for OFETs and OPVs. ACS Macro Lett. 2012, 1, 437¨C440. "
814,CC1=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C2=CC(C3=NSN=C3C(C4=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C5=CC(F)=C(C6=C(F)C=C(C)S6)S5)S4)=C7)=C7C8=NSN=C82)S1,PNTz4TF2,5.38,3.53,0.82,19.3,0.67,10.5,"Kawashima, K.; Fukuhara, T.; Suda, Y.; Suzuki, Y.; Koganezawa, T.; Yoshida, H.; Ohkita, H.; Osaka, I.; Takimiya, K. Implication of Fluorine Atom on Electronic Properties, Ordering Structures, and Photovoltaic Performance in Naphthobisthiadiazole-Based Semiconducting Polymers. J. Am. Chem. Soc. 2016, 138, 10265¨C10275. "
815,CC1=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C2=CC(C3=NSN=C3C(C4=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C5=C(F)C(F)=C(C6=C(F)C(F)=C(C)S6)S5)S4)=C7)=C7C8=NSN=C82)S1,PNTz4TF4,5.49,3.56,0.93,10.5,0.66,6.5,"Kawashima, K.; Fukuhara, T.; Suda, Y.; Suzuki, Y.; Koganezawa, T.; Yoshida, H.; Ohkita, H.; Osaka, I.; Takimiya, K. Implication of Fluorine Atom on Electronic Properties, Ordering Structures, and Photovoltaic Performance in Naphthobisthiadiazole-Based Semiconducting Polymers. J. Am. Chem. Soc. 2016, 138, 10265¨C10275. "
816,CC(S1)=CC2=C1C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=CC=C(C6=CC(CCCCCC)=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9,PBDT-DTBT,5.26,3.1,1,5.8,0.346,2.11,"Wang, M.; Hu, X.; Liu, P.; Li, W.; Gong, X.; Huang, F.; Cao, Y. Donor-Acceptor Conjugated Polymer Based on naphtho[1,2-c:5,6-c]bis[1,2,5]thiadiazole for HighPerformance Polymer Solar Cells. J. Am. Chem. Soc. 2011, 133, 9638¨C9641. "
817,CC(S1)=CC2=C1C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=CC6=C(C=C(C7=CC(CCCCCC)=C(C)S7)C8=NSN=C86)C9=NSN=C59)S4)S%10)C%10=C2C%11=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%11,PBDT-DTNT,5.19,3.26,0.8,11.71,0.61,6,"Wang, M.; Hu, X.; Liu, P.; Li, W.; Gong, X.; Huang, F.; Cao, Y. Donor-Acceptor Conjugated Polymer Based on naphtho[1,2-c:5,6-c]bis[1,2,5]thiadiazole for HighPerformance Polymer Solar Cells. J. Am. Chem. Soc. 2011, 133, 9638¨C9641. "
818,CC1=CC(CC(CCCC)CC)=C(C2=NC(SC(C3=C(CC(CCCC)CC)C=C(C4=C(CC(CCCCCC)CCCC)C=C(C5=CC(C6=NSN=C6C(C7=CC(CC(CCCCCC)CCCC)=C(C)S7)=C8)=C8C9=NSN=C95)S4)S3)=N%10)=C%10S2)S1,PTzNTz-EHBO,5.41,3.45,0.84,16,0.67,9,"Saito, M.; Osaka, I.; Suzuki, Y.; Takimiya, K.; Okabe, T.; Ikeda, S.; Asano, T. Highly Efficient and Stable Solar Cells Based on Thiazolothiazole and Naphthobisthiadiazole Copolymers. Sci. Rep. 2015, 5, 14202/1¨C9. "
819,CC1=CC(CC(CCCC)CC)=C(C2=NC(SC(C3=C(CC(CCCC)CC)C=C(C4=C(CC(CCCCCC)CCCCCCCC)C=C(C5=CC(C6=NSN=C6C(C7=CC(CC(CCCCCC)CCCCCCCC)=C(C)S7)=C8)=C8C9=NSN=C95)S4)S3)=N%10)=C%10S2)S1,PTzNTz-EHHD,5.4,3.46,0.84,15.6,0.67,8.8,"Saito, M.; Osaka, I.; Suzuki, Y.; Takimiya, K.; Okabe, T.; Ikeda, S.; Asano, T. Highly Efficient and Stable Solar Cells Based on Thiazolothiazole and Naphthobisthiadiazole Copolymers. Sci. Rep. 2015, 5, 14202/1¨C9. "
820,CC1=CC(CC(CCCC)CCCCCC)=C(C2=NC(SC(C3=C(CC(CCCC)CCCCCC)C=C(C4=C(CC(CCCCCC)CCCC)C=C(C5=CC(C6=NSN=C6C(C7=CC(CC(CCCCCC)CCCC)=C(C)S7)=C8)=C8C9=NSN=C95)S4)S3)=N%10)=C%10S2)S1,PTzNTz-BOBO,5.4,3.46,0.84,16.6,0.63,8.8,"Saito, M.; Osaka, I.; Suzuki, Y.; Takimiya, K.; Okabe, T.; Ikeda, S.; Asano, T. Highly Efficient and Stable Solar Cells Based on Thiazolothiazole and Naphthobisthiadiazole Copolymers. Sci. Rep. 2015, 5, 14202/1¨C9. "
821,CC1=CC(CC(CCCC)CCCCCC)=C(C2=NC(SC(C3=C(CC(CCCC)CCCCCC)C=C(C4=C(CC(CCCCCC)CCCCCCCC)C=C(C5=CC(C6=NSN=C6C(C7=CC(CC(CCCCCC)CCCCCCCC)=C(C)S7)=C8)=C8C9=NSN=C95)S4)S3)=N%10)=C%10S2)S1,PTzNTz-BOHD,5.41,3.44,0.84,9.8,0.63,5.2,"Saito, M.; Osaka, I.; Suzuki, Y.; Takimiya, K.; Okabe, T.; Ikeda, S.; Asano, T. Highly Efficient and Stable Solar Cells Based on Thiazolothiazole and Naphthobisthiadiazole Copolymers. Sci. Rep. 2015, 5, 14202/1¨C9. "
822,CC1=CC=C(C(C=CC(C2=CC(CCCCCCCCCCCC)=C(C3=CC=C(C4=CC(C5=NSN=C5C(C6=CC=C(C7=C(CCCCCCCCCCCC)C=C(C)S7)S6)=C8)=C8C9=NSN=C94)S3)S2)=C%10)=C%10C%11(CCCCCCCC)CCCCCCCC)C%11=C1,PF-C12NT,5.47,3.79,0.87,12.19,0.614,6.51,"Liu, L. Q.; Zhang, G. C.; Liu, P.; Zhang, J.; Dong, S.; Wang, M.; Ma, Y. G.; Yip, H. L.; Huang, F. Donor-Acceptor-Type Copolymers Based on a naphtho[1,2-c:5,6-c]bis(1,2,5-Thiadiazole Scaffold for High-Efficiency Polymer Solar Cells. Chem. -Asian J. 2014, 9, 2104¨C2112. "
823,CC1=CC=C(C(C=CC(C2=CC(CCCCCCCCCCCC)=C(C3=CC=C(C4=CC(C5=NSN=C5C(C6=CC=C(C7=C(CCCCCCCCCCCC)C=C(C)S7)S6)=C8)=C8C9=NSN=C94)S3)S2)=C%10)=C%10/C%11=C(CC(CCCCCCCC)CCCCCC)/CCCCCCCCCCCC)C%11=C1,PAF-C12NT,5.4,3.85,0.69,8.45,0.625,3.64,"Liu, L. Q.; Zhang, G. C.; Liu, P.; Zhang, J.; Dong, S.; Wang, M.; Ma, Y. G.; Yip, H. L.; Huang, F. Donor-Acceptor-Type Copolymers Based on a naphtho[1,2-c:5,6-c]bis(1,2,5-Thiadiazole Scaffold for High-Efficiency Polymer Solar Cells. Chem. -Asian J. 2014, 9, 2104¨C2112. "
824,CC1=CC=C(C(C=CC(C2=CC(CCCCCCCCCCCC)=C(C3=CC=C(C4=CC(C5=NSN=C5C(C6=CC=C(C7=C(CCCCCCCCCCCC)C=C(C)S7)S6)=C8)=C8C9=NSN=C94)S3)S2)=C%10)=C%10N%11C(CCCCCCCC)CCCCCCCC)C%11=C1,PCz-C12NT,5.35,3.72,0.76,11.31,0.564,4.85,"Liu, L. Q.; Zhang, G. C.; Liu, P.; Zhang, J.; Dong, S.; Wang, M.; Ma, Y. G.; Yip, H. L.; Huang, F. Donor-Acceptor-Type Copolymers Based on a naphtho[1,2-c:5,6-c]bis(1,2,5-Thiadiazole Scaffold for High-Efficiency Polymer Solar Cells. Chem. -Asian J. 2014, 9, 2104¨C2112. "
825,CC1=CC(CCCCCCCCCCCC)=C(S1)C(S2)=CC=C2C3=CC(C4=NSN=C45)=C(C6=NSN=C63)C=C5C7=CC=C(S7)C(S8)=C(CCCCCCCCCCCC)C=C8C9=CC(C(C%10=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%10)=C(SC(C)=C%11)C%11=C%12C%13=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%13)=C%12S9,PBDT-C12NT,5.19,3.68,0.68,10.74,0.685,5,"Liu, L. Q.; Zhang, G. C.; Liu, P.; Zhang, J.; Dong, S.; Wang, M.; Ma, Y. G.; Yip, H. L.; Huang, F. Donor-Acceptor-Type Copolymers Based on a naphtho[1,2-c:5,6-c]bis(1,2,5-Thiadiazole Scaffold for High-Efficiency Polymer Solar Cells. Chem. -Asian J. 2014, 9, 2104¨C2112. "
826,CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C)S4)S3)S2)S1,PQT-12,5.1,3.1,0.61,4.31,0.44,1.15,"Moul¨¦, a J.; Allard, S.; Moul¨¦, A. J.; Kronenberg, N. M.; Allard, S.; Tsami, A.; Kronenberg, N. M.; Tsami, A.; Scherf, U.; Scherf, U.; Meerholz, K.; Meerholz, K. Effect of Polymer Nanoparticle Formation on the Efficiency of Polythiophene Based ¡°BulkHeterojunction¡± Solar Cells. J. Phys. Chem. C 2008, 112, 12583¨C12589. "
827,CC1=CC2=C(C(C3=CC(OCC(CCCC)CC)=CC=C3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC6=C(C=C(C7=CC(CC(CC)CCCC)=C(C)S7)C8=NSN=C86)C9=NSN=C59)S4)S%10)C%10=C2C%11=CC(OCC(CC)CCCC)=CC=C%11)S1,PN1,5.39,3.75,0.85,8.65,0.378,2.78,"Liu, L.; Zhang, G.; He, B.; Huang, F. Polymer Solar Cells Based on the Copolymers of Naphtho[1,2-c:5,6-c]bis(1,2,5-Thiadiazole and Alkoxylphenyl Substituted Benzodithiophene with High Open-Circuit Voltages. Chinese J. Chem. 2015, 33, 902¨C908. "
828,CC1=CC(C(C2=CC=C(CCCCCCCC)C=C2)(C3=CC=C(CCCCCCCC)C=C3)C4=CC(C(SC(C5=C(C[C@H](CCCC)CC)C=C(C6=CC7=C(C=C(C8=CC(C[C@H](CC)CCCC)=C(C)S8)C9=NSN=C97)C%10=NSN=C6%10)S5)=C%11)=C%11C%12(C%13=CC=C(CCCCCCCC)C=C%13)C%14=CC=C(CCCCCCCC)C=C%14)=C%12C=C4%15)=C%15S1,PIDT-EHNT,5.48,3.79,0.86,4.33,0.4,1.49,"Wang, M.; Hu, X.; Liu, P.; Li, W.; Gong, X.; Huang, F.; Cao, Y. Design and Synthesis of Copolymers of Indacenodithiophene and Naphtho[1,2?c:5,6?c]bis(1,2,5-thiadiazole for Polymer Solar Cells. Macromolecules 2013, 46, 3950?3958. "
829,CC1=CC(C(C2=CC=C(CCCCCCCC)C=C2)(C3=CC=C(CCCCCCCC)C=C3)C4=CC(C(SC(C5=C(CCCCCC)C=C(C6=CC7=C(C=C(C8=CC(CCCCCC)=C(C)S8)C9=NSN=C97)C%10=NSN=C6%10)S5)=C%11)=C%11C%12(C%13=CC=C(CCCCCCCC)C=C%13)C%14=CC=C(CCCCCCCC)C=C%14)=C%12C=C4%15)=C%15S1,PIDT-DTNT,5.48,3.83,0.8,8.26,0.45,2.97,"Wang, M.; Hu, X.; Liu, P.; Li, W.; Gong, X.; Huang, F.; Cao, Y. Design and Synthesis of Copolymers of Indacenodithiophene and Naphtho[1,2?c:5,6?c]bis(1,2,5-thiadiazole for Polymer Solar Cells. Macromolecules 2013, 46, 3950?3958. "
830,CC1=CC(C(C2=CC=C(CCCCCCCC)C=C2)(C3=CC=C(CCCCCCCC)C=C3)C4=CC(C(SC(C5=CC(CCCCCCCCCCCC)=C(C6=CC=C(C7=CC8=C(C=C(C9=CC=C(C%10=C(CCCCCCCCCCCC)C=C(C)S%10)S9)C%11=NSN=C%118)C%12=NSN=C7%12)S6)S5)=C%13)=C%13C%14(C%15=CC=C(CCCCCCCC)C=C%15)C%16=CC=C(CCCCCCCC)C=C%16)=C%14C=C4%17)=C%17S1,PIDT-C12NT,5.52,3.88,0.9,10.21,0.55,5.05,"Wang, M.; Hu, X.; Liu, P.; Li, W.; Gong, X.; Huang, F.; Cao, Y. Design and Synthesis of Copolymers of Indacenodithiophene and Naphtho[1,2?c:5,6?c]bis(1,2,5-thiadiazole for Polymer Solar Cells. Macromolecules 2013, 46, 3950?3958. "
831,CC1=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C2=CC(SC(C3=C(CC(CCCCCCCCCC)CCCCCCCC)C=C(C4=CC5=C(C=C(C)C6=NSN=C65)C7=NSN=C47)S3)=C8)=C8S2)S1,NT812,5.29,3.4,0.72,19.09,0.729,10.33,"Jin, Y.; Chen, Z.; Dong, S.; Zheng, N.; Ying, L.; Jiang, X. F.; Liu, F.; Huang, F.; Cao, Y. A Novel Naphtho[1,2-c:5,6-c¡ä]Bis([1,2,5]Thiadiazole-Based Narrow-Bandgap ¦Ð-Conjugated Polymer with Power Conversion Efficiency Over 10%. Adv. Mater. 2016, 28, 9811¨C9818. "
832,CC1=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(C2=CC(SC(C3=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C4=CC5=C(C=C(C)C6=NSN=C65)C7=NSN=C47)S3)=C8)=C8S2)S1,NT1014,5.29,3.4,0.77,7.25,0.529,3.03,"Jin, Y.; Chen, Z.; Dong, S.; Zheng, N.; Ying, L.; Jiang, X. F.; Liu, F.; Huang, F.; Cao, Y. A Novel Naphtho[1,2-c:5,6-c¡ä]Bis([1,2,5]Thiadiazole-Based Narrow-Bandgap ¦Ð-Conjugated Polymer with Power Conversion Efficiency Over 10%. Adv. Mater. 2016, 28, 9811¨C9818. "
833,CC(S1)=C(CC(CCCCCCCC)CCCCCC)C=C1C(C2=NSN=C23)=CC4=C3C=C(C5=CC(C[C@H](CCCCCC)CCCCCCCC)=C(C6=CC7=C(C(C(CCCCCCCCCCCC)=CC8=C9SC(C)=C8)=C9C(CCCCCCCCCCCC)=C7)S6)S5)C%10=NSN=C%104,Pƒ¿NDTDTNT,5.4,3.64,0.8,15.55,0.644,8.01,"Cheng, S. W.; Chiou, D. Y.; Tsai, C. E.; Liang, W. W.; Lai, Y. Y.; Hsu, J. Y.; Hsu, C. S.; Osaka, I.; Takimiya, K.; Cheng, Y. J. Angular-Shaped 4,9-Dialkyl?¦Á- and?¦Â-Naphthodithiophene-Based Donor-Acceptor Copolymers: Investigation of Isomeric Structural Effects on Molecular Properties and Performance of Field-Effect Transistors and Photovoltaics. Adv. Funct. Mater. 2015, 25, 6131¨C6143. "
834,CC(S1)=C(CC(CCCCCCCC)CCCCCC)C=C1C(C2=NSN=C23)=CC4=C3C=C(C5=CC(C[C@H](CCCCCC)CCCCCCCC)=C(C6=CC7=C(C=C(CCCCCCCCCCCC)C8=C7C(CCCCCCCCCCCC)=CC9=C8C=C(C)S9)S6)S5)C%10=NSN=C%104,PƒÀNDTDTNT,5.46,3.64,0.8,8.41,0.535,3.6,"Cheng, S. W.; Chiou, D. Y.; Tsai, C. E.; Liang, W. W.; Lai, Y. Y.; Hsu, J. Y.; Hsu, C. S.; Osaka, I.; Takimiya, K.; Cheng, Y. J. Angular-Shaped 4,9-Dialkyl?¦Á- and?¦Â-Naphthodithiophene-Based Donor-Acceptor Copolymers: Investigation of Isomeric Structural Effects on Molecular Properties and Performance of Field-Effect Transistors and Photovoltaics. Adv. Funct. Mater. 2015, 25, 6131¨C6143. "
835,CC1=CC=C(N(C2=CC=C(C3=CC(C4=NSN=C4C(C)=C5)=C5C6=NSN=C63)C=C2)C7=CC=C(CCCCCCCC)C=C7)C=C1,poly(CR-TPA),5.55,2.6,0.79,6.87,0.4,2.15,"Yasuda, T.; Shinohara, Y.; Kusagaki, Y.; Matsuda, T.; Han, L.; Ishi-I, T. Synthesis and Photovoltaic Properties of Naphthobisthiadiazole-Triphenylamine-Based DonorAcceptor ¦Ð-Conjugated Polymer. Polymer 2015, 58, 139¨C145. "
836,CC1=CC=C(N(C2=CC=C(C3=CC(C(C=CC=C4)=C4C(C)=C5)=C5C6=C3C=CC=C6)C=C2)C7=CC=C(CCCCCCCC)C=C7)C=C1,poly(NTD-TPA),5.4,3.37,0.76,6.02,0.33,1.52,"Yasuda, T.; Shinohara, Y.; Kusagaki, Y.; Matsuda, T.; Han, L.; Ishi-I, T. Synthesis and Photovoltaic Properties of Naphthobisthiadiazole-Triphenylamine-Based DonorAcceptor ¦Ð-Conjugated Polymer. Polymer 2015, 58, 139¨C145. "
837,CC1=CC2=C(C(SC(C3=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C4=CN=C(C5=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C)S5)C6=NSN=C64)S3)=C7)=C7C8=C2SC(C(CCCCCCCC)CCCCCCCC)=C8)S1,BTT-TP,5.6,3.85,0.993,0.764,0.468,0.35,"Al-Naamani, E.; Ide, M.; Gopal, A.; Saeki, A.; Osaka, I.; Seki, S. Study of Photoelectric Conversion in Benzotrithiophene-Based Conjugated Semiconducting Polymers. J. Photopolym. Sci. Technol. 2015, 28, 605¨C610. "
838,CC1=CC2=C(C(SC(C3=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C4=C(F)C(F)=C(C5=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C)S5)C6=NSN=C64)S3)=C7)=C7C8=C2SC(C(CCCCCCCC)CCCCCCCC)=C8)S1,BTT-FT,5.52,3.74,0.919,2.04,0.54,1.01,"Al-Naamani, E.; Ide, M.; Gopal, A.; Saeki, A.; Osaka, I.; Seki, S. Study of Photoelectric Conversion in Benzotrithiophene-Based Conjugated Semiconducting Polymers. J. Photopolym. Sci. Technol. 2015, 28, 605¨C610. "
839,CC1=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C(S1)C(C2=NSN=C23)=CC4=C3C=C(C5=NSN=C54)C(S6)=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C6C7=CC(CCCCCCCCCCCC)=C(S7)C8=CC(C9=C%10SC(C(CCCCCCCC)CCCCCCCC)=C9)=C(S8)C%11=C%10C=C(C%12=C(CCCCCCCCCCCC)C=C(C)S%12)S%11,BTT-NTz,5.41,3.73,0.755,5.98,0.605,2.73,"Al-Naamani, E.; Ide, M.; Gopal, A.; Saeki, A.; Osaka, I.; Seki, S. Study of Photoelectric Conversion in Benzotrithiophene-Based Conjugated Semiconducting Polymers. J. Photopolym. Sci. Technol. 2015, 28, 605¨C610. "
840,CC1=CC=C(C2=C(C(OCC(CCCCCC)CCCC)=O)C=C(C3=CC(C(OCC(CCCC)CCCCCC)=O)=C(C4=CC=C(C)S4)S3)S2)S1,PDCBT,4.9,3,0.91,11,0.72,7.2,"Zhang, M.; Guo, X.; Ma, W.; Ade, H.; Hou, J. A Polythiophene Derivative with Superior Properties for Practical Application in Polymer Solar Cells. Adv. Mater. 2014, 26, 5880¨C5885. "
841,CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C6=C7C(C(F)=C(C(OCC(CCCC)CC)=O)S7)=C(C8=CC9=C(C(C%10=CC=C(CC(CCCC)CC)S%10)=C(C=C(C)S%11)C%11=C9C%12=CC=C(CC(CCCC)CC)S%12)S8)S6)S%13)C%13=C4C%14=CC=C(CC(CC)CCCC)S%14)S3)S1,rr-PTB7-Th,5.2,3.68,0.78,15.35,0.583,7.04,"Kim, H.; Lim, B.; Heo, H.; Nam, G.; Lee, H.; Lee, J. Y.; Lee, J.; Lee, Y. High-Efficiency Organic Photovoltaics with Two-Dimensional Conjugated BenzodithiopheneBased Regioregular Polymers. Chem. Mater. 2017, 29, 4301¨C4310. "
842,CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C(C=C(C6=C7C(C(F)=C(C(OCC(CCCC)CC)=O)S7)=C(C8=CC9=C(C(C%10=CC=C(SCC(CCCC)CC)S%10)=C(C=C(C)S%11)C%11=C9C%12=CC=C(SCC(CCCC)CC)S%12)S8)S6)S%13)C%13=C4C%14=CC=C(CC(CC)CCCC)S%14)S3)S1,rr-PTBS,5.22,3.84,0.82,19.63,0.633,10.31,"Kim, H.; Lim, B.; Heo, H.; Nam, G.; Lee, H.; Lee, J. Y.; Lee, J.; Lee, Y. High-Efficiency Organic Photovoltaics with Two-Dimensional Conjugated BenzodithiopheneBased Regioregular Polymers. Chem. Mater. 2017, 29, 4301¨C4310. "
843,CC1=CC(CCCCCCCC)=C(C2=CC=C(C3=C(CCCCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1,P3TI,5.82,3.83,0.7,13.1,0.69,6.3,"Wang, E.; Ma, Z.; Zhang, Z.; Vandewal, K.; Henriksson, P.; Ingan?s, O.; Zhang, F.; Andersson, M. R. An Easily Accessible Isoindigo-Based Polymer for High-Performance Polymer Solar Cells. J. Am. Chem. Soc. 2011, 133, 14244¨C14247. "
844,CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C)S3)C3=C2OCC(CCCC)CC)S1,O-PBDT,5.31,2.94,0.83,4.18,0.45,1.56,"Lee, D.; Hubijar, E.; Kalaw, G. J. D.; Ferraris, J. P. Enhanced and Tunable OpenCircuit Voltage Using Dialkylthio benzo[1,2-b:4,5-b¡ä]dithiophene in Polymer Solar Cells. Chem. Mater. 2012, 24, 2534¨C2540. "
845,CC(S1)=CC2=C1C(SCC(CCCC)CC)=C(C=C(C3=CC4=C(C(OCC(CC)CCCC)=C(C=C(C)S5)C5=C4OCC(CCCC)CC)S3)S6)C6=C2SCC(CCCC)CC,SO-PBDT,5.36,3.11,0.91,4.4,0.43,1.73,"Lee, D.; Hubijar, E.; Kalaw, G. J. D.; Ferraris, J. P. Enhanced and Tunable OpenCircuit Voltage Using Dialkylthio benzo[1,2-b:4,5-b¡ä]dithiophene in Polymer Solar Cells. Chem. Mater. 2012, 24, 2534¨C2540. "
846,CC1=CC2=C(C(SCC(CCCC)CC)=C(C=C(C)S3)C3=C2SCC(CCCC)CC)S1,S-PBDT,5.41,3.26,0.99,7.66,0.53,4,"Lee, D.; Hubijar, E.; Kalaw, G. J. D.; Ferraris, J. P. Enhanced and Tunable OpenCircuit Voltage Using Dialkylthio benzo[1,2-b:4,5-b¡ä]dithiophene in Polymer Solar Cells. Chem. Mater. 2012, 24, 2534¨C2540. "
847,CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C)S4)C4=C2C5=CC=C(CC(CCCC)CC)S5)S1,PBDTT,5.44,3.46,0.93,11.95,0.55,6.12,"Kang, T. E.; Kim, T.; Wang, C.; Yoo, S.; Kim, B. J. Poly(benzodithiophene Homopolymer for High-Performance Polymer Solar Cells with Open-Circuit Voltage of near 1 V: A Superior Candidate to Substitute for poly(3-Hexylthiophene as Wide Bandgap Polymer. Chem. Mater. 2015, 27, 2653¨C2658. "
848,CC1=CC(CC(CCCCCCCC)CCCCCC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1,P3HDTTT,5.3,3.4,0.82,6.33,0.66,3.4,"Hou, J.; Chen, T. L.; Zhang, S.; Huo, L.; Sista, S.; Yang, Y. An Easy and Effective Method to Modulate Molecular Energy Level of poly(3-Alkylthiophene for High-Voc Polymer Solar Cells. Macromolecules 2009, 42, 9217¨C9219. "
849,CC1=CC(C(OCC(CCCC)CC)=O)=C(C2=CC=C(C)S2)S1,PT-C1,5.15,2.96,0.81,5.31,0.392,1.69,"Zhang, M.; Guo, X.; Yang, Y.; Zhang, J.; Zhang, Z.-G.; Li, Y. Downwards Tuning the HOMO Level of Polythiophene by Carboxylate Substitution for High Open-CircuitVoltage Polymer Solar Cells. Polym. Chem. 2011, 2, 2900¨C2906. "
850,CC1=CC(C(OCC(CCCC)CC)=O)=C(C2=CC=C(S2)C3=CC=C(C)S3)S1,PT-C2,5.11,2.95,0.81,5.44,0.484,2.14,"Zhang, M.; Guo, X.; Yang, Y.; Zhang, J.; Zhang, Z.-G.; Li, Y. Downwards Tuning the HOMO Level of Polythiophene by Carboxylate Substitution for High Open-CircuitVoltage Polymer Solar Cells. Polym. Chem. 2011, 2, 2900¨C2906. "
851,CC1=CC(C(OCC(CCCCCCCC)CCCCCC)=O)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1,PT-C3,5.1,2.98,0.77,7.22,0.584,3.25,"Zhang, M.; Guo, X.; Yang, Y.; Zhang, J.; Zhang, Z.-G.; Li, Y. Downwards Tuning the HOMO Level of Polythiophene by Carboxylate Substitution for High Open-CircuitVoltage Polymer Solar Cells. Polym. Chem. 2011, 2, 2900¨C2906. "
852,CC1=CC(SCCCCCC)=C(C)S1,P3HST,4.9,3.08,0.63,1.27,0.34,0.34,"Huo, L.; Zhou, Y.; Li, Y. Alkylthio-Substituted Polythiophene: Absorption and Photovoltaic Properties. Macromol. Rapid Commun. 2009, 30, 925¨C931. "
853,CC1=CC(CCCCCC)=C(C2=CC=C(C3=C(CCCCCC)C=C(C)S3)S2)S1,P3HST-co-Th,5.02,3.19,0.63,2.32,0.34,0.5,"Huo, L.; Zhou, Y.; Li, Y. Alkylthio-Substituted Polythiophene: Absorption and Photovoltaic Properties. Macromol. Rapid Commun. 2009, 30, 925¨C931. "
854,CC1=CC(CCCCCC)=C(C2=CC=C(C3=C(CCCCCC)C=C(C)S3)S2)S1,C6-TT,5.25,3.05,0.75,2.5,0.34,0.6,"Koppe, M.; Scharber, M.; Brabec, C.; Duffy, W.; Heeney, M.; McCulloch, I. Polyterthiophenes as Donors for Polymer Solar Cells. Adv. Funct. Mater. 2007, 17, 1371¨C1376. "
855,CC1=CC=C(/C=C/C2=CC=C(C3=CC=C4C(C=CC(C)=C4OCCCCCCCCCC)=C3OCCCCCCCCCC)S2)S1,PBTDN,5.12,2.9,0.83,9.2,0.41,3.2,"Cha, H.; Kim, H. N.; An, T. K.; Kang, M. S.; Kwon, S. K.; Kim, Y. H.; Park, C. E. Effects of Cyano-Substituents on the Molecular Packing Structures of Conjugated Polymers for Bulk-Heterojunction Solar Cells. ACS Appl. Mater. Interfaces 2014, 6, 15774¨C15782. "
856,CC1=CC=C(/C(C#N)=C/C2=CC=C(C3=CC=C4C(C=CC(C)=C4OCCCCCCCCCC)=C3OCCCCCCCCCC)S2)S1,PBTADN,5.36,3.34,0.89,7.4,0.514,3.4,"Cha, H.; Kim, H. N.; An, T. K.; Kang, M. S.; Kwon, S. K.; Kim, Y. H.; Park, C. E. Effects of Cyano-Substituents on the Molecular Packing Structures of Conjugated Polymers for Bulk-Heterojunction Solar Cells. ACS Appl. Mater. Interfaces 2014, 6, 15774¨C15782. "
857,CC1=CC(C2=CC=C(CCCCCCCC)C=C2)=C(C)S1,POPT,5.34,3.58,0.56,5.16,0.6,1.71,"Cho, C.-H.; Kang, H.; Kang, T. E.; Cho, H.-H.; Yoon, S. C.; Jeon, M.-K.; Kim, B. J. Controlling Side-Chain Density of Electron Donating Polymers for Improving Their Packing Structure and Photovoltaic Performance. Chem. Commun. 2011, 47, 3577¨C3579. "
858,CC1=CC(C2=CC=C(CCCCCCCC)C=C2)=C(C3=CC=C(C4=CC=C(C)S4)S3)S1,POPTT,5.43,3.5,0.63,6.83,0.4,1.73,"Cho, C.-H.; Kang, H.; Kang, T. E.; Cho, H.-H.; Yoon, S. C.; Jeon, M.-K.; Kim, B. J. Controlling Side-Chain Density of Electron Donating Polymers for Improving Their Packing Structure and Photovoltaic Performance. Chem. Commun. 2011, 47, 3577¨C3579. "
859,CC1=CC(C2=CC=C(CCCCCCCC)C=C2)=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)S1,POPQT,5.49,3.52,0.71,8.67,0.56,3.44,"Cho, C.-H.; Kang, H.; Kang, T. E.; Cho, H.-H.; Yoon, S. C.; Jeon, M.-K.; Kim, B. J. Controlling Side-Chain Density of Electron Donating Polymers for Improving Their Packing Structure and Photovoltaic Performance. Chem. Commun. 2011, 47, 3577¨C3579. "
860,CC1=CC=C(S1)C(S2)=CC3=C2C(OCC(CCCC)CC)=C(C=C(C)S4)C4=C3OCC(CCCC)CC,P1,5.22,3.21,0.62,6.92,0.66,2.85,"Tan, Z.; Imae, I.; Komaguchi, K.; Ooyama, Y.; Ohshita, J.; Harima, Y. Effects of???- Conjugated Side Chains on Properties and Performances of Photovoltaic Copolymers. Synth. Met. 2014, 187, 30¨C36. "
861,CC1=C(/C=C/C2=CC=CS2)C=C(S1)C(S3)=CC4=C3C(OCC(CCCC)CC)=C(C=C(C)S5)C5=C4OCC(CCCC)CC,P2,5.22,3.26,0.64,9.3,0.58,3.44,"Tan, Z.; Imae, I.; Komaguchi, K.; Ooyama, Y.; Ohshita, J.; Harima, Y. Effects of???- Conjugated Side Chains on Properties and Performances of Photovoltaic Copolymers. Synth. Met. 2014, 187, 30¨C36. "
862,CC1=C(/C=C(C#N)/C2=CC=CS2)C=C(S1)C(S3)=CC4=C3C(OCC(CCCC)CC)=C(C=C(C)S5)C5=C4OCC(CCCC)CC,P3,5.37,3.47,0.73,11.49,0.53,4.49,"Tan, Z.; Imae, I.; Komaguchi, K.; Ooyama, Y.; Ohshita, J.; Harima, Y. Effects of???- Conjugated Side Chains on Properties and Performances of Photovoltaic Copolymers. Synth. Met. 2014, 187, 30¨C36. "
863,CC1=C(C(OC)=O)C=C(S1)C(S2)=CC3=C2C(OCC(CCCC)CC)=C(C=C(C)S4)C4=C3OCC(CCCC)CC,PBDT-3MT,5.43,3.36,0.86,10.5,0.5,4.52,"Cho, M. J.; Seo, J.; Kim, K. H.; Choi, D. H.; Prasad, P. N. Enhanced Performance of Organic Photovoltaic Cells Fabricated with a Methyl Thiophene- 3-CarboxylateContaining Alternating Conjugated Copolymer. Macromol. Rapid Commun. 2012, 33, 146?151. "
864,CC1=CC2=C(OCC(CCCC)CC)C3=C(C=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)C(OCC(CCCC)CC)=C2S1,PBDT-BT,5.37,3.25,0.82,5.86,0.458,2.2,"Kim, H. G.; Kim, M.; Clement, J. A.; Lee, J.; Shin, J.; Hwang, H.; Sin, D. H.; Cho, K. Energy Level Engineering of Donor Polymers via Inductive and Resonance Effects for Polymer Solar Cells: Effects of Cyano and Alkoxy Substituents. Chem. Mater. 2015, 27, 6858¨C6868. "
865,CC1=CC2=C(OCC(CCCC)CC)C3=C(C=C(C4=C(CCCCCCCCCCCC)C(C#N)=C(C5=C(C#N)C(CCCCCCCCCCCC)=C(C)S5)S4)S3)C(OCC(CCCC)CC)=C2S1,PBDT-BTC,5.58,3.53,0.98,1.27,0.414,0.55,"Kim, H. G.; Kim, M.; Clement, J. A.; Lee, J.; Shin, J.; Hwang, H.; Sin, D. H.; Cho, K. Energy Level Engineering of Donor Polymers via Inductive and Resonance Effects for Polymer Solar Cells: Effects of Cyano and Alkoxy Substituents. Chem. Mater. 2015, 27, 6858¨C6868. "
866,CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C(OCCCCCCCCCCCC)C(C#N)=C(C4=C(C#N)C(OCCCCCCCCCCCC)=C(C)S4)S3)S5)C5=C2OCC(CC)CCCC,PBDT-BTCox,5.5,3.51,0.86,10.1,0.584,5.06,"Kim, H. G.; Kim, M.; Clement, J. A.; Lee, J.; Shin, J.; Hwang, H.; Sin, D. H.; Cho, K. Energy Level Engineering of Donor Polymers via Inductive and Resonance Effects for Polymer Solar Cells: Effects of Cyano and Alkoxy Substituents. Chem. Mater. 2015, 27, 6858¨C6868. "
867,CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(C3=CC4=C(OCC(CCCC)CC)C(SC(C)=C5)=C5C(OCC(CCCC)CC)=C4S3)S1,PTB7,5.15,3.31,0.74,14.5,0.69,7.4,"Liang, Y.; Xu, Z.; Xia, J.; Tsai, S. T.; Wu, Y.; Li, G.; Ray, C.; Yu, L. For the Bright Future-Bulk Heterojunction Polymer Solar Cells with Power Conversion Efficiency of 7.4%. Adv. Mater. 2010, 22, 135¨C138. "
868,CC1=C(F)C(F)=C(S1)C(S2)=CC3=C2C(OCC(CCCC)CC)=C(C=C(C)S4)C4=C3OCC(CCCC)CC,PBDT[2F]T,5.05,2.95,0.9,10.7,0.72,7,"Wolf, J.; Cruciani, F.; El Labban, A.; Beaujuge, P. M. Wide Band-Gap 3,4- Difluorothiophene-Based Polymer with 7% Solar Cell Efficiency: An Alternative to P3HT. Chem. Mater. 2015, 27, 4184¨C4187. "
869,CC1=CC=C(S1)C(S2)=CC3=C2C(OCC(CCCC)CC)=C(C=C(C)S4)C4=C3OCC(CCCC)CC,PBDT[2H]T,5.32,3.24,0.8,6.3,0.58,2.9,"Wolf, J.; Cruciani, F.; El Labban, A.; Beaujuge, P. M. Wide Band-Gap 3,4- Difluorothiophene-Based Polymer with 7% Solar Cell Efficiency: An Alternative to P3HT. Chem. Mater. 2015, 27, 4184¨C4187. "
870,CC1=C(CCCCCCCCCCCC)C=C(S1)C(S2)=CC(CCCCCCCCCCCC)=C2C3=C(C(N(CC(CC)CCCC)C4=O)=O)C4=C(C)S3,PBTTPD,5.56,3.1,0.95,8.02,0.62,4.7,"Yuan, M. C.; Chiu, M. Y.; Liu, S. P.; Chen, C. M.; Wei, K. H. A thieno[3,4- c ]Pyrrole-4,6-Dione-Based Donor-Acceptor Polymer Exhibiting High Crystallinity for Photovoltaic Applications. Macromolecules 2010, 43, 6936¨C6938. "
871,CC1=C2C(C(N(CC(CCCCCCCC)CCCCCC)C2=O)=O)=C(C3=CC=C(C4=C(CCCCCCCC)C(SC(C5=CC=C(C)S5)=C6CCCCCCCC)=C6S4)S3)S1,PDTTTPD,5.54,3,0.85,8.99,0.67,5.1,"Chen, G.-Y.; Cheng, Y.-H.; Chou, Y.-J.; Su, M.-S.; Chen, C.-M.; Wei, K.-H. Crystalline Conjugated Polymer Containing Fused 2,5-Di(thiophen-2-ylthieno[2,3- b]thiophene and thieno[3,4-c]pyrrole-4,6-Dione Units for Bulk Heterojunction Solar Cells. Chem. Commun. 2011, 47, 5064¨C5066. "
872,CC1=C(CCCCCCCCCCCC)C=C(C2=CC(CCCCCCCCCCCC)=C(C3=C(C(N(C(CCCCCCCC)CCCCCCCC)C4=O)=O)C4=C(C)S3)S2)S1,PBTTPD,5.66,3.86,0.9,5.01,0.42,1.9,"Jo, J.; Pron, A.; Berrouard, P.; Leong, W. L.; Yuen, J. D.; Moon, J. S.; Leclerc, M.; Heeger, A. J. A New Terthiophene-Thienopyrrolodione Copolymer-Based Bulk Heterojunction Solar Cell with High Open-Circuit Voltage. Adv. Energy Mater. 2012, 2, 1397¨C1403."
873,CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)S1,PTTTPD,5.66,3.86,0.92,10.51,0.63,6.1,"Jo, J.; Pron, A.; Berrouard, P.; Leong, W. L.; Yuen, J. D.; Moon, J. S.; Leclerc, M.; Heeger, A. J. A New Terthiophene-Thienopyrrolodione Copolymer-Based Bulk Heterojunction Solar Cell with High Open-Circuit Voltage. Adv. Energy Mater. 2012, 2, 1397¨C1403."
874,CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)S1,PTTTPD-C8C8 (P1),5.66,3.86,0.87,9.5,0.6,4.96,"Najari, A.; Beaupr¨¦, S.; Allard, N.; Ouattara, M.; Pouliot, J. R.; Charest, P.; Besner, S.; Simoneau, M.; Leclerc, M. Thieno, Furo, and Selenopheno[3,4-C]pyrrole-4,6-Dione Copolymers: Air-Processed Polymer Solar Cells with Power Conversion Efficiency up to 7.1%. Adv. Energy Mater. 2015, 5, 1501213/1¨C9. "
875,CC1=C2C(C(N(CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)S1,PTTTPD-C8 (P2),5.56,3.73,0.81,6.7,0.59,3.2,"Najari, A.; Beaupr¨¦, S.; Allard, N.; Ouattara, M.; Pouliot, J. R.; Charest, P.; Besner, S.; Simoneau, M.; Leclerc, M. Thieno, Furo, and Selenopheno[3,4-C]pyrrole-4,6-Dione Copolymers: Air-Processed Polymer Solar Cells with Power Conversion Efficiency up to 7.1%. Adv. Energy Mater. 2015, 5, 1501213/1¨C9. "
876,CC1=C2C(C(N(COCCOC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)S1,PTTTPD-EG (P3),5.31,3.54,0.76,4.91,0.56,2.09,"Najari, A.; Beaupr¨¦, S.; Allard, N.; Ouattara, M.; Pouliot, J. R.; Charest, P.; Besner, S.; Simoneau, M.; Leclerc, M. Thieno, Furo, and Selenopheno[3,4-C]pyrrole-4,6-Dione Copolymers: Air-Processed Polymer Solar Cells with Power Conversion Efficiency up to 7.1%. Adv. Energy Mater. 2015, 5, 1501213/1¨C9. "
877,CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)[Se]1,PTTSPD-C8C8 (P4),5.57,3.69,0.88,8.8,0.66,5.11,"Najari, A.; Beaupr¨¦, S.; Allard, N.; Ouattara, M.; Pouliot, J. R.; Charest, P.; Besner, S.; Simoneau, M.; Leclerc, M. Thieno, Furo, and Selenopheno[3,4-C]pyrrole-4,6-Dione Copolymers: Air-Processed Polymer Solar Cells with Power Conversion Efficiency up to 7.1%. Adv. Energy Mater. 2015, 5, 1501213/1¨C9. "
878,CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)O1,PTTFPD-C8C8 (P5),5.65,3.8,0.81,1.57,0.39,0.5,"Najari, A.; Beaupr¨¦, S.; Allard, N.; Ouattara, M.; Pouliot, J. R.; Charest, P.; Besner, S.; Simoneau, M.; Leclerc, M. Thieno, Furo, and Selenopheno[3,4-C]pyrrole-4,6-Dione Copolymers: Air-Processed Polymer Solar Cells with Power Conversion Efficiency up to 7.1%. Adv. Energy Mater. 2015, 5, 1501213/1¨C9. "
879,CC1=C2C(C(N(CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)S3)O1,PTTFPD-C8 (P6),5.54,3.75,0.8,6.76,0.63,3.4,"Najari, A.; Beaupr¨¦, S.; Allard, N.; Ouattara, M.; Pouliot, J. R.; Charest, P.; Besner, S.; Simoneau, M.; Leclerc, M. Thieno, Furo, and Selenopheno[3,4-C]pyrrole-4,6-Dione Copolymers: Air-Processed Polymer Solar Cells with Power Conversion Efficiency up to 7.1%. Adv. Energy Mater. 2015, 5, 1501213/1¨C9. "
880,CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)[Se]4)S3)S1,PTSTPD-C8C8 (P7),5.49,3.82,0.88,8.14,0.61,4.37,"Najari, A.; Beaupr¨¦, S.; Allard, N.; Ouattara, M.; Pouliot, J. R.; Charest, P.; Besner, S.; Simoneau, M.; Leclerc, M. Thieno, Furo, and Selenopheno[3,4-C]pyrrole-4,6-Dione Copolymers: Air-Processed Polymer Solar Cells with Power Conversion Efficiency up to 7.1%. Adv. Energy Mater. 2015, 5, 1501213/1¨C9. "
881,CC1=C2C(C(N(C(CCCCCCCC)CCCCCCCC)C2=O)=O)=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)[Se]4)S3)[Se]1,PTSTPD-C8C8 (P8),5.48,3.69,0.87,7.75,0.68,4.59,"Najari, A.; Beaupr¨¦, S.; Allard, N.; Ouattara, M.; Pouliot, J. R.; Charest, P.; Besner, S.; Simoneau, M.; Leclerc, M. Thieno, Furo, and Selenopheno[3,4-C]pyrrole-4,6-Dione Copolymers: Air-Processed Polymer Solar Cells with Power Conversion Efficiency up to 7.1%. Adv. Energy Mater. 2015, 5, 1501213/1¨C9. "
882,CC1=C2C(C(N(CCCCCCCC)C2=O)=O)=C(C3=CC4=C(C(SC(C)=C5)=C5[Si]4(CC(CC)CCCC)CC(CC)CCCC)S3)[Se]1,PSBTSPD-C8 (P9),5.55,3.82,0.85,13.17,0.64,7.13,"Najari, A.; Beaupr¨¦, S.; Allard, N.; Ouattara, M.; Pouliot, J. R.; Charest, P.; Besner, S.; Simoneau, M.; Leclerc, M. Thieno, Furo, and Selenopheno[3,4-C]pyrrole-4,6-Dione Copolymers: Air-Processed Polymer Solar Cells with Power Conversion Efficiency up to 7.1%. Adv. Energy Mater. 2015, 5, 1501213/1¨C9. "
883,CC1=CC=C(S1)C(S2)=CC3=C2C(N=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C4=O)=O)C4=N5)=C5C6=C3C=C(C)S6,P(PTQD-Th),5.73,3.76,0.92,10.76,0.56,5.54,"Keshtov, M. L.; Kuklin, S. A.; Chen, F. C.; Khokhlov, A. R.; Peregudov, A. S.; Siddiqui, S. A.; Sharma, G. D. Two New D-A Conjugated Polymers P(PTQD-Th and P(PTQD-2Th with Same 9-(2-Octyldodecyl-8H-pyrrolo[3,4-b]bisthieno[2,3-f:3¡ä,2¡ä-h]quinoxaline-8,10(9H-Dione Acceptor and Different Donor Units for BHJ Polymer Solar Cells Application. Org. Electron. 2015, 24, 137¨C146. "
884,CC1=CC(C(C=C(C2=CC=C(C3=CC=C(C)S3)S2)S4)=C4C5=C6N=C7C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C7=O)=O)=N5)=C6S1,P(PTQD-2Th),5.54,3.8,0.8,11.82,0.6,5.67,"Keshtov, M. L.; Kuklin, S. A.; Chen, F. C.; Khokhlov, A. R.; Peregudov, A. S.; Siddiqui, S. A.; Sharma, G. D. Two New D-A Conjugated Polymers P(PTQD-Th and P(PTQD-2Th with Same 9-(2-Octyldodecyl-8H-pyrrolo[3,4-b]bisthieno[2,3-f:3¡ä,2¡ä-h]quinoxaline-8,10(9H-Dione Acceptor and Different Donor Units for BHJ Polymer Solar Cells Application. Org. Electron. 2015, 24, 137¨C146. "
885,CC1=CC(N(CC(CCCCCC)CCCC)C(C2=C3SC(C4=CC(C(OCC(CCCC)CC)=C(SC(C)=C5)C5=C6OCC(CCCC)CC)=C6S4)=C2)=O)=C3S1,PPDT1,5.27,2.68,0.87,8.3,0.453,3.28,"Schneider, A. M.; Lu, L.; Manley, E. F.; Zheng, T.; Sharapov, V.; Xu, T.; Marks, T. J.; Chen, L. X.; Yu, L. Wide Bandgap OPV Polymers Based on Pyridinonedithiophene Unit with Efficiency >5%. Chem. Sci. 2015, 6, 4860¨C4866. "
886,CC1=CC(N(CC(CCCCCC)CCCC)C(C2=C3SC(C4=CC(C(CCC(CCCC)CC)=C(SC(C)=C5)C5=C6CCC(CCCC)CC)=C6S4)=C2)=O)=C3S1,PPDT2,5.47,2.68,0.85,9.26,0.521,4.08,"Schneider, A. M.; Lu, L.; Manley, E. F.; Zheng, T.; Sharapov, V.; Xu, T.; Marks, T. J.; Chen, L. X.; Yu, L. Wide Bandgap OPV Polymers Based on Pyridinonedithiophene Unit with Efficiency >5%. Chem. Sci. 2015, 6, 4860¨C4866. "
887,CC1=CC(N(CC(CCCCCC)CCCC)C(C2=C3SC(C4=CC(C(C5=CC=C(CC(CC)CCCC)S5)=C(SC(C)=C6)C6=C7C8=CC=C(CC(CC)CCCC)S8)=C7S4)=C2)=O)=C3S1,PPDT3,5.36,2.83,0.89,8.5,0.706,5.33,"Schneider, A. M.; Lu, L.; Manley, E. F.; Zheng, T.; Sharapov, V.; Xu, T.; Marks, T. J.; Chen, L. X.; Yu, L. Wide Bandgap OPV Polymers Based on Pyridinonedithiophene Unit with Efficiency >5%. Chem. Sci. 2015, 6, 4860¨C4866. "
888,CC1=CC(N(CC(CCCCCC)CCCC)C(C2=C3SC(C4=CC(CCCCCC)=C(C5=C(CCCCCC)C=C(C)S5)S4)=C2)=O)=C3S1,PPDT4,5.59,2.77,0.86,3.5,0.316,0.95,"Schneider, A. M.; Lu, L.; Manley, E. F.; Zheng, T.; Sharapov, V.; Xu, T.; Marks, T. J.; Chen, L. X.; Yu, L. Wide Bandgap OPV Polymers Based on Pyridinonedithiophene Unit with Efficiency >5%. Chem. Sci. 2015, 6, 4860¨C4866. "
889,O=C(C1=C2SC(C3=CC(C(N(C[C@H](CCCCCCCCCC)CCCCCCCC)C4=C5SC(C6=CC7=C(C(OC[C@@H](CC)CCCC)=C(C=C(C)S8)C8=C7OC[C@@H](CCCC)CC)S6)=C4)=O)=C5S3)=C1)N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C9=C2SC(C)=C9,PBDT-BDTP (P1),5.53,2.68,0.89,10.37,0.547,5.05,"Ding, L.; Lu, F.; Qian, L.; Cao, J.; Feng, Y.; Du, B. D-A Copolymers Containing Lactam Moieties for Polymer Solar Cells. Polym. Chem. 2015, 6, 7373¨C7376. "
890,O=C(C1=C2SC(C3=CC(C(N(C[C@H](CCCCCCCCCC)CCCCCCCC)C4=C5SC=C4C6=CC=C(C)[Se]6)=O)=C5S3)=C1)N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C7=C2SC(C)=C7,PS-BDTP (P2),5.51,2.8,0.91,9.96,0.745,6.76,"Ding, L.; Lu, F.; Qian, L.; Cao, J.; Feng, Y.; Du, B. D-A Copolymers Containing Lactam Moieties for Polymer Solar Cells. Polym. Chem. 2015, 6, 7373¨C7376. "
891,CC1=CC(N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C(C2=C3SC(C4=CC5=C(C(OC[C@H](CC)CCCC)=C(C=C(C)S6)C6=C5OC[C@@H](CCCC)CC)S4)=C2)=O)=C3S1,PDTPO-BDTO,5.38,3.37,0.93,10.4,0.706,6.84,"Hao, M.; Luo, G.; Shi, K.; Xie, G.; Wu, K.; Wu, H.; Yu, G.; Cao, Y.; Yang, C. Dithieno[3,2-b:2¡¯,3¡¯-d]pyridin-5(4H-One-Based Polymers with Bandgap up to 2.02 eV for High Performance Field-Effect Transistors and Polymer Solar Cells with OpenCircuit Voltage up to 0.98 V and Efficiency up to 6.84%. J. Mater. Chem. A 2015, 3, 20516¨C20526. "
892,CC1=CC(N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C(C2=C3SC(C4=CC5=C(C(C6=CC=C(CC(CCCC)CC)S6)=C(C=C(C)S7)C7=C5C8=CC=C(C[C@@H](CCCC)CC)S8)S4)=C2)=O)=C3S1,PDTPO-BDTT,5.44,3.55,0.96,10.1,0.705,6.84,"Hao, M.; Luo, G.; Shi, K.; Xie, G.; Wu, K.; Wu, H.; Yu, G.; Cao, Y.; Yang, C. Dithieno[3,2-b:2¡¯,3¡¯-d]pyridin-5(4H-One-Based Polymers with Bandgap up to 2.02 eV for High Performance Field-Effect Transistors and Polymer Solar Cells with OpenCircuit Voltage up to 0.98 V and Efficiency up to 6.84%. J. Mater. Chem. A 2015, 3, 20516¨C20526. "
893,CC(S1)=CC=C1C2=C(OCC(CCCCCC)CCCCCCCC)C=C(C3=CC=C(C4=CC=C(C)C5=NSN=C45)S3)C(OCC(CCCCCCCC)CCCCCC)=C2,PPDTBT,5.29,3.57,0.81,10.4,0.61,5.08,"Nguyen, T. L.; Choi, H.; Ko, S.-J.; Uddin, M. A.; Walker, B.; Yum, S.; Jeong, J.-E.; Yun, M. H.; Shin, T. J.; Hwang, S.; Kim, J. Y.; Woo, H. Y. Semi-Crystalline Photovoltaic Polymers with Efficiency Exceeding 9% in a ~300 nm Thick Conventional Single-Cell Device. Energy Environ. Sci. 2014, 7, 3040¨C3051. "
894,CC(S1)=CC=C1C2=C(OCC(CCCCCC)CCCCCCCC)C=C(C3=CC=C(C4=C(F)C=C(C)C5=NSN=C45)S3)C(OCC(CCCCCCCC)CCCCCC)=C2,PPDTFBT,5.35,3.63,0.81,10.2,0.62,5.11,"Nguyen, T. L.; Choi, H.; Ko, S.-J.; Uddin, M. A.; Walker, B.; Yum, S.; Jeong, J.-E.; Yun, M. H.; Shin, T. J.; Hwang, S.; Kim, J. Y.; Woo, H. Y. Semi-Crystalline Photovoltaic Polymers with Efficiency Exceeding 9% in a ~300 nm Thick Conventional Single-Cell Device. Energy Environ. Sci. 2014, 7, 3040¨C3051. "
895,CC(S1)=CC=C1C2=C(OCC(CCCCCC)CCCCCCCC)C=C(C3=CC=C(C4=C(F)C(F)=C(C)C5=NSN=C45)S3)C(OCC(CCCCCCCC)CCCCCC)=C2,PPDT2FBT,5.45,3.69,0.86,11.4,0.74,7.26,"Nguyen, T. L.; Choi, H.; Ko, S.-J.; Uddin, M. A.; Walker, B.; Yum, S.; Jeong, J.-E.; Yun, M. H.; Shin, T. J.; Hwang, S.; Kim, J. Y.; Woo, H. Y. Semi-Crystalline Photovoltaic Polymers with Efficiency Exceeding 9% in a ~300 nm Thick Conventional Single-Cell Device. Energy Environ. Sci. 2014, 7, 3040¨C3051. "
896,O=C(C1=C2SC(C3=CC(C(N(C[C@H](CCCCCCCCCC)CCCCCCCC)C4=C5SC=C4C6=CC=C(C)S6)=O)=C5S3)=C1)N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C7=C2SC(C)=C7,PThBDTP,5.52,2.74,0.96,12.59,0.755,9.13,"Cao, J.; Qian, L.; Lu, F.; Zhang, J.; Feng, Y.; Qiu, X.; Yip, H.-L.; Ding, L. A Lactam Building Block for Efficient Polymer Solar Cells. Chem. Commun. 2015, 51, 11830¨C11833. "
897,CC1=C2C(N=C(CCCCCCCC)S2)=C(C3=CC=C(C4=CC=C(C)C=C4C5(CCCCCC)CCCCCC)C5=C3)S1,PFTTz,5.58,3.55,0.91,7.2,0.4,2.64,"Jo, J. W.; Kim, S. S.; Jo, W. H. Synthesis of thieno[3,4-d]thiazole-Based Conjugated Polymers and HOMO Level Tuning for High V OC Photovoltaic Cell. Org. Electron.2012, 13, 1322¨C1328. "
898,CC1=C2C(N=C(CCCCCCCC)S2)=C(C3=CC=C(C4=CC=C(C)C=C4N5C(CCCCCC)CCCCCC)C5=C3)S1,PCTTz,5.46,3.56,0.76,2.27,0.41,0.71,"Jo, J. W.; Kim, S. S.; Jo, W. H. Synthesis of thieno[3,4-d]thiazole-Based Conjugated Polymers and HOMO Level Tuning for High V OC Photovoltaic Cell. Org. Electron.2012, 13, 1322¨C1328. "
899,CC1=C2C(N=C(CCCCCCCC)S2)=C(C3=CC4=C(C(OCC(CCCC)CC)=C(C=C(C)S5)C5=C4OCC(CC)CCCC)S3)S1,PBTTz,5.24,3.57,0.52,4.64,0.58,1.41,"Jo, J. W.; Kim, S. S.; Jo, W. H. Synthesis of thieno[3,4-d]thiazole-Based Conjugated Polymers and HOMO Level Tuning for High V OC Photovoltaic Cell. Org. Electron.2012, 13, 1322¨C1328. "
900,CC1=CC=C(C(C2(CCCCCC)CCCCCC)=C1)C3=C2C=C(C4=CC=C(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NSN=C86)S5)C=C4C9(CCCCCC)CCCCCC)C9=C3,PIFTBT6,5.49,3.46,0.98,3.25,0.31,0.97,"Zheng, Q.; Jung, B. J.; Sun, J.; Katz, H. E. Ladder-Type Oligo- P -PhenyleneContaining Copolymers with High Open-Circuit Voltages and Ambient Photovoltaic Activity. J. Am. Chem. Soc. 2010, 132, 5394¨C5404. "
901,CC1=CC=C(C(C2(CCCCCCCCCC)CCCCCCCCCC)=C1)C3=C2C=C(C4=CC=C(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NSN=C86)S5)C=C4C9(CCCCCCCCCC)CCCCCCCCCC)C9=C3,PIFTBT10,5.45,3.36,1,6.1,0.4,2.44,"Zheng, Q.; Jung, B. J.; Sun, J.; Katz, H. E. Ladder-Type Oligo- P -PhenyleneContaining Copolymers with High Open-Circuit Voltages and Ambient Photovoltaic Activity. J. Am. Chem. Soc. 2010, 132, 5394¨C5404. "
902,CC1=CC=C(C(C2(CCCCCCCCCC)CCCCCCCCCC)=C1)C3=C2C=C(C4=CC=C(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NC(C9=CC=CC=C9)C(C%10=CC=CC=C%10)N=C86)S5)C=C4C%11(CCCCCCCCCC)CCCCCCCCCC)C%11=C3,PIFDTQ10,5.47,3.44,1,7.57,0.4,3.04,"Zheng, Q.; Jung, B. J.; Sun, J.; Katz, H. E. Ladder-Type Oligo- P -PhenyleneContaining Copolymers with High Open-Circuit Voltages and Ambient Photovoltaic Activity. J. Am. Chem. Soc. 2010, 132, 5394¨C5404. "
903,CC1=CC=C(S1)C(C2=NSN=C23)=CC=C3C4=CC=C(C5=CC=C6C7=CC8=C(C=C7C(CCCCCC)(CCCCCC)C6=C5)C9=CC%10=C(C(C=CC(C%11=CC=C(C)C=C%11)=C%12)=C%12C%10(CCCCCC)CCCCCC)C=C9C8(CCCCCC)CCCCCC)S4,P3FTBT6,5.45,3.45,1.04,10.3,0.42,4.5,"Zheng, Q.; Jung, B. J.; Sun, J.; Katz, H. E. Ladder-Type Oligo- P -PhenyleneContaining Copolymers with High Open-Circuit Voltages and Ambient Photovoltaic Activity. J. Am. Chem. Soc. 2010, 132, 5394¨C5404. "
904,CC1=CC=C(C2=CC=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5C6(CC(CC)CCCC)CC(CCCC)CC)C6=C2)S1,PITBT,5.48,3.66,0.94,12.51,0.502,5.92,"Wang, M.; Cai, D.; Yin, Z.; Chen, S. C.; Du, C. F.; Zheng, Q. AsymmetricIndenothiophene-Based Copolymers for Bulk Heterojunction Solar Cells with 9.14% Efficiency. Adv. Mater. 2016, 28, 3359¨C3365. "
905,CC1=CC=C(C2=CC=C(C(SC(C3=C(F)C=C(C)C4=NSN=C43)=C5)=C5C6(CC(CC)CCCC)CC(CCCC)CC)C6=C2)S1,PITFBT,5.5,3.68,0.9,15.36,0.659,9.14,"Wang, M.; Cai, D.; Yin, Z.; Chen, S. C.; Du, C. F.; Zheng, Q. AsymmetricIndenothiophene-Based Copolymers for Bulk Heterojunction Solar Cells with 9.14% Efficiency. Adv. Mater. 2016, 28, 3359¨C3365. "
906,CC1=CC=C(S1)C(C2=NSN=C23)=C(OCCCCCCCC)C(OCCCCCCCC)=C3C4=CC=C(C5=CC(N(CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)S4,HXS-1,5.21,3.35,0.81,9.8,0.69,5.4,"Ruiping, Q.; Weiwei, L.; Cuihong, L.; Chun, D.; Veit, C.; Schleiermacher, H.-F.; Andersson, M.; Zhishan, B.; Zhengping, L.; Ingan?s, O.; Wuerfel, U.; Fengling, Z. A Planar Copolymer for High Efficiency Polymer Solar Cells. J. Am. Chem. Soc. 2009, 131, 14612¨C14613. "
907,CC1=C([H])C=C(C(S2)=C3C(C(N(CCCCCCCC)C3=O)=O)=C2C4=CC([H])=C(C5=CC(N(C(CCCCCCCC)CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)S4)S1,PCDTTPD,5.71,3.74,1.07,4.72,0.36,1.82,"Najari, A.; Berrouard, P.; Ottone, C.; Boivin, M.; Zou, Y.; Gendron, D.; Caron, W.; Legros, P.; Allen, C. N.; Leclerc, M. High Open-Circuit Voltage Solar Cells Based on New Thieno[3,4-c]pyrrole-4,6-dione and 2,7-Carbazole Copolymers. Macromolecules2012, 45, 1833¨C1838. "
908,CC1=C(CCCCCCCC)C=C(C(S2)=C3C(C(N(CCCCCCCC)C3=O)=O)=C2C4=CC(CCCCCCCC)=C(C5=CC(N(C(CCCCCCCC)CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)S4)S1,PCDTTPD-ic,5.47,3.39,1.01,0.56,0.25,0.14,"Najari, A.; Berrouard, P.; Ottone, C.; Boivin, M.; Zou, Y.; Gendron, D.; Caron, W.; Legros, P.; Allen, C. N.; Leclerc, M. High Open-Circuit Voltage Solar Cells Based on New Thieno[3,4-c]pyrrole-4,6-dione and 2,7-Carbazole Copolymers. Macromolecules2012, 45, 1833¨C1838. "
909,CC1=C([H])C=C(C(S2)=C3C(C(N(CC(CCCCCCCC)CCCCCC)C3=O)=O)=C2C4=CC([H])=C(C5=CC(N(C(CCCCCCCC)CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)S4)S1,PCDTTPD-C6C8,5.5,3.5,1,0.35,0.39,0.13,"Najari, A.; Berrouard, P.; Ottone, C.; Boivin, M.; Zou, Y.; Gendron, D.; Caron, W.; Legros, P.; Allen, C. N.; Leclerc, M. High Open-Circuit Voltage Solar Cells Based on New Thieno[3,4-c]pyrrole-4,6-dione and 2,7-Carbazole Copolymers. Macromolecules2012, 45, 1833¨C1838. "
910,CC1=CC=C(C(S2)=C3C(C(N(CC(CCCCCCCC)CCCCCC)C3=O)=O)=C2C4=CC=C(C5=CC(N(C(CCCCCCCC)CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)S4)S1,PCTTPD,5.72,3.69,0.94,2.7,0.45,1.14,"Uddin, M. A.; Kim, T.; Yum, S.; Choi, H.; Hwang, S.; Kim, J. Y.; Woo, H. Y. 2,7-Carbazole and thieno[3,4-c]pyrrole-4,6-Dione Based Copolymers with Deep Highest Occupied Molecular Orbital for Photovoltaic Cells. Curr. Appl. Phys. 2015, 15, 654¨C661. "
911,CC1=CC=C(C(C=C2)=C(N3C(CCCCCCCC)CCCCCCCC)C=C2C4=CC5=C(C=C(C6=C(C(N(CC(CCCCCCCC)CCCCCC)C7=O)=O)C7=C(C8=CC9=C(C=C(C)S9)S8)S6)S5)S4)C3=C1,PCTTTPD,5.67,3.65,0.9,3.86,0.36,1.25,"Uddin, M. A.; Kim, T.; Yum, S.; Choi, H.; Hwang, S.; Kim, J. Y.; Woo, H. Y. 2,7-Carbazole and thieno[3,4-c]pyrrole-4,6-Dione Based Copolymers with Deep Highest Occupied Molecular Orbital for Photovoltaic Cells. Curr. Appl. Phys. 2015, 15, 654¨C661. "
912,CC1=CC=C(C(C=C2)=C(N3C(CCCCCCCC)CCCCCCCC)C=C2C4=CC=C(C5=CC=C(C6=C(C(N(CC(CCCCCCCC)CCCCCC)C7=O)=O)C7=C(C8=CC=C(C9=CC=C(C)S9)S8)S6)S5)S4)C3=C1,PCBTTPD,5.57,3.66,0.86,7.79,0.51,3.42,"Uddin, M. A.; Kim, T.; Yum, S.; Choi, H.; Hwang, S.; Kim, J. Y.; Woo, H. Y. 2,7-Carbazole and thieno[3,4-c]pyrrole-4,6-Dione Based Copolymers with Deep Highest Occupied Molecular Orbital for Photovoltaic Cells. Curr. Appl. Phys. 2015, 15, 654¨C661. "
913,CC1=C2C(N=C(C3=CC(OCC(CCCC)CC)=CC=C3)C(C4=CC=CC(OCC(CCCC)CC)=C4)=N2)=C(C5=CSC6=C5C(C=C(CCCCCC)S7)=C7C8=CC9=C(C=C86)N(CCCCCC)C(C9=C%10)=CC%11=C%10C(SC(CCCCCC)=C%12)=C%12C%13=C%11SC(C)=C%13)C=C1,PTTDBC-PhQC8,5.31,3.42,0.88,7.13,0.42,2.63,"Li, Z.; Zang, Y.; Chueh, C.; Cho, N.; Lu, J.; Wang, X.; Huang, J.; Li, C.; Yu, J.; Jen, A. K. Tetrathienodibenzocarbazole Based Donor ? Acceptor Type Wide Band-Gap Copolymers for Polymer Solar Cell Applications. Macromolecules 2014, 47, 7407¨C7415. "
914,CC1=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C(C2=CSC3=C2C(C=C(CCCCCC)S4)=C4C5=CC6=C(C=C53)N(CCCCCC)C(C6=C7)=CC8=C7C(SC(CCCCCC)=C9)=C9C%10=C8SC(C)=C%10)C%11=NSN=C1%11,PTTDBC-BTC12,5.35,3.41,0.93,8.78,0.55,4.5,"Li, Z.; Zang, Y.; Chueh, C.; Cho, N.; Lu, J.; Wang, X.; Huang, J.; Li, C.; Yu, J.; Jen, A. K. Tetrathienodibenzocarbazole Based Donor ? Acceptor Type Wide Band-Gap Copolymers for Polymer Solar Cell Applications. Macromolecules 2014, 47, 7407¨C7415. "
915,CC1=CC(C2(CCCCCC)CCCCCC)=C(C=C1)C3=C2C=C(C(C=C4C(C5=CC=C(C6=CC=C(C7=CC=C(C8=CC=C(C)S8)C9=NSN=C97)S6)C=C5C4(CCCCCC)CCCCCC)=C%10)=C%10N%11CC(CC)CCCC)C%11=C3,PC1,5.41,3.67,0.88,5.77,0.441,2.45,"Wang, L.; Cai, D.; Yin, Z.; Tang, C.; Chen, S.-C.; Zheng, Q. DiindenocarbazoleBased Large Bandgap Copolymers for High-Performance Organic Solar Cells with Large Open Circuit Voltages. Polym. Chem. 2014, 5, 6847¨C6856."
916,CC1=CC(C2(CCCCCC)CCCCCC)=C(C=C1)C3=C2C=C(C(C=C4C(C5=CC=C(C6=CC=C(C7=C(OCCCC)C(OCCCC)=C(C8=CC=C(C)S8)C9=NSN=C97)S6)C=C5C4(CCCCCC)CCCCCC)=C%10)=C%10N%11CC)C%11=C3,PC2,5.43,3.56,0.94,12.84,0.587,7.26,"Wang, L.; Cai, D.; Yin, Z.; Tang, C.; Chen, S.-C.; Zheng, Q. DiindenocarbazoleBased Large Bandgap Copolymers for High-Performance Organic Solar Cells with Large Open Circuit Voltages. Polym. Chem. 2014, 5, 6847¨C6856."
917,CC1=CC(C2(CCCCCC)CCCCCC)=C(C=C1)C3=C2C=C(C(C=C4C(C5=CC=C(C6=CC=C(C7=C(OCCCC)C(OCCCC)=C(C8=CC=C(C)S8)C9=NSN=C97)S6)C=C5C4(CCCCCC)CCCCCC)=C%10)=C%10N%11CC(CC)CCCC)C%11=C3,PC3,5.44,3.65,0.93,11.18,0.633,6.68,"Wang, L.; Cai, D.; Yin, Z.; Tang, C.; Chen, S.-C.; Zheng, Q. DiindenocarbazoleBased Large Bandgap Copolymers for High-Performance Organic Solar Cells with Large Open Circuit Voltages. Polym. Chem. 2014, 5, 6847¨C6856."
918,CC1=C(F)C=C(C2=CC(F)=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)C=C2N7CC(CCCCCC)CCCCCCCC)C7=C1,HD-PDFC-DTBT,5.32,3.3,0.93,14.11,0.563,7.39,"Wei, H.; Chao, Y.; Kang, C.; Li, C.; Lu, H.; Gong, X.; Dong, H.; Hu, W.; Hsu, C.; Bo, Z. High-Effi Ciency Large-Bandgap Material for Polymer Solar Cells. Macromol. Rapid Commun. 2015, 36, 84¨C89. "
919,CC1=CC(N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C2=C3C=CC(C)=C2)=C3C=C1,PCz,5.6,3.6,0.71,0.26,0.37,0.07,"Li, J.; Dierschke, F.; Wu, J.; Grimsdale, A. C.; M¨¹llen, K. Poly(2,7-Carbazole and Perylene Tetracarboxydiimide: A Promising Donor/acceptor Pair for Polymer Solar Cells. J. Mater. Chem. 2006, 16, 96¨C100. "
920,CC(C=C1)=CC=C1C2=C3C=C(OCCCCCCCC)C(OCCCCCCCC)=CC3=C(C4=CC=C(C5=CC=C(C6=C(OCCCCCCCC)C(OCCCCCCCC)=C(C7=CC=C(C)S7)C8=NSN=C86)S5)C=C4)C9=C2C=C(OCCCCCCCC)C(OCCCCCCCC)=C9,PAn-BTBT (P1),5.4,3.28,0.96,4.4,0.53,2.23,"Gong, X.; Li, C.; Lu, Z.; Li, G.; Mei, Q.; Fang, T.; Bo, Z. Anthracene-Containing Wide-Band-Gap Conjugated Polymers for High-Open-Circuit-Voltage Polymer Solar Cells. Macromol. Rapid Commun. 2013, 34, 1163¨C1168. "
921,CC(C=C1)=CC=C1C2=C3C=C(OCCCCCCCC)C(OCCCCCCCC)=CC3=C(C4=CC=C(C5=CC=C(C6=C(N=C(C7=CC(OCCCCCCCC)=CC=C7)C(C8=CC=CC(OCCCCCCCC)=C8)=N9)C9=C(C%10=CC=C(C)S%10)C=C6)S5)C=C4)C%11=C2C=C(OCCCCCCCC)C(OCCCCCCCC)=C%11,PAn-BTBT (P2),5.3,3.19,0.89,3,0.53,1.42,"Gong, X.; Li, C.; Lu, Z.; Li, G.; Mei, Q.; Fang, T.; Bo, Z. Anthracene-Containing Wide-Band-Gap Conjugated Polymers for High-Open-Circuit-Voltage Polymer Solar Cells. Macromol. Rapid Commun. 2013, 34, 1163¨C1168. "
922,CC1=CC=C(C(C=C(C2=CC=C(C3=C(OCCCCCCCC)C(OCCCCCCCC)=C(C4=CC=C(C)S4)C5=NSN=C35)S2)C=C6)=C6C7=C(C(OCC(CCCC)CC)=O)SC(C(OCC(CCCC)CC)=O)=C78)C8=C1,PTP27-DBT,5.4,2.91,0.82,10.2,0.41,3.5,"Huang, J.; Xiao, B.; Wang, J.; Wang, Y.; Peng, X.; Miao, X.; Pan, Q.; Mo, Y.; Deng, W.; Wu, H.; Cao, Y. Synthesis and Characterizations of poly(3,6-Thienophenanthrene and poly(2,7-Thienophenanthrene and Their Applications in Polymer Light-Emitting Devices and Solar Cells. Org. Electron. 2014, 15, 2311¨C2321. "
923,CC1=CC=C(C(C=CC(C2=CC=C(C3=C(OCCCCCCCC)C(OCCCCCCCC)=C(C4=CC=C(C)S4)C5=NSN=C35)S2)=C6)=C6C7=C(C(OCC(CCCC)CC)=O)SC(C(OCC(CCCC)CC)=O)=C78)C8=C1,PTP36-DBT,5.7,3.18,0.79,4.4,0.268,0.9,"Huang, J.; Xiao, B.; Wang, J.; Wang, Y.; Peng, X.; Miao, X.; Pan, Q.; Mo, Y.; Deng, W.; Wu, H.; Cao, Y. Synthesis and Characterizations of poly(3,6-Thienophenanthrene and poly(2,7-Thienophenanthrene and Their Applications in Polymer Light-Emitting Devices and Solar Cells. Org. Electron. 2014, 15, 2311¨C2321. "
924,CC1=CC=C(C2=C(C(N(CC(CC)CCCC)C3=O)=O)C3=C(C4=CC=C(C5=CC(C(OCCCCCCCCCCCC)=C(SC(C)=C6)C6=C7OCCCCCCCCCCCC)=C7S5)S4)C=C2)S1,PPhIBDT-C12 (P2),5.36,3.02,0.8,3.43,0.547,1.5,"Huang, J.; Wang, X.; Zhan, C.; Zhao, Y.; Sun, Y.; Pei, Q.; Liu, Y.; Yao, J. Wide Band Gap Copolymers Based on Phthalimide: Synthesis, Characterization, and Photovoltaic Properties with 3.70% Efficiency. Polym. Chem. 2013, 4, 2174¨C2182. "
925,CC1=CC=C(C2=C(C(N(CC(CC)CCCC)C3=O)=O)C3=C(C4=CC=C(C5=CC(C(C6=CC=C(CC(CCCC)CC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(CC(CCCC)CC)S9)=C8S5)S4)C=C2)S1,PPhIBDT-ThEH (P3),5.57,3.07,0.89,7.01,0.586,3.7,"Huang, J.; Wang, X.; Zhan, C.; Zhao, Y.; Sun, Y.; Pei, Q.; Liu, Y.; Yao, J. Wide Band Gap Copolymers Based on Phthalimide: Synthesis, Characterization, and Photovoltaic Properties with 3.70% Efficiency. Polym. Chem. 2013, 4, 2174¨C2182. "
926,CC(S1)=CC(CC(CCCC)CC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CCCC)CC)C=C(/C=C/C)S4,PTTEHV,5.4,3.53,0.53,5.02,0.39,1.19,"Subramaniyan, S.; Xin, H.; Kim, F. S.; Murari, N. M.; Courtright, B. A. E.; Jenekhe, S. A. Thiazolothiazole Donor-Acceptor Conjugated Polymer Semiconductors for Photovoltaic Applications. Macromolecules 2014, 47, 4199¨C4209. "
927,CC(S1)=CC(CC(CCCC)CC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CCCC)CC)C=C(C5=CC(N(C(CC(CC)CCCC)CC(CCCC)CC)C6=C7C=CC(C)=C6)=C7C=C5)S4,PCEHTT,5.32,3.44,0.69,5,0.25,0.87,"Subramaniyan, S.; Xin, H.; Kim, F. S.; Murari, N. M.; Courtright, B. A. E.; Jenekhe, S. A. Thiazolothiazole Donor-Acceptor Conjugated Polymer Semiconductors for Photovoltaic Applications. Macromolecules 2014, 47, 4199¨C4209. "
928,CC(S1)=CC(CCCCCCCC)=C1C2=NC(S3)=C(S2)N=C3C4=C(CCCCCCCC)C=C(C5=C(CCCCCCCC)C=C(C6=CC(CCCCCCCC)=C(C)S6)S5)S4,PBTOTT,5.16,3.34,0.75,5.3,0.25,1.03,"Subramaniyan, S.; Xin, H.; Kim, F. S.; Murari, N. M.; Courtright, B. A. E.; Jenekhe, S. A. Thiazolothiazole Donor-Acceptor Conjugated Polymer Semiconductors for Photovoltaic Applications. Macromolecules 2014, 47, 4199¨C4209. "
929,CC(S1)=CC(CC(CC)CCCC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CC)CCCC)C=C(C5=CC6=C(C(SC(C)=C7)=C7C6(C[C@H](CC)CCCC)CC(CC)CCCC)S5)S4,PCPEHTT,5.01,3.3,0.73,9.68,0.34,2.41,"Subramaniyan, S.; Xin, H.; Kim, F. S.; Murari, N. M.; Courtright, B. A. E.; Jenekhe, S. A. Thiazolothiazole Donor-Acceptor Conjugated Polymer Semiconductors for Photovoltaic Applications. Macromolecules 2014, 47, 4199¨C4209. "
930,CC(S1)=CC(OCCCCCCCC)=C1C2=NC(S3)=C(S2)N=C3C4=C(OCCCCCCCC)C=C(C5=C(CCCCCCCC)C=C(C6=CC(CCCCCCCC)=C(C)S6)S5)S4,PBTOxTT,4.91,2.77,0.53,5.54,0.31,0.94,"Subramaniyan, S.; Xin, H.; Kim, F. S.; Murari, N. M.; Courtright, B. A. E.; Jenekhe, S. A. Thiazolothiazole Donor-Acceptor Conjugated Polymer Semiconductors for Photovoltaic Applications. Macromolecules 2014, 47, 4199¨C4209. "
931,CC(S1)=CC(CC(CCCC)CC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CCCC)CC)C=C(S4)C5=CC6=C(C(SC(C)=C7)=C7N6CC(CCCCCCCC)CCCCCC)S5,PPEHTT,4.91,3.18,0.5,4.41,0.36,0.82,"Subramaniyan, S.; Xin, H.; Kim, F. S.; Murari, N. M.; Courtright, B. A. E.; Jenekhe, S. A. Thiazolothiazole Donor-Acceptor Conjugated Polymer Semiconductors for Photovoltaic Applications. Macromolecules 2014, 47, 4199¨C4209. "
932,CC(S1)=CC(CC(CCCC)CC)=C1C2=NC(S3)=C(S2)N=C3C4=C(C[C@@H](CCCC)CC)C=C(S4)C5=CC6=C(OC[C@@H](CCCCCC)CCCC)C7=C(C=C(C)S7)C(OCC(CCCCCC)CCCC)=C6S5,PDEHTT,5.65,3.68,0.74,10.8,0.7,5.71,"Subramaniyan, S.; Xin, H.; Kim, F. S.; Murari, N. M.; Courtright, B. A. E.; Jenekhe, S. A. Thiazolothiazole Donor-Acceptor Conjugated Polymer Semiconductors for Photovoltaic Applications. Macromolecules 2014, 47, 4199¨C4209. "
933,CC(S1)=CC=C1C2=CC(N3C[C@@H](CCCC)CCCCCC)=C(C(C(N(CC(CCCC)CCCCCC)C4=O)=CC(C5=CC=C(S5)C6=CC7=C(OC[C@@H](CCCCCC)CCCC)C8=C(C=C(C)S8)C(OCC(CCCCCC)CCCC)=C7S6)=C9)=C9C3=O)C4=C2,POAPPO-BDT (Pa),5.41,3.28,0.92,8.19,0.602,4.54,"Liu, M.; Liang, Y.; Chen, P.; Chen, D.; Liu, K.; Li, Y.; Liu, S.; Gong, X.; Huang, F.; Su, S.-J.; Cao, Y. Three Pyrido[2,3,4,5-lmn]phenanthridine Derivatives and Their Large Band Gap Copolymers for Organic Solar Cells. J. Mater. Chem. A 2014, 2, 321¨C325. "
934,CC(S1)=CC=C1C2=CC3=C(C(C(N(CC(CCCC)CCCCCC)C4=O)=CC(C5=CC=C(S5)C6=CC7=C(OC[C@@H](CCCCCC)CCCC)C8=C(C=C(C)S8)C(OCC(CCCCCC)CCCC)=C7S6)=C9)=C9C(OCC(CCCCCC)CCCC)=N3)C4=C2,POAPPO-BDT (Pb),5.34,3.15,0.66,1.51,0.462,0.46,"Liu, M.; Liang, Y.; Chen, P.; Chen, D.; Liu, K.; Li, Y.; Liu, S.; Gong, X.; Huang, F.; Su, S.-J.; Cao, Y. Three Pyrido[2,3,4,5-lmn]phenanthridine Derivatives and Their Large Band Gap Copolymers for Organic Solar Cells. J. Mater. Chem. A 2014, 2, 321¨C325. "
935,CC(S1)=CC=C1C2=CC3=C(C(C(N=C4OCC(CCCCCC)CCCC)=CC(C5=CC=C(S5)C6=CC7=C(OC[C@@H](CCCCCC)CCCC)C8=C(C=C(C)S8)C(OCC(CCCCCC)CCCC)=C7S6)=C9)=C9C(OCC(CCCCCC)CCCC)=N3)C4=C2,POAPPO-BDT (Pc),5.3,3.09,0.66,5.46,0.596,2.15,"Liu, M.; Liang, Y.; Chen, P.; Chen, D.; Liu, K.; Li, Y.; Liu, S.; Gong, X.; Huang, F.; Su, S.-J.; Cao, Y. Three Pyrido[2,3,4,5-lmn]phenanthridine Derivatives and Their Large Band Gap Copolymers for Organic Solar Cells. J. Mater. Chem. A 2014, 2, 321¨C325. "
936,O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(OC[C@@H](CC)CCCC)=C5C(SC(C)=C5)=C4OCC(CC)CCCC)=C21)=O,PBDTTPD,5.56,3.75,0.93,10.89,0.7,7.1,"A?ch, B. R.; Lu, J.; Beaupr¨¦, S.; Leclerc, M.; Tao, Y. Control of the Active Layer Nanomorphology by Using Co-Additives towards High-Performance Bulk Heterojunction Solar Cells. Org. Electron. 2012, 13, 1736¨C1741. "
937,O=C1N(C(CCCCCCCC)CCCCCCCC)C(C2=C(C)SC(C3=CC4=C(OC[C@@H](CC)CCCC)C5=CC(SC(C)=C6)=C6C(OC[C@@H](CC)CCCC)=C5C=C4S3)=C21)=O,PNDTTPD (P1),5.3,3.5,0.69,11.54,0.5,4,"Sanjaykumar, S. R.; Badgujar, S.; Song, C. E.; Shin, W. S.; Moon, S. J.; Kang, I. N.; Lee, J.; Cho, S.; Lee, S. K.; Lee, J. C. Synthesis and Characterization of a Novel Naphthodithiophene-Based Copolymer for Use in Polymer Solar Cells. Macromolecules2012, 45, 6938¨C6945. "
938,O=C1N(C(CCCCCCCC)CCCCCCCC)C(C2=C(C)SC(C3=CC4=C(OC[C@@H](CC)CCCC)C(SC(C)=C5)=C5C(OCC(CC)CCCC)=C4S3)=C21)=O,PBDTTPD (P2),5.47,3.59,0.78,8.37,0.52,3.4,"Sanjaykumar, S. R.; Badgujar, S.; Song, C. E.; Shin, W. S.; Moon, S. J.; Kang, I. N.; Lee, J.; Cho, S.; Lee, S. K.; Lee, J. C. Synthesis and Characterization of a Novel Naphthodithiophene-Based Copolymer for Use in Polymer Solar Cells. Macromolecules2012, 45, 6938¨C6945. "
939,O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(OC[C@@H](CC)CCCC)=C5C(SC(C)=C5)=C4OCC(CC)CCCC)=C21)=O,PBDTTPD,5.43,3.4,0.87,9.1,0.538,4.2,"Zhang, Y.; Hau, S. K.; Yip, H. L.; Sun, Y.; Acton, O.; Jen, A. K. Y. Efficient Polymer Solar Cells Based on the Copolymers of Benzodithiophene and Thienopyrroledione. Chem. Mater. 2010, 22, 2696¨C2698. "
940,CC1=C(C(N(CCCCCCCC)C2=O)=O)C2=C(C(S3)=C(CCCCCC)C(CCCCCC)=C3C4=C(C(N(CCCCCCCC)C5=O)=O)C5=C(C6=CC(C(C7=CC=C(CC(CCCC)CC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(C[C@@H](CCCC)CC)S%10)=C9S6)S4)S1,PBDTT-LTPD,5.62,3.43,1,14.32,0.52,7.59,"Xia, B.; Lu, K.; Zhao, Y.; Zhang, J.; Yuan, L.; Zhu, L.; Yi, Y.; Wei, Z. LinkedAcceptor Type Conjugated Polymer for High Performance Organic Photovoltaics with an Open-Circuit Voltage Exceeding 1 V. Adv. Sci. 2015, 2, 1500021/1¨C9. "
941,CC1=CC2=C(C(C(OCC(CCCCCCCCCC)CCCCCCCCCCCC)=NC(C=C3)=C4C5=C3C6=C7SC(C8=CC=C(C9=C(C(N(CC(CCCC)CC)C%10=O)=O)C%10=C(C%11=CC=C(C)S%11)S9)S8)=C6)=C4C%12=C2C=CC%13=C%12C5=C7C(OCC(CCCCCCCCCC)CCCCCCCCCCCC)=N%13)S1,PTAC-TPD (P1),5.35,3.51,0.89,8.1,0.67,4.8,"He, B.; Pun, A. B.; Klivansky, L. M.; McGough, A. M.; Ye, Y.; Zhu, J.; Guo, J.; Teat, S. J.; Liu, Y. Thiophene Fused Azacoronenes: Regioselective Synthesis, SelfOrganization, Charge Transport and Its Incorporation in Conjugated Polymers. Chem. Mater. 2014, 26, 3920¨C3927. "
942,CC1=CC(N(C2=CC=C(OCCCCCCCC)C=C2)C3=C4C=CC(/C=C/C)=C3)=C4C=C1,PCV,5.61,2.83,0.85,0.889,0.464,0.4,"Leclerc, N.; Michaud, A.; Sirois, K.; Morin, J. F.; Leclerc, M. Synthesis of 2,7-Carbazolenevinylene-Based Copolymers and Characterization of Their Photovoltaic Properties. Adv. Funct. Mater. 2006, 16, 1694¨C1704. "
943,C/C=C/C1=CC(N(C2=CC=C(OCCCCCCCC)C=C2)C3=C4C=CC(/C=C/C5=CC=C(C)S5)=C3)=C4C=C1,PCVT,5.52,2.92,0.7,1.076,0.445,0.4,"Leclerc, N.; Michaud, A.; Sirois, K.; Morin, J. F.; Leclerc, M. Synthesis of 2,7-Carbazolenevinylene-Based Copolymers and Characterization of Their Photovoltaic Properties. Adv. Funct. Mater. 2006, 16, 1694¨C1704. "
944,C/C=C/C1=CC(N(C2=CC=C(OCCCCCCCC)C=C2)C3=C4C=CC(/C=C/C5=C(CCCCCCCC)C=C(C6=CC(CCCCCCCC)=C(C)S6)S5)=C3)=C4C=C1,PCVTT,5.49,3.02,0.55,0.859,0.484,0.3,"Leclerc, N.; Michaud, A.; Sirois, K.; Morin, J. F.; Leclerc, M. Synthesis of 2,7-Carbazolenevinylene-Based Copolymers and Characterization of Their Photovoltaic Properties. Adv. Funct. Mater. 2006, 16, 1694¨C1704. "
945,C/C=C/C1=CC(N(C2=CC=C(OCCCCCCCC)C=C2)C3=C4C=CC(/C=C/C5=C(CCCCCCCC)C=C(C6=CC=C(C7=CC=C(C8=CC(CCCCCCCC)=C(C)S8)S7)S6)S5)=C3)=C4C=C1,PCVTTTT,5.4,2.96,0.5,0.761,0.432,0.2,"Leclerc, N.; Michaud, A.; Sirois, K.; Morin, J. F.; Leclerc, M. Synthesis of 2,7-Carbazolenevinylene-Based Copolymers and Characterization of Their Photovoltaic Properties. Adv. Funct. Mater. 2006, 16, 1694¨C1704. "
946,C/C=C/C1=CC(N(C2=CC=C(OCCCCCCCC)C=C2)C3=C4C=CC(/C=C/C5=CC=C(C6=CC=C(C7=C(CCCCCC)C(CCCCCC)=C(C8=CC=C(C9=CC=C(C)S9)S8)S7(=O)=O)S6)S5)=C3)=C4C=C1,PCPTDO,5.5,3.5,0.8,1.558,0.546,0.8,"Leclerc, N.; Michaud, A.; Sirois, K.; Morin, J. F.; Leclerc, M. Synthesis of 2,7-Carbazolenevinylene-Based Copolymers and Characterization of Their Photovoltaic Properties. Adv. Funct. Mater. 2006, 16, 1694¨C1704. "
947,O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(C5=CC=C(CC(CC)CCCC)O5)=C6C(SC(C)=C6)=C4C7=CC=C(C[C@H](CCCC)CC)O7)=C21)=O,PBDT(F)TPD,4.85,2.76,0.9,7.8,0.42,3,"Warnan, J.; El Labban, A.; Cabanetos, C.; Hoke, E. T.; Shukla, P. K.; Risko, C.; Br¨¦das, J. L.; McGehee, M. D.; Beaujuge, P. M. Ring Substituents Mediate the Morphology of PBDTTPD-PCBM Bulk-Heterojunction Solar Cells. Chem. Mater. 2014, 26, 2299¨C2306. "
948,O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(C5=CC=C(CC(CC)CCCC)S5)=C6C(SC(C)=C6)=C4C7=CC=C(C[C@H](CCCC)CC)S7)=C21)=O,PBDT(T)TPD,5.01,2.76,1,11.1,0.58,6.5,"Warnan, J.; El Labban, A.; Cabanetos, C.; Hoke, E. T.; Shukla, P. K.; Risko, C.; Br¨¦das, J. L.; McGehee, M. D.; Beaujuge, P. M. Ring Substituents Mediate the Morphology of PBDTTPD-PCBM Bulk-Heterojunction Solar Cells. Chem. Mater. 2014, 26, 2299¨C2306. "
949,O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(C5=CC=C(CC(CC)CCCC)[Se]5)=C6C(SC(C)=C6)=C4C7=CC=C(C[C@H](CCCC)CC)[Se]7)=C21)=O,PBDT(S)TPD,4.98,2.76,0.98,8.7,0.48,4.7,"Warnan, J.; El Labban, A.; Cabanetos, C.; Hoke, E. T.; Shukla, P. K.; Risko, C.; Br¨¦das, J. L.; McGehee, M. D.; Beaujuge, P. M. Ring Substituents Mediate the Morphology of PBDTTPD-PCBM Bulk-Heterojunction Solar Cells. Chem. Mater. 2014, 26, 2299¨C2306. "
950,CC1=CC2=C(C3=CC=C(CC(CCCC)CCCCCC)S3)C(S4)=C(C(C5=CC=C(CC(CCCC)CCCCCC)S5)=C2S1)C=C4C6=CC=C(S6)C7=CC8=C(C=C(C9=CC=C(C)S9)C%10=NN(CCCCCCCC)N=C%108)C%11=NN(CCCCCCCC)N=C7%11,PBDT-TZNT (P1),5.21,3.31,0.88,7.42,0.51,3.35,"Dong, Y.; Hu, X.; Duan, C.; Liu, P.; Liu, S.; Lan, L.; Chen, D.; Ying, L.; Su, S.; Gong, X.; Huang, F.; Cao, Y. A Series of New Medium-Bandgap Conjugated Polymers Based on naphtho[1,2-c:5,6-c]bis(2-Octyl-[1,2,3]triazole for High-Performance Polymer SolarCells. Adv. Mater. 2013, 25, 3683¨C3688. "
951,CC1=CC2=C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)C(S4)=C(C(C5=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S5)=C2S1)C=C4C6=CC=C(S6)C7=CC8=C(C=C(C9=CC=C(C)S9)C%10=NN(CCCCCCCC)N=C%108)C%11=NN(CCCCCCCC)N=C7%11,PBDT-TZNT (P2),5.23,3.3,0.92,11.71,0.65,7.11,"Dong, Y.; Hu, X.; Duan, C.; Liu, P.; Liu, S.; Lan, L.; Chen, D.; Ying, L.; Su, S.; Gong, X.; Huang, F.; Cao, Y. A Series of New Medium-Bandgap Conjugated Polymers Based on naphtho[1,2-c:5,6-c]bis(2-Octyl-[1,2,3]triazole for High-Performance Polymer SolarCells. Adv. Mater. 2013, 25, 3683¨C3688. "
952,CC1=CC2=C(C3=C(CCCCCCCCCC)C=C(CCCCCCCCCC)S3)C(S4)=C(C(C5=C(CCCCCCCCCC)C=C(CCCCCCCCCC)S5)=C2S1)C=C4C6=CC=C(S6)C7=CC8=C(C=C(C9=CC=C(C)S9)C%10=NN(CCCCCCCC)N=C%108)C%11=NN(CCCCCCCC)N=C7%11,PBDT-TZNT (P3),5.21,3.31,0.84,3.59,0.49,1.5,"Dong, Y.; Hu, X.; Duan, C.; Liu, P.; Liu, S.; Lan, L.; Chen, D.; Ying, L.; Su, S.; Gong, X.; Huang, F.; Cao, Y. A Series of New Medium-Bandgap Conjugated Polymers Based on naphtho[1,2-c:5,6-c]bis(2-Octyl-[1,2,3]triazole for High-Performance Polymer SolarCells. Adv. Mater. 2013, 25, 3683¨C3688. "
953,CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC(C(SC[C@H](CCCCCC)CCCC)=C(SC(C)=C5)C5=C6SCC(CCCCCC)CCCC)=C6S4)O3)C7=NN(CC(CCCCCC)CCCC)N=C27)O1,PBDTFBZO,5.38,3.28,0.91,11.81,0.582,6.25,"Li, K.; Li, Z.; Feng, K.; Xu, X.; Wang, L.; Peng, Q. Development of Large Band-Gap Conjugated Copolymers for Efficient Regular Single and Tandem Organic Solar Cells. J. Am. Chem. Soc. 2013, 135, 13549¨C13557. "
954,CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC(C(SC[C@H](CCCCCC)CCCC)=C(SC(C)=C5)C5=C6SCC(CCCCCC)CCCC)=C6S4)S3)C7=NN(CC(CCCCCC)CCCC)N=C27)S1,PBDTFBZS,5.32,3.26,0.88,12.36,0.712,7.74,"Li, K.; Li, Z.; Feng, K.; Xu, X.; Wang, L.; Peng, Q. Development of Large Band-Gap Conjugated Copolymers for Efficient Regular Single and Tandem Organic Solar Cells. J. Am. Chem. Soc. 2013, 135, 13549¨C13557. "
955,CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=CC(C(CCC(CCCCCC)CCCC)=C(SC(C)=C5)C5=C6CCC(CCCCCC)CCCC)=C6S4)S3)C7=NN(CC(CCCCCC)CCCC)N=C27)S1,FTAZ,5.45,3.45,0.85,8.89,0.759,5.75,"Li, W.; Yan, L.; Zhou, H.; You, W. A General Approach toward Electron Deficient Triazole Units to Construct Conjugated Polymers for Solar Cells. Chem. Mater. 2015, 27, 6470¨C6476."
956,CC1=CC=C(C2=NN=C(C3=CC=C(C4=CC(C(CCC(CCCCCC)CCCC)=C(SC(C)=C5)C5=C6CCC(CCCCCC)CCCC)=C6S4)S3)C7=NN(CC(CCCCCC)CCCC)N=C27)S1,PrzTAZ,5.66,3.73,0.96,8.33,0.597,4.75,"Li, W.; Yan, L.; Zhou, H.; You, W. A General Approach toward Electron Deficient Triazole Units to Construct Conjugated Polymers for Solar Cells. Chem. Mater. 2015, 27, 6470¨C6476."
957,CC1=CC=C(C2=C(C#N)N=C(C3=CC=C(C4=CC(C(CCC(CCCCCC)CCCC)=C(SC(C)=C5)C5=C6CCC(CCCCCC)CCCC)=C6S4)S3)C7=NN(CC(CCCCCC)CCCC)N=C27)S1,PBnDT?PyCNTAZ,5.67,3.83,0.965,10.92,0.714,7.52,"Li, W.; Yan, L.; Zhou, H.; You, W. A General Approach toward Electron Deficient Triazole Units to Construct Conjugated Polymers for Solar Cells. Chem. Mater. 2015, 27, 6470¨C6476."
958,CC1=CC=C(C2=C(C#N)C(C#N)=C(C3=CC=C(C4=CC(C(CCC(CCCCCC)CCCC)=C(SC(C)=C5)C5=C6CCC(CCCCCC)CCCC)=C6S4)S3)C7=NN(CC(CCCCCC)CCCC)N=C27)S1,CNTAZ,5.73,3.96,1.03,8.97,0.599,5.53,"Li, W.; Yan, L.; Zhou, H.; You, W. A General Approach toward Electron Deficient Triazole Units to Construct Conjugated Polymers for Solar Cells. Chem. Mater. 2015, 27, 6470¨C6476."
959,CC1=CC=C(C2=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C(C3=CC=C(C4=CC(C(C5=CC(F)=C(CC(CC)CCCC)C(F)=C5)=C(SC(C)=C6)C6=C7C8=CC(F)=C(CC(CCCC)CC)C(F)=C8)=C7S4)S3)C9=NSN=C29)S1,PTFBDT-BZS,5.5,3.69,0.89,12.67,0.73,8.24,"Li, G.; Gong, X.; Zhang, J.; Liu, Y.; Feng, S.; Li, C.; Bo, Z. 4-Alkyl-3,5-Difluorophenyl-Substituted Benzodithiophene-Based Wide Band Gap Polymers for HighEfficiency Polymer Solar Cells. ACS Appl. Mater. Interfaces 2016, 8, 3686¨C3692. "
960,CC1=CC=C(C2=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C(C3=CC=C(C4=CC(C(C5=CC(F)=C(CC(CC)CCCC)C(F)=C5)=C(SC(C)=C6)C6=C7C8=CC(F)=C(CC(CCCC)CC)C(F)=C8)=C7S4)S3)C9=NON=C29)S1,PTFBDT-BZO,5.62,3.8,0.96,9.24,0.64,5.67,"Li, G.; Gong, X.; Zhang, J.; Liu, Y.; Feng, S.; Li, C.; Bo, Z. 4-Alkyl-3,5-Difluorophenyl-Substituted Benzodithiophene-Based Wide Band Gap Polymers for HighEfficiency Polymer Solar Cells. ACS Appl. Mater. Interfaces 2016, 8, 3686¨C3692. "
961,CC1=CC=C(C2=C(C(N(CCCCCCCC)C3=O)=O)C3=C(C4=CC=C(C5=CC(C(C6=CC=C(CC(CC)CCCC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(CC(CC)CCCC)S9)=C8S5)S4)C%10=NN(CCCCCCCC)N=C2%10)S1,PTZBIBDT,5.34,3.46,0.87,13.5,0.74,8.63,"Lan, L.; Chen, Z.; Hu, Q.; Ying, L.; Zhu, R.; Liu, F.; Russell, T. P.; Huang, F.; Cao, Y. High-Performance Polymer Solar Cells Based on a Wide-Bandgap Polymer Containing Pyrrolo[3,4-F]benzotriazole-5,7-Dione with a Power Conversion Efficiency of 8.63%. Adv. Sci. 2016, 3, 1600032/1¨C7. "
962,CC1=CC=C(C(C2=C3SC(C(OCC(CCCCCC)CCCC)=O)=C2)=C4C(C=C(C(OCC(CCCCCC)CCCC)=O)S4)=C3C5=CC=C(C6=CC(C(OCC(CC)CCCC)=C(SC(C)=C7)C7=C8OCC(CCCC)CC)=C8S6)S5)S1,PV-BDTC1,5.56,3.49,0.93,5.9,0.594,3.25,"Tao, Q.; Liu, T.; Duan, linrui; Cai, yufeng; Xiong, W.; Wang, P.; Tan, H.; Lei, G.; Pei, Y.; Zhu, W.; Yang, R.; Sun, Y. Wide Bandgap Copolymers with Vertical Benzodithiophene Dicarboxylate for High-Performance Polymer Solar Cells with Efficiency up to 7.49%. J. Mater. Chem. A 2016, 4, 18792¨C18803. "
963,CC1=CC=C(C(C2=C3SC(C(OCC(CCCCCC)CCCC)=O)=C2)=C4C(C=C(C(OCC(CCCCCC)CCCC)=O)S4)=C3C5=CC=C(C6=CC(C(C7=CC=C(CC(CC)CCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(CC(CCCC)CC)S%10)=C9S6)S5)S1,PV-BDTC2,5.67,3.58,1.03,10.37,0.7,7.49,"Tao, Q.; Liu, T.; Duan, linrui; Cai, yufeng; Xiong, W.; Wang, P.; Tan, H.; Lei, G.; Pei, Y.; Zhu, W.; Yang, R.; Sun, Y. Wide Bandgap Copolymers with Vertical Benzodithiophene Dicarboxylate for High-Performance Polymer Solar Cells with Efficiency up to 7.49%. J. Mater. Chem. A 2016, 4, 18792¨C18803. "
964,CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC(CC(CC)CCCC)=C(F)S7)=C(SC(C)=C8)C8=C9C%10=CC(CC(CC)CCCC)=C(F)S%10)=C9S6)S5)S1,PBDTBDD (PM6),5.45,3.65,0.98,12.7,0.74,9.2,"Zhang, M.; Guo, X.; Ma, W.; Ade, H.; Hou, J. A Large-Bandgap Conjugated Polymer for Versatile Photovoltaic Applications with High Performance. Adv. Mater. 2015, 27, 4655¨C4660. "
965,CC1=CC=C(C2=CC=C(C3=NN(CCCCCCCC)N=C32)C4=CC=C(C5=CC(C(C6=CC=C(CC(CCCCCCCC)CCCCCC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(CC(CCCCCCCC)CCCCCC)S9)=C8S5)S4)S1,PBDT-HBTA,5.13,3.16,0.58,7.41,0.565,2.43,"Min, J.; Zhang, Z. G.; Zhang, S.; Li, Y. Conjugated Side-Chain-Isolated D-A Copolymers Based on benzo[1,2-b:4,5-b¡¯]dithiophene-Alt-Dithienylbenzotriazole: Synthesis and Photovoltaic Properties. Chem. Mater. 2012, 24, 3247¨C3254. "
966,CC1=CC=C(C2=C(F)C(F)=C(C3=NN(CCCCCCCC)N=C32)C4=CC=C(C5=CC(C(C6=CC=C(CC(CCCCCCCC)CCCCCC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(CC(CCCCCCCC)CCCCCC)S9)=C8S5)S4)S1,PBDT-FBTA,5.26,3.08,0.75,11.9,0.672,6,"Min, J.; Zhang, Z. G.; Zhang, S.; Li, Y. Conjugated Side-Chain-Isolated D-A Copolymers Based on benzo[1,2-b:4,5-b¡¯]dithiophene-Alt-Dithienylbenzotriazole: Synthesis and Photovoltaic Properties. Chem. Mater. 2012, 24, 3247¨C3254. "
967,CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(SC[C@@H](CC)CCCC)O7)=C(SC(C)=C8)C8=C9C%10=CC=C(SCC(CCCC)CC)O%10)=C9S6)S5)S1,PBDT(O)-T1,5.31,3.45,0.83,9.6,0.495,4.01,"Xue, X.; Fan, B.; Liu, T.; Sun, X.; Huo, L.; Ha, S. R.; Choi, H.; Kim, T.; Kim, J. Y.; Wei, D.; Yu, M.; Jin, Q.; Sun, Y. Influence of Aromatic Heterocycle of Conjugated Side Chains on Photovoltaic Performance of Benzodithiophene-Based Wide-Bandgap Polymers. Polym. Chem. 2016, 7, 4036¨C4045. "
968,CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(SC[C@@H](CC)CCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(SCC(CCCC)CC)S%10)=C9S6)S5)S1,PBDT(S)-T1,5.52,3.56,0.9,12.3,0.711,7.48,"Xue, X.; Fan, B.; Liu, T.; Sun, X.; Huo, L.; Ha, S. R.; Choi, H.; Kim, T.; Kim, J. Y.; Wei, D.; Yu, M.; Jin, Q.; Sun, Y. Influence of Aromatic Heterocycle of Conjugated Side Chains on Photovoltaic Performance of Benzodithiophene-Based Wide-Bandgap Polymers. Polym. Chem. 2016, 7, 4036¨C4045. "
969,CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(SC[C@@H](CC)CCCC)[Se]7)=C(SC(C)=C8)C8=C9C%10=CC=C(SCC(CCCC)CC)[Se]%10)=C9S6)S5)S1,PBDT(Se)-T1,5.53,3.59,0.92,13.1,0.721,8.52,"Xue, X.; Fan, B.; Liu, T.; Sun, X.; Huo, L.; Ha, S. R.; Choi, H.; Kim, T.; Kim, J. Y.; Wei, D.; Yu, M.; Jin, Q.; Sun, Y. Influence of Aromatic Heterocycle of Conjugated Side Chains on Photovoltaic Performance of Benzodithiophene-Based Wide-Bandgap Polymers. Polym. Chem. 2016, 7, 4036¨C4045. "
970,CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3C=C1,PCDTBT,5.5,3.6,0.88,10.6,0.66,6.1,"Park, S. H.; Roy, A.; Beaupr¨¦, S.; Cho, S.; Coates, N.; Moon, J. S.; Moses, D.; Leclerc, M.; Lee, K.; Heeger, A. J. Bulk Heterojunction Solar Cells with Internal Quantum Efficiency Approaching 100%. Nat. Photonics 2009, 3, 297¨C303. "
971,CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(SC[C@@H](CC)CCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(SCC(CCCC)CC)S%10)=C9S6)S5)S1,PBDT(S)-T1,5.52,3.56,0.89,12.3,0.676,7.4,"Xue, X.; Liu, T.; Meng, X.; Sun, X.; Huo, L.; Ma, W.; Sun, Y. Enhanced Open-Circuit Voltage in Methoxyl Substituted Benzodithiophene-Based Polymer Solar Cells. Sci. China Chem. 2017, 60, 243¨C250. "
972,CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC(OC)=C(SC[C@@H](CC)CCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC(OC)=C(SCC(CCCC)CC)S%10)=C9S6)S5)S1,POBDT(S)-T1,5.65,3.55,0.98,12.9,0.722,9.2,"Xue, X.; Liu, T.; Meng, X.; Sun, X.; Huo, L.; Ma, W.; Sun, Y. Enhanced Open-Circuit Voltage in Methoxyl Substituted Benzodithiophene-Based Polymer Solar Cells. Sci. China Chem. 2017, 60, 243¨C250. "
973,CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)OC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(CCCCCCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(CCCCCCCC)S%10)=C9S6)S5)S1,PBDT-O1,5.51,3.52,0.87,9.4,0.64,5.2,"Huang, X.; Weng, K.; Huo, L.; Fan, B.; Yang, C.; Sun, X.; Sun, Y. Effects of a Heteroatomic Benzothienothiophenedione Acceptor on the Properties of a Series of Wide-Bandgap Photovoltaic Polymers. J. Mater. Chem. C 2016, 4, 9052¨C9059. "
974,CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(CCCCCCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(CCCCCCCC)S%10)=C9S6)S5)S1,PBDT-ST1,5.53,3.57,0.91,13.7,0.747,9,"Huang, X.; Weng, K.; Huo, L.; Fan, B.; Yang, C.; Sun, X.; Sun, Y. Effects of a Heteroatomic Benzothienothiophenedione Acceptor on the Properties of a Series of Wide-Bandgap Photovoltaic Polymers. J. Mater. Chem. C 2016, 4, 9052¨C9059. "
975,CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)[Se]C(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC(C(C7=CC=C(CCCCCCCC)S7)=C(SC(C)=C8)C8=C9C%10=CC=C(CCCCCCCC)S%10)=C9S6)S5)S1,PBDT-Se1,5.46,3.53,0.86,13.1,0.747,8.3,"Huang, X.; Weng, K.; Huo, L.; Fan, B.; Yang, C.; Sun, X.; Sun, Y. Effects of a Heteroatomic Benzothienothiophenedione Acceptor on the Properties of a Series of Wide-Bandgap Photovoltaic Polymers. J. Mater. Chem. C 2016, 4, 9052¨C9059. "
976,CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCC)CC)SC(C[C@@H](CCCC)CC)=C4C3=O)=O)=C2C5=CC=C(C6=CC7=C(C8=C(C9=CC=C(CCCCCCCC)S9)C(SC%10=C%11SC(C)=C%10)=C%11C(C%12=CC=C(CCCCCCCC)S%12)=C8S7)S6)S5)S1,PDBT-T1,5.4,3.4,0.92,14.11,0.75,9.74,"Huo, L.; Liu, T.; Sun, X.; Cai, Y.; Heeger, A. J.; Sun, Y. Single-Junction Organic Solar Cells Based on a Novel Wide-Bandgap Polymer with Efficiency of 9.7%. Adv. Mater. 2015, 27, 2938¨C2944. "
977,CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCCCC)CCCCCCCC)SC(C[C@@H](CCCCCC)CCCCCCCC)=C4C3=O)=O)=C2C5=CC=C(C6=CC7=C(C8=CC=C(SCC(C)C)S8)C(SC(C)=C9)=C9C(C%10=CC=C(SCC(C)C)S%10)=C7S6)S5)S1,PBT1-MP,5.49,3.46,0.98,12.9,0.725,8.7,"Liu, T.; Pan, X.; Meng, X.; Liu, Y.; Wei, D.; Ma, W.; Huo, L.; Sun, X.; Lee, T. H.; Huang, M.; Choi, H.; Kim, J. Y.; Choy, W. C. H.; Sun, Y. Alkyl Side-Chain Engineering in Wide-Bandgap Copolymers Leading to Power Conversion Efficiencies over 10%. Adv. Mater. 2017, 29, 1604251/1¨C7. "
978,CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CCCCCC)CCCC)SC(C[C@@H](CCCCCC)CCCC)=C4C3=O)=O)=C2C5=CC=C(C6=CC7=C(C8=CC=C(SC[C@@H](CC)CCCC)S8)C(SC(C)=C9)=C9C(C%10=CC=C(SCC(CC)CCCC)S%10)=C7S6)S5)S1,PBT1-EH,5.43,3.43,0.97,14.21,0.75,10.3,"Liu, T.; Pan, X.; Meng, X.; Liu, Y.; Wei, D.; Ma, W.; Huo, L.; Sun, X.; Lee, T. H.; Huang, M.; Choi, H.; Kim, J. Y.; Choy, W. C. H.; Sun, Y. Alkyl Side-Chain Engineering in Wide-Bandgap Copolymers Leading to Power Conversion Efficiencies over 10%. Adv. Mater. 2017, 29, 1604251/1¨C7. "
979,CC1=CC=C(C(S2)=C3C(C(C4=C(C[C@@H](CC)CCCC)SC(C[C@@H](CC)CCCC)=C4C3=O)=O)=C2C5=CC=C(C6=CC7=C(C8=CC=C(SC[C@H](CCCCCC)CCCC)S8)C(SC(C)=C9)=C9C(C%10=CC=C(SCC(CCCCCC)CCCC)S%10)=C7S6)S5)S1,PBT1-BO,5.4,3.41,0.93,13.03,0.675,8.1,"Liu, T.; Pan, X.; Meng, X.; Liu, Y.; Wei, D.; Ma, W.; Huo, L.; Sun, X.; Lee, T. H.; Huang, M.; Choi, H.; Kim, J. Y.; Choy, W. C. H.; Sun, Y. Alkyl Side-Chain Engineering in Wide-Bandgap Copolymers Leading to Power Conversion Efficiencies over 10%. Adv. Mater. 2017, 29, 1604251/1¨C7. "
980,CC1=CC(C(C2=CC=C(CCCCCC)C=C2)(C3=CC=C(CCCCCC)C=C3)C4=CC(C(SC(C5=CC6=C(C(C=CC(C)=C7)=C7S6(=O)=O)C=C5)=C8)=C8C9(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)=C9C=C4%12)=C%12S1,PIDT-SO,5.4,3.03,0.97,6.96,0.34,2.31,"He, R.; Xu, J.; Yang, Y.; Cai, P.; Chen, D.; Ying, L.; Yang, W.; Cao, Y. Dibenzothiophene-S,S-Dioxide Based Medium-Band-Gap Polymers for Efficient Bulk Heterojunction Solar Cells. Org. Electron. 2014, 15, 2950¨C2958. "
981,CC1=CC(C(C2=CC=C(CCCCCC)C=C2)(C3=CC=C(CCCCCC)C=C3)C4=CC(C(SC(C5=CC(CCCCCC)=C(C6=CC7=C(C(C=CC(C8=C(CCCCCC)C=C(C)S8)=C9)=C9S7(=O)=O)C=C6)S5)=C%10)=C%10C%11(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)=C%11C=C4%14)=C%14S1,PIDT-DHTSO,5.33,3.05,0.95,8.2,0.48,3.81,"He, R.; Xu, J.; Yang, Y.; Cai, P.; Chen, D.; Ying, L.; Yang, W.; Cao, Y. Dibenzothiophene-S,S-Dioxide Based Medium-Band-Gap Polymers for Efficient Bulk Heterojunction Solar Cells. Org. Electron. 2014, 15, 2950¨C2958. "
982,CC(S1)=CC2=C1C(OCC(CCCC)CC)=C3C(SC(C4=CC5=C(C6=CC(C(N(CC(CCCCCCCC)CCCCCC)C7=C8SC(C)=C7)=O)=C8C=C6C(N5CC(CCCCCCCC)CCCCCC)=O)S4)=C3)=C2OCC(CCCC)CC,PBDT-TPTI (P1),5.45,2.68,0.9,9.26,0.636,5.3,"Liao, Q.; Cao, J.; Xiao, Z.; Liao, J.; Ding, L. Donor¨Cacceptor Conjugated Polymers Based on a Pentacyclic Aromatic Lactam Acceptor Unit for Polymer Solar Cells. Phys. Chem. Chem. Phys. 2013, 15, 19990¨C19993. "
983,CC(S1)=CC2=C1C3=C(C(N2CC(CCCCCC)CCCCCCCC)=O)C=C(C(C(N4CC(CCCCCCCC)CCCCCC)=O)=C3)C5=C4C=C(S5)C6=CC7=C(C(SC(C)=C8)=C8[Si]7(CC(CCCC)CC)CC(CCCC)CC)S6,PSB-TPTI (P3),5.33,2.72,0.87,7.62,0.549,3.64,"Liao, Q.; Cao, J.; Xiao, Z.; Liao, J.; Ding, L. Donor¨Cacceptor Conjugated Polymers Based on a Pentacyclic Aromatic Lactam Acceptor Unit for Polymer Solar Cells. Phys. Chem. Chem. Phys. 2013, 15, 19990¨C19993. "
984,CC(S1)=CC2=C1C3=C(C(N2CC(CC)CCCC)=O)C=C(C(C(N4CC(CCCC)CC)=O)=C3)C5=C4C=C(S5)C6=CC7=C(C(SC(C)=C8)=C8[Si]7(CC(CCCC)CC)CC(CCCC)CC)S6,PSB-TPTI (P4),5.34,2.69,0.8,10.31,0.422,3.48,"Liao, Q.; Cao, J.; Xiao, Z.; Liao, J.; Ding, L. Donor¨Cacceptor Conjugated Polymers Based on a Pentacyclic Aromatic Lactam Acceptor Unit for Polymer Solar Cells. Phys. Chem. Chem. Phys. 2013, 15, 19990¨C19993. "
985,O=C(N1CC(CCCCCCCCCC)CCCCCCCC)C2=CC3=C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C4=C3SC5=C4SC(C)=C5)=O)C=C2C6=C1C(SC(C7=CC8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CCCC)CC)=C8S7)=C%10)=C%10S6,PBDTTTP,5.43,2.6,0.98,8.12,0.695,5.53,"Cao, J.; Qian, L.; Ding, L. A Heptacyclic Acceptor Unit Developed for D¨CA Copolymers Used in Polymer Solar Cells. Polym. Chem. 2016, 7, 1027¨C1030. "
986,CC1=CC2=C(C(C=C(SC3=C4C=C5C(C(SC(C6=C(OCCCCCC)C(OCCCCCC)=C(C)C7=NSN=C76)=C8)=C8C5(C9=CC=C(CCCCCC)C=C9)C%10=CC=C(CCCCCC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)S1,PSBT,5.4,3.59,0.94,11.11,0.496,5.18,"Wang, L.; Cai, D.; Tang, C.; Wang, M.; Yin, Z.; Zheng, Q. Improved Synthesis and Photovoltaic Performance of Donor¨Cacceptor Copolymers Based on DibenzothiopheneCored Ladder-Type Heptacyclic Units. J. Mater. Chem. C 2015, 3, 5631¨C5641. "
987,CC1=CC2=C(C(C=C(SC3=C4C=C5C(C(SC(C6=C(OCCCCCCCC)C(OCCCCCCCC)=C(C)C7=NON=C76)=C8)=C8C5(C9=CC=C(CCCCCC)C=C9)C%10=CC=C(CCCCCC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)S1,PSBO,5.48,3.66,0.96,8.6,0.401,3.29,"Wang, L.; Cai, D.; Tang, C.; Wang, M.; Yin, Z.; Zheng, Q. Improved Synthesis and Photovoltaic Performance of Donor¨Cacceptor Copolymers Based on DibenzothiopheneCored Ladder-Type Heptacyclic Units. J. Mater. Chem. C 2015, 3, 5631¨C5641. "
988,CC1=CC2=C(C(C=C(SC3=C4C=C5C(C(SC(C6=CC=C(C7=C(OCCCCCCCCCC)C(OCCCCCCCCCC)=C(C8=CC=C(C)S8)C9=NSN=C97)S6)=C%10)=C%10C5(C%11=CC=C(CCCCCC)C=C%11)C%12=CC=C(CCCCCC)C=C%12)=C3)C4=C%13)=C%13C2(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15)S1,PSDTBT,5.38,3.56,0.9,9.5,0.413,3.52,"Wang, L.; Cai, D.; Tang, C.; Wang, M.; Yin, Z.; Zheng, Q. Improved Synthesis and Photovoltaic Performance of Donor¨Cacceptor Copolymers Based on DibenzothiopheneCored Ladder-Type Heptacyclic Units. J. Mater. Chem. C 2015, 3, 5631¨C5641. "
989,CC(S1)=CC2=C1C3=C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)C4=C(C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C5=C6SC(C7=CC=C(C)S7)=C5)=O)=C6C=C4)C=C3,PThTITI,5.57,2.6,0.96,8.28,0.698,5.53,"Qian, L.; Cao, J.; Ding, L. A Hexacyclic Ladder-Type Building Block for HighPerformance D¨CA Copolymers. J. Mater. Chem. A 2015, 3, 24211¨C24214. "
990,CC(S1)=CC2=C1C3=C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)C4=C(C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C5=C6SC(C7=CC=C(C)[Se]7)=C5)=O)=C6C=C4)C=C3,PSeTITI,5.54,2.78,0.94,9.35,0.705,6.17,"Qian, L.; Cao, J.; Ding, L. A Hexacyclic Ladder-Type Building Block for HighPerformance D¨CA Copolymers. J. Mater. Chem. A 2015, 3, 24211¨C24214. "
991,CC(S1)=CC2=C1C(SC3=C4SC5=C3C(N(CC(CCCCCCCC)CCCCCCCCCC)C6=C5SC(C7=CC=C(C)S7)=C6)=O)=C4C(N2CC(CCCCCCCC)CCCCCCCCCC)=O,PThTD1,5.36,2.56,0.87,9.67,0.716,6.02,"Cao, J.; Zuo, C.; Du, B.; Qiu, X.; Ding, L. Hexacyclic Lactam Building Blocks for Highly Efficient Polymer Solar Cells. Chem. Commun. 2015, 51, 12122¨C12125. "
992,CC(S1)=CC2=C1C(SC3=C4SC5=C3C(N(CC(CCCCCCCC)CCCCCC)C6=C5SC(C7=CC=C(C)S7)=C6)=O)=C4C(N2CC(CCCCCCCC)CCCCCC)=O,PThTD2,5.3,2.63,0.85,11.95,0.68,6.9,"Cao, J.; Zuo, C.; Du, B.; Qiu, X.; Ding, L. Hexacyclic Lactam Building Blocks for Highly Efficient Polymer Solar Cells. Chem. Commun. 2015, 51, 12122¨C12125. "
993,CC(S1)=CC2=C1C(SC3=C4SC5=C3C(N(CC(CCCCCCCC)CCCCCCCCCC)C6=C5SC(C7=CC=C(C)[Se]7)=C6)=O)=C4C(N2CC(CCCCCCCC)CCCCCCCCCC)=O,PSeTD1,5.34,2.7,0.83,10.92,0.687,6.22,"Cao, J.; Zuo, C.; Du, B.; Qiu, X.; Ding, L. Hexacyclic Lactam Building Blocks for Highly Efficient Polymer Solar Cells. Chem. Commun. 2015, 51, 12122¨C12125. "
994,CC(S1)=CC2=C1C(SC3=C4SC5=C3C(N(CC(CCCCCCCC)CCCCCC)C6=C5SC(C7=CC=C(C)[Se]7)=C6)=O)=C4C(N2CC(CCCCCCCC)CCCCCC)=O,PSeTD2,5.31,2.74,0.85,13.55,0.711,8.18,"Cao, J.; Zuo, C.; Du, B.; Qiu, X.; Ding, L. Hexacyclic Lactam Building Blocks for Highly Efficient Polymer Solar Cells. Chem. Commun. 2015, 51, 12122¨C12125. "
995,CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NON=C75)S4)=C2)=C3C=C1,PCDTQx,5.46,3.42,0.95,3,0.56,1.8,"Blouin, N.; Michaud, A.; Gendron, D.; Wakim, S.; Blair, E.; Neagu-Plesu, R.; Bellet¨ºte, M.; Durocher, G.; Tao, Y.; Leclerc, M. Toward a Rational Design of poly(2,7-Carbazole Derivatives for Solar Cells. J. Am. Chem. Soc. 2008, 130, 732¨C742. "
996,CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CN=C(C6=CC=C(C)S6)C7=NC=CN=C75)S4)=C2)=C3C=C1,PCDTTPP,5.52,3.67,0.9,2.6,0.44,1.1,"Blouin, N.; Michaud, A.; Gendron, D.; Wakim, S.; Blair, E.; Neagu-Plesu, R.; Bellet¨ºte, M.; Durocher, G.; Tao, Y.; Leclerc, M. Toward a Rational Design of poly(2,7-Carbazole Derivatives for Solar Cells. J. Am. Chem. Soc. 2008, 130, 732¨C742. "
997,CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CN=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3C=C1,PCDTPT,5.53,3.8,0.71,2.9,0.32,0.7,"Blouin, N.; Michaud, A.; Gendron, D.; Wakim, S.; Blair, E.; Neagu-Plesu, R.; Bellet¨ºte, M.; Durocher, G.; Tao, Y.; Leclerc, M. Toward a Rational Design of poly(2,7-Carbazole Derivatives for Solar Cells. J. Am. Chem. Soc. 2008, 130, 732¨C742. "
998,CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NC=CN=C75)S4)=C2)=C3C=C1,PCDTBX,5.47,3.65,0.96,3.7,0.6,2.4,"Blouin, N.; Michaud, A.; Gendron, D.; Wakim, S.; Blair, E.; Neagu-Plesu, R.; Bellet¨ºte, M.; Durocher, G.; Tao, Y.; Leclerc, M. Toward a Rational Design of poly(2,7-Carbazole Derivatives for Solar Cells. J. Am. Chem. Soc. 2008, 130, 732¨C742. "
999,CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CN=C(C6=CC=C(C)S6)C7=NON=C75)S4)=C2)=C3C=C1,PCDTPX,5.55,3.93,0.85,1.4,0.6,0.8,"Blouin, N.; Michaud, A.; Gendron, D.; Wakim, S.; Blair, E.; Neagu-Plesu, R.; Bellet¨ºte, M.; Durocher, G.; Tao, Y.; Leclerc, M. Toward a Rational Design of poly(2,7-Carbazole Derivatives for Solar Cells. J. Am. Chem. Soc. 2008, 130, 732¨C742. "
1000,O=C1N(CC(CCCCCCCCCC)CCCCCCCC)C(C2=C(C3=C(CCCCCCCCCC)C=C(C4=CC5=C(C(C=C(C6=CC=C(CC(CCCC)CC)S6)C7=C8SC(C)=C7)=C8C=C5C9=CC=C(C[C@H](CCCC)CC)S9)S4)S3)SC(C%10=C(CCCCCCCCCC)C=C(C)S%10)=C21)=O,PzNDTT-TPD1,5.55,3.52,0.86,12.73,0.68,7.5,"Zhu, X.; Fang, J.; Lu, K.; Zhang, J.; Zhu, L.; Zhao, Y.; Shuai, Z.; Wei, Z. Naphtho[1,2-b:5,6-b¡ä]dithiophene Based Two-Dimensional Conjugated Polymers for Highly Efficient Thick-Film Inverted Polymer Solar Cells. Chem. Mater. 2014, 26, 6947¨C6954. "
1001,CC(S1)=C(CCCCCCCCCC)C=C1C2=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C3=O)=O)C3=C(S2)C4=CC(CCCCCCCCCC)=C(C5=CC6=C(C(C=C(C7=CC=C(CC(CCCC)CC)S7)C8=C9SC(C)=C8)=C9C=C6C%10=CC=C(C[C@H](CCCC)CC)S%10)S5)S4,PzNDTT-TPD2,5.58,3.48,0.88,6.09,0.69,3.68,"Zhu, X.; Fang, J.; Lu, K.; Zhang, J.; Zhu, L.; Zhao, Y.; Shuai, Z.; Wei, Z. Naphtho[1,2-b:5,6-b¡ä]dithiophene Based Two-Dimensional Conjugated Polymers for Highly Efficient Thick-Film Inverted Polymer Solar Cells. Chem. Mater. 2014, 26, 6947¨C6954. "
1002,CC1=CC(C(C2=CC=C(CCCCCC)C=C2)(C3=CC=C(CCCCCC)C=C3)C4=CC(C(SC(C5=CC6=C(C(SC(C)=C7)=C7N(CC(CCCCCCCCCC)CCCCCCCC)C6=O)S5)=C8)=C8C9(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)=C9C=C4%12)=C%12S1,PDTPO-IDTT,5.31,3.27,0.94,9.14,0.64,5.47,"Gao, W.; Liu, T.; Hao, M.; Wu, K.; Zhang, C.; Sun, Y.; Yang, C. Dithieno[3,2-b:2¡ä,3¡ä-D]pyridin-5(4H-One Based D¨CA Type Copolymers with Wide Bandgaps of up to 2.05eV to Achieve Solar Cell Efficiencies of up to 7.33%. Chem. Sci. 2016, 7, 6167¨C6175. "
1003,CC1=CC(N(CC(CCCCCCCCCC)CCCCCCCC)C2=O)=C(S1)C3=C2C=C(C(S4)=CC5=C4C(C6(C7=CC=C(CCCCCC)C=C7)C8=CC=C(CCCCCC)C=C8)=C(S5)C9=C6C=C(C%10=C(C%11(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)C%14=C(C=C(C)S%14)S%10)C%11=C9)S3,PDTPO-IDT,5.32,3.27,0.97,10.55,0.71,7.33,"Gao, W.; Liu, T.; Hao, M.; Wu, K.; Zhang, C.; Sun, Y.; Yang, C. Dithieno[3,2-b:2¡ä,3¡ä-D]pyridin-5(4H-One Based D¨CA Type Copolymers with Wide Bandgaps of up to 2.05eV to Achieve Solar Cell Efficiencies of up to 7.33%. Chem. Sci. 2016, 7, 6167¨C6175. "
1004,CC1=CC2=C(C3=CC(C(C4=CC=C(CCCCCC)C=C4)(C5=CC=C(CCCCCC)C=C5)C6=C7SC(C8=CC=C(C)C9=C8N=C%10C(C(C=C(CCCCCCCC)C=C%11)=C%11C%12=C%10C=C(CCCCCCCC)C=C%12)=N9)=C6)=C7C=C3C2(C%13=CC=C(CCCCCC)C=C%13)C%14=CC=C(CCCCCC)C=C%14)S1,PIDT-OHBPz,5.27,3.31,0.83,8,0.566,3.75,"He, R.; Yu, L.; Cai, P.; Peng, F.; Xu, J.; Ying, L.; Chen, J.; Yang, W.; Cao, Y. Narrow-Band-Gap Conjugated Polymers Based on 2,7-Dioctyl- Substituted Dibenzo[a,c]Phenazine Derivatives for Polymer Solar Cells. Macromolecules 2014, 47, 2921¨C2928. "
1005,CC1=CC2=C(C3=CC(C(C4=CC=C(CCCCCC)C=C4)(C5=CC=C(CCCCCC)C=C5)C6=C7SC(C8=C(F)C(F)=C(C)C9=C8N=C%10C(C(C=C(CCCCCCCC)C=C%11)=C%11C%12=C%10C=C(CCCCCCCC)C=C%12)=N9)=C6)=C7C=C3C2(C%13=CC=C(CCCCCC)C=C%13)C%14=CC=C(CCCCCC)C=C%14)S1,PIDT-OFBPz,5.45,3.56,0.97,8.96,0.59,5.13,"He, R.; Yu, L.; Cai, P.; Peng, F.; Xu, J.; Ying, L.; Chen, J.; Yang, W.; Cao, Y. Narrow-Band-Gap Conjugated Polymers Based on 2,7-Dioctyl- Substituted Dibenzo[a,c]Phenazine Derivatives for Polymer Solar Cells. Macromolecules 2014, 47, 2921¨C2928. "
1006,CC1=CC2=C(C3=CC(C(C4=CC=C(CCCCCC)C=C4)(C5=CC=C(CCCCCC)C=C5)C6=C7SC(C8=CN=C(C)C9=C8N=C%10C(C(C=C(CCCCCCCC)C=C%11)=C%11C%12=C%10C=C(CCCCCCCC)C=C%12)=N9)=C6)=C7C=C3C2(C%13=CC=C(CCCCCC)C=C%13)C%14=CC=C(CCCCCC)C=C%14)S1,PIDT-OBPQ,5.3,3.58,0.86,8.97,0.509,3.93,"He, R.; Yu, L.; Cai, P.; Peng, F.; Xu, J.; Ying, L.; Chen, J.; Yang, W.; Cao, Y. Narrow-Band-Gap Conjugated Polymers Based on 2,7-Dioctyl- Substituted Dibenzo[a,c]Phenazine Derivatives for Polymer Solar Cells. Macromolecules 2014, 47, 2921¨C2928. "
1007,CC1=CC2=C(C(C=CC3=C4C=CC5=C3SC(C6=C(CCCCCCCCCCCC)C=C(C7=CC=C(/C(C(N8CC(CCCCCCCCCC)CCCCCCCC)=O)=C9C(N(CC(CCCCCCCC)CCCCCCCCCC)C%10=C\9C=CC(C%11=CC(CCCCCCCCCCCC)=C(C)S%11)=C%10)=O)C8=C7)S6)=C5)=C4C=C2)S1,P-PDT-IID12OD,5.45,3.85,0.8,9.99,0.63,5.06,"Nishinaga, S.; Mori, H.; Nishihara, Y. Phenanthrodithiophene-Isoindigo Copolymers: Effect of Side Chains on Their Molecular Order and Solar Cell Performance. Macromolecules 2015, 48, 2875¨C2885. "
1008,CC1=CC2=C(C(C=CC3=C4C=CC5=C3SC(C6=C(CCCCCCCCCCCC)C=C(C7=CC=C(/C(C(N8CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C9C(N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C%10=C\9C=CC(C%11=CC(CCCCCCCCCCCC)=C(C)S%11)=C%10)=O)C8=C7)S6)=C5)=C4C=C2)S1,P-PDT-IID12DT,5.45,3.85,0.82,6.63,0.57,3.1,"Nishinaga, S.; Mori, H.; Nishihara, Y. Phenanthrodithiophene-Isoindigo Copolymers: Effect of Side Chains on Their Molecular Order and Solar Cell Performance. Macromolecules 2015, 48, 2875¨C2885. "
1009,CC1=CC2=C(C(C=CC3=C4C=CC5=C3SC(C6=C(CC(CCCC)CCCCCC)C=C(C7=CC=C(/C(C(N8CC(CCCC)CCCCCC)=O)=C9C(N(CC(CCCCCC)CCCC)C%10=C\9C=CC(C%11=CC(CC(CCCCCC)CCCC)=C(C)S%11)=C%10)=O)C8=C7)S6)=C5)=C4C=C2)S1,P-PDT-IIDBOBO,5.5,3.81,0.82,10.7,0.6,5.28,"Nishinaga, S.; Mori, H.; Nishihara, Y. Phenanthrodithiophene-Isoindigo Copolymers: Effect of Side Chains on Their Molecular Order and Solar Cell Performance. Macromolecules 2015, 48, 2875¨C2885. "
1010,CC1=CC2=C(C(C=CC3=C4C=CC5=C3SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C7=CC=C(/C(C(N8CC(CCCCCCCC)CCCCCC)=O)=C9C(N(CC(CCCCCC)CCCCCCCC)C%10=C\9C=CC(C%11=CC(CC(CCCCCC)CCCCCCCC)=C(C)S%11)=C%10)=O)C8=C7)S6)=C5)=C4C=C2)S1,P-PDT-IIDHDHD,5.51,3.86,0.9,2.05,0.59,1.09,"Nishinaga, S.; Mori, H.; Nishihara, Y. Phenanthrodithiophene-Isoindigo Copolymers: Effect of Side Chains on Their Molecular Order and Solar Cell Performance. Macromolecules 2015, 48, 2875¨C2885. "
1011,O=C(N(CC(CC)CCCC)C(C1=CC=C(C2=CC=C(C3=CC4=C(C(C=C(C(C5=CC=C(CCCCCC)C=C5)(C6=CC=C(CCCCCC)C=C6)C7=C8SC(C)=C7)C8=C9)=C9C4(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)S3)S2)S1)=C%12%13)C%12=C(C%14=CC=C(C)S%14)N(CC(CC)CCCC)C%13=O,PTPTDP,5.25,3.6,0.75,10.3,0.54,4.2,"Yu, C. Y.; Chen, C. P.; Chan, S. H.; Hwang, G. W.; Ting, C. Thiophene/Phenylene/Thiophene-Based Low-Bandgap Conjugated Polymers for Efficient near-Infrared Photovoltaic Applications. Chem. Mater. 2009, 21, 3262¨C3269. "
1012,CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(SC(CCCCCC)=C5)=C(C6=C(C(N(CC(CC)CCCC)C7=O)=O)C7=C(C8=C9C(C=C(CCCCCC)S9)=C(C)S8)S6)S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11,PBDT_TEH-TBTT_EHi (P1),4.64,3.1,0.6,17.77,0.631,6.7,"Zhang, C.; Li, H.; Wang, J.; Zhang, Y.; Qiao, Y.; Huang, D.; Di, C.; Zhan, X.; Zhu, X.; Zhu, D. Low-Bandgap thieno[3,4-c]pyrrole-4,6-Dione-Polymers for HighPerformance Solar Cells with Significantly Enhanced Photocurrents. J. Mater. Chem. A2015, 3, 11194¨C11198. "
1013,CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(C=C(CCCCCC)S5)=C(C6=C(C(N(CC(CC)CCCC)C7=O)=O)C7=C(C8=C9C(SC(CCCCCC)=C9)=C(C)S8)S6)S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11,PBDT_TEH-TBTT_HDo (P2),4.63,3.17,0.6,15.21,0.486,4.45,"Zhang, C.; Li, H.; Wang, J.; Zhang, Y.; Qiao, Y.; Huang, D.; Di, C.; Zhan, X.; Zhu, X.; Zhu, D. Low-Bandgap thieno[3,4-c]pyrrole-4,6-Dione-Polymers for HighPerformance Solar Cells with Significantly Enhanced Photocurrents. J. Mater. Chem. A2015, 3, 11194¨C11198. "
1014,CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(SC(CCCCCC)=C5)=C(C6=C(C(N(CC(CCCCCCCC)CCCCCC)C7=O)=O)C7=C(C8=C9C(C=C(CCCCCC)S9)=C(C)S8)S6)S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11,PBDT_TEH-TBT_HD (P3),4.78,3.22,0.633,18.15,0.652,7.5,"Zhang, C.; Li, H.; Wang, J.; Zhang, Y.; Qiao, Y.; Huang, D.; Di, C.; Zhan, X.; Zhu, X.; Zhu, D. Low-Bandgap thieno[3,4-c]pyrrole-4,6-Dione-Polymers for HighPerformance Solar Cells with Significantly Enhanced Photocurrents. J. Mater. Chem. A2015, 3, 11194¨C11198. "
1015,CC1=CC(C(C2=CC(CCCCCC)=C(CC(CC)CCCC)S2)=C(SC(C3=CC(F)=C(C)C4=NSN=C43)=C5)C5=C6C7=CC(CCCCCC)=C(CC(CCCC)CC)S7)=C6S1,BFR2,5.2,3.61,0.89,7.25,0.606,3.91,"Qin, T.; Zajaczkowski, W.; Pisula, W.; Baumgarten, M.; Chen, M.; Gao, M.; Wilson, G.; Easton, C. D.; Mu, K.; Watkins, S. E. Tailored Donor ? Acceptor Polymers with an A ? D1 ? A ? D2 Structure: Controlling Intermolecular Interactions to Enable Enhanced Polymer Photovoltaic Devices. J. Am. Chem. Soc. 2014, 136, 6049¨C6055. "
1016,CC(S1)=CC(C1=C2C3=CC(CCCCCC)=C(CC(CCCC)CC)S3)=C(C4=CC(CCCCCC)=C(CC(CCCC)CC)S4)C5=C2C=C(S5)C(C6=NSN=C67)=C(F)C=C7C8=CC9=C(C%10=CC(CCCCCC)=C(CC(CCCC)CC)S%10)C%11=C(C(C%12=CC(CCCCCC)=C(CC(CC)CCCC)S%12)=C9S8)C=C(C%13=CC(F)=C(C)C%14=NSN=C%14%13)S%11,BFS3,5.2,3.62,0.9,10.82,0.608,5.92,"Qin, T.; Zajaczkowski, W.; Pisula, W.; Baumgarten, M.; Chen, M.; Gao, M.; Wilson, G.; Easton, C. D.; Mu, K.; Watkins, S. E. Tailored Donor ? Acceptor Polymers with an A ? D1 ? A ? D2 Structure: Controlling Intermolecular Interactions to Enable Enhanced Polymer Photovoltaic Devices. J. Am. Chem. Soc. 2014, 136, 6049¨C6055. "
1017,CC(S1)=CC(C1=C2C3=CC=C(CC(CCCC)CC)S3)=C(C4=CC=C(CC(CCCC)CC)S4)C5=C2C=C(S5)C(C6=NSN=C67)=C(F)C=C7C8=CC9=C(C%10=CC(CCCCCC)=C(CC(CCCC)CC)S%10)C%11=C(C(C%12=CC(CCCCCC)=C(CC(CC)CCCC)S%12)=C9S8)C=C(C%13=CC(F)=C(C)C%14=NSN=C%14%13)S%11,BFS4,5.15,3.59,0.9,13.19,0.603,7.16,"Qin, T.; Zajaczkowski, W.; Pisula, W.; Baumgarten, M.; Chen, M.; Gao, M.; Wilson, G.; Easton, C. D.; Mu, K.; Watkins, S. E. Tailored Donor ? Acceptor Polymers with an A ? D1 ? A ? D2 Structure: Controlling Intermolecular Interactions to Enable Enhanced Polymer Photovoltaic Devices. J. Am. Chem. Soc. 2014, 136, 6049¨C6055. "
1018,CC(S1)=CC(C1=C2C3=CC=C(CC(CCCC)CC)S3)=C(C4=CC=C(CC(CCCC)CC)S4)C5=C2C=C(S5)C(C6=NSN=C67)=C(F)C=C7C8=CC9=C(C%10=CC(CCCCCC)=C(CC(CCCC)CC)S%10)C%11=C(C(C%12=CC(CCCCCC)=C(CC(CC)CCCC)S%12)=C9S8)C=C(C%13=CC(F)=C(C)C%14=NSN=C%14%13)S%11,BFS4b,5.15,3.59,0.9,14.2,0.611,7.8,"Qin, T.; Zajaczkowski, W.; Pisula, W.; Baumgarten, M.; Chen, M.; Gao, M.; Wilson, G.; Easton, C. D.; Mu, K.; Watkins, S. E. Tailored Donor ? Acceptor Polymers with an A ? D1 ? A ? D2 Structure: Controlling Intermolecular Interactions to Enable Enhanced Polymer Photovoltaic Devices. J. Am. Chem. Soc. 2014, 136, 6049¨C6055. "
1019,O=C(OCC(CC)CCCC)C1=CC2=C(C)SC(C3=CC4=C(OCC(CCCC)CC)C(SC(C)=C5)=C5C(OCC(CCCC)CC)=C4S3)=C2S1,PBDTTT-E,5.04,3.19,0.66,11.53,0.547,4.16,"Huo, L.; Zhang, S.; Guo, X.; Xu, F.; Li, Y.; Hou, J. Replacing Alkoxy Groups with Alkylthienyl Groups: A Feasible Approach to Improve the Properties of Photovoltaic Polymers. Angew. Chem. Int. Ed. 2011, 50, 9697¨C9702. "
1020,O=C(OCC(CC)CCCC)C1=CC2=C(C)SC(C3=CC4=C(C5=CC=C(CC(CCCC)CC)S5)C(SC(C)=C6)=C6C(C7=CC=C(CC(CC)CCCC)S7)=C4S3)=C2S1,PBDTTT-E-T,5.09,3.22,0.68,14.59,0.626,6.21,"Huo, L.; Zhang, S.; Guo, X.; Xu, F.; Li, Y.; Hou, J. Replacing Alkoxy Groups with Alkylthienyl Groups: A Feasible Approach to Improve the Properties of Photovoltaic Polymers. Angew. Chem. Int. Ed. 2011, 50, 9697¨C9702. "
1021,O=C(C(CCCC)CC)C1=CC2=C(C)SC(C3=CC4=C(OCC(CCCC)CC)C(SC(C)=C5)=C5C(OCC(CCCC)CC)=C4S3)=C2S1,PBDTTT-C,5.07,3.21,0.7,15.51,0.592,6.43,"Huo, L.; Zhang, S.; Guo, X.; Xu, F.; Li, Y.; Hou, J. Replacing Alkoxy Groups with Alkylthienyl Groups: A Feasible Approach to Improve the Properties of Photovoltaic Polymers. Angew. Chem. Int. Ed. 2011, 50, 9697¨C9702. "
1022,O=C([C@@H](CC)CCCC)C1=CC2=C(C)SC(C3=CC4=C(C5=CC=C(CC(CCCC)CC)S5)C(SC(C)=C6)=C6C(C7=CC=C(CC(CC)CCCC)S7)=C4S3)=C2S1,PBDTTT-C-T,5.11,3.25,0.74,17.48,0.587,7.59,"Huo, L.; Zhang, S.; Guo, X.; Xu, F.; Li, Y.; Hou, J. Replacing Alkoxy Groups with Alkylthienyl Groups: A Feasible Approach to Improve the Properties of Photovoltaic Polymers. Angew. Chem. Int. Ed. 2011, 50, 9697¨C9702. "
1023,CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC(CCCCCC)=C(C4=CC=C(C5=C(CCCCCC)C=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CC)CCCC,PBDTBT (Z3),4.8,2.95,0.84,6.28,0.369,1.95,"Hou, J.; Chen, H.-Y.; Zhang, S.; Yang, Y. Synthesis and Photovoltaic Properties of Two Benzo[1,2-b:3,4-b¡ä]dithiophene-Based Conjugated Polymers. J. Phys. Chem. C 2009, 113, 21202¨C21207. "
1024,CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC(OCCCCCC)=C(C4=CC=C(C5=C(OCCCCCC)C=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CC)CCCC,PBDTBT (Z4),5.2,3.65,0.4,5.27,0.606,1.28,"Hou, J.; Chen, H.-Y.; Zhang, S.; Yang, Y. Synthesis and Photovoltaic Properties of Two Benzo[1,2-b:3,4-b¡ä]dithiophene-Based Conjugated Polymers. J. Phys. Chem. C 2009, 113, 21202¨C21207. "
1025,CC(S1)=CC=C1C2=C(C(C3=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C3C4=O)=O)C4=C(S2)C5=CC=C(C6=CC7=C(C8=CC(SCCCC)=C(SCCCCCC)S8)C9=C(C=C(C)S9)C(C%10=CC(SCCCC)=C(SCCCCCC)S%10)=C7S6)S5,PDST-BDD,5.52,3.69,1,10.8,0.551,5.95,"Yao, H.; Zhang, H.; Ye, L.; Zhao, W.; Zhang, S.; Hou, J. Dialkylthio Substitution: An Effective Method to Modulate the Molecular Energy Levels of 2D-BDT Photovoltaic Polymers. ACS Appl. Mater. Interfaces 2016, 8, 3575¨C3583. "
1026,CC(S1)=CC=C1C2=C(C(C3=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C3C4=O)=O)C4=C(S2)C5=CC=C(C6=CC7=C(C8=CC=C(CC(CC)CCCC)S8)C9=C(C=C(C)S9)C(C%10=CC=C(CC(CCCC)CC)S%10)=C7S6)S5,PBDT-BDD,5.3,3.5,0.86,10.68,0.723,6.67,"Yao, H.; Zhang, H.; Ye, L.; Zhao, W.; Zhang, S.; Hou, J. Dialkylthio Substitution: An Effective Method to Modulate the Molecular Energy Levels of 2D-BDT Photovoltaic Polymers. ACS Appl. Mater. Interfaces 2016, 8, 3575¨C3583. "
1027,CC1=C2C(SC(C(OCC(CC)CCCC)=O)=C2F)=C(C3=CC4=C(C5=CC(SCCCC)=C(SCCCCCC)S5)C6=C(C=C(C)S6)C(C7=CC(SCCCC)=C(SCCCCCC)S7)=C4S3)S1,PDST-TT,5.5,3.87,0.98,10.15,0.45,4.48,"Yao, H.; Zhang, H.; Ye, L.; Zhao, W.; Zhang, S.; Hou, J. Dialkylthio Substitution: An Effective Method to Modulate the Molecular Energy Levels of 2D-BDT Photovoltaic Polymers. ACS Appl. Mater. Interfaces 2016, 8, 3575¨C3583. "
1028,CC(S1)=CC2=C1C(C3=CC(SCCCC)=C(SCCCCCC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CC(CCCCCCCC)CCCCCC)C6=O)S4)S8)C8=C2C9=CC(SCCCC)=C(SCCCCCC)S9,PDST-DPP,5.47,4.01,0.88,6.59,0.541,3.14,"Yao, H.; Zhang, H.; Ye, L.; Zhao, W.; Zhang, S.; Hou, J. Dialkylthio Substitution: An Effective Method to Modulate the Molecular Energy Levels of 2D-BDT Photovoltaic Polymers. ACS Appl. Mater. Interfaces 2016, 8, 3575¨C3583. "
1029,CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=NN=C(C6=CC=C(C)S6)C7=NON=C75)S4)=C2)=C3C=C1,P1,5.7,4.15,0.82,1.52,0.38,0.47,"Gendron, D.; Morin, P. O.; Najari, A.; Leclerc, M. Synthesis of New Pyridazine-Based Monomers and Related Polymers for Photovoltaic Applications. Macromol. Rapid Commun. 2010, 31, 1090¨C1094. "
1030,CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=NN=C(C6=CC=C(C)S6)C7=NC=CN=C75)S4)=C2)=C3C=C1,P2,5.73,3.88,0.66,0.55,0.35,0.13,"Gendron, D.; Morin, P. O.; Najari, A.; Leclerc, M. Synthesis of New Pyridazine-Based Monomers and Related Polymers for Photovoltaic Applications. Macromol. Rapid Commun. 2010, 31, 1090¨C1094. "
1031,CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=NN=C(C6=CC=C(C)S6)C7=NC(CCCCCCCC)=C(CCCCCCCC)N=C75)S4)=C2)=C3C=C1,P3,5.76,3.99,0.91,0.86,0.44,0.37,"Gendron, D.; Morin, P. O.; Najari, A.; Leclerc, M. Synthesis of New Pyridazine-Based Monomers and Related Polymers for Photovoltaic Applications. Macromol. Rapid Commun. 2010, 31, 1090¨C1094. "
1032,CC(S1)=CC2=C1C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(C(OCC(CCCCCCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(SCC(CCCC)CC)S9,PBT-S,5.01,2.98,0.64,14.9,0.703,6.7,"Li, S.; Ye, L.; Wang, Q.; Zhang, S.; Zhao, W.; Hou, J. Improving the Open-Circuit Voltage of Alkylthio-Substituted Photovoltaic Polymers via Post-Oxidation. Org. Electron. 2016, 28, 39¨C46. "
1033,CC(S1)=CC2=C1C(C3=CC=C(S(CC(CCCC)CC)(=O)=O)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(C(OCC(CCCCCCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(S(CC(CCCC)CC)(=O)=O)S9,PBT-SO2-M,5.23,3.16,0.81,5.95,0.379,1.82,"Li, S.; Ye, L.; Wang, Q.; Zhang, S.; Zhao, W.; Hou, J. Improving the Open-Circuit Voltage of Alkylthio-Substituted Photovoltaic Polymers via Post-Oxidation. Org. Electron. 2016, 28, 39¨C46. "
1034,CC(S1)=CC2=C1C(C3=CC=C(S(CC(CCCC)CC)(=O)=O)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(C(OCC(CCCCCCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(S(CC(CCCC)CC)(=O)=O)S9,PBT-SO2-H,5.16,3.14,0.71,14.6,0.629,6.52,"Li, S.; Ye, L.; Wang, Q.; Zhang, S.; Zhao, W.; Hou, J. Improving the Open-Circuit Voltage of Alkylthio-Substituted Photovoltaic Polymers via Post-Oxidation. Org. Electron. 2016, 28, 39¨C46. "
1035,CC1=CC2=C(S1)C(C3=CC=C(CC(CCCC)CC)S3)=C4C(SC(C5=CC=C(C6=C(C(F)=C(C(OCCC(CCCCCC)CCCCCCCC)=O)S7)C7=C(C8=CC=C(C)S8)S6)S5)=C4)=C2C9=CC=C(CC(CC)CCCC)S9,PBT-T,4.95,3.12,0.6,13.7,0.677,5.56,"Zhang, M.; Guo, X.; Ma, W.; Zhang, S.; Huo, L.; Ade, H.; Hou, J. An Easy and Effective Method to Modulate Molecular Energy Level of the Polymer Based on Benzodithiophene for the Application in Polymer Solar Cells. Adv. Mater. 2014, 26, 2089¨C2095. "
1036,CC1=CC2=C(S1)C(C3=CC=CC(OCC(CCCC)CC)=C3)=C4C(SC(C5=CC=C(C6=C(C(F)=C(C(OCCC(CCCCCC)CCCCCCCC)=O)S7)C7=C(C8=CC=C(C)S8)S6)S5)=C4)=C2C9=CC=CC(OCC(CC)CCCC)=C9,PBT-OP,5.17,3.14,0.78,13.4,0.718,7.5,"Zhang, M.; Guo, X.; Ma, W.; Zhang, S.; Huo, L.; Ade, H.; Hou, J. An Easy and Effective Method to Modulate Molecular Energy Level of the Polymer Based on Benzodithiophene for the Application in Polymer Solar Cells. Adv. Mater. 2014, 26, 2089¨C2095. "
1037,CC1=CC2=C(S1)C(C3=NC=C(CCCCCCCCCC)S3)=C4C(SC(C5=C(C(N(CCCCCCCC)C6=O)=O)C6=C(C)S5)=C4)=C2C7=NC=C(CCCCCCCCCC)S7,PBDT-Tz-TPD (P1),5.65,3.84,0.82,1.05,0.32,0.27,"Xiao, Z.; Subbiah, J.; Sun, K.; Ji, S.; Jones, D. J.; Holmes, A. B.; Wong, W. W. H. Thiazolyl Substituted Benzodithiophene Copolymers: Synthesis, Properties and Photovoltaic Applications. J. Mater. Chem. C 2014, 2, 1306¨C1313. "
1038,CC1=CC2=C(S1)C(C3=NC=C(CCCCCCCCCC)S3)=C4C(SC(C5=CC=C(C6=C7C(C(N6CC(CC)CCCC)=O)=C(C8=CC=C(C)S8)N(CC(CC)CCCC)C7=O)S5)=C4)=C2C9=NC=C(CCCCCCCCCC)S9,PBDT-Tz-DPP (P2),5.18,3.84,0.44,7.6,0.49,1.63,"Xiao, Z.; Subbiah, J.; Sun, K.; Ji, S.; Jones, D. J.; Holmes, A. B.; Wong, W. W. H. Thiazolyl Substituted Benzodithiophene Copolymers: Synthesis, Properties and Photovoltaic Applications. J. Mater. Chem. C 2014, 2, 1306¨C1313. "
1039,CC1=CC2=C(S1)C(C3=NC=C(CCCCCCCCCC)S3)=C4C(SC(C5=C(SC(C(OCCCCCCCCCCCC)=O)=C6)C6=C(C)S5)=C4)=C2C7=NC=C(CCCCCCCCCC)S7,PBDT-Tz-TT (P3),5.09,3.84,0.44,9.5,0.55,2.3,"Xiao, Z.; Subbiah, J.; Sun, K.; Ji, S.; Jones, D. J.; Holmes, A. B.; Wong, W. W. H. Thiazolyl Substituted Benzodithiophene Copolymers: Synthesis, Properties and Photovoltaic Applications. J. Mater. Chem. C 2014, 2, 1306¨C1313. "
1040,O=C(OCC(CC)CCCC)C1=C(F)C2=C(C3=CC4=C(C(C5=CC(SC(CC(CC)CCCC)=C6)=C6S5)=C(C=C(C)S7)C7=C4C8=CC(SC(CC(CCCC)CC)=C9)=C9S8)S3)SC(C)=C2S1,PTTBDT-FTT,5.31,3.76,0.77,14.7,0.68,7.71,"Kim, J.-H.; Song, C. E.; Kim, B.; Kang, I.; Shin, W. S.; Hwang, D. Thieno[3,2-b]thiophene-Substituted Benzo[1,2-b?:4,5-b¡ä]dithiophene as a Promising Building Block for Low Bandgap Semiconducting Polymers for High-Performance Single and Tandem Organic Photovoltaic Cells. Chem. Mater. 2014, 26, 1234¨C1242. "
1041,O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(/C=C/C6=CC=C(SCC(CC)CCCC)S6)S5)=C(C=C(C)S7)C7=C4C8=CC=C(/C=C/C9=CC=C(SC[C@H](CCCC)CC)S9)S8)S3)=C2S1,PBT-TVT,5.29,3.76,0.81,16,0.627,8.13,"Yao, H.; Zhang, H.; Ye, L.; Zhao, W.; Zhang, S.; Hou, J. Molecular Design and Application of a Photovoltaic Polymer with Improved Optical Properties and Molecular Energy Levels. Macromolecules 2015, 48, 3493¨C3499. "
1042,CC(S1)=CC2=C1C(C3=CC(C=C(CC(CCCC)CCCCCC)C=C4)=C4S3)=C(C=C(C5=C(CC(CC)CCCC)C=C(C6=C(F)C(F)=C(C7=CC(CC(CCCC)CC)=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC(C=C(CC(CCCC)CCCCCC)C=C%11)=C%11S%10,PBDTBzT-DTffBT,5.47,3.73,0.9,12.93,0.627,7.3,"Wang, J.; Xiao, M.; Chen, W.; Qiu, M.; Du, Z.; Zhu, W.; Wen, S.; Wang, N.; Yang, R. Extending Pi-Conjugation System with Benzene: An Effective Method to Improve the Properties of Benzodithiophene-Based Polymer for Highly Efficient Organic Solar Cells. Macromolecules 2014, 47, 7823¨C7830. "
1043,CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9,PBDTT-DTffBT,5.36,3.6,0.94,9.83,0.579,5.35,"Wang, J.; Xiao, M.; Chen, W.; Qiu, M.; Du, Z.; Zhu, W.; Wen, S.; Wang, N.; Yang, R. Extending Pi-Conjugation System with Benzene: An Effective Method to Improve the Properties of Benzodithiophene-Based Polymer for Highly Efficient Organic Solar Cells. Macromolecules 2014, 47, 7823¨C7830. "
1044,CC(S1)=CC2=C1C(C3=CC=C(C4=CC(OCCCCCCCC)=C(OCCCCCCCC)C(OCCCCCCCC)=C4)S3)=C(C=C(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC=C(C%11=CC(OCCCCCCCC)=C(OCCCCCCCC)C(OCCCCCCCC)=C%11)S%10,PTOBDTDTBT,5.4,3.73,0.8,11.94,0.651,6.21,"Han, L.; Bao, X.; Hu, T.; Du, Z.; Chen, W.; Zhu, D.; Liu, Q.; Sun, M.; Yang, R. Novel Donor¨CAcceptor Polymer Containing 4,7-Bis(thiophen-2-ylbenzo[c][1,2,5]thiadiazole for Polymer Solar Cells with Power Conversion Efficiency of 6.21%. Macromol. Rapid Commun. 2014, 35, 1153?1157. "
1045,CC(S1)=CC2=C1C(C3=CC(C4=CC=C(CCCCCCCCCCCC)S4)=C(C5=CC=C(CCCCCCCCCCCC)S5)S3)=C(C=C(C6=CC=C(C7=NN=C(C8=CC=C(C)S8)N=N7)S6)S9)C9=C2C%10=CC(C%11=CC=C(CCCCCCCCCCCC)S%11)=C(C%12=CC=C(CCCCCCCCCCCC)S%12)S%10,PQ1,5.61,3.65,1.01,2.12,0.507,1.08,"Liu, Q.; Bao, X.; Han, L.; Gu, C.; Qiu, M.; Du, Z.; Sheng, R.; Sun, M.; Yang, R. Improved Open-Circuit Voltage of Benzodithiophene Based Polymer Solar Cells Using Bulky Terthiophene Side Group. Sol. Energy Mater. Sol. Cells 2015, 138, 26¨C34. "
1046,CC(S1)=CC2=C1C(C3=CC(C4=CC=C(CCCCCCCCCCCC)S4)=C(C5=CC=C(CCCCCCCCCCCC)S5)S3)=C(C=C(C6=CC=C(C7=CC=C(C8=CC=C(C)S8)S7)S6)S9)C9=C2C%10=CC(C%11=CC=C(CCCCCCCCCCCC)S%11)=C(C%12=CC=C(CCCCCCCCCCCC)S%12)S%10,PQ2,5.28,3.31,0.8,7.68,0.621,3.8,"Liu, Q.; Bao, X.; Han, L.; Gu, C.; Qiu, M.; Du, Z.; Sheng, R.; Sun, M.; Yang, R. Improved Open-Circuit Voltage of Benzodithiophene Based Polymer Solar Cells Using Bulky Terthiophene Side Group. Sol. Energy Mater. Sol. Cells 2015, 138, 26¨C34. "
1047,CC(S1)=CC2=C1C(C3=CC(C4=CC=C(CCCCCCCCCCCC)S4)=C(C5=CC=C(CCCCCCCCCCCC)S5)S3)=C(C=C(C6=CC=C(C7=C8C(C(N7CC(CC)CCCC)=O)=C(C9=CC=C(C)S9)N(CC(CCCC)CC)C8=O)S6)S%10)C%10=C2C%11=CC(C%12=CC=C(CCCCCCCCCCCC)S%12)=C(C%13=CC=C(CCCCCCCCCCCC)S%13)S%11,PQ3,5.31,4.02,0.78,2.67,0.524,1.09,"Liu, Q.; Bao, X.; Han, L.; Gu, C.; Qiu, M.; Du, Z.; Sheng, R.; Sun, M.; Yang, R. Improved Open-Circuit Voltage of Benzodithiophene Based Polymer Solar Cells Using Bulky Terthiophene Side Group. Sol. Energy Mater. Sol. Cells 2015, 138, 26¨C34. "
1048,CC(S1)=CC2=C1C(C3=CC(C4=CC=C(CCCCCCCCCCCC)S4)=C(C5=CC=C(CCCCCCCCCCCC)S5)S3)=C(C=C(C6=C(CCCCCC)C=C(C7=C(F)C(F)=C(C8=CC(CCCCCC)=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC(C%12=CC=C(CCCCCCCCCCCC)S%12)=C(C%13=CC=C(CCCCCCCCCCCC)S%13)S%11,PQ4,5.59,3.86,0.94,6.17,0.488,2.83,"Liu, Q.; Bao, X.; Han, L.; Gu, C.; Qiu, M.; Du, Z.; Sheng, R.; Sun, M.; Yang, R. Improved Open-Circuit Voltage of Benzodithiophene Based Polymer Solar Cells Using Bulky Terthiophene Side Group. Sol. Energy Mater. Sol. Cells 2015, 138, 26¨C34. "
1049,CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCC)CCCCCC)S9,PBDT2FBT-T1,5.47,3.58,0.98,9.62,0.597,5.46,"Lee, J.; Kim, J. H.; Moon, B.; Kim, H. G.; Kim, M.; Shin, J.; Hwang, H.; Cho, K. Two-Dimensionally Extended?¦Ð-Conjugation of Donor-Acceptor Copolymers via Oligothienyl Side Chains for Efficient Polymer Solar Cells. Macromolecules 2015, 48, 1723¨C1735. "
1050,CC(S1)=CC2=C1C(C3=CC=C(C4=CC=C(CC(CCCCCC)CCCC)S4)S3)=C(C=C(C5=C(CC(CC)CCCC)C=C(C6=C(F)C(F)=C(C7=CC(CC(CCCC)CC)=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC=C(C%11=CC=C(CC(CCCC)CCCCCC)S%11)S%10,PBDT2FBT-T2,5.37,3.61,0.9,10.6,0.547,5.22,"Lee, J.; Kim, J. H.; Moon, B.; Kim, H. G.; Kim, M.; Shin, J.; Hwang, H.; Cho, K. Two-Dimensionally Extended?¦Ð-Conjugation of Donor-Acceptor Copolymers via Oligothienyl Side Chains for Efficient Polymer Solar Cells. Macromolecules 2015, 48, 1723¨C1735. "
1051,CC(S1)=CC2=C1C(C3=CC=C(C4=CC=C(C5=CC=C(CC(CCCCCC)CCCC)S5)S4)S3)=C(C=C(C6=C(CC(CC)CCCC)C=C(C7=C(F)C(F)=C(C8=CC(CC(CCCC)CC)=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC=C(C%12=CC=C(C%13=CC=C(CC(CCCC)CCCCCC)S%13)S%12)S%11,PBDT2FBT-T3,5.31,3.62,0.86,12.3,0.614,6.48,"Lee, J.; Kim, J. H.; Moon, B.; Kim, H. G.; Kim, M.; Shin, J.; Hwang, H.; Cho, K. Two-Dimensionally Extended?¦Ð-Conjugation of Donor-Acceptor Copolymers via Oligothienyl Side Chains for Efficient Polymer Solar Cells. Macromolecules 2015, 48, 1723¨C1735. "
1052,CC(S1)=CC2=C1C(C3=CC=C(C4=CC=C(C5=CC=C(C6=CC=C(CC(CCCCCC)CCCC)S6)S5)S4)S3)=C(C=C(C7=C(CC(CC)CCCC)C=C(C8=C(F)C(F)=C(C9=CC(CC(CCCC)CC)=C(C)S9)C%10=NSN=C%108)S7)S%11)C%11=C2C%12=CC=C(C%13=CC=C(C%14=CC=C(C%15=CC=C(CC(CCCC)CCCCCC)S%15)S%14)S%13)S%12,PBDT2FBT-T4,5.3,3.63,0.84,6.35,0.405,2.17,"Lee, J.; Kim, J. H.; Moon, B.; Kim, H. G.; Kim, M.; Shin, J.; Hwang, H.; Cho, K. Two-Dimensionally Extended?¦Ð-Conjugation of Donor-Acceptor Copolymers via Oligothienyl Side Chains for Efficient Polymer Solar Cells. Macromolecules 2015, 48, 1723¨C1735. "
1053,CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=C4C(C=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2C#C[Si](C(C)C)(C(C)C)C(C)C)S1,PTIPS-BDT-TT (P1),5.6,3.91,0.82,12.75,0.55,5.76,"Bathula, C.; Song, C. E.; Badgujar, S.; Hong, S.-J.; Kang, I.-N.; Moon, S.-J.; Lee, J.; Cho, S.; Shim, H.-K.; Lee, S. K. New TIPS-Substituted benzo[1,2-b:4,5-b¡ä]dithiopheneBased Copolymers for Application in Polymer Solar Cells. J. Mater. Chem. 2012, 22, 22224¨C22232. "
1054,CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=C4C(C(F)=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2C#C[Si](C(C)C)(C(C)C)C(C)C)S1,PTIPS-BDT-TT (P3),5.6,3.89,0.79,9.47,0.55,4.11,"Bathula, C.; Song, C. E.; Badgujar, S.; Hong, S.-J.; Kang, I.-N.; Moon, S.-J.; Lee, J.; Cho, S.; Shim, H.-K.; Lee, S. K. New TIPS-Substituted benzo[1,2-b:4,5-b¡ä]dithiopheneBased Copolymers for Application in Polymer Solar Cells. J. Mater. Chem. 2012, 22, 22224¨C22232. "
1055,CC1=CC2=C(C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C(C=C(C3=C4C(C=C(C(C(CC)CCCC)=O)S4)=C(C)S3)S5)C5=C2C#C[Si](C(C)C)(C(C)C)C(C)C)S1,PTIPS-BDT-TT (P2),5.61,3.94,0.78,8.38,0.48,3.16,"Bathula, C.; Song, C. E.; Badgujar, S.; Hong, S.-J.; Kang, I.-N.; Moon, S.-J.; Lee, J.; Cho, S.; Shim, H.-K.; Lee, S. K. New TIPS-Substituted benzo[1,2-b:4,5-b¡ä]dithiopheneBased Copolymers for Application in Polymer Solar Cells. J. Mater. Chem. 2012, 22, 22224¨C22232. "
1056,CC1=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3C=C1,PC-DTBT,5.48,3.46,0.8,7.66,0.5,3.05,"Zhou, E.; Cong, J.; Yamakawa, S.; Wei, Q.; Nakamura, M.; Tajima, K.; Yang, C.; Hashimoto, K. Synthesis of thieno[3,4-b]pyrazine-Based and 2,1,3-BenzothiadiazoleBased Donor-Acceptor Copolymers and Their Application in Photovoltaic Devices. Macromolecules 2010, 43, 2873¨C2879. "
1057,CC1=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C2=C3C=CC(C4=CC=C(C5=C6C(N=C(C)C(C)=N6)=C(C7=CC=C(C)S7)S5)S4)=C2)=C3C=C1,TP3,5.24,3.45,0.56,4.41,0.41,1.02,"Zhou, E.; Cong, J.; Yamakawa, S.; Wei, Q.; Nakamura, M.; Tajima, K.; Yang, C.; Hashimoto, K. Synthesis of thieno[3,4-b]pyrazine-Based and 2,1,3-BenzothiadiazoleBased Donor-Acceptor Copolymers and Their Application in Photovoltaic Devices. Macromolecules 2010, 43, 2873¨C2879. "
1058,CC1=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C2=C3C=CC(C4=CC=C(C5=C6C(N=C(C7=CC=CC=C7)C(C8=CC=CC=C8)=N6)=C(C9=CC=C(C)S9)S5)S4)=C2)=C3C=C1,TP4,5.23,3.55,0.62,3.94,0.37,0.9,"Zhou, E.; Cong, J.; Yamakawa, S.; Wei, Q.; Nakamura, M.; Tajima, K.; Yang, C.; Hashimoto, K. Synthesis of thieno[3,4-b]pyrazine-Based and 2,1,3-BenzothiadiazoleBased Donor-Acceptor Copolymers and Their Application in Photovoltaic Devices. Macromolecules 2010, 43, 2873¨C2879. "
1059,CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NSN=C64)S3)C=C2C7(CC(CC)CCCC)CC(CC)CCCC)C7=C1,PF-DTBT,5.56,3.47,1.02,5.12,0.51,2.67,"Zhou, E.; Cong, J.; Yamakawa, S.; Wei, Q.; Nakamura, M.; Tajima, K.; Yang, C.; Hashimoto, K. Synthesis of thieno[3,4-b]pyrazine-Based and 2,1,3-BenzothiadiazoleBased Donor-Acceptor Copolymers and Their Application in Photovoltaic Devices. Macromolecules 2010, 43, 2873¨C2879. "
1060,CC1=CC=C(C2=CC=C(C3=CC=C(C4=C(N=C(C)C(C)=N5)C5=C(C6=CC=C(C)S6)S4)S3)C=C2C7(CC(CC)CCCC)CC(CC)CCCC)C7=C1,TP1,5.26,3.45,0.6,3.97,0.57,1.37,"Zhou, E.; Cong, J.; Yamakawa, S.; Wei, Q.; Nakamura, M.; Tajima, K.; Yang, C.; Hashimoto, K. Synthesis of thieno[3,4-b]pyrazine-Based and 2,1,3-BenzothiadiazoleBased Donor-Acceptor Copolymers and Their Application in Photovoltaic Devices. Macromolecules 2010, 43, 2873¨C2879. "
1061,CC1=CC=C(C2=CC=C(C3=CC=C(C4=C(N=C(C5=CC=CC=C5)C(C6=CC=CC=C6)=N7)C7=C(C8=CC=C(C)S8)S4)S3)C=C2C9(CC(CC)CCCC)CC(CC)CCCC)C9=C1,TP2,5.27,3.53,0.64,4.07,0.34,0.89,"Zhou, E.; Cong, J.; Yamakawa, S.; Wei, Q.; Nakamura, M.; Tajima, K.; Yang, C.; Hashimoto, K. Synthesis of thieno[3,4-b]pyrazine-Based and 2,1,3-BenzothiadiazoleBased Donor-Acceptor Copolymers and Their Application in Photovoltaic Devices. Macromolecules 2010, 43, 2873¨C2879. "
1062,CC1=CC=C(C2=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C3=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=CC=C38)=C8C=C2N9C(CCCCCCCCCC)CCCCCCCCCC)C9=C1,PIC-DTBT,5.45,3.55,0.94,3.77,0.41,1.47,"Zhou, E.; Cong, J.; Yamakawa, S.; Wei, Q.; Nakamura, M.; Tajima, K.; Yang, C.; Hashimoto, K. Synthesis of thieno[3,4-b]pyrazine-Based and 2,1,3-BenzothiadiazoleBased Donor-Acceptor Copolymers and Their Application in Photovoltaic Devices. Macromolecules 2010, 43, 2873¨C2879. "
1063,CC1=CC=C(C2=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C3=CC(C4=CC=C(C5=C(N=C(C)C(C)=N6)C6=C(C7=CC=C(C)S7)S5)S4)=CC=C38)=C8C=C2N9C(CCCCCCCCCC)CCCCCCCCCC)C9=C1,TP5,5.3,3.47,0.68,2.55,0.49,0.84,"Zhou, E.; Cong, J.; Yamakawa, S.; Wei, Q.; Nakamura, M.; Tajima, K.; Yang, C.; Hashimoto, K. Synthesis of thieno[3,4-b]pyrazine-Based and 2,1,3-BenzothiadiazoleBased Donor-Acceptor Copolymers and Their Application in Photovoltaic Devices. Macromolecules 2010, 43, 2873¨C2879. "
1064,CC1=CC=C(C2=CC(N(C(CCCCCCCCCC)CCCCCCCCCC)C3=CC(C4=CC=C(C5=C(N=C(C6=CC=CC=C6)C(C7=CC=CC=C7)=N8)C8=C(C9=CC=C(C)S9)S5)S4)=CC=C3%10)=C%10C=C2N%11C(CCCCCCCCCC)CCCCCCCCCC)C%11=C1,TP6,5.32,3.59,0.7,3.94,0.46,1.27,"Zhou, E.; Cong, J.; Yamakawa, S.; Wei, Q.; Nakamura, M.; Tajima, K.; Yang, C.; Hashimoto, K. Synthesis of thieno[3,4-b]pyrazine-Based and 2,1,3-BenzothiadiazoleBased Donor-Acceptor Copolymers and Their Application in Photovoltaic Devices. Macromolecules 2010, 43, 2873¨C2879. "
1065,CC1=C2C(C=C(S(=O)(CC(CC)CCCC)=O)S2)=C(C3=CC4=C(C(OCC(CC)CCCC)=C(C=C(C)S5)C5=C4OCC(CC)CCCC)S3)S1,PBDTTT-S,5.12,3.49,0.76,14.1,0.58,6.22,"Huang, Y.; Huo, L.; Zhang, S.; Guo, X.; Han, C. C.; Li, Y.; Hou, J. Sulfonyl: A New Application of Electron-Withdrawing Substituent in Highly Efficient Photovoltaic Polymer. Chem. Commun. 2011, 47, 8904¨C8906. "
1066,CC1=C2C(C=C(C(OCC(CC)CCCC)=O)S2)=C(C3=CC4=C(C(OCCCCCCCC)=C(C=C(C)S5)C5=C4OCCCCCCCC)S3)S1,PTB2,4.94,3.22,0.58,14.1,0.624,5.1,"Carsten, B.; Szarko, J. M.; Son, H. J.; Wang, W.; Lu, L.; He, F.; Rolczynski, B. S.; Lou, S. J.; Chen, L. X.; Yu, L. Examining the Effect of the Dipole Moment on Charge Separation in Donor¨CAcceptor Polymers for Organic Photovoltaic Applications. J. Am. Chem. Soc. 2011, 133, 20468¨C20475. "
1067,O=C(OCC(CC)CCCC)C1=CC2=C(C)SC(C3=C(F)C4=C(C(OCC(CC)CCCC)=C(C(F)=C(C)S5)C5=C4OCC(CC)CCCC)S3)=C2S1,PTBF2,5.41,3.6,0.68,11.1,0.422,3.2,"Carsten, B.; Szarko, J. M.; Son, H. J.; Wang, W.; Lu, L.; He, F.; Rolczynski, B. S.; Lou, S. J.; Chen, L. X.; Yu, L. Examining the Effect of the Dipole Moment on Charge Separation in Donor¨CAcceptor Polymers for Organic Photovoltaic Applications. J. Am. Chem. Soc. 2011, 133, 20468¨C20475. "
1068,O=C(OCC(CCCCCC)CCCC)C1=CC2=C(C3=CC4=C(C(OCC(CCCCCC)CCCC)=C(C=C(C)S5)C5=C4OCC(CCCCCC)CCCC)S3)SC(C6=C(SC(C(OCC(CCCCCC)CCCC)=O)=C7)C7=C(C)S6)=C2S1,PBB3,4.95,3.28,0.63,6.37,0.51,2.04,"Carsten, B.; Szarko, J. M.; Son, H. J.; Wang, W.; Lu, L.; He, F.; Rolczynski, B. S.; Lou, S. J.; Chen, L. X.; Yu, L. Examining the Effect of the Dipole Moment on Charge Separation in Donor¨CAcceptor Polymers for Organic Photovoltaic Applications. J. Am. Chem. Soc. 2011, 133, 20468¨C20475. "
1069,CC1=C(C(SC(C(CCCCCCC)=O)=C2)=C2C3=O)C3=C(C4=CC5=C(C(OCC(CC)CCCC)=C(C=C(C)S6)C6=C5OCC(CC)CCCC)S4)S1,PBDT-CPDTO (P1),5.44,3.15,0.86,4.97,0.55,2.72,"Zhang, W.; Cao, J. M.; Liu, Y.; Xiao, Z.; Zhu, W. G.; Zuo, Q. Q.; Ding, L. M. Using Cyclopenta [2,1-b:3,4-c¡¯] Dithiophene-4-One as a Building Block for Low-Bandgap Conjugated Copolymers Applied in Solar Cells. Macromol. Rapid Commun. 2012, 33, 1574¨C1579. "
1070,CC1=C(C(SC(C(CCCCCCC)=O)=C2)=C2C3=O)C3=C(C4=CC5=C(C(SC(C)=C6)=C6[Si]5(CC(CC)CCCC)CC(CC)CCCC)S4)S1,PSB-CPDTO (P2),5.41,3.34,0.89,4.13,0.51,2.2,"Zhang, W.; Cao, J. M.; Liu, Y.; Xiao, Z.; Zhu, W. G.; Zuo, Q. Q.; Ding, L. M. Using Cyclopenta [2,1-b:3,4-c¡¯] Dithiophene-4-One as a Building Block for Low-Bandgap Conjugated Copolymers Applied in Solar Cells. Macromol. Rapid Commun. 2012, 33, 1574¨C1579. "
1071,CC1=C(C(SC(C(CCCCCCC)=O)=C2)=C2C3=O)C3=C(C4=CC(N(C(CCCCCCCC)CCCCCCCC)C5=C6C=CC(C)=C5)=C6C=C4)S1,PCz-CPDTO (P3),5.79,3.04,0.74,0.43,0.35,0.13,"Zhang, W.; Cao, J. M.; Liu, Y.; Xiao, Z.; Zhu, W. G.; Zuo, Q. Q.; Ding, L. M. Using Cyclopenta [2,1-b:3,4-c¡¯] Dithiophene-4-One as a Building Block for Low-Bandgap Conjugated Copolymers Applied in Solar Cells. Macromol. Rapid Commun. 2012, 33, 1574¨C1579. "
1072,CC1=C(C(SC(C(CCCCCCC)=O)=C2)=C2C3=O)C3=C(C4=CC(C(CCCCCCCC)(CCCCCCCC)C5=C6C=CC(C)=C5)=C6C=C4)S1,PFL-CPDTO (P4),5.92,3.06,0.68,0.11,0.28,0.03,"Zhang, W.; Cao, J. M.; Liu, Y.; Xiao, Z.; Zhu, W. G.; Zuo, Q. Q.; Ding, L. M. Using Cyclopenta [2,1-b:3,4-c¡¯] Dithiophene-4-One as a Building Block for Low-Bandgap Conjugated Copolymers Applied in Solar Cells. Macromol. Rapid Commun. 2012, 33, 1574¨C1579. "
1073,CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1,PBnDT-DTBT,5.4,3.13,0.87,10.03,0.573,5,"Zhou, H.; Yang, L.; Stuart, A. C.; Price, S. C.; Liu, S.; You, W. Development of Fluorinated Benzothiadiazole as a Structural Unit for a Polymer Solar Cell of 7% Efficiency. Angew. Chem. Int. Ed. 2011, 50, 2995¨C2998. "
1074,CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=C(F)C(F)=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1,PBnDT-DTffBT,5.54,3.33,0.91,12.91,0.612,7.2,"Zhou, H.; Yang, L.; Stuart, A. C.; Price, S. C.; Liu, S.; You, W. Development of Fluorinated Benzothiadiazole as a Structural Unit for a Polymer Solar Cell of 7% Efficiency. Angew. Chem. Int. Ed. 2011, 50, 2995¨C2998. "
1075,CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CC)CCCC)S1,PBDT-DODTBT,5.17,3.61,0.76,8.96,0.59,4.02,"Ding, P.; Chu, C. C.; Liu, B.; Peng, B.; Zou, Y.; He, Y.; Zhou, K.; Hsu, C. S. A HighMobility Low-Bandgap Copolymer for Efficient Solar Cells. Macromol. Chem. Phys. 2010, 211, 2555¨C2561. "
1076,CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC(/C=C/C4=C(CCCCCC)C=C(C5=CC=C(C6=CC(CCCCCC)=CS6)C7=NSN=C75)S4)=C(C)S3)S8)C8=C2OCC(CC)CCCC)S1,PTG1,5.56,3.63,0.84,10.59,0.49,4.32,"Gu, Z.; Shen, P.; Tsang, S.-W.; Tao, Y.; Zhao, B.; Tang, P.; Nie, Y.; Fang, Y.; Tan, S. Development of a New Benzo(1,2-b:4,5-b¡¯dithiophene-Based Copolymer with Conjugated Dithienylbenzothiadiazole-Vinylene Side Chains for Efficient Solar Cells. Chem. Commun. 2011, 47, 9381¨C9383. "
1077,CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC(/C=C/C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(C[C@@H](CCCC)CC)=CS6)C7=NSN=C75)S4)=C(C)S3)S8)C8=C2OCC(CC)CCCC)S1,P(BDT-TBTF),5.36,3.19,0.88,13.21,0.534,6.21,"Shen, P.; Bin, H.; Xiao, L.; Li, Y. Enhancing Photovoltaic Performance of Copolymers Containing Thiophene Unit with D-A Conjugated Side Chain by Rational Molecular Design. Macromolecules 2013, 46, 9575¨C9586. "
1078,CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(N(C4=CC=C(C)C=C4)C5=CC=C(C6=CC=C(C7=CC=C(C8=CC=C(CCCCCCCC)S8)C9=NSN=C97)S6)C=C5)C=C3)S%10)C%10=C2OCC(CC)CCCC)S1,PBDT-TPA (P1),5.38,3.57,0.86,9.4,0.39,3.17,"Nie, K.; Tan, H.; Deng, X.; Wang, Y.; Chen, Q.; Huang, Y.; Liu, Y.; Yang, C.; Huang, Z.; Zhu, M.; Zhu, W. Reduced-Bandgap Triphenylamine-Alt-benzo[1,2-b:4,5- b¡ä]dithiophene Copolymers Pending Benzothiadiazole or Diketopyrrolopyrrole Units for Efficient Polymer Solar Cells. J. Polym. Sci. Part A Polym. Chem. 2013, 51, 4103¨C4110. "
1079,CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(N(C4=CC=C(C)C=C4)C5=CC=C(C6=CC=C(C7=C8C(C(N7CC(CCCC)CC)=O)=C(C9=CC=C(C%10=CC=C(CCCCCCCC)S%10)S9)N(CC(CC)CCCC)C8=O)S6)C=C5)C=C3)S%11)C%11=C2OCC(CC)CCCC)S1,PBDT-TPA (P2),5.22,3.53,0.8,10.77,0.35,3.05,"Nie, K.; Tan, H.; Deng, X.; Wang, Y.; Chen, Q.; Huang, Y.; Liu, Y.; Yang, C.; Huang, Z.; Zhu, M.; Zhu, W. Reduced-Bandgap Triphenylamine-Alt-benzo[1,2-b:4,5- b¡ä]dithiophene Copolymers Pending Benzothiadiazole or Diketopyrrolopyrrole Units for Efficient Polymer Solar Cells. J. Polym. Sci. Part A Polym. Chem. 2013, 51, 4103¨C4110. "
1080,CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(N(C4=CC=C(C5=CC=C(C6=CC=C(CCCCCCCC)S6)C7=NSN=C75)S4)C8=CC=C(C)C=C8)C=C3)S9)C9=C2OCC(CC)CCCC)S1,PDPAT-BDT-BT,5.42,3.6,0.87,7.61,0.498,3.27,"Su, W.; Fan, Q.; Xiao, M.; Chen, J.; Zhou, P.; Liu, B.; Tan, H.; Liu, Y.; Yang, R.; Zhu, W. Improved Photovoltaic Performance of a Side-Chain D-A Polymer in Polymer Solar Cells by Shortening the Phenyl Spacer between the D and A Units. Macromol. Chem. Phys. 2014, 215, 2075¨C2083. "
1081,CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCCCCCCCCCCC)S9)S1,PBDT-OBT,5.32,3.58,0.82,12.53,0.549,5.64,"Peng, Q.; Liu, X.; Su, D.; Fu, G.; Xu, J.; Dai, L. Novel benzo[1,2-b:4,5- b¡ä]dithiophene-Benzothiadiazole Derivatives with Variable Side Chains for HighPerformance Solar Cells. Adv. Mater. 2011, 23, 4554¨C4558. "
1082,CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=C(CCCCCCCC)C=C(C5=CC(F)=C(C6=CC(CCCCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCCCCCCCCCCC)S9)S1,PBDT-FBT,5.41,3.72,0.86,12.05,0.599,6.21,"Peng, Q.; Liu, X.; Su, D.; Fu, G.; Xu, J.; Dai, L. Novel benzo[1,2-b:4,5- b¡ä]dithiophene-Benzothiadiazole Derivatives with Variable Side Chains for HighPerformance Solar Cells. Adv. Mater. 2011, 23, 4554¨C4558. "
1083,CC1=CC(N(C2=CC=C(N(C3=CC=C(OCC(CCCCCC)CCCC)C=C3)C4=CC=C(OCC(CCCCCC)CCCC)C=C4)C=C2)C5=C6C=CC(C7=CC=C(C8=C(N=C(C9=CC=CC=C9)C(C%10=CC=CC=C%10)=N%11)C%11=C(C%12=CC=C(C)S%12)C%13=NSN=C%138)S7)=C5)=C6C=C1,P3,4.8,3.7,0.41,5.16,0.29,0.61,"Yi, H.; Johnson, R. G.; Iraqi, A.; Mohamad, D.; Royce, R.; Lidzey, D. G. Narrow Energy Gap Polymers with Absorptions up to 1200 Nm and Their Photovoltaic Properties. Macromol. Rapid Commun. 2008, 29, 1804¨C1809. "
1084,CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CCC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1,PBnDT-FTAZ,5.46,3.42,0.78,7.8,0.544,4.1,"Li, W.; Yang, L.; Tumbleston, J. R.; Yan, L.; Ade, H.; You, W. Controlling Molecular Weight of a High Efficiency Donor-Acceptor Conjugated Polymer and Understanding Its Significant Impact on Photovoltaic Properties. Adv. Mater. 2014, 26, 4456¨C4462. "
1085,CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CCC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1,PBnDT-FTAZ,5.51,3.48,0.76,11.4,0.642,5.8,"Li, W.; Yang, L.; Tumbleston, J. R.; Yan, L.; Ade, H.; You, W. Controlling Molecular Weight of a High Efficiency Donor-Acceptor Conjugated Polymer and Understanding Its Significant Impact on Photovoltaic Properties. Adv. Mater. 2014, 26, 4456¨C4462. "
1086,CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CCC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1,PBnDT-FTAZ,5.59,3.57,0.78,13.3,0.705,7.7,"Li, W.; Yang, L.; Tumbleston, J. R.; Yan, L.; Ade, H.; You, W. Controlling Molecular Weight of a High Efficiency Donor-Acceptor Conjugated Polymer and Understanding Its Significant Impact on Photovoltaic Properties. Adv. Mater. 2014, 26, 4456¨C4462. "
1087,CC1=CC2=C(C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CCC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC)S1,PBnDT-FTAZ,5.51,3.49,0.75,12.7,0.633,6.4,"Li, W.; Yang, L.; Tumbleston, J. R.; Yan, L.; Ade, H.; You, W. Controlling Molecular Weight of a High Efficiency Donor-Acceptor Conjugated Polymer and Understanding Its Significant Impact on Photovoltaic Properties. Adv. Mater. 2014, 26, 4456¨C4462. "
1088,CC1=C(C[C@@H](CCCC)CC)C=C(S1)C(C2=NSN=C23)=NC=C3C4=CC(C[C@@H](CC)CCCC)=C(S4)C5=CC(C(C=C(CCCCCCCC)C(CCCCCCCC)=C6)=C6C7=C8SC(C)=C7)=C8S5,PNDT-DTPyT,5.36,3.42,0.71,14.16,0.617,6.2,"Zhou, H.; Yang, L.; Price, S. C.; Knight, K. J.; You, W. Enhanced Photovoltaic Performance of Low-Bandgap Polymers with Deep LUMO Levels. Angew. Chem. Int. Ed. 2010, 49, 7992¨C7995. "
1089,CC1=C(C[C@@H](CCCC)CC)C=C(S1)C(C2=NSN=C23)=NC=C3C4=CC(C[C@@H](CC)CCCC)=C(S4)C5=CC(C(N=C(CCCCCCCC)C(CCCCCCCC)=N6)=C6C7=C8SC(C)=C7)=C8S5,PQDT-DTPyT,5.5,3.44,0.75,13.49,0.551,5.57,"Zhou, H.; Yang, L.; Price, S. C.; Knight, K. J.; You, W. Enhanced Photovoltaic Performance of Low-Bandgap Polymers with Deep LUMO Levels. Angew. Chem. Int. Ed. 2010, 49, 7992¨C7995. "
1090,CC1=C(C[C@@H](CCCC)CC)C=C(S1)C(C2=NSN=C23)=NC=C3C4=CC(C[C@@H](CC)CCCC)=C(S4)C5=CC(C(CCC(CCCCCC)CCCC)=C(SC(C)=C6)C6=C7CCC(CCCC)CCCCCC)=C7S5,PBnDT-DTPyT,5.47,3.44,0.85,12.78,0.582,6.32,"Zhou, H.; Yang, L.; Price, S. C.; Knight, K. J.; You, W. Enhanced Photovoltaic Performance of Low-Bandgap Polymers with Deep LUMO Levels. Angew. Chem. Int. Ed. 2010, 49, 7992¨C7995. "
1091,CC1=CC2=C(C=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NN(C(CCCCCCCC)CCCCCCCC)N=C64)S3)S7)C7=C2)S1,PBDT-DTBTz,5.26,3.29,0.77,7.87,0.48,2.88,"Kim, J. H.; Song, C. E.; Shin, N.; Kang, H.; Wood, S.; Kang, I. N.; Kim, B. J.; Kim, B.; Kim, J. S.; Shin, W. S.; Hwang, D. H. High-Crystalline Medium-Band-Gap Polymers Consisting of Benzodithiophene and Benzotriazole Derivatives for Organic Photovoltaic Cells. ACS Appl. Mater. Interfaces 2013, 5, 12820¨C12831. "
1092,CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(C(C=CC(CCCCCCCC)=C5)=C5C4=O)=O)=C(C)S3)O6)C6=C2OCC(CC)CCCC)O1,PBDFNTDO,5.33,3.4,0.87,9.14,0.592,4.71,"Chen, X.; Liu, B.; Zou, Y.; Xiao, L.; Guo, X.; He, Y.; Li, Y. A New benzo[1,2-b:4,5- b¡ä]difuran-Based Copolymer for Efficient Polymer Solar Cells. J. Mater. Chem. 2012, 22, 17724. "
1093,CC1=CC2=C(C(C3=CC=C(OCC(CCCC)CCCCCC)C(F)=C3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(OCC(CCCCCC)CCCC)C(F)=C9)S1,PBDTPF-DTBT,5.39,3.66,0.82,13.11,0.653,7.02,"Chen, W.; Du, Z.; Han, L.; Xiao, M.; Shen, W.; Wang, T.; Zhou, Y.; Yang, R. Efficient Polymer Solar Cells Based on a New benzo[1,2-b:4,5-b¡ä]dithiophene Derivative with Fluorinated Alkoxyphenyl Side Chain. J. Mater. Chem. A 2015, 3, 3130¨C3135. "
1094,CC1=CC2=C(C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S1,BDT-BT-2T,5.18,3.55,0.75,11.2,0.64,5.4,"Duan, C.; Furlan, A.; Van Franeker, J. J.; Willems, R. E. M.; Wienk, M. M.; Janssen, R. A. J. Wide-Bandgap Benzodithiophene-Benzothiadiazole Copolymers for Highly Efficient Multijunction Polymer Solar Cells. Adv. Mater. 2015, 27, 4461¨C4468. "
1095,CC1=CC2=C(C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S1,BDT-FBT-2T,5.33,3.63,0.85,13.3,0.68,7.7,"Duan, C.; Furlan, A.; Van Franeker, J. J.; Willems, R. E. M.; Wienk, M. M.; Janssen, R. A. J. Wide-Bandgap Benzodithiophene-Benzothiadiazole Copolymers for Highly Efficient Multijunction Polymer Solar Cells. Adv. Mater. 2015, 27, 4461¨C4468. "
1096,CC1=CC2=C(C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)O6)C7=NSN=C75)O4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S1,BDT-BT-2Fu,5.36,3.59,0.86,7.9,0.55,3.7,"Duan, C.; Furlan, A.; Van Franeker, J. J.; Willems, R. E. M.; Wienk, M. M.; Janssen, R. A. J. Wide-Bandgap Benzodithiophene-Benzothiadiazole Copolymers for Highly Efficient Multijunction Polymer Solar Cells. Adv. Mater. 2015, 27, 4461¨C4468. "
1097,CC1=CC2=C(C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)O6)C7=NSN=C75)O4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S1,BDT-FBT-2Fu,5.28,3.6,0.86,8.7,0.59,4.4,"Duan, C.; Furlan, A.; Van Franeker, J. J.; Willems, R. E. M.; Wienk, M. M.; Janssen, R. A. J. Wide-Bandgap Benzodithiophene-Benzothiadiazole Copolymers for Highly Efficient Multijunction Polymer Solar Cells. Adv. Mater. 2015, 27, 4461¨C4468. "
1098,CC1=CC2=C(C(C3=CC(CCCCCC)=C(C4=C(CCCCCC)C=C(CCCCCC)S4)S3)=C(C=C(C5=C(F)C(F)=C(C)C6=NSN=C65)S7)C7=C2C8=CC(CCCCCC)=C(C9=C(CCCCCC)C=C(CCCCCC)S9)S8)S1,PBDT-ffBT (P1),5.64,3.39,0.55,3.19,0.29,0.51,"Kularatne, R. S.; Taenzler, F. J.; Magurudeniya, H. D.; Du, J.; Murphy, J. W.; Sheina, E. E.; Gnade, B. E.; Biewer, M. C.; Stefan, M. C. Structural Variation of Donor-Acceptor Copolymers Containing Benzodithiophene with Bithienyl Substituents to Achieve High Open Circuit Voltage in Bulk Heterojunction Solar Cells. J. Mater. Chem. A 2013, 1, 15535¨C15543. "
1099,CC1=CC2=C(C(C3=CC(CCCCCC)=C(C4=C(CCCCCC)C=C(CCCCCC)S4)S3)=C(C=C(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC(CCCCCC)=C(C%11=C(CCCCCC)C=C(CCCCCC)S%11)S%10)S1,PBDT-BT (P2),5.47,3.13,1.03,7.05,0.48,3.52,"Kularatne, R. S.; Taenzler, F. J.; Magurudeniya, H. D.; Du, J.; Murphy, J. W.; Sheina, E. E.; Gnade, B. E.; Biewer, M. C.; Stefan, M. C. Structural Variation of Donor-Acceptor Copolymers Containing Benzodithiophene with Bithienyl Substituents to Achieve High Open Circuit Voltage in Bulk Heterojunction Solar Cells. J. Mater. Chem. A 2013, 1, 15535¨C15543. "
1100,CC1=CC2=C(C(C3=CC(CCCCCC)=C(C4=C(CCCCCC)C=C(CCCCCC)S4)S3)=C(C=C(C5=CC=C(C6=C(F)C(F)=C(C7=CC=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC(CCCCCC)=C(C%11=C(CCCCCC)C=C(CCCCCC)S%11)S%10)S1,PBDT-TffBT (P3),5.52,3.15,0.86,7.72,0.43,2.93,"Kularatne, R. S.; Taenzler, F. J.; Magurudeniya, H. D.; Du, J.; Murphy, J. W.; Sheina, E. E.; Gnade, B. E.; Biewer, M. C.; Stefan, M. C. Structural Variation of Donor-Acceptor Copolymers Containing Benzodithiophene with Bithienyl Substituents to Achieve High Open Circuit Voltage in Bulk Heterojunction Solar Cells. J. Mater. Chem. A 2013, 1, 15535¨C15543. "
1101,CC1=CC2=C(C(C3=CC=C(CCC(CCCCCC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCC(CCCC)CCCCCC)S9)S1,PBDT2FBT,5.6,3.59,0.94,7.21,0.519,3.47,"Lee, J.; Kim, M.; Kang, B.; Jo, S. B.; Kim, H. G.; Shin, J.; Cho, K. Side-Chain Engineering for Fine-Tuning of Energy Levels and Nanoscale Morphology in Polymer Solar Cells. Adv. Energy Mater. 2014, 4, 1400087/1¨C12. "
1102,CC1=CC2=C(C(C3=CC=C(OCC(CCCCCC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(OCC(CCCC)CCCCCC)S9)S1,PBDT2FBT-O,5.48,3.59,0.9,7.87,0.647,4.53,"Lee, J.; Kim, M.; Kang, B.; Jo, S. B.; Kim, H. G.; Shin, J.; Cho, K. Side-Chain Engineering for Fine-Tuning of Energy Levels and Nanoscale Morphology in Polymer Solar Cells. Adv. Energy Mater. 2014, 4, 1400087/1¨C12. "
1103,CC1=CC2=C(C(C3=CC=C(C[C@@H](CCCC)CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCC)CCCC)S9)S1,PBDT2FBT-T,5.55,3.58,0.98,10.6,0.578,6.37,"Lee, J.; Kim, M.; Kang, B.; Jo, S. B.; Kim, H. G.; Shin, J.; Cho, K. Side-Chain Engineering for Fine-Tuning of Energy Levels and Nanoscale Morphology in Polymer Solar Cells. Adv. Energy Mater. 2014, 4, 1400087/1¨C12. "
1104,CC1=CC2=C(C(C3=CC=C(OC[C@@H](CCCC)CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(OCC(CCCCCC)CCCC)S9)S1,PBDT2FBT-T-O,5.41,3.69,0.84,7.87,0.528,3.65,"Lee, J.; Kim, M.; Kang, B.; Jo, S. B.; Kim, H. G.; Shin, J.; Cho, K. Side-Chain Engineering for Fine-Tuning of Energy Levels and Nanoscale Morphology in Polymer Solar Cells. Adv. Energy Mater. 2014, 4, 1400087/1¨C12. "
1105,CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C([Se]C(C(OCC(CC)CCCC)=O)=C4)=C(C)[Se]3)S5)C5=C2OCC(CCCC)CC)S1,PSeB1,5.05,3.27,0.602,15.4,0.59,5.47,"Saadeh, H. a; Lu, L.; He, F.; Bullock, J. E.; Wang, W.; Carsten, B.; Yu, L. Polyselenopheno 3,4-b Selenophene for Highly Efficient Bulk Heterojunction Solar Cells. ACS Macro Lett. 2012, 1, 361¨C365. "
1106,CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C([Se]C(C(OCC(CC)CCCC)=O)=C4)=C(C)[Se]3)[Se]5)C5=C2OCC(CCCC)CC)[Se]1,PSeB2,5.04,3.26,0.64,16.8,0.64,6.87,"Saadeh, H. a; Lu, L.; He, F.; Bullock, J. E.; Wang, W.; Carsten, B.; Yu, L. Polyselenopheno 3,4-b Selenophene for Highly Efficient Bulk Heterojunction Solar Cells. ACS Macro Lett. 2012, 1, 361¨C365. "
1107,CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C(SC(C(OCC(CC)CCCC)=O)=C4)=C(C)S3)[Se]5)C5=C2OCC(CCCC)CC)[Se]1,PSeB3,5.05,3.27,0.635,14.6,0.66,6.13,"Saadeh, H. a; Lu, L.; He, F.; Bullock, J. E.; Wang, W.; Carsten, B.; Yu, L. Polyselenopheno 3,4-b Selenophene for Highly Efficient Bulk Heterojunction Solar Cells. ACS Macro Lett. 2012, 1, 361¨C365. "
1108,O=C1N(CC(CCCCCC)CCCCCCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC=C(C)S5)S4)N(CC(CCCCCCCC)CCCCCC)C3=O,PDPP3T,5.17,3.61,0.65,11.8,0.6,4.7,"Bijleveld, J. C.; Zoombelt, A. P.; Mathijssen, S. G. J.; Wienk, M. M.; Turbiez, M.; de Leeuw, D. M.; Janssen, R. A. J. Poly (Diketopyrrolopyrrole- Terthiophene for Ambipolar Logic and Photovoltaics. J. Am. Chem. Soc. 2009, 131, 16616¨C16617. "
1109,CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1,PBDTTTBO,5.46,3.68,0.85,11.8,0.59,5.9,"Jiang, J. M.; Raghunath, P.; Lin, H. K.; Lin, Y. C.; Lin, M. C.; Wei, K. H. Location and Number of Selenium Atoms in Two-Dimensional Conjugated Polymers Affect Their Band-Gap Energies and Photovoltaic Performance. Macromolecules 2014, 47, 7070¨C 7080. "
1110,CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=N[Se]N=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1,PBDTTTBS,5.29,3.6,0.66,10.1,0.5,3.3,"Jiang, J. M.; Raghunath, P.; Lin, H. K.; Lin, Y. C.; Lin, M. C.; Wei, K. H. Location and Number of Selenium Atoms in Two-Dimensional Conjugated Polymers Affect Their Band-Gap Energies and Photovoltaic Performance. Macromolecules 2014, 47, 7070¨C 7080. "
1111,CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)[Se]6)C7=NSN=C75)[Se]4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1,PBDTTTBO,5.4,3.71,0.79,11.9,0.5,4.7,"Jiang, J. M.; Raghunath, P.; Lin, H. K.; Lin, Y. C.; Lin, M. C.; Wei, K. H. Location and Number of Selenium Atoms in Two-Dimensional Conjugated Polymers Affect Their Band-Gap Energies and Photovoltaic Performance. Macromolecules 2014, 47, 7070¨C 7080. "
1112,CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)[Se]3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)[Se]9)S1,PBDTSTBO,5.46,3.68,0.86,13.9,0.64,7.6,"Jiang, J. M.; Raghunath, P.; Lin, H. K.; Lin, Y. C.; Lin, M. C.; Wei, K. H. Location and Number of Selenium Atoms in Two-Dimensional Conjugated Polymers Affect Their Band-Gap Energies and Photovoltaic Performance. Macromolecules 2014, 47, 7070¨C 7080. "
1113,CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)[Se]6)C7=N[Se]N=C75)[Se]4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1,PBDTTSBS,5.29,3.73,0.67,9.5,0.49,3,"Jiang, J. M.; Raghunath, P.; Lin, H. K.; Lin, Y. C.; Lin, M. C.; Wei, K. H. Location and Number of Selenium Atoms in Two-Dimensional Conjugated Polymers Affect Their Band-Gap Energies and Photovoltaic Performance. Macromolecules 2014, 47, 7070¨C 7080. "
1114,CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)[Se]3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=N[Se]N=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)[Se]9)S1,PBDTSTBS,5.29,3.6,0.67,11.4,0.52,4,"Jiang, J. M.; Raghunath, P.; Lin, H. K.; Lin, Y. C.; Lin, M. C.; Wei, K. H. Location and Number of Selenium Atoms in Two-Dimensional Conjugated Polymers Affect Their Band-Gap Energies and Photovoltaic Performance. Macromolecules 2014, 47, 7070¨C 7080. "
1115,CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)[Se]3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)[Se]6)C7=NSN=C75)[Se]4)S8)C8=C2C9=CC=C(CC(CC)CCCC)[Se]9)S1,PBDTSSBO,5.4,3.71,0.78,10,0.42,3.3,"Jiang, J. M.; Raghunath, P.; Lin, H. K.; Lin, Y. C.; Lin, M. C.; Wei, K. H. Location and Number of Selenium Atoms in Two-Dimensional Conjugated Polymers Affect Their Band-Gap Energies and Photovoltaic Performance. Macromolecules 2014, 47, 7070¨C 7080. "
1116,CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)[Se]3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)[Se]6)C7=N[Se]N=C75)[Se]4)S8)C8=C2C9=CC=C(CC(CC)CCCC)[Se]9)S1,PBDTSSBS,5.29,3.73,0.66,8.3,0.44,2.4,"Jiang, J. M.; Raghunath, P.; Lin, H. K.; Lin, Y. C.; Lin, M. C.; Wei, K. H. Location and Number of Selenium Atoms in Two-Dimensional Conjugated Polymers Affect Their Band-Gap Energies and Photovoltaic Performance. Macromolecules 2014, 47, 7070¨C 7080. "
1117,CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1,PBDTBT,5.34,3.23,0.88,10.73,0.536,5.06,"Shen, P.; Bin, H.; Zhang, Y.; Li, Y. Synthesis and Optoelectronic Properties of New D¨CA Copolymers Based on Fluorinated Benzothiadiazole and Benzoselenadiazole. Polym. Chem. 2014, 5, 567¨C577. "
1118,CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=N[Se]N=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1,PBDTBSe,5.3,3.47,0.81,5.36,0.506,2.2,"Shen, P.; Bin, H.; Zhang, Y.; Li, Y. Synthesis and Optoelectronic Properties of New D¨CA Copolymers Based on Fluorinated Benzothiadiazole and Benzoselenadiazole. Polym. Chem. 2014, 5, 567¨C577. "
1119,CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)O5)C6=NON=C64)O3)S7)C7=C2OCC(CC)CCCC)S1,PBDT-DFBO,5.34,3.43,0.83,10.6,0.647,5.9,"Wang, Y.; Liu, Y.; Chen, S.; Peng, R.; Ge, Z. Significant Enhancement of Polymer Solar Cell Performance via Side- Chain Engineering and Simple Solvent Treatment. Chem. Mater. 2013, 25, 3196¨C3204. "
1120,CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)O6)C7=NON=C75)O4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1,PBDTT-DFBO,5.44,3.59,0.86,9.1,0.586,4.8,"Wang, Y.; Liu, Y.; Chen, S.; Peng, R.; Ge, Z. Significant Enhancement of Polymer Solar Cell Performance via Side- Chain Engineering and Simple Solvent Treatment. Chem. Mater. 2013, 25, 3196¨C3204. "
1121,CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)O3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)O6)C7=NON=C75)O4)S8)C8=C2C9=CC=C(CC(CC)CCCC)O9)S1,PBDTF-DFBO,5.4,3.61,0.83,12.7,0.62,6.6,"Wang, Y.; Liu, Y.; Chen, S.; Peng, R.; Ge, Z. Significant Enhancement of Polymer Solar Cell Performance via Side- Chain Engineering and Simple Solvent Treatment. Chem. Mater. 2013, 25, 3196¨C3204. "
1122,O=C1/C(C2=CC=C(C(S3)=CC(CCCCCCCCCC)=C3C(O4)=C(CCCCCCCCCC)C(C4=C5)=CC6=C5C(CCCCCCCCCC)=C(C7=C(CCCCCCCCCC)C=C(C)S7)O6)C=C2N1CC(CCCCCCCC)CCCCCCCCCC)=C8C(N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C9=C/8C=CC(C)=C9)=O,PinBDFID,5.7,3.8,0.737,1.66,0.486,0.59,"Kobilka, B. M.; Dubrovskiy, A. V.; Ewan, M. D.; Tomlinson, A. L.; Larock, R. C.; Chaudhary, S.; Jeffries-EL, M. Synthesis of 3,7-Diiodo-2,6-Di(thiophen-2-ylbenzo[1,2- b:4,5-b¡ä]difurans: Functional Building Blocks for the Design of New Conjugated Polymers. Chem. Commun. 2012, 48, 8919¨C8921. "
1123,O=C1/C(C2=CC=C(C(S3)=C(CCCCCCCCCC)C=C3C(O4)=C(CCCCCCCCCC)C(C4=C5)=CC6=C5C(CCCCCCCCCC)=C(C7=CC(CCCCCCCCCC)=C(C)S7)O6)C=C2N1CC(CCCCCCCC)CCCCCCCCCC)=C8C(N(C[C@@H](CCCCCCCCCC)CCCCCCCC)C9=C/8C=CC(C)=C9)=O,PoutBDFID,5.7,3.8,0.641,1.306,0.36,0.3,"Kobilka, B. M.; Dubrovskiy, A. V.; Ewan, M. D.; Tomlinson, A. L.; Larock, R. C.; Chaudhary, S.; Jeffries-EL, M. Synthesis of 3,7-Diiodo-2,6-Di(thiophen-2-ylbenzo[1,2- b:4,5-b¡ä]difurans: Functional Building Blocks for the Design of New Conjugated Polymers. Chem. Commun. 2012, 48, 8919¨C8921. "
1124,O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(OC[C@@H](CC)CCCC)=C5C(SC(C)=C5)=C4OCC(CC)CCCC)=C21)=O,P1,5.39,3.56,0.888,8,0.67,4.8,"Braunecker, W. A.; Owczarczyk, Z. R.; Garcia, A.; Kopidakis, N.; Larsen, R. E.; Hammond, S. R.; Ginley, D. S.; Olson, D. C. Benzodithiophene and Imide-Based Copolymers for Photovoltaic Applications. Chem. Mater. 2012, 24, 1346¨C1356. "
1125,O=C1N(CCCCCCCC)C(C2=C(C)SC(C(S3)=CC4=C3C(CC[C@@H](CC)CCCC)=C5C(SC(C)=C5)=C4CCC(CC)CCCC)=C21)=O,P2,5.67,3.74,1.005,2,0.39,0.8,"Braunecker, W. A.; Owczarczyk, Z. R.; Garcia, A.; Kopidakis, N.; Larsen, R. E.; Hammond, S. R.; Ginley, D. S.; Olson, D. C. Benzodithiophene and Imide-Based Copolymers for Photovoltaic Applications. Chem. Mater. 2012, 24, 1346¨C1356. "
1126,CC1=C(C=C(C(N(CCCCCCCC)C2=O)=O)C2=C3)C3=C(S1)C(S4)=CC5=C4C(OC[C@@H](CC)CCCC)=C6C(SC(C)=C6)=C5OCC(CC)CCCC,P4,5.37,3.94,0.792,5,0.52,2.1,"Braunecker, W. A.; Owczarczyk, Z. R.; Garcia, A.; Kopidakis, N.; Larsen, R. E.; Hammond, S. R.; Ginley, D. S.; Olson, D. C. Benzodithiophene and Imide-Based Copolymers for Photovoltaic Applications. Chem. Mater. 2012, 24, 1346¨C1356. "
1127,CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC,PBDT-TPD (P1),5.56,3.75,0.94,10.8,0.51,5.2,"Najari, A.; Beaupr¨¦, S.; Berrouard, P.; Zou, Y.; Pouliot, J. R.; Lepage-P¨¦russe, C.; Leclerc, M. Synthesis and Characterization of New thieno[3,4-c]pyrrole-4,6-Dione Derivatives for Photovoltaic Applications. Adv. Funct. Mater. 2011, 21, 718¨C728. "
1128,CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CC(CCCC)CC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC,PBDT-TPD (P2),5.66,3.87,0.96,6.2,0.43,2.6,"Najari, A.; Beaupr¨¦, S.; Berrouard, P.; Zou, Y.; Pouliot, J. R.; Lepage-P¨¦russe, C.; Leclerc, M. Synthesis and Characterization of New thieno[3,4-c]pyrrole-4,6-Dione Derivatives for Photovoltaic Applications. Adv. Funct. Mater. 2011, 21, 718¨C728. "
1129,CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC,PBDT-TPD (P3),5.6,3.82,0.93,10,0.51,4.8,"Najari, A.; Beaupr¨¦, S.; Berrouard, P.; Zou, Y.; Pouliot, J. R.; Lepage-P¨¦russe, C.; Leclerc, M. Synthesis and Characterization of New thieno[3,4-c]pyrrole-4,6-Dione Derivatives for Photovoltaic Applications. Adv. Funct. Mater. 2011, 21, 718¨C728. "
1130,CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=C5C(C(N(CC(CC)CCCC)C5=O)=O)=C(C6=CC=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC,PBDT-TPD (P5),5.49,3.7,0.76,2.9,0.43,0.95,"Najari, A.; Beaupr¨¦, S.; Berrouard, P.; Zou, Y.; Pouliot, J. R.; Lepage-P¨¦russe, C.; Leclerc, M. Synthesis and Characterization of New thieno[3,4-c]pyrrole-4,6-Dione Derivatives for Photovoltaic Applications. Adv. Funct. Mater. 2011, 21, 718¨C728. "
1131,CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC(CCCCCCCC)=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C6=C(CCCCCCCC)C=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC,PBDT-TPD (P7),5.56,3.7,0.89,7.6,0.57,3.9,"Najari, A.; Beaupr¨¦, S.; Berrouard, P.; Zou, Y.; Pouliot, J. R.; Lepage-P¨¦russe, C.; Leclerc, M. Synthesis and Characterization of New thieno[3,4-c]pyrrole-4,6-Dione Derivatives for Photovoltaic Applications. Adv. Funct. Mater. 2011, 21, 718¨C728. "
1132,CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC(CC)=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C6=C(CC)C=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC,PBDT-TPD (P8),5.54,3.78,0.76,9,0.51,3.5,"Najari, A.; Beaupr¨¦, S.; Berrouard, P.; Zou, Y.; Pouliot, J. R.; Lepage-P¨¦russe, C.; Leclerc, M. Synthesis and Characterization of New thieno[3,4-c]pyrrole-4,6-Dione Derivatives for Photovoltaic Applications. Adv. Funct. Mater. 2011, 21, 718¨C728. "
1133,CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C(CCCCCCCC)C=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C6=CC(CCCCCCCC)=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC,PBDT-TPD (P9),5.66,3.83,0.66,1.2,0.26,0.2,"Najari, A.; Beaupr¨¦, S.; Berrouard, P.; Zou, Y.; Pouliot, J. R.; Lepage-P¨¦russe, C.; Leclerc, M. Synthesis and Characterization of New thieno[3,4-c]pyrrole-4,6-Dione Derivatives for Photovoltaic Applications. Adv. Funct. Mater. 2011, 21, 718¨C728. "
1134,CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC(CCCCCCCC)=C(C4=C5C(C(N(CCCCCCCCCCCC)C5=O)=O)=C(C6=C(CCCCCCCC)C=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC,PBDT-TPD (P10),5.56,3.7,0.87,7.2,0.58,3.6,"Najari, A.; Beaupr¨¦, S.; Berrouard, P.; Zou, Y.; Pouliot, J. R.; Lepage-P¨¦russe, C.; Leclerc, M. Synthesis and Characterization of New thieno[3,4-c]pyrrole-4,6-Dione Derivatives for Photovoltaic Applications. Adv. Funct. Mater. 2011, 21, 718¨C728. "
1135,CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C(CCCCCCCC)C=C(C4=C5C(C(N(CCCCCCCCCCCC)C5=O)=O)=C(C6=CC(CCCCCCCC)=C(C)S6)S4)S3)S7)C7=C2OCC(CCCC)CC,PBDT-TPD (P11),5.73,3.78,0.92,2.3,0.34,0.7,"Najari, A.; Beaupr¨¦, S.; Berrouard, P.; Zou, Y.; Pouliot, J. R.; Lepage-P¨¦russe, C.; Leclerc, M. Synthesis and Characterization of New thieno[3,4-c]pyrrole-4,6-Dione Derivatives for Photovoltaic Applications. Adv. Funct. Mater. 2011, 21, 718¨C728. "
1136,CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(C(C)=O)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7,TPO(CO)(2EH/C1),5.41,3.62,1.05,10.3,0.57,6.1,"Warnan, J.; Bude, R.; Labban, A. El; Li, L.; Beaujuge, P. M. Electron-De Fi Cient N - Alkyloyl Derivatives of Thieno[3,4 - c ]Pyrrole-4,6- Dione Yield E Ffi Cient Polymer Solar Cells with Open-Circuit Voltages >1V. Chem. Mater. 2014, 26, 2829¨C2835. "
1137,CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(C(CCC)=O)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7,TPO(CO)(2EH/C3),5.41,3.62,1.08,10.7,0.57,6.5,"Warnan, J.; Bude, R.; Labban, A. El; Li, L.; Beaujuge, P. M. Electron-De Fi Cient N - Alkyloyl Derivatives of Thieno[3,4 - c ]Pyrrole-4,6- Dione Yield E Ffi Cient Polymer Solar Cells with Open-Circuit Voltages >1V. Chem. Mater. 2014, 26, 2829¨C2835. "
1138,CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(C(CCCCCCC)=O)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7,TPO(CO)(2EH/C7),5.41,3.62,1.05,10.6,0.6,6.7,"Warnan, J.; Bude, R.; Labban, A. El; Li, L.; Beaujuge, P. M. Electron-De Fi Cient N - Alkyloyl Derivatives of Thieno[3,4 - c ]Pyrrole-4,6- Dione Yield E Ffi Cient Polymer Solar Cells with Open-Circuit Voltages >1V. Chem. Mater. 2014, 26, 2829¨C2835. "
1139,CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(C(CCCCCCCCCCC)=O)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7,TPO(CO)(2EH/C11),5.41,3.62,1.06,7.7,0.57,4.6,"Warnan, J.; Bude, R.; Labban, A. El; Li, L.; Beaujuge, P. M. Electron-De Fi Cient N - Alkyloyl Derivatives of Thieno[3,4 - c ]Pyrrole-4,6- Dione Yield E Ffi Cient Polymer Solar Cells with Open-Circuit Voltages >1V. Chem. Mater. 2014, 26, 2829¨C2835. "
1140,CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(C(CCCCCCCCCCCCC)=O)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7,TPO(CO)(2EH/C13),5.41,3.62,1.05,7,0.56,4.1,"Warnan, J.; Bude, R.; Labban, A. El; Li, L.; Beaujuge, P. M. Electron-De Fi Cient N - Alkyloyl Derivatives of Thieno[3,4 - c ]Pyrrole-4,6- Dione Yield E Ffi Cient Polymer Solar Cells with Open-Circuit Voltages >1V. Chem. Mater. 2014, 26, 2829¨C2835. "
1141,CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7,TPD(2EH/C8),5.29,3.41,1,11.1,0.58,6.5,"Warnan, J.; Bude, R.; Labban, A. El; Li, L.; Beaujuge, P. M. Electron-De Fi Cient N - Alkyloyl Derivatives of Thieno[3,4 - c ]Pyrrole-4,6- Dione Yield E Ffi Cient Polymer Solar Cells with Open-Circuit Voltages >1V. Chem. Mater. 2014, 26, 2829¨C2835. "
1142,CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C6C(C(N(CCCCCCCC)C6=O)=O)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1,PBDTTPD,5.54,3.52,0.99,8.7,0.453,3.87,"Lu, K.; Fang, J.; Yan, H.; Zhu, X.; Yi, Y.; Wei, Z. A Facile Strategy to Enhance Absorption Coefficient and Photovoltaic Performance of Two-Dimensional Benzo [1,2-b:4,5-b¡¯]dithiophene and thieno[3,4-C]pyrrole-4,6-Dione Polymers via Subtle Chemical Structure Variations. Org. Electron. 2013, 14, 2652¨C2661. "
1143,CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=C6C(C(N(CCCCCCCC)C6=O)=O)=C(C7=CC(CCCCCC)=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1,PBDTTPD-HT,5.3,3.59,0.92,10.94,0.604,6.08,"Lu, K.; Fang, J.; Yan, H.; Zhu, X.; Yi, Y.; Wei, Z. A Facile Strategy to Enhance Absorption Coefficient and Photovoltaic Performance of Two-Dimensional Benzo [1,2-b:4,5-b¡¯]dithiophene and thieno[3,4-C]pyrrole-4,6-Dione Polymers via Subtle Chemical Structure Variations. Org. Electron. 2013, 14, 2652¨C2661. "
1144,O=C(N1C2=CC=C(OCC(CCCCCCCCCC)CCCCCCCC)C=C23)C(C4=CC=C(C5=CC=C(C)S5)S4)=C6C7=C1C3=C(C8=CC=C(C)S8)C(N7C9=C6C=C(OCC(CCCCCCCC)CCCCCCCCCC)C=C9)=O,INDT-T,4.24,3.02,0.59,6.88,0.58,2.35,"Fallon, K. J.; Wijeyasinghe, N.; Yaacobi-Gross, N.; Ashraf, R. S.; Freeman, D. M. E.; Palgrave, R. G.; Al-Hashimi, M.; Marks, T. J.; McCulloch, I.; Anthopoulos, T. D.; Bronstein, H. A Nature-Inspired Conjugated Polymer for High Performance Transistors and Solar Cells. Macromolecules 2015, 48, 5148¨C5154. "
1145,CC1=CC2=C(C(C3=CC(CCCCCC)=C(C4=C(CCCCCC)C=C(CCCCCC)S4)S3)=C(C=C(C5=CC=C(C)C6=NSN=C56)S7)C7=C2C8=CC(CCCCCC)=C(C9=C(CCCCCC)C=C(CCCCCC)S9)S8)S1,PBDTBT (P1),5.53,3.57,1,5.36,0.47,2.54,"Kularatne, R. S.; Sista, P.; Nguyen, H. Q.; Bhatt, M. P.; Biewer, M. C.; Stefan, M. C. Donor-Acceptor Semiconducting Polymers Containing Benzodithiophene with Bithienyl Substituents. Macromolecules 2012, 45, 7855¨C7862. "
1146,CC1=CC2=C(C(C3=CC(CCCCCC)=C(C4=C(CCCCCC)C=C(CCCCCC)S4)S3)=C(C=C(C5=C(C(N(CCCCCC)C6=O)=O)C6=C(C)S5)S7)C7=C2C8=CC(CCCCCC)=C(C9=C(CCCCCC)C=C(CCCCCC)S9)S8)S1,PBDTTPD (P2),5.52,3.48,0.91,3.22,0.45,1.33,"Kularatne, R. S.; Sista, P.; Nguyen, H. Q.; Bhatt, M. P.; Biewer, M. C.; Stefan, M. C. Donor-Acceptor Semiconducting Polymers Containing Benzodithiophene with Bithienyl Substituents. Macromolecules 2012, 45, 7855¨C7862. "
1147,CC1=CC2=C(C(C3=CC=C(C4=CC=CC(OCC(CC)CCCC)=C4)S3)=C(C=C(C5=CC=C(C6=C7C(C(N(CC(CCCC)CC)C7=O)=O)=C(C8=CC=C(C)S8)S6)S5)S9)C9=C2C%10=CC=C(C%11=CC(OCC(CCCC)CC)=CC=C%11)S%10)S1,P1,5.42,3.66,0.96,13.2,0.559,7.14,"Kranthiraja, K.; Gunasekar, K.; Cho, W.; Song, M.; Park, Y. G.; Lee, J. Y.; Shin, Y.; Kang, I.; Kim, A.; Kim, H.; Kim, B.; Jin, S. ¨CH. Alkoxyphenylthiophene Linked Benzodithiophene Based Medium Band Gap Polymers for Organic Photovoltaics: Efficiency Improvement upon Methanol Treatment Depends on the Planarity of Backbone. Macromolecules 2014, 47, 7060?7069. "
1148,CC1=CC2=C(C(C3=CC=C(C4=CC=CC(OCC(CC)CCCC)=C4)S3)=C(C=C(C5=CC=C(C6=C(OCCCCCCCC)C(OCCCCCCCC)=C(C7=CC=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC=C(C%11=CC(OCC(CCCC)CC)=CC=C%11)S%10)S1,P2,5.34,3.6,0.72,7.4,0.341,1.82,"Kranthiraja, K.; Gunasekar, K.; Cho, W.; Song, M.; Park, Y. G.; Lee, J. Y.; Shin, Y.; Kang, I.; Kim, A.; Kim, H.; Kim, B.; Jin, S. ¨CH. Alkoxyphenylthiophene Linked Benzodithiophene Based Medium Band Gap Polymers for Organic Photovoltaics: Efficiency Improvement upon Methanol Treatment Depends on the Planarity of Backbone. Macromolecules 2014, 47, 7060?7069. "
1149,CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C6=O)=O)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1,PBDTT-DTTPD,5.43,3.55,0.89,8.05,0.68,4.82,"Chung, H.-S.; Lee, W.-H.; Song, C. E.; Shin, Y.; Kim, J.; Lee, S. K.; Shin, W. S.; Moon, S.-J.; Kang, I.-N. Highly Conjugated Side-Chain-Substituted Benzo[1,2-b:4,5-b¡¯]dithiophene-Based Conjugated Polymers for Use in Polymer Solar Cells. Macromolecules 2014, 47, 97¨C105. "
1150,CC1=CC2=C(C(C3=CC=C(/C=C/C4=CC=C(CC(CC)CCCC)S4)S3)=C(C=C(C5=CC=C(C6=C7C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C7=O)=O)=C(C8=CC=C(C)S8)S6)S5)S9)C9=C2C%10=CC=C(/C=C/C%11=CC=C(CC(CCCC)CC)S%11)S%10)S1,PBDTTVT-DTTPD,5.4,3.53,0.87,10.9,0.63,6.04,"Chung, H.-S.; Lee, W.-H.; Song, C. E.; Shin, Y.; Kim, J.; Lee, S. K.; Shin, W. S.; Moon, S.-J.; Kang, I.-N. Highly Conjugated Side-Chain-Substituted Benzo[1,2-b:4,5-b¡¯]dithiophene-Based Conjugated Polymers for Use in Polymer Solar Cells. Macromolecules 2014, 47, 97¨C105. "
1151,CC1=CC2=C(C(OCC(CCCCCC)CCCC)=C(C=C(C3=C4C(C=C(C(OC)=O)C(C(OC)=O)=C4)=C(C)S3)S5)C5=C2OCC(CCCC)CCCCCC)S1,P1,5.59,3.48,0.87,6.69,0.46,2.74,"Douglas, J. D.; Griffini, G.; Holcombe, T. W.; Young, E. P.; Lee, O. P.; Chen, M. S.; Fr¨¦chet, J. M. J. Functionalized Isothianaphthene Monomers That Promote Quinoidal Character in Donor-Acceptor Copolymers for Organic Photovoltaics. Macromolecules2012, 45, 4069¨C4074. "
1152,CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C=C(C(N(CCCCCCCC)C5=O)=O)C5=C4)=C(C)S3)S6)C6=C2OCC(CC)CCCC)S1,P2a,5.66,3.63,0.71,7.7,0.53,2.94,"Douglas, J. D.; Griffini, G.; Holcombe, T. W.; Young, E. P.; Lee, O. P.; Chen, M. S.; Fr¨¦chet, J. M. J. Functionalized Isothianaphthene Monomers That Promote Quinoidal Character in Donor-Acceptor Copolymers for Organic Photovoltaics. Macromolecules2012, 45, 4069¨C4074. "
1153,CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(N(CC(CC)CCCC)C5=O)=O)C5=C4)=C(C)S3)S6)C6=C2OCCCCCCCC)S1,P2b,5.63,3.63,0.78,7.05,0.55,3.07,"Douglas, J. D.; Griffini, G.; Holcombe, T. W.; Young, E. P.; Lee, O. P.; Chen, M. S.; Fr¨¦chet, J. M. J. Functionalized Isothianaphthene Monomers That Promote Quinoidal Character in Donor-Acceptor Copolymers for Organic Photovoltaics. Macromolecules2012, 45, 4069¨C4074. "
1154,CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C=C(C(N(CC(CC)CCCC)C5=O)=O)C5=C4)=C(C)S3)S6)C6=C2OCC(CC)CCCC)S1,P2c,5.69,3.64,0.76,8.46,0.47,3.04,"Douglas, J. D.; Griffini, G.; Holcombe, T. W.; Young, E. P.; Lee, O. P.; Chen, M. S.; Fr¨¦chet, J. M. J. Functionalized Isothianaphthene Monomers That Promote Quinoidal Character in Donor-Acceptor Copolymers for Organic Photovoltaics. Macromolecules2012, 45, 4069¨C4074. "
1155,CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(N(CCCCCCCC)C5=O)=O)C5=C4)=C(C)S3)S6)C6=C2OCCCCCCCC)S1,P3,5.64,3.66,0.75,3.66,0.48,1.36,"Douglas, J. D.; Griffini, G.; Holcombe, T. W.; Young, E. P.; Lee, O. P.; Chen, M. S.; Fr¨¦chet, J. M. J. Functionalized Isothianaphthene Monomers That Promote Quinoidal Character in Donor-Acceptor Copolymers for Organic Photovoltaics. Macromolecules2012, 45, 4069¨C4074. "
1156,CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(C(N5CCCCCCCC)=O)=C4C5=O)=C(C)S3)S6)C6=C2OCCCCCCCC)S1,POBDTPD,5.23,4,0.7,10.6,0.64,4.7,"Kim, S.; Kim, Y.; Yun, H.; Kang, I.; Yoon, Y.; Shin, N.; Son, H. J.; Kim, H.; Ko, M. J.; Kim, B.; Kim, K.; Kim, Y.; Kwon, S. N - Octyl-2,7-Dithia-5-Azacyclopenta [a] Pentalene-4,6-Dione-Based Low Band Gap Polymers for Efficient Solar Cells.Macromolecules 2013, 46, 3861?3869. "
1157,CC1=CC2=C(C(OC[C@@H](CCCC)CC)=C(C=C(C3=C4C(SC(C(N5CCCCCCCC)=O)=C4C5=O)=C(C)S3)S6)C6=C2OCC(CC)CCCC)S1,PEBDTPO,5.37,4.06,0.72,13.5,0.54,5.3,"Kim, S.; Kim, Y.; Yun, H.; Kang, I.; Yoon, Y.; Shin, N.; Son, H. J.; Kim, H.; Ko, M. J.; Kim, B.; Kim, K.; Kim, Y.; Kwon, S. N - Octyl-2,7-Dithia-5-Azacyclopenta [a] Pentalene-4,6-Dione-Based Low Band Gap Polymers for Efficient Solar Cells.Macromolecules 2013, 46, 3861?3869. "
1158,CC1=CC2=C(C(OC[C@@H](CCCCCCCC)CCCCCC)=C(C=C(C3=CC=C(C4=C(C=C(C(N(CC(CCCC)CC)C5=O)=O)C5=C6)C6=C(C7=CC=C(C)S7)S4)S3)S8)C8=C2OCC(CCCCCC)CCCCCCCC)S1,PBDTTID,5.4,3.78,0.8,6.5,0.6,3.12,"Wu, Y.; Jing, Y.; Guo, X.; Zhang, S.; Zhang, M.; Huo, L.; Hou, J. A thieno[3,4-f]isoindole-5,7-Dione Based Copolymer for Polymer Solar Cells. Polym. Chem. 2013, 4, 536¨C541. "
1159,CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(CCCCCCCC)S4(=O)=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC,PID1,5.44,3.55,0.85,7.06,0.547,3.28,"Xu, T.; Lu, L.; Zheng, T.; Szarko, J. M.; Schneider, A.; Chen, L. X.; Yu, L. Tuning the Polarizability in Donor Polymers with a Thiophenesaccharin Unit for Organic Photovoltaic Applications. Adv. Funct. Mater. 2014, 24, 3432¨C3437. "
1160,CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(CC(CC)CCCC)S4(=O)=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC,PID2,5.52,3.4,0.88,5.94,0.586,3.05,"Xu, T.; Lu, L.; Zheng, T.; Szarko, J. M.; Schneider, A.; Chen, L. X.; Yu, L. Tuning the Polarizability in Donor Polymers with a Thiophenesaccharin Unit for Organic Photovoltaic Applications. Adv. Funct. Mater. 2014, 24, 3432¨C3437. "
1161,CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC,PPB1,5.38,3.55,0.86,10.4,0.666,5.97,"Xu, T.; Lu, L.; Zheng, T.; Szarko, J. M.; Schneider, A.; Chen, L. X.; Yu, L. Tuning the Polarizability in Donor Polymers with a Thiophenesaccharin Unit for Organic Photovoltaic Applications. Adv. Funct. Mater. 2014, 24, 3432¨C3437. "
1162,CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(CC(CC)CCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC,PPB2,5.4,3.55,0.88,8.23,0.622,4.48,"Xu, T.; Lu, L.; Zheng, T.; Szarko, J. M.; Schneider, A.; Chen, L. X.; Yu, L. Tuning the Polarizability in Donor Polymers with a Thiophenesaccharin Unit for Organic Photovoltaic Applications. Adv. Funct. Mater. 2014, 24, 3432¨C3437. "
1163,CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(CC(C(OCC)=O)(C(OCC)=O)C4)=C(C)S3)S5)C5=C2OCC(CCCC)CC,PBTCT,5.25,2.75,0.62,3.39,0.53,1.13,"Kim, B. G.; Ma, X.; Chen, C.; Ie, Y.; Coir, E. W.; Hashemi, H.; Aso, Y.; Green, P. F.; Kieffer, J.; Kim, J. Energy Level Modulation of HOMO, LUMO, and Band-Gap in Conjugated Polymers for Organic Photovoltaic Applications. Adv. Funct. Mater. 2013, 23, 439¨C445. "
1164,CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C=CC4=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC,PBTCTO,5.4,3.42,0.72,8.76,0.62,3.9,"Kim, B. G.; Ma, X.; Chen, C.; Ie, Y.; Coir, E. W.; Hashemi, H.; Aso, Y.; Green, P. F.; Kieffer, J.; Kim, J. Energy Level Modulation of HOMO, LUMO, and Band-Gap in Conjugated Polymers for Organic Photovoltaic Applications. Adv. Funct. Mater. 2013, 23, 439¨C445. "
1165,CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(/C(C4=O)=C(C)/C)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC,PBTPDO,5.42,3.51,0.73,10.68,0.62,4.84,"Kim, B. G.; Ma, X.; Chen, C.; Ie, Y.; Coir, E. W.; Hashemi, H.; Aso, Y.; Green, P. F.; Kieffer, J.; Kim, J. Energy Level Modulation of HOMO, LUMO, and Band-Gap in Conjugated Polymers for Organic Photovoltaic Applications. Adv. Funct. Mater. 2013, 23, 439¨C445. "
1166,CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(C(F)(F)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC,PBTFDO,5.45,3.92,0.79,1.2,0.45,0.27,"Kim, B. G.; Ma, X.; Chen, C.; Ie, Y.; Coir, E. W.; Hashemi, H.; Aso, Y.; Green, P. F.; Kieffer, J.; Kim, J. Energy Level Modulation of HOMO, LUMO, and Band-Gap in Conjugated Polymers for Organic Photovoltaic Applications. Adv. Funct. Mater. 2013, 23, 439¨C445. "
1167,CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(C5=CC=C(CCCCCCCC)C=C5)C4=O)=O)=C(C)S3)S6)C6=C2OCC(CCCC)CC,PBT8PT,5.36,3.51,0.88,12.37,0.62,6.78,"Kim, B. G.; Ma, X.; Chen, C.; Ie, Y.; Coir, E. W.; Hashemi, H.; Aso, Y.; Green, P. F.; Kieffer, J.; Kim, J. Energy Level Modulation of HOMO, LUMO, and Band-Gap in Conjugated Polymers for Organic Photovoltaic Applications. Adv. Funct. Mater. 2013, 23, 439¨C445. "
1168,CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(C(N(C6=CC=C(CCCCCCCC)C=C6)C5=O)=O)=C(C)S4)S7)C7=C2C8=CC=C(CC(CC)CCCC)S8,PTP8,5.59,3.62,0.96,11,0.585,6.18,"Yuan, J.; Dong, H.; Li, M.; Huang, X.; Zhong, J.; Li, Y.; Ma, W. High Polymer/fullerene Ratio Realized in Efficient Polymer Solar Cells by Tailoring of the Polymer Side-Chains. Adv. Mater. 2014, 26, 3624¨C3630."
1169,CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(C(C(C=C(CCCCCCCC)C=C6)=C6C5=O)=O)=C(C)S4)S7)C7=C2C8=CC=C(CC(CC)CCCC)S8,PTN8,5.6,3.81,0.97,8.28,0.417,3.35,"Yuan, J.; Liu, Y.; Dong, H.; Shi, X.; Liu, Z.; Li, Y.; Ma, W. The Effect of Molecular Geometry on the Polymer/fullerene Ratio in Polymer Solar Cells. Polym. Chem. 2015, 6, 7550¨C7557. "
1170,CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(C(SC(CCCCCC)=C5)=C5C4=O)=O)=C(C)S3)S6)C6=C2OCC(CC)CCCC,P1,5.49,3.53,0.87,4.75,0.45,2.18,"Cao, J.; Zhang, W.; Xiao, Z.; Liao, L.; Zhu, W.; Zuo, Q.; Ding, L. Synthesis and Photovoltaic Properties of Low Band Gap Polymers Containing Benzo[1,2-b:4,5-c¡¯]dithiophene-4,8-dione. Macromolecules 2012, 45, 1710?1714. "
1171,O=C1N(CCCCCCCCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C(C=C5)=CC6=C5C7=CC=C(C)C=C7N6C(CCCCCCCCCC)CCCCCCCCCC)S4)N(CCCCCCCCCC)C3=O,PCBTDPP,5.4,3.9,0.77,9.1,0.55,3.8,"Jo, J.; Gendron, D.; Najari, A.; Moon, J. S.; Cho, S.; Leclerc, M.; Heeger, A. J. Bulk Heterojunction Solar Cells Based on a Low-Bandgap Carbazole- Diketopyrrolopyrrole Copolymer. Appl. Phys. Lett. 2010, 97, 2008¨C2011. "
1172,CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)C=C3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CC)CCCC)SC(CC(CCCC)CC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)O9)C9=C2C%10=CC=C(CC(CC)CCCC)C=C%10)O1,PBDF-T1,4.74,2.54,0.91,13.49,0.755,9.23,"Huo, L.; Liu, T.; Fan, B.; Zhao, Z.; Sun, X.; Wei, D.; Yu, M.; Liu, Y.; Sun, Y. Organic Solar Cells Based on a 2D Benzo[1,2-b:4,5-b¡ä]difuran-Conjugated Polymer with HighPower Conversion Efficiency. Adv. Mater. 2015, 27, 6969¨C6975. "
1173,CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)C=C3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CC)CCCC)SC(CC(CCCC)CC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC=C(CC(CC)CCCC)C=C%10)S1,PBDT-T1,4.8,2.52,0.86,13.13,0.718,8.12,"Huo, L.; Liu, T.; Fan, B.; Zhao, Z.; Sun, X.; Wei, D.; Yu, M.; Liu, Y.; Sun, Y. Organic Solar Cells Based on a 2D Benzo[1,2-b:4,5-b¡ä]difuran-Conjugated Polymer with HighPower Conversion Efficiency. Adv. Mater. 2015, 27, 6969¨C6975. "
1174,CC1=CC=C(C2=CC=C(C)C3=C2N=C(C4=CC=C(OCCCCCCCC)C=C4)C(C5=CC=C(OCCCCCCCC)C=C5)=N3)S1,P(T-QX),5.57,3.92,0.79,6.3,0.659,3.3,"Fu, Y.; Cha, H.; Song, S.; Lee, G. Y.; Eon Park, C.; Park, T. Low-Bandgap Quinoxaline-Based D - A-Type Copolymers: Synthesis, Characterization, and Photovoltaic Properties. J. Polym. Sci. Part A Polym. Chem. 2013, 51, 372¨C382. "
1175,CC(C1=C2N=C(C3=CC=C(OCCCCCCCC)C=C3)C(C4=CC=C(OCCCCCCCC)C=C4)=N1)=CC=C2C5=CC6=C(C(OCC(CCCC)CC)=C(C=C(C)S7)C7=C6OCC(CC)CCCC)S5,P(BDT-Qx),5.41,3.63,0.77,5,0.503,1.9,"Fu, Y.; Cha, H.; Song, S.; Lee, G. Y.; Eon Park, C.; Park, T. Low-Bandgap Quinoxaline-Based D - A-Type Copolymers: Synthesis, Characterization, and Photovoltaic Properties. J. Polym. Sci. Part A Polym. Chem. 2013, 51, 372¨C382. "
1176,CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCC(CC)CCCC)=C(OCC(CCCC)CC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7,P(BDT-DTQx),5.43,3.75,0.65,6.3,0.552,2.3,"Fu, Y.; Cha, H.; Song, S.; Lee, G. Y.; Eon Park, C.; Park, T. Low-Bandgap Quinoxaline-Based D - A-Type Copolymers: Synthesis, Characterization, and Photovoltaic Properties. J. Polym. Sci. Part A Polym. Chem. 2013, 51, 372¨C382. "
1177,CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCCCCCCCC)=C(OCCCCCCCC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(C9=CC(CCCCCCCC)=CS9)C=C8)C(C%10=CC=C(C%11=CC(CCCCCCCC)=CS%11)C=C%10)=N7,PBDT-PTQ,5.11,3.64,0.65,12.5,0.54,4.39,"Qin, H.; Li, L.; Liang, T.; Peng, X.; Peng, J.; Cao, Y. Donor-Acceptor (Donor Polymers with Differently Conjugated Side Groups at the Acceptor Units for Photovoltaics. J. Polym. Sci. Part A Polym. Chem. 2013, 51, 1565¨C1572. "
1178,CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCCCCCCCC)=C(OCCCCCCCC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(C9=CC(CCCCCCCC)=C(C%10=CC(CCCCCCCC)=CS%10)S9)C=C8)C(C%11=CC=C(C%12=CC(CCCCCCCC)=C(C%13=CC(CCCCCCCC)=CS%13)S%12)C=C%11)=N7,PBDT-PTTQ,5.18,3.62,0.66,10.53,0.52,3.58,"Qin, H.; Li, L.; Liang, T.; Peng, X.; Peng, J.; Cao, Y. Donor-Acceptor (Donor Polymers with Differently Conjugated Side Groups at the Acceptor Units for Photovoltaics. J. Polym. Sci. Part A Polym. Chem. 2013, 51, 1565¨C1572. "
1179,CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCCCCCCCC)=C(OCCCCCCCC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(CCCCCC)S8)C(C9=CC=C(CCCCCC)S9)=N7,PBDT-TQ,4.99,3.62,0.72,8.13,0.45,2.62,"Qin, H.; Li, L.; Liang, T.; Peng, X.; Peng, J.; Cao, Y. Donor-Acceptor (Donor Polymers with Differently Conjugated Side Groups at the Acceptor Units for Photovoltaics. J. Polym. Sci. Part A Polym. Chem. 2013, 51, 1565¨C1572. "
1180,CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCCCCCCCC)=C(OCCCCCCCC)C6=C5C=C(C)S6)C7=C2N=C(C(S8)=CC=C8C9=CC(CCCCCCCC)=CS9)C(C%10=CC=C(S%10)C%11=CC(CCCCCCCC)=CS%11)=N7,PBDT-TTQ,5.08,3.61,0.62,4.8,0.51,1.52,"Qin, H.; Li, L.; Liang, T.; Peng, X.; Peng, J.; Cao, Y. Donor-Acceptor (Donor Polymers with Differently Conjugated Side Groups at the Acceptor Units for Photovoltaics. J. Polym. Sci. Part A Polym. Chem. 2013, 51, 1565¨C1572. "
1181,CC(S1)=CC=C1C2=C(N=C(C[C@@H](CCCC)CC)C(CC(CC)CCCC)=N3)C3=C(C(S4)=CC=C4C(S5)=CC(C5=C6OCCCCCCCCCCCC)=C(OCCCCCCCCCCCC)C7=C6C=C(C)S7)C8=NSN=C82,PBDT-DTQx,5.16,3.68,0.72,11.47,0.62,5.12,"Keshtov, M. L.; Marochkin, D. V.; Kochurov, V. S.; Khokhlov, A. R.; Koukaras, E. N.; Sharma, G. D. Synthesis and Characterization of a Low Band Gap Quinoxaline Based D¨CA Copolymer and Its Application as a Donor for Bulk Heterojunction Polymer Solar Cells. Polym. Chem. 2013, 4, 4033¨C4044. "
1182,CC(S1)=CC=C1C2=C(N=C(C3=CC(OCCCCCC)=CC=C3)C(C4=CC=CC(OCCCCCC)=C4)=N5)C5=C(C(S6)=CC=C6C(S7)=CC(C7=C8OCC(CC)CCCC)=C(OCC(CCCC)CC)C9=C8C=C(C)S9)C(F)=C2F,PBDT-TFQ,5.52,3.3,0.76,17.9,0.576,8,"Chen, H. C.; Chen, Y. H.; Liu, C. C.; Chien, Y. C.; Chou, S. W.; Chou, P. T. Prominent Short-Circuit Currents of Fluorinated Quinoxaline-Based Copolymer Solar Cells with a Power Conversion Efficiency of 8.0%. Chem. Mater. 2012, 24, 4766¨C4772. "
1183,CC(S1)=CC=C1C2=C(N=C(C3=CC(OC[C@H](CC)CCCC)=CC=C3)C(C4=CC=CC(OCC(CC)CCCC)=C4)=N5)C5=C(C(S6)=CC=C6C(S7)=CC(C7=C8OCC(CC)CCCC)=C(OCC(CCCC)CC)C9=C8C=C(C)S9)C=C2,PBDTDTQx-O,5.12,3.38,0.71,7,0.615,3.06,"Duan, R.; Ye, L.; Guo, X.; Huang, Y.; Wang, P.; Zhang, S.; Zhang, J.; Huo, L.; Hou, J. Application of Two-Dimensional Conjugated Benzo[1,2- b?:4,5- b¡ä]dithiophene in Quinoxaline-Based Photovoltaic Polymers. Macromolecules 2012, 45, 3032¨C3038. "
1184,CC(S1)=CC=C1C2=C(N=C(C3=CC(OC[C@H](CC)CCCC)=CC=C3)C(C4=CC=CC(OCC(CC)CCCC)=C4)=N5)C5=C(C(S6)=CC=C6C(S7)=CC(C7=C8C9=CC=C(CC(CC)CCCC)S9)=C(C%10=CC=C(CC(CCCC)CC)S%10)C%11=C8C=C(C)S%11)C=C2,PBDTDTQx-T,5.12,3.45,0.76,10.13,0.643,5,"Duan, R.; Ye, L.; Guo, X.; Huang, Y.; Wang, P.; Zhang, S.; Zhang, J.; Huo, L.; Hou, J. Application of Two-Dimensional Conjugated Benzo[1,2- b?:4,5- b¡ä]dithiophene in Quinoxaline-Based Photovoltaic Polymers. Macromolecules 2012, 45, 3032¨C3038. "
1185,CC1=CC2=C(C(C3=CC=C(CCCCCC)S3)=C(C=C(C4=CC=C(C)C5=C4N=C(C6=CC=C(CCCCCC)S6)C(C7=CC=C(CCCCCC)S7)=N5)S8)C8=C2C9=CC=C(CCCCCC)S9)S1,PBDT-DTQx,5.35,3.6,0.83,11.71,0.4,3.9,"Wang, K.; Zhang, Z.; Fu, Q.; Li, Y. Synthesis and Photovoltaic Properties of a D ¨C A Copolymer Based on the 2 , 3-Di ( 5-Hexylthio- Phen-2-yl Quinoxaline Acceptor Unit. Macromol. Chem. Phys. 2014, 215, 597?603. "
1186,CC(S1)=CC=C1C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCC(CCCC)CC)=C(OC[C@H](CC)CCCC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=C(OC)C=C8)C(C9=CC=C(OC)C=C9)=N7,PBDTDT(Qx-2)-O,5.29,2.77,0.91,9.38,0.52,4.44,"Su, W.; Xiao, M.; Fan, Q.; Zhong, J.; Chen, J.; Dang, D.; Shi, J.; Xiong, W.; Duan, X.; Tan, H.; Liu, Y.; Zhu, W. Significantly Increasing Open-Circuit Voltage of the benzo[1,2-b:4,5-b¡ä]dithiophene-Alt-5,8-Dithienyl-Quinoxaline Copolymers Based PSCs by Appending Dioctyloxy Chains at 6,7-Positions of Quinoxaline. Org. Electron. 2015, 17, 129¨C137. "
1187,CC(S1)=CC=C1C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=C(OC)C=C%10)C(C%11=CC=C(OC)C=C%11)=N9,PBDTDT(Qx-2)-T,5.41,2.92,0.95,10.82,0.614,6.31,"Su, W.; Xiao, M.; Fan, Q.; Zhong, J.; Chen, J.; Dang, D.; Shi, J.; Xiong, W.; Duan, X.; Tan, H.; Liu, Y.; Zhu, W. Significantly Increasing Open-Circuit Voltage of the benzo[1,2-b:4,5-b¡ä]dithiophene-Alt-5,8-Dithienyl-Quinoxaline Copolymers Based PSCs by Appending Dioctyloxy Chains at 6,7-Positions of Quinoxaline. Org. Electron. 2015, 17, 129¨C137. "
1188,CC(S1)=CC=C1C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=CC=C%10)C(C%11=CC=CC=C%11)=N9,PBDTDT(Qx-3)-T,5.51,3.57,0.94,11.28,0.647,6.9,"Fan, Q.; Xiao, M.; Liu, Y.; Su, W.; Gao, H.; Tan, H.; Wang, Y.; Lei, G.; Yang, R.; Zhu, W. Improved Photovoltaic Performance of 2D-Conjugated Benzodithiophene-Based Polymer by the Side Chain Engineering at Quinoxaline. Polym. Chem. 2015, 6, 4290¨C4298. "
1189,O=C1N(CCCCCCCC)C(C2=CC=C(C3=CC=C([Ge](CCCC)(CCCC)C4=C5C=CC(C)=C4)C5=C3)S2)=C6C1=C(C7=CC=C(C)S7)N(CCCCCCCC)C6=O,PGFDTDPP (C4),5.38,3.7,0.76,4.1,0.62,1.5,"Allard, N.; A?ch, R. B.; Gendron, D.; Boudreault, P. L. T.; Tessier, C.; Alem, S.; Tse, S. C.; Tao, Y.; Leclerc, M. Germafluorenes: New Heterocycles for Plastic Electronics. Macromolecules 2010, 43, 2328¨C2333. "
1190,CC1=CC([Ge](CCCCCCCC)(CCCCCCCC)C2=C3C=CC(C4=CC=C(C(N(CCCCCCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CCCCCCCC)C6=O)S4)=C2)=C3C=C1,PGFDTDPP (C8),5.38,3.64,0.76,2.8,0.56,1.2,"Allard, N.; A?ch, R. B.; Gendron, D.; Boudreault, P. L. T.; Tessier, C.; Alem, S.; Tse, S. C.; Tao, Y.; Leclerc, M. Germafluorenes: New Heterocycles for Plastic Electronics. Macromolecules 2010, 43, 2328¨C2333. "
1191,CC1=CC([Ge](CCCCCCCC)(CCCCCCCC)C2=C3C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)C=C2)=C3C=C1,PGFDTBT,5.38,3.91,0.79,6.9,0.51,2.8,"Allard, N.; A?ch, R. B.; Gendron, D.; Boudreault, P. L. T.; Tessier, C.; Alem, S.; Tse, S. C.; Tao, Y.; Leclerc, M. Germafluorenes: New Heterocycles for Plastic Electronics. Macromolecules 2010, 43, 2328¨C2333. "
1192,CC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CCCCCCCCCCCC)S6)=C(C7=CC=C(CCCCCCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=CC=C%10)C(C%11=CC=CC=C%11)=N9,P0F,4.98,3.18,0.832,6.37,0.54,2.9,"Yang, P.; Yuan, M.; Zeigler, D. F.; Watkins, S. E.; Lee, J. A.; Luscombe, C. K. Influence of Fluorine Substituents on the Film Dielectric Constant and Open-Circuit Voltage in Organic Photovoltaics. J. Mater. Chem. C 2014, 2, 3278¨C3284. "
1193,CC(S1)=CC=C1C2=C(F)C=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CCCCCCCCCCCC)S6)=C(C7=CC=C(CCCCCCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=CC=C%10)C(C%11=CC=CC=C%11)=N9,P1F,5.07,3.27,0.872,6.52,0.55,3.1,"Yang, P.; Yuan, M.; Zeigler, D. F.; Watkins, S. E.; Lee, J. A.; Luscombe, C. K. Influence of Fluorine Substituents on the Film Dielectric Constant and Open-Circuit Voltage in Organic Photovoltaics. J. Mater. Chem. C 2014, 2, 3278¨C3284. "
1194,CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CCCCCCCCCCCC)S6)=C(C7=CC=C(CCCCCCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=CC=C%10)C(C%11=CC=CC=C%11)=N9,P2F,5.08,3.27,0.914,6.84,0.59,3.7,"Yang, P.; Yuan, M.; Zeigler, D. F.; Watkins, S. E.; Lee, J. A.; Luscombe, C. K. Influence of Fluorine Substituents on the Film Dielectric Constant and Open-Circuit Voltage in Organic Photovoltaics. J. Mater. Chem. C 2014, 2, 3278¨C3284. "
1195,CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(OC[C@H](CCCC)CC)C=C6)=C(C7=CC=C(OCC(CC)CCCC)C=C7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=C(OC[C@@H](CC)CCCC)C=C%10)C(C%11=CC=C(OCC(CC)CCCC)C=C%11)=N9,PBDT-DFQX-PP,5.35,3.53,0.89,8.66,0.514,3.96,"Wang, M.; Ma, D.; Shi, K.; Shi, S.; Chen, S.; Huang, C.; Qiao, Z.; Zhang, Z.-G.; Li, Y.; Li, X.; Wang, H. The Role of Conjugated Side Chains in High Performance Photovoltaic Polymers. J. Mater. Chem. A 2015, 3, 2802¨C2814. "
1196,CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(C[C@H](CCCC)CC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=C(OC[C@@H](CC)CCCC)C=C%10)C(C%11=CC=C(OCC(CC)CCCC)C=C%11)=N9,PBDT-DFQX-TP,5.25,3.52,0.82,12.34,0.601,6.08,"Wang, M.; Ma, D.; Shi, K.; Shi, S.; Chen, S.; Huang, C.; Qiao, Z.; Zhang, Z.-G.; Li, Y.; Li, X.; Wang, H. The Role of Conjugated Side Chains in High Performance Photovoltaic Polymers. J. Mater. Chem. A 2015, 3, 2802¨C2814. "
1197,CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(OC[C@H](CCCC)CC)C=C6)=C(C7=CC=C(OCC(CC)CCCC)C=C7)C8=C5C=C(C)S8)C9=C2N=C(C(S%10)=CC=C%10C[C@@H](CC)CCCC)C(C%11=CC=C(S%11)CC(CC)CCCC)=N9,PBDT-DFQX-PT,5.29,3.58,0.85,12.13,0.635,6.54,"Wang, M.; Ma, D.; Shi, K.; Shi, S.; Chen, S.; Huang, C.; Qiao, Z.; Zhang, Z.-G.; Li, Y.; Li, X.; Wang, H. The Role of Conjugated Side Chains in High Performance Photovoltaic Polymers. J. Mater. Chem. A 2015, 3, 2802¨C2814. "
1198,CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(C[C@H](CCCC)CC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C(S%10)=CC=C%10C[C@@H](CC)CCCC)C(C%11=CC=C(S%11)CC(CC)CCCC)=N9,PBDT-DFQX-TT,5.2,3.5,0.86,12.77,0.699,7.68,"Wang, M.; Ma, D.; Shi, K.; Shi, S.; Chen, S.; Huang, C.; Qiao, Z.; Zhang, Z.-G.; Li, Y.; Li, X.; Wang, H. The Role of Conjugated Side Chains in High Performance Photovoltaic Polymers. J. Mater. Chem. A 2015, 3, 2802¨C2814. "
1199,CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CCCCCCCC)S6)=C(C7=CC=C(CCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC(OCCCCCCCC)=CC=C%10)C(C%11=CC=CC(OCCCCCCCC)=C%11)=N9,PFQBDT-TR1,5.89,3.61,0.84,11.1,0.61,5.7,"Tessarolo, M.; Gedefaw, D.; Bolognesi, M.; Liscio, F.; Henriksson, P.; Zhuang, W.; Milita, S.; Muccini, M.; Wang, E.; Seri, M.; Andersson, M. R. Structural Tuning of Quinoxaline-Benzodithiophene Copolymers via Alkyl Side Chain Manipulation: Synthesis, Characterization and Photovoltaic Properties. J. Mater. Chem. A 2014, 2, 11162¨C11170. "
1200,CC(S1)=CC=C1C2=C(F)C(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC(CCCCCC)=C(CCCCCC)S6)=C(C7=CC(CCCCCC)=C(CCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC(OCCCCCCCC)=CC=C%10)C(C%11=CC=CC(OCCCCCCCC)=C%11)=N9,PFQBDT-T2R2,5.87,3.63,0.96,6.5,0.54,3.4,"Tessarolo, M.; Gedefaw, D.; Bolognesi, M.; Liscio, F.; Henriksson, P.; Zhuang, W.; Milita, S.; Muccini, M.; Wang, E.; Seri, M.; Andersson, M. R. Structural Tuning of Quinoxaline-Benzodithiophene Copolymers via Alkyl Side Chain Manipulation: Synthesis, Characterization and Photovoltaic Properties. J. Mater. Chem. A 2014, 2, 11162¨C11170. "
1201,CC(S1)=CC=C1C2=CC(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CCCC)CC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC(OCCCCCCCC)=CC=C%10)C(C%11=CC=CC(OCCCCCCCC)=C%11)=N9,PBDTTFTQ-EH,5.29,3.05,0.78,13.2,0.708,7.29,"Wu, H.; Zhao, B.; Wang, W.; Guo, Z.; Wei, W.; An, Z.; Gao, C.; Chen, H.; Xiao, B.; Xie, Y.; Wu, H.; Cao, Y. Side Chain Modification: An Effective Approach to Modulate the Energy Level of Benzodithiophene Based Polymers for High-Performance Solar Cells. J. Mater. Chem. A 2015, 3, 18115¨C18126. "
1202,CC(S1)=CC=C1C2=CC(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CCCC)CC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=C(CCCCCCCC)S%10)C(C%11=CC=C(CCCCCCCC)S%11)=N9,PBDTTFTQ-DO,5.37,3.03,0.88,11.4,0.759,7.61,"Wu, H.; Zhao, B.; Wang, W.; Guo, Z.; Wei, W.; An, Z.; Gao, C.; Chen, H.; Xiao, B.; Xie, Y.; Wu, H.; Cao, Y. Side Chain Modification: An Effective Approach to Modulate the Energy Level of Benzodithiophene Based Polymers for High-Performance Solar Cells. J. Mater. Chem. A 2015, 3, 18115¨C18126. "
1203,CC(S1)=CC=C1C2=CC(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC(CCCCCCCC)=C(CCCCCCCC)S6)=C(C7=CC(CCCCCCCC)=C(CCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC(OCCCCCCCC)=CC=C%10)C(C%11=CC=CC(OCCCCCCCC)=C%11)=N9,PBDTTFTTQ-EH,5.12,3.03,0.72,13.4,0.708,6.82,"Wu, H.; Zhao, B.; Wang, W.; Guo, Z.; Wei, W.; An, Z.; Gao, C.; Chen, H.; Xiao, B.; Xie, Y.; Wu, H.; Cao, Y. Side Chain Modification: An Effective Approach to Modulate the Energy Level of Benzodithiophene Based Polymers for High-Performance Solar Cells. J. Mater. Chem. A 2015, 3, 18115¨C18126. "
1204,CC(S1)=CC=C1C2=CC(F)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC(CCCCCCCC)=C(CCCCCCCC)S6)=C(C7=CC(CCCCCCCC)=C(CCCCCCCC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=C(CCCCCCCC)S%10)C(C%11=CC=C(CCCCCCCC)S%11)=N9,PBDTTFTTQ-DO,5.31,2.99,0.85,11.3,0.757,7.25,"Wu, H.; Zhao, B.; Wang, W.; Guo, Z.; Wei, W.; An, Z.; Gao, C.; Chen, H.; Xiao, B.; Xie, Y.; Wu, H.; Cao, Y. Side Chain Modification: An Effective Approach to Modulate the Energy Level of Benzodithiophene Based Polymers for High-Performance Solar Cells. J. Mater. Chem. A 2015, 3, 18115¨C18126. "
1205,CC(S1)=CC=C1C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCC(CC)CCCCCC)=C(OC[C@@H](CCCCCC)CC)C6=C5C=C(C)S6)C7=C2N=C(C8=CC=CC(C=C9)=C8C%10=C9C=CC=C%10%11)C%11=N7,PTTPPz-BDT,5.29,3.08,0.74,9.79,0.582,4.25,"Fan, Q.; Liu, Y.; Xiao, M.; Tan, H.; Wang, Y.; Su, W.; Yu, D.; Yang, R.; Zhu, W. Donor-Acceptor Copolymers Based on benzo[1,2-b:4,5-b¡ä]dithiophene and Pyrene-Fused Phenazine for High-Performance Polymer Solar Cells. Org. Electron. 2014, 15, 3375¨C3383. "
1206,CC(S1)=CC=C1C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCCCC)S6)=C(C7=CC=C(C[C@@H](CCCCCC)CC)S7)C8=C5C=C(C)S8)C9=C2N=C(C%10=CC=CC(C=C%11)=C%10C%12=C%11C=CC=C%12%13)C%13=N9,PTTPPz-BDTT,5.34,3.15,0.7,11.1,0.625,4.86,"Fan, Q.; Liu, Y.; Xiao, M.; Tan, H.; Wang, Y.; Su, W.; Yu, D.; Yang, R.; Zhu, W. Donor-Acceptor Copolymers Based on benzo[1,2-b:4,5-b¡ä]dithiophene and Pyrene-Fused Phenazine for High-Performance Polymer Solar Cells. Org. Electron. 2014, 15, 3375¨C3383. "
1207,CC(S1)=CC=C1C2=C3C(C(N(CC(CC)CCCC)C3=O)=O)=C(C(S4)=CC=C4C(S5)=CC(C5=C6C7=CC(CCCCCCCC)=C(CCCCCCCC)S7)=C(C8=CC(CCCCCCCC)=C(CCCCCCCC)S8)C9=C6C=C(C)S9)C%10=C2N=C(C%11=CC(OCCCCCCCC)=CC=C%11)C(C%12=CC=CC(OCCCCCCCC)=C%12)=N%10,PBDT-PQD1,5.97,3.79,0.98,10.4,0.48,4.9,"Xu, X.; Wang, C.; B?cke, O.; James, D. I.; Bini, K.; Olsson, E.; Andersson, M. R.; Fahlman, M.; Wang, E. Pyrrolo[3,4-g]quinoxaline-6,8-Dione-Based Conjugated Copolymers for Bulk Heterojunction Solar Cells with High Photovoltages. Polym. Chem.2015, 6, 4624¨C4633. "
1208,CC(S1)=CC=C1C2=C3C(C(N(CC(CC)CCCC)C3=O)=O)=C(C(S4)=CC=C4C(S5)=CC(C5=C6C7=CC=C(CC(CCCC)CC)S7)=C(C8=CC=C(CC(CC)CCCC)S8)C9=C6C=C(C)S9)C%10=C2N=C(C%11=CC(OCCCCCCCC)=CC=C%11)C(C%12=CC=CC(OCCCCCCCC)=C%12)=N%10,PBDT-PQD2,5.96,3.74,1.08,7.6,0.43,3.5,"Xu, X.; Wang, C.; B?cke, O.; James, D. I.; Bini, K.; Olsson, E.; Andersson, M. R.; Fahlman, M.; Wang, E. Pyrrolo[3,4-g]quinoxaline-6,8-Dione-Based Conjugated Copolymers for Bulk Heterojunction Solar Cells with High Photovoltages. Polym. Chem.2015, 6, 4624¨C4633. "
1209,CC(S1)=CC=C1C2=C3C(C(N(CC(CC)CCCC)C3=O)=O)=C(C(S4)=CC=C4C(S5)=CC(C5=C6OCC(CCCC)CC)=C(OCC(CC)CCCC)C7=C6C=C(C)S7)C8=C2N=C(C9=CC(OCCCCCCCC)=CC=C9)C(C%10=CC=CC(OCCCCCCCC)=C%10)=N8,PBDT-PQD3,5.82,3.72,1.03,7.3,0.39,2.9,"Xu, X.; Wang, C.; B?cke, O.; James, D. I.; Bini, K.; Olsson, E.; Andersson, M. R.; Fahlman, M.; Wang, E. Pyrrolo[3,4-g]quinoxaline-6,8-Dione-Based Conjugated Copolymers for Bulk Heterojunction Solar Cells with High Photovoltages. Polym. Chem.2015, 6, 4624¨C4633. "
1210,CC(S1)=CC=C1C2=C3C(C(N(CC(CC)CCCC)C3=O)=O)=C(C(S4)=CC=C4C5=CC=C(C)S5)C6=C2N=C(C7=CC(OCCCCCCCC)=CC=C7)C(C8=CC=CC(OCCCCCCCC)=C8)=N6,PT-PQD,5.83,3.83,1,7.7,0.38,2.9,"Xu, X.; Wang, C.; B?cke, O.; James, D. I.; Bini, K.; Olsson, E.; Andersson, M. R.; Fahlman, M.; Wang, E. Pyrrolo[3,4-g]quinoxaline-6,8-Dione-Based Conjugated Copolymers for Bulk Heterojunction Solar Cells with High Photovoltages. Polym. Chem.2015, 6, 4624¨C4633. "
1211,CC1=CC=C(C(N(CC(CCCCCCCC)CCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5CCCCCCCC)=C(CCCCCCCC)C6=C5C=C(C)S6)N7CC(CCCCCC)CCCCCCCC)C7=O)S1,O-HD,5.15,3.28,0.71,9.4,0.61,4.1,"Li, Z.; Zhang, Y.; Tsang, S. W.; Du, X.; Zhou, J.; Tao, Y.; Ding, J. Alkyl Side Chain Impact on the Charge Transport and Photovoltaic Properties of Benzodithiophene and Diketopyrrolopyrrole-Based Copolymers. J. Phys. Chem. C 2011, 115, 18002¨C18009. "
1212,CC1=CC=C(C(N(CC(CCCC)CCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5CCC(CCCC)CCCCC)=C(CCC(CCCCC)CCCC)C6=C5C=C(C)S6)N7CC(CCCCCC)CCCC)C7=O)S1,BO-BO,5.14,3.34,0.59,3.4,0.46,0.93,"Li, Z.; Zhang, Y.; Tsang, S. W.; Du, X.; Zhou, J.; Tao, Y.; Ding, J. Alkyl Side Chain Impact on the Charge Transport and Photovoltaic Properties of Benzodithiophene and Diketopyrrolopyrrole-Based Copolymers. J. Phys. Chem. C 2011, 115, 18002¨C18009. "
1213,CC1=CC=C(C(N(CCCCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5CCC(CCCCCCCC)CCCCC)=C(CCC(CCCCC)CCCCCCCC)C6=C5C=C(C)S6)N7CCCCCCCC)C7=O)S1,PU-O,5.1,3.31,0.62,5.2,0.43,1.4,"Li, Z.; Zhang, Y.; Tsang, S. W.; Du, X.; Zhou, J.; Tao, Y.; Ding, J. Alkyl Side Chain Impact on the Charge Transport and Photovoltaic Properties of Benzodithiophene and Diketopyrrolopyrrole-Based Copolymers. J. Phys. Chem. C 2011, 115, 18002¨C18009. "
1214,CC1=CC=C(C(N(CC(CCCCCC)CCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCCCCCCCCCCCC)=C(OCCCCCCCCCCCC)C6=C5C=C(C)S6)N7CC(CCCC)CCCCCC)C7=O)S1,PBDT-DPP (P1),5.3,3.8,0.64,11.27,0.602,4.35,"Morse, G. E.; Tournebize, A.; Rivaton, A.; Chass¨¦, T.; Taviot-Gueho, C.; Blouin, N.; Lozman, O. R.; Tierney, S. The Effect of Polymer Solubilizing Side-Chains on Solar Cell Stability. Phys. Chem. Chem. Phys. 2015, 17, 11884¨C11897. "
1215,CC1=CC=C(C(N(CC(CCCCCC)CCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C6=C5C=C(C)S6)N7CC(CCCC)CCCCCC)C7=O)S1,PBDT-DPP (P2),5.3,3.8,0.7,12.1,0.524,4.43,"Morse, G. E.; Tournebize, A.; Rivaton, A.; Chass¨¦, T.; Taviot-Gueho, C.; Blouin, N.; Lozman, O. R.; Tierney, S. The Effect of Polymer Solubilizing Side-Chains on Solar Cell Stability. Phys. Chem. Chem. Phys. 2015, 17, 11884¨C11897. "
1216,CC1=CC=C(C(N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5)=CC6=C5C=C(C)S6)N7CC(CCCCCCCCCCCC)CCCCCCCCCC)C7=O)S1,PBDT-DPP (P3),5.4,3.9,0.68,8.75,0.453,2.69,"Morse, G. E.; Tournebize, A.; Rivaton, A.; Chass¨¦, T.; Taviot-Gueho, C.; Blouin, N.; Lozman, O. R.; Tierney, S. The Effect of Polymer Solubilizing Side-Chains on Solar Cell Stability. Phys. Chem. Chem. Phys. 2015, 17, 11884¨C11897. "
1217,CC1=CC=C(C(N(CC(CCCCCC)CCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCC)S6)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C5C=C(C)S8)N9CC(CCCC)CCCCCC)C9=O)S1,PBDT-DPP (P4),5.4,3.9,0.66,13.6,0.329,2.95,"Morse, G. E.; Tournebize, A.; Rivaton, A.; Chass¨¦, T.; Taviot-Gueho, C.; Blouin, N.; Lozman, O. R.; Tierney, S. The Effect of Polymer Solubilizing Side-Chains on Solar Cell Stability. Phys. Chem. Chem. Phys. 2015, 17, 11884¨C11897. "
1218,CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCC)O6)=C(C7=CC=C(CC(CC)CCCC)O7)C8=C5C=C(C)S8)N9CC(CC)CCCC)C9=O)S1,PBDTF-DPP,5.16,3.64,0.69,10.46,0.489,3.5,"Wang, Y.; Yang, F.; Liu, Y.; Peng, R.; Chen, S.; Ge, Z. New Alkylfuranyl-Substituted Benzo[1,2-b:4,5-b¡ä]Dithiophene-Based Donor ? Acceptor Polymers for Highly Efficient Solar Cells. Macromolecules 2013, 46, 1368¨C1375. "
1219,CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(O3)=CC=C3C(S4)=CC(C4=C5C6=CC=C(CC(CC)CCCC)O6)=C(C7=CC=C(CC(CC)CCCC)O7)C8=C5C=C(C)S8)N9CC(CC)CCCC)C9=O)O1,PBDTF-DPPF,5.24,3.74,0.72,12.64,0.565,5.1,"Wang, Y.; Yang, F.; Liu, Y.; Peng, R.; Chen, S.; Ge, Z. New Alkylfuranyl-Substituted Benzo[1,2-b:4,5-b¡ä]Dithiophene-Based Donor ? Acceptor Polymers for Highly Efficient Solar Cells. Macromolecules 2013, 46, 1368¨C1375. "
1220,CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5OCC(CC)CCCC)=C(OCC(CC)CCCC)C6=C5C=C(C)S6)N7CC(CC)CCCC)C7=O)S1,PBDT-DPP,5.05,3.4,0.62,3.87,0.4,1,"Wang, Y.; Yang, F.; Liu, Y.; Peng, R.; Chen, S.; Ge, Z. New Alkylfuranyl-Substituted Benzo[1,2-b:4,5-b¡ä]Dithiophene-Based Donor ? Acceptor Polymers for Highly Efficient Solar Cells. Macromolecules 2013, 46, 1368¨C1375. "
1221,CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(O3)=CC=C3C(S4)=CC(C4=C5OCC(CC)CCCC)=C(OCC(CC)CCCC)C6=C5C=C(C)S6)N7CC(CC)CCCC)C7=O)O1,PBDT-DPPF,5.15,3.44,0.63,8.78,0.533,2.9,"Wang, Y.; Yang, F.; Liu, Y.; Peng, R.; Chen, S.; Ge, Z. New Alkylfuranyl-Substituted Benzo[1,2-b:4,5-b¡ä]Dithiophene-Based Donor ? Acceptor Polymers for Highly Efficient Solar Cells. Macromolecules 2013, 46, 1368¨C1375. "
1222,O=C1N(CC(CC)CCCC)C(C2=CC=C(C3=CC=C4C(N(C(CCCCCCCCCC)CCCCCCCCCC)C5=C4C=CC(C)=C5)=C3)S2)=C6C1=C(C7=CC=C(C)S7)N(CC(CC)CCCC)C6=O,PC-DTDPP,5.42,3.64,0.76,5.35,0.56,2.26,"Zhou, E.; Yamakawa, S.; Tajima, K.; Yang, C.; Hashimoto, K. Synthesis and Photovoltaic Properties of Diketopyrrolopyrrole-Based Donor-Acceptor Copolymers. Chem. Mater. 2009, 21, 4055¨C4061."
1223,O=C1N(CCCCCCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC=C6C(C(CCCCCCCC)(CCCCCCCC)C7=C6C=CC(C)=C7)=C5)S4)N(CCCCCCCC)C3=O,PF-DTDPP,5.35,3.66,0.74,2.51,0.47,0.88,"Zhou, E.; Yamakawa, S.; Tajima, K.; Yang, C.; Hashimoto, K. Synthesis and Photovoltaic Properties of Diketopyrrolopyrrole-Based Donor-Acceptor Copolymers. Chem. Mater. 2009, 21, 4055¨C4061."
1224,O=C1N(C[C@@H](CCCC)CC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC(N(C(C[C@@H](CCCC)CC)CC(CCCC)CC)C6=C7SC(C)=C6)=C7S5)S4)N(C[C@H](CC)CCCC)C3=O,PDTP-DTDPP,5.02,3.64,0.44,4.47,0.57,1.12,"Zhou, E.; Yamakawa, S.; Tajima, K.; Yang, C.; Hashimoto, K. Synthesis and Photovoltaic Properties of Diketopyrrolopyrrole-Based Donor-Acceptor Copolymers. Chem. Mater. 2009, 21, 4055¨C4061."
1225,CC1=CC2=C(C(C3=CC(C=C(CC(CC)CCCC)C=C4)=C4S3)=C(C=C(C5=CC=C(C6=C(OCC(CC(CC)CCCC)(CC(CCCC)CC)CO7)C7=C(C8=CC=C(C)C9=NSN=C89)S6)C%10=NSN=C5%10)S%11)C%11=C2C%12=CC(C=C(CC(CCCC)CC)C=C%13)=C%13S%12)S1,P1,5.2,3.56,0.81,6.27,0.369,1.93,"Chakravarthi, N.; Gunasekar, K.; Jin, S.-H.; Lee, J. H. Synthesis and Photovoltaic Properties of 2D ¦Ð-Conjugated Polymers Based on Alkylbenzothiophene Substituted Benzodithiophene Donor Unit with Titanium Sub-Oxide (TiOX as an Interlayer in the Bulk Heterojunction Device Structure. J. Inorg. Organomet. Polym. Mater. 2015, 25, 107¨C117. "
1226,CC1=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C6=CC(C=C(CC(CCCC)CC)C=C7)=C7S6)=C(C8=CC(C=C(CC(CC)CCCC)C=C9)=C9S8)C%10=C5C=C(C)S%10)N%11CC(CCCCCCCC)CCCCCC)C%11=O)S1,P2,5.26,3.89,0.78,5.15,0.581,2.6,"Chakravarthi, N.; Gunasekar, K.; Jin, S.-H.; Lee, J. H. Synthesis and Photovoltaic Properties of 2D ¦Ð-Conjugated Polymers Based on Alkylbenzothiophene Substituted Benzodithiophene Donor Unit with Titanium Sub-Oxide (TiOX as an Interlayer in the Bulk Heterojunction Device Structure. J. Inorg. Organomet. Polym. Mater. 2015, 25, 107¨C117. "
1227,CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C#CC6=CC(C7=CC=C(OCC(CCCC)CC)C=C7)=CC=C6)=C(C#CC8=C([H])C(C9=CC=C(OCC(CCCC)CC)C=C9)=CC=C8[H])C%10=C5C=C(C)S%10)N%11CC(CC)CCCC)C%11=O)S1,PBDTBPA(H)-DPP,5.25,3.86,0.74,13.17,0.57,5.58,"Chakravarthi, N.; Gunasekar, K.; Kranthiraja, K.; Kim, T.; Cho, W.; Kim, C. S.; Kim, D.-H.; Song, M.; Jin, S.-H. The Effect of With/without Resonance-Mediated Interactions on the Organic Solar Cell Performance of New 2D ¦Ð-Conjugated Polymers. Polym. Chem.2015, 6, 7149¨C7159. "
1228,CC1=CC=C(C(N(CC(CCCC)CC)C2=O)=C(C2=C(C(S3)=CC=C3C(S4)=CC(C4=C5C#CC6=C(F)C(C7=CC=C(OCC(CCCC)CC)C=C7)=CC=C6F)=C(C#CC8=C(F)C(C9=CC=C(OCC(CCCC)CC)C=C9)=CC=C8F)C%10=C5C=C(C)S%10)N%11CC(CC)CCCC)C%11=O)S1,PBDTBPA(F)-DPP,5.2,3.91,0.68,9.89,0.5,4.04,"Chakravarthi, N.; Gunasekar, K.; Kranthiraja, K.; Kim, T.; Cho, W.; Kim, C. S.; Kim, D.-H.; Song, M.; Jin, S.-H. The Effect of With/without Resonance-Mediated Interactions on the Organic Solar Cell Performance of New 2D ¦Ð-Conjugated Polymers. Polym. Chem.2015, 6, 7149¨C7159. "
1229,CC1=CC=C(C(N(CCCCCCCCCCCCC2=CC=C(C3=CC=C(C#N)C=C3)C=C2)C4=O)=C(C4=C(C(S5)=CC=C5C6=CC(C(OCC(CC)CCCC)=C(SC(C)=C7)C7=C8OCC(CC)CCCC)=C8S6)N9CCCCCCCCCCCCC%10=CC=C(C%11=CC=C(C#N)C=C%11)C=C%10)C9=O)S1,PBDTDPPcbp,5.39,3.57,0.68,4.11,0.448,1.3,"Han, Y.; Chen, L.; Chen, Y. Diketopyrrolopyrrole-Based Liquid Crystalline Conjugated Donor-Acceptor Copolymers with Reduced Band Gap for Polymer Solar Cells. J. Polym. Sci. Part A Polym. Chem. 2013, 51, 258¨C266. "
1230,CC1=CC=C(C(N(CCCCCCCCCCCCC2=CC=C(C3=CC=C(C#N)C=C3)C=C2)C4=O)=C(C4=C(C(S5)=CC=C5C6=CC7=C(C8=CC=C(C)C=C8N7C(CCCCCCCC)CCCCCCCC)C=C6)N9CCCCCCCCCCCCC%10=CC=C(C%11=CC=C(C#N)C=C%11)C=C%10)C9=O)S1,PCBTDPPcbp,5.43,3.38,0.8,4.72,0.319,1.2,"Han, Y.; Chen, L.; Chen, Y. Diketopyrrolopyrrole-Based Liquid Crystalline Conjugated Donor-Acceptor Copolymers with Reduced Band Gap for Polymer Solar Cells. J. Polym. Sci. Part A Polym. Chem. 2013, 51, 258¨C266. "
1231,CC1=CN=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C2=O)=C3C2=C(C4=NC=C(C5=CC(C=C(SC(C)=C6)C6=C7)=C7S5)S4)N(C[C@H](CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1,PDPP2TzBDT,5.51,3.98,0.98,6.2,0.53,3.2,"Li, W.; Hendriks, K. H.; Furlan, A.; Wienk, M. M.; Janssen, R. A. J. High Quantum Efficiencies in Polymer Solar Cells at Energy Losses below 0.6 eV. J. Am. Chem. Soc.2015, 137, 2231¨C2234. "
1232,CC1=CN=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C2=O)=C3C2=C(C4=NC=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)N(C[C@H](CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1,PDPP2Tz2T,5.46,3.99,0.92,8.8,0.63,5.1,"Li, W.; Hendriks, K. H.; Furlan, A.; Wienk, M. M.; Janssen, R. A. J. High Quantum Efficiencies in Polymer Solar Cells at Energy Losses below 0.6 eV. J. Am. Chem. Soc.2015, 137, 2231¨C2234. "
1233,CC1=CN=C(C(N(CC(CCCCCC)CCCC)C2=O)=C3C2=C(C4=NC=C(C5=CC(N(CC(CC)CCCC)C6=C7SC(C)=C6)=C7S5)S4)N(C[C@H](CCCCCC)CCCC)C3=O)S1,PDPP2TzDTP,5.18,3.9,0.69,14.9,0.54,5.6,"Li, W.; Hendriks, K. H.; Furlan, A.; Wienk, M. M.; Janssen, R. A. J. High Quantum Efficiencies in Polymer Solar Cells at Energy Losses below 0.6 eV. J. Am. Chem. Soc.2015, 137, 2231¨C2234. "
1234,CC1=C(CC(CCCCCC)CCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCC)CCCCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)C6=NSN=C62)S1,PffBT-T4-2HD,5.21,3.56,0.73,14.8,0.644,7.2,"Hu, H.; Jiang, K.; Yang, G.; Liu, J.; Li, Z.; Lin, H.; Liu, Y.; Zhao, J.; Zhang, J.; Huang, F.; Qu, Y.; Ma, W.; Yan, H. Terthiophene-Based D-A Polymer with an Asymmetric Arrangement of Alkyl Chains That Enables Efficient Polymer Solar Cells. J. Am. Chem. Soc. 2015, 137, 14149¨C14157. "
1235,CC1=C(CC(CCCCCC)CCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCC)CCCCCCCC)=C(C4=CC=C(C)S4)S3)C5=NSN=C52)S1,"PffBT-T3(1,3)",5.35,3.75,0.77,10.6,0.453,3.9,"Hu, H.; Jiang, K.; Yang, G.; Liu, J.; Li, Z.; Lin, H.; Liu, Y.; Zhao, J.; Zhang, J.; Huang, F.; Qu, Y.; Ma, W.; Yan, H. Terthiophene-Based D-A Polymer with an Asymmetric Arrangement of Alkyl Chains That Enables Efficient Polymer Solar Cells. J. Am. Chem. Soc. 2015, 137, 14149¨C14157. "
1236,FC(C(F)=C(C1=CC(CC(CCCCCC)CCCCCCCC)=C(C2=CC(CC(CCCCCCCC)CCCCCC)=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)S2)S1)C7=NSN=C78)=C8C9=CC(CC(CCCCCC)CCCCCCCC)=C(C%10=CC(CC(CCCCCC)CCCCCCCC)=C(C)S%10)S9,"PffBT-T3((1,2)-1",5.31,3.68,0.82,18.5,0.641,10,"Hu, H.; Jiang, K.; Yang, G.; Liu, J.; Li, Z.; Lin, H.; Liu, Y.; Zhao, J.; Zhang, J.; Huang, F.; Qu, Y.; Ma, W.; Yan, H. Terthiophene-Based D-A Polymer with an Asymmetric Arrangement of Alkyl Chains That Enables Efficient Polymer Solar Cells. J. Am. Chem. Soc. 2015, 137, 14149¨C14157. "
1237,FC(C(F)=C(C1=CC(CC(CCCCCC)CCCCCCCC)=C(C2=CC(CC(CCCCCCC)CCCCCC)=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)S2)S1)C7=NSN=C78)=C8C9=CC(CC(CCCCCC)CCCCCCCC)=C(C%10=CC(CC(CCCCCC)CCCCCCC)=C(C)S%10)S9,"PffBT-T3(1,2)-2",5.31,3.68,0.82,18.7,0.683,10.7,"Hu, H.; Jiang, K.; Yang, G.; Liu, J.; Li, Z.; Lin, H.; Liu, Y.; Zhao, J.; Zhang, J.; Huang, F.; Qu, Y.; Ma, W.; Yan, H. Terthiophene-Based D-A Polymer with an Asymmetric Arrangement of Alkyl Chains That Enables Efficient Polymer Solar Cells. J. Am. Chem. Soc. 2015, 137, 14149¨C14157. "
1238,CC1=C(CC(CCCCCCCCCCCCCC)CCCCCCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCCCCCC)CCCCCCCCCCCCCC)=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S3)C8=NSN=C82)S1,PffBT-T2,5.38,3.77,0.88,10.1,0.486,4.5,"Hu, H.; Jiang, K.; Yang, G.; Liu, J.; Li, Z.; Lin, H.; Liu, Y.; Zhao, J.; Zhang, J.; Huang, F.; Qu, Y.; Ma, W.; Yan, H. Terthiophene-Based D-A Polymer with an Asymmetric Arrangement of Alkyl Chains That Enables Efficient Polymer Solar Cells. J. Am. Chem. Soc. 2015, 137, 14149¨C14157. "
1239,CC(S1)=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C1C2=CC3=C(C4=NSN=C42)C=C(C5=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(C6=CC(CCCCCCCCCCCC)=C(C7=NC8=CC9=C(N=C(C%10=C(CCCCCCCCCCCC)C=C(C)S%10)S9)C=C8S7)S6)S5)C%11=NSN=C3%11,EC12-DT,5.51,3.8,0.861,13.3,0.575,6.59,"Al-Naamani, E.; Gopal, A.; Ide, M.; Osaka, I.; Saeki, A. Exploring Alkyl Chains in Benzobisthiazole-Naphthobisthiadiazole Polymers: Impact on Solar-Cell Performance, Crystalline Structures, and Optoelectronics. ACS Appl. Mater. Interfaces 2017, 9, 37702¨C37711. "
1240,CC(S1)=C(CC(CCCCCCCC)CCCCCCCCCC)C=C1C2=CC3=C(C4=NSN=C42)C=C(C5=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C6=CC(CCCCCCCCCCCC)=C(C7=NC8=CC9=C(N=C(C%10=C(CCCCCCCCCCCC)C=C(C)S%10)S9)C=C8S7)S6)S5)C%11=NSN=C3%11,EC12-OD,5.5,3.77,0.873,7.37,0.564,3.63,"Al-Naamani, E.; Gopal, A.; Ide, M.; Osaka, I.; Saeki, A. Exploring Alkyl Chains in Benzobisthiazole-Naphthobisthiadiazole Polymers: Impact on Solar-Cell Performance, Crystalline Structures, and Optoelectronics. ACS Appl. Mater. Interfaces 2017, 9, 37702¨C37711. "
1241,CC(S1)=C(CC(CCCCCCCC)CCCCCC)C=C1C2=CC3=C(C4=NSN=C42)C=C(C5=CC(CC(CCCCCC)CCCCCCCC)=C(C6=CC(CC(CCCCCC)CCCCCCCC)=C(C7=NC8=CC9=C(N=C(C%10=C(CC(CCCCCCCC)CCCCCC)C=C(C)S%10)S9)C=C8S7)S6)S5)C%11=NSN=C3%11,EHD-HD,5.57,3.85,0.931,4.32,0.629,2.53,"Al-Naamani, E.; Gopal, A.; Ide, M.; Osaka, I.; Saeki, A. Exploring Alkyl Chains in Benzobisthiazole-Naphthobisthiadiazole Polymers: Impact on Solar-Cell Performance, Crystalline Structures, and Optoelectronics. ACS Appl. Mater. Interfaces 2017, 9, 37702¨C37711. "
1242,CC(S1)=C(CC(CCCC)CCCCCC)C=C1C2=CC3=C(C4=NSN=C42)C=C(C5=CC(CC(CCCCCC)CCCC)=C(C6=CC(CC(CCCCCC)CCCCCCCC)=C(C7=NC8=CC9=C(N=C(C%10=C(CC(CCCCCCCC)CCCCCC)C=C(C)S%10)S9)C=C8S7)S6)S5)C%11=NSN=C3%11,EHD-BO,5.45,3.76,0.811,9.3,0.491,3.7,"Al-Naamani, E.; Gopal, A.; Ide, M.; Osaka, I.; Saeki, A. Exploring Alkyl Chains in Benzobisthiazole-Naphthobisthiadiazole Polymers: Impact on Solar-Cell Performance, Crystalline Structures, and Optoelectronics. ACS Appl. Mater. Interfaces 2017, 9, 37702¨C37711. "
1243,CC(S1)=C(CC(CCCC)CCCCCC)C=C1C2=CC3=C(C4=NSN=C42)C=C(C5=CC(CC(CCCCCC)CCCC)=C(C6=CC(CC(CCCCCC)CCCC)=C(C7=NC8=CC9=C(N=C(C%10=C(CC(CCCC)CCCCCC)C=C(C)S%10)S9)C=C8S7)S6)S5)C%11=NSN=C3%11,EBO-BO,5.44,3.76,0.834,8.61,0.43,3.09,"Al-Naamani, E.; Gopal, A.; Ide, M.; Osaka, I.; Saeki, A. Exploring Alkyl Chains in Benzobisthiazole-Naphthobisthiadiazole Polymers: Impact on Solar-Cell Performance, Crystalline Structures, and Optoelectronics. ACS Appl. Mater. Interfaces 2017, 9, 37702¨C37711. "
1244,CC1=CC=C(/C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C(N3CC(CCCCCCCCCC)CCCCCCCC)=O)/C4=C3C=C(C=C4)C5=CC=C(C)S5)C2=C1,PT-ID1,5.49,3.91,0.87,1.76,0.6,0.92,"Zhang, G.; Fu, Y.; Xie, Z.; Zhang, Q. Synthesis and Photovoltaic Properties of New Low Bandgap Isoindigo-Based Conjugated Polymers. Macromolecules 2011, 44, 1414¨C1420. "
1245,CC1=CC=C(/C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C(N3CC(CCCCCCCCCC)CCCCCCCC)=O)/C4=C3C=C(C=C4)C5=CC(SC(C)=C6)=C6S5)C2=C1,PTT-ID1,5.43,3.88,0.84,3.9,0.53,1.74,"Zhang, G.; Fu, Y.; Xie, Z.; Zhang, Q. Synthesis and Photovoltaic Properties of New Low Bandgap Isoindigo-Based Conjugated Polymers. Macromolecules 2011, 44, 1414¨C1420. "
1246,CC1=CC2=C(OCC(CC)CCCC)C(S3)=C(C(OCC(CC)CCCC)=C2S1)C=C3C4=CC5=C(/C(C(N5CC(CC)CCCC)=O)=C6C(N(CC(CCCC)CC)C7=CC(C)=CC=C7\6)=O)C=C4,PBDT-ID,5.2,3.66,0.71,7.93,0.34,1.91,"Zhang, G.; Fu, Y.; Xie, Z.; Zhang, Q. Synthesis and Photovoltaic Properties of New Low Bandgap Isoindigo-Based Conjugated Polymers. Macromolecules 2011, 44, 1414¨C1420. "
1247,CC1=CC2=C(OCC(CC)CCCC)C(S3)=C(C(OCC(CCCC)CC)=C2S1)C=C3C4=CC=C(/C(C(N5CC(CCCCCCCCCC)CCCCCCCC)=O)=C/C6=CC=C(C7=CC=C(/C=C8C(C=CC(C)=C9)=C9N(CC(CCCCCCCCCC)CCCCCCCC)C/8=O)S7)S6)C5=C4,PBDT?IBTI,5.24,3.72,0.77,11.71,0.71,6.41,"Li, S. G.; Yuan, Z. C.; Yuan, J. Y.; Deng, P.; Zhang, Q.; Sun, B. Q. An Expanded Isoindigo Unit as a New Building Block for a Conjugated Polymer Leading to HighPerformance Solar Cells. J. Mater. Chem. A 2014, 2, 5427¨C5433. "
1248,O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCC)CCCCCCCC)C4=CC(C5=CC(C)=C(C6=C(C)C=C(C)S6)S5)=CC=C4/3)=O,PMIM,5.93,3.84,0.73,6.24,0.36,1.64,"Zhuang, W.; Bolognesi, M.; Seri, M.; Henriksson, P.; Gedefaw, D.; Kroon, R.; Jarvid, M.; Lundin, A.; Wang, E.; Muccini, M.; Andersson, M. R. Influence of Incorporating Different Electron-Rich Thiophene-Based Units on the Photovoltaic Properties of Isoindigo-Based Conjugated Polymers: An Experimental and DFT Study. Macromolecules 2013, 46, 8488?8499. "
1249,O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCC)CCCCCCCC)C4=CC(C5=CC(C)=C(C6=CC=C(C7=C(C)C=C(C)S7)S6)S5)=CC=C4/3)=O,PT-MIM,5.78,3.83,0.7,10.56,0.48,3.55,"Zhuang, W.; Bolognesi, M.; Seri, M.; Henriksson, P.; Gedefaw, D.; Kroon, R.; Jarvid, M.; Lundin, A.; Wang, E.; Muccini, M.; Andersson, M. R. Influence of Incorporating Different Electron-Rich Thiophene-Based Units on the Photovoltaic Properties of Isoindigo-Based Conjugated Polymers: An Experimental and DFT Study. Macromolecules 2013, 46, 8488?8499. "
1250,O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCC)CCCCCCCC)C4=CC(C5=CC(C)=C(C6=CC7=C(OCC(CCCC)CC)C8=C(C=C(C9=C(C)C=C(C)S9)S8)C(OCC(CCCC)CC)=C7S6)S5)=CC=C4/3)=O,PBDTO-MIM,5.87,3.91,0.73,10.7,0.64,4.98,"Zhuang, W.; Bolognesi, M.; Seri, M.; Henriksson, P.; Gedefaw, D.; Kroon, R.; Jarvid, M.; Lundin, A.; Wang, E.; Muccini, M.; Andersson, M. R. Influence of Incorporating Different Electron-Rich Thiophene-Based Units on the Photovoltaic Properties of Isoindigo-Based Conjugated Polymers: An Experimental and DFT Study. Macromolecules 2013, 46, 8488?8499. "
1251,O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCC)CCCCCCCC)C4=CC(C5=CC(C)=C(C6=CC7=C(CCC(CCCC)CCCCCC)C8=C(C=C(C9=C(C)C=C(C)S9)S8)C(CCC(CCCC)CCCCCC)=C7S6)S5)=CC=C4/3)=O,PBDTA-MIM,5.94,3.81,0.8,10.2,0.65,5.36,"Zhuang, W.; Bolognesi, M.; Seri, M.; Henriksson, P.; Gedefaw, D.; Kroon, R.; Jarvid, M.; Lundin, A.; Wang, E.; Muccini, M.; Andersson, M. R. Influence of Incorporating Different Electron-Rich Thiophene-Based Units on the Photovoltaic Properties of Isoindigo-Based Conjugated Polymers: An Experimental and DFT Study. Macromolecules 2013, 46, 8488?8499. "
1252,CC1=CC2=C(OCC(CC)CCCC)C(S3)=C(C(OCC(CC)CCCC)=C2S1)C=C3C4=CC5=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCC)CCCCCCCC)C7=CC(C)=CC=C7\6)=O)C=C4,PBDT-ID,5.81,4.18,0.85,6.4,0.52,2.8,"Ma, Z.; Dang, D.; Tang, Z.; Gedefaw, D.; Bergqvist, J.; Zhu, W.; Mammo, W.; Andersson, M. R.; Ingan?s, O.; Zhang, F.; Wang, E. A Facile Method to Enhance Photovoltaic Performance of Benzodithiophene- Isoindigo Polymers by Inserting Bithiophene Spacer. Adv. Energy Mater. 2014, 4, 1301455/1¨C6. "
1253,CC1=CC2=C(OCC(CC)CCCC)C3=C(C(OCC(CC)CCCC)=C2S1)C=C(C4=CC=C(C5=CC6=C(/C(C(N6CC(CCCCCCCC)CCCCCC)=O)=C7C(N(CC(CCCCCC)CCCCCCCC)C8=CC(C9=CC=C(C)S9)=CC=C8\7)=O)C=C5)S4)S3,PBDT-TIT,5.75,4.08,0.79,9.38,0.66,4.85,"Ma, Z.; Dang, D.; Tang, Z.; Gedefaw, D.; Bergqvist, J.; Zhu, W.; Mammo, W.; Andersson, M. R.; Ingan?s, O.; Zhang, F.; Wang, E. A Facile Method to Enhance Photovoltaic Performance of Benzodithiophene- Isoindigo Polymers by Inserting Bithiophene Spacer. Adv. Energy Mater. 2014, 4, 1301455/1¨C6. "
1254,O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C3=CC(CCCCCCCC)=C(S3)C(S4)=CC=C4C5=CC(C(OC[C@H](CC)CCCC)=C(SC(C6=CC=C(C7=C(CCCCCCCC)C=C(C)S7)S6)=C8)C8=C9OCC(CC)CCCC)=C9S5)C=C2)=C%10C(N(CC(CCCCCC)CCCCCCCC)C%11=CC(C)=CC=C%11/%10)=O,PBDT-BTI,5.62,3.99,0.72,14.96,0.68,7.31,"Ma, Z.; Dang, D.; Tang, Z.; Gedefaw, D.; Bergqvist, J.; Zhu, W.; Mammo, W.; Andersson, M. R.; Ingan?s, O.; Zhang, F.; Wang, E. A Facile Method to Enhance Photovoltaic Performance of Benzodithiophene- Isoindigo Polymers by Inserting Bithiophene Spacer. Adv. Energy Mater. 2014, 4, 1301455/1¨C6. "
1255,O=C(N1CC(CCCCCCCC)CCCCCC)/C(C2=C1C=C(C3=CC(CCCCCCCC)=C(S3)C4=CC(CCCCCCCC)=C(S4)C(S5)=CC=C5C6=CC(C(OC[C@@H](CC)CCCC)=C(SC(C7=CC=C(C8=C(CCCCCCCC)C=C(C9=C(CCCCCCCC)C=C(C)S9)S8)S7)=C%10)C%10=C%11OCC(CC)CCCC)=C%11S6)C=C2)=C%12C(N(CC(CCCCCC)CCCCCCCC)C%13=CC(C)=CC=C%13/%12)=O,PBDT-TTI,5.62,3.99,0.66,11.82,0.52,3.98,"Ma, Z.; Dang, D.; Tang, Z.; Gedefaw, D.; Bergqvist, J.; Zhu, W.; Mammo, W.; Andersson, M. R.; Ingan?s, O.; Zhang, F.; Wang, E. A Facile Method to Enhance Photovoltaic Performance of Benzodithiophene- Isoindigo Polymers by Inserting Bithiophene Spacer. Adv. Energy Mater. 2014, 4, 1301455/1¨C6. "
1256,O=C1N(CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC(N(C(C[C@@H](CCCC)CC)CC(CCCC)CC)C6=C7SC(C)=C6)=C7S5)S4)N(CCCC)C3=O,PDTP-DTDPP(Bu),4.9,3.63,0.38,14.87,0.48,2.71,"Zhou, E.; Wei, Q.; Yamakawa, S.; Zhang, Y.; Tajima, K.; Yang, C.; Hashimoto, K. Diketopyrrolopyrrole-Based Semiconducting Polymer for Photovoltaic Device with Photocurrent Response Wavelengths up to 1.1 ¦Ìm. Macromolecules 2010, 43, 821¨C826. "
1257,O=C(N1CC(CCCCCCCC)CCCCCCCCCC)/C(C2=C1C=C(C(S3)=CC=C3C4=CC(C(C5=CC=C(CC(CC)CCCC)S5)=C(SC(C6=CC=C(C)S6)=C7)C7=C8C9=CC=C(CC(CC)CCCC)S9)=C8S4)C=C2)=C%10C(N(CC(CCCCCCCCCC)CCCCCCCC)C%11=CC(C)=CC=C%11/%10)=O,PBDT-IIG,5.38,3.35,0.85,10.48,0.658,5.86,"Lu, C.; Chen, H. C.; Chuang, W. T.; Hsu, Y. H.; Chen, W. C.; Chou, P. T. Interplay of Molecular Orientation, Film Formation, and Optoelectronic Properties on Isoindigo- and Thienoisoindigo-Based Copolymers for Organic Field Effect Transistor and Organic Photovoltaic Applications. Chem. Mater. 2015, 27, 6837¨C6847. "
1258,O=C1/C(C2=C(C=C(C(S3)=CC=C3C4=CC(C(C5=CC=C(CC(CC)CCCC)S5)=C(SC(C6=CC=C(C)S6)=C7)C7=C8C9=CC=C(CC(CC)CCCC)S9)=C8S4)S2)N1CC(CCCCCCCC)CCCCCCCCCC)=C%10C(N(CC(CCCCCCCCCC)CCCCCCCC)C%11=C/%10SC(C)=C%11)=O,PBDT-TIIG,4.96,3.29,0.38,11.74,0.572,2.55,"Lu, C.; Chen, H. C.; Chuang, W. T.; Hsu, Y. H.; Chen, W. C.; Chou, P. T. Interplay of Molecular Orientation, Film Formation, and Optoelectronic Properties on Isoindigo- and Thienoisoindigo-Based Copolymers for Organic Field Effect Transistor and Organic Photovoltaic Applications. Chem. Mater. 2015, 27, 6837¨C6847. "
1259,O=C(N1CC(CC)CCCC)/C(C2=C1C=C(C(S3)=CC=C3C4=CC(C(C5=CC(CCCCCCCC)=C(CCCCCCCC)S5)=C(SC(C)=C6)C6=C7C8=CC(CCCCCCCC)=C(CCCCCCCC)S8)=C7S4)C=C2)=C9C(N(CC(CCCC)CC)C%10=CC(C%11=CC=C(C)S%11)=CC=C%10/9)=O,PBDTT?ID,5.52,3.92,0.88,8.95,0.6,4.76,"Yang, Y.; Wu, R.; Wang, X.; Xu, X.; Li, Z.; Li, K.; Peng, Q. Isoindigo Fluorination to Enhance Photovoltaic Performance of Donor-Acceptor Conjugated Copolymers. Chem. Commun. 2014, 50, 439¨C441. "
1260,O=C(N1CC(CC)CCCC)/C(C2=C1C(F)=C(C(S3)=CC=C3C4=CC(C(C5=CC(CCCCCCCC)=C(CCCCCCCC)S5)=C(SC(C)=C6)C6=C7C8=CC(CCCCCCCC)=C(CCCCCCCC)S8)=C7S4)C=C2)=C9C(N(CC(CCCC)CC)C%10=C(F)C(C%11=CC=C(C)S%11)=CC=C%10/9)=O,PBDTT?FID,5.64,4.06,0.92,11.3,0.68,7.04,"Yang, Y.; Wu, R.; Wang, X.; Xu, X.; Li, Z.; Li, K.; Peng, Q. Isoindigo Fluorination to Enhance Photovoltaic Performance of Donor-Acceptor Conjugated Copolymers. Chem. Commun. 2014, 50, 439¨C441. "
1261,CC1=CC(C(C#CC2=CC=C(CCCCCCCCCC)C=C2)=C(SC(C)=C3)C3=C4C#CC5=CC=C(CCCCCCCCCC)C=C5)=C4S1,P1,5.62,3.9,0.75,4,0.34,1.05,"Sista, P.; Nguyen, H.; Murphy, J. W.; Hao, J.; Dei, D. K.; Palaniappan, K.; Servello, J.; Kularatne, R. S.; Gnade, B. E.; Xue, B.; Dastoor, P. C.; Biewer, M. C.; Stefan, M. C. Synthesis and Electronic Properties of Semiconducting Polymers Containing Benzodithiophene with Alkyl Phenylethynyl Substituents. Macromolecules 2010, 43, 8063¨C8070. "
1262,CC1=CC(C(C#CC2=CC=C(CCCCCCCCCCCCCCCC)C=C2)=C(SC(C)=C3)C3=C4C#CC5=CC=C(CCCCCCCCCCCCCCCC)C=C5)=C4S1,P2,5.61,3.87,0.85,3.3,0.33,0.47,"Sista, P.; Nguyen, H.; Murphy, J. W.; Hao, J.; Dei, D. K.; Palaniappan, K.; Servello, J.; Kularatne, R. S.; Gnade, B. E.; Xue, B.; Dastoor, P. C.; Biewer, M. C.; Stefan, M. C. Synthesis and Electronic Properties of Semiconducting Polymers Containing Benzodithiophene with Alkyl Phenylethynyl Substituents. Macromolecules 2010, 43, 8063¨C8070. "
1263,CC(O1)=CC(C1=C(C#CC2=CC=C(CCCCCCCCCC)C=C2)C3=C4OC(C)=C3)=C4C#CC5=CC=C(CCCCCCCCCC)C=C5,P1,5.39,3.32,0.83,3.71,0.39,1.19,"Sista, P.; Huang, P.; Gunathilake, S. S.; Bhatt, M. P.; Kularatne, R. S.; Stefan, M. C.; Biewer, M. C. Synthesis and Optoelectronic Properties of Novel Benzodifuran Semiconducting Polymers. J. Polym. Sci. Part A Polym. Chem. 2012, 50, 4316¨C4324. "
1264,CC(O1)=CC(C1=C(C#CC2=CC=C(CCCCCCCCCC)C=C2)C3=C4OC(C(S5)=CC(C5=C(C#CC6=CC=C(CCCCCCCCCC)C=C6)C7=C8SC(C)=C7)=C8C#CC9=CC=C(CCCCCCCCCC)C=C9)=C3)=C4C#CC%10=CC=C(CCCCCCCCCC)C=C%10,P2,5.3,3.26,0.81,2.24,0.44,0.79,"Sista, P.; Huang, P.; Gunathilake, S. S.; Bhatt, M. P.; Kularatne, R. S.; Stefan, M. C.; Biewer, M. C. Synthesis and Optoelectronic Properties of Novel Benzodifuran Semiconducting Polymers. J. Polym. Sci. Part A Polym. Chem. 2012, 50, 4316¨C4324. "
1265,CC1=CC2=C(C=C(OC(C3=CC=C(/C(C(N4CC(CCCCCCCC)CCCCCCCCCC)=O)=C5C(N(CC(CCCCCCCCCC)CCCCCCCC)C6=C\5C=CC(C)=C6)=O)C4=C3)=C7)C7=C2)O1,syn-PBDFID,5.63,3.9,0.85,2.89,0.59,1.44,"Hu, C.; Fu, Y.; Li, S.; Xie, Z.; Zhang, Q. Synthesis and Photovoltaic Properties of New Conjugated Polymers Based on Syn- and Anti-Benzodifuran. Polym. Chem. 2012, 3, 2949¨C2955. "
1266,CC1=CC2=C(C=C(C=C(C3=CC=C(/C(C(N4CC(CCCCCCCC)CCCCCCCCCC)=O)=C5C(N(CC(CCCCCCCCCC)CCCCCCCC)C6=C\5C=CC(C)=C6)=O)C4=C3)O7)C7=C2)O1,anti-PBDFID,5.49,3.85,0.75,1.74,0.48,0.65,"Hu, C.; Fu, Y.; Li, S.; Xie, Z.; Zhang, Q. Synthesis and Photovoltaic Properties of New Conjugated Polymers Based on Syn- and Anti-Benzodifuran. Polym. Chem. 2012, 3, 2949¨C2955. "
1267,O=C1C(C2=C(C3=CC=C(C)O3)N1CC(CCCC)CC)=C(C(O4)=CC=C4C(S5)=CC(CCCCCCCCCC)=C5C(O6)=C(CCCCCCCCCC)C(C6=C7)=CC8=C7C(CCCCCCCCCC)=C(C9=C(CCCCCCCCCC)C=C(C)S9)O8)N(C[C@@H](CC)CCCC)C2=O,P1,5.5,3.7,0.69,7,0.6,2.89,"Kobilka, B. M.; Hale, B. J.; Ewan, M. D.; Dubrovskiy, A. V.; Nelson, T. L.; Duzhko, V.; Jeffries-EL, M. Influence of Heteroatoms on Photovoltaic Performance of Donor¨Cacceptor Copolymers Based on 2,6-Di(thiophen-2-ylbenzo[1,2-b:4,5-b¡ä]difurans and Diketopyrrolopyrrole. Polym. Chem. 2013, 4, 5329¨C5336. "
1268,O=C1C(C2=C(C3=CC=C(C)O3)N1CCCCCCCCCCCCCC)=C(C(O4)=CC=C4C(S5)=CC(CCCCCCCCCC)=C5C(O6)=C(CCCCCCCCCC)C(C6=C7)=CC8=C7C(CCCCCCCCCC)=C(C9=C(CCCCCCCCCC)C=C(C)S9)O8)N(CCCCCCCCCCCCCC)C2=O,P2,5.5,3.8,0.65,7.7,0.57,2.81,"Kobilka, B. M.; Hale, B. J.; Ewan, M. D.; Dubrovskiy, A. V.; Nelson, T. L.; Duzhko, V.; Jeffries-EL, M. Influence of Heteroatoms on Photovoltaic Performance of Donor¨Cacceptor Copolymers Based on 2,6-Di(thiophen-2-ylbenzo[1,2-b:4,5-b¡ä]difurans and Diketopyrrolopyrrole. Polym. Chem. 2013, 4, 5329¨C5336. "
1269,O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCC)CC)=C(C(S4)=CC=C4C(S5)=CC(CCCCCCCCCC)=C5C(O6)=C(CCCCCCCCCC)C(C6=C7)=CC8=C7C(CCCCCCCCCC)=C(C9=C(CCCCCCCCCC)C=C(C)S9)O8)N(CC(CCCC)CC)C2=O,P3,5.6,3.8,0.66,7.4,0.47,2.28,"Kobilka, B. M.; Hale, B. J.; Ewan, M. D.; Dubrovskiy, A. V.; Nelson, T. L.; Duzhko, V.; Jeffries-EL, M. Influence of Heteroatoms on Photovoltaic Performance of Donor¨Cacceptor Copolymers Based on 2,6-Di(thiophen-2-ylbenzo[1,2-b:4,5-b¡ä]difurans and Diketopyrrolopyrrole. Polym. Chem. 2013, 4, 5329¨C5336. "
1270,O=C1C(C2=C(C3=CC=C(C)S3)N1CCCCCCCCCCCCCC)=C(C(S4)=CC=C4C(S5)=CC(CCCCCCCCCC)=C5C(O6)=C(CCCCCCCCCC)C(C6=C7)=CC8=C7C(CCCCCCCCCC)=C(C9=C(CCCCCCCCCC)C=C(C)S9)O8)N(CCCCCCCCCCCCCC)C2=O,P4,5.6,3.7,0.59,4.2,0.39,0.97,"Kobilka, B. M.; Hale, B. J.; Ewan, M. D.; Dubrovskiy, A. V.; Nelson, T. L.; Duzhko, V.; Jeffries-EL, M. Influence of Heteroatoms on Photovoltaic Performance of Donor¨Cacceptor Copolymers Based on 2,6-Di(thiophen-2-ylbenzo[1,2-b:4,5-b¡ä]difurans and Diketopyrrolopyrrole. Polym. Chem. 2013, 4, 5329¨C5336. "
1271,CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(C(C(CC)CCCC)=O)=C4)=C(C)S3)O5)C5=C2OCCCCCCCC)O1,PBDFTT-C,5.03,3.63,0.54,13.13,0.6,4.26,"Huo, L.; Li, Z.; Guo, X.; Wu, Y.; Zhang, M.; Ye, L.; Zhang, S.; Hou, J. BenzodifuranAlt-Thienothiophene Based Low Band Gap Copolymers: Substituent Effects on Their Molecular Energy Levels and Photovoltaic Properties. Polym. Chem. 2013, 4, 3047¨C3056. "
1272,CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(C(OCC(CC)CCCC)=O)=C4F)=C(C)S3)O5)C5=C2OCCCCCCCC)O1,PBDFTT-EF,5.07,3.61,0.61,15.75,0.538,5.17,"Huo, L.; Li, Z.; Guo, X.; Wu, Y.; Zhang, M.; Ye, L.; Zhang, S.; Hou, J. BenzodifuranAlt-Thienothiophene Based Low Band Gap Copolymers: Substituent Effects on Their Molecular Energy Levels and Photovoltaic Properties. Polym. Chem. 2013, 4, 3047¨C3056. "
1273,CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(C(C(CC)CCCC)=O)=C4F)=C(C)S3)O5)C5=C2OCCCCCCCC)O1,PBDFTT-CF,5.11,3.6,0.63,13.88,0.598,5.23,"Huo, L.; Li, Z.; Guo, X.; Wu, Y.; Zhang, M.; Ye, L.; Zhang, S.; Hou, J. BenzodifuranAlt-Thienothiophene Based Low Band Gap Copolymers: Substituent Effects on Their Molecular Energy Levels and Photovoltaic Properties. Polym. Chem. 2013, 4, 3047¨C3056. "
1274,CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(S(=O)(CC(CC)CCCC)=O)=C4)=C(C)S3)O5)C5=C2OCCCCCCCC)O1,PBDFTT-S,5.25,3.61,0.59,14.21,0.607,5.08,"Huo, L.; Li, Z.; Guo, X.; Wu, Y.; Zhang, M.; Ye, L.; Zhang, S.; Hou, J. BenzodifuranAlt-Thienothiophene Based Low Band Gap Copolymers: Substituent Effects on Their Molecular Energy Levels and Photovoltaic Properties. Polym. Chem. 2013, 4, 3047¨C3056. "
1275,CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(SC(C(OCC(CC)CCCC)=O)=C4C#N)=C(C)S3)O5)C5=C2OCCCCCCCC)O1,PBDFTT-ECN,5.44,3.7,0.87,5.88,0.446,2.28,"Huo, L.; Li, Z.; Guo, X.; Wu, Y.; Zhang, M.; Ye, L.; Zhang, S.; Hou, J. BenzodifuranAlt-Thienothiophene Based Low Band Gap Copolymers: Substituent Effects on Their Molecular Energy Levels and Photovoltaic Properties. Polym. Chem. 2013, 4, 3047¨C3056. "
1276,CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(F)=C(C(C(CC)CCCC)=O)S4)=C(C)S3)O5)C5=C2OCC(CCCC)CC)O1,PBDFTT-CF-O,4.98,3.18,0.63,13.87,0.597,5.22,"Huo, L.; Ye, L.; Wu, Y.; Li, Z.; Guo, X.; Zhang, M.; Zhang, S.; Hou, J. Conjugated and Nonconjugated Substitution Effect on Photovoltaic Properties of Benzodifuran-Based Photovoltaic Polymers. Macromolecules 2012, 45, 6923¨C6929. "
1277,CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(C(CC)CCCC)=O)S5)=C(C)S4)O6)C6=C2C7=CC=C(CC(CCCC)CC)S7)O1,PBDFTT-CF-T,5.21,3.2,0.78,13.04,0.616,6.26,"Huo, L.; Ye, L.; Wu, Y.; Li, Z.; Guo, X.; Zhang, M.; Zhang, S.; Hou, J. Conjugated and Nonconjugated Substitution Effect on Photovoltaic Properties of Benzodifuran-Based Photovoltaic Polymers. Macromolecules 2012, 45, 6923¨C6929. "
1278,CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=C5C(SC(C(C(CC)CCCC)=O)=C5F)=C(C)S4)S6)C6=C2C7=CC=C(CCCCCCCCCCCC)S7)S1,P1,5.15,3.36,0.73,6.04,0.54,2.55,"Huang, P.; Du, J.; Gunathilake, S. S.; Rainbolt, E. A.; Murphy, J. W.; Black, K. T.; Barrera, D.; Hsu, J. W. P.; Gnade, B. E.; Stefan, M. C.; Biewer, M. C. Benzodifuran and Benzodithiophene Donor¨Cacceptor Polymers for Bulk Heterojunction Solar Cells. J. Mater. Chem. A 2015, 3, 6980¨C6989. "
1279,CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)O3)=C(C=C(C4=C5C(SC(C(C(CC)CCCC)=O)=C5F)=C(C)S4)S6)C6=C2C7=CC=C(CCCCCCCCCCCC)O7)S1,P2,5.07,3.29,0.67,6.32,0.59,2.61,"Huang, P.; Du, J.; Gunathilake, S. S.; Rainbolt, E. A.; Murphy, J. W.; Black, K. T.; Barrera, D.; Hsu, J. W. P.; Gnade, B. E.; Stefan, M. C.; Biewer, M. C. Benzodifuran and Benzodithiophene Donor¨Cacceptor Polymers for Bulk Heterojunction Solar Cells. J. Mater. Chem. A 2015, 3, 6980¨C6989. "
1280,CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=C5C(SC(C(C(CC)CCCC)=O)=C5F)=C(C)S4)O6)C6=C2C7=CC=C(CCCCCCCCCCCC)S7)O1,P3,5.18,3.53,0.68,7.83,0.6,3.34,"Huang, P.; Du, J.; Gunathilake, S. S.; Rainbolt, E. A.; Murphy, J. W.; Black, K. T.; Barrera, D.; Hsu, J. W. P.; Gnade, B. E.; Stefan, M. C.; Biewer, M. C. Benzodifuran and Benzodithiophene Donor¨Cacceptor Polymers for Bulk Heterojunction Solar Cells. J. Mater. Chem. A 2015, 3, 6980¨C6989. "
1281,CC1=CC2=C(C(C3=CC=C(CCCCCCCCCCCC)O3)=C(C=C(C4=C5C(SC(C(C(CC)CCCC)=O)=C5F)=C(C)S4)O6)C6=C2C7=CC=C(CCCCCCCCCCCC)O7)O1,P4,5.12,3.56,0.65,12.11,0.64,5.23,"Huang, P.; Du, J.; Gunathilake, S. S.; Rainbolt, E. A.; Murphy, J. W.; Black, K. T.; Barrera, D.; Hsu, J. W. P.; Gnade, B. E.; Stefan, M. C.; Biewer, M. C. Benzodifuran and Benzodithiophene Donor¨Cacceptor Polymers for Bulk Heterojunction Solar Cells. J. Mater. Chem. A 2015, 3, 6980¨C6989. "
1282,CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCC)C4=O)=O)=C(C)S3)O5)C5=C2OCC(CC)CCCC)O1,BDF(2EH/C7),5.41,3.44,0.94,10.8,0.65,6.6,"Warnan, J.; Cabanetos, C.; Labban, A. El; Hansen, M. R.; Tassone, C.; Toney, M. F.; Beaujuge, P. M. Ordering Effects in Benzo[1,2-b?:4,5-b¡ä]difuran-thieno[3,4-c]Pyrrole-4,6-Dione Polymers with >7% Solar Cell Efficiency. Adv. Mater. 2014, 26, 4357¨C4362."
1283,CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)O5)C5=C2OCC(CC)CCCC)O1,BDF(2EH/C8),5.41,3.44,0.97,11.2,0.68,7.4,"Warnan, J.; Cabanetos, C.; Labban, A. El; Hansen, M. R.; Tassone, C.; Toney, M. F.; Beaujuge, P. M. Ordering Effects in Benzo[1,2-b?:4,5-b¡ä]difuran-thieno[3,4-c]Pyrrole-4,6-Dione Polymers with >7% Solar Cell Efficiency. Adv. Mater. 2014, 26, 4357¨C4362."
1284,CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCCC)C4=O)=O)=C(C)S3)O5)C5=C2OCC(CC)CCCC)O1,BDF(2EH/C9),5.41,3.44,0.93,11.3,0.69,7.3,"Warnan, J.; Cabanetos, C.; Labban, A. El; Hansen, M. R.; Tassone, C.; Toney, M. F.; Beaujuge, P. M. Ordering Effects in Benzo[1,2-b?:4,5-b¡ä]difuran-thieno[3,4-c]Pyrrole-4,6-Dione Polymers with >7% Solar Cell Efficiency. Adv. Mater. 2014, 26, 4357¨C4362."
1285,CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCCCC)C4=O)=O)=C(C)S3)O5)C5=C2OCC(CC)CCCC)O1,BDF(2EH/C10),5.41,3.44,0.94,11.2,0.6,6.3,"Warnan, J.; Cabanetos, C.; Labban, A. El; Hansen, M. R.; Tassone, C.; Toney, M. F.; Beaujuge, P. M. Ordering Effects in Benzo[1,2-b?:4,5-b¡ä]difuran-thieno[3,4-c]Pyrrole-4,6-Dione Polymers with >7% Solar Cell Efficiency. Adv. Mater. 2014, 26, 4357¨C4362."
1286,CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CC)CCCC)S1,BDT(2EH/C8),5.29,3.44,0.94,12,0.61,7.1,"Warnan, J.; Cabanetos, C.; Labban, A. El; Hansen, M. R.; Tassone, C.; Toney, M. F.; Beaujuge, P. M. Ordering Effects in Benzo[1,2-b?:4,5-b¡ä]difuran-thieno[3,4-c]Pyrrole-4,6-Dione Polymers with >7% Solar Cell Efficiency. Adv. Mater. 2014, 26, 4357¨C4362."
1287,O=C1N(CC(CC)CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC6=C(C(OCCCCCCCC)=C(C=C(C)S7)C7=C6OCCCCCCCC)S5)S4)N(CC(CCCC)CC)C3=O,PDPP-BDT,5.16,3.51,0.68,8.4,0.443,2.53,"Huo, L.; Hou, J.; Chen, H. Y.; Zhang, S.; Jiang, Y.; Chen, T. L.; Yang, Y. Bandgap and Molecular Level Control of the Low-Bandgap Polymers Based on 3,6-Dithiophen-2-yl-2,5-dihydropyrrolo[3,4-c]pyrrole-1,4-Dione toward Highly Efficient Polymer Solar Cells. Macromolecules 2009, 42, 6564¨C6571. "
1288,O=C1N(CC(CC)CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC(C(C(CCCCC)CC)=C(C(CCCCC)CC)C6=C7SC(C)=C6)=C7S5)S4)N(CC(CCCC)CC)C3=O,PDPP-BDP,5.21,3.63,0.68,10.1,0.627,4.31,"Huo, L.; Hou, J.; Chen, H. Y.; Zhang, S.; Jiang, Y.; Chen, T. L.; Yang, Y. Bandgap and Molecular Level Control of the Low-Bandgap Polymers Based on 3,6-Dithiophen-2-yl-2,5-dihydropyrrolo[3,4-c]pyrrole-1,4-Dione toward Highly Efficient Polymer Solar Cells. Macromolecules 2009, 42, 6564¨C6571. "
1289,CC1=CC2=C(C(C3=CC(CCCCCCCC)=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC(OCCCCCCCC)=CC=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N7)S4)O%10)C%10=C2C%11=CC(CCCCCCCC)=C(CCCCCCCC)S%11)O1,P1,5.25,3.2,0.83,5.28,0.51,2.22,"Cong, Z.; Zhao, B.; Wu, H.; Guo, Z.; Wang, W.; Luo, G.; Xu, J.; Xia, Y.; Gao, C.; An, Z. Synthesis of Copolymers Based on benzo[1,2-b:4,5-b¡ä]difuran and Fluorinated Quinoxaline Derivatives and Their Photovoltaic Properties. Polymer 2015, 67, 55¨C62. "
1290,CC1=CC2=C(C(C3=CC(CCCCCCCC)=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC(OCCCCCCCC)=CC=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N7)S4)O%10)C%10=C2C%11=CC(CCCCCCCC)=C(CCCCCCCC)S%11)O1,P2,5.3,3.25,0.83,8.74,0.612,4.44,"Cong, Z.; Zhao, B.; Wu, H.; Guo, Z.; Wang, W.; Luo, G.; Xu, J.; Xia, Y.; Gao, C.; An, Z. Synthesis of Copolymers Based on benzo[1,2-b:4,5-b¡ä]difuran and Fluorinated Quinoxaline Derivatives and Their Photovoltaic Properties. Polymer 2015, 67, 55¨C62. "
1291,CC(S1)=CC2=C1C3=C(C(CC(CCCC)CCCC)=C(C4=C(C=C(C5=C6C(SC(C(OCC(CCCCCC)CCCC)=O)=C6F)=C(C)S5)S4)S7)C7=C3CC(CCCC)CCCC)S2,PTDBD2,5.24,3.57,0.89,13,0.653,7.6,"Son, H. J.; Lu, L.; Chen, W.; Xu, T.; Zheng, T.; Carsten, B.; Strzalka, J.; Darling, S. B.; Chen, L. X.; Yu, L. Synthesis and Photovoltaic Effect in dithieno[2,3-d:2¡ä,3¡ä-d¡ä]benzo[1,2-b:4,5-b¡ä]dithiophene-Based Conjugated Polymers. Adv. Mater. 2013, 25, 838¨C843. "
1292,CC(S1)=CC2=C1C3=C(C(CC(CCCC)CCCC)=C(C4=C(C=C(C5=C6C(SC(C(OC(CC(CC)CCCC)CCC(CCCC)CC)=O)=C6F)=C(C)S5)S4)S7)C7=C3CC(CCCC)CCCC)S2,PTDBD3,5.3,3.63,0.88,10.7,0.521,4.9,"Son, H. J.; Lu, L.; Chen, W.; Xu, T.; Zheng, T.; Carsten, B.; Strzalka, J.; Darling, S. B.; Chen, L. X.; Yu, L. Synthesis and Photovoltaic Effect in dithieno[2,3-d:2¡ä,3¡ä-d¡ä]benzo[1,2-b:4,5-b¡ä]dithiophene-Based Conjugated Polymers. Adv. Mater. 2013, 25, 838¨C843. "
1293,CC(S1)=CC2=C1C3=C(C(OCC(CCCC)CCCCCC)=C(C4=C(C=C(C5=C6C(C(F)=C(C(OCC(CCCCCC)CCCC)=O)S6)=C(C)S5)S4)S7)C7=C3OCC(CCCCCC)CCCC)S2,PTR5b,5.18,3.28,0.65,12.2,0.63,5,"Zheng, T.; Yu, L. Roles of Quinoidal Character, Regioregularity, and Polydispersity in Determining the Photovoltaic Performance of Conjugated Copolymers. Macromolecules2014, 47, 6252?6259. "
1294,CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(S1)C(S3)=CC(S4)=C3C(C4=C5OCC(CCCCCC)CCCC)=C(OCC(CCCC)CC)C6=C5C7=C(C8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CC)CCCC)=C8S7)S6,PTR7a,5.2,3,0.2,0.28,0.25,0.01,"Zheng, T.; Yu, L. Roles of Quinoidal Character, Regioregularity, and Polydispersity in Determining the Photovoltaic Performance of Conjugated Copolymers. Macromolecules2014, 47, 6252?6259. "
1295,CC1=C(C(F)=C(C(OCC(CCCCCC)CCCC)=O)S2)C2=C(S1)C(S3)=CC(S4)=C3C(C4=C5OCC(CCCCCC)CCCC)=C(OCC(CCCC)CCCCCC)C6=C5C7=C(C8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CC)CCCC)=C8S7)S6,PTR7b,5.22,2.99,0.3,0.96,0.288,0.08,"Zheng, T.; Yu, L. Roles of Quinoidal Character, Regioregularity, and Polydispersity in Determining the Photovoltaic Performance of Conjugated Copolymers. Macromolecules2014, 47, 6252?6259. "
1296,CC1=C(C(F)=C(C(OCC(CC)CCCC)=O)S2)C2=C(C(S3)=CC(C3=C4OC[C@H](CC)CCCC)=C(OCC(CCCC)CC)C(S5)=C4C(S6)=C5C(C6=C7OCC(CCCCCC)CCCC)=C(OCC(CCCC)CC)C8=C7C9=C(C%10=C(OCC(CCCC)CC)C%11=C(C=C(C)S%11)C(OCC(CC)CCCC)=C%10S9)S8)S1,PTR9a,5.23,3.04,0.71,7.23,0.546,2.8,"Zheng, T.; Yu, L. Roles of Quinoidal Character, Regioregularity, and Polydispersity in Determining the Photovoltaic Performance of Conjugated Copolymers. Macromolecules2014, 47, 6252?6259. "
1297,CC1=C(C(F)=C(C(OCC(CCCCCC)CCCC)=O)S2)C2=C(C(S3)=CC(C3=C4OC[C@H](CC)CCCC)=C(OCC(CCCC)CC)C(S5)=C4C(S6)=C5C(C6=C7OCC(CCCCCC)CCCC)=C(OCC(CCCC)CCCCCC)C8=C7C9=C(C%10=C(OCC(CCCC)CC)C%11=C(C=C(C)S%11)C(OCC(CC)CCCC)=C%10S9)S8)S1,PTR9b,5.32,3.01,0.71,5.22,0.54,2,"Zheng, T.; Yu, L. Roles of Quinoidal Character, Regioregularity, and Polydispersity in Determining the Photovoltaic Performance of Conjugated Copolymers. Macromolecules2014, 47, 6252?6259. "
1298,CC(S1)=CC2=C1C3=C(C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C(C5=C(C=C(C6=C7C(C=C(C(C(CC)CCCC)=O)S7)=C(C)S6)S5)S8)C8=C3C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S2,pDTBDT-TTEH,5.29,3.66,0.72,15.77,0.594,6.74,"Shin, N.; Yun, H.-J.; Yoon, Y.; Son, H. J.; Ju, S.-Y.; Kwon, S.-K.; Kim, B.; Kim, Y.-H. Highly Stable Polymer Solar Cells Based on Poly(dithienobenzodithiophene-coThienothiophene. Macromolecules 2015, 48, 3890¨C3899. "
1299,CC(S1)=CC2=C1C3=C(C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C(C5=C(C=C(C6=C7C(C8=C(C(N(CCCCCCCC)C8=O)=O)S7)=C(C)S6)S5)S9)C9=C3C%10=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%10)S2,pDTBDT-DTPD,5.53,3.87,0.79,6.64,0.539,2.83,"Shin, N.; Yun, H.-J.; Yoon, Y.; Son, H. J.; Ju, S.-Y.; Kwon, S.-K.; Kim, B.; Kim, Y.-H. Highly Stable Polymer Solar Cells Based on Poly(dithienobenzodithiophene-coThienothiophene. Macromolecules 2015, 48, 3890¨C3899. "
1300,CC(S1)=CC2=C1C3=C(C(OCC(CCCCCCCC)CCCCCC)=C(C4=C(C=C(C5=CC=C(C6=C7C(C(N6CC(CCCCCCCC)CCCCCC)=O)=C(C8=CC=C(C)S8)N(CC(CCCCCC)CCCCCCCC)C7=O)S5)S4)S9)C9=C3OCC(CCCCCC)CCCCCCCC)S2,PBT-HD-DPP-C16,5.13,3.65,0.62,6.41,0.609,2.42,"Sun, S.; Zhang, P.; Li, J.; Li, Y.; Wang, J.; Zhang, S.; Xia, Y.; Meng, X.; Fan, D.; Chu, J Synthetically Controlling the Optoelectronic Properties of dithieno[2,3-d:2¡ä,3¡ä-d¡ä]benzo[1,2-b:4,5-b¡ä]dithiophene-Alt-Diketopyrrolopyrrole-Conjugated Polymers for Efficient Solar Cells. J. Mater. Chem. A 2014, 2, 15316¨C15325. "
1301,CC(S1)=CC2=C1C3=C(C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C(C5=C(C=C(C6=CC=C(C7=C8C(C(N7CC(CCCC)CCCCCC)=O)=C(C9=CC=C(C)S9)N(CC(CCCCCC)CCCC)C8=O)S6)S5)S%10)C%10=C3C%11=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%11)S2,PBT-T-DPP-C12,5.19,3.72,0.65,12.61,0.634,5.19,"Sun, S.; Zhang, P.; Li, J.; Li, Y.; Wang, J.; Zhang, S.; Xia, Y.; Meng, X.; Fan, D.; Chu, J Synthetically Controlling the Optoelectronic Properties of dithieno[2,3-d:2¡ä,3¡ä-d¡ä]benzo[1,2-b:4,5-b¡ä]dithiophene-Alt-Diketopyrrolopyrrole-Conjugated Polymers for Efficient Solar Cells. J. Mater. Chem. A 2014, 2, 15316¨C15325. "
1302,O=C(N1CC(CCCCCCCCCC)CCCCCCCCCCCC)C(C2=C1C3=CC=C(S3)C4=CC(C(OCC(CC)CCCC)=C(SC(C)=C5)C5=C6OCC(CCCC)CC)=C6S4)=C(C7=CC=C(C)S7)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C2=O,PDPPBDT,5.37,3.39,0.741,7.33,0.61,3.31,"Ryu, T. I.; Yoon, Y.; Kim, J.-H.; Hwang, D.-H.; Ko, M. J.; Lee, D.-K.; Kim, J. Y.; Kim, H.; Park, N.-G.; Kim, B.; Son, H. J. Simultaneous Enhancement of Solar Cell Efficiency and Photostability via Chemical Tuning of Electron Donating Units in Diketopyrrolopyrrole-Based Push-Pull Type Polymers. Macromolecules 2014, 47, 6270¨C6280. "
1303,O=C(N1CC(CCCCCCCCCC)CCCCCCCCCCCC)C(C2=C1C3=CC=C(S3)C(S4)=CC5=C4C6=C(C=C(C)S6)S5)=C(C7=CC=C(C)S7)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C2=O,PDPPDTT,5.36,3.59,0.7,13.64,0.64,6.11,"Ryu, T. I.; Yoon, Y.; Kim, J.-H.; Hwang, D.-H.; Ko, M. J.; Lee, D.-K.; Kim, J. Y.; Kim, H.; Park, N.-G.; Kim, B.; Son, H. J. Simultaneous Enhancement of Solar Cell Efficiency and Photostability via Chemical Tuning of Electron Donating Units in Diketopyrrolopyrrole-Based Push-Pull Type Polymers. Macromolecules 2014, 47, 6270¨C6280. "
1304,CC(S1)=CC2=C1C3=C(C(CC(CC)CCCCC)=C(C4=C(C=C(C5=CC=C(C6=C7C(C(N6CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C8=CC=C(C)S8)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C7=O)S5)S4)S9)C9=C3CC(CCCCC)CC)S2,PDPPDTBDT,5.35,3.35,0.745,9.8,0.65,4.75,"Ryu, T. I.; Yoon, Y.; Kim, J.-H.; Hwang, D.-H.; Ko, M. J.; Lee, D.-K.; Kim, J. Y.; Kim, H.; Park, N.-G.; Kim, B.; Son, H. J. Simultaneous Enhancement of Solar Cell Efficiency and Photostability via Chemical Tuning of Electron Donating Units in Diketopyrrolopyrrole-Based Push-Pull Type Polymers. Macromolecules 2014, 47, 6270¨C6280. "
1305,CC(S1)=CC2=C1C3=C(C(OCC(CC)CCCC)=C(C4=C(C=C(C5=CC=C(/C(C(N6CC(CCCCCC)CCCCCCCC)=O)=C7C(C=CC(C)=C8)=C8N(CC(CCCCCC)CCCCCCCC)C/7=O)C6=C5)S4)S9)C9=C3OCC(CCCC)CC)S2,PDTBDT-ID,5.38,3.8,0.7,12.58,0.503,4.43,"Xia, Y.; Zhang, H.; Li, J.; Tong, J.; Zhang, P.; Yang, C. Synthesis of dithieno[2,3-d:2¡¯,3¡¯-d¡¯]benzo[1,2-b:4,5-b¡¯]dithiophene -Alt-Isoindigo Conjugated Polymer and Enhancement of Photovoltaic Property with Diphenyl Sulfide Additives. J. Polym. Res.2015, 22, 633/1¨C8 . "
1306,CC(S1)=CC2=C1C3=C(C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C(C5=C(C=C(C6=C(CCCCCC)C=C(C7=CC(C8=NSN=C8C(C9=CC(CCCCCC)=C(C)S9)=C%10)=C%10C%11=NSN=C%117)S6)S5)S%12)C%12=C3C%13=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%13)S2,PDTBDT-DTNT,5.51,3.9,0.65,17.51,0.66,7.52,"Guo, P.; Xia, Y.; Huang, F.; Luo, G.; Li, J.; Zhang, P.; Zhu, Y.; Yang, C.; Wu, H.; Cao, Y. An Alkylthieno-2-Yl Flanked dithieno[2,3-d:2¡ä,3¡ä-d¡ä]benzo[1,2-b:4,5-b¡ä]dithiopheneBased Low Band Gap Conjugated Polymer for High Performance Photovoltaic Solar Cells. RSC Adv. 2015, 5, 12879¨C12885. "
1307,CC(S1)=CC2=C1C3=C(C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C(C5=C(C=C(C6=C(CCCCCCCCCCCC)C([P@](C7=C8SC(C)=C7CCCCCCCCCCCC)(C9=CC=CC=C9)=O)=C8S6)S5)S%10)C%10=C3C%11=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%11)S2,PDTP-DTBDT,5.44,3.01,0.83,15.1,0.543,6.81,"Kim, Y. J.; Kim, M.-J.; An, T. K.; Kim, Y.-H.; Park, C. E. A New Multi-Functional Conjugated Polymer for Use in High-Performance Bulk Heterojunction Solar Cells. Chem. Commun. 2015, 51, 11572¨C11575. "
1308,O=C1N(CC(CC)CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=C(C6=CC=C(C[C@H](CCCC)CC)S6)C=C(C7=CC(C8=CC=C(C[C@@H](CCCC)CC)S8)=C(C)S7)S5)S4)N(CC(CCCC)CC)C3=O,P4TDPP,5.17,3.62,0.65,8.05,0.46,2.43,"Tsai, J. H.; Lee, W. Y.; Chen, W. C.; Yu, C. Y.; Hwang, G. W.; Ting, C. New TwoDimensional Thiophene-Acceptor Conjugated Copolymers for Field Effect Transistor and Photovoltaic Cell Applications. Chem. Mater. 2010, 22, 3290¨C3299. "
1309,CC1=CC=C(C2=C(C3=CC=C(C[C@H](CCCC)CC)S3)C=C(C4=CC(C5=CC=C(CC(CCCC)CC)S5)=C(C)S4)S2)C6=NSN=C16,P4TBT,5.52,3.24,0.9,4.71,0.33,1.39,"Tsai, J. H.; Lee, W. Y.; Chen, W. C.; Yu, C. Y.; Hwang, G. W.; Ting, C. New TwoDimensional Thiophene-Acceptor Conjugated Copolymers for Field Effect Transistor and Photovoltaic Cell Applications. Chem. Mater. 2010, 22, 3290¨C3299. "
1310,CC[C@@H](CCCC)CC(S1)=CC=C1C2=C(C(S3)=CC=C3C4=CC=C(C5=CC=C(C)S5)C6=NSN=C64)SC(C7=CC(C8=CC=C(CC(CCCC)CC)S8)=C(C)S7)=C2,P4TDTBT,5.04,3.38,0.57,6.28,0.36,1.28,"Tsai, J. H.; Lee, W. Y.; Chen, W. C.; Yu, C. Y.; Hwang, G. W.; Ting, C. New TwoDimensional Thiophene-Acceptor Conjugated Copolymers for Field Effect Transistor and Photovoltaic Cell Applications. Chem. Mater. 2010, 22, 3290¨C3299. "
1311,CC[C@@H](CCCC)CC(S1)=CC=C1C2=C(C(S3)=CC=C3C4=CC=C(C5=CC=C(C)S5)C6=C4N=C(C7=CC=C(OCC(CC)CCCC)C=C7)C(C8=CC=C(OCC(CCCC)CC)C=C8)=N6)SC(C9=CC(C%10=CC=C(CC(CCCC)CC)S%10)=C(C)S9)=C2,P4TPDTQ,5.28,3.22,0.69,5.39,0.35,1.29,"Tsai, J. H.; Lee, W. Y.; Chen, W. C.; Yu, C. Y.; Hwang, G. W.; Ting, C. New TwoDimensional Thiophene-Acceptor Conjugated Copolymers for Field Effect Transistor and Photovoltaic Cell Applications. Chem. Mater. 2010, 22, 3290¨C3299. "
1312,CC1=CC([Ge](CC(CCCCCCCCCC)CCCCCCCC)(CC(CCCCCCCC)CCCCCCCCCC)C2=C3SC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1,P(Ge-DTBT),5.05,3.27,0.66,7.95,0.68,3.51,"Casey, A.; Dimitrov, S. D.; Shakya-Tuladhar, P.; Fei, Z.; Nguyen, M.; Han, Y.; Anthopoulos, T. D.; Durrant, J. R.; Heeney, M. Effect of Systematically Tuning Conjugated Donor Polymer Lowest Unoccupied Molecular Orbital Levels via Cyano Substitution on Organic Photovoltaic Device Performance. Chem. Mater. 2016, 28, 5110¨C5120. "
1313,CC1=CC([Ge](CC(CCCCCCCCCC)CCCCCCCC)(CC(CCCCCCCC)CCCCCCCCCC)C2=C3SC(C4=CC=C(C5=CC(C#N)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1,P(Ge-DTCNBT),5.11,3.54,0.68,14.83,0.7,6.55,"Casey, A.; Dimitrov, S. D.; Shakya-Tuladhar, P.; Fei, Z.; Nguyen, M.; Han, Y.; Anthopoulos, T. D.; Durrant, J. R.; Heeney, M. Effect of Systematically Tuning Conjugated Donor Polymer Lowest Unoccupied Molecular Orbital Levels via Cyano Substitution on Organic Photovoltaic Device Performance. Chem. Mater. 2016, 28, 5110¨C5120. "
1314,CC1=CC([Ge](CC(CCCCCCCCCC)CCCCCCCC)(CC(CCCCCCCC)CCCCCCCCCC)C2=C3SC(C4=CC=C(C5=C(C#N)C(C#N)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1,P(Ge-CTDCNBT),5.14,3.77,0.68,2.99,0.36,0.63,"Casey, A.; Dimitrov, S. D.; Shakya-Tuladhar, P.; Fei, Z.; Nguyen, M.; Han, Y.; Anthopoulos, T. D.; Durrant, J. R.; Heeney, M. Effect of Systematically Tuning Conjugated Donor Polymer Lowest Unoccupied Molecular Orbital Levels via Cyano Substitution on Organic Photovoltaic Device Performance. Chem. Mater. 2016, 28, 5110¨C5120. "
1315,CC1=CC(SC2=C3C=C4C(/C(C(N4CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C5C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C6=C\5C=C7C(C(SC(C8=CC=C(C)S8)=C9)=C9S7)=C6)=O)=C2)=C3S1,TBTIT-h,5.1,3.5,0.72,17.7,0.71,9.1,"Yue, W.; Ashraf, R. S.; Nielsen, C. B.; Collado-Fregoso, E.; Niazi, M. R.; Yousaf, S. A.; Kirkus, M.; Chen, H. Y.; Amassian, A.; Durrant, J. R.; McCulloch, I. A Thieno[3,2-b][1]benzothiophene Isoindigo Building Block for Additive- and Annealing-Free HighPerformance Polymer Solar Cells. Adv. Mater. 2015, 27, 4702¨C4707. "
1316,CC1=CC(SC2=C3C=C4C(/C(C(N4CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C5C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C6=C\5C=C7C(C(SC(C8=CC=C(C)S8)=C9)=C9S7)=C6)=O)=C2)=C3S1,TBTIT-i,5.2,3.6,0.73,13.6,0.54,5.3,"Yue, W.; Ashraf, R. S.; Nielsen, C. B.; Collado-Fregoso, E.; Niazi, M. R.; Yousaf, S. A.; Kirkus, M.; Chen, H. Y.; Amassian, A.; Durrant, J. R.; McCulloch, I. A Thieno[3,2-b][1]benzothiophene Isoindigo Building Block for Additive- and Annealing-Free HighPerformance Polymer Solar Cells. Adv. Mater. 2015, 27, 4702¨C4707. "
1317,CC1=CC(CCCCCCCCCCCC)=C(C2=NC3=CC(SC(C4=C(CCCCCCCCCCCC)C=C(C5=C(CCCCCCCCCCCC)C=C(C6=CC=C7C(N(CC(CCCCCC)CCCCCCCC)C(/C7=C8C(SC(C9=CC(CCCCCCCCCCCC)=C(C)S9)=C%10)=C%10N(CC(CCCCCC)CCCCCCCC)C\8=O)=O)=C6F)S5)S4)=N%11)=C%11C=C3S2)S1,F-BT2,5.44,3.95,0.64,4.48,0.57,1.66,"Ide, M.; Saeki, A. Fluorinated Benzothienoisoindigo Copolymers for Organic Solar Cells: A Comparative Study on Polymer Orientation and Device Performance. Chem. Lett.2017, 46, 1133¨C1136. "
1318,O=S(N(CC(CCCCCCCCCCCCCC)CCCCCCCCCCCCCC)C1=C2SC(C)=C1)(C3=C2SC(C4=CC=C(C5=CC=C(C)S5)S4)=C3)=O,BTSA5,5.39,3.55,0.85,9.5,0.682,5.5,"Melkonyan, F. S.; Zhao, W.; Drees, M.; Eastham, N. D.; Leonardi, M. J.; Butler, M. R.; Chen, Z.; Yu, X.; Chang, R. P. H.; Ratner, M. A.; Facchetti, A. F.; Marks, T. J. Bithiophenesulfonamide Building Block for ¦Ð-Conjugated Donor-Acceptor Semiconductors. J. Am. Chem. Soc. 2016, 138, 6944¨C6947. "
1319,CC1=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(S1)C2=NC3=NC(S4)=C(N=C3S2)N=C4C5=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C(C6=C(CCCCCC)C=C(C7=CC(CCCCCC)=C(C)S7)S6)S5,P-PDTz-Tdt-HH,5.59,3.84,0.83,4.86,0.45,1.82,"Ie, Y.; Sasada, S.; Karakawa, M.; Aso, Y. Pyradinodithiazole: An Electron-Accepting Monomer Unit for Hole-Transporting and Electron-Transporting Conjugated Copolymers. Org. Lett. 2015, 17, 4580¨C4583. "
1320,CC1=CC=C(C2=CC=C(C3=C4C(C(N3CC(CCCCCC)CCCCCCCC)=O)=C(C5=CC=C(C)S5)N(CC(CCCCCCCC)CCCCCC)C4=O)S2)S1,TTT,5.27,3.89,0.7,10.05,0.548,4.01,"Homyak, P.; Liu, Y.; Liu, F.; Russel, T. P.; Coughlin, E. B. Systematic Variation of Fluorinated Diketopyrrolopyrrole Low Bandgap Conjugated Polymers: Synthesis by Direct Arylation Polymerization and Characterization and Performance in Organic Photovoltaics and Organic Field-Effect Transistors. Macromolecules 2015, 48, 6978¨C6986. "
1321,O=C(N1CC(CCCCCC)CCCCCCCC)C(C2=C1C(S3)=CC=C3C4=CC=C(C)C=C4)=C(C5=CC=C(C)S5)N(CC(CCCCCCCC)CCCCCC)C2=O,TPT,5.32,3.84,0.76,12.86,0.399,4.37,"Homyak, P.; Liu, Y.; Liu, F.; Russel, T. P.; Coughlin, E. B. Systematic Variation of Fluorinated Diketopyrrolopyrrole Low Bandgap Conjugated Polymers: Synthesis by Direct Arylation Polymerization and Characterization and Performance in Organic Photovoltaics and Organic Field-Effect Transistors. Macromolecules 2015, 48, 6978¨C6986. "
1322,O=C(N1CC(CCCCCC)CCCCCCCC)C(C2=C1C(S3)=CC=C3C4=C(F)C(F)=C(C)S4)=C(C5=CC=C(C)S5)N(CC(CCCCCCCC)CCCCCC)C2=O,TTfT,5.44,4.06,0.7,3.17,0.53,1.25,"Homyak, P.; Liu, Y.; Liu, F.; Russel, T. P.; Coughlin, E. B. Systematic Variation of Fluorinated Diketopyrrolopyrrole Low Bandgap Conjugated Polymers: Synthesis by Direct Arylation Polymerization and Characterization and Performance in Organic Photovoltaics and Organic Field-Effect Transistors. Macromolecules 2015, 48, 6978¨C6986. "
1323,O=C(N1CC(CCCCCC)CCCCCCCC)C(C2=C1C(S3)=CC=C3C4=CC(F)=C(C)C=C4F)=C(C5=CC=C(C)S5)N(CC(CCCCCCCC)CCCCCC)C2=O,TPfT,5.45,3.98,0.83,6.14,0.449,2.4,"Homyak, P.; Liu, Y.; Liu, F.; Russel, T. P.; Coughlin, E. B. Systematic Variation of Fluorinated Diketopyrrolopyrrole Low Bandgap Conjugated Polymers: Synthesis by Direct Arylation Polymerization and Characterization and Performance in Organic Photovoltaics and Organic Field-Effect Transistors. Macromolecules 2015, 48, 6978¨C6986. "
1324,CC1=CC=C(C2=CC=C(/C(C(N3CC(CCCCCC)CCCCCCCC)=O)=C4C(N(CC(CCCCCCCC)CCCCCC)C5=C\4C=CC(C)=C5)=O)C3=C2)S1,P[T-iI(HD)]-4,5.21,3.59,0.9,5.8,0.55,2.9,"Grand, C.; Baek, S.; Lai, T. H.; Deb, N.; Zajaczkowski, W.; Stalder, R.; M¨¹llen, K.; Pisula, W.; Bucknall, D. G.; So, F.; Reynolds, J. R. Structure-Property Relationships Directing Transport and Charge Separation in Isoindigo Polymers. Macromolecules 2016, 49, 4008¨C4022. "
1325,O=C(N1CC(CCCCCC)CCCCCCCC)/C(C(C1=C2)=CC=C2C3=CC(CCCCCC)=C(C4=CC=C(C5=C(CCCCCC)C=C(C)S5)S4)S3)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C/6C=CC(C)=C7)=O,P[T3(C6)-iI(HD)]-2,5.29,3.71,0.7,15.2,0.62,6.6,"Grand, C.; Baek, S.; Lai, T. H.; Deb, N.; Zajaczkowski, W.; Stalder, R.; M¨¹llen, K.; Pisula, W.; Bucknall, D. G.; So, F.; Reynolds, J. R. Structure-Property Relationships Directing Transport and Charge Separation in Isoindigo Polymers. Macromolecules 2016, 49, 4008¨C4022. "
1326,CC1=CC(SC2=C3C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8S5)=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)=C3S1,PDTBDT-BZ,5.3,3.2,0.83,10.28,0.649,5.54,"Lee, H. S.; Song, H. G.; Jung, H.; Kim, M. H.; Cho, C.; Lee, J. Y.; Park, S.; Son, H. J.; Yun, H. J.; Kwon, S. K.; Kim, Y. H.; Kim, B. Effects of Backbone Planarity and Tightly Packed Alkyl Chains in the Donor-Acceptor Polymers for High Photostability. Macromolecules 2016, 49, 7844¨C7856. "
1327,CC1=CC(SC2=C3C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C5C(C(SC(C6=C(F)C=C(C)C7=NSN=C76)=C8)=C8S5)=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)=C3S1,PDTBDT-BZF,5.4,3.3,0.88,11.47,0.735,7.42,"Lee, H. S.; Song, H. G.; Jung, H.; Kim, M. H.; Cho, C.; Lee, J. Y.; Park, S.; Son, H. J.; Yun, H. J.; Kwon, S. K.; Kim, Y. H.; Kim, B. Effects of Backbone Planarity and Tightly Packed Alkyl Chains in the Donor-Acceptor Polymers for High Photostability. Macromolecules 2016, 49, 7844¨C7856. "
1328,CC1=CC(SC2=C3C(C4=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S4)=C5C(C(SC(C6=C(F)C(F)=C(C)C7=NSN=C76)=C8)=C8S5)=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)=C3S1,PDTBDT-BZF2,5.4,3.3,0.9,10.02,0.605,5.46,"Lee, H. S.; Song, H. G.; Jung, H.; Kim, M. H.; Cho, C.; Lee, J. Y.; Park, S.; Son, H. J.; Yun, H. J.; Kwon, S. K.; Kim, Y. H.; Kim, B. Effects of Backbone Planarity and Tightly Packed Alkyl Chains in the Donor-Acceptor Polymers for High Photostability. Macromolecules 2016, 49, 7844¨C7856. "
1329,CC1=CC(CCCCCCCCCCCC)=C(C#CC#CC2=C(CCCCCCCCCCCC)C=C(C3=CC=C(C(N(CC(CCCCCC)CCCC)C4=O)=C5C4=C(C6=CC=C(C)S6)N(CC(CCCC)CCCCCC)C5=O)S3)S2)S1,DP3,5.16,3.46,0.674,7.06,0.573,2.73,"Eckstein, B. J.; Melkonyan, F. S.; Zhou, N.; Manley, E. F.; Smith, J.; Timalsina, A.; Chang, R. P. H.; Chen, L. X.; Facchetti, A.; Marks, T. J. Buta-1,3-Diyne-Based ¦Ð-Conjugated Polymers for Organic Transistors and Solar Cells. Macromolecules 2017, 50, 1430¨C1441. "
1330,CC1=CC(CC(CCCC)CC)=C(C#CC#CC2=C(CC(CC)CCCC)C=C(C3=CC=C(C(N(CC(CCCCCC)CCCC)C4=O)=C5C4=C(C6=CC=C(C)S6)N(CC(CCCC)CCCCCC)C5=O)S3)S2)S1,DP4,5.25,3.59,0.697,8.37,0.643,3.75,"Eckstein, B. J.; Melkonyan, F. S.; Zhou, N.; Manley, E. F.; Smith, J.; Timalsina, A.; Chang, R. P. H.; Chen, L. X.; Facchetti, A.; Marks, T. J. Buta-1,3-Diyne-Based ¦Ð-Conjugated Polymers for Organic Transistors and Solar Cells. Macromolecules 2017, 50, 1430¨C1441. "
1331,FC(C=CC=C1)=C1/N=C/C(N2)=CC=C2C3=NC4=C(C)C=CC(C5=CC6=C(C7=CC=C(CCCCCCCC)S7)C(SC(C)=C8)=C8C(C9=CC=C(CCCCCCCC)S9)=C6S5)=C4N=C3C%10=CC=C(/C=N/C%11=C(F)C=CC=C%11)N%10,PTF1,4.97,3.81,0.72,4.97,0.29,1.04,"Singh, A.; Singh, R.; Lin, C. M.; Pola, M. K.; Chang, C. K.; Wei, K. H.; Lin, H. C. Novel Fluoride-Substituted Donor/acceptor Polymers Containing Benzodithiophene and Quinoxaline Units for Use in Low-band Gap Solar Cells. Eur. Polym. J. 2016, 82, 334¨C346. "
1332,FC(C=CC=C1)=C1/N=C/C(N2)=CC=C2C3=NC4=C(C)C=CC(C5=CC6=C(OCCCCCCCC)C(SC(C)=C7)=C7C(OCCCCCCCC)=C6S5)=C4N=C3C8=CC=C(/C=N/C9=C(F)C=CC=C9)N8,POF1,4.84,3.67,0.79,5.17,0.3,1.22,"Singh, A.; Singh, R.; Lin, C. M.; Pola, M. K.; Chang, C. K.; Wei, K. H.; Lin, H. C. Novel Fluoride-Substituted Donor/acceptor Polymers Containing Benzodithiophene and Quinoxaline Units for Use in Low-band Gap Solar Cells. Eur. Polym. J. 2016, 82, 334¨C346. "
1333,FC(C=CC=C1F)=C1/N=C/C(N2)=CC=C2C3=NC4=C(C)C=CC(C5=CC6=C(C7=CC=C(CCCCCCCC)S7)C(SC(C)=C8)=C8C(C9=CC=C(CCCCCCCC)S9)=C6S5)=C4N=C3C%10=CC=C(/C=N/C%11=C(F)C=CC=C%11F)N%10,PTF2,4.88,3.74,0.72,8.7,0.34,2.13,"Singh, A.; Singh, R.; Lin, C. M.; Pola, M. K.; Chang, C. K.; Wei, K. H.; Lin, H. C. Novel Fluoride-Substituted Donor/acceptor Polymers Containing Benzodithiophene and Quinoxaline Units for Use in Low-band Gap Solar Cells. Eur. Polym. J. 2016, 82, 334¨C346. "
1334,FC(C=CC=C1F)=C1/N=C/C(N2)=CC=C2C3=NC4=C(C)C=CC(C5=CC6=C(OCCCCCCCC)C(SC(C)=C7)=C7C(OCCCCCCCC)=C6S5)=C4N=C3C8=CC=C(/C=N/C9=C(F)C=CC=C9F)N8,POF2,4.78,3.62,0.77,5.25,0.4,1.6,"Singh, A.; Singh, R.; Lin, C. M.; Pola, M. K.; Chang, C. K.; Wei, K. H.; Lin, H. C. Novel Fluoride-Substituted Donor/acceptor Polymers Containing Benzodithiophene and Quinoxaline Units for Use in Low-band Gap Solar Cells. Eur. Polym. J. 2016, 82, 334¨C346. "
1335,CC1=CC(C(CC(CCCC)CC)(CC(CCCC)CC)C2=C3SC(C4=CC=C(C)C5=NSN=C45)=C2)=C3S1,PCPDTBT,5.3,3.55,0.61,15.73,0.53,5.12,"Lee, J. K.; Ma, W. L.; Brabec, C. J.; Yuen, J.; Moon, J. S.; Kim, J. Y.; Lee, K.; Bazan, G. C.; Heeger, A. J. Processing Additives for Improved Efficiency from Bulk Heterojunction Solar Cells. J. Am. Chem. Soc. 2008, 130, 3619¨C3623. "
1336,O=C1N(CC(CC)CCCC)C(C2=CC=C(C)S2)=C3C1=C(C4=CC=C(C5=CC(C(CCCCCCCC)(CCCCCCCC)C6=C7SC(C)=C6)=C7S5)S4)N(CC(CCCC)CC)C3=O,PCTDPP,4.95,3.31,0.47,10.87,0.45,2.27,"Chen, G. Y.; Chiang, C. ¨CM.; Kekuda, D.; Lan, S. C.; Chu, C. -W.; Wei, K. ¨CH. Synthesis and Characterization of a Narrow-Bandgap Polymer Containing Alternating Cyclopentadithiophene and Diketo-Pyrrolo-Pyrrole Units for Solar Cell Applications. J. Polym. Sci. Part A Polym. Chem. 2010, 48, 1669¨C1675. "
1337,CC1=CC(C(OCC(CC)CCCC)=C(SC(C2=C(CCCCCCCC)C=C(C3=C(F)C(F)=C(C4=CC(CCCCCCCC)=C(C)S4)C5=C3N=C(C6=CC=CC7=CC=CC8=C67)C8=N5)S2)=C9)C9=C%10OCC(CC)CCCC)=C%10S1,MBDT1,5.54,3.78,0.77,10.75,0.57,4.72,"Fang, T.; Lu, Z.; Lu, H.; Li, C.; Li, G.; Kang, C.; Bo, Z. The Enhanced Photovoltaic Performance of Fluorinated Acenaphtho[1,2-b]Quinoxaline Based Low Band Gap Polymer. Polymer 2015, 71, 43¨C50. "
1338,CC1=CC(C(OCC(CC)CCCC)=C(SC(C2=C(CCCCCCCC)C=C(C3=C(OCCCCCCCC)C(OCCCCCCCC)=C(C4=CC(CCCCCCCC)=C(C)S4)C5=C3N=C(C6=CC=CC7=CC=CC8=C67)C8=N5)S2)=C9)C9=C%10OCC(CC)CCCC)=C%10S1,MBDT2,5.43,3.53,0.75,4.41,0.5,1.65,"Fang, T.; Lu, Z.; Lu, H.; Li, C.; Li, G.; Kang, C.; Bo, Z. The Enhanced Photovoltaic Performance of Fluorinated Acenaphtho[1,2-b]Quinoxaline Based Low Band Gap Polymer. Polymer 2015, 71, 43¨C50. "
1339,CC1=CC=C(C2=CC=C(C3=C4C(C(N(C(CCCCCCCC)CCCCCCCC)C4=O)=O)=C(C)S3)S2)S1,PBTTPD,5.51,3.36,0.9,10.38,0.64,5.98,"Jung, J. W.; Russell, T. P.; Jo, W. H. Highly Crystalline Low Band Gap Polymer Based on Thieno[3,4-c]pyrrole-4,6-Dione for High-Performance Polymer Solar Cells with a >400 nm Thick Active Layer. ACS Appl. Mater. Interfaces 2015, 7, 13666¨C13674. "
1340,CC1=CC=C(/C=C/C2=CC=C(C3=C4C(C(N(C(CCCCCCCC)CCCCCCCC)C4=O)=O)=C(C)S3)S2)S1,PTVTPD,5.48,3.32,0.88,12.32,0.66,7.16,"Jung, J. W.; Russell, T. P.; Jo, W. H. Highly Crystalline Low Band Gap Polymer Based on Thieno[3,4-c]pyrrole-4,6-Dione for High-Performance Polymer Solar Cells with a >400 nm Thick Active Layer. ACS Appl. Mater. Interfaces 2015, 7, 13666¨C13674. "
1341,CC1=CC(CCCCCCCC)=C(C2=NC3=CC4=C(N=C(C5=C(CCCCCCCC)C=C(C6=CC=C(C(C=CC(C)=C7)=C7N8C(CCCCCCCC)CCCCCCCC)C8=C6)S5)S4)C=C3S2)S1,PBBTz-Cz,5.7,3.2,0.74,4.21,0.3,0.95,"Tsuji, M.; Saeki, A.; Koizumi, Y.; Matsuyama, N.; Vijayakumar, C.; Seki, S. Benzobisthiazole as Weak Donor for Improved Photovoltaic Performance: Microwave Conductivity Technique Assisted Molecular Engineering. Adv. Funct. Mater. 2014, 24, 28¨C36. "
1342,CC1=CC2=C3C(SC(C(CCCCCCCCCCC)CCCCCCCCCCCC)=C3)=C4C(SC(C5=C(CC(CCCC)CC)C=C(C6=C(F)C(F)=C(C7=CC(CC(CC)CCCC)=C(C)S7)C8=NSN=C86)S5)=C4)=C2S1,BTT-DTFFBT,5.24,3.54,0.78,11.79,0.61,5.61,"Zhao, X.; Lv, H.; Yang, D.; Li, Z.; Chen, Z.; Yang, X. A Novel Crystallizable Low Band Gap Polymer for High-Efficiency Polymer Photovoltaic Cells. J. Polym. Sci. Part A Polym. Chem. 2016, 54, 44¨C48. "
1343,CC(S1)=CC(CCCCCCCCCCCC)=C1C2=NC3=CC4=C(N=C(C5=C(CCCCCCCCCCCC)C=C(C6=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C(C7=CC=C(C8=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C)S8)C9=NSN=C79)S6)S5)S4)C=C3S2,PBBTZBT,5.7,3.9,0.801,12.43,0.674,6.53,"Saeki, A.; Tsuji, M.; Yoshikawa, S.; Gopal, A.; Seki, S. Boosting Photovoltaic Performance of a Benzobisthiazole Based Copolymer: A Device Approach Using a Zinc Oxide Electron Transport Layer. J. Mater. Chem. A 2014, 2, 6075¨C6080. "
1344,CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5C2(CC(CC)CCCC)CC(CC)CCCC)S1,PCPDTBT,5.3,3.55,0.65,11.8,0.456,3.5,"Zhu, Z.; Waller, D.; Gaudiana, R.; Morana, M.; M¨¹hlbacher, D.; Scharber, M.; Brabec, C. Panchromatic Conjugated Polymers Containing Alternating Donor/Acceptor Units for Photovoltaic Applications. Macromolecules 2007, 40, 1981¨C1986. "
1345,CC1=CC2=C(C(SC(C3=CC(F)=C(C)C4=NSN=C34)=C5)=C5C2(CC(CCCC)CC)CC(CCCC)CC)S1,PCPDTFBT,5.15,3.71,0.76,15,0.51,5.81,"Zhang, Y.; Zou, J.; Cheuh, C. C.; Yip, H. L.; Jen, A. K. Y. Significant Improved Performance of Photovoltaic Cells Made from a Partially Fluorinated Cyclopentadithiophene/benzothiadiazole Conjugated Polymer. Macromolecules 2012, 45, 5427¨C5435."
1346,CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=CC=C(C)C8=NSN=C78)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)S1,a-PTPTBT-SA,5.36,3.52,0.85,11.2,0.672,6.41,"Chen, Y.-C.; Yu, C.-Y.; Fan, Y.-L.; Hung, L.-I.; Chen, C.-P.; Ting, C. Low-Bandgap Conjugated Polymer for High Efficient Photovoltaic Applications. Chem. Commun. 2010, 46, 6503¨C6505. "
1347,CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(CCCCCC)C4=O)=O)S3)=C6)=C6[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1,PBTIGe-C6,5.39,3.64,0.774,11.96,0.502,4.77,"Guo, X.; Zhou, N.; Lou, S. J.; Hennek, J. W.; Ponce Ortiz, R.; Butler, M. R.; Boudreault, P. L. T.; Strzalka, J.; Morin, P. O.; Leclerc, M.; L¨®pez Navarrete, J. T.; Ratner, M. A.; Chen, L. X.; Chang, R. P. H.; Facchetti, A.; Marks, T. J. Bithiopheneimide-Dithienosilole/dithienogermole Copolymers for Efficient Solar Cells: Information from Structure-Property-Device Performance Correlations and Comparison to thieno[3,4-c]Pyrrole-4,6-Dione Analogues. J. Am. Chem. Soc. 2012, 134, 18427¨C18439. "
1348,CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(CCCCCCCC)C4=O)=O)S3)=C6)=C6[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1,PBTIGe-C8,5.38,3.63,0.745,11.62,0.472,4.32,"Guo, X.; Zhou, N.; Lou, S. J.; Hennek, J. W.; Ponce Ortiz, R.; Butler, M. R.; Boudreault, P. L. T.; Strzalka, J.; Morin, P. O.; Leclerc, M.; L¨®pez Navarrete, J. T.; Ratner, M. A.; Chen, L. X.; Chang, R. P. H.; Facchetti, A.; Marks, T. J. Bithiopheneimide-Dithienosilole/dithienogermole Copolymers for Efficient Solar Cells: Information from Structure-Property-Device Performance Correlations and Comparison to thieno[3,4-c]Pyrrole-4,6-Dione Analogues. J. Am. Chem. Soc. 2012, 134, 18427¨C18439. "
1349,CC1=CC2=C(C(SC(C3=CC4=C(C(SC(C)=C5)=C5C(N(C[C@@H](CC)CCCC)C4=O)=O)S3)=C6)=C6[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1,PBTIGe-EH,5.38,3.62,0.769,9.97,0.467,3.62,"Guo, X.; Zhou, N.; Lou, S. J.; Hennek, J. W.; Ponce Ortiz, R.; Butler, M. R.; Boudreault, P. L. T.; Strzalka, J.; Morin, P. O.; Leclerc, M.; L¨®pez Navarrete, J. T.; Ratner, M. A.; Chen, L. X.; Chang, R. P. H.; Facchetti, A.; Marks, T. J. Bithiopheneimide-Dithienosilole/dithienogermole Copolymers for Efficient Solar Cells: Information from Structure-Property-Device Performance Correlations and Comparison to thieno[3,4-c]Pyrrole-4,6-Dione Analogues. J. Am. Chem. Soc. 2012, 134, 18427¨C18439. "
1350,CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1,PGeBTBT,4.78,3.31,0.57,18.6,0.43,4.5,"Fei, Z.; Kim, J. S.; Smith, J.; Domingo, E. B.; Anthopoulos, T. D.; Stingelin, N.; Watkins, S. E.; Kim, J.-S.; Heeney, M. A Low Band Gap Co-Polymer of Dithienogermole and 2,1,3-Benzothiadiazole by Suzuki Polycondensation and Its Application in Transistor and Photovoltaic Cells. J. Mater. Chem. 2011, 21, 16257¨C16263. "
1351,CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(OCCCCCCCCCCCC)=O)S4)=C(C)S3)S5)C5=C2OCCCCCCCC)S1,PTB1,4.9,3.2,0.56,15.6,0.63,5.6,"Liang, Y.; Wu, Y.; Feng, D.; Tsai, S.-T.; Son, H.-J.; Li, G.; Yu, L. Development of New Semiconducting Polymers for High Performance Solar Cells. J. Am. Chem. Soc.2008, 131, 56¨C57. "
1352,CC1=CC2=C(C(SC(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)=C5)=C5[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1,P-Ge,5.6,3.91,0.85,12.6,0.68,7.3,"Amb, C. M.; Chen, S.; Graham, K. R.; Subbiah, J.; Small, C. E.; So, F.; Reynolds, J. R. Dithienogermole as a Fused Electron Donor in Bulk Heterojunction Solar Cells. J. Am. Chem. Soc. 2011, 133, 10062¨C10065. "
1353,CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5[Ge]2(CCCCCCCC)CCCCCCCC)S1,PGe1-C8,5.21,3.85,0.53,7.8,0.36,1.5,"Gendron, D.; Morin, P.-O.; Berrouard, P.; Allard, N.; A?ch, B. R.; Garon, C. N.; Tao, Y.; Leclerc, M. Synthesis and Photovoltaic Properties of Poly(dithieno[3,2-b?:2¡ä,3¡ä-d]Germole Derivatives. Macromolecules 2011, 44, 7188¨C7193. "
1354,CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1,PGe1-EH,5.22,3.93,0.52,10.5,0.53,2.9,"Gendron, D.; Morin, P.-O.; Berrouard, P.; Allard, N.; A?ch, B. R.; Garon, C. N.; Tao, Y.; Leclerc, M. Synthesis and Photovoltaic Properties of Poly(dithieno[3,2-b?:2¡ä,3¡ä-d]Germole Derivatives. Macromolecules 2011, 44, 7188¨C7193. "
1355,CC1=CC2=C(C(SC(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)=C5)=C5[Ge]2(CC(CCCC)CC)C[C@H](CCCC)CC)S1,PGe2,5.66,3.93,0.8,9.7,0.53,4.1,"Gendron, D.; Morin, P.-O.; Berrouard, P.; Allard, N.; A?ch, B. R.; Garon, C. N.; Tao, Y.; Leclerc, M. Synthesis and Photovoltaic Properties of Poly(dithieno[3,2-b?:2¡ä,3¡ä-d]Germole Derivatives. Macromolecules 2011, 44, 7188¨C7193. "
1356,CC1=CC(C=C(OCC(CC)CCCC)C2=C3C(OCC(CC)CCCC)=CC4=C2SC(C5=C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C6=O)=O)C6=C(C)S5)=C4)=C3S1,PzNDTTPD,5.38,3.43,0.91,9.03,0.64,5.26,"Shi, S.; Jiang, P.; Yu, S.; Wang, L.; Wang, X.; Wang, M.; Wang, H.; Li, Y.; Li, X. Efficient Polymer Solar Cells Based on a Broad Bandgap D¨CA Copolymer of ¡°zigzag¡± Naphthodithiophene and thieno[3,4-c]pyrrole-4,6-Dione. J. Mater. Chem. A 2013, 1, 1540¨C1543. "
1357,CC1=CC(C=C(OCC(CC)CCCC)C2=C3C(OCC(CC)CCCC)=CC4=C2SC(C5=CC=C(C6=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C(C7=CC=C(C)S7)C8=NSN=C86)S5)=C4)=C3S1,PzNDTDTBT,5.15,3.43,0.6,8.88,0.605,3.22,"Shi, S.; Xie, X.; Jiang, P.; Chen, S.; Wang, L.; Wang, M.; Wang, H.; Li, X.; Yu, G.; Li, Y. Naphtho[1,2-b:5,6-b¡ä]dithiophene-Based Donor-Acceptor Copolymer Semiconductors for High-Mobility Field-Effect Transistors and Efficient Polymer Solar Cells. Macromolecules 2013, 46, 3358¨C3366. "
1358,CC1=CC(C=C(OCC(CC)CCCC)C2=C3C(OCC(CC)CCCC)=CC4=C2SC(C5=CC=C(C6=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C(C7=CC=C(C)S7)C8=NON=C86)S5)=C4)=C3S1,PzNDTDTBO,5.3,3.38,0.74,10.46,0.655,5.07,"Shi, S.; Xie, X.; Jiang, P.; Chen, S.; Wang, L.; Wang, M.; Wang, H.; Li, X.; Yu, G.; Li, Y. Naphtho[1,2-b:5,6-b¡ä]dithiophene-Based Donor-Acceptor Copolymer Semiconductors for High-Mobility Field-Effect Transistors and Efficient Polymer Solar Cells. Macromolecules 2013, 46, 3358¨C3366. "
1359,CC1=CC(C=C(OCC(CCCC)CC)C2=C3C(OCC(CCCC)CC)=CC4=C2SC(C5=C6C(C=C(C(C(CC)CCCC)=O)S6)=C(C)S5)=C4)=C3S1,P1,4.86,3.26,0.55,11.99,0.38,2.51,"Bathula, C.; Song, C. E.; Badgujar, S.; Hong, S.-J.; Park, S. Y.; Shin, W. S.; Lee, J.-C.; Cho, S.; Ahn, T.; Moon, S.-J.; Lee, S. K. Naphtho[1,2-b:5,6-b¡ä]dithiophene-Based Copolymers for Applications to Polymer Solar Cells. Polym. Chem. 2013, 4, 2132¨C2139. "
1360,CC1=CC(C=C(OCC(CCCC)CC)C2=C3C(OCC(CCCC)CC)=CC4=C2SC(C5=C6C(C(F)=C(C(C(CC)CCCC)=O)S6)=C(C)S5)=C4)=C3S1,P2,5.03,3.34,0.71,13.52,0.51,4.88,"Bathula, C.; Song, C. E.; Badgujar, S.; Hong, S.-J.; Park, S. Y.; Shin, W. S.; Lee, J.-C.; Cho, S.; Ahn, T.; Moon, S.-J.; Lee, S. K. Naphtho[1,2-b:5,6-b¡ä]dithiophene-Based Copolymers for Applications to Polymer Solar Cells. Polym. Chem. 2013, 4, 2132¨C2139. "
1361,CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=CC=C(C)C8=C7N=C(C9=CC=CC=C9)C(C%10=CC=CC=C%10)=N8)=C5)C6=C%11)=C%11C2(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)S1,PIDT-diphQ,5.33,3.52,0.87,10.9,0.6,5.69,"Zhang, Y.; Zou, J.; Yip, H.-L.; Chen, K.-S.; Zeigler, D. F.; Sun, Y.; Jen, A. K.-Y. Indacenodithiophene and Quinoxaline-Based Conjugated Polymers for Highly Efficient Polymer Solar Cells. Chem. Mater. 2011, 23, 2289¨C2291. "
1362,CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=CC=C(C)C8=C7N=C(C9=C%10C=CC=C9)C(C%11=CC=CC=C%11%10)=N8)=C5)C6=C%12)=C%12C2(C%13=CC=C(CCCCCC)C=C%13)C%14=CC=C(CCCCCC)C=C%14)S1,PIDT-phanQ,5.28,3.61,0.87,11.2,0.64,6.24,"Zhang, Y.; Zou, J.; Yip, H.-L.; Chen, K.-S.; Zeigler, D. F.; Sun, Y.; Jen, A. K.-Y. Indacenodithiophene and Quinoxaline-Based Conjugated Polymers for Highly Efficient Polymer Solar Cells. Chem. Mater. 2011, 23, 2289¨C2291. "
1363,CC1=CC2=C(C(C=C(C(CCCCCCCCCCCC)(CCCCCCCCCCCC)C3=C4SC(C5=CC=C(C6=C(CCCCCC)N=C(C7=NC(CCCCCC)=C(C8=CC=C(C)S8)S7)S6)S5)=C3)C4=C9)=C9C2(CCCCCCCCCCCC)CCCCCCCCCCCC)S1,PIDT-BTz,5.26,2.8,0.9,7.43,0.414,2.77,"Zhang, M.; Guo, X.; Wang, X.; Wang, H.; Li, Y. Synthesis and Photovoltaic Properties of D-A Copolymers Based on Alkyl-Substituted Indacenodithiophene Donor Unit. Chem. Mater. 2011, 23, 4264¨C4270. "
1364,CC1=CC2=C(C(C=C(C(CCCCCCCCCCCC)(CCCCCCCCCCCC)C3=C4SC(C5=CC=C(C6=NC(SC(C7=CC=C(C)S7)=N8)=C8S6)S5)=C3)C4=C9)=C9C2(CCCCCCCCCCCC)CCCCCCCCCCCC)S1,PIDT-TTz,5.21,2.94,0.89,13.3,0.489,5.79,"Zhang, M.; Guo, X.; Wang, X.; Wang, H.; Li, Y. Synthesis and Photovoltaic Properties of D-A Copolymers Based on Alkyl-Substituted Indacenodithiophene Donor Unit. Chem. Mater. 2011, 23, 4264¨C4270. "
1365,CC1=CC2=C(C(C=C(C(CCCCCCCCCCCC)(CCCCCCCCCCCC)C3=C4SC(C5=CC=C(C6=NN=C(C7=CC=C(C)S7)N=N6)S5)=C3)C4=C8)=C8C2(CCCCCCCCCCCC)CCCCCCCCCCCC)S1,PIDT-TZ,5.22,2.97,0.9,8.85,0.381,3.04,"Zhang, M.; Guo, X.; Wang, X.; Wang, H.; Li, Y. Synthesis and Photovoltaic Properties of D-A Copolymers Based on Alkyl-Substituted Indacenodithiophene Donor Unit. Chem. Mater. 2011, 23, 4264¨C4270. "
1366,CC1=CC2=C(C(C=C(C(CCCCCCCCCCCC)(CCCCCCCCCCCC)C3=C4SC(C5=CC=C(C6=CC=C(C7=CC=C(C)S7)C8=NSN=C86)S5)=C3)C4=C9)=C9C2(CCCCCCCCCCCC)CCCCCCCCCCCC)S1,PIDT-DTBT,5.24,3.1,0.82,13.27,0.567,6.17,"Zhang, M.; Guo, X.; Wang, X.; Wang, H.; Li, Y. Synthesis and Photovoltaic Properties of D-A Copolymers Based on Alkyl-Substituted Indacenodithiophene Donor Unit. Chem. Mater. 2011, 23, 4264¨C4270. "
1367,CC1=CC2=C(C(C=C(C(C3=CC=C(OCCCCCCCC)C=C3)(C4=CC=C(OCCCCCCCC)C=C4)C5=C6[Se]C(C7=CC=C(C)C8=NSN=C78)=C5)C6=C9)=C9C2(C%10=CC=C(OCCCCCCCC)C=C%10)C%11=CC=C(OCCCCCCCC)C=C%11)[Se]1,PIDSBT-OCH8,5.28,3.45,0.76,8.45,0.41,2.6,"Chang, H. H.; Tsai, C. E.; Lai, Y. Y.; Liang, W. W.; Hsu, S. L.; Hsu, C. S.; Cheng, Y. J. A New Pentacyclic Indacenodiselenophene Arene and Its Donor-Acceptor Copolymers for Solution-Processable Polymer Solar Cells and Transistors: Synthesis, Characterization, and Investigation of Alkyl/alkoxy Side-Chain Effect. Macromolecules 2013, 46, 7715¨C7726. "
1368,CC1=CC2=C(C(C=C(C(C3=CC=C(OCCCCCCCC)C=C3)(C4=CC=C(OCCCCCCCC)C=C4)C5=C6[Se]C(C7=C(F)C(F)=C(C)C8=NSN=C78)=C5)C6=C9)=C9C2(C%10=CC=C(OCCCCCCCC)C=C%10)C%11=CC=C(OCCCCCCCC)C=C%11)[Se]1,PIDSFBT-OCH8,5.32,3.57,0.86,6.72,0.32,1.9,"Chang, H. H.; Tsai, C. E.; Lai, Y. Y.; Liang, W. W.; Hsu, S. L.; Hsu, C. S.; Cheng, Y. J. A New Pentacyclic Indacenodiselenophene Arene and Its Donor-Acceptor Copolymers for Solution-Processable Polymer Solar Cells and Transistors: Synthesis, Characterization, and Investigation of Alkyl/alkoxy Side-Chain Effect. Macromolecules 2013, 46, 7715¨C7726. "
1369,CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6[Se]C(C7=CC=C(C)C8=NSN=C78)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)[Se]1,PIDSBT-C6,5.28,3.51,0.76,11.24,0.45,3.9,"Chang, H. H.; Tsai, C. E.; Lai, Y. Y.; Liang, W. W.; Hsu, S. L.; Hsu, C. S.; Cheng, Y. J. A New Pentacyclic Indacenodiselenophene Arene and Its Donor-Acceptor Copolymers for Solution-Processable Polymer Solar Cells and Transistors: Synthesis, Characterization, and Investigation of Alkyl/alkoxy Side-Chain Effect. Macromolecules 2013, 46, 7715¨C7726. "
1370,CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6[Se]C(C7=C(F)C(F)=C(C)C8=NSN=C78)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)[Se]1,PIDSFBT-C6,5.38,3.61,0.84,9.67,0.47,3.8,"Chang, H. H.; Tsai, C. E.; Lai, Y. Y.; Liang, W. W.; Hsu, S. L.; Hsu, C. S.; Cheng, Y. J. A New Pentacyclic Indacenodiselenophene Arene and Its Donor-Acceptor Copolymers for Solution-Processable Polymer Solar Cells and Transistors: Synthesis, Characterization, and Investigation of Alkyl/alkoxy Side-Chain Effect. Macromolecules 2013, 46, 7715¨C7726. "
1371,CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=C(F)C(F)=C(C)C8=NSN=C87)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)S1,PIDT-DFBT,5.35,3.4,0.97,11.2,0.554,6.02,"Intemann, J. J.; Yao, K.; Yip, H. L.; Xu, Y. X.; Li, Y. X.; Liang, P. W.; Ding, F. Z.; Li, X.; Jen, A. K. Y. Molecular Weight Effect on the Absorption, Charge Carrier Mobility, and Photovoltaic Performance of an Indacenodiselenophene-Based Ladder-Type Polymer. Chem. Mater. 2013, 25, 3188¨C3195."
1372,CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6[Se]C(C7=C(F)C(F)=C(C)C8=NSN=C87)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)[Se]1,PIDSe-DFBTL,5.34,3.48,0.9,12.1,0.503,5.48,"Intemann, J. J.; Yao, K.; Yip, H. L.; Xu, Y. X.; Li, Y. X.; Liang, P. W.; Ding, F. Z.; Li, X.; Jen, A. K. Y. Molecular Weight Effect on the Absorption, Charge Carrier Mobility, and Photovoltaic Performance of an Indacenodiselenophene-Based Ladder-Type Polymer. Chem. Mater. 2013, 25, 3188¨C3195."
1373,CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6[Se]C(C7=C(F)C(F)=C(C)C8=NSN=C87)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)[Se]1,PIDSe-DFBTM,5.34,3.47,0.89,12.9,0.532,6.11,"Intemann, J. J.; Yao, K.; Yip, H. L.; Xu, Y. X.; Li, Y. X.; Liang, P. W.; Ding, F. Z.; Li, X.; Jen, A. K. Y. Molecular Weight Effect on the Absorption, Charge Carrier Mobility, and Photovoltaic Performance of an Indacenodiselenophene-Based Ladder-Type Polymer. Chem. Mater. 2013, 25, 3188¨C3195."
1374,CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6[Se]C(C7=C(F)C(F)=C(C)C8=NSN=C87)=C5)C6=C9)=C9C2(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)[Se]1,PIDSe-DFBTH,5.33,3.48,0.89,13.7,0.563,6.79,"Intemann, J. J.; Yao, K.; Yip, H. L.; Xu, Y. X.; Li, Y. X.; Liang, P. W.; Ding, F. Z.; Li, X.; Jen, A. K. Y. Molecular Weight Effect on the Absorption, Charge Carrier Mobility, and Photovoltaic Performance of an Indacenodiselenophene-Based Ladder-Type Polymer. Chem. Mater. 2013, 25, 3188¨C3195."
1375,CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(SC(C(C(CC)CCCC)=O)=C4)=C(C)S3)S5)C5=C2OCC(CC)CCCC)S1,PBDTTT-C,5.12,3.55,0.7,14.7,0.64,6.58,"Hou, J.; Chen, H.-Y. H.-Y.; Zhang, S.; Chen, R. I.; Yang, Y.; Wu, Y.; Li, G. Synthesis of a Low Band Gap Polymer and Its Application in Highly Efficient Polymer Solar Cells. J. Am. Chem. Soc. 2009, 131, 15586¨C15587. "
1376,CC1=CC=C(C2=CC3=C(C(SC4=C5C(CCCCCCCC)(CCCCCCCC)C6=C4C=CC(C)=C6)=C5C3(CCCCCCCC)CCCCCCCC)C=C2)C7=NSN=C17,PDIDTBT,5.51,3.07,0.7,3.3,0.33,0.76,"Chen, C. H.; Cheng, Y. J.; Dubosc, M.; Hsieh, C. H.; Chu, C. C.; Hsu, C. S. Alternating and Diblock Donor-Acceptor Conjugated Polymers Based on diindeno[1,2-b:2¡ä,1¡ä-D]thiophene Structure: Synthesis, Characterization, and Photovoltaic Applications. Chem. -Asian J. 2010, 5, 2483¨C2492. "
1377,CC1=CC(C2(CCCCCCCC)CCCCCCCC)=C(C=C1)C3=C2C(C4(CCCCCCCC)CCCCCCCC)=C(S3)C5=C4C=C(C=C5)C6=CC=C(C)S6,PTDIDT,5.36,3.23,0.7,5.3,0.44,1.65,"Chen, C. H.; Cheng, Y. J.; Dubosc, M.; Hsieh, C. H.; Chu, C. C.; Hsu, C. S. Alternating and Diblock Donor-Acceptor Conjugated Polymers Based on diindeno[1,2-b:2¡ä,1¡ä-D]thiophene Structure: Synthesis, Characterization, and Photovoltaic Applications. Chem. -Asian J. 2010, 5, 2483¨C2492. "
1378,CC1=CC(C2(CCCCCCCC)CCCCCCCC)=C(C=C1)C3=C2C(C4(CCCCCCCC)CCCCCCCC)=C(S3)C5=C4C=C(C=C5)C6=CC=C(C7=CC=C(C8=CC=C(C)S8)C9=NSN=C79)S6,PDIDTDTBT,5.35,3.32,0.68,6.2,0.47,2,"Chen, C. H.; Cheng, Y. J.; Dubosc, M.; Hsieh, C. H.; Chu, C. C.; Hsu, C. S. Alternating and Diblock Donor-Acceptor Conjugated Polymers Based on diindeno[1,2-b:2¡ä,1¡ä-D]thiophene Structure: Synthesis, Characterization, and Photovoltaic Applications. Chem. -Asian J. 2010, 5, 2483¨C2492. "
1379,CC1=CC(N2C(CCCCCCCC)CCCCCCCC)=C(S1)C(C2=C3)=CC4=C3C5=C(N4C(CCCCCCCC)CCCCCCCC)C=C(C6=CC=C(C)C7=NSN=C76)S5,PBDPTBT,5.11,3.25,0.6,10.34,0.497,3.08,"Tseng, C. A.; Wu, J. S.; Lin, T. Y.; Kao, W. S.; Wu, C. E.; Hsu, S. L.; Liao, Y. Y.; Hsu, C. S.; Huang, H. Y.; Hsieh, Y. Z.; Cheng, Y. J. A Pentacyclic Nitrogen-Bridged Thienyl-Phenylene-Thienyl Arene for Donor-Acceptor Copolymers: Synthesis, Characterization, and Applications in Field-Effect Transistors and Polymer Solar Cells. Chem. -Asian J. 2012, 7, 2102¨C2110. "
1380,CC1=CC(N2C(CCCCCCCC)CCCCCCCC)=C(S1)C(C2=C3)=CC4=C3C5=C(N4C(CCCCCCCC)CCCCCCCC)C=C(C6=C(C(N(CC(CC)CCCC)C7=O)=O)C7=C(C)S6)S5,PBDPTFPP,4.89,3.41,0.75,9.69,0.512,3.72,"Tseng, C. A.; Wu, J. S.; Lin, T. Y.; Kao, W. S.; Wu, C. E.; Hsu, S. L.; Liao, Y. Y.; Hsu, C. S.; Huang, H. Y.; Hsieh, Y. Z.; Cheng, Y. J. A Pentacyclic Nitrogen-Bridged Thienyl-Phenylene-Thienyl Arene for Donor-Acceptor Copolymers: Synthesis, Characterization, and Applications in Field-Effect Transistors and Polymer Solar Cells. Chem. -Asian J. 2012, 7, 2102¨C2110. "
1381,CC1=CC(N2C(CCCCCCCC)CCCCCCCC)=C(S1)C(C2=C3)=CC4=C3C5=C(N4C(CCCCCCCC)CCCCCCCC)C=C(C6=CC=C(C7=C8C(C(N7CC(CC)CCCC)=O)=C(C9=CC=C(C)S9)N(CC(CC)CCCC)C8=O)S6)S5,PBDPTTPD,5.14,3.13,0.56,4.95,0.485,1.34,"Tseng, C. A.; Wu, J. S.; Lin, T. Y.; Kao, W. S.; Wu, C. E.; Hsu, S. L.; Liao, Y. Y.; Hsu, C. S.; Huang, H. Y.; Hsieh, Y. Z.; Cheng, Y. J. A Pentacyclic Nitrogen-Bridged Thienyl-Phenylene-Thienyl Arene for Donor-Acceptor Copolymers: Synthesis, Characterization, and Applications in Field-Effect Transistors and Polymer Solar Cells. Chem. -Asian J. 2012, 7, 2102¨C2110. "
1382,FC1=C(COOCC(CCCC)CC)SC2=C(C)SC(C3=CC(C4=C5SC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C4)=C(S3)C6=C5C=C(C7=C(C8=C9SC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C8)C=C(C)S7)C9=C6)=C21,PTAT-2,5.12,3.32,0.77,1,0.46,0.37,"He, F.; Wang, W.; Chen, W.; Xu, T.; Darling, S. B.; Strzalka, J.; Liu, Y.; Yu, L. Tetrathienoanthracene-Based Copolymers for Efficient Solar Cells. J. Am. Chem. Soc.2011, 133, 3284¨C3287. "
1383,FC1=C(COOCC(CCCC)CC)SC2=C(C)SC(C3=CC(C4=C5SC(CC(CCCC)CCCCCC)=C4)=C(S3)C6=C5C=C(C7=C(C8=C9SC(CC(CCCC)CCCCCC)=C8)C=C(C)S7)C9=C6)=C21,PTAT-3,5.04,3.28,0.66,15,0.58,5.62,"He, F.; Wang, W.; Chen, W.; Xu, T.; Darling, S. B.; Strzalka, J.; Liu, Y.; Yu, L. Tetrathienoanthracene-Based Copolymers for Efficient Solar Cells. J. Am. Chem. Soc.2011, 133, 3284¨C3287. "
1384,FC1=C(COOCC(CCCC)CC)SC2=C(C)SC(C3=CC(C4=C5SC(CC(CC)CCCCCCCC)=C4)=C(S3)C6=C5C=C(C7=C(C8=C9SC(CC(CC)CCCCCCCC)=C8)C=C(C)S7)C9=C6)=C21,PTAT-4,5.08,3.31,0.62,9.6,0.5,2.98,"He, F.; Wang, W.; Chen, W.; Xu, T.; Darling, S. B.; Strzalka, J.; Liu, Y.; Yu, L. Tetrathienoanthracene-Based Copolymers for Efficient Solar Cells. J. Am. Chem. Soc.2011, 133, 3284¨C3287. "
1385,CC1=CC2=C(OCC(CCCC)CCCCCC)C(SC(C3=C(C(F)=C(COOCC(CC)CCCC)S4)C4=C(C)S3)=C5)=C5C(OCC(CCCCCC)CCCC)=C2S1,PTB-8,5.24,3.34,0.83,5.7,0.59,2.78,"He, F.; Wang, W.; Chen, W.; Xu, T.; Darling, S. B.; Strzalka, J.; Liu, Y.; Yu, L. Tetrathienoanthracene-Based Copolymers for Efficient Solar Cells. J. Am. Chem. Soc.2011, 133, 3284¨C3287. "
1386,CC1=CC(SC2=C3[Ge](CC(CC)CCCC)(CC(CCCC)CC)C4=C2SC5=C4SC(C6=C(C(N(CCCCCCCC)C7=O)=O)C7=C(C)S6)=C5)=C3S1,pDTTG-TPD,5.68,3.88,0.81,13.85,0.64,7.2,"Zhong, H.; Li, Z.; Deledalle, F.; Fregoso, E. C.; Shahid, M.; Fei, Z.; Nielsen, C. B.; Yaacobi-Gross, N.; Rossbauer, S.; Anthopoulos, T. D.; Durrant, J. R.; Heeney, M. Fused Dithienogermolodithiophene Low Band Gap Polymers for High-Performance Organic Solar Cells without Processing Additives. J. Am. Chem. Soc. 2013, 135, 2040¨C2043. "
1387,CC1=CC2=C(C(C3=NSN=C3C4=C5N(CCCCCCCCCCCC)C6=C4SC(C7=CC8=C(C(C=CC(C)=C9)=C9C8(CCCCCCCC)CCCCCCCC)C=C7)=C6)=C5N2CCCCCCCCCCCC)S1,PFDTPBT,5.11,2.64,0.74,8.37,0.5,3.11,"Cheng, Y. J.; Ho, Y. J.; Chen, C. H.; Kao, W. S.; Wu, C. E.; Hsu, S. L.; Hsu, C. S. Synthesis, Photophysical and Photovoltaic Properties of Conjugated Polymers Containing Fused Donor-Acceptor Dithienopyrrolobenzothiadiazole and Dithienopyrroloquinoxaline Arenes. Macromolecules 2012, 45, 2690¨C2698. "
1388,CC1=CC2=C(C(C3=NSN=C3C4=C5N(CCCCCCCCCCCC)C6=C4SC(C7=CC8=C(C(C=CC(C)=C9)=C9N8C(CCCCCCCC)CCCCCCCC)C=C7)=C6)=C5N2CCCCCCCCCCCC)S1,PCDTPBT,5.06,2.67,0.72,7.47,0.47,2.54,"Cheng, Y. J.; Ho, Y. J.; Chen, C. H.; Kao, W. S.; Wu, C. E.; Hsu, S. L.; Hsu, C. S. Synthesis, Photophysical and Photovoltaic Properties of Conjugated Polymers Containing Fused Donor-Acceptor Dithienopyrrolobenzothiadiazole and Dithienopyrroloquinoxaline Arenes. Macromolecules 2012, 45, 2690¨C2698. "
1389,CC1=CC2=C(C(C3=NSN=C3C4=C5N(CCCCCCCCCCCC)C6=C4SC(C7=CC(C(CC(CC)CCCC)(CC(CCCC)CC)C8=C9SC(C)=C8)=C9S7)=C6)=C5N2CCCCCCCCCCCC)S1,PCPDTDTPBT,4.9,2.82,0.48,6.23,0.45,1.35,"Cheng, Y. J.; Ho, Y. J.; Chen, C. H.; Kao, W. S.; Wu, C. E.; Hsu, S. L.; Hsu, C. S. Synthesis, Photophysical and Photovoltaic Properties of Conjugated Polymers Containing Fused Donor-Acceptor Dithienopyrrolobenzothiadiazole and Dithienopyrroloquinoxaline Arenes. Macromolecules 2012, 45, 2690¨C2698. "
1390,CC1=CC2=C(C(C(N=C(C3=CC=CC=C3)C(C4=CC=CC=C4)=N5)=C5C6=C7N(CCCCCCCCCCCC)C8=C6SC(C9=CC%10=C(C(C=CC(C)=C%11)=C%11C%10(CCCCCCCC)CCCCCCCC)C=C9)=C8)=C7N2CCCCCCCCCCCC)S1,PFDTPQX,5.06,2.61,0.72,8.62,0.55,3.4,"Cheng, Y. J.; Ho, Y. J.; Chen, C. H.; Kao, W. S.; Wu, C. E.; Hsu, S. L.; Hsu, C. S. Synthesis, Photophysical and Photovoltaic Properties of Conjugated Polymers Containing Fused Donor-Acceptor Dithienopyrrolobenzothiadiazole and Dithienopyrroloquinoxaline Arenes. Macromolecules 2012, 45, 2690¨C2698. "
1391,CC1=CC2=C(C(C(N=C(C3=CC=CC=C3)C(C4=CC=CC=C4)=N5)=C5C6=C7N(CCCCCCCCCCCC)C8=C6SC(C9=CC%10=C(C(C=CC(C)=C%11)=C%11N%10C(CCCCCCCC)CCCCCCCC)C=C9)=C8)=C7N2CCCCCCCCCCCC)S1,PCDTPQX,5.02,2.64,0.7,8.27,0.51,2.95,"Cheng, Y. J.; Ho, Y. J.; Chen, C. H.; Kao, W. S.; Wu, C. E.; Hsu, S. L.; Hsu, C. S. Synthesis, Photophysical and Photovoltaic Properties of Conjugated Polymers Containing Fused Donor-Acceptor Dithienopyrrolobenzothiadiazole and Dithienopyrroloquinoxaline Arenes. Macromolecules 2012, 45, 2690¨C2698. "
1392,CC1=CC2=C(C(C(N=C(C3=CC=CC=C3)C(C4=CC=CC=C4)=N5)=C5C6=C7N(CCCCCCCCCCCC)C8=C6SC(C9=CC(C(CC(CC)CCCC)(CC(CCCC)CC)C%10=C%11SC(C)=C%10)=C%11S9)=C8)=C7N2CCCCCCCCCCCC)S1,PCPDTDTPQX,4.88,2.71,0.5,5.64,0.49,1.38,"Cheng, Y. J.; Ho, Y. J.; Chen, C. H.; Kao, W. S.; Wu, C. E.; Hsu, S. L.; Hsu, C. S. Synthesis, Photophysical and Photovoltaic Properties of Conjugated Polymers Containing Fused Donor-Acceptor Dithienopyrrolobenzothiadiazole and Dithienopyrroloquinoxaline Arenes. Macromolecules 2012, 45, 2690¨C2698. "
1393,CC1=CC2=C(C3=CC(C(N(CC(CCCCCCCC)CCCCCC)C4=C5SC(C6=CC=C(C)S6)=C4)=O)=C5C=C3C(N2CC(CCCCCC)CCCCCCCC)=O)S1,PThTPTI,5.42,2.77,0.87,13.69,0.656,7.8,"Cao, J.; Liao, Q.; Du, X.; Chen, J.; Xiao, Z.; Zuo, Q.; Ding, L. A Pentacyclic Aromatic Lactam Building Block for Efficient Polymer Solar Cells. Energy Environ. Sci. 2013, 6, 3224¨C3228. "
1394,CC1=CC2=C(C3=CC(C(N(CC(CCCCCCCC)CCCCCC)C4=C5SC(C6=CC=C(C)[Se]6)=C4)=O)=C5C=C3C(N2CC(CCCCCC)CCCCCCCC)=O)S1,PSeTPTI,5.41,2.88,0.85,11.1,0.64,6.04,"Cao, J. M.; Chen, S.; Qi, Z.; Xiao, Z.; Wang, J. Z.; Ding, L. M. An Efficient Selenophene-Containing Conjugated Copolymer for Organic Solar Cells. RSC Adv. 2014, 4, 5085¨C5087. "
1395,CC(S1)=C2C(C(N(CCCCCCCC)C2=O)=O)=C1C3=CC(C(C4=CC=C(OCCCCCCCC)C=C4)(C5=CC=C(OCCCCCCCC)C=C5)C6=C7SC8=C6SC9=C8C(C%10=CC=C(OCCCCCCCC)C=C%10)(C%11=CC=C(OCCCCCCCC)C=C%11)C%12=C9SC(C)=C%12)=C7S3,PDTCTTTPD,5.3,3.13,0.72,8.35,0.43,2.59,"Cheng, Y. J.; Chen, C. H.; Lin, T. Y.; Hsu, C. S. Dithienocyclopentathieno[3,2-b]thiophene Hexacyclic Arene for Solution-Processed Organic Field-Effect Transistors and Photovoltaic Applications. Chem. -Asian J. 2012, 7, 818¨C825. "
1396,CC1=CC(C2(C3=CC=C(OCCCCCCCC)C=C3)C4=CC=C(OCCCCCCCC)C=C4)=C(S1)C5=C2C(S6)=C(S5)C7=C6C8=C(C7(C9=CC=C(OCCCCCCCC)C=C9)C%10=CC=C(OCCCCCCCC)C=C%10)C=C(C%11=CC=C(C)C%12=NSN=C%11%12)S8,PDTCTTBT,5.08,3.38,0.64,8.03,0.5,2.57,"Cheng, Y. J.; Chen, C. H.; Lin, T. Y.; Hsu, C. S. Dithienocyclopentathieno[3,2-b]thiophene Hexacyclic Arene for Solution-Processed Organic Field-Effect Transistors and Photovoltaic Applications. Chem. -Asian J. 2012, 7, 818¨C825. "
1397,CC1=CC(C2(C3=CC=C(OCCCCCCCC)C=C3)C4=CC=C(OCCCCCCCC)C=C4)=C(S1)C5=C2C(S6)=C(S5)C7=C6C8=C(C7(C9=CC=C(OCCCCCCCC)C=C9)C%10=CC=C(OCCCCCCCC)C=C%10)C=C(C%11=C(N=C(C(C=CC=C%12)=C%12C%13=C%14C=CC=C%13)C%14=N%15)C%15=C(C)C=C%11)S8,PDTCTTPQX,5.04,3.46,0.62,7.33,0.42,1.91,"Cheng, Y. J.; Chen, C. H.; Lin, T. Y.; Hsu, C. S. Dithienocyclopentathieno[3,2-b]thiophene Hexacyclic Arene for Solution-Processed Organic Field-Effect Transistors and Photovoltaic Applications. Chem. -Asian J. 2012, 7, 818¨C825. "
1398,CC(S1)=CC2=C1C3=C(C(OCC(CCCCCC)CCCCCCCC)=C(C4=C(C=C(C5=C6C(SC(C(CC(CC)CCCC)=O)=C6)=C(C)S5)S4)S7)C7=C3OCC(CCCCCCCC)CCCCCC)S2,PDTT,5.15,2.95,0.68,9.85,0.54,3.64,"Wu, Y.; Li, Z.; Guo, X.; Fan, H.; Huo, L.; Hou, J. Synthesis and Application of dithieno[2,3-d:2¡ä,3¡ä-d¡ä]benzo[1,2-b:4,5-b¡ä]dithiophene in Conjugated Polymer. J. Mater. Chem. 2012, 22, 21362¨C21365. "
1399,CC1=CC(C2(C3=CC=C(CCCCCC)C=C3)C4=CC=C(CCCCCC)C=C4)=C(S1)C5=C2C(S6)=C(S5)C7=C6C8=C(C7(C9=CC=C(CCCCCC)C=C9)C%10=CC=C(CCCCCC)C=C%10)C=C(C%11=CC=C(C)C%12=NSN=C%11%12)S8,P4TBT,5.2,3.7,0.59,9.1,0.49,2.5,"Bronstein, H.; Ashraf, R. S.; Kim, Y.; White, A. J. P.; Anthopoulos, T.; Song, K.; James, D.; Zhang, W.; McCulloch, I. Synthesis of a Novel Fused Thiophene-thieno[3,2-b]thiophene-Thiophene Donor Monomer and Co-Polymer for Use in OPV and OFETs. Macromol. Rapid Commun. 2011, 32, 1664¨C1668. "
1400,CC1=CC(C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C2=C3SC4=C2SC5=C4C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C6=C5SC(C7=CC=C(C)C8=NSN=C87)=C6)=C3S1,DTBTBT-Bz,5.2,3.4,0.92,6.78,0.6,3.7,"Biniek, L.; Schroeder, B. C.; Donaghey, J. E.; Yaacobi-Gross, N.; Ashraf, R. S.; Soon, Y. W.; Nielsen, C. B.; Durrant, J. R.; Anthopoulos, T. D.; McCulloch, I. New Fused BisThienobenzothienothiophene Copolymers and Their Use in Organic Solar Cells and Transistors. Macromolecules 2013, 46, 727¨C735. "
1401,CC1=CC(C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C2=C3SC4=C2SC5=C4C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C6=C5SC(C7=CC=C(C)S7)=C6)=C3S1,DTBTBT-T,4.9,2.7,0.7,8.1,0.59,3.3,"Biniek, L.; Schroeder, B. C.; Donaghey, J. E.; Yaacobi-Gross, N.; Ashraf, R. S.; Soon, Y. W.; Nielsen, C. B.; Durrant, J. R.; Anthopoulos, T. D.; McCulloch, I. New Fused BisThienobenzothienothiophene Copolymers and Their Use in Organic Solar Cells and Transistors. Macromolecules 2013, 46, 727¨C735. "
1402,CC1=CC(C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C2=C3SC4=C2SC5=C4C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C6=C5SC(C7=CC(SC(C)=C8)=C8S7)=C6)=C3S1,DTBTBT-TT,4.9,4.9,0.66,6.41,0.56,2.3,"Biniek, L.; Schroeder, B. C.; Donaghey, J. E.; Yaacobi-Gross, N.; Ashraf, R. S.; Soon, Y. W.; Nielsen, C. B.; Durrant, J. R.; Anthopoulos, T. D.; McCulloch, I. New Fused BisThienobenzothienothiophene Copolymers and Their Use in Organic Solar Cells and Transistors. Macromolecules 2013, 46, 727¨C735. "
1403,CC1=CC(C(CCCCCCCCCCCC)=C(CCCCCCCCCCCC)C2=C3C=C4C(C(SC(C5=CC=C(C)C6=NSN=C65)=C7)=C7C(CCCCCCCCCCCC)=C4CCCCCCCCCCCC)=C2)=C3S1,DTAT-Bz,5.3,3.5,0.94,4.55,0.64,2.7,"Biniek, L.; Schroeder, B. C.; Donaghey, J. E.; Yaacobi-Gross, N.; Ashraf, R. S.; Soon, Y. W.; Nielsen, C. B.; Durrant, J. R.; Anthopoulos, T. D.; McCulloch, I. New Fused BisThienobenzothienothiophene Copolymers and Their Use in Organic Solar Cells and Transistors. Macromolecules 2013, 46, 727¨C735. "
1404,CC1=CC=C2C(C(C3=CC=C(OCCCCCCCC)C=C3)(C4=CC=C(OCCCCCCCC)C=C4)C5=C2SC6=C5SC7=C6C(C8=CC=C(OCCCCCCCC)C=C8)(C9=CC=C(OCCCCCCCC)C=C9)C%10=C7C=CC(C%11=CC=C(C)C%12=NSN=C%11%12)=C%10)=C1,PDITTBT,5.52,3.23,0.88,7.46,0.414,2.7,"Cheng, Y.-J.; Cheng, S.-W.; Chang, C.-Y.; Kao, W.-S.; Liao, M.-H.; Hsu, C.-S. Diindenothieno[2,3-b]thiophene Arene for Efficient Organic Photovoltaics with an Extra High Open-Circuit Voltage of 1.14 eV. Chem. Commun. 2012, 48, 3203¨C3205."
1405,CC1=CC=C2C(C(C3=CC=C(OCCCCCCCC)C=C3)(C4=CC=C(OCCCCCCCC)C=C4)C5=C2SC6=C5SC7=C6C(C8=CC=C(OCCCCCCCC)C=C8)(C9=CC=C(OCCCCCCCC)C=C9)C%10=C7C=CC(C%11=CC=C(C%12=CC=C(C%13=CC=C(C)S%13)C%14=NSN=C%12%14)S%11)=C%10)=C1,PDITTDTBT,5.4,3.36,0.92,10.71,0.584,5.8,"Cheng, Y.-J.; Cheng, S.-W.; Chang, C.-Y.; Kao, W.-S.; Liao, M.-H.; Hsu, C.-S. Diindenothieno[2,3-b]thiophene Arene for Efficient Organic Photovoltaics with an Extra High Open-Circuit Voltage of 1.14 eV. Chem. Commun. 2012, 48, 3203¨C3205."
1406,CC1=CC2=C(C(C=C(C(CCCCCCCC)(CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8C5(C9=CC=C(OCC(CCCC)CC)C=C9)C%10=CC=C(OCC(CCCC)CC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(OCC(CCCC)CC)C=C%12)C%13=CC=C(OCC(CCCC)CC)C=C%13)S1,PFDCTBT,5.32,3.55,0.77,9.5,0.38,2.8,"Wu, J.-S.; Cheng, Y.-J.; Dubosc, M.; Hsieh, C.-H.; Chang, C.-Y.; Hsu, C.-S. Donor¨Cacceptor Polymers Based on Multi-Fused Heptacyclic Structures: Synthesis, Characterization and Photovoltaic Applications. Chem. Commun. 2010, 46, 3259¨C3261. "
1407,CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8C5(C9=CC=C(OCC(CCCC)CC)C=C9)C%10=CC=C(OCC(CCCC)CC)C=C%10)=C3)C4=C%11)=C%11C2(C%12=CC=C(OCC(CCCC)CC)C=C%12)C%13=CC=C(OCC(CCCC)CC)C=C%13)S1,PCDCTBT,5.38,3.61,0.8,10.7,0.43,3.7,"Wu, J.-S.; Cheng, Y.-J.; Dubosc, M.; Hsieh, C.-H.; Chang, C.-Y.; Hsu, C.-S. Donor¨Cacceptor Polymers Based on Multi-Fused Heptacyclic Structures: Synthesis, Characterization and Photovoltaic Applications. Chem. Commun. 2010, 46, 3259¨C3261. "
1408,CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C67)=C8)=C8C5(CCCCCCCC)CCCCCCCC)=C3)C4=C9)=C9C2(CCCCCCCC)CCCCCCCC)S1,PCDCTBT-C8,5.31,3.67,0.74,10.3,0.6,4.59,"Cheng, Y. J.; Wu, J. S.; Shih, P. I.; Chang, C. Y.; Jwo, P. C.; Kao, W. S.; Hsu, C. S. Carbazole-Based Ladder-Type Heptacylic Arene with Aliphatic Side Chains Leading to Enhanced Efficiency of Organic Photovoltaics. Chem. Mater. 2011, 23, 2361¨C2369. "
1409,CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C7=CC=C(C8=CC=C(C)S8)C9=NSN=C79)S6)=C%10)=C%10C5(CCCCCCCC)CCCCCCCC)=C3)C4=C%11)=C%11C2(CCCCCCCC)CCCCCCCC)S1,PCDCTDTBT-C8,5.31,3.65,0.74,9.2,0.52,3.53,"Cheng, Y. J.; Wu, J. S.; Shih, P. I.; Chang, C. Y.; Jwo, P. C.; Kao, W. S.; Hsu, C. S. Carbazole-Based Ladder-Type Heptacylic Arene with Aliphatic Side Chains Leading to Enhanced Efficiency of Organic Photovoltaics. Chem. Mater. 2011, 23, 2361¨C2369. "
1410,CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C7=C8C(C(N7CCCCCCCC)=O)=C(C9=CC=C(C)S9)N(CCCCCCCC)C8=O)S6)=C%10)=C%10C5(CCCCCCCC)CCCCCCCC)=C3)C4=C%11)=C%11C2(CCCCCCCC)CCCCCCCC)S1,PCDCTDTDPP-C8,5.24,3.87,0.7,6.7,0.5,2.35,"Cheng, Y. J.; Wu, J. S.; Shih, P. I.; Chang, C. Y.; Jwo, P. C.; Kao, W. S.; Hsu, C. S. Carbazole-Based Ladder-Type Heptacylic Arene with Aliphatic Side Chains Leading to Enhanced Efficiency of Organic Photovoltaics. Chem. Mater. 2011, 23, 2361¨C2369. "
1411,CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=C6N=C(C8=CC=CC=C8)C(C9=CC=CC=C9)=N7)=C%10)=C%10C5(CCCCCCCC)CCCCCCCC)=C3)C4=C%11)=C%11C2(CCCCCCCC)CCCCCCCC)S1,PCDCTQX-C8,5.25,3.53,0.78,5.8,0.4,1.8,"Cheng, Y. J.; Wu, J. S.; Shih, P. I.; Chang, C. Y.; Jwo, P. C.; Kao, W. S.; Hsu, C. S. Carbazole-Based Ladder-Type Heptacylic Arene with Aliphatic Side Chains Leading to Enhanced Efficiency of Organic Photovoltaics. Chem. Mater. 2011, 23, 2361¨C2369. "
1412,CC1=CC2=C(C(C=C(C(CCCCCCCC)(CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8C5(CCCCCCCC)CCCCCCCC)=C3)C4=C9)=C9C2(CCCCCCCC)CCCCCCCC)S1,PFDCTBT-C8,5.3,3.55,0.83,12.57,0.668,7,"Chang, C. Y.; Cheng, Y. J.; Hung, S. H.; Wu, J. S.; Kao, W. S.; Lee, C. H.; Hsu, C. S. Combination of Molecular, Morphological, and Interfacial Engineering to Achieve Highly Efficient and Stable Plastic Solar Cells. Adv. Mater. 2012, 24, 549¨C553. "
1413,CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8N5CC(CC)CCCC)=C3)C4=C9)=C9N2CC(CC)CCCC)S1,PDTPCBT,4.76,3.29,0.5,10.5,0.499,2.6,"Wu, J. S.; Cheng, Y. J.; Lin, T. Y.; Chang, C. Y.; Shih, P. I.; Hsu, C. S. Dithienocarbazole-Based Ladder-Type Heptacyclic Arenes with Silicon, Carbon, and Nitrogen Bridges: Synthesis, Molecular Properties, Field-Effect Transistors, and Photovoltaic Applications. Adv. Funct. Mater. 2012, 22, 1711¨C1722. "
1414,CC1=CC2=C(C(C=C(N(C(CCCCCCCC)CCCCCCCC)C3=C4C=C5C(C(SC(C6=CC=C(C)C7=NSN=C76)=C8)=C8C5(CCCCCCCC)CCCCCCCC)=C3)C4=C9)=C9C2(CCCCCCCC)CCCCCCCC)S1,PDTCCBT,5.31,3.67,0.74,10.3,0.6,4.6,"Wu, J. S.; Cheng, Y. J.; Lin, T. Y.; Chang, C. Y.; Shih, P. I.; Hsu, C. S. Dithienocarbazole-Based Ladder-Type Heptacyclic Arenes with Silicon, Carbon, and Nitrogen Bridges: Synthesis, Molecular Properties, Field-Effect Transistors, and Photovoltaic Applications. Adv. Funct. Mater. 2012, 22, 1711¨C1722. "
1415,CC1=CC2=C(C(SC3=C4C=C5C(C(C(C6=CC=C(OCCCCCCCC)C=C6)(C7=CC=C(OCCCCCCCC)C=C7)C8=C9SC(C%10=C%11C(C(N(CCCCCCCC)C%11=O)=O)=C(C)S%10)=C8)=C9S5)=C3)=C4C2(C%12=CC=C(OCCCCCCCC)C=C%12)C%13=CC=C(OCCCCCCCC)C=C%13)S1,PBDCPDT-TPD,5.36,3.2,0.87,12.21,0.622,6.6,"Chen, Y. L.; Chang, C. Y.; Cheng, Y. J.; Hsu, C. S. Synthesis of a New Ladder-Type Benzodi(cyclopentadithiophene Arene with Forced Planarization Leading to an Enhanced Efficiency of Organic Photovoltaics. Chem. Mater. 2012, 24, 3964¨C3971. "
1416,CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=C4C(C(N(CC(C#CC#CC#CC#CC#C)CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCCCCCCCCCCCC.[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH],PBDTDPT1,5.42,3.6,0.93,6.58,0.56,3.42,"Zhang, G.; Fu, Y.; Zhang, Q.; Xie, Z. Benzo[1,2-b:4,5-b¡ä]dithiopheneDioxopyrrolothiophen Copolymers for High Performance Solar Cells. Chem. Commun.2010, 46, 4997¨C4999. "
1417,CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CC(C#CC#CC#CC#CC#C)CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC.[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH].[HH],PBDTDPT2,5.44,3.58,0.91,10.34,0.51,4.79,"Zhang, G.; Fu, Y.; Zhang, Q.; Xie, Z. Benzo[1,2-b:4,5-b¡ä]dithiopheneDioxopyrrolothiophen Copolymers for High Performance Solar Cells. Chem. Commun.2010, 46, 4997¨C4999. "
1418,CC1=CC2=C(C(SC3=C4C=C5C(C(C(C6=CC=C(OCCCCCCCC)C=C6)(C7=CC=C(OCCCCCCCC)C=C7)C8=C9SC(C%10=C(F)C(F)=C(C)C%11=NSN=C%11%10)=C8)=C9S5)=C3)=C4C2(C%12=CC=C(OCCCCCCCC)C=C%12)C%13=CC=C(OCCCCCCCC)C=C%13)S1,PBDCPDT?FBT,5.35,3.48,0.81,12.82,0.555,5.76,"Chen, Y.-L.; Kao, W.-S.; Tsai, C.-E.; Lai, Y.-Y.; Cheng, Y.-J.; Hsu, C.-S. A New Ladder-Type Benzodi(cyclopentadithiophene-Based Donor¨Cacceptor Polymer and a Modified Hole-Collecting PEDOT:PSS Layer to Achieve Tandem Solar Cells with an Open-Circuit Voltage of 1.62 V. Chem. Commun. 2013, 49, 7702¨C7704. "
1419,CC1=CC=C(C2=CC(S3)=C(S2)C4=C3C5=CC(C6(C7=CC=C(OCCCCCCCC)C=C7)C8=CC=C(OCCCCCCCC)C=C8)=C(C=C5C4(C9=CC=C(OCCCCCCCC)C=C9)C%10=CC=C(OCCCCCCCC)C=C%10)C%11=C6C(S%12)=C(S%11)C=C%12C)C%13=NSN=C1%13,PIDTTBT,5.3,3.4,0.84,8.32,0.55,3.8,"Chang, H. H.; Tsai, C. E.; Lai, Y. Y.; Chiou, D. Y.; Hsu, S. L.; Hsu, C. S.; Cheng, Y. J. Synthesis, Molecular and Photovoltaic Properties of Donor-Acceptor Conjugated Polymers Incorporating a New Heptacylic indacenodithieno[3,2-b] Thiophene Arene. Macromolecules 2012, 45, 9282¨C9291. "
1420,CC1=C(F)C(F)=C(C2=CC(S3)=C(S2)C4=C3C5=CC(C6(C7=CC=C(OCCCCCCCC)C=C7)C8=CC=C(OCCCCCCCC)C=C8)=C(C=C5C4(C9=CC=C(OCCCCCCCC)C=C9)C%10=CC=C(OCCCCCCCC)C=C%10)C%11=C6C(S%12)=C(S%11)C=C%12C)C%13=NSN=C1%13,PIDTTFBT,5.43,3.5,0.9,10.08,0.46,4.2,"Chang, H. H.; Tsai, C. E.; Lai, Y. Y.; Chiou, D. Y.; Hsu, S. L.; Hsu, C. S.; Cheng, Y. J. Synthesis, Molecular and Photovoltaic Properties of Donor-Acceptor Conjugated Polymers Incorporating a New Heptacylic indacenodithieno[3,2-b] Thiophene Arene. Macromolecules 2012, 45, 9282¨C9291. "
1421,CC1=CC(SC2=C3C(C4=CC=C(OCCCCCCCC)C=C4)(C5=CC=C(OCCCCCCCC)C=C5)C6=C2C=C(C(C7=CC=C(OCCCCCCCC)C=C7)(C8=CC=C(OCCCCCCCC)C=C8)C9=C%10SC%11=C9SC(C%12=C(C(N(CCCCCCCC)C%13=O)=O)C%13=C(C)S%12)=C%11)C%10=C6)=C3S1,PIDTTTPD,5.45,3.18,0.9,7.99,0.6,4.3,"Chang, H. H.; Tsai, C. E.; Lai, Y. Y.; Chiou, D. Y.; Hsu, S. L.; Hsu, C. S.; Cheng, Y. J. Synthesis, Molecular and Photovoltaic Properties of Donor-Acceptor Conjugated Polymers Incorporating a New Heptacylic indacenodithieno[3,2-b] Thiophene Arene. Macromolecules 2012, 45, 9282¨C9291. "
1422,CC1=CC2=C(C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6C=C7C(C(SC8=C9SC(C%10=C(F)C(F)=C(C)C%11=NSN=C%11%10)=C8)=C9C7(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)=C5)=C6S2)S1,PIDTT-DFBT,5.3,3.5,0.95,12.21,0.61,7.03,"Xu, Y. X.; Chueh, C. C.; Yip, H. L.; Ding, F. Z.; Li, Y. X.; Li, C. Z.; Li, X.; Chen, W. C.; Jen, A. K. Y. Improved Charge Transport and Absorption Coefficient in indacenodithieno[3,2-b]thiophene-Based Ladder-Type Polymer Leading to Highly Efficient Polymer Solar Cells. Adv. Mater. 2012, 24, 6356¨C6361. "
1423,CC1=CC=C(C2=CC(C(C3=CC=C(OCCCCCCCC)C=C3)(C4=CC=C(OCCCCCCCC)C=C4)C5=C6C=C7C(C(SC8=C9C(CCCCCCCC)(CCCCCCCC)C%10=CC%11=C(C(C%12=CC=C(OCCCCCCCC)C=C%12)(C%13=CC=C(OCCCCCCCC)C=C%13)C%14=C%11SC(C)=C%14)C=C8%10)=C9C7(CCCCCCCC)CCCCCCCC)=C5)=C6S2)C%15=NSN=C1%15,PTPTPTBT,5.24,3.38,0.76,12.1,0.64,5.9,"Cheng, Y. J.; Chen, C. H.; Lin, Y. S.; Chang, C. Y.; Hsu, C. S. Ladder-Type Nonacyclic Structure Consisting of Alternate Thiophene and Benzene Units for Efficient Conventional and Inverted Organic Photovoltaics. Chem. Mater. 2011, 23, 5068¨C5075. "
1424,CC1=C(N=C(C2=CC=CC=C2)C(C3=CC=CC=C3)=N4)C4=C(C5=CC(C(C6=CC=C(OCCCCCCCC)C=C6)(C7=CC=C(OCCCCCCCC)C=C7)C8=C9C=C%10C(C(SC%11=C%12C(CCCCCCCC)(CCCCCCCC)C%13=CC%14=C(C(C%15=CC=C(OCCCCCCCC)C=C%15)(C%16=CC=C(OCCCCCCCC)C=C%16)C%17=C%14SC(C)=C%17)C=C%11%13)=C%12C%10(CCCCCCCC)CCCCCCCC)=C8)=C9S5)C=C1,PTPTPTQX,5.21,3.3,0.74,10.2,0.62,4.7,"Cheng, Y. J.; Chen, C. H.; Lin, Y. S.; Chang, C. Y.; Hsu, C. S. Ladder-Type Nonacyclic Structure Consisting of Alternate Thiophene and Benzene Units for Efficient Conventional and Inverted Organic Photovoltaics. Chem. Mater. 2011, 23, 5068¨C5075. "
1425,CC1=C(F)C(F)=C(C(S2)=CC3=C2C(S4)=C(C3(C5=CC=C(CCCCCC)C=C5)C6=CC=C(CCCCCC)C=C6)C7=C4C(C8(C9=CC=C(CCCCCC)C=C9)C%10=CC=C(CCCCCC)C=C%10)=C(S7)C(C8=C%11)=CC%12=C%11C(S%13)=C(C%12(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15)C%16=C%13C(C(C%17=CC=C(CCCCCC)C=C%17)(C%18=CC=C(CCCCCC)C=C%18)C%19=C%20SC(C)=C%19)=C%20S%16)C%21=NSN=C1%21,PIDTCPDT-DFBT,5.05,3.28,0.75,14.59,0.59,6.46,"Li, Y.; Yao, K.; Yip, H. L.; Ding, F. Z.; Xu, Y. X.; Li, X.; Chen, Y.; Jen, A. K. Y. Eleven-Membered Fused-Ring Low Band-Gap Polymer with Enhanced Charge Carrier Mobility and Photovoltaic Performance. Adv. Funct. Mater. 2014, 24, 3631¨C3638. "
1426,CC1=CC(CCCCCC)=C(S1)C2=CC3=C(C(C(C4=CC=C(CCCCCC)C=C4)(C5=CC=C(CCCCCC)C=C5)C6=C7C=C8C(C(SC9=C%10SC(C%11=C(CCCCCC)C=C(C%12=C(F)C(F)=C(C)C%13=NSN=C%13%12)S%11)=C9)=C%10C8(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15)=C6)=C7S3)S2,PIDTT-T-DFBT,5.15,3.2,0.92,10.4,0.54,5.26,"Li, Y.; Yao, K.; Yip, H. L.; Ding, F. Z.; Xu, Y. X.; Li, X.; Chen, Y.; Jen, A. K. Y. Eleven-Membered Fused-Ring Low Band-Gap Polymer with Enhanced Charge Carrier Mobility and Photovoltaic Performance. Adv. Funct. Mater. 2014, 24, 3631¨C3638. "
1427,CC1=CC2=C(C(SC(C3=C(F)C(F)=C(C)C4=NSN=C34)=C5)=C5C2(CC(CC)CCCC)CC(CC)CCCC)S1,PCPDTDFBT,5.34,3.52,0.85,12.6,0.52,5.6,"You, J.; Dou, L.; Yoshimura, K.; Kato, T.; Ohya, K.; Moriarty, T.; Emery, K.; Chen, C. C.; Gao, J.; Li, G.; Yang, Y. A Polymer Tandem Solar Cell with 10.6% Power Conversion Efficiency. Nat. Commun. 2013, 4, 1410¨C1446. "
1428,CC1=CC(C(CCC(CCCC(C)C)C)(CCC(CCCC(C)C)C)O2)=C(C3=C2C=C(C4=C(F)C(F)=C(C)C5=NSN=C45)S3)S1,PDTPDFBT,5.26,3.61,0.68,17.8,0.65,7.9,"You, J.; Dou, L.; Yoshimura, K.; Kato, T.; Ohya, K.; Moriarty, T.; Emery, K.; Chen, C. C.; Gao, J.; Li, G.; Yang, Y. A Polymer Tandem Solar Cell with 10.6% Power Conversion Efficiency. Nat. Commun. 2013, 4, 1410¨C1446. "
1429,CC1=CC2=C(C(OC(CCCCC)CCCCC)=C(C=C(C3=CC=C(C)C4=NON=C43)S5)C5=C2OC(CCCCC)CCCCC)S1,PBDT-BOZ,5.34,3.45,0.887,13.6,0.508,6.05,"Nie, W.; MacNeill, C. M.; Li, Y.; Noftle, R. E.; Carroll, D. L.; Coffin, R. C. A Soluble High Molecular Weight Copolymer of Benzo[1,2-b:4,5-b¡ä]dithiophene and Benzoxadiazole for Efficient Organic Photovoltaics. Macromol. Rapid Commun. 2011, 32, 1163¨C1168. "
1430,CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=N[Se]N=C75)S4)=C2)=C3C=C1,PCzDBSe,5.28,3.55,0.75,7.23,0.45,2.58,"Zhao, W.; Cai, W.; Xu, R.; Yang, W.; Gong, X.; Wu, H.; Cao, Y. Novel Conjugated Alternating Copolymer Based on 2,7-Carbazole and 2,1,3-Benzoselenadiazole. Polymer2010, 51, 3196¨C3202. "
1431,CC1=CC(C(CCCCCCCC)(CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NN(CCCCCCCCCCCC)N=C75)S4)=C2)=C3C=C1,PF-DTBTA,5.67,3.43,1,2.64,0.515,1.3,"Zhang, L.; He, C.; Chen, J.; Yuan, P.; Huang, L.; Zhang, C.; Cai, W.; Liu, Z.; Cao, Y. Bulk-Heterojunction Solar Cells with Benzotriazole-Based Copolymers as Electron Donors: Largely Improved Photovoltaic Parameters by Using PFN/AL Bilayer Cathode. Macromolecules 2010, 43, 9771¨C9778."
1432,CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NN(CCCCCCCCCCCC)N=C75)S4)=C2)=C3C=C1,PCz-DTBTA,5.54,3.36,0.9,4.68,0.653,2.75,"Zhang, L.; He, C.; Chen, J.; Yuan, P.; Huang, L.; Zhang, C.; Cai, W.; Liu, Z.; Cao, Y. Bulk-Heterojunction Solar Cells with Benzotriazole-Based Copolymers as Electron Donors: Largely Improved Photovoltaic Parameters by Using PFN/AL Bilayer Cathode. Macromolecules 2010, 43, 9771¨C9778."
1433,CC(S1)=CC=C1C(C2=NN(CCCCCCCCCCCC)N=C23)=CC=C3C(S4)=CC=C4C5=C(OCCCCCCCC)C=C(C)C(OCCCCCCCC)=C5,PPh-DTBTA,5.2,3.33,0.55,4.5,0.561,1.39,"Zhang, L.; He, C.; Chen, J.; Yuan, P.; Huang, L.; Zhang, C.; Cai, W.; Liu, Z.; Cao, Y. Bulk-Heterojunction Solar Cells with Benzotriazole-Based Copolymers as Electron Donors: Largely Improved Photovoltaic Parameters by Using PFN/AL Bilayer Cathode. Macromolecules 2010, 43, 9771¨C9778."
1434,CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NC(C)(C)N=C75)S4)=C2)=C3C=C1,PCDTMBI,5.47,3.82,0.65,10,0.48,3.12,"Song, S.; Jin, Y.; Park, S. H.; Cho, S.; Kim, I.; Lee, K.; Heeger, A. J.; Suh, H. A LowBandgap Alternating Copolymer Containing the Dimethylbenzimidazole Moiety. J. Mater. Chem. 2010, 20, 6517¨C6523. "
1435,CC(S1)=CC=C1C(C2=NC(C)(C)N=C23)=CC=C3C(S4)=CC=C4C5=CC6=C(C(C(C7(CC(CC)CCCC)CC(CC)CCCC)=CC(C)=C8)=C8C=C6)C7=C5,PCPPDTMBI,5.54,3.88,0.47,4.48,0.32,0.67,"Song, S.; Jin, Y.; Park, S. H.; Cho, S.; Kim, I.; Lee, K.; Heeger, A. J.; Suh, H. A LowBandgap Alternating Copolymer Containing the Dimethylbenzimidazole Moiety. J. Mater. Chem. 2010, 20, 6517¨C6523. "
1436,CC(S1)=CC=C1C(C2=NC(C)(C)N=C23)=CC=C3C(S4)=CC=C4C5=CC=C(C6=CC=C(C)C=C6C7(CC(CC)CCCC)CC(CC)CCCC)C7=C5,PFDTMBI,5.61,3.97,0.56,2.44,0.31,0.42,"Song, S.; Jin, Y.; Park, S. H.; Cho, S.; Kim, I.; Lee, K.; Heeger, A. J.; Suh, H. A LowBandgap Alternating Copolymer Containing the Dimethylbenzimidazole Moiety. J. Mater. Chem. 2010, 20, 6517¨C6523. "
1437,CC1=C2C(C(N(CCCCCCCCCCCC)C2=O)=O)=C(C3=C(OCCCCCCCCCCCC)C=C(C4=CC(OCCCCCCCCCCCC)=C(C)S4)S3)S1,P1,4.85,3.35,0.41,7.39,0.48,1.54,"Guo, X.; Xin, H.; Kim, F. S.; Liyanage, A. D. T.; Jenekhe, S. A.; Watson, M. D. Thieno[3,4-c]Pyrrole-4,6-Dione-Based Donor?Acceptor Conjugated Polymers for Solar Cells. Macromolecules 2011, 44, 269¨C277. "
1438,CC1=C2C(C(N(CC(CCCCCC)CCCC)C2=O)=O)=C(C3=C(OCCCCCCCCCCCC)C=C(C4=CC(OCCCCCCCCCCCC)=C(C)S4)S3)S1,P2,5.05,3.53,0.59,1.59,0.54,0.64,"Guo, X.; Xin, H.; Kim, F. S.; Liyanage, A. D. T.; Jenekhe, S. A.; Watson, M. D. Thieno[3,4-c]Pyrrole-4,6-Dione-Based Donor?Acceptor Conjugated Polymers for Solar Cells. Macromolecules 2011, 44, 269¨C277. "
1439,CC1=C2C(C(N(CCCCCCCCCCCC)C2=O)=O)=C(C3=CC(C(CCCCCCCC)(CCCCCCCC)C4=C5SC(C)=C4)=C5S3)S1,P3,5.26,3.59,0.76,8.12,0.5,3.15,"Guo, X.; Xin, H.; Kim, F. S.; Liyanage, A. D. T.; Jenekhe, S. A.; Watson, M. D. Thieno[3,4-c]Pyrrole-4,6-Dione-Based Donor?Acceptor Conjugated Polymers for Solar Cells. Macromolecules 2011, 44, 269¨C277. "
1440,CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC(C(CCCCCCCC)(CCCCCCCC)C5=C6C=CC(C)=C5)=C6C=C4)S3)C7=C2N=C(C8=CC=CC=C8)C(C9=CC=CC=C9)=N7)S1,N-P7,5.37,3.42,0.99,9.72,0.574,5.5,"Kitazawa, D.; Watanabe, N.; Yamamoto, S.; Tsukamoto, J. Quinoxaline-Based???-Conjugated Donor Polymer for Highly Efficient Organic Thin-Film Solar Cells. Appl. Phys. Lett. 2009, 95, 93¨C96. "
1441,CC1=CC2=C(C3=C4C=C(C5=CC=C(C6=C(N=C(C7=CC=C(OCCCCCCCC)C=C7)C(C8=CC=C(OCCCCCCCC)C=C8)=N9)C9=C(C%10=CC=C(C)S%10)C=C6)S5)C=C3CC2)C(N4C(CCCCCCCC)CCCCCCCC)=C1,PECz-DTQx,5.15,3.45,0.81,11.4,0.658,6.07,"He, Z.; Zhang, C.; Xu, X.; Zhang, L.; Huang, L.; Chen, J.; Wu, H.; Cao, Y. Largely Enhanced Efficiency with a PFN/Al Bilayer Cathode in High Efficiency Bulk Heterojunction Photovoltaic Cells with a Low Bandgap Polycarbazole Donor. Adv. Mater.2011, 23, 3086¨C3089. "
1442,CC1=CC=C(C2=C(N=C(C3=CC(OCCCCCCCC)=CC=C3)C(C4=CC=CC(OCCCCCCCC)=C4)=N5)C5=C(C)C=C2)S1,TQ1,5.7,3.3,0.89,10.5,0.64,6,"Wang, E.; Hou, L.; Wang, Z.; Hellstr?m, S.; Zhang, F.; Ingan?s, O.; Andersson, M. R. An Easily Synthesized Blue Polymer for High-Performance Polymer Solar Cells. Adv. Mater. 2010, 22, 5240¨C5244. "
1443,O=C1C(C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C3=CC4=C(C=C(C5=CC=C(C)S5)S4)S3)N1CC(CCCCCCCCCC)CCCCCCCC)=C2C6=CC7=C(C=C(C)S7)S6,PTT-DPP (P1),5.06,3.68,0.58,15,0.61,5.4,"Bronstein, H.; Chen, Z.; Ashraf, R. S.; Zhang, W.; Du, J.; Durrant, J. R.; Shakya Tuladhar, P.; Song, K.; Watkins, S. E.; Geerts, Y.; Wienk, M. M.; Janssen, R. A. J.; Anthopoulos, T.; Sirringhaus, H.; Heeney, M.; McCulloch, I. Thieno[3,2-b]thiopheneDiketopyrrolopyrrole-Containing Polymers for High-Performance Organic Field-Effect Transistors and Organic Photovoltaic Devices. J. Am. Chem. Soc. 2011, 133, 3272¨C3275. "
1444,O=C1C(C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C3=CC4=C(C=C(C)S4)S3)N1CC(CCCCCCCCCC)CCCCCCCC)=C2C5=CC6=C(C=C(C)S6)S5,PTT-DPP (P2),5.04,3.76,0.57,8.9,0.59,3,"Bronstein, H.; Chen, Z.; Ashraf, R. S.; Zhang, W.; Du, J.; Durrant, J. R.; Shakya Tuladhar, P.; Song, K.; Watkins, S. E.; Geerts, Y.; Wienk, M. M.; Janssen, R. A. J.; Anthopoulos, T.; Sirringhaus, H.; Heeney, M.; McCulloch, I. Thieno[3,2-b]thiopheneDiketopyrrolopyrrole-Containing Polymers for High-Performance Organic Field-Effect Transistors and Organic Photovoltaic Devices. J. Am. Chem. Soc. 2011, 133, 3272¨C3275. "
1445,CC1=CC=C(C2=C(CCCCCC)N=C(C3=NC(CCCCCC)=C(C4=CC=C(C5=CC6=C(C(C=CC(C)=C7)=C7N6C(CCCCCCCC)CCCCCCCC)C=C5)S4)S3)S2)S1,P1,5.44,2.91,0.82,1.24,0.296,0.3,"Zhang, M.; Fan, H.; Guo, X.; He, Y.; Zhang, Z.; Min, J.; Zhang, J.; Zhao, G.; Zhan, X.; Li, Y. Synthesis and Photovoltaic Properties of Bithiazole-Based Donor-Acceptor Copolymers. Macromolecules 2010, 43, 5706¨C5712. "
1446,CC1=CC=C(C2=C(CCCCCC)N=C(C3=NC(CCCCCC)=C(C4=CC=C(C5=CC(N(CC(CCCC)CC)C6=C7SC(C)=C6)=C7S5)S4)S3)S2)S1,P2,4.76,2.79,0.28,0.51,0.337,0.06,"Zhang, M.; Fan, H.; Guo, X.; He, Y.; Zhang, Z.; Min, J.; Zhang, J.; Zhao, G.; Zhan, X.; Li, Y. Synthesis and Photovoltaic Properties of Bithiazole-Based Donor-Acceptor Copolymers. Macromolecules 2010, 43, 5706¨C5712. "
1447,CC1=C(CCCCCC)C=C(C2=NN=C(C3=CC(CCCCCC)=C(C4=CC(C(CCCCCC)(CCCCCC)C5=C6SC(C)=C5)=C6S4)S3)N=N2)S1,PCPDTTTz,5.34,3.48,0.75,12.2,0.59,5.4,"Li, Z.; Ding, J.; Song, N.; Lu, J.; Tao, Y. Development of a New s-Tetrazine-Based Copolymer for Efficient Solar Cells. J. Am. Chem. Soc. 2010, 132, 13160¨C13161. "
1448,CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5N2C(CCCCCCCC)CCCCCCCC)S1,PDTPBT-C8,4.89,3.08,0.43,6.19,0.46,1.23,"Yue, W.; Zhao, Y.; Shao, S.; Tian, H.; Xie, Z.; Geng, Y.; Wang, F. Novel NIRAbsorbing Conjugated Polymers for Efficient Polymer Solar Cells: Effect of Alkyl Chain Length on Device Performance. J. Mater. Chem. 2009, 19, 2199¨C2206. "
1449,CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5N2C(CCCCCC)CCCCCC)S1,PDTPBT-C6,4.86,3.07,0.43,11.1,0.43,2.06,"Yue, W.; Zhao, Y.; Shao, S.; Tian, H.; Xie, Z.; Geng, Y.; Wang, F. Novel NIRAbsorbing Conjugated Polymers for Efficient Polymer Solar Cells: Effect of Alkyl Chain Length on Device Performance. J. Mater. Chem. 2009, 19, 2199¨C2206. "
1450,CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5N2C(CCCCC)CCCCC)S1,PDTPBT-C5,4.81,3.08,0.54,11.9,0.44,2.8,"Yue, W.; Zhao, Y.; Shao, S.; Tian, H.; Xie, Z.; Geng, Y.; Wang, F. Novel NIRAbsorbing Conjugated Polymers for Efficient Polymer Solar Cells: Effect of Alkyl Chain Length on Device Performance. J. Mater. Chem. 2009, 19, 2199¨C2206. "
1451,CC1=CC2=C(C(SC(C3=C(C(N(CCCCCCCC)C4=O)=O)C4=C(C)S3)=C5)=C5C2(CC(CC)CCCC)CC(CCCC)CC)S1,PDTC,5.43,3.25,0.8,10.04,0.47,3.74,"Zhang, Y.; Zou, J.; Yip, H.-L.; Sun, Y.; Davies, J. A.; Chen, K.-S.; Acton, O.; Jen, A. K.-Y. Conjugated Polymers Based on C, Si and N-Bridged Dithiophene and Thienopyrroledione Units: Synthesis, Field-Effect Transistors and Bulk Heterojunction Polymer Solar Cells. J. Mater. Chem. 2011, 21, 3895¨C3902. "
1452,CC1=CC2=C(C(SC(C3=C(C(N(CCCCCCCC)C4=O)=O)C4=C(C)S3)=C5)=C5N2C(CC(CC)CCCC)CC(CCCC)CC)S1,PDTP,5.16,3.08,0.76,4.69,0.53,1.69,"Zhang, Y.; Zou, J.; Yip, H.-L.; Sun, Y.; Davies, J. A.; Chen, K.-S.; Acton, O.; Jen, A. K.-Y. Conjugated Polymers Based on C, Si and N-Bridged Dithiophene and Thienopyrroledione Units: Synthesis, Field-Effect Transistors and Bulk Heterojunction Polymer Solar Cells. J. Mater. Chem. 2011, 21, 3895¨C3902. "
1453,CC1=CC=C(C2=CC3=C(C4=CC(N(CC(CCCCCCCCCC)CCCCCCCC)C5=C6SC(C)=C5)=C6C=C4N3CC(CCCCCCCCCC)CCCCCCCC)S2)C7=NSN=C71,P1,4.9,3.5,0.36,4.2,0.536,0.8,"Donaghey, J. E.; Ashraf, R. S.; Kim, Y.; Huang, Z. G.; Nielsen, C. B.; Zhang, W.; Schroeder, B.; Grenier, C. R. G.; Brown, C. T.; D¡¯Angelo, P.; Smith, J.; Watkins, S.; Song, K.; Anthopoulos, T. D.; Durrant, J. R.; Williams, C. K.; McCulloch, I. Pyrroloindacenodithiophene Containing Polymers for Organic Field Effect Transistors and Organic Photovoltaics. J. Mater. Chem. 2011, 21, 18744¨C18752. "
1454,CC1=C(F)C(F)=C(C2=CC3=C(C4=CC(N(CC(CCCCCCCCCC)CCCCCCCC)C5=C6SC(C)=C5)=C6C=C4N3CC(CCCCCCCCCC)CCCCCCCC)S2)C7=NSN=C71,P2,4.9,3.4,0.44,3.69,0.4,0.7,"Donaghey, J. E.; Ashraf, R. S.; Kim, Y.; Huang, Z. G.; Nielsen, C. B.; Zhang, W.; Schroeder, B.; Grenier, C. R. G.; Brown, C. T.; D¡¯Angelo, P.; Smith, J.; Watkins, S.; Song, K.; Anthopoulos, T. D.; Durrant, J. R.; Williams, C. K.; McCulloch, I. Pyrroloindacenodithiophene Containing Polymers for Organic Field Effect Transistors and Organic Photovoltaics. J. Mater. Chem. 2011, 21, 18744¨C18752. "
1455,CC(S1)=CC2=C1C3=C(N2CC(CCCCCCCCCC)CCCCCCCC)C=C(C(N4CC(CCCCCCCCCC)CCCCCCCC)=C3)C5=C4C=C(S5)C6=C7C(C(N(CCCCCCCC)C7=O)=O)=C(C)S6,P3,5.1,3.4,0.58,4.04,0.478,1.1,"Donaghey, J. E.; Ashraf, R. S.; Kim, Y.; Huang, Z. G.; Nielsen, C. B.; Zhang, W.; Schroeder, B.; Grenier, C. R. G.; Brown, C. T.; D¡¯Angelo, P.; Smith, J.; Watkins, S.; Song, K.; Anthopoulos, T. D.; Durrant, J. R.; Williams, C. K.; McCulloch, I. Pyrroloindacenodithiophene Containing Polymers for Organic Field Effect Transistors and Organic Photovoltaics. J. Mater. Chem. 2011, 21, 18744¨C18752. "
1456,CC(S1)=CC2=C1C3=C(N2CC(CCCCCCCCCC)CCCCCCCC)C=C(C(N4CC(CCCCCCCCCC)CCCCCCCC)=C3)C5=C4C=C(S5)C6=C7C(C(N(CC(CC)CCCC)C7=O)=O)=C(C8=C(C(N(CC(CC)CCCC)C9=O)=O)C9=C(C)S8)S6,P4,5.1,3.5,0.77,4.62,0.688,2.5,"Donaghey, J. E.; Ashraf, R. S.; Kim, Y.; Huang, Z. G.; Nielsen, C. B.; Zhang, W.; Schroeder, B.; Grenier, C. R. G.; Brown, C. T.; D¡¯Angelo, P.; Smith, J.; Watkins, S.; Song, K.; Anthopoulos, T. D.; Durrant, J. R.; Williams, C. K.; McCulloch, I. Pyrroloindacenodithiophene Containing Polymers for Organic Field Effect Transistors and Organic Photovoltaics. J. Mater. Chem. 2011, 21, 18744¨C18752. "
1457,CC(S1)=CC(CCCCCCCCCCCC)=C1C2=NC3=CC4=C(N=C(C5=C(CCCCCCCCCCCC)C=C(C6=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C(C7=CN=C(C8=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C)S8)C9=NSN=C79)S6)S5)S4)C=C3S2,PBBTz-PT,5.54,3.84,0.761,5.91,0.48,2.3,"Gopal, A.; Saeki, A.; Ide, M.; Seki, S. Fluorination of Benzothiadiazole?Benzobisthiazole Copolymer Leads to Additive-Free Processing with Meliorated Solar Cell Performance. ACS Sustainable Chem. Eng. 2014, 2, 2613?2622. "
1458,CC(S1)=CC(CCCCCCCCCCCC)=C1C2=NC3=CC4=C(N=C(C5=C(CCCCCCCCCCCC)C=C(C6=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)C=C(C7=C(F)C(F)=C(C8=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C)S8)C9=NSN=C79)S6)S5)S4)C=C3S2,PBBTz-FT,5.42,3.69,0.881,10.88,0.649,6.37,"Gopal, A.; Saeki, A.; Ide, M.; Seki, S. Fluorination of Benzothiadiazole?Benzobisthiazole Copolymer Leads to Additive-Free Processing with Meliorated Solar Cell Performance. ACS Sustainable Chem. Eng. 2014, 2, 2613?2622. "
1459,CC1=CC2=C(C(SC(C)=C3)=C3C(C4=CC=C(CC(CCCCCCCC)CCCCCC)S4)=C2C5=CC=C(CC(CCCCCC)CCCCCCCC)S5)S1,HMPBDT,5.7,2.65,0.76,0.34,0.4,0.1,"Xiao, S.; Stuart, A. C.; Liu, S.; You, W. Conjugated Polymers Based on benzo[2,1-b:3,4- b¡ä]Dithiophene with Low-Lying Highest Occupied Molecular Orbital Energy Levels for Organic Photovoltaics. ACS Appl. Mater. Interfaces 2009, 1, 1613¨C1621."
1460,CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5C(C6=CC=C(CC(CCCCCCCC)CCCCCC)S6)=C2C7=CC=C(CC(CCCCCC)CCCCCCCC)S7)S1,PBDTBT,5.34,3.16,0.72,2.06,0.42,0.6,"Xiao, S.; Stuart, A. C.; Liu, S.; You, W. Conjugated Polymers Based on benzo[2,1-b:3,4- b¡ä]Dithiophene with Low-Lying Highest Occupied Molecular Orbital Energy Levels for Organic Photovoltaics. ACS Appl. Mater. Interfaces 2009, 1, 1613¨C1621."
1461,CC1=CC2=C(C(SC(C)=C3)=C3C(C4=C5C=C(CC(CCCCCCCC)CCCCCC)S4)=C2C6=C5C=C(CC(CCCCCC)CCCCCCCC)S6)S1,HMPQTN,5.39,2.72,0.76,5.02,0.531,2.03,"Xiao, S.; Stuart, A. C.; Liu, S.; Zhou, H.; You, W. Conjugated Polymer Based on Polycyclic Aromatics for Bulk Heterojunction Organic Solar Cells: A Case Study of Quadrathienonaphthalene Polymers with 2% Efficiency. Adv. Funct. Mater. 2010, 20, 635¨C643. "
1462,CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C43)=C5)=C5C(C6=C7C=C(CC(CCCCCCCC)CCCCCC)S6)=C2C8=C7C=C(CC(CCCCCC)CCCCCCCC)S8)S1,PQTNBT,5.38,3.34,0.72,5.69,0.503,2.06,"Xiao, S.; Stuart, A. C.; Liu, S.; Zhou, H.; You, W. Conjugated Polymer Based on Polycyclic Aromatics for Bulk Heterojunction Organic Solar Cells: A Case Study of Quadrathienonaphthalene Polymers with 2% Efficiency. Adv. Funct. Mater. 2010, 20, 635¨C643. "
1463,CC1=CC(C(CCCCCCCC)(CCCCCCCC)C2=CC(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=C4N=C(C7=CC=C(CCCCCCCC)S7)C(C8=CC=C(CCCCCCCC)S8)=N6)S3)=CC=C29)=C9C=C1,PFTTQx,5.26,3.4,0.9,7.4,0.59,4.4,"Zhang, J.; Cai, W.; Huang, F.; Wang, E.; Zhong, C.; Liu, S.; Wang, M.; Duan, C.; Yang, T.; Cao, Y. Synthesis of Quinoxaline-Based Donor-Acceptor Narrow-Band-Gap Polymers and Their Cyclized Derivatives for Bulk-Heterojunction Polymer Solar Cell Applications. Macromolecules 2011, 44, 894¨C901. "
1464,CC1=CC(C(CCCCCCCC)(CCCCCCCC)C2=CC(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=C4N=C(C7=C8C=C(CCCCCCCC)S7)C(C9=C8C=C(CCCCCCCC)S9)=N6)S3)=CC=C2%10)=C%10C=C1,PFTTPz,5.21,3.53,0.85,4.7,0.51,2.1,"Zhang, J.; Cai, W.; Huang, F.; Wang, E.; Zhong, C.; Liu, S.; Wang, M.; Duan, C.; Yang, T.; Cao, Y. Synthesis of Quinoxaline-Based Donor-Acceptor Narrow-Band-Gap Polymers and Their Cyclized Derivatives for Bulk-Heterojunction Polymer Solar Cell Applications. Macromolecules 2011, 44, 894¨C901. "
1465,CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=CC(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=C4N=C(C7=CC=C(CCCCCCCC)S7)C(C8=CC=C(CCCCCCCC)S8)=N6)S3)=CC=C29)=C9C=C1,PCzTTQx,5.23,3.33,0.88,6.6,0.53,3.5,"Zhang, J.; Cai, W.; Huang, F.; Wang, E.; Zhong, C.; Liu, S.; Wang, M.; Duan, C.; Yang, T.; Cao, Y. Synthesis of Quinoxaline-Based Donor-Acceptor Narrow-Band-Gap Polymers and Their Cyclized Derivatives for Bulk-Heterojunction Polymer Solar Cell Applications. Macromolecules 2011, 44, 894¨C901. "
1466,CC1=CC(N(C(CCCCCCCC)CCCCCCCC)C2=CC(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=C4N=C(C7=C8C=C(CCCCCCCC)S7)C(C9=C8C=C(CCCCCCCC)S9)=N6)S3)=CC=C2%10)=C%10C=C1,PCzTTPz,5.17,3.51,0.75,6.4,0.54,3,"Zhang, J.; Cai, W.; Huang, F.; Wang, E.; Zhong, C.; Liu, S.; Wang, M.; Duan, C.; Yang, T.; Cao, Y. Synthesis of Quinoxaline-Based Donor-Acceptor Narrow-Band-Gap Polymers and Their Cyclized Derivatives for Bulk-Heterojunction Polymer Solar Cell Applications. Macromolecules 2011, 44, 894¨C901. "
1467,CC1=CC2=C(C(C=CC(C3=CC=C(N(C4=CC=C(/C=C\C5=CC=C(C=C(C#N)C#N)S5)C=C4)C6=CC=C(C)C=C6)C=C3)=C7)=C7C2(CCCCCCCC)CCCCCCCC)C=C1,PFDCN,5.3,3.43,0.99,9.62,0.5,4.74,"Huang, F.; Chen, K.-S.; Yip, H.-L.; Hau, S. K.; Acton, O.; Zhang, Y.; Luo, J.; Jen, A. K.-Y. Development of New Conjugated Polymers with Donor-Pi-Bridge-Acceptor Side Chains for High Performance Solar Cells. J. Am. Chem. Soc. 2009, 131, 13886¨C13887. "
1468,CC1=CC2=C(C(C=CC(C3=CC=C(N(C4=CC=C(/C=C\C5=CC=C(C=C6C(N(CC)C(N(CC)C6=O)=S)=O)S5)C=C4)C7=CC=C(C)C=C7)C=C3)=C8)=C8C2(CCCCCCCC)CCCCCCCC)C=C1,PFPDT,5.26,3.5,0.99,9.61,0.46,4.37,"Huang, F.; Chen, K.-S.; Yip, H.-L.; Hau, S. K.; Acton, O.; Zhang, Y.; Luo, J.; Jen, A. K.-Y. Development of New Conjugated Polymers with Donor-Pi-Bridge-Acceptor Side Chains for High Performance Solar Cells. J. Am. Chem. Soc. 2009, 131, 13886¨C13887. "
1469,CC1=CC(/C=C/C2=CC=C(/C=C(C(OCCCCCCCC)=O)/C#N)S2)=C(C3=CC=C(C(C=CC(C)=C4)=C4C5(CCCCCCCC)CCCCCCCC)C5=C3)S1,P2,5.51,2.53,0.8,1.45,0.41,0.48,"Fan, H.; Zhang, Z.; Li, Y.; Zhan, X. Copolymers of Fluorene and Thiophene with Conjugated Side Chain for Polymer Solar Cells: Effect of Pendant Acceptors. J. Polym. Sci. Part A Polym. Chem. 2011, 49, 1462¨C1470. "
1470,CC1=CC(/C=C/C2=CC=C(/C=C(C#N)/C#N)S2)=C(C3=CC=C(C(C=CC(C)=C4)=C4C5(CCCCCCCC)CCCCCCCC)C5=C3)S1,P3,5.51,2.54,0.9,4.33,0.34,1.33,"Fan, H.; Zhang, Z.; Li, Y.; Zhan, X. Copolymers of Fluorene and Thiophene with Conjugated Side Chain for Polymer Solar Cells: Effect of Pendant Acceptors. J. Polym. Sci. Part A Polym. Chem. 2011, 49, 1462¨C1470. "
1471,CC1=CC2=C(C(SC(C3=CC=C(N(C4=CC=C(C)C=C4)C5=CC=C(/C=C\C6=CC=C(/C=C(C#N)/C#N)S6)C=C5)C=C3)=C7)=C7C2(CC(CC)CCCC)CC(CC)CCCC)S1,CPDT-co-TPADCN,5.08,3.38,0.64,4.45,0.4,1.14,"Cheng, Y. J.; Hung, L. -C.; Cao, F. -Y.; Kao, W. -S.; Chang, C. -Y.; Hsu, C. ¨CS. Alternating Copolymers Incorporating Cyclopenta[2,1-b:3,4-b¡¯]dithiophene Unit and Organic Dyes for Photovoltaic Applications. J. Polym. Sci. Part A Polym. Chem. 2011, 49, 1791¨C1801. "
1472,CC1=CC2=C(C(SC(C3=CC=C(N(C4=CC=C(C)C=C4)C5=CC=C(/C=C\C6=CC=C(/C=C7C(N(CC)C(N(CC)C\7=O)=S)=O)S6)C=C5)C=C3)=C8)=C8C2(CC(CC)CCCC)CC(CC)CCCC)S1,CPDT-co-TPADTA,5.06,3.37,0.62,4.65,0.41,1.18,"Cheng, Y. J.; Hung, L. -C.; Cao, F. -Y.; Kao, W. -S.; Chang, C. -Y.; Hsu, C. ¨CS. Alternating Copolymers Incorporating Cyclopenta[2,1-b:3,4-b¡¯]dithiophene Unit and Organic Dyes for Photovoltaic Applications. J. Polym. Sci. Part A Polym. Chem. 2011, 49, 1791¨C1801. "
1473,CC1=CC2=C(C(SC(C3=CC=C(N(C4=CC=C(C)C=C4)C5=CC=C(/C=C\C6=CC=C(/C(C#N)=C(C#N)/C#N)S6)C=C5)C=C3)=C7)=C7C2(CC(CC)CCCC)CC(CC)CCCC)S1,CPDT-co-TPATCN,5.06,3.72,0.58,1.26,0.32,0.22,"Cheng, Y. J.; Hung, L. -C.; Cao, F. -Y.; Kao, W. -S.; Chang, C. -Y.; Hsu, C. ¨CS. Alternating Copolymers Incorporating Cyclopenta[2,1-b:3,4-b¡¯]dithiophene Unit and Organic Dyes for Photovoltaic Applications. J. Polym. Sci. Part A Polym. Chem. 2011, 49, 1791¨C1801. "
1474,CC1=CC2=C(C(SC(C3=CC(C(CCCCCC)(CCCCCC)C4=C5C=CC(N(C6=CC=C(C(C=CC(C)=C7)=C7C8(CCCCCC)CCCCCC)C8=C6)C9=CC=C(/C=C\C%10=CC=C(/C=C(C#N)\C#N)S%10)C=C9)=C4)=C5C=C3)=C%11)=C%11C2(CC(CC)CCCC)CC(CC)CCCC)S1,CPDT-co-FADCN,5.2,3.4,0.79,3.51,0.49,1.36,"Cheng, Y. J.; Hung, L. -C.; Cao, F. -Y.; Kao, W. -S.; Chang, C. -Y.; Hsu, C. ¨CS. Alternating Copolymers Incorporating Cyclopenta[2,1-b:3,4-b¡¯]dithiophene Unit and Organic Dyes for Photovoltaic Applications. J. Polym. Sci. Part A Polym. Chem. 2011, 49, 1791¨C1801. "
1475,CC1=CC2=C(C(SC(C3=CC(C(CCCCCC)(CCCCCC)C4=C5C=CC(N(C6=CC=C(C(C=CC(C)=C7)=C7C8(CCCCCC)CCCCCC)C8=C6)C9=CC=C(/C=C\C%10=CC=C(/C=C%11C(N(CC)C(N(CC)C\%11=O)=S)=O)S%10)C=C9)=C4)=C5C=C3)=C%12)=C%12C2(CC(CC)CCCC)CC(CC)CCCC)S1,CPDT-co-FADTA,5.21,3.52,0.7,4.57,0.43,1.38,"Cheng, Y. J.; Hung, L. -C.; Cao, F. -Y.; Kao, W. -S.; Chang, C. -Y.; Hsu, C. ¨CS. Alternating Copolymers Incorporating Cyclopenta[2,1-b:3,4-b¡¯]dithiophene Unit and Organic Dyes for Photovoltaic Applications. J. Polym. Sci. Part A Polym. Chem. 2011, 49, 1791¨C1801. "
1476,CC1=CC2=C(C(SC(C3=CC(C(CCCCCC)(CCCCCC)C4=C5C=CC(N(C6=CC=C(C(C=CC(C)=C7)=C7C8(CCCCCC)CCCCCC)C8=C6)C9=CC=C(/C=C\C%10=CC=C(/C(C#N)=C(C#N)\C#N)S%10)C=C9)=C4)=C5C=C3)=C%11)=C%11C2(CC(CC)CCCC)CC(CC)CCCC)S1,CPDT-co-FATCN,5.17,3.83,0.7,1.17,0.38,0.31,"Cheng, Y. J.; Hung, L. -C.; Cao, F. -Y.; Kao, W. -S.; Chang, C. -Y.; Hsu, C. ¨CS. Alternating Copolymers Incorporating Cyclopenta[2,1-b:3,4-b¡¯]dithiophene Unit and Organic Dyes for Photovoltaic Applications. J. Polym. Sci. Part A Polym. Chem. 2011, 49, 1791¨C1801. "
1477,CC1=C(CCCCCC)C(CCCCCC)=C(C2=NN=C(C3=C(CCCCCC)C(CCCCCC)=C(C4=CC=C(C)S4)S3)O2)S1,P1,5.55,3.26,0.81,0.713,0.498,0.28,"Higashihara, T.; Wu, H. C.; Mizobe, T.; Lu, C.; Ueda, M.; Chen, W. C. Synthesis of Thiophene-Based ¦Ð-Conjugated Polymers Containing Oxadiazole or Thiadiazole Moieties and Their Application to Organic Photovoltaics. Macromolecules 2012, 45, 9046¨C9055. "
1478,CC1=C(CCCCCC)C(CCCCCC)=C(C2=NN=C(C3=C(CCCCCC)C(CCCCCC)=C(C4=CC=C(C)S4)S3)S2)S1,P2,5.33,3.23,0.8,6.6,0.576,3.04,"Higashihara, T.; Wu, H. C.; Mizobe, T.; Lu, C.; Ueda, M.; Chen, W. C. Synthesis of Thiophene-Based ¦Ð-Conjugated Polymers Containing Oxadiazole or Thiadiazole Moieties and Their Application to Organic Photovoltaics. Macromolecules 2012, 45, 9046¨C9055. "
1479,CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(/C=C/C)S3)C3=C2OCCCCCCCCCCCC,H3,5.07,3.04,0.56,1.16,0.38,0.25,"Hou, J.; Park, M.; Zhang, S.; Yao, Y.; Chen, L.-M.; Li, J.-H.; Yang, Y. Bandgap and Molecular Energy Level Control of Conjugated Polymer Photovoltaic Materials Based on Benzo[1,2- B?:4,5- B¡¯]dithiophene. Macromolecules 2008, 41, 6012¨C6018. "
1480,CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=CC=C(C)S3)S4)C4=C2OCCCCCCCCCCCC,H6,5.05,2.99,0.75,3.78,0.56,1.6,"Hou, J.; Park, M.; Zhang, S.; Yao, Y.; Chen, L.-M.; Li, J.-H.; Yang, Y. Bandgap and Molecular Energy Level Control of Conjugated Polymer Photovoltaic Materials Based on Benzo[1,2- B?:4,5- B¡¯]dithiophene. Macromolecules 2008, 41, 6012¨C6018. "
1481,CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=C4C(OCCO4)=C(C)S3)S5)C5=C2OCCCCCCCCCCCC,H8,4.56,2.59,0.37,2.46,0.4,0.36,"Hou, J.; Park, M.; Zhang, S.; Yao, Y.; Chen, L.-M.; Li, J.-H.; Yang, Y. Bandgap and Molecular Energy Level Control of Conjugated Polymer Photovoltaic Materials Based on Benzo[1,2- B?:4,5- B¡¯]dithiophene. Macromolecules 2008, 41, 6012¨C6018. "
1482,CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=CC=C(C)C4=C3N=C(C5=CC=CC=C5)C(C6=CC=CC=C6)=N4)S7)C7=C2OCCCCCCCCCCCC,H1,4.78,3.15,0.6,1.54,0.26,0.23,"Hou, J.; Park, M.; Zhang, S.; Yao, Y.; Chen, L.-M.; Li, J.-H.; Yang, Y. Bandgap and Molecular Energy Level Control of Conjugated Polymer Photovoltaic Materials Based on Benzo[1,2- B?:4,5- B¡¯]dithiophene. Macromolecules 2008, 41, 6012¨C6018. "
1483,CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=CC=C(C)C4=NSN=C43)S5)C5=C2OCCCCCCCCCCCC,H7,5.1,3.4,0.68,2.97,0.44,0.9,"Hou, J.; Park, M.; Zhang, S.; Yao, Y.; Chen, L.-M.; Li, J.-H.; Yang, Y. Bandgap and Molecular Energy Level Control of Conjugated Polymer Photovoltaic Materials Based on Benzo[1,2- B?:4,5- B¡¯]dithiophene. Macromolecules 2008, 41, 6012¨C6018. "
1484,CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=C4C(N=CC=N4)=C(C)S3)S5)C5=C2OCCCCCCCCCCCC,H9,4.65,3.6,0.22,1.41,0.35,0.11,"Hou, J.; Park, M.; Zhang, S.; Yao, Y.; Chen, L.-M.; Li, J.-H.; Yang, Y. Bandgap and Molecular Energy Level Control of Conjugated Polymer Photovoltaic Materials Based on Benzo[1,2- B?:4,5- B¡¯]dithiophene. Macromolecules 2008, 41, 6012¨C6018. "
1485,CC(S1)=CC2=C1C(OCCCCCCCCCCCC)=C(C=C(C3=CC=C(C)C4=N[Se]N=C43)S5)C5=C2OCCCCCCCCCCCC,H11,4.88,3.36,0.55,1.05,0.32,0.18,"Hou, J.; Park, M.; Zhang, S.; Yao, Y.; Chen, L.-M.; Li, J.-H.; Yang, Y. Bandgap and Molecular Energy Level Control of Conjugated Polymer Photovoltaic Materials Based on Benzo[1,2- B?:4,5- B¡¯]dithiophene. Macromolecules 2008, 41, 6012¨C6018. "
1486,CC1=CC(CCC(CC)CCCCC)=C(C2=CC=C(C3=C(CCC(CCCCC)CC)C=C(C4=CC=C(C5=C(N=C(C6=CC=C(OCCC(CCCCC)CC)C=C6)C(C7=CC=C(OCCC(CC)CCCCC)C=C7)=N8)C8=C(C9=CC=C(C)S9)C=C5)S4)S3)S2)S1,P3TDTQ,5.37,3.67,0.67,1.82,0.46,0.56,"Lee, W.; Lee, S. K.; Son, S. K.; Choi, J.; Shin, W. S.; Kim, K.; Lee, S.; Moon, S.; Kang, I. Synthesis and Characterization of New Selenophene-Based Conjugated Polymers for Organic Photovoltaic Cells. Macromolecules 2012, 45, 1303?1312. "
1487,CC1=CC(CCC(CC)CCCCC)=C(C2=CC=C(C3=C(CCC(CCCCC)CC)C=C(C4=CC=C(C5=C(N=C(C6=CC=C(OCCC(CCCCC)CC)C=C6)C(C7=CC=C(OCCC(CC)CCCCC)C=C7)=N8)C8=C(C9=CC=C(C)S9)C=C5)S4)[Se]3)[Se]2)[Se]1,P3SDTQ,5.35,3.72,0.63,2.48,0.45,0.72,"Lee, W.; Lee, S. K.; Son, S. K.; Choi, J.; Shin, W. S.; Kim, K.; Lee, S.; Moon, S.; Kang, I. Synthesis and Characterization of New Selenophene-Based Conjugated Polymers for Organic Photovoltaic Cells. Macromolecules 2012, 45, 1303?1312. "
1488,CC1=CC(CCC(CC)CCCCC)=C(C2=CC=C(C3=C(CCC(CCCCC)CC)C=C(C4=CC=C(C5=C6C(C(N5CC(CC)CCCC)=O)=C(C7=CC=C(C)S7)N(CC(CC)CCCC)C6=O)S4)S3)S2)S1,P3TDTDPP,5.21,3.94,0.54,10.65,0.56,3.18,"Lee, W.; Lee, S. K.; Son, S. K.; Choi, J.; Shin, W. S.; Kim, K.; Lee, S.; Moon, S.; Kang, I. Synthesis and Characterization of New Selenophene-Based Conjugated Polymers for Organic Photovoltaic Cells. Macromolecules 2012, 45, 1303?1312. "
1489,CC1=CC(CCC(CC)CCCCC)=C(C2=CC=C(C3=C(CCC(CCCCC)CC)C=C(C4=CC=C(C5=C6C(C(N5CC(CC)CCCC)=O)=C(C7=CC=C(C)S7)N(CC(CC)CCCC)C6=O)S4)[Se]3)[Se]2)[Se]1,P3SDTDPP,5.16,3.91,0.51,12.33,0.45,2.81,"Lee, W.; Lee, S. K.; Son, S. K.; Choi, J.; Shin, W. S.; Kim, K.; Lee, S.; Moon, S.; Kang, I. Synthesis and Characterization of New Selenophene-Based Conjugated Polymers for Organic Photovoltaic Cells. Macromolecules 2012, 45, 1303?1312. "
1490,FC1=C(C)C2=NSN=C2C(C3=CC=C(C4=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C5=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C6=CC=C(C)[Se]6)S5)S4)[Se]3)=C1F,P(FBT-alt-Se2Th2),5.39,3.7,0.7,15.8,0.664,7.34,"Wu, J.-S.; Jheng, J.-F.; Chang, J.-Y.; Lai, Y.-Y.; Wu, K.-Y.; Wang, C.-L.; Hsu, C.-S. Synthesis and Morphological Studies of a poly(5,6-Difluorobenzo-2,1,3-Thiadiazole-4,7-Diyl-Alt-Quaterchalcogenophene Copolymer with 7.3% Polymer Solar Cell Efficiency. Polym. Chem. 2014, 5, 6472¨C6479. "
1491,CC1=C(CCCCCCCCCCCC)C(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1,H12,5.28,3.33,0.77,6.09,0.53,2.49,"Jo, J. W.; Jung, J. W.; Wang, H. W.; Kim, P.; Russell, T. P.; Jo, W. H. Fluorination of Polythiophene Derivatives for High Performance Organic Photovoltaics. Chem. Mater.2014, 26, 4214¨C4220. "
1492,CC1=C(CC(CC)CCCC)C(CC(CCCC)CC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1,HEH,5.27,3.31,0.8,4.04,0.43,1.39,"Jo, J. W.; Jung, J. W.; Wang, H. W.; Kim, P.; Russell, T. P.; Jo, W. H. Fluorination of Polythiophene Derivatives for High Performance Organic Photovoltaics. Chem. Mater.2014, 26, 4214¨C4220. "
1493,CC1=C(CCCCCCCCCCCC)C(CCCCCCCCCCCC)=C(C2=CC(F)=C(C3=C(F)C=C(C)S3)S2)S1,F12,5.4,3.45,0.84,5.93,0.61,3.04,"Jo, J. W.; Jung, J. W.; Wang, H. W.; Kim, P.; Russell, T. P.; Jo, W. H. Fluorination of Polythiophene Derivatives for High Performance Organic Photovoltaics. Chem. Mater.2014, 26, 4214¨C4220. "
1494,CC1=C(CC(CC)CCCC)C(CC(CCCC)CC)=C(C2=CC(F)=C(C3=C(F)C=C(C)S3)S2)S1,FEH,5.42,3.51,0.87,9.82,0.61,5.2,"Jo, J. W.; Jung, J. W.; Wang, H. W.; Kim, P.; Russell, T. P.; Jo, W. H. Fluorination of Polythiophene Derivatives for High Performance Organic Photovoltaics. Chem. Mater.2014, 26, 4214¨C4220. "
1495,CC1=CC2=C(C(SC(C3=C(F)C(F)=C(C4=CC=C(C5=C(F)C(F)=C(C)S5)C6=NSN=C46)S3)=C7)=C7[Ge]2(CC(CCCCCCCC)CCCCCCCCCC)CC(CCCCCCCCCC)CCCCCCCC)S1,PGeTFDTBT,5.28,3.72,0.71,13.51,0.57,5.47,"Fei, Z.; Shahid, M.; Yaacobi-Gross, N.; Rossbauer, S.; Zhong, H.; Watkins, S. E.; Anthopoulos, T. D.; Heeney, M. Thiophene Fluorination to Enhance Photovoltaic Performance in Low Band Gap Donor¨Cacceptor Polymers. Chem. Commun. 2012, 48, 11130¨C11132. "
1496,CC1=CC2=C(C(SC(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NSN=C46)S3)=C7)=C7[Ge]2(CC(CCCCCCCC)CCCCCCCCCC)CC(CCCCCCCCCC)CCCCCCCC)S1,PGeDTBT,5.04,3.47,0.66,7.46,0.68,3.51,"Fei, Z.; Shahid, M.; Yaacobi-Gross, N.; Rossbauer, S.; Zhong, H.; Watkins, S. E.; Anthopoulos, T. D.; Heeney, M. Thiophene Fluorination to Enhance Photovoltaic Performance in Low Band Gap Donor¨Cacceptor Polymers. Chem. Commun. 2012, 48, 11130¨C11132. "
1497,CC1=C(SCCCCCCCC)C=C(C2=CC(SCCCCCCCC)=C(C3=C4C(C=C(C(CCCCCCCC)=O)S4)=C(C)S3)S2)S1,PK,4.8,3.49,0.454,4.82,0.51,1.11,"Morvillo, P.; Diana, R.; Fontanesi, C.; Ricciardi, R.; Lanzi, M.; Mucci, A.; Tassinari, F.; Schenetti, L.; Minarini, C.; Parenti, F. Low Band Gap Polymers for Application in Solar Cells: Synthesis and Characterization of Thienothiophene¨Cthiophene Copolymers. Polym. Chem. 2014, 5, 2391¨C2400. "
1498,CC1=C(SCCCCCCCC)C=C(C2=CC(SCCCCCCCC)=C(C3=C4C(C=C(C(OCCCCCCCC)=O)S4)=C(C)S3)S2)S1,PE,4.77,3.46,0.387,5.56,0.4,0.87,"Morvillo, P.; Diana, R.; Fontanesi, C.; Ricciardi, R.; Lanzi, M.; Mucci, A.; Tassinari, F.; Schenetti, L.; Minarini, C.; Parenti, F. Low Band Gap Polymers for Application in Solar Cells: Synthesis and Characterization of Thienothiophene¨Cthiophene Copolymers. Polym. Chem. 2014, 5, 2391¨C2400. "
1499,CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC(CCCCCCCCCCCC)=C(C6=CC=C(C7=CC=C(C8=C(CCCCCCCCCCCC)C=C(C)[Se]8)[Se]7)[Se]6)[Se]5)[Se]4)[Se]3)[Se]2)[Se]1,PQS,5.2,3.47,0.57,8.6,0.48,2.37,"Lee, W. H.; Lee, S. K.; Shin, W. S.; Moon, S. J.; Lee, S. H.; Kang, I. N. Synthesis and Photovolatic Properties of New Poly(quarterselenophene and Poly(quarterselenopheneAlt-Quarterthiophenes. Sol. Energy Mater. Sol. Cells 2013, 117, 161¨C167."
1500,CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC(CCCCCCCCCCCC)=C(C6=CC=C(C7=CC=C(C8=C(CCCCCCCCCCCC)C=C(C)[Se]8)[Se]7)[Se]6)[Se]5)S4)S3)S2)S1,PQSQT,5.17,3.31,0.44,9.77,0.51,2.22,"Lee, W. H.; Lee, S. K.; Shin, W. S.; Moon, S. J.; Lee, S. H.; Kang, I. N. Synthesis and Photovolatic Properties of New Poly(quarterselenophene and Poly(quarterselenopheneAlt-Quarterthiophenes. Sol. Energy Mater. Sol. Cells 2013, 117, 161¨C167."
1501,O=C1C2=C(C=C(CCCCCC)C(CCCCCC)=C2)C(C3=C(C)SC(C4=CC5=C(C(OCC(CCCC)CC)=C(C=C(C)S6)C6=C5OCC(CCCC)CC)S4)=C31)=O,BDT-C6,5.4,3.5,0.83,1.81,0.3,0.45,"Ie, Y.; Huang, J.; Uetani, Y.; Karakawa, M.; Aso, Y. Synthesis, Properties, and Photovoltaic Performances of Donor-Acceptor Copolymers Having DioxocycloalkeneAnnelated Thiophenes as Acceptor Monomer Units. Macromolecules 2012, 45, 4564¨C4571. "
1502,CC1=CC2=C(C(SC(C3=CC(CCCCCCCC)=C(C4=CC=C(C5=C(CCCCCCCC)C=C(C)S5)C6=NSN=C46)S3)=C7)=C7N2C8=CC=C(CCCCCCCC)C=C8)S1,PDTPTBT,5.27,3.57,0.55,8.91,0.421,2.04,"Tamilavan, V.; Song, M.; Kim, S.; Agneeswari, R.; Kang, J. W.; Hyun, M. H. Synthesis of N-[4-Octylphenyl]dithieno[3,2-b:2¡ä,3¡ä-d]pyrrole- Based Broad Absorbing Polymers and Their Photovoltaic Applications. Polymer 2013, 54, 3198¨C3205. "
1503,CC(S1)=CC2=C1C(C3=CC(CCCCCC)=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C)C5=NSN=C54)S6)C6=C2C7=CC(CCCCCC)=C(CC(CCCC)CC)S7,PBDT-BT,5.45,3.7,0.92,15.4,0.64,9.4,"Subbiah, J.; Purushothaman, B.; Chen, M.; Qin, T.; Gao, M.; Vak, D.; Scholes, F. H.; Chen, X.; Watkins, S. E.; Wilson, G. J.; Holmes, A. B.; Wong, W. W. H.; Jones, D. J. Organic Solar Cells Using a High-Molecular-Weight Benzodithiophene-Benzothiadiazole Copolymer with an Efficiency of 9.4%. Adv. Mater. 2015, 27, 702¨C705. "
1504,CC1=C(CCCCCC)C(CCCCCC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1,PDHTT,5.15,3.19,0.716,8.54,0.66,4.2,"Ko, S.; Verploegen, E.; Hong, S.; Mondal, R.; Hoke, E. T.; Toney, M. F.; McGehee, M. D.; Bao, Z. 3,4-Disubstituted Polyalkylthiophenes for High-Performance Thin-Film Transistors and Photovoltaics. J. Am. Chem. Soc. 2011, 133, 16722¨C16725. "
1505,CC1=C(CCCCCCCC)C(CCCCCCCC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1,PDOTT,5.14,3.17,0.754,7.96,0.67,4.23,"Ko, S.; Verploegen, E.; Hong, S.; Mondal, R.; Hoke, E. T.; Toney, M. F.; McGehee, M. D.; Bao, Z. 3,4-Disubstituted Polyalkylthiophenes for High-Performance Thin-Film Transistors and Photovoltaics. J. Am. Chem. Soc. 2011, 133, 16722¨C16725. "
1506,CC1=C(CCCCCCCCCCCC)C(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C)S3)S2)S1,PDDTT,5.17,3.18,0.771,6.42,0.65,3.53,"Ko, S.; Verploegen, E.; Hong, S.; Mondal, R.; Hoke, E. T.; Toney, M. F.; McGehee, M. D.; Bao, Z. 3,4-Disubstituted Polyalkylthiophenes for High-Performance Thin-Film Transistors and Photovoltaics. J. Am. Chem. Soc. 2011, 133, 16722¨C16725. "
1507,CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(/C=C/C)S3)C4=NSN=C24)S1,PDTBTV,5.01,3.03,0.43,3.15,0.335,0.46,"Cardone, A.; Martinelli, C.; Losurdo, M.; Dilonardo, E.; Bruno, G.; Scavia, G.; Destri, S.; Cosma, P.; Salamandra, L.; Reale, A.; Di Carlo, A.; Aguirre, A.; Mili¨¢n-Medina, B.; Gierschner, J.; Farinola, G. M. Fluoro-Functionalization of Vinylene Units in a Polyarylenevinylene for Polymer Solar Cells. J. Mater. Chem. A 2013, 1, 715¨C727. "
1508,CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(/C(F)=C(F)/C)S3)C4=NSN=C24)S1,PDTBTFV,5.2,3.14,0.83,4.32,0.346,1.24,"Cardone, A.; Martinelli, C.; Losurdo, M.; Dilonardo, E.; Bruno, G.; Scavia, G.; Destri, S.; Cosma, P.; Salamandra, L.; Reale, A.; Di Carlo, A.; Aguirre, A.; Mili¨¢n-Medina, B.; Gierschner, J.; Farinola, G. M. Fluoro-Functionalization of Vinylene Units in a Polyarylenevinylene for Polymer Solar Cells. J. Mater. Chem. A 2013, 1, 715¨C727. "
1509,CC1=NC2=C(C=C(OC(/C=C/C3=C(CCCCCCCCCCCC)C(CCCCCCCCCCCC)=C(/C=C/C)S3)=N4)C4=C2)O1,PTVcBBO,5.19,3.02,0.35,0.12,0.26,0.01,"Mike, J. F.; Nalwa, K.; Makowski, A. J.; Putnam, D.; Tomlinson, A. L.; Chaudhary, S.; Jeffries-EL, M. Synthesis, Characterization and Photovoltaic Properties of Poly(thiophenevinylene-Alt-Benzobisoxazoles. Phys. Chem. Chem. Phys. 2011, 13, 1338¨C1344. "
1510,CC1=NC2=C(C=C(N=C(/C=C/C3=C(CCCCCCCCCCCC)C(CCCCCCCCCCCC)=C(/C=C/C)S3)O4)C4=C2)O1,PTVtBBO,5.14,3.1,0.4,0.66,0.31,0.08,"Mike, J. F.; Nalwa, K.; Makowski, A. J.; Putnam, D.; Tomlinson, A. L.; Chaudhary, S.; Jeffries-EL, M. Synthesis, Characterization and Photovoltaic Properties of Poly(thiophenevinylene-Alt-Benzobisoxazoles. Phys. Chem. Chem. Phys. 2011, 13, 1338¨C1344. "
1511,CC1=CC(CCCCCCCCCCCC)=C(/C=C/C2=C(CCCCCCCCCCCC)C=C(C)S2)S1,PEBT,5.3,3.65,0.57,2.33,0.4,0.53,"Jang, S.-Y.; Lim, B.; Yu, B.-K.; Kim, J.; Baeg, K.-J.; Khim, D.; Kim, D.-Y. Synthesis and Characterization of Low-Band-Gap Poly(thienylenevinylene Derivatives for Polymer Solar Cells. J. Mater. Chem. 2011, 21, 11822¨C11830. "
1512,CC1=CC(CCCCCCCCCCCC)=C(/C=C/C2=C(CCCCCCCCCCCC)C=C(C3=CC=C(C)C4=NSN=C34)S2)S1,PEBTBT,4.89,3.69,0.45,4.16,0.57,1.07,"Jang, S.-Y.; Lim, B.; Yu, B.-K.; Kim, J.; Baeg, K.-J.; Khim, D.; Kim, D.-Y. Synthesis and Characterization of Low-Band-Gap Poly(thienylenevinylene Derivatives for Polymer Solar Cells. J. Mater. Chem. 2011, 21, 11822¨C11830. "
1513,CC1=CC(CCCCCCCCCCCC)=C(/C=C/C2=C(CCCCCCCCCCCC)C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NSN=C46)S3)S2)S1,PEBTBTTBT,4.95,3.39,0.6,4.41,0.4,1.04,"Jang, S.-Y.; Lim, B.; Yu, B.-K.; Kim, J.; Baeg, K.-J.; Khim, D.; Kim, D.-Y. Synthesis and Characterization of Low-Band-Gap Poly(thienylenevinylene Derivatives for Polymer Solar Cells. J. Mater. Chem. 2011, 21, 11822¨C11830. "
1514,CC1=CC2=C(C(C=CC(C3=CC(/C=C/C4=CC=C(/C=C(C(OCCCCCCCC)=O)\C#N)S4)=C(C)S3)=C5)=C5N2C(CCCCCCCC)CCCCCCCC)C=C1,PCzTh-TVCN,5.57,3.39,0.99,3.72,0.361,1.33,"Zhang, Z.-G.; Fan, H.; Min, J.; Zhang, S.; Zhang, J.; Zhang, M.; Guo, X.; Zhan, X.; Li, Y. Synthesis and Photovoltaic Properties of Copolymers of Carbazole and Thiophene with Conjugated Side Chain Containing Acceptor End Groups. Polym. Chem. 2011, 2, 1678¨C1687. "
1515,CC1=CC2=C(C(C=CC(C3=CC(/C=C/C4=CC=C(/C=C(C#N)\C#N)S4)=C(C)S3)=C5)=C5N2C(CCCCCCCC)CCCCCCCC)C=C1,PCzTh-TVDCN,5.6,3.55,1.03,5.75,0.365,2.16,"Zhang, Z.-G.; Fan, H.; Min, J.; Zhang, S.; Zhang, J.; Zhang, M.; Guo, X.; Zhan, X.; Li, Y. Synthesis and Photovoltaic Properties of Copolymers of Carbazole and Thiophene with Conjugated Side Chain Containing Acceptor End Groups. Polym. Chem. 2011, 2, 1678¨C1687. "
1516,CC1=CC2=C(C(C=CC(C3=CC(/C=C/C4=CC=C(/C=C5C(N(CC)C(N(CC)C/5=O)=S)=O)S4)=C(C)S3)=C6)=C6N2C(CCCCCCCC)CCCCCCCC)C=C1,PCzTh-TVDT,5.59,3.65,0.96,4.67,0.291,1.3,"Zhang, Z.-G.; Fan, H.; Min, J.; Zhang, S.; Zhang, J.; Zhang, M.; Guo, X.; Zhan, X.; Li, Y. Synthesis and Photovoltaic Properties of Copolymers of Carbazole and Thiophene with Conjugated Side Chain Containing Acceptor End Groups. Polym. Chem. 2011, 2, 1678¨C1687. "
1517,CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC=C(C6=C7C(C(N6CC(CCCC)CC)=O)=C(C8=CC=C(C)S8)N(CC(CC)CCCC)C7=O)S5)S4)S3)S2)S1,PQTDPP,5.19,3.64,0.58,7.16,0.55,2.28,"Son, S. K.; Kim, B. S.; Lee, C.-Y.; Lee, J. S.; Cho, J. H.; Ko, M. J.; Lee, D.-K.; Kim, H.; Choi, D. H.; Kim, K. Synthesis and Photovoltaic Properties of Low Band Gap Quarterthiophenes-Alt-Diketopyrrolopyrroles Polymers Having High Hole Mobility. Sol. Energy Mater. Sol. Cells 2012, 104, 185¨C192. "
1518,CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(/C=C/C3=CC=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC=C(C6=C7C(C(N6CC(CCCC)CC)=O)=C(C8=CC=C(C)S8)N(CC(CC)CCCC)C7=O)S5)S4)S3)S2)S1,PQTVTDPP,5.05,3.66,0.5,7.6,0.51,1.97,"Son, S. K.; Kim, B. S.; Lee, C.-Y.; Lee, J. S.; Cho, J. H.; Ko, M. J.; Lee, D.-K.; Kim, H.; Choi, D. H.; Kim, K. Synthesis and Photovoltaic Properties of Low Band Gap Quarterthiophenes-Alt-Diketopyrrolopyrroles Polymers Having High Hole Mobility. Sol. Energy Mater. Sol. Cells 2012, 104, 185¨C192. "
1519,CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(C(C=C(CCCCCC)C=C5)=C5C4=O)=O)=C(C)S3)S6)C6=C2OCC(CCCC)CC)S1,PBDTNTDO-1,5.14,3.28,0.81,4.71,0.287,1.09,"Cui, C.; Fan, H.; Guo, X.; Zhang, M.; He, Y.; Zhan, X.; Li, Y. Synthesis and Photovoltaic Properties of D¨CA Copolymers of Benzodithiophene and naphtho[2,3-c]thiophene-4,9-Dione. Polym. Chem. 2012, 3, 99¨C104. "
1520,CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(C(C=C(C(C)(C)C)C=C5)=C5C4=O)=O)=C(C)S3)S6)C6=C2OCC(CCCC)CC)S1,PBDTNTDO-2,5.19,3.3,0.88,5.67,0.305,1.52,"Cui, C.; Fan, H.; Guo, X.; Zhang, M.; He, Y.; Zhan, X.; Li, Y. Synthesis and Photovoltaic Properties of D¨CA Copolymers of Benzodithiophene and naphtho[2,3-c]thiophene-4,9-Dione. Polym. Chem. 2012, 3, 99¨C104. "
1521,CC1=CC2=C(OCC(CCCC)CC)C3=C(C=C(C4=C5C(C(C(C=C(OCCCCCCCC)C(OCCCCCCCC)=C6)=C6C5=O)=O)=C(C)S4)S3)C(OCC(CC)CCCC)=C2S1,PBDTNTDO-C1,5.19,3.38,0.87,4.42,0.508,1.96,"Chen, X.; Liu, B.; Zou, Y.; Tang, W.; Li, Y.; Xiao, D. Copolymers from naphtho[2,3-c]thiophene-4,9-Dione Derivatives and Benzodithiophene: Synthesis and Photovoltaic Applications. RSC Adv. 2012, 2, 7439¨C7448. "
1522,CC1=CC2=C(OCC(CCCC)CC)C3=C(C=C(C4=C5C(C(C(C=C(OCCCCCCCC)C=C6)=C6C5=O)=O)=C(C)S4)S3)C(OCC(CC)CCCC)=C2S1,PBDTNTDO-C2,5.23,3.33,0.71,4.21,0.34,1.01,"Chen, X.; Liu, B.; Zou, Y.; Tang, W.; Li, Y.; Xiao, D. Copolymers from naphtho[2,3-c]thiophene-4,9-Dione Derivatives and Benzodithiophene: Synthesis and Photovoltaic Applications. RSC Adv. 2012, 2, 7439¨C7448. "
1523,CC1=CC2=C(OCC(CCCC)CC)C3=C(C=C(C4=C5C(C(C(C=C(CCCCCCCC)C=C6)=C6C5=O)=O)=C(C)S4)S3)C(OCC(CC)CCCC)=C2S1,PBDTNTDO-C3,5.27,3.39,0.81,4.93,0.552,2.21,"Chen, X.; Liu, B.; Zou, Y.; Tang, W.; Li, Y.; Xiao, D. Copolymers from naphtho[2,3-c]thiophene-4,9-Dione Derivatives and Benzodithiophene: Synthesis and Photovoltaic Applications. RSC Adv. 2012, 2, 7439¨C7448. "
1524,CC1=CC2=C(C3=CC=C(CC(CC)CCCC)S3)C4=C(C=C(C5=CC=C(C(N(CC(CCCC)CCCCCC)C6=O)=C7C6=C(C8=CC=C(C)S8)N(CC(CCCCCC)CCCC)C7=O)S5)S4)C(C9=CC=C(CC(CCCC)CC)S9)=C2S1,PBDTT-DPP,5.3,3.63,0.73,14,0.65,6.6,"Dou, L.; Gao, J.; Richard, E.; You, J.; Chen, C. C.; Cha, K. C.; He, Y.; Li, G.; Yang, Y. Systematic Investigation of Benzodithiophene- and Diketopyrrolopyrrole- Based LowBandgap Polymers Designed for Single Junction and Tandem Polymer Solar Cells. J. Am. Chem. Soc. 2012, 134, 10071¨C10079. "
1525,CC1=CC2=C(C(C=C3)=CC=C3CC(CC)CCCC)C4=C(C=C(C5=CC=C(C(N(CC(CCCC)CCCCCC)C6=O)=C7C6=C(C8=CC=C(C)S8)N(CC(CCCCCC)CCCC)C7=O)S5)S4)C(C(C=C9)=CC=C9CC(CCCC)CC)=C2S1,PBDTP-DPP,5.35,3.56,0.76,13.6,0.6,6.2,"Dou, L.; Gao, J.; Richard, E.; You, J.; Chen, C. C.; Cha, K. C.; He, Y.; Li, G.; Yang, Y. Systematic Investigation of Benzodithiophene- and Diketopyrrolopyrrole- Based LowBandgap Polymers Designed for Single Junction and Tandem Polymer Solar Cells. J. Am. Chem. Soc. 2012, 134, 10071¨C10079. "
1526,CC1=CC2=C(C3=CC=C(CC(CC)CCCC)S3)C4=C(C=C(C5=CC=C(C(N(CC(CCCC)CC)C6=O)=C7C6=C(C8=CC=C(C)O8)N(CC(CC)CCCC)C7=O)O5)S4)C(C9=CC=C(CC(CCCC)CC)S9)=C2S1,PBDTT-FDPP,5.26,3.64,0.77,13.8,0.55,5.8,"Dou, L.; Gao, J.; Richard, E.; You, J.; Chen, C. C.; Cha, K. C.; He, Y.; Li, G.; Yang, Y. Systematic Investigation of Benzodithiophene- and Diketopyrrolopyrrole- Based LowBandgap Polymers Designed for Single Junction and Tandem Polymer Solar Cells. J. Am. Chem. Soc. 2012, 134, 10071¨C10079. "
1527,CC1=CC2=C(C(C=C3)=CC=C3CC(CC)CCCC)C4=C(C=C(C5=CC=C(C(N(CC(CCCC)CCCCCC)C6=O)=C7C6=C(C8=CC=C(C)O8)N(CC(CCCCCC)CCCC)C7=O)O5)S4)C(C(C=C9)=CC=C9CC(CCCC)CC)=C2S1,PBDTP-FDPP,5.33,3.57,0.77,7.42,0.59,3.3,"Dou, L.; Gao, J.; Richard, E.; You, J.; Chen, C. C.; Cha, K. C.; He, Y.; Li, G.; Yang, Y. Systematic Investigation of Benzodithiophene- and Diketopyrrolopyrrole- Based LowBandgap Polymers Designed for Single Junction and Tandem Polymer Solar Cells. J. Am. Chem. Soc. 2012, 134, 10071¨C10079. "
1528,CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=NC(/C=C/C4=C(CCCCCC)C=C(C5=CC=C(C6=CC(CCCCCC)=CS6)C7=NSN=C75)S4)=C(C)S3)S8)C8=C2OCC(CC)CCCC)S1,PT-Tz-DTBT,5.58,3.65,0.76,7.75,0.45,2.63,"Liu, X.; Huang, Y.; Cao, Z.; Weng, C.; Chen, H.; Tan, S. Synthesis and Photovoltaic Properties of Copolymers Based on benzo[1,2-b:4,5-b¡ä]dithiophene and Thiazole with Different Conjugated Side Groups. Polym. Chem. 2013, 4, 4737¨C4745. "
1529,CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=NC(/C=C/C4=C(CCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CCCCCC)=CS6)C7=NSN=C75)S4)=C(C)S3)S8)C8=C2OCC(CC)CCCC)S1,PT-Tz-DTffBT,5.59,3.57,0.88,10.11,0.5,4.42,"Liu, X.; Huang, Y.; Cao, Z.; Weng, C.; Chen, H.; Tan, S. Synthesis and Photovoltaic Properties of Copolymers Based on benzo[1,2-b:4,5-b¡ä]dithiophene and Thiazole with Different Conjugated Side Groups. Polym. Chem. 2013, 4, 4737¨C4745. "
1530,CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC,PBDTPTD,5.56,3.76,0.85,9.81,0.66,5.5,"Zou, Y.; Najari, A.; Berrouard, P.; Beaupre, S.; A?ch, B. R.; Tao, Y.; Leclerc, M. A Thieno[3,4-c]pyrrole-4, 6-Dione-Based Copolymer for Efficient Solar Cells. J. Am. Chem. Soc. 2010, 132, 5330¨C5331. "
1531,CC1=CC=C(C2=C(CCCCCC)N=C(C3=NC(CCCCCC)=C(C4=CC=C(C5=CC6=C(C(OCCCCCCCC)=C(OCCCCCCCC)C7=C6C=C(C)S7)S5)S4)S3)S2)S1,PBdT-BTz,5.16,2.82,0.88,5.2,0.613,2.81,"Zhang, M.; Sun, Y.; Guo, X.; Cui, C.; He, Y.; Li, Y. Synthesis and Characterization of Dioctyloxybenzo[1,2-b:4,3-b¡ä]dithiophene-Containing Copolymers for Polymer Solar Cells. Macromolecules 2011, 44, 7625¨C7631. "
1532,CC1=C(CCCCCC)C=C(C(S2)=NC3=C2N=C(S3)C4=CC(CCCCCC)=C(C5=CC6=C(C(OCCCCCCCC)=C(OCCCCCCCC)C7=C6C=C(C)S7)S5)S4)S1,PBdT-TTz,5.19,2.9,0.9,5.5,0.687,3.4,"Zhang, M.; Sun, Y.; Guo, X.; Cui, C.; He, Y.; Li, Y. Synthesis and Characterization of Dioctyloxybenzo[1,2-b:4,3-b¡ä]dithiophene-Containing Copolymers for Polymer Solar Cells. Macromolecules 2011, 44, 7625¨C7631. "
1533,CC1=C(CCCCCC)C=C(C2=CC=C(C3=NSN=C32)C4=CC(CCCCCC)=C(C5=CC6=C(C(OCCCCCCCC)=C(OCCCCCCCC)C7=C6C=C(C)S7)S5)S4)S1,PBdT-DTBT,5.09,3.1,0.8,4.58,0.307,1.13,"Zhang, M.; Sun, Y.; Guo, X.; Cui, C.; He, Y.; Li, Y. Synthesis and Characterization of Dioctyloxybenzo[1,2-b:4,3-b¡ä]dithiophene-Containing Copolymers for Polymer Solar Cells. Macromolecules 2011, 44, 7625¨C7631. "
1534,CC1=CC2=C(S1)C(OCCCCCCCC)=C(OCCCCCCCC)C3=C2C=C(S3)C4=CC=C(C5=C6C(C(N5CC(CCCC)CC)=O)=C(C7=CC=C(C)S7)N(CC(CC)CCCC)C6=O)S4,PBdT-DPP,5.01,3.36,0.71,3.28,0.561,1.31,"Zhang, M.; Sun, Y.; Guo, X.; Cui, C.; He, Y.; Li, Y. Synthesis and Characterization of Dioctyloxybenzo[1,2-b:4,3-b¡ä]dithiophene-Containing Copolymers for Polymer Solar Cells. Macromolecules 2011, 44, 7625¨C7631. "
1535,CC1=CC2=C(C3=CC=C(CC(CC)CCCC)[Se]3)C(SC(C4=CC=C(C5=C(OCC(CCCCCCC)(CCCCCCC)CO6)C6=C(C7=CC=C(C)C8=NSN=C78)S5)C9=NSN=C49)=C%10)=C%10C(C%11=CC=C(CC(CC)CCCC)[Se]%11)=C2S1,P1,5.34,3.7,0.65,11.72,0.587,4.51,"Chakravarthi, N.; Kranthiraja, K.; Song, M.; Gunasekar, K.; Jeong, P.; Moon, S. J.; Suk Shin, W.; Kang, I. N.; Lee, J. W.; Jin, S. H. New Alkylselenyl Substituted Benzodithiophene-Based Solution-Processable 2D ¦Ð-Conjugated Polymers for Bulk Heterojunction Polymer Solar Cell Applications. Sol. Energy Mater. Sol. Cells 2014, 122, 136¨C145."
1536,CC1=CC2=C(C3=CC=C(CC(CC)CCCC)[Se]3)C(SC(C4=C(C(N(CC(CC)CCCC)C5=O)=O)C5=C(C)S4)=C6)=C6C(C7=CC=C(CC(CC)CCCC)[Se]7)=C2S1,P2,5.73,3.88,0.68,9.94,0.528,3.58,"Chakravarthi, N.; Kranthiraja, K.; Song, M.; Gunasekar, K.; Jeong, P.; Moon, S. J.; Suk Shin, W.; Kang, I. N.; Lee, J. W.; Jin, S. H. New Alkylselenyl Substituted Benzodithiophene-Based Solution-Processable 2D ¦Ð-Conjugated Polymers for Bulk Heterojunction Polymer Solar Cell Applications. Sol. Energy Mater. Sol. Cells 2014, 122, 136¨C145."
1537,CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C(CC(CCCC)CC)C=C(C4=NN=C(C5=CC(CC(CCCC)CC)=C(C)S5)N=N4)S3)S6)C6=C2OCC(CCCC)CC)S1,PBDT-TTz,5.42,3.58,0.92,6.21,0.58,3.32,"Wen, S.; Dong, Q.; Cheng, W.; Li, P.; Xu, B.; Tian, W. A benzo[1,2-b:4,5-b¡¯]dithiophene-Based Copolymer with Deep HOMO Level for Efficient Polymer Solar Cells. Sol. Energy Mater. Sol. Cells 2012, 100, 239¨C245. "
1538,CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=CC(/C=C/C4=CC=C(C5=CC=C(C6=C7C(C(N6CC(CC)CCCC)=O)=C(C8=CC=CS8)N(CC(CC)CCCC)C7=O)S5)S4)=C(C)S3)S9)C9=C2OCC(CCCC)CC)S1,PBDT-TDPP-S,5.34,3.52,0.84,10.04,0.56,4.89,"Tan, H.; Deng, X.; Yu, J.; Zhao, B.; Wang, Y.; Liu, Y.; Zhu, W.; Wu, H.; Cao, Y. A Novel benzo[1,2- b:4,5- B¡ä]dithiophene-Based Conjugated Polymer with a Pendant Diketopyrrolopyrrole Unit for High-Performance Solar Cells. Macromolecules 2013, 46, 113¨C118. "
1539,CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC4=C(/C(C(N4CC(CCCCCC)CCCCCCCC)=O)=C5C(N(CC(CCCCCC)CCCCCCCC)C6=C\5C=CC(C)=C6)=O)C=C3)S7)C7=C2OCC(CCCC)CC)S1,PBDT-I,5.82,3.88,0.84,3.9,0.46,1.53,"Ma, Z.; Wang, E.; Jarvid, M. E.; Henriksson, P.; Ingan?s, O.; Zhang, F.; Andersson, M. R. Synthesis and Characterization of Benzodithiophene¨Cisoindigo Polymers for Solar Cells. J. Mater. Chem. 2012, 22, 2306¨C2314. "
1540,CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(C4=CC5=C(/C(C(N5CC(CCCCCC)CCCCCCCC)=O)=C6C(N(CC(CCCCCC)CCCCCCCC)C7=C\6C=CC(C8=CC=C(C)S8)=C7)=O)C=C4)S3)S9)C9=C2OCC(CCCC)CC)S1,PBDT-TIT,5.78,3.91,0.79,7.87,0.68,4.22,"Ma, Z.; Wang, E.; Jarvid, M. E.; Henriksson, P.; Ingan?s, O.; Zhang, F.; Andersson, M. R. Synthesis and Characterization of Benzodithiophene¨Cisoindigo Polymers for Solar Cells. J. Mater. Chem. 2012, 22, 2306¨C2314. "
1541,CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=C(CCCCCCCC)C=C(C4=CC5=C(/C(C(N5CC(CCCCCC)CCCCCCCC)=O)=C6C(N(CC(CCCCCC)CCCCCCCC)C7=C\6C=CC(C8=CC(CCCCCCCC)=C(C)S8)=C7)=O)C=C4)S3)S9)C9=C2OCC(CCCC)CC)S1,PBDT-OIO,5.74,3.91,0.73,3.15,0.6,1.39,"Ma, Z.; Wang, E.; Jarvid, M. E.; Henriksson, P.; Ingan?s, O.; Zhang, F.; Andersson, M. R. Synthesis and Characterization of Benzodithiophene¨Cisoindigo Polymers for Solar Cells. J. Mater. Chem. 2012, 22, 2306¨C2314. "
1542,CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=C4C(SC(C(C(CC)CCCC)=O)=C4)=C(C)S3)O5)C5=C2OCC(CC)CCCC)O1,PBDFTT-C,5.27,3.69,0.66,10.45,0.638,4.4,"Liu, B.; Chen, X.; Zou, Y.; He, Y.; Xiao, L.; Xu, X.; Li, L.; Li, Y. A benzo[1,2-b:4,5-b¡ä]difuran- and Thieno-[3,4-b]thiophene-Based Low Bandgap Copolymer for Photovoltaic Applications. Polym. Chem. 2013, 4, 470¨C476. "
1543,CC(C1=NSN=C12)=CC=C2C3=CC(C4=C5SC(C(CCCCCCCC)CCCCCCCC)=C4)=C(S3)C6=C5C=C(C)S6,PBTT-BT (P1),5.09,3.34,0.81,6.07,0.44,2.18,"Nielsen, C. B.; Schroeder, B. C.; Hadipour, A.; Rand, B. P.; Watkins, S. E.; McCulloch, I. A Benzotrithiophene-Based Low Band Gap Polymer for Polymer Solar Cells with High Open-Circuit Voltage. J. Mater. Chem. 2011, 21, 17642¨C17645. "
1544,CC1=CC(C2=C3SC(CCCCCCCCCCCCCCCC)=C2)=C(S1)C4=C3C=C(C5=C6C(C(N(CCCCCCCCCCCC)C6=O)=O)=C(C)S5)S4,PBTTDPP,4.96,3.69,0.67,2.79,0.43,0.8,"Bian, L.; Miao, J.; Hai, J.; Zhu, E.; Yu, J.; Ge, G.; Wu, H.; Tang, W. RSC Advances Benzotrithiophene Polymers with Tuneable Bandgap for Photovoltaic Applications. RSC Adv. 2014, 4, 53939¨C53945. "
1545,CC1=CC(C2=C3SC(CCCCCCCCCCCCCCCC)=C2)=C(S1)C4=C3C=C(C5=CC(OCCCCCCCCCCCCCCCCCCCC)=C(C6=NC(SC(C7=C(OCCCCCCCCCCCCCCCCCCCC)C=C(C)S7)=N8)=C8S6)S5)S4,PBTTTTz,5.15,3.52,0.62,3.09,0.56,1.07,"Bian, L.; Miao, J.; Hai, J.; Zhu, E.; Yu, J.; Ge, G.; Wu, H.; Tang, W. RSC Advances Benzotrithiophene Polymers with Tuneable Bandgap for Photovoltaic Applications. RSC Adv. 2014, 4, 53939¨C53945. "
1546,CC1=CC(C2=C3SC(CCCCCCCCCCCCCCCC)=C2)=C(S1)C4=C3C=C(C5=C6C(C(N(CCCCCCCCCCCC)C6=O)=O)=C(C)S5)S4,PBTTTPD,5.41,3.61,0.79,2.64,0.37,0.78,"Bian, L.; Miao, J.; Hai, J.; Zhu, E.; Yu, J.; Ge, G.; Wu, H.; Tang, W. RSC Advances Benzotrithiophene Polymers with Tuneable Bandgap for Photovoltaic Applications. RSC Adv. 2014, 4, 53939¨C53945. "
1547,CC1=CC(C2=C3SC(CCCCCCCCCCCCCCCC)=C2)=C(S1)C4=C3C=C(C5=CC=C(C6=C7C(N=C(C8=CC(OCCCCCCCCCCCC)=C(OCCCCCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCCCCCC)C(OCCCCCCCCCCCC)=C9)=N7)=C(C%10=CC=C(C)S%10)C%11=NSN=C6%11)S5)S4,PBTTTzQx,4.8,3.6,0.43,3.16,0.48,0.65,"Bian, L.; Miao, J.; Hai, J.; Zhu, E.; Yu, J.; Ge, G.; Wu, H.; Tang, W. RSC Advances Benzotrithiophene Polymers with Tuneable Bandgap for Photovoltaic Applications. RSC Adv. 2014, 4, 53939¨C53945. "
1548,CC1=CC2=C(C(SC(C3=C(CCCCCC)N=C(C4=NC(CCCCCC)=C(C)S4)S3)=C5)C5C6=C2C=C(C(CCCCCCCCCCC)CCCCCCCCCCCC)S6)S1,BTT-BTz,5.65,3.6,0.81,10.9,0.57,5.06,"Zhao, X.; Yang, D.; Lv, H.; Yin, L.; Yang, X. New Benzotrithiophene Derivative with a Broad Band Gap for High Performance Polymer Solar Cells. Polym. Chem. 2013, 4, 57¨C60. "
1549,CC1=CC2=C(C(SC(C3=CC=C(C)C4=NSN=C34)=C5)=C5C6=C2C=C(OCC(CCCC)CC)C(OCC(CCCC)CC)=C6)S1,PNB-3,5.22,3.44,0.66,2.76,0.34,0.62,"Wang, B.; Tsang, S.-W.; Zhang, W.; Tao, Y.; Wong, M. S. Naphthodithiophene-2,1,3-Benzothiadiazole Copolymers for Bulk Heterojunction Solar Cells. Chem. Commun. 2011, 47, 9471¨C9473. "
1550,CC1=CC2=C(C(SC(C3=C(CCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCC)=C(C)S5)C6=NSN=C46)S3)=C7)=C7C8=C2C=C(OCC(CCCC)CC)C(OCC(CCCC)CC)=C8)S1,PNB-4,5.14,3.54,0.64,13.5,0.62,5.27,"Wang, B.; Tsang, S.-W.; Zhang, W.; Tao, Y.; Wong, M. S. Naphthodithiophene-2,1,3-Benzothiadiazole Copolymers for Bulk Heterojunction Solar Cells. Chem. Commun. 2011, 47, 9471¨C9473. "
1551,CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)C6=NSN=C62)S1,PffBT4T-2OD,5.34,3.69,0.77,18.4,0.74,10.5,"Liu, Y.; Zhao, J.; Li, Z.; Mu, C.; Ma, W.; Hu, H.; Jiang, K.; Lin, H.; Ade, H.; Yan, H. Aggregation and Morphology Control Enables Multiple Cases of High-Efficiency Polymer Solar Cells. Nat. Commun. 2014, 5, 5293/1¨C8. "
1552,CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=CC=C(C3=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C4=CC(F)=C(C5=C(F)C=C(C)S5)S4)S3)C6=NSN=C62)S1,PffBT4T-2OD,5.2,3.57,0.77,18.2,0.74,10.4,"Liu, Y.; Zhao, J.; Li, Z.; Mu, C.; Ma, W.; Hu, H.; Jiang, K.; Lin, H.; Ade, H.; Yan, H. Aggregation and Morphology Control Enables Multiple Cases of High-Efficiency Polymer Solar Cells. Nat. Commun. 2014, 5, 5293/1¨C8. "
1553,CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)C6=NSN=C62)S1,PffBT4T-2OD,5.34,3.69,0.76,17.9,0.65,9,"Liu, Y.; Zhao, J.; Li, Z.; Mu, C.; Ma, W.; Hu, H.; Jiang, K.; Lin, H.; Ade, H.; Yan, H. Aggregation and Morphology Control Enables Multiple Cases of High-Efficiency Polymer Solar Cells. Nat. Commun. 2014, 5, 5293/1¨C8. "
1554,CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)C6=NSN=C62)S1,PffBT4T-2OD,5.34,3.69,0.72,16.7,0.63,7.7,"Liu, Y.; Zhao, J.; Li, Z.; Mu, C.; Ma, W.; Hu, H.; Jiang, K.; Lin, H.; Ade, H.; Yan, H. Aggregation and Morphology Control Enables Multiple Cases of High-Efficiency Polymer Solar Cells. Nat. Commun. 2014, 5, 5293/1¨C8. "
1555,CC1=C(C[C@@H](CCCCCCCC)CCCCCCCCCC)C=C(C2=CC(C3=NSN=C3C(C4=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)=C7)=C7C8=NSN=C82)S1,PNTz4T-2OD,5.24,3.71,0.76,19.8,0.68,10.1,"Liu, Y.; Zhao, J.; Li, Z.; Mu, C.; Ma, W.; Hu, H.; Jiang, K.; Lin, H.; Ade, H.; Yan, H. Aggregation and Morphology Control Enables Multiple Cases of High-Efficiency Polymer Solar Cells. Nat. Commun. 2014, 5, 5293/1¨C8. "
1556,CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CC)CCCC)SC(CC(CC)CCCC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC=C(CC(CCCC)CC)S%10,PBDTBDD,5.23,3.43,0.86,10.68,0.723,6.67,"Qian, D.; Ye, L.; Zhang, M.; Liang, Y.; Li, L.; Huang, Y.; Guo, X.; Zhang, S.; Tan, Z.; Hou, J. Design, Application, and Morphology Study of a New Photovoltaic Polymer with Strong Aggregation in Solution State. Macromolecules 2012, 45, 9611¨C9617. "
1557,CC1=C2C(SC(C(OCC(CC)CCCC)=O)=C2F)=C(C3=CC4=C(C5=CC=C(CC(CCCC)CC)O5)C6=C(C=C(C)S6)C(C7=CC=C(CC(CC)CCCC)O7)=C4S3)S1,PBDTTT-EFF,5.19,3.64,0.693,11.77,0.648,5.28,"Zhang, S.; Ye, L.; Zhao, W.; Liu, D.; Yao, H.; Hou, J. Side Chain Selection for Designing Highly Efficient Photovoltaic Polymers with 2D-Conjugated Structure. Macromolecules 2014, 47, 4653¨C4659. "
1558,CC1=C2C(SC(C(OCC(CC)CCCC)=O)=C2F)=C(C3=CC4=C(C5=CC=C(CC(CCCC)CC)S5)C6=C(C=C(C)S6)C(C7=CC=C(CC(CC)CCCC)S7)=C4S3)S1,PBDTTT-EFT,5.24,3.66,0.784,16.86,0.682,9,"Zhang, S.; Ye, L.; Zhao, W.; Liu, D.; Yao, H.; Hou, J. Side Chain Selection for Designing Highly Efficient Photovoltaic Polymers with 2D-Conjugated Structure. Macromolecules 2014, 47, 4653¨C4659. "
1559,CC1=C2C(SC(C(OCC(CC)CCCC)=O)=C2F)=C(C3=CC4=C(C5=CC=C(CC(CCCC)CC)[Se]5)C6=C(C=C(C)S6)C(C7=CC=C(CC(CC)CCCC)[Se]7)=C4S3)S1,PBDTTT-EFS,5.29,3.71,0.807,16.57,0.656,8.78,"Zhang, S.; Ye, L.; Zhao, W.; Liu, D.; Yao, H.; Hou, J. Side Chain Selection for Designing Highly Efficient Photovoltaic Polymers with 2D-Conjugated Structure. Macromolecules 2014, 47, 4653¨C4659. "
1560,CC1=CC2=C(C3=CC=C(C4=CC=C(C5=C(OCC(CC)CCCC)C(OCC(CCCC)CC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)C=C3C(CCCCCCCC)(CCCCCCCC)O2)C=C1,PDBPTBT-2,5.51,3.49,0.9,6.1,0.59,3.28,"Zhou, Y.; Li, M.; Guo, Y.; Lau, H.; Song, J.; Bo, Z.; Wang, H. Dibenzopyran-Based Wide Band Gap Conjugated Copolymers: Structural Design and Application for Polymer Solar Cells. ACS Appl. Mater. Interfaces 2016, 8, 31348¨C31358. "
1561,CC1=CC2=C(C3=CC=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)C=C3C(CCCCCCCC)(CCCCCCCC)O2)C=C1,PDBPTBT-3,5.44,3.46,0.8,8.03,0.62,3.99,"Zhou, Y.; Li, M.; Guo, Y.; Lau, H.; Song, J.; Bo, Z.; Wang, H. Dibenzopyran-Based Wide Band Gap Conjugated Copolymers: Structural Design and Application for Polymer Solar Cells. ACS Appl. Mater. Interfaces 2016, 8, 31348¨C31358. "
1562,CC1=CC2=C(C3=CC=C(C4=CC=C(C5=C(OCCCCCCCC)C=C(C6=CC=C(C)S6)C7=NSN=C75)S4)C=C3C(CCCCCCCC)(CCCCCCCC)O2)C=C1,PDBPTBT-4,5.32,3.5,0.75,9.42,0.58,4.1,"Zhou, Y.; Li, M.; Guo, Y.; Lau, H.; Song, J.; Bo, Z.; Wang, H. Dibenzopyran-Based Wide Band Gap Conjugated Copolymers: Structural Design and Application for Polymer Solar Cells. ACS Appl. Mater. Interfaces 2016, 8, 31348¨C31358. "
1563,CC1=CC2=C(C3=CC=C(C4=CC=C(C5=C(OCCCCCCCC)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)C=C3C(CCCCCCCC)(CCCCCCCC)O2)C=C1,PDBPTBT-5,5.57,3.63,0.96,11.09,0.67,7.06,"Zhou, Y.; Li, M.; Guo, Y.; Lau, H.; Song, J.; Bo, Z.; Wang, H. Dibenzopyran-Based Wide Band Gap Conjugated Copolymers: Structural Design and Application for Polymer Solar Cells. ACS Appl. Mater. Interfaces 2016, 8, 31348¨C31358. "
1564,CC(S1)=CC2=C1C(C3=CC=C(C4=CC=C(OCC(CCCC)CC)C=C4)S3)=C(C=C(C5=C(CCCCCCCC)C=C(C6=C(C(N(CC(CC)CCCC)C7=O)=O)C7=C(C8=CC(CCCCCCCC)=C(C)S8)S6)S5)S9)C9=C2C%10=CC=C(C%11=CC=C(OCC(CCCC)CC)C=C%11)S%10,P1,5.41,3.59,0.81,9.96,0.538,4.35,"Kranthiraja, K.; Park, S. H.; Kim, H.; Gunasekar, K.; Han, G.; Kim, B. J.; Kim, C. S.; Kim, S.; Lee, H.; Nishikubo, R.; Saeki, A.; Jin, S. H.; Song, M. Accomplishment of Multifunctional ¦Ð-Conjugated Polymers by Regulating the Degree of Side-Chain Fluorination for Efficient Dopant-Free Ambient-Stable Perovskite Solar Cells and Organic Solar Cells. ACS Appl. Mater. Interfaces 2017, 9, 36053¨C36060. "
1565,CC(S1)=CC2=C1C(C3=CC=C(C4=CC=C(OCC(CCCC)CC)C(F)=C4)S3)=C(C=C(C5=C(CCCCCCCC)C=C(C6=C(C(N(CC(CC)CCCC)C7=O)=O)C7=C(C8=CC(CCCCCCCC)=C(C)S8)S6)S5)S9)C9=C2C%10=CC=C(C%11=CC(F)=C(OCC(CCCC)CC)C=C%11)S%10,P2,5.43,3.61,0.82,15.1,0.642,7.93,"Kranthiraja, K.; Park, S. H.; Kim, H.; Gunasekar, K.; Han, G.; Kim, B. J.; Kim, C. S.; Kim, S.; Lee, H.; Nishikubo, R.; Saeki, A.; Jin, S. H.; Song, M. Accomplishment of Multifunctional ¦Ð-Conjugated Polymers by Regulating the Degree of Side-Chain Fluorination for Efficient Dopant-Free Ambient-Stable Perovskite Solar Cells and Organic Solar Cells. ACS Appl. Mater. Interfaces 2017, 9, 36053¨C36060. "
1566,CC1=CC2=C(C(C3=CC=C(S3)C4=CC(F)=C(C(F)=C4)OCC(CC)CCCC)=C5C=C(SC5=C2C6=CC=C(S6)C7=CC(F)=C(C(F)=C7)OCC(CC)CCCC)C8=C(C=C(S8)C9=C(C%10=C(S9)C%11=CC(CCCCCCCC)=C(S%11)C)C(N(C%10=O)CC(CCCC)CC)=O)CCCCCCCC)S1,P3,5.5,3.68,1,13.25,0.556,7.43,"Kranthiraja, K.; Park, S. H.; Kim, H.; Gunasekar, K.; Han, G.; Kim, B. J.; Kim, C. S.; Kim, S.; Lee, H.; Nishikubo, R.; Saeki, A.; Jin, S. H.; Song, M. Accomplishment of Multifunctional ¦Ð-Conjugated Polymers by Regulating the Degree of Side-Chain Fluorination for Efficient Dopant-Free Ambient-Stable Perovskite Solar Cells and Organic Solar Cells. ACS Appl. Mater. Interfaces 2017, 9, 36053¨C36060. "
1567,CC1=CC(OCC(CCCCCCCC)CCCCCC)=C(C2=CC=C(C3=C(F)C(F)=C(C4=CC=C(C)S4)C5=NSN=C35)S2)C=C1OCC(CCCCCC)CCCCCCCC,P0,5.34,3.59,0.768,15.79,0.636,7.8,"Zhang, Z.; Liu, Y.; Zhang, J.; Feng, S.; Wu, L.; Gong, X.; Xu, X.; Chen, X.; Bo, Z. Enhancing the Efficiency of Polymer Solar Cells by Incorporation of 2,5-Difluorobenzene Units into the Polymer Backbone via Random Copolymerization. ACS Appl. Mater. Interfaces 2017, 9, 23775¨C23781. "
1568,CC1=CC(SC2=C3SC(C4=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C5=CC=C(C6=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1,PBT,4.87,3.3,0.57,4.23,0.4,1,"Kim, I.-B.; Jang, S.-Y.; Kim, Y.-A.; Kang, R.; Kim, I.-S.; Ko, D.-K.; Kim, D.-Y. The Effect of Fluorine Substitution on the Molecular Interactions and Performance in Polymer Solar Cells. ACS Appl. Mater. Interfaces 2017, 9, 24011¨C24019. "
1569,CC1=CC(SC2=C3SC(C4=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C5=C(F)C=C(C6=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1,PFBT,4.91,3.35,0.67,12.15,0.67,6,"Kim, I.-B.; Jang, S.-Y.; Kim, Y.-A.; Kang, R.; Kim, I.-S.; Ko, D.-K.; Kim, D.-Y. The Effect of Fluorine Substitution on the Molecular Interactions and Performance in Polymer Solar Cells. ACS Appl. Mater. Interfaces 2017, 9, 24011¨C24019. "
1570,CC1=CC(SC2=C3SC(C4=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C)S6)C7=NSN=C75)S4)=C2)=C3S1,PDFBT,5.11,3.52,0.73,14.32,0.69,7.3,"Kim, I.-B.; Jang, S.-Y.; Kim, Y.-A.; Kang, R.; Kim, I.-S.; Ko, D.-K.; Kim, D.-Y. The Effect of Fluorine Substitution on the Molecular Interactions and Performance in Polymer Solar Cells. ACS Appl. Mater. Interfaces 2017, 9, 24011¨C24019. "
1571,CC1=C(OCC(CCCCCCCC)CCCCCC)C(F)=C(C2=CC=C(C)S2)C3=NSN=C31,P1-0,5.56,3.83,0.8,13.38,0.68,7.25,"Gong, X.; Li, G.; Wu, Y.; Zhang, J.; Feng, S.; Liu, Y.; Li, C.; Ma, W.; Bo, Z. Enhancing the Performance of Polymer Solar Cells by Using Donor Polymers Carrying Discretely Distributed Side Chains. ACS Appl. Mater. Interfaces 2017, 9, 24020¨C24026. "
1572,CC1=C(C(N(CC(CC)CCCC)C2=O)=O)C2=C(C3=NSN=C31)C4=CC(S5)=C(S4)C6=C5C7=C(C6(C8=CC=CC(CCCCCC)=C8)C9=CC(CCCCCC)=CC=C9)C=C%10C%11=C(C(SC(C)=C%12)=C%12S%11)C(C%13=CC(CCCCCC)=CC=C%13)(C%14=CC=CC(CCCCCC)=C%14)C%10=C7,PIDTT-TID,5.89,3.84,1,12.6,0.53,6.7,"Wang, C.; Xu, X.; Zhang, W.; Bergqvist, J.; Xia, Y.; Meng, X.; Bini, K.; Ma, W.; Yartsev, A.; Vandewal, K.; Andersson, M. R.; Ingan?s, O.; Fahlman, M.; Wang, E. Low Band Gap Polymer Solar Cells with Minimal Voltage Losses. Adv. Energy Mater. 2016, 6, 1600148/1¨C10."
1573,CC1=C(F)C=C(C2=C(CC(CC)CCCC)C=C(C3=C4C(C(C5=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C5C4=O)=O)=C(C6=CC(CC(CCCC)CC)=C(C7=CC(F)=C(C)S7)S6)S3)S2)S1,PBDD-ff4T,5.42,3.53,0.95,13.2,0.73,9.2,"Fan, Q.; Su, W.; Guo, X.; Guo, B.; Li, W.; Zhang, Y.; Wang, K.; Zhang, M.; Li, Y. A New Polythiophene Derivative for High Efficiency Polymer Solar Cells with PCE over 9%. Adv. Energy Mater. 2016, 6, 1600430/1¨C7. "
1574,CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CC(CCCCCCCCCC)CCCCCCCC)C6=O)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1,PBDPP-OD,5.27,3.86,0.74,4.3,0.67,2.13,"Ye, L.; Jiao, X.; Zhang, S.; Yao, H.; Qin, Y.; Ade, H.; Hou, J. Control of Mesoscale Morphology and Photovoltaic Performance in Diketopyrrolopyrrole-Based Small Band Gap Terpolymers. Adv. Energy Mater. 2017, 7, 1601138/1¨C9. "
1575,CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CC)CCCC)SC(CC(CCCC)CC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC=C(CC(CC)CCCC)S%10)S1,PBDB-TT0,5.47,3.54,0.886,11.75,0.699,7.28,"Jeong, M.; Chen, S.; Lee, S. M.; Wang, Z.; Yang, Y.; Zhang, Z. G.; Zhang, C.; Xiao, M.; Li, Y.; Yang, C. Feasible D1-A-D2-A Random Copolymers for Simultaneous HighPerformance Fullerene and Nonfullerene Solar Cells. Adv. Energy Mater. 2017, 7, 1702166/1¨C13. "
1576,CC(S1)=CC2=C1C(C3=CC(F)=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7)S4)S%10)C%10=C2C%11=CC(F)=C(CC(CCCC)CC)S%11,PBQ-4,5.05,3.3,0.9,13.58,0.702,8.55,"Liu, D.; Zhao, W.; Zhang, S.; Ye, L.; Zheng, Z.; Cui, Y.; Chen, Y.; Hou, J. Highly Efficient Photovoltaic Polymers Based on Benzodithiophene and Quinoxaline with Deeper HOMO Levels. Macromolecules 2015, 48, 5172¨C5178. "
1577,CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CC)S%11,PBQ-1,4.66,2.95,0.64,12.56,0.701,5.63,"Liu, D.; Zhao, W.; Zhang, S.; Ye, L.; Zheng, Z.; Cui, Y.; Chen, Y.; Hou, J. Highly Efficient Photovoltaic Polymers Based on Benzodithiophene and Quinoxaline with Deeper HOMO Levels. Macromolecules 2015, 48, 5172¨C5178. "
1578,CC(S1)=CC2=C1C(C3=CC(F)=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7)S4)S%10)C%10=C2C%11=CC(F)=C(CC(CCCC)CC)S%11,PBQ-2,4.86,3.15,0.76,13.05,0.633,6.25,"Liu, D.; Zhao, W.; Zhang, S.; Ye, L.; Zheng, Z.; Cui, Y.; Chen, Y.; Hou, J. Highly Efficient Photovoltaic Polymers Based on Benzodithiophene and Quinoxaline with Deeper HOMO Levels. Macromolecules 2015, 48, 5172¨C5178. "
1579,CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CC)S%11,PBQ-3,4.92,3.21,0.8,13.6,0.677,7.39,"Liu, D.; Zhao, W.; Zhang, S.; Ye, L.; Zheng, Z.; Cui, Y.; Chen, Y.; Hou, J. Highly Efficient Photovoltaic Polymers Based on Benzodithiophene and Quinoxaline with Deeper HOMO Levels. Macromolecules 2015, 48, 5172¨C5178. "
1580,CC1=CC2=C(C(OCCCCCCCCCC=C)=C(C=C(C3=C4C(SC(C(OCC(CC)CCCC)=O)=C4F)=C(C)S3)S5)C5=C2OCCCCCCCCCC=C)S1,PTB7-TV,5.15,3.24,0.75,15.75,0.72,8.55,"Meng, B.; Wang, Z.; Ma, W.; Xie, Z.; Liu, J.; Wang, L. A Cross-Linkable Donor Polymer as the Underlying Layer to Tune the Active Layer Morphology of Polymer Solar Cells. Adv. Funct. Mater. 2016, 26, 226¨C232. "
1581,CC1=CC=C(C2=CC3=C(C=C(C4=CC=C(C5=CC(C(C6=CC=C(CC(CCCC)CCCCCC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(CC(CCCC)CCCCCC)S9)=C8S5)S4)C%10=C3N=C(C%11=CC=C(CCCCCCCC)S%11)C(C%12=CC=C(CCCCCCCC)S%12)=N%10)C%13=C2N=C(C%14=CC=C(CCCCCCCC)S%14)C(C%15=CC=C(CCCCCCCC)S%15)=N%13)S1,PBDT-NQx,5.24,3.42,0.8,11.03,0.601,5.3,"Yu, T.; Xu, X.; Zhang, G.; Wan, J.; Li, Y.; Peng, Q. Wide Bandgap Copolymers Based on Quinoxalino[6,5-f].quinoxaline for Highly Efficient Nonfullerene Polymer Solar Cells. Adv. Funct. Mater. 2017, 27, 1701491/1¨C11. "
1582,CC1=CC=C(C2=CC3=C(C=C(C4=CC=C(C5=CC(C(C6=CC=C(SCC(CCCC)CCCCCC)S6)=C(SC(C)=C7)C7=C8C9=CC=C(SCC(CCCC)CCCCCC)S9)=C8S5)S4)C%10=C3N=C(C%11=CC=C(CCCCCCCC)S%11)C(C%12=CC=C(CCCCCCCC)S%12)=N%10)C%13=C2N=C(C%14=CC=C(CCCCCCCC)S%14)C(C%15=CC=C(CCCCCCCC)S%15)=N%13)S1,PBDTS-NQx,5.31,3.46,0.85,12.71,0.653,7.05,"Yu, T.; Xu, X.; Zhang, G.; Wan, J.; Li, Y.; Peng, Q. Wide Bandgap Copolymers Based on Quinoxalino[6,5-f].quinoxaline for Highly Efficient Nonfullerene Polymer Solar Cells. Adv. Funct. Mater. 2017, 27, 1701491/1¨C11. "
1583,CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC5=C(C=C(C6=CC=C(C)S6)S5)S4)N(CC(CCCCCCCCCC)CCCCCCCC)C3=O)S1,PDPPTT-2T,4.8,3.44,0.6,15.8,0.64,6.1,"Ji, Y.; Xiao, C.; Wang, Q.; Zhang, J.; Li, C.; Wu, Y.; Wei, Z.; Zhan, X.; Hu, W.; Wang, Z.; Janssen, R. A. J.; Li, W. Asymmetric Diketopyrrolopyrrole Conjugated Polymers for Field-Effect Transistors and Polymer Solar Cells Processed from a Nonchlorinated Solvent. Adv. Mater. 2016, 28, 943¨C950. "
1584,CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCC)CCCCCC)=O)=C(C4=CC(C)=C(C5=CC=C(C)S5)S4)N(CC(CCCCCC)CCCCCCCC)C3=O)S1,PDPPMT-2T,4.8,3.46,0.62,15.8,0.66,6.5,"Ji, Y.; Xiao, C.; Wang, Q.; Zhang, J.; Li, C.; Wu, Y.; Wei, Z.; Zhan, X.; Hu, W.; Wang, Z.; Janssen, R. A. J.; Li, W. Asymmetric Diketopyrrolopyrrole Conjugated Polymers for Field-Effect Transistors and Polymer Solar Cells Processed from a Nonchlorinated Solvent. Adv. Mater. 2016, 28, 943¨C950. "
1585,CC1=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)S3)C6=NON=C62)S1,PffBX4T-2OD,5.51,3.85,0.875,15.8,0.66,9.4,"Zhao, J.; Li, Y.; Hunt, A.; Zhang, J.; Yao, H.; Li, Z.; Zhang, J.; Huang, F.; Ade, H.; Yan, H. A Difluorobenzoxadiazole Building Block for Efficient Polymer Solar Cells. Adv. Mater. 2016, 28, 1868¨C1873. "
1586,O=C(N1CC(CCCCCCCCCC)CCCCCCCCCCCC)C2C=C(C)SC2C3=C(C(SC(C(SC(C4=CC=C(C5=CC=C(C)S5)S4)=C6)=C6C(N7CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C8C7=O)=C8S3)C1=O,PTBI2T,5.7,3.22,1.05,8.2,0.66,5.6,"Saito, M.; Osaka, I.; Suda, Y.; Yoshida, H.; Takimiya, K. Dithienylthienothiophenebisimide, a Versatile Electron-Deficient Unit for Semiconducting Polymers. Adv. Mater. 2016, 28, 6921¨C6925. "
1587,O=C(N1CC(CCCCCC)CCCCCCCC)C2C=C(C)SC2C3=C(C(SC(C(SC(C4=C(CCCCCCCCCCCC)C=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)S4)=C6)=C6C(N7CC(CCCCCC)CCCCCCCC)=O)=C8C7=O)=C8S3)C1=O,PTBI2TR,5.58,3.31,1,10.9,0.65,8,"Saito, M.; Osaka, I.; Suda, Y.; Yoshida, H.; Takimiya, K. Dithienylthienothiophenebisimide, a Versatile Electron-Deficient Unit for Semiconducting Polymers. Adv. Mater. 2016, 28, 6921¨C6925. "
1588,O=C(N1CC(CCCCCCCCCC)CCCCCCCCCCCC)C2C=C(C)SC2C3=C(C(SC(C(SC(C4=CC(SC(C)=C5)=C5S4)=C6)=C6C(N7CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C8C7=O)=C8S3)C1=O,PTBITT,5.85,3.4,1.07,4.2,0.53,2.4,"Saito, M.; Osaka, I.; Suda, Y.; Yoshida, H.; Takimiya, K. Dithienylthienothiophenebisimide, a Versatile Electron-Deficient Unit for Semiconducting Polymers. Adv. Mater. 2016, 28, 6921¨C6925. "
1589,O=C(N1CC(CCCCCCCCCC)CCCCCCCCCCCC)C2C=C(C)SC2C3=C(C(SC(C(SC(C4=CN=C(C5=NC=C(C)S5)S4)=C6)=C6C(N7CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C8C7=O)=C8S3)C1=O,PTBI2Tz,6.12,3.56,0.4,0.34,0.32,0.05,"Saito, M.; Osaka, I.; Suda, Y.; Yoshida, H.; Takimiya, K. Dithienylthienothiophenebisimide, a Versatile Electron-Deficient Unit for Semiconducting Polymers. Adv. Mater. 2016, 28, 6921¨C6925. "
1590,CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2C8=CC=CC=C8,PBDTDTBT-H,5.03,3.3,0.83,13.92,0.665,7.68,"Liu, D.; Zhu, Q.; Gu, C.; Wang, J.; Qiu, M.; Chen, W.; Bao, X.; Sun, M.; Yang, R. High-Performance Photovoltaic Polymers Employing Symmetry-Breaking Building Blocks. Adv. Mater. 2016, 28, 8490¨C8498. "
1591,CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2C8=CC=C(OCC(CC)CCCC)C=C8,PBDTDTBT-R,5.01,3.29,0.84,13.64,0.717,8.22,"Liu, D.; Zhu, Q.; Gu, C.; Wang, J.; Qiu, M.; Chen, W.; Bao, X.; Sun, M.; Yang, R. High-Performance Photovoltaic Polymers Employing Symmetry-Breaking Building Blocks. Adv. Mater. 2016, 28, 8490¨C8498. "
1592,CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=C(F)C(F)=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2C8=CC=CC=C8,PBDTDTffBT-H,5.06,3.3,0.88,14.92,0.719,9.44,"Liu, D.; Zhu, Q.; Gu, C.; Wang, J.; Qiu, M.; Chen, W.; Bao, X.; Sun, M.; Yang, R. High-Performance Photovoltaic Polymers Employing Symmetry-Breaking Building Blocks. Adv. Mater. 2016, 28, 8490¨C8498. "
1593,CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=C(F)C(F)=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2C8=CC=C(OCC(CC)CCCC)C=C8,PBDTDTffBT-R,5.03,3.28,0.88,13.98,0.739,9.09,"Liu, D.; Zhu, Q.; Gu, C.; Wang, J.; Qiu, M.; Chen, W.; Bao, X.; Sun, M.; Yang, R. High-Performance Photovoltaic Polymers Employing Symmetry-Breaking Building Blocks. Adv. Mater. 2016, 28, 8490¨C8498. "
1594,CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C4C(C(F)=C(C(OCC(CC)CCCC)=O)S4)=C(C)S3)S5)C5=C2C6=CC=CC=C6,PBDTTT-H,5.1,3.42,0.8,17.37,0.675,9.38,"Liu, D.; Zhu, Q.; Gu, C.; Wang, J.; Qiu, M.; Chen, W.; Bao, X.; Sun, M.; Yang, R. High-Performance Photovoltaic Polymers Employing Symmetry-Breaking Building Blocks. Adv. Mater. 2016, 28, 8490¨C8498. "
1595,CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C4C(C(F)=C(C(OCC(CC)CCCC)=O)S4)=C(C)S3)S5)C5=C2C6=CC=C(OCC(CC)CCCC)C=C6,PBDTTT-R,5.06,3.39,0.82,12.1,0.576,5.72,"Liu, D.; Zhu, Q.; Gu, C.; Wang, J.; Qiu, M.; Chen, W.; Bao, X.; Sun, M.; Yang, R. High-Performance Photovoltaic Polymers Employing Symmetry-Breaking Building Blocks. Adv. Mater. 2016, 28, 8490¨C8498. "
1596,CC1=CC=C(C2=CC(CC(CCCC)CCCCCC)=C(C3=C(OCC(CCCCC)CCC)C=C(C)S3)S2)C4=NSN=C41,P1,4.94,3.56,0.53,16.1,0.57,4.9,"Shi, S.; Liao, Q.; Tang, Y.; Guo, H.; Zhou, X.; Wang, Y.; Yang, T.; Liang, Y.; Cheng, X.; Liu, F.; Guo, X. Head-to-Head Linkage Containing Bithiophene-Based Polymeric Semiconductors for Highly Efficient Polymer Solar Cells. Adv. Mater. 2016, 28, 9969¨C9977. "
1597,CC1=CC(F)=C(C2=CC(CC(CCCC)CCCCCC)=C(C3=C(OCC(CCCCC)CCC)C=C(C)S3)S2)C4=NSN=C41,P2,5.13,3.76,0.6,18.04,0.65,6.88,"Shi, S.; Liao, Q.; Tang, Y.; Guo, H.; Zhou, X.; Wang, Y.; Yang, T.; Liang, Y.; Cheng, X.; Liu, F.; Guo, X. Head-to-Head Linkage Containing Bithiophene-Based Polymeric Semiconductors for Highly Efficient Polymer Solar Cells. Adv. Mater. 2016, 28, 9969¨C9977. "
1598,CC1=C(F)C(F)=C(C2=CC(CC(CCCC)CCCCCC)=C(C3=C(OCC(CCCCC)CCC)C=C(C)S3)S2)C4=NSN=C41,P3,5.2,3.74,0.66,20.69,0.71,9.76,"Shi, S.; Liao, Q.; Tang, Y.; Guo, H.; Zhou, X.; Wang, Y.; Yang, T.; Liang, Y.; Cheng, X.; Liu, F.; Guo, X. Head-to-Head Linkage Containing Bithiophene-Based Polymeric Semiconductors for Highly Efficient Polymer Solar Cells. Adv. Mater. 2016, 28, 9969¨C9977. "
1599,CC1=CC2=C(C(C3=CC=C(C4=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C5)=C5C=C4)S3)=C(C=C(C6=C(CCCCCCCC)C=C(C7=CC=C(C8=CC(CCCCCCCC)=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC=C(C%12=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C%13)=C%13C=C%12)S%11)S1,P1,5.05,3.45,0.65,10.58,0.593,4.11,"Kranthiraja, K.; Gunasekar, K.; Kim, H.; Cho, A. N.; Park, N. G.; Kim, S.; Kim, B. J.; Nishikubo, R.; Saeki, A.; Song, M.; Jin, S. H. High-Performance Long-Term-Stable Dopant-Free Perovskite Solar Cells and Additive-Free Organic Solar Cells by Employing Newly Designed Multirole ¦Ð-Conjugated Polymers. Adv. Mater. 2017, 29, 1700183/1¨C8. "
1600,CC1=CC2=C(C(C3=CC=C(C4=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C5)=C5C=C4)S3)=C(C=C(C6=C(CCCCCCCC)C=C(C7=CC(F)=C(C8=CC(CCCCCCCC)=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC=C(C%12=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C%13)=C%13C=C%12)S%11)S1,P2,5.09,3.49,0.73,12.87,0.602,5.73,"Kranthiraja, K.; Gunasekar, K.; Kim, H.; Cho, A. N.; Park, N. G.; Kim, S.; Kim, B. J.; Nishikubo, R.; Saeki, A.; Song, M.; Jin, S. H. High-Performance Long-Term-Stable Dopant-Free Perovskite Solar Cells and Additive-Free Organic Solar Cells by Employing Newly Designed Multirole ¦Ð-Conjugated Polymers. Adv. Mater. 2017, 29, 1700183/1¨C8. "
1601,CC1=CC2=C(C(C3=CC=C(C4=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C5)=C5C=C4)S3)=C(C=C(C6=C(CCCCCCCC)C=C(C7=C(F)C(F)=C(C8=CC(CCCCCCCC)=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC=C(C%12=CC(C=CC(OCC(CCCCCCCC)CCCCCC)=C%13)=C%13C=C%12)S%11)S1,P3,5.06,3.41,0.82,14.41,0.7,8.26,"Kranthiraja, K.; Gunasekar, K.; Kim, H.; Cho, A. N.; Park, N. G.; Kim, S.; Kim, B. J.; Nishikubo, R.; Saeki, A.; Song, M.; Jin, S. H. High-Performance Long-Term-Stable Dopant-Free Perovskite Solar Cells and Additive-Free Organic Solar Cells by Employing Newly Designed Multirole ¦Ð-Conjugated Polymers. Adv. Mater. 2017, 29, 1700183/1¨C8. "
1602,CC1=CC(N(CCCCCCCC)C(C2=CC3=CN=C(/C=C4C(C=CC(C5=CC6=C(C(C7=CC(CCCCCCCC)=C(CCCCCCCC)S7)=C(C=C(C)S8)C8=C6C9=CC(CCCCCCCC)=C(CCCCCCCC)S9)S5)=C%10)=C%10N(CCCCCCCC)C\4=O)C=N3)=O)=C2C=C1,PzIIG-BDT2TC8,5.48,3.64,1.01,7.93,0.656,5.26,"Li, J.-L.; Chai, Y.-F.; Wang, W. V.; Shi, Z.-F.; Xu, Z.-G.; Zhang, H.-L. PyrazineFused Isoindigo: A New Building Block for Polymer Solar Cells with High Open Circuit Voltage. Chem. Commun. 2017, 53, 5882¨C5885. "
1603,CC1=CC(N(CCCCCCCC)C(C2=CC3=CN=C(/C=C4C(C=CC(C5=CC6=C(S5)C7=C(C(C8=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S8)=C(C(SC(C)=C9)=C9S%10)C%10=C7C%11=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S%11)S6)=C%12)=C%12N(CCCCCCCC)C\4=O)C=N3)=O)=C2C=C1,PzIIG-BTT2TC10,5.4,3.58,0.94,5.89,0.608,3.36,"Li, J.-L.; Chai, Y.-F.; Wang, W. V.; Shi, Z.-F.; Xu, Z.-G.; Zhang, H.-L. PyrazineFused Isoindigo: A New Building Block for Polymer Solar Cells with High Open Circuit Voltage. Chem. Commun. 2017, 53, 5882¨C5885. "
1604,CC(S1)=CC2=C1C(C3=CC(OC)=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC(OC)=C(CC(CC)CCCC)S%10,PMOT5,5.28,3.22,0.96,13.45,0.71,9.25,"Huang, W.; Li, M.; Zhang, L.; Yang, T.; Zhang, Z.; Zeng, H.; Zhang, X.; Dang, L.; Liang, Y. Molecular Engineering on Conjugated Side Chain for Polymer Solar Cells with Improved Efficiency and Accessibility. Chem. Mater. 2016, 28, 5887¨C5895. "
1605,CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(C(C6=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C6C7=O)=O)C7=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC=C(CC(CC)CCCC)S%10,PBDTBDD,5.16,3.11,0.84,12.45,0.65,6.77,"Huang, W.; Li, M.; Zhang, L.; Yang, T.; Zhang, Z.; Zeng, H.; Zhang, X.; Dang, L.; Liang, Y. Molecular Engineering on Conjugated Side Chain for Polymer Solar Cells with Improved Efficiency and Accessibility. Chem. Mater. 2016, 28, 5887¨C5895. "
1606,CC(S1)=CC2=C1C(C3=CC(OC)=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC(OCCCCCCCC)=CC=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N7)S4)S%10)C%10=C2C%11=CC(OC)=C(CC(CC)CCCC)S%11,PMOT2,5.22,3.21,0.88,13.18,0.69,8.01,"Huang, W.; Li, M.; Zhang, L.; Yang, T.; Zhang, Z.; Zeng, H.; Zhang, X.; Dang, L.; Liang, Y. Molecular Engineering on Conjugated Side Chain for Polymer Solar Cells with Improved Efficiency and Accessibility. Chem. Mater. 2016, 28, 5887¨C5895. "
1607,CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC(OCCCCCCCC)=CC=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N7)S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11,PBQ-3,5.1,3.15,0.81,11.73,0.68,6.48,"Huang, W.; Li, M.; Zhang, L.; Yang, T.; Zhang, Z.; Zeng, H.; Zhang, X.; Dang, L.; Liang, Y. Molecular Engineering on Conjugated Side Chain for Polymer Solar Cells with Improved Efficiency and Accessibility. Chem. Mater. 2016, 28, 5887¨C5895. "
1608,CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(C=C(S(=O)(CC(CCCCCC)CCCCCCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(CC(CCCC)CC)S7,PBDTTT-S-T,5.29,3.68,0.81,12.27,0.62,5.93,"Wu, Y.; Li, Z.; Ma, W.; Huang, Y.; Huo, L.; Guo, X.; Zhang, M.; Ade, H.; Hou, J. PDT-S-T: A New Polymer with Optimized Molecular Conformation for Controlled Aggregation and ¦Ð-¦Ð Stacking and Its Application in Efficient Photovoltaic Devices. Adv. Mater. 2013, 25, 3449¨C3455. "
1609,CC1=C(C=C(S(=O)(CC(CCCCCC)CCCCCCCC)=O)S2)C2=C(C3=CC4=C(S3)C5=C(C6=CC=C(C[C@H](CCCC)CC)S6)C7=C(C(SC(C)=C8)=C8S7)C(C9=CC=C(C[C@@H](CCCC)CC)S9)=C5S4)S1,PDT-S-T,5.21,3.68,0.73,16.63,0.641,7.79,"Wu, Y.; Li, Z.; Ma, W.; Huang, Y.; Huo, L.; Guo, X.; Zhang, M.; Ade, H.; Hou, J. PDT-S-T: A New Polymer with Optimized Molecular Conformation for Controlled Aggregation and ¦Ð-¦Ð Stacking and Its Application in Efficient Photovoltaic Devices. Adv. Mater. 2013, 25, 3449¨C3455. "
1610,CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(Cl)=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC=C(CC(CCCC)CCCCCC)S9,PBDTBO-CIBTDD,5.47,3.7,0.76,16.79,0.717,9.11,"Mo, D.; Wang, H.; Chen, H.; Qu, S.; Chao, P.; Yang, Z.; Tian, L.; Su, Y. A.; Gao, Y.; Yang, B.; Chen, W.; He, F. Chlorination of Low-Band-Gap Polymers: Toward HighPerformance Polymer Solar Cells. Chem. Mater. 2017, 29, 2819¨C2830. "
1611,CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(Cl)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC=C(CC(CCCC)CCCCCC)S9,PBDTBO-CIBTEH,5.5,3.73,0.79,13.33,0.631,6.88,"Mo, D.; Wang, H.; Chen, H.; Qu, S.; Chao, P.; Yang, Z.; Tian, L.; Su, Y. A.; Gao, Y.; Yang, B.; Chen, W.; He, F. Chlorination of Low-Band-Gap Polymers: Toward HighPerformance Polymer Solar Cells. Chem. Mater. 2017, 29, 2819¨C2830. "
1612,CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCCCC)CCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(Cl)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC=C(CC(CCCCCCCC)CCCCCC)S9,PBDTHD-CIBTEH,5.53,3.71,0.78,10.94,0.644,5.46,"Mo, D.; Wang, H.; Chen, H.; Qu, S.; Chao, P.; Yang, Z.; Tian, L.; Su, Y. A.; Gao, Y.; Yang, B.; Chen, W.; He, F. Chlorination of Low-Band-Gap Polymers: Toward HighPerformance Polymer Solar Cells. Chem. Mater. 2017, 29, 2819¨C2830. "
1613,CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCCCC)CCCCCC)S3)=C(C=C(C4=CC=C(C5=CC(Cl)=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC=C(CC(CCCCCCCC)CCCCCC)S9,PBDTHD-CIBTDD,5.53,3.71,0.68,11.69,0.623,4.95,"Mo, D.; Wang, H.; Chen, H.; Qu, S.; Chao, P.; Yang, Z.; Tian, L.; Su, Y. A.; Gao, Y.; Yang, B.; Chen, W.; He, F. Chlorination of Low-Band-Gap Polymers: Toward HighPerformance Polymer Solar Cells. Chem. Mater. 2017, 29, 2819¨C2830. "
1614,CC(S1)=CC2=C1C(C3=CC=CC(OCC(CCCC)CC)=C3)=C(C=C(C4=CC=C(C5=C6C(C(C7=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C7C6=O)=O)=C(C8=CC=C(C)S8)S5)S4)S9)C9=C2C%10=CC=CC(OCC(CCCC)CC)=C%10,PBPD-Th,5.42,3.36,0.95,12.4,0.71,8.4,"Xu, Z.; Fan, Q.; Meng, X.; Guo, X.; Su, W.; Ma, W.; Zhang, M.; Li, Y. SeleniumContaining Medium Bandgap Copolymer for Bulk Heterojunction Polymer Solar Cells with High Efficiency of 9.8%. Chem. Mater. 2017, 29, 4811¨C4818."
1615,CC(S1)=CC2=C1C(C3=CC=CC(OCC(CCCC)CC)=C3)=C(C=C(C4=CC=C(C5=C6C(C(C7=C(CC(CCCC)CC)SC(CC(CC)CCCC)=C7C6=O)=O)=C(C8=CC=C(C)[Se]8)S5)[Se]4)S9)C9=C2C%10=CC=CC(OCC(CCCC)CC)=C%10,PBPD-Se,5.35,3.31,0.9,14.9,0.73,9.8,"Xu, Z.; Fan, Q.; Meng, X.; Guo, X.; Su, W.; Ma, W.; Zhang, M.; Li, Y. SeleniumContaining Medium Bandgap Copolymer for Bulk Heterojunction Polymer Solar Cells with High Efficiency of 9.8%. Chem. Mater. 2017, 29, 4811¨C4818."
1616,CC(S1)=CC2=C1C(C3=CC=C(OCC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(C(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(OCC(CCCC)CC)S7,PBDTT-O-TT-CF,5.31,3.33,0.78,16.5,0.68,8.68,"Cui, C.; He, Z.; Wu, Y.; Cheng, X.; Wu, H.; Li, Y.; Cao, Y.; Wong, W.-Y. HighPerformance Polymer Solar Cells Based on a 2D-Conjugated Polymer with an Alkylthio Side-Chain. Energy Environ. Sci. 2016, 9, 885¨C891. "
1617,CC(S1)=CC2=C1C(C3=CC=C(SCC(CC)CCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(C(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7,PBDTT-S-TT-CF,5.44,3.31,0.89,15.1,0.71,9.58,"Cui, C.; He, Z.; Wu, Y.; Cheng, X.; Wu, H.; Li, Y.; Cao, Y.; Wong, W.-Y. HighPerformance Polymer Solar Cells Based on a 2D-Conjugated Polymer with an Alkylthio Side-Chain. Energy Environ. Sci. 2016, 9, 885¨C891. "
1618,CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=CC8=C(C(C9=CC=C(C)S9)=C(C=C(C)S%10)C%10=C8C%11=CC=C(/C=C/C%12=CC=C(C%13=CC(/C(C(N%14CC(CCCCCCCC)CCCCCCCCCC)=O)=C%15C(N(CC(CCCCCCCCCC)CCCCCCCC)C%16=C\%15C=CC=C%16)=O)=C%14C=C%13)S%12)S%11)S7)=C5)C6=C%17)=C%17C2(C%18=CC=C(CCCCCC)C=C%18)C%19=CC=C(CCCCCC)C=C%19)S1,PIDTBDTID,5.47,3.72,0.87,7.24,0.42,2.66,"Peng, W.; Tan, H.; Xiao, M.; Chen, J.; Tao, Q.; Duan, X.; Wang, Y.; Liu, Y.; Yang, R.; Zhu, W. Synthesis and Characterization of Novel Indacenodithiophene-Based Narrow Band-Gap Polymers with Pendant Isoindigo Units for Polymer Solar Cells. Eur. Polym. J.2016, 81, 307¨C315. "
1619,CC1=CC2=C(C(C=C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6SC(C7=CC8=C(C(C9=CC=C(/C=C/C%10=CC=C(C%11=CC=C(/C(C(N%12CC(CCCCCCCCCC)CCCCCCCC)=O)=C%13C(N(CC(CCCCCCCC)CCCCCCCCCC)C%14=C\%13C=CC=C%14)=O)C%12=C%11)S%10)S9)=C(C=C(C)S%15)C%15=C8C%16=CC=C(/C=C/C%17=CC=C(C%18=CC(/C(C(N%19CC(CCCCCCCC)CCCCCCCCCC)=O)=C%20C(N(CC(CCCCCCCCCC)CCCCCCCC)C%21=C\%20C=CC=C%21)=O)=C%19C=C%18)S%17)S%16)S7)=C5)C6=C%22)=C%22C2(C%23=CC=C(CCCCCC)C=C%23)C%24=CC=C(CCCCCC)C=C%24)S1,PIDTBDT(ID)2,5.53,3.8,0.93,6.34,0.423,2.5,"Peng, W.; Tan, H.; Xiao, M.; Chen, J.; Tao, Q.; Duan, X.; Wang, Y.; Liu, Y.; Yang, R.; Zhu, W. Synthesis and Characterization of Novel Indacenodithiophene-Based Narrow Band-Gap Polymers with Pendant Isoindigo Units for Polymer Solar Cells. Eur. Polym. J.2016, 81, 307¨C315. "
1620,CC1=CC2=C(C(OCC(CC)CCCC)=C(C=C(C3=CC=C(N(C4=CC=CC=C4)C5=CC=C(C6=NC(SC(C7=CC=C(N(C8=CC=C(C)C=C8)C9=CC=CC=C9)C=C7)=N%10)=C%10S6)C=C5)C=C3)S%11)C%11=C2OCC(CCCC)CC)S1,P1,5.26,2.86,0.6,3.08,0.33,0.61,"Xie, Y.; Peng, Z.; Jia, T.; Zhang, H.; Hou, Q.; Luo, S.; Zeng, R.; Hou, L. Triphenylamine¨Cthiazolothiazole¨Cbenzodithiophene Based Conjugated Copolymers for Polymer Solar Cells. J. Mater. Sci. Mater. Electron. 2016, 27, 4705¨C4710. "
1621,CC1=CC2=C(C(OCCCCCCCCCCCC)=C(C=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)C6=NN(CCCCCCCCCCCC)N=C64)S3)S7)C7=C2OCCCCCCCCCCCC)S1,P1,5.14,3.69,0.6,7.83,0.609,3,"Zhou, D.; Chen, K.; Zhong, X.; Li, M.; Qin, Y.; Zhao, Y. Novel benzo(1,2-b:4,5-b¡¯)dithiophene-Based Donor¨Cacceptor Conjugated Polymes for Polymer Solar Cells. J. Mater. Sci. Mater. Electron. 2016, 27, 9920¨C9928. "
1622,CC1=CC2=C(C(OCCCCCCCCCCCC)=C(C=C(C3=C(CCCCCCCCCCCC)C=C(C4=C(N=C(C)C(C)=N5)C5=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)C7=NN(CCCCCCCCCCCC)N=C74)S3)S8)C8=C2OCCCCCCCCCCCC)S1,P2,5.18,3.57,0.6,6.99,0.588,2.28,"Zhou, D.; Chen, K.; Zhong, X.; Li, M.; Qin, Y.; Zhao, Y. Novel benzo(1,2-b:4,5-b¡¯)dithiophene-Based Donor¨Cacceptor Conjugated Polymes for Polymer Solar Cells. J. Mater. Sci. Mater. Electron. 2016, 27, 9920¨C9928. "
1623,O=C(OCC(CC)CCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(C(C5=CC=C(SCCCCCCCC)S5)=C(C=C(C6=C(SC(C(OCC(CC)CCCC)=O)=C7F)C7=C(C8=CC9=C(C(C%10=CC=C(SCCCCCCCC)S%10)=C(C=C(C)S%11)C%11=C9C%12=CC=C(SCCCCCCCC)S%12)S8)S6)S%13)C%13=C4C%14=CC=C(SCCCCCCCC)S%14)S3)=C2S1,PBDT-TSR,5.3,3.45,0.804,17.79,0.706,10.2,"Yao, H.; Zhao, W.; Zheng, Z.; Cui, Y.; Zhang, J.; Wei, Z.; Hou, J. PBDT-TSR: A Highly Efficient Conjugated Polymer for Polymer Solar Cells with a Regioregular Structure. J. Mater. Chem. A 2016, 4, 1708¨C1713. "
1624,CC1=CC=C(C2=C3C(C(N2CC(CCCCCC)CCCCCCCC)=O)=C(C4=CC=C(C5=C(OCCO6)C6=C(C)S5)S4)N(CC(CCCCCCCC)CCCCCC)C3=O)S1,PDPP[T]2-EDOT,5.73,3.66,0.32,15.5,0.5,2.6,"Wang, C.; Mueller, C. J.; Gann, E.; Liu, A. C. Y.; Thelakkat, M.; McNeill, C. R. EDOT¨Cdiketopyrrolopyrrole Copolymers for Polymer Solar Cells. J. Mater. Chem. A2016, 4, 3477¨C3486. "
1625,CC1=CC=C(C2=C3C(C(N2CC(CCCCCC)CCCCCCCC)=O)=C(C4=CC=C(C5=C(OCCO6)C6=C(C)S5)C=N4)N(CC(CCCCCCCC)CCCCCC)C3=O)N=C1,PDPP[Py]2-EDOT,6.07,3.74,0.8,5.1,0.54,2.4,"Wang, C.; Mueller, C. J.; Gann, E.; Liu, A. C. Y.; Thelakkat, M.; McNeill, C. R. EDOT¨Cdiketopyrrolopyrrole Copolymers for Polymer Solar Cells. J. Mater. Chem. A2016, 4, 3477¨C3486. "
1626,CC1=CC=C(C2=C3C(C(N2CC(CCCCCC)CCCCCCCC)=O)=C(C4=CC=C(C5=C(OCCO6)C6=C(C)S5)C=C4)N(CC(CCCCCCCC)CCCCCC)C3=O)C=C1,PDPP[Ph]2-EDOT,5.89,3.53,0.91,4.4,0.43,1.8,"Wang, C.; Mueller, C. J.; Gann, E.; Liu, A. C. Y.; Thelakkat, M.; McNeill, C. R. EDOT¨Cdiketopyrrolopyrrole Copolymers for Polymer Solar Cells. J. Mater. Chem. A2016, 4, 3477¨C3486. "
1627,CC1=CC(C(OCC(CCCC)CC)=C(SC(C2=CC=C(C3=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C4=O)=O)C4=C(C=C(C5=CC=C(C)S5)C(C(N6CC(CCCCCCCC)CCCCCCCCCC)=O)=C7C6=O)C7=C3)S2)=C8)C8=C9OCC(CC)CCCC)=C9S1,PBDTA-INDI,5.41,3.29,0.93,8.51,0.637,5.04,"Li, Z.; Feng, K.; Liu, J.; Mei, J.; Li, Y.; Peng, Q. Large Band-Gap Copolymers Based on a 1,2,5,6-Naphthalenediimide Unit for Polymer Solar Cells with High Open Circuit Voltages and Power Conversion Efficiencies. J. Mater. Chem. A 2016, 4, 7372¨C7381. "
1628,CC1=CC(C(C2=CC=C(CC(CCCC)CC)S2)=C(SC(C3=CC=C(C4=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C5=O)=O)C5=C(C=C(C6=CC=C(C)S6)C(C(N7CC(CCCCCCCC)CCCCCCCCCC)=O)=C8C7=O)C8=C4)S3)=C9)C9=C%10C%11=CC=C(CC(CC)CCCC)S%11)=C%10S1,PBDTT-INDI,5.47,3.46,0.96,10.26,0.645,6.35,"Li, Z.; Feng, K.; Liu, J.; Mei, J.; Li, Y.; Peng, Q. Large Band-Gap Copolymers Based on a 1,2,5,6-Naphthalenediimide Unit for Polymer Solar Cells with High Open Circuit Voltages and Power Conversion Efficiencies. J. Mater. Chem. A 2016, 4, 7372¨C7381. "
1629,O=C(OCC(CCCCCCCCCC)CCCCCCCC)C1=C(C2=CC=C(C3=CC=C(C4=CC=C(C)S4)C5=NSN=C53)S2)SC(C6=CC(C(OCC(CCCCCCCC)CCCCCCCCCC)=O)=C(C)S6)=C1,P1,5.6,3.88,0.85,2.79,0.6,1.43,"Liu, Y.; Zhao, W.; Wu, Y.; Zhang, J.; Li, G.; Li, W.; Ma, W.; Hou, J.; Bo, Z. Enhancing the Power Conversion Efficiency of Polymer Solar Cells to 9.26% by a Synergistic Effect of Fluoro and Carboxylate Substitution. J. Mater. Chem. A 2016, 4, 8097¨C8104. "
1630,O=C(OCC(CCCCCCCCCC)CCCCCCCC)C1=C(C2=CC=C(C3=C(F)C(F)=C(C4=CC=C(C)S4)C5=NSN=C53)S2)SC(C6=CC(C(OCC(CCCCCCCC)CCCCCCCCCC)=O)=C(C)S6)=C1,P2,5.72,3.95,0.87,14.91,0.71,9.26,"Liu, Y.; Zhao, W.; Wu, Y.; Zhang, J.; Li, G.; Li, W.; Ma, W.; Hou, J.; Bo, Z. Enhancing the Power Conversion Efficiency of Polymer Solar Cells to 9.26% by a Synergistic Effect of Fluoro and Carboxylate Substitution. J. Mater. Chem. A 2016, 4, 8097¨C8104. "
1631,CC(S1)=CC2=C1C(C3=CC=C(C[C@H](CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(S(=O)(CC(CCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(C[C@@H](CCCC)CC)S9,PBDTDTTT-S-T,5.04,3.68,0.69,16.35,0.663,7.48,"Huang, Y.; Guo, X.; Liu, F.; Huo, L.; Chen, Y.; Russell, T. P.; Han, C. C.; Li, Y.; Hou, J. Improving the Ordering and Photovoltaic Properties by Extending ¦Ð-Conjugated Area of Electron-Donating Units in Polymers with D-A Structure. Adv. Mater. 2012, 24, 3383¨C3389. "
1632,CC1=CC=C(C2=CC(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6C=C7C(C(SC(C8=CC=C(C9=C%10C(N=C(C%11=CC(OCCCCCCCC)=CC=C%11)C(C%12=CC=CC(OCCCCCCCC)=C%12)=N%10)=C(C%13=CC=C(C%14=C(N=C(C%15=CC(OCCCCCCCC)=CC=C%15)C(C%16=CC=CC(OCCCCCCCC)=C%16)=N%17)C%17=C(C)C=C%14)S%13)C=C9)S8)=C%18)=C%18C7(C%19=CC=C(CCCCCC)C=C%19)C%20=CC=C(CCCCCC)C=C%20)=C5)=C6S2)S1,PIDT-DTQ-T,5.33,3.29,0.86,11.42,0.658,6.41,"Dang, D.; Zhou, P.; Duan, linrui; Bao, X.; Yang, R.; Zhu, W. An Efficient Method to Achieve the Balanced Open Circuit Voltage and Short Circuit Current Density in Polymers Solar Cells. J. Mater. Chem. A 2016, 4, 8291¨C8297. "
1633,CC1=CC=C(C2=CC(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6C=C7C(C(SC(C8=CC=C(C9=C%10C(N=C(C%11=CC(OCCCCCCCC)=CC=C%11)C(C%12=CC=CC(OCCCCCCCC)=C%12)=N%10)=C(C%13=CC(SC(C%14=C(N=C(C%15=CC(OCCCCCCCC)=CC=C%15)C(C%16=CC=CC(OCCCCCCCC)=C%16)=N%17)C%17=C(C)C=C%14)=C%18)=C%18S%13)C=C9)S8)=C%19)=C%19C7(C%20=CC=C(CCCCCC)C=C%20)C%21=CC=C(CCCCCC)C=C%21)=C5)=C6S2)S1,PIDT-DTQ-TT,5.29,3.27,0.83,12.43,0.653,6.63,"Dang, D.; Zhou, P.; Duan, linrui; Bao, X.; Yang, R.; Zhu, W. An Efficient Method to Achieve the Balanced Open Circuit Voltage and Short Circuit Current Density in Polymers Solar Cells. J. Mater. Chem. A 2016, 4, 8291¨C8297. "
1634,CC1=CC2=C(C(C3=CC=CC(OCC(CC)CCCC)=C3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CCCC)CC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=CC(OCC(CC)CCCC)=C7)S1,PBTF-OP,5.45,3.34,0.86,16.4,0.622,9,"Li, W.; Guo, B.; Chang, C.; Guo, X.; Zhang, M.; Li, Y. Efficient Polymer Solar Cells Based on a Copolymer of Meta-Alkoxy-Phenyl-Substituted Benzodithiophene and thieno[3,4-b]thiophene. J. Mater. Chem. A 2016, 4, 10135¨C10141. "
1635,CC1=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C2=O)=C3C2=C(C4=CC=C(C5=CC(F)=C(C6=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C7=O)=C8C7=C(C9=CC=C(C%10=CC(N(CC(CC)CCCC)C%11=C%12C=C(F)C(C)=C%11)=C%12C=C%10F)S9)N(CC(CCCCCC)CCCCCCCC)C8=O)S6)C=C5F)S4)N(CC(CCCCCC)CCCCCCCC)C3=O)S1,PCDPP,5.44,3.89,0.86,16,0.65,9.02,"Liu, Y.; Li, G.; Zhang, Z.; Wu, L.; Chen, J.; Xu, X.; Chen, X.; Ma, W.; Bo, Z. An Effective Way to Reduce Energy Loss and Enhance Open-Circuit Voltage in Polymer Solar Cells Based on a Diketopyrrolopyrrole Polymer Containing Three Regular Alternating Units. J. Mater. Chem. A 2016, 4 (34), 13265¨C13270. "
1636,CC1=CC2=C(C(C3=CC4=C(C=C(CC(CCCCCC)CCCCCCCC)S4)S3)=C(C=C(C5=C(CC(CC)CCCC)C=C(C6=CC=C(C7=CC(CC(CCCC)CC)=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC%11=C(C=C(CC(CCCCCC)CCCCCCCC)S%11)S%10)S1,PF0,5.29,3.58,0.74,11.76,0.655,5.7,"Li, Z.; Zhang, T.; Xin, Y.; Zhao, X.; Yang, D.; Wu, F.; Yang, X. Synergistic Effect of Fluorination and Regio-Regularity on the Long-Term Thermal Stability of Polymer Solar Cells. J. Mater. Chem. A 2016, 4, 18598¨C18606. "
1637,CC1=CC2=C(C(C3=CC4=C(C=C(CC(CCCCCC)CCCCCCCC)S4)S3)=C(C=C(C5=C(CC(CC)CCCC)C=C(C6=C(F)C=C(C7=CC(CC(CCCC)CC)=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC%11=C(C=C(CC(CCCCCC)CCCCCCCC)S%11)S%10)S1,PF1,5.39,3.7,0.8,11.85,0.662,6.29,"Li, Z.; Zhang, T.; Xin, Y.; Zhao, X.; Yang, D.; Wu, F.; Yang, X. Synergistic Effect of Fluorination and Regio-Regularity on the Long-Term Thermal Stability of Polymer Solar Cells. J. Mater. Chem. A 2016, 4, 18598¨C18606. "
1638,CC1=CC2=C(C(C3=CC4=C(C=C(CC(CCCCCC)CCCCCCCC)S4)S3)=C(C=C(C5=C(CC(CC)CCCC)C=C(C6=C(F)C(F)=C(C7=CC(CC(CCCC)CC)=C(C)S7)C8=NSN=C86)S5)S9)C9=C2C%10=CC%11=C(C=C(CC(CCCCCC)CCCCCCCC)S%11)S%10)S1,PF2,5.48,3.73,0.86,11.67,0.653,6.54,"Li, Z.; Zhang, T.; Xin, Y.; Zhao, X.; Yang, D.; Wu, F.; Yang, X. Synergistic Effect of Fluorination and Regio-Regularity on the Long-Term Thermal Stability of Polymer Solar Cells. J. Mater. Chem. A 2016, 4, 18598¨C18606. "
1639,CC1=CC2=C(C(C(C3=CC=C(CCCCCC)C=C3)(C4=CC=C(CCCCCC)C=C4)C5=C6C=C7C(C(SC8=C9SC(C%10=CC%11=C(C=C(C)S%11)S%10)=C8)=C9C7(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)=C5)=C6S2)S1,PIDTT-TT,5.35,3.11,0.96,10.96,0.65,7.08,"Lee, W.; Jung, J. W. A Wide Band Gap Polymer Based on indacenodithieno[3,2-b]thiophene for High-Performance Bulk Heterojunction Polymer Solar Cells. J. Mater. Chem. A 2017, 5, 712¨C719. "
1640,CC1=CC(/C(C2=C3C=C4C(C(SC(C5=C(F)C(F)=C(C)C6=NSN=C65)=C7)=C7/C4=C/C(CCCCCC)CCCCCCCC)=C2)=C/C(CCCCCC)CCCCCCCC)=C3S1,PIDTV-ffBT,5.23,3.69,0.7,17.1,0.61,7.3,"Fan, Q.; Su, W.; Guo, X.; Zhang, X.; Xu, Z.; Guo, B.; Jiang, L.; Zhang, M.; Li, Y. A 1,1¡ä-Vinylene-Fused Indacenodithiophene-Based Low Bandgap Polymer for Efficient Polymer Solar Cells. J. Mater. Chem. A 2017, 5, 5106¨C5114. "
1641,CC1=CC=C(C2=C3C(C(N2CC(CCCC)CC)=O)=C(C4=CC=C(C5=C(CC(CCCCCC)CCCCCCCC)C=C(C6=C(F)C=C(C7=CC(F)=C(C8=CC(CC(CCCCCCCC)CCCCCC)=C(C)S8)C=C7N=N9)C9=C6)S5)S4)N(CC(CC)CCCC)C3=O)S1,PDFBC-DPP,5.35,3.82,0.8,13.15,0.68,7.33,"Zeng, Z.; Zhang, Z.; Zhao, B.; Liu, H.; Sun, X.; Wang, G.; Zhang, J.; Tan, S. Rational Design of a Difluorobenzo[c]cinnoline-Based Low-Bandgap Copolymer for HighPerformance Polymer Solar Cells. J. Mater. Chem. A 2017, 5, 7300¨C7304. "
1642,FC1=C(C2=CC(C3=CC=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)S3)=C(C)S2)C4=NSN=C4C(C5=CC(C6=CC=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)S6)=C(C7=CC=C(C8=CC=C(C)S8)S7)S5)=C1F,P-2T,5.27,3.1,0.76,17.48,0.595,7.91,"He, M.; Li, M.; Dong, X.; Tian, H.; Tong, H.; Liu, J.; Xie, Z.; Geng, Y.; Wang, F. A Difluorobenzothiadiazole-Based Conjugated Polymer with Alkylthiophene as the Side Chains for Efficient, Additive-Free and Thick-Film Polymer Solar Cells. J. Mater. Chem. A 2017, 5, 20473¨C20481. "
1643,FC1=C(C2=CC(C3=CC=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)S3)=C(C)S2)C4=NSN=C4C(C5=CC(C6=CC=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)S6)=C(C7=CC(SC(C)=C8)=C8S7)S5)=C1F,P-TT,5.3,3.13,0.8,18.15,0.686,9.96,"He, M.; Li, M.; Dong, X.; Tian, H.; Tong, H.; Liu, J.; Xie, Z.; Geng, Y.; Wang, F. A Difluorobenzothiadiazole-Based Conjugated Polymer with Alkylthiophene as the Side Chains for Efficient, Additive-Free and Thick-Film Polymer Solar Cells. J. Mater. Chem. A 2017, 5, 20473¨C20481. "
1644,CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(F)C=C8)C(C9=CC=C(F)C=C9)=N7)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CC)S%11)S1,PBDTT-DTFPQx,5.52,3.86,0.87,11.4,0.73,7.2,"Fan, Q.; Jiang, H.; Liu, Y.; Su, W.; Tan, H.; Wang, Y.; Yang, R.; Zhu, W. Efficient Polymer Solar Cells Based on a New Quinoxaline Derivative with Fluorinated Phenyl Side Chain. J. Mater. Chem. C 2016, 4, 2606¨C2613. "
1645,CC1=CC2=C(C3=CC(N(C)C4=C5C=C6C(C7=CC=C(C8=CC=C(C9=C(OCCCCCC)C(OCCCCCC)=C(C%10=CC=C(C)S%10)C%11=NSN=C%119)S8)C=C7C6(CCCCCC)CCCCCC)=C4)=C5C=C3C2(CCCCCC)CCCCCC)C=C1,PC1BT6,5.48,3.59,0.95,14,0.552,7.34,"Tu, Q.; Cai, D.; Wang, L.; Wei, J.; Shang, Q.; Chen, S.; Ma, Y.; Yin, Z.; Tang, C.; Zheng, Q. Side-Chain Engineering of Diindenocarbazole-Based Large Bandgap Copolymers toward High Performance Polymer Solar Cells. J. Mater. Chem. C 2016, 4, 6160¨C6168. "
1646,CC1=CC2=C(C3=CC(N(CC)C4=C5C=C6C(C7=CC=C(C8=CC=C(C9=C(OCCCCCC)C(OCCCCCC)=C(C%10=CC=C(C)S%10)C%11=NSN=C%119)S8)C=C7C6(CCCCCC)CCCCCC)=C4)=C5C=C3C2(CCCCCC)CCCCCC)C=C1,PC2BT6,5.49,3.56,0.99,13.11,0.51,6.62,"Tu, Q.; Cai, D.; Wang, L.; Wei, J.; Shang, Q.; Chen, S.; Ma, Y.; Yin, Z.; Tang, C.; Zheng, Q. Side-Chain Engineering of Diindenocarbazole-Based Large Bandgap Copolymers toward High Performance Polymer Solar Cells. J. Mater. Chem. C 2016, 4, 6160¨C6168. "
1647,CC1=CC2=C(C3=CC(N(CCCCCC)C4=C5C=C6C(C7=CC=C(C8=CC=C(C9=C(OCCCCCC)C(OCCCCCC)=C(C%10=CC=C(C)S%10)C%11=NSN=C%119)S8)C=C7C6(CCCCCC)CCCCCC)=C4)=C5C=C3C2(CCCCCC)CCCCCC)C=C1,PC6BT6,5.49,3.56,0.98,12.91,0.505,6.39,"Tu, Q.; Cai, D.; Wang, L.; Wei, J.; Shang, Q.; Chen, S.; Ma, Y.; Yin, Z.; Tang, C.; Zheng, Q. Side-Chain Engineering of Diindenocarbazole-Based Large Bandgap Copolymers toward High Performance Polymer Solar Cells. J. Mater. Chem. C 2016, 4, 6160¨C6168. "
1648,CC1=CC2=C(C3=CC(N(CC)C4=C5C=C6C(C7=CC=C(C8=CC=C(C9=C(OCCCCCC)C(OCCCCCC)=C(C%10=CC=C(C)S%10)C%11=NSN=C%119)S8)C=C7C6(CCCC)CCCC)=C4)=C5C=C3C2(CCCC)CCCC)C=C1,PNC2C4BT6,5.48,3.63,0.99,13.24,0.509,6.67,"Tu, Q.; Cai, D.; Wang, L.; Wei, J.; Shang, Q.; Chen, S.; Ma, Y.; Yin, Z.; Tang, C.; Zheng, Q. Side-Chain Engineering of Diindenocarbazole-Based Large Bandgap Copolymers toward High Performance Polymer Solar Cells. J. Mater. Chem. C 2016, 4, 6160¨C6168. "
1649,CC1=CC2=C(C3=CC(N(CC)C4=C5C=C6C(C7=CC=C(C8=C(CCCCCC)C=C(C9=CC=C(C%10=CC(CCCCCC)=C(C)S%10)C%11=NSN=C%119)S8)C=C7C6(CCCCCC)CCCCCC)=C4)=C5C=C3C2(CCCCCC)CCCCCC)C=C1,PC2BT,5.54,3.61,1.01,10.48,0.38,4.02,"Tu, Q.; Cai, D.; Wang, L.; Wei, J.; Shang, Q.; Chen, S.; Ma, Y.; Yin, Z.; Tang, C.; Zheng, Q. Side-Chain Engineering of Diindenocarbazole-Based Large Bandgap Copolymers toward High Performance Polymer Solar Cells. J. Mater. Chem. C 2016, 4, 6160¨C6168. "
1650,CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=CC=C(C)C4=NSN=C43)S5)C5=C2OCC(CCCCCCCC)CCCCCC,PBDTBT,5.22,3.68,0.76,5.32,0.423,1.71,"Huang, Y.; Liu, F.; Guo, X.; Zhang, W.; Gu, Y.; Zhang, J.; Han, C. C.; Russell, T. P.; Hou, J. Manipulating Backbone Structure to Enhance Low Band Gap Polymer Photovoltaic Performance. Adv. Energy Mater. 2013, 3, 930¨C937. "
1651,CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CC)CCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CC)CCCC,PBDTDTBT,5.24,3.68,0.79,13.56,0.691,7.4,"Huang, Y.; Liu, F.; Guo, X.; Zhang, W.; Gu, Y.; Zhang, J.; Han, C. C.; Russell, T. P.; Hou, J. Manipulating Backbone Structure to Enhance Low Band Gap Polymer Photovoltaic Performance. Adv. Energy Mater. 2013, 3, 930¨C937. "
1652,CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(SC(C(OCC(CCCC)CC)=O)=C6)C6=C(C7=CC=C(C)S7)C8=NN(CC(CC)CCCC)N=C85)S4)S9)C9=C2C%10=CC=C(CC(CCCC)CC)S%10)S1,PBDTT-BTAZT-1,5.11,3.12,0.75,14.11,0.624,6.95,"Zhou, P.; Yang, Y.; Chen, X.; Zhang, Z.-G.; Li, Y. Designing Thiophene-Fused Benzotriazole Unit as an Electron Acceptor to Build D-A Copolymers for Polymer Solar Cells. J. Mater. Chem. C 2017, 5, 2951¨C2957. "
1653,CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(SC(C(CC(CCCC)CC)=O)=C6)C6=C(C7=CC=C(C)S7)C8=NN(CC(CC)CCCC)N=C85)S4)S9)C9=C2C%10=CC=C(CC(CCCC)CC)S%10)S1,PBDTT-BTAZT-2,5.13,3.14,0.75,12.73,0.624,6.16,"Zhou, P.; Yang, Y.; Chen, X.; Zhang, Z.-G.; Li, Y. Designing Thiophene-Fused Benzotriazole Unit as an Electron Acceptor to Build D-A Copolymers for Polymer Solar Cells. J. Mater. Chem. C 2017, 5, 2951¨C2957. "
1654,CC1=CC(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C2=C3C=C4C(C(C=C(C(C5=CC=C(OCCCCCCCC)C=C5)(C6=CC=C(OCCCCCCCC)C=C6)C7=C8C=C9C(C(SC(C%10=CC=C(C)C%11=NSN=C%11%10)=C%12)=C%12N9CC(CCCCCCCCCCCC)CCCCCCCCCC)=C7)C8=C%13)=C%13C4(C%14=CC=C(OCCCCCCCC)C=C%14)C%15=CC=C(OCCCCCCCC)C=C%15)=C2)=C3S1,PIDTI-BT,5.3,3.76,0.82,8.99,0.546,4.02,"Zhao, B.; Yan, C.; Wang, Z.; Huang, H.; Hu, Y.; Cheng, P.; Yi, M.; Huang, C.; Zhan, X.; Huang, W. Ladder-Type Nonacyclic indacenodithieno[3,2-b]indole for Highly Efficient Organic Field-Effect Transistors and Organic Photovoltaics. J. Mater. Chem. C2017, 5, 8988¨C8998. "
1655,CC1=CC(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C2=C3C=C4C(C(C=C(C(C5=CC=C(OCCCCCCCC)C=C5)(C6=CC=C(OCCCCCCCC)C=C6)C7=C8C=C9C(C(SC(C%10=CC=C(C%11=CC=C(C%12=CC=C(C)S%12)C%13=NSN=C%13%11)S%10)=C%14)=C%14N9CC(CCCCCCCCCCCC)CCCCCCCCCC)=C7)C8=C%15)=C%15C4(C%16=CC=C(OCCCCCCCC)C=C%16)C%17=CC=C(OCCCCCCCC)C=C%17)=C2)=C3S1,PIDTI-DTBT,5.26,3.74,0.8,9.07,0.514,3.72,"Zhao, B.; Yan, C.; Wang, Z.; Huang, H.; Hu, Y.; Cheng, P.; Yi, M.; Huang, C.; Zhan, X.; Huang, W. Ladder-Type Nonacyclic indacenodithieno[3,2-b]indole for Highly Efficient Organic Field-Effect Transistors and Organic Photovoltaics. J. Mater. Chem. C2017, 5, 8988¨C8998. "
1656,CC1=CC=C(C2=C(OCC(CCCCCCCC)CCCCCC)C=C(C3=CC=C(C4=CC5=C(C=C(C)C6=NSN=C65)C7=NSN=C47)S3)C(OCC(CCCCCCCC)CCCCCC)=C2)S1,h-PPDTNTz,5.3,3.79,0.7,13.4,0.49,4.6,"Li, Y.; Lee, T. H.; Kim, J.; Park, S. Y.; Song, S.; Hwang, S.; Kim, J. Y.; Woo, H. Y. Thiophene and Naphtho[1,2-c:5,6-c]bis[1,2,5]thiadiazole Based Alternating Copolymers for Polymer Solar Cells. J. Photopolym. Sci. Technol. 2016, 29, 553¨C559. "
1657,CC1=CC=C(C2=C(OCC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C3=CC=C(C4=CC5=C(C=C(C)C6=NSN=C65)C7=NSN=C47)S3)C(OCC(CCCCCCCCCC)CCCCCCCCCCCC)=C2)S1,d-PPDTNTz,5.38,3.76,0.72,14,0.66,6.66,"Li, Y.; Lee, T. H.; Kim, J.; Park, S. Y.; Song, S.; Hwang, S.; Kim, J. Y.; Woo, H. Y. Thiophene and Naphtho[1,2-c:5,6-c]bis[1,2,5]thiadiazole Based Alternating Copolymers for Polymer Solar Cells. J. Photopolym. Sci. Technol. 2016, 29, 553¨C559. "
1658,CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(/C=C/C6=CC=C(C)S6)S5)O4)N(CC(CCCCCCCCCC)CCCCCCCC)C3=O)O1,PDVF-8,5.19,3.63,0.65,8.58,0.641,3.57,"Zhou, W.; Yu, C.; Chen, H.; Jia, T.; Zhang, W.; Yu, G.; Li, F. Improving the Photovoltaic Performance of Polymer Solar Cells Based on Furan-Flanked Diketopyrrolopyrrole Copolymers via Tuning the Alkyl Side Chain. J. Phys. Chem. C2016, 120, 4824¨C4832. "
1659,CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(/C=C/C6=CC=C(C)S6)S5)O4)N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C3=O)O1,PDVF-10,5.23,3.67,0.65,10.56,0.666,4.56,"Zhou, W.; Yu, C.; Chen, H.; Jia, T.; Zhang, W.; Yu, G.; Li, F. Improving the Photovoltaic Performance of Polymer Solar Cells Based on Furan-Flanked Diketopyrrolopyrrole Copolymers via Tuning the Alkyl Side Chain. J. Phys. Chem. C2016, 120, 4824¨C4832. "
1660,CC(S1)=CC2=C1C(C=CC=C3)=C3/C2=C(C4=C5C=C(C6=CC7=C(OCCCCCCCCCCCCCCCCCCCC)C8=C(C=C(C)S8)C(OCCCCCCCCCCCCCCCCCCCC)=C7S6)S4)/C9=C5C=CC=C9,PtBTPBDT,5.29,3.83,0.68,9.09,0.63,4.03,"Chiu, C. Y.; Wang, H.; Phan, H.; Shiratori, K.; Nguyen, T. Q.; Hawker, C. J. Twisted Olefinic Building Blocks for Low Bandgap Polymers in Solar Cells and Ambipolar FieldEffect Transistors. J. Polym. Sci. Part A Polym. Chem. 2016, 54, 889¨C899. "
1661,CC1=CC(C2=C/3C=CC(F)=C2)=C(S1)C3=C(C4=C5C=C(C6=CC7=C(OCCCCCCCCCCCCCCCCCCCC)C8=C(C=C(C)S8)C(OCCCCCCCCCCCCCCCCCCCC)=C7S6)S4)/C9=C5C=C(F)C=C9,PtFBTPBDT,5.42,3.97,0.83,5.79,0.64,3.11,"Chiu, C. Y.; Wang, H.; Phan, H.; Shiratori, K.; Nguyen, T. Q.; Hawker, C. J. Twisted Olefinic Building Blocks for Low Bandgap Polymers in Solar Cells and Ambipolar FieldEffect Transistors. J. Polym. Sci. Part A Polym. Chem. 2016, 54, 889¨C899. "
1662,CC1=CC(C(C=CC=C2)=C2/C3=C4C(SC(C5=CC=C(C6=C7C(C(N6CCCCCCCCCCCCCCCCCCCC)=O)=C(C8=CC=C(C)S8)N(CCCCCCCCCCCCCCCCCCCC)C7=O)S5)=C9)=C9C%10=C\4C=CC=C%10)=C3S1,PtBTPDPP,5.2,3.99,0.6,2.47,0.61,0.94,"Chiu, C. Y.; Wang, H.; Phan, H.; Shiratori, K.; Nguyen, T. Q.; Hawker, C. J. Twisted Olefinic Building Blocks for Low Bandgap Polymers in Solar Cells and Ambipolar FieldEffect Transistors. J. Polym. Sci. Part A Polym. Chem. 2016, 54, 889¨C899. "
1663,CC1=CC(C(C=CC=C2)=C2/C3=C4C(SC(C5=CC(C(C6=CC=C(CCCCCC)C=C6)(C7=CC=C(CCCCCC)C=C7)C8=C9C=C%10C(C(SC(C)=C%11)=C%11C%10(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)=C8)=C9S5)=C%14)=C%14C%15=C\4C=CC=C%15)=C3S1,PtBTPIDT,5.28,3.78,0.77,10.01,0.45,3.64,"Chiu, C. Y.; Wang, H.; Phan, H.; Shiratori, K.; Nguyen, T. Q.; Hawker, C. J. Twisted Olefinic Building Blocks for Low Bandgap Polymers in Solar Cells and Ambipolar FieldEffect Transistors. J. Polym. Sci. Part A Polym. Chem. 2016, 54, 889¨C899. "
1664,CC(S1)=CC(C2=C/3C=CC=C2)=C1C3=C4C(SC(C5=CC(C(OCCCCCCCCCCCCCCCCCCCC)=C(SC(C)=C6)C6=C7OCCCCCCCCCCCCCCCCCCCC)=C7S5)=C8)=C8C9=C/4C=CC=C9,PcBTPBDT,5.29,3.81,0.66,3.4,0.53,1.23,"Chiu, C. Y.; Wang, H.; Phan, H.; Shiratori, K.; Nguyen, T. Q.; Hawker, C. J. Twisted Olefinic Building Blocks for Low Bandgap Polymers in Solar Cells and Ambipolar FieldEffect Transistors. J. Polym. Sci. Part A Polym. Chem. 2016, 54, 889¨C899. "
1665,CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC(C(C=C(C)S5)=C5C6=NC(C(N(CC(CCCCCCCC)CCCCCCCCCC)C7=O)=O)=C7N=C68)=C8S4)S3)C9=NSN=C92)S1,P1,5.44,3.84,0.84,11.74,0.63,6.21,"Keshtov, M. L.; Kuklin, S. A.; Godovsky, D. Y.; Khokhlov, A. R.; Kurchania, R.; Chen, F. C.; Koukaras, E. N.; Sharma, G. D. New Alternating D-A1-D-A2copolymer Containing Two Electron-Deficient Moieties Based on Benzothiadiazole and 9-(2-Octyldodecyl)-8H-pyrrolo[3,4-b]bisthieno[2,3-f:3¡¯,2¡¯-h]quinoxaline-8,10(9H)-Dione for Efficient Polymer Solar Cells. J. Polym. Sci. Part A Polym. Chem. 2016, 54, 155¨C168. "
1666,CC1=C(CCC(C)CCCC(C)C)C=C(C2=C(C3=C4C5=CC=CC4=CC=C3)C5=C(C6=CC(CCC(C)CCCC(C)C)=C(C7=CC8=C(C=C(C)S8)S7)S6)S2(=O)=O)S1,PTSSO-TT,5.4,3.8,0.71,11.86,0.45,3.79,"Shin, Y.-R.; Lee, W.-H.; Park, J. B.; Kim, J.-H.; Lee, S. K.; Shin, W. S.; Hwang, D.-H.; Kang, I.-N. Synthesis and Characterization of New Low Band-Gap Polymers Containing Electron-Accepting acenaphtho[1,2-C]thiophene-S,S-Dioxide Groups. J. Polym. Sci. Part A Polym. Chem. 2016, 54, 498¨C506. "
1667,CC1=C(CCC(C)CCCC(C)C)C=C(C2=C(C3=C4C5=CC=CC4=CC=C3)C5=C(C6=CC(CCC(C)CCCC(C)C)=C(C7=CC8=C(C(OCC(CCCC)CC)=C(C=C(C)S9)C9=C8OCC(CC)CCCC)S7)S6)S2(=O)=O)S1,PTSSO-BDT,5.5,3.9,0.72,7.78,0.35,1.93,"Shin, Y.-R.; Lee, W.-H.; Park, J. B.; Kim, J.-H.; Lee, S. K.; Shin, W. S.; Hwang, D.-H.; Kang, I.-N. Synthesis and Characterization of New Low Band-Gap Polymers Containing Electron-Accepting acenaphtho[1,2-C]thiophene-S,S-Dioxide Groups. J. Polym. Sci. Part A Polym. Chem. 2016, 54, 498¨C506. "
1668,CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC5=C(C(C6=CC=C(CC(CCCC)CC)S6)=C(C=C(C)S7)C7=C5C8=CC=C(CC(CC)CCCC)S8)S4)S3)C9=C2N=C(C%10=CC=C(OCCC(C)CCCC(C)C)C(OCCC(C)CCCC(C)C)=C%10)C(C%11=CC(OCCC(C)CCCC(C)C)=C(OCCC(C)CCCC(C)C)C=C%11)=N9)S1,PQx,5.4,3.58,0.85,8.96,0.52,3.97,"Jo, E.; Park, J. B.; Lee, W.-H.; Kim, J.-H.; Jung, I. H.; Hwang, D.-H.; Kang, I.-N. Synthesis and Characterization of a New Phenanthrenequinoxaline-Based Polymer for Organic Solar Cells. J. Polym. Sci. Part A Polym. Chem. 2016, 54, 2804¨C2810. "
1669,CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC5=C(C(C6=CC=C(CC(CCCC)CC)S6)=C(C=C(C)S7)C7=C5C8=CC=C(CC(CC)CCCC)S8)S4)S3)C9=C2N=C(C%10=C%11C=C(OCCC(C)CCCC(C)C)C(OCCC(C)CCCC(C)C)=C%10)C(C%12=CC(OCCC(C)CCCC(C)C)=C(OCCC(C)CCCC(C)C)C=C%12%11)=N9)S1,PphQx,5.4,3.64,0.8,10.85,0.58,5.03,"Jo, E.; Park, J. B.; Lee, W.-H.; Kim, J.-H.; Jung, I. H.; Hwang, D.-H.; Kang, I.-N. Synthesis and Characterization of a New Phenanthrenequinoxaline-Based Polymer for Organic Solar Cells. J. Polym. Sci. Part A Polym. Chem. 2016, 54, 2804¨C2810. "
1670,CC1=CC2=C(C(C3=C(F)C(F)=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCCCC)C5=C(C=C(C6=C(C(N(CC(CCCCCCCC)CCCCCC)C7=O)=O)C7=C(C8=CC9=C(C(CCCCCCCC)=C(C)S9)S8)S6)S5)S4)S%10)C%10=C2C%11=C(F)C(F)=C(CC(CCCC)CC)S%11)S1,PBDT(ff)-ttTPD,5.65,3.49,0.98,12.49,0.61,7.45,"Kim, J.; Park, J. B.; Lee, W. H.; Kim, J. H.; Hwang, D. H.; Kang, I. N. HighPerformance Fluorine-Containing BDT-Based Copolymer for Organic Solar Cells with a High Open Circuit Voltage. J. Polym. Sci. Part A Polym. Chem. 2017, 55, 2506¨C2512. "
1671,CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCCCC)C5=C(C=C(C6=C(C(N(CC(CCCCCCCC)CCCCCC)C7=O)=O)C7=C(C8=CC9=C(C(CCCCCCCC)=C(C)S9)S8)S6)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CC)S%11)S1,PBDTT-ttTPD,5.45,3.58,0.84,12.07,0.67,6.79,"Kim, J.; Park, J. B.; Lee, W. H.; Kim, J. H.; Hwang, D. H.; Kang, I. N. HighPerformance Fluorine-Containing BDT-Based Copolymer for Organic Solar Cells with a High Open Circuit Voltage. J. Polym. Sci. Part A Polym. Chem. 2017, 55, 2506¨C2512. "
1672,CC1=CC2=C(C(C3=C(OC)C(OC)=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=C(OC)C(OC)=C(CC(CC)CCCC)S9)S1,PBDTOT-FBT,5.46,3.55,0.92,8.71,0.603,4.84,"Wang, W.; Chen, L.; Wang, G.; Zhang, Z.; Li, Y. Synthesis and Optoelectronic Properties of Copolymers with Conjugated 2-(2-Ethylhexyl)-3,4-Dimethoxythiophene Side Chains. Macromol. Chem. Phys. 2016, 217, 1586¨C1599. "
1673,CC1=CC2=C(C(C3=C(OC)C(OC)=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=CC=C(C6=CC(CCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=C(OC)C(OC)=C(CC(CC)CCCC)S9)S1,PBDTOT-BT,5.25,3.54,0.88,7.6,0.369,2.47,"Wang, W.; Chen, L.; Wang, G.; Zhang, Z.; Li, Y. Synthesis and Optoelectronic Properties of Copolymers with Conjugated 2-(2-Ethylhexyl)-3,4-Dimethoxythiophene Side Chains. Macromol. Chem. Phys. 2016, 217, 1586¨C1599. "
1674,CC1=CC2=C(C(C3=C(OC)C(OC)=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C(N(CC(CC)CCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CC(CC)CCCC)C6=O)S4)S8)C8=C2C9=C(OC)C(OC)=C(CC(CC)CCCC)S9)S1,PBDTOT-DPP,5.2,3.52,0.78,8.29,0.472,3.05,"Wang, W.; Chen, L.; Wang, G.; Zhang, Z.; Li, Y. Synthesis and Optoelectronic Properties of Copolymers with Conjugated 2-(2-Ethylhexyl)-3,4-Dimethoxythiophene Side Chains. Macromol. Chem. Phys. 2016, 217, 1586¨C1599. "
1675,CC(S1)=CC2=C1C(OC[C@H](CCCC)CC)=C(C=C(C3=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C4=O)=C5C4=C(C6=CC=C(C)S6)N(CC(CCCCCC)CCCCCCCC)C5=O)S3)S7)C7=C2OC[C@H](CCCC)CC,PBDPP-1,5.29,3.84,0.69,6.5,0.63,2.83,"Zhang, S.; Ye, L.; Wang, Q.; Li, Z.; Guo, X.; Huo, L.; Fan, H.; Hou, J. Enhanced Photovoltaic Performance of Diketopyrrolopyrrole (DPP Based Polymer with Extended ¦Ð -Conjugation. J. Phys. Chem. C 2013, 117, 9550?9557. "
1676,CC(S1)=CC2=C1C(C3=CC=C(C[C@H](CCCC)CC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CC(CCCCCC)CCCCCCCC)C6=O)S4)S8)C8=C2C9=CC=C(C[C@H](CCCC)CC)S9,PBDPP-2,5.29,3.84,0.73,8.42,0.68,4.23,"Zhang, S.; Ye, L.; Wang, Q.; Li, Z.; Guo, X.; Huo, L.; Fan, H.; Hou, J. Enhanced Photovoltaic Performance of Diketopyrrolopyrrole (DPP Based Polymer with Extended ¦Ð -Conjugation. J. Phys. Chem. C 2013, 117, 9550?9557. "
1677,CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC5=C(C=C(C(N(CC(CCCCCC)CCCCCCCC)C6=O)=C7C6=C(C8=CC9=C(C=C(C)S9)S8)N(CC(CCCCCC)CCCCCCCC)C7=O)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CC)S%11,PBDPP-3,5.05,3.62,0.63,16.25,0.6,6.18,"Zhang, S.; Ye, L.; Wang, Q.; Li, Z.; Guo, X.; Huo, L.; Fan, H.; Hou, J. Enhanced Photovoltaic Performance of Diketopyrrolopyrrole (DPP Based Polymer with Extended ¦Ð -Conjugation. J. Phys. Chem. C 2013, 117, 9550?9557. "
1678,CC1=CC2=C(C(C3=CC(CCCCCCCC)=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(CCCCCCCCC)N=C(C6=NC(CCCCCCCCC)=C(C7=CC=C(C)S7)S6)S5)S4)S8)C8=C2C9=CC(CCCCCCCC)=C(CCCCCCCC)S9)S1,PBDTBTz-T,4.95,2.82,0.92,10.53,0.629,6.15,"Wang, K.; Guo, X.; Guo, B.; Li, W.; Zhang, M.; Li, Y. Broad Bandgap D-A Copolymer Based on Bithiazole Acceptor Unit for Application in High-Performance Polymer Solar Cells with Lower Fullerene Content. Macromol. Rapid Commun. 2016, 37, 1066¨C1073. "
1679,CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=CC=C(C3=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C(F)=C5F)S4)S3)C7=NSN=C72)S1,PBT-2TPF4,5.63,3.88,0.854,10.93,0.606,5.7,"Liao, X.; Wu, F.; An, Y.; Xie, Q.; Chen, L.; Chen, Y. Novel Copolymers Based Tetrafluorobenzene and Difluorobenzothiadiazole for Organic Solar Cells with Prominent Open Circuit Voltage and Stability. Macromol. Rapid Commun. 2017, 38, 1600556/1¨C7. "
1680,CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C(F)=C5F)S4)S3)C7=NSN=C72)S1,PffBT-2TPF4,5.84,4.07,1.017,6.73,0.526,3.6,"Liao, X.; Wu, F.; An, Y.; Xie, Q.; Chen, L.; Chen, Y. Novel Copolymers Based Tetrafluorobenzene and Difluorobenzothiadiazole for Organic Solar Cells with Prominent Open Circuit Voltage and Stability. Macromol. Rapid Commun. 2017, 38, 1600556/1¨C7. "
1681,CC1=C(CC(CC)CCCC)C=C(C2=C(C(C3=C(CC(CC)CCCC)SC(CC(CCCC)CC)=C3C4=O)=O)C4=C(C5=CC(CC(CC)CCCC)=C(C6=CC=C(C7=CC=C(C)S7)S6)S5)S2)S1,PBDD4T,5.3,3.27,0.86,11.16,0.68,6.53,"Zhang, S.; Qin, Y.; Uddin, M. A.; Jang, B.; Zhao, W.; Liu, D.; Woo, H. Y.; Hou, J. A Fluorinated Polythiophene Derivative with Stabilized Backbone Conformation for Highly Efficient Fullerene and Non-Fullerene Polymer Solar Cells. Macromolecules 2016, 49, 2993¨C3000. "
1682,CC1=C(CC(CC)CCCC)C=C(C2=C(C(C3=C(CC(CC)CCCC)SC(CC(CCCC)CC)=C3C4=O)=O)C4=C(C5=CC(CC(CC)CCCC)=C(C6=CC(F)=C(C7=C(F)C=C(C)S7)S6)S5)S2)S1,PBDD4T-2F,5.39,3.61,0.88,15.13,0.68,9.04,"Zhang, S.; Qin, Y.; Uddin, M. A.; Jang, B.; Zhao, W.; Liu, D.; Woo, H. Y.; Hou, J. A Fluorinated Polythiophene Derivative with Stabilized Backbone Conformation for Highly Efficient Fullerene and Non-Fullerene Polymer Solar Cells. Macromolecules 2016, 49, 2993¨C3000. "
1683,CC1=CC=C(C2=CC=C(C3=CC=C(C4=C5C(C(N4CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C6=CC=C(C)S6)N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C5=O)S3)S2)S1,P(BT-DPP),5.17,3.55,0.64,3.65,0.63,1.48,"Wang, L.; Qiao, Z.; Gao, C.; Liu, J.; Zhang, Z. G.; Li, X.; Li, Y.; Wang, H. EndCapping Effect of quinoxalino[2,3-b¡ä]porphyrin on Donor-Acceptor Copolymer and Improved Performance of Polymer Solar Cells. Macromolecules 2016, 49, 3723¨C3732. "
1684,CC1=CC=C(C2=CC=C(C3=CC=C(C4=C5C(C(N4CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C6=CC=C(C)S6)N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C5=O)S3)S2)S1,P(BT-DPP)-T,5.22,3.52,0.64,6.22,0.62,2.45,"Wang, L.; Qiao, Z.; Gao, C.; Liu, J.; Zhang, Z. G.; Li, X.; Li, Y.; Wang, H. EndCapping Effect of quinoxalino[2,3-b¡ä]porphyrin on Donor-Acceptor Copolymer and Improved Performance of Polymer Solar Cells. Macromolecules 2016, 49, 3723¨C3732. "
1685,CC1=CC2=C(C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC6=C(C(SC(C7=CC(CC(CCCC)CC)=C(C)S7)=C8)=C8C9=NON=C96)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CCCCCC)S%11)S1,PBDTfDTBO-L,5.51,3.56,0.76,3.97,0.455,1.37,"Lee, J.; Sin, D. H.; Clement, J. A.; Kulshreshtha, C.; Kim, H. G.; Song, E.; Shin, J.; Hwang, H.; Cho, K. Medium-Bandgap Conjugated Polymers Containing Fused Dithienobenzochalcogenadiazoles: Chalcogen Atom Effects on Organic Photovoltaics. Macromolecules 2016, 49, 9358¨C9370. "
1686,CC1=CC2=C(C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC6=C(C(SC(C7=CC(CC(CCCC)CC)=C(C)S7)=C8)=C8C9=NSN=C96)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CCCCCC)S%11)S1,PBDTfDTBT-L,5.44,3.54,0.86,8.72,0.61,4.58,"Lee, J.; Sin, D. H.; Clement, J. A.; Kulshreshtha, C.; Kim, H. G.; Song, E.; Shin, J.; Hwang, H.; Cho, K. Medium-Bandgap Conjugated Polymers Containing Fused Dithienobenzochalcogenadiazoles: Chalcogen Atom Effects on Organic Photovoltaics. Macromolecules 2016, 49, 9358¨C9370. "
1687,CC1=CC2=C(C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC6=C(C(SC(C7=CC(CC(CCCC)CC)=C(C)S7)=C8)=C8C9=N[Se]N=C96)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CCCC)CCCCCC)S%11)S1,PBDTfDTBS-L,5.4,3.55,0.82,9.66,0.674,5.34,"Lee, J.; Sin, D. H.; Clement, J. A.; Kulshreshtha, C.; Kim, H. G.; Song, E.; Shin, J.; Hwang, H.; Cho, K. Medium-Bandgap Conjugated Polymers Containing Fused Dithienobenzochalcogenadiazoles: Chalcogen Atom Effects on Organic Photovoltaics. Macromolecules 2016, 49, 9358¨C9370. "
1688,CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C(C#N)C(OCC(CCCC)CC)=C(C5=C(OCC(CC)CCCC)C(C#N)=C(C)S5)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7)S1,P1,5.6,3.78,1,8.76,0.58,5.06,"Huang, J.; Tang, Y.; Gao, K.; Liu, F.; Guo, H.; Russell, T. P.; Yang, T.; Liang, Y.; Cheng, X.; Guo, X. Head-to-Head Linkage Containing Dialkoxybithiophene-Based Polymeric Semiconductors for Polymer Solar Cells with Large Open- Circuit Voltages. Macromolecules 2017, 50, 137¨C150. "
1689,CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C(C#N)C(OCCCCCCCCCC)=C(C5=C(OCCCCCCCCCC)C(C#N)=C(C)S5)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7)S1,P2,5.54,3.77,0.9,10.31,0.54,5,"Huang, J.; Tang, Y.; Gao, K.; Liu, F.; Guo, H.; Russell, T. P.; Yang, T.; Liang, Y.; Cheng, X.; Guo, X. Head-to-Head Linkage Containing Dialkoxybithiophene-Based Polymeric Semiconductors for Polymer Solar Cells with Large Open- Circuit Voltages. Macromolecules 2017, 50, 137¨C150. "
1690,CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C(C#N)C(OCCCCCCCCCCCC)=C(C5=C(OCCCCCCCCCCCC)C(C#N)=C(C)S5)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7)S1,P3,5.56,3.78,0.92,12.21,0.64,7.13,"Huang, J.; Tang, Y.; Gao, K.; Liu, F.; Guo, H.; Russell, T. P.; Yang, T.; Liang, Y.; Cheng, X.; Guo, X. Head-to-Head Linkage Containing Dialkoxybithiophene-Based Polymeric Semiconductors for Polymer Solar Cells with Large Open- Circuit Voltages. Macromolecules 2017, 50, 137¨C150. "
1691,CC1=CC2=C(C(C3=CC(C(CC(CCCC)CC)(CC(CC)CCCC)C4=C5C=CC=C4)=C5C=C3)=C(C=C(C6=CC=C(C7=CC=C(C8=CC=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC(C(CC(CCCC)CC)(CC(CCCC)CC)C%12=C%13C=CC=C%12)=C%13C=C%11)S1,PFBDT-DTBT,5.41,3.6,0.9,13.26,0.598,7.13,"Song, X.; Zhang, Y.; Li, Y.; Li, F.; Bao, X.; Ding, D.; Sun, M.; Yang, R. Fluorene Side-Chained Benzodithiophene Polymers for Low Energy Loss Solar Cells. Macromolecules 2017, 50, 6880¨C6887. "
1692,CC1=CC2=C(C(C3=CC(C(CC(CCCC)CC)(CC(CC)CCCC)C4=C5C=CC=C4)=C5C=C3)=C(C=C(C6=CC=C(C7=C(F)C(F)=C(C8=CC=C(C)S8)C9=NSN=C97)S6)S%10)C%10=C2C%11=CC(C(CC(CCCC)CC)(CC(CCCC)CC)C%12=C%13C=CC=C%12)=C%13C=C%11)S1,PFBDT-DTffBT,5.82,3.7,0.96,13.24,0.577,7.33,"Song, X.; Zhang, Y.; Li, Y.; Li, F.; Bao, X.; Ding, D.; Sun, M.; Yang, R. Fluorene Side-Chained Benzodithiophene Polymers for Low Energy Loss Solar Cells. Macromolecules 2017, 50, 6880¨C6887. "
1693,CC1=CC(N(C2=CC=C(OCC(CCCCCCCCCCCC)CCCCCCCCCC)C=C2)B(F)F)=C(C(N=CC(C3=CC(OC)=C(C4=C(OC)C=C(C)S4)S3)=C5)=C5N(B(F)F)C6=CC=C(OCC(CCCCCCCCCC)CCCCCCCCCCCC)C=C6)N=C1,P2-Ome,5.46,3.48,0.76,7.59,0.506,2.92,"Long, X.; Dou, C.; Liu, J.; Wang, L. Fine-Tuning LUMO Energy Levels of Conjugated Polymers Containing a B¡ûN Unit. Macromolecules 2017, 50, 8521¨C8528. "
1694,CC1=CC2=C(C(C3=CC(OCCCCCC)=CC(OCCCCCC)=C3)=C(C=C(C4=CC=C(C5=C(CCCCCCCCC)N=C(C6=NC(CCCCCCCCC)=C(C7=CC=C(C)S7)S6)S5)S4)S8)C8=C2C9=CC(OCCCCCC)=CC(OCCCCCC)=C9)S1,PTZ6,5.36,3.36,0.96,10.9,0.767,8.1,"Guo, B.; Li, W.; Guo, X.; Meng, X.; Ma, W.; Zhang, M.; Li, Y. A Novel Wide Bandgap Conjugated Polymer (2.0 eV) Based on Bithiazole for High Efficiency Polymer Solar Cells. Nano Energy 2017, 34, 556¨C561. "
1695,CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC=C(N(C5=CC=C(C)C=C5)C6=CC=C(OCCCCCCCC)C=C6)C=C4)S3)C7=NON=C27)S1,P1,5.15,3.09,0.7,2.06,0.43,0.86,"Zhang, B.; Chen, G.; Xu, J.; Yang, W. Feasible Energy Level Tuning in Polymer Solar Cells Based on Broad Band-Gap Polytriphenylamine. New J. Chem. 2015, 40, 402¨C412. "
1696,CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC=C(N(C5=CC=C(C)C=C5)C6=CC=C(CCCCCCCC)C=C6)C=C4)S3)C7=NON=C27)S1,P2,5.23,3.08,0.8,4.84,0.5,2.22,"Zhang, B.; Chen, G.; Xu, J.; Yang, W. Feasible Energy Level Tuning in Polymer Solar Cells Based on Broad Band-Gap Polytriphenylamine. New J. Chem. 2015, 40, 402¨C412. "
1697,CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC=C(N(C5=CC=C(C)C=C5)C6=CC=C(C(F)(F)F)C=C6)C=C4)S3)C7=NON=C27)S1,P3,5.41,3.08,0.95,2.57,0.36,1.28,"Zhang, B.; Chen, G.; Xu, J.; Yang, W. Feasible Energy Level Tuning in Polymer Solar Cells Based on Broad Band-Gap Polytriphenylamine. New J. Chem. 2015, 40, 402¨C412. "
1698,CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC=C(N(C5=CC=C(C)C=C5)C6=CC(C(F)(F)F)=CC(C(F)(F)F)=C6)C=C4)S3)C7=NON=C27)S1,P4,5.46,3.09,1,1.87,0.38,1.05,"Zhang, B.; Chen, G.; Xu, J.; Yang, W. Feasible Energy Level Tuning in Polymer Solar Cells Based on Broad Band-Gap Polytriphenylamine. New J. Chem. 2015, 40, 402¨C412. "
1699,CC(S1)=CC2=C1C(CC(CCCC)CCCCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=C4N=C(C7=CC=C(OCCCCCCCC)C=C7)C(C8=CC=C(OCCCCCCCC)C=C8)=N6)S3)S9)C9=C2CC(CCCCCC)CCCC,PBDTFQ-T,6,4.23,0.84,9.18,0.67,5.68,"Gedefaw, D.; Tessarolo, M.; Zhuang, W.; Kroon, R.; Wang, E.; Bolognesi, M.; Seri, M.; Muccini, M.; Andersson, M. R. Conjugated Polymers Based on Benzodithiophene and Fluorinated Quinoxaline for Bulk Heterojunction Solar Cells: Thiophene versus thieno[3,2-b]thiophene as ¦Ð-Conjugated Spacers. Polym. Chem. 2014, 5, 2083?2093. "
1700,CC(S1)=CC2=C1C(CC(CCCC)CCCCCC)=C(C=C(C3=CC4=C(C=C(C5=C(F)C(F)=C(C6=CC7=C(C=C(C)S7)S6)C8=C5N=C(C9=CC=C(OCCCCCCCC)C=C9)C(C%10=CC=C(OCCCCCCCC)C=C%10)=N8)S4)S3)S%11)C%11=C2CC(CCCCCC)CCCC,PBDTFQ-TT,5.9,4.23,0.82,10.87,0.59,5.6,"Gedefaw, D.; Tessarolo, M.; Zhuang, W.; Kroon, R.; Wang, E.; Bolognesi, M.; Seri, M.; Muccini, M.; Andersson, M. R. Conjugated Polymers Based on Benzodithiophene and Fluorinated Quinoxaline for Bulk Heterojunction Solar Cells: Thiophene versus thieno[3,2-b]thiophene as ¦Ð-Conjugated Spacers. Polym. Chem. 2014, 5, 2083?2093. "
1701,O=C(N1CC(CCCCCCCC)CCCCCCCCCC)C2=C(C(C=CC3=C4C5=C(C=C(C6=CC=C(C)S6)S5)N(CC(CCCCCCCCCC)CCCCCCCC)C3=O)=C4C=C2)C7=C1C=C(C)S7,PThzTITI,5.64,2.78,1.08,1.6,0.568,0.98,"Xiao, N.; Qian, L.; Cao, J.; Zhao, X.; Han, A.; Ding, L. A Zigzag Fused-Ring Building Block for Polymer Solar Cells. New J. Chem. 2016, 40, 4895¨C4898. "
1702,O=C(N1CC(CCCCCCCC)CCCCCCCCCC)C2=C(C(C=CC3=C4C5=C(C=C(C6=CC=C(C)[Se]6)S5)N(CC(CCCCCCCCCC)CCCCCCCC)C3=O)=C4C=C2)C7=C1C=C(C)S7,PSezTITI,5.65,2.82,1.05,3.75,0.596,2.36,"Xiao, N.; Qian, L.; Cao, J.; Zhao, X.; Han, A.; Ding, L. A Zigzag Fused-Ring Building Block for Polymer Solar Cells. New J. Chem. 2016, 40, 4895¨C4898. "
1703,CC1=CC=C(C2=C3C(SC(CCCCCCCC)=C3)=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C)C6=NSN=C65)S4)C7=C2SC(CCCCCCCC)=C7)S1,PVB1,5.51,3.52,1,6.8,0.42,2.84,"Wen, S.; Xiao, M.; Shen, W.; Gu, C.; Zhu, D.; Yang, R. Incorporating a Vertical BDT Unit in Conjugated Polymers for Drastically Improving the Open- Circuit Voltage of Polymer Solar Cells. New J. Chem. 2016, 40, 5300¨C5305. "
1704,CC1=CC=C(C2=C3C(SC(CCCCCCCC)=C3)=C(C4=CC=C(C5=C6C(C(N(CC(CC)CCCC)C6=O)=O)=C(C)S5)S4)C7=C2SC(CCCCCCCC)=C7)S1,PVB2,5.64,3.54,1.09,5.33,0.35,2.05,"Wen, S.; Xiao, M.; Shen, W.; Gu, C.; Zhu, D.; Yang, R. Incorporating a Vertical BDT Unit in Conjugated Polymers for Drastically Improving the Open- Circuit Voltage of Polymer Solar Cells. New J. Chem. 2016, 40, 5300¨C5305. "
1705,CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(C(N(CCCCCCCC)C6=O)=O)C6=C(C7=CC=C(C8=CC=C(C9=C(C(N(CCCCCCCC)C%10=O)=O)C%10=C(C%11=CC=C(C)S%11)N9CC(CCCCCCCC)CCCCCCCCCC)S8)S7)N5C[C@@H](CCCCCCCC)CCCCCCCCCC)S4)S%12)C%12=C2C%13=CC=C(CC(CCCC)CC)S%13)S1,P(BDTT-BTBDPPD),5.44,3.34,0.9,7.99,0.64,4.62,"Tamilavan, V.; Kim, S.; Sung, J. Y.; Lee, D. Y.; Cho, S.; Jin, Y.; Jeong, J.; Park, S. H.; Hyun, M. H. Effects of the Incorporation of Bithiophene instead of Thiophene between the pyrrolo[3,4-c]pyrrole-1,3-Dione Units of a bis(pyrrolo[3,4-c]pyrrole-1,3- Dione)-Based Polymer for Polymer Solar Cells. New J. Chem. 2016, 40, 10153¨C10160. "
1706,CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=CC3=C(C(SC(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC=C(C)S5)S4)=C6)=C6C7=NON=C73)S2)S1,PDTfBO-T,5.5,3.66,0.93,11.1,0.543,5.63,"Wang, H.; Zhu, Y.; Liu, Z.; Zhang, L.; Chen, J.; Cao, Y. Alternating Dithienobenzoxadiazole-Based Conjugated Polymers for Field-Effect Transistors and Polymer Solar Cells. Org. Electron. 2016, 31, 1¨C10. "
1707,CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=CC3=C(C(SC(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)=C7)=C7C8=NON=C83)S2)S1,PDTfBO-DT,5.48,3.62,0.89,10.3,0.61,5.61,"Wang, H.; Zhu, Y.; Liu, Z.; Zhang, L.; Chen, J.; Cao, Y. Alternating Dithienobenzoxadiazole-Based Conjugated Polymers for Field-Effect Transistors and Polymer Solar Cells. Org. Electron. 2016, 31, 1¨C10. "
1708,CC1=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C2=CC3=C(C(SC(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC6=C(C=C(C)S6)S5)S4)=C7)=C7C8=NON=C83)S2)S1,PDTfBO-TT,5.39,3.5,0.87,9.69,0.664,5.6,"Wang, H.; Zhu, Y.; Liu, Z.; Zhang, L.; Chen, J.; Cao, Y. Alternating Dithienobenzoxadiazole-Based Conjugated Polymers for Field-Effect Transistors and Polymer Solar Cells. Org. Electron. 2016, 31, 1¨C10. "
1709,CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)C=C6)C=C5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1,poly(DPP-alt-BP),5.5,3.82,0.75,7.25,0.362,1.97,"Kim, S. B.; Um, H. A.; Kim, H. J.; Cho, M. J.; Choi, D. H. A DiketopyrrolopyrroleBased Regular Terpolymer Bearing Two Different ¦Ð-Extended Donor Units and Its Application in Solar Cells. Org. Electron. 2016, 31, 198¨C206. "
1710,CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1,poly(DPP-alt-BT),5.27,3.94,0.63,9.83,0.52,3.21,"Kim, S. B.; Um, H. A.; Kim, H. J.; Cho, M. J.; Choi, D. H. A DiketopyrrolopyrroleBased Regular Terpolymer Bearing Two Different ¦Ð-Extended Donor Units and Its Application in Solar Cells. Org. Electron. 2016, 31, 198¨C206. "
1711,CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C7=CC=C(C8=C9C(C(N8CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C%10=CC=C(C%11=CC=C(C%12=CC=C(C)C=C%12)C=C%11)S%10)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C9=O)S7)S6)S5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1,poly(DPP4T-alt-TBP),5.42,3.9,0.71,10.08,0.633,4.54,"Kim, S. B.; Um, H. A.; Kim, H. J.; Cho, M. J.; Choi, D. H. A DiketopyrrolopyrroleBased Regular Terpolymer Bearing Two Different ¦Ð-Extended Donor Units and Its Application in Solar Cells. Org. Electron. 2016, 31, 198¨C206. "
1712,CC1=CC=C(S1)C2=CC3=C(C(C4=CC=C(CC(CCCC)CC)S4)=C(C=C(C5=CC=C(C6=CC=C(C7=CC=C(C8=C(N=C(C9=CC(OCCCCCCCC)=CC=C9)C(C%10=CC=CC(OCCCCCCCC)=C%10)=N%11)C%11=C(C)C=C8)S7)C%12=C6N=C(C%13=CC=CC(OCCCCCCCC)=C%13)C(C%14=CC(OCCCCCCCC)=CC=C%14)=N%12)S5)S%15)C%15=C3C%16=CC=C(CC(CCCC)CC)S%16)S2,PBDT-DTQ,5.19,3.29,0.67,10.37,0.555,3.84,"Dang, D.; Wang, X.; Zhi, Y.; Meng, L.; Bao, X.; Yang, R.; Zhu, W. Synthesis and Characterization of D-A-A Type Regular Terpolymers with Narrowed Band-Gap and Their Application in High Performance Polymer Solar Cells. Org. Electron. 2016, 32, 237¨C243. "
1713,CC(C=C1)=C2C(N=C(C3=CC(OCCCCCCCC)=CC=C3)C(C4=CC=CC(OCCCCCCCC)=C4)=N2)=C1C(S5)=CC=C5C(C6=C7N=C(C8=CC=CC(OCCCCCCCC)=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N6)=CC=C7C%10=CC=C(S%10)C%11=CC%12=C(C%13=CC%14=C(C(SC(C%15=CC=C(C)S%15)=C%16)=C%16C%14(C%17=CC=C(CCCCCC)C=C%17)C%18=CC=C(CCCCCC)C=C%18)C=C%13C%12(C%19=CC=C(CCCCCC)C=C%19)C%20=CC=C(CCCCCC)C=C%20)S%11,PIDT-DTQ,5.33,3.28,0.86,11.42,0.658,6.41,"Dang, D.; Wang, X.; Zhi, Y.; Meng, L.; Bao, X.; Yang, R.; Zhu, W. Synthesis and Characterization of D-A-A Type Regular Terpolymers with Narrowed Band-Gap and Their Application in High Performance Polymer Solar Cells. Org. Electron. 2016, 32, 237¨C243. "
1714,CC1=C(CC(CCCCCCCC)CCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCC)CCCCCCCC)=C(C4=CC=C(C)S4)S3)C5=NSN=C52)S1,P8,5,3.46,0.73,14.76,0.621,6.73,"Tang, D.; Liu, Y.; Zhang, Z.; Shu, Q.; Wang, B.; Fan, J.; Song, B. Donor-Acceptor Polymers Based on 5,6-Difluoro-benzo[1,2,5]thiadiazole for High Performance Solar Cells. Org. Electron. 2016, 33, 187¨C193. "
1715,CC1=C(CC(CCCCCCCC)CCCCCC)C=C(C2=C(F)C(F)=C(C3=CC(CC(CCCCCC)CCCCCCCC)=C(C4=CC=C(C)[Se]4)S3)C5=NSN=C52)S1,P9,5.14,3.54,0.75,14.15,0.646,6.84,"Tang, D.; Liu, Y.; Zhang, Z.; Shu, Q.; Wang, B.; Fan, J.; Song, B. Donor-Acceptor Polymers Based on 5,6-Difluoro-benzo[1,2,5]thiadiazole for High Performance Solar Cells. Org. Electron. 2016, 33, 187¨C193. "
1716,CC1=CC(/C=C/C2=CC=C(C3=CC=C(N(C4=CC=CC=C4)C5=CC=CC=C5)C=C3)S2)=C(C6=CC=C(C7=CC=C(C8=C9C(C(N8CC(CC)CCCC)=O)=C(C%10=CC=C(C%11=CC=C(C)S%11)S%10)N(CC(CCCC)CC)C9=O)S7)S6)S1,r-PTTDPP50,5.16,3.89,0.632,9.81,0.374,2.32,"Li, W. C.; Liu, Y. R.; Chen, J. H.; Chang, W. C.; Sah, P. T.; Chan, L. H. Two-Dimensional Conjugated Copolymers Composed of Diketopyrrolopyrrole, Thiophene, and Thiophene with Side Chains for Binary and Ternary Polymer Solar Cells. Org. Electron. 2016, 33, 213¨C220."
1717,O=C1C(C2=C(C3=CC=C(C4=CC(SC(C)=C5)=C5S4)S3)N1CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(C6=CC=C(C)S6)N(C[C@@H](CCCCCCCCCCCC)CCCCCCCCCC)C2=O,DT-PDPP2T-TT,5.1,3.7,0.72,11.79,0.65,5.55,"Kim, Y. J.; Jang, W.; Ahn, S.; Park, C. E.; Wang, D. H. Dramatically Enhanced Performances and Ideally Controlled Nano-Morphology via Co-Solvent Processing in Low Bandgap Polymer Solar Cells. Org. Electron. 2016, 34, 42¨C49. "
1718,O=C(N1CC(CCCCCCCC)CCCCCCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCCCCCC)CCCCCCCC)C4=C/3C=CC(C5=CC=C(C6=CC=C(C)S6)S5)=C4)=O,PIIDBT,5.54,3.97,0.87,8.51,0.619,4.58,"Park, G. E.; Choi, S.; Shin, J.; Cho, M. J.; Choi, D. H. Isoindigo-Based Polymer Solar Cells with High Open Circuit Voltages up to 1.01 v. Org. Electron. 2016, 34, 157¨C163. "
1719,O=C(N1CC(CCCCCCCC)CCCCCCCCCC)/C(C2=C1C=C(C)C=C2)=C3C(N(CC(CCCCCCCCCC)CCCCCCCC)C4=C/3C=CC(C5=CC(F)=C(C6=C(F)C=C(C)S6)S5)=C4)=O,PIIDFBT,5.79,4.18,1.01,9.11,0.672,6.21,"Park, G. E.; Choi, S.; Shin, J.; Cho, M. J.; Choi, D. H. Isoindigo-Based Polymer Solar Cells with High Open Circuit Voltages up to 1.01 v. Org. Electron. 2016, 34, 157¨C163. "
1720,O=C1N(CC(CCCCCCCCCC)CCCCCCCC)C(C2=C(C3=CC=C(C4=CC=C(C)S4)S3)SC(C5=CC=C(S5)C6=CC=C(C7=CC8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CCCC)CC)=C8S7)S6)=C21)=O,P1,5.39,3.52,0.81,6.11,0.67,3.3,"Liu, S.; Bao, X.; Li, W.; Wu, K.; Xie, G.; Yang, R.; Yang, C. Benzo[1,2-b:4,5-b¡ä]dithiophene and thieno[3,4-c]pyrrole-4,6-Dione Based Donor-¦Ð-Acceptor Conjugated Polymers for High Performance Solar Cells by Rational Structure Modulation. Macromolecules 2015, 48, 2948¨C2957. "
1721,O=C1N(CC(CCCCCCCCCC)CCCCCCCC)C(C2=C(C3=CC(SC(C)=C4)=C4S3)SC(C5=CC(S6)=C(S5)C=C6C7=CC8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CCCC)CC)=C8S7)=C21)=O,P2,5.47,3.4,0.88,9.3,0.68,5.55,"Liu, S.; Bao, X.; Li, W.; Wu, K.; Xie, G.; Yang, R.; Yang, C. Benzo[1,2-b:4,5-b¡ä]dithiophene and thieno[3,4-c]pyrrole-4,6-Dione Based Donor-¦Ð-Acceptor Conjugated Polymers for High Performance Solar Cells by Rational Structure Modulation. Macromolecules 2015, 48, 2948¨C2957. "
1722,O=C1N(CC(CCCC)CCCCCC)C(C2=C(C3=CC(SC(C)=C4CCCCCC)=C4S3)SC(C5=CC6=C(S5)C(CCCCCC)=C(C7=CC8=C(OCC(CCCC)CC)C9=C(C=C(C)S9)C(OCC(CCCC)CC)=C8S7)S6)=C21)=O,P3,5.42,3.52,0.83,10.6,0.65,5.77,"Liu, S.; Bao, X.; Li, W.; Wu, K.; Xie, G.; Yang, R.; Yang, C. Benzo[1,2-b:4,5-b¡ä]dithiophene and thieno[3,4-c]pyrrole-4,6-Dione Based Donor-¦Ð-Acceptor Conjugated Polymers for High Performance Solar Cells by Rational Structure Modulation. Macromolecules 2015, 48, 2948¨C2957. "
1723,O=C1N(CC(CCCCCCCCCC)CCCCCCCC)C(C2=C(C3=CC(SC(C)=C4CCCCCC)=C4S3)SC(C5=CC6=C(S5)C(CCCCCC)=C(C7=CC8=C(C9=CC=C(CC(CCCC)CC)S9)C%10=C(C=C(C)S%10)C(C%11=CC=C(CC(CCCC)CC)S%11)=C8S7)S6)=C21)=O,P4,5.38,3.47,0.86,13.7,0.66,7.71,"Liu, S.; Bao, X.; Li, W.; Wu, K.; Xie, G.; Yang, R.; Yang, C. Benzo[1,2-b:4,5-b¡ä]dithiophene and thieno[3,4-c]pyrrole-4,6-Dione Based Donor-¦Ð-Acceptor Conjugated Polymers for High Performance Solar Cells by Rational Structure Modulation. Macromolecules 2015, 48, 2948¨C2957. "
1724,CC1=CC2=C(C3=C4C5=C6C=C(C7=C(C)C=C(C)C=C7C)C=C5C8=C9C4=C(C(C%10=CC(C%11=CC=C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C%12=O)=C%13C%12=C(C%14=CC=C(C)S%14)N(CC(CCCCCCCC)CCCCCCCCCC)C%13=O)S%11)=C%15)=C%15C9=CC(C%16=C(C)C=C(C)C=C%16C)=C8)C%17=C3C(C2=CC(C%18=C(C)C=C(C)C=C%18C)=C%19)=C%19C%20=C%17C%10=CC(C%21=C(C)C=C(C)C=C%21C)=C%20)C6=C1,PHBCDPPC20,5.32,3.67,0.92,6.53,0.353,2.12,"Gao, C.; Qiao, Z.; Shi, K.; Chen, S.; Li, Y.; Yu, G.; Li, X.; Wang, H. Hexa-PeriHexabenzocoronene and Diketopyrrolopyrrole Based D-A Conjugated Copolymers for Organic Field Effect Transistor and Polymer Solar Cells. Org. Electron. 2016, 38, 245¨C255. "
1725,CC1=CC2=C(C3=C4C5=C6C=C(C7=C(C)C=C(C)C=C7C)C=C5C8=C9C4=C(C(C%10=CC(C%11=CC=C(C(N(CC(CC)CCCC)C%12=O)=C%13C%12=C(C%14=CC=C(C)S%14)N(CC(CC)CCCC)C%13=O)S%11)=C%15)=C%15C9=CC(C%16=C(C)C=C(C)C=C%16C)=C8)C%17=C3C(C2=CC(C%18=C(C)C=C(C)C=C%18C)=C%19)=C%19C%20=C%17C%10=CC(C%21=C(C)C=C(C)C=C%21C)=C%20)C6=C1,PHBCDPPC8,5.28,3.62,0.86,10.38,0.318,2.85,"Gao, C.; Qiao, Z.; Shi, K.; Chen, S.; Li, Y.; Yu, G.; Li, X.; Wang, H. Hexa-PeriHexabenzocoronene and Diketopyrrolopyrrole Based D-A Conjugated Copolymers for Organic Field Effect Transistor and Polymer Solar Cells. Org. Electron. 2016, 38, 245¨C255. "
1726,CC1=CC2=C(C3=C4C5=C6C=C(C7=C(C)C=C(C)C=C7C)C=C5C8=C9C4=C(C(C%10=CC(C%11=CC=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C%12=O)=C%13C%12=C(C%14=CC=C(C)O%14)N(CC(CCCCCCCCCC)CCCCCCCC)C%13=O)O%11)=C%15)=C%15C9=CC(C%16=C(C)C=C(C)C=C%16C)=C8)C%17=C3C(C2=CC(C%18=C(C)C=C(C)C=C%18C)=C%19)=C%19C%20=C%17C%10=CC(C%21=C(C)C=C(C)C=C%21C)=C%20)C6=C1,PHBCDPPF,5.3,3.61,0.88,6.39,0.336,1.89,"Gao, C.; Qiao, Z.; Shi, K.; Chen, S.; Li, Y.; Yu, G.; Li, X.; Wang, H. Hexa-PeriHexabenzocoronene and Diketopyrrolopyrrole Based D-A Conjugated Copolymers for Organic Field Effect Transistor and Polymer Solar Cells. Org. Electron. 2016, 38, 245¨C255. "
1727,CC1=CC2=C(C3=C4C5=C6C=C(C7=C(C)C=C(C)C=C7C)C=C5C8=C9C4=C(C(C%10=CC(C%11=CC=C(C%12=CC=C(C(N(CC(CCCCCCCCCC)CCCCCCCC)C%13=O)=C%14C%13=C(C%15=CC=C(C%16=CC=C(C)S%16)S%15)N(CC(CCCCCCCCCC)CCCCCCCC)C%14=O)S%12)S%11)=C%17)=C%17C9=CC(C%18=C(C)C=C(C)C=C%18C)=C8)C%19=C3C(C2=CC(C%20=C(C)C=C(C)C=C%20C)=C%21)=C%21C%22=C%19C%10=CC(C%23=C(C)C=C(C)C=C%23C)=C%22)C6=C1,PHBCDPPDT,5.19,3.63,0.79,10.5,0.331,2.74,"Gao, C.; Qiao, Z.; Shi, K.; Chen, S.; Li, Y.; Yu, G.; Li, X.; Wang, H. Hexa-PeriHexabenzocoronene and Diketopyrrolopyrrole Based D-A Conjugated Copolymers for Organic Field Effect Transistor and Polymer Solar Cells. Org. Electron. 2016, 38, 245¨C255. "
1728,CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC(C(C=C(C)S5)=C5C6=NC(C(N(CC(CCCCCCCC)CCCCCCCCCC)C7=O)=O)=C7N=C68)=C8S4)S3)C9=NSN=C29)S1,P1,5.44,3.84,0.86,11.92,0.64,6.56,"Keshtov, M. L.; Khokhlov, A. R.; Kuklin, S. A.; Osipov, S. A.; Radychev, N. A.; Buzin, M. I.; Sharma, G. D. Benzothiadiazole-pyrrolo[3,4-b]dithieno[2,3-f:3¡ä,2¡ä-h]quinoxalindione-Based Random Terpolymer Incorporating Strong and Weak Electron Accepting [1,2,5]thiadiazolo[3,4g]quinoxalinefor Polymer Solar Cells. Org. Electron. 2017, 41, 1¨C8. "
1729,CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C6C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C6=O)=O)=C(C7=CC(SC(C8=C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C9=O)=O)C9=C(C%10=CC=C(C)S%10)N8CCCCCCCC)=C%11)=C%11S7)N5CCCCCCCC)S4)S%12)C%12=C2C%13=CC=C(CC(CC)CCCC)S%13)S1,P(BDTT-TTBDPPD),5.42,3.36,0.9,8.94,0.67,5.37,"Tamilavan, V.; Kim, S.; Sung, J.; Lee, D. Y.; Cho, S.; Jin, Y.; Jeong, J.; Park, S. H.; Hyun, M. H. Enhanced Photovoltaic Performances of bis(pyrrolo[3,4-c]pyrrole-1,3-Dione)-Based Wide Band Gap Polymer via the Incorporation of an Appropriate Spacer Unit between pyrrolo[3,4-c]pyrrole-1,3-Dione Units. Org. Electron. 2017, 42, 34¨C41. "
1730,CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC(CCCCCC)=C(C5=CC=C(C6=C(CCCCCC)C=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1,PA,5.76,3.94,0.855,8.669,0.506,3.75,"Hong, N. J.; Lee, Y. S.; Park, J. H.; Na, S. I.; Choe, J. C.; Zong, K. Investigations into Inward Positioned 3,3¡ä-Dihexylditheinylbenzothiadiazole (DTBTh)-Benzodithiophene (BDT) Based Polymer Solar Cells by Controlling Molecular Weight and Alkyl Side Chain. Org. Electron. 2017, 42, 293¨C302. "
1731,CC(S1)=CC(CCCCCC)=C1C(C2=NSN=C23)=CC=C3C(S4)=C(CCCCCC)C=C4C(S5)=CC(C5=C6C7=CC=C(CCCCCCCCC)S7)=C(C8=CC=C(CCCCCCCCC)S8)C9=C6C=CS9,PB,5.66,3.85,0.769,6.9,0.456,2.42,"Hong, N. J.; Lee, Y. S.; Park, J. H.; Na, S. I.; Choe, J. C.; Zong, K. Investigations into Inward Positioned 3,3¡ä-Dihexylditheinylbenzothiadiazole (DTBTh)-Benzodithiophene (BDT) Based Polymer Solar Cells by Controlling Molecular Weight and Alkyl Side Chain. Org. Electron. 2017, 42, 293¨C302. "
1732,CC1=CC2=C(C(C3=CC=C(CC(CCCC)CCCCCC)S3)=C(C=C(C4=CC=C(C)C5=NSN=C54)S6)C6=C2C7=CC=C(CC(CCCCCC)CCCC)S7)S1,PC,5.71,3.93,0.861,6.914,0.38,2.26,"Hong, N. J.; Lee, Y. S.; Park, J. H.; Na, S. I.; Choe, J. C.; Zong, K. Investigations into Inward Positioned 3,3¡ä-Dihexylditheinylbenzothiadiazole (DTBTh)-Benzodithiophene (BDT) Based Polymer Solar Cells by Controlling Molecular Weight and Alkyl Side Chain. Org. Electron. 2017, 42, 293¨C302. "
1733,CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC5=C(C(C=C(C(C6=CC=C(CCCCCC)C=C6)(C7=CC=C(CCCCCC)C=C7)C8=C9SC(C)=C8)C9=C%10)=C%10C5(C%11=CC=C(CCCCCC)C=C%11)C%12=CC=C(CCCCCC)C=C%12)S4)S3)C%13=NC(C%14=CC(F)=CC(OCCCCCCCC)=C%14)=C(C%15=CC(OCCCCCCCC)=CC(F)=C%15)N=C2%13)S1,PHF,5.36,3.62,0.84,12.46,0.69,7.2,"Gong, X.; Li, G.; Chen, J.; Feng, S.; Ma, D.; Hou, R.; Li, C.; Ma, W.; Bo, Z. Insights into the in Fl Uence of Fl Uorination Positions on Polymer Donor Materials on Photovoltaic Performance. Org. Electron. 2017, 46, 115¨C120. "
1734,CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=CC5=C(C(C=C(C(C6=CC=C(CCCCCC)C=C6)(C7=CC=C(CCCCCC)C=C7)C8=C9SC(C)=C8)C9=C%10)=C%10C5(C%11=CC=C(CCCCCC)C=C%11)C%12=CC=C(CCCCCC)C=C%12)S4)S3)C%13=NC(C%14=CC=CC(OCCCCCCCC)=C%14)=C(C%15=CC(OCCCCCCCC)=CC=C%15)N=C2%13)S1,PFH,5.43,3.61,0.93,9.57,0.7,6.19,"Gong, X.; Li, G.; Chen, J.; Feng, S.; Ma, D.; Hou, R.; Li, C.; Ma, W.; Bo, Z. Insights into the in Fl Uence of Fl Uorination Positions on Polymer Donor Materials on Photovoltaic Performance. Org. Electron. 2017, 46, 115¨C120. "
1735,CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=CC5=C(C(C=C(C(C6=CC=C(CCCCCC)C=C6)(C7=CC=C(CCCCCC)C=C7)C8=C9SC(C)=C8)C9=C%10)=C%10C5(C%11=CC=C(CCCCCC)C=C%11)C%12=CC=C(CCCCCC)C=C%12)S4)S3)C%13=NC(C%14=CC(F)=CC(OCCCCCCCC)=C%14)=C(C%15=CC(OCCCCCCCC)=CC(F)=C%15)N=C2%13)S1,PFF,5.43,3.69,0.92,4.61,0.68,2.9,"Gong, X.; Li, G.; Chen, J.; Feng, S.; Ma, D.; Hou, R.; Li, C.; Ma, W.; Bo, Z. Insights into the in Fl Uence of Fl Uorination Positions on Polymer Donor Materials on Photovoltaic Performance. Org. Electron. 2017, 46, 115¨C120. "
1736,CC1=C2N=C(C3=CC(C(C(F)=CC(F)=C4)=C4C5(CCCCCCCCCCCC)CCCCCCCCCCCC)=C5C=C3)C(C6=CC=C(C(CCCCCCCCCCCC)(CCCCCCCCCCCC)C7=C8C(F)=CC(F)=C7)C8=C6)=NC2=C(C9=CC=C(C%10=CC=C(C%11=CC=C(C)S%11)C%12=NSN=C%10%12)S9)C%13=NSN=C1%13,P,5.25,3.83,0.65,16.12,0.72,7.54,"Keshtov, M. L.; Kuklin, S. A.; Khokhlov, A. R.; Osipov, S. N.; Radychev, N. A.; Godovskiy, D. Y.; Konstantinov, I. O.; Chen, F. C.; Koukaras, E. N.; Sharma, G. D. Polymer Solar Cells Based Low Bandgap A1-D-A2-D Terpolymer Based on Fl Uorinated Thiadiazoloquinoxaline and Benzothiadiazole Acceptors with Energy Loss Less than 0.5 eV. Org. Electron. 2017, 46, 192¨C202. "
1737,CC1=CC2=C(C(OCCCCCCCCCCCC)=C(C=C(C3=C(CCCCCCCCCCCC)C=C(C4=C5C(N=C(C(N=C(C(CC)CCCCCCCCCCCCCCCC)S6)=C6C7=C8N=C(C(CC)CCCCCCCCCCCCCCCC)S7)C8=N5)=C(C9=CC(CCCCCCCCCCCC)=C(C)S9)C%10=NSN=C4%10)S3)S%11)C%11=C2OCCCCCCCCCCCC)S1,P1,5.34,3.88,0.9,12.62,0.64,7.27,"Keshtov, M. L.; Kuklin, S. A.; Radychev, N. A.; Nikolaev, A. Y.; Ostapov, I. E.; Krayushkin, M. M.; Konstantinov, I. O.; Koukaras, E. N.; Sharma, A.; Sharma, G. D. New Low Bandgap near-IR Conjugated D ¨C A Copolymers for BHJ Polymer Solar Cell. Phys. Chem. Chem. Phys. 2016, 18, 8389¨C8400. "
1738,CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C(C(N(CCCCCCCC)C5=O)=O)C5=C(C)S4)S6)C6=C2C7=CC=C(CC(CC)CCCC)S7)S1,PBDT-TPD,5.53,3.46,0.46,10.5,0.392,1.92,"Kotturappa, C. G.; Gopikrishna, M. M.; Rao, D.; Ramamurthy, P. C. Design and Synthesis of Thieno [3,4-c] Pyrrole-4,6-Dione Based Conjugated Copolymers for Organic Solar Cells. Polym. Int. 2017, 66, 1206¨C1213. "
1739,CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(C(N(CCCCCCCC)C6=O)=O)C6=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1,PBDT-Th-TPD,5.41,3.42,0.74,4.17,0.361,1.11,"Kotturappa, C. G.; Gopikrishna, M. M.; Rao, D.; Ramamurthy, P. C. Design and Synthesis of Thieno [3,4-c] Pyrrole-4,6-Dione Based Conjugated Copolymers for Organic Solar Cells. Polym. Int. 2017, 66, 1206¨C1213. "
1740,CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC5=C(C=C(C6=C(C(N(CCCCCCCC)C7=O)=O)C7=C(C8=CC9=C(C=C(C)S9)S8)S6)S5)S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11)S1,PBDT-TT-TPD,5.21,3.02,0.74,4.88,0.372,1.36,"Kotturappa, C. G.; Gopikrishna, M. M.; Rao, D.; Ramamurthy, P. C. Design and Synthesis of Thieno [3,4-c] Pyrrole-4,6-Dione Based Conjugated Copolymers for Organic Solar Cells. Polym. Int. 2017, 66, 1206¨C1213. "
1741,CC1=CC=C(C2=C3C(C(N2CC(CC)CCCC)=O)=C(C4=CC=C(C5=CC(N(CC(CCCCCC)CCCCCCCC)C(C6=CC(C(SC(C)=C7)=C7N(CC(CCCCCCCC)CCCCCC)C8=O)=C8C=C69)=O)=C9S5)S4)N(CC(CCCC)CC)C3=O)S1,PDPP2TPCL,5.06,3.89,0.77,9.5,0.64,4.7,"Feng, G.; Xu, Y.; Xiao, C.; Zhang, J.; Zhang, X.; Li, C.; Wei, Z.; Hu, W.; Wang, Z.; Li, W. Poly(Pentacyclic Lactam-alt-Diketopyrrolopyrrole) for Field-Effect Transistors and Polymer Solar Cells Processed from Non-Chlorinated Solvents. Polym. Chem. 2016, 7, 164¨C170. "
1742,CC1=CC(SC(C(SC2=C3SC(C4=C(CCCCCCCCCCCCCC)C=C(C5=CC(CCCCCCCCCCCCCC)=C(C)S5)S4)=C2)=C3C(N6OCC(CCCCCCCCCC)CCCCCCCC)=O)=C7C6=O)=C7S1,PTTABT,5.3,3.12,0.69,10.19,0.658,4.65,"He, D.; Qian, L.; Ding, L. A Pentacyclic Building Block Containing an Azepine-2,7-Dione Moiety for Polymer Solar Cells. Polym. Chem. 2016, 7, 2329¨C2332. "
1743,CC1=CC(SC(C(SC2=C3SC(C4=CC5=C(C(C6=CC=C(CC(CC)CCCC)S6)=C(C=C(C)S7)C7=C5C8=CC=C(CC(CC)CCCC)S8)S4)=C2)=C3C(N9OCC(CCCCCCCCCC)CCCCCCCC)=O)=C%10C9=O)=C%10S1,PTTABDT,5.33,3.03,0.79,10.52,0.654,5.46,"He, D.; Qian, L.; Ding, L. A Pentacyclic Building Block Containing an Azepine-2,7-Dione Moiety for Polymer Solar Cells. Polym. Chem. 2016, 7, 2329¨C2332. "
1744,CC(S1)=CC2=C1C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(OCCCCCCCCCCCC)=O)S4)=C(C)S3)S5)C5=C2OCCCCCCCC,PTB1,4.9,3.2,0.58,12.5,0.654,4.76,"Liang, Y.; Feng, D.; Wu, Y.; Tsai, S.-T. T.; Li, G.; Ray, C.; Yu, L. Highly Efficient Solar Cell Polymers Developed via Fine-Tuning of Structural and Electronic Properties. J. Am. Chem. Soc. 2009, 131, 7792¨C7799. "
1745,CC(S1)=CC2=C1C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCCCCCCCC,PTB2,4.94,3.22,0.6,12.8,0.663,5.1,"Liang, Y.; Feng, D.; Wu, Y.; Tsai, S.-T. T.; Li, G.; Ray, C.; Yu, L. Highly Efficient Solar Cell Polymers Developed via Fine-Tuning of Structural and Electronic Properties. J. Am. Chem. Soc. 2009, 131, 7792¨C7799. "
1746,CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C=C(C(OCCCCCCCC)=O)S4)=C(C)S3)S5)C5=C2OCC(CCCC)CC,PTB5,5.01,3.24,0.68,10.3,0.431,3.02,"Liang, Y.; Feng, D.; Wu, Y.; Tsai, S.-T. T.; Li, G.; Ray, C.; Yu, L. Highly Efficient Solar Cell Polymers Developed via Fine-Tuning of Structural and Electronic Properties. J. Am. Chem. Soc. 2009, 131, 7792¨C7799. "
1747,CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C=C(C(OCC(CCCCCC)CCCC)=O)S4)=C(C)S3)S5)C5=C2OCC(CCCC)CC,PTB6,5.01,3.17,0.62,7.74,0.47,2.26,"Liang, Y.; Feng, D.; Wu, Y.; Tsai, S.-T. T.; Li, G.; Ray, C.; Yu, L. Highly Efficient Solar Cell Polymers Developed via Fine-Tuning of Structural and Electronic Properties. J. Am. Chem. Soc. 2009, 131, 7792¨C7799. "
1748,CC(S1)=CC2=C1C(CCCCCCCC)=C(C=C(C3=C4C(C=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2CCCCCCCC,PTB3,5.04,3.29,0.74,13.1,0.568,5.53,"Liang, Y.; Feng, D.; Wu, Y.; Tsai, S.-T. T.; Li, G.; Ray, C.; Yu, L. Highly Efficient Solar Cell Polymers Developed via Fine-Tuning of Structural and Electronic Properties. J. Am. Chem. Soc. 2009, 131, 7792¨C7799. "
1749,CC(S1)=CC2=C1C(OCCCCCCCC)=C(C=C(C3=C4C(C(F)=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCCCCCCCC,PTB4,5.12,3.31,0.74,13,0.614,5.9,"Liang, Y.; Feng, D.; Wu, Y.; Tsai, S.-T. T.; Li, G.; Ray, C.; Yu, L. Highly Efficient Solar Cell Polymers Developed via Fine-Tuning of Structural and Electronic Properties. J. Am. Chem. Soc. 2009, 131, 7792¨C7799. "
1750,CC1=CC(C(C(CC(CCCCCCCC)CCCCCCCCCC)=CC2=C3C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S2)=C3C(CC(CCCCCCCCCC)CCCCCCCC)=C8)=C8S1,"P4,9-BNDTDTFBT",5.55,3.7,0.88,11.56,0.71,7.23,"Chiou, D.; Cao, F.; Hsu, J.; Tsai, C.; Lai, Y.; Jeng, U.; Zhang, J.; Yan, H.; Su, C.; Cheng, Y. Synthesis and Side-Chain Isomeric Effect of 4,9-/5,10-Dialkylated-¦Â-AngularShaped Naphthodithiophenes-Based Donor¨CAcceptor Copolymers for Polymer Solar Cells and Field-Effect Transistors. Polym. Chem. 2017, 8, 2334¨C2345. "
1751,CC1=CC(C(C=C(CC(CCCCCCCC)CCCCCCCCCC)C2=C3C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S2)=C3C=C8CC(CCCCCCCCCC)CCCCCCCC)=C8S1,"P5,10-BNDTDTFBT",5.49,3.61,0.74,12.42,0.605,5.56,"Chiou, D.; Cao, F.; Hsu, J.; Tsai, C.; Lai, Y.; Jeng, U.; Zhang, J.; Yan, H.; Su, C.; Cheng, Y. Synthesis and Side-Chain Isomeric Effect of 4,9-/5,10-Dialkylated-¦Â-AngularShaped Naphthodithiophenes-Based Donor¨CAcceptor Copolymers for Polymer Solar Cells and Field-Effect Transistors. Polym. Chem. 2017, 8, 2334¨C2345. "
1752,CC1=CC2=C(C(SC(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=C4N=C7C(C(C=CC=C8)=C8C9=C7C=CC=C9)=N6)S3)=C%10)=C%10C(OCC(CC)CCCC)=C2OCC(CC)CCCC)S1,P(BDP-DTPz),5.27,3.75,0.859,11.1,0.653,6.2,"Jeon, S. J.; Nam, S. J.; Han, Y. W.; Lee, T. H.; Moon, D. K. Molecular Design Through Computational Simulation on the Benzo[2,1-b;3,4-b¡¯]Dithiophene Based Highly Ordered Donor Material for Efficient Polymer Solar Cells. Polym. Chem. 2017, 8, 2979¨C2989."
1753,CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCC(CCCCCC)CCCCCCCC)C(OCC(CCCCCCCC)CCCCCC)=C(C)C5=NSN=C54)S3)C6=NSN=C62)S1,P1,5.64,3.96,0.89,12.32,0.62,6.87,"Kini, G. P.; Hoang, Q. V.; Song, C. E.; Lee, S. K.; Shin, W. S.; So, W.; Uddin, M. A.; Woo, H. Y.; Lee, J. Thiophene-Benzothiadiazole Based D¨CA1¨CD¨CA2 Type Alternating Copolymers for Polymer Solar Cells. Polym. Chem. 2017, 8, 3622¨C3631. "
1754,CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCCC(CCCCCCCC)CCCCCC)C(OCCC(CCCCCCCC)CCCCCC)=C(C)C5=NSN=C54)S3)C6=NSN=C62)S1,P2,5.53,3.87,0.85,14.49,0.67,8.27,"Kini, G. P.; Hoang, Q. V.; Song, C. E.; Lee, S. K.; Shin, W. S.; So, W.; Uddin, M. A.; Woo, H. Y.; Lee, J. Thiophene-Benzothiadiazole Based D¨CA1¨CD¨CA2 Type Alternating Copolymers for Polymer Solar Cells. Polym. Chem. 2017, 8, 3622¨C3631. "
1755,CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCCC(CCCCCCCC)CCCCCCCC)C(OCCC(CCCCCCCC)CCCCCCCC)=C(C)C5=NSN=C54)S3)C6=NSN=C62)S1,P3,5.57,3.9,0.84,13.89,0.67,7.84,"Kini, G. P.; Hoang, Q. V.; Song, C. E.; Lee, S. K.; Shin, W. S.; So, W.; Uddin, M. A.; Woo, H. Y.; Lee, J. Thiophene-Benzothiadiazole Based D¨CA1¨CD¨CA2 Type Alternating Copolymers for Polymer Solar Cells. Polym. Chem. 2017, 8, 3622¨C3631. "
1756,CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCCC(CCCCCCCCCC)CCCCCCCC)C(OCCC(CCCCCCCCCC)CCCCCCCC)=C(C)C5=NSN=C54)S3)C6=NSN=C62)S1,P4,5.57,3.89,0.84,12.81,0.69,7.38,"Kini, G. P.; Hoang, Q. V.; Song, C. E.; Lee, S. K.; Shin, W. S.; So, W.; Uddin, M. A.; Woo, H. Y.; Lee, J. Thiophene-Benzothiadiazole Based D¨CA1¨CD¨CA2 Type Alternating Copolymers for Polymer Solar Cells. Polym. Chem. 2017, 8, 3622¨C3631. "
1757,CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCCC(CCCCCCCCCC)CCCCCCCCCC)C(OCCC(CCCCCCCCCC)CCCCCCCCCC)=C(C)C5=NSN=C54)S3)C6=NSN=C62)S1,P5,5.61,3.95,0.86,10.61,0.69,6.28,"Kini, G. P.; Hoang, Q. V.; Song, C. E.; Lee, S. K.; Shin, W. S.; So, W.; Uddin, M. A.; Woo, H. Y.; Lee, J. Thiophene-Benzothiadiazole Based D¨CA1¨CD¨CA2 Type Alternating Copolymers for Polymer Solar Cells. Polym. Chem. 2017, 8, 3622¨C3631. "
1758,CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(CC(CC)CCCC)S8)C(C9=CC=C(CC(CC)CCCC)S9)=N7)S4)S%10)C%10=C2C%11=CC=C(SCC(CC)CCCC)S%11)S1,PBDT-DFQX-TTSEH,5.48,3.46,0.85,12.58,0.661,7.02,"Zhao, M.; Qiao, Z.; Chen, X.; Jiang, C.; Li, X.; Li, Y.; Wang, H. High Photovoltaic Performance of As-Cast Devices Based on New Quinoxaline-Based Donor¨CAcceptor Copolymers. Polym. Chem. 2017, 8, 5688¨C5697. "
1759,CC1=CC2=C(C(C3=CC=C(SCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(CC(CC)CCCC)S8)C(C9=CC=C(CC(CC)CCCC)S9)=N7)S4)S%10)C%10=C2C%11=CC=C(SCCCCCCCC)S%11)S1,PBDT-DFQX-TTSC8,5.37,3.47,0.85,14.63,0.682,8.51,"Zhao, M.; Qiao, Z.; Chen, X.; Jiang, C.; Li, X.; Li, Y.; Wang, H. High Photovoltaic Performance of As-Cast Devices Based on New Quinoxaline-Based Donor¨CAcceptor Copolymers. Polym. Chem. 2017, 8, 5688¨C5697. "
1760,CC1=CC2=C(C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=NN=C(C5=CC=C(C)S5)C(C(N6CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C4C6=O)S3)S7)C7=C2OCC(CC)CCCC)S1,P1,5.22,3.6,0.86,5.96,0.53,2.71,"Zhang, G.; Zhang, J.; Ding, G.; Guo, J.; Lu, H.; Qiu, L.; Ma, W. Synthesis and Photovoltaic Application of Low-Bandgap Conjugated Polymers by Incorporating Highly Electron-deficient Pyrrolo[3,4-d]Pyridazine-5,7-Dione Units. Polymer 2016, 93, 213¨C220. "
1761,CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=NN=C(C6=CC=C(C)S6)C(C(N7CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C5C7=O)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9)S1,P2,5.34,3.6,0.9,6.16,0.62,3.48,"Zhang, G.; Zhang, J.; Ding, G.; Guo, J.; Lu, H.; Qiu, L.; Ma, W. Synthesis and Photovoltaic Application of Low-Bandgap Conjugated Polymers by Incorporating Highly Electron-deficient Pyrrolo[3,4-d]Pyridazine-5,7-Dione Units. Polymer 2016, 93, 213¨C220. "
1762,CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)[Se]6)[Se]5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1,PDPP-SS,5.25,3.97,0.6,6.46,0.65,2.51,"Lee, J. H.; Park, G. E.; Choi, S.; Lee, D. H.; Um, H. A.; Shin, J.; Cho, M. J.; Choi, D. H. Effect of the Thiophene and Selenophene Moiety in Regular Terpolymers on the Performance of Thin Film Transistors and Polymer Solar Cells. Polymer 2016, 94, 43¨C52. "
1763,CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCC)CCCCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1,PDPP-TT,5.31,3.9,0.64,7.26,0.73,3.43,"Lee, J. H.; Park, G. E.; Choi, S.; Lee, D. H.; Um, H. A.; Shin, J.; Cho, M. J.; Choi, D. H. Effect of the Thiophene and Selenophene Moiety in Regular Terpolymers on the Performance of Thin Film Transistors and Polymer Solar Cells. Polymer 2016, 94, 43¨C52. "
1764,CC1=CC2=C(OCC(CC)CCCC)C(OCC(CCCC)CC)=C3C(SC(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)=C3)=C2S1,PBDPBT-T,5.31,3.48,0.88,8.5,0.577,4.32,"Lee, T. H.; Choi, M. H.; Jeon, S. J.; Moon, D. K. Correlation of Intermolecular Packing Distance and Crystallinity of D-A Polymers according to ¦Ð-Spacer for Polymer Solar Cells. Polymer 2016, 99, 756¨C766. "
1765,CC1=CC2=C(OCC(CC)CCCC)C(OCC(CCCC)CC)=C3C(SC(C4=CC(SC(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC(SC(C)=C7)=C7S6)C8=NSN=C85)=C9)=C9S4)=C3)=C2S1,PBDPBT-TT,5.29,3.32,0.8,5.6,0.476,2.13,"Lee, T. H.; Choi, M. H.; Jeon, S. J.; Moon, D. K. Correlation of Intermolecular Packing Distance and Crystallinity of D-A Polymers according to ¦Ð-Spacer for Polymer Solar Cells. Polymer 2016, 99, 756¨C766. "
1766,CC1=CC2=C(OCC(CC)CCCC)C(OCC(CCCC)CC)=C3C(SC(C4=CC=C(C5=CC=C(C6=C(OCCCCCCCC)C(OCCCCCCCC)=C(C7=CC=C(C8=CC=C(C)S8)S7)C9=NSN=C96)S5)S4)=C3)=C2S1,PBDPBT-biT,5.35,3.5,0.88,8.6,0.594,4.5,"Lee, T. H.; Choi, M. H.; Jeon, S. J.; Moon, D. K. Correlation of Intermolecular Packing Distance and Crystallinity of D-A Polymers according to ¦Ð-Spacer for Polymer Solar Cells. Polymer 2016, 99, 756¨C766. "
1767,CC1=CC=C(C2=CC=C(C3=CC=C(C4=C(OCCCCCCCCCCCCCC)C(OCCCCCCCCCCCCCC)=C(C)C5=NN(CCCCCCCCCCCCCC)N=C54)S3)C6=NSN=C62)S1,BTzDTBT,5.2,3.55,0.51,10.31,0.56,2.92,"Nguyen, T. L.; Choi, H.; Ko, S.; Kim, T.; Uddin, M. A.; Hwang, S.; Kim, J. Y.; Woo, H. Y. Semi-Crystalline A1¨CD¨CA2-Type Copolymers for Efficient Polymer Solar Cells. Polym. J. 2017, 49, 141¨C148. "
1768,CC1=CC=C(C2=C(F)C=C(C3=CC=C(C4=C(OCCCCCCCCCCCCCC)C(OCCCCCCCCCCCCCC)=C(C)C5=NN(CCCCCCCCCCCCCC)N=C54)S3)C6=NSN=C62)S1,BTzDTFBT,5.3,3.65,0.62,12.7,0.65,5.14,"Nguyen, T. L.; Choi, H.; Ko, S.; Kim, T.; Uddin, M. A.; Hwang, S.; Kim, J. Y.; Woo, H. Y. Semi-Crystalline A1¨CD¨CA2-Type Copolymers for Efficient Polymer Solar Cells. Polym. J. 2017, 49, 141¨C148. "
1769,CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=C(OCCCCCCCCCCCCCC)C(OCCCCCCCCCCCCCC)=C(C)C5=NN(CCCCCCCCCCCCCC)N=C54)S3)C6=NSN=C62)S1,BTzDT2FBT,5.4,3.74,0.75,14.64,0.64,7,"Nguyen, T. L.; Choi, H.; Ko, S.; Kim, T.; Uddin, M. A.; Hwang, S.; Kim, J. Y.; Woo, H. Y. Semi-Crystalline A1¨CD¨CA2-Type Copolymers for Efficient Polymer Solar Cells. Polym. J. 2017, 49, 141¨C148. "
1770,CC1=CC=C(C2=C(OCC(CCCC)CC)C=C(C3=CC=C(C4=C(CCCCCC)C=C(C(N(CC(CC)CCCC)C5=O)=C6C5=C(C7=CC(CCCCCC)=C(C)S7)N(CC(CC)CCCC)C6=O)S4)S3)C(OCC(CC)CCCC)=C2)S1,PDPPHT-TBT,5.24,3.66,0.63,11.66,0.48,3.51,"Guo, H.; Shen, T.; Wu, F.; Wang, G.; Ye, L.; Liu, Z.; Zhao, B.; Tan, S. Controlling the Morphology and Hole Mobility of Terpolymers for Polymer Solar Cells. RSC Adv. 2016, 6, 13177¨C13184. "
1771,O=C1N(CC(CC)CCCC)C(C2=CC(CCCCCC)=C(C)S2)=C3C(N(CC(CC)CCCC)C(C4=CC(CCCCCC)=C(S4)C5=CC6=C(C(C7=CC=C(CC(CC)CCCC)S7)=C(C=C(C)S8)C8=C6C9=CC=C(CC(CC)CCCC)S9)S5)=C31)=O,PDPPHT-BDTT,5.4,3.53,0.77,7.26,0.44,2.46,"Guo, H.; Shen, T.; Wu, F.; Wang, G.; Ye, L.; Liu, Z.; Zhao, B.; Tan, S. Controlling the Morphology and Hole Mobility of Terpolymers for Polymer Solar Cells. RSC Adv. 2016, 6, 13177¨C13184. "
1772,CC1=CC2=C(C(C3=CC=C(OCCCCCCCC)C(OCCCCCCCC)=C3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C57)S4)S8)C8=C2C9=CC(OCCCCCCCC)=C(OCCCCCCCC)C=C9)S1,PBBDTBT,5.43,3.67,0.73,8.94,0.7,4.57,"Zhang, Z.; Zhang, X.; Zhang, J.; Gong, X.; Liu, Y.; Lu, H. Efficient Polymer Solar Cells Processed by Environmentally Friendly Halogen-Free Solvents. RSC Adv. 2016, 6, 39074¨C39079. "
1773,CC(S1)=CC2=C1C(C3=CC=C(SCCCCCCCC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CCCC)CC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCCCCCCCC)S7,PBDT-TS1,5.29,3.69,0.81,17.55,0.672,9.52,"Zhang, S.; Uddin, M. A.; Zhao, W.; Ye, L.; Woo, H. Y.; Liu, D.; Yang, B.; Yao, H.; Cui, Y.; Hou, J. Optimization of Side Chains in Alkylthiothiophene-Substituted benzo[1,2-b:4,5-b¡ä]dithiophene-Based Photovoltaic Polymers. Polym. Chem. 2015, 6, 2752¨C2760. "
1774,CC(S1)=CC2=C1C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CCCC)CC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCC(CC)CCCC)S7,PBDT-TS2,5.29,3.7,0.81,16.52,0.623,8.37,"Zhang, S.; Uddin, M. A.; Zhao, W.; Ye, L.; Woo, H. Y.; Liu, D.; Yang, B.; Yao, H.; Cui, Y.; Hou, J. Optimization of Side Chains in Alkylthiothiophene-Substituted benzo[1,2-b:4,5-b¡ä]dithiophene-Based Photovoltaic Polymers. Polym. Chem. 2015, 6, 2752¨C2760. "
1775,CC(S1)=CC2=C1C(C3=CC=C(SCCC(C)CCCC(C)C)S3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CCCC)CC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCCC(C)CCCC(C)C)S7,PBDT-TS3,5.29,3.68,0.81,16.22,0.56,7.36,"Zhang, S.; Uddin, M. A.; Zhao, W.; Ye, L.; Woo, H. Y.; Liu, D.; Yang, B.; Yao, H.; Cui, Y.; Hou, J. Optimization of Side Chains in Alkylthiothiophene-Substituted benzo[1,2-b:4,5-b¡ä]dithiophene-Based Photovoltaic Polymers. Polym. Chem. 2015, 6, 2752¨C2760. "
1776,CC1=CC2=C(C(C3=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S3)=C(C=C(C4=CC5=C(C(SC(C)=C6)=C6C7=NON=C75)S4)S8)C8=C2C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)S1,PBDTT-fDTBO,5.64,3.73,1.05,5.53,0.496,2.88,"Ding, D.; Wang, J.; Chen, W.; Qiu, M.; Ren, J. Novel Wide Band Gap Polymers Based on Dithienobenzoxadiazole for Polymer Solar Cells with High Open Circuit Voltages over 1 V. RSC Adv. 2016, 6, 51419¨C51425. "
1777,CC1=CC2=C(C(OCC(CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=CC4=C(C(SC(C)=C5)=C5C6=NON=C64)S3)S7)C7=C2OCC(CCCCCCCCCC)CCCCCCCC)S1,PBDTO-fDTBO,5.56,3.57,1.02,5.41,0.507,2.8,"Ding, D.; Wang, J.; Chen, W.; Qiu, M.; Ren, J. Novel Wide Band Gap Polymers Based on Dithienobenzoxadiazole for Polymer Solar Cells with High Open Circuit Voltages over 1 V. RSC Adv. 2016, 6, 51419¨C51425. "
1778,CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC5=C(C6=CC=C(OCC(CCCC)CC)C(F)=C6)C7=C(C=C(C)O7)C(C8=CC(F)=C(OCC(CC)CCCC)C=C8)=C5S4)S3)C9=NSN=C92)S1,TBFPF-BT,5.28,3.6,0.8,12.12,0.71,6.8,"He, D.; Qiu, L.; Zhang, Z.; Li, Y.; Pan, C.; Zou, Y. Two New Fluorinated Copolymers Based on Thieno[2,3-f]Benzofuran for Efficient Polymer Solar Cells. RSC Adv. 2016, 6, 62923¨C62933. "
1779,CC1=CC=C(C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=CC=C(C4=CC5=C(C6=CC=C(OCC(CCCC)CC)C(F)=C6)C7=C(C=C(C)S7)C(C8=CC(F)=C(OCC(CC)CCCC)C=C8)=C5O4)S3)C9=NON=C92)S1,TBFPF-BO,5.38,3.69,0.89,10.35,0.65,5.98,"He, D.; Qiu, L.; Zhang, Z.; Li, Y.; Pan, C.; Zou, Y. Two New Fluorinated Copolymers Based on Thieno[2,3-f]Benzofuran for Efficient Polymer Solar Cells. RSC Adv. 2016, 6, 62923¨C62933. "
1780,CC1=C2C(C(N1CC(CCCCCCCCCC)CCCCCCCC)=O)=C(C3=CC=C(C4=CC=C(C5=C(CCCCCC)C=C(C6=C(C(N(CCCCCCCC)C7=O)=O)C7=C(C8=CC(CCCCCC)=C(C9=CC=C(C%10=CC=C(C)S%10)S9)S8)S6)S5)S4)S3)N(CC(CCCCCCCC)CCCCCCCCCC)C2=O,P1,5.12,3.56,0.58,12.98,0.583,4.36,"Lu, M.; Wang, W.; Lv, W.; Yan, S.; Zhang, T.; Zhen, H. Simple Synthesis of Novel Terthiophene-Based D¨CA1¨CD¨CA2 Polymers for Polymer Solar Cells. RSC Adv. 2016, 6, 86276¨C86284. "
1781,CC1=C2C(C(N1CC(CCCCCCCCCC)CCCCCCCC)=O)=C(C3=CC=C(C4=CC=C(C5=C(CCCCCC)C=C(C6=CC=C(C7=CC(CCCCCC)=C(C8=CC=C(C9=CC=C(C)S9)S8)S7)C%10=NSN=C%106)S5)S4)S3)N(CC(CCCCCCCC)CCCCCCCCCC)C2=O,P2,5.14,3.58,0.61,9.33,0.645,3.66,"Lu, M.; Wang, W.; Lv, W.; Yan, S.; Zhang, T.; Zhen, H. Simple Synthesis of Novel Terthiophene-Based D¨CA1¨CD¨CA2 Polymers for Polymer Solar Cells. RSC Adv. 2016, 6, 86276¨C86284. "
1782,CC1=C2C(C(N1CC(CCCCCCCCCC)CCCCCCCC)=O)=C(C3=CC=C(C4=CC=C(C5=C(CCCCCC)C=C(C6=C(F)C(F)=C(C7=CC(CCCCCC)=C(C8=CC=C(C9=CC=C(C)S9)S8)S7)C%10=NSN=C%106)S5)S4)S3)N(CC(CCCCCCCC)CCCCCCCCCC)C2=O,P3,5.22,3.75,0.62,1.6,0.451,0.45,"Lu, M.; Wang, W.; Lv, W.; Yan, S.; Zhang, T.; Zhen, H. Simple Synthesis of Novel Terthiophene-Based D¨CA1¨CD¨CA2 Polymers for Polymer Solar Cells. RSC Adv. 2016, 6, 86276¨C86284. "
1783,CC1=C2C(C(N1CC(CCCCCCCCCC)CCCCCCCC)=O)=C(C3=CC=C(C4=C(CCCCCC)C=C(C5=C(C(N(CCCCCCCC)C6=O)=O)C6=C(C7=CC(CCCCCC)=C(C8=CC=C(C)S8)S7)S5)S4)S3)N(CC(CCCCCCCC)CCCCCCCCCC)C2=O,P4,5.24,3.64,0.72,5.93,0.653,2.79,"Lu, M.; Wang, W.; Lv, W.; Yan, S.; Zhang, T.; Zhen, H. Simple Synthesis of Novel Terthiophene-Based D¨CA1¨CD¨CA2 Polymers for Polymer Solar Cells. RSC Adv. 2016, 6, 86276¨C86284. "
1784,CC1=CC2=C(C(C3=CC=C(SCC(CCCCCC)CCCCCCCC)C=C3)=C(C=C(C4=C(F)C(F)=C(C)C5=NSN=C54)S6)C6=C2C7=CC=C(SCC(CCCCCC)CCCCCCCC)C=C7)S1,PSB-DFBT,5.39,3.54,0.76,6.39,0.39,1.88,"Liu, H.; Zhang, Z.; Zeng, Z.; Zhao, B.; Tan, S. Design and Synthesis of the Polymers Based on Alkylthiophenyl Side Chains and Variant Acceptor Moieties for Polymer Solar Cells. RSC Adv. 2016, 6, 95306¨C95313. "
1785,CC1=CC2=C(C(C3=CC=C(SCC(CCCCCC)CCCCCCCC)C=C3)=C(C=C(C4=C(CCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(SCC(CCCCCC)CCCCCCCC)C=C9)S1,PSB-DTDFBT,5.3,3.55,0.58,2.97,0.28,0.48,"Liu, H.; Zhang, Z.; Zeng, Z.; Zhao, B.; Tan, S. Design and Synthesis of the Polymers Based on Alkylthiophenyl Side Chains and Variant Acceptor Moieties for Polymer Solar Cells. RSC Adv. 2016, 6, 95306¨C95313. "
1786,CC1=CC2=C(C(C3=CC=C(SCC(CCCCCC)CCCCCCCC)C=C3)=C(C=C(C4=C5C(C(F)=C(C(OCC(CC)CCCC)=O)S5)=C(C)S4)S6)C6=C2C7=CC=C(SCC(CCCCCC)CCCCCCCC)C=C7)S1,PSB-FTT,5.21,3.41,0.82,9.5,0.57,4.45,"Liu, H.; Zhang, Z.; Zeng, Z.; Zhao, B.; Tan, S. Design and Synthesis of the Polymers Based on Alkylthiophenyl Side Chains and Variant Acceptor Moieties for Polymer Solar Cells. RSC Adv. 2016, 6, 95306¨C95313. "
1787,CC1=CC2=C(C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=C5C(C(N(CCCCCCCCCCCC)C5=O)=O)=C(C6=CC=C(C7=C(CCCCCCCC)C(CCCCCCCC)=C(C8=CC=C(C9=C%10C(C(N(CCCCCCCCCCCC)C%10=O)=O)=C(C)S9)S8)S7)S6)S4)S%11)C%11=C2C%12=CC=C(CC(CC)CCCC)S%12)S1,LGC-D013,5.56,3.72,0.87,11.29,0.731,7.22,"Bang, S.-M.; Kang, S.; Lee, Y.-S.; Lim, B.; Heo, H.; Lee, J.; Lee, Y.; Na, S.-I. A Novel Random Terpolymer for High-Efficiency Bulk-Heterojunction Polymer Solar Cells. RSC Adv. 2017, 7, 1975¨C1980. "
1788,CC1=C(F)C(F)=C(C2=CC=C(C)S2)C3=C1N=C(C4=CC=CC(OCCCCCCCC)=C4)C(C5=CC(OCCCCCCCC)=CC=C5)=N3,TQF2-1,6.18,3.7,0.93,8.5,0.58,4.6,"Genene, Z.; Wang, J.; Xu, X.; Yang, R.; Mammo, W.; Wang, E. A Comparative Study of the Photovoltaic Performances of Terpolymers and Ternary Systems. RSC Adv. 2017, 7, 17959¨C17967. "
1789,CC1=CC2=C(/C(C(N2CC(CCCCCC)CCCCCCCC)=O)=C3C(N(CC(CCCCCC)CCCCCCCC)C4=CC(C5=CC=C(C)S5)=CC=C4\3)=O)C=C1,PTI-1,5.78,3.95,0.88,6.8,0.62,3.7,"Genene, Z.; Wang, J.; Xu, X.; Yang, R.; Mammo, W.; Wang, E. A Comparative Study of the Photovoltaic Performances of Terpolymers and Ternary Systems. RSC Adv. 2017, 7, 17959¨C17967. "
1790,CC1=CC=C(C2=C(F)C(F)=C(C3=CC=C(C4=CC=C5C(N(CC(CCCCCCCC)CCCCCC)C(/C5=C6C(C=CC(C)=C7)=C7N(CC(CCCCCC)CCCCCCCC)C\6=O)=O)=C4)S3)C8=C2N=C(C9=CC=CC(OCCCCCCCC)=C9)C(C%10=CC(OCCCCCCCC)=CC=C%10)=N8)S1,PR11,5.88,3.98,0.92,7.6,0.57,4,"Genene, Z.; Wang, J.; Xu, X.; Yang, R.; Mammo, W.; Wang, E. A Comparative Study of the Photovoltaic Performances of Terpolymers and Ternary Systems. RSC Adv. 2017, 7, 17959¨C17967. "
1791,CC1=CC2=C(C(C(C3=CC=C(OCC(CC)CCCC)C=C3)(C4=CC=C(OCC(CCCC)CC)C=C4)C5=C6C=C7C(C(SC8=C9SC(C%10=CC=C(C%11=CC=C(C%12=CC=C(C)S%12)C%13=NON=C%11%13)S%10)=C8)=C9C7(C%14=CC=C(OCC(CCCC)CC)C=C%14)C%15=CC=C(OCC(CC)CCCC)C=C%15)=C5)=C6S2)S1,PIDTT-DTBO,5.36,3.69,0.88,10.5,0.497,4.6,"Cai, P.; Xu, X.; Sun, J.; Chen, J.; Cao, Y. Effects of Including Electron-Withdrawing Atoms on the Physical and Photovoltaic Properties of indacenodithieno[3,2-b]thiopheneBased Donor¨Cacceptor Polymers: Towards an Acceptor Design for Efficient Polymer Solar Cells. RSC Adv. 2017, 7, 20440¨C20450. "
1792,CC1=CC2=C(C(C(C3=CC=C(OCC(CC)CCCC)C=C3)(C4=CC=C(OCC(CCCC)CC)C=C4)C5=C6C=C7C(C(SC8=C9SC(C%10=CC=C(C%11=CC=C(C%12=CC=C(C)S%12)C%13=NSN=C%11%13)S%10)=C8)=C9C7(C%14=CC=C(OCC(CCCC)CC)C=C%14)C%15=CC=C(OCC(CC)CCCC)C=C%15)=C5)=C6S2)S1,PIDTT-DTBT,5.31,3.67,0.86,10.2,0.56,4.91,"Cai, P.; Xu, X.; Sun, J.; Chen, J.; Cao, Y. Effects of Including Electron-Withdrawing Atoms on the Physical and Photovoltaic Properties of indacenodithieno[3,2-b]thiopheneBased Donor¨Cacceptor Polymers: Towards an Acceptor Design for Efficient Polymer Solar Cells. RSC Adv. 2017, 7, 20440¨C20450. "
1793,CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C(F)C(F)=C(C)C5=NSN=C54)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7)S1,PBDTS-FBT,5.49,3.46,0.8,6.65,0.303,1.42,"Zhang, X.; Chen, L.; Wang, G.; Zhang, Z. G.; Li, Y.; Shen, P. Synthesis and Photovoltaic Properties of Alkylthiothienyl-Substituted benzo[1,2-b:4,5-b¡ä]dithiophene D-A Copolymers with Different Accepting Units. Synth. Met. 2016, 211, 121¨C131. "
1794,CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(SCC(CCCC)CC)S9)S1,PBDTS-DTFBT,5.47,3.54,0.83,8.27,0.464,3.19,"Zhang, X.; Chen, L.; Wang, G.; Zhang, Z. G.; Li, Y.; Shen, P. Synthesis and Photovoltaic Properties of Alkylthiothienyl-Substituted benzo[1,2-b:4,5-b¡ä]dithiophene D-A Copolymers with Different Accepting Units. Synth. Met. 2016, 211, 121¨C131. "
1795,CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=C5C(C(N(CC(CC)CCCC)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(SCC(CCCC)CC)S7)S1,PBDT-TPD,5.51,3.34,0.93,5.23,0.416,2.14,"Zhang, X.; Chen, L.; Wang, G.; Zhang, Z. G.; Li, Y.; Shen, P. Synthesis and Photovoltaic Properties of Alkylthiothienyl-Substituted benzo[1,2-b:4,5-b¡ä]dithiophene D-A Copolymers with Different Accepting Units. Synth. Met. 2016, 211, 121¨C131. "
1796,CC1=CC2=C(C(C3=CC=C(SCC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C(N5CC(CC)CCCC)=O)=C(C7=CC=C(C)S7)N(CC(CCCC)CC)C6=O)S4)S8)C8=C2C9=CC=C(SCC(CCCC)CC)S9)S1,PBDTS-DPP,5.3,3.45,0.78,7.79,0.396,2.41,"Zhang, X.; Chen, L.; Wang, G.; Zhang, Z. G.; Li, Y.; Shen, P. Synthesis and Photovoltaic Properties of Alkylthiothienyl-Substituted benzo[1,2-b:4,5-b¡ä]dithiophene D-A Copolymers with Different Accepting Units. Synth. Met. 2016, 211, 121¨C131. "
1797,CC1=CC(CCCCCCCCCCCC)=C(C2=CC(SC3=C4SC(C5=C(CCCCCCCCCCCC)C=C(C6=CC=C(C(N(CC(CCCC)CC)C7=O)=C8C7=C(C9=CC=C(C)S9)N(CC(CC)CCCC)C8=O)S6)S5)=C3)=C4S2)S1,PDTTDPP-EH,5.11,3.69,0.54,8,0.51,2.22,"Choi, S.; Park, G. E.; Shin, J.; Um, H. A.; Cho, M. J.; Choi, D. H. DithienothiopheneDiketopyrrolopyrrole-Containing Copolymers with Alkyl Side-Chain and Their Application to Polymer Solar Cells. Synth. Met. 2016, 212, 167¨C173. "
1798,CC1=CC(CCCCCCCCCCCC)=C(C2=CC(SC3=C4SC(C5=C(CCCCCCCCCCCC)C=C(C6=CC=C(C(N(CC(CCCC)CCCCCC)C7=O)=C8C7=C(C9=CC=C(C)S9)N(CC(CCCCCC)CCCC)C8=O)S6)S5)=C3)=C4S2)S1,PDTTDPP-BO,5.16,3.77,0.55,10.01,0.54,2.93,"Choi, S.; Park, G. E.; Shin, J.; Um, H. A.; Cho, M. J.; Choi, D. H. DithienothiopheneDiketopyrrolopyrrole-Containing Copolymers with Alkyl Side-Chain and Their Application to Polymer Solar Cells. Synth. Met. 2016, 212, 167¨C173. "
1799,O=C(CCCCCCC)C1=C(F)C2=C(C)SC(C3=CC4=C(OCC(CCCC)CC)C(SC(C)=C5)=C5C(OCC(CCCC)CC)=C4S3)=C2S1,PBDTTT-CF,5.22,3.45,0.76,15.2,0.669,7.73," Chen, H.-Y.; Hou, J.; Zhang, S.; Liang, Y.; Yang, G.; Yang, Y.; Yu, L.; Wu, Y.; Li, G. Polymer Solar Cells with Enhanced Open-Circuit Voltage and Efficiency. Nat. Photonics2009, 3, 649¨C653. "
1800,CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CC(CCCC)CC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC,PBDTTPD-P1,5.48,3.73,0.87,8.1,0.56,4,"Piliego, C.; Holcombe, T. W.; Douglas, J. D.; Woo, C. H.; Beaujuge, P. M.; Fr¨¦chet, J. M. J. Synthetic Control of Structural Order in N-Alkylthieno[3,4-c]Pyrrole-4,6-DioneBased Polymers for Efficient Solar Cells. J. Am. Chem. Soc. 2010, 132, 7595¨C7597. "
1801,CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCC(C)CCCC(C)C)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC,PBDTTPD-P2,5.57,3.87,0.81,9.7,0.67,5.7,"Piliego, C.; Holcombe, T. W.; Douglas, J. D.; Woo, C. H.; Beaujuge, P. M.; Fr¨¦chet, J. M. J. Synthetic Control of Structural Order in N-Alkylthieno[3,4-c]Pyrrole-4,6-DioneBased Polymers for Efficient Solar Cells. J. Am. Chem. Soc. 2010, 132, 7595¨C7597. "
1802,CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(N(CCCCCCCC)C4=O)=O)=C(C)S3)S5)C5=C2OCC(CCCC)CC,PBDTTPD-P3,5.4,3.67,0.85,11.5,0.68,6.8,"Piliego, C.; Holcombe, T. W.; Douglas, J. D.; Woo, C. H.; Beaujuge, P. M.; Fr¨¦chet, J. M. J. Synthetic Control of Structural Order in N-Alkylthieno[3,4-c]Pyrrole-4,6-DioneBased Polymers for Efficient Solar Cells. J. Am. Chem. Soc. 2010, 132, 7595¨C7597. "
1803,CC1=CC=C(C2=CC3=C(C(SC(C4=CC=C(C)C5=NSN=C54)=C6)=C6N3C(CCCCCCCC)CCCCCCCC)C=C2)S1,PTTIBT,5.32,3.5,0.62,3.28,0.42,0.85,"Jeong, I.; Kim, J.; Kim, J.; Lee, J.; Lee, D. Y.; Kim, I.; Park, S. H.; Suh, H. 6-(2- Thienyl)-4H-thieno[3,2-b]indole Based Conjugated Polymers with Low Bandgaps for Organic Solar Cells. Synth. Met. 2016, 213, 25¨C33. "
1804,CC1=CC=C(C2=CC3=C(C(SC(C4=CC=C(C)C5=NC(C)(C)N=C54)=C6)=C6N3C(CCCCCCCC)CCCCCCCC)C=C2)S1,PTTIMBI,5.29,3.61,0.69,7.1,0.53,2.6,"Jeong, I.; Kim, J.; Kim, J.; Lee, J.; Lee, D. Y.; Kim, I.; Park, S. H.; Suh, H. 6-(2- Thienyl)-4H-thieno[3,2-b]indole Based Conjugated Polymers with Low Bandgaps for Organic Solar Cells. Synth. Met. 2016, 213, 25¨C33. "
1805,CC1=CC(N(CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=CC(OCCCCCCCC)=C8)C(C9=CC(OCCCCCCCC)=CC=C9)=N7)S4)=C2)=C3C=C1,P1,5.49,3.5,0.87,3.77,0.46,1.51,"Lu, Z.; Zhang, J.; Li, C.; Feng, F.; Bo, Z. The Effect of Meta-Substituted or ParaSubstituted Phenyl as Side Chains on the Performance of Polymer Solar Cells. Synth. Met. 2016, 220, 402¨C409. "
1806,CC1=CC(N(CCCCCCCC)C2=C3C=CC(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=C5N=C(C8=CC=C(OCCCCCCCC)C=C8)C(C9=CC=C(OCCCCCCCC)C=C9)=N7)S4)=C2)=C3C=C1,P2,5.41,3.39,0.86,7.48,0.52,3.33,"Lu, Z.; Zhang, J.; Li, C.; Feng, F.; Bo, Z. The Effect of Meta-Substituted or ParaSubstituted Phenyl as Side Chains on the Performance of Polymer Solar Cells. Synth. Met. 2016, 220, 402¨C409. "
1807,CC1=CC2=C(C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(/C=C(C(OCC(CCCCCCCC)CCCCCCCCCC)=O)/C#N)S4)=C(C)S3)S5)C5=C2OCCCCCCCC)S1,BDT8TT,5.76,3.51,0.77,4.5,0.473,1.63,"Kim, Y. J.; Ahn, E. S.; Hwang, M. C.; Park, C. E.; Kim, Y. H. A BenzodithiopheneThienothiophene Derivative with Cyano Acrylate Side Chain: A Novel Donor Polymer with Deep HOMO Level for P-N Heterojunction Solar Cells. Thin Solid Films 2016, 603, 165¨C172."
1808,CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CC(CC)CCCC)S7,PBDT-T8-TPD,5.61,3.76,1,9.79,0.63,6.17,"Yuan, J.; Zhai, Z.; Dong, H.; Li, J.; Jiang, Z.; Li, Y.; Ma, W. Efficient Polymer Solar Cells with a High Open Circuit Voltage of 1 Volt. Adv. Funct. Mater. 2013, 23, 885¨C892. "
1809,CC(S1)=CC2=C1C(C3=CC=C(CCCCCCCCCC)S3)=C(C=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CCCCCCCCCC)S7,PBDT-T10-TPD,5.47,3.67,0.92,8.92,0.55,4.51,"Yuan, J.; Zhai, Z.; Dong, H.; Li, J.; Jiang, Z.; Li, Y.; Ma, W. Efficient Polymer Solar Cells with a High Open Circuit Voltage of 1 Volt. Adv. Funct. Mater. 2013, 23, 885¨C892. "
1810,CC(S1)=CC2=C1C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C)S4)S6)C6=C2C7=CC=C(CCCCCCCCCCCC)S7,PBDT-T12-TPD,5.56,3.74,0.95,8.94,0.532,4.5,"Yuan, J.; Zhai, Z.; Dong, H.; Li, J.; Jiang, Z.; Li, Y.; Ma, W. Efficient Polymer Solar Cells with a High Open Circuit Voltage of 1 Volt. Adv. Funct. Mater. 2013, 23, 885¨C892. "
1811,CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCC)CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCC)CCCCCCCC)S9,PBDTDTBT-p,5.09,3.45,0.67,9.63,0.54,3.48,"Yao, H.; Ye, L.; Fan, B.; Huo, L.; Hou, J. Influence of the Alkyl Substitution Position on Photovoltaic Properties of 2D-BDT-Based Conjugated Polymers. Sci. China Mater.2015, 58, 213¨C222. "
1812,CC(S1)=CC2=C1C(C3=CC(CCCCCCCC)=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC(CCCCCCCC)=C(CCCCCCCC)S9,PBDTDTBT-o,5.11,3.43,0.75,11.82,0.65,5.76,"Yao, H.; Ye, L.; Fan, B.; Huo, L.; Hou, J. Influence of the Alkyl Substitution Position on Photovoltaic Properties of 2D-BDT-Based Conjugated Polymers. Sci. China Mater.2015, 58, 213¨C222. "
1813,CC(S1)=CC2=C1C(C3=C(CCCCCCCC)C=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=C(CCCCCCCC)C=C(CCCCCCCC)S9,PBDTDTBT-m,5.31,3.56,0.9,10.81,0.53,5.16,"Yao, H.; Ye, L.; Fan, B.; Huo, L.; Hou, J. Influence of the Alkyl Substitution Position on Photovoltaic Properties of 2D-BDT-Based Conjugated Polymers. Sci. China Mater.2015, 58, 213¨C222. "
1814,CC(S1)=CC2=C1C(OCCCCCCCC)=C(C=C(C3=C4C(C=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCCCCCCCC,PTBF0,4.94,3.22,0.58,14.1,0.624,5.1,"Son, H. J.; Wang, W.; Xu, T.; Liang, Y.; Wu, Y.; Li, G.; Yu, L. Synthesis of Fluorinated Polythienothiophene-co-Benzodithiophenes and Effect of Fluorination on the Photovoltaic Properties. J. Am. Chem. Soc. 2011, 133, 1885¨C1894. "
1815,CC(S1)=CC2=C1C(OCC(CC)CCCC)=C(C=C(C3=C4C(C(F)=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCC(CC)CCCC,PTBF1,5.15,3.31,0.74,14,0.603,6.2,"Son, H. J.; Wang, W.; Xu, T.; Liang, Y.; Wu, Y.; Li, G.; Yu, L. Synthesis of Fluorinated Polythienothiophene-co-Benzodithiophenes and Effect of Fluorination on the Photovoltaic Properties. J. Am. Chem. Soc. 2011, 133, 1885¨C1894. "
1816,CC(S1)=C(F)C2=C1C(OCC(CC)CCCC)=C(C(F)=C(C3=C4C(C(F)=C(C(OCC(CCCC)CC)=O)S4)=C(C)S3)S5)C5=C2OCC(CC)CCCC,PTBF3,5.48,3.59,0.75,9.1,0.394,2.7,"Son, H. J.; Wang, W.; Xu, T.; Liang, Y.; Wu, Y.; Li, G.; Yu, L. Synthesis of Fluorinated Polythienothiophene-co-Benzodithiophenes and Effect of Fluorination on the Photovoltaic Properties. J. Am. Chem. Soc. 2011, 133, 1885¨C1894. "
1817,CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(C(OCC(CCCCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)S9,PBT-0F,4.9,3.29,0.56,12.2,0.667,4.5,"Zhang, M.; Guo, X.; Zhang, S.; Hou, J. Synergistic Effect of Fluorination on Molecular Energy Level Modulation in Highly Efficient Photovoltaic Polymers. Adv. Mater. 2014, 26, 1118¨C1123. "
1818,CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C(F)=C(C(OCC(CCCCCC)CCCCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)S9,PBT-1F,4.95,3.29,0.6,14.3,0.657,5.6,"Zhang, M.; Guo, X.; Zhang, S.; Hou, J. Synergistic Effect of Fluorination on Molecular Energy Level Modulation in Highly Efficient Photovoltaic Polymers. Adv. Mater. 2014, 26, 1118¨C1123. "
1819,CC(S1)=CC2=C1C(C3=CC(F)=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C=C(C(OCC(CCCCCCCC)CCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC(F)=C(CC(CCCC)CC)S9,PBT-2F,5.15,3.29,0.74,14.4,0.677,7.2,"Zhang, M.; Guo, X.; Zhang, S.; Hou, J. Synergistic Effect of Fluorination on Molecular Energy Level Modulation in Highly Efficient Photovoltaic Polymers. Adv. Mater. 2014, 26, 1118¨C1123. "
1820,CC(S1)=CC2=C1C(C3=CC(F)=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C6C(C(F)=C(C(OCC(CCCCCCCC)CCCCCC)=O)S6)=C(C7=CC=C(C)S7)S5)S4)S8)C8=C2C9=CC(F)=C(CC(CCCC)CC)S9,PBT-3F,5.2,3.29,0.78,15.2,0.724,8.6,"Zhang, M.; Guo, X.; Zhang, S.; Hou, J. Synergistic Effect of Fluorination on Molecular Energy Level Modulation in Highly Efficient Photovoltaic Polymers. Adv. Mater. 2014, 26, 1118¨C1123. "
1821,CC(S1)=CC2=C1C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NN(CC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCC)CCCCCC,PBnDT-HTAZ,5.29,2.87,0.7,11.14,0.552,4.36,"Price, S. C.; Stuart, A. C.; Yang, L.; Zhou, H.; You, W. Fluorine Substituted Conjugated Polymer of Medium Band Gap Yields 7% Efficiency in Polymer-Fullerene Solar Cells. J. Am. Chem. Soc. 2011, 133, 4625¨C4631. "
1822,CC(S1)=CC2=C1C(CCC(CCCCCC)CCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCC)CCCCCC,PBnDT-FTAZ,5.36,3.05,0.79,11.83,0.729,7.1,"Price, S. C.; Stuart, A. C.; Yang, L.; Zhou, H.; You, W. Fluorine Substituted Conjugated Polymer of Medium Band Gap Yields 7% Efficiency in Polymer-Fullerene Solar Cells. J. Am. Chem. Soc. 2011, 133, 4625¨C4631. "
1823,CC(O1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CCCC)CC)=C(C)S5)C6=NSN=C64)S3)O7)C7=C2OCC(CCCC)CC,PBDFDTBT,5.1,3.5,0.78,11.77,0.546,5.01,"Huo, L.; Huang, Y.; Fan, B.; Guo, X.; Jing, Y.; Zhang, M.; Li, Y.; Hou, J. Synthesis of a 4,8-Dialkoxy-benzo[1,2-b:4,5-b¡ä]difuran Unit and Its Application in Photovoltaic Polymer. Chem. Commun. 2012, 48, 3318¨C3320. "
1824,CC(O1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)O7)C7=C2OCC(CCCC)CC,PBDFDODTBT,5.11,3.38,0.69,9.87,0.653,4.45,"Liu, B.; Chen, X.; Zou, Y.; Xiao, L.; Xu, X.; He, Y.; Li, L.; Li, Y. Benzo[1,2-b:4,5-B¡¯]difuran-Based Donor-Acceptor Copolymers for Polymer Solar Cells. Macromolecules2012, 45, 6898¨C6905."
1825,CC(O1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NN(CCCCCCCC)N=C64)S3)O7)C7=C2OCC(CCCC)CC,PBDFDTBTz,4.99,3.06,0.44,4.92,0.575,1.24,"Liu, B.; Chen, X.; Zou, Y.; Xiao, L.; Xu, X.; He, Y.; Li, L.; Li, Y. Benzo[1,2-b:4,5-B¡¯]difuran-Based Donor-Acceptor Copolymers for Polymer Solar Cells. Macromolecules2012, 45, 6898¨C6905."
1826,CC(O1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NON=C64)S3)O7)C7=C2OCC(CCCC)CC,PBDFDTBO,5.19,3.49,0.82,5.04,0.7,2.88,"Liu, B.; Chen, X.; Zou, Y.; Xiao, L.; Xu, X.; He, Y.; Li, L.; Li, Y. Benzo[1,2-b:4,5-B¡¯]difuran-Based Donor-Acceptor Copolymers for Polymer Solar Cells. Macromolecules2012, 45, 6898¨C6905."
1827,CC(S1)=CC2=C1C(C3=CC=C(CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCCCCC)S9,PBDTT-BT,5.26,3.59,0.88,5.83,0.36,1.85,"Zhang, Y.; Gao, L.; He, C.; Sun, Q.; Li, Y. Synthesis and Photovoltaic Properties of Two-Dimension-Conjugated D¨CA Copolymers Based on Benzodithiophene or Benzodifuran Units. Polym. Chem. 2013, 4, 1474¨C1481. "
1828,CC(S1)=CC2=C1C(C3=CC=C(CCCCCC)O3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCCCCC)O9,PBDTF-BT,5.24,3.54,0.85,8.41,0.403,2.88,"Zhang, Y.; Gao, L.; He, C.; Sun, Q.; Li, Y. Synthesis and Photovoltaic Properties of Two-Dimension-Conjugated D¨CA Copolymers Based on Benzodithiophene or Benzodifuran Units. Polym. Chem. 2013, 4, 1474¨C1481. "
1829,CC(O1)=CC2=C1C(C3=CC=C(CCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)O8)C8=C2C9=CC=C(CCCCCC)S9,PBDFT-BT,5.08,3.4,0.73,9.94,0.609,4.42,"Zhang, Y.; Gao, L.; He, C.; Sun, Q.; Li, Y. Synthesis and Photovoltaic Properties of Two-Dimension-Conjugated D¨CA Copolymers Based on Benzodithiophene or Benzodifuran Units. Polym. Chem. 2013, 4, 1474¨C1481. "
1830,CC(O1)=CC2=C1C(C3=CC=C(CCCCCC)O3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)O8)C8=C2C9=CC=C(CCCCCC)O9,PBDFF-BT,5.11,3.5,0.8,5.84,0.556,2.6,"Zhang, Y.; Gao, L.; He, C.; Sun, Q.; Li, Y. Synthesis and Photovoltaic Properties of Two-Dimension-Conjugated D¨CA Copolymers Based on Benzodithiophene or Benzodifuran Units. Polym. Chem. 2013, 4, 1474¨C1481. "
1831,CC(O1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC(F)=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)C6=NSN=C64)S3)O7)C7=C2OCC(CCCC)CC,PBDFFBT,5.33,3.73,0.62,9.17,0.584,3.3,"Xiao, L.; Liu, B.; Chen, X.; Li, Y.; Tang, W.; Zou, Y. Fluorine Substituted Benzothiazole-Based Low Bandgap Polymers for Photovoltaic Applications. RSC Adv.2013, 3, 11869¨C11876. "
1832,CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC(F)=C(C5=CC(CCCCCCCCCCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CCCC)CC,PBDTFBT,5.3,3.66,0.72,9.31,0.6,4,"Xiao, L.; Liu, B.; Chen, X.; Li, Y.; Tang, W.; Zou, Y. Fluorine Substituted Benzothiazole-Based Low Bandgap Polymers for Photovoltaic Applications. RSC Adv.2013, 3, 11869¨C11876. "
1833,CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NON=C64)S3)S7)C7=C2OCC(CCCC)CC,PBDTBO,5.27,3.53,0.86,10.4,0.644,5.7,"Jiang, J.-M.; Yang, P.-A.; Chen, H.-C.; Wei, K.-H. Synthesis, Characterization, and Photovoltaic Properties of a Low-Bandgap Copolymer Based on 2,1,3-Benzooxadiazole. Chem. Commun. 2011, 47, 8877¨C8879. "
1834,CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NN(CCCCCCCC)N=C64)S3)S7)C7=C2OCC(CCCC)CC,PBDTDTBTz,5.06,3.11,0.61,4.5,0.62,1.7,"Zhang, Z.; Peng, B.; Liu, B.; Pan, C.; Li, Y.; He, Y.; Zhou, K.; Zou, Y. Copolymers from Benzodithiophene and Benzotriazole: Synthesis and Photovoltaic Applications. Polym. Chem. 2010, 1, 1441¨C1447. "
1835,CC(O1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)O8)C8=C2C9=CC=C(CC(CCCC)CC)S9,PBDTTDTBO,5.25,3.56,0.84,11.45,0.613,5.9,"Liu, B.; Chen, X.; He, Y.; Li, Y.; Xu, X.; Xiao, L.; Li, L.; Zou, Y. New Alkylthienyl Substituted benzo[1,2-b:4,5-b¡ä]dithiophene-Based Polymers for High Performance Solar Cells. J. Mater. Chem. A 2013, 1, 570¨C577. "
1836,CC(O1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)O8)C8=C2C9=CC=C(CC(CCCC)CC)S9,PBDTTDTBT,5.15,3.49,0.75,10.29,0.64,4.94,"Liu, B.; Chen, X.; He, Y.; Li, Y.; Xu, X.; Xiao, L.; Li, L.; Zou, Y. New Alkylthienyl Substituted benzo[1,2-b:4,5-b¡ä]dithiophene-Based Polymers for High Performance Solar Cells. J. Mater. Chem. A 2013, 1, 570¨C577. "
1837,CC(O1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NN(CCCCCCCC)N=C75)S4)O8)C8=C2C9=CC=C(CC(CCCC)CC)S9,PBDTTDTBTz,4.92,3.14,0.54,9.47,0.606,3.1,"Liu, B.; Chen, X.; He, Y.; Li, Y.; Xu, X.; Xiao, L.; Li, L.; Zou, Y. New Alkylthienyl Substituted benzo[1,2-b:4,5-b¡ä]dithiophene-Based Polymers for High Performance Solar Cells. J. Mater. Chem. A 2013, 1, 570¨C577. "
1838,CC(S1)=CC2=C1C(OCC(CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=N[Se]N=C64)S3)S7)C7=C2OCC(CCCCCCCCCC)CCCCCCCC,PBDT?DTBSe,5.18,3.63,0.6,13.58,0.64,5.18,"Zhou, E.; Cong, J.; Hashimoto, K.; Tajima, K. A Benzoselenadiazole-Based Low Band Gap Polymer: Synthesis and Photovoltaic Application. Macromolecules 2013, 46, 763¨C768. "
1839,CC(S1)=CC2=C1C(OCC(CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CCCCCCCCCC)CCCCCCCC,PBDT?DTBT,5.26,3.54,0.72,11.16,0.62,5.01,"Zhou, E.; Cong, J.; Hashimoto, K.; Tajima, K. A Benzoselenadiazole-Based Low Band Gap Polymer: Synthesis and Photovoltaic Application. Macromolecules 2013, 46, 763¨C768. "
1840,CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)S3)=C(C=C(C4=CC=C(C5=C(F)C=C(C6=CC=C(C)S6)C7=N[Se]N=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCCCCCCCC)CCCCCCCCCC)S9,PBDT-T-FBSe,5.19,3.59,0.78,11.8,0.54,5,"Li, Y.; Pan, Z.; Miao, L.; Xing, Y.; Li, C.; Chen, Y. Fluoro-Benzoselenadiazole-Based Low Band Gap Polymers for High Efficiency Organic Solar Cells. Polym. Chem. 2014, 5, 330¨C334. "
1841,CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CN=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)S9,PIDT-T-FBSe,5.41,3.85,0.75,14.07,0.459,4.84,"Yuan, J.; Huang, X.; Dong, H.; Lu, J.; Yang, T.; Li, Y.; Gallagher, A.; Ma, W. Structure, Band Gap and Energy Level Modulations for Obtaining Efficient Materials in Inverted Polymer Solar Cells. Org. Electron. 2013, 14, 635¨C643. "
1842,CC(S1)=CC2=C1C(C3=CC=C(CCCCCCCCCCCC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=CN=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CCCCCCCCCCCC)S9,PBPT-12,5.44,3.91,0.75,12.56,0.542,5.11,"Yuan, J.; Huang, X.; Dong, H.; Lu, J.; Yang, T.; Li, Y.; Gallagher, A.; Ma, W. Structure, Band Gap and Energy Level Modulations for Obtaining Efficient Materials in Inverted Polymer Solar Cells. Org. Electron. 2013, 14, 635¨C643. "
1843,CC(S1)=CC2=C1C(C3=C(CCCCCCCC)C=C(CCCCCCCC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=C(CCCCCCCC)C=C(CCCCCCCC)S9,PBDTTBT,5.31,3.56,0.92,10.7,0.575,5.66,"Huo, L.; Hou, J.; Zhang, S.; Chen, H. Y.; Yang, Y. A Poh benzo[1,2-6:4,5-b¡ä]dithiophene Derivative with Deep HOMO Level and Its Application in HighPerformance Polymer Solar Cells. Angew. Chem. Int. Ed. 2010, 49, 1500¨C1503. "
1844,CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)C=C3)=C(C=C(C4=C(CC(CCCC)CC)C=C(C5=CC=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)C=C9,PBDTP-DTBT,5.35,3.65,0.88,12.94,0.709,8.07,"Zhang, M.; Gu, Y.; Guo, X.; Liu, F.; Zhang, S.; Huo, L.; Russell, T. P.; Hou, J. Efficient Polymer Solar Cells Based on Benzothiadiazole and Alkylphenyl Substituted Benzodithiophene with a Power Conversion Efficiency over 8%. Adv. Mater. 2013, 25, 4944¨C4949. "
1845,CC(S1)=CC2=C1C(C3=CC=C(OCC(CCCC)CC)C=C3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)S8)C8=C2C9=CC=C(OCC(CC)CCCC)C=C9,PBDTPO-DTBO,5.56,3.91,0.89,11,0.64,6.2,"Yuan, J.; Xiao, L.; Liu, B.; Li, Y.; He, Y.; Pan, C.; Zou, Y. New Alkoxylphenyl Substituted benzo[1,2-b:4,5-b¡¯] Dithiophene-Based Polymers: Synthesis and Application in Solar Cells. J. Mater. Chem. A 2013, 1, 10639¨C10645. "
1846,CC(S1)=CC2=C1C(C3=CC=C(OCC(CCCC)CC)C=C3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(OCC(CC)CCCC)C=C9,PBDTPO-DTBT,5.46,3.84,0.78,9.3,0.47,3.4,"Yuan, J.; Xiao, L.; Liu, B.; Li, Y.; He, Y.; Pan, C.; Zou, Y. New Alkoxylphenyl Substituted benzo[1,2-b:4,5-b¡¯] Dithiophene-Based Polymers: Synthesis and Application in Solar Cells. J. Mater. Chem. A 2013, 1, 10639¨C10645. "
1847,CC(S1)=CC2=C1C(C3=CC=C(OCC(CCCC)CC)C=C3)=C(C=C(C4=C(CCCCCCCCCCCC)C=C(C5=C(F)C=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(OCC(CC)CCCC)C=C9,PBDTPO-FBT,5.43,3.9,0.7,7.23,0.471,2.7,"Xiao, L.; Yuan, J.; Zou, Y.; Liu, B.; Jiang, J.; Wang, Y.; Jiang, L.; Li, Y. F. A New Polymer from Fluorinated Benzothiadiazole and Alkoxylphenyl Substituted benzo[1,2-b:4,5-b¡ä]dithiophene: Synthesis and Photovoltaic Applications. Synth. Met. 2014, 187, 201¨C208. "
1848,CC1=CC=C(C2=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C3=CC(C4=NSN=C4C(C5=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C6=CC=C(C)S6)S5)=C7)=C7C8=NSN=C83)S2)S1,PNTz4T,5.14,3.46,0.71,19.4,0.734,10.1,"Vohra, V.; Kawashima, K.; Kakara, T.; Koganezawa, T.; Osaka, I.; Takimiya, K.; Murata, H. Efficient Inverted Polymer Solar Cells Employing Favourable Molecular Orientation. Nat. Photonics 2015, 9, 403¨C408. "
1849,CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9,PBDTTBO,5.46,3.68,0.86,12.8,0.67,7.4,"Jiang, J. M.; Lin, H. K.; Lin, Y. C.; Chen, H. C.; Lan, S. C.; Chang, C. K.; Wei, K. H. Side Chain Structure Affects the Photovoltaic Performance of Two-Dimensional Conjugated Polymers. Macromolecules 2014, 47, 70¨C78. "
1850,CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)C=C3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)S8)C8=C2C(C=C9)=CC=C9CC(CC)CCCC,PBDTPBO,5.4,3.62,0.85,11.8,0.64,6.4,"Jiang, J. M.; Lin, H. K.; Lin, Y. C.; Chen, H. C.; Lan, S. C.; Chang, C. K.; Wei, K. H. Side Chain Structure Affects the Photovoltaic Performance of Two-Dimensional Conjugated Polymers. Macromolecules 2014, 47, 70¨C78. "
1851,CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)O3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NON=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)O9,PBDTFBO,5.38,3.6,0.81,11.2,0.6,5.4,"Jiang, J. M.; Lin, H. K.; Lin, Y. C.; Chen, H. C.; Lan, S. C.; Chang, C. K.; Wei, K. H. Side Chain Structure Affects the Photovoltaic Performance of Two-Dimensional Conjugated Polymers. Macromolecules 2014, 47, 70¨C78. "
1852,CC1=CC2=C(C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(OCCCCCCCC)C(OCCCCCCCC)=C(C6=CC=C(C)S6)C7=NSN=C57)S4)O8)C8=C2C9=CC=C(CC(CCCC)CC)S9)S1,PTBFTDTBT,5.2,3.57,0.78,13.51,0.61,6.42,"Fan, L.; Cui, R.; Guo, X.; Qian, D.; Qiu, B.; Yuan, J.; Li, Y.; Huang, W.; Yang, J.; Liu, W.; Xu, X.; Li, L.; Zou, Y. A New Two-Dimensional Donor/acceptor Copolymer Based on 4,8-bis(2¡ä-ethylhexylthiophenethieno[2,3-f]benzofuran for High-Performance Polymer Solar Cells. J. Mater. Chem. C 2014, 2, 5651¨C5659. "
1853,CC(S1)=CC2=C1C(CCC(CCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=C(F)C(F)=C(C5=CC(C[C@@H](CCCC)CC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CC[C@H](CCCCCC)CCCC,DTffBT,5.53,3.8,0.9,12.2,0.621,7.16,"Stuart, A. C.; Tumbleston, J. R.; Zhou, H.; Li, W.; Liu, S.; Ade, H.; You, W. Fluorine Substituents Reduce Charge Recombination and Drive Structure and Morphology Development in Polymer Solar Cells. J. Am. Chem. Soc. 2013, 135, 1806¨C1815. "
1854,CC(S1)=CC2=C1C(CCC(CCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=CC=C(C5=CC(CC(CCCC)CC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC,DTBT,5.42,3.77,0.78,11.7,0.476,4.53,"Stuart, A. C.; Tumbleston, J. R.; Zhou, H.; Li, W.; Liu, S.; Ade, H.; You, W. Fluorine Substituents Reduce Charge Recombination and Drive Structure and Morphology Development in Polymer Solar Cells. J. Am. Chem. Soc. 2013, 135, 1806¨C1815. "
1855,CC(S1)=CC2=C1C(CCC(CCCC)CCCCCC)=C(C=C(C3=C(CC(CC)CCCC)C=C(C4=C(F)C=C(C5=CC(CC(CCCC)CC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CCC(CCCCCC)CCCC,DTfBT,5.48,3.81,0.85,11.5,0.522,5.22,"Stuart, A. C.; Tumbleston, J. R.; Zhou, H.; Li, W.; Liu, S.; Ade, H.; You, W. Fluorine Substituents Reduce Charge Recombination and Drive Structure and Morphology Development in Polymer Solar Cells. J. Am. Chem. Soc. 2013, 135, 1806¨C1815. "
1856,CC(S1)=CC2=C1C(CCC(CCCCC)CCCCCCCC)=C(C=C(C3=C(CCCCCCCC)C=C(C4=C(F)C(F)=C(C5=CC(CCCCCCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2CC[C@H](CCCCC)CCCCCCCC,PTBDTDTBT,5.48,3.92,0.69,8.89,0.554,3.4,"Li, Z.; Lu, J.; Tse, S.-C.; Zhou, J.; Du, X.; Tao, Y.; Ding, J. Synthesis and Applications of Difluorobenzothiadiazole Based Conjugated Polymers for Organic Photovoltaics. J. Mater. Chem. 2011, 21, 3226¨C3233."
1857,CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCC)CC)S3)=C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCC)CC)S9,PTBDTffDTBT,5.46,3.72,0.86,12.17,0.46,4.8,"Wu, F.; Zha, D.; Chen, L.; Chen, Y. Photovoltaics of Donor-Acceptor Polymers Based on Benzodithiophene with Lateral Thiophenyl and Fluorinated Benzothiadiazole. J. Polym. Sci. Part A Polym. Chem. 2013, 51, 1506¨C1511. "
1858,CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCC)CC)S3)=C(C=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCC)CC)S9,PTBDTDTBT,5.29,3.67,0.68,6.69,0.42,1.9,"Wu, F.; Zha, D.; Chen, L.; Chen, Y. Photovoltaics of Donor-Acceptor Polymers Based on Benzodithiophene with Lateral Thiophenyl and Fluorinated Benzothiadiazole. J. Polym. Sci. Part A Polym. Chem. 2013, 51, 1506¨C1511. "
1859,CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CCCCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CCCCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)S9,PBDT_TEH-DT_H-BTff,5.33,3.61,0.68,11.87,0.552,4.46,"Wang, N.; Chen, Z.; Wei, W.; Jiang, Z. Fluorinated Benzothiadiazole-Based Conjugated Polymers for High-Performance Polymer Solar Cells without Any Processing Additives or Post-Treatments. J. Am. Chem. Soc. 2013, 135, 17060¨C17068. "
1860,CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=C(CC(CC)CCCC)C=C(C5=C(F)C(F)=C(C6=CC(CC(CCCC)CC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCC)CC)S9,PBDT_TEH-DT_EH-BTff,5.34,3.58,0.76,13.17,0.619,6.2,"Wang, N.; Chen, Z.; Wei, W.; Jiang, Z. Fluorinated Benzothiadiazole-Based Conjugated Polymers for High-Performance Polymer Solar Cells without Any Processing Additives or Post-Treatments. J. Am. Chem. Soc. 2013, 135, 17060¨C17068. "
1861,CC(S1)=CC2=C1C(OCC(CCCCCCCC)CCCCCC)=C(C=C(C3=C(CCCCCC)C=C(C4=C(F)C(F)=C(C5=CC(CCCCCC)=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OCC(CCCCCCCC)CCCCCC,PBDT_TEH-HDO_H-BTff,5.31,3.61,0.78,15.38,0.692,8.3,"Wang, N.; Chen, Z.; Wei, W.; Jiang, Z. Fluorinated Benzothiadiazole-Based Conjugated Polymers for High-Performance Polymer Solar Cells without Any Processing Additives or Post-Treatments. J. Am. Chem. Soc. 2013, 135, 17060¨C17068. "
1862,CC(S1)=CC2=C1C(CCC(CCCC)CCCCCC)=C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C)S5)C6=NN(CC(CCCCCC)CCCC)N=C64)S3)S7)C7=C2CCC(CCCC)CCCCCC,PBnDT-FTAZ,5.36,3.36,0.79,11.83,0.729,6.81,"Tumbleston, J. R.; Stuart, A. C.; Gann, E.; You, W.; Ade, H. Fluorinated Polymer Yields High Organic Solar Cell Performance for a Wide Range of Morphologies. Adv. Funct. Mater. 2013, 23, 3463¨C3470. "
1863,CC(S1)=CC2=C1C(OC[C@H](CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)O5)C6=NSN=C64)O3)S7)C7=C2OC[C@H](CCCC)CC,PFBT-BDT,5.44,3.48,0.94,6.5,0.46,2.81,"Wang, X.; Chen, S.; Sun, Y.; Zhang, M.; Li, Y.; Li, X.; Wang, H. A Furan-Bridged D-¦Ð-A Copolymer with Deep HOMO Level: Synthesis and Application in Polymer Solar Cells. Polym. Chem. 2011, 2, 2872¨C2877. "
1864,CC(S1)=CC2=C1C(OC[C@H](CCCC)CC)=C(C=C(C3=CC=C(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC=C(C)S5)C6=NSN=C64)S3)S7)C7=C2OC[C@H](CCCC)CC,P(BDT-T-BT),5.35,3.53,0.82,9.45,0.48,3.72,"Wang, X.; Sun, Y.; Chen, S.; Guo, X.; Zhang, M.; Li, X.; Li, Y.; Wang, H. Effects of ¦Ð-Conjugated Bridges on Photovoltaic Properties of Donor-¦Ð-Acceptor Conjugated Copolymers. Macromolecules 2012, 45, 1208¨C1216. "
1865,CC(S1)=CC2=C1C(OC[C@@H](CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=CC(SC(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC(SC(C)=C6)=C6S5)C7=NSN=C74)=C8)=C8S3)S9)C9=C2OC[C@H](CCCCCCCC)CCCCCCCCCC,P(BDT-TT-BT),5.21,3.43,0.69,11.34,0.63,4.93,"Wang, X.; Sun, Y.; Chen, S.; Guo, X.; Zhang, M.; Li, X.; Li, Y.; Wang, H. Effects of ¦Ð-Conjugated Bridges on Photovoltaic Properties of Donor-¦Ð-Acceptor Conjugated Copolymers. Macromolecules 2012, 45, 1208¨C1216. "
1866,CC(S1)=CC2=C1C(OC[C@H](CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=CC(SC(C4=C(OCCCCCCCC)C(OCCCCCCCC)=C(C5=CC(SC(C)=C6)=C6S5)C7=NON=C74)=C8)=C8S3)S9)C9=C2OC[C@H](CCCCCCCC)CCCCCCCCCC,P(BDT-TT-BO),5.31,3.54,0.76,13.87,0.666,7.05,"Wang, X.; Jiang, P.; Chen, Y.; Luo, H.; Zhang, Z.; Wang, H.; Li, X.; Yu, G.; Li, Y. Thieno[3,2-b]Thiophene-Bridged D-¦Ð-A Polymer Semiconductor Based on benzo[1,2-b:4,5- b¡ä]dithiophene and Benzoxadiazole. Macromolecules 2013, 46, 4805¨C4812. "
1867,CC(S1)=CC2=C1C(OC[C@@H](CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=C(CCCCCC)C(SC(C4=CC=C(C5=CC(SC(C)=C6CCCCCC)=C6S5)C7=NSN=C74)=C8)=C8S3)S9)C9=C2OC[C@H](CCCCCCCC)CCCCCCCCCC,P(BDT-TT-HBT),5.29,3.59,0.72,10.12,0.6,4.37,"Wang, X. C.; Zhang, Z. G.; Luo, H.; Chen, S.; Yu, S. Q.; Wang, H. Q.; Li, X. Y.; Yu, G.; Li, Y. F. Effects of Fluorination on the Properties of Thieno 3,2-B Thiophene-Bridged Donor-Pi-Acceptor Polymer Semiconductors. Polym. Chem. 2014, 5, 502¨C511. "
1868,CC(S1)=CC2=C1C(OC[C@@H](CCCCCCCCCC)CCCCCCCC)=C(C=C(C3=C(CCCCCC)C(SC(C4=C(F)C(F)=C(C5=CC(SC(C)=C6CCCCCC)=C6S5)C7=NSN=C74)=C8)=C8S3)S9)C9=C2OC[C@H](CCCCCCCC)CCCCCCCCCC,P(BDT-TT-FBT),5.37,3.64,0.81,8,0.55,3.56,"Wang, X. C.; Zhang, Z. G.; Luo, H.; Chen, S.; Yu, S. Q.; Wang, H. Q.; Li, X. Y.; Yu, G.; Li, Y. F. Effects of Fluorination on the Properties of Thieno 3,2-B Thiophene-Bridged Donor-Pi-Acceptor Polymer Semiconductors. Polym. Chem. 2014, 5, 502¨C511. "
1869,CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCCCC)CCCCCC)S3)=C(C=C(C4=C(CCCCCCCCCCC)C(SC(C5=CC=C(C6=CC(SC(C)=C7CCCCCCCCCCC)=C7S6)C8=NSN=C85)=C9)=C9S4)S%10)C%10=C2C%11=CC=C(CC(CCCCCCCC)CCCCCC)S%11,PBDTT?DTTBT,5.11,3.46,0.78,12.46,0.62,6.03,"Guo, X.; Zhang, M.; Huo, L.; Xu, F.; Wu, Y.; Hou, J. Design, Synthesis and Photovoltaic Properties of a New D¨C¦Ð¨CA Polymer with Extended ¦Ð-Bridge Units. J. Mater. Chem. 2012, 22, 21024¨C21031. "
1870,CC(S1)=CC2=C1C(C3=CC=C(CC(CCCCCCCC)CCCCCC)S3)=C(C=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC=C(C6=CC(CCCCCCCCCCCC)=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CCCCCC)CCCCCCCC)S9,PBDTT?DTBT,5.15,3.52,0.82,5.78,0.495,2.34,"Guo, X.; Zhang, M.; Huo, L.; Xu, F.; Wu, Y.; Hou, J. Design, Synthesis and Photovoltaic Properties of a New D¨C¦Ð¨CA Polymer with Extended ¦Ð-Bridge Units. J. Mater. Chem. 2012, 22, 21024¨C21031. "
1871,CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC=C(C5=C(OCC(CC)CCCC)C(OCC(CCCC)CC)=C(C6=CC=C(C)S6)C7=NSN=C75)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9,PBDT?TBT,5.27,3.48,0.96,9.1,0.518,4.9,"Zuo, G.; Li, Z.; Zhang, M.; Guo, X.; Wu, Y.; Zhang, S.; Peng, B.; Wei, W.; Hou, J. Influence of the Backbone Conformation of Conjugated Polymers on Morphology and Photovoltaic Properties. Polym. Chem. 2014, 5, 1976¨C1981. "
1872,CC(S1)=CC2=C1C(C3=CC=C(CC(CC)CCCC)S3)=C(C=C(C4=CC(SC(C5=C(OCC(CCCCCC)CCCC)C(OCC(CCCC)CCCCCC)=C(C6=CC7=C(S6)C=C(C)S7)C8=NSN=C85)=C9)=C9S4)S%10)C%10=C2C%11=CC=C(CC(CC)CCCC)S%11,PBDT?TTBT,5.09,3.36,0.8,11.83,0.666,6.3,"Zuo, G.; Li, Z.; Zhang, M.; Guo, X.; Wu, Y.; Zhang, S.; Peng, B.; Wei, W.; Hou, J. Influence of the Backbone Conformation of Conjugated Polymers on Morphology and Photovoltaic Properties. Polym. Chem. 2014, 5, 1976¨C1981. "
1873,CC1=CC(CCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCC)CCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1,PTzBT-10HD,5.21,3.41,0.81,10.2,0.62,5.2,"Osaka, I.; Saito, M.; Koganezawa, T.; Takimiya, K. Thiophene-Thiazolothiazole Copolymers: Significant Impact of Side Chain Composition on Backbone Orientation and Solar Cell Performances. Adv. Mater. 2014, 26, 331¨C338. "
1874,CC1=CC(CCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCC)C=C(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1,PTzBT-10OD,5.2,3.4,0.84,8.5,0.54,3.8,"Osaka, I.; Saito, M.; Koganezawa, T.; Takimiya, K. Thiophene-Thiazolothiazole Copolymers: Significant Impact of Side Chain Composition on Backbone Orientation and Solar Cell Performances. Adv. Mater. 2014, 26, 331¨C338. "
1875,CC1=CC(CCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1,PTzBT-12HD,5.2,3.4,0.81,10,0.6,4.8,"Osaka, I.; Saito, M.; Koganezawa, T.; Takimiya, K. Thiophene-Thiazolothiazole Copolymers: Significant Impact of Side Chain Composition on Backbone Orientation and Solar Cell Performances. Adv. Mater. 2014, 26, 331¨C338. "
1876,CC1=CC(CCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCCCC)CCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1,PTzBT-12OD,5.21,3.41,0.82,11.3,0.62,5.8,"Osaka, I.; Saito, M.; Koganezawa, T.; Takimiya, K. Thiophene-Thiazolothiazole Copolymers: Significant Impact of Side Chain Composition on Backbone Orientation and Solar Cell Performances. Adv. Mater. 2014, 26, 331¨C338. "
1877,CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCCCC)CCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1,PTzBT-14OD,5.21,3.41,0.82,9.8,0.64,5.1,"Osaka, I.; Saito, M.; Koganezawa, T.; Takimiya, K. Thiophene-Thiazolothiazole Copolymers: Significant Impact of Side Chain Composition on Backbone Orientation and Solar Cell Performances. Adv. Mater. 2014, 26, 331¨C338. "
1878,CC1=CC(CC(CC)CCCC)=C(C2=NC(SC(C3=C(CC(CC)CCCC)C=C(C4=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCCCC)CCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1,PTzBT-EHOD,5.21,3.41,0.88,10.3,0.64,5.8,"Osaka, I.; Saito, M.; Koganezawa, T.; Takimiya, K. Thiophene-Thiazolothiazole Copolymers: Significant Impact of Side Chain Composition on Backbone Orientation and Solar Cell Performances. Adv. Mater. 2014, 26, 331¨C338. "
1879,CC1=CC(CC(CCCCCC)CCCC)=C(C2=NC(SC(C3=C(CC(CCCCCC)CCCC)C=C(C4=CC(CC(CCCC)CCCCCC)=C(C5=NC(SC(C6=C(CC(CCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1,PTzBT-BOBO,5.23,3.43,0.89,10.5,0.63,5.9,"Osaka, I.; Saito, M.; Koganezawa, T.; Takimiya, K. Thiophene-Thiazolothiazole Copolymers: Significant Impact of Side Chain Composition on Backbone Orientation and Solar Cell Performances. Adv. Mater. 2014, 26, 331¨C338. "
1880,CC1=CC(CC(CCCCCC)CCCC)=C(C2=NC(SC(C3=C(CC(CCCCCC)CCCC)C=C(C4=CC(CC(CCCCCCCC)CCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1,PTzBT-BOHD,5.23,3.43,0.89,11.4,0.65,6.7,"Osaka, I.; Saito, M.; Koganezawa, T.; Takimiya, K. Thiophene-Thiazolothiazole Copolymers: Significant Impact of Side Chain Composition on Backbone Orientation and Solar Cell Performances. Adv. Mater. 2014, 26, 331¨C338. "
1881,CC1=CC(CC(CCCCCC)CCCC)=C(C2=NC(SC(C3=C(CC(CCCCCC)CCCC)C=C(C4=CC(CC(CCCCCCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1,PTzBT-BOOD,5.23,3.43,0.9,8.5,0.62,4.7,"Osaka, I.; Saito, M.; Koganezawa, T.; Takimiya, K. Thiophene-Thiazolothiazole Copolymers: Significant Impact of Side Chain Composition on Backbone Orientation and Solar Cell Performances. Adv. Mater. 2014, 26, 331¨C338. "
1882,CC1=CC(CCCCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCCCC)C=C(C4=CC(CC(CCCCCC)CCCCCCCC)=C(C5=NC(SC(C6=C(CC(CCCCCCCC)CCCCCC)C=C(C)S6)=N7)=C7S5)S4)S3)=N8)=C8S2)S1,PTzBT-14HD,5.21,3.41,0.84,10.6,0.64,5.7,"Osaka, I.; Saito, M.; Mori, H.; Koganezawa, T.; Takimiya, K. Drastic Change of Molecular Orientation in a Thiazolothiazole Copolymer by Molecular-Weight Control and Blending with PC61BM Leads to High Efficiencies in Solar Cells. Adv. Mater. 2012, 24, 425¨C430. "
1883,CC1=CC(CCCCCCCCCCCCCC)=C(C2=CC(CCCCCCCCCCCCCC)=C(C3=NC(SC(C4=C(CCCCCCCCCCCCCC)C=C(C5=C(CCCCCCCCCCCCCC)C=C(C)S5)S4)=N6)=C6S3)S2)S1,PTzQT-14,5.1,3.3,0.64,6,0.43,1.6,"Osaka, I.; Saito, M.; Mori, H.; Koganezawa, T.; Takimiya, K. Drastic Change of Molecular Orientation in a Thiazolothiazole Copolymer by Molecular-Weight Control and Blending with PC61BM Leads to High Efficiencies in Solar Cells. Adv. Mater. 2012, 24, 425¨C430. "
1884,CC1=CC(C(CCCCCCCC)CCCCCC)=C(C2=NC(SC(C3=C(C(CCCCCCCC)CCCCCC)C=C(C)S3)=N4)=C4S2)S1,PTzBT-HD,5.3,3.5,0.96,2.3,0.37,0.8,"Osaka, I.; Saito, M.; Mori, H.; Koganezawa, T.; Takimiya, K. Drastic Change of Molecular Orientation in a Thiazolothiazole Copolymer by Molecular-Weight Control and Blending with PC61BM Leads to High Efficiencies in Solar Cells. Adv. Mater. 2012, 24, 425¨C430. "
1885,CC(S1)=CC2=C1C(OCCCCCC)=C(C=C(C3=CC=C(C(N(CCCCCC)C4=O)=C5C4=C(C6=CC=C(C)C=C6)N(CCCCCC)C5=O)C=C3)S7)C7=C2OCCCCCC,PDPP-BBT,5.47,3.74,0.78,3.73,0.52,1.51,"Kanimozhi, C.; Balraju, P.; Sharma, G. D.; Patil, S. Synthesis of Diketopyrrolopyrrole-Containing Copolymers: A Study of Their Optical and Photovoltaic Properties. J. Phys. Chem. B 2010, 114, 3095¨C3103. "
1886,CC(S1)=CC2=C1C(OCCCCCC)=C(C=C(C3=CC=C(C(N(CCCCCC)C4=O)=C5C4=C(C6=CC=C(C)S6)N(CCCCCC)C5=O)S3)S7)C7=C2OCCCCCC,TDPP-BBT,5.15,3.69,0.74,6.72,0.56,2.78,"Kanimozhi, C.; Balraju, P.; Sharma, G. D.; Patil, S. Synthesis of Diketopyrrolopyrrole-Containing Copolymers: A Study of Their Optical and Photovoltaic Properties. J. Phys. Chem. B 2010, 114, 3095¨C3103. "
1887,CC1=CC=C(C2=CN=C(C3=C4C(C(N3CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C5=CC=C(C6=CC=C(C)S6)C=N5)N(CC(CCCCCCCCCC)CCCCCCCC)C4=O)C=C2)S1,PBTPyDPP,5.77,3.86,0.92,7.96,0.658,4.88,"Jung, J. W.; Liu, F.; Russell, T. P.; Jo, W. H. Synthesis of Pyridine-Capped Diketopyrrolopyrrole and Its Use as a Building Block of Low Band-Gap Polymers for Efficient Polymer Solar Cells. Chem. Commun. 2013, 49, 8495¨C8497. "
1888,O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCC)=C(C4=CC=C(C5=CC=C(C)S5)S4)N(CC(CCCCCC)CCCCCCCC)C2=O,PDPP3T,5.3,3.74,0.67,15.4,0.69,7.1,"Hendriks, K. H.; Heintges, G. H. L.; Gevaerts, V. S.; Wienk, M. M.; Janssen, R. A. J. High-Molecular-Weight Regular Alternating Diketopyrrolopyrrole-Based Terpolymers for Efficient Organic Solar Cells. Angew. Chem. Int. Ed. 2013, 52, 8341¨C8344. "
1889,O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCC)=C(C4=CC=C(C5=CC=C(C)C=C5)S4)N(CC(CCCCCC)CCCCCCCC)C2=O,PDPPTPT,5.48,3.66,0.8,14,0.67,7.4,"Hendriks, K. H.; Heintges, G. H. L.; Gevaerts, V. S.; Wienk, M. M.; Janssen, R. A. J. High-Molecular-Weight Regular Alternating Diketopyrrolopyrrole-Based Terpolymers for Efficient Organic Solar Cells. Angew. Chem. Int. Ed. 2013, 52, 8341¨C8344. "
1890,O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCC)=C(C4=CC=C(C5=CC=C(C6=CC=C(S6)C7=C8C(C(N7CC(CCCCCCCC)CCCCCC)=O)=C(C9=CC=C(C%10=CC=C(C)S%10)S9)N(CC(CCCCCC)CCCCCCCC)C8=O)C=C5)S4)N(CC(CCCCCC)CCCCCCCC)C2=O,PDPP3TaltTPT,5.16,3.73,0.75,15.9,0.67,8,"Hendriks, K. H.; Heintges, G. H. L.; Gevaerts, V. S.; Wienk, M. M.; Janssen, R. A. J. High-Molecular-Weight Regular Alternating Diketopyrrolopyrrole-Based Terpolymers for Efficient Organic Solar Cells. Angew. Chem. Int. Ed. 2013, 52, 8341¨C8344. "
1891,O=C1C(C2=C(C3=CC4=C(C=C(C)S4)S3)N1CCCC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC6=C(C=C(C7=CC=C(C)S7)S6)S5)N(CCCC(CCCCCCCC)CCCCCCCCCC)C2=O,C3-DPPTTT,5.08,3.69,0.57,23.5,0.66,8.8,"Ashraf, R. S.; Meager, I.; Nikolka, M.; Kirkus, M.; Planells, M.; Schroeder, B. C.; Holliday, S.; Hurhangee, M.; Nielsen, C. B.; Sirringhaus, H.; McCulloch, I. Chalcogenophene Comonomer Comparison in Small Band Gap DiketopyrrolopyrroleBased Conjugated Polymers for High-Performing Field-Effect Transistors and Organic Solar Cells. J. Am. Chem. Soc. 2015, 137, 1314¨C1321. "
1892,O=C1C(C2=C(C3=CC4=C(C=C(C)S4)S3)N1CCCC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC6=C(C=C(C7=CC=C(C)[Se]7)S6)S5)N(CCCC(CCCCCCCC)CCCCCCCCCC)C2=O,C3-DPPTTSe,5.07,3.7,0.56,21.5,0.63,7.6,"Ashraf, R. S.; Meager, I.; Nikolka, M.; Kirkus, M.; Planells, M.; Schroeder, B. C.; Holliday, S.; Hurhangee, M.; Nielsen, C. B.; Sirringhaus, H.; McCulloch, I. Chalcogenophene Comonomer Comparison in Small Band Gap DiketopyrrolopyrroleBased Conjugated Polymers for High-Performing Field-Effect Transistors and Organic Solar Cells. J. Am. Chem. Soc. 2015, 137, 1314¨C1321. "
1893,O=C1C(C2=C(C3=CC4=C(C=C(C)S4)S3)N1CCCC(CCCCCCCCCC)CCCCCCCC)=C(C5=CC6=C(C=C(C7=CC=C(C)[Te]7)S6)S5)N(CCCC(CCCCCCCC)CCCCCCCCCC)C2=O,C3-DPPTTTe,5.05,3.73,0.52,21.7,0.63,7.1,"Ashraf, R. S.; Meager, I.; Nikolka, M.; Kirkus, M.; Planells, M.; Schroeder, B. C.; Holliday, S.; Hurhangee, M.; Nielsen, C. B.; Sirringhaus, H.; McCulloch, I. Chalcogenophene Comonomer Comparison in Small Band Gap DiketopyrrolopyrroleBased Conjugated Polymers for High-Performing Field-Effect Transistors and Organic Solar Cells. J. Am. Chem. Soc. 2015, 137, 1314¨C1321. "
1894,CC1=CC=C(C2=CC=C(C(N(CCCCCCCCCCCC)C3=O)=C4C3=C(C5=CC=C(C)O5)N(CCCCCCCCCCCC)C4=O)O2)S1,PDPP2FT-C12,5.2,3.8,0.65,12.2,0.6,5.2,"Yiu, A. T.; Beaujuge, P. M.; Lee, O. P.; Woo, C. H.; Toney, M. F.; Fr¨¦chet, J. M. J. Side-Chain Tunability of Furan-Containing Low-Band-Gap Polymers Provides Control of Structural Order in Efficient Solar Cells. J. Am. Chem. Soc. 2012, 134, 2180¨C2185."
1895,CC1=CC=C(C2=CC=C(C(N(CCCCCCCCCCCCCC)C3=O)=C4C3=C(C5=CC=C(C)O5)N(CCCCCCCCCCCCCC)C4=O)O2)S1,PDPP2FT-C14,5.2,3.8,0.65,14.8,0.64,6.5,"Yiu, A. T.; Beaujuge, P. M.; Lee, O. P.; Woo, C. H.; Toney, M. F.; Fr¨¦chet, J. M. J. Side-Chain Tunability of Furan-Containing Low-Band-Gap Polymers Provides Control of Structural Order in Efficient Solar Cells. J. Am. Chem. Soc. 2012, 134, 2180¨C2185."
1896,CC1=CC=C(C2=CC=C(C(N(CCCCCCCCCCCCCCCC)C3=O)=C4C3=C(C5=CC=C(C)O5)N(CCCCCCCCCCCCCCCC)C4=O)O2)S1,PDPP2FT-C16,5.3,3.9,0.65,12.3,0.69,6.2,"Yiu, A. T.; Beaujuge, P. M.; Lee, O. P.; Woo, C. H.; Toney, M. F.; Fr¨¦chet, J. M. J. Side-Chain Tunability of Furan-Containing Low-Band-Gap Polymers Provides Control of Structural Order in Efficient Solar Cells. J. Am. Chem. Soc. 2012, 134, 2180¨C2185."
1897,CC1=CC=C(C2=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C=C(C3=CC(C4=NON=C4C(C5=CC(CC(CCCCCCCCCCCC)CCCCCCCCCC)=C(C6=CC=C(C)S6)S5)=C7)=C7C8=NON=C83)S2)S1,PNOz4T,5.48,3.65,0.96,14.5,0.64,8.9,"Kawashima, K.; Tamai, Y.; Ohkita, H.; Osaka, I.; Takimiya, K. High-Efficiency Polymer Solar Cells with Small Photon Energy Loss. Nat. Commun. 2015, 6, 10085/1¨C9. "
1898,CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCC)CCCC)C5=O)=C6C5=C(C7=CC=C(C)O7)N(CC(CCCCCC)CCCC)C6=O)O4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9,PBDTT-FDPP,5.26,3.64,0.77,10.9,0.56,4.7,"Dou, L.; Chang, W. H.; Gao, J.; Chen, C. C.; You, J.; Yang, Y. A Selenium-Substituted Low-Bandgap Polymer with Versatile Photovoltaic Applications. Adv. Mater. 2013, 25, 825¨C831. "
1899,CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCC)CCCC)C5=O)=C6C5=C(C7=CC=C(C)S7)N(CC(CCCCCC)CCCC)C6=O)S4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9,PBDTT-DPP,5.3,3.63,0.73,13.7,0.65,6.5,"Dou, L.; Chang, W. H.; Gao, J.; Chen, C. C.; You, J.; Yang, Y. A Selenium-Substituted Low-Bandgap Polymer with Versatile Photovoltaic Applications. Adv. Mater. 2013, 25, 825¨C831. "
1900,CC(S1)=CC2=C1C(C3=CC=C(CC(CCCC)CC)S3)=C(C=C(C4=CC=C(C(N(CC(CCCCCC)CCCC)C5=O)=C6C5=C(C7=CC=C(C)[Se]7)N(CC(CCCCCC)CCCC)C6=O)[Se]4)S8)C8=C2C9=CC=C(CC(CC)CCCC)S9,PBDTT-SeDPP,5.25,3.7,0.69,16.8,0.62,7.2,"Dou, L.; Chang, W. H.; Gao, J.; Chen, C. C.; You, J.; Yang, Y. A Selenium-Substituted Low-Bandgap Polymer with Versatile Photovoltaic Applications. Adv. Mater. 2013, 25, 825¨C831. "
1901,O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCCCCCC)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)C=C6)C=C5)S4)N(CC(CCCCCCCCCC)CCCCCCCC)C2=O,PDPP2TBP,5.39,3.76,0.8,11.5,0.63,5.7,"Li, W.; Furlan, A.; Roelofs, W. S. C.; Hendriks, K. H.; van Pruissen, G. W. P.; Wienk, M. M.; Janssen, R. A. J. Wide Band Gap Diketopyrrolopyrrole-Based Conjugated Polymers Incorporating Biphenyl Units Applied in Polymer Solar Cells. Chem. Commun. 2014, 50, 679¨C681. "
1902,O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCCCCCC)=C(C4=CC=C(C5=CC=C(C6=CC(F)=C(C)C=C6)C=C5F)S4)N(CC(CCCCCCCCCC)CCCCCCCC)C2=O,F1-PDPP2TBP,5.44,3.85,0.89,6.7,0.62,3.7,"Li, W.; Furlan, A.; Roelofs, W. S. C.; Hendriks, K. H.; van Pruissen, G. W. P.; Wienk, M. M.; Janssen, R. A. J. Wide Band Gap Diketopyrrolopyrrole-Based Conjugated Polymers Incorporating Biphenyl Units Applied in Polymer Solar Cells. Chem. Commun. 2014, 50, 679¨C681. "
1903,O=C1C(C2=C(C3=CC=C(C)S3)N1CC(CCCCCCCC)CCCCCCCCCC)=C(C4=CC=C(C5=CC(F)=C(C6=CC=C(C)C=C6F)C=C5)S4)N(CC(CCCCCCCCCC)CCCCCCCC)C2=O,F2-PDPP2TBP,5.48,3.78,0.93,7.7,0.56,4.1,"Li, W.; Furlan, A.; Roelofs, W. S. C.; Hendriks, K. H.; van Pruissen, G. W. P.; Wienk, M. M.; Janssen, R. A. J. Wide Band Gap Diketopyrrolopyrrole-Based Conjugated Polymers Incorporating Biphenyl Units Applied in Polymer Solar Cells. Chem. Commun. 2014, 50, 679¨C681. "
1904,O=C1N(CC(CCCCCCCC)CCCCCCCCCC)C(C2=CC=C(C3=CC(C=CC(C)=C4)=C4C=C3)S2)=C5C(N(CC(CCCCCCCC)CCCCCCCCCC)C(C6=CC=C(C)S6)=C51)=O,PDPPTNT,5.29,3.79,0.76,11.8,0.52,4.7,"Sonar, P.; Singh, S. P.; Li, Y.; Ooi, Z.-E.; Ha, T.; Wong, I.; Soh, M. S.; Dodabalapur, A. High Mobility Organic Thin Film Transistor and Efficient Photovoltaic Devices Using Versatile Donor¨Cacceptor Polymer Semiconductor by Molecular Design. Energy Environ. Sci. 2011, 4, 2288¨C2296. "
1905,CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C)C=C5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1,DT-PDPPTPT,5.4,3.86,0.81,6.6,0.59,3.2,"Li, W.; Hendriks, K. H.; Furlan, A.; Roelofs, W. S. C.; Wienk, M. M.; Janssen, R. A. J. Universal Correlation between Fibril Width and Quantum Efficiency in Diketopyrrolopyrrole-Based Polymer Solar Cells. J. Am. Chem. Soc. 2013, 135, 18942¨C 18948. "
1906,CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C)S5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1,DT-PDPP3T,5.25,3.89,0.65,10.6,0.71,4.8,"Li, W.; Hendriks, K. H.; Furlan, A.; Roelofs, W. S. C.; Wienk, M. M.; Janssen, R. A. J. Universal Correlation between Fibril Width and Quantum Efficiency in Diketopyrrolopyrrole-Based Polymer Solar Cells. J. Am. Chem. Soc. 2013, 135, 18942¨C 18948. "
1907,CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C(C=CC(C)=C6)=C6S7)C7=C5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1,DT-PDPP2T-DBT,5.36,3.74,0.76,10.2,0.68,5.3,"Li, W.; Hendriks, K. H.; Furlan, A.; Roelofs, W. S. C.; Wienk, M. M.; Janssen, R. A. J. Universal Correlation between Fibril Width and Quantum Efficiency in Diketopyrrolopyrrole-Based Polymer Solar Cells. J. Am. Chem. Soc. 2013, 135, 18942¨C 18948. "
1908,CC1=CC=C(C2=C3C(C(N2CC(CCCCCCCCCCCC)CCCCCCCCCC)=O)=C(C4=CC=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C3=O)S1,DT-PDPP4T,5.09,3.66,0.64,16,0.69,7.1,"Li, W.; Hendriks, K. H.; Furlan, A.; Roelofs, W. S. C.; Wienk, M. M.; Janssen, R. A. J. Universal Correlation between Fibril Width and Quantum Efficiency in Diketopyrrolopyrrole-Based Polymer Solar Cells. J. Am. Chem. Soc. 2013, 135, 18942¨C 18948. "
1909,CC1=C2C(C(N1CC(CCCCCCCC)CCCCCC)=O)=C(C3=CC=C(C4=CC=C(C5=C6C(C(N(C(CCCCCCCC)CCCCCCCC)C6=O)=O)=C(C7=CC=C(C8=CC=C(C)S8)S7)S5)S4)S3)N(CC(CCCCCCCC)CCCCCC)C2=O,reg-PDPP/TPDalt2T,5.78,3.84,0.78,9.6,0.68,5.3,"Hendriks, K. H.; Heintges, G. H. L.; Wienk, M. M.; Janssen, R. A. J. Comparing Random and Regular Diketopyrrolopyrrole¨Cbithiophene¨Cthienopyrrolodione Terpolymers for Organic Photovoltaics. J. Mater. Chem. A 2014, 2, 17899¨C17905. "
1910,CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(C(C=C(CCCCCC)C(CCCCCC)=C5)=C5C4=O)=O)=C(C)S3)S6)C6=C2OCC(CCCC)CC,BDT-C6,5.23,3.37,0.83,1.81,0.3,0.45,"Ie, Y.; Aso, Y. Development of Donor-Acceptor Copolymers Based on Dioxocycloalkene-Annelated Thiophenes as Acceptor Units for Organic Photovoltaic Materials. Polym. J. 2017, 49, 13¨C22. "
1911,CC(S1)=CC2=C1C(OCC(CCCC)CC)=C(C=C(C3=C4C(C(C5=C(CCCCCC)SC(CCCCCC)=C5C4=O)=O)=C(C)S3)S6)C6=C2OCC(CCCC)CC,BDT-T6,5.32,3.4,0.87,2.64,0.33,0.73,"Ie, Y.; Aso, Y. Development of Donor-Acceptor Copolymers Based on Dioxocycloalkene-Annelated Thiophenes as Acceptor Units for Organic Photovoltaic Materials. Polym. J. 2017, 49, 13¨C22. "
1912,CC1=CC2=C(OCC(CCCC)CC)C(S3)=C(C(OCC(CCCC)CC)=C2S1)C=C3C4=CC(C(N(CC(CCCCCC)CCCC)C5=O)=O)=C(S4)C6=C5C=C(C)S6,BTI-BDT,5.41,2.3,0.88,9.69,0.518,4.39,"Zhou, N.; Guo, X.; Ortiz, R. P.; Li, S.; Zhang, S.; Chang, R. P. H.; Facchetti, A.; Marks, T. J. Bithiophene Imide and Benzodithiophene Copolymers for Efficient Inverted Polymer Solar Cells. Adv. Mater. 2012, 24, 2242¨C2248. "
1913,CC1=CC2=C(OCCCCCCCCCCCC)C(S3)=C(C(OCCCCCCCCCCCC)=C2S1)C=C3C4=CC(C(N(CC(CCCCCC)CCCCCCCC)C5=O)=O)=C(S4)C6=C5C=C(C)S6,BTI-BDT(2),5.39,2.54,0.92,9.62,0.62,5.5,"Zhou, N.; Guo, X.; Ortiz, R. P.; Li, S.; Zhang, S.; Chang, R. P. H.; Facchetti, A.; Marks, T. J. Bithiophene Imide and Benzodithiophene Copolymers for Efficient Inverted Polymer Solar Cells. Adv. Mater. 2012, 24, 2242¨C2248. "
1914,CC1=CC(CCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C5C(N(CC(CCCCCCCC)CCCCCC)C(/C5=C6C(SC(C)=C7)=C7N(CC(CCCCCC)CCCCCCCC)C\6=O)=O)=C4)S3)=N8)=C8S2)S1,‚s‚s1,5.35,3.94,0.56,2.83,0.38,0.6,"Ide, M.; Saeki, A.; Koizumi, Y.; Koganezawa, T.; Seki, S. Molecular Engineering of Benzothienoisoindigo Copolymers Allowing Highly Preferential Face-on Orientations. J. Mater. Chem. A 2015, 3, 21578¨C21585. "
1915,CC1=CC(CCCCCCCCCCCC)=C(C2=NC(SC(C3=C(CCCCCCCCCCCC)C=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC=C6C(N(CC(CCCCCCCC)CCCCCC)C(/C6=C7C(SC(C8=CC(CCCCCCCCCCCC)=C(C)S8)=C9)=C9N(CC(CCCCCC)CCCCCCCC)C\7=O)=O)=C5)S4)S3)=N%10)=C%10S2)S1,TT2,5.43,3.98,0.58,8.54,0.69,3.4,"Ide, M.; Saeki, A.; Koizumi, Y.; Koganezawa, T.; Seki, S. Molecular Engineering of Benzothienoisoindigo Copolymers Allowing Highly Preferential Face-on Orientations. J. Mater. Chem. A 2015, 3, 21578¨C21585. "
1916,CC1=CC(CCCCCCCCCCCC)=C(C2=NC(C=C(SC(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C5C(N(CC(CCCCCCCC)CCCCCC)C(/C5=C6C(SC(C)=C7)=C7N(CC(CCCCCC)CCCCCCCC)C\6=O)=O)=C4)S3)=N8)C8=C9)=C9S2)S1,BT1,5.5,3.98,0.73,6.72,0.67,3.29,"Ide, M.; Saeki, A.; Koizumi, Y.; Koganezawa, T.; Seki, S. Molecular Engineering of Benzothienoisoindigo Copolymers Allowing Highly Preferential Face-on Orientations. J. Mater. Chem. A 2015, 3, 21578¨C21585. "
1917,CC1=CC(CCCCCCCCCCCC)=C(C2=NC(C=C(SC(C3=C(CCCCCCCCCCCC)C=C(C4=C(CCCCCCCCCCCC)C=C(C5=CC=C6C(N(CC(CCCCCCCC)CCCCCC)C(/C6=C7C(SC(C8=CC(CCCCCCCCCCCC)=C(C)S8)=C9)=C9N(CC(CCCCCC)CCCCCCCC)C\7=O)=O)=C5)S4)S3)=N%10)C%10=C%11)=C%11S2)S1,BT2,5.41,3.92,0.62,10.07,0.67,4.18,"Ide, M.; Saeki, A.; Koizumi, Y.; Koganezawa, T.; Seki, S. Molecular Engineering of Benzothienoisoindigo Copolymers Allowing Highly Preferential Face-on Orientations. J. Mater. Chem. A 2015, 3, 21578¨C21585. "
1918,O=C(N1CC(CCCC)CC)/C(C2=C1C=C(C)S2)=C3C(N(CC(CC)CCCC)C4=C/3SC(C5=CC6=C(OCC(CCCC)CC)C7=C(C=C(C)S7)C(OCC(CCCC)CC)=C6S5)=C4)=O,IP1,4.9,3.8,0.39,3.26,0.4,0.51,"Ide, M.; Koizumi, Y.; Saeki, A.; Izumiya, Y.; Ohkita, H.; Ito, S.; Seki, S. Near-Infrared Absorbing Thienoisoindigo-Based Copolymers for Organic Photovoltaics. J. Phys. Chem. C 2013, 117, 26859¨C26870. "
1919,O=C(N1CC(CCCC)CC)/C(C2=C1C=C(C)S2)=C3C(N(CC(CC)CCCC)C4=C/3SC(C5=CC6=C(C(SC(C)=C7)=C7C6(CC(CCCC)CC)CC(CCCC)CC)S5)=C4)=O,IP2,4.8,3.8,0.3,1.73,0.52,0.27,"Ide, M.; Koizumi, Y.; Saeki, A.; Izumiya, Y.; Ohkita, H.; Ito, S.; Seki, S. Near-Infrared Absorbing Thienoisoindigo-Based Copolymers for Organic Photovoltaics. J. Phys. Chem. C 2013, 117, 26859¨C26870. "
1920,O=C(N1CC(CCCC)CC)/C(C2=C1C=C(C)S2)=C3C(N(CC(CC)CCCC)C4=C/3SC(C5=CC(C(CCCCCCCC)(CCCCCCCC)C6=CC(C)=CC=C67)=C7C=C5)=C4)=O,IP3,5.4,3.8,0.73,3.22,0.53,1.3,"Ide, M.; Koizumi, Y.; Saeki, A.; Izumiya, Y.; Ohkita, H.; Ito, S.; Seki, S. Near-Infrared Absorbing Thienoisoindigo-Based Copolymers for Organic Photovoltaics. J. Phys. Chem. C 2013, 117, 26859¨C26870. "
1921,CC1=CC(CCCCCC)=C(C2=CC=C(C3=C(CCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1,IsoC6,5.58,3.93,0.69,12.3,0.58,5.2,"Grand, C.; Zajaczkowski, W.; Deb, N.; Lo, C. K.; Hernandez, J. L.; Bucknall, D. G.; M¨¹llen, K.; Pisula, W.; Reynolds, J. R. Morphology Control in Films of Isoindigo Polymers by Side-Chain and Molecular Weight Effects. ACS Appl. Mater. Interfaces 2017, 9, 13357¨C13368. "
1922,CC1=CC(CCCCCCCC)=C(C2=CC=C(C3=C(CCCCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1,IsoC8,5.58,3.9,0.7,12.7,0.57,5.6,"Grand, C.; Zajaczkowski, W.; Deb, N.; Lo, C. K.; Hernandez, J. L.; Bucknall, D. G.; M¨¹llen, K.; Pisula, W.; Reynolds, J. R. Morphology Control in Films of Isoindigo Polymers by Side-Chain and Molecular Weight Effects. ACS Appl. Mater. Interfaces 2017, 9, 13357¨C13368. "
1923,CC1=CC(CCCCCCCCCC)=C(C2=CC=C(C3=C(CCCCCCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1,IsoC10,5.6,4.06,0.63,11.6,0.54,4.2,"Grand, C.; Zajaczkowski, W.; Deb, N.; Lo, C. K.; Hernandez, J. L.; Bucknall, D. G.; M¨¹llen, K.; Pisula, W.; Reynolds, J. R. Morphology Control in Films of Isoindigo Polymers by Side-Chain and Molecular Weight Effects. ACS Appl. Mater. Interfaces 2017, 9, 13357¨C13368. "
1924,CC1=CC(CCCCCCCCCCCC)=C(C2=CC=C(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1,IsoC12,5.55,3.84,0.66,11.3,0.52,4.1,"Grand, C.; Zajaczkowski, W.; Deb, N.; Lo, C. K.; Hernandez, J. L.; Bucknall, D. G.; M¨¹llen, K.; Pisula, W.; Reynolds, J. R. Morphology Control in Films of Isoindigo Polymers by Side-Chain and Molecular Weight Effects. ACS Appl. Mater. Interfaces 2017, 9, 13357¨C13368. "
1925,CC1=CC(CC(CCCC)CC)=C(C2=CC=C(C3=C(CC(CCCC)CC)C=C(C4=CC=C(/C(C(N5CC(CCCCCCCC)CCCCCC)=O)=C6C(N(CC(CCCCCCCC)CCCCCC)C7=C\6C=CC(C)=C7)=O)C5=C4)S3)S2)S1,Iso2EH,5.81,3.93,0.88,0.8,0.58,0.3,"Grand, C.; Zajaczkowski, W.; Deb, N.; Lo, C. K.; Hernandez, J. L.; Bucknall, D. G.; M¨¹llen, K.; Pisula, W.; Reynolds, J. R. Morphology Control in Films of Isoindigo Polymers by Side-Chain and Molecular Weight Effects. ACS Appl. Mater. Interfaces 2017, 9, 13357¨C13368. "
1926,CCCCC(CC)CC1=CSC(C2=CC=C(C3=CC(CC(CC)CCCC)=C(C4=CC5=C(C6=CC(F)=C(CC(CC)CCCC)S6)C6=C(C=CS6)C(C6=CC(F)=C(CC(CC)CCCC)S6)=C5S4)S3)C3=NSN=C23)=C1,PBT,?5.45,?3.37,0.79,25.6,63.3,12.9," T. Lin, Y. Hai, Y. Luo, L. Feng, T. Jia, J. Wu, R. Ma, T.A. Dela Pe?a, Y. Li, Z. Xing, M. Li, M. Wang, B. Xiao, K.S. Wong, S. Liu, G. Li, Isomerization of Benzothiadiazole Yields a Promising Polymer Donor and Organic Solar Cells with Efficiency of 19.0%, Advanced Materials n/a (n.d.) 2312311. https://doi.org/10.1002/adma.202312311."
1927,CCCCC(CC)CC1=CSC(C2=CC=C(C3=CC(CC(CC)CCCC)=C(C4=CC5=C(C6=CC(F)=C(CC(CC)CCCC)S6)C6=C(C=CS6)C(C6=CC(F)=C(CC(CC)CCCC)S6)=C5S4)S3)C3N=NSC23)=C1,PiBT,?5.53,?3.17,0.87,28.2,77.3,19," T. Lin, Y. Hai, Y. Luo, L. Feng, T. Jia, J. Wu, R. Ma, T.A. Dela Pe?a, Y. Li, Z. Xing, M. Li, M. Wang, B. Xiao, K.S. Wong, S. Liu, G. Li, Isomerization of Benzothiadiazole Yields a Promising Polymer Donor and Organic Solar Cells with Efficiency of 19.0%, Advanced Materials n/a (n.d.) 2312311. https://doi.org/10.1002/adma.202312311."
1928,CCCCCCCCCCCC1=CSC2=C1SC(C1=CC(/C=N\OCC(CCCCCC)CCCCCCCC)=C(C3=CC4=C(S3)C(CCCCCCCCCCC)=C(C3=CC5=C(S3)C(C3=CC(Cl)=C(CC(CC)CCCC)S3)=C3C=CSC3=C5C3=CC(Cl)=C(CC(CC)CCCC)S3)S4)S1)=C2,PTO-HD,?5.51,?3.58,0.806,23.24,74.19,13.89," L. Hu, L. Wang, L. Ye, B. Zhao, S. Tan, Polymer donors based on alkyloxime-substituted thiophene and 6-undecylthiopheno[3,2-b"
1929,CCCCCCCCCCCC1=CSC2=C1SC(C1=CC(/C=N\OCC(CCCC)CCCCCC)=C(C3=CC4=C(S3)C(CCCCCCCCCCC)=C(C3=CC5=C(S3)C(C3=CC(Cl)=C(CC(CC)CCCC)S3)=C3C=CSC3=C5C3=CC(Cl)=C(CC(CC)CCCC)S3)S4)S1)=C2,PTO-BO,?5.47,?3.61,0.799,22.74,67.67,12.29," L. Hu, L. Wang, L. Ye, B. Zhao, S. Tan, Polymer donors based on alkyloxime-substituted thiophene and 6-undecylthiopheno[3,2-b"
1930,CCCCCCCCCCCCC(CCCCCCCCCC)CC1=C(C)SC(C2=CC3=C(S2)C2=C(C=C(C4=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(C5=CC(F)=C(C6=C(F)C=C(C)S6)S5)S4)S2)C2=C3N=CC=N2)=C1,PQx4T-2F,?5.40,?3.45,0.84,25.78,73.65,15.95," X. Wang, Z. Zhang, L. Kong, M. Luo, M. Chen, L. Zhang, J. Chen, Dithienoquinoxaline-quaterthiophene wide bandgap donor polymers with strong interchain aggregation for efficient organic solar cells processed with a non-halogenated solvent, J. Mater. Chem. A (2024). https://doi.org/10.1039/D3TA08020J."
1931,CCCCCCCCCCCCC(CCCCCCCCCC)CC1=C(C)SC(C2=CC3=C(S2)C2=C(C=C(C4=CC(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(C5=CC=C(C6=CC=C(C)S6)S5)S4)S2)C2=C3N=CC=N2)=C1,PQx4T,?5.30,?3.35,0.82,24.82,65.37,13.3," X. Wang, Z. Zhang, L. Kong, M. Luo, M. Chen, L. Zhang, J. Chen, Dithienoquinoxaline-quaterthiophene wide bandgap donor polymers with strong interchain aggregation for efficient organic solar cells processed with a non-halogenated solvent, J. Mater. Chem. A (2024). https://doi.org/10.1039/D3TA08020J."
1932,CCCCCCCCCCCC1=CSC2=C1SC(C1=CN=C(C3=CC4=C(S3)C(CCCCCCCCCCC)=C(C3=CC5=C(C6=CC(F)=C(CC(CC)CCCC)S6)C6=C(C=CS6)C(C6=CC(F)=C(CC(CC)CCCC)S6)=C5C3)S4)C3=NSN=C13)=C2,PBDTF-ttPTZ,,,0.715,23.87,65.60? ,11.03," G. Xu, X. Huang, H. Mao, L. Zhang, L. Zhang, S. Yu, H. Tempel, X. Liao, Y. Chen, Novel Narrow Band-Gap Copolymers Based on Pyridinthiadiazole for Semitransparent Organic Solar Cells, J. Phys. Chem. C 128 (2024) 1893¨C1900. https://doi.org/10.1021/acs.jpcc.3c06864."
1933,CCCCC(CC)CC1=CC=C(C2=C3C=C(C4=NC(Cl)=CS4)SC3=C(C3=CC=C(CC(CC)CCCC)S3)C3=C2SC=C3)S1,PJ-1,?5.54,?3.54,0.864,66.1,26.08,15.01," H. Lu, H. Wang, G. Ran, W. Liu, H. Huang, X. Jiang, Y. Liu, X. Xu, Z. Bo, Chlorinated Thiazole-Based Low-Cost Polymer Donors for High Efficiency Binary and Ternary Organic Solar Cells, CCS Chemistry 0 (2023) 1¨C10. https://doi.org/10.31635/ccschem.023.202303239."
1934,CCCCCCCCCCC(CCCCCCCC)CN1C(=O)C2=C(C1=O)C1=C(CC(C3=CC(CC(CC)CCCC)=C(C4=CC5=C(C6=CC=C(CC(CC)CCCC)S6)C6=C(C=CS6)C(C6=CC=C(CC(CC)CCCC)S6)=C5S4)S3)=C1)C1=C2C=C(C2=CC(CC(CC)CCCC)=CS2)C1,PBTID?,-5.53,-3.54,0.87,26.1,69.6,15.8," L. Zhang, Z. Zhang, H. Liang, X. Guo, M. Zhang, A Non-Halogenated Polymer Donor Based on Imide Unit for Organic Solar Cells with Efficiency Nearly 16%, Chinese Journal of Chemistry 41 (2023) 2095¨C2102. https://doi.org/10.1002/cjoc.202300007."
1935,CCCCCCCCC(CCCCCC)COC1=CC2=NSN=C2C(C2=CC=C(C3=C(F)C=C(C4=CC=CS4)C(F)=C3)S2)=C1OCC(CCCCCC)CCCCCCCC,PDTBTBz-2F,-5.56,¨C3.64,0.87,21.69,65.5,12.37," Y. Kong, S. Ju, H. Qin, M.H. Jee, S. Xia, J. Ren, C. Gao, J. Yuan, W. Su, H.Y. Woo, Y. Li, Semicrystalline Unfused Polymer Donors with Backbone Halogenation toward Cost-Effective Organic Solar Cells?, Chinese Journal of Chemistry n/a (n.d.). https://doi.org/10.1002/cjoc.202300547."
1936,CCCCCCCCC(CCCCCC)COC1=CC2=NSN=C2C(C2=CC=C(C3=CC=C(C4=CC=CS4)C=C3)S2)=C1OCC(CCCCCC)CCCCCCCC,PDTBTBz-2H,-5.42,¨C3.45,0.77,21.82,57.6,9.73," Y. Kong, S. Ju, H. Qin, M.H. Jee, S. Xia, J. Ren, C. Gao, J. Yuan, W. Su, H.Y. Woo, Y. Li, Semicrystalline Unfused Polymer Donors with Backbone Halogenation toward Cost-Effective Organic Solar Cells?, Chinese Journal of Chemistry n/a (n.d.). https://doi.org/10.1002/cjoc.202300547."
1937,CCCCCCCCC(CCCCCC)CN1C(=O)C2=CC(C3=CC=C4C(=C3)C(=O)N(CC(CCCCCC)CCCCCCCC)C3=C4SC(C4=CC5=C(S4)C(C4=CC=C(CC(CC)CCCC)S4)=C4C=CSC4=C5C4=CC=C(CC(CC)CCCC)S4)=C3)=CC=C2C2=C1C=CS2,PBDT-PiQ,?5.40,?3.34,0.85,20.82,63.51,11.28," J.-W. Ha, B. Park, S.-J. Ko, D.-H. Hwang, Highly crystalline polycyclic aromatic lactam-based regioregular wide-band gap polymer donors for organic solar cells, J. Mater. Chem. C 12 (2023) 80¨C87. https://doi.org/10.1039/D3TC02994H."
1938,CCCCCCCCC(CCCCCC)CC1=C(F)C=C(C2=C3C=C(C)SC3=C(C3=CC(F)=C(CC(CCCCCC)CCCCCCCC)S3)C3=C2SC(C2=C(CCCCCC)C=C(C4=CC5=C(S4)C4=C(C=C(C6=CC(CCCCCC)=C(C)S6)S4)C4=C5C=C5C(=O)N(CCCC)C(=O)C5=C4)S2)=C3)S1,PNDT2,,,0.861,26.33,0.8,18.13," M. Su, M. Lin, S. Mo, J. Chen, X. Shen, Y. Xiao, M. Wang, J. Gao, L. Dang, X. Huang, F. He, Q. Wu, Manipulating the Alkyl Chains of Naphthodithiophene Imide-Based Polymers to Concurrently Boost the Efficiency and Stability of Organic Solar Cells, ACS Appl. Mater. Interfaces 15 (2023) 37371¨C37380. https://doi.org/10.1021/acsami.3c05668."
1939,CCCCCCCCC(CCCCCC)CC1=C(F)C=C(C2=C3C=C(C)SC3=C(C3=CC(F)=C(CC(CCCCCC)CCCCCCCC)S3)C3=C2SC(C2=C(CCCCCC)C=C(C4=CC5=C(S4)C4=C(C=C(C6=CC(CCCCCC)=C(C)S6)S4)C4=C5C=C5C(=O)N(CC)C(=O)C5=C4)S2)=C3)S1,PNDT1,,,0.865,25.85,0.772,17.27," M. Su, M. Lin, S. Mo, J. Chen, X. Shen, Y. Xiao, M. Wang, J. Gao, L. Dang, X. Huang, F. He, Q. Wu, Manipulating the Alkyl Chains of Naphthodithiophene Imide-Based Polymers to Concurrently Boost the Efficiency and Stability of Organic Solar Cells, ACS Appl. Mater. Interfaces 15 (2023) 37371¨C37380. https://doi.org/10.1021/acsami.3c05668."
1940,CCCCCCC(CCCC)CSC1=C(SCC(CCCC)CCCCCC)C=C2C(=O)C3=C(C4=CC=C(C5=CC6=C(S5)C(C5=CC(F)=C(CC(CC)CCCC)S5)=C5C=C(C)SC5=C6C5=CC(F)=C(CC(CC)CCCC)S5)S4)SC(C4=CC=C(C)S4)=C3CC2=C1,PBN-SBO,?5.39,?3.58,0.851,25.84,0.738,16.22," K. Hu, H. Yang, H. Cao, H. Fan, X. Li, C. Cui, Y. Li, Flexible side-chain optimization in polymer donor enables improved photovoltaic performance, Organic Electronics 116 (2023) 106765. https://doi.org/10.1016/j.orgel.2023.106765."
1941,CCCCC(CC)CSC1=C(SCC(CC)CCCC)C=C2C(=O)C3=C(C4=CC=C(C5=CC6=C(S5)C(C5=CC(F)=C(CC(CC)CCCC)S5)=C5C=C(C)SC5=C6C5=CC(F)=C(CC(CC)CCCC)S5)S4)SC(C4=CC=C(C)S4)=C3CC2=C1,PBN-S ,?5.33,?3.48,0.848,24.71,0.614,12.86," K. Hu, H. Yang, H. Cao, H. Fan, X. Li, C. Cui, Y. Li, Flexible side-chain optimization in polymer donor enables improved photovoltaic performance, Organic Electronics 116 (2023) 106765. https://doi.org/10.1016/j.orgel.2023.106765."
1942,CCCCC(CC)CC1=CSC(C2=CN=C(C3=CC(CC(CC)CCCC)=C(C4=CC5=C(C6=CC=C(CC(CC)CCCC)S6)C6=C(C=CS6)C(C6=CC=C(CC(CC)CCCC)S6)=C5S4)S3)C=N2)=C1,PZ2,-5.48,-3.69,0.817,60.01,22.88,11.21," J. Zheng, C. Jin, X. Tang, K. Li, P. Shen, C. Weng, Effect of diazine isomers on photovoltaic properties of simple and efficient wide band gap polymer donor materials, Organic Electronics 125 (2024) 106964. https://doi.org/10.1016/j.orgel.2023.106964."
1943,CCCCC(CC)CC1=CSC(C2=CC=C(C3=CC(CC(CC)CCCC)=C(C4=CC5=C(C6=CC=C(CC(CC)CCCC)S6)C6=C(C=CS6)C(C6=CC=C(CC(CC)CCCC)S6)=C5S4)S3)N=N2)=C1,PZ3,-5.5,-3.68,0.83,60.5,21.44,10.77," J. Zheng, C. Jin, X. Tang, K. Li, P. Shen, C. Weng, Effect of diazine isomers on photovoltaic properties of simple and efficient wide band gap polymer donor materials, Organic Electronics 125 (2024) 106964. https://doi.org/10.1016/j.orgel.2023.106964."
1944,CCCCCCCCC(CCCCCC)CSC1=CC=C(C2=C3C=C(C4=C(CC(CCCC)CCCCCC)C=C(C5=CC6=C(S5)C5=C(C=C(C7=CC(CC(CCCC)CCCCCC)=CS7)S5)C5=NSN=C56)S4)SC3=C(C3=CC=C(SCC(CCCCCC)CCCCCCCC)C=C3)C3=C2SC=C3)C=C1,Z4,¨C5.59,¨C3.41,0.807,26.27,71.06,15.12," M. Zhang, H. Liu, Y. Liu, M. Zeng, B. Zhao, S. Tan, Side Chain Engineering of Two-Dimensional Polymeric Donors for High-Efficiency Organic Solar Cells, Energy Fuels 37 (2023) 6122¨C6128. https://doi.org/10.1021/acs.energyfuels.3c00526."
1945,CCCCCCCCC(CCCCCC)CSC1=CC=C(C2=CC=C(C3=C4C=C(C5=C(CC(CCCC)CCCCCC)C=C(C6=CC7=C(S6)C6=C(C=C(C8=CC(CC(CCCC)CCCCCC)=CS8)S6)C6=NSN=C67)S5)SC4=C(C4=CC=C(C5=CC=C(SCC(CCCCCC)CCCCCCCC)C=C5)S4)C4=C3SC=C4)S2)C=C1,Z3,¨C5.42,¨C3.38,0.798,20.07,66.71,10.68," M. Zhang, H. Liu, Y. Liu, M. Zeng, B. Zhao, S. Tan, Side Chain Engineering of Two-Dimensional Polymeric Donors for High-Efficiency Organic Solar Cells, Energy Fuels 37 (2023) 6122¨C6128. https://doi.org/10.1021/acs.energyfuels.3c00526."
1946,CCCCC(CC)CC1=C(F)C=C(C2=C3C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=CS6)C6=NC(C7=CC(Cl)=C(CC(CC)CCCC)S7)=C(C7=CC(Cl)=C(CC(CC)CCCC)S7)N=C65)S4)SC3=C(C3=CC(F)=C(CC(CC)CCCC)S3)C3=C2SC=C3)S1,PBDQx-¦Â-Cl,¨C5.64,¨C3.93,0.85,24.84,68.33,14.49," M. Pu, Y. Zhu, P. Tan, Y. Zhu, X. Lai, H. Chen, J. Qu, F. He, Chlorination and Position Isomerization to Enhance the Photovoltaic Performance of Polymer Donors, Macromolecules 56 (2023) 5865¨C5872. https://doi.org/10.1021/acs.macromol.3c01416."
1947,CCCCCCCCC(CCCCCC)COC(=O)c1cc(C)sc1-c1nc2sc(-c3sc(-c4cc(CC(CCCC)CCCCCC)c(-c5nc6sc(-c7sc(C)cc7CC(CCCC)CCCCCC)nc6s5)s4)cc3C(=O)OCC(CCCCCC)CCCCCCCC)nc2s1,PTzBTE,-5.47,-3,0.87,23.8,0.72,14.9," K. Yamanaka, M. Saito, T. Koganezawa, H. Saito, H.D. Kim, H. Ohkita, I. Osaka, Interplay Between ¦Ð-Conjugated Polymer Donors and Acceptors Determines Crystalline Order of Their Blends and Photovoltaic Performance, Advanced Energy Materials 13 (2023) 2203443. https://doi.org/10.1002/aenm.202203443."
1948,CCCCCCCCC(CCCCCC)CN1N=C2C(=N1)C(C1=CC=C(C3=CC4=C(S3)C3=C(C(=O)N4CC(CCCC)CCCCCC)C4=C(C=CS4)N(CC(CCCC)CCCCCC)C3=O)S1)=C(F)C(F)=C2C1=CC=CS1,P3,?5.38,?3.51,0.742,22.8,74.3,12.56," S. Shen, Q. Tu, H. Tao, Y. Ma, Q. Zheng, Side-chain engineering of wide-bandgap copolymers based on two different electron-deficient units for high-performance polymer solar cells, Polym. Chem. 14 (2023) 4227¨C4234. https://doi.org/10.1039/D3PY00540B."
1949,CCCCCCCCC(CCCCCC)CN1N=C2C(=N1)C(C1=CC=C(C3=CC4=C(S3)C3=C(C(=O)N4CC(CCCCCC)CCCCCCCC)C4=C(C=CS4)N(CC(CCCCCC)CCCCCCCC)C3=O)S1)=C(F)C(F)=C2C1=CC=CS1,P1,?5.41,?3.49,0.766,18.12,73.72,10.37," S. Shen, Q. Tu, H. Tao, Y. Ma, Q. Zheng, Side-chain engineering of wide-bandgap copolymers based on two different electron-deficient units for high-performance polymer solar cells, Polym. Chem. 14 (2023) 4227¨C4234. https://doi.org/10.1039/D3PY00540B."
1950,CCCCCCCCCCC(CCCCCCCC)CN1C(=O)C2=CC3=C(C=C2C2=C1C=C(C1=CC4=C(S1)C(C1=CC=C(CC(CC)CCCC)S1)=C1C=CSC1=C4C1=CC=C(CC(CC)CCCC)S1)S2)C(=O)N(CC(CCCCCCCC)CCCCCCCCCC)C1=C3SC=C1,P(TPTI-BDT),?5.30,?3.26,0.86,20,70,11.7," N. Sato, S. Hwang, Y. Tsuchii, T. Yasuda, Fused polycyclic lactam-based ¦Ð-conjugated polymers for efficient nonfullerene organic solar cells, J. Mater. Chem. A 11 (2023) 9840¨C9845. https://doi.org/10.1039/D3TA01127E."
1951,CCCCCCCCCCC(CCCCCCCC)CN1C(=O)C2=C(SC(C3=CC4=C(S3)C3=C(C=C(C5=CC6=C(S5)C(C5=CC=C(CC(CC)CCCC)S5)=C5C=CSC5=C6C5=CC=C(CC(CC)CCCC)S5)S3)N(CC(CCCCCCCC)CCCCCCCCCC)C4=O)=C2)C2=C1C=CS2,P(2DTP-BDT),?5.35,?3.38,0.93,15.8,68,9.2," N. Sato, S. Hwang, Y. Tsuchii, T. Yasuda, Fused polycyclic lactam-based ¦Ð-conjugated polymers for efficient nonfullerene organic solar cells, J. Mater. Chem. A 11 (2023) 9840¨C9845. https://doi.org/10.1039/D3TA01127E."
1952,CCCCCCCCC(CCCCCC)CC1=C(C2=CC3=C(C4=CC(F)=C(CC(CC)CCCC)S4)C4=C(C=CS4)C(C4=CC(F)=C(CC(CC)CCCC)S4)=C3S2)SC(C2=CC3=C(S2)C2=C(C=C(C4=CC(CC(CCCC)CCCCCC)=CS4)S2)C2=N[Se]N=C23)=C1,PSe-HD,¨C5.50,¨C3.49,0.852,25.76,67.66,14.85," H. Tang, J. Ning, K. Wang, H. Liu, X. Lu, S. Tan, M. Huang, B. Zhao, Dithienobenzoselenadiazole-Based Polymer Donors with Tuned Side Chains for Efficient Polymer Solar Cells, ACS Appl. Energy Mater. 6 (2023) 4079¨C4088. https://doi.org/10.1021/acsaem.3c00392."
1953,CCCCCCC(CCCC)CC1=CSC(C2=CC3=C(S2)C2=C(C=C(C4=CC(CC(CCCC)CCCCCC)=C(C5=CC6=C(C7=CC(F)=C(CC(CC)CCCC)S7)C7=C(C=CS7)C(C7=CC(F)=C(CC(CC)CCCC)S7)=C6S5)S4)S2)C2=N[Se]N=C23)=C1,PSe-BO,¨C5.45,¨C3.29,0.845,23.63,65.48,13.07," H. Tang, J. Ning, K. Wang, H. Liu, X. Lu, S. Tan, M. Huang, B. Zhao, Dithienobenzoselenadiazole-Based Polymer Donors with Tuned Side Chains for Efficient Polymer Solar Cells, ACS Appl. Energy Mater. 6 (2023) 4079¨C4088. https://doi.org/10.1021/acsaem.3c00392."
1954,CCCCC(CC)CC1=C(F)C=C(C2=C3C=C(C4=C(F)C=C(C5=C6C(=O)C7=C(CC(CC)CCCC)SC(CC(CC)CCCC)=C7C(=O)C6=C(C6=CC(F)=CS6)S5)S4)SC3=C(C3=CC(F)=C(CC(CC)CCCC)S3)C3=C2SC=C3)S1,PM6-F,-5.62,-3.74,0.93,21.71,66.56,13.44," F. Weng, J. Liao, Z. Huang, L. Zeng, P. Zheng, G. Xu, H. Zhao, Y. Xu, Fluorination strategy on ¦Ð-bridge of polymer donor for efficient photovoltaic performance, Journal of Power Sources 580 (2023) 233331. https://doi.org/10.1016/j.jpowsour.2023.233331."
1955,CCCCCCCCc1cc(-c2cc3c(s2)c2sc(-c4cc(CCCCCCCC)c(-c5cc6c(-c7cc(Cl)c(CC(CCCCCC)CCCCCCCC)s7)c7sc(C)cc7c(-c7cc(Cl)c(CC(CCCCCC)CCCCCCCC)s7)c6s5)s4)cc2c2c(F)c(F)c(F)c(F)c32)sc1C,PFNT-Cl,-5.51,-3.53,0.842,26.03,0.8,17.53," J. Chen, D. Li, M. Su, Y. Xiao, H. Chen, M. Lin, X. Qiao, L. Dang, X.-C. Huang, F. He, Q. Wu, A Multifluorination Strategy Toward Wide Bandgap Polymers for Highly Efficient Organic Solar Cells, Angewandte Chemie International Edition 62 (2023) e202215930. https://doi.org/10.1002/anie.202215930."
1956,CCCCCCCCC1=CSC(C2=C3C(=O)N(C)C(=O)C3=C(C3=CC(CCCCCCCC)=C(C4=CC5=C(C6=CC(F)=C(CC(CC)CCCC)S6)C6=C(C=CS6)C(C6=CC(F)=C(CC(CC)CCCC)S6)=C5S4)S3)S2)=C1,PTTB-F ,,,0.882,26.56,77.08,18.06," L.-Y. Xu, Y. Gao, W. Wang, Y. Shao, M. Chen, X. Yang, Y. Fu, M. Zhang, X. Lu, R. Sun, J. Min, A facile synthetic approach based on thieno[3,4-c"
1957,CCCCCCCCC1=CSC(C2=C3C(=O)N(C)C(=O)C3=C(C3=CC(CCCCCCCC)=C(C4=CC5=C(C6=CC=C(CC(CC)CCCC)S6)C6=C(C=CS6)C(C6=CC=C(CC(CC)CCCC)S6)=C5S4)S3)S2)=C1,PTTB-H ,,,0.827,24.49,65.88,13.34," L.-Y. Xu, Y. Gao, W. Wang, Y. Shao, M. Chen, X. Yang, Y. Fu, M. Zhang, X. Lu, R. Sun, J. Min, A facile synthetic approach based on thieno[3,4-c"
1958,CCCCCCCCC(CCCCCC)CN1N=C2C(=N1)C(C1=CC=C(C3=CC4=C(O3)C(C3=CC=C(SCC(CC)CCCC)C(F)=C3)=C3C=C(C)OC3=C4C3=CC=C(SCC(CC)CCCC)C(F)=C3)S1)=C(F)C(F)=C2C1=CC=C(C)O1,PBDF-TF-BTz ,,,0.857,24.8,77.78,17.01," Y. Gao, Z. Xiao, M. Cui, M.I. Saidaminov, F. Tan, L. Shang, W. Li, C. Qin, L. Ding, Asymmetric ¦°-Bridge Engineering Enables High-Permittivity Benzo[1,2-B:4,5-b¡ä"
1959,CCCCCCCCC(CCCCCC)CN1N=C2C(=N1)C(C1=CC=C(C3=CC4=C(O3)C(C3=CC=C(SCC(CC)CCCC)C(F)=C3)=C3C=C(C)OC3=C4C3=CC=C(SCC(CC)CCCC)C(F)=C3)S1)=C(F)C(F)=C2C1=CC=C(C)S1,BDF-dT-BTz ,,,0.852,24.32,75.21,16.03," Y. Gao, Z. Xiao, M. Cui, M.I. Saidaminov, F. Tan, L. Shang, W. Li, C. Qin, L. Ding, Asymmetric ¦°-Bridge Engineering Enables High-Permittivity Benzo[1,2-B:4,5-b¡ä"
1960,CCCCCCCCC(CCCCCC)CN1N=C2C(=N1)C(C1=CC=C(C3=CC4=C(O3)C(C3=CC=C(SCC(CC)CCCC)C(F)=C3)=C3C=C(C)OC3=C4C3=CC=C(SCC(CC)CCCC)C(F)=C3)O1)=C(F)C(F)=C2C1=CC=C(C)O1,PBDF-dF-BTz ,,,0.863,23.08,74.42,15.59," Y. Gao, Z. Xiao, M. Cui, M.I. Saidaminov, F. Tan, L. Shang, W. Li, C. Qin, L. Ding, Asymmetric ¦°-Bridge Engineering Enables High-Permittivity Benzo[1,2-B:4,5-b¡ä"
1961,CCCCCCCCC(CCCCCC)CN1N=C2C(=N1)C(C1=CC(F)=C(C3=CC4=C(C5=CC=C(CC(CC)CCCC)S5)C5=C(C=C(C)S5)C(C5=CC=C(CC(CC)CCCC)S5)=C4S3)S1)=C(F)C(F)=C2C1=CC(F)=CS1,J52-FTh,?5.51,?3.68,0.92,21.29,68,13.32," J. Liao, F. Weng, P. Zheng, G. Xu, L. Zeng, Z. Huang, T. Deng, Y. Pang, S. Wu, J. Chen, H. Zhao, Y. Xu, Enhanced efficiency of polymer solar cells via simple fluorination on the ¦Ð-bridge of polymer donors, Organic Electronics 108 (2022) 106611. https://doi.org/10.1016/j.orgel.2022.106611."
1962,CCCCCCCCC(CCCCCC)CC1=C(F)C=C(C2=C3C=C(C4=CC=C(C)S4)SC3=C(C3=CC(F)=C(CC(CCCCCC)CCCCCCCC)S3)C3=C2SC(C2=CC=C(C4=C(CC(CC)CCCC)C=C(C5=C6C7=CC=C8C(=O)N(CCCC)C(=O)C9=C8C7=C(C=C9)C6=C(C6=CC(CC(CC)CCCC)=C(C)S6)S5)S4)S2)=C3)S1,PNTB-HD?,,,0.854,26.88,0.79,18.15," Q. Jiang, P. Han, H. Ning, J. Jiang, H. Chen, Y. Xiao, C.-R. Ye, J. Chen, M. Lin, F. He, X.-C. Huang, Q. Wu, Reducing steric hindrance around electronegative atom in polymer simultaneously enhanced efficiency and stability of organic solar cells, Nano Energy 101 (2022) 107611. https://doi.org/10.1016/j.nanoen.2022.107611."
1963,CCCCCCC(CCCC)CC1=C(F)C=C(C2=C3C=C(C4=CC=C(C)S4)SC3=C(C3=CC(F)=C(CC(CCCC)CCCCCC)S3)C3=C2SC(C2=CC=C(C4=C(CC(CC)CCCC)C=C(C5=C6C7=CC=C8C(=O)N(CC(CC)CCCC)C(=O)C9=C8C7=C(C=C9)C6=C(C6=CC(CC(CC)CCCC)=C(C)S6)S5)S4)S2)=C3)S1,PNTB-2T,,,0.841,26.07,0.765,16.77," Q. Jiang, P. Han, H. Ning, J. Jiang, H. Chen, Y. Xiao, C.-R. Ye, J. Chen, M. Lin, F. He, X.-C. Huang, Q. Wu, Reducing steric hindrance around electronegative atom in polymer simultaneously enhanced efficiency and stability of organic solar cells, Nano Energy 101 (2022) 107611. https://doi.org/10.1016/j.nanoen.2022.107611."
1964,CCCCCCCCC1=C(C)SC(C2=C(Cl)N=C(C3=CC(CCCCCCCC)=C(C4=CC5=C(S4)C(C4=CC(Cl)=C(CC(CC)CCCC)S4)=C4C=CSC4=C5C4=CC(Cl)=C(CC(C)CC)S4)S3)S2)=C1,PBTTz3Cl,-5.56,-3.6,0.888,26.6,77.81,18.38," Y. Shao, Y. Gao, R. Sun, M. Zhang, J. Min, A Versatile and Low-Cost Polymer Donor Based on 4-Chlorothiazole for Highly Efficient Polymer Solar Cells, Advanced Materials 35 (2023) 2208750. https://doi.org/10.1002/adma.202208750."
1965,CCCCCCCCC(CCCCCC)COC(=O)c1cc(-c2ccc(-c3c(F)c(F)c(-c4ccc(C)s4)c4nn(CC(CCCCCC)CCCCCCCC)nc34)s2)sc1C,PBTz-TC,?5.47,?3.52,0.84,20.91,72.69,12.81," J. Deng, S. Huang, J. Liu, D. Zhou, L. Zhao, L. Liu, B. Huang, Y. Cheng, C. Yang, F. Wu, L. Chen, Layer-by-layer and non-halogenated solvent processing of benzodithiophene-free simple polymer donors for organic solar cells, Chemical Engineering Journal 443 (2022) 136515. https://doi.org/10.1016/j.cej.2022.136515."
1966,CCCCCCCCC(CCCCCC)COC(=O)c1cc(-c2ccc(-c3c(F)c(F)c(-c4ccc(C)s4)c4nn(CC(CCCCCC)CCCCCCCC)nc34)s2)sc1-c1ccc(C)s1,PBTz-TTC,?5.38,?3.51,0.84,18.47,61.4,9.52," J. Deng, S. Huang, J. Liu, D. Zhou, L. Zhao, L. Liu, B. Huang, Y. Cheng, C. Yang, F. Wu, L. Chen, Layer-by-layer and non-halogenated solvent processing of benzodithiophene-free simple polymer donors for organic solar cells, Chemical Engineering Journal 443 (2022) 136515. https://doi.org/10.1016/j.cej.2022.136515."
1967,CCCCC(CC)CC1=C(Cl)C=C(C2=C3C=C(C4=C(F)C=C(C5=C6C(=O)C7=C(CC(CC)CCCC)SC(CC(CC)CCCC)=C7C(=O)C6=C(C6=CC(F)=C(C)S6)S5)S4)SC3=C(C3=CC(Cl)=C(CC(CC)CCCC)S3)C3=C2SC=C3)S1,PM7-F,?5.65,?3.75,0.94,20.79,68.87,13.46," J. Liao, F. Weng, Z. Huang, L. Zeng, P. Zheng, G. Xu, H. Zhao, Y. Xu, Fluorine-Substituted ¦Ð-Bridge through a Simple Method for Efficient Polymer Donor, Solar RRL 6 (2022) 2200697. https://doi.org/10.1002/solr.202200697."
1968,CCCCCCCCCCCCC1=C(C)SC2=C1C1=C(SC(C3=CC4=C(C5=NC(CCCCCCCCCCC)=C(CCCCCCCCCCC)S5)C5=C(C=CS5)C(C5=NC(CCCCCCCCCCC)=C(CCCCCCCCCCC)S5)=C4S3)=C1CCCCCCCCCCCC)C1=CC3=C(C=C12)C(=O)C1=C(CC(CC)CCCC)SC(CC(CC)CCCC)=C1C3=O,P126,?5.53,?3.35,0.89,23.52,0.72,15.07," M.L. Keshtov, I.O. Konstantinov, A.R. Khokhlov, S.A. Kuklin, V.G. Alekseev, I.E. Ostapov, Y. Zou, R. Singhal, H. Dahiya, G.D. Sharma, New wide band gap ¦Ð-conjugated copolymers based on anthra[1,2-b: 4,3-b¡¯: 6,7-c¡¯¡¯"
1969,CCCCCCCCCCCCC1=C(CC)SC2=C1C1=C(SC(C3=CC4=C(C5=CC=C(CC(CC)CCCC)S5)C5=C(C=C(CC)S5)C(C5=CC=C(CC(CC)CCCC)S5)=C4S3)=C1CCCCCCCCCCCC)C1=CC3=C(C=C12)C(=O)C1=C(CC(CC)CCCC)SC(CC(CC)CCCC)=C1C3=O,P127,?5.47,?3.34,0.82,22.24,0.67,12.27," M.L. Keshtov, I.O. Konstantinov, A.R. Khokhlov, S.A. Kuklin, V.G. Alekseev, I.E. Ostapov, Y. Zou, R. Singhal, H. Dahiya, G.D. Sharma, New wide band gap ¦Ð-conjugated copolymers based on anthra[1,2-b: 4,3-b¡¯: 6,7-c¡¯¡¯"
1970,CCCCC(CC)CC1=CSC(C2=CC(F)=C(C3=CC(CC(CC)CCCC)=C(C4=CC5=C(C6=CC(F)=C(CC(CC)CCCC)S6)C6=C(C=CS6)C(C6=CC(F)=C(CC(CC)CCCC)S6)=C5S4)S3)C=C2F)=C1,PBDT-2FBn,?5.52,?3.50,0.858,18,60.2,9.3," G.P. Kini, Y.W. Han, S.J. Jeon, E.J. Lee, Y.J. Lee, M. Goh, D.K. Moon, Tailoring Microstructure and Morphology via Sequential Fluorination to Enhance the Photovoltaic Performance of Low-Cost Polymer Donors for Organic Solar Cells, Macromolecular Rapid Communications 43 (2022) 2200070. https://doi.org/10.1002/marc.202200070."
1971,CCCCCCC(CCCC)CCC1=CSC(C2=CC3=C(S2)C2=C(C=C(C4=CC(CCC(CCCC)CCCCCC)=C(C5=CC6=C(C7=CC(F)=C(CC(CC)CCCC)S7)C7=C(C=C(C)S7)C(C7=CC(F)=C(CC(CC)CCCC)S7)=C6S5)S4)S2)C(=O)O3)=C1,L3,,,0.864,26.97,76.4,17.81," Z. Ou, J. Qin, K. Jin, J. Zhang, L. Zhang, C. Yi, Z. Jin, Q. Song, K. Sun, J. Yang, Z. Xiao, L. Ding, Engineering of the alkyl chain branching point on a lactone polymer donor yields 17.81% efficiency, J. Mater. Chem. A 10 (2022) 3314¨C3320. https://doi.org/10.1039/D1TA10233H."
1972,CCCCCCC(CCCC)Cc1cc(-c2nc3cc4sc(-c5cc(CC(CCCC)CCCCCC)c(-c6cc7c(-c8ccc(CC(CC)CCCC)s8)c8sc(C)cc8c(-c8ccc(CC(CC)CCCC)s8)c7s6)s5)nc4cc3s2)sc1C,PNBTz1,-5.44,-2.88,0.85,24,0.72,14," N. Nakao, S. Ogawa, H.D. Kim, H. Ohkita, T. Mikie, M. Saito, I. Osaka, Pronounced Backbone Coplanarization by ¦Ð-Extension in a Sterically Hindered Conjugated Polymer System Leads to Higher Photovoltaic Performance in Non-Fullerene Solar Cells, ACS Appl. Mater. Interfaces 13 (2021) 56420¨C56429. https://doi.org/10.1021/acsami.1c17199."
1973,CCCCCCCCCCC(CCCCCCCC)Cc1ccc(-c2c3cc(-c4cnc(-c5cc6c(s5)-c5sc7c8c(sc7c5C6(c5ccc(CCCCCC)cc5)c5ccc(CCCCCC)cc5)-c5sc(-c6ncc(C)c7nsnc67)cc5C8(c5ccc(CCCCCC)cc5)c5ccc(CCCCCC)cc5)c5nsnc45)sc3c(-c3ccc(CC(CCCCCCCC)CCCCCCCCCC)s3)c3cc(C)sc23)s1,PL2,?5.49,?3.98,0.69,23.3,62.66,10.12," W. Liu, S. Sun, L. Zhou, Y. Cui, W. Zhang, J. Hou, F. Liu, S. Xu, X. Zhu, Design of Near-Infrared Nonfullerene Acceptor with Ultralow Nonradiative Voltage Loss for High-Performance Semitransparent Ternary Organic Solar Cells, Angewandte Chemie International Edition n/a (n.d.) e202116111. https://doi.org/10.1002/anie.202116111."
1974,S=C(N(CC)C/1=O)SC1=C/C2=CC(CCCCCCCC)=C(C3=CC=C(C4=C(CCCCCCCC)C=C(C5=CC(C(C6=CC=C(C(CCCCCCCC)CCCCCCC)S6)=C(SC(C7=CC(CCCCCCCC)=C(C8=CC=C(C9=C(CCCCCCCC)C=C(/C=C%10SC(N(CC)C\%10=O)=S)S9)S8)S7)=C%11)C%11=C%12C%13=CC=C(CC(CCCCCC)CCCCCCCC)S%13)=C%12S5)S4)S3)S2,DR3TBDTT-HD,,,,,,,
1975,CCCCCCC(C=C(C1=CC(CCCCCC)=C(/C=C2C(C(C=CC=C3)=C3C\2=O)=O)S1)S4)=C4C(S5)=CC6=C5C(C7=CC=C(CCCCCC)S7)=C(C=C(C8=C(CCCCCC)C=C(C9=CC(CCCCCC)=C(/C=C%10C(C(C=CC=C%11)=C%11C\%10=O)=O)S9)S8)S%12)C%12=C6C%13=CC=C(CCCCCC)S%13,D2,,,0.96,11.92,0.59,6.79,"	Zhou J, et al. Solution-Processed and High-Performance Organic Solar Cells Using Small Molecules with a Benzodithiophene Unit. Journal of the American Chemical Society 135, 8484-8487 (2013)."
1976,O=C(C(C=CC=C1)=C1C/2=O)C2=C\C(S3)=CC(CCCCCC)=C3C(S4)=CC5=C4C(C6=CC=C(CCCCCC)S6)=C(C=C(C7=C(CCCCCC)C=C(/C=C8C(C(C=CC=C9)=C9C/8=O)=O)S7)S%10)C%10=C5C%11=CC=C(CCCCCC)S%11,D1,,,0.92,11.05,0.66,6.75,"	Shen S, et al. Solution-Processable Organic Molecule Photovoltaic Materials with Bithienyl-benzodithiophene Central Unit and Indenedione End Groups. Chemistry of Materials 25, 2274-2281 (2013)."
1977,O=C(C(C=CC=C1)=C1C/2=O)C2=C\C(S3)=CC(CCCCCC)=C3C(S4)=CC5=C4C(OCC(CC)CCCC)=C(C=C(C6=C(CCCCCC)C=C(/C=C7C(C(C=CC=C8)=C8C/7=O)=O)S6)S9)C9=C5OCC(CC)CCCC,DO1,,,1.03,10.07,0.55,5.67,"	Shen S, et al. Solution-Processable Organic Molecule Photovoltaic Materials with Bithienyl-benzodithiophene Central Unit and Indenedione End Groups. Chemistry of Materials 25, 2274-2281 (2013)."
1978,CCCCCCC(C=C(C1=CC(CCCCCC)=C(/C=C2C(C(C=CC=C3)=C3C\2=O)=O)S1)S4)=C4C(S5)=CC6=C5C(OCC(CC)CCCC)=C(C=C(C7=C(CCCCCC)C=C(C8=CC(CCCCCC)=C(/C=C9C(C(C=CC=C%10)=C%10C\9=O)=O)S8)S7)S%11)C%11=C6OCC(CC)CCCC,DO2,,,0.91,9.47,0.48,4.15,"	Shen S, et al. Solution-Processable Organic Molecule Photovoltaic Materials with Bithienyl-benzodithiophene Central Unit and Indenedione End Groups. Chemistry of Materials 25, 2274-2281 (2013)."
1979,CC1=CC=CC(N(C2=CC=CC=C2)C(C=C3)=CC=C3C4=CC=C(N(C5=CC=CC=C5)C6=CC(C)=CC=C6)C=C4)=C1,TPD,,,0.92,8.58,0.65,5.11,"	Shen S, et al. Solution-Processable Organic Molecule Photovoltaic Materials with Bithienyl-benzodithiophene Central Unit and Indenedione End Groups. Chemistry of Materials 25, 2274-2281 (2013)."
1980,C1(C2=CC=C(C3=CC=C(C4=CC=C(C5=CC=C(C6=CC=CC=C6)C=C5)C=C4)C=C3)C=C2)=CC=CC=C1,p-6P,,,0.67,3.04,0.53,1.08,"Osasa T, Yamamoto S, Matsumura M. Formation of a bulk-heterojunction structure in organic solar cells by annealing stacked amorphous and microcrystalline layers. Advanced Functional Materials 17, 2937-2942 (2007)."
1981,Cl[Al](N1/C(C2=C(C=CC=C2)/C1=N/3)=N\4)N5C(/N=C6N=C3C7=C\6C=CC=C7)=C8C(C=CC=C8)=C5/N=C9C%10=C(C=CC=C%10)C4=N/9,ClAlP,,,0.42,0.96,----,0.18,"Jiang X, Dai J, Wang H, Geng Y, Yan D. Organic photovoltaic cells using hexadecafluorophthalocyaninatocopper (F16CuPc) as electron acceptor material. Chemical Physics Letters 446, 329-332 (2007)."
1982,N#C/C(C#N)=C1C=C(/C=C/C2=CC=C(/C=C/C3=CC=C(N(C4=CC=CC=C4)C5=CC=CC=C5)C=C3)C=C2)OC(/C=C/C6=CC=C(/C=C/C7=CC=C(N(C8=CC=CC=C8)C9=CC=CC=C9)C=C7)C=C6)=C\1,TPA-DCM-TPA,,,0.68,6.2,0.5,2.15,"Bailey-Salzman RF, Rand BP, Forrest SR. Near-infrared sensitive small molecule organic photovoltaic cells based on chloroaluminum phthalocyanine. Applied Physics Letters 91,  (2007)."
1983,CC(C=C1)=CC=C1N(C2=CC=C(C3=CC=C(N(C4=CC=CC=C4)C5=CC=C(C)C=C5)C=C3)C=C2)C(C=C6)=CC=C6C(CC7)SC7C(CC8)SC8C9=CC%10=C(C=C9)C%11=CC=C(C)C=C%11C%10(CCCCCCCC)CCCCCCCC.CC.CC,PF8-TPD-T2,,,0.9,2.14,0.41,0.79,"He C, et al. Synthesis and photovoltaic properties of a solution-processable organic molecule containing triphenylamine and DCM moieties. Journal of Physical Chemistry C 111, 8661-8666 (2007)."
1984,O=CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC=CS4)S3)S2)S1,4T-CHO,,,0.61,0.99,0.52,0.33,"Li J, Osasa T, Hirayama Y, Sano T, Wakisaka K, Matsumura M. Organic solar cells consisting of stacked amine-thiophene copolymer and 3,4,9,10-perylenetetracarboxyl-bis-benzimidazole layers. Solar Energy Materials and Solar Cells 91, 745-750 (2007)."
1985,O=CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC=C(C5=CC=CS5)S4)S3)S2)S1,5T-CHO,,,2.45,1.9,0.46,2.76,"Liu P, et al. Organic photovoltaic devices with high open-circuit voltage based on oligothiophene derivatives. Chinese Chemical Letters 18, 437-440 (2007)."
1986,C1(N2C(C=CC(C3=CC=C(N(C4=CC=CC=C4)C5=CC=CC=C5)C=C3)=C6)=C6C7=C2C=CC(C8=CC=C(N(C9=CC=CC=C9)C%10=CC=CC=C%10)C=C8)=C7)=CC=C(C%11=CC=C(N%12C(C=CC(C%13=CC=C(N(C%14=CC=CC=C%14)C%15=CC=CC=C%15)C=C%13)=C%16)=C%16C%17=C%12C=CC(C%18=CC=C(N(C%19=CC=CC=C%19)C%20=CC=CC=C%20)C=C%18)=C%17)S%11)S1,G2-DTP-G2,,,2.31,2.49,0.42,2.9,"Liu P, et al. Organic photovoltaic devices with high open-circuit voltage based on oligothiophene derivatives. Chinese Chemical Letters 18, 437-440 (2007)."
1987,C1(C2=CC=C(C3=CC=C(N4C(C=CC(C5=CC=C(N(C6=CC=CC=C6)C7=CC=CC=C7)C=C5)=C8)=C8C9=C4C=CC(C%10=CC=C(N(C%11=CC=CC=C%11)C%12=CC=CC=C%12)C=C%10)=C9)S3)S2)=CC=C(N%13C(C=CC(C%14=CC=C(N(C%15=CC=CC=C%15)C%16=CC=CC=C%16)C=C%14)=C%17)=C%17C%18=C%13C=CC(C%19=CC=C(N(C%20=CC=CC=C%20)C%21=CC=CC=C%21)C=C%19)=C%18)S1,G2-TTP-G2,,,0.85,1.08,0.31,0.28,"	Lu J, Xia PF, Lo PK, Tao Y, Wong MS. Synthesis and properties of multi-triarylamine-substituted carbazole-based dendrimers with an oligothiophene core for potential applications in organic solar cells and light-emitting diodes. Chemistry of Materials 18, 6194-6203 (2006)."
1988,C1(C2=CC=C(C3=CC=C(C4=CC=C(N5C(C=CC(C6=CC=C(N(C7=CC=CC=C7)C8=CC=CC=C8)C=C6)=C9)=C9C%10=C5C=CC(C%11=CC=C(N(C%12=CC=CC=C%12)C%13=CC=CC=C%13)C=C%11)=C%10)S4)S3)S2)=CC=C(N%14C(C=CC(C%15=CC=C(N(C%16=CC=CC=C%16)C%17=CC=CC=C%17)C=C%15)=C%18)=C%18C%19=C%14C=CC(C%20=CC=C(N(C%21=CC=CC=C%21)C%22=CC=CC=C%22)C=C%20)=C%19)S1,G2-QTP-G2,,,0.82,1.01,0.35,0.29,"	Lu J, Xia PF, Lo PK, Tao Y, Wong MS. Synthesis and properties of multi-triarylamine-substituted carbazole-based dendrimers with an oligothiophene core for potential applications in organic solar cells and light-emitting diodes. Chemistry of Materials 18, 6194-6203 (2006)."
1989,C1(C2=CC=C(C3=CC=C(C4=CC=C(C5=CC=C(N6C(C=CC(C7=CC=C(N(C8=CC=CC=C8)C9=CC=CC=C9)C=C7)=C%10)=C%10C%11=C6C=CC(C%12=CC=C(N(C%13=CC=CC=C%13)C%14=CC=CC=C%14)C=C%12)=C%11)S5)S4)S3)S2)=CC=C(N%15C(C=CC(C%16=CC=C(N(C%17=CC=CC=C%17)C%18=CC=CC=C%18)C=C%16)=C%19)=C%19C%20=C%15C=CC(C%21=CC=C(N(C%22=CC=CC=C%22)C%23=CC=CC=C%23)C=C%21)=C%20)S1,G2-PTP-G2,,,0.88,0.81,0.3,0.22,"	Lu J, Xia PF, Lo PK, Tao Y, Wong MS. Synthesis and properties of multi-triarylamine-substituted carbazole-based dendrimers with an oligothiophene core for potential applications in organic solar cells and light-emitting diodes. Chemistry of Materials 18, 6194-6203 (2006)."
1990,C=CC1=CC=C(S1)C(S2)=CC=C2C3=CC=C(S3)C4=CC=CS4,V4T,,,0.83,0.86,0.3,0.22,"	Lu J, Xia PF, Lo PK, Tao Y, Wong MS. Synthesis and properties of multi-triarylamine-substituted carbazole-based dendrimers with an oligothiophene core for potential applications in organic solar cells and light-emitting diodes. Chemistry of Materials 18, 6194-6203 (2006)."
1991,C=CC1=CC=C(S1)C(S2)=CC=C2C3=CC=C(S3)C4=CC=C(C5=CC=CS5)S4,V5T,,,2.07,1.98,0.44,2.32,"	Liu P, Li Q, Huang M, Pan W, Deng W. High open circuit voltage organic photovoltaic cells based on oligothiophene derivatives. Applied Physics Letters 89,  (2006)."
1992,C12=C(C3=CC=CC=C3)C4=C(C5=CC=CC=C5)C6=CC=CC=C6C(C7=CC=CC=C7)=C4C(C8=CC=CC=C8)=C1C=CC=C2,rubrene,,,1.87,1.92,0.58,2.67,"	Liu P, Li Q, Huang M, Pan W, Deng W. High open circuit voltage organic photovoltaic cells based on oligothiophene derivatives. Applied Physics Letters 89,  (2006)."
1993,C/C=C/C1=CC(OC)=C(C)C=C1OCCC(C)CCCC(C)C,MDMO-PPV,,,0.91,3.2,0.53,1.5,"	Taima T, Sakai J, Yamanari T, Saito K. Realization of large open-circuit photovoltage in organic thin-film solar cells by controlling measurement environment. Japanese Journal of Applied Physics Part 2-Letters & Express Letters 45, L995-L997 (2006)."
1994,CCCCCCC(S1)=CC=C1C2=C(C3=CC=C(CCCCCC)S3)SC(C(S4)=CC=C4C5=CC(C6=CC=C(C7=CC(C8=CC=C(CCCCCC)S8)=C(C9=CC=C(CCCCCC)S9)S7)S6)=CC(C%10=CC=C(C%11=CC(C%12=CC=C(CCCCCC)S%12)=C(C%13=CC=C(CCCCCC)S%13)S%11)S%10)=C5)=C2,3G1-1S,,,0.77,7.6,0.51,3,"	Taima T, Sakai J, Yamanari T, Saito K. Realization of large open-circuit photovoltage in organic thin-film solar cells by controlling measurement environment. Japanese Journal of Applied Physics Part 2-Letters & Express Letters 45, L995-L997 (2006)."
1995,CCCCCCC(S1)=CC=C1C2=C(C3=CC=C(CCCCCC)S3)SC(C(S4)=CC=C4C(S5)=CC=C5C6=CC(C7=CC=C(C8=CC=C(C9=CC(C%10=CC=C(CCCCCC)S%10)=C(C%11=CC=C(CCCCCC)S%11)C9)S8)S7)=CC(C%12=CC=C(C%13=CC=C(C%14=CC(C%15=CC=C(CCCCCC)S%15)=C(C%16=CC=C(CCCCCC)S%16)C%14)S%13)S%12)=C6)=C2,3G2-1S,,,0.91,0.64,0.25,0.17,"	Kopidakis N, et al. Bulk heterojunction organic photovoltaic devices based on phenyl-cored thiophene dendrimers. Applied Physics Letters 89,  (2006)."
1996,CCCCCCC(S1)=CC=C1C2=C(C3=CC=C(CCCCCC)S3)SC(C(S4)=CC=C4C5=C(C6=CC=C(C7=CC(C8=CC=C(CCCCCC)S8)=C(C9=CC=C(CCCCCC)S9)S7)S6)C=C(C%10=CC=C(C%11=CC(C%12=CC=C(CCCCCC)S%12)=C(C%13=CC=C(CCCCCC)S%13)S%11)S%10)C(C%14=CC=C(C%15=CC(C%16=CC=C(CCCCCC)S%16)=C(C%17=CC=C(CCCCCC)S%17)S%15)S%14)=C5)=C2,4G1-1S,,,0.8,0.96,0.26,0.21,"	Kopidakis N, et al. Bulk heterojunction organic photovoltaic devices based on phenyl-cored thiophene dendrimers. Applied Physics Letters 89,  (2006)."
1997,CCCCCCC(S1)=CC=C1C2=C(C3=CC=C(CCCCCC)S3)SC(C(S4)=CC=C4C(S5)=CC=C5C6=C(C7=CC=C(C8=CC=C(C9=CC(C%10=CC=C(CCCCCC)S%10)=C(C%11=CC=C(CCCCCC)S%11)S9)S8)S7)C=C(C%12=CC=C(C%13=CC=C(C%14=CC(C%15=CC=C(CCCCCC)S%15)=C(C%16=CC=C(CCCCCC)S%16)S%14)S%13)S%12)C(C%17=CC=C(C%18=CC=C(C%19=CC(C%20=CC=C(CCCCCC)S%20)=C(C%21=CC=C(CCCCCC)S%21)S%19)S%18)S%17)=C6)=C2,4G1-2S,,,0.87,0.21,0.26,0.05,"	Kopidakis N, et al. Bulk heterojunction organic photovoltaic devices based on phenyl-cored thiophene dendrimers. Applied Physics Letters 89,  (2006)."
1998,CCCCCCC(S1)=CC=C1C2=C(C3=CC=C(CCCCCC)S3)SC(C(S4)=CC=C4C(S5)=CC=C5C(S6)=CC=C6C7=C(C8=CC=C(C9=CC=C(C%10=CC=C(C%11=CC(C%12=CC=C(CCCCCC)S%12)=C(C%13=CC=C(CCCCCC)S%13)S%11)S%10)S9)S8)C=C(C%14=CC=C(C%15=CC=C(C%16=CC=C(C%17=CC(C%18=CC=C(CCCCCC)S%18)=C(C%19=CC=C(CCCCCC)S%19)S%17)S%16)S%15)S%14)C(C%20=CC=C(C%21=CC=C(C%22=CC=C(C%23=CC(C%24=CC=C(CCCCCC)S%24)=C(C%25=CC=C(CCCCCC)S%25)S%23)S%22)S%21)S%20)=C7)=C2,4G1-3S,,,0.78,0.68,0.27,0.14,"	Kopidakis N, et al. Bulk heterojunction organic photovoltaic devices based on phenyl-cored thiophene dendrimers. Applied Physics Letters 89,  (2006)."
1999,CC1=CC=CC(N(C2=CC=CC=C2)C(C=C3)=CC=C3N(C4=CC=C(N(C5=CC=CC=C5)C6=CC(C)=CC=C6)C=C4)C7=CC=C(N(C8=CC=CC=C8)C9=CC(C)=CC=C9)C=C7)=C1,m-MTDATA,,,0.86,1.93,0.33,0.57,"	Kopidakis N, et al. Bulk heterojunction organic photovoltaic devices based on phenyl-cored thiophene dendrimers. Applied Physics Letters 89,  (2006)."
2000,CCCCCCC(S1)=CC=C1C(S2)=CC=C2C(S3)=CC=C3[Si](C4=CC=C(C5=CC=C(C6=CC=C(CCCCCC)S6)S5)S4)(C7=CC=C(C8=CC=C(C9=CC=C(CCCCCC)S9)S8)S7)C%10=CC=C(C%11=CC=C(C%12=CC=C(CCCCCC)S%12)S%11)S%10,1,,,1.05,0.55,0.3,1.03,"	Chen LL, Li WL, Wei HZ, Chu B, Li B. Organic ultraviolet photovoltaic diodes based on copper phthalocyanine as an electron acceptor. Solar Energy Materials and Solar Cells 90, 1788-1796 (2006)."
2001,CCCCCSC(S1)=CC=C1C(S2)=CC=C2C(S3)=CC=C3[Si](C4=CC=C(C5=CC=C(C6=CC=C(SCCCCC)S6)S5)S4)(C7=CC=C(C8=CC=C(C9=CC=C(SCCCCC)S9)S8)S7)C%10=CC=C(C%11=CC=C(C%12=CC=C(SCCCCC)S%12)S%11)S%10,2,,,0.66,0.36,0.46,0.2,"	Roquet S, de Bettignies R, Leriche P, Cravino A, Roncali J. Three-dimensional tetra(oligothienyl)silanes as donor material for organic solar cells. Journal of Materials Chemistry 16, 3040-3045 (2006)."
2002,CCC(C1=N/2)=C(CC)C2=C\C3=C(CC)C(CC)=C4N3[Pt]N5/C(C(CC)=C(CC)/C5=C/1)=C\C(C(CC)=C/6CC)=NC6=C/4,PtOEP,,,0.85,1.13,0.24,0.29,"	Roquet S, de Bettignies R, Leriche P, Cravino A, Roncali J. Three-dimensional tetra(oligothienyl)silanes as donor material for organic solar cells. Journal of Materials Chemistry 16, 3040-3045 (2006)."
2003,C12=CC=CC=C1C=C3C(C=C(C=C(C=CC=C4)C4=C5)C5=C3)=C2,pentacene,,,0.66,5.6,0.57,2.1,"	Shao Y, Yang Y. Efficient organic heterojunction photovoltaic cells based on triplet materials. Advanced Materials 17, 2841-+ (2005)."
2004,CCN1C2=C(C=CC=C2)C3=C1C=CC(N(C4=CC(C)=CC=C4)C(C=C5)=CC=C5N(C6=CC=C(N(C7=CC(C)=CC=C7)C8=CC(C(C=CC=C9)=C9N%10CC)=C%10C=C8)C=C6)C%11=CC=C(N(C%12=CC(C(C=CC=C%13)=C%13N%14CC)=C%14C=C%12)C%15=CC(C)=CC=C%15)C=C%11)=C3,PCATA,,,0.25,11.1,0.57,2.8,"Potscavage WJ, Yoo S, Domercq B, Kippelen B. Encapsulation of pentacene/C-60 organic solar cells with Al2O3 deposited by atomic layer deposition. Applied Physics Letters 90,  (2007)."
2005,COC1=CC=C(N(C2=CC=C(OC)C=C2)C3=CC=C(C4=CC=C(N(C5=CC=C(OC)C=C5)C6=CC=C(OC)C=C6)C=C4)C=C3)C=C1,MeO-TPD,,,1.1,0.07,0.29,2.03,"	Li JY, Lee CS, Lee ST. Efficient UV-sensitive organic photovoltaic devices using a starburst amine as electron donor. Journal of Materials Chemistry 15, 3268-3271 (2005)."
2006,CN1C(/C(C2=CC=C(OC)C=C2)=C3N=C(/C(C4=CC=C(OC)C=C4)=C(C=C/5)\N([Zn])C5=C6\C7=CC=C(OC)C=C7)C=C\3)=CC=C1/C(C8=CC=C(OC)C=C8)=C9C=CC6=N/9,Zntpp(OMe)2,,,0.45,6.55,0.49,1.44,"	Maennig B, et al. Organic p-i-n solar cells. Applied Physics a-Materials Science & Processing 79, 1-14 (2004)."
2007,CN1C(/C(C2=CC=C(Cl)C=C2)=C3N=C(/C(C4=CC=C(Cl)C=C4)=C(C=C/5)\N([H])C5=C6\C7=CC=CN=C7)C=C\3)=CC=C1/C(C8=CC=C(Cl)C=C8)=C9C=CC6=N/9.[H+],H2pyp3p(Cl),,,0.33,----,0.34,1.15,"	Takahashi K, Kuraya N, Yamaguchi T, Komura T, Murata K. Three-layer organic solar cell with high-power conversion efficiency of 3.5%. Solar Energy Materials and Solar Cells 61, 403-416 (2000)."
2008,CN1C(/C(C2=CC=C(Cl)C=C2)=C3N=C(/C(C4=CC=C(Cl)C=C4)=C(C=C/5)\N([Zn])C5=C6\C7=CC=C(Cl)C=C7)C=C\3)=CC=C1/C(C8=CC=C(Cl)C=C8)=C9C=CC6=N/9,Zntpp(Cl),,,0.47,----,0.32,0.82,"	Takahashi K, Kuraya N, Yamaguchi T, Komura T, Murata K. Three-layer organic solar cell with high-power conversion efficiency of 3.5%. Solar Energy Materials and Solar Cells 61, 403-416 (2000)."
2009,CN1C(/C(C2=CC=CC=C2)=C3N=C(/C(C4=CC=CC=C4)=C(C=C/5)\N([Zn])C5=C6\C7=CC=CC=C7)C=C\3)=CC=C1/C(C8=CC=CC=C8)=C9C=CC6=N/9,Zntpp,,,0.28,----,0.27,0.2,"	Takahashi K, Kuraya N, Yamaguchi T, Komura T, Murata K. Three-layer organic solar cell with high-power conversion efficiency of 3.5%. Solar Energy Materials and Solar Cells 61, 403-416 (2000)."
2010,CN1C(/C(C2=CC=C(Cl)C=C2)=C3N=C(/C(C4=CC=C(Cl)C=C4)=C(C=C/5)\N([H])C5=C6\C7=CC=C(Cl)C=C7)C=C\3)=CC=C1/C(C8=CC=C(Cl)C=C8)=C9C=CC6=N/9.[H+],H2tpp(Cl),,,0.24,----,0.35,0.51,"	Takahashi K, Kuraya N, Yamaguchi T, Komura T, Murata K. Three-layer organic solar cell with high-power conversion efficiency of 3.5%. Solar Energy Materials and Solar Cells 61, 403-416 (2000)."
2011,CN1C(/C(C2=CC=CC=C2)=C3N=C(/C(C4=CC=CC=C4)=C(C=C/5)\N([H])C5=C6\C7=CC=CC=C7)C=C\3)=CC=C1/C(C8=CC=CC=C8)=C9C=CC6=N/9.[H+],H2tpp,,,0.46,----,0.29,0.44,"	Takahashi K, Kuraya N, Yamaguchi T, Komura T, Murata K. Three-layer organic solar cell with high-power conversion efficiency of 3.5%. Solar Energy Materials and Solar Cells 61, 403-416 (2000)."
2012,CN1C(/C(C2=CC=C(OC)C=C2)=C3N=C(/C(C4=CC=C(OC)C=C4)=C(C=C/5)\N([H])C5=C6\C7=CC=C(OC)C=C7)C=C\3)=CC=C1/C(C8=CC=C(OC)C=C8)=C9C=CC6=N/9.[H+],H2tpp(OMe),,,0.48,----,0.38,1.32,"	Takahashi K, Kuraya N, Yamaguchi T, Komura T, Murata K. Three-layer organic solar cell with high-power conversion efficiency of 3.5%. Solar Energy Materials and Solar Cells 61, 403-416 (2000)."
2013,O=C1C2=CC(C)=CC=C2NC3=C1C=C(NC(C=CC(C)=C4)=C4C5=O)C5=C3,"2,9-dimethyl quinacridone",,,0.47,----,0.4,2.79,"	Takahashi K, Kuraya N, Yamaguchi T, Komura T, Murata K. Three-layer organic solar cell with high-power conversion efficiency of 3.5%. Solar Energy Materials and Solar Cells 61, 403-416 (2000)."
2014,O=C(O)CN(C/1=O)C(SC1=C/C=C2SC3=CC=CC=C3N\2CC)=S,BTh-Rh,,,0.52,6.7*10-3,0.41,0.07,"	Manabe K, Kusabayashi S, Yokoyama M. LONG-LIFE ORGANIC SOLAR-CELL FABRICATION USING QUINACRIDONE PIGMENT. Chemistry Letters, 609-612 (1987)."
2015,O=C1N(CC)C(S/C1=C\C=C2C=CN(CC)C3=C\2C=CC=C3)=S,Q-Rh,,,0.66,0.24,0.56,0.12,"	Chamberlain GA. ORGANIC P-N-JUNCTION SOLAR-CELLS. Molecular Crystals and Liquid Crystals 93, 369-379 (1983)."
2016,O=C1N(CC)C(S/C1=C\C=C2N(CC)C3=CC=CC=C3N/2CC)=S,Bim-Rh,,,0.25,0.62,0.3,0.09,"	Chamberlain GA. ORGANIC P-N-JUNCTION SOLAR-CELLS. Molecular Crystals and Liquid Crystals 93, 369-379 (1983)."
2017,[O-]C1=C(C2=CC=C(N(CC)CC)C=C2O)C(C1C3C(O)=CC(N(CC)CC)C=C3)=O,OHSq,,,0.53,0.31,0.32,0.11,"	Chamberlain GA. ORGANIC P-N-JUNCTION SOLAR-CELLS. Molecular Crystals and Liquid Crystals 93, 369-379 (1983)."
2018,CCCCC1(CCCC)C2=C(C=CC(C3=CC=C(C4=C(C5=C(C6=CC=C(C7=CC(C(CCCC)(CCCC)C8=C9C=CC=C8)=C9C=C7)S6)C%10=NSN=C%10C(C%11=CC=C(C%12=CC=C(C(C=CC=C%13)=C%13C%14(CCCC)CCCC)C%14=C%12)S%11)=C5)C=C(C%15=CC=C(C%16=CC=C(C(C=CC=C%17)=C%17C%18(CCCC)CCCC)C%18=C%16)S%15)C%19=NSN=C%194)S3)=C2)C%20=CC=CC=C%201,DFTBT,,,---,---,---,0.2,"	Merritt VY, Hovel HJ. ORGANIC SOLAR-CELLS OF HYDROXY SQUARYLIUM. Applied Physics Letters 29, 414-415 (1976)."
2019,CCCCCCCCC(C1=C2C=CC=C1)(CCCCCCCC)C3=C2C=CC(C4=CC=C(S4)C(C5=NSN=C56)=CC=C6C7=CC=C(S7)C8=CC=C(C(C=CC(C9=CC=C(C%10=C(C%11=C(C%12=CC=C(C%13=CC=C%14C(C(CCCCCCCC)(CCCCCCCC)C%15=C%14C=CC(C%16=CC=C(C%17=CC=C(C%18SC(C%19=CC(C(CCCCCCCC)(CCCCCCCC)C%20=C%21C=CC=C%20)=C%21C=C%19)CC%18)C%22=NSN=C%17%22)S%16)=C%15)=C%13)S%12)C%23=NSN=C%23C(C%24=CC=C(C%25=CC=C(C(C=CC(C%26=CC=C(C%27=CC=C(C%28CCC(C%29=CC=C(C(C=CC=C%30)=C%30C%31C(CCCCCCC)CCCCCCC)C%31=C%29)S%28)C%32=NSN=C%32%27)C%26)=C%33)=C%33C%34(CCCCCCCC)CCCCCCC)C%34=C%25)S%24)=C%11)C=C(C%35=CC=C(C%36=CC=C(C(C=CC(C%37=CC=C(C%38=CC=C(C%39=CC=C(C%40=CC%41=C(C(C=CC=C%42)=C%42C%41(CCCCCCCC)CCCCCCCC)C=C%40)S%39)C%43=NSN=C%38%43)S%37)=C%44)=C%44C%45(CCCCCCCC)CCCCCCC)C%45=C%36)S%35)C%46=NSN=C%46%10)S9)=C%47)=C%47C%48C(CCCCCCC)CCCCCCC)C%48=C8)=C3,SFTBT,,,1.09,2.47,0.27,0.74,"	Ni D, Zhao B, Shi T, Ma S, Tu G, Wu H. Monodisperse Low-Bandgap Macromolecule-Based 5,5 '-Bibenzo c 1,2,5 thiadiazole Swivel Cruciform for Organic Solar Cells. Acs Macro Letters 2, 621-624 (2013)."
2020,O=C1N(CC(CC)CCCC)C(C2=CC=C(C3=CC=C(CCCCCC)C=C3)S2)=C4C1=C(C5=CSC(C6=CC=C(CCCCCC)C=C6)=C5)N(CC(CC)CCCC)C4=O,DPP-TP6,,,1.08,6.75,0.43,3.14,"	Ni D, Zhao B, Shi T, Ma S, Tu G, Wu H. Monodisperse Low-Bandgap Macromolecule-Based 5,5 '-Bibenzo c 1,2,5 thiadiazole Swivel Cruciform for Organic Solar Cells. Acs Macro Letters 2, 621-624 (2013)."
2021,O=C1N(CC(CC)CCCC)C(C2=CC=C(C3=CC=C(CCCCCCCCCCCC)C=C3)S2)=C4C1=C(C5=CSC(C6=CC=C(CCCCCCCCCCCC)C=C6)=C5)N(CC(CC)CCCC)C4=O,DPP-TP12,,,0.93,8.32,0.55,4.25,"	Shin W, Yasuda T, Watanabe G, Yang YS, Adachi C. Self-Organizing Mesomorphic Diketopyrrolopyrrole Derivatives for Efficient Solution-Processed Organic Solar Cells. Chemistry of Materials 25, 2549-2556 (2013)."
2022,CCCCCCC(S1)=CC=C1C(S2)=CC=C2C(S3)=CC=C3C(S4)=NC5C4N=C(C6=CC=C(C7=CC=C(C8=CC=C(CCCCCC)S8)S7)S6)S5,RTzR,,,0.93,3.82,0.36,1.25,"	Shin W, Yasuda T, Watanabe G, Yang YS, Adachi C. Self-Organizing Mesomorphic Diketopyrrolopyrrole Derivatives for Efficient Solution-Processed Organic Solar Cells. Chemistry of Materials 25, 2549-2556 (2013)."
2023,C1(C2=C(C3=CC=CC=C31)C=CC4=C52)=CC=C5C6=CC=C7C8=C6C4=CC=C8C9=CC=CC=C97,DIP,,,0.65,7.85,0.31,1.57,"	Nazim M, Ameen S, Akhtar MS, Lee Y-S, Shin H-S. Novel thiazolothiazole based linear chromophore for small molecule organic solar cells. Chemical Physics Letters 574, 89-93 (2013)."
2024,CCCCCCCCCCCCC1=C(C2=CC=C(N(C3=CC=CC=C3)C4=CC=CC=C4)C=C2)SC(C5=CC=C(C6=CC(CCCCCCCCCCCC)=C(C7=CC=C(C=C7)N(C8=CC=CC=C8)C9=CC=CC=C9)S6)C%10=NSN=C%105)=C1,P1,,,0.91,8.4,51.9,4.1,"	Wagner J, et al. High Fill Factor and Open Circuit Voltage in Organic Photovoltaic Cells with Diindenoperylene as Donor Material. Advanced Functional Materials 20, 4295-4303 (2010)."
2025,CCCCOC1=CC=C(N(C2=CC=C(OCCCC)C=C2)C3=CC=C(/C=C/C(S4)=CC=C4/C=C/C5=CC=C(/C=C/C6=CC=C(/C=C/C7=CC=C(N(C8=CC=C(OCCCC)C=C8)C9=CC=C(OCCCC)C=C9)C=C7)S6)C%10=NSN=C%105)C=C3)C=C1,P2,,,0.86,3.23,38,1.04,"	Shang H, Fan H, Shi Q, Li S, Li Y, Zhan X. Solution processable D-A-D molecules based on triphenylamine for efficient organic solar cells. Solar Energy Materials and Solar Cells 94, 457-464 (2010)."
2026,C1(C(C2=CC=CC=C2)=CC=C3)=C3C4=N/C1=C\C5=C6C(C(C7=CC=CC=C7)=CC=C6)=C8N5[Zn]N9/C(C%10=C(C(C%11=CC=CC=C%11)=CC=C%10)/C9=C/4)=C\C(C%12=C/%13C=CC=C%12C%14=CC=CC=C%14)=NC%13=C/8,Ph-ZnPc,,,0.62,1.89,36,0.42,"	Shang H, Fan H, Shi Q, Li S, Li Y, Zhan X. Solution processable D-A-D molecules based on triphenylamine for efficient organic solar cells. Solar Energy Materials and Solar Cells 94, 457-464 (2010)."
2027,C1(C(C2=CC=CC3=C2C=CC=C3)=CC=C4)=C4C5=N/C1=N\C6=C7C(C(C8=CC=CC9=C8C=CC=C9)=CC=C7)=C%10N6[Zn]N%11/C(C%12=C(C(C%13=CC=CC%14=C%13C=CC=C%14)=CC=C%12)/C%11=N/5)=N\C(C%15=C/%16C=CC=C%15C%17=CC=CC%18=C%17C=CC=C%18)=NC%16=N/%10,N-ZnPc,,,0.68,-4.19,64,1.82,"	Bruder I, et al. Theoretical and experimental investigation on the influence of the molecular polarizability of novel zinc phthalocyanine derivatives on the open circuit voltage of organic hetero-junction solar cells. Solar Energy Materials and Solar Cells 94, 310-316 (2010)."
2028,C1(C(C2=C(C=CC=C3)C3=CC4=C2C=CC=C4)=CC=C5)=C5C6=N/C1=N\C7=C8C(C(C9=C(C=CC=C%10)C%10=CC%11=C9C=CC=C%11)=CC=C8)=C%12N7[Zn]N%13/C(C%14=C(C(C%15=C(C=CC=C%16)C%16=CC%17=C%15C=CC=C%17)=CC=C%14)/C%13=N/6)=N\C(C%18=C/%19C=CC=C%18C%20=C(C=CC=C%21)C%21=CC%22=C%20C=CC=C%22)=NC%19=N/%12,A-ZnPc,,,0.76,-3.24,60,1.48,"	Bruder I, et al. Theoretical and experimental investigation on the influence of the molecular polarizability of novel zinc phthalocyanine derivatives on the open circuit voltage of organic hetero-junction solar cells. Solar Energy Materials and Solar Cells 94, 310-316 (2010)."
2029,CC(C)[Si](C(C)C)(C(C)C)C#CC1=C(C=CC(C2=CC=C(C3=CC=CS3)S2)=C4)C4=C(C#C[Si](C(C)C)(C(C)C)C(C)C)C5=CC=C(C6=CC=C(C7=CC=CS7)S6)C=C51,TIPSAntBT,,,0.79,-0.03,22,0.005,"	Bruder I, et al. Theoretical and experimental investigation on the influence of the molecular polarizability of novel zinc phthalocyanine derivatives on the open circuit voltage of organic hetero-junction solar cells. Solar Energy Materials and Solar Cells 94, 310-316 (2010)."
2030,CC(C)[Si](C(C)C)(C(C)C)C#CC1=C(C=CC(C2=CC(C=CC=C3)=C3C=C2)=C4)C4=C(C#C[Si](C(C)C)(C(C)C)C(C)C)C5=CC=C(C6=CC(C=CC=C7)=C7C=C6)C=C51,TIPSAntNa,,,0.78,4.55,40.3,1.4,"	Chung DS, et al. Solution-Processed Organic Photovoltaic Cells with Anthracene Derivatives. Chemsuschem 3, 742-748 (2010)."
2031,CCC1=C(SC(C2=CC=C(C3=CC=C(C4=C(CC)C(CC)=C(C5=CC=C(/C=C(C#N)/C#N)S5)S4)S3)S2)=C1CC)C6=CC=C(/C=C(C#N)/C#N)S6,DCV6T-Eth,,,0.97,0.4,36.6,0.14,"	Chung DS, et al. Solution-Processed Organic Photovoltaic Cells with Anthracene Derivatives. Chemsuschem 3, 742-748 (2010)."
2032,C1(N(C2=CC=CC=C2)C3=CC=CC=C3)=CC=C(C4=CC=C(C(C=C5)=CC=C5N(C6=CC=CC=C6)C7=CC=CC=C7)C8=NSN=C48)C=C1,BTD-TPA,,,0.9,6.5,64,3.8,"	Wynands D, et al. Correlation between morphology and performance of low bandgap oligothiophene:C60 mixed heterojunctions in organic solar cells. Journal of Applied Physics 107,  (2010)."
2033,C1(N(C2=CC=CC=C2)C3=CC=CC=C3)=CC=C(/C=C/C4=CC=C(/C=C/C(C=C5)=CC=C5N(C6=CC=CC=C6)C7=CC=CC=C7)C8=NSN=C48)C=C1,BTD-ETPA,,,0.87,1.53,32,0.43,"	Yasuda T, Ishi-i T, Han L. Benzothiadiazole-Triphenylamine Derivatives as Donor Materials for Bulk-Heterojunction Organic Solar Cells. Journal of Photopolymer Science and Technology 23, 307-312 (2010)."
2034,C1(N(C2=CC=CC=C2)C3=CC=CC=C3)=CC=C(C(S4)=CC=C4C5=CC=C(C6=CC=C(C(C=C7)=CC=C7N(C8=CC=CC=C8)C9=CC=CC=C9)S6)C%10=NSN=C5%10)C=C1,BTD-Th-TPA,,,0.86,1.53,33,0.44,"	Yasuda T, Ishi-i T, Han L. Benzothiadiazole-Triphenylamine Derivatives as Donor Materials for Bulk-Heterojunction Organic Solar Cells. Journal of Photopolymer Science and Technology 23, 307-312 (2010)."
2035,O=C(N1CC(CC)CCCC)/C(C2=C1C=C(C3=CC=C(N(C4=CC=CC=C4)C5=CC=CC=C5)C=C3)C=C2)=C6C(N(CC(CC)CCCC)C7=C/6C=CC(C8=CC=C(N(C9=CC=CC=C9)C%10=CC=CC=C%10)C=C8)=C7)=O,M1,,,0.81,3.57,34,1,"	Yasuda T, Ishi-i T, Han L. Benzothiadiazole-Triphenylamine Derivatives as Donor Materials for Bulk-Heterojunction Organic Solar Cells. Journal of Photopolymer Science and Technology 23, 307-312 (2010)."
2036,CC(O[C@@H]1C[C@@](C)(O)C(C(C)(C)C1)=C=C/C(C)=C/C=C/C(C)=C/C=C/C=C(C)/C=C/C=C(C)/CC[C@]23C(C)C[C@H](O)C[C@@]2(C)O3)=O,fucoxanthin,,,0.78,2.94,36.5,0.84,"	Yang M, Chen X, Zou Y, Pan C, Liu B, Zhong H. A solution-processable D-A-D small molecule based on isoindigo for organic solar cells. Journal of Materials Science 48, 1014-1020 (2013)."
2037,C/C(/C=C/C1=C(C)CCCC1(C)C)=C\C=C\C(C)=C\C=C\C=C(C)\C=C\C=C(C)\C=C\C2=C(C)CCCC2(C)C,¦Â-carotene,,,0.7,0.7,28,0.14,"	Wang X-F, et al. Natural Photosynthetic Carotenoids for Solution-Processed Organic Bulk-Heterojunction Solar Cells. Journal of Physical Chemistry C 117, 804-811 (2013)."
2038,C/C(/C=C/C=C(C)/C=C/C=C(C)/C)=C\C=C\C(C)=C\C=C\C=C(C)\C=C\C=C(C)\C=C\C=C(C)\CC/C=C(C)/C,lycopene,,,0.63,0.86,28,0.15,"	Wang X-F, et al. Natural Photosynthetic Carotenoids for Solution-Processed Organic Bulk-Heterojunction Solar Cells. Journal of Physical Chemistry C 117, 804-811 (2013)."
2039,C1(N(C2=CC=CC=C2)C3=CC=CC=C3)=CC=C(C4=NC(SC(C5=CC=C(N(C6=CC=CC=C6)C7=CC=CC=C7)C=C5)=N8)C8S4)C=C1,T0,,,0.45,1.39,52,0.33,"	Wang X-F, et al. Natural Photosynthetic Carotenoids for Solution-Processed Organic Bulk-Heterojunction Solar Cells. Journal of Physical Chemistry C 117, 804-811 (2013)."
2040,CCCCCCCCCCCCC1=C(SC(C2=CC=C(N(C3=CC=CC=C3)C4=CC=CC=C4)C=C2)=C1)C5=NC(SC(C6=C(CCCCCCCCCCCC)C=C(C7=CC=C(N(C8=CC=CC=C8)C9=CC=CC=C9)C=C7)S6)=N%10)C%10S5,T1,,,0.94,5.2,41.5,2.19,"	Cheng P, Shi Q, Lin Y, Li Y, Zhan X. Evolved structure of thiazolothiazole based small molecules towards enhanced efficiency in organic solar cells. Organic Electronics 14, 599-606 (2013)."
2041,CCCCCCC1=CC=C(C2=CC=C(C3=CC=C(C4=CC=C(C5=CC=C(CCCCCC)S5)S4)S3)S2)S1,DH5T,,,0.91,7.9,45,3.73,"	Cheng P, Shi Q, Lin Y, Li Y, Zhan X. Evolved structure of thiazolothiazole based small molecules towards enhanced efficiency in organic solar cells. Organic Electronics 14, 599-606 (2013)."
2042,CCCCCCCCCCCCC1=C(C2=CC=C(S2)C3=NC(SC(C4=CC=C(C5=C(CCCCCCCCCCCC)C=C(C6=CC=C(N(C7=CC=CC=C7)C8=CC=CC=C8)C=C6)S5)S4)=N9)C9S3)SC(C%10=CC=C(N(C%11=CC=CC=C%11)C%12=CC=CC=C%12)C=C%10)=C1,T2,,,0.51,4.25,37,0.8,"	Kong JA, Lim E, Lee KK, Lee S, Kim SH. A benzothiadiazole-based oligothiophene for vacuum-deposited organic photovoltaic cells. Solar Energy Materials and Solar Cells 94, 2057-2063 (2010)."
2043,CC(C=C1)=CC=C1N(C2=CC=C(C)C=C2)C(C=C3)=CC(C4=C/5C=CC(N(C6=CC=C(C)C=C6)C7=CC=C(C)C=C7)=C4)=C3C5=C(C#N)/C#N,1,,,0.85,9.74,3.89,4.05,"	Cheng P, Shi Q, Lin Y, Li Y, Zhan X. Evolved structure of thiazolothiazole based small molecules towards enhanced efficiency in organic solar cells. Organic Electronics 14, 599-606 (2013)."
2044,N#C/C(C#N)=C/C1=CC=C(C2=CC=C(/C=C/C3=CC=C(C4=CC=C(N(C5=CC=CC=C5)C6=CC=CC=C6)C=C4)S3)S2)S1,8,,,0.99,7.64,53,4.04,"	Chi L-C, et al. Donor-acceptor small molecule with coplanar and rigid pi-bridge for efficient organic solar cells. Solar Energy Materials and Solar Cells 109, 33-39 (2013)."
2045,N#C/C(C#N)=C/C1=CC=C(C2=CC=C(/C=C/C(S3)=CC=C3C4=CC=C(C5=CC=C(N(C6=CC=CC=C6)C7=CC=CC=C7)C=C5)S4)S2)S1,9,,,0.68,4.98,60,2.02,"	Kwok EC-H, Tsang DP-K, Chan M-Y, Yam VW-W. Organic Photovoltaic Devices Based on a New Class of Oligothienylenevinylene Derivatives as Donor Materials. Chemistry-a European Journal 19, 2757-2767 (2013)."
2046,N#C/C(C#N)=C\C1=CC=C(C2=CC=C(/C=C/C3=CC=C(/C=C/C4=CC=C(C5=CC=C(N(C6=CC=CC=C6)C7=CC=CC=C7)C=C5)S4)S3)S2)S1,10,,,0.76,3.39,52,1.33,"	Kwok EC-H, Tsang DP-K, Chan M-Y, Yam VW-W. Organic Photovoltaic Devices Based on a New Class of Oligothienylenevinylene Derivatives as Donor Materials. Chemistry-a European Journal 19, 2757-2767 (2013)."
2047,N#C/C(C#N)=C\C1=CC=C(C2=CC=C(/C=C/C3=CC=C(C4=CC=C(C5=CC=C(N(C6=CC=CC=C6)C7=CC=CC=C7)C=C5)S4)S3)S2)S1,11,,,0.61,4.39,53,1.43,"	Kwok EC-H, Tsang DP-K, Chan M-Y, Yam VW-W. Organic Photovoltaic Devices Based on a New Class of Oligothienylenevinylene Derivatives as Donor Materials. Chemistry-a European Journal 19, 2757-2767 (2013)."
2048,N#C/C(C1=CC=C(N(C2=CC=CC=C2)C3=C(C=CC=C4)C4=CC=C3)C=C1)=C(C#N)\C5=CC=C(N(C6=C(C=CC=C7)C7=CC=C6)C8=CC=CC=C8)C=C5,NPAFN,,,0.79,3.32,45,1.2,"	Kwok EC-H, Tsang DP-K, Chan M-Y, Yam VW-W. Organic Photovoltaic Devices Based on a New Class of Oligothienylenevinylene Derivatives as Donor Materials. Chemistry-a European Journal 19, 2757-2767 (2013)."
2049,CCCCC(CC)CN1C(C2=CC=C(C3=CC=CC=C3)S2)=C4C(N(CC(CC)CCCC)C(C(S5)=CC=C5C(C=C6)=CC=C6N(C7=CC=C(C8=CC=C(C9=C%10C(C(N9CC(CC)CCCC)=O)=C(C%11=CC=C(C%12=CC=CC=C%12)S%11)N(CC(CC)CCCC)C%10=O)S8)C=C7)C%13=CC=C(C%14=CC=C(C%15=C%16C(C(N%15CC(CC)CCCC)=O)=C(C%17=CC=C(C%18=CC=CC=C%18)S%17)N(CC(CC)CCCC)C%16=O)S%14)C=C%13)=C4C1=O)=O,(P-DPP)3TPA,,,0.97,3.95,60.19,2.3,"	Liu S-W, et al. Enhancement in open circuit voltage of organic photovoltaic devices through control of deposition rate of donor material. Solar Energy Materials and Solar Cells 109, 280-287 (2013)."
2050,CCCCC(CC)CN1C(C2=CC=C(C3=CC=C(F)C=C3)S2)=C4C(N(CC(CC)CCCC)C(C(S5)=CC=C5C(C=C6)=CC=C6N(C7=CC=C(C8=CC=C(C9=C%10C(C(N9CC(CC)CCCC)=O)=C(C%11=CC=C(C%12=CC=C(F)C=C%12)S%11)N(CC(CC)CCCC)C%10=O)S8)C=C7)C%13=CC=C(C%14=CC=C(C%15=C%16C(C(N%15CC(CC)CCCC)=O)=C(C%17=CC=C(C%18=CC=C(F)C=C%18)S%17)N(CC(CC)CCCC)C%16=O)S%14)C=C%13)=C4C1=O)=O,(4-FP-DPP)3TPA,,,0.72,7.94,52,2.98,"	Pan J-Y, et al. Star-Shaped D-A Small Molecules Based on Diketopyrrolopyrrole and Triphenylamine for Efficient Solution-Processed Organic Solar Cells. Acs Applied Materials & Interfaces 5, 972-980 (2013)."
2051,CCCCCCC1=CC=C(C2=CC=C(C3=CC=C(C4=CC=C(C5=CC=C(CCCCCC)S5)S4)C6=NSN=C63)S2)S1,DH5TB,,,0.76,5.14,42,1.63,"	Pan J-Y, et al. Star-Shaped D-A Small Molecules Based on Diketopyrrolopyrrole and Triphenylamine for Efficient Solution-Processed Organic Solar Cells. Acs Applied Materials & Interfaces 5, 972-980 (2013)."
2052,CCCCC(CC)CN1C(C2=CC=C(C3=CC=C(CCCC)C=C3)S2)=C4C(N(CC(CC)CCCC)C(C(S5)=CC=C5C(C=C6)=CC=C6N(C7=CC=C(C8=CC=C(C9=C%10C(C(N9CC(CC)CCCC)=O)=C(C%11=CC=C(C%12=CC=C(CCCC)C=C%12)S%11)N(CC(CC)CCCC)C%10=O)S8)C=C7)C%13=CC=C(C%14=CC=C(C%15=C%16C(C(N%15CC(CC)CCCC)=O)=C(C%17=CC=C(C%18=CC=C(CCCC)C=C%18)S%17)N(CC(CC)CCCC)C%16=O)S%14)C=C%13)=C4C1=O)=O,(4-BuP-DPP)3TPA,,,0.53,4.75,38,0.97,"	Kong JA, Lim E, Lee KK, Lee S, Kim SH. A benzothiadiazole-based oligothiophene for vacuum-deposited organic photovoltaic cells. Solar Energy Materials and Solar Cells 94, 2057-2063 (2010)."
2053,ClB1N2C(C(C=C(Cl)C(Cl)=C3)=C3/C2=N/C4=NC5C6=C4C=C(Cl)C(Cl)=C6)=NC7=C8C(C=C(Cl)C(Cl)=C8)=C(N5)N17,Cl6SubPc,,,0.8,5.83,42,1.98,"	Pan J-Y, et al. Star-Shaped D-A Small Molecules Based on Diketopyrrolopyrrole and Triphenylamine for Efficient Solution-Processed Organic Solar Cells. Acs Applied Materials & Interfaces 5, 972-980 (2013)."
2054,N#C/C(C#N)=C\C(S1)=CC=C1C(C=C2)=CC=C2N(C3=CC=C(C4=CC=C(/C=C(C#N)\C#N)S4)C=C3)C5=CC=C(C6=CC=C(/C=C(C#N)\C#N)S6)C=C5,TDCV¨CTPA,,,4.54,1.47,52,3.44,"	Sullivan P, et al. Ultra-High Voltage Multijunction Organic Solar Cells for Low-Power Electronic Applications. Advanced Energy Materials 3, 239-244 (2013)."
2055,O=C(C(C=CC=C1)=C1C/2=O)C2=C/C3=CC=C(S3)C(S4)=CC=C4N5C6=C(C=CC=C6)C7=C5C=CC=C7,InTTCz,,,0.78,6.6,55,2.5,"	Bernede JC, et al. MoO3/CuI hybrid buffer layer for the optimization of organic solar cells based on a donor-acceptor triphenylamine. Solar Energy Materials and Solar Cells 110, 107-114 (2013)."
2056,O=C(C(C=CC=C1)=C1C/2=O)C2=C/C3=CC=C(S3)C(S4)=CC=C4N(C5=CC=C(C)C=C5)C6=CC=C(C)C=C6,InTTD,,,0.9,-0.27,24,0.059,"	Hirade M, Yasuda T, Adachi C. Effects of Intramolecular Donor-Acceptor Interactions on Bimolecular Recombination in Small-Molecule Organic Photovoltaic Cells. Journal of Physical Chemistry C 117, 4986-4991 (2013)."
2057,O=C(C(C=CC=C1)=C1/C/2=C(C#N)/C#N)C2=C/C3=CC=C(S3)C(S4)=CC=C4N(C5=CC=C(C)C=C5)C6=CC=C(C)C=C6,InCNTTD,,,0.71,-2.69,32,0.62,"	Hirade M, Yasuda T, Adachi C. Effects of Intramolecular Donor-Acceptor Interactions on Bimolecular Recombination in Small-Molecule Organic Photovoltaic Cells. Journal of Physical Chemistry C 117, 4986-4991 (2013)."
2058,CCCCC(CC)CC1=CC=C(C2=CC=C(C3=CC=C(C4=CC=C(CCCCCCCCCCC[Si](C)(O[Si](C)(CCCCCCCCCCCC5=CC=C(C6=CC=C(C7=CC=C(C8=CC=C(CC(CC)CCCC)S8)S7)S6)S5)C)C)S4)S3)S2)S1,D1,,,0.82,-3.95,38,1.22,"	Hirade M, Yasuda T, Adachi C. Effects of Intramolecular Donor-Acceptor Interactions on Bimolecular Recombination in Small-Molecule Organic Photovoltaic Cells. Journal of Physical Chemistry C 117, 4986-4991 (2013)."
2059,C1(C=CC=C2)=C2C3=N/C1=N\C4=C5C(C=CC=C5)=C6N4[Sn]N7/C(C8=C(C=CC=C8)/C7=N/3)=N\C(C9=C/%10C=CC=C9)=NC%10=N/6,SnPc,,,0.68,3.2,40,0.9,"	Troshin PA, et al. Quaterthiophene-based multipods as promising materials for solution-processible organic solar cells and field effect transistors. Solar Energy Materials and Solar Cells 94, 2064-2072 (2010)."
2060,Cl[Sn](N1/C(C2=C(C=C(C=CC=C3)C3=C2)/C1=N/4)=N\5)(Cl)N6C(/N=C7N=C4C8=C\7C=C(C=CC=C9)C9=C8)=C%10C(C=C(C=CC=C%11)C%11=C%10)=C6/N=C%12C%13=C(C=C(C=CC=C%14)C%14=C%13)C5=N/%12,SnNcCl2,,,0.25,9,50,0.8,"	Pandey R, Kerner RA, Menke SM, Holst J, Josyula KVB, Holmes RJ. Tin naphthalocyanine complexes for infrared absorption in organic photovoltaic cells. Organic Electronics 14, 804-808 (2013)."
2061,O=C(OCCCCCCCC)/C(C#N)=C/C(S1)=CC=C1C(S2)=CC=C2/C=C/C(C=C3)=CC=C3N(C4=CC=C(/C=C/C5=CC=C(C6=CC=C(/C=C(C#N)/C(OCCCCCCCC)=O)S6)S5)C=C4)C7=CC=C(/C=C/C8=CC=C(C9=CC=C(/C=C(C#N)/C(OCCCCCCCC)=O)S9)S8)C=C7,S(TPA-bTV-CA),,,0.38,9,53,1.2,"	Pandey R, Kerner RA, Menke SM, Holst J, Josyula KVB, Holmes RJ. Tin naphthalocyanine complexes for infrared absorption in organic photovoltaic cells. Organic Electronics 14, 804-808 (2013)."
2062,CCCCCCC(S1)=CC=C1C2=CC=C(S2)C(S3)=CC=C3C(N(CC(CC)CCCC)C4=O)=C(C4=C(C5=CC=C(C6=CC=C(C7=CC=C(CCCCCC)S7)S6)S5)N8CC(CC)CCCC)C8=O,SMDPPEH,,,0.91,4.64,50,2.1,"	Shen S, Gao L, He C, Zhang Z, Sun Q, Li Y. A star-shaped oligothiophene with triphenylamine as core and octyl cyanoacetate as end groups for solution-processed organic solar cells. Organic Electronics 14, 875-881 (2013)."
2063,C1(N(C2=CC=CC=C2)C3=C(C=CC=C4)C4=CC=C3)=CC=C(C5=CC=C(N(C6=CC=CC=C6)C7=C(C=CC=C8)C8=CC=C7)C=C5)C=C1,NPB,,,0.72,10.19,36,2.62,"	Akaba T, Yonezawa K, Kamioka H, Yasuda T, Han L, Moritomo Y. Carrier formation dynamics of a small-molecular organic photovoltaic. Applied Physics Letters 102,  (2013)."
2064,CCCCC(CC)CC1=CC=C(C(S2)=CC=C2C3=CC=C(C4=CC=C(CCCCCCCCCCC[Si](C)(O[Si](C)(CCC[Si](CCC[Si](C)(C)O[Si](C)(C)CCCCCCCCCCCC5=CC=C(S5)C6=CC=C(C7=CC=C(C8=CC=C(S8)CC(CC)CCCC)S7)S6)(CCC[Si](C)(C)O[Si](C)(C)CCCCCCCCCCCC9=CC=C(S9)C%10=CC=C(C%11=CC=C(C%12=CC=C(S%12)CC(CC)CCCC)S%11)S%10)CCC[Si](C)(C)O[Si](C)(CCCCCCCCCCCC%13=CC=C(S%13)C%14=CC=C(S%14)C%15=CC=C(C%16=CC=C(S%16)CC(CC)CCCC)S%15)C)C)C)S4)S3)S1,D2,,,0.825,6.5,42,2.25,"	Jin F, et al. The influence of donor material on achieving high photovoltaic response for organic bulk heterojunction cells with small ratio donor component. Organic Electronics 14, 1130-1135 (2013)."
2065,C1(C2=CC=C(N3C4=C(C5=C3C=CC=C5)C=CC=C4)C=C2)=CC=C(N6C7=C(C8=C6C=CC=C8)C=CC=C7)C=C1,CBP,,,0.6,1.3,35,0.27,"	Troshin PA, et al. Quaterthiophene-based multipods as promising materials for solution-processible organic solar cells and field effect transistors. Solar Energy Materials and Solar Cells 94, 2064-2072 (2010)."
2066,CCCCCCC1=CC=C(C(S2)=CC=C2C3=CC=C(C4=CC=C(CCCCCCCCCCC[Si](C)(O[Si](C)(CCC[Si](CCC[Si](C)(C)O[Si](C)(C)CCCCCCCCCCCC5=CC=C(S5)C6=CC=C(C7=CC=C(C8=CC=C(S8)CCCCCC)S7)S6)(CCC[Si](C)(C)O[Si](C)(C)CCCCCCCCCCCC9=CC=C(S9)C%10=CC=C(C%11=CC=C(C%12=CC=C(S%12)CCCCCC)S%11)S%10)CCC[Si](C)(C)O[Si](C)(CCCCCCCCCCCC%13=CC=C(S%13)C%14=CC=C(S%14)C%15=CC=C(C%16=CC=C(S%16)CCCCCC)S%15)C)C)C)S4)S3)S1,D3,,,1.167,3,29,1.01,"	Jin F, et al. The influence of donor material on achieving high photovoltaic response for organic bulk heterojunction cells with small ratio donor component. Organic Electronics 14, 1130-1135 (2013)."
2067,CCCCCCCCC(CCCCCCCC)N1C2=C(C=C(C3=CC=CC=C3)C=C2)C(C1=C4)=CC=C4C(S5)=CC=C5C(C6=NSN=C67)=CC=C7C8=CC=C(S8)C9=CC=CC=C9,PCDTBT,,,0.36,0.45,29,0.05,"	Troshin PA, et al. Quaterthiophene-based multipods as promising materials for solution-processible organic solar cells and field effect transistors. Solar Energy Materials and Solar Cells 94, 2064-2072 (2010)."
2068,N(C1=CC=C(C2=CC=C3C=CC=CC3=C2)C=C1)(C4=CC=C(C5=CC=C6C=CC=CC6=C5)C=C4)C7=CC=C(C8=CC=C9C=CC=CC9=C8)C=C7,2-TNPA,,,0.89,12.67,67,7.6,"	Baek S-W, Noh J, Lee C-H, Kim B, Seo M-K, Lee J-Y. Plasmonic Forward Scattering Effect in Organic Solar Cells: A Powerful Optical Engineering Method. Scientific Reports 3,  (2013)."
2069,CC1(C)C2=C(C=CC=C2)N(CC)/C1=C\C=C\C3=[N+](CC)C4=CC=CC=C4C3(C)C.FP(F)(F)(F)F.[F-],Cy3-P,,,0.91,1.24,34,0.39,"	Kwon J, Kim MK, Hong J-P, Lee W, Lee S, Hong J-I. A Multifunctional Material Based on Triphenylamine and a Naphthyl Unit for Organic Light-Emitting Diodes, Organic Solar Cells, and Organic Thin-Film Transistors. Bulletin of the Korean Chemical Society 34, 1355-1360 (2013)."
2070,CCCCCCOC1=CC=C(C#CC2=CC=C(C3=CC=C(C4=CC=C(C#CC5=CC=C(OCCCCCC)C(OCCCCCC)=C5)S4)C6=NSN=C63)S2)C=C1OCCCCCC,SM1,,,0.88,6.2,67.8,3.7,"	Berner E, et al. Influence of crystalline titanium oxide layer smoothness on the performance of inverted organic bilayer solar cells. Applied Physics Letters 102,  (2013)."
2071,FC(F)(COC1=C(OCC(F)(F)F)C(OCC(F)(F)F)=C(OCC(F)(F)F)C2=C1/C3=N/C4=C(C(OCC(F)(F)F)=C(OCC(F)(F)F)C(OCC(F)(F)F)=C5OCC(F)(F)F)C5=C(/N=C6N=C7C8=C\6C(OCC(F)(F)F)=C(OCC(F)(F)F)C(OCC(F)(F)F)=C8OCC(F)(F)F)N4[Zn]N9/C(C%10=C(C(OCC(F)(F)F)=C(OCC(F)(F)F)C(OCC(F)(F)F)=C%10OCC(F)(F)F)/C9=N/7)=N\C2=N3)F,(4TFEO)4ZnPc,,,0.88,2.2,34,0.66,"	Wu Z, Fan B, Xue F, Adachi C, Ouyang J. Organic molecules based on dithienyl-2,1,3-benzothiadiazole as new donor materials for solution-processed organic photovoltaic cells. Solar Energy Materials and Solar Cells 94, 2230-2237 (2010)."
2072,FC(COC1=CC2=C(/N=C3C4=C(C=C(OCC(F)(F)F)C(OCC(F)(F)F)=C4)C5=N/3)N([Zn]6)C(/N=C7N=C(/N=C(C8=C/9C=C(OCC(F)(F)F)C(OCC(F)(F)F)=C8)\N6C9=N/5)C%10=C\7C=C(OCC(F)(F)F)C(OCC(F)(F)F)=C%10)=C2C=C1OCC(F)(F)F)(F)F,(2TFEO)4ZnPc,,,0.1,7.2*10-4,24,1.6*10-5,"	Yamada I, Iida N, Hayashi Y, Soga T, Shibata N. Phthalocyanine with Trifluoroethoxy Substituents for Organic Solar Cells. Japanese Journal of Applied Physics 52,  (2013)."
2073,FC(COC1=CC=CC2=C(/N=C3N=C(/N=C(C4=C/5C=CC=C4OCC(F)(F)F)\N6C5=N/7)C8=C\3C(OCC(F)(F)F)=CC=C8)N([Zn]6)C(/N=C9C%10=C(C(OCC(F)(F)F)=CC=C%10)C7=N/9)=C21)(F)F,(a-TFEO)4ZnPc,,,0.05,4.1*10-4,35,0.6*10-5,"	Yamada I, Iida N, Hayashi Y, Soga T, Shibata N. Phthalocyanine with Trifluoroethoxy Substituents for Organic Solar Cells. Japanese Journal of Applied Physics 52,  (2013)."
2074,FC(COC1=CC2=C(/N=C3C4=C(C=C(OCC(F)(F)F)C=C4)C5=N/3)N([Zn]6)C(/N=C7N=C(/N=C(C8=C/9C=CC(OCC(F)(F)F)=C8)\N6C9=N/5)C%10=C\7C=C(OCC(F)(F)F)C=C%10)=C2C=C1)(F)F,(b-TFEO)4ZnPc,,,0.06,2.0*10-4,23,0.2*10-5,"	Yamada I, Iida N, Hayashi Y, Soga T, Shibata N. Phthalocyanine with Trifluoroethoxy Substituents for Organic Solar Cells. Japanese Journal of Applied Physics 52,  (2013)."
2075,[O-]C(/C(C1=O)=C2C(O)=C/C(C=C\2O)=[N+](CCCC(C)C)/CCCC(C)C)=C1C3=C(O)C=C(N(CCCC(C)C)CCCC(C)C)C=C3O,DiPSQ(OH)2,,,0.07,2.5*10-4,25,4.1*10-5,"	Yamada I, Iida N, Hayashi Y, Soga T, Shibata N. Phthalocyanine with Trifluoroethoxy Substituents for Organic Solar Cells. Japanese Journal of Applied Physics 52,  (2013)."
2076,CCCCCCOC1=CC=C(C#CC2=CC=C(C#CC3=CC=C(C4=CC=C(C5=CC=C(C#CC6=CC=C(C#CC7=CC=C(OCCCCCC)C(OCCCCCC)=C7)C=C6)S5)C8=NSN=C84)S3)C=C2)C=C1OCCCCCC,SM2,,,0.55,5.7,51.9,1.54,"	Spencer SD, et al. The effect of controllable thin film crystal growth on the aggregation of a novel high panchromaticity squaraine viable for organic solar cells. Solar Energy Materials and Solar Cells 112, 202-208 (2013)."
2077,C1(C=CC=C2)=C2C3=N/C1=N\C4=C5C(C=CC=C5)=C6N4[Zn]N7/C(C8=C(C=CC=C8)/C7=N/3)=N\C(C9=C/%10C=CC=C9)=NC%10=N/6,ZnPc,,,0.74,0.69,27,0.14,"	Wu Z, Fan B, Xue F, Adachi C, Ouyang J. Organic molecules based on dithienyl-2,1,3-benzothiadiazole as new donor materials for solution-processed organic photovoltaic cells. Solar Energy Materials and Solar Cells 94, 2230-2237 (2010)."
2078,CCCC(C(CCC)=C1C2=CC=CC=C2)=C(C3=CC=CC=C3)C4=C1C5=C6C(C7=CC=C64)=C(C8=C9C7=CC=C%10C9=C(C%11=C%10C(C%12=CC=CC=C%12)=C(CCC)C(CCC)=C%11C%13=CC=CC=C%13)C=C8)C=C5,P4©\Ph4©\DIP,,,0.6,10.5,58,3.7,"	Kim I, Haverinen HM, Li J, Jabbour GE. Enhanced power conversion efficiency of p-i-n type organic solar cells by employing a p-layer of palladium phthalocyanine. Applied Physics Letters 97,  (2010)."
2079,C1(C=C2N3)=CC=CC=C1C=C2NC4=C3C=C(C=CC=C5)C5=C4,NDP,,,0.99,2.9,76.2,1.92,"	Meiss J, Hummert M, Ziehlke H, Leo K, Riede M. Organic solar cells with very high fill factor and voltage using tetrapropyl-tetraphenyl-diindenoperylene as green donor. Physica Status Solidi-Rapid Research Letters 4, 329-331 (2010)."
2080,N(C1=CC=C(C2=CC=CS2)C=C1)(C3=CC=C(C4=CC=CS4)C=C3)C5=CC=C(C6=CC=CS6)C=C5,TTPA,,,0.44,3.42,59.74,0.9,"	Zhang M, Wang H, Tang CW. Effect of the highest occupied molecular orbital energy level offset on organic heterojunction photovoltaic cells. Applied Physics Letters 97,  (2010)."
2081,CCCCCCN1C2=C(C=C(C3=CC=C(C4=CC=C(/C=C(C#N)/C(O)=O)S4)S3)C=C2)C5=C1C=CC(C6=CC=C(C7=CC=C(/C=C(C(O)=O)\C#N)S7)S6)=C5,D1,,,0.96,3.8,49,1.8,"	Kageyama H, Ohishi H, Tanaka M, Ohmori Y, Shirota Y. Organic Photovoltaic Devices Using an Amorphous Molecular Material With High Hole Drift Mobility, Tris 4-(2-thienyl)phenyl amine. Ieee Journal of Selected Topics in Quantum Electronics 16, 1528-1536 (2010)."
2082,CC1=C(/C=C2N=C(/C=C(C(CC)=C/3C)\NC3=C/C(C(CC)=C/4C)=NC4=C/5)C(C)=C\2CC)NC5=C1CC,HOX,,,0.56,1.76,27,0.27,"	Sahu D, et al. Synthesis and application of H-Bonded cross-linking polymers containing a conjugated pyridyl H-Acceptor side-chain polymer and various carbazole-based H-Donor dyes bearing symmetrical cyanoacrylic acids for organic solar cells. Polymer 51, 6182-6192 (2010)."
2083,CCC1=C(CC)C(/C=C(C(CC)=C/2CC)\NC2=C/C(C(CC)=C/3CC)=NC3=C/4)=N/C1=C\C5=C(CC)C(CC)=C4N5,HOEP,,,0.48,7.97,38,1.45,"	Xu Z-X, Roy VAL, Liu Z-T, Lee CS. Importance of molecular alignment for organic photovoltaic devices. Applied Physics Letters 97,  (2010)."
2084,C1(N(C2=CC=C(N3C(C=CC=C4)=C4C5=C3C=CC=C5)C=C2)C6=CC=C(N7C(C=CC=C8)=C8C9=C7C=CC=C9)C=C6)=CC=C(N%10C(C=CC=C%11)=C%11C%12=C%10C=CC=C%12)C=C1,TCTA,,,0.5,5.49,28,0.78,"	Xu Z-X, Roy VAL, Liu Z-T, Lee CS. Importance of molecular alignment for organic photovoltaic devices. Applied Physics Letters 97,  (2010)."
2085,C1(C(C2=CC=C(C=CC=C3)C3=C2)=C(C=CC=C4)C4=C5C6=CC=C(C=CC=C7)C7=C6)=C5C=CC=C1,ADN,,,0.89,3.05,49.39,1.34,"	Zhang M, Wang H, Tang CW. Effect of the highest occupied molecular orbital energy level offset on organic heterojunction photovoltaic cells. Applied Physics Letters 97,  (2010)."
2086,CC(C1=C(N/2CCCC)C=CC=C1)(C)C2=C/C=C3C(C(C=CC=C4)=C4/C\3=C5C(C(C=CC=C6)=C6C\5=O)=O)=O,HB094,,,0.97,2.53,38.21,0.94,"	Zhang M, Wang H, Tang CW. Effect of the highest occupied molecular orbital energy level offset on organic heterojunction photovoltaic cells. Applied Physics Letters 97,  (2010)."
2087,CCCCCCCCC(CCCCCCCC)N1C2=C(C=C(C3=CC=C(C4=CC=C(/C=C(C#N)/C(O)=O)S4)S3)C=C2)C5=C1C=CC(C6=CC=C(C7=CC=C(/C=C(C(O)=O)\C#N)S7)S6)=C5,D2,,,0.53,5,29,0.85,"	Kronenberg NM, et al. Direct Comparison of Highly Efficient Solution- and Vacuum-Processed Organic Solar Cells Based on Merocyanine Dyes. Advanced Materials 22, 4193-+ (2010)."
2088,CC(C1=C(N/2CCC3)C3=CC=C1)(C)C2=C/C=C4C(C(C=CC=C5)=C5/C\4=C(C#N)\C#N)=O,HB194,,,0.57,1.4,30,0.24,"	Sahu D, et al. Synthesis and application of H-Bonded cross-linking polymers containing a conjugated pyridyl H-Acceptor side-chain polymer and various carbazole-based H-Donor dyes bearing symmetrical cyanoacrylic acids for organic solar cells. Polymer 51, 6182-6192 (2010)."
2089,CC(C1=C(N/2C)C=CC=C1)(C)C2=C/C=C3C(C)=C(C#N)C(N(C)C\3=O)=O,HB226,,,0.57,6,40.5,1.5,"	Kronenberg NM, et al. Direct Comparison of Highly Efficient Solution- and Vacuum-Processed Organic Solar Cells Based on Merocyanine Dyes. Advanced Materials 22, 4193-+ (2010)."
2090,CC(C1=C(N/2CCCC)C=CC=C1)(C)C2=C/C=C3C(C(C=CC=C4)=C4/C\3=C(C#N)\C#N)=O,MD376,,,0.65,9,41,2.6,"	Kronenberg NM, et al. Direct Comparison of Highly Efficient Solution- and Vacuum-Processed Organic Solar Cells Based on Merocyanine Dyes. Advanced Materials 22, 4193-+ (2010)."
2091,CCCCCCCCC1=CSC(C(C2=NSN=C23)=CC=C3C(S4)=CC(CCCCCCCC)=C4C(C=C5)=CC=C5OC6=CC7=C(/N=C8C9=C(C=C(OC%10=CC=C(C%11=C(CCCCCCCC)C=C(C%12=CC=C(C%13=CC(CCCCCCCC)=CS%13)C%14=NSN=C%14%12)S%11)C=C%10)C=C9)C%15=N/8)N([Zn]%16)C(/[Zn]=C%17N=C(/N=C(C%18=C/%19C=CC(OC%20=CC=C(C%21=C(CCCCCCCC)C=C(C%22=CC=C(C%23=CC(CCCCCCCC)=CS%23)C%24=NSN=C%24%22)S%21)C=C%20)=C%18)\N%16C%19=N/%15)C%25=C\%17C=C(OC%26=CC=C(C%27=C(CCCCCCCC)C=C(C%28=CC=C(C%29=CC(CCCCCCCC)=CS%29)C%30=NSN=C%30%28)S%27)C=C%26)C=C%25)=C7C=C6)=C1,ZnPc-TDA,,,0.78,11,46,4.5,"	Kronenberg NM, et al. Direct Comparison of Highly Efficient Solution- and Vacuum-Processed Organic Solar Cells Based on Merocyanine Dyes. Advanced Materials 22, 4193-+ (2010)."
2092,CCCCCCCCCCCCC1=C(C2=CC=C(N(C3=CC=CC=C3)C4=CC=CC=C4)C=C2)SC(C5=CC=C(C6=CC(CCCCCCCCCCCC)=C(C7=CC=C(N(C8=CC=CC=C8)C9=CC=CC=C9)C=C7)S6)C%10=NSN=C%105)=C1,TTBTT,,,0.68,2.26,28,0.42,"	Liang F, et al. Donor-acceptor conjugates-functionalized zinc phthalocyanine: Towards broad absorption and application in organic solar cells. Solar Energy Materials and Solar Cells 94, 1803-1808 (2010)."
2093,CCCCCCCCC(CCCCCCCC)N1C2=C(C=C(C3=C(CCCCCC)C=C(C4=CC=C(C5=CC=C(/C=C(C(O)=O)\C#N)S5)S4)S3)C=C2)C6=C1C=CC(C7=C(CCCCCC)C=C(C8=CC=C(C9=CC=C(/C=C(C(O)=O)\C#N)S9)S8)S7)=C6,D3,,,0.93,7.49,41,2.86,"	Fan H, Shang H, Li Y, Zhan X. Efficiency enhancement in small molecule bulk heterojunction organic solar cells via additive. Applied Physics Letters 97,  (2010)."
2094,O=C1C2=CC=CC=C2N(CC(CC)CCCC)C3=C1C=C(N(CC(CC)CCCC)C(C=CC=C4)=C4C5=O)C5=C3,QA,,,0.59,1.13,24,0.16,"	Sahu D, et al. Synthesis and application of H-Bonded cross-linking polymers containing a conjugated pyridyl H-Acceptor side-chain polymer and various carbazole-based H-Donor dyes bearing symmetrical cyanoacrylic acids for organic solar cells. Polymer 51, 6182-6192 (2010)."
2095,O=C1C2=CC(C3=CC=C(C4=CC=C(CCCCCC)S4)S3)=CC=C2N(CC(CC)CCCC)C5=C1C=C(N(CC(CC)CCCC)C(C=CC(C6=CC=C(C7=CC=C(CCCCCC)S7)S6)=C8)=C8C9=O)C9=C5,QA-BT,,,0.2,0.94,28,0.05,"	Chen JJ-A, et al. Quinacridone-Based Molecular Donors for Solution Processed Bulk-Heterojunction Organic Solar Cells. Acs Applied Materials & Interfaces 2, 2679-2686 (2010)."
2096,O=C1C2=CC(C3=CC=C(C4=CC=C(C5=CC=C(CCCCCC)S5)C6=NSN=C64)S3)=CC=C2N(CC(CC)CCCC)C7=C1C=C(N(CC(CC)CCCC)C(C=CC(C8=CC=C(C9=CC=C(C%10=CC=C(CCCCCC)S%10)C%11=NSN=C%119)S8)=C%12)=C%12C%13=O)C%13=C7,QA-BTD,,,0.8,5.67,40,1.84,"	Chen JJ-A, et al. Quinacridone-Based Molecular Donors for Solution Processed Bulk-Heterojunction Organic Solar Cells. Acs Applied Materials & Interfaces 2, 2679-2686 (2010)."
2097,CCCCCCCCC1=C(C2=CC(CCCCCCCC)=C(C3=CC(CCCCCCCC)=C(C4=CC=C(C5=C(CCCCCCCC)C=C(C6=C(CCCCCCCC)C=C(C7=C(CCCCCCCC)C=C(/C=C(C#N)/C#N)S7)S6)S5)S4)S3)S2)SC(/C=C(C#N)\C#N)=C1,DCN7T,,,0.72,8.87,0.35,2.22,"	Chen JJ-A, et al. Quinacridone-Based Molecular Donors for Solution Processed Bulk-Heterojunction Organic Solar Cells. Acs Applied Materials & Interfaces 2, 2679-2686 (2010)."
2098,N(C1=CC=C(C2=C3C=CC=CC3=CC=C2)C=C1)(C4=CC=C(C5=C6C=CC=CC6=CC=C5)C=C4)C7=CC=C(C8=C9C=CC=CC9=CC=C8)C=C7,1-TNPA,,,0.88,12.4,34,3.7,"	Yin B, et al. Solution-processed bulk heterojunction organic solar cells based on an oligothiophene derivative. Applied Physics Letters 97,  (2010)."
2099,CCCCCCN1C2=C(C=C(C3=C(CCCCCC)C=C(C4=CC=C(C5=CC=C(/C=C(C(O)=O)\C#N)S5)S4)S3)C=C2)C6=C1C=CC(C7=C(CCCCCC)C=C(C8=CC=C(C9=CC=C(/C=C(C(O)=O)\C#N)S9)S8)S7)=C6,D4,,,0.87,1.35,38,0.45,"	Kwon J, et al. 4,4 ',4 ''-Tris(4-naphthalen-1-yl-phenyl)amine as a multifunctional material for organic light-emitting diodes, organic solar cells, and organic thin-film transistors. Organic Electronics 11, 1288-1295 (2010)."
2100,C12=CC=CC=C1C=C3C(C=C(C=C4)C5=C3C=CC6=CC=CC4=C56)=C2,NP,,,0.55,1.9,29,0.31,"	Sahu D, et al. Synthesis and application of H-Bonded cross-linking polymers containing a conjugated pyridyl H-Acceptor side-chain polymer and various carbazole-based H-Donor dyes bearing symmetrical cyanoacrylic acids for organic solar cells. Polymer 51, 6182-6192 (2010)."
2101,O=C1C(C2=NC3=CC=CC=C3S2)=CC4=C(O1)C=C(N(CC)CC)C=C4,C6,,,0.59,1.9,42,0.48,"	Kwon J, et al. Naphtho 2,3,a pyrene as an efficient multifunctional organic semiconductor for organic solar cells, organic light-emitting diodes, and organic thin-film transistors. Organic Electronics 11, 1103-1110 (2010)."
2102,CC1=CC=CC(N(C2=CC=CC=C2)C3=CC=C(N(C4=CC/C(C=C4)=C(C5=CC(C)=CC=C5)/C6=CC=CC=C6)C7=CC=C(N(C8=CC=CC=C8)C9=CC(C)=CC=C9)C=C7)C=C3)=C1,MTDATA,,,0.34,1.6,37,0.19,"	Ismail YAM, Soga T, Jimbo T. Photovoltaic Properties of Bulk Heterojunction Organic Solar Cell Composed of Coumarin 6 Dye as Light Harvester and Donor Material. Japanese Journal of Applied Physics 49,  (2010)."
2103,CCCCCCCC(C1C2=C(C3=C1C=CC=C3)C=CC(C4=CC(C5=CC(C6=CC(C(CCCCCCCC)(CCCCCCCC)C7=C8C=CC=C7)=C8C=C6)=C9)=C%10C(C%11=C%12C(C%13=CC(C%14=CC(C(CCCCCCCC)(CCCCCCCC)C%15=C%16C=CC=C%15)=C%16C=C%14)=CC%17=C%13C%18=C%19C%20=C(C(C%21=C%19C%17=CC(C%22=CC(C(CCCCCCCC)(CCCCCCCC)C%23=C%24C=CC=C%23)=C%24C=C%22)=C%21)=CC(C%25=CC(C(CCCCCCCC)(CCCCCCCC)C%26=C%27C=CC=C%26)=C%27C=C%25)=C%28)C%28=C9C5=C%20C%10=C%18%12)=CC(C%29=CC(C(CCCCCCCC)(CCCCCCCC)C%30=C%31C=CC=C%30)=C%31C=C%29)=C%11)=C4)=C2)CCCCCCC,4,,,1.85,0.0593,41,3.74,"	Su Z, Chu B, Li W. High efficient organic ultraviolet photovoltaic devices based on gallium complex. Solid-State Electronics 54, 605-608 (2010)."
2104,CCCCCCCCC1(CCCCCCCC)C2=C(C3=C1C=CC=C3)C=CC(C4=CC(C5=CC=CC6=C7C8=C9C%10=C(C(C(C%11=CC(C%12=CC(C(CCCCCCCC)(CCCCCCCC)C%13=C%14C=CC=C%13)=C%14C=C%12)=CC%15=C%11%16)=CC=C%17)=C%17C%18=CC=CC(C8=CC=C7)=C%18%10)C%16=C%19C9=C65)=C%19C%15=C4)=C2,5,,,0.61,-0.17,32,0.03,"	Wong WWH, et al. Solution Processable Fluorenyl Hexa-peri-hexabenzocoronenes in Organic Field-Effect Transistors and Solar Cells. Advanced Functional Materials 20, 927-938 (2010)."
2105,CCCCCCCCC1(CCCCCCCC)C2=C(C3=C1C=CC=C3)C=CC(C4=CC5=C6C7=C8C9=C(C(C(C%10=CC=CC%11=C%10%12)=CC(C%13=CC(C(CCCCCCCC)(CCCCCCCC)C%14=C%15C=CC=C%14)=C%15C=C%13)=C%16)=C%16C%17=CC=CC(C7=CC=C6)=C%179)C%12=C%18C8=C5C(C%19=C%18C%11=CC=C%19)=C4)=C2,6,,,0.87,-2.03,60,1.06,"	Wong WWH, et al. Solution Processable Fluorenyl Hexa-peri-hexabenzocoronenes in Organic Field-Effect Transistors and Solar Cells. Advanced Functional Materials 20, 927-938 (2010)."
2106,CCCCCCCCC1=C(/C=C/C2=CC=CC=C2)SC(/C=C/C3=C(CCCCCCCC)C(CCCCCCCC)=C(C=C)S3)=C1CCCCCCCC,PDOTV,,,0.9,-2.68,61,1.46,"	Wong WWH, et al. Solution Processable Fluorenyl Hexa-peri-hexabenzocoronenes in Organic Field-Effect Transistors and Solar Cells. Advanced Functional Materials 20, 927-938 (2010)."
2107,CCCCCCC1=CSC(C2=CC=C(/C=C/C3=CC=C(N(C4=CC=CC=C4)C5=CC=C(/C=C/C6=CC=C(C7=CC(CCCCCC)=CS7)C8=NSN=C86)C=C5)C=C3)C9=NSN=C92)=C1,B(TPA-BT-HT),,,0.498,-0.748,48,0.18,"	Horie M, et al. Poly(thienylenevinylene) prepared by ring-opening metathesis polymerization: Performance as a donor in bulk heterojunction organic photovoltaic devices. Polymer 51, 1541-1547 (2010)."
2108,C1(C=CC=C2)=C2C3=N/C1=N\C4=C5C(C=CC=C5)=C6N4[Ni]N7/C(C8=C(C=CC=C8)/C7=N/3)=N\C(C9=C/%10C=CC=C9)=NC%10=N/6,NiPc,,,0.96,5.5,37,1.96,"	Yang Y, et al. Solution-Processable Organic Molecule with Triphenylamine Core and Two Benzothiadiazole-Thiophene Arms for Photovoltaic Application. Journal of Physical Chemistry C 114, 3701-3706 (2010)."
2109,C1(C=CC=C2)=C2C3=N/C1=N\C4=C5C(C=CC=C5)=C6N4[Fe]N7/C(C8=C(C=CC=C8)/C7=N/3)=N\C(C9=C/%10C=CC=C9)=NC%10=N/6,FePc,,,0.44,-2.67,55,0.64,"	Bruder I, et al. What determines the performance of metal phthalocyanines (MPc, M = Zn, Cu, Ni, Fe) in organic heterojunction solar cells? A combined experimental and theoretical investigation. Organic Electronics 11, 377-387 (2010)."
2110,C12=CC3=C(C=C(C4=CC=CC=C4)O3)C=C1C=C5C(C=C(C6=CC=CC=C6)O5)=C2,5b,,,0.16,-1.06,42,0.07,"	Bruder I, et al. What determines the performance of metal phthalocyanines (MPc, M = Zn, Cu, Ni, Fe) in organic heterojunction solar cells? A combined experimental and theoretical investigation. Organic Electronics 11, 377-387 (2010)."
2111,CC1=C(O[Pt]OC2=C(C)C=C(C)C3=CC=CN=C23)C4=NC=CC=C4C(C)=C1,Pt(Me2q)2,,,0.69,2.98,64,1.31,"	Nakano M, Mori H, Shinamura S, Takimiya K. Naphtho[2,3-b:6,7-b¡ä]dichalcogenophenes: Syntheses, Characterizations, and Chalcogene Atom Effects on Organic Field-Effect Transistor and Organic Photovoltaic Devices. Chemistry of Materials 24, 190-198 (2012)."
2112,CCCCCCC(S1)=CC=C1C2=CC=C(S2)C(S3)=CC=C3C(C4=NSN=C45)=CC=C5C(C=C6)=CC=C6N(C7=CC=C(C8=CC=C(C9=CC=C(C%10=CC=C(C%11=CC=C(CCCCCC)S%11)S%10)S9)C%12=NSN=C%128)C=C7)C%13=CC=C(C%14=CC=C(C%15=CC=C(C%16=CC=C(C%17=CC=C(CCCCCC)S%17)S%16)S%15)C%18=NSN=C%18%14)C=C%13,S(TPA-BT-HTT),,,0.42,14.8,38,2.4,"	Low KH, Xu ZX, Xiang HF, Chui SS, Roy VA, Che CM. Bis(5,7-dimethyl-8-hydroxyquinolinato)platinum(II) complex for efficient organic heterojunction solar cells. Chemistry, an Asian journal 6, 3223-3229 (2011)."
2113,CCCCCCC1=C(SC(C2=CC=C(C3=CC(CCCCCC)=C(/C=C/C4=CC=C(N(C5=CC=CC=C5)C6=CC=CC=C6)C=C4)S3)C7=NSN=C72)=C1)/C=C/C8=CC=C(N(C9=CC=CC=C9)C%10=CC=CC=C%10)C=C8,TPA-HT-BT,,,0.87,9.51,52,4.3,"	Shang H, Fan H, Liu Y, Hu W, Li Y, Zhan X. A solution-processable star-shaped molecule for high-performance organic solar cells. Advanced materials 23, 1554-1557 (2011)."
2114,CCCCCCC(C(SC(C1=CC=C(C2=CC(SC(/C=C/C3=CC=C(N(C4=CC=CC=C4)C5=CC=CC=C5)C=C3)=C6CCCCCC)=C6S2)C7=NSN=C71)=C8)=C8S9)=C9/C=C/C%10=CC=C(N(C%11=CC=CC=C%11)C%12=CC=CC=C%12)C=C%10,TPA-HTT-BT,,,0.79,4.84,37.5,1.44,"	Deng D, et al. Triphenylamine-containing linear D-A-D molecules with benzothiadiazole as acceptor unit for bulk-heterojunction organic solar cells. Organic Electronics 12, 614-622 (2011)."
2115,CCCCCCC(C(SC(C1=CC=C(C2=CC(SC(/C=C/C3=CC=C(N(C4=CC=C(OCCCCCCCC)C=C4)C5=CC=C(OCCCCCCCC)C=C5)C=C3)=C6CCCCCC)=C6S2)C7=NSN=C71)=C8)=C8S9)=C9/C=C/C%10=CC=C(N(C%11=CC=C(OCCCCCCCC)C=C%11)C%12=CC=C(OCCCCCCCC)C=C%12)C=C%10,boTPA-HTT-BT,,,0.74,5.71,34,1.44,"	Deng D, et al. Triphenylamine-containing linear D-A-D molecules with benzothiadiazole as acceptor unit for bulk-heterojunction organic solar cells. Organic Electronics 12, 614-622 (2011)."
2116,O=S(C1C=CC2=C3N([Cu]N4/C(C(C=CC(S(=O)(O[Na])=O)=C5)=C5/C4=N/C(C6=C/7C(S(=O)(O[Na])=O)=CC=C6)=NC7=N/3)=N\C8=N/C(C9=C8C=C(S(=O)(O[Na])=O)C=C9)=N\%10)C%10C2=C1)(O[Na])=O,TSCuPc,,,0.61,3.61,34.2,0.75,"	Deng D, et al. Triphenylamine-containing linear D-A-D molecules with benzothiadiazole as acceptor unit for bulk-heterojunction organic solar cells. Organic Electronics 12, 614-622 (2011)."
2117,N#C/C(C#N)=C\C1=CC=C(C2=CC=C(C3=CC=C(C4=CC=C(C5=CC=C(/C=C(C#N)/C#N)S5)S4)S3)S2)S1,DCV5T,,,0.52,1.47,41,0.32,"	Schumann S, Hatton RA, Jones TS. Organic Photovoltaic Devices Based on Water-Soluble Copper Phthalocyanine. The Journal of Physical Chemistry C 115, 4916-4921 (2011)."
2118,CCCCC(C=C(/C([H])=C(C#N)\C#N)S1)=C1C2=CC(CCCC)=C(S2)C3=CC=C(C4=CC=C(C5=C(CCCC)C=C(C6=C(CCCC)C=C(/C([H])=C(C#N)\C#N)S6)S5)S4)S3,DCV6T-Bu,,,0.97,5.1,52,2.6,"	Fitzner R, et al. Dicyanovinyl-Substituted Oligothiophenes: Structure-Property Relationships and Application in Vacuum-Processed Small Molecule Organic Solar Cells. Advanced Functional Materials 21, 897-910 (2011)."
2119,N#C/C(C#N)=C/C1=CC=C(C2=CC=C(C3=CC=C(C4=CC=C(C5=CC=C(C6=CC=C(/C=C(C#N)/C#N)S6)S5)S4)S3)S2)S1,DCV6T,,,0.81,4,67,2,"	Levichkova M, et al. Dicyanovinyl sexithiophene as donor material in organic planar heterojunction solar cells: Morphological, optical, and electrical properties. Organic Electronics 12, 2243-2252 (2011)."
2120,CC12C3(C)SC(/C=C/C4=CC=C(N(C5=CC=C(/C=C/C6=CC=C(N(C7=CC=CC=C7)C8=CC=CC=C8)C=C6)C=C5)C9=CC=C(/C=C/C%10=CC=C(N(C%11=CC=CC=C%11)C%12=CC=CC=C%12)C=C%10)C=C9)C=C4)=CC3=C(C(F)(F)C(F)(F)C%13(F)F)C%13=C1C=C(/C=C/C%14=CC=C(N(C%15=CC=C(/C=C/C%16=CC=C(N(C%17=CC=CC=C%17)C%18=CC=CC=C%18)C=C%16)C=C%15)C%19=CC=C(/C=C/C%20=CC=C(N(C%21=CC=CC=C%21)C%22=CC=CC=C%22)C=C%20)C=C%19)C=C%14)S2,TP-G2,,,0.91,4.8,64,2.8,"	Fitzner R, et al. Dicyanovinyl-Substituted Oligothiophenes: Structure-Property Relationships and Application in Vacuum-Processed Small Molecule Organic Solar Cells. Advanced Functional Materials 21, 897-910 (2011)."
2121,CC12C3(C)SC(C4=CC=C(/C=C/C5=CC=C(N(C6=CC=CC=C6)C7=CC=CC=C7)C=C5)C=C4)=CC3=C(C(F)(F)C(F)(F)C8(F)F)C8=C1C=C(C9=CC=C(/C=C/C%10=CC=C(N(C%11=CC=CC=C%11)C%12=CC=CC=C%12)C=C%10)C=C9)S2,TPB-G1,,,0.58,0.42,25.3,0.06,"	Fan C, et al. Synthesis and organic photovoltaic (OPV) properties of triphenylamine derivatives based on a hexafluorocyclopentene ¡°core¡±. Solar Energy Materials and Solar Cells 95, 992-1000 (2011)."
2122,CC12C3(C)SC(C4=CC=C(/C=C/C5=CC=C(N(C6=CC=C(/C=C/C7=CC=C(N(C8=CC=CC=C8)C9=CC=CC=C9)C=C7)C=C6)C%10=CC=C(/C=C/C%11=CC=C(N(C%12=CC=CC=C%12)C%13=CC=CC=C%13)C=C%11)C=C%10)C=C5)C=C4)=CC3=C(C(F)(F)C(F)(F)C%14(F)F)C%14=C1C=C(C%15=CC=C(/C=C/C%16=CC=C(N(C%17=CC=C(/C=C/C%18=CC=C(N(C%19=CC=CC=C%19)C%20=CC=CC=C%20)C=C%18)C=C%17)C%21=CC=C(/C=C/C%22=CC=C(N(C%23=CC=CC=C%23)C%24=CC=CC=C%24)C=C%22)C=C%21)C=C%16)C=C%15)S2,TPB-G2,,,0.8,0.51,25.3,0.1,"	Fan C, et al. Synthesis and organic photovoltaic (OPV) properties of triphenylamine derivatives based on a hexafluorocyclopentene ¡°core¡±. Solar Energy Materials and Solar Cells 95, 992-1000 (2011)."
2123,O=[Ti]12(N3C4=C(C=CC=C5)C5=C3N=C(C6=C7C=CC=C6)N2C7=N8)N9C(C(C=CC=C%10)=C%10C9=N4)=NC%11=C%12C(C=CC=C%12)=C8N1%11,TiOPc,,,0.64,0.94,30.4,0.18,"	Fan C, et al. Synthesis and organic photovoltaic (OPV) properties of triphenylamine derivatives based on a hexafluorocyclopentene ¡°core¡±. Solar Energy Materials and Solar Cells 95, 992-1000 (2011)."
2124,CCCCCCC1=C(/C=C(C#N)/C#N)SC(C(S2)=CC(CCCCCC)=C2C(C=C3)=CC=C3N(C4=CC=C(C5=C(CCCCCC)C=C(C6=CC(CCCCCC)=C(/C=C(C#N)/C#N)S6)S5)C=C4)C7=CC=C(C8=C(CCCCCC)C=C(C9=CC(CCCCCC)=C(/C=C(C#N)/C#N)S9)S8)C=C7)=C1,S(TPA-bT-DCN),,,0.74,4.2,38,1.2,"	Obata N, Sato Y, Nakamura E, Matsuo Y. Small-Molecule-Based Organic Photovoltaic Devices Covering Visible and Near-Infrared Absorption through Phase Transition of Titanylphthalocyanine Induced by Solvent Exposure. Japanese Journal of Applied Physics 50, 121603 (2011)."
2125,CCCCCCC1=C(/C=C(C#N)/C#N)SC(C(S2)=CC(CCCCCC)=C2/C=C/C(C=C3)=CC=C3N(C4=CC=C(/C=C/C5=C(CCCCCC)C=C(C6=CC(CCCCCC)=C(/C=C(C#N)/C#N)S6)S5)C=C4)C7=CC=C(/C=C/C8=C(CCCCCC)C=C(C9=CC(CCCCCC)=C(/C=C(C#N)/C#N)S9)S8)C=C7)=C1,S(TPA-bTV-DCN),,,0.84,5.21,30.8,1.4,"	Zhang J, et al. Solution-Processable Star-Shaped Molecules with Triphenylamine Core and Dicyanovinyl Endgroups for Organic Solar Cells?. Chemistry of Materials 23, 817-822 (2011)."
2126,CCCCC(CC)CN1C(C=CC(/C=C(C#N)\C#N)=C2)=C2C3=C1C=CC(/C=C(C#N)\C#N)=C3,1,,,0.88,7.76,43.9,3,"	Zhang J, et al. Solution-Processable Star-Shaped Molecules with Triphenylamine Core and Dicyanovinyl Endgroups for Organic Solar Cells?. Chemistry of Materials 23, 817-822 (2011)."
2127,CCCCC(CC)CC1(CC(CC)CCCC)C(C=C(/C=C(C#N)\C#N)S2)=C2C3=C1C=C(/C=C(C#N)\C#N)S3,2,,,0.154,0.86,28,0.05,"	Yassin A, Rousseau T, Leriche P, Cravino A, Roncali J. Evaluation of bis-dicyanovinyl short-chain conjugated systems as donor materials for organic solar cells. Solar Energy Materials and Solar Cells 95, 462-468 (2011)."
2128,CCCCC(CC)CN1C(C=C(/C=C(C#N)\C#N)S2)=C2C3=C1C=C(/C=C(C#N)\C#N)S3,3,,,0.63,0.014,15,0.0013,"	Yassin A, Rousseau T, Leriche P, Cravino A, Roncali J. Evaluation of bis-dicyanovinyl short-chain conjugated systems as donor materials for organic solar cells. Solar Energy Materials and Solar Cells 95, 462-468 (2011)."
2129,CCCCCCCCC(CCCCCCCC)N1C2=CC(C3=CC=CC=C3)=CC=C2C4=CC=C(C5=CC=C(C6=CC=C(C7=CC=C(C8=CC=C(C9=CC=C(C%10=CC=CC=C%10)S9)S8)C%11=NC(CCCCCC)(CCCCCC)N=C%117)S6)S5)C=C41,A-PCBBTHBI,,,0.515,1.21,39,0.24,"	Yassin A, Rousseau T, Leriche P, Cravino A, Roncali J. Evaluation of bis-dicyanovinyl short-chain conjugated systems as donor materials for organic solar cells. Solar Energy Materials and Solar Cells 95, 462-468 (2011)."
2130,CCCCC1=C(CCCC)C(C2=CC=CC=C2)=C3C(C4=C5C(C6=CC=C53)=C(C7=CC=C(C8=C(C9=CC=CC=C9)C(CCCC)=C(CCCC)C(C%10=CC=CC=C%10)=C8%11)C%12=C%11C=CC6=C%127)C=C4)=C1C%13=CC=CC=C%13,Bu4-Ph4-DIP,,,0.12,5.18,30,0.27,"	Song S, Heum Park S, Jin Y, Kim I, Lee K, Suh H. Copolymer derived from dihexyl-2H-benzimidazole and carbazole for organic photovoltaic cells. Solar Energy Materials and Solar Cells 95, 521-528 (2011)."
2131,CCCCC(C=C(C1=CC=C(C2=CC(CCCC)=C(C3=CC=C(C(C(F)(F)F)=O)S3)S2)C4=NSN=C41)S5)=C5C6=CC=C(C(C(F)(F)F)=O)S6,2,,,0.97,3.7,57,2,"	Meiss J, Hummert M, Petrich A, Pfuetzner S, Leo K, Riede M. Tetrabutyl-tetraphenyl-diindenoperylene derivatives as alternative green donor in bulk heterojunction organic solar cells. Solar Energy Materials and Solar Cells 95, 630-635 (2011)."
2132,O=C(C(F)(F)F)C1=CC=C(S1)C(S2)=CC=C2C(C3=NSN=C34)=CC=C4C(S5)=CC=C5C6=CC=C(C(C(F)(F)F)=O)S6,3,,,1.17,4.04,33,1.56,"	Steinberger SM, Amaresh; Reinold, Egon. A-D-A-D-A-Type Oligothiophenes for Vacuum-Deposited Organic Solar Cells. Organic Letters 13, 90-93 (2011)."
2133,N#C/C(C#N)=C\C1=CC([Si]2(C3=CC=CC=C3)C4=CC=CC=C4)=C(S1)C5=C2C=C(C6=CC=C(N(C7=CC=CC=C7)C8=CC=CC=C8)C=C6)S5,TPDCDTS,,,1.1,4.38,30,1.45,"	Steinberger SM, Amaresh; Reinold, Egon. A-D-A-D-A-Type Oligothiophenes for Vacuum-Deposited Organic Solar Cells. Organic Letters 13, 90-93 (2011)."
2134,O=C1C2=C3C(C(N1)=O)=CC4=C5C3=C(C6=C7C5=C8C9=C4C=C(C%10=CC=C(C%11=CC=C(C%12=CC=C(N(C%13=CC=CC=C%13)C%14=CC=CC=C%14)C=C%12)S%11)S%10)S9)C(C(SC(C%15=CC=C(C%16=CC=C(C%17=CC=C(N(C%18=CC=CC=C%18)C%19=CC=CC=C%19)C=C%17)S%16)S%15)=C%20)=C%20C6=CC(C(NC%21=O)=O)=C7C%21=C8)=C2,FPTTPA,,,0.83,9.53,48,3.82,"	Lin HW, et al. A new donor-acceptor molecule with uniaxial anisotropy for efficient vacuum-deposited organic solar cells. Chemical communications 47, 7872-7874 (2011)."
2135,O=C1C2=C3C(C(N1CCCCCC)=O)=CC4=C5C3=C(C6=C7C5=C8C9=C4C=C(C%10=CC(CCCCCC)=C(C%11=CC(CCCCCC)=C(C%12=CC=C(N(C%13=CC=CC=C%13)C%14=CC=CC=C%14)C=C%12)S%11)S%10)S9)C(C(SC(C%15=CC(CCCCCC)=C(C%16=CC(CCCCCC)=C(C%17=CC=C(N(C%18=CC=CC=C%18)C%19=CC=CC=C%19)C=C%17)S%16)S%15)=C%20)=C%20C6=CC(C(N(CCCCCC)C%21=O)=O)=C7C%21=C8)=C2,FP3HTTPA,,,0.776,5.94,30.8,1.42,"	Choi H, Paek S, Song J, Kim C, Cho N, Ko J. Synthesis of annulated thiophene perylene bisimide analogues: their applications to bulk heterojunction organic solar cells. Chemical communications 47, 5509-5511 (2011)."
2136,O=C1C2=C3C(C(N1C(CCCCCC)CCCCCC)=O)=CC=C4C3=C(C(C=CC(C(N(C(CCCCCC)CCCCCC)C5=O)=O)=C6C5=C7)=C6C4=C7C8=CC=C(C9=CC=C(C%10=CC=C(C%11=CC=C(N(C%12=CC=CC=C%12)C%13=CC=CC=C%13)C=C%11)S%10)S9)S8)C(C%14=CC=C(C%15=CC=C(C%16=CC=C(C%17=CC=C(N(C%18=CC=CC=C%18)C%19=CC=CC=C%19)C=C%17)S%16)S%15)S%14)=C2,PTPA,,,0.96,2.53,33.3,0.81,"	Choi H, Paek S, Song J, Kim C, Cho N, Ko J. Synthesis of annulated thiophene perylene bisimide analogues: their applications to bulk heterojunction organic solar cells. Chemical communications 47, 5509-5511 (2011)."
2137,N#C/C(C#N)=C1C=C(/C=C/C2=CC=C(/C=C/C3=CC=C(N(C4=CC=CC=C4)C5=CC=CC=C5)C=C3)C=C2)OC(/C=C/C6=CC=C(/C=C/C7=CC=C(N(C8=CC=CC=C8)C9=CC=CC=C9)C=C7)C=C6)=C\1,TPA¨CDCM¨CTPA,,,0.575,0.83,27.2,0.13,"	Choi H, Paek S, Song J, Kim C, Cho N, Ko J. Synthesis of annulated thiophene perylene bisimide analogues: their applications to bulk heterojunction organic solar cells. Chemical communications 47, 5509-5511 (2011)."
2138,N#C/C(C#N)=C1C=C(/C=C/C2=CC=C(/C=C/C3=CC=C(N(C4=CC=CC=C4)C5=CC=CC=C5)C=C3)S2)OC(/C=C/C6=CC=C(/C=C/C7=CC=C(N(C8=CC=CC=C8)C9=CC=CC=C9)C=C7)S6)=C/1,TPA¨CTV¨CPM,,,0.71,5.07,38,1.4,"	Zhang J, Wu G, He C, Deng D, Li Y. Triphenylamine-containing D¨CA¨CD molecules with (dicyanomethylene)pyran as an acceptor unit for bulk-heterojunction organic solar cells. Journal of Materials Chemistry 21, 3768 (2011)."
2139,CCCCCCC1=C(/C=C/C2=CC=C(N(C3=CC=CC=C3)C4=CC=CC=C4)C=C2)SC(/C=C/C(OC(/C=C/C5=CC(CCCCCC)=C(/C=C/C6=CC=C(N(C7=CC=CC=C7)C8=CC=CC=C8)C=C6)S5)=C/9)=CC9=C(C#N)/C#N)=C1,TPA¨CHTV¨CPM,,,0.79,5.94,44,2.06,"	Zhang J, Wu G, He C, Deng D, Li Y. Triphenylamine-containing D¨CA¨CD molecules with (dicyanomethylene)pyran as an acceptor unit for bulk-heterojunction organic solar cells. Journal of Materials Chemistry 21, 3768 (2011)."
2140,O=C(C1N2C=CC=C1)O[Ir]32N(C=C4)C(C5=C3C=CC=C5)C6=C4C=CC=C6,1,,,0.78,6.78,39,2.1,"	Zhang J, Wu G, He C, Deng D, Li Y. Triphenylamine-containing D¨CA¨CD molecules with (dicyanomethylene)pyran as an acceptor unit for bulk-heterojunction organic solar cells. Journal of Materials Chemistry 21, 3768 (2011)."
2141,O=C(C1N2C=CC=C1)O[Ir]32N(C=C4)C(C5=C3C=C(N(C6=CC=CC=C6)C7=CC=CC=C7)C=C5)C8=C4C=CC=C8,2,,,0.46,2.32,42,0.45,"	Lee W, Kwon T-H, Kwon J, Kim J-y, Lee C, Hong J-I. Effect of main ligands on organic photovoltaic performance of Ir(iii) complexes. New Journal of Chemistry 35, 2557 (2011)."
2142,O=C(C1N2C=CC=C1)O[Ir]32N(C=C4)C(C5=C3C=C6C7=C5C=CC8=CC=CC(C=C6)=C87)C9=C4C=CC=C9,3,,,0.44,2.65,43,0.5,"	Lee W, Kwon T-H, Kwon J, Kim J-y, Lee C, Hong J-I. Effect of main ligands on organic photovoltaic performance of Ir(iii) complexes. New Journal of Chemistry 35, 2557 (2011)."
2143,O=C(OCC)/C(C#N)=C/C(S1)=CC(CCCCCCCC)=C1C2=CC(CCCCCCCC)=C(S2)C3=CC(CCCCCCCC)=C(C4=CC=C(C5=C(CCCCCCCC)C=C(C6=C(CCCCCCCC)C=C(C7=C(CCCCCCCC)C=C(/C=C(C#N)/C(OCC)=O)S7)S6)S5)S4)S3,DCAE7T,,,0.45,2.17,34,0.34,"	Lee W, Kwon T-H, Kwon J, Kim J-y, Lee C, Hong J-I. Effect of main ligands on organic photovoltaic performance of Ir(iii) complexes. New Journal of Chemistry 35, 2557 (2011)."
2144,O=C(OCCCCCCCC)/C(C#N)=C/C(S1)=CC(CCCCCCCC)=C1C2=CC(CCCCCCCC)=C(S2)C3=CC(CCCCCCCC)=C(C4=CC=C(C5=C(CCCCCCCC)C=C(C6=C(CCCCCCCC)C=C(C7=C(CCCCCCCC)C=C(/C=C(C#N)/C(OCCCCCCCC)=O)S7)S6)S5)S4)S3,DCAO7T,,,0.88,9.94,51,4.46,"	Liu Y, et al. Spin-Coated Small Molecules for High Performance Solar Cells. Advanced Energy Materials 1, 771-775 (2011)."
2145,O=C(OCC(CC)CCCC)/C(C#N)=C/C(S1)=CC(CCCCCCCC)=C1C2=CC(CCCCCCCC)=C(S2)C3=CC(CCCCCCCC)=C(C4=CC=C(C5=C(CCCCCCCC)C=C(C6=C(CCCCCCCC)C=C(C7=C(CCCCCCCC)C=C(/C=C(C#N)/C(OCC(CC)CCCC)=O)S7)S6)S5)S4)S3,DCAEH7T,,,0.86,10.74,55,5.08,"	Liu Y, et al. Spin-Coated Small Molecules for High Performance Solar Cells. Advanced Energy Materials 1, 771-775 (2011)."
2146,[O-]C(/C1=C2[N+](CCCCCC)=C(/C=N/N(C3=CC=CC=C3)C4=CC=CC=C4)C=C\2)=C(C5=CC=C(/C=N/N(C6=CC=CC=C6)C7=CC=CC=C7)N5CCCCCC)C1=O,SQ,,,0.93,9.91,49.1,4.52,"	Liu Y, et al. Spin-Coated Small Molecules for High Performance Solar Cells. Advanced Energy Materials 1, 771-775 (2011)."
2147,C1(N(C2=CC=C(/C=C/C3=CC=C(C4=CC=C(N(C5=CC=CC=C5)C6=CC=CC=C6)C=C4)C7=NSN=C73)C=C2)C8=CC=CC=C8)=CC=CC=C1,TPA-BT,,,0.6,7.84,39,1.79,"	Peh RJ, Lu Y, Zhao F, Lee C-LK, Kwan WL. Vacuum-free processed transparent inverted organic solar cells with spray-coated PEDOT:PSS anode. Solar Energy Materials and Solar Cells 95, 3579-3584 (2011)."
2148,C1(N(C2=CC=C(C3=CC=C(/C=C/C4=CC=C(N(C5=CC=CC=C5)C6=CC=CC=C6)C=C4)C7=NSN=C37)C=C2)C8=CC=C(C9=CC=C(/C=C/C%10=CC=C(N(C%11=CC=CC=C%11)C%12=CC=CC=C%12)C=C%10)C%13=NSN=C9%13)C=C8)=CC=CC=C1,b-TPA-BT,,,0.86,4.29,36,1.33,"	Zhang J, Yang Y, He C, Deng D, Li Z, Li Y. Effect of molecular spatial configuration on the photovoltaic properties of triphenylamine-containing D¨CA structured organic molecules. Journal of Physics D: Applied Physics 44, 475101 (2011)."
2149,C1(N(C2=CC=C(C3=CC=C(/C=C/C4=CC=C(N(C5=CC=CC=C5)C6=CC=CC=C6)C=C4)C7=NSN=C37)C=C2)C8=CC=C(C9=CC=C(/C=C/C%10=CC=C(N(C%11=CC=CC=C%11)C%12=CC=CC=C%12)C=C%10)C%13=NSN=C9%13)C=C8)=CC=C(C%14=CC=C(/C=C/C%15=CC=C(N(C%16=CC=CC=C%16)C%17=CC=CC=C%17)C=C%15)C%18=NSN=C%14%18)C=C1,t-TPA-BT,,,0.89,6.28,40,2.23,"	Zhang J, Yang Y, He C, Deng D, Li Z, Li Y. Effect of molecular spatial configuration on the photovoltaic properties of triphenylamine-containing D¨CA structured organic molecules. Journal of Physics D: Applied Physics 44, 475101 (2011)."
2150,C1(N(C2=CC=C(/C=C/C3=CC=C(/C=C/C4=CC=C(N(C5=CC=CC=C5)C6=CC=CC=C6)C=C4)C7=NSN=C73)C=C2)C8=CC=C(/C=C/C9=CC=C(/C=C/C%10=CC=C(N(C%11=CC=CC=C%11)C%12=CC=CC=C%12)C=C%10)C%13=NSN=C%139)C=C8)=CC=C(/C=C/C%14=CC=C(/C=C/C%15=CC=C(N(C%16=CC=CC=C%16)C%17=CC=CC=C%17)C=C%15)C%18=NSN=C%18%14)C=C1,S(TPA-BT),,,0.92,7.77,44,3.14,"	Zhang J, Yang Y, He C, Deng D, Li Z, Li Y. Effect of molecular spatial configuration on the photovoltaic properties of triphenylamine-containing D¨CA structured organic molecules. Journal of Physics D: Applied Physics 44, 475101 (2011)."
2151,C12=CC3=C(C=C(C4=CC=CC=C4)[Se]3)C=C1C=C5C(C=C(C6=CC=CC=C6)[Se]5)=C2,6b,,,0.84,9.1,44.1,3.37,"	Zhang J, Yang Y, He C, Deng D, Li Z, Li Y. Effect of molecular spatial configuration on the photovoltaic properties of triphenylamine-containing D¨CA structured organic molecules. Journal of Physics D: Applied Physics 44, 475101 (2011)."
2152,CCCCCCCCC(C=C(C1=C(CCCCCCCC)C=C(C2=C(CCCCCCCC)C=C(/C=C(C#N)\C#N)S2)S1)S3)=C3C4=CC=C(C5=C(CCCCCCCC)C=C(C6=C(CCCCCCCC)C=C(C7=C(CCCCCCCC)C=C(/C=C(C#N)\C#N)S7)S6)S5)S4,1,,,0.46,3.03,59,0.83,"	Nakano M, Mori H, Shinamura S, Takimiya K. Naphtho[2,3-b:6,7-b¡ä]dichalcogenophenes: Syntheses, Characterizations, and Chalcogene Atom Effects on Organic Field-Effect Transistor and Organic Photovoltaic Devices. Chemistry of Materials 24, 190-198 (2012)."
2153,CCCCCCCCC(C=C(C1=C(CCCCCCCC)C=C(C2=C(CCCCCCCC)C=C(/C=C(C(N3CC)=O)\C(N(CC)C3=S)=O)S2)S1)S4)=C4C5=CC=C(C6=C(CCCCCCCC)C=C(C7=C(CCCCCCCC)C=C(C8=C(CCCCCCCC)C=C(/C=C(C(N9CC)=O)\C(N(CC)C9=S)=O)S8)S7)S6)S5,2,,,0.72,6,34,1.64,"	Demeter D, Rousseau T, Leriche P, Cauchy T, Po R, Roncali J. Manipulation of the Open-Circuit Voltage of Organic Solar Cells by Desymmetrization of the Structure of Acceptor-Donor-Acceptor Molecules. Advanced Functional Materials 21, 4379-4387 (2011)."
2154,CCCCCCCCC(C=C(C1=C(CCCCCCCC)C=C(C2=C(CCCCCCCC)C=C(/C=C(C(N3CC)=O)\C(N(CC)C3=S)=O)S2)S1)S4)=C4C5=CC=C(C6=C(CCCCCCCC)C=C(C7=C(CCCCCCCC)C=C(C8=C(CCCCCCCC)C=C(/C=C(C#N)\C#N)S8)S7)S6)S5,3,,,0.51,2.16,28,0.36,"	Demeter D, Rousseau T, Leriche P, Cauchy T, Po R, Roncali J. Manipulation of the Open-Circuit Voltage of Organic Solar Cells by Desymmetrization of the Structure of Acceptor-Donor-Acceptor Molecules. Advanced Functional Materials 21, 4379-4387 (2011)."
2155,CCCCCCCC[Si]1(CCCCCCCC)C2=C(SC(C3=CC(CCCCCCCC)=C(C4=CC=C(C5=C(CCCCCCCC)C=C(/C=C(C#N)/C(OCCCCCCCC)=O)S5)S4)S3)=C2)C6=C1C=C(C7=CC(CCCCCCCC)=C(C8=CC=C(C9=C(CCCCCCCC)C=C(/C=C(C#N)/C(OCCCCCCCC)=O)S9)S8)S7)S6,DCAO3TSi,,,0.81,3.7,36,1.21,"	Demeter D, Rousseau T, Leriche P, Cauchy T, Po R, Roncali J. Manipulation of the Open-Circuit Voltage of Organic Solar Cells by Desymmetrization of the Structure of Acceptor-Donor-Acceptor Molecules. Advanced Functional Materials 21, 4379-4387 (2011)."
2156,F[B-]([N+]1=C(C2=CC=CC=C2)C(C=CC=C3)=C3C1=N4)(F)N5C4=C(C=CC=C6)C6=C5C7=CC=CC=C7,Ph2-benz-bodipy,,,0.8,11.51,64,5.84,"	Zhou J, et al. A Planar Small Molecule with Dithienosilole Core for High Efficiency Solution-Processed Organic Photovoltaic Cells. Chemistry of Materials 23, 4666-4668 (2011)."
2157,O=C(C1=CC2=C3N4[Cu](N5C6=NC4=C2C=C1)(N7C(C(C=C(C(O)=O)C=C8)=C8C7=N9)=NC5C%10=C6C=C(C(O)=O)C=C%10)N%11C9C(C=C(C(O)=O)C=C%12)=C%12C%11=N3)O,CuTcPc,,,0.81,5.8,53,2.3,"	Meiss J, Holzmueller F, Gresser R, Leo K, Riede M. Near-infrared absorbing semitransparent organic solar cells. Applied Physics Letters 99, 193307 (2011)."
2158,C1(C2=C(/N=C3N=C(C4=CC=CC=C4)C=C\3C5=CC=CC=C5)NC(C6=CC=CC=C6)=C2)=CC=CC=C1,ADPM,,,0.54,0.825,32.3,0.14,"	Zhang T, et al. Soluble Copper Phthalocyanine Applied for Organic Solar Cells. Journal of Nanoscience and Nanotechnology 11, 9641-9644 (2011)."
2159,FB(F)N1C(C2=CC=CC=C2)=CC(C3=CC=CC=C3)=C1/N=C4N=C(C5=CC=CC=C5)C=C\4C6=CC=CC=C6,BF2-ADPM,,,0.207,5.53,48.7,0.56,"	Leblebici SY, Catane L, Barclay DE, Olson T, Chen TL, Ma B. Near-infrared azadipyrromethenes as electron donor for efficient planar heterojunction organic solar cells. ACS applied materials & interfaces 3, 4469-4474 (2011)."
2160,C1(C2=C(/N=C3N=C(C4=C5C=CC=C4)C=C\3C6=CC=CC=C6)N(B7O5)C(C8=C(O7)C=CC=C8)=C2)=CC=CC=C1,BO-ADPM,,,0.469,3.088,47.5,0.69,"	Leblebici SY, Catane L, Barclay DE, Olson T, Chen TL, Ma B. Near-infrared azadipyrromethenes as electron donor for efficient planar heterojunction organic solar cells. ACS applied materials & interfaces 3, 4469-4474 (2011)."
2161,CCCCC1=C(SC(C2=CC=C(/C=C(C#N)\C#N)S2)=C1CCCC)C3=CC=C(C4=C(CCCC)C(CCCC)=C(C5=CC=C(/C=C(C#N)\C#N)S5)S4)S3,DCV5T,,,0.796,5.882,56.2,2.63,"	Leblebici SY, Catane L, Barclay DE, Olson T, Chen TL, Ma B. Near-infrared azadipyrromethenes as electron donor for efficient planar heterojunction organic solar cells. ACS applied materials & interfaces 3, 4469-4474 (2011)."
2162,CCCCC1=C(SC(C2=CC=C(/C=C(C#N)\C#N)S2)=C1CCCC)C3=CC=C(C4=C(CCCC)C(CCCC)=C(C5=CC=C(/C=C(C#N)\C#N)S5)S4)[Se]3,1,,,1.02,7,43,3.47,"	Haid S, Mishra A, Uhrich C, Pfeiffer M, B?uerle P. Dicyanovinylene-Substituted Selenophene¨CThiophene Co-oligomers for Small-Molecule Organic Solar Cells. Chemistry of Materials 23, 4435-4444 (2011)."
2163,CCCCC1=C(SC(C2=CC=C(/C=C(C#N)\C#N)[Se]2)=C1CCCC)C3=CC=C(C4=C(CCCC)C(CCCC)=C(C5=CC=C(/C=C(C#N)\C#N)[Se]5)S4)S3,2,,,0.99,5.5,48,3.09,"	Haid S, Mishra A, Uhrich C, Pfeiffer M, B?uerle P. Dicyanovinylene-Substituted Selenophene¨CThiophene Co-oligomers for Small-Molecule Organic Solar Cells. Chemistry of Materials 23, 4435-4444 (2011)."
2164,CCCCC1=C(SC(C2=CC=C(/C=C(C#N)\C#N)[Se]2)=C1CCCC)C3=CC=C(C4=C(CCCC)C(CCCC)=C(C5=CC=C(/C=C(C#N)\C#N)[Se]5)S4)[Se]3,3,,,1,7,39,2.93,"	Haid S, Mishra A, Uhrich C, Pfeiffer M, B?uerle P. Dicyanovinylene-Substituted Selenophene¨CThiophene Co-oligomers for Small-Molecule Organic Solar Cells. Chemistry of Materials 23, 4435-4444 (2011)."
2165,CC(C=C1)=CC=C1N(C2=CC=C(C)C=C2)C3=CC=C(C4=CC=C(/C=C(C#N)/C#N)C5=NSN=C54)S3,DTDCTB,,,0.95,5.4,46,2.53,"	Haid S, Mishra A, Uhrich C, Pfeiffer M, B?uerle P. Dicyanovinylene-Substituted Selenophene¨CThiophene Co-oligomers for Small-Molecule Organic Solar Cells. Chemistry of Materials 23, 4435-4444 (2011)."
2166,OC1=CC(N(C2=CC=CC3=C2C=CC=C3)C4=CC=CC=C4)=CC(O)=C1C5C([O-])C(C6=C(O)C=C(N(C7=CC=CC8=C7C=CC=C8)C9=CC=CC=C9)C=C6O)C5[O-],1-NPSQ,,,,,,5.81,"	Lin LY, et al. A low-energy-gap organic dye for high-performance small-molecule organic solar cells. Journal of the American Chemical Society 133, 15822-15825 (2011)."
2167,CCCCCCCC[Si]1(CCCCCCCC)C(C=C(C2=CC=C(/C=C(C#N)/C#N)C3=NSN=C23)S4)=C4C5=C1C=C(C6=CC=C(/C=C(C#N)/C#N)C7=NSN=C76)S5,BDCDTS,,,0.9,10,64,5.7,"	Wei G, et al. Arylamine-based squaraine donors for use in organic solar cells. Nano letters 11, 4261-4264 (2011)."
2168,O=C1N(CC(CC)CCCO)C(C2=CC=C(C3=CC=C(C(F)(F)F)C=C3)S2)=C4C(N(CC(CC)CCCO)C(C5=CC=C(C6=CC=C(C(F)(F)F)C=C6)S5)=C41)=O,EH-DPP-TFP,,,0.43,0.73,24,0.07,"	Lin L-Y, Lu C-W, Huang W-C, Chen Y-H, Lin H-W, Wong K-T. New AADAA-type electron donors for small molecule organic solar cells. Organic letters 13, 4962-4965 (2011)."
2169,O=C1N(CC(CC)CCCO)C(C2=CC=C(C=CC3=CC=C(C(F)(F)F)C=C3)S2)=C4C(N(CC(CC)CCCO)C(C5=CC=C(C=CC6=CC=C(C(F)(F)F)C=C6)S5)=C41)=O,EH-DPP-TFPV,,,0.46,2.19,34,0.3,"	Kylberg W, et al. Synthesis, thin-film morphology, and comparative study of bulk and bilayer heterojunction organic photovoltaic devices using soluble diketopyrrolopyrrole molecules. Energy & Environmental Science 4, 3617 (2011)."
2170,FC1=CC=CC2=C1C3=N/C2=N\C4=C5C(C=CC=C5F)=C6N4[Zn]N7/C(C(C=CC=C8F)C8/C7=N/C(C9=C/%10C(F)=CC=C9)=NC%10=N/6)=N\3,F4-ZnPc,,,0.86,7.65,51,3.4,"	Kylberg W, et al. Synthesis, thin-film morphology, and comparative study of bulk and bilayer heterojunction organic photovoltaic devices using soluble diketopyrrolopyrrole molecules. Energy & Environmental Science 4, 3617 (2011)."
2171,CCCCC1=C(SC(/C=C(C#N)/C#N)=C1)C2=CC(CCCC)=C(C3=CC=C(C4=CC=C(C5=C(CCCC)C=C(C6=C(CCCC)C=C(/C=C(C#N)/C#N)S6)S5)S4)S3)S2,DCV6T,,,0.66,8.3,64,3.9,"	Riede M, et al. Efficient Organic Tandem Solar Cells based on Small Molecules. Advanced Functional Materials 21, 3019-3028 (2011)."
2172,C1(/C2=N/C(C3=CC=CC=C3/4)=NC4=N/C5=C(C=CC=C6)C6=C(N5)/N=C(C7=CC=CC=C78)\N=C8/N=C9\N2)=C9C=CC=C1,H2Pc,,,0.88,8.3,66,4.3,"	Riede M, et al. Efficient Organic Tandem Solar Cells based on Small Molecules. Advanced Functional Materials 21, 3019-3028 (2011)."
2173,N12/C(C(C=CC=C3)=C3/C2=N/C(C4=CC=CC=C4/5)=NC5=N/6)=N\C7=N/C(C8=CC=CC=C87)=N\C9=C%10C(C=CC=C%10)=C6N9[Pb]1,PbPc,,,0.5,10.6,47,2.5,"	Kaji T, et al. Co-evaporant induced crystalline donor: acceptor blends in organic solar cells. Advanced materials 23, 3320-3325 (2011)."
2174,Cl[Al]1N2/C(C(C=CC=C3)=C3/C2=N/C(C4=CC=CC=C4/5)=NC5=N/6)=N\C7=N/C(C8=CC=CC=C87)=N\C9=C%10C(C=CC=C%10)=C6N19,AlPcCl,,,0.28,4.9,50,0.68,"	Kaji T, et al. Co-evaporant induced crystalline donor: acceptor blends in organic solar cells. Advanced materials 23, 3320-3325 (2011)."
2175,CCCCCCC1=C(C2=CC=CS2)SC(C3=CC=C(S3)/C=C/C4=CC(C(C#N)C#N)C=C(/C=C/C5=CC=C(C6=C(CCCCCC)C(CCCCCC)=C(C7=CC=CS7)S6)S5)O4)=C1CCCCCC,T3PM,,,0.59,3,43,0.76,"	Kaji T, et al. Co-evaporant induced crystalline donor: acceptor blends in organic solar cells. Advanced materials 23, 3320-3325 (2011)."
2176,C1(C2=C(C3=CC=CC=C3)N=NC4=C2C=CC=C4C5=CC=C(C6=CC=CC7=C6N=NC(C8=CC=CC=C8)=C7C9=CC=CC=C9)C=C5)=CC=CC=C1,p8-BCB,,,0.3,3.26,35,0.34,"	Bern¨¨de JC, et al. Influence of the highest occupied molecular orbital energy level of the donor material on the effectiveness of the anode buffer layer in organic solar cells. physica status solidi (a) 208, 1989-1994 (2011)."
2177,C1(C2=CC=CC3=C2N=NC(C4=CC=CC=C4)=C3C5=CC=CC=C5)=CC=CC(C6=C(N=NC(C7=CC=CC=C7)=C8C9=CC=CC=C9)C8=CC=C6)=C1,m8-BCB,,,0.77,8.84,59,4.39,"	Tsuji H, Yokoi Y, Sato Y, Tanaka H, Nakamura E. Bis-cinnolines as n-type semiconducting material with high electron mobility and thermal stability and their application in organic photovoltaic cells. Chemistry, an Asian journal 6, 2005-2008 (2011)."
2178,C1(C2=C(C3=CC=CC=C3)N=NC4=C2C=CC=C4C5=CC=CC6=C5N=NC(C7=CC=CC=C7)=C6C8=CC=CC=C8)=CC=CC=C1,8-BC,,,0.77,9.31,56,4.37,"	Tsuji H, Yokoi Y, Sato Y, Tanaka H, Nakamura E. Bis-cinnolines as n-type semiconducting material with high electron mobility and thermal stability and their application in organic photovoltaic cells. Chemistry, an Asian journal 6, 2005-2008 (2011)."
2179,C1(C=CC=C2)=C2C(C3=CC=C(C4=C(C5=CC=CC=C5)N=NC6=C4C=CC=C6)C=C3)=C(C7=CC=CC=C7)N=N1,p4-BCB,,,0.77,8.3,56,4,"	Tsuji H, Yokoi Y, Sato Y, Tanaka H, Nakamura E. Bis-cinnolines as n-type semiconducting material with high electron mobility and thermal stability and their application in organic photovoltaic cells. Chemistry, an Asian journal 6, 2005-2008 (2011)."
2180,O=C(N1CCC(C)CCCC(C)CCCC(C)C)C(C2=C1C3=CC=C(S3)C4=C(C=CC=C5)C5=C(C=CC=C6)C6=C4)=C(C7=CC=C(C8=C(C=CC=C9)C9=C(C=CC=C%10)C%10=C8)S7)N(CCC(C)CCCC(C)CCCC(C)C)C2=O,SPDPP,,,0.46,8.35,50,2.31,"	Tsuji H, Yokoi Y, Sato Y, Tanaka H, Nakamura E. Bis-cinnolines as n-type semiconducting material with high electron mobility and thermal stability and their application in organic photovoltaic cells. Chemistry, an Asian journal 6, 2005-2008 (2011)."
2181,O=C(N1CCC(C)CCCC(C)CCCC(C)C)C(C2=C1C3=CC=C(S3)C#CC4=C(C=CC=C5)C5=C(C=CC=C6)C6=C4)=C(C7=CC=C(C#CC8=C(C=CC=C9)C9=C(C=CC=C%10)C%10=C8)S7)N(CCC(C)CCCC(C)CCCC(C)C)C2=O,TPDPP,,,0.92,2.79,27,0.69,"	Wu Z, Li A, Fan B, Xue F, Adachi C, Ouyang J. Phenanthrene-functionalized 3,6-dithiophen-2-yl-2,5- dihydropyrrolo[3,4¨Cc]pyrrole-1,4-diones as donor molecules for solution-processed organic photovoltaic cells. Solar Energy Materials and Solar Cells 95, 2516-2523 (2011)."
2182,CC[P-](CC)(CC)[Pt](C1=CC=CC=C1)([P-](CC)(CC)CC)C#CC2=CC=C(S2)C(C=C3)=CC=C3N(C4=CC=C(C5=CC=C(C#C[Pt]([P-](CC)(CC)CC)([P-](CC)(CC)CC)C6=CC=CC=C6)S5)C=C4)C7=CC=C(C8=CC=C(C#C[Pt]([P-](CC)(CC)CC)([P-](CC)(CC)CC)C9=CC=CC=C9)S8)C=C7,M2,,,0.77,3.92,57,1.71,"	Wu Z, Li A, Fan B, Xue F, Adachi C, Ouyang J. Phenanthrene-functionalized 3,6-dithiophen-2-yl-2,5- dihydropyrrolo[3,4¨Cc]pyrrole-1,4-diones as donor molecules for solution-processed organic photovoltaic cells. Solar Energy Materials and Solar Cells 95, 2516-2523 (2011)."
2183,CCCCCCC1=CC=C(S1)C(S2)=CC=C2C3=CC=C(S3)C(C=C4)=CC=C4N(C5=CC=C(C6=CC=C(/C=C(C#N)\C#N)S6)C=C5)C7=CC=C(C8=CC=C(C9=CC=C(C%10=CC=C(CCCCCC)S%10)S9)S8)C=C7,3,,,0.65,2.35,27,0.41,"	Wang Q, et al. Platinum-acetylide polymers with higher dimensionality for organic solar cells. Chemistry, an Asian journal 6, 1766-1777 (2011)."
2184,CCCCCCC1=CC=C(S1)C(S2)=CC=C2C3=CC=C(S3)C(C=C4)=CC=C4N(C5=CC=C(C6=CC=C(/C=C(C#N)\C#N)S6)C=C5)C7=CC=C(C8=CC=C(/C=C(C#N)\C#N)S8)C=C7,4,,,0.85,5.3,39,1.8,"	Ripaud E, Rousseau T, Leriche P, Roncali J. Unsymmetrical Triphenylamine-Oligothiophene Hybrid Conjugated Systems as Donor Materials for High-Voltage Solution-Processed Organic Solar Cells. Advanced Energy Materials 1, 540-545 (2011)."
2185,O=C1C2=C(C=CC=C2)NC(C1=C3)=CC4=C3NC5=C(C4=O)C=CC=C5,QA,,,1.07,5.83,31,2.02,"	Ripaud E, Rousseau T, Leriche P, Roncali J. Unsymmetrical Triphenylamine-Oligothiophene Hybrid Conjugated Systems as Donor Materials for High-Voltage Solution-Processed Organic Solar Cells. Advanced Energy Materials 1, 540-545 (2011)."
2186,N#C/C(C#N)=C(C1=CC=C(C2=CC=C(N(C3=CC=CC=C3)C4=CC=CC=C4)C=C2)S1)/C(C5=CC=C(S5)C6=CC=C(C=C6)N(C7=CC=CC=C7)C8=CC=CC=C8)=C(C#N)\C#N,1a,,,0.79,2.34,44,0.83,"	Chen TL, Chen JJ-A, Catane L, Ma B. Fully solution processed p-i-n organic solar cells with an industrial pigment ¨C Quinacridone. Organic Electronics 12, 1126-1131 (2011)."
2187,C1(N(C2=CC=CC=C2)C3=C(C=CC=C4)C4=CC=C3)=CC=C(C5=CC=C(N(C6=CC=CC7=C6C=CC=C7)C8=CC=CC=C8)C=C5)C=C1,¦Á -NPD,,,0.97,3.06,33,1.08,"	Antoine Leli¨¨ge PB, Th¨¦odulf Rousseau, and Jean Roncali. Triphenylamine/Tetracyanobutadiene-Based D-A-D ¦Ð-Conjugated Systems as Molecular Donors for Organic Solar Cells. Organic Letters 13, 3098-3101 (2011)."
2188,C12=CC=CC=C1C(C3=CC=C(N(C4=CC=C(C5=CC=CC=C5)C=C4)C6=CC=C(C7=CC=CC=C7)C=C6)C=C3)(C8=CC=C(N(C9=CC=C(C%10=CC=CC=C%10)C=C9)C%11=CC=C(C%12=CC=CC=C%12)C=C%11)C=C8)C%13=CC=CC=C2%13,BPAPF,,,0.83,2.6,51,1.1,"	Tress W, Leo K, Riede M. Influence of Hole-Transport Layers and Donor Materials on Open-Circuit Voltage and Shape of I-V Curves of Organic Solar Cells. Advanced Functional Materials 21, 2140-2149 (2011)."
2189,CCCCCCC(S1)=CC=C1C2=CC=C(S2)C3=CC=C(C4=CC=C(C5=CC=C(C6=CC=C(CCCCCC)S6)S5)S4)S3,DH6T,,,0.95,2.3,49,1,"	Tress W, Leo K, Riede M. Influence of Hole-Transport Layers and Donor Materials on Open-Circuit Voltage and Shape of I-V Curves of Organic Solar Cells. Advanced Functional Materials 21, 2140-2149 (2011)."
2190,C12=CC=CN=C1C(O[Pt]OC3=CC=CC4=CC=CN=C34)=CC=C2,Ptq2,,,0.36,0.097,24,0.01,"	Muhammad FF, Sulaiman K. Photovoltaic performance of organic solar cells based on DH6T/PCBM thin film active layers. Thin Solid Films 519, 5230-5233 (2011)."
2191,ClB1N2/C3=N\C4=NC(/N=C(C5=C6C=CC=C5)\N1C6N=C2C7=C3C=CC=C7)=C8C4C=CC=C8,SubPc,,,0.25,2.3,30,0.17,"	Low KH, Xu ZX, Xiang HF, Chui SS, Roy VA, Che CM. Bis(5,7-dimethyl-8-hydroxyquinolinato)platinum(II) complex for efficient organic heterojunction solar cells. Chemistry, an Asian journal 6, 3223-3229 (2011)."
2192,CC1(COCCCCCCOCC2=C(C)SC(C3=C(CCCCCC)C=C(C)S3)=C2)COC1,P3HT-Ox10,,,,,,4.4,"	Menke SM, Luhman WA, Holmes RJ. Tailored exciton diffusion in organic photovoltaic cells for enhanced power conversion efficiency. Nat. Mater. 12, 152-157 (2013)."
2193,CC1=CC=C(C2=C1C=CC=C23)C4=CC=CC5=C4C3=CC=C5CCC6=CC=C(C7=CC=C(C8=NSN=C87)C9=CC=C(CCC(C=C%10)=CC%11=C%10C(C=CC(C)=C%12)=C%12C%11(CCCCCCCC)CCCCCCCC)S9)S6,PFDTBT_10Per,,,0.63,2.23,46,1.07,"	Brotas G, Farinhas J, Ferreira Q, Morgado J, Charas A. Nanostructured layers of a new cross-linkable poly(3-hexylthiophene) in organic photovoltaic cells. Synth. Met. 162, 2052-2058 (2012)."
2194,CC1=CC=C(C2=C1C=CC=C23)C4=CC=CC5=C4C3=CC=C5CCC6=CC=C(C7=CC=C(C8=NSN=C87)C9=CC=C(CCC%10=CC=C(C(C=C%11)=CC%12=C%11C(C=CC(C%13=CC=C(C)S%13)=C%14)=C%14C%12(CCCCCCCC)CCCCCCCC)S%10)S9)S6,PFD2TBT_10Per,,,0.81,9.61,41,3.16,"	Kim J-H, et al. Introduction of Perylene Units for Enhanced Interchain Interaction in Conjugated Polymers for Organic Photovoltaic Devices. Macromolecules 45, 2367-2376 (2012)."
2195,CCCCCCC1=C(C2=CC=C(C=C2)N(C3=CC=CC=C3)C4=CC=CC=C4)SC(C5=NC(CCCCCC)=C(C6=CC=C(C=C6)N(C7=CC=CC=C7)C8=CC=CC=C8)S5)=N1,1,,,0.76,9.68,38,2.82,"	Kim J-H, et al. Introduction of Perylene Units for Enhanced Interchain Interaction in Conjugated Polymers for Organic Photovoltaic Devices. Macromolecules 45, 2367-2376 (2012)."
2196,CCCCCCC1=C(C2=CC=C(C3=CC=C(C=C3)N(C4=CC=CC=C4)C5=CC=CC=C5)S2)SC(C6=NC(CCCCCC)=C(C7=CC=C(C8=CC=C(C=C8)N(C9=CC=CC=C9)C%10=CC=CC=C%10)S7)S6)=N1,2,,,0.71,3.42,30.1,0.73,"	Lin Y, et al. Small molecules based on bithiazole for solution-processed organic solar cells. Org. Electron. 13, 673-680 (2012)."
2197,CCCCCCC1=C(C2=CC=C(C3=CC=C(C4=CC=C(N(C5=CC=CC=C5)C6=CC=CC=C6)C=C4)S3)S2)SC(C7=NC(CCCCCC)=C(C8=CC=C(C9=CC=C(C%10=CC(N(C%11=CC=CC=C%11)C%12=CC=CC=C%12)=CC=C%10)S9)S8)S7)=N1,3,,,0.81,4.69,33.5,1.27,"	Lin Y, et al. Small molecules based on bithiazole for solution-processed organic solar cells. Org. Electron. 13, 673-680 (2012)."
2198,FB(F)N1C(/N=C2N=C(C3=CC=CC=C3)C=C\2C4=CC=CC=C4)=C(C5=CC=CC=C5)C=C1C6=CC=CC=C6,Ph4-bodipy,,,0.84,7.72,40.2,2.61,"	Lin Y, et al. Small molecules based on bithiazole for solution-processed organic solar cells. Org. Electron. 13, 673-680 (2012)."
2199,C[Lr]1(C)C(C=CC=C2)=C2C3N1C4=CC=CC=C4N3C5=CC=CC=C5,(pbi)2Ir(acac),,,0.92,3,33,0.8,"	Mueller T, Gresser R, Leo K, Riede M. Organic solar cells based on a novel infrared absorbing aza-bodipy dye. Sol. Energy Mater. Sol. Cells 99, 176-181 (2012)."
2200,C12=C(C3=CC=CC=C3)C4=C(C5=CC=CC=C5)C6=CC=CC=C6C(C7=CC=CC=C78)=C4C8=C1C=CC=C2,2a,,,0.81,4.64,44,1.65,"	Wang N, Yu J, Zheng Y, Guan Z, Jiang Y. Organic Photovoltaic Cells Based on a Medium-Bandgap Phosphorescent Material and C-60. J. Phys. Chem. C 116, 5887-5891 (2012)."
2201,FC1=CC=C2C(C3=C4C(C=CC=C4)=C(C5=CC=C(F)C=C5)C6=C(C7=CC=C(F)C=C7)C8=CC=CC=C8C2=C36)=C1,2b,,,0.955,1.295,56.3,1.58,"	Gu X, Luhman WA, Yagodkin E, Holmes RJ, Douglas CJ. Diarylindenotetracenes via a Selective Cross-Coupling/C-H Functionalization: Electron Donors for Organic Photovoltaic Cells. Org. Lett. 14, 1390-1393 (2012)."
2202,COC1=CC=C(C2=C3C(C4=C5C(C=CC=C5)=C3C6=CC=C(OC)C=C6)=C(C7=CC(OC)=CC=C74)C8=CC=CC=C28)C=C1,2f,,,1.12,1.259,43.7,1.4,"	Gu X, Luhman WA, Yagodkin E, Holmes RJ, Douglas CJ. Diarylindenotetracenes via a Selective Cross-Coupling/C-H Functionalization: Electron Donors for Organic Photovoltaic Cells. Org. Lett. 14, 1390-1393 (2012)."
2203,COC1=CC(OC)=C(C2=C3C(C=CC=C3)=C(C4=CC(OC)=CC(OC)=C4)C5=C(C6=CC(OC)=CC(OC)=C6)C7=CC=CC=C7C8=C25)C8=C1,2g,,,0.81,1.341,38.1,0.94,"	Gu X, Luhman WA, Yagodkin E, Holmes RJ, Douglas CJ. Diarylindenotetracenes via a Selective Cross-Coupling/C-H Functionalization: Electron Donors for Organic Photovoltaic Cells. Org. Lett. 14, 1390-1393 (2012)."
2204,COC1=C(OC)C(OC)=CC(C2=C3C(C4=C5C(C=CC=C5)=C3C6=CC(OC)=C(OC)C(OC)=C6)=C(C7=C(OC)C(OC)=C(OC)C=C74)C8=CC=CC=C28)=C1,2h,,,0.702,2.314,53.6,1.12,"	Gu X, Luhman WA, Yagodkin E, Holmes RJ, Douglas CJ. Diarylindenotetracenes via a Selective Cross-Coupling/C-H Functionalization: Electron Donors for Organic Photovoltaic Cells. Org. Lett. 14, 1390-1393 (2012)."
2205,CCN(C1=CC=CC=C1)C2=CC=C(/C=C/C(C(C)(C)O/3)=C(C#N)C3=C(C#N)/C#N)C=C2,3a,,,0.834,1.177,40.8,0.91,"	Gu X, Luhman WA, Yagodkin E, Holmes RJ, Douglas CJ. Diarylindenotetracenes via a Selective Cross-Coupling/C-H Functionalization: Electron Donors for Organic Photovoltaic Cells. Org. Lett. 14, 1390-1393 (2012)."
2206,CCN(C1=CC=CC=C1S2)C3=C2C=C(/C=C/C(C(C)(C)O/4)=C(C#N)C4=C(C#N)/C#N)C=C3,3b,,,0.82,0.26,30,0.064,"	Cho MJ, et al. Tricyanofuran-based donor-acceptor type chromophores for bulk heterojunction organic solar cells. Sol. Energy Mater. Sol. Cells 98, 71-77 (2012)."
2207,CC(O/1)(C)C(/C=C/C2=CC=C(C=C2)N(C3=CC=CC=C3)C4=CC=CC=C4)=C(C#N)C1=C(C#N)/C#N,5a,,,0.85,6.01,29,1.47,"	Cho MJ, et al. Tricyanofuran-based donor-acceptor type chromophores for bulk heterojunction organic solar cells. Sol. Energy Mater. Sol. Cells 98, 71-77 (2012)."
2208,CC(O/1)(C)C(/C=C/C2=CC=C(C=C2)N(C3=CC=C(C(C)(C)C)C=C3)C4=CC=C(C(C)(C)C)C=C4)=C(C#N)C1=C(C#N)/C#N,5b,,,93,8.74,30,2.44,"	Cho MJ, et al. Tricyanofuran-based donor-acceptor type chromophores for bulk heterojunction organic solar cells. Sol. Energy Mater. Sol. Cells 98, 71-77 (2012)."
2209,CCCCCCCCCCC1=C(C2=CN=C(C3=NC=C(C(S4)=C(CCCCCCCCCC)C=C4C(C=C5)=CC=C5N(C6=CC=CC=C6)C7=CC=CC=C7)S3)S2)SC(C(C=C8)=CC=C8N(C9=CC=CC=C9)C%10=CC=CC=C%10)=C1,M1,,,0.87,1.11,28,0.27,"	Cho MJ, et al. Tricyanofuran-based donor-acceptor type chromophores for bulk heterojunction organic solar cells. Sol. Energy Mater. Sol. Cells 98, 71-77 (2012)."
2210,CCCCCCCCCCC1=C(C(S2)=NC3=C2N=C(C(S4)=C(CCCCCCCCCC)C=C4C(C=C5)=CC=C5N(C6=CC=CC=C6)C7=CC=CC=C7)S3)SC(C(C=C8)=CC=C8N(C9=CC=CC=C9)C%10=CC=CC=C%10)=C1,M2,,,0.94,4.05,27,1.03,"	Dutta P, Yang W, Eom SH, Lee S-H. Synthesis and characterization of triphenylamine flanked thiazole-based small molecules for high performance solution processed organic solar cells. Org. Electron. 13, 273-282 (2012)."
2211,CCCCCCCCCCC1=C(C(S2)=CC3=C2C4=C(C=C3)C5=C(C=C(C6=C(CCCCCCCCCC)C=C(C7=CC=CC8=NSN=C87)S6)S5)C=C4)SC(C9=CC=CC%10=NSN=C%109)=C1,BNB,,,0.92,6.36,35,2.05,"	Dutta P, Yang W, Eom SH, Lee S-H. Synthesis and characterization of triphenylamine flanked thiazole-based small molecules for high performance solution processed organic solar cells. Org. Electron. 13, 273-282 (2012)."
2212,CCCCCCCCCCC1=C(C(S2)=CC3=C2C4=C(C=C3)C5=C(C=C(C6=C(CCCCCCCCCC)C=C(C7=CC=C(C(C=C8)=CC=C8N(C9=CC=CC=C9)C%10=CC=CC=C%10)C%11=NSN=C%117)S6)S5)C=C4)SC(C%12=CC=C(C(C=C%13)=CC=C%13N(C%14=CC=CC=C%14)C%15=CC=CC=C%15)C%16=NSN=C%16%12)=C1,TBNBT,,,0.93,3.79,28,0.98,"	Dutta P, Yang W, Eom SH, Lee W-H, Kang IN, Lee S-H. Development of naphtho 1,2-b:5,6-b ' dithiophene based novel small molecules for efficient bulk-heterojunction organic solar cells. Chem. Commun. 48, 573-575 (2012)."
2213,C12=CC(C=C(C=C(C3=CC=CC=C3)S4)C4=C5)=C5C=C1C=C(C6=CC=CC=C6)S2,1b,,,0.95,6.18,37,2.2,"	Dutta P, Yang W, Eom SH, Lee W-H, Kang IN, Lee S-H. Development of naphtho 1,2-b:5,6-b ' dithiophene based novel small molecules for efficient bulk-heterojunction organic solar cells. Chem. Commun. 48, 573-575 (2012)."
2214,O=C(N1C2CCCCC2)C3=C(/C=C/C4=CC=C(/C=C([N+]#[C-])/C5=CC=C([N+]([O-])=O)C=C5)C=C4)C=CC(/C=C/C6=CC=C(/C=C([N+]#[C-])/C7=CC=C([N+]([O-])=O)C=C7)C=C6)=C3C1=O,SM,,,0.52,3.16,60,0.98,"	Nakano M, Mori H, Shinamura S, Takimiya K. Naphtho 2,3-b:6,7-b ' dichalcogenophenes: Syntheses, Characterizations, and Chalcogene Atom Effects on Organic Field-Effect Transistor and Organic Photovoltaic Devices. Chem. Mater. 24, 190-198 (2012)."
2215,N#C/C([N+]#[C-])=C1C=C(/C=C/C(C=C2)=CC=C2/C=C/C(C=C3)=CC=C3N(C4=CC=CC=C4)C5=CC=CC=C5)OC(/C=C/C(C=C6)=CC=C6/C=C/C(C=C7)=CC=C7N(C8=CC=CC=C8)C9=CC=CC=C9)=C\1,TPA¨CDCM¨CTPA,,,0.84,8.8,56,4.14,"	Sharma GD, Mikroyannidis JA, Kurchania R, Thomas KRJ. Organic bulk heterojunction solar cells based on solution processable small molecules (A-pi-A) featuring 2-(4-nitrophenyl) acrylonitrile acceptors and phthalimide-based pi-linkers. Journal of Materials Chemistry 22, 13986-13995 (2012)."
2216,N#C/C([N+]#[C-])=C1C=C(/C=C/C2=CC=C(/C=C/C3=CC=C(N(C4=CC=CC=C4)C5=CC=CC=C5)C=C3)S2)OC(/C=C/C6=CC=C(/C=C/C7=CC=C(N(C8=CC=CC=C8)C9=CC=CC=C9)C=C7)S6)=C/1,TPA¨CTV¨CPM,,,0.71,5.07,38,1.4,"	Zhang J, Wu G, He C, Deng D, Li Y. Triphenylamine-containing D-A-D molecules with (dicyanomethylene)pyran as an acceptor unit for bulk-heterojunction organic solar cells. J. Mater. Chem. 21, 3768-3774 (2011)."
2217,CCCCCCC1=C(/C=C/C2=CC=C(N(C3=CC=CC=C3)C4=CC=CC=C4)C=C2)SC(/C=C/C5=C/C(C=C(/C=C/C6=CC(CCCCCC)=C(/C=C/C7=CC=C(N(C8=CC=CC=C8)C9=CC=CC=C9)C=C7)S6)O5)=C(C#N)\[N+]#[C-])=C1,TPA¨CHTV¨CPM,,,0.79,5.94,44,2.06,"	Zhang J, Wu G, He C, Deng D, Li Y. Triphenylamine-containing D-A-D molecules with (dicyanomethylene)pyran as an acceptor unit for bulk-heterojunction organic solar cells. J. Mater. Chem. 21, 3768-3774 (2011)."
2218,CCCCCCC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(C4=NSN=C45)=CC=C5C(S6)=CC=C6C(C=C7)=CC=C7N(C8=CC9=C(C(C=CC=C%10)=C%10C9(C)C)C=C8)C%11=CC(C%12(C)C)=C(C=C%11)C%13=C%12C=CC=C%13)S2,1,,,0.78,6.78,39,2.1,"	Zhang J, Wu G, He C, Deng D, Li Y. Triphenylamine-containing D-A-D molecules with (dicyanomethylene)pyran as an acceptor unit for bulk-heterojunction organic solar cells. J. Mater. Chem. 21, 3768-3774 (2011)."
2219,CCCCCCC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(C4=NSN=C45)=CC(F)=C5C(S6)=CC=C6C(C=C7)=CC=C7N(C8=CC9=C(C(C=CC=C%10)=C%10C9(C)C)C=C8)C%11=CC(C%12(C)C)=C(C=C%11)C%13=C%12C=CC=C%13)S2,2,,,0.82,10.52,42,3.54,"	Paek S, Cho N, Song K, Jun M-J, Lee JK, Ko J. Efficient Organic Semiconductors Containing Fluorine-Substituted Benzothiadiazole for Solution-Processed Small Molecule Organic Solar Cells. J. Phys. Chem. C 116, 23205-23213 (2012)."
2220,CCCCCCC(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C(C4=NSN=C45)=C(F)C(F)=C5C(S6)=CC=C6C(C=C7)=CC=C7N(C8=CC9=C(C(C=CC=C%10)=C%10C9(C)C)C=C8)C%11=CC(C%12(C)C)=C(C=C%11)C%13=C%12C=CC=C%13)S2,3,,,0.85,10.55,44,3.73,"	Paek S, Cho N, Song K, Jun M-J, Lee JK, Ko J. Efficient Organic Semiconductors Containing Fluorine-Substituted Benzothiadiazole for Solution-Processed Small Molecule Organic Solar Cells. J. Phys. Chem. C 116, 23205-23213 (2012)."
2221,C1([Si](C2=CC=CC=C2)(C3=CC=CC=C3)C4=CC=CC=C4)=CC=C([Si](C5=CC=CC=C5)(C6=CC=CC=C6)C7=CC=CC=C7)C=C1,UGH2,,,0.88,10.76,44,4.24,"	Paek S, Cho N, Song K, Jun M-J, Lee JK, Ko J. Efficient Organic Semiconductors Containing Fluorine-Substituted Benzothiadiazole for Solution-Processed Small Molecule Organic Solar Cells. J. Phys. Chem. C 116, 23205-23213 (2012)."
2222,CCCCCCC1=C(C2=CC=C(C(C3=NSN=C34)=CC=C4C5=CC=C(C6=C(CCCCCC)C=CS6)S5)S2)SC=C1,¦Â-DH5TB(1),,,,,,4.4,"	Menke SM, Luhman WA, Holmes RJ. Tailored exciton diffusion in organic photovoltaic cells for enhanced power conversion efficiency. Nat. Mater. 12, 152-157 (2013)."
2223,CCCCCCC1=C(C2=CC=C(C(C3=NSN=C34)=CC=C4C5=CC=C(C6=CC(CCCCCC)=CS6)S5)S2)SC=C1,¦Â-DH5TB(2),,,0.52,4.04,36,0.76,"	Lim E, et al. Solution-processable oligothiophenes with solubilizing beta-alkyl groups for organic photovoltaic cells. Sol. Energy Mater. Sol. Cells 107, 165-174 (2012)."
2224,CCCCCCC1=CC=C(C2=CC=C(C(C3=NSN=C34)=CC=C4C5=CC=C(C6=CC=C(CCCCCC)S6)S5)S2)S1,¦Á-DH5TB,,,0.6,4.69,35,0.98,"	Lim E, et al. Solution-processable oligothiophenes with solubilizing beta-alkyl groups for organic photovoltaic cells. Sol. Energy Mater. Sol. Cells 107, 165-174 (2012)."
2225,CCCCCCC1=CC=C(C2=CC=C(C3=CC=C(C4=CC=C(C5=CC=C(CCCCCC)S5)S4)S3)S2)S1,¦Á-DH5T,,,0.55,4.75,34,0.89,"	Lim E, et al. Solution-processable oligothiophenes with solubilizing beta-alkyl groups for organic photovoltaic cells. Sol. Energy Mater. Sol. Cells 107, 165-174 (2012)."
2226,CCCCCCCCC(CCCCCCCC)N1C2=C(C3=C1C=C(CCC4=CC=C(C5=CC=C(C6=CC=C(CCC7=C(CC=C8CC=C9C%10=CC=CC=C%10)C(C8=C9C=C%11)=C%11C=C7)S6)C%12=NSN=C%125)S4)C=C3)C=CC(C%13=CC=CC=C%13)=C2,PCDTBT-5Pyr,,,0.51,4.25,37,0.8,"	Lim E, et al. Solution-processable oligothiophenes with solubilizing beta-alkyl groups for organic photovoltaic cells. Sol. Energy Mater. Sol. Cells 107, 165-174 (2012)."
2227,CCCCC(CC)CC(S1)=CC=C1C2=C(C=C(C3=CC=C(C4=CC=C(C5=CC=C(C6=CC=CS6)S5)C7=NSN=C74)S3)S8)C8=C(C9=CC=C(CC(CC)CCCC)S9)C%10=C2SC(C%11=CC=CS%11)=C%10,PBDTDTBT,,,0.74,10.6,41,3.22,"	Kim J-H, et al. Incorporation of Pyrene Units to Improve Hole Mobility in Conjugated Polymers for Organic Solar Cells. Macromolecules 45, 8628-8638 (2012)."
2228,CCCCC(CC)CC(S1)=CC=C1C2=C(C=C(CCC3=CC=C(C4=CC=C(C5=CC=C(CCC6=CC=C7C8=C9C(C=C7)=C(C%10=CC=CS%10)C=CC9=CC=C68)S5)C%11=NSN=C%114)S3)S%12)C%12=C(C%13=CC=C(CC(CC)CCCC)S%13)C%14=C2SC(C%15=CC=CS%15)=C%14,PBDTDTBT-10Pyr,,,0.82,8.84,46,3.34,"	Kim J-H, et al. Incorporation of Pyrene Units to Improve Hole Mobility in Conjugated Polymers for Organic Solar Cells. Macromolecules 45, 8628-8638 (2012)."
2229,O=C(N1CC(CC)CCCC)C(C2=C1C3=CC=C(C)S3)=C(C4=CC=C(C5=CC=C(C6=C(C(OCCCCCCCC)=O)C(C(OCCCCCCCC)=O)=C(C7=CC=C(C)S7)S6)S5)S4)N(CC(CC)CCCC)C2=O,PCTDPP,,,0.87,10.93,53,5.04,"	Kim J-H, et al. Incorporation of Pyrene Units to Improve Hole Mobility in Conjugated Polymers for Organic Solar Cells. Macromolecules 45, 8628-8638 (2012)."
2230,CCCCC(CC)COC1=C(C=C(C2=CC=C(C3=CC=C(N(C4=CC=CC=C4)C5=CC=CC=C5)C=C3)C6=NSN=C62)S7)C7=C(OCC(CC)CCCC)C8=C1SC(C9=CC=C(C%10=CC=C(N(C%11=CC=CC=C%11)C%12=CC=CC=C%12)C=C%10)C%13=NSN=C%139)=C8,BDT(TBT)2,,,0.62,10.2,51,3.2,"	Zuo L, Cao Z, Hu X, Gu Z, Pan H, Chen H. Immerse precipitation as an efficient protocol to optimize morphology and performance of organic solar cells. Appl. Phys. Lett. 101,  (2012)."
2231,O=C(OCCCCCCCC)/C([N+]#[C-])=C/C1=CC(CCCCCCCC)=C(C(S2)=CC=C2C3=C(CCCCCCCC)C=C(C4=CC5=C(OCC(CC)CCCC)C6=C(C=C(C7=CC(CCCCCCCC)=C(C8=CC=C(C9=C(CCCCCCCC)C=C(/C=C([N+]#[C-])/C(OCCCCCCCC)=O)S9)S8)S7)S6)C(OCC(CC)CCCC)=C5S4)S3)S1,DCAO3TBDT,,,0.89,7.94,40,2.83,"	Dutta P, Kim J, Eom SH, Lee W-H, Kang IN, Lee S-H. An Easily Accessible Donor-pi-Acceptor-Conjugated Small Molecule from a 4,8-Dialkoxybenzo 1,2-b:4,5-b ' dithiophene Unit for Efficient Solution-Processed Organic Solar Cells. ACS Appl. Mater. Interfaces 4, 6668-6674 (2012)."
2232,CCCCCCCCC1=C(C(S2)=CC=C2C3=C(CCCCCCCC)C=C(C4=CC5=C(OCC(CC)CCCC)C6=C(C=C(C7=CC(CCCCCCCC)=C(C8=CC=C(C9=C(CCCCCCCC)C=C(/C=C(S%10)/C(N(CC)C%10=S)=O)S9)S8)S7)S6)C(OCC(CC)CCCC)=C5S4)S3)SC(/C=C(S%11)/C(N(CC)C%11=S)=O)=C1,DR3TBDT,,,0.95,8,60,4.56,"	Zhou J, et al. Small Molecules Based on Benzo 1,2-b:4,5-b ' dithiophene Unit for High-Performance Solution-Processed Organic Solar Cells. J. Am. Chem. Soc. 134, 16345-16351 (2012)."
2233,[C-]#[N+]/C(C#N)=C\C1=CC=C(C([Se]2)=CC=C2C([Se]3)=CC=C3C4=CC=C(/C=C([N+]#[C-])\C#N)[Se]4)[Se]1,DCV4S,,,0.93,12.21,65,7.38,"	Zhou J, et al. Small Molecules Based on Benzo 1,2-b:4,5-b ' dithiophene Unit for High-Performance Solution-Processed Organic Solar Cells. J. Am. Chem. Soc. 134, 16345-16351 (2012)."
2234,[C-]#[N+]/C(C#N)=C\C1=CC=C(C([Se]2)=CC=C2C([Se]3)=CC=C3C([Se]4)=CC=C4C5=CC=C(/C=C([N+]#[C-])\C#N)[Se]5)[Se]1,DCV5S,,,0.95,4.8,53,2.4,"	Haid S, Mishra A, Weil M, Uhrich C, Pfeiffer M, Baeuerle P. Synthesis and Structure-Property Correlations of Dicyanovinyl-Substituted Oligoselenophenes and their Application in Organic Solar Cells. Adv. Funct. Mater. 22, 4322-4333 (2012)."
2235,CCCCCCC1=C(/C=C([N+]#[C-])/C#N)SC2=C1SC(/C=C/C(C=C3)=CC=C3N(C4=CC=C(/C=C/C5=C(CCCCCC)C6=C(C(CCCCCC)=C(/C=C([N+]#[C-])/C#N)S6)S5)C=C4)C7=CC=C(/C=C/C8=C(CCCCCC)C9=C(C(CCCCCC)=C(/C=C([N+]#[C-])/[N+]#[C-])S9)S8)C=C7)=C2CCCCCC,S(TPA¨CDHT¨CDCN),,,0.91,7.1,53,3.4,"	Haid S, Mishra A, Weil M, Uhrich C, Pfeiffer M, Baeuerle P. Synthesis and Structure-Property Correlations of Dicyanovinyl-Substituted Oligoselenophenes and their Application in Organic Solar Cells. Adv. Funct. Mater. 22, 4322-4333 (2012)."
2236,IC1=CC=C(/C(C2=C(C)C=C(/C=C/CCCCCC3=CC=C(C=O)S3)N2B(F)F)=C4N=C(/C=C/CCCCCC5=CC=C(C=O)S5)C=C/4C)C=C1,TB1,,,0.96,6.8,43.5,2.87,"	Deng D, Shen S, Zhang J, He C, Zhang Z, Li Y. Solution-processable star-shaped photovoltaic organic molecule with triphenylamine core and thieno 3,2-b thiophene-dicyanovinyl arms. Org. Electron. 13, 2546-2552 (2012)."
2237,IC1=CC=C(/C(C2=C(C)C=C(/C=C/CCCCCC3=CC=C(C4=CC=C(C=O)S4)S3)N2B(F)F)=C5N=C(/C=C/CCCCCC6=CC=C(C7=CC=C(C=O)S7)S6)C=C/5C)C=C1,TB2,,,0.76,5.84,31,1.4,"	Bura T, et al. High-Performance Solution-Processed Solar Cells and Ambipolar Behavior in Organic Field-Effect Transistors with Thienyl-BODIPY Scaffoldings. J. Am. Chem. Soc. 134, 17404-17407 (2012)."
2238,IC1=CC=C(/C(C2=C(C)C=C(/C=C/OCCOCCOC3=CC=C(C4=CC=C(C=O)S4)S3)N2B(F)F)=C5N=C(/C=C/OCCOCCOC6=CC=C(C7=CC=C(C=O)S7)S6)C=C/5C)C=C1,TB3,,,0.7,14.3,47,4.7,"	Bura T, et al. High-Performance Solution-Processed Solar Cells and Ambipolar Behavior in Organic Field-Effect Transistors with Thienyl-BODIPY Scaffoldings. J. Am. Chem. Soc. 134, 17404-17407 (2012)."
2239,IC1=CC=C(/C(C2=C(C)C=C(/C=C/OCCOCCOCCC3=CC=C(C4=CC=C(C=O)S4)S3)N2B(F)F)=C5N=C(/C=C/OCCOCCOCCC6=CC=C(C7=CC=C(C=O)S7)S6)C=C/5C)C=C1,TB4,,,0.56,5.1,30,0.9,"	Bura T, et al. High-Performance Solution-Processed Solar Cells and Ambipolar Behavior in Organic Field-Effect Transistors with Thienyl-BODIPY Scaffoldings. J. Am. Chem. Soc. 134, 17404-17407 (2012)."
2240,O=C1N(CC(CC)CCCC)C(C2=CC=C(C3=CC=C4C=CC=CC4=C3)S2)C5C1=C(C6=CC=C(C7=CC=C8C=CC=CC8=C7)S6)N(CC(CC)CCCC)C5=O,M1,,,0.55,8.5,32,1.5,"	Bura T, et al. High-Performance Solution-Processed Solar Cells and Ambipolar Behavior in Organic Field-Effect Transistors with Thienyl-BODIPY Scaffoldings. J. Am. Chem. Soc. 134, 17404-17407 (2012)."
2241,O=C1N(CC(CC)CCCC)C(C2=CC=C(C3=CC(CCCCCC)=CS3)S2)C4C1=C(C5=CC=C(C6=CC(CCCCCC)=CS6)S5)N(CC(CC)CCCC)C4=O,M2,,,0.88,6.83,43.3,2.59,"	Liu Y, et al. Solution processable low bandgap small molecule donors with naphthalene end-groups for organic solar cells. Synth. Met. 162, 1665-1671 (2012)."
2242,O=C1N(CC(CC)CCCC)C(C2=CC=C(C3=CC(CCCCCC)=C(C4=CC=C5C=CC=CC5=C4)S3)S2)C6C1=C(C7=CC=C(C8=CC(CCCCCC)=C(C9=CC=C%10C=CC=CC%10=C9)S8)S7)N(CC(CC)CCCC)C6=O,M3,,,0.83,5.14,37.4,1.6,"	Liu Y, et al. Solution processable low bandgap small molecule donors with naphthalene end-groups for organic solar cells. Synth. Met. 162, 1665-1671 (2012)."
2243,C1(C2=N/C3=C\C4=C5C=CC=CC5=C(/C=C(N=C6/C=C(N/C7=C\2)/C8=C7C=CC=C8)/C9=C6C=CC=C9)N4)=C3C=CC=C1,BP,,,0.81,6.57,44.7,2.37,"	Liu Y, et al. Solution processable low bandgap small molecule donors with naphthalene end-groups for organic solar cells. Synth. Met. 162, 1665-1671 (2012)."
2244,CCCCCCCCC(C1=C2C=CC(C3=CC=C(C4=CC=C(C5=CC=C(C6=CC=CC=C6)S5)C7=NN(CC(CC)CCCC)N=C74)S3)=C1)(CCCCCCCC)C(C2=N8)=NC9=C8C(CCCCCCCC)(CCCCCCCC)C%10=CC(C%11=CC=CC=C%11)=CC=C%109,PIPY¨CDTBTA,,,0.76,8.91,65,4.41,"	Tsuji H, Ota Y, Furukawa S, Mitsui C, Sato Y, Nakamura E. Tripyridyltruxenes: Thermally Stable Cathode Buffer Materials for Organic Thin-Film Solar Cells. Asian Journal of Organic Chemistry 1, 34-37 (2012)."
2245,C1(N(C2=CC=C(C3=CC=C(C4=CC=C(C5=CC=C(C6=CC=C(C(C7)=CC=C7C8=CC=C(C=C8)N(C9=CC=CC=C9)C%10=CC=CC=C%10)S6)C%11=NSN=C%115)S4)S3)C=C2)C%12=CC=CC=C%12)=CC=CC=C1,1,,,0.78,2.05,48,0.77,"	Liu X, et al. Development of a new diindenopyrazine-benzotriazole copolymer for multifunctional application in organic field-effect transistors, polymer solar cells and light-emitting diodes. Org. Electron. 13, 1671-1679 (2012)."
2246,FC1=C(C2=CC=C(C(S3)=CC=C3C4=CC=C(C=C4)N(C5=CC=CC=C5)C6=CC=CC=C6)S2)C7=NSN=C7C(C8=CC=C(C(S9)=CC=C9C%10=CC=C(C=C%10)N(C%11=CC=CC=C%11)C%12=CC=CC=C%12)S8)=C1,2,,,0.81,7.65,38,2.38,"	Cho N, Song K, Lee JK, Ko J. Facile Synthesis of Fluorine-Substituted Benzothiadiazole-Based Organic Semiconductors and Their Use in Solution-Processed Small-Molecule Organic Solar Cells. Chemistry-a European Journal 18, 11433-11439 (2012)."
2247,FC1=C(C2=CC=C(C(S3)=CC=C3C4=CC=C(C=C4)N(C5=CC=CC=C5)C6=CC=CC=C6)S2)C7=NSN=C7C(C8=CC=C(C(S9)=CC=C9C%10=CC=C(C=C%10)N(C%11=CC=CC=C%11)C%12=CC=CC=C%12)S8)=C1F,3,,,0.85,8.51,41,2.95,"	Cho N, Song K, Lee JK, Ko J. Facile Synthesis of Fluorine-Substituted Benzothiadiazole-Based Organic Semiconductors and Their Use in Solution-Processed Small-Molecule Organic Solar Cells. Chemistry-a European Journal 18, 11433-11439 (2012)."
2248,N#C/C(C#N)=C\C(C1=NSN=C12)=CC=C2C3=CC=C(N(C4=CC=CC=C4)C5=CC=CC=C5)S3,DPDCTB,,,0.81,8.03,42,2.74,"	Cho N, Song K, Lee JK, Ko J. Facile Synthesis of Fluorine-Substituted Benzothiadiazole-Based Organic Semiconductors and Their Use in Solution-Processed Small-Molecule Organic Solar Cells. Chemistry-a European Journal 18, 11433-11439 (2012)."
2249,CC(C=C1)=CC=C1N(C(C=C2)=CC=C2C3=CC=C(/C=C(C#N)\C#N)C4=NSN=C43)C5=CC=C(C)C=C5,DTDCPB,,,0.88,12.99,49,5.6,"	Chen Y-H, et al. Vacuum-Deposited Small-Molecule Organic Solar Cells with High Power Conversion Efficiencies by Judicious Molecular Design and Device Optimization. J. Am. Chem. Soc. 134, 13616-13623 (2012)."
2250,OC1=C(C2C([O-])C(C3=C(O)C=C(C=C3O)N(C4=CC=CC=C4)C5=CC=CC=C5)C2[O-])C(O)=CC(N(C6=CC=CC=C6)C7=CC=CC=C7)=C1,DPSQ,,,0.93,13.48,53,6.6,"	Chen Y-H, et al. Vacuum-Deposited Small-Molecule Organic Solar Cells with High Power Conversion Efficiencies by Judicious Molecular Design and Device Optimization. J. Am. Chem. Soc. 134, 13616-13623 (2012)."
2251,FC1=C(C(S2)=CC3=C2C(SC(C(C4=NSN=C45)=C(F)C=C5C6=CC=C(C7=CC=C(CCCCCC)S7)S6)=C8)=C8[Si]3(CC(CC)CCCC)CC(CC)CCCC)C9=NSN=C9C(C%10=CC=C(C%11=CC=C(CCCCCC)S%11)S%10)=C1,p©\DTS(PTTh2)2,,,0.96,7,71,4.8,"	Zimmerman JD, et al. Independent Control of Bulk and Interfacial Morphologies of Small Molecular Weight Organic Heterojunction Solar Cells. Nano Lett. 12, 4366-4371 (2012)."
2252,CCCCCCN1C(/C=C(C#N)/C2=CC=C([N+]([O-])=O)C=C2)=CC=C1N=NC3=CC=C(N=NC4=CC=C(/C=C(C#N)/C5=CC=C([N+]([O-])=O)C=C5)N4CCCCCC)C=C3,P,,,0.82,10.8,65,5.8,"	van der Poll TS, Love JA, Thuc-Quyen N, Bazan GC. Non-Basic High-Performance Molecules for Solution-Processed Organic Solar Cells. Adv. Mater. 24, 3646-3649 (2012)."
2253,CCCCC(CC)CN1C(/C=C(C#N)/C2=CC=C([N+]([O-])=O)C=C2)=CC=C1N=NC3=CC(C(C=C(N=NC4=CC=C(/C=C(C#N)/C5=CC=C([N+]([O-])=O)C=C5)N4CC(CC)CCCC)C=C6)=C6N7CCCCCC)=C7C=C3,C,,,0.94,5.36,0.48,2.41,"	Sharma GD, Mikroyannidis JA, Sharma SS, Thomas KRJ. Bulk heterojunction organic photovoltaic devices based on small molecules featuring pyrrole and carbazole and 2-(4-nitrophenyl)acrylonitrile acceptor segments as donor and fullerene derivatives as acceptor. Dyes and Pigments 94, 320-329 (2012)."
2254,CC1=C(C2=CC=C(C3=CC=C(C4=CC=C(C5=C(C)C(C)=C(/C=C(C#N)\[N+]#[C-])S5)S4)S3)S2)SC(/C=C([N+]#[C-])\C#N)=C1C,1,,,0.86,7,52,3.13,"	Sharma GD, Mikroyannidis JA, Sharma SS, Thomas KRJ. Bulk heterojunction organic photovoltaic devices based on small molecules featuring pyrrole and carbazole and 2-(4-nitrophenyl)acrylonitrile acceptor segments as donor and fullerene derivatives as acceptor. Dyes and Pigments 94, 320-329 (2012)."
2255,CC1=C(C2=CC=C(/C=C([N+]#[C-])\C#N)S2)SC(C3=CC=C(C4=C(C)C(C)=C(C5=CC=C(/C=C(C#N)\[N+]#[C-])S5)S4)S3)=C1C,2,,,0.91,9.6,63,4.8,"	Fitzner R, et al. Correlation of pi-Conjugated Oligomer Structure with Film Morphology and Organic Solar Cell Performance. J. Am. Chem. Soc. 134, 11064-11067 (2012)."
2256,CC1=C(C2=CC=C(C3=CC=C(/C=C(C#N)\[N+]#[C-])S3)S2)SC(C4=CC=C(C5=CC=C(/C=C([N+]#[C-])\C#N)S5)S4)=C1C,3,,,0.95,9.4,62,4.8,"	Fitzner R, et al. Correlation of pi-Conjugated Oligomer Structure with Film Morphology and Organic Solar Cell Performance. J. Am. Chem. Soc. 134, 11064-11067 (2012)."
2257,CCCCCCCCOC(C(OCCCCCCCC)=C1)=CC(C1=C(C2=CC=C(C3=CC(C(CCCCCCCCC)(CCCCCCCCC)C4=C5C=CC(C6=CC=C(C(C7=CC=C(C)C=C7)C8=CC=C(C9=CC(C(CCCCCCCCC)(CCCCCCCCC)C%10=C%11C=CC(C)=C%10)=C%11C=C9)C=C8)C=C6)=C4)=C5C=C3)S2)C=C%12)=C%12C%13=CC=C(C)S%13,P1a,,,0.95,11.5,63,6.9,"	Fitzner R, et al. Correlation of pi-Conjugated Oligomer Structure with Film Morphology and Organic Solar Cell Performance. J. Am. Chem. Soc. 134, 11064-11067 (2012)."
2258,CC1(C)C2=C(C=CC=C2)C3=CC=C(N(C4=CC=C(C(C=CC=C5)=C5C6(C)C)C6=C4)C7=CC=C(C=C(C8=CC=C([N+]([O-])=O)S8)S9)C9=C7)C=C31,1,,,0.84,4.6,54,2.3,"	Mangold H, Howard IA, Janietz S, Laquai F. Controlled energy shuttling in terpolymers enabling independent optimization of absorption and transport properties in organic solar cell materials. Appl. Phys. Lett. 101,  (2012)."
2259,CC1(C)C2=C(C=CC=C2)C3=CC=C(N(C4=CC=C(C(C=CC=C5)=C5C6(C)C)C6=C4)C7=CC=C(C=C(C8=CC=C(/C=C/C(OC(C(C)(C)C)=C/9)=CC9=C(C#N)/C#N)S8)S%10)C%10=C7)C=C31,2,,,0.75,8.54,33,2.14,"	Kim J, Cho N, Ko HM, Kim C, Lee JK, Ko J. Push-pull organic semiconductors comprising of bis-dimethylfluorenyl amino benzo b thiophene donor and various acceptors for solution processed small molecule organic solar cells. Sol. Energy Mater. Sol. Cells 102, 159-166 (2012)."
2260,CC1(C)C2=C(C=CC=C2)C3=CC=C(N(C4=CC=C(C(C=CC=C5)=C5C6(C)C)C6=C4)C7=CC=C(C=C(C8=CC=C(/C=C/C9=C(C#N)/C(OC9(C)C)=C(C#N)\C#N)S8)S%10)C%10=C7)C=C31,3,,,79,8.22,34,2.22,"	Kim J, Cho N, Ko HM, Kim C, Lee JK, Ko J. Push-pull organic semiconductors comprising of bis-dimethylfluorenyl amino benzo b thiophene donor and various acceptors for solution processed small molecule organic solar cells. Sol. Energy Mater. Sol. Cells 102, 159-166 (2012)."
2261,CC(S1)=CC(CCCCCCCC)=C1C2=C(CCCCCCCC)C=C(C(S3)=CC=C3C4=CC=C(C(S5)=CC(CCCCCCCC)=C5C(S6)=C(CCCCCCCC)C=C6C(C=C7)=CC=C7C(C(N(CC(CC)CCCC)C8=O)=O)=C8C9=CC=C(C)C=C9)S4)S2,PMLTQT,,,0.8,9.64,42,3.22,"	Kim J, Cho N, Ko HM, Kim C, Lee JK, Ko J. Push-pull organic semiconductors comprising of bis-dimethylfluorenyl amino benzo b thiophene donor and various acceptors for solution processed small molecule organic solar cells. Sol. Energy Mater. Sol. Cells 102, 159-166 (2012)."
2262,CC1=CC=C(C(S2)=CC3=C2C=C(C(S4)=CC=C4C(S5)=CC(CCCCCCCC)=C5C(C=C6)=CC=C6C(C(N(CC(CC)CCCC)C7=O)=O)=C7C8=CC=C(C9=C(CCCCCCCC)C=C(C)S9)C=C8)S3)S1,PMLT2T,,,0.7,7.9,19,0.85,"	Chan L-H, Juang S-Y, Chen M-C, Lin Y-J. A new series of random conjugated copolymers containing 3,4-diphenyl-maleimide and thiophene units for organic photovoltaic cell applications. Polymer 53, 2334-2346 (2012)."
2263,CC1=CC=C(C2=CC(S3)=C(S2)C4=C3C=C(C(S5)=CC=C5C(S6)=CC(CCCCCCCC)=C6C(C=C7)=CC=C7C(C(N(CC(CC)CCCC)C8=O)=O)=C8C9=CC=C(C%10=C(CCCCCCCC)C=C(C)S%10)C=C9)S4)S1,PMLT3T,,,0.7,7.9,20,1.08,"	Chan L-H, Juang S-Y, Chen M-C, Lin Y-J. A new series of random conjugated copolymers containing 3,4-diphenyl-maleimide and thiophene units for organic photovoltaic cell applications. Polymer 53, 2334-2346 (2012)."
2264,CC1=C(CCCCCC)C=C(C2=CC=C(/C(C3=CC=C(/C(C4=CC=C(C5=CC(CCCCCC)=C(C)S5)C=C4)=C6N=C7C=C\6)N3[Zn]N8/C(C=C/C8=C7\C9=CC=C(C%10=CC(CCCCCC)=C(C)S%10)C=C9)=C%11/C%12=CC=C(C%13=CC(CCCCCC)=C(C)S%13)C=C%12)=C%14C=CC%11=N\%14)C=C2)S1,TTP1,,,0.74,7.4,22,1.2,"	Chan L-H, Juang S-Y, Chen M-C, Lin Y-J. A new series of random conjugated copolymers containing 3,4-diphenyl-maleimide and thiophene units for organic photovoltaic cell applications. Polymer 53, 2334-2346 (2012)."
2265,CC1=C(CCCCCC)C=C(C2=CC=C(C3=CC=C(/C(C4=CC=C5N4[Zn]N6/C(C=C/C6=C7\C8=CC=C(C9=CC=C(C%10=CC(CCCCCC)=C(C)S%10)S9)C=C8)=C(C%11=CC=C(C%12=CC=C(C%13=CC(CCCCCC)=C(C)S%13)S%12)C=C%11)\C(C=C/%14)=NC%14=C5\C%15=CC=C(C%16=CC=C(C%17=CC(CCCCCC)=C(C)S%17)S%16)C=C%15)=C%18N=C7C=C/%18)C=C3)S2)S1,TTP2,,,0.688,2.143,,0.45,"	Cho EH, Chae SH, Kim K, Lee SJ, Joo J. Photovoltaic characteristics of organic solar cells using Zn-porphyrin derivatives with controlled pi-conjugation structures. Synth. Met. 162, 813-819 (2012)."
2266,CC1=C(CCCCCC)C=C(C2=CC=C(C3=CC=C(C4=CC=C(/C(C5=CC=C(/C(C6=CC=C(C7=CC=C(C8=CC=C(C9=CC(CCCCCC)=C(C)S9)S8)S7)C=C6)=C%10N=C%11C=C\%10)N5[Zn]N%12/C(C=C/C%12=C%11\C%13=CC=C(C%14=CC=C(C%15=CC=C(C%16=CC(CCCCCC)=C(C)S%16)S%15)S%14)C=C%13)=C%17/C%18=CC=C(C%19=CC=C(C%20=CC=C(C%21=CC(CCCCCC)=C(C)S%21)S%20)S%19)C=C%18)=C%22C=CC%17=N\%22)C=C4)S3)S2)S1,TTP3,,,0.664,1.951,,0.36,"	Cho EH, Chae SH, Kim K, Lee SJ, Joo J. Photovoltaic characteristics of organic solar cells using Zn-porphyrin derivatives with controlled pi-conjugation structures. Synth. Met. 162, 813-819 (2012)."
2267,CC1=C(CCCCCC)C=C(C2=CC=C(C#C/C(C3=N/C(C=C3)=C4/C5=CC=CC=C5)=C(C=C/6)/N7C6=C(C8=CC=CC=C8)/C(C=C/9)=NC9=C(C#CC%10=CC=C(C%11=CC(CCCCCC)=C(C)S%11)S%10)/C%12=CC=C4N%12[Zn]7)S2)S1,TTP4,,,0.653,1.847,,0.32,"	Cho EH, Chae SH, Kim K, Lee SJ, Joo J. Photovoltaic characteristics of organic solar cells using Zn-porphyrin derivatives with controlled pi-conjugation structures. Synth. Met. 162, 813-819 (2012)."
2268,CCCCCCC1=CC=C(C2=CC=C(C3=CC(S(C4=C5C=CC(C6=CC=C(C7=CC=C(CCCCCC)C=C7)S6)=C4)(=O)=O)=C5C=C3)S2)C=C1,37HPTDBTSO,,,0.556,5.287,,1,"	Cho EH, Chae SH, Kim K, Lee SJ, Joo J. Photovoltaic characteristics of organic solar cells using Zn-porphyrin derivatives with controlled pi-conjugation structures. Synth. Met. 162, 813-819 (2012)."
2269,CC1=C(CCCCCC)C=C(C2=CC=C(C#C/C(C3=N/C(C=C3)=C4/C5=C(OCCCCCC)C=CC=C5OCCCCCC)=C(C=C/6)/N7C6=C(C8=C(OCCCCCC)C=CC=C8OCCCCCC)/C(C=C/9)=NC9=C(C#CC%10=CC=C(C%11=CC(CCCCCC)=C(C)S%11)S%10)/C%12=CC=C4N%12[Zn]7)S2)S1,TTP5,,,0.85,2.75,35,0.84,"	Fujii S, et al. Synthesis of novel thiophene-phenylene oligomer derivatives with a dibenzothiophene-5,5-dioxide core for use in organic solar cells. Phys. Status Solidi B-Basic Solid State Phys. 249, 2648-2651 (2012)."
2270,CC1(C)C2=C(C3=C1C=CC=C3)C=CC(N(C4=CC(C(C)(C)C5=C6C=CC=C5)=C6C=C4)C7=CC=C(C8=CC=C(C9=CC=C([N+]([O-])=O)S9)S8)C=C7)=C2,1,,,0.621,4.129,,0.76,"	Cho EH, Chae SH, Kim K, Lee SJ, Joo J. Photovoltaic characteristics of organic solar cells using Zn-porphyrin derivatives with controlled pi-conjugation structures. Synth. Met. 162, 813-819 (2012)."
2271,CC1(C)C2=C(C3=C1C=CC=C3)C=CC(N(C4=CC(C(C)(C)C5=C6C=CC=C5)=C6C=C4)C7=CC=C(C8=CC=C(C9=CC=C(/C=C/C(OC(C(C)(C)C)=C/%10)=CC%10=C(C#N)/C#N)S9)S8)C=C7)=C2,2,,,0.83,8.19,40,2.7,"	Cho N, Kim J, Song K, Lee JK, Ko J. Synthesis and characterization of push-pull organic semiconductors with various acceptors for solution-processed small molecule organic solar cells. Tetrahedron 68, 4029-4036 (2012)."
2272,CC1(C)C2=C(C3=C1C=CC=C3)C=CC(N(C4=CC(C(C)(C)C5=C6C=CC=C5)=C6C=C4)C7=CC=C(C8=CC=C(C9=CC=C(/C=C/C%10=C([N+]#[C-])/C(OC%10(C)C)=C(C#N)\[N+]#[C-])S9)S8)C=C7)=C2,3,,,0.85,6.8,35,2.01,"	Cho N, Kim J, Song K, Lee JK, Ko J. Synthesis and characterization of push-pull organic semiconductors with various acceptors for solution-processed small molecule organic solar cells. Tetrahedron 68, 4029-4036 (2012)."
2273,CCCCCCC(S1)=CC=C1C2=CC=C(C3=CC=C(C(N(CCCCCC)C4=O)=C(C4=C(C5=CC=C(C6=CC=C(C7=CC=C(CCCCCC)S7)S6)S5)N8CCCCCC)C8=O)S3)S2,DPPTh,,,0.8,6.26,33,1.68,"	Cho N, Kim J, Song K, Lee JK, Ko J. Synthesis and characterization of push-pull organic semiconductors with various acceptors for solution-processed small molecule organic solar cells. Tetrahedron 68, 4029-4036 (2012)."
2274,CCCCCCC(S1)=CC=C1C2=CC=C(C(C=C3)=CC=C3C(N(CCCCCC)C4=O)=C(C4=C(C5=CC=C(C6=CC=C(C7=CC=C(CCCCCC)S7)S6)C=C5)N8CCCCCC)C8=O)S2,DPPPhe,,,0.47,4.2,40,0.79,"	Seo JH. Electronic properties of small molecule-diketopyrrolopyrrole derivatives and a correlation with the open circuit voltage in organic solar cells. Synth. Met. 162, 748-752 (2012)."
2275,O=C1N(CCCCCC)C(C2=NC(C3=CC=C(C4=CC=C(CCCCCC)S4)S3)=CC=C2)=C5C1=C(C6=CC=C(C7=CC=C(C8=CC=C(CCCCCC)S8)S7)N=C6)N(CCCCCC)C5=O,DPPPyr,,,0.87,4.5,37,1.45,"	Seo JH. Electronic properties of small molecule-diketopyrrolopyrrole derivatives and a correlation with the open circuit voltage in organic solar cells. Synth. Met. 162, 748-752 (2012)."
2276,CCCCCCCCCCC1=C(SC(C2=CC(CCCCCCCCCC)=C(C3=CC4=C(C(C=CC5=C6SC(C7=C(CCCCCCCCCC)C=C(C8=CC(CCCCCCCCCC)=C(S8)C(S9)=NC%10=C9N=C(S%10)C(S%11)=C(CCCCCCCCCC)C=C%11C(C=C%12)=CC=C%12N(C%13=CC=CC=C%13)C%14=CC=CC=C%14)S7)=C5)=C6C=C4)S3)S2)=C1)C(S%15)=NC%16=C%15N=C(S%16)C(S%17)=C(CCCCCCCCCC)C=C%17C(C=C%18)=CC=C%18N(C%19=CC=CC=C%19)C%20=CC=CC=C%20,NDT(TTz)2,,,0.5,2.7,41,0.55,"	Seo JH. Electronic properties of small molecule-diketopyrrolopyrrole derivatives and a correlation with the open circuit voltage in organic solar cells. Synth. Met. 162, 748-752 (2012)."
2277,C12=CC3=C(C4=CC=CC=C4)C5=CC6=CC=CC=C6C=C5C(C7=CC=CC=C7)=C3C=C1C=CC=C2,DP-penta,,,0.75,5.1,38,1.44,"	Dutta P, Park H, Lee W-H, Kang I-N, Lee S-H. A crystalline D-pi-A organic small molecule with naphtho 1,2-b:5,6-b ' dithiophene-core for solution processed organic solar cells. Org. Electron. 13, 3183-3194 (2012)."
2278,C12=CC3=C(C4=CC=C(C5=CC=CC=C5)C=C4)C6=CC7=CC=CC=C7C=C6C(C8=CC=C(C9=CC=CC=C9)C=C8)=C3C=C1C=CC=C2,DB-penta,,,0.71,1.22,40.8,0.35,"	Chou C-T, Lin C-H, Tai Y, Liu C-HJ, Chen L-C, Chen K-H. Stacking Orientation Mediation of Pentacene and Derivatives for High Open-Circuit Voltage Organic Solar Cells. J. Phys. Chem. Lett. 3, 1079-1083 (2012)."
2279,N#C/C(C#N)=C\C1=CC=C(C(S2)=CC=C2C3=CC=C(C4=CC=C(/C=C(C#N)\C#N)S4)S3)S1,DCV4T,,,0.83,1.46,55,0.71,"	Chou C-T, Lin C-H, Tai Y, Liu C-HJ, Chen L-C, Chen K-H. Stacking Orientation Mediation of Pentacene and Derivatives for High Open-Circuit Voltage Organic Solar Cells. J. Phys. Chem. Lett. 3, 1079-1083 (2012)."
2280,CC(C=C1)=CC=C1N(C2=CC=C(C3=NC=C(/C=C(C#N)\C#N)C=N3)S2)C4=CC=C(C)C=C4,DTDCTP,,,0.98,6.49,48.4,3,"	Koerner C, et al. Probing the effect of substrate heating during deposition of DCV4T:C-60 blend layers for organic solar cells. Org. Electron. 13, 623-631 (2012)."
2281,CCCCCCCCN1N=C2C(C3=CC=C(/C=C/C4=CC=C(N(C5=CC=CC=C5)C6=CC=C(OCC(CC)CCCC)C=C6)C=C4)S3)=CC=C(C7=CC=C(/C=C/C8=CC=C(N(C9=CC=CC=C9)C%10=CC=C(OCC(CC)CCCC)C=C%10)C=C8)S7)C2=N1,TPA¨CDTBTz¨CTPA,,,0.94,11.3,52,5.5,"	Lin H-W, et al. Device Engineering for Highly Efficient Top-Illuminated Organic Solar Cells with Microcavity Structures. Adv. Mater. 24, 2269-2272 (2012)."
2282,CCCCCCC1=C(/C=C/C2=C3C(OCCO3)=C(/C=C/C4=C(CCCCCC)C(CCCCCC)=C(/C=C(C#N)/C#N)S4)S2)SC(/C=C(C#N)/C#N)=C1CCCCCC,smL01,,,0.74,4.34,29,0.93,"	Liu B, Zou Y-p, Long M, He Y-h, Zhong H, Li Y-f. Synthesis and photovoltaic properties of a solution-processable organic molecule containing dithienylbenzotriazole and triphenylamine. Synth. Met. 162, 630-635 (2012)."
2283,C12=CC3=CC4=CC=CC=C4C=C3C=C1C=CC=C2,Tetracene,,,1.01,¡ª,63.7,3.5,"	Montcada NF, et al. High open circuit voltage in efficient thiophene-based small molecule solution processed organic solar cells. Org. Electron. 14, 2826-2832 (2013)."
2284,CCCCC(CC)CC1(CC(CC)CCCC)C2=C(C3=NC(C(CC(CC)CCCC)(CC(CC)CCCC)C4=C5C=CC(C6=CC=CC=C6)=C4)=C5N=C31)C=CC(C7=CC=C(C8=CC=C(C9=CC=C(C%10=CC=CC=C%10)C9)C%11=NSN=C%118)S7)=C2,PIPYDBT,,,0.69,2.4,56,0.94,"	Graham KR, et al. Re-evaluating the Role of Sterics and Electronic Coupling in Determining the Open-Circuit Voltage of Organic Solar Cells. Adv. Mater. 25, 6076-6082 (2013)."
2285,CCCCC(CC)CC1(CC(CC)CCCC)C2=C(C3=NC(C(CC(CC)CCCC)(CC(CC)CCCC)C4=C5C=CC(C6=CC=CC=C6)=C4)=C5N=C31)C=CC(C7=CC=C(C8=C9N=C(C%10=CC=CC=C%10)C(C%11=CC=CC=C%11)=NC9=C(C%12=CC=C(C%13=CC=CC=C%13)S%12)C=C8)S7)=C2,PIPYDTQ,,,0.81,3.51,43.5,1.23,"	Chen S, et al. Ladder-type Diindenopyrazine Based Conjugated Copolymers for Organic Solar Cells with High Open-circuit Voltages. Chin. J. Chem . 31, 1409-1417 (2013)."
2286,CCCCC(CC)CC1(CC(CC)CCCC)C2=C(C3=NC(C(CC(CC)CCCC)(CC(CC)CCCC)C4=C5C=CC(C6=CC=CC=C6)=C4)=C5N=C31)C=CC(C7=CC=C(C8=C9N=C(C%10=CC=C(F)C=C%10)C(C%11=CC=C(F)C=C%11)=NC9=C(C%12=CC=C(C%13=CC=CC=C%13)S%12)C=C8)S7)=C2,PIPYDFTQ,,,1,5.73,44.2,2.53,"	Chen S, et al. Ladder-type Diindenopyrazine Based Conjugated Copolymers for Organic Solar Cells with High Open-circuit Voltages. Chin. J. Chem . 31, 1409-1417 (2013)."
2287,O=C(C1=C2C(/C=C/C3=CC=C(/C=C(C4=CC=C([N+]([O-])=O)C=C4)\C#N)C=C3)=CC=C1/C=C/C5=CC=C(/C=C(C6=CC=C([N+]([O-])=O)C=C6)\C#N)C=C5)N(C7CCCCC7)C2=O,SM,,,0.94,4,38.4,1.45,"	Chen S, et al. Ladder-type Diindenopyrazine Based Conjugated Copolymers for Organic Solar Cells with High Open-circuit Voltages. Chin. J. Chem . 31, 1409-1417 (2013)."
2288,C1(/C=C\C2=NC(C3C(C=CC=C4)=C4C5N3)C6=C2C=CC=C6)=C7C(C=CC=C7)=C(C8=NC(/C=C\5)C9=C8C=CC=C9)N1,BPc,,,0.84,8.8,56,4.14,"	Sharma GD, Mikroyannidis JA, Kurchania R, Thomas KRJ. Organic bulk heterojunction solar cells based on solution processable small molecules (A-pi-A) featuring 2-(4-nitrophenyl) acrylonitrile acceptors and phthalimide-based pi-linkers. Journal of Materials Chemistry 22, 13986-13995 (2012)."
2289,CCCCCCC(S1)=CC=C1C2=CC(C3=C4SC(C5=CC=C(CCCCCC)S5)=C3)=C(S2)C(C4=C6)=CC7=C6C8=C(C7(CCCCCC)CCCCCC)C9=C(C(CCCCCC)(CCCCCC)C%10=C9C=C%11C(C(SC(C%12=CC=C(CCCCCC)S%12)=C%13)=C%13C%14=C%11SC(C%15=CC=C(CCCCCC)S%15)=C%14)=C%10)C%16=C8C(CCCCCC)(CCCCCC)C%17=C%16C=C%18C(C(SC(C%19=CC=C(CCCCCC)S%19)=C%20)=C%20C%21=C%18SC(C%22=CC=C(CCCCCC)S%22)=C%21)=C%17,1a,,,0.36,1.14,40,0.16,"	Saeki H, Misaki M, Kuzuhara D, Yamada H, Ueda Y. Fabrication of Phase-Separated Benzoporphycene/ 6,6 -Phenyl-C-61-Butyric Acid Methyl Ester Films for Use in Organic Photovoltaic Cells. Jpn. J. Appl. Phys. 52,  (2013)."
2290,CCCCCCC(C1=C2C=C3C(C(SC(C4=CC=C(C5=CC=C(CCCCCC)S5)S4)=C6)=C6C7=C3SC(C8=CC=C(C9=CC=C(CCCCCC)S9)S8)=C7)=C1)(CCCCCC)C%10=C2C(C(CCCCCC)(CCCCCC)C%11=C%12C=C%13C(C(SC(C%14=CC=C(C%15=CC=C(CCCCCC)S%15)S%14)=C%16)=C%16C%17=C%13SC(C%18=CC=C(C%19=CC=C(CCCCCC)S%19)S%18)=C%17)=C%11)=C%12C%20=C%10C%21=C(C=C(C(SC(C%22=CC=C(C%23=CC=C(CCCCCC)S%23)S%22)=C%24)=C%24C%25=C%26SC(C%27=CC=C(C%28=CC=C(CCCCCC)S%28)S%27)=C%25)C%26=C%21)C%20(CCCCCC)CCCCCC,1b,,,1.07,2.31,27,0.67,"	Yang X, Zheng Q, Tang C, Cai D, Chen S-C, Ma Y. Star-shaped chromophores based on a benzodithiophene fused truxene core for solution processed organic solar cells. Dyes and Pigments 99, 366-373 (2013)."
2291,CCCCCCC(C1=C2C=C3C(C(SC(C4=CC=C(C5=CC=C(C6=CC=C(CCCCCC)S6)S5)S4)=C7)=C7C8=C3SC(C9=CC=C(C%10=CC=C(C%11=CC=C(CCCCCC)S%11)S%10)S9)=C8)=C1)(CCCCCC)C%12=C2C(C(CCCCCC)(CCCCCC)C%13=C%14C=C%15C(C(SC(C%16=CC=C(C%17=CC=C(C%18=CC=C(CCCCCC)S%18)S%17)S%16)=C%19)=C%19C%20=C%15SC(C%21=CC=C(C%22=CC=C(C%23=CC=C(CCCCCC)S%23)S%22)S%21)=C%20)=C%13)=C%14C%24=C%12C%25=C(C=C(C(SC(C%26=CC=C(C%27=CC=C(C%28=CC=C(CCCCCC)S%28)S%27)S%26)=C%29)=C%29C%30=C%31SC(C%32=CC=C(C%33=CC=C(C%34=CC=C(CCCCCC)S%34)S%33)S%32)=C%30)C%31=C%25)C%24(CCCCCC)CCCCCC,1c,,,0.95,4.63,29.1,1.28,"	Yang X, Zheng Q, Tang C, Cai D, Chen S-C, Ma Y. Star-shaped chromophores based on a benzodithiophene fused truxene core for solution processed organic solar cells. Dyes and Pigments 99, 366-373 (2013)."
2292,CCCCCCC(C1=C2C=C3C(C(SC(C4=CC=C(C5=CC=C(C6=CC=C(CCCCCC)S6)C7=NSN=C75)S4)=C8)=C8C9=C3SC(C%10=CC=C(C%11=CC=C(C%12=CC=C(CCCCCC)S%12)C%13=NSN=C%13%11)S%10)=C9)=C1)(CCCCCC)C%14=C2C(C(CCCCCC)(CCCCCC)C%15=C%16C=C%17C(C(SC(C%18=CC=C(C%19=CC=C(C%20=CC=C(CCCCCC)S%20)C%21=NSN=C%21%19)S%18)=C%22)=C%22C%23=C%17SC(C%24=CC=C(C%25=CC=C(C%26=CC=C(CCCCCC)S%26)C%27=NSN=C%27%25)S%24)=C%23)=C%15)=C%16C%28=C%14C%29=C(C=C(C(SC(C%30=CC=C(C%31=CC=C(C%32=CC=C(CCCCCC)S%32)C%33=NSN=C%33%31)S%30)=C%34)=C%34C%35=C%36SC(C%37=CC=C(C%38=CC=C(C%39=CC=C(CCCCCC)S%39)C%40=NSN=C%40%38)S%37)=C%35)C%36=C%29)C%28(CCCCCC)CCCCCC,1d,,,0.97,7.08,34.9,2.4,"	Yang X, Zheng Q, Tang C, Cai D, Chen S-C, Ma Y. Star-shaped chromophores based on a benzodithiophene fused truxene core for solution processed organic solar cells. Dyes and Pigments 99, 366-373 (2013)."
2293,CCCCC1=C(C2=CC=C(/C=C(C#N)/C#N)S2)SC(C3=CC=C(C4=C(CCCC)C(CCCC)=C(C5=CC=C(/C=C(C#N)/C#N)S5)S4)S3)=C1CCCC,DCV5T-Bu4,,,0.86,5.67,31,1.51,"	Yang X, Zheng Q, Tang C, Cai D, Chen S-C, Ma Y. Star-shaped chromophores based on a benzodithiophene fused truxene core for solution processed organic solar cells. Dyes and Pigments 99, 366-373 (2013)."
2294,O=C(OCCCCCCCC)/C(C#N)=C\C1=CC(CCCCCCCC)=C(C2=CC(CCCCCCCC)=C(C3=CC(CCCCCCCC)=C(C(S4)=CC(C4=C5C6=CC=C(CCCCCCCC)S6)=C(C7=CC=C(CCCCCCCC)S7)C8=C5SC(C9=C(CCCCCCCC)C=C(C%10=C(CCCCCCCC)C=C(C%11=C(CCCCCCCC)C=C(C(C#N)C(OCCCCCCCC)=O)S%11)S%10)S9)=C8)S3)S2)S1,TBDTCNR,,,1.11,6.5,41,3,"	Schulz GL, et al. Optimization of solution-processed oligothiophene:fullerene based organic solar cells by using solvent additives. Beilstein Journal of Nanotechnology 4, 680-689 (2013)."
2295,N#C/C(C#N)=C/C1=CC(CCCCCCCC)=C(C2=CC(CCCCCCCC)=C(C3=CC(CCCCCCCC)=C(C(S4)=CC(C4=C5C6=CC=C(CCCCCCCC)S6)=C(C7=CC=C(CCCCCCCC)S7)C8=C5SC(C9=C(CCCCCCCC)C=C(C%10=C(CCCCCCCC)C=C(C%11=C(CCCCCCCC)C=C(C(C#N)C#N)S%11)S%10)S9)=C8)S3)S2)S1,TBDTCN,,,0.9,9.08,66,5.42,"	Patra D, et al. 2-Alkyl-5-thienyl-Substituted Benzo 1,2-b:4,5-b ' dithiophene-Based Donor Molecules for Solution-Processed Organic Solar Cells. ACS Appl. Mater. Interfaces 5, 9494-9500 (2013)."
2296,O=C1N(CC(CC)CCCC)C(C2=CC=CS2)=C3C1=C(C4=CC=C(C5=CC=C(C6=CC(C7=CC=C(C8=CC=C(C(N9CC(CC)CCCC)=C%10C(N(CC(CC)CCCC)C(C%11=CC=CS%11)=C%10C9=O)=O)S8)S7)=CC(C%12=CC=C(C%13=CC=C(C(N%14CC(CC)CCCC)=C%15C(N(CC(CC)CCCC)C(C%16=CC=CS%16)=C%15C%14=O)=O)S%13)S%12)=C6)S5)S4)N(CC(CC)CCCC)C3=O,3D-T-P,,,0.91,5.17,46,2.13,"	Patra D, et al. 2-Alkyl-5-thienyl-Substituted Benzo 1,2-b:4,5-b ' dithiophene-Based Donor Molecules for Solution-Processed Organic Solar Cells. ACS Appl. Mater. Interfaces 5, 9494-9500 (2013)."
2297,CCCCCCC1=C(C2=CC(C3=C(CCCCCC)C=C(C4=CC=C(C(N5CC(CC)CCCC)=C6C(N(CC(CC)CCCC)C(C7=CC=CS7)=C6C5=O)=O)S4)S3)=CC(C8=C(CCCCCC)C=C(C9=CC=C(C(N%10CC(CC)CCCC)=C%11C(N(CC(CC)CCCC)C(C%12=CC=CS%12)=C%11C%10=O)=O)S9)S8)=C2)SC(C%13=CSC(C(N(CC(CC)CCCC)C%14=O)=C%15C%14=C(C%16=CC=CS%16)N(CC(CC)CCCC)C%15=O)=C%13)=C1,3D-HT-P,,,0.68,4.8,33,1.16,"	Zhang S, et al. Phenyl-1,3,5-Trithienyl-Diketopyrrolopyrrole: A Molecular Backbone Potentially Affording High Efficiency for Solution-Processed Small-Molecule Organic Solar Cells through Judicious Molecular Design. Chemistry-an Asian Journal 8, 2407-2416 (2013)."
2298,O=C1C(CC(CC)CCCC)C(C2=CC=CS2)=C3C(C(CC(CC)CCCC)C(C4=CC=C(C5=CC=C(C6=CC(C7=CC=CS7)=CC(C8=CC=C(C9=CC=C(C%10=C%11C(C(CC(CC)CCCC)C(C%12=CC=CS%12)=C%11C(C%10CC(CC)CCCC)=O)=O)S9)S8)=C6)S5)S4)=C13)=O,2D-T-P,,,0.84,4.45,33,1.24,"	Zhang S, et al. Phenyl-1,3,5-Trithienyl-Diketopyrrolopyrrole: A Molecular Backbone Potentially Affording High Efficiency for Solution-Processed Small-Molecule Organic Solar Cells through Judicious Molecular Design. Chemistry-an Asian Journal 8, 2407-2416 (2013)."
2299,O=C1C(CC(CC)CCCC)C(C2=CC=C(C(S3)=CC(C3=C4C5=CC=C(CC(CC)CCCC)S5)=C(C6=CC=C(CC(CC)CCCC)S6)C7=C4C=C(C8=CC=C(C9=CC(C%10=CC=C(C(S%11)=CC(C%11=C%12C%13=CC=C(CC(CC)CCCC)S%13)=C(C%14=CC=C(CC(CC)CCCC)S%14)C%15=C%12C=CS%15)S%10)=CC(C%16=CC=C(C(C%17)=CC%18=C%17C(C%19=CC=C(CC(CC)CCCC)S%19)=C%20C=C(C%21=CC=C(C(C(CC(CC)CCCC)C(C%22=C(C%23=CC=CS%23)C%24CC(CC)CCCC)=O)=C%22C%24=O)S%21)CC%20=C%18C%25=CC=C(CC(CC)CCCC)S%25)S%16)=C9)S8)S7)S2)=C%26C(C(CC(CC)CCCC)C(C%27=CC=CS%27)=C1%26)=O,2D-B-T-P,,,0.7,3.87,29.9,0.81,"	Zhang S, et al. Phenyl-1,3,5-Trithienyl-Diketopyrrolopyrrole: A Molecular Backbone Potentially Affording High Efficiency for Solution-Processed Small-Molecule Organic Solar Cells through Judicious Molecular Design. Chemistry-an Asian Journal 8, 2407-2416 (2013)."
2300,O=C1N(CC(CC)CCCC)C(C2=CC=C(C(S3)=CC(C3=C4C5=CC=C(CC(CC)CCCC)S5)=C(C6=CC=C(CC(CC)CCCC)S6)C7=C4C=C(C8=CC=C(C9=CC(C%10=CC=C(C(S%11)=CC(C%11=C%12C%13=CC=C(CC(CC)CCCC)S%13)=C(C%14=CC=C(CC(CC)CCCC)S%14)C%15=C%12C=C(C%16=CC=C(C(C(CC(CC)CCCC)C(C%17=C(C%18=CC=CS%18)C%19CC(CC)CCCC)=O)=C%17C%19=O)S%16)S%15)S%10)=CC(C%20=CC=C(C(C%21)=CC%22=C%21C(C%23=CC=C(CC(CC)CCCC)S%23)=C%24C=C(C%25=CC=C(C(C(CC(CC)CCCC)C(C%26=C(C%27=CC=CS%27)C%28CC(CC)CCCC)=O)=C%26C%28=O)S%25)CC%24=C%22C%29=CC=C(CC(CC)CCCC)S%29)S%20)=C9)S8)S7)S2)=C%30C1=C(C%31=CC=CS%31)N(CC(CC)CCCC)C%30=O,3D-B-T-P,,,0.74,5.57,45.3,1.86,"	Zhang S, et al. Phenyl-1,3,5-Trithienyl-Diketopyrrolopyrrole: A Molecular Backbone Potentially Affording High Efficiency for Solution-Processed Small-Molecule Organic Solar Cells through Judicious Molecular Design. Chemistry-an Asian Journal 8, 2407-2416 (2013)."
2301,Cl[In]1N2C3=C4C=CC=CC4=C2/N=C5C6=C(C=CC=C6)C(/N=C7C8=C(C=CC=C8)/C(N/71)=N/C9=N/C(C%10=C9C=CC=C%10)=N\3)=N/5,ClInPc,,,0.77,7.69,59,3.6,"	Zhang S, et al. Phenyl-1,3,5-Trithienyl-Diketopyrrolopyrrole: A Molecular Backbone Potentially Affording High Efficiency for Solution-Processed Small-Molecule Organic Solar Cells through Judicious Molecular Design. Chemistry-an Asian Journal 8, 2407-2416 (2013)."
2302,O=C1N(CC(CC)CCCC)C(C2=CC=C(C3=CC4=C(N(CCCCCC)C5=C4C(N(CCCCCC)C6=C7C=CC=C6)=C7C8=C5C9=C(N8CCCCCC)C=CC=C9)C=C3)S2)=C%10C1=C(C%11=CC=C(C%12=CC%13=C(N(CCCCCC)C%14=C%13C(N(CCCCCC)C%15=C%16C=CC=C%15)=C%16C%17=C%14C%18=C(N%17CCCCCC)C=CC=C%18)C=C%12)S%11)N(CC(CC)CCCC)C%10=O,1,,,1.07,8.43,40,3.62,"	Sutty S, Williams G, Aziz H. Role of the donor material and the donor-acceptor mixing ratio in increasing the efficiency of Schottky junction organic solar cells. Org. Electron. 14, 2392-2400 (2013)."
2303,O=C1N(CC(CC)CCCC)C(C2=CC=C(C3=CC4=C(C=C3)C5=C(C6=C(N(CCCCCC)C7=C6C=CC=C7)C8=C5N(CCCCCC)C9=C8C=CC=C9)N4CCCCCC)S2)=C%10C1=C(C%11=CC=C(C%12=CC%13=C(C=C%12)C%14=C(C%15=C(N(CCCCCC)C%16=C%15C=CC=C%16)C%17=C%14N(CCCCCC)C%18=C%17C=CC=C%18)N%13CCCCCC)S%11)N(CC(CC)CCCC)C%10=O,2,,,0.63,14.6,58,5.3,"	Bura T, Leclerc N, Bechara R, Leveque P, Heiser T, Ziessel R. Triazatruxene-Diketopyrrolopyrrole Dumbbell-Shaped Molecules as Photoactive Electron Donor for High-Efficiency Solution Processed Organic Solar Cells. Adv. Energy Mater. 3, 1118-1124 (2013)."
2304,CCCCC(CC)CC1=CC=C(C2=C3C(C=C(C4=CC=C(C(N5CC(CC)CCCC)=C6C(N(CC(CC)CCCC)C(C7=CC=CS7)=C6C5=O)=O)S4)S3)=C(C8=CC=C(CC(CC)CCCC)S8)C9=C2C=C(C%10=CC=C(C(N%11CC(CC)CCCC)=C%12C(N(CC(CC)CCCC)C(C%13=CC=CS%13)=C%12C%11=O)=O)S%10)S9)S1,BDT-2DPP,,,0.65,13.1,52,4.4,"	Bura T, Leclerc N, Bechara R, Leveque P, Heiser T, Ziessel R. Triazatruxene-Diketopyrrolopyrrole Dumbbell-Shaped Molecules as Photoactive Electron Donor for High-Efficiency Solution Processed Organic Solar Cells. Adv. Energy Mater. 3, 1118-1124 (2013)."
2305,CC1=CC=C(N(C2=CC=C(C)C=C2)C3=CC=C(C4=CC(/C=C/C5=C(CCCCCC)C=C(C6=CC=C(C7=CSC=C7CCCCCC)C8=NSN=C86)S5)=C(OCC(CC)CCCC)C(/C=C/C9=C(CCCCCC)C=C(C%10=CC=C(C%11=CC(CCCCCC)=CS%11)C%12=NSN=C%12%10)S9)=C4)C=C3)C=C1,TPA-DTBT,,,0.84,11.97,57.6,5.79,"	Lin Y, Ma L, Li Y, Liu Y, Zhu D, Zhan X. A Solution-Processable Small Molecule Based on Benzodithiophene and Diketopyrrolopyrrole for High-Performance Organic Solar Cells. Adv. Energy Mater. 3, 1166-1170 (2013)."
2306,CC1=CC=C(N(C2=CC=C(C)C=C2)C3=CC=C(C4=CC(/C=C/C5=C(CCCCCC)C=C(C6=CC=C(C7=CC(CCCCCC)=C(C8=CC=C(CCCCCCCCCCCCCC)S8)S7)C9=NSN=C96)S5)=C(OCC(CC)CCCC)C(/C=C/C%10=C(CCCCCC)C=C(C%11=CC=C(C%12=CSC(C%13=CC=C(CCCCCCCCCCCCCC)S%13)=C%12CCCCCC)C%14=NSN=C%14%11)S%10)=C4)C=C3)C=C1,TPA-DTBT-TH,,,0.92,5.66,35,1.85,"	Wang C, et al. Synthesis and photovoltaic properties of organic small molecules containing triphenylamine and benzothiadiazole moieties with different terminal groups. Dyes and Pigments 98, 464-470 (2013)."
2307,O=C(OCCCCCCCC)/C(C#N)=C/C1=C(CCCCCC)C(C2=CC=C(C3=CC(CCCCCC)=C(/C=C/C4=CC(C5=CC=C(N(C6=CC=C(C)C=C6)C7=CC=C(C)C=C7)C=C5)=CC(/C=C/C8=C(CCCCCC)C=C(C9=CC=C(C%10=CC(CCCCCC)=C(/C=C(C#N)/C(OCCCCCCCC)=O)S%10)C%11=NSN=C%119)S8)=C4OCC(CC)CCCC)S3)C%12=NSN=C%122)=CS1,TPA-DTBT-CAO,,,0.76,4.3,25,0.83,"	Wang C, et al. Synthesis and photovoltaic properties of organic small molecules containing triphenylamine and benzothiadiazole moieties with different terminal groups. Dyes and Pigments 98, 464-470 (2013)."
2308,CCCCCCCCOC1=C(C2=CC=CS2)C3=N[Se]N=C3C(C4=CC=C(C5=CC=C(N(C6=CC=C(C7=CC=C(C8=C(OCCCCCCCC)C(OCCCCCCCC)=C(C9=CC=CS9)C%10=N[Se]N=C%108)S7)C=C6)C%11=CC=C(C%12=CC=C(C%13=C(OCCCCCCCC)C(OCCCCCCCC)=C(C%14=CC=CS%14)C%15=N[Se]N=C%15%13)S%12)C=C%11)C=C5)S4)=C1OCCCCCCCC,M1,,,0.84,4.71,26,1.02,"	Wang C, et al. Synthesis and photovoltaic properties of organic small molecules containing triphenylamine and benzothiadiazole moieties with different terminal groups. Dyes and Pigments 98, 464-470 (2013)."
2309,O=C1N(CC(CCCCCCCC)CCCCCCCCCC)C(C2=CC=C(C#CC3=C(C4=C56)C=CC6=CC=CC5=CC=C4C=C3)S2)=C7C1=C(C8=CC=C(C#CC9=C(C%10=C%11%12)C=CC%12=CC=CC%11=CC=C%10C=C9)S8)N(CC(CCCCCCCC)CCCCCCCCCC)C7=O,OD-DPP-A-PY,,,0.91,4.54,37.2,1.54,"	Guo X, Xiao L, Tang W, Liu B, Cui R, Zou Y. Synthesis and characterization of a new solution-processable star-shaped small molecule based on 5,6-bis(n-octyloxy)-2,1,3-benzoselenadiazole for organic solar cells. Journal of Materials Science 48, 5833-5839 (2013)."
2310,O=C1N(CC(CCCCCC)CCCCCCCC)C(C2=CC=C(C#CC3=C(C4=C56)C=CC6=CC=CC5=CC=C4C=C3)S2)=C7C1=C(C8=CC=C(C#CC9=C(C%10=C%11%12)C=CC%12=CC=CC%11=CC=C%10C=C9)S8)N(CC(CCCCCC)CCCCCCCC)C7=O,HD-DPP-A-PY,,,0.87,6.2,41.9,1.96,"	Mun J-W, et al. Acetylene-bridged D-A-D type small molecule comprising pyrene and diketopyrrolopyrrole for high efficiency organic solar cells. Org. Electron. 14, 2341-2347 (2013)."
2311,O=C1N(CC(CCCCCCCC)CCCCCCCCCC)C(C2=CC=C(C3=C(C4=C56)C=CC6=CC=CC5=CC=C4C=C3)S2)=C7C1=C(C8=CC=C(C9=C(C%10=C%11%12)C=CC%12=CC=CC%11=CC=C%10C=C9)S8)N(CC(CCCCCCCC)CCCCCCCCCC)C7=O,OD-DPP-PY,,,0.85,8.89,41.7,2.95,"	Mun J-W, et al. Acetylene-bridged D-A-D type small molecule comprising pyrene and diketopyrrolopyrrole for high efficiency organic solar cells. Org. Electron. 14, 2341-2347 (2013)."
2312,O=C1N(CC(CC)CCCC)C2=C(C=CC(C3=CC(CC(CC)CCCC)=C(C4=CC=C(C=C4)N(C5=CC=CC=C5)C6=CC=CC=C6)S3)=C2)/C1=C7C(N(CC(CC)CCCC)C8=C\7C=CC(C9=CC(CC(CC)CCCC)=C(C%10=CC=C(C=C%10)N(C%11=CC=CC=C%11)C%12=CC=CC=C%12)S9)=C8)=O,I(TPA)2,,,0.79,2.38,27.2,0.46,"	Mun J-W, et al. Acetylene-bridged D-A-D type small molecule comprising pyrene and diketopyrrolopyrrole for high efficiency organic solar cells. Org. Electron. 14, 2341-2347 (2013)."
2313,O=C1N(CC(CC)CCCC)C(C2=CC=CS2)=C3C1=C(C4=CC=C(C5=CC=C(C6=CC=C(C(S7)=CC=C7C(N8CC(CC)CCCC)=C9C(N(CC(CC)CCCC)C(C%10=CC=CS%10)=C9C8=O)=O)S6)S5)S4)N(CC(CC)CCCC)C3=O,T2(TDPP)2,,,1,2.35,26,0.61,"	Liu Q, et al. Low HOMO isoindigo based small molecule for high open-circuit voltage 1.0V solution processed organic solar cells. Synth. Met. 178, 38-43 (2013)."
2314,O=C1N(CC(CC)CCCC)C(C2=CC=CS2)=C3C1=C(C4=CC=C(C5=CC6=C(C=C(C(S7)=CC=C7C(N8CC(CC)CCCC)=C9C(N(CC(CC)CCCC)C(C%10=CC=CS%10)=C9C8=O)=O)S6)S5)S4)N(CC(CC)CCCC)C3=O,TT(TDPP)2,,,0.78,6.8,57,3,"	Choi YS, Jo WH. A strategy to enhance both V-OC and J(SC) of A-D-A type small molecules based on diketopyrrolopyrrole for high efficient organic solar cells. Org. Electron. 14, 1621-1628 (2013)."
2315,O=C1N(CC(CC)CCCC)C(C2=CC=CS2)=C3C1=C(C4=CC=C(C5=CC=C(C6=CC=C(C(S7)=CC=C7C(N8CC(CC)CCCC)=C9C(N(CC(CC)CCCC)C(C%10=CC=CS%10)=C9C8=O)=O)C=C6)C=C5)S4)N(CC(CC)CCCC)C3=O,Ph2(TDPP)2,,,0.81,9.3,53,4,"	Choi YS, Jo WH. A strategy to enhance both V-OC and J(SC) of A-D-A type small molecules based on diketopyrrolopyrrole for high efficient organic solar cells. Org. Electron. 14, 1621-1628 (2013)."
2316,O=C1N(CC(CC)CCCC)C(C2=CC=CS2)=C3C1=C(C4=CC=C(C5=CC6=CC=C(C(S7)=CC=C7C(N8CC(CC)CCCC)=C9C(N(CC(CC)CCCC)C(C%10=CC=CS%10)=C9C8=O)=O)C=C6C=C5)S4)N(CC(CC)CCCC)C3=O,NPT(TDPP)2,,,0.86,8.3,53,3.8,"	Choi YS, Jo WH. A strategy to enhance both V-OC and J(SC) of A-D-A type small molecules based on diketopyrrolopyrrole for high efficient organic solar cells. Org. Electron. 14, 1621-1628 (2013)."
2317,C1(C=CC=C2)=C2C3=N/C1=N\C4=C5C(C=CC=C5)=C6N4[Cu]N7/C(C8=C(C=CC=C8)/C7=N/3)=N\C(C9=C/%10C=CC=C9)=NC%10=N/6,CuPc,,,0.87,9.5,53,4.4,"	Choi YS, Jo WH. A strategy to enhance both V-OC and J(SC) of A-D-A type small molecules based on diketopyrrolopyrrole for high efficient organic solar cells. Org. Electron. 14, 1621-1628 (2013)."
2318,CC1=CC=C(C2=CC3=C(C(C=CC(C4=CC=C(C5=CC=C(C6=CC=C(C7=CC=C(C)C=C7)S6)C8=NN(C9=CC(F)=C(OCC(CCCCCCCC)CCCCCCCCCC)C(F)=C9)N=C85)S4)=C%10)=C%10N3C(CCCCCCCC)CCCCCCCC)C=C2)C=C1,PCDTPBt,,,0.49,17.82,40,3.51,"	Chou D-W, Chen K-L, Huang C-J, Tsao Y-J, Chen W-R, Meen T-H. Efficient small-molecule organic solar cells incorporating a doped buffer layer. Thin Solid Films 536, 235-239 (2013)."
2319,O=C(NC(C(C#N)=C/1C)=O)C1=C/C2=CC(CCCCCC)=C(C(S3)=CC(CCCCCCCC)=C3C4=CC=C(C=C4)N(C5=CC=CC=C5)C6=CC=CC=C6)S2,2,,,0.82,6.4,70,4.6,"	Klein MFG, et al. Carbazole-Phenylbenzotriazole Copolymers as Absorber Material in Organic Solar Cells. Macromolecules 46, 3870-3878 (2013)."
2320,O=C(N(CC(CC)CCCC)C(C(C#N)=C/1C)=O)C1=C/C2=CC=C(C(S3)=CC=C3C4=CC=C(C=C4)N(C5=CC=CC=C5)C6=CC=CC=C6)S2,1,,,0.96,5.1,49,2.4,"	Kumar RJ, Subbiah J, Holmes AB. Enhancement of efficiency in organic photovoltaic devices containing self-complementary hydrogen-bonding domains. Beilstein Journal of Organic Chemistry 9, 1102-1110 (2013)."
2321,C12=NSN=C1C(C3=CC=C(C=C3)N(C4=CC=CC=C4)C5=CC=CC=C5)=CC=C2C6=CC=C(C=C6)N(C7=CC=CC=C7)C8=CC=CC=C8,BTD¨CTPA,,,0.87,6.77,38,2.25,"	Kumar RJ, Subbiah J, Holmes AB. Enhancement of efficiency in organic photovoltaic devices containing self-complementary hydrogen-bonding domains. Beilstein Journal of Organic Chemistry 9, 1102-1110 (2013)."
2322,N#C/C(C1=CC2=C(C=C1)C3=C(C=C(N(C4=CC=CC=C4)C5=CC=CC=C5)C=C3)C26C(C=CC=C7)=C7C8=C6C=CC=C8)=C(C#N)\C9=CC%10=C(C=C9)C%11=C(C=C(N(C%12=CC=CC=C%12)C%13=CC=CC=C%13)C=C%11)C%10%14C(C=CC=C%15)=C%15C%16=C%14C=CC=C%16,PhSPFN,,,0.87,1.53,32,0.43,"	Yasuda T, Shinohara Y, Matsuda T, Han L, Ishi-i T. Improved power conversion efficiency of bulk-heterojunction organic solar cells using a benzothiadiazole-triphenylamine polymer. Journal of Materials Chemistry 22, 2539-2544 (2012)."
2323,CCCCCCCCC1=CC=C(N(C2=CC=C(C3=CC=C(C4=CC=CC=C4)C5=NSN=C53)C=C2)C6=CC=C(C7=CC=CC=C7)C=C6)C=C1,Poly(BTD-TPA),,,0.91,3.92,56,2,"	Liu S-W, Lin C-F. Improvement in the open-circuit voltage of an organic photovoltaic device through selection of a suitable and low-lying highest occupied molecular orbital for the electron donor layer. J. Mater. Res. 28, 1442-1448 (2013)."
2324,CCCCCCC1=C(C#CC#CC2=C(CCCCCC)C=C(C(C3=NSN=C34)=CC=C4C(C=C5)=CC=C5N(C6=CC=CC=C6)C7=CC=CC=C7)S2)SC(C(C8=NSN=C89)=CC=C9C(C=C%10)=CC=C%10N(C%11=CC=CC=C%11)C%12=CC=CC=C%12)=C1,1,,,0.92,7.45,39,2.65,"	Yasuda T, Shinohara Y, Matsuda T, Han L, Ishi-i T. Improved power conversion efficiency of bulk-heterojunction organic solar cells using a benzothiadiazole-triphenylamine polymer. Journal of Materials Chemistry 22, 2539-2544 (2012)."
2325,CCCCCCC1=C(C#CC2=CC=C(C#CC3=C(CCCCCC)C=C(C(C4=NSN=C45)=CC=C5C(C=C6)=CC=C6N(C7=CC=CC=C7)C8=CC=CC=C8)S3)S2)SC(C(C9=NSN=C9%10)=CC=C%10C(C=C%11)=CC=C%11N(C%12=CC=CC=C%12)C%13=CC=CC=C%13)=C1,2,,,0.97,7.85,41,3.11,"	Liu Q, et al. Oligothiophene-Bridged Bis(arylene ethynylene) Small Molecules for Solution-Processible Organic Solar Cells with High Open-Circuit Voltage. Chemistry-an Asian Journal 8, 1892-1900 (2013)."
2326,CCCCCCC1=C(C#CC2=CC=C(C3=CC=C(C#CC4=C(CCCCCC)C=C(C(C5=NSN=C56)=CC=C6C(C=C7)=CC=C7N(C8=CC=CC=C8)C9=CC=CC=C9)S4)S3)S2)SC(C(C%10=NSN=C%10%11)=CC=C%11C(C=C%12)=CC=C%12N(C%13=CC=CC=C%13)C%14=CC=CC=C%14)=C1,3,,,0.91,7.96,44,3.19,"	Liu Q, et al. Oligothiophene-Bridged Bis(arylene ethynylene) Small Molecules for Solution-Processible Organic Solar Cells with High Open-Circuit Voltage. Chemistry-an Asian Journal 8, 1892-1900 (2013)."
2327,CCCCCCC1=C(C#CC2=CC=C(C3=CC=C(C4=CC=C(C#CC5=C(CCCCCC)C=C(C(C6=NSN=C67)=CC=C7C(C=C8)=CC=C8N(C9=CC=CC=C9)C%10=CC=CC=C%10)S5)S4)S3)S2)SC(C(C%11=NSN=C%11%12)=CC=C%12C(C=C%13)=CC=C%13N(C%14=CC=CC=C%14)C%15=CC=CC=C%15)=C1,4,,,0.94,7.75,42,3.07,"	Liu Q, et al. Oligothiophene-Bridged Bis(arylene ethynylene) Small Molecules for Solution-Processible Organic Solar Cells with High Open-Circuit Voltage. Chemistry-an Asian Journal 8, 1892-1900 (2013)."
2328,CCCCCCCCC(CCCCCCCC)N1C2=CC(C)=CC=C2C3=C1C=C(C4=CC=C(C5=CC=C(C6=CC=C(C7=CC=C8C(NC9=C8C=CC(C%10=CC=C(C%11=CC=C(C%12=CC=C(C)S%12)C%13=NSN=C%13%11)S%10)=C9)=C7)S6)C%14=NSN=C%145)S4)C=C3,P(C49C1-DTBT),,,0.96,8.08,48,3.68,"	Liu Q, et al. Oligothiophene-Bridged Bis(arylene ethynylene) Small Molecules for Solution-Processible Organic Solar Cells with High Open-Circuit Voltage. Chemistry-an Asian Journal 8, 1892-1900 (2013)."
2329,CC1(C)C2=CC=CC3=C2N4C5=C(C3(C)C)C=CC=C5C(C)(C)C6=C4C1=CC(C7=CC=C(C8=CC=C(/C=C(C#N)\C#N)S8)S7)=C6,1,,,0.94,13.5,48,6.1,"	Cha H, Lee GY, Fu Y, Kim YJ, Park CE, Park T. Simultaneously Grasping and Self-Organizing Photoactive Polymers for Highly Reproducible Organic Solar Cells with Improved Efficiency. Adv. Energy Mater. 3, 1018-1024 (2013)."
2330,N#C/C(C#N)=C\C(S1)=CC=C1C2=CC=C(C3=CC=C(C=C3)N(C4=CC=CC=C4)C5=CC=CC=C5)S2,2,,,0.89,10.8,42,4.04,"	Do K, Kim C, Song K, Yun SJ, Lee JK, Ko J. Efficient planar organic semiconductors containing fused triphenylamine for solution processed small molecule organic solar cells. Sol. Energy Mater. Sol. Cells 115, 52-57 (2013)."
2331,N#C/C(C#N)=C\C(S1)=CC=C1C2=CC=C(C(S3)=CC=C3C4=CC=C(C=C4)N(C5=CC=CC=C5)C6=CC=CC=C6)S2,1,,,0.89,10.36,34,3.05,"	Do K, Kim C, Song K, Yun SJ, Lee JK, Ko J. Efficient planar organic semiconductors containing fused triphenylamine for solution processed small molecule organic solar cells. Sol. Energy Mater. Sol. Cells 115, 52-57 (2013)."
2332,N#C/C(C#N)=C/C(S1)=CC2=C1SC(C3=CC=C(C=C3)N(C4=CC=CC=C4)C5=CC=CC=C5)=C2,2,,,0.74,7.28,32,1.72,"	Lee JK, Lee S, Yun SJ. Effects of Fused Thiophene Bridges in Organic Semiconductors for Solution-Processed Small-Molecule Organic Solar Cells. Bull. Korean Chem. Soc. 34, 2148-2154 (2013)."
2333,N#CC(C#N)=CC(S1)=CC2=C1C(S3)=C(S2)C=C3C4=CC=C(C=C4)N(C5=CC=CC=C5)C6=CC=CC=C6,3,,,0.8,7.58,35,2.09,"	Lee JK, Lee S, Yun SJ. Effects of Fused Thiophene Bridges in Organic Semiconductors for Solution-Processed Small-Molecule Organic Solar Cells. Bull. Korean Chem. Soc. 34, 2148-2154 (2013)."
2334,CC([Si](C#CC1=C2C=C(C3=CC=C(C4=CC=C(C5=CC=C(C=C5)N(C6=CC=CC=C6)C7=CC=CC=C7)S4)S3)C=CC2=C(C#C[Si](C(C)C)(C(C)C)C(C)C)C8=CC(C9=CC=C(C%10=CC=C(C%11=CC=C(C=C%11)N(C%12=CC=CC=C%12)C%13=CC=CC=C%13)S%10)S9)=CC=C18)(C(C)C)C(C)C)C,TIPSAntBT¨CTPA,,,0.74,7.6,31,1.8,"	Lee JK, Lee S, Yun SJ. Effects of Fused Thiophene Bridges in Organic Semiconductors for Solution-Processed Small-Molecule Organic Solar Cells. Bull. Korean Chem. Soc. 34, 2148-2154 (2013)."
2335,CC([Si](C#CC1=C2C=C(C3=CC=C(C4=CC=C(C5=CC=C(N(C6=CC(C(C)(C)C7=C8C=CC=C7)=C8C=C6)C9=CC(C(C)(C)C%10=C%11C=CC=C%10)=C%11C=C9)C=C5)S4)S3)C=CC2=C(C#C[Si](C(C)C)(C(C)C)C(C)C)C%12=CC(C%13=CC=C(C%14=CC=C(C%15=CC=C(N(C%16=CC(C(C)(C)C%17=C%18C=CC=C%17)=C%18C=C%16)C%19=CC(C(C)(C)C%20=C%21C=CC=C%20)=C%21C=C%19)C=C%15)S%14)S%13)=CC=C1%12)(C(C)C)C(C)C)C,TIPSAntBT¨CbisDMFA,,,0.72,6.07,40,1.97,"	Choi H, Ko HM, Cho N, Song K, Lee JK, Ko J. Electron-Rich Anthracene Semiconductors Containing Triarylamine for Solution-Processed Small-Molecule Organic Solar Cells. ChemSusChem 5, 2045-2052 (2012)."
2336,CCCCCCCCOC1=C(C2=CC=C(C3=CC=C(/C(C#N)=C/C4=CC=C(N(C5=CC=CC=C5)C6=CC=CC=C6)C=C4)C=C3)S2)C7=NSN=C7C(C8=CC=C(C9=CC=C(/C(C#N)=C/C%10=CC=C(N(C%11=CC=CC=C%11)C%12=CC=CC=C%12)C=C%10)C=C9)S8)=C1OCCCCCCCC,BDCTBT,,,0.85,8.58,41,2.96,"	Choi H, Ko HM, Cho N, Song K, Lee JK, Ko J. Electron-Rich Anthracene Semiconductors Containing Triarylamine for Solution-Processed Small-Molecule Organic Solar Cells. ChemSusChem 5, 2045-2052 (2012)."
2337,CCCCCCCCOC1=C(C2=CC=C(C3=CC=C(/C=C/C4=CC=C(C=C4)N(C5=CC=CC=C5)C6=CC=CC=C6)C=C3)S2)C7=NSN=C7C(C8=CC=C(C9=CC=C(/C=C/C%10=CC=C(C=C%10)N(C%11=CC=CC=C%11)C%12=CC=CC=C%12)C=C9)S8)=C1OCCCCCCCC,BDETBT,,,1.04,11.2,33,3.85,"	Zeng S, et al. D-pi-A-pi-D type benzothiadiazole-triphenylamine based small molecules containing cyano on the pi-bridge for solution-processed organic solar cells with high open-circuit voltage. Chem. Commun. 48, 10627-10629 (2012)."
2338,O=C(OCC(CC)CCCC)/C(C#N)=C/C1=CC=C(C2=CC=C(C3=CC=C(C4=CC=C(N(C5=CC=C(C6=CC=C(C7=CC=C(C8=CC=C(/C=C(C#N)/C(OCC(CC)CCCC)=O)S8)S7)S6)C=C5)C9=CC=C(C%10=CC=C(C%11=CC=C(C%12=CC=C(/C=C(C#N)/C(OCC(CC)CCCC)=O)S%12)S%11)S%10)C=C9)C=C4)S3)S2)S1,S(TPA-3T-CA),,,0.94,6.33,33,1.99,"	Zeng S, et al. D-pi-A-pi-D type benzothiadiazole-triphenylamine based small molecules containing cyano on the pi-bridge for solution-processed organic solar cells with high open-circuit voltage. Chem. Commun. 48, 10627-10629 (2012)."
2339,N#C/C(C#N)=C/C1=CC=C(C2=CC=C(N(C3=CC=CC=C3)C4=CC=CC=C4)C=C2)S1,1,,,0.88,7.3,56,3.6,"	Lin Y, Zhang Z-G, Bai H, Li Y, Zhan X. A star-shaped oligothiophene end-capped with alkyl cyanoacetate groups for solution-processed organic solar cells. Chem. Commun. 48, 9655-9657 (2012)."
2340,N#C/C(C#N)=C(C1=C2C=C(C3=CC=C(N(C4=CC=CC=C4)C5=CC=CC=C5)C=C3)S1)\C6=C2C=CC=C6,2,,,0.92,5.77,42,2.53,"	Leliege A, Le Regent C-H, Allain M, Blanchard P, Roncali J. Structural modulation of internal charge transfer in small molecular donors for organic solar cells. Chem. Commun. 48, 8907-8909 (2012)."
2341,C1(C2=C(C3=C45)C=CC5=CC=CC4=CC=C3C=C2)=CC=C(C6=C(C7=C89)C=CC9=CC=CC8=CC=C7C=C6)S1,1s,,,0.97,5.32,52,2.97,"	Leliege A, Le Regent C-H, Allain M, Blanchard P, Roncali J. Structural modulation of internal charge transfer in small molecular donors for organic solar cells. Chem. Commun. 48, 8907-8909 (2012)."
2342,C1(C2=CC=C(C3=CC=C(C4=C(C5=C67)C=CC7=CC=CC6=CC=C5C=C4)S3)S2)=CC=C(C8=C(C9=C%10%11)C=CC%11=CC=CC%10=CC=C9C=C8)S1,3s,,,0.71,2.12,56,0.83,"	Kwon J, et al. Pyrene end-capped oligothiophene derivatives for organic thin-film transistors and organic solar cells. New J. Chem. 36, 1813-1818 (2012)."
2343,OC1=CC=C(C2=CC=C(C3=CC=C(C4=CC=C(C5=CC(N(C(CCCCCCCC)CCCCCCCC)C6=C7C=CC(C8=CC=C(O)C=C8)=C6)=C7C=C5)S4)C9=NSN=C93)S2)C=C1,OH-PCDTBT,,,0.85,3.24,44,1.2,"	Kwon J, et al. Pyrene end-capped oligothiophene derivatives for organic thin-film transistors and organic solar cells. New J. Chem. 36, 1813-1818 (2012)."
2344,CCCCCCCCC(N1C2=C(C3=C1C=C(C4=CC=CC=C4)C=C3)C=CC(C5=CC=C(C6=CC=C(C7=CC=C(C8=CC=CC=C8)S7)C9=NSN=C96)S5)=C2)CCCCCCCC,H-PCDTBT,,,0.9,10.39,45,4.21,"	Shim C, Kim M, Ihn S-G, Choi YS, Kim Y, Cho K. Controlled nanomorphology of PCDTBT-fullerene blends via polymer end-group functionalization for high efficiency organic solar cells. Chem. Commun. 48, 7206-7208 (2012)."
2345,FC(C1=CC=C(C2=CC=C(C3=CC=C(C4=CC=C(C5=CC(N(C(CCCCCCCC)CCCCCCCC)C6=C7C=CC(C8=CC=C(C(F)(F)F)C=C8)=C6)=C7C=C5)S4)C9=NSN=C93)S2)C=C1)(F)F,CF3-PCDTBT,,,0.91,11.22,45,4.82,"	Shim C, Kim M, Ihn S-G, Choi YS, Kim Y, Cho K. Controlled nanomorphology of PCDTBT-fullerene blends via polymer end-group functionalization for high efficiency organic solar cells. Chem. Commun. 48, 7206-7208 (2012)."
2346,CCCCCCCCCCC1=C(C2=CN=C(C3=NC=C(C4=C(CCCCCCCCCC)C=C(C5=CC(CCCCCCCCCC)=C(C6=CC7=C(C8=CC=C(C=C(C9=C(CCCCCCCCCC)C=C(C%10=CC(CCCCCCCCCC)=C(C%11=CN=C(C%12=NC=C(C%13=C(CCCCCCCCCC)C=CS%13)S%12)S%11)S%10)S9)S%14)C%14=C8C=C7)S6)S5)S4)S3)S2)SC=C1,M3,,,0.91,12.24,54,6.02,"	Shim C, Kim M, Ihn S-G, Choi YS, Kim Y, Cho K. Controlled nanomorphology of PCDTBT-fullerene blends via polymer end-group functionalization for high efficiency organic solar cells. Chem. Commun. 48, 7206-7208 (2012)."
2347,CCCCCCCCCCC1=C(C2=CC3=CC=C(C4=C(C=C5)C=C(C6=C(CCCCCCCCCC)C=C(C7=CC(CCCCCCCCCC)=C(C8=CN=C(C9=NC=C(C%10=C(CCCCCCCCCC)C=C(C%11=CC=C(C=C%11)N(C%12=CC=CC=C%12)C%13=CC=CC=C%13)S%10)S9)S8)S7)S6)S4)C5=C3S2)SC(C%14=CC(CCCCCCCCCC)=C(C%15=CN=C(C%16=NC=C(C%17=C(CCCCCCCCCC)C=C(C%18=CC=C(C=C%18)N(C%19=CC=CC=C%19)C%20=CC=CC=C%20)S%17)S%16)S%15)S%14)=C1,M4,,,0.8,3.35,41,1.09,"	Dutta P, Yang W, Lee W-H, Kang IN, Lee S-H. Novel naphtho 1,2-b:5,6-b ' dithiophene core linear donor-pi-acceptor conjugated small molecules with thiophene-bridged bithiazole acceptor: design, synthesis, and their application in bulk heterojunction organic solar cells. Journal of Materials Chemistry 22, 10840-10851 (2012)."
2348,O=C1N(CC(CCCCCCCC)CCCCCCCCCC)C(C2=CC=C(C3=CC4=C(C=C(CCCCCCCCCC)S5)C5=C(C=C(C)S6)C6=C4S3)S2)=C7C1=C(C8=CC=C(C9=CC%10=C%11C(C=C(CCCCCCCCCCCCCCCC)S%11)=C(C=C(C%12=CC=C(C)C%13=NSN=C%13%12)S%14)C%14=C%10S9)S8)N(CC(CCCCCCCC)CCCCCCCCCC)C7=O,P1,,,0.76,4.47,48,1.62,"	Dutta P, Yang W, Lee W-H, Kang IN, Lee S-H. Novel naphtho 1,2-b:5,6-b ' dithiophene core linear donor-pi-acceptor conjugated small molecules with thiophene-bridged bithiazole acceptor: design, synthesis, and their application in bulk heterojunction organic solar cells. Journal of Materials Chemistry 22, 10840-10851 (2012)."
2349,O=C1C2=C(C)SC(C3=CC4=C(C=C(CCCCCCCCCCCCCCCC)S5)C5=C(C=C(C6=CC=C(C(N(CC(CCCCCCCC)CCCCCCCCCC)C7=O)=C8C7=C(C9=CC=C(C%10=CC%11=C(C=C(CCCCCCCCCCCCCCCC)S%12)C%12=C(C=C(C)S%13)C%13=C%11S%10)S9)N(CC(CCCCCCCC)CCCCCCCCCC)C8=O)S6)S%14)C%14=C4S3)=C2C(N1CCCCCCCC)=O,P2,,,0.68,10.95,69,5.14,"	Nielsen CB, et al. Random benzotrithiophene-based donor-acceptor copolymers for efficient organic photovoltaic devices. Chem. Commun. 48, 5832-5834 (2012)."
2350,O=C1N(CC(CCCCCCCC)CCCCCCCCCC)C(C2=CC=C(C3=CC4=C(C=C(CCCCCCCCCCCCCCCC)S5)C5=C(C=C(C)S6)C6=C4S3)S2)=C7C1=C(C8=CC=C(C9=CC%10=C%11C(C=C(CCCCCCCCCCCCCCCC)S%11)=C(C=C(C(CCCCCCCC)(C)CCCCCCCC)S%12)C%12=C%10S9)S8)N(CC(CCCCCCCC)CCCCCCCCCC)C7=O,P3,,,0.72,8.87,66,4.23,"	Nielsen CB, et al. Random benzotrithiophene-based donor-acceptor copolymers for efficient organic photovoltaic devices. Chem. Commun. 48, 5832-5834 (2012)."
2351,O=C1N(CC(CCCCCCCC)CCCCCCCCCC)C(C2=CC=C(C3=CC4=C(C=C(CCCCCCCCCCCCCCCC)S5)C5=C(C=C(C)S6)C6=C4S3)S2)=C7C1=C(C8=CC=C(C9=CC%10=C%11C(C=C(CCCCCCCCCCCCCCCC)S%11)=C(C=C(C(CCCCCCCC)(C)CCCCCCCC)S%12)C%12=C%10S9)S8)N(CC(CCCCCCCC)CCCCCCCCCC)C7=O,P4,,,0.68,11.1,61,4.58,"	Nielsen CB, et al. Random benzotrithiophene-based donor-acceptor copolymers for efficient organic photovoltaic devices. Chem. Commun. 48, 5832-5834 (2012)."
2352,C1(/C2=N/3)=C(C=CC=C1)/C4=N/C5=N/C(C6=C5C=CC=C6)=N\C(N7[Pb]N42)=C8C=CC=CC8=C7/N=C9C%10=C(C=CC=C%10)C3=N/9,CuI (0.5)¨CPbPc (30),,,0.66,12.07,53,4.28,"	Nielsen CB, et al. Random benzotrithiophene-based donor-acceptor copolymers for efficient organic photovoltaic devices. Chem. Commun. 48, 5832-5834 (2012)."
2353,N#C/C(C#N)=C/C1=CC=C(C2=CC3=CC=C(N(C4=CC(C(C)(C)C5=C6C=CC=C5)=C6C=C4)C7=CC(C(C)(C)C8=C9C=CC=C8)=C9C=C7)C=C3S2)S1,1,,,0.46,8.85,63,2.58,"	Shim H-S, et al. Enhancement of near-infrared absorption with high fill factor in lead phthalocyanine-based organic solar cells. Journal of Materials Chemistry 22, 9077-9081 (2012)."
2354,N#C/C(C#N)=C/C1=CC=C(C2=CC=C(C3=CC=C(N(C4=CC(C(C)(C)C5=C6C=CC=C5)=C6C=C4)C7=CC(C(C)(C)C8=C9C=CC=C8)=C9C=C7)C=C3)S2)S1,2,,,0.95,10.05,42,4.01,"	Kim J, Ko HM, Cho N, Paek S, Lee JK, Ko J. Efficient small molecule organic semiconductor containing bis-dimethylfluorenyl amino benzo b thiophene for high open circuit voltage in high efficiency solution processed organic solar cell. Rsc Advances 2, 2692-2695 (2012)."
2355,CC1=C(CCCCCC)C=C(C2=CC=C(C3=CC=C(C4=CC=C(C5=C(CCCCCC)C=C(C6=CC(C(CCCCCOC7=CC=C(C8=CC=C(C9=CC=C(OCCCCCC)C=C9)C=C8)C=C7)(CCCCCOC%10=CC=C(C%11=CC=C(C%12=CC=C(OCCCCCC)C=C%12)C=C%11)C=C%10)C%13=C%14C=CC(C)=C%13)=C%14C=C6)S5)S4)C%15=CSC=C%153)S2)S1,PFtpTDTBT-b,,,0.91,9,44,3.58,"	Kim J, Ko HM, Cho N, Paek S, Lee JK, Ko J. Efficient small molecule organic semiconductor containing bis-dimethylfluorenyl amino benzo b thiophene for high open circuit voltage in high efficiency solution processed organic solar cell. Rsc Advances 2, 2692-2695 (2012)."
2356,O=C1N(CCCC)C(C2=CC=C(C3=CC=C(C4=CC=C(CCCCCC)S4)S3)C=C2)=C5C1=C(C6=CC=C(C7=CC=C(C8=CC=C(CCCCCC)S8)S7)C=C6)N(CCCC)C5=O,D2,,,0.751,4.06,44.4,1.35,"	Yao K, et al. Tuning the photovoltaic parameters of thiophene-linked donor-acceptor liquid crystalline copolymers for organic photovoltaics. Polymer Chemistry 3, 710-717 (2012)."
2357,CCCCCCCCCCCCC1=C(C2=NC(SC(C3=C(CCCCCCCCCCCC)C=C(C4=CC=C(C=C4)N(C5=CC=CC=C5)C6=CC=CC=C6)S3)=N7)=C7S2)SC(C8=CC=C(C=C8)N(C9=CC=CC=C9)C%10=CC=CC=C%10)=C1,TT©\TTPA,,,0.84,9.26,48,3.72,"	Walker B, Han X, Kim C, Sellinger A, Thuc-Quyen N. Solution-Processed Organic Solar Cells from Dye Molecules: An Investigation of Diketopyrrolopyrrole:Vinazene Heterojunctions. ACS Appl. Mater. Interfaces 4, 244-250 (2012)."
2358,N#C/C(C#N)=C/C1=CN=C(C2=CC=C(N(C3=CC=CC=C3)C4=CC=CC=C4)S2)N=C1,DTDCTP,,,0.91,9.39,43.7,3.73,"	Shi Q, Cheng P, Li Y, Zhan X. A Solution Processable D-A-D Molecule based on Thiazolothiazole for High Performance Organic Solar Cells. Adv. Energy Mater. 2, 63-67 (2012)."
2359,N#CC(C1=O)=C(C)/C(C(N1CC(CC)CCCC)=O)=C/C2=CC=C(C3=CC=C(C4=CC=C(N(C5=CC=CC=C5)C6=CC=CC=C6)C=C4)S3)S2,1,,,0.95,12.1,56,6.4,"	Chiu S-W, et al. A donor-acceptor-acceptor molecule for vacuum-processed organic solar cells with a power conversion efficiency of 6.4%. Chem. Commun. 48, 1857-1859 (2012)."
2360,N#C/C(C#N)=C/C1=CC=C(C2=CC=C(C3=CC=C(N(C4=CC=CC=C4)C5=CC=CC=C5)C=C3)S2)S1,2,,,0.92,6.87,41.5,2.62,"	Gupta A, et al. Absorption enhancement of oligothiophene dyes through the use of a cyanopyridone acceptor group in solution-processed organic solar cells. Chem. Commun. 48, 1889-1891 (2012)."
2361,CCCCCCC1=CSC(C2=CC=C(C3=CC(CCCCCC)=C(/C=C/C4=CC=C(N(C5=CC=C(/C=C/C6=C(CCCCCC)C=C(C7=CC=C(C8=CC(CCCCCC)=CS8)C9=NSN=C97)S6)C=C5)C%10=CC=C(/C=C/C%11=C(CCCCCC)C=C(C%12=CC=C(C%13=CC(CCCCCC)=CS%13)C%14=NSN=C%14%12)S%11)C=C%10)C=C4)S3)C%15=NSN=C%152)=C1,S(TPA-TBTT),,,0.98,4.7,36,1.64,"	Gupta A, et al. Absorption enhancement of oligothiophene dyes through the use of a cyanopyridone acceptor group in solution-processed organic solar cells. Chem. Commun. 48, 1889-1891 (2012)."
2362,CCCCCCC1=C(/C=C\C2=CC=C(C=C2)N(C3=CC=CC=C3)C4=CC=CC=C4)SC(C5=CC=C(C6=CC(CCCCCC)=C(/C=C/C7=CC=C(N(C8=CC=C(/C=C/C9=C(CCCCCC)C=C(C%10=CC=C(C%11=CC(CCCCCC)=C(/C=C/C%12=CC=C(N(C%13=CC=CC=C%13)C%14=CC=CC=C%14)C=C%12)S%11)C%15=NSN=C%15%10)S9)C=C8)C%16=CC=C(/C=C/C%17=C(CCCCCC)C=C(C%18=CC=C(C%19=CC(CCCCCC)=C(/C=C/C%20=CC=C(N(C%21=CCCC=C%21)C%22=CC=CC=C%22)C=C%20)S%19)C%23=NSN=C%23%18)S%17)C=C%16)C=C7)S6)C%24=NSN=C%245)=C1,S(TPA-TBTT-TPA),,,0.75,6.41,39,1.9,"	Zhang J, et al. Solution-processable star-shaped photovoltaic organic molecules based on triphenylamine and benzothiadiazole with longer pi-bridge. Org. Electron. 13, 166-172 (2012)."
2363,CCCCCCC1=CC=C(C=C1)C2(C3=CC=C(CCCCCC)C=C3)C4=CC5=C(C(C6=CC=C(CCCCCC)C=C6)(C7=CC=C(CCCCCC)C=C7)C8=C5SC9=C8SC(C%10=CC=CS%10)=C9)C=C4C%11=C2C(SC(C%12=C(CCCCCC)C=C(C%13=C(F)C(F)=C(C%14=CC(CCCCCC)=C(C%15=CC=CS%15)S%14)C%16=NSN=C%13%16)S%12)=C%17)=C%17S%11,PIDTT©\DFBT©\T,,,0.71,5.41,32,1.23,"	Zhang J, et al. Solution-processable star-shaped photovoltaic organic molecules based on triphenylamine and benzothiadiazole with longer pi-bridge. Org. Electron. 13, 166-172 (2012)."
2364,CCCCCCC1=CC=C(C=C1)C2(C3=CC=C(CCCCCC)C=C3)C4=CC5=C(C(C6=CC=C(CCCCCC)C=C6)(C7=CC=C(CCCCCC)C=C7)C8=C5SC9=C8SC(C%10=CC=CS%10)=C9)C=C4C%11=C2C(SC(C%12=C(CCCCCCCC)C%13=C(C=C(C%14=C(F)C(F)=C(C%15=CC%16=C(C(CCCCCCCC)=C(C%17=CC=CS%17)S%16)S%15)C%18=NSN=C%14%18)S%13)S%12)=C%19)=C%19S%11,PIDTT©\DFBT©\TT,,,0.91,9.5,50,4.4,"	Intemann JJ, et al. Highly Efficient Inverted Organic Solar Cells Through Material and Interfacial Engineering of Indacenodithieno 3,2-b thiophene- Based Polymers and Devices. Adv. Funct. Mater. 24, 1465-1473 (2014)."
2365,CCCCC(CC)C(C1=CC2=C(C(S3)=CC(C3=C4)=CC5=C4C=C(C6=C7C(C=C(C(C(CC)CCCC)=O)S7)=C(C)S6)S5)SC(C(S8)=CC(C8=C9OCCCCCCC=C)=C(OCCCCCCC=C)C%10=C9C=C(C)S%10)=C2S1)=O,PBDTTT,,,0.96,11.9,63,7.2,"	Intemann JJ, et al. Highly Efficient Inverted Organic Solar Cells Through Material and Interfacial Engineering of Indacenodithieno 3,2-b thiophene- Based Polymers and Devices. Adv. Funct. Mater. 24, 1465-1473 (2014)."
2366,CC([Si](C#CC1=C(C=CC=C2)C2=C3C4=C5C(C=C3)=C(C#C[Si](C(C)C)(C(C)C)C(C)C)C6=CC=CC=C6C5=CC=C41)(C(C)C)C(C)C)C,TIPS©\DBC,,,0.75,12.52,38.6,3.6,"	Chen L, Li X, Chen Y. Inter-crosslinking through both donor and acceptor with unsaturated bonds for highly efficient and stable organic solar cells. Polymer Chemistry 4, 5637-5644 (2013)."
2367,Cl[In]1N2C3=C4C=CC=CC4=C2/N=C5C6=C(C=CC=C6)C(/N=C7C8=C(C=CC=C8)/C(N/71)=N/C9=N/C(C%10=C9C=CC=C%10)=N\3)=N/5,InClPc,,,0.64,4.88,51,1.58,"	Scholes FH, et al. Intraphase Microstructure-Understanding the Impact on Organic Solar Cell Performance. Adv. Funct. Mater. 23, 5655-5662 (2013)."
2368,O=C(C1=C(C2=C3C=C(C4=C(CCCCCCCCCC)C=C(C5=CC=CS5)S4)S2)SC(C(S6)=C(CCCCCCCCCC)C=C6C(S7)=CC(C7=C8C9=CC=C(CC(CC)CCCC)S9)=C(C%10=CC=C(CC(CC)CCCC)S%10)C%11=C8C=C(S%11)C%12=CC=CS%12)=C1)N(CC(CCCCCCCC)CCCCCC)C3=O,PBTIBDTT,,,0.62,7.05,45,2,"	Abe Y, Yokoyama T, Matsuo Y. Low-LUMO 56 pi-electron fullerene acceptors bearing electron-withdrawing cyano groups for small-molecule organic solar cells. Org. Electron. 14, 3306-3311 (2013)."
2369,O=C(C1=C(C2=C3C=C(C4=C(CCCCCCCCCC)C=C(C5=CC=CS5)S4)S2)SC(C(S6)=C(CCCCCCCCCC)C=C6C(S7)=CC(C7=C8C9=CC=C(SCC(CC)CCCC)S9)=C(C%10=CC=C(SCC(CC)CCCC)S%10)C%11=C8C=C(S%11)C%12=CC=CS%12)=C1)N(CC(CCCCCCCC)CCCCCC)C3=O,PBTIBDTT-S,,,0.91,14.53,71.29,9.42,"	Yang DL, et al. Novel wide band gap copolymers featuring excellent comprehensive performance towards the practical application for organic solar cells. Polymer Chemistry 8, 4332-4338 (2017)."
2370,O=C(N1CC(CCCC)CC)C(C2=C1C3=CC=C(C4=CC=CO4)S3)=C(C5=CC=C(C6=CC=CO6)S5)N(CC(CCCC)CC)C2=O,1,,,0.96,11.98,69.76,8.02,"	Yang DL, et al. Novel wide band gap copolymers featuring excellent comprehensive performance towards the practical application for organic solar cells. Polymer Chemistry 8, 4332-4338 (2017)."
2371,O=C(N1CC(CCCC)CC)C(C2=C1C3=CC=C(C4=CC5=C(C=CC=C5)S4)S3)=C(C6=CC=C(C7=CC8=C(C=CC=C8)S7)S6)N(CC(CCCC)CC)C2=O,2,,,0.702,4.77,45,1.52,"	Fernandez D, et al. Understanding the Limiting Factors of Solvent-Annealed Small-Molecule Bulk-Heterojunction Organic Solar Cells from a Chemical Perspective. Chemsuschem 10, 3118-3134 (2017)."
2372,O=C(N1CC(CCCC)CC)C(C2=C1C3=CC=C(C4=CC=C(N(C5=CC=C(OCCCCCC)C=C5)C6=CC=C(OCCCCCC)C=C6)C=C4)S3)=C(C7=CC=C(C8=CC=C(N(C9=CC=C(OCCCCCC)C=C9)C%10=CC=C(OCCCCCC)C=C%10)C=C8)S7)N(CC(CCCC)CC)C2=O,3,,,0.608,2.78,55,0.93,"	Fernandez D, et al. Understanding the Limiting Factors of Solvent-Annealed Small-Molecule Bulk-Heterojunction Organic Solar Cells from a Chemical Perspective. Chemsuschem 10, 3118-3134 (2017)."
2373,O=C(N1CC(CCCC)CC)C(C2=C1C3=CC=C(C4=CC=C(C(F)(F)F)C=C4)S3)=C(C5=CC=C(C6=CC=C(C(F)(F)F)C=C6)S5)N(CC(CCCC)CC)C2=O,4,,,0.628,4.8,44,1.32,"	Fernandez D, et al. Understanding the Limiting Factors of Solvent-Annealed Small-Molecule Bulk-Heterojunction Organic Solar Cells from a Chemical Perspective. Chemsuschem 10, 3118-3134 (2017)."
2374,O=C(N1CC(CCCC)CC)C(C2=C1C3=CC=C(C4=CC(F)=C(F)C(F)=C4)S3)=C(C5=CC=C(C6=CC(F)=C(F)C(F)=C6)S5)N(CC(CCCC)CC)C2=O,5,,,1.06,2.84,45,1.34,"	Fernandez D, et al. Understanding the Limiting Factors of Solvent-Annealed Small-Molecule Bulk-Heterojunction Organic Solar Cells from a Chemical Perspective. Chemsuschem 10, 3118-3134 (2017)."
2375,S=C(N(CC)C/1=O)SC1=C\C2=CC(CCCCCCCC)=C(C3=CC=C(C4=C(CCCCCCCC)C=C(C5=CC6=C(C=C(C7=CC(CCCCCCCC)=C(C8=CC=C(C9=C(CCCCCCCC)C=C(C%10=CC%11=C(C(C%12=CC=C(CC(CCCC)CC)S%12)=C(C=C(C(S%13)=CC(CCCCCCCC)=C%13C%14=CC=C(S%14)C(S%15)=C(CCCCCCCC)C=C%15C(C%16=NSN=C%16%17)=CC%18=C%17C=C(C%19=NSN=C%19%18)C%20=CC(CCCCCCCC)=C(S%20)C(S%21)=CC=C%21C%22=C(CCCCCCCC)C=C(S%22)/C=C%23SC(N(CC)C/%23=O)=S)S%24)C%24=C%11C%25=CC=C(CC(CCCC)CC)S%25)S%10)S9)S8)S7)C%26=NSN=C%266)C%27=NSN=C5%27)S4)S3)S2,BDTTNTTR,,,0.964,1.11,25,0.27,"	Fernandez D, et al. Understanding the Limiting Factors of Solvent-Annealed Small-Molecule Bulk-Heterojunction Organic Solar Cells from a Chemical Perspective. Chemsuschem 10, 3118-3134 (2017)."
2376,CCC(CCCC)COC1=C2C(C=C(C3=CC4=C(C(OCC(CCCC)CC)=C(C=C(C5=C6C(C(C(C)(C)C6=O)=O)=C(C7=CC=CS7)S5)S8)C8=C4OCC(CCCC)CC)S3)S2)=C(OCC(CCCC)CC)C9=C1C=C(S9)C%10=CC=CS%10,P(EH),,,0.89,15.7,71.7,10.02,"	Wan J, Xu X, Zhang G, Li Y, Feng K, Peng Q. Highly efficient halogen-free solvent processed small-molecule organic solar cells enabled by material design and device engineering. Energ. Environ. Sci. 10, 1739-1745 (2017)."
2377,CCC(CCCC)COC1=C(C=C(C2=CC3=C(C(OCC(CCCC)CC)=C(C=C(C4=C5C(C(C(C)(C)C5=O)=O)=C(C6=CC=CS6)S4)S7)C7=C3OCCCCCCCCCCCC)S2)S8)C8=C(OCCCCCCCCCCCC)C9=C1SC(C%10=CC=CS%10)=C9,P(C12),,,0.89,7.2,0.61,3.9,"	Oosterhout SD, et al. Molecular engineering to improve carrier lifetimes for organic photovoltaic devices with thick active layers. Organic Electronics 47, 57-65 (2017)."
2378,O=S(C1=C(C23C4=CC(C5=CC=C(N6C(C=CC=C7)=C7C8=C6C=CC=C8)C=C5)=CC=C4C9=C2C=C(C%10=CC=C(N%11C(C=CC=C%12)=C%12C%13=C%11C=CC=C%13)C=C%10)C=C9)C=CC=C1)(C%14=CC=CC=C%143)=O,1,,,0.83,5.8,0.54,2.6,"	Oosterhout SD, et al. Molecular engineering to improve carrier lifetimes for organic photovoltaic devices with thick active layers. Organic Electronics 47, 57-65 (2017)."
2379,O=S(C1=C(C23C4=CC(C5=CC=C(N(C6=CC=CC=C6)C7=CC=CC=C7)C=C5)=CC=C4C8=C2C=C(C9=CC=C(N(C%10=CC=CC=C%10)C%11=CC=CC=C%11)C=C9)C=C8)C=CC=C1)(C%12=CC=CC=C%123)=O,3,,,4.17¡À0.09,1.08¡À0.01,0.29¡À0.01,1.31¡À0.04,"	Chan C-Y, Wong Y-C, Chan M-Y, Cheung S-H, So S-K, Yam VW-W. Hole-transporting spirothioxanthene derivatives as donor materials for efficient small-molecule-based organic photovoltaic devices. Chem. Mater. 26, 6585-6594 (2014)."
2380,S=C(N(CC)C/1=O)SC1=C/C2=CC(CCCCCCCC)=C(C3=CC=C(C4=C(CCCCCCCC)C=C(C5SC(C(SCC(CC)CCCC)=C(C=C(C(S6)=CC(CCCCCCCC)=C6C7=CC=C(S7)C(S8)=C(CCCCCCCC)C=C8/C=C(S9)/C(N(CC)C9=S)=O)S%10)C%10=C%11SCC(CC)CCCC)=C%11C5)S4)S3)S2,DR3TSBDT,,,0.94¡À0.01,10.83¡À0.14,0.53¡À0.01,5.40¡À0.06,"	Chan C-Y, Wong Y-C, Chan M-Y, Cheung S-H, So S-K, Yam VW-W. Hole-transporting spirothioxanthene derivatives as donor materials for efficient small-molecule-based organic photovoltaic devices. Chem. Mater. 26, 6585-6594 (2014)."
2381,CC1=CC(CCCCCC)=C(S1)C2=CC=C(C3=C(CCCCCC)C=C(C4=CC(C5(CCCCCC)CCCCCC)=C(C6=C5C=C(C7=CC=C(N(C8=CC=C(/C=C(C#N)/C9=CC=C(/C=C(C#N)\C#N)S9)C=C8)C%10=CC=C(C%11=CC(C%12(CCCCCC)CCCCCC)=C(C%13=C%12C=C(C)C=C%13)C=C%11)C=C%10)C=C7)C=C6)C=C4)S3)C%14=NSN=C%142,BT-F-TPA,,,0.91¡À0.01,14.45¡À0.18,0.73¡À0.01,9.60¡À0.35,"	Kan B, et al. Solution-Processed Organic Solar Cells Based on Dialkylthiol-Substituted Benzodithiophene Unit with Efficiency near 10%. Journal of the American Chemical Society 136, 15529-15532 (2014)."
2382,CC1=CC2=C3N4[Cu]N5/C(C(C=C(C)C=C6)=C6/C5=N/C(C7=C/8C=CC(C)=C7)=NC8=N/3)=N\C9=N/C(C%10=C9C=CC(C)=C%10)=N\C4=C2C=C1,CuMePc,,,0.82,1.8,29,0.43,"	Nayak A, Sreekanth PSR, Sahu SK, Sahu D. Structural Tuning of Low Band Gap Intermolecular Push/Pull Side-chain Polymers for Organic Photovoltaic Applications. Chinese Journal of Polymer Science 35, 1073-1085 (2017)."
2383,CCCCCCC1=CSC(C2=CC=C(C3=CC=C(C4=CC=C(C5=CC(CCCCCC)=CS5)S4)S3)S2)=C1,¦Â-DH5T,,,0.533,9.85,63.8,3.35,"	Qu D, Guo R, Yue S, Wu Y, Yan P, Cheng G. Planar heterojunction organic photovoltaic cells based on tetramethyl substituted copper(II) phthalocyanine treated with thermal annealing. Journal of Physics D-Applied Physics 47,  (2014)."
2384,CC1=CC(CCCCCC)=C(S1)C2=CC=C(C3=C(CCCCCC)C=C(C4=CC(N5C(CCCCCC)CCCCCC)=C(C6=C5C=C(C7=CC=C(N(C8=CC=C(/C=C(C#N)/C9=CC=C(/C=C(C#N)\C#N)S9)C=C8)C%10=CC=C(C%11=CC(N%12C(CCCCCC)CCCCCC)=C(C%13=C%12C=C(C)C=C%13)C=C%11)C=C%10)C=C7)C=C6)C=C4)S3)C%14=NSN=C%142,BT-CZ-TPA,,,0.45,3.19,0.32,0.46,"	Lim E. Solution-Processable Organic Photovoltaic Cell Based on the Oligothiophene with Solubilizing beta-alkyl Groups. Molecular Crystals and Liquid Crystals 602, 251-257 (2014)."
2385,CCCCCCCCCC1=C(C(S2)=CC3=C2C=CC=C3)SC(C4=CC5=C(/C(C(N5CCC(CC)CCCC)=O)=C6C(N(CCC(CC)CCCC)C7=C\6C=CC(C8=CC(CCCCCCCCC)=C(C9=CC(C=CC=C%10)=C%10S9)S8)=C7)=O)C=C4)=C1,BT-T-ID,,,0.76,2.9,30,0.66,"	Nayak A, Sreekanth PSR, Sahu SK, Sahu D. Structural Tuning of Low Band Gap Intermolecular Push/Pull Side-chain Polymers for Organic Photovoltaic Applications. Chinese Journal of Polymer Science 35, 1073-1085 (2017)."
2386,CCCCCCCCCC1=C(C(S2)=CC3=C2C=CC=C3)SC(C4=C(CCCCCCCCC)C=C(C5=C(CCCCCCCCC)C=C(C6=CC7=C(/C(C(N7CCC(CC)CCCC)=O)=C8C(N(CCC(CC)CCCC)C9=C\8C=CC(C%10=C(CCCCCCCCC)C=C(C%11=CC(CCCCCCCCC)=C(C%12=CC(CCCCCCCCC)=C(C%13=CC(C=CC=C%14)=C%14S%13)S%12)S%11)S%10)=C9)=O)C=C6)S5)S4)=C1,BT-T3-ID,,,0.84,4.9,0.42,1.7,"	Ren Y, Hailey AK, Hiszpanski AM, Loo YL. lsoindigo-Containing Molecular Semiconductors: Effect of Backbone Extension on Molecular Organization and Organic Solar Cell Performance. Chemistry of Materials 26, 6570-6577 (2014)."
2387,CCCCCCC1=CC=C(C2=CC=C(C3=CC=C(C4=CN=C(C5=CSC6=C5[Si](CCCCCC)(CCCCCC)C7=C6SC(C8=CC=C(N(C9=CC=C(C(S%10)=CC%11=C%10C%12=C(C(C%13=NC=C(C%14=CC=C(C%15=CC=C(C%16=CC=C(CCCCCC)S%16)S%15)S%14)C%17=NSN=C%17%13)=CS%12)[Si]%11(CCCCCC)CCCCCC)C=C9)C%18=CC=C(C(S%19)=CC%20=C%19C%21=C(C(C%22=NC=C(C%23=CC=C(C%24=CC=C(C%25=CC=C(CCCCCC)S%25)S%24)S%23)C%26=NSN=C%26%22)=CS%21)[Si]%20(CCCCCC)CCCCCC)C=C%18)C=C8)=C7)C%27=NSN=C4%27)S3)S2)S1,TPA-[DTS-PyBTTh3]3,,,0.91,6,0.4,2.2,"	Ren Y, Hailey AK, Hiszpanski AM, Loo YL. lsoindigo-Containing Molecular Semiconductors: Effect of Backbone Extension on Molecular Organization and Organic Solar Cell Performance. Chemistry of Materials 26, 6570-6577 (2014)."
2388,CCCCCCC1=C(C2=CC=C(C3=C(CCCCCC)C=C(/C=C(C#N)/C(OCCCCCC)=O)S3)S2)SC(C4=CC5=C(N6C7=C(C8(C)C)C=C(C9=CC(CCCCCC)=C(C%10=CC=C(C%11=C(CCCCCC)C=C(/C=C(C(OCCCCCC)=O)\C#N)S%11)S%10)S9)C=C7C(C)(C)C%12=C6C(C5(C)C)=CC(C%13=CC(CCCCCC)=C(C%14=CC=C(C%15=C(CCCCCC)C=C(/C=C(C(OCCCCCC)=O)/C#N)S%15)S%14)S%13)=C%12)C8=C4)=C1,DMM-TPA-[T3HCA]3,,,0.7,10.66,0.52,3.88,"	Lim K, Lee SY, Song K, Sharma GD, Ko J. Synthesis and properties of low bandgap star molecules TPA- DTS-PyBTTh3 (3) and DMM-TPA DTS-PyBTTh3 (3) for solution-processed bulk heterojunction organic solar cells. Journal of Materials Chemistry C 2, 8412-8422 (2014)."
2389,O=C(C1=C(C2=CC=C(C3=CC=C(CCCCCC)S3)S2)SC(C(S4)=CC5=C4C6=C(C=C(C7=C(C(N8C)=O)C(C8=O)=C(C9=CC=C(C%10=CC=C(CCCCCC)S%10)S9)S7)S6)[Si](CC(CC)CCCC)5CC(CC)CCCC)=C1%11)N(C)C%11=O,DTS(MeTPD2THex)2,,,0.85,8.91,0.47,3.55,"	Paek S, Choi H, Sim J, Song K, Lee JK, Ko J. Efficient Organic Solar Cells with Star-Shaped Small Molecules Comprising of Planar Donating Core and Accepting Edges. Journal of Physical Chemistry C 118, 27193-27200 (2014)."
2390,CCCCCCCCCC1=C(C(S2)=CC3=C2C=CC=C3)SC(C4=C(CCCCCCCCC)C=C(C5=CC6=C(/C(C(N6CCC(CC)CCCC)=O)=C7C(N(CCC(CC)CCCC)C8=C\7C=CC(C9=CC(CCCCCCCCC)=C(C%10=CC(CCCCCCCCC)=C(C%11=CC(C=CC=C%12)=C%12S%11)S%10)S9)=C8)=O)C=C5)S4)=C1,BT-T2-ID,,,0.93,6.4,0.52,3.1,"	Choi YS, Shin TJ, Jo WH. Small Molecules Based on Thieno 3,4-c pyrrole-4,6-dione for High Open-Circuit Voltage (V-OC) Organic Photovoltaics: Effect of Different Positions of Alkyl Substitution on Molecular Packing and Photovoltaic Performance. Acs Applied Materials & Interfaces 6, 20035-20042 (2014)."
2391,CCCCCCC1=C(C2=CC=C(C3=C(CCCCCC)C=C(/C=C(C#N)/C#N)S3)S2)SC(C4=CC5=C(N6C7=C(C8(C)C)C=C(C9=CC(CCCCCC)=C(C%10=CC=C(C%11=C(CCCCCC)C=C(/C=C(C#N)/C#N)S%11)S%10)S9)C=C7C(C)(C)C%12=C6C(C5(C)C)=CC(C%13=CC(CCCCCC)=C(C%14=CC=C(C%15=C(CCCCCC)C=C(/C=C(C#N)/C#N)S%15)S%14)S%13)=C%12)C8=C4)=C1,DMM-TPA-[T3MMN]3,,,0.9,8.7,0.43,3.4,"	Ren Y, Hailey AK, Hiszpanski AM, Loo YL. lsoindigo-Containing Molecular Semiconductors: Effect of Backbone Extension on Molecular Organization and Organic Solar Cell Performance. Chemistry of Materials 26, 6570-6577 (2014)."
2392,C/C(C1=CC=C(C2=CC=C(C3=CC([Si]4(CCCCCCCC)CCCCCCCC)=C(C5=C4C=C(C6=CC=C(C7=CC=C(/C(C)=C(C#N)/C#N)S7)S6)S5)S3)S2)S1)=C(C#N)\C#N,DTS(Oct)2-(2T-DCV-Me)2,,,0.86,10.22,0.47,4.18,"	Paek S, Choi H, Sim J, Song K, Lee JK, Ko J. Efficient Organic Solar Cells with Star-Shaped Small Molecules Comprising of Planar Donating Core and Accepting Edges. Journal of Physical Chemistry C 118, 27193-27200 (2014)."
2393,CCCCCCC1=CC=C(C2=CC=C(C3=CC=C(C4=CN=C(C5=CSC6=C5[Si](CCCCCC)(CCCCCC)C7=C6SC(C8=CC9=C(N%10C%11=C(C%12(C)C)C=C(C(S%13)=CC%14=C%13C%15=C(C(C%16=NC=C(C%17=CC=C(C%18=CC=C(C%19=CC=C(CCCCCC)S%19)S%18)S%17)C%20=NSN=C%20%16)=CS%15)[Si]%14(CCCCCC)CCCCCC)C=C%11C(C)(C)C%21=C%10C(C9(C)C)=CC(C(S%22)=CC%23=C%22C%24=C(C(C%25=NC=C(C%26=CC=C(C%27=CC=C(C%28=CC=C(CCCCCC)S%28)S%27)S%26)C%29=NSN=C%29%25)=CS%24)[Si]%23(CCCCCC)CCCCCC)=C%21)C%12=C8)=C7)C%30=NSN=C4%30)S3)S2)S1,DMM-TPA[DTS-PyBTTh3]3,,,0.85,10.2,0.63,5.44,"	Luponosov YN, Min J, Ameri T, Brabec CJ, Ponomarenko SA. A new dithienosilole-based oligothiophene with methyldicyanovinyl groups for high performance solution-processed organic solar cells. Organic Electronics 15, 3800-3804 (2014)."
2394,O=C(C1=C(C2=CC=C(C3=CC=CS3)S2)SC(C(S4)=CC5=C4C6=C(C=C(C7=C(C(N8CCCCCC)=O)C(C8=O)=C(C9=CC=C(C%10=CC=CS%10)S9)S7)S6)[Si](CC(CC)CCCC)5CC(CC)CCCC)=C1%11)N(CCCCCC)C%11=O,DTS(HexTPD2T)2,,,0.78,12.84,0.58,5.81,"	Lim K, Lee SY, Song K, Sharma GD, Ko J. Synthesis and properties of low bandgap star molecules TPA- DTS-PyBTTh3 (3) and DMM-TPA DTS-PyBTTh3 (3) for solution-processed bulk heterojunction organic solar cells. Journal of Materials Chemistry C 2, 8412-8422 (2014)."
2395,S=C(N(CC)C/1=O)SC1=C\C2=CC(CCCCCCCC)=C(C3=CC=C(C4=C(CCCCCCCC)C=C(C5=CC6=C(C=C(C7=CC(CCCCCCCC)=C(C8=CC=C(C9=C(CCCCCCCC)C=C(C%10=CC%11=C(C(C%12=CC=C(SCC(CCCC)CC)S%12)=C(C=C(C(S%13)=CC(CCCCCCCC)=C%13C%14=CC=C(S%14)C(S%15)=C(CCCCCCCC)C=C%15C(C%16=NSN=C%16%17)=CC%18=C%17C=C(C%19=NSN=C%19%18)C%20=CC(CCCCCCCC)=C(S%20)C(S%21)=CC=C%21C%22=C(CCCCCCCC)C=C(S%22)/C=C%23SC(N(CC)C/%23=O)=S)S%24)C%24=C%11C%25=CC=C(SCC(CCCC)CC)S%25)S%10)S9)S8)S7)C%26=NSN=C%266)C%27=NSN=C5%27)S4)S3)S2,BDTSTNTTR,,,0.94,11.8,0.54,6,"	Choi YS, Shin TJ, Jo WH. Small Molecules Based on Thieno 3,4-c pyrrole-4,6-dione for High Open-Circuit Voltage (V-OC) Organic Photovoltaics: Effect of Different Positions of Alkyl Substitution on Molecular Packing and Photovoltaic Performance. Acs Applied Materials & Interfaces 6, 20035-20042 (2014)."
2396,O=S(C1=C(C23C4=CC(C5=CC=C(N6C(C=CC(C(C)(C)C)=C7)=C7C8=C6C=CC(C(C)(C)C)=C8)C=C5)=CC=C4C9=C2C=C(C%10=CC=C(N%11C(C=CC(C(C)(C)C)=C%12)=C%12C%13=C%11C=CC(C(C)(C)C)=C%13)C=C%10)C=C9)C=CC=C1)(C%14=CC=CC=C%143)=O,2,,,0.93,16.21,0.765,11.53,"	Wan J, Xu X, Zhang G, Li Y, Feng K, Peng Q. Highly efficient halogen-free solvent processed small-molecule organic solar cells enabled by material design and device engineering. Energ. Environ. Sci. 10, 1739-1745 (2017)."
2397,C1(C23C4=CC=CC=C4SC5=C3C=CC=C5)=CC(C6=CC=C(N(C7=CC=CC=C7)C8=CC=CC=C8)C=C6)=CC=C1C9=C2C=C(C%10=CC=C(N(C%11=CC=CC=C%11)C%12=CC=CC=C%12)C=C%10)C=C9,4,,,1.16,8.35,0.37,3.58,"	Chan C-Y, Wong Y-C, Chan M-Y, Cheung S-H, So S-K, Yam VW-W. Hole-transporting spirothioxanthene derivatives as donor materials for efficient small-molecule-based organic photovoltaic devices. Chem. Mater. 26, 6585-6594 (2014)."
2398,S=C(N(C/1=O)CC)SC1=C\C2=CC(CCCCCCCC)=C(C3=CC=C(C4=C(CCCCCCCC)C=C(C5=CC6=C(C(C7=CC=C(/C=C/C8=CC=C(CC(CCCCCCCC)CCCCCC)S8)S7)=C(C=C(C9=CC(CCCCCCCC)=C(C%10=CC=C(C%11=C(CCCCCCCC)C=C(/C=C%12SC(N(CC)C/%12=O)=S)S%11)S%10)S9)S%13)C%13=C6C%14=CC=C(/C=C/C%15=CC=C(CC(CCCCCCCC)CCCCCC)S%15)S%14)S5)S4)S3)S2,DR3TBDTTV,,,0.95,10.94,0.48,4.99,"	Chan C-Y, Wong Y-C, Chan M-Y, Cheung S-H, So S-K, Yam VW-W. Hole-transporting spirothioxanthene derivatives as donor materials for efficient small-molecule-based organic photovoltaic devices. Chem. Mater. 26, 6585-6594 (2014)."
2399,O=C1C(C2=C(O)C=C(N(CCCCCC)CCCCCC)C=C2O)=C([O-])/C1=C(C(O)=C/3)\C(O)=CC3=[N+](CCCCCC)\CCCCCC,SQ2,,,0.88,10.22,69.1,5.71,"	Zhu K, et al. A two-dimension-conjugated small molecule for efficient ternary organic solar cells. Organic Electronics 48, 179-187 (2017)."
2400,CCCCCCC(C1=C2/C(N/C1=C\3)=N/C(C4=C/5C(CCCCCC)=CC=C4CCCCCC)=NC5=N/C6=C7C(C(CCCCCC)=CC=C7CCCCCC)=C(/N=C8N=C3C9=C\8C(CCCCCC)=CC=C9CCCCCC)N6)=CC=C2CCCCCC,C6TBTAPH2,,,0.88,5.48,31,1.5,"	Bruck S, et al. Structure-property relationship of anilino-squaraines in organic solar cells. Physical chemistry chemical physics : PCCP 16, 1067-1077 (2014)."
2401,CCCCCCC(C1=C2/C(N/C1=N\3)=N/C(C4=C/5C(CCCCCC)=CC=C4CCCCCC)=NC5=N/C6=C7C(C(CCCCCC)=CC=C7CCCCCC)=C(/N=C8N=C3C9=C\8C(CCCCCC)=CC=C9CCCCCC)N6)=CC=C2CCCCCC,C6PcH2,,,0.73,10.5,60,4.5,"	Dao Q-D, et al. Efficiency enhancement in solution processed small-molecule based organic solar cells utilizing various phthalocyanine¨Ctetrabenzoporphyrin hybrid macrocycles. Organic Electronics 23, 44-52 (2015)."
2402,CCCCC(CC)COC1=C(C=C(C2=C(F)C=C(C3=CC=C(C4=CC=C(CCCCCC)S4)S3)C5=NSN=C52)S6)C6=C(OCC(CC)CCCC)C7=C1SC(C8=C(F)C=C(C9=CC=C(C%10=CC=C(CCCCCC)S%10)S9)C%11=NSN=C%118)=C7,1,,,0.73,9.5,53,3.7,"	Dao Q-D, et al. Efficiency enhancement in solution processed small-molecule based organic solar cells utilizing various phthalocyanine¨Ctetrabenzoporphyrin hybrid macrocycles. Organic Electronics 23, 44-52 (2015)."
2403,FC1=C(C2=CC3=C(C#C[Si](C(C)C)(C(C)C)C(C)C)C4=C(C=C(C5=C(F)C=C(C6=CC=C(C7=CC=C(CCCCCC)S7)S6)C8=NSN=C85)S4)C(C#C[Si](C(C)C)(C(C)C)C(C)C)=C3S2)C9=NSN=C9C(C%10=CC=C(C%11=CC=C(CCCCCC)S%11)S%10)=C1,2,,,0.74,10.22,54,4.08,"	Do K, Cho N, Siddiqui SA, Singh SP, Sharma GD, Ko J. New D-A-D-A-D push¨Cpull organic semiconductors with different benzo[1,2-b:4, 5-b¡ä] dithiophene cores for solution processed bulk heterojunction solar cells. Dyes and Pigments 120, 126-135 (2015)."
2404,CCCCC(CC)COC1=C2C(C=C(C3=CC(CCCCCCCC)=C(C4=CC=C(C5=C(CCCCCCCC)C=C(/C=C(S/C6=C(C#N)/C#N)\C(N6CCCCCCCC)=O)S5)S4)S3)S2)=C(OCC(CC)CCCC)C7=C1C=C(C8=CC(CCCCCCCC)=C(C9=CC=C(C%10=C(CCCCCCCC)C=C(/C=C(S/C%11=C(C#N)/C#N)\C(N%11CCCCCCCC)=O)S%10)S9)S8)S7,D(T3-DCRD)-BDT,,,0.94,10.44,58,5.69,"	Do K, Cho N, Siddiqui SA, Singh SP, Sharma GD, Ko J. New D-A-D-A-D push¨Cpull organic semiconductors with different benzo[1,2-b:4, 5-b¡ä] dithiophene cores for solution processed bulk heterojunction solar cells. Dyes and Pigments 120, 126-135 (2015)."
2405,CCCCCCCCC1=C(C2=CC=C(C3=C(CCCCCCCC)C=C(/C=C(S/C4=C(C#N)/C#N)\C(N4CCCCCCCC)=O)S3)S2)SC(C5=CC6=C(C7=CC=C(CC(CC)CCCC)S7)C8=C(C=C(C9=CC(CCCCCCCC)=C(C%10=CC=C(C%11=C(CCCCCCCC)C=C(/C=C(S/C%12=C(C#N)/C#N)\C(N%12CCCCCCCC)=O)S%11)S%10)S9)S8)C(C%13=CC=C(S%13)CC(CC)CCCC)=C6S5)=C1,D(T3-DCRD)-BDTT,,,0.93,2.44,49,1.1,"	Fan Q, et al. Acceptor-donor-acceptor small molecules containing benzo[1,2-b:4,5-b']dithiophene and rhodanine units for solution processed organic solar cells. Dyes and Pigments 116, 13-19 (2015)."
2406,N#C/C(C#N)=C(/C(C1=CC=C(C2=NC3=CC=CC=C3S2)C=C1)=C(C#N)\C#N)/C4=CC=C(N(C5=CC=CC=C5)C6=CC=CC=C6)C=C4,BT3,,,0.96,3.69,55,1.94,"	Fan Q, et al. Acceptor-donor-acceptor small molecules containing benzo[1,2-b:4,5-b']dithiophene and rhodanine units for solution processed organic solar cells. Dyes and Pigments 116, 13-19 (2015)."
2407,N#C/C(C#N)=C(/C(C1=CC=C(N(C2=CC=CC=C2)C3=CC=CC=C3)C=C1)=C4C=C/C(C=C\4)=C(C#N)\C#N)\C5=CC=C(C6=NC7=CC=CC=C7S6)C=C5,BT4,,,0.92,8.2,50,3.77,"	Gautam P, Misra R, Siddiqui SA, Sharma GD. Donor¨Cacceptor¨C¦Ð¨Cacceptor based charge transfer chromophore as electron donors for solution processed small molecule organic bulk heterojunction solar cells. Organic Electronics 19, 76-82 (2015)."
2408,N#C/C(C#N)=C(C1=CC=C(C#CC2=C(C=CC=C3)C3=CC4=C2C=CC=C4)C5=NSN=C15)\C(C6=CC=C(N(C7=CC=CC=C7)C8=CC=CC=C8)C=C6)=C(C#N)\C#N,BDT3,,,0.84,10.82,58,5.27,"	Gautam P, Misra R, Siddiqui SA, Sharma GD. Donor¨Cacceptor¨C¦Ð¨Cacceptor based charge transfer chromophore as electron donors for solution processed small molecule organic bulk heterojunction solar cells. Organic Electronics 19, 76-82 (2015)."
2409,CCCCC(CC)CC1=C(C2=NC(SC(C3=C(CC(CC)CCCC)C=C(C4=C(CCCCCCCC)C=C(C5=CC=C(C6=CC(CCCCCCCC)=C(C7=CC=C(CCCCCC)S7)S6)C8=NSN=C85)S4)S3)=N9)=C9S2)SC(C%10=C(CCCCCCCC)C=C(C%11=CC=C(C%12=CC(CCCCCCCC)=C(C%13=CC=C(CCCCCC)S%13)S%12)C%14=NSN=C%14%11)S%10)=C1,DTTz-DTBTT,,,0.9,9.48,54,4.61,"	Gautam P, Misra R, Siddiqui SA, Sharma GD. Unsymmetrical Donor-Acceptor-Acceptor-pi-Donor Type Benzothiadiazole-Based Small Molecule for a Solution Processed Bulk Heterojunction Organic Solar Cell. ACS Appl Mater Interfaces 7, 10283-10292 (2015)."
2410,CCCCC(CC)CN(C1=O)C(C2=CC=C(C#CC3=CC=C(C=O)C=C3)S2)=C4C1=C(C5=CC=C(C#CC6=CC=C(C=O)C=C6)S5)N(CC(CC)CCCC)C4=O,DPP-BZ,,,0.66,5.11,48.3,1.64,"	Chen Y, et al. New small molecules with thiazolothiazole and benzothiadiazole acceptors for solution-processed organic solar cells. New Journal of Chemistry 38, 1559 (2014)."
2411,CCCCCCC(C=C1)=CC=C1C2(C3=CC=C(CCCCCC)C=C3)C4=C(SC5=C4SC(C6=C(F)C(F)=C(C7=CC=C(C8=CC=C(CCCCCC)S8)S7)C9=NSN=C69)=C5)C%10=C2C=C(C(SC%11=C%12SC(C%13=C(F)C(F)=C(C%14=CC=C(C%15=CC=C(CCCCCC)S%15)S%14)C%16=NSN=C%13%16)=C%11)=C%12C(C%17=CC=C(CCCCCC)C=C%17)%18C%19=CC=C(CCCCCC)C=C%19)C%18=C%10,IDTT-DFBT-BT,,,0.84,4.42,47.2,1.76,"	Ghosh SS, Serrano LA, Ebenhoch B, Rotello VM, Cooke G, Samuel IDW. Organic solar cells based on acceptor-functionalized diketopyrrolopyrrole derivatives. Journal of Photonics for Energy 5, 057215 (2015)."
2412,CCCCCCC(C=C1)=CC=C1C2(C3=CC=C(CCCCCC)C=C3)C4=C(SC5=C4SC(C6=C(F)C=C(C7=CC=C(C8=CC=C(CCCCCC)S8)S7)C9=NSN=C69)=C5)C%10=C2C=C(C(SC%11=C%12SC(C%13=C(F)C=C(C%14=CC=C(C%15=CC=C(CCCCCC)S%15)S%14)C%16=NSN=C%13%16)=C%11)=C%12C(C%17=CC=C(CCCCCC)C=C%17)%18C%19=CC=C(CCCCCC)C=C%19)C%18=C%10,IDTT-FBT-TT,,,0.91,10,46,4.37,"	Intemann JJ, et al. Enhanced Performance of Organic Solar Cells with Increased End Group Dipole Moment in Indacenodithieno[3,2-b]thiophene-Based Molecules. Advanced Functional Materials 25, 4889-4897 (2015)."
2413,CCCCCCC(C=C1)=CC=C1C2(C3=CC=C(CCCCCC)C=C3)C4=C(SC5=C4SC(C6=C(F)C=C(C7=CC8=C(C=C(CCCCCC)S8)S7)C9=NSN=C69)=C5)C%10=C2C=C(C(SC%11=C%12SC(C%13=C(F)C=C(C%14=CC%15=C(C=C(CCCCCC)S%15)S%14)C%16=NSN=C%13%16)=C%11)=C%12C(C%17=CC=C(CCCCCC)C=C%17)%18C%19=CC=C(CCCCCC)C=C%19)C%18=C%10,IDTT-FBT-BT,,,0.99,11.7,50,5.75,"	Intemann JJ, et al. Enhanced Performance of Organic Solar Cells with Increased End Group Dipole Moment in Indacenodithieno[3,2-b]thiophene-Based Molecules. Advanced Functional Materials 25, 4889-4897 (2015)."
2414,CCCCCCC(C=C1)=CC=C1C2(C3=CC=C(CCCCCC)C=C3)C4=C(SC5=C4SC(C6=C(F)C=C(C7=CC=C(C8=CC=C(C9=CC=C(CCCCCC)S9)S8)S7)C%10=NSN=C6%10)=C5)C%11=C2C=C(C(SC%12=C%13SC(C%14=C(F)C=C(C%15=CC=C(C%16=CC=C(C%17=CC=C(CCCCCC)S%17)S%16)S%15)C%18=NSN=C%14%18)=C%12)=C%13C(C%19=CC=C(CCCCCC)C=C%19)%20C%21=CC=C(CCCCCC)C=C%21)C%20=C%11,IDTT-FBT-3T,,,0.96,12,53,6.12,"	Intemann JJ, et al. Enhanced Performance of Organic Solar Cells with Increased End Group Dipole Moment in Indacenodithieno[3,2-b]thiophene-Based Molecules. Advanced Functional Materials 25, 4889-4897 (2015)."
2415,CCCCC(CC)COC1=C(C=C(C2=C(CCCCCCCC)C=C(C3=CC=C(C4=CC=C(CCCCCCCC)S4)C5=NSN=C35)S2)S6)C6=C(OCC(CC)CCCC)C7=C1SC(C8=C(CCCCCCCC)C=C(C9=CC=C(C%10=CC=C(CCCCCCCC)S%10)C%11=NSN=C9%11)S8)=C7,DRTBTTBDT,,,0.95,12.4,55,6.54,"	Intemann JJ, et al. Enhanced Performance of Organic Solar Cells with Increased End Group Dipole Moment in Indacenodithieno[3,2-b]thiophene-Based Molecules. Advanced Functional Materials 25, 4889-4897 (2015)."
2416,CC(C)CCCC(C)CCC1(CCC(C)CCCC(C)C)C(C=C(C2=CC=C(C3=C4C(C(N3CC(CCCC)CC)=O)=C(C5=CC=CS5)N(CC(CCCC)CC)C4=O)S2)S6)=C6C(SC(C7=CC=C(C8=C9C(C(N8CC(CCCC)CC)=O)=C(C%10=CC=CS%10)N(CC(CCCC)CC)C9=O)S7)=C%11)=C%11O1,DTPDPP,,,0.7,4.15,35,1.01,"	Chen Y, et al. Two-dimensional benzodithiophene and benzothiadiazole based solution-processed small molecular organic field-effect transistors & solar cells. Journal of Materials Chemistry C 2, 3921 (2014)."
2417,O=C1C(C2=C(C3=CC=C(C4=CC(S5)=C(S4)C6=C5C(CC(CC)CCCC)=C(C(SC=C7C8=CC=C(C9=C%10C(C(N9C(C)CCCCCC)=O)=C(C%11=CC=CS%11)N(C(C)CCCCCC)C%10=O)S8)=C7S%12)C%12=C6CC(CC)CCCC)S3)N1C(C)CCCCCC)=C(C%13=CC=CS%13)N(C(C)CCCCCC)C2=O,DTBDTDPPeEH,,,0.8,14.12,61,6.88,"	Jung JW, Russell TP, Jo WH. A Small Molecule Composed of Dithienopyran and Diketopyrrolopyrrole as Versatile Electron Donor Compatible with Both Fullerene and Nonfullerene Electron Acceptors for High Performance Organic Solar Cells. Chemistry of Materials 27, 4865-4870 (2015)."
2418,O=C1C(C2=C(C3=CC=C(C4=CC(S5)=C(S4)C6=C5C(CC(CC)CCCC)=C(C(SC=C7C8=CC=C(C9=C%10C(C(N9C(CCC)CCCCCCCC)=O)=C(C%11=CC=CS%11)N(C(CCC)CCCCCCCC)C%10=O)S8)=C7S%12)C%12=C6CC(CC)CCCC)S3)N1C(CCC)CCCCCCC)=C(C%13=CC=CS%13)N(C(CCC)CCCCCCCC)C2=O,DTBDTDPPeBO,,,0.85,9.9,51.3,4.35,"	Jung M, et al. Structural and morphological tuning of dithienobenzodithiophene-core small molecules for efficient solution processed organic solar cells. Dyes and Pigments 115, 23-34 (2015)."
2419,CCCCCCCCC(S1)=CC=C1C(C2=NSN=C32)=CC=C3C4=CC(CCCCCCCC)=C(S4)C5=CC6=C(C7=CC=C(CC(CC)CCCC)S7)C8=C(C=C(C9=C(CCCCCCCC)C=C(C%10=CC=C(C%11=CC=C(CCCCCCCC)S%11)C%12=NSN=C%10%12)S9)S8)C(C%13=CSC(CC(CC)CCCC)=C%13)=C6S5,DRTBTTBDTT,,,0.82,7.3,45.2,2.69,"	Jung M, et al. Structural and morphological tuning of dithienobenzodithiophene-core small molecules for efficient solution processed organic solar cells. Dyes and Pigments 115, 23-34 (2015)."
2420,CCCCC(CC)COC1=C(C=C(C2=CC3=C(S2)C4=C(C=C(/C=C(C#N)\C#N)S4)C3(CCCCCC)CCCCCC)S5)C5=C(OCC(CC)CCCC)C6=C1SC(C7=CC8=C(S7)C9=C(C=C(/C=C(C#N)\C#N)S9)C8(CCCCCC)CCCCCC)=C6,VC89,,,0.89,2.07,29,0.54,"	Chen Y, et al. Two-dimensional benzodithiophene and benzothiadiazole based solution-processed small molecular organic field-effect transistors & solar cells. Journal of Materials Chemistry C 2, 3921 (2014)."
2421,CCCCCCCCN1C2=C(SC(C3=CC(CCCCCCCC)=C(C4=CC=C(C5=CC(CCCCCCCC)=C(CC6CC(N(CCCCCCCC)C6=O)=S)S5)S4)S3)=C2)C7=C1C=C(C8=CC(CCCCCCCC)=C(C9=CC=C(C%10=CC(CCCCCCCC)=C(CC%11CC(N(CCCCCCCC)C%11=O)=S)S%10)S9)S8)S7,DR3TDTN,,,0.92,11.56,62,6.66,"	Kumar CV, Cabau L, Viterisi A, Biswas S, Sharma GD, Palomares E. Solvent Annealing Control of Bulk Heterojunction Organic Solar Cells with 6.6% Efficiency Based on a Benzodithiophene Donor Core and Dicyano Acceptor Units. The Journal of Physical Chemistry C 119, 20871-20879 (2015)."
2422,CCCCN1C2=CC=CC=C2OC3=C1C=CC(C4=CC=C(/C=C/C(CC(C)(C)C/5)=CC5=C(C#N)/C#N)S4)=C3,POZ4,,,0.67,8.22,55,3.03,"	Li M, et al. Dithienopyrrole Based Small Molecule with Low Band Gap for Organic Solar Cells. Chin. J. Chem. 33, 852-858 (2015)."
2423,CCCCCCCCC1=C(C2=CC=C(C3=C(CCCCCCCC)C=C(/C=C(C(N4CC)=O)/C(N(CC)C4=S)=O)S3)S2)SC(C5=CC6=C(C=C5)C7=C(C=C(C8=CC(CCCCCCCC)=C(C9=CC=C(C%10=C(CCCCCCCC)C=C(/C=C(C(N%11CC)=O)/C(N(CC)C%11=S)=O)S%10)S9)S8)C=C7)N6C(CCCCCC)C)=C1,DTB3TCz,,,0.847,10.5,40.3,3.58,"	Cheng M, Yang X, Chen C, Tan Q, Sun L. Molecular engineering of small molecules donor materials based on phenoxazine core unit for solution-processed organic solar cells. J. Mater. Chem. A 2, 10465-10469 (2014)."
2424,N#C/C(C#N)=C1CC(C)(C)CC(/C=C/C(S2)=CC=C2C3=CC=C4C(N(CCCC)C(C=CC(C5=CC=C(/C=C/C(CC(C)(C)C/6)=CC6=C(C#N)/C#N)S5)=C7)=C7O4)=C3)=C\1,POZ6,,,0.91,11.8,49,5.26,"	Li M, et al. A low bandgap carbazole based small molecule for organic solar cells. Organic Electronics 24, 89-95 (2015)."
2425,N#C/C(C#N)=C\C1=CC=C(C(C=C2)=CC=C2N(C3=CC=CC=C3)C4=CC=CC5=C4C=CC=C5)S1,2a,,,0.862,13.1,49.6,5.6,"	Cheng M, Yang X, Chen C, Tan Q, Sun L. Molecular engineering of small molecules donor materials based on phenoxazine core unit for solution-processed organic solar cells. J. Mater. Chem. A 2, 10465-10469 (2014)."
2426,N#C/C(C#N)=C\C1=CC=C(C(C=C2)=CC=C2N(C3=CC4=C(C=CC=C4)C=C3)C5=CC=CC=C5)S1,2b,,,0.8,6.2,40,2.2,"	Mohamed S, Demeter D, Laffitte J-A, Blanchard P, Roncali J. Structure-properties relationships in triarylamine-based donor-acceptor molecules containing naphtyl groups as donor material for organic solar cells. Scientific reports 5, 9031 (2015)."
2427,N#C/C(C#N)=C\C1=CC=C(C(C=C2)=CC=C2N(C3=CC4=C(C=CC=C4)C=C3)C5=CC=CC6=C5C=CC=C6)S1,3ab,,,0.83,7.8,47,3.38,"	Mohamed S, Demeter D, Laffitte J-A, Blanchard P, Roncali J. Structure-properties relationships in triarylamine-based donor-acceptor molecules containing naphtyl groups as donor material for organic solar cells. Scientific reports 5, 9031 (2015)."
2428,N#C/C(C#N)=C\C1=CC=C(C(C=C2)=CC=C2N(C3=CC4=C(C=CC=C4)C=C3)C5=CC=C(C=CC=C6)C6=C5)S1,4bb,,,0.96,4,0.39,1.66,"	Mohamed S, Demeter D, Laffitte J-A, Blanchard P, Roncali J. Structure-properties relationships in triarylamine-based donor-acceptor molecules containing naphtyl groups as donor material for organic solar cells. Scientific reports 5, 9031 (2015)."
2429,N#C/C(C#N)=C\C1=CC=C(C(C=C2)=CC3=C2N(C4CCCC43)C5=CC=C(C)C=C5)S1,LC151,,,0.92,3.3,40,1.35,"	Mohamed S, Demeter D, Laffitte J-A, Blanchard P, Roncali J. Structure-properties relationships in triarylamine-based donor-acceptor molecules containing naphtyl groups as donor material for organic solar cells. Scientific reports 5, 9031 (2015)."
2430,CC(C=C1)=CC=C1N(C2CCCC23)C4=C3C=C(C5=CC=C(C6=CC=C(/C=C(C#N)/C#N)S6)S5)C=C4,LC163,,,0.915,8.33,43.79,3.34,"	Montcada NF, Cabau L, Kumar CV, Cambarau W, Palomares E. Indoline as electron donor unit in ¡°Push¨CPull¡± organic small molecules for solution processed organic solar cells: Effect of the molecular ¦Ð-bridge on device efficiency. Organic Electronics 20, 15-23 (2015)."
2431,CC(C=C1)=CC=C1N(C2CCCC23)C4=C3C=C(C5=CC6=C(C7=C(C6(CCCCCC)CCCCCC)C=C(/C=C(C#N)/C#N)S7)S5)C=C4,VC63,,,0.753,5.44,41.88,1.72,"	Montcada NF, Cabau L, Kumar CV, Cambarau W, Palomares E. Indoline as electron donor unit in ¡°Push¨CPull¡± organic small molecules for solution processed organic solar cells: Effect of the molecular ¦Ð-bridge on device efficiency. Organic Electronics 20, 15-23 (2015)."
2432,CC(C=C1)=CC=C1N(C2CCCC23)C4=C3C=C(C5=CC=C(C6=CC=C(/C=C(C#N)/C#N)S6)C7=NSN=C75)C=C4,VC64,,,0.729,3.05,38.33,0.85,"	Montcada NF, Cabau L, Kumar CV, Cambarau W, Palomares E. Indoline as electron donor unit in ¡°Push¨CPull¡± organic small molecules for solution processed organic solar cells: Effect of the molecular ¦Ð-bridge on device efficiency. Organic Electronics 20, 15-23 (2015)."
2433,CCCCCCC1=CC=C(C2=CC=C(C3=CC=C(/C(C#N)=C(C(C=C4)=CC=C4C5=CC=C(C6=CC=C(CCCCCC)S6)S5)\C#N)C=C3)S2)S1,RCNR,,,0.809,6.42,49.98,2.45,"	Montcada NF, Cabau L, Kumar CV, Cambarau W, Palomares E. Indoline as electron donor unit in ¡°Push¨CPull¡± organic small molecules for solution processed organic solar cells: Effect of the molecular ¦Ð-bridge on device efficiency. Organic Electronics 20, 15-23 (2015)."
2434,CCCCCCCCC1=C(C2=CC=C(C3=C(CCCCCCCC)C=C(/C=C(S4)/C(N(CC)C4=S)=O)S3)S2)SC(C5=CC6=C(C=C5)C7=C(C=C(C8=CC(CCCCCCCC)=C(C9=CC=C(C%10=C(CCCCCCCC)C=C(/C=C(S%11)/C(N(CC)C%11=S)=O)S%10)S9)S8)C=C7)C6(CC(CC)CCCC)CC(CC)CCCC)=C1,DR3TDTC,,,0.792,9.68,35,2.69,"	Nazim M, Ameen S, Seo HK, Shin HS. Effective D-A-D type chromophore of fumaronitrile-core and terminal alkylated bithiophene for solution-processed small molecule organic solar cells. Scientific reports 5, 11143 (2015)."
2435,N#C/C(C#N)=C\C1=CC=C(S1)C2=CC=C(N(C3=CC=CC=C3)C4=CC=CC=C4)C=C2,DPTMM,,,0.85,2.74,30,0.71,"	Ni W, et al. Dithienosilole-Based Small-Molecule Organic Solar Cells with an Efficiency over 8%: Investigation of the Relationship between the Molecular Structure and Photovoltaic Performance. Chemistry of Materials 27, 6077-6084 (2015)."
2436,CCCCCCCCC1=C(C2=CC=C(C3=C(CCCCCCCC)C=C(/C=C(S4)/C(N(CC)C4=S)=O)S3)S2)SC(C5=CC6=C(C=C5)C7=C(C=C(C8=CC(CCCCCCCC)=C(C9=CC=C(C%10=C(CCCCCCCC)C=C(/C=C(S%11)/C(N(CC)C%11=S)=O)S%10)S9)S8)C=C7)[Si]6(CC(CC)CCCC)CC(CC)CCCC)=C1,DR3TDTS,,,0.99,6.29,64,4,"	Choi JW, et al. Exploiting the potential of 2-((5-(4-(diphenylamino)phenyl)thiophen-2-yl)methylene)malononitrile as an efficient donor molecule in vacuum-processed bulk-heterojunction organic solar cells. RSC Advances 4, 5236 (2014)."
2437,CCCCCCC1=C(C2=CC=C(C3=C(CCCCCC)C=C(C4=C(CCCCCC)C=C(C5=CC=C(/C(C(N6CC(CC)CCCC)=O)=C7C(C(CC(C)CCCC)C8=C\7C=C(F)C=C8)=O)C6=C5)S4)S3)S2)SC(C9=CC(CCCCCC)=C(C%10=CC=C(/C(C(N%11CC(CC)CCCC)=O)=C%12C(C(CC(C)CCCC)C%13=C\%12C=C(F)C=C%13)=O)C%11=C%10)S9)=C1,M1,,,0.82,13.67,69,7.8,"	Ni W, et al. Dithienosilole-Based Small-Molecule Organic Solar Cells with an Efficiency over 8%: Investigation of the Relationship between the Molecular Structure and Photovoltaic Performance. Chemistry of Materials 27, 6077-6084 (2015)."
2438,CCCCCCC1=C(C2=CC=C(C3=CC(C4=CC=C(C5=C(CCCCCC)C=C(C6=C(CCCCC)C=C(C7=CC=C(/C(C(N8CC(CC)CCCC)=O)=C9C(C(CC(C)CCCC)C%10=C\9C=C(F)C=C%10)=O)C8=C7)S6)S5)S4)=CC(C%11=CC=C(C%12=C(CCCCCC)C=C(C%13=C(CCCCC)C=C(C%14=CC=C(/C(C(N%15CC(CC)CCCC)=O)=C%16C(C(CC(C)CCCC)C%17=C\%16C=C(F)C=C%17)=O)C%15=C%14)S%13)S%12)S%11)=C3)S2)SC(C%18=C(CCCCC)C=C(C%19=CC=C(/C(C(N%20CC(CC)CCCC)=O)=C%21C(C(CC(C)CCCC)C%22=C\%21C=C(F)C=C%22)=O)C%20=C%19)S%18)=C1,M2,,,0.7,4.11,53.4,1.54,"	Ouhib F, et al. Linear and propeller-like fluoro-isoindigo based donor¨Cacceptor small molecules for organic solar cells. Organic Electronics 20, 76-88 (2015)."
2439,CCCCCCC1=CC=C(C2=CC=C(C3=CC=C(C4=CC=C(C5=CC(C(NNC6=O)=O)=C6C=C5)S4)S3)S2)S1,HexLQPH,,,0.97,4.29,53.3,2.23,"	Ouhib F, et al. Linear and propeller-like fluoro-isoindigo based donor¨Cacceptor small molecules for organic solar cells. Organic Electronics 20, 76-88 (2015)."
2440,CCCCCCC1=CC=C(C2=CC=C(C3=CC=C(C4=CC=C(C5=CC(C(OC)=O)=C(C(OC)=O)C=C5)S4)S3)S2)S1,HexLQPME,,,0.7,6.6,48,2.24,"	Shewmon NT, et al. Enhancement in Organic Photovoltaic Efficiency through the Synergistic Interplay of Molecular Donor Hydrogen Bonding and ¦Ð-Stacking. Advanced Electronic Materials 25, 5166-5177 (2015)."
2441,CCC(CCCC)CN(C1)C(C2=CC=C(C3=CC=C(C4=NC(C5=CC=C(C6=CC=C(C(N(CC(CCCC)CC)C7)=C8C7=C(C(S9)=CC=C9C%10=CC=C(N(C%11=CC=C(C(C)(C)C)C=C%11)C%12=CC=C(C(C)(C)C)C=C%12)C=C%10)N(CC(CCCC)CC)C8)S6)C=C5)=NC(C%13=CC=C(C%14=CC=C(C(N(CC(CCCC)CC)C%15)=C%16C%15=C(C(S%17)=CC=C%17C%18=CC=C(N(C%19=CC=C(C(C)(C)C)C=C%19)C%20=CC=C(C(C)(C)C)C=C%20)C=C%18)N(CC(CCCC)CC)C%16)S%14)C=C%13)=N4)C=C3)S2)=C%21C1=C(C(S%22)=CC=C%22C%23=CC=C(N(C%24=CC=C(C(C)(C)C)C=C%24)C%25=CC=C(C(C)(C)C)C=C%25)C=C%23)N(CC(CCCC)CC)C%21,TDPP-TPA,,,0.71,3.8,32,0.88,"	Shewmon NT, et al. Enhancement in Organic Photovoltaic Efficiency through the Synergistic Interplay of Molecular Donor Hydrogen Bonding and ¦Ð-Stacking. Advanced Electronic Materials 25, 5166-5177 (2015)."
2442,CCC(CCCC)CN(C1)C(C(C=C2)=CC=C2C3=CC=C(C4=NC(C5=CC=C(C6=CC=C(C(N(CC(CCCC)CC)C7)=C8C7=C(C(C=C9)=CC=C9C%10=CC=C(N(C%11=CC=C(C(C)(C)C)C=C%11)C%12=CC=C(C(C)(C)C)C=C%12)C=C%10)N(CC(CCCC)CC)C8)C=C6)C=C5)=NC(C%13=CC=C(C%14=CC=C(C(N(CC(CCCC)CC)C%15)=C%16C%15=C(C%17=CC=C(C%18=CC=C(N(C%19=CC=C(C(C)(C)C)C=C%19)C%20=CC=C(C(C)(C)C)C=C%20)C=C%18)C=C%17)N(CC(CCCC)CC)C%16)C=C%14)C=C%13)=N4)C=C3)=C%21C1=C(C%22=CC=C(C%23=CC=C(N(C%24=CC=C(C(C)(C)C)C=C%24)C%25=CC=C(C(C)(C)C)C=C%25)C=C%23)C=C%22)N(CC(CCCC)CC)C%21,PDPP-TPA,,,0.73,6.34,34,1.57,"	Shiau S-Y, Chang C-H, Chen W-J, Wang H-J, Jeng R-J, Lee R-H. Star-shaped organic semiconductors with planar triazine core and diketopyrrolopyrrole branches for solution-processed small-molecule organic solar cells. Dyes and Pigments 115, 35-49 (2015)."
2443,CCC(CCCC)CN(C1)C(C(C=C2)=CC=C2C3=CC=C(C4=NC(C5=CC=C(C6=CC=C(C(N(CC(CCCC)CC)C7)=C8C7=C(C(C=C9)=CC=C9C%10=CC=C(N%11C%12=CC=C(C(C)(C)C)C=C%12C%13=C%11C=CC(C(C)(C)C)=C%13)C=C%10)N(CC(CCCC)CC)C8)C=C6)C=C5)=NC(C%14=CC=C(C%15=CC=C(C(N(CC(CCCC)CC)C%16)=C%17C%16=C(C%18=CC=C(C%19=CC=C(N(C%20=CC=C(C(C)(C)C)C=C%20%21)C%22=C%21C=C(C(C)(C)C)C=C%22)C=C%19)C=C%18)N(CC(CCCC)CC)C%17)C=C%15)C=C%14)=N4)C=C3)=C%23C1=C(C%24=CC=C(C%25=CC=C(N%26C%27=CC=C(C(C)(C)C)C=C%27C%28=C%26C=CC(C(C)(C)C)=C%28)C=C%25)C=C%24)N(CC(CCCC)CC)C%23,PDPP-Cz,,,0.61,5.85,32,1.14,"	Shiau S-Y, Chang C-H, Chen W-J, Wang H-J, Jeng R-J, Lee R-H. Star-shaped organic semiconductors with planar triazine core and diketopyrrolopyrrole branches for solution-processed small-molecule organic solar cells. Dyes and Pigments 115, 35-49 (2015)."
2444,CCCCC(CC)CC(S1)=CC=C1C2=C(C=C(C3=C(CCCCCCCC)C=C(C4=C(CCCCCCCC)C=C(C5=CC=C(/C=C(C(OCC(CCCC)CC)=O)\C#N)S5)S4)S3)S6)C6=C(C7=CC=C(CC(CC)CCCC)S7)C8=C2SC(C9=C(CCCCCCCC)C=C(C%10=C(CCCCCCCC)C=C(C%11=CC=C(/C=C(C(OCC(CCCC)CC)=O)\C#N)S%11)S%10)S9)=C8,DCA3T(T-BDT),,,0.5,2.75,28,0.39,"	Shiau S-Y, Chang C-H, Chen W-J, Wang H-J, Jeng R-J, Lee R-H. Star-shaped organic semiconductors with planar triazine core and diketopyrrolopyrrole branches for solution-processed small-molecule organic solar cells. Dyes and Pigments 115, 35-49 (2015)."
2445,CCCCCCCCC1=C(C2=CC=C(C3=CC(CCCCCCCC)=C(/C=C4C(N(CCCCCCCC)C(S\4)=S)=O)S3)S2)SC(C5=CC6=C(C7=CC=C(CC(CC)CCCC)S7)C8=C(C=C(C9=CC(CCCCCCCC)=C(C%10=CC=C(C%11=CC(CCCCCCCC)=C(/C=C%12C(N(CCCCCCCC)C(S\%12)=S)=O)S%11)S%10)S9)S8)C(C%13=CC=C(CC(CC)CCCC)S%13)=C6S5)=C1,SMPV1,,,0.95,9.16,70,11.11,"	Du Z, et al. High efficiency solution-processed two-dimensional small molecule organic solar cells obtained via low-temperature thermal annealing. J. Mater. Chem. A 2, 15904-15911 (2014)."
2446,CC1=C(CC)C2=N/C1=C\C3=C(CC)C(C)=C(/C=C([C@H]4C)\N=C(C(CC5)=C(C5=C/6C)NC6=C/2)C4CCC(OC)=O)N3,1a,,,0.93,10.59,72,6.74,"	Sun Q, et al. Revealing the effect of donor/acceptor intermolecular arrangement on organic solar cells performance based on two-dimensional conjugated small molecule as electron donor. Organic Electronics 24, 30-36 (2015)."
2447,CC1=C(CC)C2=N/C1=C\C3=C(C(C)=O)C(C)=C(/C=C([C@H]4C)\N=C(C(CC5)=C(C5=C/6C)NC6=C/2)C4CCC(OC)=O)N3,1b,,,0.6,3.25,34,0.68,"	Tamiaki H, Tanaka T, Wang X-F. Photophysical properties of synthetic monomer, dimer, trimer, and tetramer of chlorophyll derivatives and their application to organic solar cells. Journal of Photochemistry and Photobiology A: Chemistry 313, 19-26 (2015)."
2448,CC1=C(CC)C2=N/C1=C\C3=C(CC)C(C)=C(/C=C([C@H]4C)\N=C(C(CC5=O)=C(C5=C/6C)NC6=C/2)C4CCC(OC)=O)N3,1c,,,0.7,4.47,35,1.17,"	Tamiaki H, Tanaka T, Wang X-F. Photophysical properties of synthetic monomer, dimer, trimer, and tetramer of chlorophyll derivatives and their application to organic solar cells. Journal of Photochemistry and Photobiology A: Chemistry 313, 19-26 (2015)."
2449,CC1=C(CC)C2=N/C1=C\C3=C(C(C)=O)C(C)=C(/C=C([C@H]4C)\N=C(C(CC5=O)=C(C5=C/6C)NC6=C/2)C4CCC(OC)=O)N3,1d,,,0.76,5.76,34,1.49,"	Tamiaki H, Tanaka T, Wang X-F. Photophysical properties of synthetic monomer, dimer, trimer, and tetramer of chlorophyll derivatives and their application to organic solar cells. Journal of Photochemistry and Photobiology A: Chemistry 313, 19-26 (2015)."
2450,CCC(CCCC)CC1=CC=C(C2=C3C(C=C(C4=C(CCCCCCCC)C=C(/C=C5C(N(CC(CCCC)CC)C(C(C#N)=C/5C)=O)=O)S4)S3)=C(C6=CC=C(CC(CC)CCCC)S6)C7=C2C=C(C8=C(CCCCCCCC)C=C(/C=C9C(N(CC(CCCC)CC)C(C(C#N)=C/9C)=O)=O)S8)S7)S1,1TBM,,,0.84,5.53,34,1.52,"	Tamiaki H, Tanaka T, Wang X-F. Photophysical properties of synthetic monomer, dimer, trimer, and tetramer of chlorophyll derivatives and their application to organic solar cells. Journal of Photochemistry and Photobiology A: Chemistry 313, 19-26 (2015)."
2451,CCC(CCCC)CC1=CC=C(C2=C3C(C=C(C4=CC(CCCCCCCC)=C(C5=C(CCCCCCCC)C=C(/C=C6C(N(CC(CCCC)CC)C(C(C#N)=C/6C)=O)=O)S5)S4)S3)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C2C=C(C9=CC(CCCCCCCC)=C(C%10=C(CCCCCCCC)C=C(/C=C%11C(N(CC(CCCC)CC)C(C(C#N)=C/%11C)=O)=O)S%10)S9)S8)S1,2TBM,,,0.82,3.49,33.2,0.95,"	Tang A, Zhan C, Yao J. Series of Quinoidal Methyl-Dioxocyano-Pyridine Based ¦Ð-Extended Narrow-Bandgap Oligomers for Solution-Processed Small-Molecule Organic Solar Cells. Chemistry of Materials 27, 4719-4730 (2015)."
2452,CCC(CCCC)CC1=CC=C(C2=C3C(C=C(C4=CC(CCCCCCCC)=C(C5=CC=C(C6=C(CCCCCCCC)C=C(/C=C7C(N(CC(CCCC)CC)C(C(C#N)=C/7C)=O)=O)S6)S5)S4)S3)=C(C8=CC=C(CC(CC)CCCC)S8)C9=C2C=C(C%10=CC(CCCCCCCC)=C(C%11=CC=C(C%12=C(CCCCCCCC)C=C(/C=C%13C(N(CC(CCCC)CC)C(C(C#N)=C/%13C)=O)=O)S%12)S%11)S%10)S9)S1,3TBM,,,0.79,6.66,35.1,1.85,"	Tang A, Zhan C, Yao J. Series of Quinoidal Methyl-Dioxocyano-Pyridine Based ¦Ð-Extended Narrow-Bandgap Oligomers for Solution-Processed Small-Molecule Organic Solar Cells. Chemistry of Materials 27, 4719-4730 (2015)."
2453,CCC(CCCC)CC1=CC=C(C2=C3C(C=C(C4=CC(CCCCCCCC)=C(C5=CC(CCCCCCCC)=C(C6=C(CCCCCCCC)C=C(C7=C(CCCCCCCC)C=C(/C=C8C(N(CC(CCCC)CC)C(C(C#N)=C\8C)=O)=O)S7)S6)S5)S4)S3)=C(C9=CC=C(CC(CC)CCCC)S9)C%10=C2C=C(C%11=CC(CCCCCCCC)=C(C%12=CC(CCCCCCCC)=C(C%13=C(CCCCCCCC)C=C(C%14=C(CCCCCCCC)C=C(/C=C%15C(N(CC(CCCC)CC)C(C(C#N)=C\%15C)=O)=O)S%14)S%13)S%12)S%11)S%10)S1,4TBM,,,0.79,14.38,55.4,6.29,"	Tang A, Zhan C, Yao J. Series of Quinoidal Methyl-Dioxocyano-Pyridine Based ¦Ð-Extended Narrow-Bandgap Oligomers for Solution-Processed Small-Molecule Organic Solar Cells. Chemistry of Materials 27, 4719-4730 (2015)."
2454,CCC(CCCC)CC1=CC=C(C2=C3C(C=C(C4=CC(CCCCCCCC)=C(C5=CC(CCCCCCCC)=C(C6=CC=C(C7=C(CCCCCCCC)C=C(C8=C(CCCCCCCC)C=C(/C=C9C(N(CC(CCCC)CC)C(C(C#N)=C\9C)=O)=O)S8)S7)S6)S5)S4)S3)=C(C%10=CC=C(CC(CC)CCCC)S%10)C%11=C2C=C(C%12=CC(CCCCCCCC)=C(C%13=CC(CCCCCCCC)=C(C%14=CC=C(C%15=C(CCCCCCCC)C=C(C%16=C(CCCCCCCC)C=C(/C=C%17C(N(CC(CCCC)CC)C(C(C#N)=C\%17C)=O)=O)S%16)S%15)S%14)S%13)S%12)S%11)S1,5TBM,,,0.78,5.01,40.2,1.56,"	Tang A, Zhan C, Yao J. Series of Quinoidal Methyl-Dioxocyano-Pyridine Based ¦Ð-Extended Narrow-Bandgap Oligomers for Solution-Processed Small-Molecule Organic Solar Cells. Chemistry of Materials 27, 4719-4730 (2015)."
2455,S=C(S/1)N(C2=CC=CC=C2OC)C(C1=C\C=C\C3=CC=CC=C3[N+]([O-])=O)=O,TH-2,,,0.81,9.62,68.7,5.35,"	Tang A, Zhan C, Yao J. Series of Quinoidal Methyl-Dioxocyano-Pyridine Based ¦Ð-Extended Narrow-Bandgap Oligomers for Solution-Processed Small-Molecule Organic Solar Cells. Chemistry of Materials 27, 4719-4730 (2015)."
2456,O=C(N(CC(CCCC)CC)C1=C/2SC(C#CC3=CC=C(N4C(C=CC=C5)=C5C6=C4C=CC=C6)C=C3)=C1)C2=C7C8=C(C=C(C#CC9=CC=C(N%10C(C=CC=C%11)=C%11C%12=C%10C=CC=C%12)C=C9)S8)N(CC(CCCC)CC)C/7=O,TII-PCz,,,0.41,3.52,34,0.49,"	Toumi AL, et al. Optimum Compromise Between Optical Absorption And Electrical Property Of the Planar Multi-Heterojunction Organic Solar Cells Based with New Thiazol Derivative, the (2-Thioxo-3-N-(2-Methoxyphenyl) Thiazolidin-4-One), as Electron Donor. Surface Review and Letters 22, 1550025 (2015)."
2457,O=C(N(CC(CCCC)CC)C1=C/2SC(C#CC3=CC=C(N(C4=CC=CC=C4)C5=CC=CC=C5)C=C3)=C1)C2=C6C7=C(C=C(C#CC8=CC=C(N(C9=CC=CC=C9)C%10=CC=CC=C%10)C=C8)S7)N(CC(CCCC)CC)C/6=O,TII-TPA,,,0.99,4.11,29.9,1.52,"	Vybornyi O, et al. Solution-processable thienoisoindigo-based molecular donors for organic solar cells with high open-circuit voltage. Dyes and Pigments 115, 17-22 (2015)."
2458,CCCCCCC1=CC=C(C2=CC=C(C3=C(F)C(F)=C(C4=CC5=C(C(C=C(C(C(CCCCCC)C)(C(CCCCCC)C)C6=C7SC(C8=CC=C(C9=C%10C(C(C9C(CCCCCC)C)=O)=C(C%11=CC=C(C(S%12)=CC%13=C%12C%14=CC(C%15(C(CCCCCC)C)C(CCCCCC)C)=C(C=C%14C%13(C(CCCCCC)C)C(CCCCCC)C)C%16=C%15C=C(C%17=C(F)C(F)=C(C%18=NSN=C%18%17)C%19=CC=C(C%20=CC=C(CCCCCC)S%20)S%19)S%16)S%11)C(C(CCCCCC)C)C%10=O)S8)=C6)C7=C%21)=C%21C5(C(CCCCCC)C)C(CCCCCC)C)S4)C%22=NSN=C3%22)S2)S1,DPPFB,,,0.82,5.48,39.8,2.23,"	Vybornyi O, et al. Solution-processable thienoisoindigo-based molecular donors for organic solar cells with high open-circuit voltage. Dyes and Pigments 115, 17-22 (2015)."
2459,O=C1C(C(C(C2C(CCCCCC)C)=O)=C(C3=CC=C(C4=CC(C(S5)=CC6=C5C7=CC(C8(C(CCCCCC)C)C(CCCCCC)C)=C(C=C7C6(C(CCCCCC)C)C(CCCCCC)C)C9=C8C=C(C%10=CC=C(C%11=C(F)C(F)=C(C%12=NSN=C%12%11)C%13=CC=C(C%14=CC=C(CCCCCC)S%14)S%13)S%10)S9)=CS4)S3)C1C(CCCCCC)C)=C2C%15=CC=C(C%16=CC=C(C(S%17)=CC%18=C%17C%19=CC(C%20(C(CCCCCC)C)C(CCCCCC)C)=C(C=C%19C%18(C(CCCCCC)C)C(CCCCCC)C)C%21=C%20C=C(C%22=CC=C(C%23=C(F)C(F)=C(C%24=NSN=C%24%23)C%25=CC=C(C%26=CC=C(CCCCCC)S%26)S%25)S%22)S%21)S%16)S%15,DPPFBT,,,0.76,9.88,69,5.21,"	Wang J-L, et al. Solution-Processed Diketopyrrolopyrrole-Containing Small-Molecule Organic Solar Cells with 7.0% Efficiency: In-Depth Investigation on the Effects of Structure Modification and Solvent Vapor Annealing. Chemistry of Materials 27, 4338-4348 (2015)."
2460,O=C1C(C(C(C2C(CCCCCC)C)=O)=C(C3=NC=C(C4=CC(C(S5)=CC6=C5C7=CC(C8(C(CCCCCC)C)C(CCCCCC)C)=C(C=C7C6(C(CCCCCC)C)C(CCCCCC)C)C9=C8C=C(C%10=CC=C(C%11=C(F)C(F)=C(C%12=NSN=C%12%11)C%13=CC=C(C%14=CC=C(CCCCCC)S%14)S%13)S%10)S9)=CS4)S3)C1C(CCCCCC)C)=C2C%15=NC=C(C%16=CC=C(C(S%17)=CC%18=C%17C%19=CC(C%20(C(CCCCCC)C)C(CCCCCC)C)=C(C=C%19C%18(C(CCCCCC)C)C(CCCCCC)C)C%21=C%20C=C(C%22=CC=C(C%23=C(F)C(F)=C(C%24=NSN=C%24%23)C%25=CC=C(C%26=CC=C(CCCCCC)S%26)S%25)S%22)S%21)S%16)S%15,NDPPFBT,,,0.76,10.51,60.85,4.83,"	Wang J-L, et al. Solution-Processed Diketopyrrolopyrrole-Containing Small-Molecule Organic Solar Cells with 7.0% Efficiency: In-Depth Investigation on the Effects of Structure Modification and Solvent Vapor Annealing. Chemistry of Materials 27, 4338-4348 (2015)."
2461,CC(CCCCCC)C1=CC=C(C2=C(C=C(C3=C(F)C=C(C4=CC=C(C5=CC=C(CCCCCC)S5)S4)C6=NSN=C36)S7)C7=C(C8=CC=C(C(CCCCCC)C)S8)C9=C2SC(C%10=C(F)C=C(C%11=CC=C(C%12=CC=C(CCCCCC)S%12)S%11)C%13=NSN=C%10%13)=C9)S1,BDT-BTF,,,0.88,10.71,71.6,6.86,"	Wang J-L, et al. Solution-Processed Diketopyrrolopyrrole-Containing Small-Molecule Organic Solar Cells with 7.0% Efficiency: In-Depth Investigation on the Effects of Structure Modification and Solvent Vapor Annealing. Chemistry of Materials 27, 4338-4348 (2015)."
2462,O=C1C(C2=C(O)C=C(N(C(C)CC)CCC)C=C2O)=C([O-])/C1=C(C(O)=C/3)\C(O)=CC3=[N+](CCC)\C(C)CC,SQ3,,,0.85,10.48,66,5.88,"	Wang K, Guo B, Xu Z, Guo X, Zhang M, Li Y. Solution-Processable Organic Molecule for High-Performance Organic Solar Cells with Low Acceptor Content. ACS Appl Mater Interfaces 7, 24686-24693 (2015)."
2463,COC1C=CC2=C(C3=CC=C(OCCOCCOCCOC)C=C3)C(N4[B](F)(F)N21)=CC=C4C5=CC6=C(C7=CC=C(CC(CC)CC)S7)C8=C(C=C(C9=CC=C%10N9[B](F)(F)N%11C(C=CC%11OC)=C%10C%12=CC=C(OCCOCCOCCOC)C=C%12)S8)C(C%13=CC=C(CC(CC)CC)S%13)=C6S5,BDTT-BODIPY,,,0.76,7.75,32,1.85,"	Bruck S, et al. Structure-property relationship of anilino-squaraines in organic solar cells. Physical chemistry chemical physics : PCCP 16, 1067-1077 (2014)."
2464,COC1=[N]2C(C=C1)=C(C3=CC=C(OCCOCCOCCOC)C=C3)C4=CC=C(C5=CC(C6(CCCCCCCC)CCCCCCCC)=C(C(C6=C7)=CC=C7C8=CC=C9N8[B](F)(F)[N]%10=C(OC)C=CC%10=C9C%11=CC=C(OCCOCCOCCOC)C=C%11)C=C5)N4[B]2(F)F,FL-BODIPY,,,0.97,10.55,46.5,4.75,"	Xiao L, et al. A-D-A Type Small Molecules Based on Boron Dipyrromethene for Solution-Processed Organic Solar Cells. Chemistry, an Asian journal 10, 1513-1518 (2015)."
2465,CCC(CCCC)CC1=CC=C(C2=C(C=C(C3=C(F)C(F)=C(C4=CC5=C(S4)C(C6=CC=C(CC(CCCC)CC)S6)=C(C=CS7)C7=C5C8=CC=C(CC(CCCC)CC)S8)C9=NSN=C39)S%10)C%10=C(C%11=CC=C(CC(CCCC)CC)S%11)C%12=C2SC(C%13=C(F)C(F)=C(C%14=CC%15=C(C%16=CC=C(CC(CCCC)CC)S%16)C%17=C(C=CS%17)C(C%18=CC=C(CC(CCCC)CC)S%18)=C%15S%14)C%19=NSN=C%19%13)=C%12)S1,O-BDTdFBT,,,0.99,3.49,43.49,1.51,"	Xiao L, et al. A-D-A Type Small Molecules Based on Boron Dipyrromethene for Solution-Processed Organic Solar Cells. Chemistry, an Asian journal 10, 1513-1518 (2015)."
2466,CC(C=C1)=CC=C1N(C2=CC=C(C)C=C2)C3=CC=C(C4=CC=C(C5=CC(CCCCCC)=C(C#CC6=CC=C(C#CC7=C(CCCCCC)C=C(C8=CC=C(C(C=C9)=CC=C9N(C%10=CC=C(C)C=C%10)C%11=CC=C(C)C=C%11)C%12=NSN=C8%12)S7)C=C6)S5)C%13=NSN=C%134)C=C3,1,,,0.97,11.48,70,7.81,"	Yuan L, et al. Oligomeric Donor Material for High-Efficiency Organic Solar Cells: Breaking Down a Polymer. Adv Mater 27, 4229-4233 (2015)."
2467,CC(C=C1)=CC=C1N(C2=CC=C(C)C=C2)C3=CC=C(C4=CC=C(C5=CC(CCCCCC)=C(C#CC(S6)=CC7=C6C(SC(C#CC8=C(CCCCCC)C=C(C9=CC=C(C(C=C%10)=CC=C%10N(C%11=CC=C(C)C=C%11)C%12=CC=C(C)C=C%12)C%13=NSN=C9%13)S8)=C%14)=C%14C7(CCCCCCCCCCCC)CCCCCCCCCCCC)S5)C%15=NSN=C%154)C=C3,2,,,0.93,7.04,44,2.87,"	Zhan H, et al. Organic donor materials based on Bis(arylene ethynylene)s for bulk heterojunction organic solar cells with high V(oc) values. Chemistry, an Asian journal 10, 1017-1024 (2015)."
2468,CC(C1=CC=C(C2=C3C(C=C(C4=CC(C5=C(C(N6CCCCCCCC)=O)C(C6=O)=C(C7=CC=CS7)S5)=CS4)S3)=C(C8=CC=C(C(CCCCCC)C)[Se]8)C9=C2C=C(C%10=CC(C%11=C(C(N%12CCCCCCCC)=O)C(C%12=O)=C(C%13=CC=CS%13)S%11)=CS%10)S9)[Se]1)CCCCCC,BDTSe-TTPD,,,0.94,7.24,48,3.28,"	Zhan H, et al. Organic donor materials based on Bis(arylene ethynylene)s for bulk heterojunction organic solar cells with high V(oc) values. Chemistry, an Asian journal 10, 1017-1024 (2015)."
2469,CC(C=C1)=CC=C1N(C2=CC=C(C)C=C2)C3=CC=C(C4=CC=C(C5=CC(CCCCCC)=C(C#CC6=CC=C(N(C7=CC=C(C)C=C7)C(C=C8)=CC=C8C#CC9=C(CCCCCC)C=C(C%10=CC=C(C(C=C%11)=CC=C%11N(C%12=CC=C(C)C=C%12)C%13=CC=C(C)C=C%13)C%14=NSN=C%10%14)S9)C=C6)S5)C%15=NSN=C%154)C=C3,3,,,0.9,10.5,46.3,4.37,"	Kim YJ, et al. A high-performance solution-processed small molecule: alkylselenophene-substituted benzodithiophene organic solar cell. J. Mater. Chem. C 2, 4937-4946 (2014)."
2470,CCCCCCC1=C(C#CC2=CC=C(C#CC3=C(CCCCCC)C=C(C4=CC=C(C5=CC=C(C(C=C6)=CC=C6N(C7=CC=C(C)C=C7)C8=CC=C(C)C=C8)S5)C9=NSN=C49)S3)C=C2)SC(C%10=CC=C(C%11=CC=C(C(C=C%12)=CC=C%12N(C%13=CC=C(C)C=C%13)C%14=CC=C(C)C=C%14)S%11)C%15=NSN=C%10%15)=C1,4,,,0.96,5.96,44,2.51,"	Zhan H, et al. Organic donor materials based on Bis(arylene ethynylene)s for bulk heterojunction organic solar cells with high V(oc) values. Chemistry, an Asian journal 10, 1017-1024 (2015)."
2471,O=C(N(CCCCCCCC)C1=O)C2=CC=CC(C2=C1C=C3)=C3C4=CC=C(C5=CC=C(N(C(C=C6)=CC=C6C7=CC=C(C8=C(C=CC=C9C(N(CCCCCCCC)C%10=O)=O)C9=C%10C=C8)S7)C(C=C%11)=CC=C%11C%12=CC=C(C%13=C(C=CC=C%14C(N(CCCCCCCC)C%15=O)=O)C%14=C%15C=C%13)S%12)C=C5)S4,SM3,,,0.85,6.45,43,2.36,"	Zhan H, et al. Organic donor materials based on Bis(arylene ethynylene)s for bulk heterojunction organic solar cells with high V(oc) values. Chemistry, an Asian journal 10, 1017-1024 (2015)."
2472,O=C(N(CCCCCCCC)C1=O)C2=CC=C(C3=CC=C(C4=C(CCCCCCCC)C(CCCCCCCC)=C(C5=CC=C(C6=CC=C(N(C(C=C7)=CC=C7C8=CC=C(C9=C(CCCCCCCC)C(CCCCCCCC)=C(C%10=CC=C(C%11=CC=C(C(N(CCCCCCCC)C%12=O)=O)C%13=C%12C=CC=C%13%11)S%10)S9)S8)C(C=C%14)=CC=C%14C%15=CC=C(C%16=C(CCCCCCCC)C(CCCCCCCC)=C(C%17=CC=C(C%18=CC=C(C(N(CCCCCCCC)C%19=O)=O)C%20=C%19C=CC=C%20%18)S%17)S%16)S%15)C=C6)S5)S4)S3)C%21=CC=CC1=C%212,SM4,,,0.9,6.29,34,1.96,"	Zhang J, et al. Synthesis of star-shaped small molecules carrying peripheral 1,8-naphthalimide functional groups and their applications in organic solar cells. Dyes and Pigments 115, 181-189 (2015)."
2473,C1(C2=CC=C(C(C3=CC=CN3[Ni]4)=C5N4CC=C5)S2)=CC=C(C(C=C6)=CC=C6N(C7=CC=CC=C7)C8=CC=CC=C8)C9=NSN=C19,8,,,0.94,6.38,39,2.32,"	Zhang J, et al. Synthesis of star-shaped small molecules carrying peripheral 1,8-naphthalimide functional groups and their applications in organic solar cells. Dyes and Pigments 115, 181-189 (2015)."
2474,C12=C(C(C=C3)=CC=C2)C(C3=C(C(S4)=CC5=C4C(SC(C6=C7C8=C(C=CC9=C8C(C=C7)=CC=C9)C=C6)=C%10)=C%10S5)C=C%11)=C%11C=C1,DDT,,,0.59,1.04,25,0.15,"	Zou L, Guan S, Li L, Zhao L. Dipyrrin-based complexes for solution-processed organic solar cells. Chemical Research in Chinese Universities 31, 801-808 (2015)."
2475,C1(C2=CC=C(C(C3=CC=CN3[Zn]4)=C5N4CC=C5)S2)=CC=C(C(C=C6)=CC=C6N(C7=CC=CC=C7)C8=CC=CC=C8)C9=NSN=C19,9,,,0.98,9.24,40,3.6,"	Kwon J, Kim T-M, Oh H-S, Kim J-J, Hong J-I. Vacuum processable donor material based on dithieno[3,2-b:2¡ä,3¡ä-d]thiophene and pyrene for efficient organic solar cells. RSC Adv. 4, 24453-24457 (2014)."
2476,C1(C2=CC=C(C(C3=CC=CN3[Pd]4)=C5N4CC=C5)S2)=CC=C(C(C=C6)=CC=C6N(C7=CC=CC=C7)C8=CC=CC=C8)C9=NSN=C19,10,,,0.41,1.13,25,0.12,"	Zou L, Guan S, Li L, Zhao L. Dipyrrin-based complexes for solution-processed organic solar cells. Chemical Research in Chinese Universities 31, 801-808 (2015)."
2477,F[B]1(F)N(CC=C2)C2=C(C3=CC=CN31)C4=CC=C(C5=CC=C(C(C=C6)=CC=C6N(C7=CC=CC=C7)C8=CC=CC=C8)C9=NSN=C59)S4,11,,,0.47,0.75,24,0.085,"	Zou L, Guan S, Li L, Zhao L. Dipyrrin-based complexes for solution-processed organic solar cells. Chemical Research in Chinese Universities 31, 801-808 (2015)."
2478,CCCCCCCC1=C(C2=CC(CCCCCCC)=C(C3=CC(CCCCCCC)=C(C4=CC=C(C5=C(CCCCCCC)C=C(C6=C(CCCCCCC)C=C(C7=C(CCCCCCC)C=C(/C=C8C(N(CC)/C(S/8)=C(C#N)/C#N)=O)S7)S6)S5)[Se]4)S3)S2)SC(/C=C9C(N(CC)/C(S/9)=C(C#N)/C#N)=O)=C1,DRCN7T-Se,,,0.81,3.03,24,0.58,"	Zou L, Guan S, Li L, Zhao L. Dipyrrin-based complexes for solution-processed organic solar cells. Chemical Research in Chinese Universities 31, 801-808 (2015)."
2479,N#C/C(C#N)=C(CCC1)/C=C1C2=CC=C(C3=C/C(CCC3)=C(C#N)\C#N)S2,DCC3T,,,0.913,13.06,69.6,8.3,"	Zuo Y, et al. A small molecule with selenophene as the central block for high performance solution-processed organic solar cells. Organic Electronics 19, 98-104 (2015)."
2480,N#C/C(C#N)=C(CCC1)/C=C1C2=CC=C(C3=C(C)C(C)=C(C4=CC=C(C5=C/C(CCC5)=C(C#N)\C#N)S4)S3)S2,DCC3T-Me,,,1,5.3,56,3,"	Fitzner R, Mena-Osteritz E, Walzer K, Pfeiffer M, B?uerle P. A-D-A-Type Oligothiophenes for Small Molecule Organic Solar Cells: Extending the ¦Ð-System by Introduction of Ring-Locked Double Bonds. Advanced Functional Materials 25, 1845-1856 (2015)."
2481,CC(CCCCCC)C1=CC=C(C2=C(C=C(C3=CC=C(C4=C5C(C(N4C(CCCCCC)C)=O)=C(C6=CC=C(C7=CC=CC=C7)S6)N(C(CCCCCC)C)C5=O)S3)S8)C8=C(C9=CC=C(C(CCCCCC)C)S9)C%10=C2SC(C%11=CC=C(C%12=C%13C(C(N%12C(CCCCCC)C)=O)=C(C%14=CC=C(C%15=CC=CC=C%15)S%14)N(C(CCCCCC)C)C%13=O)S%11)=C%10)S1,BDTT-(DPP)2-B,,,0.99,8.5,53,4.4,"	Fitzner R, Mena-Osteritz E, Walzer K, Pfeiffer M, B?uerle P. A-D-A-Type Oligothiophenes for Small Molecule Organic Solar Cells: Extending the ¦Ð-System by Introduction of Ring-Locked Double Bonds. Advanced Functional Materials 25, 1845-1856 (2015)."
2482,CC(CCCCCC)C1=CC=C(C2=C(C=C(C3=CC=C(C4=C5C(C(N4C(CCCCCC)C)=O)=C(C6=CC=C(C7=CC=C(F)C=C7)S6)N(C(CCCCCC)C)C5=O)S3)S8)C8=C(C9=CC=C(C(CCCCCC)C)S9)C%10=C2SC(C%11=CC=C(C%12=C%13C(C(N%12C(CCCCCC)C)=O)=C(C%14=CC=C(C%15=CC=C(F)C=C%15)S%14)N(C(CCCCCC)C)C%13=O)S%11)=C%10)S1,BDTT-(DPP)2-F,,,0.7,10.21,51,3.3,"	Kim JH, et al. Controlling the Morphology of BDTT-DPP-Based Small Molecules via End-Group Functionalization for Highly Efficient Single and Tandem Organic Photovoltaic Cells. ACS Appl Mater Interfaces 7, 23866-23875 (2015)."
2483,CC(CCCCCC)C1=CC=C(C2=C(C=C(C3=CC=C(C4=C5C(C(N4C(CCCCCC)C)=O)=C(C6=CC=C(C7=CC=C(C(F)(F)F)C=C7)S6)N(C(CCCCCC)C)C5=O)S3)S8)C8=C(C9=CC=C(C(CCCCCC)C)S9)C%10=C2SC(C%11=CC=C(C%12=C%13C(C(N%12C(CCCCCC)C)=O)=C(C%14=CC=C(C%15=CC=C(C(F)(F)F)C=C%15)S%14)N(C(CCCCCC)C)C%13=O)S%11)=C%10)S1,BDTT-(DPP)2-CF3,,,0.69,12.48,58,4.64,"	Kim JH, et al. Controlling the Morphology of BDTT-DPP-Based Small Molecules via End-Group Functionalization for Highly Efficient Single and Tandem Organic Photovoltaic Cells. ACS Appl Mater Interfaces 7, 23866-23875 (2015)."
2484,O=C(N1C(CCCCCC)C)C(C(C(N2C(CCCCCC)C)=O)=C1C(S3)=CC=C3C(C=C4)=CC=C4C(C=C5)=CC=C5N(C6=CC=CC=C6)C7=CC=CC=C7)=C2C(S8)=CC=C8C(C=C9)=CC=C9C(C=C%10)=CC=C%10N(C%11=CC=CC=C%11)C%12=CC=CC=C%12,SM1,,,0.69,13.6,64,5.87,"	Kim JH, et al. Controlling the Morphology of BDTT-DPP-Based Small Molecules via End-Group Functionalization for Highly Efficient Single and Tandem Organic Photovoltaic Cells. ACS Appl Mater Interfaces 7, 23866-23875 (2015)."
2485,O=C(N1C(CCCCCC)C)C(C(C(N2C(CCCCCC)C)=O)=C1C(S3)=CC=C3C4=CC=C(/C=C\C(C=C5)=CC=C5N(C6=CC=CC=C6)C7=CC=CC=C7)C=C4)=C2C(S8)=CC=C8C9=CC=C(/C=C\C(C=C%10)=CC=C%10N(C%11=CC=CC=C%11)C%12=CC=CC=C%12)C=C9,SM2,,,0.88,8.62,36,2.74,"	Ji C, et al. Linkage effects of linear D¨C¦Ð¨CA¨C¦Ð¨CD type diketopyrrolopyrrole-triphenylamine based solution-processable organic small molecule photovoltaic materials. Journal of Materials Chemistry C 2, 4019 (2014)."
2486,O=C(N1C(CCCCCC)C)C(C(C(N2C(CCCCCC)C)=O)=C1C(S3)=CC=C3C4=CC=C(C#CC(C=C5)=CC=C5N(C6=CC=CC=C6)C7=CC=CC=C7)C=C4)=C2C(S8)=CC=C8C9=CC=C(C#CC(C=C%10)=CC=C%10N(C%11=CC=CC=C%11)C%12=CC=CC=C%12)C=C9,SM3,,,0.84,11.9,38,3.76,"	Ji C, et al. Linkage effects of linear D¨C¦Ð¨CA¨C¦Ð¨CD type diketopyrrolopyrrole-triphenylamine based solution-processable organic small molecule photovoltaic materials. Journal of Materials Chemistry C 2, 4019 (2014)."
2487,O=C(N1C(CCCCCC)C)C(C(C(N2C(CCCCCC)C)=O)=C1C(S3)=CC=C3C4=CC=C(/C(C#N)=C\C(C=C5)=CC=C5N(C6=CC=CC=C6)C7=CC=CC=C7)C=C4)=C2C(S8)=CC=C8C9=CC=C(/C(C#N)=C\C(C=C%10)=CC=C%10N(C%11=CC=CC=C%11)C%12=CC=CC=C%12)C=C9,SM4,,,0.93,10.3,32,3.1,"	Ji C, et al. Linkage effects of linear D¨C¦Ð¨CA¨C¦Ð¨CD type diketopyrrolopyrrole-triphenylamine based solution-processable organic small molecule photovoltaic materials. Journal of Materials Chemistry C 2, 4019 (2014)."
2488,CCCCCCC(C=C(C1=C(CCCCCC)C=C(/C=C(CCCCCC)\C#N)S1)S2)=C2C(S3)=CC4=C3C(S5)=C([Si]4(CCCCCC)CCCCCC)C=C5C(S6)=CC=C6C(C=C7)=CC=C7N(C8=CC=CC=C8)C9=CC=CC=C9,1,,,0.9,9.73,33,2.92,"	Ji C, et al. Linkage effects of linear D¨C¦Ð¨CA¨C¦Ð¨CD type diketopyrrolopyrrole-triphenylamine based solution-processable organic small molecule photovoltaic materials. Journal of Materials Chemistry C 2, 4019 (2014)."
2489,CCCCCCC(C=C(C1=C(CCCCCC)C=C(/C=C(C#N)\C#N)S1)S2)=C2C(S3)=CC4=C3C(S5)=C([Si]4(CCCCCC)CCCCCC)C=C5C(S6)=CC=C6C(C=C7)=CC=C7N(C8=CC=CC=C8)C9=CC=CC=C9,2,,,0.79,5.57,38,1.67,"	Paek S, Lee JK, Ko J. Synthesis and photovoltaic characteristics of push¨Cpull organic semiconductors containing an electron-rich dithienosilole bridge for solution-processed small-molecule organic solar cells. Solar Energy Materials and Solar Cells 120, 209-217 (2014)."
2490,CCCCCCC(C=C(C1=C(CCCCCC)C=C(/C=C(CCCCCC)\C#N)S1)S2)=C2C(S3)=CC4=C3C(S5)=C([Si]4(CCCCCC)CCCCCC)C=C5C(S6)=CC=C6C(C=C7)=CC=C7N(C8=CC9=C(C(C)(C)C%10=C9C=CC=C%10)C=C8)C%11=CC(C(C)(C)C%12=C%13C=CC=C%12)=C%13C=C%11,3,,,0.8,6.46,37,1.92,"	Paek S, Lee JK, Ko J. Synthesis and photovoltaic characteristics of push¨Cpull organic semiconductors containing an electron-rich dithienosilole bridge for solution-processed small-molecule organic solar cells. Solar Energy Materials and Solar Cells 120, 209-217 (2014)."
2491,CCCCCCC(C=C(C1=C(CCCCCC)C=C(/C=C(C#N)\C#N)S1)S2)=C2C(S3)=CC4=C3C(S5)=C([Si]4(CCCCCC)CCCCCC)C=C5C(S6)=CC=C6C(C=C7)=CC=C7N(C8=CC9=C(C(C)(C)C%10=C9C=CC=C%10)C=C8)C%11=CC(C(C)(C)C%12=C%13C=CC=C%12)=C%13C=C%11,4,,,0.81,6.22,40,2.02,"	Paek S, Lee JK, Ko J. Synthesis and photovoltaic characteristics of push¨Cpull organic semiconductors containing an electron-rich dithienosilole bridge for solution-processed small-molecule organic solar cells. Solar Energy Materials and Solar Cells 120, 209-217 (2014)."
2492,O=C(N(CCCCCC)C1=O)C2=CC(OC(C=C3)=CC=C3C(C4=CC=CC=C4)C5=CC=CC=C5)=C6C7=C(OC(C=C8)=CC=C8C(C9=CC=CC=C9)C%10=CC=CC=C%10)C=C%11C%12=C(C(N(CCCCCC)C%11=O)=O)C=C(OC(C=C%13)=CC=C%13C(C%14=CC=CC=C%14)C%15=CC=CC=C%15)C(C%16=C6C2=C1C=C%16OC(C=C%17)=CC=C%17C(C%18=CC=CC=C%18)C%19=CC=CC=C%19)=C7%12,1,,,0.81,7.31,40,2.34,"	Paek S, Lee JK, Ko J. Synthesis and photovoltaic characteristics of push¨Cpull organic semiconductors containing an electron-rich dithienosilole bridge for solution-processed small-molecule organic solar cells. Solar Energy Materials and Solar Cells 120, 209-217 (2014)."
2493,O=C(N(CCCCCC)C1=O)C2=CC(OC3=CC=C(C4=CC(C56C7=C(C8=C6C=CC=C8)C=CC=C7)=C(C9=C5C=C(C(C=C%10)=CC=C%10C(C%11=CC=CC=C%11)C%12=CC=CC=C%12)C=C9)C=C4)C=C3)=C%13C%14=C(OC%15=CC=C(C%16=CC(C%17%18C%19=C(C%20=C%18C=CC=C%20)C=CC=C%19)=C(C%21=C%17C=C(C(C=C%22)=CC=C%22C(C%23=CC=CC=C%23)C%24=CC=CC=C%24)C=C%21)C=C%16)C=C%15)C=C%25C%26=C(C(N(CCCCCC)C%25=O)=O)C=C(OC%27=CC=C(C%28=CC(C%29%30C%31=C(C%32=C%30C=CC=C%32)C=CC=C%31)=C(C%33=C%29C=C(C(C=C%34)=CC=C%34C(C%35=CC=CC=C%35)C%36=CC=CC=C%36)C=C%33)C=C%28)C=C%27)C(C%37=C%13C2=C1C=C%37OC%38=CC=C(C%39=CC(C%40%41C%42=C(C%43=C%41C=CC=C%43)C=CC=C%42)=C(C%44=C%40C=C(C(C=C%45)=CC=C%45C(C%46=CC=CC=C%46)C%47=CC=CC=C%47)C=C%44)C=C%39)C=C%38)=C%14%26,2,,,0.79,9.06,46,3.29,"	Chan C-Y, Wong Y-C, Wong H-L, Chan M-Y, Wing-Wah Yam V. A new class of three-dimensional, p-type, spirobifluorene-modified perylene diimide derivatives for small molecular-based bulk heterojunction organic photovoltaic devices. Journal of Materials Chemistry C 2, 7656 (2014)."
2494,O=C(N(CCCCCC)C1=O)C2=CC(OC3=CC=C(C4=CC(C56C7=C(C8=C6C=CC(C(C)(C)C)=C8)C=CC=C7)=C(C9=C5C=C(C(C=C%10)=CC=C%10C(C%11=CC=CC=C%11)C%12=CC=CC=C%12)C=C9)C=C4)C=C3)=C%13C%14=C(OC%15=CC=C(C%16=CC(C%17%18C%19=C(C%20=C%18C=CC(C(C)(C)C)=C%20)C=CC=C%19)=C(C%21=C%17C=C(C(C=C%22)=CC=C%22C(C%23=CC=CC=C%23)C%24=CC=CC=C%24)C=C%21)C=C%16)C=C%15)C=C%25C%26=C(C(N(CCCCCC)C%25=O)=O)C=C(OC%27=CC=C(C%28=CC(C%29%30C%31=C(C%32=C%30C=C(C(C)(C)C)C=C%32)C=CC=C%31)=C(C%33=C%29C=C(C(C=C%34)=CC=C%34C(C%35=CC=CC=C%35)C%36=CC=CC=C%36)C=C%33)C=C%28)C=C%27)C(C%37=C%13C2=C1C=C%37OC%38=CC=C(C%39=CC(C%40%41C%42=C(C%43=C%41C=CC(C(C)(C)C)=C%43)C=CC=C%42)=C(C%44=C%40C=C(C(C=C%45)=CC=C%45C(C%46=CC=CC=C%46)C%47=CC=CC=C%47)C=C%44)C=C%39)C=C%38)=C%14%26,3,,,0.96,10.15,38,3.7,"	Chan C-Y, Wong Y-C, Wong H-L, Chan M-Y, Wing-Wah Yam V. A new class of three-dimensional, p-type, spirobifluorene-modified perylene diimide derivatives for small molecular-based bulk heterojunction organic photovoltaic devices. Journal of Materials Chemistry C 2, 7656 (2014)."
2495,O=C(N(CCCCCC)C1=O)C2=CC=C3C4=CC=C5C6=C(C(N(CCCCCC)C5=O)=O)C=C(OC7=CC=C(C8=CC(C9%10C%11=C(C%12=C%10C=C(C(C)(C)C)C=C%12)C=CC=C%11)=C(C%13=C9C=C(C(C=C%14)=CC=C%14C(C%15=CC=CC=C%15)C%16=CC=CC=C%16)C=C%13)C=C8)C=C7)C(C%17=C3C2=C1C=C%17OC%18=CC=C(C%19=CC(C%20%21C%22=C(C%23=C%21C=CC(C(C)(C)C)=C%23)C=CC=C%22)=C(C%24=C%20C=C(C(C=C%25)=CC=C%25C(C%26=CC=CC=C%26)C%27=CC=CC=C%27)C=C%24)C=C%19)C=C%18)=C46,4,,,0.94,9.74,43,3.94,"	Chan C-Y, Wong Y-C, Wong H-L, Chan M-Y, Wing-Wah Yam V. A new class of three-dimensional, p-type, spirobifluorene-modified perylene diimide derivatives for small molecular-based bulk heterojunction organic photovoltaic devices. Journal of Materials Chemistry C 2, 7656 (2014)."
2496,N#C/C(C#N)=C\C1=CC=C(C(C=C2)=CC=C2N(C3=CC=CC=C3)C4=CC=CC=C4)S1,1,,,0.87,6.43,38,2.13,"	Chan C-Y, Wong Y-C, Wong H-L, Chan M-Y, Wing-Wah Yam V. A new class of three-dimensional, p-type, spirobifluorene-modified perylene diimide derivatives for small molecular-based bulk heterojunction organic photovoltaic devices. Journal of Materials Chemistry C 2, 7656 (2014)."
2497,O=C1C(C2=C(C3=CC=C(C4=CC=C(C5=CC=C(C6=CC=C(OCCCCCCCCCCCC)C=C6)S5)S4)S3)N1CC(CCCCCCCCCC)CCCCCCCC)=C(C7=CC=C(C8=CC=C(C9=CC=C(C%10=CC=C(OCCCCCCCCCCCC)C=C%10)S9)S8)S7)N(CC(CCCCCCCCCC)CCCCCCCC)C2=O,DPP(3TP)2,,,0.92,5.8,42,2.5,"	Mohamed S, Demeter D, Laffitte J-A, Blanchard P, Roncali J. Structure-properties relationships in triarylamine-based donor-acceptor molecules containing naphtyl groups as donor material for organic solar cells. Scientific reports 5, 9031 (2015)."
2498,CCCCCCC1=C(C2=CC(CCCCCC)=C(/C=C3C(N(CC)C(S/3)=S)=O)S2)SC(C4=CC(C=CC5=CC(C6=CC(CCCCCC)=C(C7=CC(CCCCCC)=C(/C=C8C(N(CC)C(S/8)=S)=O)S7)S6)=C9)=C(C5=C9C=C%10)C%10=C4)=C1,1,,,0.76,1.82,43.2,0.59,"	Li HJ, Wang JT, Mei CY, Li WS. A new class of organic photovoltaic materials: poly(rod-coil) polymers having alternative conjugated and non-conjugated segments. Chemical communications 50, 7720-7722 (2014)."
2499,N#C/C(C#N)=C\C1=CC=C(C2=CC=C(N(C3=CC=CC=C3)C4=CC=CC=C4)C=C2)C5=NSN=C15,DPDCPB,,,1.04,3.21,33,1.1,"	Takemoto K, Kimura M. Low band gap disk-shaped donors for solution-processed organic solar cells. RSC Adv. 4, 64589-64595 (2014)."
2500,CCCCCCC(C=C1)=CC=C1C(C2=C3SC(C4=CC=C(C5=CC=C(C6=CC=C(CC(CC)CCCC)S6)S5)C7=NSN=C47)=C2)(C8=CC=C(CCCCCC)C=C8)C9=C3C=C%10C(C%11=CC=C(CCCCCC)C=C%11)(C%12=CC=C(CCCCCC)C=C%12)C(C=C(C%13=CC=C(C%14=CC=C(C%15=CC=C(CC(CC)CCCC)S%15)S%14)C%16=NSN=C%13%16)S%17)=C%17C%10=C9,BTIDTC6,,,1.01,10.9,40,4.1,"	Lin H-W, et al. Highly efficient organic solar cells using a solution-processed active layer with a small molecule donor and pristine fullerene. J. Mater. Chem. A 2, 3709-3714 (2014)."
2501,CCCCC(CC)CC1=CC=C(C2=CC=C(C3=CC=C(C(S4)=CC5=C4C6=C(C5(C7=CC=C(OCCCCCCCCCCCC)C=C7)C8=CC=C(OCCCCCCCCCCCC)C=C8)C=C9C%10=C(C=C(C%11=CC=C(C%12=CC=C(C%13=CC=C(CC(CC)CCCC)S%13)S%12)C%14=NSN=C%11%14)S%10)C(C%15=CC=C(OCCCCCCCCCCCC)C=C%15)(C%16=CC=C(OCCCCCCCCCCCC)C=C%16)C9=C6)C%17=NSN=C3%17)S2)S1,BTIDTOC12,,,0.91,11.01,48.17,4.83,"	Liu D, et al. Solution-processed, indacenodithiophene-based, small-molecule organic field-effect transistors and solar cells. Journal of Materials Chemistry C 2, 7523 (2014)."
2502,CCCCCCC1=C(C2=CC(CCCCCC)=C(/C=C3C(N(CC)C(S/3)=S)=O)S2)SC(C(C=C4C5=CC(CCCCCC)=C(C6=CC(CCCCCC)=C(/C=C7C(N(CC)C(S/7)=S)=O)S6)S5)=C8C=CC9=C(C8=C4C=C%10)C%10=CC(C(C)(C)C)=C9)=C1,2,,,0.94,10,43.3,4.06,"	Liu D, et al. Solution-processed, indacenodithiophene-based, small-molecule organic field-effect transistors and solar cells. Journal of Materials Chemistry C 2, 7523 (2014)."
2503,C/C(C1=CC=C(C2=CC=C(C3=CC(OC)=C(C(C4=C(OC)C=C(C5=CC=C(C6=CC=C(/C(C)=C(C#N)\C#N)S6)S5)C=C4)C7=C(OC)C=C(C8=CC=C(C9=CC=C(/C(C)=C(C#N)\C#N)S9)S8)C=C7)C=C3)S2)S1)=C(C#N)/C#N,N(Ph(OMe)-2T-DCV-Me)3,,,1.15,2.87,29,1,"	Takemoto K, Kimura M. Low band gap disk-shaped donors for solution-processed organic solar cells. RSC Adv. 4, 64589-64595 (2014)."
2504,CCCCCCC1=CC=C(C2=CC=C(C3=CC=C(C(S4)=NC5=C4N=C(C6=CC=C(C7=CC=C(N(C8=CC=CC=C8)C9=CC=CC=C9)C=C7)S6)S5)S3)S2)S1,TPTzR,,,0.88,9.15,54.4,4.38,"	Min J, et al. A star-shaped D¨C¦Ð¨CA small molecule based on a tris(2-methoxyphenyl)amine core for highly efficient solution-processed organic solar cells. J. Mater. Chem. C 2, 7614-7620 (2014)."
2505,O=C(/C1=C(C2=C(N3C(OCC(CC)CCCC)=O)C=CC=C2)/C3=O)N(C(OCC(CC)CCCC)=O)C4=C1C=CC(C5=CC=C(C6=CC=C(C7=CC(N(C(OCC(CC)CCCC)=O)C(/C8=C(C9=C(N%10C(OCC(CC)CCCC)=O)C=CC=C9)/C%10=O)=O)=C8C=C7)S6)S5)=C4,1,,,0.691,12.05,30,2.43,"	Nazim M, Ameen S, Akhtar MS, Seo H-K, Shin HS. Novel liquid crystalline oligomer with thiazolothiazole-acceptor for efficient BHJ small molecule organic solar cells. Synthetic Metals 187, 178-184 (2014)."
2506,O=C(/C1=C(C2=C(N3C(OCC(CC)CCCC)=O)C=CC=C2)/C3=O)N(C(OCC(CC)CCCC)=O)C4=C1C=CC(C5=CC(OCCCCCCCCCCCC)=C(C6=C(OCCCCCCCCCCCC)C=C(C7=CC(N(C(OCC(CC)CCCC)=O)C(/C8=C(C9=C(N%10C(OCC(CC)CCCC)=O)C=CC=C9)/C%10=O)=O)=C8C=C7)S6)S5)=C4,2,,,0.66,2.7,31,0.6,"	Randell NM, Douglas AF, Kelly TL. 7-Azaisoindigo as a new electron deficient component of small molecule chromophores for organic solar cells. J. Mater. Chem. A 2, 1085-1092 (2014)."
2507,CCCCN(C1=CC=CC=C1)C2=CC(O)=C(C3C([O-])C(C3[O-])C4=C(O)C=C(N(CCCC)C5=CC=CC=C5)C=C4O)C(O)=C2,SQ-BP,,,0.67,2.5,40,0.7,"	Randell NM, Douglas AF, Kelly TL. 7-Azaisoindigo as a new electron deficient component of small molecule chromophores for organic solar cells. J. Mater. Chem. A 2, 1085-1092 (2014)."
2508,CCCCCCC1=C(C2=CC(CCCCCC)=C(/C=C3C(N(CC)C(S/3)=S)=O)S2)SC(C(C=C4C5=CC(CCCCCC)=C(C6=CC(CCCCCC)=C(/C=C7C(N(CC)C(S/7)=S)=O)S6)S5)=C8C=CC9=C(C8=C4C=C%10)C%10=C(C%11=CC(CCCCCC)=C(C%12=CC(CCCCCC)=C(/C=C%13C(N(CC)C(S/%13)=S)=O)S%12)S%11)C=C9C%14=CC(CCCCCC)=C(C%15=CC(CCCCCC)=C(/C=C%16C(N(CC)C(S/%16)=S)=O)S%15)S%14)=C1,3,,,0.98,11.01,45,4.86,"	Sasabe H, Igrashi T, Sasaki Y, Chen G, Hong Z, Kido J. Soluble squaraine derivatives for 4.9% efficient organic photovoltaic cells. RSC Adv. 4, 42804-42807 (2014)."
2509,OC1=CC(N(CCCCCCCCCCCC)C2=CC=CC=C2)=CC(O)=C1C3C([O-])C(C3[O-])C4=C(O)C=C(N(CCCCCCCCCCCC)C5=CC=CC=C5)C=C4O,SQ-DP,,,1.11,5.53,38,2.3,"	Takemoto K, Kimura M. Low band gap disk-shaped donors for solution-processed organic solar cells. RSC Adv. 4, 64589-64595 (2014)."
2510,CC1=CC=C(C2=C(C3=CC=C(C)S3)C=C(C4=CC=C(C5=CC=C6C(C(NNC6=O)=O)=C5)S4)S2)S1,MeBQPH,,,0.96,5.72,36,1.97,"	Sasabe H, Igrashi T, Sasaki Y, Chen G, Hong Z, Kido J. Soluble squaraine derivatives for 4.9% efficient organic photovoltaic cells. RSC Adv. 4, 42804-42807 (2014)."
2511,CC1=CC=C(C2=C(C3=CC=C(C)S3)C=C(C4=CC=C(C5=CC=C(C(OC)=O)C(C(OC)=O)=C5)S4)S2)S1,MeBQPME,,,0.87,2.7,44,1.04,"	Schulze BM, et al. Consequences of hydrogen bonding on molecular organization and charge transport in molecular organic photovoltaic materials. J. Mater. Chem. A 2, 1541-1549 (2014)."
2512,CC1=CC=C(C2=C(C3=CC=C(C)S3)C=C(C4=CC=C(C5=CC=C6C(C(N(N(C)C6=O)C)=O)=C5)S4)S2)S1,MeBQPNMe,,,0.92,1.5,35,0.49,"	Schulze BM, et al. Consequences of hydrogen bonding on molecular organization and charge transport in molecular organic photovoltaic materials. J. Mater. Chem. A 2, 1541-1549 (2014)."
2513,O=C(N(CCCCCCCCCC)C(C1=CC=C(C2=CC(C=CN3)=C3C=C2)S1)=C45)C4=C(C6=CC=C(C7=CC(C=CN8)=C8C=C7)S6)N(CCCCCCCCCC)C5=O,CSDPP1,,,0.97,1.7,30,0.5,"	Schulze BM, et al. Consequences of hydrogen bonding on molecular organization and charge transport in molecular organic photovoltaic materials. J. Mater. Chem. A 2, 1541-1549 (2014)."
2514,O=C(N(CCCCCCCCCC)C(C1=CC=C(C2=C(C(C)C)C=C(C(C)C)C=C2C(C)C)S1)=C34)C3=C(C5=CC=C(C6=C(C(C)C)C=C(C(C)C)C=C6C(C)C)S5)N(CCCCCCCCCC)C4=O,CSDPP3,,,0.82,10.82,56,4.96,"	Sharma GD, Reddy MA, Ganesh K, Singh SP, Chandrasekharam M. Indole and triisopropyl phenyl as capping units for a diketopyrrolopyrrole (DPP) acceptor central unit: an efficient D¨CA¨CD type small molecule for organic solar cells. RSC Adv. 4, 732-742 (2014)."
2515,CC1=CC(C)=C(C2=C3C=CC4=C(C5=CC=C(NC6=NC(NC7=CC=C(C8=C9C=CC%10=C(C%11=CC=CC=C%11)C(N%12%13)C=CC%12=C(C%14=CC=CC=C%14)C%15=CC=C%16N%15[Zn]%13(N%17C(C=CC%178)=C%16C%18=CC=CC=C%18)N9%10)C=C7)=NC(N%19CCCCC%19)=N6)C=C5)C(N%20%21)C=CC%20=C(C%22=C(C)C=C(C)C=C%22C)C%23=CC=C%24N%23[Zn]%21(N%25C(C=CC%252)=C%24C%26=CC=C(C(O)=O)C=C%26)N34)C(C)=C1,P-tNp-P',,,0.9,7.34,46,3.04,"	Sharma GD, Reddy MA, Ganesh K, Singh SP, Chandrasekharam M. Indole and triisopropyl phenyl as capping units for a diketopyrrolopyrrole (DPP) acceptor central unit: an efficient D¨CA¨CD type small molecule for organic solar cells. RSC Adv. 4, 732-742 (2014)."
2516,CCCCCCC1=C(C2=CC(C)=C(/C=C3C(N(CC)C(S/3)=S)=O)S2)SC(C(C=C4C5=CC(CCCCCC)=C(C6=CC(C)=C(/C=C7C(N(CC)C(S/7)=S)=O)S6)S5)=C8C=CC9=C(C8=C4C=C%10)C%10=C(C%11=CC(CCCCCC)=C(C%12=CC(C)=C(/C=C%13C(N(CC)C(S/%13)=S)=O)S%12)S%11)C=C9C%14=CC(CCCCCC)=C(C%15=CC(C)=C(/C=C%16C(N(CC)C(S/%16)=S)=O)S%15)S%14)=C1,4,,,0.94,8.52,52,4.16,"	Sharma GD, Zervaki GE, Angaridis P, Coutsolelos AG. New solution processed bulk-heterojunction organic solar cells based on a triazine-bridged porphyrin dyad as electron donor. RSC Adv. 4, 50819-50827 (2014)."
2517,O=C1C(C2=C(C3=CC=CS3)N1CC(CC)CCCC)=C(C4=CC=C(C#CC5=CC=C(C#CC6=CC=C(C7=C8C(C(N7CC(CC)CCCC)=O)=C(C9=CC=CS9)N(CC(CC)CCCC)C8=O)S6)C%10=NSN=C%105)S4)N(CC(CC)CCCC)C2=O,DPPBT,,,1.08,8.42,41,3.7,"	Takemoto K, Kimura M. Low band gap disk-shaped donors for solution-processed organic solar cells. RSC Adv. 4, 64589-64595 (2014)."
2518,O=C1C(C2=C(C3=CC=CS3)N1CC(CC)CCCC)=C(C4=CC=C(C#CC5=NC6=C(N=C(C#CC7=CC=C(C8=C9C(C(N8CC(CC)CCCC)=O)=C(C%10=CC=CS%10)N(CC(CC)CCCC)C9=O)S7)S6)S5)S4)N(CC(CC)CCCC)C2=O,DPPTT,,,0.97,6.29,40,2.11,"	Yu C, et al. New dithienyl-diketopyrrolopyrrole-based conjugated molecules entailing electron withdrawing moieties for organic ambipolar semiconductors and photovoltaic materials. J. Mater. Chem. C 2, 10101-10109 (2014)."
2519,CCCCCCC1=CSC(C2=C(CCCCCC)C=C(C3=C(CCCCCC)C=C(C4=C(CCCCCC)C=C(C5=C(F)C(F)=C(C6=CC(CCCCCC)=C(C7=CC(CCCCCC)=C(C8=CC(CCCCCC)=C(C9=CC(CCCCCC)=CS9)S8)S7)S6)C%10=NSN=C%105)S4)S3)S2)=C1,4TA4T,,,0.99,8.28,51,3.92,"	Yu C, et al. New dithienyl-diketopyrrolopyrrole-based conjugated molecules entailing electron withdrawing moieties for organic ambipolar semiconductors and photovoltaic materials. J. Mater. Chem. C 2, 10101-10109 (2014)."
2520,CC(C)(C)C(O1)C=C(C(C)(C)C)O[Ir]21N3C=C(C4=CC=C(OC)C=C4)C=CC3C5=C2C6=C(S5)C=CC=C6,R1,,,0.83,8.02,57,3.81,"	Yuan L, Zhao Y, Lu K, Deng D, Yan W, Wei Z. Small molecules incorporating regioregular oligothiophenes and fluorinated benzothiadiazole groups for solution-processed organic solar cells. J. Mater. Chem. C 2, 5842-5849 (2014)."
2521,CC(C)(C)C(O1)C=C(C(C)(C)C)O[Ir]21N3C=C(C4=CC=C(N(C5=CC=CC=C5)C6=CC=CC=C6)C=C4)C=CC3C7=C2C8=C(S7)C=CC=C8,R2,,,0.77,4.3,35,1.2,"	Zhen H, et al. Solution-processed bulk-heterojunction organic solar cells employing Ir complexes as electron donors. Journal of Materials Chemistry A 2, 12390 (2014)."
2522,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C(C=C(C4=CC=C(C5=C6C(C(N5CC(CC)CCCC)=O)=C(C7=CC=CS7)N(CC(CC)CCCC)C6=O)S4)S8)C8C9=CC%10=C(C%11=C(C=C(C%12=CC=C(C%13=C%14C(C(N%13CC(CC)CCCC)=O)=C(C%15=CC=CS%15)N(CC(CC)CCCC)C%14=O)S%12)S%11)C%10(C%16=CC=C(CCCCCC)C=C%16)C%17=CC=C(CCCCCC)C=C%17)C=C92)C=C1,IDT-2DPP,,,0.74,6.52,42,2,"	Zhen H, et al. Solution-processed bulk-heterojunction organic solar cells employing Ir complexes as electron donors. Journal of Materials Chemistry A 2, 12390 (2014)."
2523,CC1=CC=C(C2=C(C=C(C3=CC4=C(C=C(C5=C6C(C(N(C)C6=O)=O)=C(C(S7)=CC8=C7C=CS8)S5)S4)S3)S9)C9=C(C%10=CC=C(C)S%10)C%11=C2SC=C%11)S1,PBDTT-ttTPD,,,0.88,8.53,37.6,2.82,"	Bai H, et al. A bipolar small molecule based on indacenodithiophene and diketopyrrolopyrrole for solution processed organic solar cells. J. Mater. Chem. A 2, 778-784 (2014)."
2524,CC1=C(F)C(F)=C(C2=C(C=C(C3=CC4=C(C=C(C5=C6C(C(N(C)C6=O)=O)=C(C(S7)=CC8=C7C=CS8)S5)S4)S3)S9)C9=C(C%10=C(F)C(F)=C(C)S%10)C%11=C2SC=C%11)S1,PBDTFT-ttTPD,,,0.71,7.88,49,2.74,"	Cho S-N, Lee W-H, Park JB, Kim J-H, Hwang D-H, Kang I-N. Synthesis and characterization of fluorine atom substituted new BDT-based polymers for use in organic solar cells. Synthetic Metals 210, 273-281 (2015)."
2525,CCCCC(CC)CSC1=CC=C(C2=C3C(C=C(C4=CC(CCCCCCCC)=C(C5=CC=C(C6=C(CCCCCCCC)C=C(/C=C(C(N7CC)=O)/SC7=O)S6)S5)S4)S3)=C(C8=CC=C(SCC(CC)CCCC)S8)C9=C2C=C(C%10=CC(CCCCCCCC)=C(C%11=CC=C(C%12=C(CCCCCCCC)C=C(/C=C(C(N%13CC)=O)/SC%13=O)S%12)S%11)S%10)S9)S1,BDTT-S-TR,,,0.79,8.57,48,3.27,"	Cho S-N, Lee W-H, Park JB, Kim J-H, Hwang D-H, Kang I-N. Synthesis and characterization of fluorine atom substituted new BDT-based polymers for use in organic solar cells. Synthetic Metals 210, 273-281 (2015)."
2526,NC1=CC=C(C2=CC=C(C3=CC=C(C4=CC=C(C5=CC([n+]([o-])[o-])=C(C#N)C=C5)S4)S3)S2)C=C1,C2B4TA,,,0.97,13.45,70.5,9.2,"	Cui C, et al. High-Performance Organic Solar Cells Based on a Small Molecule with Alkylthio-Thienyl-Conjugated Side Chains without Extra Treatments. Adv Mater 27, 7469-7475 (2015)."
2527,NC1=CC=C(C2=CC=C(C3=CC=C(C4=CC=C(C5=CC([n+]([o-])[o-])=C(C#N)C([n+]([o-])[o-])=C5)S4)S3)S2)C=C1,"C2,5B4TA",,,0.545,2.83,68.22,1.05,"	Zamora PP, Bieger K, Vasquez D. Effect of Nitro Groups on Electrochemical and Photovoltaic Behavior of Tris-thiophenes used in Organic Solar Cells. INTERNATIONAL JOURNAL OF ELECTROCHEMICAL SCIENCE 10, 10321-10335 (2015)."
2528,CCCCCCC1=C(SC(/C=C(C#N)\C#N)=C1CCCCCC)C#CC2=C(N34)C=CC3=C(C5=C(C)C=C(C)C=C5C)C(N67)C=CC6=C(C#CC8=C(CCCCCC)C(CCCCCC)=C(/C=C(C#N)\C#N)S8)C9=CC=C%10N9[Zn]74N%11C(C=CC%112)=C%10C%12=C(C)C=C(C)C=C%12C,1a,,,5.25,5.58,69.57,2.04,"	Zamora PP, Bieger K, Vasquez D. Effect of Nitro Groups on Electrochemical and Photovoltaic Behavior of Tris-thiophenes used in Organic Solar Cells. INTERNATIONAL JOURNAL OF ELECTROCHEMICAL SCIENCE 10, 10321-10335 (2015)."
2529,CC1=CC(C)=CC(C)=C1C2=C(C=C3)N4C3=C(C#CC5=C(CCCCCC)C(CCCCCC)=C(/C=C/C6=C(CCCCCC)C(CCCCCC)=C(/C=C(C#N)/C#N)S6)S5)C(C=C7)N8C7=C(C9=C(C)C=C(C)C=C9C)C%10=CC=C%11N%10[Zn]48N%12C2C=CC%12=C%11C#CC%13=C(CCCCCC)C(CCCCCC)=C(/C=C/C%14=C(CCCCCC)C(CCCCCC)=C(/C=C(C#N)\C#N)S%14)S%13,1b,,,0.86,5.67,28.1,1.36,"	Arrechea S, Molina-Ontoria A, Aljarilla A, de la Cruz P, Langa F, Echegoyen L. New acceptor¨C¦Ð-porphyrin¨C¦Ð-acceptor systems for solution-processed small molecule organic solar cells. Dyes and Pigments 121, 109-117 (2015)."
2530,O=C1N(C(CCCCCC)C)C(C2=CC=C(C3=CC=C(N(C4=CC=CC=C4)C5=CC=CC=C5)C=C3)S2)=C6C(N(C(CCCCCC)C)C(C7=CC=C(C8=CC=C(N(C9=CC=CC=C9)C%10=CC=CC=C%10)C=C8)S7)=C16)=O,TPA-DPP-TPA,,,0.82,10.83,35.7,3.16,"	Arrechea S, Molina-Ontoria A, Aljarilla A, de la Cruz P, Langa F, Echegoyen L. New acceptor¨C¦Ð-porphyrin¨C¦Ð-acceptor systems for solution-processed small molecule organic solar cells. Dyes and Pigments 121, 109-117 (2015)."
2531,O=C1N(C(CCCCCC)C)C(C2=CC=C(C3=CC(C4)=C(C5=C4C=CC=C5)C=C3)S2)=C6C(N(C(CCCCCC)C)C(C7=CC=C(C8=CC9=C(C%10=C(C9)C=CC=C%10)C=C8)S7)=C16)=O,FL-DPP-FL,,,0.77,5.58,34,1.45,"	Bagde SS, Park H, Yang S-n, Jin S-H, Lee S-H. Diketopyrrolopyrrole-based narrow band gap donors for efficient solution-processed organic solar cells. Chemical Physics Letters 630, 37-43 (2015)."
2532,S=C(S/C1=C/C2=CC3=C(C=C2)N(CC)C4=C3C=C(C5=CC=C(C6=CC7=C(N(CC)C8=C7C=C(/C=C(C(N9CCCCCCCC)=O)/SC9=S)C=C8)C=C6)C%10=NSN=C5%10)C=C4)N(CCCCCCCC)C1=O,ECBT,,,0.87,5.03,39,1.73,"	Bagde SS, Park H, Yang S-n, Jin S-H, Lee S-H. Diketopyrrolopyrrole-based narrow band gap donors for efficient solution-processed organic solar cells. Chemical Physics Letters 630, 37-43 (2015)."
2533,S=C(S/C1=C/C2=CC3=C(C=C2)N(CC)C4=C3C=C(C5=CC=C(C6=CC=C(C7=CC=C(C8=CC9=C(N(CC)C%10=C9C=C(/C=C(C(N%11CCCCCCCC)=O)/SC%11=S)C=C%10)C=C8)S7)C%12=NSN=C6%12)S5)C=C4)N(CCCCCCCC)C1=O,ECTBT,,,0.74,5.4,36.2,1.45,"	Castro E, Cabrera-Espinoza A, Deemer E, Echegoyen L. Low-Energy-Gap Organic Based Acceptor--Donor-Acceptor ¦Ð-Conjugated Small Molecules for Bulk-Heterojunction Organic Solar Cells. European Journal of Organic Chemistry 2015, 4629-4634 (2015)."
2534,N#C/C(C#N)=C(N=C/1C2=CC=CC=C2)\SC1=C/C3=CC=C(N(C4=CC=CC=C4)C5=CC=CC=C5)C=C3,DPPT,,,0.77,9.98,49.6,3.19,"	Castro E, Cabrera-Espinoza A, Deemer E, Echegoyen L. Low-Energy-Gap Organic Based Acceptor--Donor-Acceptor ¦Ð-Conjugated Small Molecules for Bulk-Heterojunction Organic Solar Cells. European Journal of Organic Chemistry 2015, 4629-4634 (2015)."
2535,N#C/C(C#N)=C(N=C/1C2=CC=CC=C2)\SC1=C/C3=CC=C(N(C4=CC=C(C)C=C4)C5=CC=C(C)C=C5)C=C3,DTPT,,,0.98,9.05,40,3.52,"	Chen K-W, et al. Merocyanines for vacuum-deposited small-molecule organic solar cells. Organic Electronics 26, 319-326 (2015)."
2536,N#C/C(C#N)=C(N=C/1C2=CC=CC=C2)/SC1=C/C3=CC=C(N(C4=CC=CC5=C4C=CC=C5)C6=CC=CC=C6)C=C3,1-NPPT,,,0.85,6.4,34,1.86,"	Chen K-W, et al. Merocyanines for vacuum-deposited small-molecule organic solar cells. Organic Electronics 26, 319-326 (2015)."
2537,CCCCCCC(C1=C2/C(N/C1=C\3)=C/C(C4=C/5C(CCCCCC)=CC=C4CCCCCC)=NC5=C/C6=C7C(C(CCCCCC)=CC=C7CCCCCC)=C(/C=C8N=C3C9=C\8C(CCCCCC)=CC=C9CCCCCC)N6)=CC=C2CCCCCC,C6TBPH2,,,0.87,5.64,30,1.48,"	Chen K-W, et al. Merocyanines for vacuum-deposited small-molecule organic solar cells. Organic Electronics 26, 319-326 (2015)."
2538,CCCCCCC(C1=C2/C(N/C1=C\3)=C/C(C4=C/5C(CCCCCC)=CC=C4CCCCCC)=NC5=N/C6=C7C(C(CCCCCC)=CC=C7CCCCCC)=C(/C=C8N=C3C9=C\8C(CCCCCC)=CC=C9CCCCCC)N6)=CC=C2CCCCCC,C6TBMAPH2,,,0.51,4.8,54,1.4,"	Dao Q-D, et al. Efficiency enhancement in solution processed small-molecule based organic solar cells utilizing various phthalocyanine¨Ctetrabenzoporphyrin hybrid macrocycles. Organic Electronics 23, 44-52 (2015)."
2539,CCCCCCC(C1=C2/C(N/C1=C\3)=N/C(C4=C/5C(CCCCCC)=CC=C4CCCCCC)=NC5=N/C6=C7C(C(CCCCCC)=CC=C7CCCCCC)=C(/C=C8N=C3C9=C\8C(CCCCCC)=CC=C9CCCCCC)N6)=CC=C2CCCCCC,C6TBDAPH2,,,0.67,6.4,57,2.4,"	Dao Q-D, et al. Efficiency enhancement in solution processed small-molecule based organic solar cells utilizing various phthalocyanine¨Ctetrabenzoporphyrin hybrid macrocycles. Organic Electronics 23, 44-52 (2015)."
2540,CC(C)[Si](C(C)C)(C(C)C)C1=CC2=C(C3=CC4=C(C5=N/C4=N\C6=C7C=C(C8=C9C=C([Si](C(C)C)(C(C)C)C(C)C)S8)C(C%10=C9C=C([Si](C(C)C)(C(C)C)C(C)C)S%10)=CC7=C%11/N=C(C%12=C%13C=C(C%14=C%15C=C([Si](C(C)C)(C(C)C)C(C)C)S%14)C(C%16=C%15C=C([Si](C(C)C)(C(C)C)C(C)C)S%16)=C%12)\N=C%13/N=C(C%17=C/%18C=C(C%19=C%20C=C([Si](C(C)C)(C(C)C)C(C)C)S%19)C(C%21=C%20C=C([Si](C(C)C)(C(C)C)C(C)C)S%21)=C%17)\N(C%18=N/5)[Zn]N6%11)C=C3C%22=C2C=C([Si](C(C)C)(C(C)C)C(C)C)S%22)S1,6,,,0.69,8.3,50,2.8,"	Dao Q-D, et al. Efficiency enhancement in solution processed small-molecule based organic solar cells utilizing various phthalocyanine¨Ctetrabenzoporphyrin hybrid macrocycles. Organic Electronics 23, 44-52 (2015)."
2541,FB(F)N1C(C(C2=CC=C(Br)C=C2)C3N=C(/C=C/C4=CC=C(N(CC(OCC)=O)C5=C6C=CC=C5)C6=C4)C(C(OCC7=CC=CC=C7)=O)=C3/C=C/C8=CC(C(C=CC=C9)=C9N%10CC(OCC)=O)=C%10C=C8)=C(/C=C/C%11=CC=C(N(CC(OCC)=O)C%12=C%13C=CC=C%12)C%13=C%11)C(C(OCC%14=CC=CC=C%14)=O)=C1/C=C/C%15=CC(C(C=CC=C%16)=C%16N%17CC(OCC)=O)=C%17C=C%15,TAC,,,0.7,1.7,51,0.6,"	Yan X, et al. Synthesis of an octathienyl-fused phthalocyanine as a donor material for organic solar cells. Dyes and Pigments 114, 124-128 (2015)."
2542,CCCCC(CC)COC1=C(C=C(C2=CC(C(CCCCCC)(CCCCCC)C3=C4SC(/C=C5SC(N(CC)C\5=O)=S)=C3)=C4S2)S6)C6=C(OCC(CC)CCCC)C7=C1SC(C8=CC(C(CCCCCC)(CCCCCC)C9=C%10SC(/C=C%11SC(N(CC)C\%11=O)=S)=C9)=C%10S8)=C7,BDT(CDTRH)2,,,0.85,8.17,39,2.7,"	Zhang X, Zhang Y, Chen L, Xiao Y. Star-shaped carbazole-based BODIPY derivatives with improved hole transportation and near-infrared absorption for small-molecule organic solar cells with high open-circuit voltages. RSC Advances 5, 32283-32289 (2015)."
2543,CCCCCCCCCCC(CCCCCCCC)OC1=C(OC(CCCCCCCC)CCCCCCCCCC)C=C2C(C=C(C3=CC=CS3)S4)=C4C(SC(C5=CC=C(C6=CC(OCCCCCC)=C(C=C(C7=CC=C(C8=CC=CS8)S7)C=C9)C9=C6OCCCCCC)S5)=C%10)=C%10C2=C1,PNDT-BTN,,,0.94,10.42,62,6.07,"	Kumar CV, Cabau L, Koukaras EN, Viterisi A, Sharma GD, Palomares E. Solution processed organic solar cells based on A¨CD¨CD¡ä¨CD¨CA small molecule with benzo [1, 2-b: 4, 5-b¡ä] dithiophene donor (D¡ä) unit, cyclopentadithiophene donor (D) and ethylrhodanine acceptor unit having 6% light to energy conversion efficiency. Journal of Materials Chemistry A 3, 4892-4902 (2015)."
2544,CCCCCCC1=CSC(C(C=C2)=CC=C2N(C3=CC=C(C4=CC(CCCCCC)=CS4)C=C3)C(C=C5)=CC=C5C(S6)=NC7=C6N=C(C8=CC=C(N(C9=CC=C(C%10=CC(CCCCCC)=CS%10)C=C9)C%11=CC=C(C%12=CC(CCCCCC)=CS%12)C=C%11)C=C8)S7)=C1,SM1,,,0.98,8.7,50,4.29,"	Kim YJ, Cheon YR, Jang J-W, Kim Y-H, Park CE. A potential naphtho [2, 1-b: 3, 4-b¡ä] dithiophene-based polymer with large open circuit voltage for efficient use in organic solar cells. Journal of Materials Chemistry C 3, 1904-1912 (2015)."
2545,CCCCCCCCCCCCC1=C(C2=CC=C(C(C3=CC=CC=C3)C4=CC=CC=C4)C=C2)SC(C(C=C5)=CC=C5N(C6=CC=C(C7=CC(CCCCCCCCCCCC)=C(C8=CC=C(C(C9=CC=CC=C9)C%10=CC=CC=C%10)C=C8)S7)C=C6)C(C=C%11)=CC=C%11C(S%12)=NC%13=C%12N=C(C%14=CC=C(N(C%15=CC=C(C%16=CC(CCCCCCCCCCCC)=C(C%17=CC=C(C(C%18=CC=CC=C%18)C%19=CC=CC=C%19)C=C%17)S%16)C=C%15)C%20=CC=C(C%21=CC(CCCCCCCCCCCC)=C(C%22=CC=C(C(C%23=CC=CC=C%23)C%24=CC=CC=C%24)C=C%22)S%21)C=C%20)C=C%14)S%13)=C1,SM2,,,0.82,6.28,32,1.65,"	Jia T, Peng Z, Li Q, Zhu T, Hou Q, Hou L. Synthesis of four-armed triphenylamine-based molecules and their applications in organic solar cells. New Journal of Chemistry 39, 994-1000 (2015)."
2546,CCCCCCCCCCCCC1=C(C2=CC=C(N(C3=CC=CC=C3)C4=CC=CC=C4)C=C2)SC(C(C5=NSN=C56)=CC=C6/C=C/C(C=C7)=CC=C7N(C8=CC=C(/C=C/C9=CC=C(C%10=CC(CCCCCCCCCCCC)=C(C%11=CC=C(N(C%12=CC=CC=C%12)C%13=CC=CC=C%13)C=C%11)S%10)C%14=NSN=C%149)C=C8)C%15=CC=CC=C%15)=C1,SM1,,,0.86,6.8,36,2.1,"	Jia T, Peng Z, Li Q, Zhu T, Hou Q, Hou L. Synthesis of four-armed triphenylamine-based molecules and their applications in organic solar cells. New Journal of Chemistry 39, 994-1000 (2015)."
2547,N#C/C(C#N)=C/C(C=C1)=CC=C1N(C2=CC=CC=C2)C(C=C3)=CC=C3/C=C/C4=CC=C(C5=CC(CCCCCCCCCCCC)=C(C6=CC=C(N(C7=CC=CC=C7)C8=CC=CC=C8)C=C6)S5)C9=NSN=C94,SM2,,,0.8,5.21,0.25,1.04,"	Jia T, Peng Z, Li Q, Xie Y, Hou Q, Hou L. Synthesis of triphenylamine-based molecules with cyan terminals and their application for organic solar cells. Synthetic Metals 199, 14-20 (2015)."
2548,CCCCCCC(S1)=CC=C1C(S2)=CC=C2C(O3)=CC=C3C(S4)=NC5=C4N=C(C6=CC=C(C7=CC=C(C8=CC=C(CCCCCC)S8)S7)O6)S5,RFTzR,,,0.89,5.8,0.29,1.51,"	Jia T, Peng Z, Li Q, Xie Y, Hou Q, Hou L. Synthesis of triphenylamine-based molecules with cyan terminals and their application for organic solar cells. Synthetic Metals 199, 14-20 (2015)."
2549,O=C(N(CC(CC)CCCC)C(C1=CC=C(C2=CC(C=CC=C3)=C3O2)S1)=C45)C4=C(C6=CC=C(C7=CC(C=CC=C8)=C8O7)S6)N(CC(CC)CCCC)C5=O,DPP(TBFu)2,,,0.76,10.13,34,2.72,"	Nazim M, Ameen S, Akhtar MS, Seo H-K, Shin H-S. Furan-bridged thiazolo [5, 4-d] thiazole based D¨C¦Ð¨CA¨C¦Ð¨CD type linear chromophore for solution-processed bulk-heterojunction organic solar cells. RSC Advances 5, 6286-6293 (2015)."
2550,CCCCCCC(C=C1)=CC=C1C#CC2=C3C=C(C#CC4=CC=C(CCCCCC)C=C4)C5=CC=CC6=C(C#CC7=CC=C(CCCCCC)C=C7)C8=CC(C#CC9=CC=C(CCCCCC)C=C9)=C%10C(C2=CC=C%10)=C8C3=C65,1,,,1.03,9.52,52,5.08,"	Ryan JW, Matsuo Y. Increased efficiency in small molecule organic solar cells through the use of a 56-¦Ð electron acceptor¨Cmethano indene fullerene. Scientific reports 5,  (2015)."
2551,CCCCCCCCC(S1)=CC=C1C#CC2=CC3=C(C#CC4=CC=C(CCCCCCCC)S4)C5=CC=CC6=C(C#CC7=CC=C(CCCCCCCC)S7)C=C8C(C#CC9=CC=C(CCCCCCCC)S9)=C%10C(C2=CC=C%10)=C3C8=C65,2,,,0.77,5.3,55,2.2,"	Gigu¨¨re J-B, Sariciftci NS, Morin J-F. Polycyclic anthanthrene small molecules: semiconductors for organic field-effect transistors and solar cells applications. Journal of Materials Chemistry C 3, 601-606 (2015)."
2552,CCCCCCCCC1=CC=C(C2=CC3=C(C#CC4=CC=C(CCCCCCCC)S4)C5=CC=CC6=C(C7=CC=C(CCCCCCCC)S7)C=C8C(C#CC9=CC=C(CCCCCCCC)S9)=C%10C(C2=CC=C%10)=C3C8=C65)S1,3,,,0.59,3.5,47,1,"	Gigu¨¨re J-B, Sariciftci NS, Morin J-F. Polycyclic anthanthrene small molecules: semiconductors for organic field-effect transistors and solar cells applications. Journal of Materials Chemistry C 3, 601-606 (2015)."
2553,N#C/C(C#N)=C\C1=CC=C(S1)C2=CC=C(C3=CC=C(C4=CC=C(/C=C(C#N)\C#N)S4)S3)S2,2,,,0.74,4.9,59,2.1,"	Gigu¨¨re J-B, Sariciftci NS, Morin J-F. Polycyclic anthanthrene small molecules: semiconductors for organic field-effect transistors and solar cells applications. Journal of Materials Chemistry C 3, 601-606 (2015)."
2554,CCC1(CC)C2=C(SC(C3=CC=C(/C=C(C#N)\C#N)S3)=C2)C4=C1C=C(C5=CC=C(/C=C(C#N)\C#N)S5)S4,1,,,0.88,1.74,25,0.51,"	Baert F, et al. A bridged low band gap A¨CD¨CA quaterthiophene as efficient donor for organic solar cells. Journal of Materials Chemistry C 3, 390-398 (2015)."
2555,[O-]c1c(C2=C(O)C=C(N(CC(C)C)CC(C)C)C=C2O)c([O-])c1C3=C(O)C=C(N(CC(C)C)CC(C)C)C=C3O,DIB-SQ,,,0.97,5.07,45,2.82,"	Baert F, et al. A bridged low band gap A¨CD¨CA quaterthiophene as efficient donor for organic solar cells. Journal of Materials Chemistry C 3, 390-398 (2015)."
2556,FC(C=C(C1=CC=C(C2=CC=C(CCCCCC)S2)S1)C3=NSN=C34)=C4C5=CC6=C(S5)C7=C(C=C(C(S8)=CC9=C8C(SC(C%10=C(F)C=C(C%11=CC=C(C%12=CC=C(CCCCCC)S%12)S%11)C%13=NSN=C%13%10)=C%14)=C%14[Si]9(CC(CC)CCCC)CC(CC)CCCC)S7)[Si]6(CC(CC)CCCC)CC(CC)CCCC,DTS(FBTTh2)2-homo,,,0.77,2.76,51.3,1.08,"	Wang Y, Zhao X, Zhan X. Layer by layer solution processed organic solar cells based on a small molecule donor and a polymer acceptor. Journal of Materials Chemistry C 3, 447-452 (2015)."
2557,FC(C=C(C1=CC=C(C2=CC=C(CCCCCC)S2)S1)C3=NSN=C34)=C4C5=CC6=C(S5)C7=C(C=C(C8=C(F)C=C(C9=CC=C(C%10=CC=C(CCCCCC)S%10)S9)C%11=NSN=C%118)S7)[Si]6(CC(CC)CCCC)CC(CC)CCCC,DTS(FBTTh2)2,,,0.64,11.3,61,4.5,"	Vangerven T, et al. Elucidating Batch-to-Batch Variation Caused by Homocoupled Side Products in Solution-Processable Organic Solar Cells. Chemistry of Materials 28, 9088-9098 (2016)."
2558,CCCCCCCCCCC1=C(CCCCCCCCCC)SC(C2=C3C(C(SC(C4=CC(CCCCCCCC)=C(C5=CC=C(C6=C(CCCCCCCC)C=C(/C=C7C(N(CC)C(S/7)=S)=O)S6)S5)S4)=C8)=C8S3)=C(C9=CC(CCCCCCCCCC)=C(CCCCCCCCCC)S9)C%10=C2C(SC(C%11=CC(CCCCCCCC)=C(C%12=CC=C(C%13=C(CCCCCCCC)C=C(/C=C%14C(N(CC)C(S/%14)=S)=O)S%13)S%12)S%11)=C%15)=C%15S%10)=C1,DTBDT-Rho,,,0.77,13.1,68,6.8,"	Vangerven T, et al. Elucidating Batch-to-Batch Variation Caused by Homocoupled Side Products in Solution-Processable Organic Solar Cells. Chemistry of Materials 28, 9088-9098 (2016)."
2559,CCCCCCC1=C(SC(C2=C(CCCCCC)C=C(/C=C(C#N)/C(OCCCCCCCC)=O)S2)=C1)C(S3)=CC=C3/C=C/C4=CC=C(C5=C(CCCCCC)C=C(C6=C(CCCCCC)C=C(/C=C(C#N)/C(OCCCCCCCC)=O)S6)S5)S4,S-01,,,0.81,17.2,51,7.1,"	Song HG, Kim YJ, Lee JS, Kim Y-H, Park CE, Kwon S-K. Dithienobenzodithiophene-Based Small Molecule Organic Solar Cells with over 7% Efficiency via Additive-and Thermal-Annealing-Free Processing. ACS applied materials & interfaces 8, 34353-34359 (2016)."
2560,CCCCCCC1=C(C#CC2=CC=C(C3=CC=C(C#CC4=C(CCCCCC)C=C(C5=C(CCCCCC)C=C(/C=C(C#N)/C(OCCCCCCCC)=O)S5)S4)S3)S2)SC(C6=C(CCCCCC)C=C(/C=C(C#N)/C(OCCCCCCCC)=O)S6)=C1,S-02,,,0.85,4.26,59,2.13,"	Cui C, et al. Conjugated Oligothiophene Derivatives Based on Bithiophene with Unsaturated Bonds as Building Blocks for Solution©\Processed Bulk Heterojunction Organic Solar Cells. Chemistry¨CAn Asian Journal 11, 3557-3567 (2016)."
2561,CCCCCCC1=C(C#CC(S2)=CC=C2/C=C/C3=CC=C(C#CC4=C(CCCCCC)C=C(C5=C(CCCCCC)C=C(/C=C(C#N)/C(OCCCCCCCC)=O)S5)S4)S3)SC(C6=C(CCCCCC)C=C(/C=C(C#N)/C(OCCCCCCCC)=O)S6)=C1,S-03,,,0.86,2.88,46,1.13,"	Cui C, et al. Conjugated Oligothiophene Derivatives Based on Bithiophene with Unsaturated Bonds as Building Blocks for Solution©\Processed Bulk Heterojunction Organic Solar Cells. Chemistry¨CAn Asian Journal 11, 3557-3567 (2016)."
2562,CCCCCCC1=C(C#CC(S2)=CC=C2/C=C/C3=CC=C(C#CC4=C(CCCCCC)C=C(C5=C(CCCCCC)C=C(/C=C(C#N)/C#N)S5)S4)S3)SC(C6=C(CCCCCC)C=C(/C=C(C#N)/C#N)S6)=C1,S-04,,,0.96,4.57,50,2.19,"	Cui C, et al. Conjugated Oligothiophene Derivatives Based on Bithiophene with Unsaturated Bonds as Building Blocks for Solution©\Processed Bulk Heterojunction Organic Solar Cells. Chemistry¨CAn Asian Journal 11, 3557-3567 (2016)."
2563,CCCCCCC1=C(C#CC(S2)=CC=C2/C=C/C3=CC=C(C#CC4=C(CCCCCC)C=C(C5=C(CCCCCC)C=C(/C=C6C(N(CC)C(N(CC)C\6=O)=S)=O)S5)S4)S3)SC(C7=C(CCCCCC)C=C(/C=C8C(N(CC)C(N(CC)C\8=O)=S)=O)S7)=C1,S-05,,,0.98,3.4,31,1.02,"	Cui C, et al. Conjugated Oligothiophene Derivatives Based on Bithiophene with Unsaturated Bonds as Building Blocks for Solution©\Processed Bulk Heterojunction Organic Solar Cells. Chemistry¨CAn Asian Journal 11, 3557-3567 (2016)."
2564,CCCCC(CC)CC(S1)=CC=C1C2=C3C(C=C(C4=C(CCCCCC)C5=C(C=C(C6=C(CCCCCC)C=C(/C=C7CC(C(CC8=O)=O)=C8C=C/7)S6)S5)S4)S3)=C(C9=CC=C(CC(CC)CCCC)S9)C%10=C2C=C(C%11=C(CCCCCC)C%12=C(C=C(C%13=C(CCCCCC)C=C(/C=C%14CC(C(CC%15=O)=O)=C%15C=C/%14)S%13)S%12)S%11)S%10,BTID-0F,,,0.99,4.48,28,1.22,"	Cui C, et al. Conjugated Oligothiophene Derivatives Based on Bithiophene with Unsaturated Bonds as Building Blocks for Solution©\Processed Bulk Heterojunction Organic Solar Cells. Chemistry¨CAn Asian Journal 11, 3557-3567 (2016)."
2565,CCCCCCC1=C(SC2=C1SC(C3=C(CCCCCC)C=C(/C=C4C(F)C(C(CC5=O)=O)=C5C=C/4)S3)=C2)C(S6)=CC7=C6C(C8=CC=C(CC(CCCC)CCCCCC)S8)=C(C=C(C9=C(CCCCCC)C%10=C(C=C(C%11=C(CCCCCC)C=C(/C=C%12C(F)C(C(CC%13=O)=O)=C%13C=C/%12)S%11)S%10)S9)S%14)C%14=C7C%15=CC=C(CC(CCCC)CCCCCC)S%15,BTID-1F,,,0.93,14,64,8.3,"	Deng D, et al. Fluorination-enabled optimal morphology leads to over 11% efficiency for inverted small-molecule organic solar cells. Nat. Commun. 7, 13740 (2016)."
2566,CCCCCCC1=C(SC2=C1SC(C3=C(CCCCCC)C=C(/C=C4C(F)C(C(CC5=O)=O)=C5C(F)=C/4)S3)=C2)C(S6)=CC7=C6C(C8=CC=C(CC(CCCCCC)CCCCCCCC)S8)=C(C=C(C9=C(CCCCCC)C%10=C(C=C(C%11=C(CCCCCC)C=C(/C=C%12C(F)C(C(CC%13=O)=O)=C%13C(F)=C/%12)S%11)S%10)S9)S%14)C%14=C7C%15=CC=C(CC(CCCCCC)CCCCCCCC)S%15,BTID-2F,,,0.94,15.3,72,10.4,"	Deng D, et al. Fluorination-enabled optimal morphology leads to over 11% efficiency for inverted small-molecule organic solar cells. Nat. Commun. 7, 13740 (2016)."
2567,O=C1C(C2=C(C3=CC=C(C4=CC=CC=C4)S3)N1CC(CC)CCCC)=C(C5=CC=C(C6=CC=CC=C6)S5)N(CC(CC)CCCC)C2=O,DPP-B,,,0.95,15.7,76,11.3,"	Deng D, et al. Fluorination-enabled optimal morphology leads to over 11% efficiency for inverted small-molecule organic solar cells. Nat. Commun. 7, 13740 (2016)."
2568,O=C1C(C2=C(C3=CC=C(C4=CC=C(C=CC=C5)C5=C4)S3)N1CC(CC)CCCC)=C(C6=CC=C(C7=CC=C(C=CC=C8)C8=C7)S6)N(CC(CC)CCCC)C2=O,DPP-N,,,0.63,0.69,43.4,0.2,"	Yuan J, Ma W. Diketopyrrolopyrrole based highly crystalline conjugated molecules for application in small molecule donor-polymer acceptor nonfullerene organic solar cells. Organic Electronics 39, 279-287 (2016)."
2569,O=C1C(C2=C(C3=CC=C(C4=CC(C=CC5=CC=C6)=C(C5=C6C=C7)C7=C4)S3)N1CC(CCCCCC)CCCCCCCC)=C(C8=CC=C(C9=CC(C=CC%10=CC=C%11)=C(C%10=C%11C=C%12)C%12=C9)S8)N(CC(CCCCCC)CCCCCCCC)C2=O,DPP-P,,,0.83,1.14,53.2,0.5,"	Yuan J, Ma W. Diketopyrrolopyrrole based highly crystalline conjugated molecules for application in small molecule donor-polymer acceptor nonfullerene organic solar cells. Organic Electronics 39, 279-287 (2016)."
2570,CCCCC(CC)C[Si]1(CC(CC)CCCC)C2=C(SC(C3=CC=C(C4=CC=C(C5=CC=C(CCCCCC)S5)S4)C6=C3CC(C7=CC(OCCCCCCCC)=CC=C7)C(C8=CC=CC(OCCCCCCCC)=C8)C6)=C2)C9=C1C=C(C%10=C(CC(C%11=CC=CC(OCCCCCCCC)=C%11)C(C%12=CC(OCCCCCCCC)=CC=C%12)C%13)C%13=C(C%14=CC=C(C%15=CC=C(CCCCCC)S%15)S%14)C=C%10)S9,DTS(QxHT2)2,,,0.78,4.45,58.5,2.05,"	Yuan J, Ma W. Diketopyrrolopyrrole based highly crystalline conjugated molecules for application in small molecule donor-polymer acceptor nonfullerene organic solar cells. Organic Electronics 39, 279-287 (2016)."
2571,O=C1N(CC(CC)CCCC)C(C2=CC=C(C3=CC(C(OCC)=O)=C(C(OCC)=O)S3)S2)=C4C1=C(C5=CC=C(C6=CC(C(OCC)=O)=C(C(OCC)=O)S6)S5)N(CC(CC)CCCC)C4=O,DPP(C2T)2,,,0.98,12.46,64,7.81,"	Keshtov M, et al. Synthesis and photophysical properties of semiconductor molecules D 1-AD 2-AD 1-type structure based on derivatives of quinoxaline and dithienosilole for organics solar cells. Organic Electronics 39, 361-370 (2016)."
2572,CC(C=C1)=CC=C1N(C2=CC=C(C3=CC=C(/C=C(C4=C(F)C(F)=C(C(F)(F)F)C(F)=C4F)\C#N)C5=NSN=C35)S2)C6=CC=C(C)C=C6,TFTF,,,0.97,3.58,48,1.66,"	Zhang Z, Liu W, Yan J, Shi M, Chen H. A bipolar diketopyrrolopyrrole molecule end capped with thiophene-2, 3-dicarboxylate used as both electron donor and acceptor for organic solar cells. Synthetic Metals 222, 211-218 (2016)."
2573,CC(C=C1)=CC=C1N(C2=CC=C(C3=CC=C(/C=C(C4=C(F)C(F)=C(C#N)C(F)=C4F)\C#N)C5=NSN=C35)S2)C6=CC=C(C)C=C6,CNTF,,,0.82,3.9,39,1.2,"	Fang L, et al. Fluorine-containing low-energy-gap organic dyes with low voltage losses for organic solar cells. Synthetic Metals 222, 232-239 (2016)."
2574,CC(C=C1)=CC=C1N(C2=CC=C(C3=CC=C(/C=C(C4=C(F)C(F)=NC(F)=C4F)\C#N)C5=NSN=C35)S2)C6=CC=C(C)C=C6,PRTF,,,0.88,5.4,53,2.4,"	Fang L, et al. Fluorine-containing low-energy-gap organic dyes with low voltage losses for organic solar cells. Synthetic Metals 222, 232-239 (2016)."
2575,CCCCCCC1(CCCCCC)C2=CC(C3=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C4=O)=C5C4=C(C6=CC=C(C7=CC=C(C(C=CC(C)=C8)=C8C9(CCCCCC)CCCCCC)C9=C7)S6)N(CC(CCCCCC)CCCCCCCC)C5=O)S3)=CC=C2C%10=C1C=C(C%11=CC(CCCCCC)=C(C%12=CC=C(C%13=CC=C(C%14=C(CCCCCC)C=C(C)S%14)S%13)S%12)S%11)C=C%10,P4TFDPP,,,0.9,4.7,55,2.3,"	Fang L, et al. Fluorine-containing low-energy-gap organic dyes with low voltage losses for organic solar cells. Synthetic Metals 222, 232-239 (2016)."
2576,CC1=CC(CCCCCC)=C(S1)C(S2)=CC=C2C3=CC=C(S3)C(S4)=C(CCCCCC)C=C4C5=CC=C(C6=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C7=O)=C8C7=C(C9=CC=C(C%10=CC=C(C)C=C%10)S9)N(CC(CCCCCC)CCCCCCCC)C8=O)S6)C=C5,P5TDPP,,,0.88,9.4,59,4.9,"	SambathKumar B, et al. Two Donor¨COne Acceptor Random Terpolymer Comprised of Diketopyrrolopyrrole Quaterthiophene with Various Donor ¦Ð-Linkers for Organic Photovoltaic Application. The Journal of Physical Chemistry C 120, 26609-26619 (2016)."
2577,CC1=CC(CCCCCC)=C(S1)C(S2)=CC=C2C3=CC=C(S3)C4=C(CCCCCC)C=C(C5=CC=C(S5)C6=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C7=O)=C8C7=C(C9=CC=C(C%10=CC=C(C)S%10)S9)N(CC(CCCCCC)CCCCCCCC)C8=O)S6)S4,P4TPDPP,,,0.77,8.57,61,4.1,"	SambathKumar B, et al. Two Donor¨COne Acceptor Random Terpolymer Comprised of Diketopyrrolopyrrole Quaterthiophene with Various Donor ¦Ð-Linkers for Organic Photovoltaic Application. The Journal of Physical Chemistry C 120, 26609-26619 (2016)."
2578,CC1=CC(CCCCCC)=C(S1)C(S2)=CC=C2C3=CC=C(S3)C4=C(CCCCCC)C=C(/C=C/C5=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C6=O)=C7C6=C(C8=CC=C(/C=C/C)S8)N(CC(CCCCCC)CCCCCCCC)C7=O)S5)S4,P4TVDPP,,,0.72,10.05,50,3.8,"	SambathKumar B, et al. Two Donor¨COne Acceptor Random Terpolymer Comprised of Diketopyrrolopyrrole Quaterthiophene with Various Donor ¦Ð-Linkers for Organic Photovoltaic Application. The Journal of Physical Chemistry C 120, 26609-26619 (2016)."
2579,O=C1N(CC(CC)CCCC)C(C2=CC=C(C3=CC(C(C(C=CC=C4)=C4S5)=C5N6CCCCCCCCCCCC)=C6C=C3)S2)=C7C(N(CC(CC)CCCC)C(C8=CC=C(S8)C9=CC=C(C%10=CC=C(C(N(CC(CC)CCCC)C%11=O)=C%12C%11=C(C%13=CC=C(C%14=CC(C(C(C=CC=C%15)=C%15S%16)=C%16N%17CCCCCCCCCCCC)=C%17C=C%14)S%13)N(CC(CC)CCCC)C%12=O)S%10)S9)=C71)=O,3T(DPP-BTI)2,,,0.69,9.43,44,2.9,"	SambathKumar B, et al. Two Donor¨COne Acceptor Random Terpolymer Comprised of Diketopyrrolopyrrole Quaterthiophene with Various Donor ¦Ð-Linkers for Organic Photovoltaic Application. The Journal of Physical Chemistry C 120, 26609-26619 (2016)."
2580,CCCCCCCCCCC(CCCCCCCC)/C(C1=CC=C(/C(C#CC2=CC(CCCCCC)=C(C3=CC=C(C4=C(CCCCCC)C=C(/C=C5C(N(CC)C(S/5)=S)=O)S4)S3)S2)=C6N=C7C=C\6)N1[Zn]N8/C(C=C/C8=C7\C(CCCCCCCC)CCCCCCCCCC)=C9/C#CC%10=CC(CCCCCC)=C(C%11=CC=C(C%12=C(CCCCCC)C=C(/C=C%13C(N(CC)C(S/%13)=S)=O)S%12)S%11)S%10)=C%14C=CC9=N\%14,PTTR,,,0.52,10.41,55.8,3.02,"	Qi H, et al. Novel D (A-Ar) 2 type small molecules with oligothiophene, diketopyrrolopyrrole and benzo [4, 5] thieno [2, 3-b] indole units: investigation on relationship between structure and property for organic solar cells. Tetrahedron 72, 7430-7437 (2016)."
2581,CCCCCCCCCCC(CCCCCCCC)/C(C1=CC=C(/C(C#CC2=CC(CCCCCC)=C(C3=CC=C(C4=C(CCCCCC)C=C(/C=C5C(N(CC)/C(S/5)=C(C#N)\C#N)=O)S4)S3)S2)=C6N=C7C=C\6)N1[Zn]N8/C(C=C/C8=C7\C(CCCCCCCC)CCCCCCCCCC)=C9/C#CC%10=CC(CCCCCC)=C(C%11=CC=C(C%12=C(CCCCCC)C=C(/C=C%13C(N(CC)/C(S/%13)=C(C#N)/C#N)=O)S%12)S%11)S%10)=C%14C=CC9=N\%14,PTTCNR,,,0.8,14.93,64,7.66,"	Xiao L, et al. New Terthiophene-Conjugated Porphyrin Donors for Highly Efficient Organic Solar Cells. ACS applied materials & interfaces 8, 30176-30183 (2016)."
2582,CCCCCCCCC(C=C(C1=C(CCCCCCCC)C=C(/C=C2SC(N(CC)C\2=O)=S)S1)S3)=C3C4=CC=C(S4)C5=CC=C(C6=CC=C(C7=C(CCCCCCCC)C=C(C8=C(CCCCCCCC)C=C(/C=C9C(N(CC)C(S/9)=S)=O)S8)S7)S6)S5,DERHD7T,,,0.82,14.3,70,8.21,"	Xiao L, et al. New Terthiophene-Conjugated Porphyrin Donors for Highly Efficient Organic Solar Cells. ACS applied materials & interfaces 8, 30176-30183 (2016)."
2583,FC(C(F)=C(C1=CC=C(C2=CC(C(C=CC=C3)=C3N4CCCCCCCC)=C4C=C2)S1)C5=NSN=C56)=C6C(C=C7)=CC=C7C(C8=CC=C(C9=C(F)C(F)=C(C%10=CC=C(C%11=CC=C(N(CCCCCCCC)C%12=C%13C=CC=C%12)C%13=C%11)S%10)C%14=NSN=C9%14)C=C8)C%15=CC=C(C%16=C(F)C(F)=C(C%17=CC=C(C%18=CC(C(C=CC=C%19)=C%19N%20CCCCCCCC)=C%20C=C%18)S%17)C%21=NSN=C%21%16)C=C%15,TPA(F2BT-T-3Cz)3,,,,,,6.1,"	Li Y. Photovoltaic efficiency of solution-processable organic molecules reached near 10%. Sci. China: Chem 58, 191-191 (2015)."
2584,FC(C=C(C1=CC=C(C2=CC(C(C=CC=C3)=C3N4CCCCCCCC)=C4C=C2)S1)C5=NSN=C56)=C6C(C=C7)=CC=C7C(C8=CC=C(C9=C(F)C=C(C%10=CC=C(C%11=CC=C(N(CCCCCCCC)C%12=C%13C=CC=C%12)C%13=C%11)S%10)C%14=NSN=C9%14)C=C8)C%15=CC=C(C%16=C(F)C=C(C%17=CC=C(C%18=CC(C(C=CC=C%19)=C%19N%20CCCCCCCC)=C%20C=C%18)S%17)C%21=NSN=C%21%16)C=C%15,TPA(F1BT-T-3Cz)3,,,0.96,10.55,49,4.81,"	Wang Q, et al. Photovoltaic Small Molecules of TPA (F x BT-T-Cz) 3: Tuning Open-Circuit Voltage over 1.0 V for Their Organic Solar Cells by Increasing Fluorine Substitution. ACS applied materials & interfaces 8, 30320-30327 (2016)."
2585,O=C(OC(CC)CCCCC)C1=C(C2=CC=C(C3=CC=C(C4=C5C(C(N4CC(CC)CCCC)=O)=C(C6=CC=C(C7=CC=CC=C7)S6)N(CC(CC)CCCC)C5=O)S3)S2)SC(C8=CC=C(C9=CC=C(C%10=C%11C(C(N%10CC(CC)CCCC)=O)=C(C%12=CC=C(C%13=CC=CC=C%13)S%12)N(CC(CC)CCCC)C%11=O)S9)S8)=C1,3EhT(DPP)2,,,1.01,10.86,44,4.99,"	Wang Q, et al. Photovoltaic Small Molecules of TPA (F x BT-T-Cz) 3: Tuning Open-Circuit Voltage over 1.0 V for Their Organic Solar Cells by Increasing Fluorine Substitution. ACS applied materials & interfaces 8, 30320-30327 (2016)."
2586,CC(C=C(C)C=C1C)=C1/C(C2=CC=C(/C(C#CC3=C(CCCCCC)C(CCCCCC)=C(/C=C4C(N(CC)C(S/4)=S)=O)S3)=C5N=C6C=C\5)N2[Zn]N7/C(C=C/C7=C6\C8=C(C)C=C(C)C=C8C)=C9/C#CC%10=C(CCCCCC)C(CCCCCC)=C(/C=C%11C(N(CC)C(S/%11)=S)=O)S%10)=C%12C=CC9=N\%12,1a,,,0.7,8.31,56,3.29,"	Ko EY, Choi S, Park GE, Lee DH, Cho MJ, Choi DH. Diketopyrrolopyrrole-based conjugated small molecules bearing two different acceptor moieties for organic solar cells. Synthetic Metals 221, 39-47 (2016)."
2587,CC(C=C(C)C=C1C)=C1/C(C2=CC=C(/C(C#CC3=C(CCCCCC)C(CCCCCC)=C(/C=C/C4=C(CCCCCC)C(CCCCCC)=C(/C=C5SC(N(CC)C\5=O)=S)S4)S3)=C6N=C7C=C\6)N2[Zn]N8/C(C=C/C8=C7\C9=C(C)C=C(C)C=C9C)=C%10/C#CC%11=C(CCCCCC)C(CCCCCC)=C(/C=C/C%12=C(CCCCCC)C(CCCCCC)=C(/C=C%13SC(N(CC)C\%13=O)=S)S%12)S%11)=C%14C=CC%10=N\%14,1b,,,0.85,11.36,31,3.01,"	Montcada NF, et al. High photo-current in solution processed organic solar cells based on a porphyrin core A-¦Ð-D-¦Ð-A as electron donor material. Organic Electronics 38, 330-336 (2016)."
2588,CCCCCCCCC(C=C(C1=C(CCCCCCCC)C=C(/C=C2S/C(N(CC)C\2=O)=C(C#N)/C#N)S1)S3)=C3C4=CC=C(S4)C5=CC=C(C6=CC=C(C7=C(CCCCCCCC)C=C(C8=C(CCCCCCCC)C=C(/C=C9C(N(CC)/C(S/9)=C(C#N)\C#N)=O)S8)S7)S6)S5,DRCN7T,,,0.8,13.2,40,4.24,"	Montcada NF, et al. High photo-current in solution processed organic solar cells based on a porphyrin core A-¦Ð-D-¦Ð-A as electron donor material. Organic Electronics 38, 330-336 (2016)."
2589,N#C/C(C1=CC=C([N+]([O-])=O)C=C1)=C/C(C=C2)=CC=C2N(C3=CC=CC=C3)C(C=C4)=CC=C4/C=C/C5=CC=C(C6=CC(CCCCCCCCCCCC)=C(C7=CC=C(N(C8=CC=CC=C8)C9=CC=CC=C9)C=C7)S6)C%10=NSN=C%105,SM3,,,,,,9.3,"	Li Y. Photovoltaic efficiency of solution-processable organic molecules reached near 10%. Sci. China: Chem 58, 191-191 (2015)."
2590,N#C/C(C1=CC=C([N+]([O-])=O)C=C1)=C\C(C=C2)=CC=C2N(C3=CC=CC=C3)C(C=C4)=CC=C4/C=C/C5=CC=C(C6=CC7=C(C(OCC(CC)CCCC)=C(C=C(C8=CC=C(/C=C/C9=CC=C(N(C%10=CC=CC=C%10)C%11=CC=C(/C=C(C#N)/C%12=CC=C([N+]([O-])=O)C=C%12)C=C%11)C=C9)C%13=NSN=C8%13)S%14)C%14=C7OCC(CC)CCCC)S6)C%15=NSN=C%155,SM4,,,0.85,5.22,33,1.46,"	Jia T, Peng Z, Li Q, Xie Y, Hou Q, Hou L. Synthesis of triphenylamine-based molecules with cyan terminals and their application for organic solar cells. Synthetic Metals 199, 14-20 (2015)."
2591,O=C1N(CC(CC)CCCC)C(C2=CC=C(C3=CC(C(C(C=CC=C4)=C4S5)=C5N6CCCCCCCCCCCC)=C6C=C3)S2)=C7C(N(CC(CC)CCCC)C(C8=CC=C(C9=CC=C(S9)C%10=CC=C(C%11=CC=C(C(N(CC(CC)CCCC)C%12=O)=C%13C%12=C(C%14=CC=C(C%15=CC(C(C(C=CC=C%16)=C%16S%17)=C%17N%18CCCCCCCCCCCC)=C%18C=C%15)S%14)N(CC(CC)CCCC)C%13=O)S%11)S%10)S8)=C71)=O,4T(DPP-BTI)2,,,0.78,4.89,33,1.27,"	Jia T, Peng Z, Li Q, Xie Y, Hou Q, Hou L. Synthesis of triphenylamine-based molecules with cyan terminals and their application for organic solar cells. Synthetic Metals 199, 14-20 (2015)."
2592,FC1=C(C2=CC=C(C(C3=CC=CC=C3)C4=CC=CC=C4)C=C2)C5=NSN=C5C(C6=CC=C(C7=CC=C(C8=CC=C(CCCCCC)S8)S7)S6)=C1F,TPA-DFBT3T,,,0.53,10.43,53.1,2.94,"	Qi H, et al. Novel D (A-Ar) 2 type small molecules with oligothiophene, diketopyrrolopyrrole and benzo [4, 5] thieno [2, 3-b] indole units: investigation on relationship between structure and property for organic solar cells. Tetrahedron 72, 7430-7437 (2016)."
2593,CCCCCCC(S1)=CC=C1C2=CC=C(S2)C(S3)=CC=C3C4=CC=C(C5=CC=C(C(C6=CC=CC=C6)C7=CC=CC=C7)C=C5)C8=NSN=C48,TPA-BT3T,,,0.89,5.18,34,1.54,"	Wang Y, Bai H, Cheng P, Zhang M, Zhan X. Effect of electron-withdrawing units on triphenylamine-based small molecules for solution-processed organic solar cells. Science China Chemistry 58, 331-338 (2015)."
2594,CCCCCCC(S1)=CC=C1C2=CC=C(S2)C(S3)=CC=C3C4=NC=C(C5=CC=C(C(C6=CC=CC=C6)C7=CC=CC=C7)C=C5)C8=NSN=C48,TPA-PT3T,,,0.91,8.7,37,2.89,"	Wang Y, Bai H, Cheng P, Zhang M, Zhan X. Effect of electron-withdrawing units on triphenylamine-based small molecules for solution-processed organic solar cells. Science China Chemistry 58, 331-338 (2015)."
2595,S=C(S/1)N(CC)C(C1=C\C(S2)=CC3=C2C(OCC(CC)CCCC)=C(C=C(C(S4)=CC5=C4C(OCC(CC)CCCC)=C(C=C(C(S6)=CC7=C6C(OCC(CC)CCCC)=C(C=C(/C=C8C(N(CC)C(S/8)=S)=O)S9)C9=C7OCC(CC)CCCC)S%10)C%10=C5OCC(CC)CCCC)S%11)C%11=C3OCC(CC)CCCC)=O,DRBDT3,,,0.9,4.54,33,1.34,"	Wang Y, Bai H, Cheng P, Zhang M, Zhan X. Effect of electron-withdrawing units on triphenylamine-based small molecules for solution-processed organic solar cells. Science China Chemistry 58, 331-338 (2015)."
2596,CCCCCCC(C=C(C1=C(CCCCCC)C=C(/C=C2C(N(CC)C(N(CC)C/2=O)=S)=O)S1)S3)=C3C#C[Pt]([Pt](CCCC)(CCCC)CCCC)(C#CC4=C(CCCCCC)C=C(C5=C(CCCCCC)C=C(/C=C6C(N(CC)C(N(CC)C\6=O)=S)=O)S5)S4)[Pt](CCCC)(CCCC)CCCC,S-1,,,0.99,8.26,50,4.09,"	Ni W, et al. A new oligobenzodithiophene end-capped with 3-ethyl-rhodanine groups for organic solar cells with high open-circuit voltage. Science China Chemistry 58, 339-346 (2015)."
2597,CCCCCCC1=C(C2=CC=C(S2)C#C[Pt]([Pt](CCCC)(CCCC)CCCC)(C#CC3=CC=C(C4=C(CCCCCC)C=C(C5=C(CCCCCC)C=C(/C=C6C(N(CC)C(N(CC)C\6=O)=S)=O)S5)S4)S3)[Pt](CCCC)(CCCC)CCCC)SC(C7=C(CCCCCC)C=C(/C=C8C(N(CC)C(N(CC)C/8=O)=S)=O)S7)=C1,S-2,,,0.91,3.61,28,0.88,"	Cui C, Zhang Y, Choy WC, Li H, Wong W-Y. Metallated conjugation in small-sized-molecular donors for solution-processed organic solar cells. Science China Chemistry 58, 347-356 (2015)."
2598,CCCCCCC(C=C(C1=C(CCCCCC)C=C(/C=C(C#N)/C#N)S1)S2)=C2C#C[Pt]([Pt](CCCC)(CCCC)CCCC)(C#CC3=C(CCCCCC)C=C(C4=C(CCCCCC)C=C(/C=C(C#N)/C#N)S4)S3)[Pt](CCCC)(CCCC)CCCC,S-3,,,0.93,5.89,29,1.59,"	Cui C, Zhang Y, Choy WC, Li H, Wong W-Y. Metallated conjugation in small-sized-molecular donors for solution-processed organic solar cells. Science China Chemistry 58, 347-356 (2015)."
2599,CCCCCCC1=C(C2=CC=C(S2)C#C[Pt]([Pt](CCCC)(CCCC)CCCC)(C#CC3=CC=C(C4=C(CCCCCC)C=C(C5=C(CCCCCC)C=C(/C=C(C#N)/C#N)S5)S4)S3)[Pt](CCCC)(CCCC)CCCC)SC(C6=C(CCCCCC)C=C(/C=C(C#N)/C#N)S6)=C1,S-4,,,0.6,1.22,34,0.17,"	Cui C, Zhang Y, Choy WC, Li H, Wong W-Y. Metallated conjugation in small-sized-molecular donors for solution-processed organic solar cells. Science China Chemistry 58, 347-356 (2015)."
2600,CCCCCCCCC(C=C(C1=C(CCCCCCCC)C=C(C2=CC=C(/C=C3C(N(CCCCCCCC)/C(S\3)=C(C#N)\C#N)=O)S2)S1)S4)=C4C(C=C5)=CC=C5N(C6=CC=C(C7=C(CCCCCCCC)C=C(C8=C(CCCCCCCC)C=C(C9=CC=C(/C=C%10S/C(N(CCCCCCCC)C\%10=O)=C(C#N)/C#N)S9)S8)S7)C=C6)C%11=CC=C(C%12=C(CCCCCCCC)C=C(C%13=C(CCCCCCCC)C=C(C%14=CC=C(/C=C%15C(N(CCCCCCCC)/C(S/%15)=C(C#N)\C#N)=O)S%14)S%13)S%12)C=C%11,TCNR3TTPA,,,0.92,4.88,33,1.56,"	Cui C, Zhang Y, Choy WC, Li H, Wong W-Y. Metallated conjugation in small-sized-molecular donors for solution-processed organic solar cells. Science China Chemistry 58, 347-356 (2015)."
2601,CCCCCCCCOC1=C2C(C=CS2)=C(OCCCCCCCC)C3=C1C=C(S3)C4=CC=C5C6=CC=C(C7=CC8=C(C(OCCCCCCCC)=C(C=CS9)C9=C8OCCCCCCCC)S7)C=C6C%10=NSN=C%10C5=C4,SM1,,,0.99,5.76,44,2.5,"	Zhou Y, et al. High open-circuit voltage solution-processed organic solar cells based on a star-shaped small molecule end-capped with a new rhodanine derivative. Science China Chemistry 58, 357-363 (2015)."
2602,CCCCCCCCOC1=C2C(C=CS2)=C(OCCCCCCCC)C3=C1C=C(C(S4)=CC=C4C5=CC=C6C7=CC=C(C8=CC=C(C9=CC%10=C(C(OCCCCCCCC)=C(C=CS%11)C%11=C%10OCCCCCCCC)S9)S8)C=C7C%12=NC(C)(C)N=C%12C6=C5)S3,SM2,,,0.77,0.61,30,0.15,"	Kim J, et al. 2, 2-dimethyl-2H-benzimidazole based small molecules for organic solar cells. Macromolecular Research 23, 214-222 (2015)."
2603,N#C/C(/N=C/C1=CC=C(N(C2=CC=C(OC)C=C2)C3=CC=C(OC)C=C3)S1)=C(C#N)\N=C\C4=CC=C(N(C5=CC=C(OC)C=C5)C6=CC=C(OC)C=C6)S4,T,,,0.62,1.69,27,0.28,"	Kim J, et al. 2, 2-dimethyl-2H-benzimidazole based small molecules for organic solar cells. Macromolecular Research 23, 214-222 (2015)."
2604,N#C/C(/N=C/C1=CC=C(N(C2=CC=C(OC)C=C2)C3=CC=C(OC)C=C3)C=C1)=C(C#N)\C=N\C4=CC=C(N(C5=CC=C(OC)C=C5)C6=CC=C(OC)C=C6)C=C4,P,,,0.52,4.28,36,0.89,"	Jeux V, et al. One step synthesis of DAD chromophores as active materials for organic solar cells by basic condensation. Dyes and Pigments 113, 402-408 (2015)."
2605,CC(C=C1)=CC=C1N(C2=CC=C(C3=CC=C(C4=CC=C(N(C5=CC=C(C6=CC(CCCCCCCCCCCC)=C(C7=CC=C(C(C8=CC=CC=C8)C9=CC=CC=C9)C=C7)S6)C=C5)C%10=CC=C(C)C=C%10)C=C4)C%11=NSN=C%113)C=C2)C%12=CC=C(C%13=CC(CCCCCCCCCCCC)=C(C%14=CC=C(C(C%15=CC=CC=C%15)C%16=CC=CC=C%16)C=C%14)S%13)C=C%12,(TPATh)2(MTPA)2B,,,0.84,3.65,35,1.18,"	Jeux V, et al. One step synthesis of DAD chromophores as active materials for organic solar cells by basic condensation. Dyes and Pigments 113, 402-408 (2015)."
2606,CCCCCCCCCCCCC1=C(C2=CC=C(C(C3=CC=CC=C3)C4=CC=CC=C4)C=C2)SC(C(C=C5)=CC=C5N(C6=CC=C(C7=CC=C(C8=CC=C(N(C9=CC=C(C%10=CC(CCCCCCCCCCCC)=C(C%11=CC=C(C(C%12=CC=CC=C%12)C%13=CC=CC=C%13)C=C%11)S%10)C=C9)C%14=CC=C(C%15=CC(CCCCCCCCCCCC)=C(C%16=CC=C(C(C%17=CC=CC=C%17)C%18=CC=CC=C%18)C=C%16)S%15)C=C%14)C=C8)C%19=NSN=C%197)C=C6)C%20=CC=C(C%21=CC(CCCCCCCCCCCC)=C(C%22=CC=C(C(C%23=CC=CC=C%23)C%24=CC=CC=C%24)C=C%22)S%21)C=C%20)=C1,(TPATh)4TPA2B,,,0.8,3.18,33,0.83,"	Zhen H, Peng Z, Hou L, Jia T, Li Q, Hou Q. Comparative study on triphenylamine-based bi-armed and four-armed small molecule donors for solution processed organic solar cells. Dyes and Pigments 113, 451-457 (2015)."
2607,CCCCC(CC)CC(S1)=CC=C1C2=C(C=C(C3=CC=C(/C(C(N4CC(CC)CCCC)=O)=C/C5=CC=C(C6=CC=C(CCCCCC)S6)S5)C4=C3)S7)C7=C(C8=CC=C(CC(CC)CCCC)S8)C9=C2SC(C%10=CC(N(CC(CC)CCCC)C(/C%11=C\C%12=CC=C(C%13=CC=C(CCCCCC)S%13)S%12)=O)=C%11C=C%10)=C9,TIBDT,,,0.71,4.89,37,1.3,"	Zhen H, Peng Z, Hou L, Jia T, Li Q, Hou Q. Comparative study on triphenylamine-based bi-armed and four-armed small molecule donors for solution processed organic solar cells. Dyes and Pigments 113, 451-457 (2015)."
2608,CCCCC(CC)COC1=C2C(SC(C3=C4C(SC(C(OCCCCOCC5=CC(Cl)=C(Cl)C=C5)=O)=C4F)=C(C6=CC7=C(S6)C(OCC(CC)CCCC)=C8C(SC(C9=C%10C(SC(C(OCC(CCCC)CCCCCC)=O)=C%10F)=C(C)S9)=C8)=C7OC(CC)CCCCC)S3)=C2)=C(OC(CC)CCCCC)C%11=C1SC(C)=C%11,PTBDCB25,,,0.89,7.36,60,3.94,"	Fan L, Cui R, Jiang L, Zou Y, Li Y, Qian D. A new small molecule with indolone chromophore as the electron accepting unit for efficient organic solar cells. Dyes and Pigments 113, 458-464 (2015)."
2609,FC1=CC(C2=C(C=C(C3=CC=C(C4=C5C(C(N4CC(CC)CCCC)=O)=C(C6=CC=CS6)N(CC(CC)CCCC)C5=O)S3)S7)C7=C(C8=CC=C(OCC(CC)CCCC)C(F)=C8)C9=C2SC(C%10=CC=C(C%11=C%12C(C(N%11CC(CC)CCCC)=O)=C(C%13=CC=CS%13)N(CC(CC)CCCC)C%12=O)S%10)=C9)=CC=C1OCC(CC)CCCC,M1,,,0.76,16.22,67,8.3,"	Park S, et al. Enhancement of organic photovoltaic efficiency via nanomorphology control using conjugated polymers incorporating fullerene compatible side-chains. Macromolecules 48, 337-345 (2015)."
2610,FC1=CC(C2=C(C=C(C3=CC=C(C4=C5C(C(N4CC(CC)CCCC)=O)=C(C6=CC=CS6)N(CC(CC)CCCC)C5=O)S3)O7)C7=C(C8=CC=C(OCC(CC)CCCC)C(F)=C8)C9=C2OC(C%10=CC=C(C%11=C%12C(C(N%11CC(CC)CCCC)=O)=C(C%13=CC=CS%13)N(CC(CC)CCCC)C%12=O)S%10)=C9)=CC=C1OCC(CC)CCCC,M2,,,0.88,5.5,64,3.1,"	Qian D, et al. Modulating molecular aggregation by facile heteroatom substitution of diketopyrrolopyrrole based small molecules for efficient organic solar cells. Journal of Materials Chemistry A 3, 24349-24357 (2015)."
2611,CCCCCC(CC)C(S1)=CC=C1C2=C3C(SC(C4=CC=C(C5=CC=C(C6=CC=C(C7=CC=C(CCCCCC)S7)S6)C8=NSN=C58)S4)=C3)=C(C9=CC=C(C(CC)CCCCC)S9)C%10=C2SC(C%11=CC=C(C%12=CC=C(C%13=CC=C(C%14=CC=C(CCCCCC)S%14)S%13)C%15=NSN=C%15%12)S%11)=C%10,BDT(TBTTT6)2,,,0.8,11.4,60,5.5,"	Qian D, et al. Modulating molecular aggregation by facile heteroatom substitution of diketopyrrolopyrrole based small molecules for efficient organic solar cells. Journal of Materials Chemistry A 3, 24349-24357 (2015)."
2612,CCCCCC(CC)C(S1)=CC=C1C2=C3C(SC(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(C7=CC=C(CCCCCC)S7)S6)C8=NSN=C58)S4)=C3)=C(C9=CC=C(C(CC)CCCCC)S9)C%10=C2SC(C%11=CC=C(C%12=C(F)C(F)=C(C%13=CC=C(C%14=CC=C(CCCCCC)S%14)S%13)C%15=NSN=C%15%12)S%11)=C%10,BDT(TffBTTT6)2,,,0.71,8.42,5.3,3.17,"	Liao X, Wu F, Zhang L, Chen L, Chen Y. Solution-processed small molecules based on benzodithiophene and difluorobenzothiadiazole for inverted organic solar cells. Polymer Chemistry 6, 7726-7736 (2015)."
2613,CCCCCCCCC1=C(C2=CC=C(C3=C(CCCCCCCC)C=C(/C=C4C(N(CC)C(S/4)=S)=O)S3)S2)SC(C5=CC6=C(C7=CC=C(C8=CC=C(CC(CCCCCC)CCCCCCCC)S8)S7)C(SC(C9=CC(CCCCCCCC)=C(C%10=CC=C(C%11=C(CCCCCCCC)C=C(/C=C%12SC(N(C)C\%12=O)=S)S%11)S%10)S9)=C%13)=C%13C(C%14=CC=C(C%15=CC=C(CC(CCCCCCCC)CCCCCC)S%15)S%14)=C6S5)=C1,DR3TBDT2T,,,0.73,9.13,62.5,4.17,"	Liao X, Wu F, Zhang L, Chen L, Chen Y. Solution-processed small molecules based on benzodithiophene and difluorobenzothiadiazole for inverted organic solar cells. Polymer Chemistry 6, 7726-7736 (2015)."
2614,CCCCC(CC)COC(C=C1)=CC=C1C2=CC=C(F)C(C#CC3=C(C=CS4)C4=C(C#CC5=C(F)C(C6=CC=C(OCC(CC)CCCC)C=C6)=CC=C5F)C7=C3SC=C7)=C2F,PBDTBPA(F)-DPP,,,0.91,13.2,,8.33,"	Zuo Y, et al. Device characterization and optimization of small molecule organic solar cells assisted by modelling simulation of the current¨Cvoltage characteristics. Physical Chemistry Chemical Physics 17, 19261-19267 (2015)."
2615,CCCCC(CC)COC(C=C1)=CC=C1C2=CC=CC(C#CC3=C(C=C([Sn](C)(C)C)S4)C4=C(C#CC5=CC(C6=CC=C(OCC(CC)CCCC)C=C6)=CC=C5)C7=C3SC([Sn](C)(C)C)=C7)=C2,PBDTBPA(H)-DPP,,,0.68,9.89,50,4.04,"	Chakravarthi N, et al. The effect of with/without resonance-mediated interactions on the organic solar cell performance of new 2D ¦Ð-conjugated polymers. Polymer Chemistry 6, 7149-7159 (2015)."
2616,OC1=CC(N2CCC3=C2C=CC(C#N)=C3)=CC(O)=C1C(C4=O)=C([O-])C4=CC5=[N+](CCCC)C6=C(C(C=CC=C7)=C7C=C6)C5(C)C,ASQ-5-CN,,,0.74,13.17,57,5.58,"	Chakravarthi N, et al. The effect of with/without resonance-mediated interactions on the organic solar cell performance of new 2D ¦Ð-conjugated polymers. Polymer Chemistry 6, 7149-7159 (2015)."
2617,CCCCCCCCN1C2=C(C=CC=C2)C3=C1C=CC(C4=CC=C(C5=CC=C(C(C=C6)=CC=C6C(C7=CC=C(C8=CC=C(C9=CC=C(C%10=CC(C(C=CC=C%11)=C%11N%12CCCCCCCC)=C%12C=C%10)C%13=NSN=C%139)S8)C=C7)C%14=CC=C(C%15=CC=C(C%16=CC=C(C%17=CC(C(C=CC=C%18)=C%18N%19CCCCCCCC)=C%19C=C%17)C%20=NSN=C%20%16)S%15)C=C%14)S5)C%21=NSN=C4%21)=C3,TPA(T¨CBT¨C3Cz)3,,,0.85,12.4,58,6.11,"	Yang D, et al. Cyano-substitution on the end-capping group: facile access toward asymmetrical squaraine showing strong dipole¨Cdipole interactions as a high performance small molecular organic solar cells material. J. Mater. Chem. A 3, 17704-17712 (2015)."
2618,CCCCCCCCN1C2=C(C=CC=C2)C3=C1C=CC(C(C4=NSN=C45)=CC=C5C(C=C6)=CC=C6C(C7=CC=C(C8=CC=C(C9=CC(C(C=CC=C%10)=C%10N%11CCCCCCCC)=C%11C=C9)C%12=NSN=C%128)C=C7)C%13=CC=C(C%14=CC=C(C%15=CC(C(C=CC=C%16)=C%16N%17CCCCCCCC)=C%17C=C%15)C%18=NSN=C%18%14)C=C%13)=C3,TPA(BT¨C3Cz)3,,,0.84,8.77,52,3.82,"	Zhou P, et al. Enhancing the photovoltaic performance of triphenylamine based star-shaped molecules by tuning the moiety sequence of their arms in organic solar cells. Journal of Materials Chemistry A 3, 13568-13576 (2015)."
2619,CCCCCCCCN1C2=C(C=CC=C2)C3=C1C=CC(C(S4)=CC=C4C(C5=NSN=C56)=CC=C6C(C=C7)=CC=C7C(C8=CC=C(C9=CC=C(C%10=CC=C(C%11=CC(C(C=CC=C%12)=C%12N%13CCCCCCCC)=C%13C=C%11)S%10)C%14=NSN=C%149)C=C8)C%15=CC=C(C%16=CC=C(C%17=CC=C(C%18=CC(C(C=CC=C%19)=C%19N%20CCCCCCCC)=C%20C=C%18)S%17)C%21=NSN=C%21%16)C=C%15)=C3,TPA(BT¨CT¨C3Cz)3,,,0.97,8.8,46,3.94,"	Zhou P, et al. Enhancing the photovoltaic performance of triphenylamine based star-shaped molecules by tuning the moiety sequence of their arms in organic solar cells. Journal of Materials Chemistry A 3, 13568-13576 (2015)."
2620,ClC1=C2C(C3=CC=C2Cl)=C(C=C1)C4=C3/C(N/C4=C\C5=N/C(C6=C5C=CC=C6)=C\7)=C/C(C8=C/9C=CC=C8)=NC9=C/C%10=C(C=CC=C%11)C%11=C7N%10,CABP,,,0.9,10.08,54,5.07,"	Zhou P, et al. Enhancing the photovoltaic performance of triphenylamine based star-shaped molecules by tuning the moiety sequence of their arms in organic solar cells. Journal of Materials Chemistry A 3, 13568-13576 (2015)."
2621,N#C/C(C#N)=C/C1=CC=C(C2=CC=C(N(C3=CC=CC=C3)C4=CC=CC=C4)C=C2)S1,2,,,0.65,2.5,52,0.9,"	Zhen Y, Tanaka H, Harano K, Okada S, Matsuo Y, Nakamura E. Organic Solid Solution Composed of Two Structurally Similar Porphyrins for Organic Solar Cells. Journal of the American Chemical Society 137, 2247-2252 (2015)."
2622,N#C/C(C#N)=C/C1=CC=C(C2=CC=C(N(C)C3=CC=CC=C3)C=C2)S1,1,,,0.92,5.8,42,2.5,"	Jiang Y, Cabanetos C, Allain M, Liu P, Roncali J. Manipulation of the band gap and efficiency of a minimalist push¨Cpull molecular donor for organic solar cells. Journal of Materials Chemistry C 3, 5145-5151 (2015)."
2623,CC(C=C1C)=CC(C)=C1/C(C(C2=C/3C=CC=C2)=NC3=C4\C5=CC=C(C(O)=O)C=C5)=C(N/6)\C7=C(C=CC=C7)C6=C(C8=CC=C(NC9=NC(NC%10=CC=C(/C(C%11=NC(C)C=C%11C)=C%12N(C(C)C=C/%12C)B(F)F)C=C%10)=NC(NC%13=CC=C(/C(C%14=C(C)C=C(C)N%14B(F)F)=C%15C(C)=CC(C)=N\%15)C=C%13)=N9)C=C8)\C%16=N/C(C%17=C%16C=CC=C%17)=C(C%18=C(C)C=C(C)C=C%18C)\C%19=C%20C(C=CC=C%20)=C4N%19,(PorCOOH)(BDP)2,,,0.8,7,52,3.3,"	Jiang Y, Cabanetos C, Allain M, Liu P, Roncali J. Manipulation of the band gap and efficiency of a minimalist push¨Cpull molecular donor for organic solar cells. Journal of Materials Chemistry C 3, 5145-5151 (2015)."
2624,CCCCC(CC)CN1C2=C(SC(C3=C(COCCCCC)C(OCCCCCC)=C(C4=CC=C(C5=CC=C(CCCCCC)S5)S4)C6=NSN=C36)=C2)C7=C1C(N(CC(CC)CCCC)C8=C9SC(C%10=C(OCCCCCC)C(OCCCCCC)=C(C%11=CC=C(C%12=CC=C(CCCCCC)S%12)S%11)C%13=NSN=C%13%10)=C8)=C9S7,K,,,0.9,10.48,56,5.29,"	Sharma GD, et al. A mono (carboxy) porphyrin-triazine-(bodipy) 2 triad as a donor for bulk heterojunction organic solar cells. Journal of Materials Chemistry C 3, 6209-6217 (2015)."
2625,CCCCC(CC)CN1C2=C(SC(C3=CC=C(C4=CC=C(C5=CC=C(CCCCCC)S5)S4)C6=NSN=C36)=C2)C7=C1C(N(CC(CC)CCCC)C8=C9SC(C%10=CC=C(C%11=CC=C(C%12=CC=C(CCCCCC)S%12)S%11)C%13=NSN=C%13%10)=C8)=C9S7,J,,,0.84,9.88,61,5.06,"	Jo H, et al. S, N-Heteropentacene based small molecules with A¨CD¨CA structure for solution processed organic bulk heterojunction solar cells. RSC Advances 5, 102115-102125 (2015)."
2626,O=C(N(CC)/C(S/1)=C(C#N)\C#N)C1=C\C(S2)=CC(CCCCCCCC)=C2C3=CC(CCCCCCCC)=C(S3)C(S4)=CC(CCCCCCCC)=C4C5=CC=C(C6=CC=C(C7=C(CCCCCCCC)C=C(C8=C(CCCCCCCC)C=C(C9=C(CCCCCCCC)C=C(/C=C%10C(N(CC)/C(S/%10)=C(C#N)\C#N)=O)S9)S8)S7)S6)S5,DRCN8T,,,0.82,11.13,66,6.02,"	Jo H, et al. S, N-Heteropentacene based small molecules with A¨CD¨CA structure for solution processed organic bulk heterojunction solar cells. RSC Advances 5, 102115-102125 (2015)."
2627,O=C(N(CC)/C(S/1)=C(C#N)\C#N)C1=C\C(S2)=CC(CCCCCCCC)=C2C3=CC(CCCCCCCC)=C(S3)C(S4)=CC(CCCCCCCC)=C4C5=CC(SC(C6=C(CCCCCCCC)C=C(C7=C(CCCCCCCC)C=C(C8=C(CCCCCCCC)C=C(/C=C9C(N(CC)/C(S/9)=C(C#N)\C#N)=O)S8)S7)S6)=C%10)=C%10S5,DRCN8TT,,,0.86,10.8,68,6.5,"	Zhang Q, et al. A solution-processed high performance organic solar cell using a small molecule with the thieno [3, 2-b] thiophene central unit. Chemical Communications 51, 15268-15271 (2015)."
2628,CCCCCCCCC(C=C(C1=CC=C(C2=CC(CCCCCCCC)=C(CC(C#N)C(OCCCCCCCC)=O)S2)S1)S3)=C3C(S4)=CC5=C4C(C6=CC=C(CC(CC)CCCC)S6)=C(C=C(C7=C(CCCCCCCC)C=C(C8=CC=C(C9=CC(CCCCCCCC)=C(/C=C(C(OCCCCCCCC)=O)/C#N)S9)S8)S7)S%10)C%10=C5C%11=CC=C(CC(CC)CCCC)S%11,BDT©\3T©\CNCOO,,,0.88,14.07,65.5,8.11,"	Zhang Q, et al. A solution-processed high performance organic solar cell using a small molecule with the thieno [3, 2-b] thiophene central unit. Chemical Communications 51, 15268-15271 (2015)."
2629,CCCCC(CC)CC(S1)=CC=C1C2=C(C=C(C3=C(CCCCCC)C=C(C4=C(F)C(F)=C(C5=CC(CCCCCC)=C(/C=C(C(OCC(CC)CCCC)=O)\C#N)S5)C6=NSN=C46)S3)S7)C7=C(C8=CC=C(CC(CC)CCCC)S8)C9=C2SC(C%10=C(CCCCCC)C=C(C%11=C(F)C(F)=C(C%12=CC(CCCCCCC)=C(/C=C(C(OCC(CC)CCCC)=O)\C#N)S%12)C%13=NSN=C%11%13)S%10)=C9,BDT(dFBT-ON)2,,,0.97,10.1,73,7.48,"	Zhang Y, et al. Synergistic Effect of Polymer and Small Molecules for High©\Performance Ternary Organic Solar Cells. Advanced materials 27, 1071-1076 (2015)."
2630,CCCCC(CC)CC(S1)=CC=C1C2=C(C=C(C3=C(CCCCCC)C=C(C4=C(F)C(F)=C(C5=CC(CCCCCC)=C(C6=CC=C(CC(CC)CCCC)S6)S5)C7=NSN=C47)S3)S8)C8=C(C9=CC=C(CC(CC)CCCC)S9)C%10=C2SC(C%11=C(CCCCCC)C=C(C%12=C(F)C(F)=C(C%13=CC(CCCCCC)=C(C%14=CC=C(CC(CC)CCCC)S%14)S%13)C%15=NSN=C%12%15)S%11)=C%10,BDT(dFBT-TT)2,,,0.95,7.48,50,3.54,"	Zhao Y, et al. Understanding effects of two different acceptors in one small molecule for solution processable organic solar cells. RSC Advances 5, 61703-61709 (2015)."
2631,CCCCC(CC)C[Si]1(CC(CC)CCCC)C(C=C(C2=CC(N(CCCC)C(/C3=C4C(C=CC(C5=CC=C(C6=CC=C(CCCCCC)S6)S5)=C7)=C7N(CCCC)C\4=O)=O)=C3C=C2)S8)=C8C9=C1C=C(C%10=CC=C(/C(C(N%11CCCC)=O)=C%12C(N(CCCC)C%13=C\%12C=CC(C%14=CC=C(C%15=CC=C(CCCCCC)S%15)S%14)=C%13)=O)C%11=C%10)S9,DTS(IIThThHEX)2,,,0.86,9.19,66,5.55,"	Zhao Y, et al. Understanding effects of two different acceptors in one small molecule for solution processable organic solar cells. RSC Advances 5, 61703-61709 (2015)."
2632,O=C(C1=C2C=CC=C1)C3=C2C(/C(C4=C5C=CC=C4)=C6SC=CS\6)=C5C7=C3C8=C(C=CC=C8)/C7=C9SC=CS/9,truxTTF-CO,,,0.69,11.3,0.41,3.19,"	Areephong J, San Juan RR, Payne A-J, Welch GC. A narrow band gap isoindigo based molecular donor for solution processed organic solar cells. New Journal of Chemistry 39, 5075-5079 (2015)."
2633,C1(/C(C2=C3C=CC=C2)=C4SC=CS\4)=C3C(/C(C5=C6C=CC=C5)=C7SC=CS\7)=C6C8=C1C9=C(C=CC=C9)/C8=C%10SC=CS/%10,truxTTF,,,0.5,3.24,28.7,0.47,"	Molina-Ontoria A, Gallego M, Echegoyen L, P¨¦rez EM, Mart¨ªn N. Organic solar cells based on bowl-shaped small-molecules. RSC Advances 5, 31541-31546 (2015)."
2634,FB(F)N1C(C(C2=CC=C(Br)C=C2)C3N=C(/C=C/C4=CC=C(N(CC(OCC)=O)C5=C6C=CC=C5)C6=C4)C=C3C)=C(C)C=C1C,SAC,,,0.63,4.28,31.2,0.81,"	Molina-Ontoria A, Gallego M, Echegoyen L, P¨¦rez EM, Mart¨ªn N. Organic solar cells based on bowl-shaped small-molecules. RSC Advances 5, 31541-31546 (2015)."
2635,CCCCCCOC1=C(C2=C(C=C3)N4C3=C(C#CC5=C(CCCCCC)C(CCCCCC)=C(/C=C/C6=C(CCCCCC)C(CCCCCC)=C(/C=C(C#N)/C#N)S6)S5)C(C=C7)N8C7=C(C9=C(OCCCCCC)C=CC=C9OCCCCCC)C%10=CC=C%11N%10[Zn]48N%12C2C=CC%12=C%11C#CC%13=C(CCCCCC)C(CCCCCC)=C(/C=C/C%14=C(CCCCCC)C(CCCCCC)=C(/C=C(C#N)/C#N)S%14)S%13)C(OCCCCCC)=CC=C1,1b,,,0.88,3.73,37,1.2,"	Zhang X, Zhang Y, Chen L, Xiao Y. Star-shaped carbazole-based BODIPY derivatives with improved hole transportation and near-infrared absorption for small-molecule organic solar cells with high open-circuit voltages. RSC Advances 5, 32283-32289 (2015)."
2636,O=C1N(CC(CCCC)CC)C(C2=CC=C(C3=CC=C(C4=CC5=C(C6=CC=C(C7=CC=C(S7)C8=CC=C(S8)C9=C%10C(C(N9CC(CCCC)CC)=O)=C(C%11=CC=CS%11)N(CC(CCCC)CC)C%10=O)C=C6C5%12C%13=CC=C(C%14=CC=C(S%14)C%15=CC=C(S%15)C%16=C%17C(C(N%16CC(CCCC)CC)=O)=C(C%18=CC=CS%18)N(CC(CCCC)CC)C%17=O)C=C%13C%19=C%12C=C(C%20=CC=C(S%20)C%21=CC=C(S%21)C%22=C%23C(C(N%22CC(CCCC)CC)=O)=C(C%24=CC=CS%24)N(CC(CCCC)CC)C%23=O)C=C%19)C=C4)S3)S2)=C%25C1=C(C%26=CC=CS%26)N(CC(CCCC)CC)C%25=O,SF(TDPP)4,,,0.88,13.34,0.65,7.63,"	Arrechea S, Aljarilla A, de la Cruz P, Palomares E, Sharma GD, Langa F. Efficiency improvement using bis(trifluoromethane) sulfonamide lithium salt as a chemical additive in porphyrin based organic solar cells. Nanoscale 8, 17953-17962 (2016)."
2637,S=C(N(CC)C/1=O)SC1=C/C2=CC(CCCCCCCC)=C(S2)C3=CC=C(C4=C(CCCCCCCC)C=C(S4)C(O5)=CC(C5=C6OCC(CC)CCCC)=C(OCC(CC)CCCC)C7=C6C=C(C8=CC(CCCCCCCC)=C(C9=CC=C(C(S%10)=C(CCCCCCCC)C=C%10/C=C(SC(N%11CC)=S)/C%11=O)S9)S8)S7)S3,R3T-TBFO,,,0.9,7.51,0.412,2.8,"	Dang D, et al. Spirobifluorene-cored small molecules containing four diketopyrrolopyrrole arms for solution-processed organic solar cells. Journal of Materials Science 51, 8018-8026 (2016)."
2638,O=C1N(C(CC)CCCC)C(C2=CC=C(C3=CC=C(C4=CC=C(CCCCCC)S4)S3)S2)=C5C1=C(C6=CC=C(C(C=C7)=CC=C7N(C8=CC=CC=C8)C9=CC=CC=C9)S6)N(C(CCCC)CC)C5=O,TPA(DPP),,,0.89,9.87,0.72,6.32,"	Qiu B, et al. An asymmetric small molecule based on thieno 2,3-f benzofuran for efficient organic solar cells. Organic Electronics 35, 87-94 (2016)."
2639,O=C1N(C(CC)CCCC)C(C2=CC=C(C3=CC=C(C4=CC=C(CCCCCC)S4)S3)S2)=C5C1=C(C6=CC=C(S6)C(C=C7)=CC=C7N(C8=CC=CC=C8)C9=CC=C(C%10=CC=C(C%11=C%12C(C(N%11C(CCCC)CC)=O)=C(C%13=CC=C(C%14=CC=C(C%15=CC=C(CCCCCC)S%15)S%14)S%13)N(C(CC)CCCC)C%12=O)S%10)C=C9)N(C(CCCC)CC)C5=O,TPA(DPP)2,,,0.7,3.18,0.31,0.68,"	Oh S, Lee J-C, Ahn T, Lee SK. Solution Processable Small Molecules for Application to Organic Solar Cells. Journal of Nanoscience and Nanotechnology 16, 8670-8673 (2016)."
2640,O=C1N(C(CC)CCCC)C(C2=CC=C(C3=CC=C(C4=CC=C(CCCCCC)S4)S3)S2)=C5C1=C(C6=CC=C(S6)C(C=C7)=CC=C7N(C8=CC=C(C9=CC=C(C%10=C%11C(C(N%10C(CCCC)CC)=O)=C(C%12=CC=C(C%13=CC=C(C%14=CC=C(CCCCCC)S%14)S%13)S%12)N(C(CC)CCCC)C%11=O)S9)C=C8)C%15=CC=C(C%16=CC=C(C%17=C%18C(C(N%17C(CCCC)CC)=O)=C(C%19=CC=C(C%20=CC=C(C%21=CC=C(CCCCCC)S%21)S%20)S%19)N(C(CC)CCCC)C%18=O)S%16)C=C%15)N(C(CCCC)CC)C5=O,TPA(DPP)3,,,0.69,5.06,0.34,1.19,"	Oh S, Lee J-C, Ahn T, Lee SK. Solution Processable Small Molecules for Application to Organic Solar Cells. Journal of Nanoscience and Nanotechnology 16, 8670-8673 (2016)."
2641,FC1=C(C2=CC=C(S2)C3=C(OC(CCCCCC)CCCC)C=C(C4=CC=CS4)C(OC(CCCCCC)CCCC)=C3)C5=NSN=C5C(C6=CC=C(S6)C7=C(OC(CCCCCC)CCCC)C=C(C8=CC=CS8)C(OC(CCCCCC)CCCC)=C7)=C1F,O©\1,,,0.63,5.44,0.44,1.5,"	Oh S, Lee J-C, Ahn T, Lee SK. Solution Processable Small Molecules for Application to Organic Solar Cells. Journal of Nanoscience and Nanotechnology 16, 8670-8673 (2016)."
2642,FC1=C(C2=CC=C(S2)C3=C(OC(CCCCCC)CCCC)C=C(C4=CC=CS4)C(OC(CCCCCC)CCCC)=C3)C5=NSN=C5C(C6=CC=C(S6)C7=C(OC(CCCCCC)CCCC)C=C(C8=CC=C(C9=C(F)C(F)=C(C%10=CC=C(S%10)C%11=C(OC(CCCCCC)CCCC)C=C(C%12=CC=CS%12)C(OC(CCCCCC)CCCC)=C%11)C%13=NSN=C9%13)S8)C(OC(CCCCCC)CCCC)=C7)=C1F,O©\2,,,1.04,3.92,0.25,1.02,"	Yuan L, et al. Acceptor End-Capped Oligomeric Conjugated Molecules with Broadened Absorption and Enhanced Extinction Coefficients for High-Efficiency Organic Solar Cells. Advanced Materials 28, 5980-+ (2016)."
2643,CC1=C(/C(C2=N/C(C=C2)=C3/C#CC4=C(CCCCCC)C(CCCCCC)=C(/C=C5C(N(CC)C(S/5)=S)=O)S4)=C(C=C/6)/N7C6=C(C#CC8=C(CCCCCC)C(CCCCCC)=C(/C=C9C(N(CC)C(S/9)=S)=O)S8)/C(C=C/%10)=NC%10=C(C%11=C(C)C=C(C)C=C%11C)/C%12=CC=C3N%12[Zn]7)C(C)=CC(C)=C1,1a,,,0.9,11.2,0.7,7.06,"	Yuan L, et al. Acceptor End-Capped Oligomeric Conjugated Molecules with Broadened Absorption and Enhanced Extinction Coefficients for High-Efficiency Organic Solar Cells. Advanced Materials 28, 5980-+ (2016)."
2644,FC1=C(C2=CC=C(S2)C3=C(OC(CCCCCC)CCCC)C=C(C4=CC=C(/C=C5C(C6=C(C\5=O)C=CC=C6)=O)S4)C(OC(CCCCCC)CCCC)=C3)C7=NSN=C7C(C8=CC=C(S8)C9=C(OC(CCCCCC)CCCC)C=C(C%10=CC=C(/C=C%11C(C%12=C(C\%11=O)C=CC=C%12)=O)S%10)C(OC(CCCCCC)CCCC)=C9)=C1F,M©\1,,,0.85,11.36,30.8,3.01,"	Montcada NF, et al. High photo-current in solution processed organic solar cells based on a porphyrin core A-pi-D-pi-A as electron donor material. Organic Electronics 38, 330-336 (2016)."
2645,FC1=C(C2=CC=C(S2)C3=C(OC(CCCCCC)CCCC)C=C(C4=CC=C(/C=C5C(C6=C(C\5=O)C=CC=C6)=O)S4)C(OC(CCCCCC)CCCC)=C3)C7=NSN=C7C(C8=CC=C(S8)C9=C(OC(CCCCCC)CCCC)C=C(C%10=CC=C(C%11=C(F)C(F)=C(C%12=CC=C(S%12)C%13=C(OC(CCCCCC)CCCC)C=C(C%14=CC=C(/C=C%15C(C%16=C(C\%15=O)C=CC=C%16)=O)S%14)C(OC(CCCCCC)CCCC)=C%13)C%17=NSN=C%11%17)S%10)C(OC(CCCCCC)CCCC)=C9)=C1F,M©\2,,,0.94,13.5,0.71,9.01,"	Yuan L, et al. Acceptor End-Capped Oligomeric Conjugated Molecules with Broadened Absorption and Enhanced Extinction Coefficients for High-Efficiency Organic Solar Cells. Advanced Materials 28, 5980-+ (2016)."
2646,O=C1N(CC(CCCC)CC)C(C2=CC=C(C3=CC=C(CCCCCC)C=C3)S2)=C4C1=C(C5=CC=C(C6=CC(C7=C(SC(C8=CC=C(C9=C%10C(C(N9CC(CCCC)CC)=O)=C(C%11=CC=C(C%12=CC=C(CCCCCC)C=C%12)S%11)N(CC(CCCC)CC)C%10=O)S8)=C7)C%13=C%14C=C(C(SC(C%15=CC=C(C%16=C%17C(C(N%16CC(CCCC)CC)=O)=C(C%18=CC=C(C%19=CC=C(CCCCCC)C=C%19)S%18)N(CC(CCCC)CC)C%17=O)S%15)=C%20)=C%20C%21=C%22SC(C%23=CC=C(C%24=C%25C(C(N%24CC(CCCC)CC)=O)=C(C%26=CC=C(C%27=CC=C(CCCCCC)C=C%27)S%26)N(CC(CCCC)CC)C%25=O)S%23)=C%21)C%22=C%13)=C%14S6)S5)N(CC(CCCC)CC)C4=O,TTA-DPP4,,,0.92,13.3,0.7,8.59,"	Yuan L, et al. Acceptor End-Capped Oligomeric Conjugated Molecules with Broadened Absorption and Enhanced Extinction Coefficients for High-Efficiency Organic Solar Cells. Advanced Materials 28, 5980-+ (2016)."
2647,O=C1N(CC(CCCC)CC)C(C2=CC=C(C3=CC=C(CCCCCC)C=C3)S2)=C4C1=C(C5=CC=C(C6=CC(C7=C(SC(CC(CCCC)CC)=C7)C8=C9C=C(C(SC(CC(CCCC)CC)=C%10)=C%10C%11=C%12SC(C%13=CC=C(C%14=C%15C(C(N%14CC(CCCC)CC)=O)=C(C%16=CC=C(C%17=CC=C(CCCCCC)C=C%17)S%16)N(CC(CCCC)CC)C%15=O)S%13)=C%11)C%12=C8)=C9S6)S5)N(CC(CCCC)CC)C4=O,TTA-DPP2,,,0.7,6.02,0.456,1.93,"	Komiyama H, Adachi C, Yasuda T. Star-shaped and linear pi-conjugated oligomers consisting of a tetrathienoanthracene core and multiple diketopyrrolopyrrole arms for organic solar cells. Beilstein Journal of Organic Chemistry 12, 1459-1466 (2016)."
2648,O=C1N(CCCCCCCCCC)C(C2=CC=CS2)=C3C1=C(C4=CC=C(/C=C/C5=CC=C(C6=C7C(C(N6CCCCCCCCCC)=O)=C(C8=CC=CS8)N(CCCCCCCCCC)C7=O)S5)S4)N(CCCCCCCCCC)C3=O,DPP-DPP,,,0.74,4.25,0.447,1.4,"	Komiyama H, Adachi C, Yasuda T. Star-shaped and linear pi-conjugated oligomers consisting of a tetrathienoanthracene core and multiple diketopyrrolopyrrole arms for organic solar cells. Beilstein Journal of Organic Chemistry 12, 1459-1466 (2016)."
2649,O=C1N(CCCCCCCCCC)C(C2=CC=CS2)=C3C1=C(C4=CC=C(C#CC5=CC=C(C6=C7C(C(N6CCCCCCCCCC)=O)=C(C8=CC=CS8)N(CCCCCCCCCC)C7=O)S5)S4)N(CCCCCCCCCC)C3=O,DPPTDPP,,,0.79,11.53,0.58,5.28,"	Patil Y, Misra R, Sharma A, Sharma GD. D-A-D-pi-D-A-D type diketopyrrolopyrrole based small molecule electron donors for bulk heterojunction organic solar cells. Physical Chemistry Chemical Physics 18, 16950-16957 (2016)."
2650,CCCCCCCCOC1=CC=CC(C2=NC3=C(C4=CC=C(C5=CC=C(CCCCCC)S5)S4)C=CC(C6=CC7=C(C(SC(C8=C(N=C(C9=CC=CC(OCCCCCCCC)=C9)C(C%10=CC(OCCCCCCCC)=CC=C%10)=N%11)C%11=C(C%12=CC=C(C%13=CC=C(CCCCCC)S%13)S%12)C=C8)=C%14)C%14[Si]7(C(CC)CCCCC)C(CC)CCCCC)S6)=C3N=C2C%15=CC=CC(OCCCCCCCC)=C%15)=C1,DTS(FCT2)2,,,0.91,10.84,0.56,5.52,"	Patil Y, Misra R, Sharma A, Sharma GD. D-A-D-pi-D-A-D type diketopyrrolopyrrole based small molecule electron donors for bulk heterojunction organic solar cells. Physical Chemistry Chemical Physics 18, 16950-16957 (2016)."
2651,CC1=C(/C(C2=N/C(C=C2)=C3/C#CC4=C(CCCCCC)C(CCCCCC)=C(/C=C/C5=C(CCCCCC)C(CCCCCC)=C(/C=C6C(N(CC)C(S/6)=S)=O)S5)S4)=C(C=C/7)/N8C7=C(C#CC9=C(CCCCCC)C(CCCCCC)=C(/C=C/C%10=C(CCCCCC)C(CCCCCC)=C(/C=C%11C(N(CC)C(S/%11)=S)=O)S%10)S9)/C(C=C/%12)=NC%12=C(C%13=C(C)C=C(C)C=C%13C)/C%14=CC=C3N%14[Zn]8)C(C)=CC(C)=C1,1b,,,0.76,2.69,0.29,0.59,"	Keshtov ML, Kuklin SA, Buzin MI, Godowsky DY, Khokhlov AR. Synthesis and photophysical properties of semiconductor molecules of D-1-A-D-2-A-D-1 structure on the basis of quinoxaline and dithienosilole derivatives for organic solar cells. Doklady Physical Chemistry 469, 106-110 (2016)."
2652,O=C1N(CCCCCC)C(C2=CC=C(C3=CC=C(/C4=C5C6=CC=CC=C6N(CC(CCCC)CC)C/5=O)C(N(CC(CCCC)CC)C4=O)=C3)C=C2)=C7C1=C(C8=CC=C(C9=CC=C(/C%10=C%11C%12=CC=CC=C%12N(CC(CCCC)CC)C/%11=O)C(N(CC(CCCC)CC)C%10=O)=C9)C=C8)N(CCCCCC)C7=O,DPPID,,,0.8,13.2,40.1,4.24,"	Montcada NF, et al. High photo-current in solution processed organic solar cells based on a porphyrin core A-pi-D-pi-A as electron donor material. Organic Electronics 38, 330-336 (2016)."
2653,O=C1N(CCCCCC)C(C2=CC=C(C3=CC=C(/C4=C5C(SC=C6)=C6N(CC(CCCC)CC)C/5=O)C(N(CC(CCCC)CC)C4=O)=C3)C=C2)=C7C1=C(C8=CC=C(C9=CC=C(/C%10=C%11C(SC=C%12)=C%12N(CC(CCCC)CC)C/%11=O)C(N(CC(CCCC)CC)C%10=O)=C9)C=C8)N(CCCCCC)C7=O,DPPBI,,,0.71,3.65,0.4,1.05,"	Zhao Y, et al. Diketopyrrolopyrrole based A(2)-D-A(1)-D-A(2) type small molecules for organic solar cells: Effects of substitution of benzene with thiophene. Dyes and Pigments 130, 282-290 (2016)."
2654,O=C1N(CCCCCCCC)C(C2=CC=C(S2)C3=CC=C(/C4=C5C(SC=C6)=C6N(CC(CCCC)CC)C/5=O)C(N(CC(CCCC)CC)C4=O)=C3)=C7C1=C(C8=CC=C(S8)C9=CC=C(/C%10=C%11C(SC=C%12)=C%12N(CC(CCCC)CC)C/%11=O)C(N(CC(CCCC)CC)C%10=O)=C9)N(CCCCCCCC)C7=O,DPPTBI,,,0.86,7.46,0.37,2.36,"	Zhao Y, et al. Diketopyrrolopyrrole based A(2)-D-A(1)-D-A(2) type small molecules for organic solar cells: Effects of substitution of benzene with thiophene. Dyes and Pigments 130, 282-290 (2016)."
2655,CCCCCCC1=C(SC=C1)C2=CC=C(S2)C3=NC=C(C4=CC=C(C5=C(CCCCCC)C=CS5)S4)C6=NSN=C36,DH5TPy-3,,,0.64,2.18,0.52,0.74,"	Zhao Y, et al. Diketopyrrolopyrrole based A(2)-D-A(1)-D-A(2) type small molecules for organic solar cells: Effects of substitution of benzene with thiophene. Dyes and Pigments 130, 282-290 (2016)."
2656,CCCCCCC1=CSC(C2=CC=C(C3=CN=C(C4=CC=C(C5=CC(CCCCCC)=CS5)S4)C6=NSN=C36)S2)=C1,DH5TPy-4,,,0.36,1.86,0.3,0.2,"	Cho A, Song CE, Lee SK, Shin WS, Lim E. Effects of alkyl side chain and electron-withdrawing group on benzo 1,2,5 thiadiazole-thiophene-based small molecules in organic photovoltaic cells. Journal of Materials Science 51, 6770-6780 (2016)."
2657,CCCCCCCC[Si]1(CCCCCCCC)C(C=C(C2=CC=C(C3=CC=C(C)C4=NSN=C34)S2)C=C5)=C5C6=C1C=C(C7=CC=C(C8=CC=C(C)C9=NSN=C89)S7)C=C6,SiF-BT,,,0.33,2.04,0.3,0.2,"	Cho A, Song CE, Lee SK, Shin WS, Lim E. Effects of alkyl side chain and electron-withdrawing group on benzo 1,2,5 thiadiazole-thiophene-based small molecules in organic photovoltaic cells. Journal of Materials Science 51, 6770-6780 (2016)."
2658,CCCCCCC1=C(SC=C1)C2=CC=C(S2)C3=C(F)C(F)=C(C4=CC=C(C5=C(CCCCCC)C=CS5)S4)C6=NSN=C36,2F-DH5TB-3,,,2.06,0.9,29.8,0.53,"	Mamoshina P, Vieira A, Putin E, Zhavoronkov A. Applications of Deep Learning in Biomedicine. Mol Pharm 13, 1445-1454 (2016)."
2659,FC1=C(C2=CC=C(C3=CC(CCCCCC)=CS3)S2)C4=NSN=C4C(C5=CC=C(C6=CC(CCCCCC)=CS6)S5)=C1F,2F-DH5TB-4,,,0.92,2.5,0.29,0.67,"	Cho A, Song CE, Lee SK, Shin WS, Lim E. Effects of alkyl side chain and electron-withdrawing group on benzo 1,2,5 thiadiazole-thiophene-based small molecules in organic photovoltaic cells. Journal of Materials Science 51, 6770-6780 (2016)."
2660,CCCCC(CC)CC1(CC(CC)CCCC)C2=C(SC(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C6=CC=C(CCCCCC)S6)S5)C7=NSN=C47)S3)=C2)C8=CC(C9(CC(CC)CCCC)CC(CC)CCCC)=C(C%10=C9C=C(C%11=CC=C(C%12=C(F)C(F)=C(C%13=CC=C(C%14=CC=C(CCCCCC)S%14)S%13)C%15=NSN=C%12%15)S%11)S%10)C=C81,BIT4F,,,0.89,4.13,0.3,1.11,"	Cho A, Song CE, Lee SK, Shin WS, Lim E. Effects of alkyl side chain and electron-withdrawing group on benzo 1,2,5 thiadiazole-thiophene-based small molecules in organic photovoltaic cells. Journal of Materials Science 51, 6770-6780 (2016)."
2661,CCCCC(CC)CC1(CC(CC)CCCC)C2=C(SC(C3=CC=C(C(C4=NSN=C54)=C(F)C(F)=C5C6=CC=C(S6)C7=CC8=C(S7)C9=C(C8(CC(CC)CCCC)CC(CC)CCCC)C=C(C%10=C(C%11(CC(CC)CCCC)CC(CC)CCCC)C=C(C%12=CC=C(C%13=C(F)C(F)=C(C%14=CC=C(C%15=CC=C(CCCCCC)S%15)S%14)C%16=NSN=C%13%16)S%12)S%10)C%11=C9)S3)=C2)C%17=CC(C%18(CC(CC)CCCC)CC(CC)CCCC)=C(C%19=C%18C=C(C%20=CC=C(C%21=C(F)C(F)=C(C%22=CC=C(C%23=CC=C(CCCCCC)S%23)S%22)C%24=NSN=C%21%24)S%20)S%19)C=C%171,BIT6F,,,0.89,12.2,0.763,8.27,"	Wang J-L, et al. Series of Multifluorine Substituted Oligomers for Organic Solar Cells with Efficiency over 9% and Fill Factor of 0.77 by Combination Thermal and Solvent Vapor Annealing. Journal of the American Chemical Society 138, 7687-7697 (2016)."
2662,CCCCC(CC)CC1(CC(CC)CCCC)C2=C(SC(C3=CC=C(C(C4=NSN=C54)=C(F)C(F)=C5C6=CC=C(S6)C7=CC8=C(S7)C9=C(C8(CC(CC)CCCC)CC(CC)CCCC)C=C(C%10=C(C%11(CC(CC)CCCC)CC(CC)CCCC)C=C(C%12=CC=C(C(C%13=NSN=C%14%13)=C(F)C(F)=C%14C%15=CC=C(S%15)C%16=CC%17=C(S%16)C%18=C(C%17(CC(CC)CCCC)CC(CC)CCCC)C=C(C%19=C(C%20(CC(CC)CCCC)CC(CC)CCCC)C=C(C%21=CC=C(C%22=C(F)C(F)=C(C%23=CC=C(C%24=CC=C(CCCCCC)S%24)S%23)C%25=NSN=C%22%25)S%21)S%19)C%20=C%18)S%12)S%10)C%11=C9)S3)=C2)C%26=CC(C%27(CC(CC)CCCC)CC(CC)CCCC)=C(C%28=C%27C=C(C%29=CC=C(C%30=C(F)C(F)=C(C%31=CC=C(C%32=CC=C(CCCCCC)S%32)S%31)C%33=NSN=C%30%33)S%29)S%28)C=C%261,BIT8F,,,0.89,13.39,0.7517,8.91,"	Wang J-L, et al. Series of Multifluorine Substituted Oligomers for Organic Solar Cells with Efficiency over 9% and Fill Factor of 0.77 by Combination Thermal and Solvent Vapor Annealing. Journal of the American Chemical Society 138, 7687-7697 (2016)."
2663,CCCCC(CC)CC1(CC(CC)CCCC)C2=C(SC(C3=CC=C(C(C4=NSN=C54)=C(F)C(F)=C5C6=CC=C(S6)C7=CC8=C(S7)C9=C(C8(CC(CC)CCCC)CC(CC)CCCC)C=C(C%10=C(C%11(CC(CC)CCCC)CC(CC)CCCC)C=C(C%12=CC=C(C(C%13=NSN=C%14%13)=C(F)C(F)=C%14C%15=CC=C(S%15)C%16=CC%17=C(S%16)C%18=C(C%17(CC(CC)CCCC)CC(CC)CCCC)C=C(C%19=C(C%20(CC(CC)CCCC)CC(CC)CCCC)C=C(C%21=CC=C(C(C%22=NSN=C%23%22)=C(F)C(F)=C%23C%24=CC=C(S%24)C%25=CC%26=C(S%25)C%27=C(C%26(CC(CC)CCCC)CC(CC)CCCC)C=C(C%28=C(C%29(CC(CC)CCCC)CC(CC)CCCC)C=C(C%30=CC=C(C%31=C(F)C(F)=C(C%32=CC=C(C%33=CC=C(CCCCCC)S%33)S%32)C%34=NSN=C%31%34)S%30)S%28)C%29=C%27)S%21)S%19)C%20=C%18)S%12)S%10)C%11=C9)S3)=C2)C%35=CC(C%36(CC(CC)CCCC)CC(CC)CCCC)=C(C%37=C%36C=C(C%38=CC=C(C%39=C(F)C(F)=C(C%40=CC=C(C%41=CC=C(CCCCCC)S%41)S%40)C%42=NSN=C%39%42)S%38)S%37)C=C%351,BIT10F,,,0.89,10.9,0.6907,6.67,"	Wang J-L, et al. Series of Multifluorine Substituted Oligomers for Organic Solar Cells with Efficiency over 9% and Fill Factor of 0.77 by Combination Thermal and Solvent Vapor Annealing. Journal of the American Chemical Society 138, 7687-7697 (2016)."
2664,FC1=C(C2=CC=C(C3=CC4=C(S3)C5=CC(C6(CC(CC)CCCC)CC(CC)CCCC)=C(C7=C6C=C(C8=CC=C(C9=C(F)C(F)=C(C%10=CC=C(C%11=CC=C(CCCCCC)S%11)S%10)C%12=NSN=C9%12)S8)S7)C=C5C4(CC(CC)CCCC)CC(CC)CCCC)S2)C%13=NSN=C%13C(C%14=CC=C(C%15=CC=C(CCCCCC)S%15)S%14)=C1F,PBITnF,,,0.91,11.72,0.6578,7.04,"	Wang J-L, et al. Series of Multifluorine Substituted Oligomers for Organic Solar Cells with Efficiency over 9% and Fill Factor of 0.77 by Combination Thermal and Solvent Vapor Annealing. Journal of the American Chemical Society 138, 7687-7697 (2016)."
2665,S=C(N(CC)C/1=O)SC1=C/C2=CC(CCCCCCCC)=C(C3=CC=C(S3)C4=C(CCCCCCCC)C=C(C(S5)=CC6=C5C(C7=CC=C(CC(CC)CCCC)S7)=C8C(SC(C9=CC(CCCCCCCC)=C(C%10=CC=C(C%11=C(CCCCCCCC)C=C(S%11)/C=C(SC(N%12CC)=S)/C%12=O)S%10)S9)=C8)=C6C%13=CC=C(CC(CC)CCCC)S%13)S4)S2,BDT1,,,0.89,8.64,0.5531,4.23,"	Wang J-L, et al. Series of Multifluorine Substituted Oligomers for Organic Solar Cells with Efficiency over 9% and Fill Factor of 0.77 by Combination Thermal and Solvent Vapor Annealing. Journal of the American Chemical Society 138, 7687-7697 (2016)."
2666,S=C(N(CC)C/1=O)SC1=C/C2=CC(CCCCCCCC)=C(C3=CC=C(S3)C4=C(CCCCCCCC)C=C(C(S5)=CC6=C5C(C7=CC=C(CC(CC)CCCC)S7)=C8C(SC(C(S9)=CC%10=C9C(C%11=CC=C(CC(CC)CCCC)S%11)=C%12C(SC(C%13=CC(CCCCCCCC)=C(C%14=CC=C(C%15=C(CCCCCCCC)C=C(S%15)/C=C(SC(N%16CC)=S)/C%16=O)S%14)S%13)=C%12)=C%10C%17=CC=C(CC(CC)CCCC)S%17)=C8)=C6C%18=CC=C(CC(CC)CCCC)S%18)S4)S2,BDT2,,,0.89,13.02,0.62,7.18,"	Badgujar S, et al. High-Performance Small Molecule via Tailoring Intermolecular Interactions and its Application in Large-Area Organic Photovoltaic Modules. Advanced Energy Materials 6,  (2016)."
2667,S=C(N(CC)C/1=O)SC1=C/C2=CC(CCCCCCCC)=C(C3=CC=C(S3)C4=C(CCCCCCCC)C=C(C5=CC6=C(S5)C(C7=CC=C(CC(CC)CCCC)S7)=C8C(SC(C(S9)=CC%10=C9C(C%11=CC=C(CC(CC)CCCC)S%11)=C%12C(SC(C(S%13)=CC%14=C%13C(C%15=CC=C(CC(CC)CCCC)S%15)=C%16C(SC(C%17=CC(CCCCCCCC)=C(C%18=CC=C(C%19=C(CCCCCCCC)C=C(S%19)/C=C(SC(N%20CC)=S)/C%20=O)S%18)S%17)=C%16)=C%14C%21=CC=C(CC(CC)CCCC)S%21)=C%12)=C%10C%22=CC=C(CC(CC)CCCC)S%22)=C8)=C6C%23=CC=C(CC(CC)CCCC)S%23)S4)S2,BDT3,,,0.89,13.17,0.73,8.56,"	Badgujar S, et al. High-Performance Small Molecule via Tailoring Intermolecular Interactions and its Application in Large-Area Organic Photovoltaic Modules. Advanced Energy Materials 6,  (2016)."
2668,O=N(C(C1=NON=C12)=CC=C2C(C=C3)=CC=C3N(C4=CC=C(C)C=C4)C5=CC=C(C)C=C5)=O,PNBO,,,0.9,11.34,0.7,7.14,"	Badgujar S, et al. High-Performance Small Molecule via Tailoring Intermolecular Interactions and its Application in Large-Area Organic Photovoltaic Modules. Advanced Energy Materials 6,  (2016)."
2669,CC(C=C1)=CC=C1N(C2=CC=C(C3=CC=C(N(=O)=O)C4=NON=C43)S2)C5=CC=C(C)C=C5,TNBO,,,0.97,10.2,0.515,5.1,"	Ting H-C, et al. Easy Access to NO2-Containing Donor-Acceptor-Acceptor Electron Donors for High Efficiency Small-Molecule Organic Solar Cells. Chemsuschem 9, 1433-1441 (2016)."
2670,CCCCCCCCC1=C(SC(C(S2)=CC3=C2C(C4=CC=C(CC(CC)CCCC)S4)=C5C(SC(C(S6)=CC(CCCCCCCC)=C6C7=CC(SC(C8=C(CCCCCCCC)C=C(/C=C(C(OCC(CC)CCCC)=O)\C#N)S8)=C9)=C9S7)=C5)=C3C%10=CC=C(CC(CC)CCCC)S%10)=C1)C%11=CC(SC(C%12=C(CCCCCCCC)C=C(/C=C(C(OCC(CC)CCCC)=O)\C#N)S%12)=C%13)=C%13S%11,DCATT,,,0.89,12.4,0.455,5.02,"	Ting H-C, et al. Easy Access to NO2-Containing Donor-Acceptor-Acceptor Electron Donors for High Efficiency Small-Molecule Organic Solar Cells. Chemsuschem 9, 1433-1441 (2016)."
2671,CCCCCCCCC1=C(C2=C(CCCCCCCC)C=C(C3=CC(SC(/C=C(C(OCC(CC)CCCC)=O)\C#N)=C4)=C4S3)S2)SC(C(S5)=CC6=C5C(C7=CC=C(CC(CC)CCCC)S7)=C8C(SC(C9=CC(CCCCCCCC)=C(C%10=C(CCCCCCCC)C=C(C%11=CC(SC(/C=C(C(OCC(CC)CCCC)=O)\C#N)=C%12)=C%12S%11)S%10)S9)=C8)=C6C%13=CC=C(CC(CC)CCCC)S%13)=C1,DCATT-L,,,0.89,8.83,0.66,5.2,"	Wang T, et al. Influence of a pi-bridge dependent molecular configuration on the optical and electrical characteristics of organic solar cells. Journal of Materials Chemistry A 4, 8784-8792 (2016)."
2672,CCCCCCCCC1=C(SC(C(S2)=CC3=C2C(C4=CC=C(CC(CC)CCCC)S4)=C5C(SC(C6=CC(CCCCCCCC)=C(S6)C7=CC=C(C8=C(CCCCCCCC)C=C(/C=C(SC(N9CC)=S)/C9=O)S8)S7)=C5)=C3C%10=CC=C(CC(CC)CCCC)S%10)=C1)C%11=CC=C(C%12=C(CCCCCCCC)C=C(/C=C(SC(N%13CC)=S)/C%13=O)S%12)S%11,DR3TBDTT,,,0.98,11.38,0.69,7.72,"	Wang T, et al. Influence of a pi-bridge dependent molecular configuration on the optical and electrical characteristics of organic solar cells. Journal of Materials Chemistry A 4, 8784-8792 (2016)."
2673,CCCCCCCCC1=C(SC(C(S2)=CC3=C2C(C4=CC(F)=C(CC(CC)CCCC)S4)=C5C(SC(C6=CC(CCCCCCCC)=C(S6)C7=CC=C(C8=C(CCCCCCCC)C=C(/C=C(SC(N9CC)=S)/C9=O)S8)S7)=C5)=C3C%10=CC(F)=C(CC(CC)CCCC)S%10)=C1)C%11=CC=C(C%12=C(CCCCCCCC)C=C(/C=C(SC(N%13CC)=S)/C%13=O)S%12)S%11,DR3TBDTTF,,,0.9,13.92,0.733,9.18,"	Wang Z, et al. Solution-Processed Organic Solar Cells with 9.8% Efficiency Based on a New Small Molecule Containing a 2D Fluorinated Benzodithiophene Central Unit. Advanced Electronic Materials 2,  (2016)."
2674,CCCCC(CC)CN1C2=C(C3=C1C(N4CC(CC)CCCC)=C(C5=C4C=C(C6=C(CCCCCC)C=C(C7=C(CCCCCC)C=C(/C=C(C#N)/C#N)S7)S6)S5)S3)SC(C8=C(CCCCCC)C=C(C9=C(CCCCCC)C=C(/C=C(C#N)/C#N)S9)S8)=C2,SM1,,,0.93,14.1,0.747,9.8,"	Wang Z, et al. Solution-Processed Organic Solar Cells with 9.8% Efficiency Based on a New Small Molecule Containing a 2D Fluorinated Benzodithiophene Central Unit. Advanced Electronic Materials 2,  (2016)."
2675,CCCCC(CC)CN1C2=C(C3=C1C(N4CC(CC)CCCC)=C(C5=C4C=C(C6=C(CCCCCC)C=C(C7=C(CCCCCC)C=C(/C=C(C#N)/C(OCCCCCC)=O)S7)S6)S5)S3)SC(C8=C(CCCCCC)C=C(C9=C(CCCCCC)C=C(/C=C(C#N)/C(OCCCCCC)=O)S9)S8)=C2,SM2,,,0.82,11.48,0.6,5.64,"	Tee H, Jo H, Kim D, Biswas S, Sharma GD, Ko J. The effect of acceptor end groups on the physical and photovoltaic properties of A-pi-D-pi-A type oligomers with same S, N-heteropentacene central electron donor unit for solution processed organic solar cells. Dyes and Pigments 129, 209-219 (2016)."
2676,CCCCC(CC)CN1C2=C(C3=C1C(N4CC(CC)CCCC)=C(C5=C4C=C(C6=C(CCCCCC)C=C(C7=C(CCCCCC)C=C(/C=C(C8=O)\C(C9=C8C=CC=C9)=O)S7)S6)S5)S3)SC(C%10=C(CCCCCC)C=C(C%11=C(CCCCCC)C=C(/C=C(C%12=O)/C(C%13=C%12C=CC=C%13)=O)S%11)S%10)=C2,SM3,,,0.82,9.24,0.56,4.24,"	Tee H, Jo H, Kim D, Biswas S, Sharma GD, Ko J. The effect of acceptor end groups on the physical and photovoltaic properties of A-pi-D-pi-A type oligomers with same S, N-heteropentacene central electron donor unit for solution processed organic solar cells. Dyes and Pigments 129, 209-219 (2016)."
2677,CCCCN1C(C(C2=C3C=CC=C2C1=O)=CC=C3C#CC(C4=NSN=C45)=CC=C5C#CC(C=C6)=CC=C6N(C7=CC=CC=C7)C8=CC=CC=C8)=O,TPA-BT-NPI,,,0.92,11.64,0.62,6.64,"	Tee H, Jo H, Kim D, Biswas S, Sharma GD, Ko J. The effect of acceptor end groups on the physical and photovoltaic properties of A-pi-D-pi-A type oligomers with same S, N-heteropentacene central electron donor unit for solution processed organic solar cells. Dyes and Pigments 129, 209-219 (2016)."
2678,S=C(N(CCCCCCCC)C/1=O)SC1=C/C2=CC(CCCCCCCC)=C(C3=CC=C(C4=C(CCCCCCCC)C=C(C5=CC=C(C6=CC=C(S6)C7=CC(CCCCCCCC)=C(S7)C8=CC=C(S8)C9=C(CCCCCCCC)C=C(S9)/C=C(SC(N%10CCCCCCCC)=S)/C%10=O)S5)S4)S3)S2,TTH-D3TRh,,,0.9,11.54,0.66,6.67,"	Gautam P, Misra R, Biswas S, Sharma GD. A D-pi-A1-pi-A2 push-pull small molecule donor for solution processed bulk heterojunction organic solar cells. Physical Chemistry Chemical Physics 18, 13918-13926 (2016)."
2679,S=C(N(CCCCCCCC)C/1=O)SC1=C/C2=CC(CCCCCCCC)=C(C3=CC=C(C4=C(CCCCCCCC)C=C(C5=CC(F)=C(C6=C(F)C=C(S6)C7=CC(CCCCCCCC)=C(S7)C8=CC=C(S8)C9=C(CCCCCCCC)C=C(S9)/C=C(SC(N%10CCCCCCCC)=S)/C%10=O)S5)S4)S3)S2,TTF-D3TRh,,,0.86,10.26,0.668,5.89,"	Wang Z, et al. Solution-Processable Small Molecules for High-Performance Organic Solar Cells with Rigidly Fluorinated 2,2 '-Bithiophene Central Cores. Acs Applied Materials & Interfaces 8, 11639-11648 (2016)."
2680,O=C1N(CC(CCCC)C)C(C2=CC=CS2)=C3C1=C(C4=CC=C(C5=CC=C(C6=CC=C(S6)C7=C8C(C(N7CC(CCCC)CC)=O)=C(C9=CC=CS9)N(CC(CCCC)C)C8=O)C=C5)S4)N(CC(CCCC)CC)C3=O,(TDPP)2Ph,,,0.93,11.03,0.696,7.14,"	Wang Z, et al. Solution-Processable Small Molecules for High-Performance Organic Solar Cells with Rigidly Fluorinated 2,2 '-Bithiophene Central Cores. Acs Applied Materials & Interfaces 8, 11639-11648 (2016)."
2681,S=C(N(CC)C1=O)SC1=CC2=CC(CCCCCCCC)=C(S2)C3=CC=C(S3)C4=C(CCCCCCCC)C=C(S4)C(S5)=CC6=C5C(OCCCCCCCCCCCC)=C7C(SC(C8=CC(CCCCCCCC)=C(C9=CC=C(C%10=C(CCCCCCCC)C=C(C=C(SC(N%11CC)=S)C%11=O)S%10)S9)S8)=C7)=C6OCCCCCCCCCCCC,DR3TBDTOC12,,,0.91,6.85,0.51,3.21,"	Lee JW, Choi YS, Ahn H, Jo WH. Ternary Blend Composed of Two Organic Donors and One Acceptor for Active Layer of High-Performance Organic Solar Cells. Acs Applied Materials & Interfaces 8, 10961-10967 (2016)."
2682,S=C(N(CC)C1=O)SC1=CC2=CC(CCCCCCCC)=C(S2)C3=CC=C(S3)C4=C(CCCCCCCC)C=C(S4)C(S5)=CC6=C5C(C7=CC=C(CCCCCCCCCCCC)S7)=C8C(SC(C9=CC(CCCCCCCC)=C(C%10=CC=C(C%11=C(CCCCCCCC)C=C(C=C(SC(N%12CC)=S)C%12=O)S%11)S%10)S9)=C8)=C6C%13=CC=C(CCCCCCCCCCCC)S%13,DR3TBDTTC12,,,0.88,7.38,0.6539,4.25,"	Yin X, et al. Side-chain Engineering of Benzo 1,2-b:4,5-b ' dithiophene Core-structured Small Molecules for High-Performance Organic Solar Cells. Scientific Reports 6,  (2016)."
2683,S=C(N(CC)C1=O)SC1=CC2=CC(CCCCCCCC)=C(S2)C3=CC=C(S3)C4=C(CCCCCCCC)C=C(S4)C(S5)=CC6=C5C(C7=CC=C(CSCCCCCCC)S7)=C8C(SC(C9=CC(CCCCCCCC)=C(C%10=CC=C(C%11=C(CCCCCCCC)C=C(C=C(SC(N%12CC)=S)C%12=O)S%11)S%10)S9)=C8)=C6C%13=CC=C(SCCCCCCCC)S%13,DR3TBDTTSC8,,,0.9,11.69,0.6648,6.99,"	Yin X, et al. Side-chain Engineering of Benzo 1,2-b:4,5-b ' dithiophene Core-structured Small Molecules for High-Performance Organic Solar Cells. Scientific Reports 6,  (2016)."
2684,CC/C(C1=CC=C(S1)C2=CC=C(S2)C(C=C3)=CC=C3N(C4=CC=C(C5=CSC(C6=CC=C(/C(CC)=C(C#N)\C#N)S6)=C5)C=C4)C7=CC=C(C8=CC=C(C9=CC=C(/C(CC)=C(C#N)\C#N)S9)S8)C=C7)=C(C#N)/C#N,SSO1,,,0.94,11.7,0.6161,6.78,"	Yin X, et al. Side-chain Engineering of Benzo 1,2-b:4,5-b ' dithiophene Core-structured Small Molecules for High-Performance Organic Solar Cells. Scientific Reports 6,  (2016)."
2685,C/C(C1=CC=C(S1)C2=CC=C(S2)C(C=C3OC)=CC=C3N(C4=CC=C(C5=CSC(C6=CC=C(/C(C)=C(C#N)\C#N)S6)=C5)C=C4OC)C7=CC=C(C8=CC=C(C9=CC=C(/C(C)=C(C#N)\C#N)S9)S8)C=C7OC)=C(C#N)/C#N,SSO2,,,0.942,8.59,0.495,4.01,"	Trukhanov VA, et al. Solution-processed star-shaped oligomers in normal and inverted organic solar cells. Synthetic Metals 215, 229-234 (2016)."
2686,CCCCCCC1=CC=C(C2=CC=C(C3=CC=C(C4=C(C56C7=C(C8=CC=CC=C86)C=CC=C7)C=C(C9=CC(C(F)(F)F)=CC(C(F)(F)F)=C9)C=C4)C5=C3)S2)S1,RTh-Sp-CF3,,,0.871,8.56,0.451,3.36,"	Trukhanov VA, et al. Solution-processed star-shaped oligomers in normal and inverted organic solar cells. Synthetic Metals 215, 229-234 (2016)."
2687,N#C/C(C#N)=C(CCCCCC)/C1=CC=C(S1)C2=CC=C(S2)C(C=C3OC)=CC=C3N(C4=CC=C(C5=CSC(C6=CC=C(/C(CCCCCC)=C(C#N)\C#N)S6)=C5)C=C4OC)C7=CC=C(C8=CC=C(C9=CC=C(/C(CCCCCC)=C(C#N)\C#N)S9)S8)C=C7OC,SSO3,,,0.66,8.42,0.38,2.12,"	Nazim M, Ameen S, Akhtar MS, Shin HS. Efficient spirobifluorene-core electron-donor material for application in solution-processed organic solar cells. Chemical Physics Letters 663, 137-144 (2016)."
2688,CC1(C)C(C=C(C([O-])=C2C3=C(O)C=C(N4C(CCC5)C5C6=C4C=CC=C6)C=C3O)C2=O)=[N+](CCCC)C7=CC=CC=C71,USQ-11,,,0.819,7.17,0.445,2.61,"	Trukhanov VA, et al. Solution-processed star-shaped oligomers in normal and inverted organic solar cells. Synthetic Metals 215, 229-234 (2016)."
2689,O=C1C(C2=C(O)C=C(N3C(CCC4)C4C5=C3C=CC=C5)C=C2O)=C([O-])C1=CC6=[N+](CCCC)C7=CC=CC=C7S6,USQ-12,,,0.86,10.34,0.48,4.27,"	Yang D, et al. Two different donor subunits substituted unsymmetrical squaraines for solution-processed small molecule organic solar cells. Organic Electronics 32, 179-186 (2016)."
2690,CCCCCCC1=C(C2=CC=C(C3=C(CCCCCC)C=C(C4=CC=C(CCCCCC)S4)S3)C5=NSN=C25)SC(C(S6)=CC7=C6C(OCC(CC)CCCC)=C8C(SC(C9=CC(CCCCCC)=C(C%10=CC=C(C%11=C(CCCCCC)C=C(C%12=CC=C(CCCCCC)S%12)S%11)C%13=NSN=C%10%13)S9)=C8)=C7OCC(CC)CCCC)=C1,BDT-C1,,,0.72,9.34,0.45,3.03,"	Yang D, et al. Two different donor subunits substituted unsymmetrical squaraines for solution-processed small molecule organic solar cells. Organic Electronics 32, 179-186 (2016)."
2691,FB(F)N1C(/C(C2=CC=C(OCCCCCCCC)C=C2)=C3N=CC(C4=CC=CS4)=C\3)=CC(C5=CC=CS5)=C1,BDP1,,,0.879,10.9,0.634,6.1,"	Chen C, Cheng M, Liu P, Gao J, Kloo L, Sun L. Application of benzodithiophene based A-D-A structured materials in efficient perovskite solar cells and organic solar cells. Nano Energy 23, 40-49 (2016)."
2692,FB(F)N1C(/C(C2=CC=C(OCCCCCCCC)C=C2)=C3N=CC(C4=CC=C(C5=CC=CS5)S4)=C\3)=CC(C6=CC=C(C7=CC=CS7)S6)=C1,BDP2,,,0.64,6.02,0.39,1.49,"	Liao J, et al. Novel D-A-D type dyes based on BODIPY platform for solution processed organic solar cells. Dyes and Pigments 128, 131-140 (2016)."
2693,FB(F)N1C(/C(C2=CC=C(OCCCCCCCC)C=C2)=C3N=CC(C4=CC=C(C(C)(C)C5=C6C=CC=C5)C6=C4)=C\3)=CC(C7=CC=C(C(C)(C)C8=C9C=CC=C8)C9=C7)=C1,BDP3,,,0.78,6.77,0.41,2.15,"	Liao J, et al. Novel D-A-D type dyes based on BODIPY platform for solution processed organic solar cells. Dyes and Pigments 128, 131-140 (2016)."
2694,FB(F)N1C(/C(C2=CC=C(OCCCCCCCC)C=C2)=C3N=CC(C4=CC=C(N(CCCCCCCC)C5=C6C=CC=C5)C6=C4)=C\3)=CC(C7=CC=C(N(CCCCCCCC)C8=C9C=CC=C8)C9=C7)=C1,BDP4,,,0.81,3.62,0.36,1.06,"	Liao J, et al. Novel D-A-D type dyes based on BODIPY platform for solution processed organic solar cells. Dyes and Pigments 128, 131-140 (2016)."
2695,CCCCC(CC)C[Si]1(CC(CC)CCCC)C2=C(SC(C3=C(F)C=C(C4=CC=C(C5=CC=C(CCCCCC)S5)S4)C6=NSN=C36)=C2)C7=C1C=C(C8=C(F)C=C(C9=CC=C(C%10=CC=C(CCCCCC)S%10)S9)C%11=NSN=C8%11)S7,p-DTS(FBTTh2)2,,,0.7,5.03,0.44,1.56,"	Liao J, et al. Novel D-A-D type dyes based on BODIPY platform for solution processed organic solar cells. Dyes and Pigments 128, 131-140 (2016)."
2696,O=C1N(CC(CC)CCCC)C(C2=CC=C(C#CC3=CC=C(C#CC4=CC=C(S4)C5=C6C(C(N5CC(CC)CCCC)=O)=C(C7=CC=CS7)N(CC(CC)CCCC)C6=O)C=C3)S2)=C8C1=C(C9=CC=CS9)N(CC(CC)CCCC)C8=O,BEDPP,,,0.74,17.8,0.52,6.83,"	Kim IK, Jo JH, Yun J-H. Morphology-Controlled High-Efficiency Small Molecule Organic Solar Cells without Additive Solvent Treatment. Nanomaterials (Basel, Switzerland) 6,  (2016)."
2697,O=C1N(CC(CC)CCCC)C(C2=CC=C(C#CC3=CC=C4C(C=CC(C#CC5=CC=C(S5)C6=C7C(C(N6CC(CC)CCCC)=O)=C(C8=CC=CS8)N(CC(CC)CCCC)C7=O)=C4)=C3)S2)=C9C1=C(C%10=CC=CS%10)N(CC(CC)CCCC)C9=O,NEDPP,,,0.9,4.78,0.345,1.48,"	Gao K, et al. A-pi-D-pi-A type Small Molecules Using Ethynylene Linkages for Organic Solar Cells with High Open-circuit Voltages. Chinese Journal of Chemistry 34, 353-358 (2016)."
2698,CCCCC(CC)CC1(CC(CC)CCCC)C2C3=CC=C(C4=CC=CC=C4)C=C3C(CC(CC)CCCC)(CC(CC)CCCC)C2C5=C1C=C(C6=CC(C(N7CC(CCCCCCCC)CCCCCCCCCC)=O)=C(C(SC(C8=CC=CC=C8)=C9)=C9C7=O)S6)C=C5,P1,,,0.98,6.1,0.386,2.31,"	Gao K, et al. A-pi-D-pi-A type Small Molecules Using Ethynylene Linkages for Organic Solar Cells with High Open-circuit Voltages. Chinese Journal of Chemistry 34, 353-358 (2016)."
2699,O=C(N1CC(CCCCCCCC)CCCCCCCCCC)C2=C(C(SC(C3=CC=C(C4=CC=CC=C4)S3)=C5)=C5C1=O)SC(C6=CC=C(S6)C(C=C7)=CC8=C7C9C(C8(CC(CC)CCCC)CC(CC)CCCC)C%10=CC=C(C%11=CC=CC=C%11)C=C%10C9(CC(CC)CCCC)CC(CC)CCCC)=C2,P2,,,0.44,0.26,0.33,0.04,"	Kim J, et al. Syntheses and Properties of Conjugated Polymer with Thiophene-Bridged BTI and Indenoindene Units for Organic Solar Cells. Bulletin of the Korean Chemical Society 37, 506-514 (2016)."
2700,FC1=C(C2=CC([Si](CC(CC)CCCC)(CC(CC)CCCC)C3=C4SC(C5=C6C(SC(C(C7=CC=C(OC)C=C7)=O)=C6)=C(C(S8)=CC([Si]9(CC(CC)CCCC)CC(CC)CCCC)=C8C%10=C9C=C(S%10)C%11=C(F)C=C(C%12=CC=C(C%13=CC=C(CCCCCC)S%13)S%12)C%14=NSN=C%11%14)S5)=C3)=C4S2)C%15=NSN=C%15C(C%16=CC=C(C%17=CC=C(CCCCCC)S%17)S%16)=C1,oligo-1a,,,0.8,1.59,0.39,0.49,"	Kim J, et al. Syntheses and Properties of Conjugated Polymer with Thiophene-Bridged BTI and Indenoindene Units for Organic Solar Cells. Bulletin of the Korean Chemical Society 37, 506-514 (2016)."
2701,FC1=C(C2=CC([Si](CC(CC)CCCC)(CC(CC)CCCC)C3=C4SC(C5=C6C(SC(C(C7=CC=CC=C7)=O)=C6)=C(C(S8)=CC([Si]9(CC(CC)CCCC)CC(CC)CCCC)=C8C%10=C9C=C(S%10)C%11=C(F)C=C(C%12=CC=C(C%13=CC=C(CCCCCC)S%13)S%12)C%14=NSN=C%11%14)S5)=C3)=C4S2)C%15=NSN=C%15C(C%16=CC=C(C%17=CC=C(CCCCCC)S%17)S%16)=C1,oligo-1b,,,0.56,7.16,0.47,1.88,"	Wada Y, et al. Synthesis of Thieno 3,4-b thiophene-Based Donor Molecules with Phenyl Ester Pendants for Organic Solar Cells: Control of Photovoltaic Properties via Single Substituent Replacement. Chemistryselect 1, 703-709 (2016)."
2702,FC1=C(C2=CC([Si](CC(CC)CCCC)(CC(CC)CCCC)C3=C4SC(C5=C6C(SC(C(C7=CC=C(F)C=C7)=O)=C6)=C(C(S8)=CC([Si]9(CC(CC)CCCC)CC(CC)CCCC)=C8C%10=C9C=C(S%10)C%11=C(F)C=C(C%12=CC=C(C%13=CC=C(CCCCCC)S%13)S%12)C%14=NSN=C%11%14)S5)=C3)=C4S2)C%15=NSN=C%15C(C%16=CC=C(C%17=CC=C(CCCCCC)S%17)S%16)=C1,oligo-1c,,,0.56,7,0.56,2.19,"	Wada Y, et al. Synthesis of Thieno 3,4-b thiophene-Based Donor Molecules with Phenyl Ester Pendants for Organic Solar Cells: Control of Photovoltaic Properties via Single Substituent Replacement. Chemistryselect 1, 703-709 (2016)."
2703,FC1=C(C2=CC([Si](CC(CC)CCCC)(CC(CC)CCCC)C3=C4SC(C5=C6C(SC(C(C7=CC=C(C(F)(F)F)C=C7)=O)=C6)=C(C(S8)=CC([Si]9(CC(CC)CCCC)CC(CC)CCCC)=C8C%10=C9C=C(S%10)C%11=C(F)C=C(C%12=CC=C(C%13=CC=C(CCCCCC)S%13)S%12)C%14=NSN=C%11%14)S5)=C3)=C4S2)C%15=NSN=C%15C(C%16=CC=C(C%17=CC=C(CCCCCC)S%17)S%16)=C1,oligo-1d,,,0.58,6.07,0.5,1.75,"	Wada Y, et al. Synthesis of Thieno 3,4-b thiophene-Based Donor Molecules with Phenyl Ester Pendants for Organic Solar Cells: Control of Photovoltaic Properties via Single Substituent Replacement. Chemistryselect 1, 703-709 (2016)."
2704,CCCCCCOC1=C(C2=C(C=C3)N4C3=C(C#CC5=C(CCCCCC)C(CCCCCC)=C(/C=C/C6=C(CCCCCC)C(CCCCCC)=C(/C=C7C(N(CC)C(S/7)=S)=O)S6)S5)C(C=C8)N9C8=C(C%10=C(OCCCCCC)C=CC=C%10OCCCCCC)C%11=CC=C%12N%11[Zn]49N%13C2C=CC%13=C%12C#CC%14=C(CCCCCC)C(CCCCCC)=C(/C=C/C%15=C(CCCCCC)C(CCCCCC)=C(/C=C%16C(N(CC)C(S/%16)=S)=O)S%15)S%14)C(OCCCCCC)=CC=C1,1a,,,0.6,8.17,0.53,2.58,"	Wada Y, et al. Synthesis of Thieno 3,4-b thiophene-Based Donor Molecules with Phenyl Ester Pendants for Organic Solar Cells: Control of Photovoltaic Properties via Single Substituent Replacement. Chemistryselect 1, 703-709 (2016)."
2705,FC1=C(C2=CC=C(C3=CC(C(CC(CC)CCCC)(C4=C5C=C(C(CC(CC)CCCC)(CC(CC)CCCC)C6=C7SC(C8=CC=C(C9=C(F)C(F)=C(C%10=CC=C(C%11=CC=C(CCCCCC)S%11)S%10)C%12=NSN=C9%12)O8)=C6)C7=C4)CC(CC)CCCC)=C5S3)O2)C%13=NSN=C%13C(C%14=CC=C(C%15=CC=C(CCCCCC)S%15)S%14)=C1F,BIT4FFu,,,0.93,10.67,0.54,5.14,"	Arrechea S, Aljarilla A, de la Cruz P, Palomares E, Sharma GD, Langa F. Efficiency improvement using bis(trifluoromethane) sulfonamide lithium salt as a chemical additive in porphyrin based organic solar cells. Nanoscale 8, 17953-17962 (2016)."
2706,FC1=C(C2=CC=C(C3=CC(C(CC(CC)CCCC)(C4=C5C=C(C(CC(CC)CCCC)(CC(CC)CCCC)C6=C7SC(C8=CC=C(C9=C(F)C(F)=C(C%10=CC=C(C%11=CC=C(CCCCCC)S%11)S%10)C%12=NSN=C9%12)S8)=C6)C7=C4)CC(CC)CCCC)=C5S3)S2)C%13=NSN=C%13C(C%14=CC=C(C%15=CC=C(CCCCCC)S%15)S%14)=C1F,BIT4FTh,,,0.89,11.12,0.61,6.01,"	Wang J-L, et al. Difluorobenzothiadiazole-Based Small-Molecule Organic Solar Cells with 8.7% Efficiency by Tuning of pi-Conjugated Spacers and Solvent Vapor Annealing. Advanced Functional Materials 26, 1803-1812 (2016)."
2707,FC1=C(C2=CC=C(C3=CC(C(CC(CC)CCCC)(C4=C5C=C(C(CC(CC)CCCC)(CC(CC)CCCC)C6=C7SC(C8=CC=C(C9=C(F)C(F)=C(C%10=CC=C(C%11=CC=C(CCCCCC)S%11)S%10)C%12=NSN=C9%12)[Se]8)=C6)C7=C4)CC(CC)CCCC)=C5S3)[Se]2)C%13=NSN=C%13C(C%14=CC=C(C%15=CC=C(CCCCCC)S%15)S%14)=C1F,BIT4FSe,,,0.89,13.06,0.75,8.7,"	Wang J-L, et al. Difluorobenzothiadiazole-Based Small-Molecule Organic Solar Cells with 8.7% Efficiency by Tuning of pi-Conjugated Spacers and Solvent Vapor Annealing. Advanced Functional Materials 26, 1803-1812 (2016)."
2708,CCCCCCCCC(CCCCCCCC)N(C1=C2SC(C3=CC=C(C4=CC=CC=C4)C5=NSN=C35)=C1)C6=C2C=CC(C7=CC=C(S7)C8=CC=CC=C8)=C6,PTTIBT,,,0.87,13.4,0.72,8.41,"	Wang J-L, et al. Difluorobenzothiadiazole-Based Small-Molecule Organic Solar Cells with 8.7% Efficiency by Tuning of pi-Conjugated Spacers and Solvent Vapor Annealing. Advanced Functional Materials 26, 1803-1812 (2016)."
2709,CCCCCCCCC(CCCCCCCC)N(C1=C2SC(C3=CC=C(C4=CC=CC=C4)C5=NC(C)(C)N=C35)=C1)C6=C2C=CC(C7=CC=C(S7)C8=CC=CC=C8)=C6,PTTIMBI,,,0.62,3.28,0.42,0.85,"	Jeong I, et al. 6-(2-Thienyl)-4H-thieno 3,2-b indole based conjugated polymers with low bandgaps for organic solar cells. Synthetic Metals 213, 25-33 (2016)."
2710,CCCCCCN(C1=C2C=CC(C3=CC=C(C4=CC=C(C5=CC=C(C6=CC=C(CCCCCC)S6)S5)S4)C7=NSN=C37)=C1)C8=C2N(CCCCCC)C9=CC(C%10=CC=C(C%11=CC=C(C%12=CC=C(C%13=CC=C(CCCCCC)S%13)S%12)S%11)C%14=NSN=C%10%14)=CC=C98,1,,,0.69,7.1,0.53,2.6,"	Jeong I, et al. 6-(2-Thienyl)-4H-thieno 3,2-b indole based conjugated polymers with low bandgaps for organic solar cells. Synthetic Metals 213, 25-33 (2016)."
2711,CCCCCCN(C1=C2C=CC(C3=C(F)C=C(C4=CC=C(C5=CC=C(C6=CC=C(CCCCCC)S6)S5)S4)C7=NSN=C37)=C1)C8=C2N(CCCCCC)C9=CC(C%10=C(F)C=C(C%11=CC=C(C%12=CC=C(C%13=CC=C(CCCCCC)S%13)S%12)S%11)C%14=NSN=C%10%14)=CC=C98,2,,,0.82,9.72,0.52,4.14,"	Sim J, et al. D-A-D-A-D push pull organic small molecules based on 5,10-dihydroindolo 3,2-b indole (DINI) central core donor for solution processed bulk heterojunction solar cells. Organic Electronics 30, 122-130 (2016)."
2712,O=C1N(CC(CC)CCCC)C(C2=CC=CS2)=C3C1=C(C4=CC=C(C(S5)=CC6=C5C(OCC(CC)CCCC)=C7C(SC(C8=CC=C(S8)C9=C%10C(C(N9CC(CC)CCCC)=O)=C(C%11=CC=CS%11)N(CC(CC)CCCC)C%10=O)=C7)=C6OCC(CC)CCCC)S4)N(CC(CC)CCCC)C3=O,BDT(DPP)2-T,,,0.86,10.94,0.56,5.27,"	Sim J, et al. D-A-D-A-D push pull organic small molecules based on 5,10-dihydroindolo 3,2-b indole (DINI) central core donor for solution processed bulk heterojunction solar cells. Organic Electronics 30, 122-130 (2016)."
2713,O=C1N(CC(CC)CCCC)C(C2=CC=C(C3=CC=CS3)S2)=C4C1=C(C5=CC=C(C(S6)=CC7=C6C(OCC(CC)CCCC)=C8C(SC(C9=CC=C(S9)C%10=C%11C(C(N%10CC(CC)CCCC)=O)=C(C%12=CC=C(C%13=CC=CS%13)S%12)N(CC(CC)CCCC)C%11=O)=C8)=C7OCC(CC)CCCC)S5)N(CC(CC)CCCC)C4=O,BDT(DPP)2-T2,,,0.88,8.2,0.434,3.13,"	Park S, Nam SY, Suh DH, Lee J, Lee C, Yoon SC. Solution Processed Organic Photovoltaic Cells Using D-A-D-A-D Type Small Molecular Donor Materials with Benzodithiophene and Diketopyrrolopyrrole Units. Journal of Nanoscience and Nanotechnology 16, 2787-2791 (2016)."
2714,O=C1N(CC(CC)CCCC)C(C2=CC=C(C3=CC=C(C4=CC=C(CCCCCC)S4)S3)S2)=C5C1=C(C6=CC=C(C(S7)=CC8=C7C(OCC(CC)CCCC)=C9C(SC(C%10=CC=C(S%10)C%11=C%12C(C(N%11CC(CC)CCCC)=O)=C(C%13=CC=C(C%14=CC=C(C%15=CC=C(CCCCCC)S%15)S%14)S%13)N(CC(CC)CCCC)C%12=O)=C9)=C8OCC(CC)CCCC)S6)N(CC(CC)CCCC)C5=O,BDT(DPP)2-T3Hx,,,0.78,9.72,0.442,3.36,"	Park S, Nam SY, Suh DH, Lee J, Lee C, Yoon SC. Solution Processed Organic Photovoltaic Cells Using D-A-D-A-D Type Small Molecular Donor Materials with Benzodithiophene and Diketopyrrolopyrrole Units. Journal of Nanoscience and Nanotechnology 16, 2787-2791 (2016)."
2715,CC(C=C1)=CC=C1N(C2=CC=C(C3=CC=C(/C=C4C(N(CC)C(S/4)=S)=O)C5=NSN=C53)S2)C6=CC=C(C)C=C6,DTATBTER,,,0.68,4.46,0.656,1.99,"	Park S, Nam SY, Suh DH, Lee J, Lee C, Yoon SC. Solution Processed Organic Photovoltaic Cells Using D-A-D-A-D Type Small Molecular Donor Materials with Benzodithiophene and Diketopyrrolopyrrole Units. Journal of Nanoscience and Nanotechnology 16, 2787-2791 (2016)."
2716,CC(C=C1)=CC=C1N(C2=CC=C(C3=CC=C(/C=C4C(N(CCCCCCCC)C(S/4)=S)=O)C5=NSN=C53)S2)C6=CC=C(C)C=C6,DTATBTHR,,,0.87,3.2,0.319,0.89,"	Kim N, Park S, Lee M-H, Lee J, Lee C, Yoon SC. Syntheses of D-A-A Type Small Molecular Donor Materials Having Various Electron Accepting Moiety for Organic Photovoltaic Application. Journal of Nanoscience and Nanotechnology 16, 2916-2921 (2016)."
2717,O=C1N(CC(CCCC)CCCCCC)C(C2=CC=C(S2)C#CC(C=C3)=CC=C3N(C4=CC=C(C(CC)(CC)C5=C6C=CC=C5)C6=C4)C7=CC(C(CC)(CC)C8=C9C=CC=C8)=C9C=C7)=C%10C1=C(C%11=CC=C(S%11)C#CC(C=C%12)=CC=C%12N(C%13=CC=C(C(CC)(CC)C%14=C%15C=CC=C%14)C%15=C%13)C%16=CC(C(CC)(CC)C%17=C%18C=CC=C%17)=C%18C=C%16)N(CC(CCCC)CCCCCC)C%10=O,Compound 1,,,0.88,2.95,0.315,0.82,"	Kim N, Park S, Lee M-H, Lee J, Lee C, Yoon SC. Syntheses of D-A-A Type Small Molecular Donor Materials Having Various Electron Accepting Moiety for Organic Photovoltaic Application. Journal of Nanoscience and Nanotechnology 16, 2916-2921 (2016)."
2718,O=C1N(CC(CCCC)CCCCCC)C(C2=CC=C(S2)C#CC(C=C3)=CC(C3=C4)=CC=C4N(C5=CC=C(C(CC)(CC)C6=C7C=CC=C6)C7=C5)C8=CC(C(CC)(CC)C9=C%10C=CC=C9)=C%10C=C8)=C%11C1=C(C%12=CC=C(S%12)C#CC(C=C%13)=CC(C%13=C%14)=CC=C%14N(C%15=CC=C(C(CC)(CC)C%16=C%17C=CC=C%16)C%17=C%15)C%18=CC(C(CC)(CC)C%19=C%20C=CC=C%19)=C%20C=C%18)N(CC(CCCC)CCCCCC)C%11=O,Compound 2,,,0.92,4.25,0.3993,1.56,"	Xia Y, et al. Soluble acetylenic molecular glasses based on dithienyldiketopyrrolopyrrole for organic solar cells. Dyes and Pigments 126, 96-103 (2016)."
2719,O=C1N(C(CCCCCC)CC)C(C2=CC=C(C3=C(CCCCCCCC)C=C(C4=C(CCCCCCCC)C=C(C(C(OCCCCCCCC)=O)C#N)S4)S3)S2)=C5C1=C(C6=CC=C(C7=C(CCCCCCCC)C=C(C8=C(CCCCCCCC)C=C(C(C(OCCCCCCCC)=O)C#N)S8)S7)S6)N(C(CCCCCC)CC)C5=O,DCAO2TDPP,,,0.96,6.24,0.4388,2.62,"	Xia Y, et al. Soluble acetylenic molecular glasses based on dithienyldiketopyrrolopyrrole for organic solar cells. Dyes and Pigments 126, 96-103 (2016)."
2720,O=C1N(C(CCCCCC)CC)C(C2=CC=C(C3=C(CCCCCCCC)C=C(C4=C(CCCCCCCC)C=C(C5SC(N(CCCCCCCC)C5=O)=S)S4)S3)S2)=C6C1=C(C7=CC=C(C8=C(CCCCCCCC)C=C(C9=C(CCCCCCCC)C=C(C%10SC(N(CCCCCCCC)C%10=O)=S)S9)S8)S7)N(C(CCCCCC)CC)C6=O,DOR2TDPP,,,0.76,3.12,0.46,1.09,"	Zhang H, et al. Diketopyrrolopyrrole based small molecules with near infrared absorption for solution processed organic solar cells. Dyes and Pigments 126, 173-178 (2016)."
2721,CCCCC(CC)CC1=CC=C(S1)C2=CC3=C(SC(C4=CC(CCCCCCCC)=C(C5=CC=C(C6=C(CCCCCCCC)C=C(/C=C(C(OCCCCCCCC)=O)\C#N)S6)S5)S4)=C7)C7=C(C8=CC=C(CC(CC)CCCC)S8)C=C3C9=C2C=C(C%10=CC(CCCCCCCC)=C(C%11=CC=C(C%12=C(CCCCCCCC)C=C(/C=C(C(OCCCCCCCC)=O)\C#N)S%12)S%11)S%10)S9,NDTT-CNCOO,,,0.76,5.09,0.53,2.05,"	Zhang H, et al. Diketopyrrolopyrrole based small molecules with near infrared absorption for solution processed organic solar cells. Dyes and Pigments 126, 173-178 (2016)."
2722,CCCCC(CC)CC(C=C1)=CC=C1C2=CC3=C(SC(C4=CC(CCCCCCCC)=C(C5=CC=C(C6=C(CCCCCCCC)C=C(/C=C(C(OCCCCCCCC)=O)\C#N)S6)S5)S4)=C7)C7=C(C8=CC=C(CC(CC)CCCC)C=C8)C=C3C9=C2C=C(C%10=CC(CCCCCCCC)=C(C%11=CC=C(C%12=C(CCCCCCCC)C=C(/C=C(C(OCCCCCCCC)=O)\C#N)S%12)S%11)S%10)S9,NDTP-CNCOO,,,0.91,7.4,0.699,4.71,"	Zhu X, et al. Naphtho 1,2-b:5,6-b ' dithiophene-Based Small Molecules for Thick Film Organic Solar Cells with High Fill Factors. Chemistry of Materials 28, 943-950 (2016)."
2723,CCCCCCCCOC(C=C1)=CC=C1/C(C2=CC=C(/C(C#CC3=CC=C(C4=C5C(C(N4CC(CC)CCCC)=O)=C(C6=CC=CO6)N(CC(CC)CCCC)C5=O)O3)=C7N=C8C=C\7)N2[Zn]N9/C(C=C/C9=C8\C%10=CC=C(OCCCCCCCC)C=C%10)=C%11/C#CC%12=CC=C(C%13=C%14C(C(N%13CC(CC)CCCC)=O)=C(C%15=CC=CO%15)N(CC(CC)CCCC)C%14=O)O%12)=C%16C=CC%11=N\%16,PorODPP,,,0.94,10.77,0.711,7.2,"	Zhu X, et al. Naphtho 1,2-b:5,6-b ' dithiophene-Based Small Molecules for Thick Film Organic Solar Cells with High Fill Factors. Chemistry of Materials 28, 943-950 (2016)."
2724,CCCCCCCCOC(C=C1)=CC=C1/C(C2=CC=C(/C(C#CC3=CC=C(C4=C5C(C(N4CC(CC)CCCC)=O)=C(C6=CC=C[Se]6)N(CC(CC)CCCC)C5=O)[Se]3)=C7N=C8C=C\7)N2[Zn]N9/C(C=C/C9=C8\C%10=CC=C(OCCCCCCCC)C=C%10)=C%11/C#CC%12=CC=C(C%13=C%14C(C(N%13CC(CC)CCCC)=O)=C(C%15=CC=C[Se]%15)N(CC(CC)CCCC)C%14=O)[Se]%12)=C%16C=CC%11=N\%16,PorSeDPP,,,0.81,10.52,0.5001,4.26,"	Liang T, et al. Porphyrin small molecules containing furan- and selenophene-substituted diketopyrrolopyrrole for bulk heterojunction organic solar cells. Organic Electronics 29, 127-134 (2016)."
2725,O=C(C1=C(C2=CC=C(S2)C3=CC=CC=N3)SC(C4=CC=C(S4)C5=CC=CC=N5)=C16)N(CC(CC)CCCC)C6=O,TPDTPy,,,0.71,14.93,0.5471,5.81,"	Liang T, et al. Porphyrin small molecules containing furan- and selenophene-substituted diketopyrrolopyrrole for bulk heterojunction organic solar cells. Organic Electronics 29, 127-134 (2016)."
2726,O=C1N(CC(CC)CCCC)C(C2=CC=C(S2)C3=CC=CC=N3)=C4C1=C(C5=CC=C(S5)C6=CC=CC=N6)N(CC(CC)CCCC)C4=O,DPPTPy,,,0.83,0.73,0.26,0.16,"	Kim J, Song CE, Lee SK, Lim E. TPD- and DPP-based Small Molecule Donors Containing Pyridine End Groups for Organic Photovoltaic Cells. Bulletin of the Korean Chemical Society 37, 161-165 (2016)."
2727,O=C1N(C(CC)CCCCC)C(C2=CC=CS2)=C3C1=C(C4=CC=C(S4)C(C=C5)=CC=C5N(C6=CC=CC=C6)C7=CC=CC=C7)N(CC(CC)CCCC)C3=O,TPA©\DPP,,,0.66,2.85,0.33,0.62,"	Kim J, Song CE, Lee SK, Lim E. TPD- and DPP-based Small Molecule Donors Containing Pyridine End Groups for Organic Photovoltaic Cells. Bulletin of the Korean Chemical Society 37, 161-165 (2016)."
2728,O=C1N(C(CC)CCCCC)C(C2=CC=CS2)=C3C1=C(C4=CC=C(S4)C(C=C5)=CC=C5N(C6=CC=C(C(C=C7)=CC=C7N(C8=CC=CC=C8)C9=CC=CC=C9)C=C6)C%10=CC=CC=C%10)N(CC(CC)CCCC)C3=O,DTPA©\DPP,,,0.81,6.3,0.385,1.97,"	Tan H, et al. Starburst Triphenylamine-Based Donor-Acceptor-Type Small Molecules for Solution-Processed Organic Solar Cells. European Journal of Organic Chemistry, 799-805 (2016)."
2729,O=C1N(C(CC)CCCCC)C(C2=CC=CS2)=C3C1=C(C4=CC=C(S4)C(C=C5)=CC=C5N(C6=CC=C(C(C=C7)=CC=C7N(C8=CC=CC=C8)C9=CC=CC=C9)C=C6)C%10=CC=C(C(C=C%11)=CC=C%11N(C%12=CC=CC=C%12)C%13=CC=CC=C%13)C=C%10)N(CC(CC)CCCC)C3=O,TTPA©\DPP,,,0.83,6.81,0.397,2.26,"	Tan H, et al. Starburst Triphenylamine-Based Donor-Acceptor-Type Small Molecules for Solution-Processed Organic Solar Cells. European Journal of Organic Chemistry, 799-805 (2016)."
2730,C12=CC=CC=C1C(C3=CC=CC=C43)=C5C6=C4C7=CC=CC=C7C8=C9C=CC=CC9=C%10C%11=CC=CC=C%11C%12=C%13C=CC=CC%13=C2C5=C%12C%10=C68,cHBC,,,0.83,7.13,0.419,2.47,"	Tan H, et al. Starburst Triphenylamine-Based Donor-Acceptor-Type Small Molecules for Solution-Processed Organic Solar Cells. European Journal of Organic Chemistry, 799-805 (2016)."
2731,C(C1=C2C3=C(C4=C5C(C=CC=C6)=C6O4)C7=C1C8=C(C=CC=C8)O7)(C=CC=C9)=C9C(C%10=C%11OC%12=C%10C=CC=C%12)=C2C%13=C%11C(OC%14=C%15C=CC=C%14)=C%15C%16=C%13C3=C5C%17=C%16C=CC=C%17,cTBFDBC,,,1.05,2.9,0.64,2,"	Davy NC, et al. Contorted Hexabenzocoronenes with Extended Heterocyclic Moieties Improve Visible-Light Absorption and Performance in Organic Solar Cells. Chemistry of Materials 28, 673-681 (2016)."
2732,C(C1=C2C3=C(C4=C5C(C=CC=C6)=C6S4)C7=C1C8=C(C=CC=C8)S7)(C=CC=C9)=C9C(C%10=C%11SC%12=C%10C=CC=C%12)=C2C%13=C%11C(SC%14=C%15C=CC=C%14)=C%15C%16=C%13C3=C5C%17=C%16C=CC=C%17,cTBTDBC,,,0.81,4.1,0.69,2.3,"	Davy NC, et al. Contorted Hexabenzocoronenes with Extended Heterocyclic Moieties Improve Visible-Light Absorption and Performance in Organic Solar Cells. Chemistry of Materials 28, 673-681 (2016)."
2733,CCCCC(CC)C[Si]1(CC(CC)CCCC)C2=C(SC(C3=CC=C(C4=CC=C(C5=CC=C(CCCCCC)S5)S4)C6=NSN=C36)=C2)C7=C1C=C(C8=CC=C(C9=CC=C(C%10=CC=C(CCCCCC)S%10)S9)C%11=NSN=C8%11)S7,0F,,,0.9,3.7,0.65,2.2,"	Davy NC, et al. Contorted Hexabenzocoronenes with Extended Heterocyclic Moieties Improve Visible-Light Absorption and Performance in Organic Solar Cells. Chemistry of Materials 28, 673-681 (2016)."
2734,CCCCC(CC)C[Si]1(CC(CC)CCCC)C2=C(SC(C3=C(F)C=C(C4=CC=C(C5=CC=C(CCCCCC)S5)S4)C6=NSN=C36)=C2)C7=C1C=C(C8=CC=C(C9=CC=C(C%10=CC=C(CCCCCC)S%10)S9)C%11=NSN=C8%11)S7,1F,,,0.76,4.55,0.34,1.16,"	Yun JH, et al. Enhancement of charge transport properties of small molecule semiconductors by controlling fluorine substitution and effects on photovoltaic properties of organic solar cells and perovskite solar cells. Chemical Science 7, 6649-6661 (2016)."
2735,CCCCC(CC)C[Si]1(CC(CC)CCCC)C2=C(SC(C3=C(F)C=C(C4=CC=C(C5=CC=C(CCCCCC)S5)S4)C6=NSN=C36)=C2)C7=C1C=C(C8=C(F)C=C(C9=CC=C(C%10=CC=C(CCCCCC)S%10)S9)C%11=NSN=C8%11)S7,2F,,,0.7,8.23,0.53,3.02,"	Yun JH, et al. Enhancement of charge transport properties of small molecule semiconductors by controlling fluorine substitution and effects on photovoltaic properties of organic solar cells and perovskite solar cells. Chemical Science 7, 6649-6661 (2016)."
2736,CCCCC(CC)C[Si]1(CC(CC)CCCC)C2=C(SC(C3=C(F)C=C(C4=CC=C(C5=CC=C(CCCCCC)S5)S4)C6=NSN=C36)=C2)C7=C1C=C(C8=C(F)C(F)=C(C9=CC=C(C%10=CC=C(CCCCCC)S%10)S9)C%11=NSN=C8%11)S7,3F,,,0.81,14.96,0.66,7.98,"	Yun JH, et al. Enhancement of charge transport properties of small molecule semiconductors by controlling fluorine substitution and effects on photovoltaic properties of organic solar cells and perovskite solar cells. Chemical Science 7, 6649-6661 (2016)."
2737,CCCCC(CC)C[Si]1(CC(CC)CCCC)C2=C(SC(C3=C(F)C(F)=C(C4=CC=C(C5=CC=C(CCCCCC)S5)S4)C6=NSN=C36)=C2)C7=C1C=C(C8=C(F)C(F)=C(C9=CC=C(C%10=CC=C(CCCCCC)S%10)S9)C%11=NSN=C8%11)S7,4F,,,0.78,13.42,0.62,6.59,"	Yun JH, et al. Enhancement of charge transport properties of small molecule semiconductors by controlling fluorine substitution and effects on photovoltaic properties of organic solar cells and perovskite solar cells. Chemical Science 7, 6649-6661 (2016)."
2738,CCCCCCC1=CC=C(S1)C2=C(SC(C3=CC(CCCCCC)=C(C4=CC=C(C5=C(CCCCCC)C=C(/C=C6C(C7=CC=CC=C7C\6=O)=O)S5)S4)S3)=C8)C8=C(C9=CC=C(CCCCCC)S9)C%10=C2C=C(C%11=CC(CCCCCC)=C(C%12=CC=C(C%13=C(CCCCCC)C=C(/C=C%14C(C%15=CC=CC=C%15C\%14=O)=O)S%13)S%12)S%11)S%10,BDT-3T(3-Hex)-ID,,,0.86,11.56,0.69,6.86,"	Yun JH, et al. Enhancement of charge transport properties of small molecule semiconductors by controlling fluorine substitution and effects on photovoltaic properties of organic solar cells and perovskite solar cells. Chemical Science 7, 6649-6661 (2016)."
2739,CCCCCCC1=CC=C(S1)C2=C(SC(C3=C(CCCCCC)C=C(C4=CC=C(C5=CC(CCCCCC)=C(/C=C6C(C7=CC=CC=C7C\6=O)=O)S5)S4)S3)=C8)C8=C(C9=CC=C(CCCCCC)S9)C%10=C2C=C(C%11=C(CCCCCC)C=C(C%12=CC=C(C%13=CC(CCCCCC)=C(/C=C%14C(C%15=CC=CC=C%15C\%14=O)=O)S%13)S%12)S%11)S%10,BDT-3T(4-Hex)-ID,,,0.75,4,0.353,1.06,"	Zhang J, et al. Impact of the alkyl side chain position on the photovoltaic properties of solution-processable organic molecule donor materials. Journal of Materials Chemistry A 4, 11747-11753 (2016)."
2740,CCCCCCC1=CC=C(S1)/C(C2=N/C(C=C2)=C3/C#CC4=C(CCCCCC)C(CCCCCC)=C(/C=C5C(N(CC)C(S/5)=S)=O)S4)=C(C=C/6)/N7C6=C(C#CC8=C(CCCCCC)C(CCCCCC)=C(/C=C9C(N(CC)C(S/9)=S)=O)S8)/C(C=C/%10)=NC%10=C(C%11=CC=C(CCCCCC)S%11)/C%12=CC=C3N%12[Zn]7,1a,,,0.87,10.54,0.714,6.55,"	Zhang J, et al. Impact of the alkyl side chain position on the photovoltaic properties of solution-processable organic molecule donor materials. Journal of Materials Chemistry A 4, 11747-11753 (2016)."
2741,CCCCCCC1=CC=C(S1)/C(C2=N/C(C=C2)=C3/C#CC4=C(CCCCCC)C(CCCCCC)=C(/C=C/C5=C(CCCCCC)C(CCCCCC)=C(/C=C6C(N(CC)C(S/6)=S)=O)S5)S4)=C(C=C/7)/N8C7=C(C#CC9=C(CCCCCC)C(CCCCCC)=C(/C=C/C%10=C(CCCCCC)C(CCCCCC)=C(/C=C%11C(N(CC)C(S/%11)=S)=O)S%10)S9)/C(C=C/%12)=NC%12=C(C%13=CC=C(CCCCCC)S%13)/C%14=CC=C3N%14[Zn]8,1b,,,0.99,10.74,0.62,6.59,"	Moran G, et al. CuSCN as selective contact in solution-processed small-molecule organic solar cells leads to over 7% efficient porphyrin-based device. Journal of Materials Chemistry A 4, 11009-11022 (2016)."
2742,O=C1N(CC(CC)CCCC)C(C2=CC=C(S2)C3=CC(C=C4)=C5C6=C4C=C(C7=CC=C(S7)C8=C9C(C(N8CC(CC)CCCC)=O)=C(C%10=CC=CS%10)N(CC(CC)CCCC)C9=O)C=C6C=CC5=C3)=C%11C1=C(C%12=CC=CS%12)N(CC(CC)CCCC)C%11=O,DPP2Py,,,0.94,11.67,0.66,7.24,"	Moran G, et al. CuSCN as selective contact in solution-processed small-molecule organic solar cells leads to over 7% efficient porphyrin-based device. Journal of Materials Chemistry A 4, 11009-11022 (2016)."
2743,O=C1N(CC(CC)CCCC)C(C2=CC=C(S2)C3=CC(C=C4)=C5C6=C4C=C(C7=CC=C(S7)C8=C9C(C(N8CC(CC)CCCC)=O)=C(C%10=CC=C(C%11=CC=C(CCCCCCCC)S%11)S%10)N(CC(CC)CCCC)C9=O)C=C6C=CC5=C3)=C%12C1=C(C%13=CC=C(C%14=CC=C(CCCCCCCC)S%14)S%13)N(CC(CC)CCCC)C%12=O,ThDPP2Py,,,0.85,11.13,0.6007,5.67,"	Chen J, et al. Tuning the central fused ring and terminal units to improve the photovoltaic performance of Ar(A-D)(2) type small molecules in solution-processed organic solar cells. Journal of Materials Chemistry A 4, 4952-4961 (2016)."
2744,O=C1N(CC(CC)CCCC)C(C2=CC=C(S2)C3=CC(C=C4)=C5C6=C4C=C(C7=CC=C(S7)C8=C9C(C(N8CC(CC)CCCC)=O)=C(C%10=CC=C(C%11=CC=C(N(C%12=CC=C(OCCCCCCCC)C=C%12)C%13=CC=C(OCCCCCCCC)C=C%13)C=C%11)S%10)N(CC(CC)CCCC)C9=O)C=C6C=CC5=C3)=C%14C1=C(C%15=CC=C(C%16=CC=C(N(C%17=CC=C(OCCCCCCCC)C=C%17)C%18=CC=C(OCCCCCCCC)C=C%18)C=C%16)S%15)N(CC(CC)CCCC)C%14=O,TPADPP2Py,,,0.66,15.35,0.5789,5.88,"	Chen J, et al. Tuning the central fused ring and terminal units to improve the photovoltaic performance of Ar(A-D)(2) type small molecules in solution-processed organic solar cells. Journal of Materials Chemistry A 4, 4952-4961 (2016)."
2745,CCCN1C2=C(C3=C1C(SC4=C5N(CCC)C6=C4SC(/C=C(C#N)/C#N)=C6)=C5S3)SC(/C=C(C#N)/C#N)=C2,1,,,0.62,10.77,0.6394,4.26,"	Chen J, et al. Tuning the central fused ring and terminal units to improve the photovoltaic performance of Ar(A-D)(2) type small molecules in solution-processed organic solar cells. Journal of Materials Chemistry A 4, 4952-4961 (2016)."
2746,N#C/C(C#N)=C/C1=CC2=C(C(S3)=C(C4=C3C5=C(C6=C(N5CCCC)C=C(/C=C(C#N)/C#N)S6)S4)N2CCCC)S1,2,,,0.9,10.7,0.608,5.9,"	Wetzel C, Mishra A, Mena-Osteritz E, Walzer K, Pfeiffer M, Baeuerle P. Development of strongly absorbing S,N-heterohexacene-based donor materials for efficient vacuum-processed organic solar cells. Journal of Materials Chemistry C 4, 3715-3725 (2016)."
2747,N#C/C(C#N)=C/C1=CC2=C(C(S3)=C(C4=C3C5=C(C6=C(N5CCCCC)C=C(/C=C(C#N)/C#N)S6)S4)N2CCCCC)S1,3,,,0.95,10,0.621,5.9,"	Wetzel C, Mishra A, Mena-Osteritz E, Walzer K, Pfeiffer M, Baeuerle P. Development of strongly absorbing S,N-heterohexacene-based donor materials for efficient vacuum-processed organic solar cells. Journal of Materials Chemistry C 4, 3715-3725 (2016)."
2748,CCCCCC1=C(C2=CC=C(C3=CC=C(C4=C5C(C(N4CC(CC)CCCC)=O)=C(C6=CC=C(C)S6)N(CC(CC)CCCC)C5=O)S3)S2)SC(C7=C(CCOCCOC)C=C(C)S7)=C1,P3HTT-DPP-MEO40%,,,0.96,12.2,0.606,7.1,"	Wetzel C, Mishra A, Mena-Osteritz E, Walzer K, Pfeiffer M, Baeuerle P. Development of strongly absorbing S,N-heterohexacene-based donor materials for efficient vacuum-processed organic solar cells. Journal of Materials Chemistry C 4, 3715-3725 (2016)."
2749,N#C/C(C#N)=C/C1=CC2=C(C(S3)=C(C4=C3C5=C(C6=C(N5CCCCCC)C=C(/C=C(C#N)/C#N)S6)S4)N2CCCCCC)S1,4,,,0.596,11.01,0.545,3.58,"	Gobalasingham NS, Noh S, Howard JB, Thompson BC. Influence of Surface Energy on Organic Alloy Formation in Ternary Blend Solar Cells Based on Two Donor Polymers. Acs Applied Materials & Interfaces 8, 27931-27941 (2016)."
2750,N#C/C(C#N)=C/C1=CC2=C(C(S3)=C(C4=C3C5=C(C6=C(N5CCCCCCC)C=C(/C=C(C#N)/C#N)S6)S4)N2CCCCCCC)S1,5,,,0.96,10.3,0.601,4.62,"	Wetzel C, Mishra A, Mena-Osteritz E, Walzer K, Pfeiffer M, Baeuerle P. Development of strongly absorbing S,N-heterohexacene-based donor materials for efficient vacuum-processed organic solar cells. Journal of Materials Chemistry C 4, 3715-3725 (2016)."
2751,O=C1N(C(C2=CC=C(S2)C#CC(C3=C4C=CC=C3)=C(C=CC=C5)C5=C4C#CC6=C(CCCCCCCCCCCC)C=CS6)=C7C1=C(C8=CC=C(S8)C#CC(C9=C%10C=CC=C9)=C(C=CC=C%11)C%11=C%10C#CC%12=C(CCCCCCCCCCCC)C=CS%12)N(CC(CCCC)CCCCCC)C7=O)CC(CCCC)CCCCCC,An-1,,,0.96,11.4,0.574,4.48,"	Wetzel C, Mishra A, Mena-Osteritz E, Walzer K, Pfeiffer M, Baeuerle P. Development of strongly absorbing S,N-heterohexacene-based donor materials for efficient vacuum-processed organic solar cells. Journal of Materials Chemistry C 4, 3715-3725 (2016)."
2752,O=C1N(C(C2=CC=C(C#CC3=CC=C(C#CC(C4=C5C=CC=C4)=C(C=CC=C6)C6=C5C#CC7=C(CCCCCCCCCCCC)C=CS7)C=C3)S2)=C8C1=C(C9=CC=C(C#CC%10=CC=C(C#CC(C%11=C%12C=CC=C%11)=C(C=CC=C%13)C%13=C%12C#CC%14=C(CCCCCCCCCCCC)C=CS%14)C=C%10)S9)N(CC(CCCC)CCCCCC)C8=O)CC(CCCC)CCCCCC,An-2,,,0.73,8.18,0.6459,3.86,"	Zhang C-H, et al. Effective modulation of an aryl acetylenic molecular system based on dithienyldiketopyrrolopyrrole for organic solar cells. Journal of Materials Chemistry C 4, 3757-3764 (2016)."
2753,CC1(C)C(C=C2C([O-])=C(C3=C(O)C=C(N4C(CCC5)C5C6=C4C=CC=C6)C=C3O)C2=O)=[N+](CCCC)C7=CC=CC=C71,S-SQ,,,0.87,9.24,0.63,5.07,"	Zhang C-H, et al. Effective modulation of an aryl acetylenic molecular system based on dithienyldiketopyrrolopyrrole for organic solar cells. Journal of Materials Chemistry C 4, 3757-3764 (2016)."
2754,CC1(C)C(C=C2C([O-])=C(C3=C(O)C=C(N4C(CCC5)C5C6=C4C=CC=C6)C=C3O)C2=O)=[N+](CCCC)C7=CC=C(C8=CC(C(S8)=C9C%10=CC=C(CC(CC)CCCC)S%10)=C(C%11=CC=C(CC(CC)CCCC)S%11)C%12=C9C=C(C%13=CC=CC=C%13)S%12)C=C71,BDT-SQ,,,0.79,13.45,0.52,5.52,"	Yang D, et al. An effective pi-extended squaraine for solution-processed organic solar cells with high efficiency. Journal of Materials Chemistry A 4, 18931-18941 (2016)."
2755,CC1(C)C(C=C2C([O-])=C(C3=C(O)C=C(N4C(CCC5)C5C6=C4C=CC=C6)C=C3O)C2=O)=[N+](CCCC)C7=CC=C(C8=CC(C(S8)=C9C%10=CC=C(CC(CC)CCCC)S%10)=C(C%11=CC=C(CC(CC)CCCC)S%11)C%12=C9C=C(C%13=CC=C([N+](CCCC)=C(C=C%14C([O-])=C(C%15=C(O)C=C(N%16C(CCC%17)C%17C%18=C%16C=CC=C%18)C=C%15O)C%14=O)C%19(C)C)C%19=C%13)S%12)C=C71,D-BDT-SQ,,,0.86,12.87,0.52,5.75,"	Yang D, et al. An effective pi-extended squaraine for solution-processed organic solar cells with high efficiency. Journal of Materials Chemistry A 4, 18931-18941 (2016)."
2756,O=C1N(CC(CC)CCCC)C(C2=CC=CS2)=C3C1=C(C4=CC=C(C5=CC(N(CC(CCCC)CCCCCC)C(C6=C7C=C8C(C(SC(C9=CC=C(S9)C%10=C%11C(C(N%10CC(CC)CCCC)=O)=C(C%12=CC=CS%12)N(CC(CC)CCCC)C%11=O)=C%13)C%13N(CC(CCCC)CCCCCC)C8=O)=C6)=O)=C7S5)S4)N(CC(CC)CCCC)C3=O,PCLDPP,,,0.83,14.89,0.6,7.41,"	Yang D, et al. An effective pi-extended squaraine for solution-processed organic solar cells with high efficiency. Journal of Materials Chemistry A 4, 18931-18941 (2016)."
2757,CCCCCCCCC(CCCCCCCC)N1C2=C(C3=C1C=C(C4=C(CCCCCC)C=C(C5=C(CCCCCC)C=C(/C=C(C#N)/C#N)S5)S4)S3)SC(C6=C(CCCCCC)C=C(C7=C(CCCCCC)C=C(/C=C(C#N)/C#N)S7)S6)=C2,1?DCV,,,0.89,9.7,0.56,4.8,"	Feng G, et al. All-small-molecule organic solar cells based on an electron donor incorporating binary electron-deficient units. Journal of Materials Chemistry A 4, 6056-6063 (2016)."
2758,CCCCCCCCC(CCCCCCCC)N1C2=C(C3=C1C=C(C4=C(CCCCCC)C=C(C5=C(CCCCCC)C=C(/C=C6C(C(C=CC=C7)=C7C/6=O)=O)S5)S4)S3)SC(C8=C(CCCCCC)C=C(C9=C(CCCCCC)C=C(/C=C%10C(C(C=CC=C%11)=C%11C/%10=O)=O)S9)S8)=C2,2?IN,,,0.9,13.05,0.65,7.63,"	Mishra A, et al. High performance A-D-A oligothiophene-based organic solar cells employing two-step annealing and solution-processable copper thiocyanate (CuSCN) as an interfacial hole transporting layer. Journal of Materials Chemistry A 4, 17344-17353 (2016)."
2759,O=C(C1=C(C2=CC=C(S2)C3=CC=CS3)SC(C4=CC=C(C5=CC=CS5)S4)=C16)N(CC(CC)CCCC)C6=O,TPD2T,,,0.86,14.06,0.68,8.22,"	Mishra A, et al. High performance A-D-A oligothiophene-based organic solar cells employing two-step annealing and solution-processable copper thiocyanate (CuSCN) as an interfacial hole transporting layer. Journal of Materials Chemistry A 4, 17344-17353 (2016)."
2760,CCCCC(CC)COC1=C(SC(C2=C(CCCCCCCC)C(SC(C3=CC=C(/C(C(N4CC(CCCCCC)CCCCCCCC)=O)=C(C(N5CC(CCCCCC)CCCCCCCC)=O)/C(C5=C6)=CC=C6C(S7)=CC(S8)=C7C(CCCCCCCC)=C8C9=CC=CS9)C4=C3)=C%10)=C%10S2)=C%11)C%11=C(OCC(CC)CCCC)C%12=C1C=C(C%13=CC=CS%13)S%12,PBDT-TT-IID,,,1.04,0.68,0.22,0.15,"	Lim E. Synthesis of TPD-thiophene-based small molecule donor for organic photovoltaic cells. Molecular Crystals and Liquid Crystals 635, 87-93 (2016)."
2761,CCCCCCCCC1=C(SC2=C1SC(C3=CC=C(/C(C(N4CC(CCCCCC)CCCCCCCC)=O)=C(C(N5CC(CCCCCC)CCCCCCCC)=O)/C(C5=C6)=CC=C6C(S7)=CC(S8)=C7C(CCCCCCCC)=C8C9=CC=CS9)C4=C3)=C2)C(S%10)=CC(C%10=C%11C(S%12)=CC=C%12CC(CC)CCCC)=C(C%13=CC=C(CC(CC)CCCC)S%13)C%14=C%11C=C(C%15=CC=CS%15)S%14,PBDTT-TT-IID,,,0.79,12.24,0.65,6.31,"	Zhu L, Wang M, Li B, Jiang C, Li Q. High efficiency organic photovoltaic devices based on isoindigo conjugated polymers with a thieno 3,2-b thiophene pi-bridge. Journal of Materials Chemistry A 4, 16064-16072 (2016)."
2762,CCCCC(CC)CC1=CC=C(S1)C2=C(SC(C3=CC(CCCCCCCC)=C(C4=CC=C(C5=C(CCCCCCCC)C=C(/C=C6C(N(CC)C(S/6)=S)=O)S5)S4)S3)=C7)C7=C(C8=CC=C(CC(CC)CCCC)S8)C9=C2C=C(C(S%10)=CC(C%10=C%11C%12=CC=C(CC(CC)CCCC)S%12)=C(C%13=CC=C(CC(CC)CCCC)S%13)C%14=C%11C=C(C(S%15)=CC(C%15=C%16C%17=CC=C(CC(CC)CCCC)S%17)=C(C%18=CC=C(CC(CC)CCCC)S%18)C%19=C%16C=C(C%20=CC(CCCCCCCC)=C(C%21=CC=C(C%22=C(CCCCCCCC)C=C(/C=C%23C(N(CC)C(S/%23)=S)=O)S%22)S%21)S%20)S%19)S%14)S9,BDT3TR,,,0.79,14.14,0.72,8.05,"	Zhu L, Wang M, Li B, Jiang C, Li Q. High efficiency organic photovoltaic devices based on isoindigo conjugated polymers with a thieno 3,2-b thiophene pi-bridge. Journal of Materials Chemistry A 4, 16064-16072 (2016)."
2763,O=C(N(CC)C(S/1)=S)C1=C/C2=CC(CCCCCC)=C(S2)C3=C(OCCO4)C4=C(C5=C(CCCCCC)C=C(/C=C6C(N(CC)C(S\6)=S)=O)S5)S3,DRH-2TE,,,1.06,12.1,0.55,6.96,"	Badgujar S, et al. Highly efficient and thermally stable fullerene-free organic solar cells based on a small molecule donor and acceptor. Journal of Materials Chemistry A 4, 16335-16340 (2016)."
2764,CCCCCCC1=C(SC(/C=C(C#N)/C(OCC)=O)=C1)C2=C(OCCO3)C3=C(C4=C(CCCCCC)C=C(/C=C(C#N)/C(OCC)=O)S4)S2,DECA-2TE,,,0.68,5.6,0.35,1.36,"	Antwi BY, Taylor RGD, Cameron J, Owoare RB, Kingsford-Adaboh R, Skabara PJ. Acceptor-donor-acceptor small molecules based on derivatives of 3,4-ethylenedioxythiophene for solution processed organic solar cells. Rsc Advances 6, 98797-98803 (2016)."
2765,O=C1N(CC(CC)CCCC)C(C2=CC=C(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C6C(SC(C7=CC=C(C(N8CC(CC)CCCC)=C9C(C8=O)=C(C%10=CC=C(C%11=CC=C(C(F)(F)F)C=C%11)S%10)N(CC(CC)CCCC)C9=O)S7)=C6)=C4C%12=CC=C(CC(CC)CCCC)S%12)S3)S2)=C%13C1=C(C%14=CC=C(C%15=CC=C(C(F)(F)F)C=C%15)S%14)N(CC(CC)CCCC)C%13=O,SM-CF3,,,0.9,2.99,0.39,1.05,"	Antwi BY, Taylor RGD, Cameron J, Owoare RB, Kingsford-Adaboh R, Skabara PJ. Acceptor-donor-acceptor small molecules based on derivatives of 3,4-ethylenedioxythiophene for solution processed organic solar cells. Rsc Advances 6, 98797-98803 (2016)."
2766,O=C1N(CCCCCCCCCC)C(C2=CC=CS2)=C3C1=C(C4=CC=C(C#CC5=CC=C(N(C6=CC=CC=C6)C7=CC=CC=C7)C=C5)S4)N(CCCCCCCCCC)C3=O,DPP3,,,0.881,10.72,0.568,5.31,"	Jiang B, Yao J, Zhan C. Modulating PCBM-Acceptor Crystallinity and Organic Solar Cell Performance by Judiciously Designing Small-Molecule Mainchain End-Capping Units. Acs Applied Materials & Interfaces 8, 26058-26065 (2016)."
2767,O=C1N(CCCCCCCCCC)C(C2=CC=C(C#CC3=CC=C(N(C4=CC=CC=C4)C5=CC=CC=C5)C=C3)S2)=C6C1=C(C7=CC=C(C#CC8=CC=C(N(C9=CC=CC=C9)C%10=CC=CC=C%10)C=C8)S7)N(CCCCCCCCCC)C6=O,DPP4,,,0.88,8.88,0.52,4.06,"	Patil Y, Misra R, Chen FC, Keshtov ML, Sharma GD. Symmetrical and unsymmetrical triphenylamine based diketopyrrolopyrroles and their use as donors for solution processed bulk heterojunction organic solar cells. Rsc Advances 6, 99685-99694 (2016)."
2768,CCCCC(CC)CC1(CC(CC)CCCC)C2=CC3=C(C=C2C4C1C=C(C5=CC=C(C6=CC=C(C7=C(F)C(F)=C(C8=CC=C(C9=CC=C(CCCCCCCCCCCC)S9)S8)C%10=NSN=C7%10)S6)S5)S4)C(CC(CC)CCCC)(CC(CC)CCCC)C%11=C3SC(C%12=CC=C(C%13=CC=C(C%14=C(F)C(F)=C(C%15=CC=C(C%16=CC=C(CCCCCCCCCCCC)S%16)S%15)C%17=NSN=C%14%17)S%13)S%12)=C%11,BIT4FDT,,,0.85,11.16,0.56,5.31,"	Patil Y, Misra R, Chen FC, Keshtov ML, Sharma GD. Symmetrical and unsymmetrical triphenylamine based diketopyrrolopyrroles and their use as donors for solution processed bulk heterojunction organic solar cells. Rsc Advances 6, 99685-99694 (2016)."
2769,CCCCC(CC)CC1(CC(CC)CCCC)C2=CC3=C(C=C2C4C1C=C(C5=CC(SC(C6=C(F)C(F)=C(C7=CC=C(C8=CC=C(CCCCCCCCCCCC)S8)S7)C9=NSN=C69)=C%10)=C%10S5)S4)C(CC(CC)CCCC)(CC(CC)CCCC)C%11=C3SC(C%12=CC(SC(C%13=C(F)C(F)=C(C%14=CC=C(C%15=CC=C(CCCCCCCCCCCC)S%15)S%14)C%16=NSN=C%13%16)=C%17)=C%17S%12)=C%11,BIT4FTT,,,0.88,8.83,0.73,5.71,"	Wang J-L, et al. Toward high performance indacenodithiophene-based small-molecule organic solar cells: investigation of the effect of fused aromatic bridges on the device performance. Journal of Materials Chemistry A 4, 2252-2262 (2016)."
2770,O=C1N(CC(CC)CCCC)C(C2=CC=C(C3=CC=C(/C=C(C(OCCCCCCCC)=O)\C#N)S3)S2)=C4C1=C(C5=CC=C(C(S6)=CC7=C6C(C8=CC=C(CC(CC)CCCC)S8)=C9C(SC=C9)=C7C%10=CC=C(CC(CC)CCCC)S%10)S5)N(CC(CC)CCCC)C4=O,M1,,,0.89,11.33,0.75,7.57,"	Wang J-L, et al. Toward high performance indacenodithiophene-based small-molecule organic solar cells: investigation of the effect of fused aromatic bridges on the device performance. Journal of Materials Chemistry A 4, 2252-2262 (2016)."
2771,O=C1N(CC(CC)CCCC)C(C2=CC=C(C3=CC=C(/C=C(C(OCCCCCCCC)=O)\C#N)S3)S2)=C4C1=C(C5=CC=C(C(S6)=CC7=C6C(C8=CC=C(CC(CC)CCCC)S8)=C9C(SC(C%10=CC=CS%10)=C9)=C7C%11=CC=C(CC(CC)CCCC)S%11)S5)N(CC(CC)CCCC)C4=O,M2,,,0.82,7.06,0.617,3.58,"	Huang J, et al. Terminal moiety-driven electrical performance of asymmetric small-molecule-based organic solar cells. Journal of Materials Chemistry A 4, 15688-15697 (2016)."
2772,O=C1N(CC(CC)CCCC)C(C2=CC=C(C3=CC=C(/C=C(C(OCCCCCCCC)=O)\C#N)S3)S2)=C4C1=C(C5=CC=C(C(S6)=CC7=C6C(C8=CC=C(CC(CC)CCCC)S8)=C9C(SC(C%10=CC=C(C%11=CC=C(CCCCCC)S%11)S%10)=C9)=C7C%12=CC=C(CC(CC)CCCC)S%12)S5)N(CC(CC)CCCC)C4=O,M3,,,0.74,6.65,0.623,3.06,"	Huang J, et al. Terminal moiety-driven electrical performance of asymmetric small-molecule-based organic solar cells. Journal of Materials Chemistry A 4, 15688-15697 (2016)."
2773,O=C1N(CC(CCCC)CC)C(C2=CC=C(C3=CC=CC=C3)S2)C4C1C(C5=CC=C(C6=CC=C(C(SC(C7=CC=C(C8=CC=C(C9N(CC(CCCC)CC)C(C%10C(C%11=CC=C(C%12=CC=CC=C%12)S%11)N(CC(CCCC)CC)C(C%109)=O)=O)S8)S7)=C%13C(N%14CC(CCCC)CC)=O)=C%13C%14=O)S6)S5)N(CC(CCCC)CC)C4=O,TPD(DPP)2,,,0.67,6.45,0.584,2.52,"	Huang J, et al. Terminal moiety-driven electrical performance of asymmetric small-molecule-based organic solar cells. Journal of Materials Chemistry A 4, 15688-15697 (2016)."
2774,O=C1N(CC(CC)CCCC)C(C2=CC=C(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C6C(SC(C7=CC=C(C(N8CC(CC)CCCC)=C9C(C8=O)=C(C%10=CC=C(C%11=CC=C(OC)C=C%11)S%10)N(CC(CC)CCCC)C9=O)S7)=C6)=C4C%12=CC=C(CC(CC)CCCC)S%12)S3)S2)=C%13C1=C(C%14=CC=C(C%15=CC=C(OC)C=C%15)S%14)N(CC(CC)CCCC)C%13=O,SM-OCH3,,,0.8,7.86,0.54,3.37,"	Ko EY, Choi S, Park GE, Lee DH, Cho MJ, Choi DH. Diketopyrrolopyrrole-based conjugated small molecules bearing two different acceptor moieties for organic solar cells. Synthetic Metals 221, 39-47 (2016)."
2775,O=C1N(CC(CC)CCCC)C(C2=CC=C(C3=CC=C(/C=C(C(OCCCCCCCC)=O)\C#N)S3)S2)=C4C1=C(C5=CC=C(C(S6)=CC7=C6C(C8=CC=C(CC(CC)CCCC)S8)=C9C(SC(C%10=CC=C(/C=C(C(OCCCCCCCC)=O)/C#N)S%10)=C9)=C7C%11=CC=C(CC(CC)CCCC)S%11)S5)N(CC(CC)CCCC)C4=O,M4,,,0.624,16.15,0.563,5.89,"	Jiang B, Yao J, Zhan C. Modulating PCBM-Acceptor Crystallinity and Organic Solar Cell Performance by Judiciously Designing Small-Molecule Mainchain End-Capping Units. Acs Applied Materials & Interfaces 8, 26058-26065 (2016)."
2776,O=C1N(CC(CC)CCCC)C(C2=CC=C(S2)C#CC(S3)=CC(C3=C4OCC(CC)CCCC)=C(OCC(CC)CCCC)C5=C4C=C(C#CC6=CC=C(C7=C(C(N8CC(CC)CCCC)=O)C(C(N7CC(CC)CCCC)=O)=C8C9=CC=CS9)S6)S5)=C%10C1=C(C%11=CC=CS%11)N(CC(CC)CCCC)C%10=O,DPP-E-BDT,,,0.78,2.76,0.42,0.91,"	Huang J, et al. Terminal moiety-driven electrical performance of asymmetric small-molecule-based organic solar cells. Journal of Materials Chemistry A 4, 15688-15697 (2016)."
2777,O=C1N(CC(CC)CCCC)C(C2=CC=C(S2)C#CC(S3)=CC(C3=C4C(S5)=CC=C5CC(CC)CCCC)=C(C(S6)=CC=C6CC(CC)CCCC)C7=C4C=C(C#CC8=CC=C(C9=C(C(N%10CC(CC)CCCC)=O)C(C(N9CC(CC)CCCC)=O)=C%10C%11=CC=CS%11)S8)S7)=C%12C1=C(C%13=CC=CS%13)N(CC(CC)CCCC)C%12=O,DPP-E-BDT-T,,,0.88,7.78,0.604,4.19,"	Kan Y, et al. Solution-processed small molecules with ethynylene bridges for highly efficient organic solar cells. Journal of Materials Chemistry A 4, 14720-14728 (2016)."
2778,CCCCCCC1=C(C2=CC(SC(C3=C(CCCCCC)C=C(C4=C(CCCCCCCCC)N=C(C5=NC(CCCCCCCCC)=C(C6=CC(CCCCCC)=C(S6)C(S7)=CC8=C7C=C(S8)C9=C(CCCCCC)C=C(S9)C(C=C%10)=CC=C%10N(C%11=CC=CC=C%11)C%12=CC=CC=C%12)S5)S4)S3)=C%13)=C%13S2)SC(C(C=C%14)=CC=C%14N(C%15=CC=CC=C%15)C%16=CC=CC=C%16)=C1,SM1,,,0.91,7.53,0.552,3.78,"	Kan Y, et al. Solution-processed small molecules with ethynylene bridges for highly efficient organic solar cells. Journal of Materials Chemistry A 4, 14720-14728 (2016)."
2779,O=C1N(CC(CC)CCCC)C(C2=CC=C(C3=CC4=C(C(C5=CC=C(CC(CC)CCCC)S5)=C6C(SC(C7=CC=C(C(N8CC(CC)CCCC)=C9C(C8=O)=C(C%10=CC=C(C%11=CC=C(N%12C%13=CC=CC=C%13C%14=C%12C=CC=C%14)C=C%11)S%10)N(CC(CC)CCCC)C9=O)S7)=C6)=C4C%15=CC=C(CC(CC)CCCC)S%15)S3)S2)=C%16C1=C(C%17=CC=C(C%18=CC=C(N%19C%20=CC=CC=C%20C%21=C%19C=CC=C%21)C=C%18)S%17)N(CC(CC)CCCC)C%16=O,SM-Cz,,,0.76,6.14,0.54,2.5,"	Kudrjasova J, et al. A direct arylation approach towards efficient small molecule organic solar cells. Journal of Materials Chemistry A 4, 791-795 (2016)."
2780,FC1=CC(C2=CC(CCCCCC)=C(S2)C(S3)=CC4=C3C=C(S4)C5=C(CCCCCC)C=C(S5)C(C=C6)=CC=C6N(C7=CC=CC=C7)C8=CC=CC=C8)=C9N=C(C(C%10=CC=CC=C%10)=NC9=C1C%11=CC(CCCCCC)=C(S%11)C(S%12)=CC%13=C%12C=C(S%13)C%14=C(CCCCCC)C=C(S%14)C(C=C%15)=CC=C%15N(C%16=CC=CC=C%16)C%17=CC=CC=C%17)C%18=CC=CC=C%18,SM2,,,0.846,13.33,0.548,6.26,"	Jiang B, Yao J, Zhan C. Modulating PCBM-Acceptor Crystallinity and Organic Solar Cell Performance by Judiciously Designing Small-Molecule Mainchain End-Capping Units. Acs Applied Materials & Interfaces 8, 26058-26065 (2016)."
2781,O=C(N1CC(CCCCCC)CCCCCCCC)/C(C2=C1C=C(C3=CC(CCCCCC)=C(S3)C(S4)=CC5=C4C=C(S5)C6=C(CCCCCC)C=C(S6)C(C=C7)=CC=C7N(C8=CC=CC=C8)C9=CC=CC=C9)C=C2)=C(C(N%10CC(CCCCCC)CCCCCCCC)=O)\C%11=C%10C=C(C%12=CC(CCCCCC)=C(S%12)C(S%13)=CC%14=C%13C=C(S%14)C%15=C(CCCCCC)C=C(S%15)C(C=C%16)=CC=C%16N(C%17=CC=CC=C%17)C%18=CC=CC=C%18)C=C%11,SM3,,,0.84,10.18,0.57,4.9,"	Kudrjasova J, et al. A direct arylation approach towards efficient small molecule organic solar cells. Journal of Materials Chemistry A 4, 791-795 (2016)."
2782,O=C1N(CC(CC)CCCC)C(C2=CC=CS2)=C3C1=C(C4=CC=C(C(S5)=CC6=C5C(C7=CC=C(SCCCCCCCC)S7)=C8C(SC(C9=CC=C(S9)C%10=C%11C(C(N%10CC(CC)CCCC)=O)=C(C%12=CC=CS%12)N(CC(CC)CCCC)C%11=O)=C8)=C6C%13=CC=C(SCCCCCCCC)S%13)S4)N(CC(CC)CCCC)C3=O,BDTS-2DPP,,,0.84,7.04,0.35,2.11,"	Kudrjasova J, et al. A direct arylation approach towards efficient small molecule organic solar cells. Journal of Materials Chemistry A 4, 791-795 (2016)."
2783,CCCCCCCCC1=CC=C(S1)C2=CC3=C(S2)C(SC(C4=CC=C(CCCCCCCC)S4)=C5)=C5C6=NC7=C(N=C63)C(C8=CC=C(CCCCCCCC)S8)=C9C(N=C%10C(C%11=C(SC(C%12=CC=C(CCCCCCCC)S%12)=C%11)C%13=C%10C=C(C%14=CC=C(CCCCCCCC)S%14)S%13)=N9)=C7C%15=CC=C(CCCCCCCC)S%15,B2AT,,,0.94,10.87,0.59,6.03,"	Lin Y, et al. Efficient fullerene-free organic solar cells based on fused-ring oligomer molecules. Journal of Materials Chemistry A 4, 1486-1494 (2016)."
2784,CCCCCCCCC1=CC=C(C2=CC=C(S2)C3=C4C(N=C5C(C6=C(SC(C7=CC=C(C8=CC=C(CCCCCCCC)S8)S7)=C6)C9=C5C=C(C%10=CC=C(C%11=CC=C(CCCCCCCC)S%11)S%10)S9)=N4)=C(C%12=CC=C(C%13=CC=C(CCCCCCCC)S%13)S%12)C%14=C3N=C%15C(C%16=C(SC(C%17=CC=C(C%18=CC=C(CCCCCCCC)S%18)S%17)=C%16)C%19=C%15C=C(C%20=CC=C(C%21=CC=C(CCCCCCCC)S%21)S%20)S%19)=N%14)S1,B2A2T,,,1.02,8.43,0.56,4.82,"	Zhang Y, Shi J, He X, Tu G. All-thiophene-substituted N-heteroacene electron-donor materials for efficient organic solar cells. Journal of Materials Chemistry A 4, 13519-13524 (2016)."
2785,O=C1/C(C(C(N1CC(CC)CCCC)=C2)=CC=C2C3=CC=C(/C=C/C4=CC=C(N(C5=CC=CC=C5)C6=CC=CC=C6)C=C4)C=C3)=C7C(C(N(CC(CC)CCCC)C\7=O)=C8)=CC=C8C9=CC=C(/C=C/C%10=CC=C(N(C%11=CC=CC=C%11)C%12=CC=CC=C%12)C=C%10)C=C9,(TDAEB)2iI,,,1,10.17,0.53,5.39,"	Zhang Y, Shi J, He X, Tu G. All-thiophene-substituted N-heteroacene electron-donor materials for efficient organic solar cells. Journal of Materials Chemistry A 4, 13519-13524 (2016)."
2786,O=C1/C(C(C(N1CC(CC)CCCC)=C2)=CC=C2C3=CC=C(/C(C#N)=C/C4=CC=C(N(C5=CC=CC=C5)C6=CC=CC=C6)C=C4)C=C3)=C7C(C(N(CC(CC)CCCC)C\7=O)=C8)=CC=C8C9=CC=C(/C(C#N)=C/C%10=CC=C(N(C%11=CC=CC=C%11)C%12=CC=CC=C%12)C=C%10)C=C9,(TDACB)2iI,,,0.99,7.98,0.33,2.63,"	He K, Zhang X, Ren S, Sun J. Identity Mappings in Deep Residual Networks.  (ed^(eds). Springer International Publishing (2016)."
2787,CCCCC(CC)CCOC1=C(OCCC(CC)CCCC)C(C2=CC=C(C3=CC=C(C4=C5C(C(N4CCC(CC)CCCC)=O)=C(C6=CC=C(C7=CC8=C(C(C=CC=C9)=C9C=C8)C=C7)S6)N(CCC(CC)CCCC)C5=O)S3)S2)=C%10C=C(SC(C%11=CC=C(C%12=C%13C(C(N%12CCC(CC)CCCC)=O)=C(C%14=CC=C(C%15=CC%16=C(C(C=CC=C%17)=C%17C=C%16)C=C%15)S%14)N(CCC(CC)CCCC)C%13=O)S%11)=C%18)C%18=CC%10=C1C%19=CC=C(C%20=CC=C(C%21=C%22C(C(N%21CCC(CC)CCCC)=O)=C(C%23=CC=C(C%24=CC%25=C(C(C=CC=C%26)=C%26C=C%25)C=C%24)S%23)N(CCC(CC)CCCC)C%22=O)S%20)S%19,DTNT(DPP©\PN)3,,,1.06,9.46,0.35,3.57,"	He K, Zhang X, Ren S, Sun J. Identity Mappings in Deep Residual Networks.  (ed^(eds). Springer International Publishing (2016)."
2788,CCCCC(CC)CCOC1=C(OCCC(CC)CCCC)C(C2=CC=C(C3=CC=C(C4=C5C(C(N4CCC(CC)CCCC)=O)=C(C6=CC=CS6)N(CCC(CC)CCCC)C5=O)S3)S2)=C7C=C(SC(C8=CC=C(C9=C%10C(C(N9CCC(CC)CCCC)=O)=C(C%11=CC=CS%11)N(CCC(CC)CCCC)C%10=O)S8)=C%12)C%12=CC7=C1C%13=CC=C(C%14=CC=C(C%15=C%16C(C(N%15CCC(CC)CCCC)=O)=C(C%17=CC=CS%17)N(CCC(CC)CCCC)C%16=O)S%14)S%13,DTNT©\3DPP,,,0.74,9.52,0.523,3.69,"	Tan H, et al. Two T-Shaped Donor-Acceptor Small Molecules Based on 4,9-Di(thiophen-2-yl)naphtho 2,3-b thiophene for Solution-Processed Organic Solar Cells. European Journal of Organic Chemistry, 5127-5135 (2016)."
2789,CC(S1)=CC=C1C2=C(C=CC=C3)C3=C4N=C5N([B@]6(C7=CC=CC=C7C8=C6C=CC=C8)N42)C(C9=CC=C(C)S9)=C%10C=CC=CC5%10,2c,,,0.92,8.93,0.421,3.47,"	Tan H, et al. Two T-Shaped Donor-Acceptor Small Molecules Based on 4,9-Di(thiophen-2-yl)naphtho 2,3-b thiophene for Solution-Processed Organic Solar Cells. European Journal of Organic Chemistry, 5127-5135 (2016)."
2790,CCCCCCCCC(CCCCCCCC)N1C2=CC(C3=CC=C(C4=CC=C(C5=CC=C(C6=C7C=CC=C6)C(N7CCCCCCCC)=C5)S4)C8=NSN=C38)=CC=C2C9=C1C=C(C%10=CC=C(C%11=CC=C(C%12=CC=C(C%13=C%14C=CC=C%13)C(N%14CCCCCCCC)=C%12)S%11)C%15=NSN=C%10%15)C=C9,Cz(BT-T-3Cz)2,,,0.61,8.5,0.51,2.6,"	Lorenz-Rothe M, et al. From Fluorine to FluoreneA Route to Thermally Stable aza-BODIPYs for Organic Solar Cell Application. Advanced Electronic Materials 2,  (2016)."
2791,CCCCCCCCN1C2=CC(C(S3)=CC=C3C4=CC=C(C(C=C5)=CC=C5N(C6=CC=C(C7=CC=C(C8=CC=C(C9=CC=C(C%10=C%11C=CC=C%10)C(N%11CCCCCCCC)=C9)S8)C%12=NSN=C7%12)C=C6)C%13=CC=C(C%14=CC=C(C%15=CC=C(C%16=CC=C(C%17=C%18C=CC=C%17)C(N%18CCCCCCCC)=C%16)S%15)C%19=NSN=C%14%19)C=C%13)C%20=NSN=C4%20)=CC=C2C%21=C1C=CC=C%21,TPA(BT-T-3Cz)3,,,0.95,7.36,0.417,3,"	Dang D, Zhou P, Xiao M, Yang R, Zhu W. Synthesis of multi-armed small molecules with planar terminals and their application in organic solar cells. Dyes and Pigments 133, 1-8 (2016)."
2792,CCCCCCCCN1C2=CC(C(S3)=CC=C3C4=CC=C(C5=CC6=C(C7=CC=C(C8=CC=C(C9=CC=C(C%10=CC=C(C%11=C%12C=CC=C%11)C(N%12CCCCCCCC)=C%10)S9)C%13=NSN=C8%13)C=C7C6%14C%15=CC(C%16=CC=C(C%17=CC=C(C%18=CC=C(C%19=C%20C=CC=C%19)C(N%20CCCCCCCC)=C%18)S%17)C%21=NSN=C%16%21)=CC=C%15C%22=C%14C=C(C%23=CC=C(C%24=CC=C(C%25=CC=C(C%26=C%27C=CC=C%26)C(N%27CCCCCCCC)=C%25)S%24)C%28=NSN=C%23%28)C=C%22)C=C5)C%29=NSN=C4%29)=CC=C2C%30=C1C=CC=C%30,SF(BT-T-3Cz)4,,,0.94,10.66,0.528,5.25,"	Dang D, Zhou P, Xiao M, Yang R, Zhu W. Synthesis of multi-armed small molecules with planar terminals and their application in organic solar cells. Dyes and Pigments 133, 1-8 (2016)."
2793,CCCCC(CC)CN(C1=C2SC=C1)C(/C2=C(C3=C4C=C(C5=CC=C(C6=C/C(C(N6CCCCCC)=O)=C(C=C(C7=CC=C(C8=CC(N(CC(CC)CCCC)C(/C9=C(C%10=C%11C=CS%10)/C(N%11CC(CC)CCCC)=O)=O)=C9S8)C=C7)N%12CCCCCC)\C%12=O)C=C5)S3)/C(N4CC(CC)CCCC)=O)=O,DPPTTC6,,,0.94,8.7,0.52,4.37,"	Dang D, Zhou P, Xiao M, Yang R, Zhu W. Synthesis of multi-armed small molecules with planar terminals and their application in organic solar cells. Dyes and Pigments 133, 1-8 (2016)."
2794,CCCCC(CC)CN(C1=C2SC=C1)C(/C2=C(C3=C4C=C(C5=CC=C(C6=C/C(C(N6CCCCCCCC)=O)=C(C=C(C7=CC=C(C8=CC(N(CC(CC)CCCC)C(/C9=C(C%10=C%11C=CS%10)/C(N%11CC(CC)CCCC)=O)=O)=C9S8)C=C7)N%12CCCCCCCC)\C%12=O)C=C5)S3)/C(N4CC(CC)CCCC)=O)=O,DPPTTC8,,,0.68,4.57,0.34,1.06,"	Zhao Y, et al. Influence of the positions of thiophenes and side chains on diketopyrrolopyrrole based narrow band-gap small molecules for organic solar cells. Dyes and Pigments 133, 100-108 (2016)."
2795,CCCCC(CC)CN(C1=CC=CC=C1/C2=C(C3=C4C=CC(C5=CC=C(S5)C6=C/C(C(N6CCCCCCCC)=O)=C(C=C(C7=CC=C(S7)C8=CC=C(C9=C8)N(CC(CC)CCCC)C(/C9=C(C%10=CC=CC=C%10N%11CC(CC)CCCC)/C%11=O)=O)N%12CCCCCCCC)\C%12=O)=C3)\C(N4CC(CC)CCCC)=O)C2=O,IDPPTIC8,,,0.68,7.54,0.39,2.01,"	Zhao Y, et al. Influence of the positions of thiophenes and side chains on diketopyrrolopyrrole based narrow band-gap small molecules for organic solar cells. Dyes and Pigments 133, 100-108 (2016)."
2796,O=C1N(CC(CCCC)CC)C(C2=CC=C(C3=CC=CC=C3)S2)C4C1C(C5=CC=C(C6=CC=C(C7=C8C(F)=C(C(OCC(CCCC)CC)=O)SC8=C(C9=CC=C(C%10=CC=C(C%11N(CC(CCCC)CC)C(C%12C(C%13=CC=C(C%14=CC=CC=C%14)S%13)N(CC(CCCC)CC)C(C%12%11)=O)=O)S%10)S9)S7)S6)S5)N(CC(CCCC)CC)C4=O,TT(DPP)2,,,0.68,3.3,0.42,0.93,"	Zhao Y, et al. Influence of the positions of thiophenes and side chains on diketopyrrolopyrrole based narrow band-gap small molecules for organic solar cells. Dyes and Pigments 133, 100-108 (2016)."
2797,CCCCC(CC)CN(C1=CC=CC=C1/C2=C(C3=C4C=CC(C5=CC=C(S5)C6=C/C(C(N6CC(CC)CCCC)=O)=C(C=C(C7=CC=C(S7)C8=CC=C(C9=C8)N(CC(CC)CCCC)C(/C9=C(C%10=CC=CC=C%10N%11CC(CC)CCCC)/C%11=O)=O)N%12CC(CC)CCCC)\C%12=O)=C3)\C(N4CC(CC)CCCC)=O)C2=O,IDPPTIEH,,,0.7,6.48,0.59,2.69,"	Ko EY, Choi S, Park GE, Lee DH, Cho MJ, Choi DH. Diketopyrrolopyrrole-based conjugated small molecules bearing two different acceptor moieties for organic solar cells. Synthetic Metals 221, 39-47 (2016)."
2798,CCC(CCCC)COC1=C(SC(C2=CC=C(C3=C4C(C(N3CC(CCCCCCCC)CCCCCC)=O)=C(C5=CC=C(C6=CC=CC=C6)S5)N(CC(CCCCCCCC)CCCCCC)C4=O)S2)=C7)C7=C(OCC(CCCC)CC)C8=C1C=C(C9=CC=C(C%10=C%11C(C(N%10CC(CCCCCCCC)CCCCCC)=O)=C(C%12=CC=C(C%13=CC=CC=C%13)S%12)N(CC(CCCCCCCC)CCCCCC)C%11=O)S9)S8,BDT(DPP)2,,,0.76,4.74,0.36,1.32,"	Zhao Y, et al. Influence of the positions of thiophenes and side chains on diketopyrrolopyrrole based narrow band-gap small molecules for organic solar cells. Dyes and Pigments 133, 100-108 (2016)."
2799,CCC(CC1=CC=C(S1)C2=C(SC(C3=CC=C(C4=C5C(C(N4CC(CCCCCCCC)CCCCCC)=O)=C(C6=CC=C(C7=CC=CC=C7)S6)N(CC(CCCCCCCC)CCCCCC)C5=O)S3)=C8)C8=C(C9=CC=C(CC(CCCC)CC)S9)C%10=C2C=C(C%11=CC=C(C%12=C%13C(C(N%12CC(CCCCCCCC)CCCCCC)=O)=C(C%14=CC=C(C%15=CC=CC=C%15)S%14)N(CC(CCCCCCCC)CCCCCC)C%13=O)S%11)S%10)CCCC,BDTT(DPP)2,,,0.81,3.2,0.492,1.26,"	Tao Q, et al. D(A-A ')(2) architecture: An efficient strategy to improve photovoltaic performance of small molecules for solution-processed organic solar cells. Dyes and Pigments 133, 153-160 (2016)."
2800,O=C1N(CC(CCCCCCCC)CCCCCC)C(C2=CC=C(C3=CC=C(C4=C5C(C(N(CCCCCCCC)C5=O)=O)=C(C6=CC=C(C(S7)=CC8=C7C(CC(CCCC)CC)=C9C(SC(C%10=CC=C(S%10)C%11=C(C(N(CCCCCCCC)C%12=O)=O)C%12=C(C%13=CC=C(C%14=CC=C(C%15=C%16C(C(N%15CC(CCCCCCCC)CCCCCC)=O)=C(C%17=CC=C(C%18=CC=CC=C%18)S%17)N(CC(CCCCCCCC)CCCCCC)C%16=O)S%14)S%13)S%11)=C9)=C8CC(CCCC)CC)S6)S4)S3)S2)=C%19C1=C(C%20=CC=C(C%21=CC=CC=C%21)S%20)N(CC(CCCCCCCC)CCCCCC)C%19=O,BDT(TPD-DPP)2,,,0.78,2.83,0.349,0.77,"	Tao Q, et al. D(A-A ')(2) architecture: An efficient strategy to improve photovoltaic performance of small molecules for solution-processed organic solar cells. Dyes and Pigments 133, 153-160 (2016)."
2801,CCC(CC1=CC=C(S1)C2=C(SC(C3=CC=C(S3)C4=C(C(N(CCCCCCCC)C5=O)=O)C5=C(C6=CC=C(C7=CC=C(C8=C9C(C(N8CC(CCCCCCCC)CCCCCC)=O)=C(C%10=CC=C(C%11=CC=CC=C%11)S%10)N(CC(CCCCCCCC)CCCCCC)C9=O)S7)S6)S4)=C%12)C%12=C(C%13=CC=C(CC(CCCC)CC)S%13)C%14=C2C=C(C%15=CC=C(S%15)C%16=C(C(N(CCCCCCCC)C%17=O)=O)C%17=C(C%18=CC=C(C%19=CC=C(C%20=C%21C(C(N%20CC(CCCCCCCC)CCCCCC)=O)=C(C%22=CC=C(C%23=CC=CC=C%23)S%22)N(CC(CCCCCCCC)CCCCCC)C%21=O)S%19)S%18)S%16)S%14)CCCC,BDTT(TPD-DPP)2,,,0.78,5.69,0.545,2.41,"	Tao Q, et al. D(A-A ')(2) architecture: An efficient strategy to improve photovoltaic performance of small molecules for solution-processed organic solar cells. Dyes and Pigments 133, 153-160 (2016)."
2802,O=C1N(C(CCCCCC)C)C(C2=CC=CS2)=C3C1=C(C4=CC=C(C5=C(CCCCCCCCCCCCCCC)C(SC6=C7SC8=C6SC(C9=CC=C(S9)C%10=C%11C(C(N%10C(CCCCCC)C)=O)=C(C%12=CC=CS%12)N(C(C)CCCCCC)C%11=O)=C8CCCCCCCCCCCCCCC)=C7S5)S4)N(C(C)CCCCCC)C3=O,1,,,0.77,10.83,0.509,4.25,"	Tao Q, et al. D(A-A ')(2) architecture: An efficient strategy to improve photovoltaic performance of small molecules for solution-processed organic solar cells. Dyes and Pigments 133, 153-160 (2016)."
2803,O=C1N(C(CCCCCCCCCCCCCCCCCCCCCC)C)C(C2=CC=CS2)=C3C1=C(C4=CC=C(C5=C(CCCCCCCCCCCCCCC)C(SC6=C7SC8=C6SC(C9=CC=C(S9)C%10=C%11C(C(N%10C(CCCCCCCCCCCCCCCCCCCCCC)C)=O)=C(C%12=CC=CS%12)N(C(C)CCCCCCCCCCCCCCCCCCCCCC)C%11=O)=C8CCCCCCCCCCCCCCC)=C7S5)S4)N(C(C)CCCCCCCCCCCCCCCCCCCCCC)C3=O,2,,,0.7,7.7,0.503,2.7,"	Vegiraju S, et al. Synthesis and characterization of solution-processable diketopyrrolopyrrole (DPP) and tetrathienothiophene (TTA)-based small molecules for organic thin film transistors and organic photovoltaic cells. Dyes and Pigments 133, 280-291 (2016)."
2804,O=C1N(C(C2=CC=C(C3=CC=C(C4=C(CCCCCCCCCCCCCCC)C(S5)=C(C(S6)=C5C7=C6C(CCCCCCCCCCCCCCC)=C(C8=CC=C(C9=CC=C(C%10=C%11C(C(N%10CC(CC)CCCC)=O)=C(C%12=CC=CS%12)N(CC(CC)CCCC)C%11=O)S9)S8)S7)S4)S3)S2)=C%13C1=C(C%14=CC=CS%14)N(CC(CC)CCCC)C%13=O)CC(CC)CCCC,3,,,0.76,1.8,0.584,0.8,"	Vegiraju S, et al. Synthesis and characterization of solution-processable diketopyrrolopyrrole (DPP) and tetrathienothiophene (TTA)-based small molecules for organic thin film transistors and organic photovoltaic cells. Dyes and Pigments 133, 280-291 (2016)."
2805,CCCCCCCCCCCCCCCC1=C(C2=CC=C(C3=CC=C(C4=CC=C(C5=C6C(C(N5CC(CC)CCCC)=O)=C(C7=CC=CS7)N(CC(CC)CCCC)C6=O)S4)S3)S2)SC8=C1SC9=C8SC%10=C9SC(C%11=CC=C(C%12=CC=C(C%13=CC=C(C%14=C%15C(C(N%14CC(CC)CCCC)=O)=C(C%16=CC=CS%16)N(CC(CC)CCCC)C%15=O)S%13)S%12)S%11)=C%10CCCCCCCCCCCCCCC,4,,,0.7,5.1,0.518,1.8,"	Vegiraju S, et al. Synthesis and characterization of solution-processable diketopyrrolopyrrole (DPP) and tetrathienothiophene (TTA)-based small molecules for organic thin film transistors and organic photovoltaic cells. Dyes and Pigments 133, 280-291 (2016)."
2806,CCCCCCCCCCCCCCCC1=C(C2=CC=C(C3=C4C(C(N3CC(CC)CCCC)=O)=C(C5=CC=C(C6=CC=C(CC(CC)CCCC)S6)S5)N(CC(CC)CCCC)C4=O)S2)SC7=C1SC8=C7SC9=C8SC(C%10=CC=C(C%11=C%12C(C(N%11CC(CC)CCCC)=O)=C(C%13=CC=C(C%14=CC=C(CC(CC)CCCC)S%14)S%13)N(CC(CC)CCCC)C%12=O)S%10)=C9CCCCCCCCCCCCCCC,5,,,0.63,3.6,0.387,0.9,"	Vegiraju S, et al. Synthesis and characterization of solution-processable diketopyrrolopyrrole (DPP) and tetrathienothiophene (TTA)-based small molecules for organic thin film transistors and organic photovoltaic cells. Dyes and Pigments 133, 280-291 (2016)."
2807,O=C(N(CC)/C(S/1)=C(C#N)\C#N)C1=C\C2=CC(CCCCCCCC)=C(C3=CC(CCCCCCCC)=C(C4=CC(F)=C(C5=C(F)C=C(C6=C(CCCCCCCC)C=C(C7=C(CCCCCCCC)C=C(/C=C8C(N(CC)/C(S/8)=C(C#N)/C#N)=O)S7)S6)S5)S4)S3)S2,DRCN6T-F,,,0.6,1.5,0.597,0.5,"	Vegiraju S, et al. Synthesis and characterization of solution-processable diketopyrrolopyrrole (DPP) and tetrathienothiophene (TTA)-based small molecules for organic thin film transistors and organic photovoltaic cells. Dyes and Pigments 133, 280-291 (2016)."
2808,CCCCC(CC)COC1=C(SC(C2=C(CCCCCC)C=C(C3=NN=C(C4=CC(CCCCCC)=C(C5=CC=C(CCCCCC)S5)C4)N=N3)S2)=C6)C6=C(OCC(CC)CCCC)C7=C1C=C(C8=C(CCCCCC)C=C(C9=NN=C(C%10=CC(CCCCCC)=C(C%11=CC=C(CCCCCC)S%11)S%10)N=N9)S8)S7,BDT(TTzT)2,,,0.94,4.19,0.57,2.26,"	Kan B, et al. Oligothiophene-based small molecules with 3,3 '-difluoro-2,2 '-bithiophene central unit for solution-processed organic solar cells. Organic Electronics 38, 172-179 (2016)."
2809,CCCCC(CC)COC1=C(SC(C2=C(CCCCCC)C=C(C3=CC(CCCCCC)=C(C4=NN=C(C5=CC(CCCCCC)=C(C6=CC=C(CCCCCC)S6)S5)N=N4)S3)S2)=C7)C7=C(OCC(CC)CCCC)C8=C1C=C(C9=C(CCCCCC)C=C(C%10=CC(CCCCCC)=C(C%11=NN=C(C%12=CC(CCCCCC)=C(C%13=CC=C(CCCCCC)S%13)S%12)N=N%11)S%10)S9)S8,BDT(2TTzT)2,,,0.98,9.56,0.535,5.01,"	Ma P, et al. Small molecules based on tetrazine unit for efficient performance solution-processed organic solar cells. Solar Energy Materials and Solar Cells 155, 30-37 (2016)."
2810,N#C/C(C1=C(OCCCCCCCC)C=C(/C(C#N)=C/C2=CC=C(S2)C(C=C3)=CC=C3N(C4=CC=CC=C4)C5=CC=CC=C5)C(OCCCCCCCC)=C1)=C\C6=CC=C(S6)C(C=C7)=CC=C7N(C8=CC=CC=C8)C9=CC=CC=C9,ZOPTAN-TPA,,,0.88,10.55,0.572,5.29,"	Ma P, et al. Small molecules based on tetrazine unit for efficient performance solution-processed organic solar cells. Solar Energy Materials and Solar Cells 155, 30-37 (2016)."
2811,O=C1N(CC(OCC)=O)C(C2=CC=C(/C=C/C3=CC=C(N(C4=CC=CC=C4)C5=CC=CC=C5)C=C3)C=C2)=C6C1=C(C7=CC=CC=C7)N(CC(OCC)=O)C6=O,DPP 1,,,0.92,3.87,0.3,1.07,"	Iqbal J, et al. An arylene-vinylene based donor-acceptor-donor small molecule for the donor compound in high-voltage organic solar cells. Solar Energy Materials and Solar Cells 155, 348-355 (2016)."
2812,O=C1N(CC(OCC)=O)C(C2=CC=C(/C=C/C3=CC=C(N(C4=CC=CC=C4)C5=CC=CC=C5)C=C3)C=C2)=C6C1=C(C7=CC=C(/C=C/C8=CC=C(N(C9=CC=CC=C9)C%10=CC=CC=C%10)C=C8)C=C7)N(CC(OCC)=O)C6=O,DPP 2,,,0.67,4.5,0.28,0.86,"	Honova J, et al. Thiophene-free diphenyl-amino-stilbene-diketo-pyrrolo-pyrrole derivatives as donors for organic bulk heterojunction solar cells. Chemical Papers 70, 1416-1424 (2016)."
2813,CCCCCCCCC1=C(C2=CC(CCCCCCCC)=C(C3=CC(CCCCCCCC)=C(C4=CC(F)=C(C5=C(F)C=C(C6=C(CCCCCCCC)C=C(C7=C(CCCCCCCC)C=C(C8=C(CCCCCCCC)C=C(/C=C9C(N(CC)/C(S/9)=C(C#N)/C#N)=O)S8)S7)S6)S5)S4)S3)S2)SC(/C=C%10C(N(CC)/C(S/%10)=C(C#N)\C#N)=O)=C1,DRCN8T-F,,,0.68,6.8,0.33,1.53,"	Honova J, et al. Thiophene-free diphenyl-amino-stilbene-diketo-pyrrolo-pyrrole derivatives as donors for organic bulk heterojunction solar cells. Chemical Papers 70, 1416-1424 (2016)."
2814,O=C1N(CC(OCC(CCCC)CC)=O)C(C2=CC=C(/C=C/C3=CC=C(N(C4=CC=CC=C4)C5=CC=CC=C5)C=C3)C=C2)=C6C1=C(C7=CC=CC=C7)N(CC(OCC(CCCC)CC)=O)C6=O,DPP 3,,,0.9,8.8,0.64,5.07,"	Kan B, et al. Oligothiophene-based small molecules with 3,3 '-difluoro-2,2 '-bithiophene central unit for solution-processed organic solar cells. Organic Electronics 38, 172-179 (2016)."
2815,O=C1N(CC(OCC(CCCC)CC)=O)C(C2=CC=C(/C=C/C3=CC=C(N(C4=CC=CC=C4)C5=CC=CC=C5)C=C3)C=C2)=C6C1=C(C7=CC=C(/C=C/C8=CC=C(N(C9=CC=CC=C9)C%10=CC=CC=C%10)C=C8)C=C7)N(CC(OCC(CCCC)CC)=O)C6=O,DPP 4,,,0.54,2.3,0.26,0.32,"	Honova J, et al. Thiophene-free diphenyl-amino-stilbene-diketo-pyrrolo-pyrrole derivatives as donors for organic bulk heterojunction solar cells. Chemical Papers 70, 1416-1424 (2016)."
2816,O=C1N(C(CCCC)CC)C(C2=CC=C(S2)C(S3)=CC(C3=C4C5=CC=C(C(CCCC)CC)S5)=C(C6=CC=C(C(CCCC)CC)S6)C7=C4C=C(C8=CC=C(C9=C%10C(C(N9C(CCCC)CC)=O)=C(C%11=CC=C(C%12=CC=C(F)C=C%12)S%11)N(C(CCCC)CC)C%10=O)S8)S7)=C%13C1=C(C%14=CC=C(C%15=CC=C(F)C=C%15)S%14)N(C(CCCC)CC)C%13=O,1,,,0.75,6.3,31.3,1.49,"	Honova J, et al. Thiophene-free diphenyl-amino-stilbene-diketo-pyrrolo-pyrrole derivatives as donors for organic bulk heterojunction solar cells. Chemical Papers 70, 1416-1424 (2016)."
2817,O=C1N(C(CCCC)CC)C(C2=CC=C(S2)C(S3)=CC(C3=C4C5=CC=C(C(CCCC)CC)S5)=C(C6=CC=C(C(CCCC)CC)S6)C7=C4C=C(C8=CC=C(C9=C%10C(C(N9C(CCCC)CC)=O)=C(C%11=CC=C(C%12=CC=C(C(F)(F)F)C=C%12)S%11)N(C(CCCC)CC)C%10=O)S8)S7)=C%13C1=C(C%14=CC=C(C%15=CC=C(C(F)(F)F)C=C%15)S%14)N(C(CCCC)CC)C%13=O,2,,,0.76,10.1,0.52,4,"	Furukawa S, Komiyama H, Yasuda T. Controlling Open-Circuit Voltage in Organic Solar Cells by Terminal Fluoro-Functionalization of Narrow-Bandgap pi-Conjugated Molecules. Journal of Physical Chemistry C 120, 21235-21241 (2016)."
2818,O=C1N(C(CCCC)CC)C(C2=CC=C(S2)C(S3)=CC(C3=C4C5=CC=C(C(CCCC)CC)S5)=C(C6=CC=C(C(CCCC)CC)S6)C7=C4C=C(C8=CC=C(C9=C%10C(C(N9C(CCCC)CC)=O)=C(C%11=CC=C(C%12=CC(F)=CC(F)=C%12)S%11)N(C(CCCC)CC)C%10=O)S8)S7)=C%13C1=C(C%14=CC=C(C%15=CC(F)=CC(F)=C%15)S%14)N(C(CCCC)CC)C%13=O,3,,,0.83,6.1,0.54,2.8,"	Furukawa S, Komiyama H, Yasuda T. Controlling Open-Circuit Voltage in Organic Solar Cells by Terminal Fluoro-Functionalization of Narrow-Bandgap pi-Conjugated Molecules. Journal of Physical Chemistry C 120, 21235-21241 (2016)."
2819,O=C1N(C(CCCC)CC)C(C2=CC=C(S2)C(S3)=CC(C3=C4C5=CC=C(C(CCCC)CC)S5)=C(C6=CC=C(C(CCCC)CC)S6)C7=C4C=C(C8=CC=C(C9=C%10C(C(N9C(CCCC)CC)=O)=C(C%11=CC=C(C%12=CC(C(F)(F)F)=CC(C(F)(F)F)=C%12)S%11)N(C(CCCC)CC)C%10=O)S8)S7)=C%13C1=C(C%14=CC=C(C%15=CC(C(F)(F)F)=CC(C(F)(F)F)=C%15)S%14)N(C(CCCC)CC)C%13=O,4,,,0.85,8.3,0.6,4.2,"	Furukawa S, Komiyama H, Yasuda T. Controlling Open-Circuit Voltage in Organic Solar Cells by Terminal Fluoro-Functionalization of Narrow-Bandgap pi-Conjugated Molecules. Journal of Physical Chemistry C 120, 21235-21241 (2016)."
2820,O=C1N(CCCCCCCCCC)C(C2=CC=CS2)=C3C1=C(C4=CC=C(C#CC5=CC=C(N6C7=CC=CC=C7C8=C6C=CC=C8)C=C5)S4)N(CCCCCCCCCC)C3=O,DPP5,,,0.94,2.5,0.45,1.1,"	Furukawa S, Komiyama H, Yasuda T. Controlling Open-Circuit Voltage in Organic Solar Cells by Terminal Fluoro-Functionalization of Narrow-Bandgap pi-Conjugated Molecules. Journal of Physical Chemistry C 120, 21235-21241 (2016)."
2821,O=C1N(CCCCCCCCCC)C(C2=CC=C(C#CC3=CC=C(N4C5=CC=CC=C5C6=C4C=CC=C6)C=C3)S2)=C7C1=C(C8=CC=C(C#CC9=CC=C(N%10C%11=CC=CC=C%11C%12=C%10C=CC=C%12)C=C9)S8)N(CCCCCCCCCC)C7=O,DPP6,,,0.98,8.19,0.58,4.65,"	Patil Y, Misra R, Chen FC, Sharma GD. Small molecule based N-phenyl carbazole substituted diketopyrrolopyrroles as donors for solution-processed bulk heterojunction organic solar cells. Physical Chemistry Chemical Physics 18, 22999-23005 (2016)."
2822,CCCCCCC(CC)CC1=CC=C(S1)C2=C(C3=C(S4)C=C(C5=CC=C(C6=C7C(C(N6CC(CC)CCCCCC)=O)=C(C8=CC=CS8)N(CC(CC)CCCCCC)C7=O)S5)S3)C4=C(C9=CC=C(CC(CC)CCCCCC)S9)C%10=C2SC%11=C%10SC(C%12=CC=C(C%13=C%14C(C(N%13CC(CC)CCCCCC)=O)=C(C%15=CC=CS%15)N(CC(CC)CCCCCC)C%14=O)S%12)=C%11,DT-BDT,,,0.98,9.58,0.61,5.73,"	Patil Y, Misra R, Chen FC, Sharma GD. Small molecule based N-phenyl carbazole substituted diketopyrrolopyrroles as donors for solution-processed bulk heterojunction organic solar cells. Physical Chemistry Chemical Physics 18, 22999-23005 (2016)."
2823,CCCCCCC(CC)CC1=CC=C(S1)C2=C(C=C3C4=CC=C(C5=C6C(C(N5CC(CC)CCCCCC)=O)=C(C7=CC=CS7)N(CC(CC)CCCCCC)C6=O)S4)C(S3)=C(C8=CC=C(CC(CC)CCCCCC)S8)C9=C2SC(C%10=CC=C(C%11=C%12C(C(N%11CC(CC)CCCCCC)=O)=C(C%13=CC=CS%13)N(CC(CC)CCCCCC)C%12=O)S%10)=C9,2T-BDT,,,0.848,9.76,0.48,3.98,"	Zhang X, Yao J, Zhan C. Boosting Organic Solar Cell Electrical Performance by Introducing Large Aromatics onto Small-Molecule Peripheral Side-Chains. Advanced Materials Interfaces 3,  (2016)."
2824,O=C1N(CC(CC)CCCCCC)C(C2=CC=CS2)=C(C(N3CC(CC)CCCCCC)=O)C1=C3C4=CC=C(S4)C5=CC6=C(C7=CC=C(C8=CSC(CC(CC)CCCCCC)=C8)S7)C9=C(C=C(C%10=CC=C(C%11=C%12C(C(N%11CC(CC)CCCCCC)=O)=C(C%13=CC=CS%13)N(CC(CC)CCCCCC)C%12=O)S%10)S9)C(C%14=CC=C(C%15=CSC(CC(CC)CCCCCC)=C%15)S%14)=C6S5,4T-BDT,,,0.837,11,0.558,5.15,"	Zhang X, Yao J, Zhan C. Boosting Organic Solar Cell Electrical Performance by Introducing Large Aromatics onto Small-Molecule Peripheral Side-Chains. Advanced Materials Interfaces 3,  (2016)."
2825,CC1=CC=C(C2=C(C3=CSC(C)=C3)SC(/C=C/C4=CC(C5=CC=C(C)S5)=C(C6=CSC(C)=C6)S4)=C2)S1,BSTV,,,0.799,12.17,0.621,6.04,"	Zhang X, Yao J, Zhan C. Boosting Organic Solar Cell Electrical Performance by Introducing Large Aromatics onto Small-Molecule Peripheral Side-Chains. Advanced Materials Interfaces 3,  (2016)."
2826,CC1=CC=C(C2=C(C3=CSC(C)=C3)SC(C4=CC=C(S4)/C=C/C5=CC=C(C6=CC(C7=CC=C(C)S7)=C(C8=CSC(C)=C8)S6)S5)=C2)S1,BOTV,,,0.65,5.27,0.58,1.99,"	Martinez F, et al. Classical or inverted photovoltaic cells: On the importance of the morphology of the organic layers on their power conversion efficiency. Dyes and Pigments 132, 185-193 (2016)."
2827,FC1=C(C2=CC([Si]3(CC(CC)CCCC)CC(CC)CCCC)=C(C4=C3C=C(C5=C(F)C=C(C6=CC=C(C7=CC=C(C(N(CCCCCCCC)C8=O)=O)C8=C7)S6)C9=NSN=C59)S4)S2)C%10=NSN=C%10C(C%11=CC=C(C%12=CC=C(C(N(CCCCCCCC)C%13=O)=O)C%13=C%12)S%11)=C1,DTS(FBT-Th-Pht-Oct)2,,,0.57,6.88,0.54,2.12,"	Martinez F, et al. Classical or inverted photovoltaic cells: On the importance of the morphology of the organic layers on their power conversion efficiency. Dyes and Pigments 132, 185-193 (2016)."
2828,FC1=C(C2=CC([Si]3(CC(CC)CCCC)CC(CC)CCCC)=C(C4=C3C=C(C5=C(F)C=C(C6=CC=C(C7=CC=C(C(N(CCCCCC)C8=O)=O)C8=C7)S6)C9=NSN=C59)S4)S2)C%10=NSN=C%10C(C%11=CC=C(C%12=CC=C(C(N(CCCCCC)C%13=O)=O)C%13=C%12)S%11)=C1,DTS(FBT-Th-Pht-Hex)2,,,0.867,1.7,0.47,0.7,"	San Juan RR, Payne A-J, Welch GC, Eftaiha AaF. Development of low band gap molecular donors with phthalimide terminal groups for use in solution processed organic solar cells. Dyes and Pigments 132, 369-377 (2016)."
2829,FC1=C(C2=CC=C(C3=CC=C(CCCCCC)S3)S2)C4=NN(CCCCCC)N=C4C(C5=CC([Si]6(CC(CC)CCCC)CC(CC)CCCC)=C(C7=C6C=C(C8=CC(F)=C(C9=CC=C(C%10=CC=C(CCCCCC)S%10)S9)C%11=NN(CCCCCC)N=C8%11)S7)S5)=C1.CC,K2,,,0.734,1.12,0.29,0.24,"	San Juan RR, Payne A-J, Welch GC, Eftaiha AaF. Development of low band gap molecular donors with phthalimide terminal groups for use in solution processed organic solar cells. Dyes and Pigments 132, 369-377 (2016)."
2830,CCCCCCN1N=C2C(C3=CC=C(C4=CC=C(CCCCCC)S4)S3)=CC(F)=C(C5=CC([Si]6(CC(CC)CCCC)CC(CC)CCCC)=C(C7=C6C=C(C8=C(F)C=C(C9=CC=C(C%10=CC=C(CCCCCC)S%10)S9)C%11=NN(CCCCCC)N=C8%11)S7)S5)C2=N1.CC,K3,,,0.83,11.68,0.62,6.01,"	Keshtov ML, et al. Design, synthesis and photophysical properties of D1-A-D2-A-D1-type small molecules based on fluorobenzotriazole acceptor and dithienosilole core donor for solution processed organic solar cells. Dyes and Pigments 132, 387-397 (2016)."
2831,O=C1N(CC(CCCC)CC)C(C2=CC=C(C3=CC4=C(C5=CC=C(C6=CC=C(S6)C7=C8C(C(N7CC(CCCC)CC)=O)=C(C9=CC=CS9)N(CC(CCCC)CC)C8=O)C=C5C4%10C%11=CC=C(C%12=CC=C(S%12)C%13=C%14C(C(N%13CC(CCCC)CC)=O)=C(C%15=CC=CS%15)N(CC(CCCC)CC)C%14=O)C=C%11C%16=C%10C=CC(C%17=CC=C(S%17)C%18=C%19C(C(N%18CC(CCCC)CC)=O)=C(C%20=CC=CS%20)N(CC(CCCC)CC)C%19=O)=C%16)C=C3)S2)=C%21C1=C(C%22=CC=CS%22)N(CC(CCCC)CC)C%21=O,SF(DPP)4,,,0.8,10.24,0.58,4.75,"	Keshtov ML, et al. Design, synthesis and photophysical properties of D1-A-D2-A-D1-type small molecules based on fluorobenzotriazole acceptor and dithienosilole core donor for solution processed organic solar cells. Dyes and Pigments 132, 387-397 (2016)."
2832,CCCCC(CC)COC1=C2C(C=C(C3CCC(C4=CC=C(C5=CC=C(CCCCCC)C=C5)S4)C6=NSN=C63)S2)=C(OCC(CC)CCCC)C7=C1C=C(C8CCC(C9=CC=C(C%10=CC=C(CCCCCC)C=C%10)S9)C%11=NSN=C%118)S7,BDT(PTBT)2,,,0.95,9.12,42.9,3.72,"	Dang D, et al. Spirobifluorene-cored small molecules containing four diketopyrrolopyrrole arms for solution-processed organic solar cells. Journal of Materials Science 51, 8018-8026 (2016)."
2833,O=C1C(C(C(N2CC(CCCC)CCC)=O)=C(C3=CC=CS3)N1CC(CC)CCCC)=C2C4=CC=C(S4)C5=CC=C(/C(C(N6CCCCCC)=O)=C7C(N(CCCCCC)C8=C\7C=CC(C9=CC=C(C%10=C%11C(C(N%10CC(CCCC)CCC)=O)=C(C%12=CC=CS%12)N(CC(CC)CCCC)C%11=O)S9)=C8)=O)C6=C5,DPP-Ii-DPP,,,1.22,2.88,0.81,0.52,"	Bagde SS, Park H, Lee SM, Lee SH. Influence of the terminal donor on the performance of 4,8-dialkoxybenzo 1,2-b:4,5 ' dithiophene based small molecules for efficient solution-processed organic solar cells. New J. Chem. 40, 2063-2070 (2016)."
2834,O=C(N(CC(CCCCCC)CCCC)C1=CC(C2=CC=CS2)=CC=C1/3)C3=C/C=C4C(N(CC(CCCCCC)CCCC)C5=C\4C=CC(C6=CC=CS6)=C5)=O,EBI-T,,,5.86,11.75,10.67,0.58,"	Jung JW. A low band gap conjugated small molecule based on isoindigo flanked with diketopyrrolopyrrole for efficient organic solar cells. Dyes and Pigments 137, 512-517 (2017)."
2835,O=C(N(CC(CCCCCC)CCCC)C1=CC(C2=CC=C(C3=CC=CS3)S2)=CC=C1/4)C4=C/C=C5C(N(CC(CCCCCC)CCCC)C6=C\5C=CC(C7=CC=C(C8=CC=CS8)S7)=C6)=O,EBI-2T,,,0.18,0.82,0.73,0.3,"	Le Borgne M, Quinn J, Martin J, Stingelin N, Li YN, Wantz G. New 3,3 '-(ethane-1,2-diylidene)bis(indolin-2-one) (EBI)-based small molecule semiconductors for organic solar cells. J. Mater. Chem. C 5, 5143-5153 (2017)."
2836,O=C(N(CC(CCCCCC)CCCC)C1=CC(C2=CC(C=CC=C3)=C3O2)=CC=C1/4)C4=C/C=C5C(N(CC(CCCCCC)CCCC)C6=C\5C=CC(C7=CC(C=CC=C8)=C8O7)=C6)=O,EBI-BF-C16,,,1.65,5.51,0.87,0.34,"	Le Borgne M, Quinn J, Martin J, Stingelin N, Li YN, Wantz G. New 3,3 '-(ethane-1,2-diylidene)bis(indolin-2-one) (EBI)-based small molecule semiconductors for organic solar cells. J. Mater. Chem. C 5, 5143-5153 (2017)."
2837,O=C1N(CC(CC)CCCC)C(C2=CC=C(C3=CC4=C(C(OCC(CC)CCCC)=C(C=CS5)C5=C4OCC(CC)CCCC)S3)S2)=C(C6=O)C1=C(N6CC(CC)CCCC)C7=CC=CS7,aBDT,,,0.06,0.87,0.23,0.27,"	Le Borgne M, Quinn J, Martin J, Stingelin N, Li YN, Wantz G. New 3,3 '-(ethane-1,2-diylidene)bis(indolin-2-one) (EBI)-based small molecule semiconductors for organic solar cells. J. Mater. Chem. C 5, 5143-5153 (2017)."
2838,O=C1N(CC(CC)CCCC)C(C2=CC=C(C3=CC4=C(C(OCC(CC)CCCC)=C(C=C(C5=CC=C(S5)C(N6CC(CC)CCCC)=C(C(N7CC(CC)CCCC)=O)C(C6=O)=C7C8=CC=CS8)S9)C9=C4OCC(CC)CCCC)S3)S2)=C(C%10=O)C1=C(N%10CC(CC)CCCC)C%11=CC=CS%11,BDT,,,0.4,1.74,0.81,0.27,"	Loser S, et al. Systematic evaluation of structure-property relationships in heteroacene - diketopyrrolopyrrole molecular donors for organic solar cells. J. Mater. Chem. A 5, 9217-9232 (2017)."
2839,O=C1N(CC(CC)CCCC)C(C2=CC=C(C3=CC4=C(C(OCC(CC)CCCC)=C(C=C(C5=CC=C(S5)C(N6CC(CC)CCCC)=C(C(N7CC(CC)CCCC)=O)C(C6=O)=C7C8=CC=CS8)O9)C9=C4OCC(CC)CCCC)O3)S2)=C(C%10=O)C1=C(N%10CC(CC)CCCC)C%11=CC=CS%11,BDF,,,3.6,8.67,0.85,0.49,"	Loser S, et al. Systematic evaluation of structure-property relationships in heteroacene - diketopyrrolopyrrole molecular donors for organic solar cells. J. Mater. Chem. A 5, 9217-9232 (2017)."
2840,O=C1N(CC(CC)CCCC)C(C2=CC=C(C(S3)=CC(C3=C4OCC(CC)CCCC)=CC5=C4C=C(C=C(C6=CC=C(S6)C(N7CC(CC)CCCC)=C(C(N8CC(CC)CCCC)=O)C(C7=O)=C8C9=CC=CS9)S%10)C%10=C5OCC(CC)CCCC)S2)=C(C%11=O)C1=C(N%11CC(CC)CCCC)C%12=CC=CS%12,NDT,,,3.7,8.97,0.83,0.5,"	Loser S, et al. Systematic evaluation of structure-property relationships in heteroacene - diketopyrrolopyrrole molecular donors for organic solar cells. J. Mater. Chem. A 5, 9217-9232 (2017)."
2841,O=C1N(CC(CC)CCCC)C(C2=CC=C(C3=CC4=CC(OCC(CC)CCCC)=C(C5=C(C=C6OCC(CC)CCCC)C=C(C7=CC=C(S7)C(N8CC(CC)CCCC)=C(C(N9CC(CC)CCCC)=O)C(C8=O)=C9C%10=CC=CS%10)S5)C6=C4S3)S2)=C(C%11=O)C1=C(N%11CC(CC)CCCC)C%12=CC=CS%12,zNDT,,,4.1,11.27,0.84,0.43,"	Loser S, et al. Systematic evaluation of structure-property relationships in heteroacene - diketopyrrolopyrrole molecular donors for organic solar cells. J. Mater. Chem. A 5, 9217-9232 (2017)."
2842,O=C1C2=C(C3=CC=C(C4=CC(SC(C=CC=C5)=C5N6CC(CCCC)CC)=C6C=C4)S3)N(CC(CCCC)CC)C(C2=C(C7=CC=C(C8=CC(SC9=CC=CC=C9N%10CC(CCCC)CC)=C%10C=C8)S7)N1CC(CCCC)CC)=O,DPP1,,,4.4,11.69,0.76,0.5,"	Loser S, et al. Systematic evaluation of structure-property relationships in heteroacene - diketopyrrolopyrrole molecular donors for organic solar cells. J. Mater. Chem. A 5, 9217-9232 (2017)."
2843,O=C1C2=C(C3=NC=C(C4=CC(SC(C=CC=C5)=C5N6CC(CCCC)CC)=C6C=C4)S3)N(CC(CCCC)CC)C(C2=C(C7=NC=C(C8=CC(SC9=CC=CC=C9N%10CC(CCCC)CC)=C%10C=C8)S7)N1CC(CCCC)CC)=O,DPP2,,,0.71,2.9,0.84,0.29,"	Maglione C, et al. Novel low bandgap phenothiazine functionalized DPP derivatives prepared by direct heteroarylation: Application in bulk heterojunction organic solar cells. Dyes Pigment. 141, 169-178 (2017)."
2844,CCCCCCCCCCC(CCCCCCCCCCCC)CN1C(C2=CC=C(C3=CC=CS3)S2)=C4C(N(CC(CCCCCCCCCCCC)CCCCCCCCC)C(C(S5)=CC=C5C6=CC=C(C7=CC=C(C(N(CC(CCCCCCCCCC)CCCCCCCCCCCC)C8=O)=C9C8=C(C%10=CC=C(C%11=CC=C(C%12=CC=CS%12)C=C%11C)S%10)N(CC(CCCCCCCCCCCC)CCCCCCCCCC)C9=O)S7)C=C6)=C4C1=O)=O,P(DPP-B70T30),,,0.7,3.1,0.73,0.31,"	Maglione C, et al. Novel low bandgap phenothiazine functionalized DPP derivatives prepared by direct heteroarylation: Application in bulk heterojunction organic solar cells. Dyes Pigment. 141, 169-178 (2017)."
2845,O=C1C(C(C(N2CC(CC)CCCC)=O)=C(C3=CC=CS3)N1CC(CC)CCCC)=C2C(S4)=CC=C4C5=CC6=C(C7=CC=C(/C=C/C8=CC=C(CC(CC)CCCC)[Se]8)[Se]7)C(SC(C9=CC=C(C%10=C%11C(C(N%10CC(CC)CCCC)=O)=C(C%12=CC=CS%12)N(CC(CC)CCCC)C%11=O)S9)=C%13)=C%13C(C%14=CC=C(/C=C/C%15=CC=C(CC(CC)CCCC)[Se]%15)[Se]%14)=C6S5,SeBDT©\DPP,,,5.1,12.22,0.75,0.56,"	Park S, et al. Effect of vacuum treatment in diketopyrrolopyrrole (DPP) based copolymer with ratio controlled toluene- and benzene- functional groups for efficient organic photovoltaic cells: Morphological and electrical contribution. Org. Electron. 46, 183-191 (2017)."
2846,CC(C)(C)C(C=C1)=CC2=C1N(C3=C2C=C(C(C)(C)C)C=C3)C4=CC=C(N(C5=CC=C(C6=CC7=NSN=C7N=C6)C=C5)C8=CC=C(C9=CC%10=NSN=C%10N=C9)C=C8)C=C4,CTDP,,,5.04,10.98,0.79,0.58,"	Shin Y, Song CE, Lee W-H, Lee SK, Shin WS, Kang I-N. Synthesis and Characterization of a Soluble A-D-A Molecule Containing a 2D Conjugated Selenophene-Based Side Group for Organic Solar Cells. Macromol. Rapid Commun. 38,  (2017)."
2847,CCCCC(CC)CC1(CC(CC)CCCC)C2=CC(C3=C4C=C(S3)C([Se]5)=CC=C5C6=C(F)C(F)=C(C7=CC=C(C8=CC9=C(C%10=C(C9(CC(CC)CCCC)CC(CC)CCCC)C=C(C%11=C%12C=C(C%13=CC=C(C%14=C(F)C(F)=C(C%15=CC=C(C%16=CC=C(CCCCCC)S%16)S%15)C%17=NSN=C%14%17)S%13)S%11)C(C%12(CC(CC)CCCC)CC(CC)CCCC)=C%10)S8)[Se]7)C%18=NSN=C6%18)=C(C4(CC(CC)CCCC)CC(CC)CCCC)C=C2C%19=C1C=C(C%20=CC=C(C%21=C(F)C(F)=C(C%22=CC=C(C%23=CC=C(CCCCCC)S%23)S%22)C%24=NSN=C%21%24)S%20)S%19,Th6FSe,,,1.5,4.55,0.97,0.34,"	Paramasivam M, Gupta A, Babu NJ, Bhanuprakash K, Bhosale SV, Rao VJ. Funnel shaped molecules containing benzo/pyrido 1,2,5 thiadiazole functionalities as peripheral acceptors for organic photovoltaic applications. RSC Adv. 6, 66978-66989 (2016)."
2848,CCCCC(CC)CC1(CC(CC)CCCC)C2=CC(C3=C4C=C(S3)C(S5)=CC=C5C6=C(F)C(F)=C(C7=CC=C(C8=CC9=C(C%10=C(C9(CC(CC)CCCC)CC(CC)CCCC)C=C(C%11=C%12C=C(C%13=CC=C(C%14=C(F)C(F)=C(C%15=CC=C(C%16=CC=C(CCCCCC)S%16)S%15)C%17=NSN=C%14%17)[Se]%13)S%11)C(C%12(CC(CC)CCCC)CC(CC)CCCC)=C%10)S8)S7)C%18=NSN=C6%18)=C(C4(CC(CC)CCCC)CC(CC)CCCC)C=C2C%19=C1C=C(C%20=CC=C(C%21=C(F)C(F)=C(C%22=CC=C(C%23=CC=C(CCCCCC)S%23)S%22)C%24=NSN=C%21%24)[Se]%20)S%19,Se6FTh,,,6.84,11.78,0.87,0.67,"	Wang JL, et al. Donor End-Capped Hexafluorinated Oligomers for Organic Solar Cells with 9.3% Efficiency by Engineering the Position of pi-Bridge and Sequence of Two-Step Annealing. Chem. Mat. 29, 1036-1046 (2017)."
2849,CC(C)(C)C1=CC2=C(C=C1)C3=C(C=C(C(C)(C)C)C=C3)C42C5=C(SC(C6=CC(CCCCCCCC)=C(C7=CC=C(C8=C(CCCCCCCC)C=C(/C=C9C(C(C=CC=C%10)=C%10C/9=O)=O)S8)S7)S6)=C5)C%11=C4C=C(C%12=CC(CCCCCCCC)=C(C%13=CC=C(C%14=C(CCCCCCCC)C=C(/C=C%15C(C(C=CC=C%16)=C%16C/%15=O)=O)S%14)S%13)S%12)S%11,STFYT,,,8.95,14.3,0.87,0.72,"	Wang JL, et al. Donor End-Capped Hexafluorinated Oligomers for Organic Solar Cells with 9.3% Efficiency by Engineering the Position of pi-Bridge and Sequence of Two-Step Annealing. Chem. Mat. 29, 1036-1046 (2017)."
2850,CC(C)(C)C1=CC2=C(C=C1)C3=C(C=C(C(C)(C)C)C=C3)C42C5=C(SC(C6=CC(CCCCCCCC)=C(C7=CC=C(C8=C(CCCCCCCC)C=C(/C=C9SC(N(CC)C/9=O)=S)S8)S7)S6)=C5)C%10=C4C=C(C%11=CC(CCCCCCCC)=C(C%12=CC=C(C%13=C(CCCCCCCC)C=C(/C=C%14SC(N(CC)C/%14=O)=S)S%13)S%12)S%11)S%10,STFRDN,,,6.68,12.88,0.79,0.66,"	Wang WG, et al. Development of Spiro cyclopenta 1,2-b:5,4-b ' dithiophene-4,9 '-fluorene -Based A-pi-D-pi-A Small Molecules with Different Acceptor Units for Efficient Organic Solar Cells. Acs Applied Materials & Interfaces 9, 4614-4625 (2017)."
2851,CC(C)(C)C1=CC2=C(C=C1)C3=C(C=C(C(C)(C)C)C=C3)C42C5=C(SC(C6=CC(CCCCCCCC)=C(C7=CC=C(C8=C(CCCCCCCC)C=C(/C=C9S/C(N(CC)C/9=O)=C(C#N)/C#N)S8)S7)S6)=C5)C%10=C4C=C(C%11=CC(CCCCCCCC)=C(C%12=CC=C(C%13=C(CCCCCCCC)C=C(/C=C%14S/C(N(CC)C/%14=O)=C(C#N)/C#N)S%13)S%12)S%11)S%10,STFRCN,,,3.3,7.21,0.87,0.53,"	Wang WG, et al. Development of Spiro cyclopenta 1,2-b:5,4-b ' dithiophene-4,9 '-fluorene -Based A-pi-D-pi-A Small Molecules with Different Acceptor Units for Efficient Organic Solar Cells. Acs Applied Materials & Interfaces 9, 4614-4625 (2017)."
2852,CC(C)(C)C1=CC2=C(C=C1)N(C3=C2C=C(C(C)(C)C)C=C3)C(C=C4)=CC=C4N(C5=CC=C(N(C6=C7C=C(C(C)(C)C)C=C6)C8=C7C=C(C(C)(C)C)C=C8)C=C5)C9=CC=C(C%10=CC%11=NSN=C%11C=C%10)C=C9,DCTB,,,4.33,10.08,0.88,0.49,"	Wang WG, et al. Development of Spiro cyclopenta 1,2-b:5,4-b ' dithiophene-4,9 '-fluorene -Based A-pi-D-pi-A Small Molecules with Different Acceptor Units for Efficient Organic Solar Cells. Acs Applied Materials & Interfaces 9, 4614-4625 (2017)."
2853,O=C1C(C(C(N2CC(CC)CCCC)=O)=C(C3=CC=CS3)N1CC(CC)CCCC)=C2C4=CC=C(S4)C#CC5=CC6=C(C(C=CC7=CC(C#CC8=CC=C(S8)C9=C(C(N%10CC(CC)CCCC)=O)C(C(N9CC(CC)CCCC)=O)=C%10C%11=CC=CS%11)=C%12)=C5)C7=C%12C=C6,PyrA(EH-DPP)2,,,1.06,3.8,0.87,0.32,"	Paramasivam M, Gupta A, Babu NJ, Bhanuprakash K, Bhosale SV, Rao VJ. Funnel shaped molecules containing benzo/pyrido 1,2,5 thiadiazole functionalities as peripheral acceptors for organic photovoltaic applications. RSC Adv. 6, 66978-66989 (2016)."
2854,CCC(CCCC)CC1=C(CCCCCC)C=C(S1)C2=C3C(SC(C4=CC(CCCCCC)=C(C5=CC(CCCCCC)=C(C6=CC=C(/C=C7C(N(CCCCCC)C(S\7)=O)=O)S6)S5)S4)=C3)=C(C8=CC(CCCCCC)=C(CC(CC)CCCC)S8)C9=C2SC(C%10=CC(CCCCCC)=C(C%11=CC(CCCCCC)=C(C%12=CC=C(/C=C%13C(N(CCCCCC)C(S\%13)=O)=O)S%12)S%11)S%10)=C9,BTR,,,2.73,6.31,0.85,0.51,"	Xu J-Q, et al. ADA small molecule donors based on pyrene and diketopyrrolopyrrole for organic solar cells. Sci. China Chem. 60, 561-569 (2017)."
2855,CC(C)(C)C1=CC2=C(C=C1)N(C3=C2C=C(C(C)(C)C)C=C3)C(C=C4)=CC=C4N(C5=CC=C(N(C6=C7C=C(C(C)(C)C)C=C6)C8=C7C=C(C(C)(C)C)C=C8)C=C5)C9=CC=C(C%10=CC%11=NSN=C%11N=C%10)C=C9,DCTP,,,10.1,17.1,0.782,0.75,"	Zhang GC, et al. High-Performance Ternary Organic Solar Cell Enabled by a Thick Active Layer Containing a Liquid Crystalline Small Molecule Donor. J. Am. Chem. Soc. 139, 2387-2395 (2017)."
2856,FC1=C(C(S2)=CC3=C2C4=C(C=C(C5=C(F)C=C(C6=CC=C(C7=CC=C(CCCCCC)S7)S6)C8=NSN=C85)S4)[Si]3(CC(CCCC)CC)CC(CC)CCCC)C9=NSN=C9C(C%10=CC=C(C%11=CC=C(CCCCCC)S%11)S%10)=C1,p©\DTS(FBTTH2)2,,,2.21,6.75,0.87,0.38,"	Paramasivam M, Gupta A, Babu NJ, Bhanuprakash K, Bhosale SV, Rao VJ. Funnel shaped molecules containing benzo/pyrido 1,2,5 thiadiazole functionalities as peripheral acceptors for organic photovoltaic applications. RSC Adv. 6, 66978-66989 (2016)."
2857,S=C(N(CC)C/1=O)SC1=C/C2=CC(CCCCCCCC)=C(C3=CC=C(C4=C(CCCCCCCC)C=C(C5=CC(C6(CCCCCC)CCCCCC)=C(C7=C6C=C(C8=CC(CCCCCCCC)=C(C9=CC=C(C%10=C(CCCCCCCC)C=C(/C=C(S%11)/C(N(CC)C%11=S)=O)S%10)S9)S8)S7)S5)S4)S3)S2,DR3TDTC-C6,,,10.78,21.67,0.74,0.67,"	Zhang JQ, et al. Enhancing Performance of Large-Area Organic Solar Cells with Thick Film via Ternary Strategy. Small 13, 8 (2017)."
2858,S=C(N(CC)C/1=O)SC1=C/C2=CC(CCCCCCCC)=C(C3=CC=C(C4=C(CCCCCCCC)C=C(C5=CC(C6(CCCCCCCC)CCCCCCCC)=C(C7=C6C=C(C8=CC(CCCCCCCC)=C(C9=CC=C(C%10=C(CCCCCCCC)C=C(/C=C(S%11)/C(N(CC)C%11=S)=O)S%10)S9)S8)S7)S5)S4)S3)S2,DR3TDTC-C8,,,4.04,8.7,0.8,0.57,"	Zhang YM, et al. Effects of alkyl chains on intermolecular packing and device performance in small molecule based organic solar cells. Dyes Pigment. 141, 262-268 (2017)."
2859,S=C(N(CC)C/1=O)SC1=C/C2=CC(CCCCCCCC)=C(C3=CC=C(C4=C(CCCCCCCC)C=C(C5=CC(C6(CC(CC)CCCC)CC(CC)CCCC)=C(C7=C6C=C(C8=CC(CCCCCCCC)=C(C9=CC=C(C%10=C(CCCCCCCC)C=C(/C=C(S%11)/C(N(CC)C%11=S)=O)S%10)S9)S8)S7)S5)S4)S3)S2,DR3TDTC,,,4.11,8.86,0.8,0.58,"	Zhang YM, et al. Effects of alkyl chains on intermolecular packing and device performance in small molecule based organic solar cells. Dyes Pigment. 141, 262-268 (2017)."
2860,O=C1C(C(C(N2CC(CCCCCC)CCCCCCCC)=O)=C(C3=CC=CS3)N1CC(CCCCCC)CCCCCCCC)=C2C4=CC=C(S4)C5=CC6=C(C(C=CC7=CC(C8=CC=C(C9=C%10C(C(N9CC(CCCCCC)CCCCCCCC)=O)=C(C%11=CC=CS%11)N(CC(CCCCCC)CCCCCCCC)C%10=O)S8)=C%12)=C5)C7=C%12C=C6,Pyr(HD-DPP)2,,,0.75,2.85,0.85,0.31,"	Zhang YM, et al. Effects of alkyl chains on intermolecular packing and device performance in small molecule based organic solar cells. Dyes Pigment. 141, 262-268 (2017)."
2861,O=C1C(C(C(N2CC(CC)CCCC)=O)=C(C3=CC=CS3)N1CC(CC)CCCC)=C2C4=CC=C(S4)C5=CC6=C(C(C=CC7=CC(C8=CC=C(C9=C%10C(C(N9CC(CC)CCCC)=O)=C(C%11=CC=CS%11)N(CC(CC)CCCC)C%10=O)S8)=C%12)=C5)C7=C%12C=C6,Pyr(EH-DPP)2,,,1.04,3.49,0.82,0.36,"	Xu J-Q, et al. ADA small molecule donors based on pyrene and diketopyrrolopyrrole for organic solar cells. Sci. China Chem. 60, 561-569 (2017)."
2862,CCCCC(CC)COC1=C2C(C=C(C3CCC(C4=CC=C(C5=CC=C(CCCCCC)S5)S4)C6=NSN=C63)S2)=C(OCC(CC)CCCC)C7=C1C=C(C8CCC(C9=CC=C(C%10=CC=C(CCCCCC)S%10)S9)C%11=NSN=C%118)S7,BDT(TTBT)2,,,4.16,8.67,0.85,0.57,"	Xu J-Q, et al. ADA small molecule donors based on pyrene and diketopyrrolopyrrole for organic solar cells. Sci. China Chem. 60, 561-569 (2017)."
2863,O=C1C(C2=C(C3=CC=C(C4=CC=C5C(OC(C=CC=C6)=C6N5CCCCCC)=C4)S3)N1CCCCCCCCCC)=C(C7=CC=C(C8=CC=C9C(OC(C=CC=C%10)=C%10N9CCCCCC)=C8)S7)N(CCCCCCCCCC)C2=O,CSDPP5,,,1.73,4.75,0.81,0.45,"	Bagde SS, Park H, Lee SM, Lee SH. Influence of the terminal donor on the performance of 4,8-dialkoxybenzo 1,2-b:4,5 ' dithiophene based small molecules for efficient solution-processed organic solar cells. New J. Chem. 40, 2063-2070 (2016)."
2864,O=C1C(C2=C(C3=CC=C(C4=CC=C5C(OC(C=CC=C6)=C6N5CCCCCC)=C4)S3)N1CC(CCCC)CC)=C(C7=CC=C(C8=CC=C9C(OC(C=CC=C%10)=C%10N9CCCCCC)=C8)S7)N(CC(CCCC)CC)C2=O,CSDPP6,,,2.97,7.88,0.84,0.47,"	Reddy MA, Kumar CP, Ashok A, Sharma A, Sharma GD, Chandrasekharam M. Hetero aromatic donors as effective terminal groups for DPP based organic solar cells. RSC Adv. 6, 9023-9036 (2016)."
2865,O=C1C(C2=C(C3=CC=C(C4=CC=C(N(CCCCCC)C5=C6C=CC=C5)C6=C4)S3)N1CCCCCCCCCC)=C(C7=CC=C(C8=CC=C(N(CCCCCC)C9=C%10C=CC=C9)C%10=C8)S7)N(CCCCCCCCCC)C2=O,CSDPP7,,,4.69,10.48,0.8,0.56,"	Reddy MA, Kumar CP, Ashok A, Sharma A, Sharma GD, Chandrasekharam M. Hetero aromatic donors as effective terminal groups for DPP based organic solar cells. RSC Adv. 6, 9023-9036 (2016)."
2866,O=C1C(C2=C(C3=CC=C(C4=CC=C(N(CCCCCC)C5=C6C=CC=C5)C6=C4)S3)N1CC(CC)CCCC)=C(C7=CC=C(C8=CC=C(N(CCCCCC)C9=C%10C=CC=C9)C%10=C8)S7)N(CC(CCCC)CC)C2=O,CSDPP8,,,2.42,6.34,0.91,0.42,"	Reddy MA, Kumar CP, Ashok A, Sharma A, Sharma GD, Chandrasekharam M. Hetero aromatic donors as effective terminal groups for DPP based organic solar cells. RSC Adv. 6, 9023-9036 (2016)."
2867,CCCCCCC1=CC=C(S1)C(S2)=C(CCCCCC)C=C2C3=CC(F)=C(C(S4)=CC5=C4C(SC(C6=C(F)C=C(C7=CC(CCCCCC)=C(C8=CC=C(CCCCCC)S8)S7)C9=NSN=C69)=C%10)=C%10C5(CC(CC)CCCC)CCCCCCCC)C%11=NSN=C%113,CPDT(FBTTh2)2,,,4.14,8.92,0.86,0.52,"	Reddy MA, Kumar CP, Ashok A, Sharma A, Sharma GD, Chandrasekharam M. Hetero aromatic donors as effective terminal groups for DPP based organic solar cells. RSC Adv. 6, 9023-9036 (2016)."
2868,CCCCCCC1=CC=C(S1)C(S2)=C(CCCCCC)C=C2C3=CC(F)=C(C(S4)=CC5=C4C(SC(C6=C(F)C=C(C7=CC(CCCCCC)=C(C8=CC=C(CCCCCC)S8)S7)C9=NSN=C69)=C%10)=C%10N5C(C(CCCC)CC)=O)C%11=NSN=C%113,DTP(FBTTh2)2,,,2.83,8.39,0.85,0.4,"	Verstappen P, et al. Impact of structure and homo-coupling of the central donor unit of small molecule organic semiconductors on solar cell performance. RSC Adv. 6, 32298-32307 (2016)."
2869,CCCCCCC1=CC=C(S1)C(S2)=C(CCCCCC)C=C2C3=CC(F)=C(C(S4)=CC5=C4C=C(C6=C(F)C=C(C7=CC(CCCCCC)=C(C8=CC=C(CCCCCC)S8)S7)C9=NSN=C69)S5)C%10=NSN=C%103,TT(FBTTh2)2,,,2.56,8.37,0.67,0.44,"	Verstappen P, et al. Impact of structure and homo-coupling of the central donor unit of small molecule organic semiconductors on solar cell performance. RSC Adv. 6, 32298-32307 (2016)."
2870,CCN1C(/C(SC1=S)=C/C2=CC(OCCCCCC)=C(C3=C(C=C4)N(C4C(C5CC(OCCCCCCCCCCCC)CC(OCCCCCCCCCCCC)C5)=C(C=C6)N7C6=C(C8=C(OCCCCCC)C=C(C(OCCCCCC)=C8)/C=C(S9)/C(N(CC)C9=S)=O)C%10C=C%11)[Zn]7(N%10C%11=C%12C%13CC(OCCCCCCCCCCCC)CC(OCCCCCCCCCCCC)C%13)N%14C%12=CC=C%143)C=C2OCCCCCC)=O,4a,,,2.63,9.13,0.79,0.36,"	Verstappen P, et al. Impact of structure and homo-coupling of the central donor unit of small molecule organic semiconductors on solar cell performance. RSC Adv. 6, 32298-32307 (2016)."
2871,CCN1C(/C(SC1=S)=C/C2=CC(OCCCCCC)=C(C3=C(C=C4)N(C4C(C5CCC(OCCCCCCCCCCCC)CC5)=C(C=C6)N7C6=C(C8=C(OCCCCCC)C=C(C(OCCCCCC)=C8)/C=C(S9)/C(N(CC)C9=S)=O)C%10C=C%11)[Zn]7(N%10C%11=C%12C%13CCC(OCCCCCCCCCCC)CC%13)N%14C%12=CC=C%143)C=C2OCCCCCC)=O,4b,,,3.21,7.2,0.9,0.48,"	Wang HD, et al. Structural engineering of porphyrin-based small molecules as donors for efficient organic solar cells. Chem. Sci. 7, 4301-4307 (2016)."
2872,CC1N(C=C2C(CCCCCCCC)CCCCCC)[Zn]34N5C2=CC=C5C(C6=C(OCCCCCC)C=C(C(OCCCCCC)=C6)/C=C(S7)/C(N(CC)C7=S)=O)=C(C=C8)N3C8C(C(CCCCCC)CCCCCCCC)=C(C=C9)N4C9=C1C%10=C(OCCCCCC)C=C(C(OCCCCCC)=C%10)/C=C(S%11)/C(N(CC)C%11=S)=O,4c,,,5.07,10.14,0.9,0.56,"	Wang HD, et al. Structural engineering of porphyrin-based small molecules as donors for efficient organic solar cells. Chem. Sci. 7, 4301-4307 (2016)."
2873,CCCCC(CC)CN(C1=C2SC(/C=C(C#N)\C#N)=C1)C3=C2SC4=C3N(CC(CC)CCCC)C5=C4SC(/C=C(C#N)\C#N)=C5,DTPT,,,7.7,13.32,0.91,0.64,"	Wang HD, et al. Structural engineering of porphyrin-based small molecules as donors for efficient organic solar cells. Chem. Sci. 7, 4301-4307 (2016)."
2874,CC(C=C1C)=CC(C)=C1/C2=C3N4/C(C=C/3)=C(C#CC5=CC6=C(C(SC(/C=C7SC(N(CC)C\7=O)=S)=C8)=C8C6(CCCCCC)CCCCCC)S5)\C9=N/C(C=C9)=C(C%10=C(C)C=C(C)C=C%10C)\C(N%11[Zn]4)=CC=C%11/C(C#CC%12=CC%13=C(C(SC(/C=C%14SC(N(CC)C\%14=O)=S)=C%15)=C%15C%13(CCCCCC)CCCCCC)S%12)=C%16C=CC2=N/%16,SA1,,,3.01,6.96,1.03,0.41,"	Chung CL, et al. A-D-A type organic donors employing coplanar heterocyclic cores for efficient small molecule organic solar cells. Org. Electron. 28, 229-238 (2016)."
2875,CCCCC(CC)CN(C1=C2SC(/C=C(C#N)/C#N)=C1)C3=C2SC4=C3SC5=C4N(CC(CC)CCCC)C6=C5SC(/C=C(C#N)/C#N)=C6,DTPTT,,,6.71,13.38,0.85,0.59,"	Arrechea S, Aljarilla A, de la Cruz P, Singh MK, Sharma GD, Langa F. New cyclopentadithiophene (CDT) linked porphyrin donors with different end-capping acceptors for efficient small molecule organic solar cells. J. Mater. Chem. C 5, 4742-4751 (2017)."
2876,CC(C=C1C)=CC(C)=C1/C2=C3N4/C(C=C/3)=C(C#CC5=CC6=C(C(SC(/C=C(C#N)/C#N)=C7)=C7C6(CCCCCC)CCCCCC)S5)\C8=N/C(C=C8)=C(C9=C(C)C=C(C)C=C9C)\C(N%10[Zn]4)=CC=C%10/C(C#CC%11=CC%12=C(C(SC(/C=C(C#N)\C#N)=C%13)=C%13C%12(CCCCCC)CCCCCC)S%11)=C%14C=CC2=N/%14,SA2,,,1.7,5.25,1.02,0.31,"	Chung CL, et al. A-D-A type organic donors employing coplanar heterocyclic cores for efficient small molecule organic solar cells. Org. Electron. 28, 229-238 (2016)."
2877,CCCCC(CC)CC(S1)=CC=C1C2=C3C(C=C(C4=CC=C(C5=C(F)C(F)=C(C6=CC=C(/C=C(C(OCC(CCCC)CC)=O)\C#N)S6)C7=NN(CC(CCCCCC)CCCCCCCC)N=C57)S4)S3)=C(C8=CC=C(CC(CC)CCCC)S8)C9=C2C=C(C%10=CC=C(C%11=C(F)C(F)=C(C%12=CC=C(/C=C(C(OCC(CCCC)CC)=O)\C#N)S%12)C%13=NN(CC(CCCCCC)CCCCCCCC)N=C%11%13)S%10)S9,H11,,,7.93,13.84,0.91,0.63,"	Arrechea S, Aljarilla A, de la Cruz P, Singh MK, Sharma GD, Langa F. New cyclopentadithiophene (CDT) linked porphyrin donors with different end-capping acceptors for efficient small molecule organic solar cells. J. Mater. Chem. C 5, 4742-4751 (2017)."
2878,CCCCC(CC)COC1=C2C(C=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(/C=C(C(OCC(CCCC)CC)=O)\C#N)S5)C6=NN(CC(CCCCCC)CCCCCCCC)N=C46)S3)S2)=C(OCC(CC)CCCC)C7=C1C=C(C8=CC=C(C9=C(F)C(F)=C(C%10=CC=C(/C=C(C(OCC(CCCC)CC)=O)\C#N)S%10)C%11=NN(CC(CCCCCC)CCCCCCCC)N=C9%11)S8)S7,H12,,,9.73,15.21,0.977,0.65,"	Bin HJ, et al. 9.73% Efficiency Nonfullerene All Organic Small Molecule Solar Cells with Absorption-Complementary Donor and Acceptor. J. Am. Chem. Soc. 139, 5085-5094 (2017)."
2879,CC(C)(C)C(C=C1)=CC=C1N2C3=C(C=CC=C3)C4=CC(C5=CC=C(C6=CC=C(/C=C(C#N)\C#N)C=C6)S5)=CC=C42,F1,,,5.51,10.51,0.955,0.55,"	Bin HJ, et al. 9.73% Efficiency Nonfullerene All Organic Small Molecule Solar Cells with Absorption-Complementary Donor and Acceptor. J. Am. Chem. Soc. 139, 5085-5094 (2017)."
2880,CC(C)(C)C(C=C1)=CC=C1N2C3=C(C=CC=C3)C4=CC(C5=CC=C(C6=CC=C(/C=C7C(C(C=CC=C8)=C8C\7=O)=O)C=C6)S5)=CC=C42,F2,,,4.93,9.61,1.02,0.51,"	Chang YJ, et al. Carbazole-based small molecules for vacuum-deposited organic photovoltaic devices with open-circuit voltage exceeding 1 V. Org. Electron. 47, 162-173 (2017)."
2881,CC(C)(C)C(C=C1)=CC=C1N2C3=C(C=CC=C3)C4=CC(C5=CC=C(C6=CC=C(/C=C/C7=C/C(C=C(C)O7)=C(C#N)/C#N)C=C6)S5)=CC=C42,F3,,,2.17,5.13,0.97,0.44,"	Chang YJ, et al. Carbazole-based small molecules for vacuum-deposited organic photovoltaic devices with open-circuit voltage exceeding 1 V. Org. Electron. 47, 162-173 (2017)."
2882,CC(C)(C)C(C=C1)=CC=C1N2C3=C(C=CC=C3)C4=CC(C5=CC=C(C6=CC=C(/C=C/C(OC(C)=C/7)=CC7=C8C(C(C=CC=C9)=C9C/8=O)=O)C=C6)S5)=CC=C42,F4,,,2.09,5,0.92,0.45,"	Chang YJ, et al. Carbazole-based small molecules for vacuum-deposited organic photovoltaic devices with open-circuit voltage exceeding 1 V. Org. Electron. 47, 162-173 (2017)."
2883,CCCCC(CC)CC(S1)=CC=C1C2=C3C(SC(C4=CC(CCCCCCCC)=C(C5=CC=C(C6=C(CCCCCCCC)C=C(/C=C/C7=NC(C#N)=C(C#N)N7CCCCCCCC)S6)S5)S4)=C3)=C(C8=CC=C(CC(CC)CCCC)S8)C9=C2SC(C%10=CC(CCCCCCCC)=C(C%11=CC=C(C%12=C(CCCCCCCC)C=C(/C=C/C%13=NC(C#N)=C(C#N)N%13CCCCCCCC)S%12)S%11)S%10)=C9,V-BDT,,,1.42,4.32,0.86,0.38,"	Chang YJ, et al. Carbazole-based small molecules for vacuum-deposited organic photovoltaic devices with open-circuit voltage exceeding 1 V. Org. Electron. 47, 162-173 (2017)."
2884,O=C1OC2=CC(N(CC)CC)=CC=C2C=C1C3=NC4=C(C=CC=C4)N3,Coumarin7,,,3.73,6.88,0.89,0.61,"	Chen M, et al. Vinazene end-capped acceptor-donor-acceptor type small molecule for solution-processed organic solar cells. Org. Electron. 44, 11-19 (2017)."
2885,CCCCCCC1(CCCCCC)C2=C(SC(/C=C/C3=C(CCCCCC)C(CCCCCC)=C(/C=C(C#N)/C#N)S3)=C2)C4=C1C=C(/C=C/C5=C(CCCCCC)C(CCCCCC)=C(/C=C(C#N)/C#N)S5)S4,1,,,10.28,18.72,0.73,0.75,"	Chen X, et al. Ternary Organic Solar Cells with Coumarin7 as the Donor Exhibiting over 10% Power Conversion Efficiency and a High Fill Factor of 75. ACS applied materials & interfaces,  (2017)."
2886,CCCCCCC1(CCCCCC)C2=C(SC(/C=C/C3=C(CCCCCC)C=C(/C=C(C#N)/C#N)S3)=C2)C4=C1C=C(/C=C/C5=C(CCCCCC)C=C(/C=C(C#N)/C#N)S5)S4,2,,,4,7.76,0.89,0.57,"	Dominguez R, Schulz GL, de la Cruz P, Bauerle P, Langa F. Cyclopentadithiophene-based co-oligomers for solution-processed organic solar cells. Dyes Pigment. 143, 112-122 (2017)."
2887,CCCCCCC1(CCCCCC)C2=C(SC(/C=C/C3=CC=C(/C=C(C#N)/C#N)S3)=C2)C4=C1C=C(/C=C/C5=CC=C(/C=C(C#N)/C#N)S5)S4,3,,,3.6,6.06,0.94,0.63,"	Dominguez R, Schulz GL, de la Cruz P, Bauerle P, Langa F. Cyclopentadithiophene-based co-oligomers for solution-processed organic solar cells. Dyes Pigment. 143, 112-122 (2017)."
2888,CCCCCCC1=C(SC(/C=C(C#N)\C#N)=C1CCCCCC)/C=C/C(S2)=CC3=C2C=C(/C=C/C4=C(CCCCCC)C(CCCCCC)=C(/C=C(C#N)\C#N)S4)S3,4,,,3,7.3,0.84,0.48,"	Dominguez R, Schulz GL, de la Cruz P, Bauerle P, Langa F. Cyclopentadithiophene-based co-oligomers for solution-processed organic solar cells. Dyes Pigment. 143, 112-122 (2017)."
2889,C1(C2=CC=C3C1=C(C4=C3C(C5=CC=CC=C5)=C(C=CC=C6)C6=C4C7=CC=CC=C7)C=C8)=C8C9=C%10C2=CC=C(C%11=C%12C(C%13=CC=CC=C%13)=C(C=CC=C%14)C%14=C%11C%15=CC=CC=C%15)C%10=C%12C=C9,DBP,,,1.7,3.01,1.06,0.54,"	Dominguez R, Schulz GL, de la Cruz P, Bauerle P, Langa F. Cyclopentadithiophene-based co-oligomers for solution-processed organic solar cells. Dyes Pigment. 143, 112-122 (2017)."
2890,CCCCCCCCCCCCC1=C(C2=CC(CCCCCCCCCCCC)=C(C3=NC(C=C(SC(C4=C(CCCCCCCCCCCC)C=C(C5=CC=CC=C5)S4)=N6)C6=C7)=C7S3)S2)SC(C8=CC=C9C(N(CC(CCCCCC)CCCCCCCC)C(/C9=C%10C(SC(C%11=CC(CCCCCCCCCCCC)=C(C%12=CC=CC=C%12)S%11)=C%13)=C%13N(CC(CCCCCC)CCCCCCCC)C\%10=O)=O)=C8)=C1,BT2,,,3.32,6.11,0.86,0.63,"	Gao YA, et al. Cooperative plasmon enhanced organic solar cells with thermal coevaporated Au and Ag nanoparticles. Org. Electron. 48, 336-341 (2017)."
2891,CCCCCCCCCCCCC1=C(C2=CC(CCCCCCCCCCCC)=C(C3=NC(C=C(SC(C4=C(CCCCCCCCCCCC)C=C(C5=CC=CC=C5)S4)=N6)C6=C7)=C7S3)S2)SC(C8=CC=C9C(N(CC(CCCCCC)CCCCCCCC)C(/C9=C%10C(SC(C%11=CC(CCCCCCCCCCCC)=C(C%12=CC=CC=C%12)S%11)=C%13)=C%13N(CC(CCCCCC)CCCCCCCC)C\%10=O)=O)=C8F)=C1,F-BT2,,,4.18,10.07,0.62,0.67,"	Ide M, Saeki A. Fluorinated Benzothienoisoindigo Copolymers for Organic Solar Cells: A Comparative Study on Polymer Orientation and Device Performance. Chem. Lett. 46, 1133-1136 (2017)."
2892,C1(/C=C2S/C(C=C\2)=C\C=C(S/3)\C=CC3=C\C(S4)=CC=C4/C=C\5)=CC=C5S1,TTA,,,1.66,4.48,0.64,0.57,"	Ide M, Saeki A. Fluorinated Benzothienoisoindigo Copolymers for Organic Solar Cells: A Comparative Study on Polymer Orientation and Device Performance. Chem. Lett. 46, 1133-1136 (2017)."
2893,O=C1N(CC(CC)CCCC)C(C2=CC=C(C3=CC=C(/C=C4C(N(CC)C(S/4)=S)=O)S3)O2)=C5C1=C(C6=CC=C(C7=CC=C(/C=C8C(N(CC)C(S/8)=S)=O)S7)O6)N(CC(CC)CCCC)C5=O,DPPFT-RH,,,0.16,3.1,46,0.23,"	Xi H, Wei Z, Xu W, Bo Z, Hu W, Zhu D. Organic photovoltaic cells based on tetrathia 22 annulene 2,1,2,1 /PCBM heterojunction (vol 484, pg 41, 2009). Chemical Physics Letters 485, 263-263 (2010)."
2894,CCCCCCCCC(S1)=CC=C1C2=CC=C(C3=CC4=C(C(OCC(CC)CCCC)=C5C(SC(C6=CC=C(C7=CC=C(CCCCCCCC)S7)C8=C6N=C(C9=CC=C(C%10=CC=C(N(C%11=CC=CC=C%11)C%12=CC=CC=C%12)C=C%10)C=C9)C(C%13=CC=C(C%14=CC=C(N(C%15=CC=CC=C%15)C%16=CC=CC=C%16)C=C%14)C=C%13)=N8)=C5)=C4OCC(CC)CCCC)S3)C%17=C2N=C(C%18=CC=C(C%19=CC=C(N(C%20=CC=CC=C%20)C%21=CC=CC=C%21)C=C%19)C=C%18)C(C%22=CC=C(C%23=CC=C(N(C%24=CC=CC=C%24)C%25=CC=CC=C%25)C=C%23)C=C%22)=N%17,DTPA-Q-BDT-Q-DTPA,,,0.83,6.36,33,1.77,"	Lim E. Rational design of p-bridges for ambipolar DPP-RH-based small molecules in organic photovoltaic cells. Journal of Industrial and Engineering Chemistry 45, 338-348 (2017)."
2895,O=C1C(C2=C(C3=CSC(C4=CC=C(C5=CC=C(CCCCCC)S5)S4)=C3)N1C(OC(C)(C)C)=O)=C(C6=CC=C(C7=CC=C(C8=CC=C(CCCCCC)S8)S7)S6)N(C(OC(C)(C)C)=O)C2=O,"a,a-DH6TDPP",,,0.64,6.1,31,1.22,"	Yu J, Zhu W, Tan H, Peng Q. A novel D2-A-D1-A-D2-type donor-acceptor conjugated small molecule based on a benzo 1,2-b:4,5-b ' dithiophene core for solution processed organic photovoltaic cells. Chemical Physics Letters 667, 254-259 (2017)."
2896,C1(C2=CC=C(C3=CC=C(C4=CC=CS4)S3)S2)=C(C5=CC=C(C6=CC=CS6)S5)SC(C7=CC=C(C8=CC=CS8)S7)=C1C9=CC=C(C%10=CC=C(C%11=CC=CS%11)S%10)S9,11T,,,0.67,8.42,45,2.33,"	Tamayo AB, Walker B, Nguyen T-Q. A low band gap, solution processable oligothiophene with a diketopyrrolopyrrole core for use in organic solar cells. Journal of Physical Chemistry C 112, 11545-11551 (2008)."
2897,C1(C2=CC=C(C3=CC=C(N4C(C=C(C5=CC=C(N(C6=CC=CC=C6)C7=CC=CC=C7)C=C5)C=C8)=C8C9=C4C=CC(C%10=CC=C(N(C%11=CC=CC=C%11)C%12=CC=CC=C%12)C=C%10)=C9)S3)S2)=CC=C(C%13=CC=C(C%14=CC=C(N%15C(C=C(C%16=CC=C(N(C%17=CC=CC=C%17)C%18=CC=CC=C%18)C=C%16)C=C%19)=C%19C%20=C%15C=CC(C%21=CC=C(N(C%22=CC=CC=C%22)C%23=CC=CC=C%23)C=C%21)=C%20)S%14)S%13)C%24=NSN=C1%24,G2©\OT(4)BTD©\G2,,,0.54,0.93,31,0.16,"	Ya-Nan W, et al. X-shape oligo(thiophene)s as donor materials for vacuum-deposited organic photovoltaic cells. Chinese Physics B 17, 1448-1453 (2008)."
2898,C1(C2=CC=C(S2)C3=CC=C(C4=CC=C(N5C(C=C(C6=CC=C(N(C7=CC=CC=C7)C8=CC=CC=C8)C=C6)C=C9)=C9C%10=C5C=CC(C%11=CC=C(N(C%12=CC=CC=C%12)C%13=CC=CC=C%13)C=C%11)=C%10)S4)S3)=CC=C(C(S%14)=CC=C%14C%15=CC=C(C%16=CC=C(N%17C(C=C(C%18=CC=C(N(C%19=CC=CC=C%19)C%20=CC=CC=C%20)C=C%18)C=C%21)=C%21C%22=C%17C=CC(C%23=CC=C(N(C%24=CC=CC=C%24)C%25=CC=CC=C%25)C=C%23)=C%22)S%16)S%15)C%26=NSN=C1%26,G2©\OT(6)BTD©\G2,,,0.86,1.23,26,0.27,"	Xia PF, Lu J, Kwok CH, Fukutani H, Wong MS, Tao Y. Synthesis and Properties of Monodisperse Multi-Triarylamine-Substituted Oligothiophenes and 4,7-Bis(2 '-oligothienyl)-2,1,3-benzothiadiazoles for Organic Solar Cell Applications. Journal of Polymer Science Part a-Polymer Chemistry 47, 137-148 (2009)."
2899,ClB1N2/C(C3=CC4=C(C=CC=C4)C=C3C2=N5)=N\C(C6=CC(C=CC=C7)=C7C=C6/8)=NC8=N/C9=C(C=C(C=CC=C%10)C%10=C%11)C%11=C5N19,SubNc,,,0.75,1.5,29,0.32,"	Xia PF, Lu J, Kwok CH, Fukutani H, Wong MS, Tao Y. Synthesis and Properties of Monodisperse Multi-Triarylamine-Substituted Oligothiophenes and 4,7-Bis(2 '-oligothienyl)-2,1,3-benzothiadiazoles for Organic Solar Cell Applications. Journal of Polymer Science Part a-Polymer Chemistry 47, 137-148 (2009)."
2900,CCCCCCC1=CC2=C(C3=CC(CCCCCC)=C(C4=CC(CCCCCC)=C(C5=CC(CCCCCC)=C(C6=CC(CCCCCC)=C(C7=CC(CCCCCC)=C(C8=CC(CCCCCC)=C(C9=CC(CCCCCC)=C(C%10=CC(CCCCCC)=C([H])S%10)S9)S8)S7)S6)S5)S4)S3)SC(C%11=CC(CCCCCC)=C(C%12=CC(CCCCCC)=C(C%13=CC(CCCCC)=C(C%14=CC(CCCCCC)=C(C%15=CC(CCCCCC)=C(C%16=CC(CCCCCC)=C(C%17=CC(CCCCCC)=C(C%18=CC(CCCCCC)=C([H])S%18)S%17)S%16)S%15)S%14)S%13)S%12)S%11)=C2S1,MF,,,0.79,6.1,49,2.5,"	Verreet B, et al. The characterization of chloroboron (III) subnaphthalocyanine thin films and their application as a donor material for organic solar cells. Journal of Materials Chemistry 19, 5295-5297 (2009)."
2901,C=CC(C=C1)=CC=C1N(C2=CC=C(/C=C/C3=CC=C(/C=C/C4=C/C(C=C(/C=C/C5=CC=C(/C=C/C6=CC=C(N(C7=CC=CC=C7)C8=CC=CC=C8)C=C6)C=C5)O4)=C(C#N)\C#N)C=C3)C=C2)C9=CC=C(/C=C/C%10=CC=C(/C=C/C%11=C/C(C=C(/C=C/C%12=CC=C(/C=C/C%13=CC=C(N(C%14=CC=CC=C%14)C%15=CC=CC=C%15)C=C%13)C=C%12)O%11)=C(C#N)\C#N)C=C%10)C=C9,B(TPA-DCM-TPA),,,0.54,7.42,36,1.46,"	Liang Y, et al. Regioregular Oligomer and Polymer Containing Thieno 3,4-b thiophene Moiety for Efficient Organic Solar Cells. Macromolecules 42, 1091-1098 (2009)."
2902,N(C1=CC=C(C2=CC=C(C3=CC=CC=C3)S2)C=C1)(C4=CC=C(C5=CC=C(C6=CC=CC=C6)S5)C=C4)C7=CC=C(C8=CC=C(C9=CC=CC=C9)S8)C=C7,TPTPA,,,0.77,2.37,40,0.73,"	Zhao G, et al. Solution-Processable Multiarmed Organic Molecules Containing Triphenylamine and DCM Moieties: Synthesis and Photovoltaic Properties. Journal of Physical Chemistry C 113, 2636-2642 (2009)."
2903,CCCCCCC1=C(C2=C(CCCCCC)C=C(C3=CC=C(C4=CC=C(N5C(C=C(C6=CC=C(N(C7=CC=CC=C7)C8=CC=CC=C8)C=C6)C=C9)=C9C%10=C5C=CC(C%11=CC=C(N(C%12=CC=CC=C%12)C%13=CC=CC=C%13)C=C%11)=C%10)S4)S3)S2)SC(C%14=CC=C(C%15=CC=C(N%16C(C=C(C%17=CC=C(N(C%18=CC=CC=C%18)C%19=CC=CC=C%19)C=C%17)C=C%20)=C%20C%21=C%16C=CC(C%22=CC=C(N(C%23=CC=CC=C%23)C%24=CC=CC=C%24)C=C%22)=C%21)S%15)S%14)=C1,G2©\OT(6)©\G2,,,0.92,2.6,71,1.7,"	Kageyama H, Ohishi H, Tanaka M, Ohmori Y, Shirota Y. High performance organic photovoltaic devices using amorphous molecular materials with high charge-carrier drift mobilities. Applied Physics Letters 94,  (2009)."
2904,CCCCCCC1=C(C(S2)=CC=C2C3=C(CCCCCC)C=C(C4=CC=C(C5=CC=C(N6C(C=C(C7=CC=C(N(C8=CC=CC=C8)C9=CC=CC=C9)C=C7)C=C%10)=C%10C%11=C6C=CC(C%12=CC=C(N(C%13=CC=CC=C%13)C%14=CC=CC=C%14)C=C%12)=C%11)S5)S4)S3)SC(C%15=CC=C(C%16=CC=C(N%17C(C=C(C%18=CC=C(N(C%19=CC=CC=C%19)C%20=CC=CC=C%20)C=C%18)C=C%21)=C%21C%22=C%17C=CC(C%23=CC=C(N(C%24=CC=CC=C%24)C%25=CC=CC=C%25)C=C%23)=C%22)S%16)S%15)=C1,G2©\OT(7)©\G2,,,0.63,1.55,29,0.28,"	Xia PF, Lu J, Kwok CH, Fukutani H, Wong MS, Tao Y. Synthesis and Properties of Monodisperse Multi-Triarylamine-Substituted Oligothiophenes and 4,7-Bis(2 '-oligothienyl)-2,1,3-benzothiadiazoles for Organic Solar Cell Applications. Journal of Polymer Science Part a-Polymer Chemistry 47, 137-148 (2009)."
2905,CCCCCCC1=C(C(S2)=CC=C2C(S3)=CC=C3C4=C(CCCCCC)C=C(C5=CC=C(C6=CC=C(N7C(C=C(C8=CC=C(N(C9=CC=CC=C9)C%10=CC=CC=C%10)C=C8)C=C%11)=C%11C%12=C7C=CC(C%13=CC=C(N(C%14=CC=CC=C%14)C%15=CC=CC=C%15)C=C%13)=C%12)S6)S5)S4)SC(C%16=CC=C(C%17=CC=C(N%18C(C=C(C%19=CC=C(N(C%20=CC=CC=C%20)C%21=CC=CC=C%21)C=C%19)C=C%22)=C%22C%23=C%18C=CC(C%24=CC=C(N(C%25=CC=CC=C%25)C%26=CC=CC=C%26)C=C%24)=C%23)S%17)S%16)=C1,G2©\OT(8)©\G2,,,0.61,1.64,29,0.29,"	Xia PF, Lu J, Kwok CH, Fukutani H, Wong MS, Tao Y. Synthesis and Properties of Monodisperse Multi-Triarylamine-Substituted Oligothiophenes and 4,7-Bis(2 '-oligothienyl)-2,1,3-benzothiadiazoles for Organic Solar Cell Applications. Journal of Polymer Science Part a-Polymer Chemistry 47, 137-148 (2009)."
2906,FC1=C(F)C(F)=C(F)C2=C3N([Cu]N4/C5=N\C6=N/C(C7=C6C(F)=C(F)C(F)=C7F)=N\3)C(/N=C8N=C(/N=C4/C9=C5C(F)=C(F)C(F)=C9F)C%10=C\8C(F)=C(F)C(F)=C%10F)=C21,F16CuPc,,,0.65,1.43,28,0.26,"	Xia PF, Lu J, Kwok CH, Fukutani H, Wong MS, Tao Y. Synthesis and Properties of Monodisperse Multi-Triarylamine-Substituted Oligothiophenes and 4,7-Bis(2 '-oligothienyl)-2,1,3-benzothiadiazoles for Organic Solar Cell Applications. Journal of Polymer Science Part a-Polymer Chemistry 47, 137-148 (2009)."
2907,Cl[Sn]1(Cl)N2C(/N=C3N=C4C5=C\3C=CC=C5)=C(C=CC=C6)C6=C2/N=C7C(C=CC=C8)=C8C(/N=C(C9=C/%10C=CC=C9)\N1C%10=N/4)=N/7,SnCl2Pc,,,0.78,2.89,37,0.83,"	Yu B, Zhu F, Wang H, Li G, Yan D. All-organic tunnel junctions as connecting units in tandem organic solar cell. Journal of Applied Physics 104,  (2008)."
2908,CCCCCCC1=CC=C(S1)C(S2)=CC=C2/C=C/C3=C(/C=C/C4=CC=C(C5=CC=C(CCCCCC)S5)S4)C=C(/C=C/C6=CC=C(C7=CC=C(CCCCCC)S7)S6)C(/C=C/C8=CC=C(C9=CC=C(CCCCCC)S9)S8)=C3,4(HPBT),,,0.88,2.85,55,1.38,"	Yu B, Zhu F, Wang H, Li G, Yan D. All-organic tunnel junctions as connecting units in tandem organic solar cell. Journal of Applied Physics 104,  (2008)."
2909,CC(C)[Si](C(C)C)(C(C)C)C#CC1=C2C(C=C(C=CC=C3)C3=C2)=C(C#C[Si](C(C)C)(C(C)C)C(C)C)C4=CC5=CC=CC=C5C=C41,TIPS,,,3.21,0.42,31,0.43,"	Lee TW, et al. Bulk heterojunction organic photovoltaic cell fabricated with a p-type conjugated star-shaped molecule. Chemistry Letters 37, 866-867 (2008)."
2910,CC(C)[Si](C(C)C)(C(C)C)C#CC1=C2C(C=C(C=C(OCO3)C3=C4)C4=C2)=C(C#C[Si](C(C)C)(C(C)C)C(C)C)C5=CC6=CC7=C(OCO7)C=C6C=C51,TP-5,,,0.9,1.42,33,0.42,"	Palilis LC, Lane PA, Kushto GP, Purushothaman B, Anthony JE, Kafafi ZH. Organic photovoltaic cells with high open circuit voltages based on pentacene derivatives. Organic Electronics 9, 747-752 (2008)."
2911,CC(C)[Si](C(C)C)(C(C)C)C#CC1=C2C(C=C(C=C(OC(CC)(CC)O3)C3=C4)C4=C2)=C(C#C[Si](C(C)C)(C(C)C)C(C)C)C5=CC6=CC7=C(OC(CC)(CC)O7)C=C6C=C51,EtTP-5,,,0.57,2.32,37,0.5,"	Palilis LC, Lane PA, Kushto GP, Purushothaman B, Anthony JE, Kafafi ZH. Organic photovoltaic cells with high open circuit voltages based on pentacene derivatives. Organic Electronics 9, 747-752 (2008)."
2912,N(C1=CC=C(/C=C2SC(C=CC=C3)=C3S/2)C=C1)(C4=CC=C(/C=C5SC(C=CC=C6)=C6S/5)C=C4)C7=CC=C(/C=C8SC(C=CC=C9)=C9S/8)C=C7,1,,,0.69,1.68,29,0.34,"	Palilis LC, Lane PA, Kushto GP, Purushothaman B, Anthony JE, Kafafi ZH. Organic photovoltaic cells with high open circuit voltages based on pentacene derivatives. Organic Electronics 9, 747-752 (2008)."
2913,CCCCCCC1=CSC(C2=CC=C(C3=NSN=C32)/C=C/C(C=C4)=CC=C4N(C5=CC=C(/C=C/C6=CC=C(C7=CC(CCCCCC)=CS7)C8=NSN=C68)C=C5)C9=CC=C(/C=C/C%10=CC=C(C%11=CC(CCCCCC)=CS%11)C%12=NSN=C%10%12)C=C9)=C1,P(InCzTh2BTD),,,0.4,0.87,32,0.11,"	Aleveque O, Leriche P, Cocherel N, Frere P, Cravino A, Roncali J. Star-shaped conjugated systems derived from dithiafulvenyl-derivatized triphenylamines as active materials for organic solar cells. Solar Energy Materials and Solar Cells 92, 1170-1174 (2008)."
2914,C1(/C=C/C2=CC=C(N(C3=CC=CC=C3)C4=CC=CC=C4)C=C2)=CC=C(/C=C/C5=CC=C(N(C6=CC=CC=C6)C7=CC=CC=C7)C=C5)C8=NSN=C18,7T,,,0.85,8.58,32.7,2.39,"	Zhang J, Yang Y, He C, He Y, Zhao G, Li Y. Solution-Processable Star-Shaped Photovoltaic Organic Molecule with Triphenylamine Core and Benzothiadiazole-Thiophene Arms. Macromolecules 42, 7619-7622 (2009)."
2915,C1(C2=CC=C(C3=CC=CS3)S2)=C(C4=CC=CS4)SC(C5=CC=CS5)=C1C6=CC=C(C7=CC=CS7)S6,p-OXA-X,,,0.84,1.25,34,0.35,"	He C, et al. Improving the efficiency of solution processable organic photovoltaic devices by a star-shaped molecular geometry. Journal of Materials Chemistry 18, 4085-4090 (2008)."
2916,CC(C(OCCCCCCCC)=C1)=CC(OCCCCCCCC)=C1/C=C/C(C=C2)=CC=C2/C=C/C3=CC(/C=C/C4=CC=C(/C=C/C5=CC=C(C6=NN=C(C7=CC=C(C)C=C7)O6)C=C5)C=C4)=C(/C=C/C8=CC=C(/C=C/C9=C(OCCCCCCCC)C=C(C)C(OCCCCCCCC)=C9)C=C8)C=C3/C=C/C%10=CC=C(/C=C/C%11=CC=C(C%12=NN=C(C%13=CC=C(C)C=C%13)O%12)C=C%11)C=C%10,DDBTD,,,1.18,0.63,24,0.18,"	Ya-Nan W, et al. X-shape oligo(thiophene)s as donor materials for vacuum-deposited organic photovoltaic cells. Chinese Physics B 17, 1448-1453 (2008)."
2917,CCCCCCCCC1(CCCCCCCC)C2=CC(N(C3=CC=CC=C3)C4=CC=CC=C4)=CC=C2C5=C1C=C(C=C5)C6=CC=C(S6)C7=CC=C(C8=CC=C(C9=CC%10=C(C%11=CC=C(N(C%12=CC=CC=C%12)C%13=CC=CC=C%13)C=C%11C%10(CCCCCCCC)CCCCCCCC)C=C9)S8)C%14=NSN=C%147,P6,,,0.74,1.48,51,0.57,"	Kim Y-G, et al. P-OXA-X: A new Oligo photosensitizer for organic solar cells. Solar Energy Materials and Solar Cells 92, 307-312 (2008)."
2918,C1(C2=NC3=C(C=CC=C3)N2C4=CC=CC=C4)=CC(C5=NC6=C(C=CC=C6)N5C7=CC=CC=C7)=CC(C8=NC9=C(C=CC=C9)N8C%10=CC=CC=C%10)=C1,F16CuPc,,,0.7,1.59,22.3,0.22,"	Sun M, Wang L, Du B, Xiong Y, Liu R, Cao Y. Narrow band-gap oligomer for solution-processed heterojunction organic solar cells. Synthetic Metals 158, 125-129 (2008)."
2919,CCCCCCC1=C(C2=CC=C(C(S3)=C(CCCCCC)C=C3C4=CC(CCCCCC)=C(C5=CC=C(C(S6)=C(CCCCCC)C=C6C7=CC(CCCCCC)=C(C8=CC=C(C(S9)=C(CCCCCC)C=C9C%10=CC(CCCCCC)=C(C%11=CC=C(C(S%12)=C(CCCCCC)C=C%12C%13=CC(CCCCCC)=C(C%14=CC=C(C)S%14)S%13)S%11)S%10)S8)S7)S5)S4)S2)SC(C%15=CC(CCCCCC)=C(C%16=CC=C(C%17=C(CCCCCC)C(C(C%18=CC(C(SC(C)=C%19CCCCCC)=C%19C%20=O)=C%20C=C%18%21)=O)=C%21S%17)S%16)S%15)=C1,2,,,0.35,2.08,31,0.25,"	Tripathi V, Datta D, Samal GS, Awasthi A, Kumar S. Role of exciton blocking layers in improving efficiency of copper phthalocyanine based organic solar cells. Journal of Non-Crystalline Solids 354, 2901-2904 (2008)."
2920,O=C1C2=C(SC(C)=C2CCCCCC)C3=C1C=C(C(S4)=C(C5=O)C(CCCCCC)=C4C6=CC=C(C7=C(CCCCCC)C(C8=O)=C(S7)C9=C8C=C(C(S%10)=C(C%11=O)C(CCCCCC)=C%10C%12=CC=C(C(S%13)=C(CCCCCC)C=C%13C%14=CC(CCCCCC)=C(C%15=CC=C(C(S%16)=C(CCCCCC)C=C%16C%17=CC(CCCCCC)=C(C%18=CC=C(C(S%19)=C(CCCCCC)C=C%19C%20=CC(CCCCCC)=C(C%21=CC=C(C(S%22)=C(CCCCCC)C=C%22C%23=CC(CCCCCC)=C(C%24=CC=C(C(S%25)=C(CCCCCC)C=C%25C%26=CC(CCCCCC)=C(C%27=CC=C(C)S%27)S%26)S%24)S%23)S%21)S%20)S%18)S%17)S%15)S%14)S%12)C%11=C9)S6)C5=C3,3,,,0.62,1.02,0.26,0.33,"	Zhao C, Chen X, Zhang Y, Ng M-K. 4,9-dihydro-s-indaceno 1,2-b : 5,6-b' dithiophene-4,9-dione functionalized copolymers for organic photovoltaic devices. Journal of Polymer Science Part a-Polymer Chemistry 46, 2680-2688 (2008)."
2921,O=C(C1=C(CC(CC)CCCC)SC(CC(CC)CCCC)=C12)C3=C(C4=CC(CCCCCCCC)=C(C5=CC=C(C6=C(CCCCCCCC)C=C(/C=C7SC(N(CC)C/7=O)=S)S6)S5)S4)SC(C8=CC(CCCCCCCC)=C(C9=CC=C(C%10=C(CCCCCCCC)C=C(/C=C%11SC(N(CC)C/%11=O)=S)S%10)S9)S8)=C3C2=O,DR3TBDD,,,0.54,0.72,0.33,0.26,"	Zhao C, Chen X, Zhang Y, Ng M-K. 4,9-dihydro-s-indaceno 1,2-b : 5,6-b' dithiophene-4,9-dione functionalized copolymers for organic photovoltaic devices. Journal of Polymer Science Part a-Polymer Chemistry 46, 2680-2688 (2008)."
2922,O=C1C(C2=C(C3=CC=C(C4=C(C=C(C5=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C6=O)=C7C6=C(C8=CSC(C9=CC%10=C(C(C(C=C%11)=CC=C%12)=C%12C=C%10)C%11=C9)=C8)N(CC(CCCCCC)CCCCCCCC)C7=O)S5)C(OC)=C4)OC)S3)N1CC(CCCCCC)CCCCCCCC)=C(N(CC(CC)CCCCCC)C2=O)C(S%13)=CC=C%13C%14=CC%15=C%16C%17=C(C=CC%16=C%14)C=CC=C%17C=C%15,SM1,,,0.96,14.59,66,9.23,"	Zhang H, et al. Developing high-performance small molecule organic solar cells via a large planar structure and an electron-withdrawing central unit. Chemical Communications 53, 451-454 (2017)."
2923,CCCCCCCCC1=C(CCCCCCCC)C(C(C(SC2=C3C4=C(SC(CCCCCCCC)=C4CCCCCCCC)C5=C2SC(C6=CC=C(C7=CC=C(N(CCCCCCCC)C8=C9C=CC=C8)C9=C7)C%10=NSN=C6%10)=C5)=C3S%11)=C%11C%12=C%13C=C(C%14=CC=C(C%15=CC=C(N(CCCCCCCC)C%16=C%17C=CC=C%16)C%17=C%15)C%18=NSN=C%14%18)S%12)=C%13S1,FT3,,,0.68,14.5,55,5.47,"	Qiu Z, et al. Tuning the central donor core via intramolecular noncovalent interactions based on D(A-Ar)2 type small molecules for high performance organic solar cells. Solar Energy 161, 138-147 (2018)."
2924,CCCCCCCCC1=C(CCCCCCCC)C(C(C=C(C(S2)=CC3=C2C(SC(C4=CC=C(C5=CC=C(N(CCCCCCCC)C6=C7C=CC=C6)C7=C5)C8=NSN=C48)=C9)=C9C%10=C3C(CCCCCCCC)=C(CCCCCCCC)S%10)S%11)=C%11C%12=C%13C=C(C%14=CC=C(C%15=CC=C(N(CCCCCCCC)C%16=C%17C=CC=C%16)C%17=C%15)C%18=NSN=C%14%18)S%12)=C%13S1,FT4,,,0.61,5.67,61.41,2.13,"	Zhi Y, et al. Strain-released method to enhance the photovoltaic performance in solution-processed organic solar cells. Dyes and Pigments 145, 263-269 (2017)."
2925,O=C1C(C2=C(C3=CC=C(C4=C(C=C(C5=CC=C(C(N(CC(CCCCCC)CCCCCCCC)C6=O)=C7C6=C(C8=CSC(C9=CC%10=C(C(C(C=C%11)=CC=C%12)=C%12C=C%10)C%11=C9)=C8)N(CC(CCCCCC)CCCCCCCC)C7=O)S5)C(F)=C4)F)S3)N1CC(CCCC)CCCCCCCC)=C(N(CC(CCCCCCCC)CCCCCC)C2=O)C(S%13)=CC=C%13C%14=CC%15=C%16C%17=C(C=CC%16=C%14)C=CC=C%17C=C%15,SM2,,,0.64,8.23,58.62,3.07,"	Zhi Y, et al. Strain-released method to enhance the photovoltaic performance in solution-processed organic solar cells. Dyes and Pigments 145, 263-269 (2017)."
2926,O=C(N(CC)C(N(CC)C/1=O)=S)C1=C\C2=C(CCCCCC)C=C(C3=CC(CCCCCC)=C(/C=C/C4=CC=C(N(C5=CC=C(/C=C/C6=C(CCCCCC)C=C(C7=CC(CCCCCC)=C(/C=C8C(N(CC)C(N(CC)C/8=O)=S)=O)S7)S6)C=C5)C9=CC=C(/C=C/C%10=C(CCCCCC)C=C(C%11=CC(CCCCCC)=C(/C=C(C%12=O)\C(N(C(N%12CC)=S)CC)=O)S%11)S%10)C=C9)C=C4)S3)S2,TPA-bHTV-DT,,,0.77,15.3,64,7.54,"	Qiu Z, et al. Tuning the central donor core via intramolecular noncovalent interactions based on D(A-Ar)2 type small molecules for high performance organic solar cells. Solar Energy 161, 138-147 (2018)."
2927,O=C(N1CC(CC)CCCC)C(C2=C1C3=CC=CS3)=C(C4=CC=C(C5=CC=C(/C(C(N6CCCCCC)=O)=C7C(N(CCCCCC)C8=C\7C=CC(C(S9)=CC=C9C%10=C(C(N%11CC(CC)CCCC)=O)C(C(N%10CC(CC)CCCC)=O)=C%11C%12=CC=CS%12)=C8)=O)C6=C5)S4)N(CC(CC)CCCC)C2=O,DPP-Li-DPP,,,0.92,7.87,42.4,3.07,"	Zhang J, et al. A star-shaped photovoltaic organic molecule based on 1,3-diethyl-2-thiobarbituric acid reaches a power conversion efficiency of 3.07%. Thin Solid Films 645, 129-133 (2018)."
2928,CC1(C)C2=C(C=CC(/C=C(N=C)/N=C)=C2)C3=CC=C(N(C4=CC=CC=C4)C5=CC=CC=C5)C=C31,FCN,,,0.86,11.75,58,5.86,"	Jung JW. A low band gap conjugated small molecule based on isoindigo flanked with diketopyrrolopyrrole for efficient organic solar cells. Dyes and Pigments 137, 512-517 (2017)."
2929,CC1(C)C2=C(C=CC(/C=C3SC(N(CC)C\3=O)=S)=C2)C4=CC=C(N(C5=CC=CC=C5)C6=CC=CC=C6)C=C41,SCN,,,0.86,3.17,33,1.07,"	Dalinot C, Szal¨®ki G, Dindault C, Segut O, Sanguinet L, Leriche P. Spirobifluorene based small push-pull molecules for organic photovoltaic applications. Dyes and Pigments 140, 62-69 (2017)."
2930,CCN1C(S/C(C1=O)=C\C2=CC=C(C3=CC=C(C(N(CC(CC)CCCC)C4=O)=C5C4=C(C6=CC=C(C7=CC=C(/C=C8C(N(CC)C(S/8)=S)=O)S7)S6)N(CC(CCCC)CC)C5=O)S3)S2)=S,DPP2T-RH,,,0.73,5.35,35.7,1.67,"	Dalinot C, Szal¨®ki G, Dindault C, Segut O, Sanguinet L, Leriche P. Spirobifluorene based small push-pull molecules for organic photovoltaic applications. Dyes and Pigments 140, 62-69 (2017)."
2931,C=N/C(N=C)=C\C1=CC2=C(C=C1)C3=CC=C(N(C4=CC=CC=C4)C5=CC=CC=C5)C=C3C26C7=C(C=CC(/C=C(N=C)/N=C)=C7)C8=CC=C(N(C9=CC=CC=C9)C%10=CC=CC=C%10)C=C86,FRh,,,0.61,3.94,63,1.28,"	Eom Y, Song CE, Shin WS, Lee SK, Lim E. Rational design of ¦Ð-bridges for ambipolar DPP-RH-based small molecules in organic photovoltaic cells. Journal of Industrial and Engineering Chemistry 45, 338-348 (2017)."
2932,O=C(/C(S1)=C/C2=CC3=C(C=C2)C4=CC=C(N(C5=CC=CC=C5)C6=CC=CC=C6)C=C4C37C8=CC(N(C9=CC=CC=C9)C%10=CC=CC=C%10)=CC=C8C%11=C7C=C(/C=S(C(N(CC)C%12=O)=S)/C%12=C)C=C%11)N(CC)C1=S,SRh,,,0.79,1.94,32.3,0.59,"	Dalinot C, Szal¨®ki G, Dindault C, Segut O, Sanguinet L, Leriche P. Spirobifluorene based small push-pull molecules for organic photovoltaic applications. Dyes and Pigments 140, 62-69 (2017)."
2933,O=C(C1=C(C/2=O)C=CC=C1)C2=C\C3=CC(CC(CCCC)CC)=C(C4=CC5=C(C(SC(C(S6)=C(CC(CCCC)CC)C=C6/C=C(C7=O)\C(C8=C7C=CC=C8)=O)=C9)=C9[Si]5(CCCCCCCC)CCCCCCCC)S4)S3,DINDTS,,,0.65,3.08,31.3,0.75,"	Dalinot C, Szal¨®ki G, Dindault C, Segut O, Sanguinet L, Leriche P. Spirobifluorene based small push-pull molecules for organic photovoltaic applications. Dyes and Pigments 140, 62-69 (2017)."
2934,O=C(C(/C1=C(C#N)/C#N)=C\C2=CC(CC(CCCC)CC)=C(C3=CC4=C(C(SC(C(S5)=C(CC(CCCC)CC)C=C5/C=C(/C6=C(C#N)\C#N)C(C7=C6C=CC=C7)=O)=C8)=C8[Si]4(CCCCCCCC)CCCCCCCC)S3)S2)C9=C1C=CC=C9,DINCNDTS,,,0.799,13.5,61.2,6.6,"	Chen X, et al. Impact of end-capped groups on the properties of dithienosilole-based small molecules for solution-processed organic solar cells. Dyes and Pigments 147, 183-189 (2017)."
2935,N#C/C(C#N)=C\C1=CC(SC(C=C(C2=CC(C(OCC(CCCC)CC)=C(SC(C(C=C3)=CC4=C3N(CC(CCCC)CC)C5=C(S4)C=C(/C=C(C#N)\C#N)C=C5)=C6)C6=C7OCC(CCCC)CC)=C7S2)C=C8)=C8N9CC(CCCC)CC)=C9C=C1,SM1,,,0.857,1.82,37.3,0.58,"	Chen X, et al. Impact of end-capped groups on the properties of dithienosilole-based small molecules for solution-processed organic solar cells. Dyes and Pigments 147, 183-189 (2017)."
2936,CCC(CCCC)CN1C2=C(C=C(C3=CC(C(OCC(CCCC)CC)=C(SC(C(C=C4)=CC5=C4N(CC(CCCC)CC)C6=C(S5)C=C(/C=C7C(C(C=CC=C8)=C8C\7=O)=O)C=C6)=C9)C9=C%10OCC(CCCC)CC)=C%10S3)C=C2)SC%11=C1C=CC(/C=C%12C(C(C=CC=C%13)=C%13C\%12=O)=O)=C%11,SM2,,,0.99,11.18,56,6.2,"	Revoju S, Biswas S, Eliasson B, Sharma GD. Effect of acceptor strength on optical, electrochemical and photovoltaic properties of phenothiazine-based small molecule for bulk heterojunction organic solar cells. Dyes and Pigments 149, 830-842 (2018)."
2937,CCN1C(/C(SC1=S)=C/C2=CC=C(C3=CC(N(C(CCCCCC)CCCCCCCC)C4=C5C=CC(C6=CC7=C(C(C8=CC=C(C(CC)CCCC)S8)=C(C=C(C(C=C9)=CC%10=C9C(S%11)=C(N%10C(CCCCCC)CCCCCCCC)C=C%11C%12=CC=C(/C=C(S%13)/C(N(CC)C%13=S)=O)S%12)S%14)C%14=C7C%15=CC=C(C(CC)CCCC)S%15)S6)=C4)=C5S3)S2)=O,BDT-TITRH,,,1.04,12.06,60,7.45,"	Revoju S, Biswas S, Eliasson B, Sharma GD. Effect of acceptor strength on optical, electrochemical and photovoltaic properties of phenothiazine-based small molecule for bulk heterojunction organic solar cells. Dyes and Pigments 149, 830-842 (2018)."
2938,CCN1C(/C(SC1=S)=C/C2=CC=C(C3=CC(N(C(CCCCCC)CCCCCCCC)C4=C5C=CC(C6=CC=C(C7=CC8=C(C(C9=CC=C(C(CC)CCCC)S9)=C(C=C(C%10=CC=C(C(C=C%11)=CC%12=C%11C(S%13)=C(N%12C(CCCCCC)CCCCCCCC)C=C%13C%14=CC=C(/C=C(S%15)/C(N(CC)C%15=S)=O)S%14)S%10)S%16)C%16=C8C%17=CC=C(C(CC)CCCC)S%17)S7)S6)=C4)=C5S3)S2)=O,BDT-TI2TRH,,,0.8,13.05,33.8,3.52,"	Zhou X, et al. Thieno[3,2-b]indole (TI) bridged A-¦Ð?D-¦Ð?A small molecules: Synthesis, characterizations and organic solar cell applications. Dyes and Pigments 160, 16-24 (2019)."
2939,O=C1N(CC)C(S/C1=C\C2=CC=C(C3=CC(SC(C4=CC=C(C5=CC6=C(C(C7=CC=CS7)=C(C=C(C(S8)=CC=C8C9=CC(S%10)=C(S9)C=C%10C%11=CC=C(/C=C(C(N%12CC)=O)\SC%12=S)S%11)S%13)C%13=C6C%14=CC=CS%14)S5)S4)=C%15)=C%15S3)S2)=S,BTTR,,,0.85,13.23,37.3,4.19,"	Zhou X, et al. Thieno[3,2-b]indole (TI) bridged A-¦Ð?D-¦Ð?A small molecules: Synthesis, characterizations and organic solar cell applications. Dyes and Pigments 160, 16-24 (2019)."
2940,CCCCCCC1=C(C2=CC3=C(C(C4=CC=C(CCCCCC)S4)=C(C=C(C5=C(CCCCCC)C=C(C6=CC=CC7=NSN=C76)S5)S8)C8=C3C9=CC=C(CCCCCC)S9)S2)SC(C%10=CC=CC%11=NSN=C%11%10)=C1,BDT-HTH-BT,,,0.93,13.2,65.4,8,"	Ye C, et al. High-performance organic solar cells based on a small molecule with thieno[3,2-b]thiophene as ¦Ð-bridge. Organic Electronics 53, 273-279 (2018)."
2941,CCCCCCC(S1)=CC=C1C2=C3C(C=C(C4=CC=C(C5=CC(CCCCCC)=CS5)C6=NSN=C64)S3)=C(C7=CC=C(CCCCCC)S7)C8=C2C=C(C9=CC=C(C%10=CC(CCCCCC)=CS%10)C%11=NSN=C%119)S8,BDT-BT-HTH,,,1,2.12,17.5,0.37,"	Zhang J, et al. Impact of benzothiadiazole position on the photovoltaic properties of solution-processable organic molecule materials. Synthetic Metals 234, 47-52 (2017)."
2942,N12C3N=C(C4=C5C=CC=C4)N(Cl2N67)C5=NC6=C(C=CC=C8)C8=C7N=C1C9=C3C=CC=C9,CL-BsubPc,,,0.815,6.85,61.8,3.45,"	Zhang J, et al. Impact of benzothiadiazole position on the photovoltaic properties of solution-processable organic molecule materials. Synthetic Metals 234, 47-52 (2017)."
2943,CCN1C(/C(SC1=O)=C/C2=CC=C(C(N(CC(CC)CCCC)C3=O)=C4C3=C(C5=CC=C(/C=C(SC(N6CC)=O)/C6=S)S5)N(CC(CCCC)CC)C4=O)S2)=S,DPPT-RH,,,1.09,3.83,57,2.3,"	Garner RK, et al. Boron subphthalocyanines as electron donors in outdoor lifetime monitored organic photovoltaic cells. Solar Energy Materials and Solar Cells 176, 331-335 (2018)."
2944,N#CC(C1=NSN=C12)=CC=C2C3=CC4=C(C5=C([Si]4(CCCCCCCC)CCCCCCCC)C=C(C6=CC=C(C#N)C7=NSN=C67)S5)S3,BCNDTS,,,0.41,3.56,52,0.77,"	Eom Y, Song CE, Shin WS, Lee SK, Lim E. Rational design of ¦Ð-bridges for ambipolar DPP-RH-based small molecules in organic photovoltaic cells. Journal of Industrial and Engineering Chemistry 45, 338-348 (2017)."
2945,N#CC(C1=NSN=C12)=CC=C2C3=CC4=C(C5=C(C4(CCCCCCCC)CCCCCCCC)C=C(C6=CC=C(C#N)C7=NSN=C67)S5)S3,CBC,,,1.01,8.26,47,3.92,"	Chen K-W, et al. Fluorination effects of A-D-A-type small molecules on physical property and the performance of organic solar cell. Organic Electronics 52, 342-349 (2018)."
2946,N#CC(C1=NSN=C12)=CC(F)=C2C3=CC4=C(C5=C(C4(CCCCCCCC)CCCCCCCC)C=C(C6=C(F)C=C(C#N)C7=NSN=C67)S5)S3,CBCIF,,,0.94,10.25,44,4.24,"	Chen K-W, et al. Fluorination effects of A-D-A-type small molecules on physical property and the performance of organic solar cell. Organic Electronics 52, 342-349 (2018)."
2947,CCCCCCCCC(S1)=CC=C1C2=CC=C(C3=CC=C(CCCCCCCC)S3)C4=C2N=C(C5=CC=C(C6=CC=C(N(C7=CC=CC=C7)C8=CC=CC=C8)C=C6)C=C5)C(C9=CC=C(C%10=CC=C(N(C%11=CC=CC=C%11)C%12=CC=CC=C%12)C=C%10)C=C9)=N4,TPA-Q-TPA,,,0.96,10.17,51,4.98,"	Chen K-W, et al. Fluorination effects of A-D-A-type small molecules on physical property and the performance of organic solar cell. Organic Electronics 52, 342-349 (2018)."
2948,N#CC(C1=NSN=C12)=C(F)C=C2C3=CC4=C(C5=C(C4(CCCCCCCC)CCCCCCCC)C=C(C6=CC(F)=C(C#N)C7=NSN=C67)S5)S3,CBCOF,,,0.64,2.61,25,0.42,"	Yu J, Zhu W, Tan H, Peng Q. A novel D2-A-D1-A-D2-type donor¨Cacceptor conjugated small molecule based on a benzo[1,2- b :4,5- b ¡ä]dithiophene core for solution processed organic photovoltaic cells. Chemical Physics Letters 667, 254-259 (2017)."
2949,N#CC(C1=NSN=C12)=C(F)C(F)=C2C3=CC4=C(C5=C(C4(CCCCCCCC)CCCCCCCC)C=C(C6=C(F)C(F)=C(C#N)C7=NSN=C67)S5)S3,CBCdF,,,1.02,8.12,42,3.48,"	Chen K-W, et al. Fluorination effects of A-D-A-type small molecules on physical property and the performance of organic solar cell. Organic Electronics 52, 342-349 (2018)."
2950,O=C(C1=C(C/2=O)C=CC=C1)C2=C/C3=CC(CCCCCC)=C(/C=C/C4=C(CCCCCC)C=C(C5=CC=C(C(S6)=CC(CCCCCC)=C6/C=C/C7=C(CCCCCC)C=C(/C=C(C8=O)/C(C9=C8C=CC=C9)=O)S7)S5)S4)S3,HEX-3TVT-ID,,,1.06,6.87,35,2.52,"	Chen K-W, et al. Fluorination effects of A-D-A-type small molecules on physical property and the performance of organic solar cell. Organic Electronics 52, 342-349 (2018)."
2951,O=C(C1=C(C/2=O)C=CC=C1)C2=C/C3=CC(CCCCCC)=C(/C=C/C4=CC=C(C5=C(C(CC)CCCCC)C(C(CC)CCCCC)=C(C(S6)=CC=C6/C=C/C7=C(CCCCCC)C=C(/C=C(C8=O)/C(C9=C8C=CC=C9)=O)S7)S5)S4)S3,EH-3TVT-ID,,,0.53,7.7,56.1,2.3,"	Zhang J, et al. Photovoltaic molecules based on vinylene-bridged oligothiophene applied for bulk-heterojunction organic solar cells. Journal of Energy Chemistry 27, 426-431 (2018)."
2952,O=C1C2=C(CC(CC)CCCC)SC(CC(CC)CCCC)=C2C(C3=C(C4=CC=C(/C=C5SC(N(CC)C\5=O)=S)S4)SC(C(S6)=CC=C6C7=CC8=C(C9=CC=C(SCC(CC)CCCC)S9)C%10=C(C=C(C%11=CC=C(C%12=C%13C(C(C%14=CSC=C%14C%13=O)=O)=C(C%15=CC=C(/C=C%16SC(N(CC)C\%16=O)=S)S%15)S%12)S%11)S%10)C(C%17=CC=C(SCC(CC)CCCC)S%17)=C8S7)=C31)=O,SBDT-BDD,,,0.93,7,41.8,2.7,"	Zhang J, et al. Photovoltaic molecules based on vinylene-bridged oligothiophene applied for bulk-heterojunction organic solar cells. Journal of Energy Chemistry 27, 426-431 (2018)."
2953,O=C1C(C(C(N2CC(CC)CCCC)=O)=C(C3=NC=C(C4=CC=C(CCCCCCCC)S4)C=C3)N1CC(CC)CCCC)=C2C(C=C5)=NC=C5C6=CC(F)=C(C7=C(F)C=C(C8=CN=C(C(N(CC(CC)CCCC)C9=O)=C%10C9=C(C%11=CC=C(C%12=CC=C(CCCCCCCC)S%12)C=N%11)N(CC(CC)CCCC)C%10=O)C=C8)S7)S6,FBT(PyDPP-T)2,,,0.97,16.21,69.3,10.9,"	Huo Y, et al. Dual-Accepting-Unit Design of Donor Material for All-Small-Molecule Organic Solar Cells with Efficiency Approaching 11%. Chem. Mater. 30, 8661-8668 (2018)."
2954,FC1=C(C2=C(F)C=C(C3=CC(N(CC(CC)CCCC)C(/C4=C5C(C=CC(C6=CC=C(CCCCCCCC)S6)=C7)=C7N(CC(CC)CCCC)C\5=O)=O)=C4C=C3)S2)SC(C8=CC9=C(/C(C(N9CC(CC)CCCC)=O)=C%10C(N(CC(CC)CCCC)C%11=C\%10C=CC(C%12=CC=C(CCCCCCCC)S%12)=C%11)=O)C=C8)=C1,FBT(IID-T)2,,,0.765,13.53,61.81,6.4,"	Li M, et al. Efficient chemical structure and device engineering for achieving difluorinated 2,2¡ä-bithiophene-based small molecular organic solar cells with 9.0% efficiency. J. Mater. Chem. A 6, 12493-12505 (2018)."
2955,O=C1C(C(C(N2CC(CC)CCCC)=O)=C(C3=CC=C(S3)C4=CC=C(CCCCCCCC)S4)N1CC(CC)CCCC)=C2C5=CC=C(C6=CC(F)=C(C7=C(F)C=C(C8=CC=C(C(N(CC(CC)CCCC)C9=O)=C%10C9=C(C%11=CC=C(C%12=CC=C(CCCCCCCC)S%12)S%11)N(CC(CC)CCCC)C%10=O)S8)S7)S6)S5,FBT(TDPP-T)2,,,0.785,14.74,67.26,7.78,"	Li M, et al. Efficient chemical structure and device engineering for achieving difluorinated 2,2¡ä-bithiophene-based small molecular organic solar cells with 9.0% efficiency. J. Mater. Chem. A 6, 12493-12505 (2018)."
2956,COC(C=C1)=CC=C1C2=CC3=C(O2)C=C(/C(C(F)(F)F)=C4N=C(C=C(C5=CC=C(OC)C=C5)O6)C6=C\4)N3B(F)F,BDP-1,,,0.758,16.14,73.52,9,"	Li M, et al. Efficient chemical structure and device engineering for achieving difluorinated 2,2¡ä-bithiophene-based small molecular organic solar cells with 9.0% efficiency. J. Mater. Chem. A 6, 12493-12505 (2018)."
2957,COC(C=C1)=CC=C1C2=CC3=C(O2)C=C(/C(C(C(F)(F)F)(F)F)=C4N=C(C=C(C5=CC=C(OC)C=C5)O6)C6=C\4)N3B(F)F,BDP-2,,,0.72,13.6,60,6,"	Li T-y, et al. Boron dipyrromethene (BODIPY) with meso-perfluorinated alkyl substituents as near infrared donors in organic solar cells. J. Mater. Chem. A 6, 18583-18591 (2018)."
2958,COC(C=C1)=CC=C1C2=CC3=C(O2)C=C(/C(C(C(C(F)(F)F)(F)F)(F)F)=C4N=C(C=C(C5=CC=C(OC)C=C5)O6)C6=C\4)N3B(F)F,BDP-3,,,0.76,13.6,62,6.4,"	Li T-y, et al. Boron dipyrromethene (BODIPY) with meso-perfluorinated alkyl substituents as near infrared donors in organic solar cells. J. Mater. Chem. A 6, 18583-18591 (2018)."
2959,COC(C=C1)=CC=C1N(C2=CC=C(OC)C=C2)C3=CC=C(N(C4=CC=C(OC)C=C4)C5=CC=C(OC)C=C5)C6=NSN=C63,CS03,,,0.75,13.5,60,6.1,"	Li T-y, et al. Boron dipyrromethene (BODIPY) with meso-perfluorinated alkyl substituents as near infrared donors in organic solar cells. J. Mater. Chem. A 6, 18583-18591 (2018)."
2960,[H]/C(C(S1)=CC=C1C(S2)=CC3=C2C(OCC(CC)CCCC)=C(C=C(C4=CC=C(/C([H])=C5C(C6=CC=CC=C6)=NOC/5=O)S4)S7)C7=C3OCC(CCCC)CC)=C8C(C9=CC=CC=C9)=NOC\8=O,BDT-HTOX,,,0.67,12.81,62,5.32,"	Rodr¨ªguez-Seco C, Biswas S, Sharma GD, Vidal-Ferran A, Palomares E. Benzothiadiazole Substituted Semiconductor Molecules for Organic Solar Cells: The Effect of the Solvent Annealing Over the Thin Film Hole Mobility Values. The Journal of Physical Chemistry C 122, 13782-13789 (2018)."
2961,CCCCCCCCC(CCCCCCCCCC)CN1C2=C(C=CC(C3=CC=C(C4=CC=C(/C=C/C5=CC=C(OCCCCCCCCCC)C=C5)C6=NSN=C64)S3)=C2)C7=C1C=C(C8=CC=C(C9=CC=C(/C=C/C%10=CC=C(OCCCCCCCCCC)C=C%10)C%11=NSN=C9%11)S8)C=C7,CzBT-DP,,,0.88,3.26,27.9,0.8,"	Sylvianti N, et al. New A-D-A type small molecules based on benzodithiophene derivative for organic solar cells. Molecular Crystals and Liquid Crystals 660, 66-71 (2018)."
2962,O=C(/C(S/1)=C/C2=CC(CCCCCCCC)=C(S2)C(S3)=CC(CCCCCCCC)=C3C4=CC=C(C5=C(CCCCCCCC)C=C(C6=C(CCCCCCCC)C=C(/C=C7C(N(CC)/C(S/7)=C(C#N)/C#N)=O)S6)S5)S4)N(CC)C1=C(C#N)\C#N,DRCN5T,,,0.94,1.78,38.3,0.64,"	Sylvianti N, Kim YH, Marsya MA, Kim DG, Kim JH. A-¦Ð-D-¦Ð-A type oligomer based on carbazole and benzothiadiazole for organic solar cells. Molecular Crystals and Liquid Crystals 655, 166-172 (2017)."
2963,S=C(N(CC)C/1=O)SC1=C\C(S2)=CC3=C2C(C4=CC=C(CC(CC)CCCC)S4)=C(C=C(C5=CC6=C(C(C7=CC=C(CC(CC)CCCC)S7)=C(C=C(C8=CC9=C(C(C%10=CC=C(CC(CC)CCCC)S%10)=C(C=C(/C=C%11C(N(CC)C(S/%11)=S)=O)S%12)C%12=C9C%13=CC=C(CC(CC)CCCC)S%13)S8)S%14)C%14=C6C%15=CC=C(CC(CC)CCCC)S%15)S5)S%16)C%16=C3C%17=CC=C(CC(CC)CCCC)S%17,C2,,,0.864,15.21,64.1,8.42,"	Wang Y, Chang M, Kan B, Wan X, Li C, Chen Y. All-Small-Molecule Organic Solar Cells Based on Pentathiophene Donor and Alkylated Indacenodithiophene-Based Acceptors with Efficiency over 8%. ACS Applied Energy Materials 1, 2150-2156 (2018)."
2964,S=C(N(CCCC)C/1=O)SC1=C\C(S2)=CC3=C2C(C4=CC=C(CC(CC)CCCC)S4)=C(C=C(C5=CC6=C(C(C7=CC=C(CC(CC)CCCC)S7)=C(C=C(C8=CC9=C(C(C%10=CC=C(CC(CC)CCCC)S%10)=C(C=C(/C=C%11C(N(CCCC)C(S/%11)=S)=O)S%12)C%12=C9C%13=CC=C(CC(CC)CCCC)S%13)S8)S%14)C%14=C6C%15=CC=C(CC(CC)CCCC)S%15)S5)S%16)C%16=C3C%17=CC=C(CC(CC)CCCC)S%17,C4,,,0.893,16.66,64,9.52,"	Yang L, et al. Modulating Molecular Orientation Enables Efficient Nonfullerene Small-Molecule Organic Solar Cells. Chem. Mater. 30, 2129-2134 (2018)."
2965,S=C(N(CCCCCC)C/1=O)SC1=C\C(S2)=CC3=C2C(C4=CC=C(CC(CC)CCCC)S4)=C(C=C(C5=CC6=C(C(C7=CC=C(CC(CC)CCCC)S7)=C(C=C(C8=CC9=C(C(C%10=CC=C(CC(CC)CCCC)S%10)=C(C=C(/C=C%11C(N(CCCCCC)C(S/%11)=S)=O)S%12)C%12=C9C%13=CC=C(CC(CC)CCCC)S%13)S8)S%14)C%14=C6C%15=CC=C(CC(CC)CCCC)S%15)S5)S%16)C%16=C3C%17=CC=C(CC(CC)CCCC)S%17,C6,,,0.909,18.27,68,11.24,"	Yang L, et al. Modulating Molecular Orientation Enables Efficient Nonfullerene Small-Molecule Organic Solar Cells. Chem. Mater. 30, 2129-2134 (2018)."
2966,S=C(N(CCCCCCCC)C/1=O)SC1=C\C(S2)=CC3=C2C(C4=CC=C(CC(CC)CCCC)S4)=C(C=C(C5=CC6=C(C(C7=CC=C(CC(CC)CCCC)S7)=C(C=C(C8=CC9=C(C(C%10=CC=C(CC(CC)CCCC)S%10)=C(C=C(/C=C%11C(N(CCCCCCCC)C(S/%11)=S)=O)S%12)C%12=C9C%13=CC=C(CC(CC)CCCC)S%13)S8)S%14)C%14=C6C%15=CC=C(CC(CC)CCCC)S%15)S5)S%16)C%16=C3C%17=CC=C(CC(CC)CCCC)S%17,C8,,,0..929,17.92,63,10.52,"	Yang L, et al. Modulating Molecular Orientation Enables Efficient Nonfullerene Small-Molecule Organic Solar Cells. Chem. Mater. 30, 2129-2134 (2018)."
2967,CCCCCCC(S1)=CC=C1C2=CC=C(S2)C3=CN=C(C4=NSN=C43)C5=CC([Si]6(CC(CC)CCCC)CC(CC)CCCC)=C(S5)C7=C6C=C(S7)C8=NC9=C(S8)C(C%10=CC=C(CC(CC)CCCC)S%10)=C%11C(SC(C%12=CC([Si](CC(CC)CCCC)(CC(CC)CCCC)C%13=C%14SC(C%15=NC=C(C%16=CC=C(C%17=CC=C(CCCCCC)S%17)S%16)C%18=NSN=C%18%15)=C%13)=C%14S%12)=N%11)=C9C%19=CC=C(CC(CC)CCCCC)S%19,BBTz-X,,,0.928,16.15,61,9.14,"	Yang L, et al. Modulating Molecular Orientation Enables Efficient Nonfullerene Small-Molecule Organic Solar Cells. Chem. Mater. 30, 2129-2134 (2018)."
2968,CCCCCCC(S1)=CC=C1C2=CC=C(S2)C3=CN=C(C4=NSN=C43)C5=CC([Si]6(CC(CC)CCCC)CC(CC)CCCC)=C(S5)C7=C6C=C(S7)C8=CC9=C(S8)C(C%10=CC=C(CC(CC)CCCC)S%10)=C%11C(SC(C%12=CC([Si](CC(CC)CCCC)(CC(CC)CCCC)C%13=C%14SC(C%15=NC=C(C%16=CC=C(C%17=CC=C(CCCCCC)S%17)S%16)C%18=NSN=C%18%15)=C%13)=C%14S%12)=C%11)=C9C%19=CC=C(CC(CC)CCCCC)S%19,BDT-X,,,0.84,12.27,69.5,7.2,"	Zhang S, et al. Intermediate-Sized Conjugated Donor Molecules for Organic Solar Cells: Comparison of Benzodithiophene and Benzobisthiazole-Based Cores. Chem. Mater. 29, 7880-7887 (2017)."
2969,CCCCCCC(S1)=CC=C1C2=CC=C(S2)C3=CN=C(C4=NSN=C43)C5=CC([Si]6(CC(CC)CCCC)CC(CC)CCCC)=C(S5)C7=C6C=C(S7)C8=CC=C(C9=CC([Si](CC(CC)CCCC)(CC(CC)CCCC)C%10=C%11SC(C%12=CC=C(C%13=CC([Si](CC(CC)CCCC)(CC(CC)CCCC)C%14=C%15SC(C%16=NC=C(C%17=CC=C(C%18=CC=C(CCCCCC)S%18)S%17)C%19=NSN=C%19%16)=C%14)=C%15S%13)C%20=NSN=C%20%12)=C%10)=C%11S9)C%21=NSN=C%218,X2,,,0.78,13.71,73.04,7.74,"	Zhang S, et al. Intermediate-Sized Conjugated Donor Molecules for Organic Solar Cells: Comparison of Benzodithiophene and Benzobisthiazole-Based Cores. Chem. Mater. 29, 7880-7887 (2017)."
2970,FC1(F)OC(C=C(O1)/C=C/C2=CC=C(N(C3=CC=CC=C3)C4=CC=CC=C4)C=C2)/C=C/C5=CC=C(N(C6=CC=CC=C6)C7=CC=CC=C7)C=C5,1,,,0.66,15.41,69,7.01,"	Zhang S, et al. Intermediate-Sized Conjugated Donor Molecules for Organic Solar Cells: Comparison of Benzodithiophene and Benzobisthiazole-Based Cores. Chem. Mater. 29, 7880-7887 (2017)."
2971,FB(F)N(C(/C(C1=CC=C(OCCCCCCCC)C=C1)=C2N=CC(C#CC3=CC4=C(C(OCCCCCCCC)=C(C=CS5)C5=C4OCCCCCCCC)S3)=C\2)=C6)C=C6C#CC7=CC8=C(OCCCCCCCC)C9=C(C=CS9)C(OCCCCCCCC)=C8S7,BDP-dBDT,,,1.01,9.85,42,4.14,"	Archet F, et al. Synthesis of Bioinspired Curcuminoid Small Molecules for Solution-Processed Organic Solar Cells with High Open-Circuit Voltage. ACS Energy Letters 2, 1303-1307 (2017)."
2972,FC1=C(C2=NSN=C2C(C3=CC=C(C4=CC5=C(C(C=C(C(CC(CC)CCCC)(CC(CC)CCCC)C6=C7SC(C8=CC=C(C9=C(F)C(F)=C(C%10=CC=C(C%11=CC=C(CCCCCC)S%11)S%10)C%12=NSN=C%129)S8)=C6)C7=C%13)=C%13C5(CC(CC)CCCC)CC(CC)CCCC)S4)S3)=C1F)C%14=CC=C(S%14)C%15=CC=C(CCCCCC)S%15,BIT-4F,,,0.7,12.98,62,5.61,"	Liao J, et al. BODIPY-based panchromatic chromophore for efficient organic solar cell. Organic Electronics 61, 215-222 (2018)."
2973,O=C(C(C=CC=C1)=C1C/2=O)C2=C/C(S3)=CC(CCCCCCCC)=C3C(S4)=CC5=C4C(C6=CC=C(CC(CC)CCCC)S6)=C(C=C(C7=C(CCCCCCCC)C=C(/C=C8C(C(C=CC=C9)=C9C\8=O)=O)S7)S%10)C%10=C5C%11=CC=C(CC(CC)CCCC)S%11,BDTTID,,,0.89,12.56,77.31,8.61,"	Yan J, et al. Optimized Phase Separation and Reduced Geminate Recombination in High Fill Factor Small-Molecule Organic Solar Cells. ACS Energy Letters 2, 14-21 (2016)."
2974,O=C1C2=C(C=CC=C2)C(/C1=C\C3=CC(CCCCCCCC)=C(S3)C(S4)=CC=C4C5=C(CCCCCCCC)C=C(S5)C(S6)=CC7=C6C(C8=CC=C(CC(CC)CCCC)S8)=C(C=C(C9=CC(CCCCCCCC)=C(C%10=CC=C(C%11=C(CCCCCCCC)C=C(/C=C%12C(C(C=CC=C%13)=C%13C\%12=O)=O)S%11)S%10)S9)S%14)C%14=C7C%15=CC=C(CC(CC)CCCC)S%15)=O,BDT3TID,,,1.03,10.2,53,5.54,"	Lee KC, et al. Influence of the Crystalline Nature of Small Donors Molecules on the Efficiency and Stability of Organic Photovoltaic Devices. Solar RRL 2, 1700235 (2018)."
2975,O=C(OCC(CC)CCCC)/C(C#N)=C/C(S1)=CC=C1C2=C(OCCCCCCCC)C(OCCCCCCCC)=C(C3=NSN=C32)C4=CC=C(S4)C(S5)=CC6=C5C(C7=CC=C(CC(CC)CCCC)S7)=C(C=C(C8=CC=C(C9=C(OCCCCCCCC)C(OCCCCCCCC)=C(C%10=CC=C(/C=C(C(OCC(CC)CCCC)=O)\C#N)S%10)C%11=NSN=C9%11)S8)S%12)C%12=C6C%13=CC=C(CC(CC)CCCC)S%13,SM-BT2OR,,,0.89,9.04,59,4.74,"	Lee KC, et al. Influence of the Crystalline Nature of Small Donors Molecules on the Efficiency and Stability of Organic Photovoltaic Devices. Solar RRL 2, 1700235 (2018)."
2976,O=C(OCC(CC)CCCC)/C(C#N)=C/C(S1)=C(CCCCCCCC)C=C1C2=C(F)C(F)=C(C3=NSN=C32)C4=CC(CCCCCCCC)=C(S4)C(S5)=CC6=C5C(C7=CC=C(CC(CC)CCCC)S7)=C(C=C(C8=C(CCCCCCCC)C=C(C9=C(F)C(F)=C(C%10=CC(CCCCCCCC)=C(/C=C(C(OCC(CC)CCCC)=O)\C#N)S%10)C%11=NSN=C9%11)S8)S%12)C%12=C6C%13=CC=C(CC(CC)CCCC)S%13,SM-BT2F,,,0.939,13.57,56.5,7.2,"	Qiu B, et al. Effects of Alkoxy and Fluorine Atom Substitution of Donor Molecules on the Morphology and Photovoltaic Performance of All Small Molecule Organic Solar Cells. Front Chem 6, 413 (2018)."
2977,S=C(N(CC)C/1=O)SC1=C/C2=C(CCCCCCCC)C=C(S2)C(C3=NSN=C34)=CC=C4C5=CC=C6C(SC(C=C(C7=CC=C(C8=CC(CCCCCCCC)=C(/C=C9C(N(CC)C(S/9)=S)=O)S8)C%10=NSN=C7%10)C=C%11)C%11N6CC(CC)CCCC)=C5,SM1,,,0.983,6.74,41.7,2.76,"	Qiu B, et al. Effects of Alkoxy and Fluorine Atom Substitution of Donor Molecules on the Morphology and Photovoltaic Performance of All Small Molecule Organic Solar Cells. Front Chem 6, 413 (2018)."
2978,S=C(N(CC)C/1=O)SC1=C/C2=C(CCCCCCCC)C=C(S2)C(C3=NSN=C34)=CC=C4C5=CC=C6C(SC(C=C(C7=CC=C(C8=CC(CCCCCCCC)=C(/C=C9C(N(CC)C(S/9)=S)=O)S8)C%10=NSN=C7%10)C=C%11)C%11N6CCOCCOC)=C5,SM2,,,0.81,9.38,52,3.95,"	Revoju S, Biswas S, Eliasson B, Sharma GD. Phenothiazine-based small molecules for bulk heterojunction organic solar cells; variation of side-chain polarity and length of conjugated system. Organic Electronics 65, 232-242 (2019)."
2979,S=C(N(CC)C/1=O)SC1=C/C2=C(CCCCCCCC)C=C(S2)C3=CC=C(C4=CC(CCCCCCCC)=C(S4)C5=CC=C6C(SC(C=C(C7=C(CCCCCCCC)C=C(C8=CC=C(C9=CC(CCCCCCCC)=C(/C=C%10C(N(CC)C(S/%10)=S)=O)S9)C%11=NSN=C8%11)S7)C=C%12)C%12N6CCOCCOC)=C5)C%13=NSN=C3%13,SM3,,,0.93,11.94,59,6.55,"	Revoju S, Biswas S, Eliasson B, Sharma GD. Phenothiazine-based small molecules for bulk heterojunction organic solar cells; variation of side-chain polarity and length of conjugated system. Organic Electronics 65, 232-242 (2019)."
2980,FC(C=C1)=CC=C1/C(C#N)=C/C(C=C2)=CC3=C2N(CCCCC)C4=C3C=C(/C=C(C#N)/C5=CC=C(F)C=C5)C=C4,FHCS,,,0.93,12.42,62,7.16,"	Revoju S, Biswas S, Eliasson B, Sharma GD. Phenothiazine-based small molecules for bulk heterojunction organic solar cells; variation of side-chain polarity and length of conjugated system. Organic Electronics 65, 232-242 (2019)."
2981,FC(C=C1)=CC=C1/C(C#N)=C/C(C=C2)=CC3=C2N(CC(CC)CCC)C4=C3C=C(/C=C(C#N)/C5=CC=C(F)C=C5)C=C4,FBCS,,,0.75,2.02,26.1,0.4,"	Sathiyan G, Siva G, Prakash J, Swart HC, Sakthivel P. Design and chemical engineering of carbazole-based donor small molecules for organic solar cell applications. Journal of Materials Science: Materials in Electronics 29, 14842-14851 (2018)."
2982,CCCCCN1C2=C(C=C(/C=C(C#N)/C3=CC=C([N+]([O-])=O)C=C3)C=C2)C4=C1C=CC(/C=C(C#N)/C5=CC=C([N+]([O-])=O)C=C5)=C4,NHCS,,,0.76,2.72,27.54,0.57,"	Sathiyan G, Siva G, Prakash J, Swart HC, Sakthivel P. Design and chemical engineering of carbazole-based donor small molecules for organic solar cell applications. Journal of Materials Science: Materials in Electronics 29, 14842-14851 (2018)."
2983,CCCC(CC)CN1C2=C(C=C(/C=C(C#N)/C3=CC=C([N+]([O-])=O)C=C3)C=C2)C4=C1C=CC(/C=C(C#N)/C5=CC=C([N+]([O-])=O)C=C5)=C4,NBCS,,,0.77,3.9,29.76,0.9,"	Sathiyan G, Siva G, Prakash J, Swart HC, Sakthivel P. Design and chemical engineering of carbazole-based donor small molecules for organic solar cell applications. Journal of Materials Science: Materials in Electronics 29, 14842-14851 (2018)."
2984,CC1=CC=C([Se]1)/C=C/C([Se]2)=CC=C2C3=C4C(C=C(C5=CC=C(C(N(C)C6=O)=C7C6=C(C8=CC=CS8)N(C)C7=O)S5)S4)=C(C9=CC=C(/C=C/C%10=CC=C(C)[Se]%10)[Se]9)C%11=C3C=C(C%12=CC=C(C(N(C)C%13=O)=C%14C%13=C(C%15=CC=CS%15)N(C)C%14=O)S%12)S%11,SeBDT-DPP,,,0.75,4.35,30.07,0.98,"	Sathiyan G, Siva G, Prakash J, Swart HC, Sakthivel P. Design and chemical engineering of carbazole-based donor small molecules for organic solar cell applications. Journal of Materials Science: Materials in Electronics 29, 14842-14851 (2018)."
2985,CC(C1=NSN=C12)=CC=C2C(S3)=CC=C3C(S4)=CC5=C4C(OCC(CC)CCCCCC)C(C=C(C6=CC=C(C7=CC=C(C)C8=NSN=C87)S6)S9)=C9C5OCC(CCCCCC)CC,BDT-TBT,,,0.79,10.98,58,5.04,"	Shin Y, Song CE, Lee WH, Lee SK, Shin WS, Kang IN. Synthesis and Characterization of a Soluble A-D-A Molecule Containing a 2D Conjugated Selenophene-Based Side Group for Organic Solar Cells. Macromol Rapid Commun 38,  (2017)."
2986,CCC(CCCCCC)COC1C2=C(C=C(C3=CC=C(C4=C(CCCCCC)C=C(C5=CC=C(C)C6=NSN=C56)S4)S3)S2)C(OCC(CC)CCCCCC)C7=C1C=C(C8=CC=C(C9=C(CCCCCC)C=C(C%10=CC=C(C)C%11=NSN=C%10%11)S9)S8)S7,BDT-THTBT,,,0.84,2.56,31.9,0.69,"	Sylvianti N, et al. Synthesis of Conjugated Materials Based on Benzodithiophene - Benzothiadazole and Their Application of Organic Solar Cells. Macromolecular Research 26, 552-556 (2018)."
2987,O=C(N1CC(CC)CCCC)C(C2=C1C3=CC=C(S3)C#C/C(C4=CC=C5N4[Zn]N6/C(C=C/C6=C7\C8=CC=C(CC(CC)CCCC)S8)=C(C#CC9=CC=C(C%10=C%11C(C(N%10CC(CC)CCCC)=O)=C(C%12=CC=CS%12)N(CC(CC)CCCC)C%11=O)S9)\C(C=C/%13)=NC%13=C5\C%14=CC=C(CC(CC)CCCC)S%14)=C%15N=C7C=C/%15)=C(C%16=CC=CS%16)N(CC(CC)CCCC)C2=O,DPPEZnP-TEH,,,0.82,4.2,30.1,1.04,"	Sylvianti N, et al. Synthesis of Conjugated Materials Based on Benzodithiophene - Benzothiadazole and Their Application of Organic Solar Cells. Macromolecular Research 26, 552-556 (2018)."
2988,CC(C)(C)C1=CC2=C(C=C1)C3=C(C=C(C(C)(C)C)C=C3)C24C(C=C(C5=C(CC(CC)CCCC)C=C(/C=C6C(C(C=CC=C7)=C7C/6=O)=O)S5)S8)=C8C9=C4C=C(C%10=C(CC(CC)CCCC)C=C(/C=C%11C(C(C=CC=C%12)=C%12C\%11=O)=O)S%10)S9,STFTYT,,,0.8,12.4,57.26,5.68,"	Tan W-Y, et al. Enhancing Performances of Solution-Processed Inverted Ternary Small-Molecule Organic Solar Cells: Manipulating the Host-Guest Donors and Acceptor Interaction. Solar RRL 1, 1600003 (2017)."
2989,FC1=C(C2=NSN=C2C(C3=CC4=C(C(C(CC(CC)CCCC)(CC(CC)CCCC)C5=C6C=C7C(C(SC8=C9SC(C%10=C(F)C(F)=C(C%11=CC=C(C%12=CC=C(CCCCCC)S%12)S%11)C%13=NSN=C%13%10)=C8)=C9C7(CC(CC)CCCC)CC(CC)CCCC)=C5)=C6S4)S3)=C1F)C%14=CC=C(C%15=CC=C(CCCCCC)S%15)S%14,DT4FIDTT,,,0.97,12.54,50.8,6.17,"	Wang J, et al. STFTYT: A simple and broadly absorbing small molecule for efficient organic solar cells with a very low energy loss. Organic Electronics 57, 45-52 (2018)."
2990,FC1=C(C2=NSN=C2C(C3=CC4=C(C(C(CC(CC)CCCC)(CC(CC)CCCC)C5=C6C=C7C(C(SC8=C9SC(C%10=C(F)C(F)=C(C%11=CC(SC(CCCCCC)=C%12)=C%12S%11)C%13=NSN=C%13%10)=C8)=C9C7(CC(CC)CCCC)CC(CC)CCCC)=C5)=C6S4)S3)=C1F)C%14=CC(SC(CCCCCC)=C%15)=C%15S%14,TT4FIDTT,,,0.92,13.49,74,9.15,"	Wang J-L, et al. Branched 2-Ethylhexyl Substituted Indacenodithieno[3,2-b]Thiophene Core Enabling Wide-Bandgap Small Molecule for Fullerene-Based Organic Solar Cells with 9.15% Efficiency: Effect of Length and Position of Fused Polycyclic Aromatic Units. Solar RRL 2, 1800108 (2018)."
2991,CCCCCCCCC(S1)=C(CCCCCCCC)C=C1C2=C3C(C=C(C4=NC=C(C5=CC=C(C6=CC=C(CCCCCC)S6)S5)C7=NSN=C74)S3)=C(C8=CC(CCCCCCCC)=C(CCCCCCCC)S8)C9=C2C=C(C%10=NC=C(C%11=CC=C(C%12=CC=C(CCCCCC)S%12)S%11)C%13=NSN=C%13%10)S9,BDTDPTz,,,0.94,11.17,70,7.35,"	Wang J-L, et al. Branched 2-Ethylhexyl Substituted Indacenodithieno[3,2-b]Thiophene Core Enabling Wide-Bandgap Small Molecule for Fullerene-Based Organic Solar Cells with 9.15% Efficiency: Effect of Length and Position of Fused Polycyclic Aromatic Units. Solar RRL 2, 1800108 (2018)."
2992,O=C1N(CC(CC)CCCC)C(C2=C(C3=CC=C(N(C4=CC=CC=C4)C5=CC=CC=C5)C=C3)SC(C6=CC=C(N(C7=CC=CC=C7)C8=CC=CC=C8)C=C6)=C21)=O,TPA-TPD,,,0.868,12.83,56.4,6.28,"	Wang K, et al. Synthesis of organic molecule donor for efficient organic solar cells with low acceptor content. Organic Electronics 64, 54-61 (2019)."
2993,O=C(/C(S/1)=C/CC(S2)=CC(CCCCCCCCCCCC)=C2C3=CC(SC(C4=C(CCCCCCCCCCCC)C=C(C/C=C5SC(C(C#N)C#N)N(CC)C\5=O)S4)=C6)=C6S3)N(CC)C1=C(C#N)\C#N,DRCN3TT,,,0.97,7.3,33,2.32,"	Garcias-Morales C, et al. Small Molecules Derived from Thieno[3,4-c]pyrrole-4,6-dione (TPD) and Their Use in Solution Processed Organic Solar Cells. Molecules 22,  (2017)."
2994,O=C(/C(S/1)=C/C2=CC(CCCCCCCC)=C(S2)C(S3)=CC(CCCCCCCCCCCC)=C3C4=CC(SC(C5=C(CCCCCCCCCCCC)C=C(C6=C(CCCCCCCC)C=C(/C=C7SC(C(C#N)C#N)N(CC)C\7=O)S6)S5)=C8)=C8S4)N(CC)C1=C(C#N)\C#N,DRCN5TT,,,0.94,6.15,66.6,3.85,"	Wang Y, et al. Two Thieno[3,2-b]thiophene-Based Small Molecules as Bifunctional Photoactive Materials for Organic Solar Cells. Solar RRL 2, 1700179 (2018)."
2995,[O-]C1=C(/C(/C1=C/C2=[N+](CCCC)C(C=CC=C3)=C3S2)=C(C#N)/C#N)C4=CC=C(N(CCCC)CCCC)C=C4,diCN-USQ-1,,,0.9,12.43,62.9,7.03,"	Wang Y, et al. Two Thieno[3,2-b]thiophene-Based Small Molecules as Bifunctional Photoactive Materials for Organic Solar Cells. Solar RRL 2, 1700179 (2018)."
2996,[O-]C1=C(/C(/C1=C/C2=[N+](CCCC)C(C=CC=C3)=C3S2)=C(C#N)/C#N)C4=C(O)C=C(N(CCCC)CCCC)C=C4,diCN-USQ-2,,,0.61,6.51,37,1.49,"	Wu J, et al. Central dicyanomethylene-substituted unsymmetrical squaraines and their application in organic solar cells. J. Mater. Chem. A 6, 5797-5806 (2018)."
2997,[O-]C1=C(/C(/C1=C/C2=[N+](CCCC)C(C(C=CC=C3)=C3C=C4)=C4C2(C)C)=C(C#N)/C#N)C5=C(O)C=C(N6C(CCC7)C7C8=C6C=CC=C8)C=C5,diCN-USQ-3,,,0.65,7.75,38,1.91,"	Wu J, et al. Central dicyanomethylene-substituted unsymmetrical squaraines and their application in organic solar cells. J. Mater. Chem. A 6, 5797-5806 (2018)."
2998,FC1=C(C2=CC(CCCCCCCC)=C(C3=CC4=C(C(C#C[Si](C)(C)C)=C(C=C(C5=C(CCCCCCCC)C=C(C6=C(F)C=C(C7=CC=C(C8=CC=C(CC(CCCCCCCC)CCCCCCCCCC)S8)S7)C9=NSN=C96)S5)S%10)C%10=C4C#C[Si](C(C)C)(C(C)C)C(C)C)S3)S2)C%11=NSN=C%11C(C%12=CC=C(C%13=CC=C(CC(CCCCCCCCCC)CCCCCCCC)S%13)S%12)=C1,BDTTIPS,,,0.87,10.89,49,4.58,"	Wu J, et al. Central dicyanomethylene-substituted unsymmetrical squaraines and their application in organic solar cells. J. Mater. Chem. A 6, 5797-5806 (2018)."
2999,O=C1N(CC(CC)CCCC)C(C2=C(C3=CC=C(/C=C(C4=CC=C(C5=CC=C(N(C6=CC=CC=C6)C7=CC=CC=C7)C=C5)C=C4)\C#N)S3)SC(C8=CC=C(/C=C(C9=CC=C(C%10=CC=C(N(C%11=CC=CC=C%11)C%12=CC=CC=C%12)C=C%10)C=C9)\C#N)S8)=C21)=O,TPA-PT-TPD,,,0.88,7.68,59.06,3.99,"	Xie R, et al. Diethynylbenzo[1,2-b:4,5-b¡ä]dithiophene-based small molecule and cross-conjugated copolymers for organic solar cells. Journal of Polymer Science Part A: Polymer Chemistry 55, 660-671 (2017)."
3000,O=C1N(CC(CC)CCCC)C(C2=CC=C(S2)C#CC3=C(CCCCCCCC)C=C(S3)C4=CC(CCCCCCCC)=C(C#CC5=CC=C(C(N(CC(CC)CCCC)C6=O)=C7C6=C(C8=CC=CS8)N(CC(CC)CCCC)C7=O)S5)S4)=C9C1=C(C%10=CC=CS%10)N(CC(CC)CCCC)C9=O,BT(DTDPPA)2,,,0.8,3.1,27,0.67,"	Garcias-Morales C, et al. Small Molecules Derived from Thieno[3,4-c]pyrrole-4,6-dione (TPD) and Their Use in Solution Processed Organic Solar Cells. Molecules 22,  (2017)."
3001,O=C1N(CC(CC)CCCC)C(C2=CC=C(S2)C#CC3=C(CCCCCCCC)C=C(S3)C4=CC(CCCCCCCC)=C(C#CC5=CC=C(C(N(CC(CC)CCCC)C6=O)=C7C6=C(C8=CC=C(C9=CC(C=CC=C%10)=C%10O9)S8)N(CC(CC)CCCC)C7=O)S5)S4)=C%11C1=C(C%12=CC=C(C%13=CC%14=C(C=CC=C%14)O%13)S%12)N(CC(CC)CCCC)C%11=O,BT(BFuDTDPPA)2,,,0.96,4.53,33.5,1.45,"	Yu P-P, et al. Bis(dithienyldiketopyrrolopyrrole) compounds with a diethynylbithienyl linkage for organic solar cells. Dyes and Pigments 154, 100-106 (2018)."
3002,O=C1N(CC(CC)CCCC)C(C2=CC=CS2)=C3C(N(CC(CC)CCCC)C(C4=CC=C(S4)C#CC5=C(C=CC=C6)C6=C(C#CC7=CC=C(C(N(CC(CC)CCCC)C8=O)=C9C8=C(C%10=CC=CS%10)N(CC(CC)CCCC)C9=O)S7)C%11=C5C=CC=C%11)=C31)=O,An(DTDPPA)2,,,0.81,9.05,62.8,4.6,"	Yu P-P, et al. Bis(dithienyldiketopyrrolopyrrole) compounds with a diethynylbithienyl linkage for organic solar cells. Dyes and Pigments 154, 100-106 (2018)."
3003,CCCCCCCCOC(C(OCCCCCCCC)=C(C1=CC=C(C(S2)=CC=C2C3=C(OCCCCCCCC)C(OCCCCCCCC)=C(C4=CC=CS4)C5=NSN=C53)S1)C6=NSN=C67)=C7C8=CC=CS8,S2,,,0.905,11.32,51,5.26,"	Zhang C-H, et al. An easily and environmentally friendly accessible small-molecule acetylenic donor for organic solar cells. Dyes and Pigments 160, 983-988 (2019)."
3004,O=C1N(CC(CC)CCCC)C(C2=C(C3=CC=C(/C(C#N)=C/C4=CC=C(C5=CC=C(N(C6=CC=CC=C6)C7=CC=CC=C7)C=C5)S4)S3)SC(C8=CC=C(/C(C#N)=C/C9=CC=C(C%10=CC=C(N(C%11=CC=CC=C%11)C%12=CC=CC=C%12)C=C%10)S9)S8)=C21)=O,TPA-TT-TPD,,,0.99,4.75,29.46,1.38,"	Zhang G, et al. An Open-Circuit Voltage and Power Conversion Efficiency Study of Fullerene Ternary Organic Solar Cells Based on Oligomer/Oligomer and Oligomer/Polymer. Macromol Rapid Commun 38,  (2017)."
3005,S=C(N(CC)C/1=O)SC1=C\C(S2)=CC3=C2C(OCC(CC)CCCC)=C4C(SC(C(S5)=CC6=C5C(OCC(CC)CCCC)=C(C=C(C7=CC8=C(C(OCC(CC)CCCC)=C(C=C(/C=C9C(N(CC)C(S/9)=S)=O)S%10)C%10=C8OCC(CC)CCCC)S7)S%11)C%11=C6OCC(CC)CCCC)=C4)=C3OCC(CC)CCCC,DRTB-O,,,0.74,3.6,30,0.81,"	Garcias-Morales C, et al. Small Molecules Derived from Thieno[3,4-c]pyrrole-4,6-dione (TPD) and Their Use in Solution Processed Organic Solar Cells. Molecules 22,  (2017)."
3006,FC(C=C(C1=CC=C(C2=CC=C(CCCCCC)S2)S1)C3=CSC=C34)=C4C(C=C5)=CC=C5N(C6=CC=C(C7=C(F)C=C(C8=CC=C(C9=CC=C(CCCCCC)S9)S8)C%10=NSN=C7%10)C=C6)C%11=CC=C(C%12=C(F)C=C(C%13=CC=C(C%14=CC=C(CCCCCC)S%14)S%13)C%15=NSN=C%15%12)C=C%11,3BTF-TPA,,,1.01,7.49,65,4.91,"	Zhang S, et al. Influence of the replacement of alkoxyl with alkylthienyl on photovoltaic properties of two small molecule donors for organic solar cells. Sci. China Chem. 60, 1340-1348 (2017)."
3007,FC1=C(C(C=C2)=CC=C2N(C3=CC=C(C4=C(F)C=C(C5=CC=C(C6=CC=CS6)S5)C7=NSN=C47)C=C3)C(C=C8)=CC=C8C(S9)=CC=C9C(C=C%10)=CC=C%10N(C%11=CC=C(C%12=C(F)C=C(C%13=CC=C(C%14=CC=C(CCCCCC)S%14)S%13)C%15=NSN=C%12%15)C=C%11)C%16=CC=C(C%17=C(F)C=C(C%18=CC=C(C%19=CC=C(CCCCCC)S%19)S%18)C%20=NSN=C%20%17)C=C%16)C%21=CSC=C%21C(C%22=CC=C(C%23=CC=C(CCCCCC)S%23)S%22)=C1,4BTF-DTPA-T,,,1,7.6,34.4,2.61,"	Zhi Y, et al. Triphenylamine cored electron-donors for solution-processed organic solar cells: From tri-armed molecules to tetra-armed molecules. Dyes and Pigments 153, 291-299 (2018)."
3008,O=C1C(C(C(N2CC(CC)CCCC)=O)=C(C3=CC=CS3)N1CC(CC)CCCC)=C2C(S4)=CC=C4C5=CC(C6=C7C8=C(OCCC(CC)CCCC)C=C6)=C(S5)C9=C7C(C(C8=C(OCCC(CC)CCCC)C=C%10)=C%10C%11=C%12SC(C%13=CC=C(C(N(CC(CC)CCCC)C%14=O)=C%15C%14=C(C%16=CC=CS%16)N(CC(CC)CCCC)C%15=O)S%13)=C%11)=C%12C%17=CSC=C%179,BThP-DPP,,,0.88,9.33,44.8,3.68,"	Zhi Y, et al. Triphenylamine cored electron-donors for solution-processed organic solar cells: From tri-armed molecules to tetra-armed molecules. Dyes and Pigments 153, 291-299 (2018)."
3009,O=C1C(C(C(N2CC(CC)CCCC)=O)=C(C3=CC=CS3)N1CC(CC)CCCC)=C2C(S4)=CC=C4C5=CC(C6=C7C8=C(OCCC(CC)CCCC)C=C6)=C(S5)C9=C7C(C(C8=C(OCCC(CC)CCCC)C=C%10)=C%10C%11=C%12SC(C%13=CC=C(C(N(CC(CC)CCCC)C%14=O)=C%15C%14=C(C%16=CC=CS%16)N(CC(CC)CCCC)C%15=O)S%13)=C%11)=C%12C%17=CN(CC(CC)CCCC)C=C%179,BTrP-DPP,,,0.63,7.37,52.7,2.45,"	Chen Z, et al. Synthesis and Application of Perylene-Embedded Benzoazoles for Small-Molecule Organic Solar Cells. Org Lett 20, 6376-6379 (2018)."
3010,O=C(O)CN(/C(S/1)=C2SC(N(CCCCCCCC)C\2=O)=S)CC1=C\C3=CC(C(CCC4)C4N5C6=CC=C(/C=C(C7=CC=CC=C7)/C8=CC=CC=C8)C=C6)=C5C=C3,D205,,,0.69,9.44,44.3,2.88,"	Chen Z, et al. Synthesis and Application of Perylene-Embedded Benzoazoles for Small-Molecule Organic Solar Cells. Org Lett 20, 6376-6379 (2018)."
3011,O=C(OCC(CC)CCCC)/C(C#N)=C/C(S1)=CC=C1C2=CC=C(S2)C3=C4C(OCCO4)=C(C5=CC=C(C6=CC=C(/C=C(C(OCC(CC)CCCC)=O)\C#N)S6)S5)S3,SAM-72,,,0.96,7,42,2.8,"	Duan S-N, Dall¡¯Agnese C, Ojima H, Wang X-F. Effect of solvent-induced phase separation on performance of carboxylic indoline-based small-molecule organic solar cells. Dyes and Pigments 151, 110-115 (2018)."
3012,CCN(C/1=O)C(SC1=C/C2=CC(S3)=C(C=C2)N(CC(CC)CCCC)C(C3=C4)=CC=C4C(C=C5)=CC=C5N(C6=CC=CC=C6)C7=CC=CC=C7)=S,M1,,,0.72,4.34,60.45,1.9,"	Mica NA, Almahmoud SAJ, Krishnan Jagadamma L, Cooke G, Samuel IDW. An investigation of the role acceptor side chains play in the processibility and efficiency of organic solar cells fabricated from small molecular donors featuring 3,4-ethylenedioxythiophene cores. RSC Advances 8, 39231-39240 (2018)."
3013,CCCCC(CC)CN(C(C=CC(/C=C(C#N)/C#N)=C1)=C1S2)C(C2=C3)=CC=C3C(C=C4)=CC=C4N(C5=CC=CC=C5)C6=CC=CC=C6,M2,,,0.77,9.88,63,4.79,"	Revoju S, Biswas S, Eliasson B, Sharma GD. Asymmetric triphenylamine-phenothiazine based small molecules with varying terminal acceptors for solution processed bulk-heterojunction organic solar cells. Phys Chem Chem Phys 20, 6390-6400 (2018)."
3014,CCCCC(CC)CN(C(C=CC(/C=C1C(C(C=CC=C2)=C2C\1=O)=O)=C3)=C3S4)C(C4=C5)=CC=C5C(C=C6)=CC=C6N(C7=CC=CC=C7)C8=CC=CC=C8,M3,,,0.89,10.68,65,6.18,"	Revoju S, Biswas S, Eliasson B, Sharma GD. Asymmetric triphenylamine-phenothiazine based small molecules with varying terminal acceptors for solution processed bulk-heterojunction organic solar cells. Phys Chem Chem Phys 20, 6390-6400 (2018)."
3015,CCCN(C(C=CC(C#CC1=CC=C(N(C2=CC=CC=C2)C3=CC=CC=C3)C=C1)=C4)=C4S5)C(C5=C6)=CC=C6/C(/C(C(C=C7)=CC=C7N(C8=CC=CC=C8)C9=CC=CC=C9)=C(C#N)\C#N)=C(C#N)/C#N,1,,,0.85,12.36,69,7.25,"	Revoju S, Biswas S, Eliasson B, Sharma GD. Asymmetric triphenylamine-phenothiazine based small molecules with varying terminal acceptors for solution processed bulk-heterojunction organic solar cells. Phys Chem Chem Phys 20, 6390-6400 (2018)."
3016,CCCN(C(C=CC(C#CC1=CC=C(N(C2=CC=CC=C2)C3=CC=CC=C3)C=C1)=C4)=C4S5)C(C5=C6)=CC=C6/C(/C(C(C=C7)=CC=C7N(C8=CC=CC=C8)C9=CC=CC=C9)=C%10C=C/C(C=C/%10)=C(C#N)\C#N)=C(C#N)/C#N,2,,,0.95,8.73,58,4.81,"	Rout Y, Misra R, Singhal R, Biswas S, Sharma GD. Phenothiazine-based small-molecule organic solar cells with power conversion efficiency over 7% and open circuit voltage of about 1.0 V using solvent vapor annealing. Phys Chem Chem Phys 20, 6321-6329 (2018)."
3017,CCCCCCCCC(CCCCCCCC)N1C2=C(C=CC(C3=CC=C(C4=C(N=C(C5=CC(OCCCCCCCC)=CC=C5)C(C6=CC=CC(OCCCCCCCC)=C6)=N7)C7=C(C8=CC=C(C9=CC%10=C(C(C=CC(C%11=CC=C(C%12=C(F)C=C(C%13=CC(C%14=CC%15=C(C(C=CC(C%16=CC=C(C%17=C(F)C=C(C%18=CC=CS%18)C%19=C%17N=C(C%20=CC(OCCCCCCCC)=CC=C%20)C(C%21=CC=CC(OCCCCCCCC)=C%21)=N%19)S%16)=C%22)=C%22N%15C(CCCCCCCC)CCCCCCCC)C=C%14)=CS%13)C%23C%12N=C(C%24=CC(OCCCCCCCC)=CC=C%24)C(C%25=CC=CC(OCCCCCCCC)=C%25)=N%23)S%11)=C%26)=C%26N%10C(CCCCCCCC)CCCCCCCC)C=C9)S8)C=C4F)S3)=C2)C%27=C1C=CC=C%27,PCzFTQx,,,0.99,11.98,62,7.35,"	Rout Y, Misra R, Singhal R, Biswas S, Sharma GD. Phenothiazine-based small-molecule organic solar cells with power conversion efficiency over 7% and open circuit voltage of about 1.0 V using solvent vapor annealing. Phys Chem Chem Phys 20, 6321-6329 (2018)."
3018,CCCCC(CC)CSC(S1)=CC=C1C2=C(C=C(C3=CC(SCCCCCCCC)=C(C4=CC=C(C5=C(SCCCCCCCC)C=C(/C=C6SC(N(CC)C/6=O)=S)S5)S4)S3)S7)C7=C(C8=CC=C(SCC(CC)CCCC)S8)C9=C2SC(C%10=CC(SCCCCCCCC)=C(C%11=CC=C(C%12=C(SCCCCCCCC)C=C(/C=C%13SC(N(CC)C/%13=O)=S)S%12)S%11)S%10)=C9,BDTT-S-TRS,,,0.94,9.31,59,5.19,"	Qu B, et al. An alternating polymer with fluorinated quinoxaline and 2,7-carbazole segments for photovoltaic devices. RSC Advances 7, 16041-16048 (2017)."
3019,O=C(/C(S1)=C\C2=CC=C(C3=C4C(C(C5=C(CC(CCCC)CCCCCC)SC(CC(CCCC)CCCCCC)=C5C4=O)=O)=C(C6=CC=C(C7=CC8=C(C9=CC=C(CC(CC)CCCC)S9)C%10=C(C=C(C%11=CC=C(C%12=C(C(C%13=C(CC(CCCC)CCCCCC)SC(CC(CCCC)CCCCCC)=C%13C%14=O)=O)C%14=C(C%15=CC=C(/C=C%16SC(N(CC)C/%16=O)=S)S%15)S%12)S%11)S%10)C(C%17=CC=C(CC(CC)CCCC)S%17)=C8S7)S6)S3)S2)N(CC)C1=S,BBDDR,,,0.87,13.14,70.5,8.07,"	Zou Y, Wu Y, Yang H, Dong Y, Cui C, Li Y. The effect of alkylthio side chains in oligothiophene-based donor materials for organic solar cells. Molecular Systems Design & Engineering 3, 131-141 (2018)."
3020,CCCCC(CC)CC1=CC=C(S1)C(S2)=CC=C2C3=C4C(SC(C5=CC=C(C6=C7C(C(N6CC(CC)CCCC)=O)=C(C8=CC=CS8)N(CC(CC)CCCC)C7=O)S5)=C4)=C(C9=CC=C(C%10=CC=C(CC(CC)CCCC)S%10)S9)C%11=C3SC(C%12=CC=C(C%13=C%14C(C(N%13CC(CC)CCCC)=O)=C(C%15=CC=CS%15)N(CC(CC)CCCC)C%14=O)S%12)=C%11,BTBDT(DPP)2,,,1.01,14.6,53,7.8,"	Fang J, et al. Non-fullerene organic solar cells based on a small molecule with benzo[1,2-c:4,5-c']dithiophene-4,8-dione as ¦Ð-bridge. Organic Electronics 67, 175-180 (2019)."
3021,O=C(N1CC(CC)CCCC)C(C2=C1C3=CC=C(C4=CC5=C(C6=CC7=C(C=C(SCC(CC)CCCC)S7)S6)C(SC(C8=CC=C(C9=C%10C(C(N9CC(CC)CCCC)=O)=C(C%11=CC=CS%11)N(CC(CC)CCCC)C%10=O)S8)=C%12)=C%12C(C%13=CC%14=C(C=C(SCC(CC)CCCC)S%14)S%13)=C5S4)S3)=C(C%15=CC=CS%15)N(CC(CC)CCCC)C2=O,TTSBDT(TDPP)2,,,0.94,11.72,54,5.95,"	Jung JW. A versatile small molecular electron donor with 2-dimensional conjugation structure for efficient organic solar cells compatible with both fullerene and non-fullerene electron acceptors. Dyes and Pigments 161, 214-220 (2019)."
3022,CCCCCCCCC(CCCCCCCC)N1C2=C(C=CC(C3=CC=C(C4=C(N=C(C5=CC(OCCCCCCCC)=CC=C5)C(C6=CC=CC(OCCCCCCCC)=C6)=N7)C7=C(C8=CC=C(C9=CC%10=C(C(C=CC(C%11=CC=C(C%12=CC=C(C%13=CC(C%14=CC%15=C(C(C=CC(C%16=CC=C(C%17=CC=C(C%18=CC=CS%18)C%19=C%17N=C(C%20=CC(OCCCCCCCC)=CC=C%20)C(C%21=CC=CC(OCCCCCCCC)=C%21)=N%19)S%16)=C%22)=C%22N%15C(CCCCCCCC)CCCCCCCC)C=C%14)=CS%13)C%23C%12N=C(C%24=CC(OCCCCCCCC)=CC=C%24)C(C%25=CC=CC(OCCCCCCCC)=C%25)=N%23)S%11)=C%26)=C%26N%10C(CCCCCCCC)CCCCCCCC)C=C9)S8)C=C4)S3)=C2)C%27=C1C=CC=C%27,PCzTQx,,,0.84,12.76,61,6.88,"	Lee W, Choi J, Jung JW. A solution-processed small molecule with optimal side chains for high efficiency non-fullerene organic solar cells. Dyes and Pigments 161, 283-287 (2019)."
3023,O=C1/C(C2=CC=C(C3=CC=CS3)C=C2N1CC(CC)CCCC)=C4C(N(CC(CC)CCCC)C5=C/4C=CC(C6=CC7=C(C(C8=CC=C(CC(CC)CCCC)S8)=C(C=C(C9=CC=CC=C9)S%10)C%10=C7C%11=CC=C(CC(CC)CCCC)S%11)S6)=C5)=O,P1,,,0.82,9.57,60,4.72,"	Qu B, et al. An alternating polymer with fluorinated quinoxaline and 2,7-carbazole segments for photovoltaic devices. RSC Advances 7, 16041-16048 (2017)."
3024,O=C1/C(C2=C(C=C(C3=CC=CS3)S2)N1CC(CC)CCCC)=C4C(N(CC(CC)CCCC)C5=C/4SC(C6=CC7=C(C(C8=CC=C(CC(CC)CCCC)S8)=C(C=C(C9=CC=CC=C9)S%10)C%10=C7C%11=CC=C(CC(CC)CCCC)S%11)S6)=C5)=O,P2,,,0.94,5.94,43.08,2.4,"	Liu F, Wang H, Zhang Y, Wang X, Zhang S. Synthesis of low band-gap 2D conjugated polymers and their application for organic field effect transistors and solar cells. Organic Electronics 64, 27-36 (2019)."
3025,O=C(/C/1=C/C2=CC(CCCCCC)=C(C3=CC=C(C4=C(CCCCCC)C=C(C5=CC=C(N(C6=CC=CC=C6)C7=CC=CC=C7)C=C5)S4)S3)S2)C8=CC=CC=C8C1=C(C#N)\C#N,3T,,,0.66,5.25,38.1,1.28,"	Liu F, Wang H, Zhang Y, Wang X, Zhang S. Synthesis of low band-gap 2D conjugated polymers and their application for organic field effect transistors and solar cells. Organic Electronics 64, 27-36 (2019)."
3026,O=C(/C/1=C/C2=CC(CCCCCC)=C(C3=CC(SC4=C5SC(C6=C(CCCCCC)C=C(C7=CC=C(N(C8=CC=CC=C8)C9=CC=CC=C9)C=C7)S6)=C4)=C5S3)S2)C%10=CC=CC=C%10C1=C(C#N)\C#N,DTT,,,0.86,11.9,34,3.45,"	Lim HC, Kim J-J, Jang J, Hong J-I. Effect of the ¦Ð-linker on the performance of organic photovoltaic devices based on push¨Cpull D¨C¦Ð¨CA molecules. New Journal of Chemistry 42, 11458-11464 (2018)."
3027,CCCCCCCCC(C1=C2SC(C3=CC(SC(C4=CC=CC=C4)=C5)=C5S3)=C1)(CCCCCCCC)C6=C2SC(C7=CC=CC=C7)=C6,8CDT-TT,,,0.76,9.5,33,2.38,"	Lim HC, Kim J-J, Jang J, Hong J-I. Effect of the ¦Ð-linker on the performance of organic photovoltaic devices based on push¨Cpull D¨C¦Ð¨CA molecules. New Journal of Chemistry 42, 11458-11464 (2018)."
3028,CC(C(C1=CC=C(/C=C2SC(SCCCCCC)=C(SCCCCCC)S/2)O1)=C3C)=C4N3[B-](F)(F)[N+]5=C(C)C(C6=CC=C(/C=C7SC(SCCCCCC)=C(SCCCCCC)S\7)O6)=C(C)C5=C4C8=CC=C(OC)C=C8,BODIPY-DTF,,,0.542,8.7,45,2.12,"	Madathil PK, Cho S, Choi S, Kim T-D, Lee K-S. Synthesis and Characterization of Cyclopentadithiophene and Thienothiophene-Based Polymers for Organic Thin-Film Transistors and Solar Cells. Macromolecular Research 26, 934-941 (2018)."
3029,CCCCCCCCCCCCCCCCC(C1=C2SC(C3=CC(SC(C4=CC=CC=C4)=C5)=C5S3)=C1)(CCCCCCCCCCCCCCCC)C6=C2SC(C7=CC=CC=C7)=C6,16CDT-TT,,,0.768,13.79,66.5,7.2,"	Srinivasa Rao R, Bagui A, Hanumantha Rao G, Gupta V, Singh SP. Achieving the highest efficiency using a BODIPY core decorated with dithiafulvalene wings for small molecule based solution-processed organic solar cells. Chem Commun (Camb) 53, 6953-6956 (2017)."
3030,CCCCCCC(C=C1)=CC=C1C2(C3=CC=C(CCCCCC)C=C3)C4=C(SC(C5=CC=C(/C=C6C(N(CC)C(S/6)=S)=O)C7=NSN=C75)=C4)C8=CC(C9(CCCCCCCC)CCCCCCCC)=C(C%10=C9C=C(C(SC(C%11=CC=C(/C=C%12C(N(CC)C(S/%12)=S)=O)C%13=NSN=C%13%11)=C%14)=C%14C%15(C%16=CC=C(CCCCCC)C=C%16)C%17=CC=C(CCCCCC)C=C%17)C%15=C%10)C=C82,DTFBR,,,0.58,6,53,1.84,"	Madathil PK, Cho S, Choi S, Kim T-D, Lee K-S. Synthesis and Characterization of Cyclopentadithiophene and Thienothiophene-Based Polymers for Organic Thin-Film Transistors and Solar Cells. Macromolecular Research 26, 934-941 (2018)."
3031,CC(C=C1C)=CC(C)=[C@@]1/[C@](C2=CC=C(/C(C#CC3=C(CCCCCC)C(CCCCCC)=C(/C=C/C4=C(CCCCCC)C(CCCCCC)=C(/C=C5C(N(CC)/C(S/5)=C(C#N)\C#N)=O)S4)S3)=C6N=C7C=C\6)N2[Zn]N8/C(C=C/C8=C7\C9=C(C)C=C(C)C=C9C)=C%10/C#CC%11=C(CCCCCC)C(CCCCCC)=C(/C=C/C%12=C(CCCCCC)C(CCCCCC)=C(/C=C%13C(N(CC)/C(S/%13)=C(C#N)\C#N)=O)S%12)S%11)=C%14C=CC%10=N\%14,MV72,,,1.08,6.94,32,2.42,"	Song J, Xue X, Fan B, Huo L, Sun Y. A novel bifunctional A¨CD¨CA type small molecule for efficient organic solar cells. Materials Chemistry Frontiers 2, 1626-1630 (2018)."
3032,CCCCC(CC)CC(S1)=CC=C1C2=C3C(C=C(C4=CC(CCCCCCCC)=C(C5=CC=C(C6=C(CCCCCCCC)C=C(/C=C(C(OCC(CC)CCCC)=O)\C#N)S6)S5)S4)S3)=C(C7=CC=C(CC(CC)CCCC)S7)C8=C2C=C(C9=CC(CCCCCCCC)=C(C%10=CC=C(C%11=C(CCCCCCCC)C=C(/C=C(C(OCC(CC)CCCC)=O)\C#N)S%11)S%10)S9)S8,SM1,,,0.92,11.25,39,4.03,"	Vartanian M, de la Cruz P, Biswas S, Sharma GD, Langa F. Panchromatic ternary organic solar cells with 9.44% efficiency incorporating porphyrin-based donors. Nanoscale 10, 12100-12108 (2018)."
3033,CCCCC(CC)CC(S1)=CC=C1C2=C3C(C=C(C4=CC(CCCCCCCC)=C(C5=CC=C(C6=C(CCCCCCCC)C=C(/C=C7C(N(CC)C8=C\7C=CC=C8)=O)S6)S5)S4)S3)=C(C9=CC=C(CC(CC)CCCC)S9)C%10=C2C=C(C%11=CC(CCCCCCCC)=C(C%12=CC=C(C%13=C(CCCCCCCC)C=C(/C=C%14C(C=CC=C%15)=C%15N(CC)C\%14=O)S%13)S%12)S%11)S%10,DI3T,,,0.883,7.34,61.34,3.97,"	Yang Y, et al. High-efficiency organic solar cells based on a small-molecule donor and a low-bandgap polymer acceptor with strong absorption. Journal of Materials Chemistry A 6, 9613-9622 (2018)."
3034,CCCCC(CC)CC(S1)=CC=C1C2=C3C(C=C(C4=CC(CCCCCCCC)=C(C5=CC=C(C6=C(CCCCCCCC)C=C(/C=C7C(N(CC)C8=C\7C=C(F)C(F)=C8)=O)S6)S5)S4)S3)=C(C9=CC=C(CC(CC)CCCC)S9)C%10=C2C=C(C%11=CC(CCCCCCCC)=C(C%12=CC=C(C%13=C(CCCCCCCC)C=C(/C=C%14C(C=C(F)C(F)=C%15)=C%15N(CC)C\%14=O)S%13)S%12)S%11)S%10,DI3T-2F,,,0.854,3.63,27,0.83,"	Yang Y, et al. Fluorination Triggered New Small Molecule Donor Materials for Efficient As-Cast Organic Solar Cells. Small 14, e1801542 (2018)."
3035,OC1=C(C2=C([O-])/C(C2=O)=C\C3=[N+](CCCCCC)C(C=CC(C4=CC(SC5=C6C(C7=CC=C(CCCCCC)C=C7)(C8=CC=C(CCCCCC)C=C8)C9=C5C=C(C(C%10=CC=C(CCCCCC)C=C%10)(C%11=CC=C(CCCCCC)C=C%11)C%12=C%13SC%14=C%12SC(C%15=CC=C([N+](CCCCCC)=C(/C=C%16C([O-])=C(C%17=C(O)C=C(N%18C(CCC%19)C%19C%20=C%18C=CC(C#N)=C%20)C=C%17O)C\%16=O)C%21(C)C)C%21=C%15)=C%14)C%13=C9)=C6S4)=C%22)=C%22C3(C)C)C(O)=CC(N%23C%24C(CCC%24)C%25=C%23C=CC([N+]#[C-])=C%25)=C1,D-IDTT-SQ,,,0.836,13,71.8,7.8,"	Yang Y, et al. Fluorination Triggered New Small Molecule Donor Materials for Efficient As-Cast Organic Solar Cells. Small 14, e1801542 (2018)."
3036,S=C(N(CC)C/1=O)SC1=C\C2=CC(CCCCCCCC)=C(C3=CC=C(C4=C(CCCCCCCC)C=C(C5=CC6=C(C(C7=CC=C([Si](CCC)(CCC)CCC)S7)=C(C=C(C8=CC(CCCCCCCC)=C(C9=CC=C(C%10=C(CCCCCCCC)C=C(/C=C%11SC(N(CC)C/%11=O)=S)S%10)S9)S8)S%12)C%12=C6C%13=CC=C([Si](CCC)(CCC)CCC)S%13)S5)S4)S3)S2,H21,,,0.93,14.03,54,7.05,"	Yang D, Sasabe H, Sano T, Kido J. Low-Band-Gap Small Molecule for Efficient Organic Solar Cells with a Low Energy Loss below 0.6 eV and a High Open-Circuit Voltage of over 0.9 V. ACS Energy Letters 2, 2021-2025 (2017)."
3037,CCC(CCCC)COC(/C(C#N)=C/C1=CC(CCCCCCCC)=C(C2=CC=C(C3=C(CCCCCCCC)C=C(C4=CC5=C(C(C6=CC=C([Si](CCC)(CCC)CCC)S6)=C(C=C(C7=CC(CCCCCCCC)=C(C8=CC=C(C9=C(CCCCCCCC)C=C(/C=C(C(OC(CCCC)CC)=O)/C#N)S9)S8)S7)S%10)C%10=C5C%11=CC=C([Si](CCC)(CCC)CCC)S%11)S4)S3)S2)S1)=O,H22,,,0.895,13,65.58,7.62,"	Bin H, et al. High-Efficiency All-Small-Molecule Organic Solar Cells Based on an Organic Molecule Donor with Alkylsilyl-Thienyl Conjugated Side Chains. Adv Mater 30, e1706361 (2018)."
3038,O=C1N(CC(CCCC)CC)C(C2=CC=C(C#C/C(C3=CC=C(/C(C4=CC=C(OCCCCCCCC)C=C4)=C5N=C6C=C\5)N3[Zn]N7/C(C=C/C7=C6\C#CC8=CC=C(C(N(CC(CC)CCCC)C9=O)=C%10C9=C(C%11=CC=CS%11)N(CC(CCCC)CC)C%10=O)S8)=C%12/C%13=CC=C(OCCCCCCCC)C=C%13)=C%14C=CC%12=N\%14)S2)=C%15C1=C(C%16=CC=CS%16)N(CC(CC)CCCC)C%15=O,1,,,0.942,15.38,71.15,10.29,"	Bin H, et al. High-Efficiency All-Small-Molecule Organic Solar Cells Based on an Organic Molecule Donor with Alkylsilyl-Thienyl Conjugated Side Chains. Adv Mater 30, e1706361 (2018)."
3039,O=C1N(CC(CCCC)CC)C(C2=CC=C(C#C/C(C3=CC=C(/C(C4=CC=C(OCC(CCCC)CC)C=C4)=C5N=C6C=C\5)N3[Zn]N7/C(C=C/C7=C6\C#CC8=CC=C(C(N(CC(CC)CCCC)C9=O)=C%10C9=C(C%11=CC=CS%11)N(CC(CCCC)CC)C%10=O)S8)=C%12/C%13=CC=C(OCC(CC)CCCC)C=C%13)=C%14C=CC%12=N\%14)S2)=C%15C1=C(C%16=CC=CS%16)N(CC(CC)CCCC)C%15=O,2,,,0.71,15.46,56,6.13,"	Hadmojo WT, et al. Near-Infrared Harvesting Fullerene-Free All-Small-Molecule Organic Solar Cells Based on Porphyrin Donors. ACS Sustainable Chemistry & Engineering 6, 5306-5313 (2018)."
3040,O=C1N(CC(CCCC)CC)C(C2=CC=C(C#C/C(C3=CC=C(/C(C4=CC=C(CC(CCCC)CC)S4)=C5N=C6C=C\5)N3[Zn]N7/C(C=C/C7=C6\C#CC8=CC=C(C(N(CC(CC)CCCC)C9=O)=C%10C9=C(C%11=CC=CS%11)N(CC(CCCC)CC)C%10=O)S8)=C%12/C%13=CC=C(CC(CCCC)CC)S%13)=C%14C=CC%12=N\%14)S2)=C%15C1=C(C%16=CC=CS%16)N(CC(CC)CCCC)C%15=O,3,,,0.71,14.03,53,5.21,"	Hadmojo WT, et al. Near-Infrared Harvesting Fullerene-Free All-Small-Molecule Organic Solar Cells Based on Porphyrin Donors. ACS Sustainable Chemistry & Engineering 6, 5306-5313 (2018)."
3041,CCC(CCCC)CC1=CC=C(S1)/C(C2=N/C(C=C2)=C3/C#CC4=CC=C(C(N(CC(CCCC)CC)C5=O)=C6C5=C(C7=CC=CS7)N(CC(CCCC)CC)C6=O)S4)=C(C=C/8)/N9C8=C(C#C/C(C%10=CC=C%11N%10[Zn]N%12/C(C=C/C%12=C%13\C%14=CC=C(CC(CCCC)CC)S%14)=C(C#CC%15=CC=C(C%16=C%17C(C(N%16CC(CCCC)CC)=O)=C(C%18=CC=CS%18)N(CC(CC)CCCC)C%17=O)S%15)\C(C=C/%19)=NC%19=C%11\C%20=CC=C(CC(CCCC)CC)S%20)=C%21N=C%13C=C/%21)/C(C=C/%22)=NC%22=C(C%23=CC=C(CC(CCCC)CC)S%23)/C%24=CC=C3N%24[Zn]9,ZnP2-DPP,,,0.71,11.46,51,4.08,"	Hadmojo WT, et al. Near-Infrared Harvesting Fullerene-Free All-Small-Molecule Organic Solar Cells Based on Porphyrin Donors. ACS Sustainable Chemistry & Engineering 6, 5306-5313 (2018)."
3042,COC(C=C1OC)=CC=C1C(C=C2)=CC=C2N(C3=CC=C(C4=C(OC)C=C(OC)C=C4)C=C3)C5=CC=C(N(C6=CC=C(C7=C(OC)C=C(OC)C=C7)C=C6)C8=CC=C(C9=CC=C(OC)C=C9OC)C=C8)C%10=NSN=C%105,CS01,,,0.65,19.65,66.15,8.45,"	Lai T, et al. Dimeric Porphyrin Small Molecules for Efficient Organic Solar Cells with High Photoelectron Response in the Near-Infrared Region. ACS Appl Mater Interfaces 10, 668-675 (2018)."
3043,CC(C=C1)=CC=C1N(C2=CC=C(C)C=C2)C(C=C3)=CC=C3C4(C5=CC=C(N(C6=CC=C(C)C=C6)C7=CC=C(C)C=C7)C=C5)CCCCC4,TAPC,,,0.97,16.27,63,9.94,"	Privado M, et al. Reduced Energy Offsets and Low Energy Losses Lead to Efficient (¡«10% at 1 sun) Ternary Organic Solar Cells. ACS Energy Letters 3, 2418-2424 (2018)."
3044,O=C1C2=C(C3=CC=C(C4=CC=C(/C(C#N)=C/C5=CC=C(N(CC(CC)CCCC)C(C=CC=C6)=C6S7)C7=C5)C=C4)S3)N(CC(CC)CCCC)C(C2=C(C8=CC=C(C9=CC=C(/C(C#N)=C/C%10=CC(SC(C=CC=C%11)=C%11N%12CC(CC)CCCC)=C%12C=C%10)C=C9)S8)N1CC(CC)CCCC)=O,TDPP-PTCN,,,0.9,11.35,61,6.24,"	Seo J-W, et al. Columnar-Structured Low-Concentration Donor Molecules in Bulk Heterojunction Organic Solar Cells. ACS Omega 3, 929-936 (2018)."
3045,O=C1C2=C(C3=CC=C(C4=CC=C(/C(C#N)=C/C5=CC=C(N(CC(CC)CCCC)C(C=CC=C6)=C6S7)C7=C5)C=C4)O3)N(CC(CC)CCCC)C(C2=C(C8=CC=C(C9=CC=C(/C(C#N)=C/C%10=CC(SC(C=CC=C%11)=C%11N%12CC(CC)CCCC)=C%12C=C%10)C=C9)O8)N1CC(CC)CCCC)=O,FDPP-PTCN,,,0.806,10.46,62,5.2,"	Yadagiri B, et al. D?¦Ð¨CA?¦Ð¨CD Structured Diketopyrrolopyrrole-Based Electron Donors for Solution-Processed Organic Solar Cells. ACS Omega 3, 13365-13373 (2018)."
3046,O=C1C(C2=C(C3=CC=C(C#C/C(C4=CC=C5N4[Zn]N6/C(C=C/C6=C7\C8=CC(SC(CCCCCC)=C9)=C9S8)=C(C%10=CC(SC(CCCCCC)=C%11)=C%11S%10)\C(C=C/%12)=NC%12=C5\C%13=CC(SC(CCCCCC)=C%14)=C%14S%13)=C%15N=C7C=C/%15)S3)N1CC(CC)CCCC)=C(C%16=CC=C(C#C/C(C%17=CC=C%18N%17[Zn]N%19/C(C=C/C%19=C%20\C%21=CC(SC(CCCCCC)=C%22)=C%22S%21)=C(C%23=CC(SC(CCCCCC)=C%24)=C%24S%23)\C(C=C/%25)=NC%25=C%18\C%26=CC(SC(CCCCCC)=C%27)=C%27S%26)=C%28N=C%20C=C/%28)S%16)N(CC(CC)CCCC)C2=O,VC4,,,0.795,9.42,53.5,4,"	Yadagiri B, et al. D?¦Ð¨CA?¦Ð¨CD Structured Diketopyrrolopyrrole-Based Electron Donors for Solution-Processed Organic Solar Cells. ACS Omega 3, 13365-13373 (2018)."
3047,O=C1C(C2=C(C3=CC=C(C#C/C(C4=CC=C5N4[Zn]N6/C(C=C/C6=C7\C8=C(OCCCCCCCCCCCC)C=CC=C8OCCCCCCCCCCCC)=C(C9=C(OCCCCCCCCCCCC)C=CC=C9OCCCCCCCCCCCC)\C(C=C/%10)=NC%10=C5\C%11=C(OCCCCCCCCCCCC)C=CC=C%11OCCCCCCCCCCCC)=C%12N=C7C=C/%12)S3)N1CC(CC)CCCC)=C(C%13=CC=C(C#C/C(C%14=CC=C%15N%14[Zn]N%16/C(C=C/C%16=C%17\C%18=C(OCCCCCCCCCCCC)C=CC=C%18OCCCCCCCCCCCC)=C(C%19=C(OCCCCCCCCCCCC)C=CC=C%19OCCCCCCCCCCCC)\C(C=C/%20)=NC%20=C%15\C%21=C(OCCCCCCCCCCCC)C=CC=C%21OCCCCCCCCCCCC)=C%22N=C%17C=C/%22)S%13)N(CC(CC)CCCC)C2=O,VC5,,,0.91,13.83,64,8.05,"	Cuesta V, Singhal R, de la Cruz P, Sharma GD, Langa F. Near-IR Absorbing D-A-D Zn-Porphyrin-Based Small-Molecule Donors for Organic Solar Cells with Low-Voltage Loss. ACS Appl Mater Interfaces 11, 7216-7225 (2019)."
3048,O=C1C2=C(C3=CC=C(C#C/C(C(C=C/4)=NC4=C5\C6=CC=C(SCC(CCCC)CCCCCC)S6)=C7C=C/C8=C(C9=CC=C(SCC(CCCC)CCCCCC)S9)/C%10=N/C(C=C%10)=C(C#CC%11=C(OCCCCCC)C(/C=C%12SC(N(CC)C\%12=O)=S)=CC(OCCCCCC)=C%11)\C%13=CC=C5N%13[Zn]N\78)S3)N(CC(CCCC)CCCCCC)C(C2=C(C%14=CC=C(C#C/C(C%15=CC=C%16N%15[Zn]N%17/C(C=C/C%17=C%18\C%19=CC=C(SCC(CCCC)CCCCCC)S%19)=C(C#CC%20=C(OCCCCCC)C=C(/C=C%21C(N(CC)C(S/%21)=S)=O)C(OCCCCCC)=C%20)\C(C=C/%22)=NC%22=C%16\C%23=CC=C(SCC(CCCC)CCCCCC)S%23)=C%24N=C%18C=C/%24)S%14)N1CC(CCCC)CCCCCC)=O,DPP-2TTP,,,0.79,16.98,66.3,8.89,"	Cuesta V, Singhal R, de la Cruz P, Sharma GD, Langa F. Near-IR Absorbing D-A-D Zn-Porphyrin-Based Small-Molecule Donors for Organic Solar Cells with Low-Voltage Loss. ACS Appl Mater Interfaces 11, 7216-7225 (2019)."
3049,O=C1C2=C(C3=CC=C(C#C/C(C(C=C/4)=NC4=C5\C6=CC=C(CC(CCCCCC)CCCC)S6)=C7C=C/C8=C(C9=CC=C(CC(CCCCCC)CCCC)S9)/C%10=N/C(C=C%10)=C(C#CC%11=C(OCCCCCC)C(/C=C%12SC(N(CC)C\%12=O)=S)=CC(OCCCCCC)=C%11)\C%13=CC=C5N%13[Zn]N\78)S3)N(CC(CCCC)CCCCCC)C(C2=C(C%14=CC=C(C#C/C(C%15=CC=C%16N%15[Zn]N%17/C(C=C/C%17=C%18\C%19=CC=C(CC(CCCCCC)CCCC)S%19)=C(C#CC%20=C(OCCCCCC)C=C(/C=C%21C(N(CC)C(S/%21)=S)=O)C(OCCCCCC)=C%20)\C(C=C/%22)=NC%22=C%16\C%23=CC=C(CC(CCCCCC)CCCC)S%23)=C%24N=C%18C=C/%24)S%14)N1CC(CCCC)CCCCCC)=O.CC,DPP-2TP,,,0.82,17.78,76.5,11.01,"	Piradi V, et al. Panchromatic Ternary Organic Solar Cells with Porphyrin Dimers and Absorption-Complementary Benzodithiophene-based Small Molecules. ACS Appl Mater Interfaces 11, 6283-6291 (2019)."
3050,CC1=CC(C)=CC(C)=C1/C(C2=CC=C3N2[Zn]N4/C(C=C/C4=C(C5=C(C)C=C(C)C=C5C)/C6=N/C(C=C6)=C3/C#CC7=CC(C(CCCCCC)(CCCCCC)C8=C9SC(/C=C%10C(N(CC)C(S/%10)=S)=O)=C8)=C9S7)=C%11/C#CC%12=CC%13=C(C(SC(/C=C%14SC(N(CC)C\%14=O)=S)=C%15)=C%15C%13(CCCCCC)CCCCCC)S%12)=C%16C=CC%11=N\%16,SA1,,,0.76,15.54,68.7,8,"	Piradi V, et al. Panchromatic Ternary Organic Solar Cells with Porphyrin Dimers and Absorption-Complementary Benzodithiophene-based Small Molecules. ACS Appl Mater Interfaces 11, 6283-6291 (2019)."
3051,CC1=CC(C)=CC(C)=C1/C(C2=CC=C3N2[Zn]N4/C(C=C/C4=C(C5=C(C)C=C(C)C=C5C)/C6=N/C(C=C6)=C3/C#CC7=CC(C(CCCCCC)(CCCCCC)C8=C9SC(/C=C(C#N)/C#N)=C8)=C9S7)=C%10/C#CC%11=CC%12=C(C(SC(/C=C(C#N)\C#N)=C%13)=C%13C%12(CCCCCC)CCCCCC)S%11)=C%14C=CC%10=N\%14,SA2,,,0.85,13.38,59,6.71,"	Arrechea S, Aljarilla A, de la Cruz P, Singh MK, Sharma GD, Langa F. New cyclopentadithiophene (CDT) linked porphyrin donors with different end-capping acceptors for efficient small molecule organic solar cells. J. Mater. Chem. C 5, 4742-4751 (2017)."
3052,CCCCC(CC)CC(S1)=CC=C1C2=C(SC(C3=C(C(N(CC(CC)CCCC)C4=O)=O)C4=CS3)=C2)C(S5)=CC6=C5C7=CC=C(C=C(C8=C(C9=CC=C(CC(CC)CCCC)S9)C=C(C%10=C(C(N(CC(CC)CCCC)C%11=O)=O)C%11=CS%10)S8)S%12)C%12=C7C=C6,2D-NDT(TPD)2,,,0.91,13.84,63,7.93,"	Arrechea S, Aljarilla A, de la Cruz P, Singh MK, Sharma GD, Langa F. New cyclopentadithiophene (CDT) linked porphyrin donors with different end-capping acceptors for efficient small molecule organic solar cells. J. Mater. Chem. C 5, 4742-4751 (2017)."
3053,CCCCC(CC)CC(S1)=CC=C1C2=C(SC(C3=CC=C(/C=C(C(OCC(CC)CCCC)=O)\C#N)S3)=C2)C(S4)=CC5=C4C6=CC=C(C=C(C7=C(C8=CC=C(CC(CC)CCCC)S8)C=C(C9=CC=C(/C=C(C(OCC(CC)CCCC)=O)\C#N)S9)S7)S%10)C%10=C6C=C5,2D-NDT(Ester)2,,,0.73,1.66,27.2,0.33,"	Bagde SS, Park H, Tran V-H, Lee S-H. A new 2D-naphtho[1,2-b:5,6-b¡¯]dithiophene based donor small molecules for bulk-heterojunction organic solar cells. Dyes and Pigments 163, 30-39 (2019)."
3054,CCCCC(CC)CC(S1)=CC=C1C2=C(SC(C3=CC=C(/C=C(C(NCC(CC)CCCC)=O)\C#N)S3)=C2)C(S4)=CC5=C4C6=CC=C(C=C(C7=C(C8=CC=C(CC(CC)CCCC)S8)C=C(C9=CC=C(/C=C(C(NCC(CC)CCCC)=O)\C#N)S9)S7)S%10)C%10=C6C=C5,2D-NDT(Amide)2,,,0.91,3.75,35.5,1.22,"	Bagde SS, Park H, Tran V-H, Lee S-H. A new 2D-naphtho[1,2-b:5,6-b¡¯]dithiophene based donor small molecules for bulk-heterojunction organic solar cells. Dyes and Pigments 163, 30-39 (2019)."
3055,O=C(N(CC(CCCC)CC)C(C1=CC=C(C2=CC=C(C3=CC(C(N(CC(CC)CCCC)C4=O)=O)=C4C=C3)S2)S1)=C56)C5=C(C7=CC=C(C8=CC=C(C9=CC(C(N(CC(CC)CCCC)C%10=O)=O)=C%10C=C9)S8)S7)N(CC(CCCC)CC)C6=O,PI-DPP,,,0.64,2.36,36.95,0.55,"	Bagde SS, Park H, Tran V-H, Lee S-H. A new 2D-naphtho[1,2-b:5,6-b¡¯]dithiophene based donor small molecules for bulk-heterojunction organic solar cells. Dyes and Pigments 163, 30-39 (2019)."
3056,O=C(N(CC(CCCC)CC)C(C1=CC=C(C2=CC=C(C3=CC=C(C(N4CC(CC)CCCC)=O)C5=C3C=CC=C5C4=O)S2)S1)=C67)C6=C(C8=CC=C(C9=CC=C(C%10=CC=C(C(N%11CC(CC)CCCC)=O)C%12=C%10C=CC=C%12C%11=O)S9)S8)N(CC(CCCC)CC)C7=O,NI-DPP,,,0.91,1.54,64,0.9,"	Chen M, et al. Phthalimide and Naphthalimide end-Capped Diketopyrrolopyrrole for Organic Photovoltaic Applications. Chinese Journal of Chemistry 35, 1396-1404 (2017)."
3057,CCCCCCCCC(CCCCCC)CC1=CC=C(S1)C2=C3C(SC4=C3SC(C5=C6C(C=C(CC(CC)CCCC)S6)=C(/C=C7SC(N(CC)C\7=S)=O)S5)=C4)=C(C8=CC=C(CC(CCCCCC)CCCCCCCC)S8)C9=C2SC%10=C9SC(C%11=C%12C(C=C(CC(CC)CCCC)S%12)=C(/C=C%13SC(N(CC)C\%13=S)=O)S%11)=C%10,STB-4,,,0.79,3.28,29,0.76,"	Chen M, et al. Phthalimide and Naphthalimide end-Capped Diketopyrrolopyrrole for Organic Photovoltaic Applications. Chinese Journal of Chemistry 35, 1396-1404 (2017)."
3058,S=C(/C(S1)=C/C2=C(C=C(CC(CC)CCCC)S3)C3=C(C(S4)=CC5=C4C(C6=CC=C(CC(CC)CCCC)S6)=C(C=C(C7=C8C(C=C(CC(CC)CCCC)S8)=C(/C=C9SC(N(CC)C\9=S)=O)S7)S%10)C%10=C5C%11=CC=C(CC(CC)CCCC)S%11)S2)N(CC)C1=O,STB-2,,,0.904,13.33,67,8.17,"	Liu W, Zhou Z, Vergote T, Xu S, Zhu X. A thieno[3,4-b]thiophene-based small-molecule donor with a ¦Ð-extended dithienobenzodithiophene core for efficient solution-processed organic solar cells. Materials Chemistry Frontiers 1, 2349-2355 (2017)."
3059,O=C(N1CC(CC)CCCC)C(C2=C1C(S3)=CC=C3C#C/C(C(C=C/4)=NC4=C5\C#CC6=CC=CC=C6)=C7C=C/C8=C(C#CC9=CC=CC=C9)/C%10=N/C(C=C%10)=C(C#CC%11=CC=C(C%12=C%13C(C(N%12CC(CC)CCCC)=O)=C(C%14=CC=CS%14)N(CC(CC)CCCC)C%13=O)S%11)\C%15=CC=C5N%15[Mg]N\78)=C(C%16=CC=CS%16)N(CC(CC)CCCC)C2=O,2a,,,0.901,13.12,66,7.84,"	Liu W, Zhou Z, Vergote T, Xu S, Zhu X. A thieno[3,4-b]thiophene-based small-molecule donor with a ¦Ð-extended dithienobenzodithiophene core for efficient solution-processed organic solar cells. Materials Chemistry Frontiers 1, 2349-2355 (2017)."
3060,O=C(N1CC(CC)CCCC)C(C2=C1C(S3)=CC=C3C#C/C(C(C=C/4)=NC4=C5\C#CC6=CC=C(CCCCCC)C=C6)=C7C=C/C8=C(C#CC9=CC=C(CCCCCC)C=C9)/C%10=N/C(C=C%10)=C(C#CC%11=CC=C(C%12=C%13C(C(N%12CC(CC)CCCC)=O)=C(C%14=CC=CS%14)N(CC(CC)CCCC)C%13=O)S%11)\C%15=CC=C5N%15[Mg]N\78)=C(C%16=CC=CS%16)N(CC(CC)CCCC)C2=O,2b,,,0.74,13.27,49,4.85,"	Ogumi K, Nakagawa T, Okada H, Sakai R, Wang H, Matsuo Y. Substituent effects in magnesium tetraethynylporphyrin with two diketopyrrolopyrrole units for bulk heterojunction organic solar cells. Journal of Materials Chemistry A 5, 23067-23077 (2017)."
3061,CC(C=C1)=CC=C1C2=C3C(C4=C2C=CC=C4)=C(C5=CC=CC=C5)C6=C(C7=CC=C(C)C=C7)C8=C(C=CC=C8)C6=C3C9=CC=CC=C9,TAInF2,,,0.69,14.8,56,5.73,"	Ogumi K, Nakagawa T, Okada H, Sakai R, Wang H, Matsuo Y. Substituent effects in magnesium tetraethynylporphyrin with two diketopyrrolopyrrole units for bulk heterojunction organic solar cells. Journal of Materials Chemistry A 5, 23067-23077 (2017)."
3062,O=C(N1CC(CC)CCCC)C(C2=C1C(S3)=CC=C3C#C/C(C(C=C/4)=NC4=C5\C#CC6=CC=C(C(F)(F)F)C=C6)=C7C=C/C8=C(C#CC9=CC=C(C(F)(F)F)C=C9)/C%10=N/C(C=C%10)=C(C#CC%11=CC=C(C%12=C%13C(C(N%12CC(CC)CCCC)=O)=C(C%14=CC=CS%14)N(CC(CC)CCCC)C%13=O)S%11)\C%15=CC=C5N%15[Mg]N\78)=C(C%16=CC=CS%16)N(CC(CC)CCCC)C2=O,2c,,,0.94,8.62,35.9,2.91,"	Lo Y-C, et al. The synthesis, structure, and properties of 5,6,11,12-tetraarylindeno[1,2-b]fluorenes and their applications as donors for organic photovoltaic devices. Organic Chemistry Frontiers 4, 675-681 (2017)."
3063,O=C(N1CC(CC)CCCC)C(C2=C1C(S3)=CC=C3C#C/C(C(C=C/4)=NC4=C5\C#CC6=CC=C(N(C)C)C=C6)=C7C=C/C8=C(C#CC9=CC=C(N(C)C)C=C9)/C%10=N/C(C=C%10)=C(C#CC%11=CC=C(C%12=C%13C(C(N%12CC(CC)CCCC)=O)=C(C%14=CC=CS%14)N(CC(CC)CCCC)C%13=O)S%11)\C%15=CC=C5N%15[Mg]N\78)=C(C%16=CC=CS%16)N(CC(CC)CCCC)C2=O,2d,,,0.79,4.61,45,1.65,"	Ogumi K, Nakagawa T, Okada H, Sakai R, Wang H, Matsuo Y. Substituent effects in magnesium tetraethynylporphyrin with two diketopyrrolopyrrole units for bulk heterojunction organic solar cells. Journal of Materials Chemistry A 5, 23067-23077 (2017)."
3064,CCCCCCCC(S1)=CC=C1C(S2)=CC=C2C(S3)=CC=C3C(S4)=CC=C4C5=CC=C(C(SC(C6=CC=C(C7=CC=C(C8=CC=C(CCCCCCC)S8)S7)S6)=C9)=C9C%10(CC(CC)CCCC)CC(CC)CCCC)C%10=C5,IT3T,,,0.53,12.63,46,3.06,"	Ogumi K, Nakagawa T, Okada H, Sakai R, Wang H, Matsuo Y. Substituent effects in magnesium tetraethynylporphyrin with two diketopyrrolopyrrole units for bulk heterojunction organic solar cells. Journal of Materials Chemistry A 5, 23067-23077 (2017)."
3065,CCCCCCCC(S1)=CC=C1C2=CC=C(C(C3=NSN=C34)=CC(F)=C4C(S5)=CC=C5C6=CC=C(C(SC(C7=C(F)C=C(C8=CC=C(C9=CC=C(CCCCCCC)S9)S8)C%10=NSN=C7%10)=C%11)=C%11C%12(CC(CC)CCCC)CC(CC)CCCC)C%12=C6)S2,ITFBT,,,0.753,3.29,28.6,0.71,"	Shang Q, Wang M, Wei J, Zheng Q. Indenothiophene-based asymmetric small molecules for organic solar cells. RSC Advances 7, 18144-18150 (2017)."
3066,CCCCCCCC(S1)=CC=C1C2=CC=C(C(C3=NSN=C34)=C(F)C(F)=C4C(S5)=CC=C5C6=CC=C(C(SC(C7=C(F)C(F)=C(C8=CC=C(C9=CC=C(CCCCCCC)S9)S8)C%10=NSN=C7%10)=C%11)=C%11C%12(CC(CC)CCCC)CC(CC)CCCC)C%12=C6)S2,IT2FBT,,,0.979,10.24,45.6,4.57,"	Shang Q, Wang M, Wei J, Zheng Q. Indenothiophene-based asymmetric small molecules for organic solar cells. RSC Advances 7, 18144-18150 (2017)."
3067,N#C/C(C(C=C1)=CC=C1C(S2)=CC=C2C3=C(N=C(C4=CC=CC=C4)C(C5=CC=CC=C5)=N6)C6=C(C7=CC=C(C8=CC=C(/C(C#N)=C/C9=CC=C(N(C%10=CC=CC=C%10)C%11=CC=CC=C%11)C=C9)C=C8)S7)C=C3)=C\C%12=CC=C(N(C%13=CC=CC=C%13)C%14=CC=CC=C%14)C=C%12,(TPACN)2Qx,,,1.01,6.25,30.5,1.92,"	Shang Q, Wang M, Wei J, Zheng Q. Indenothiophene-based asymmetric small molecules for organic solar cells. RSC Advances 7, 18144-18150 (2017)."
3068,FC1=C(C2=NSN=C2C(C3=CC=C(C4=CC=C(CCCCCC)S4)S3)=C1)C(S5)=CC6=C5C(SC(C7=C(F)C=C(C8=CC=C(C9=CC=C(CCCCCC)S9)S8)C%10=NSN=C%107)=C%11)=C%11[Si]6(CC(CC)CCCC)CC(CC)CCCC,p-DTS-(FBTTH2)2,,,0.95,14.08,47,6.25,"	Xie B, et al. Efficient small molecule photovoltaic donor based on 2,3-diphenyl-substituted quinoxaline core for solution-processed organic solar cells. RSC Advances 7, 23779-23786 (2017)."
3069,S=C(N(CC)C/1=O)SC1=C\C(S2)=CC3=C2C(C4=CC=C(CC(CC)CCCC)S4)=C5C(SC(C(S6)=CC7=C6C(C8=CC=C(CC(CC)CCCC)S8)=C(C=C(C9=CC%10=C(C(C%11=CC=C(CC(CC)CCCC)S%11)=C(C=C(/C=C%12C(N(CC)C(S/%12)=S)=O)S%13)C%13=C%10C%14=CC=C(CC(CC)CCCC)S%14)S9)S%15)C%15=C7C%16=CC=C(CC(CC)CCCC)S%16)=C5)=C3C%17=CC=C(CC(CC)CCCC)S%17,DRTB-T,,,0.79,11.86,69,6.5,"	Xu G, et al. n-Type conjugated electrolytes cathode interlayer with thickness-insensitivity for highly efficient organic solar cells. Journal of Materials Chemistry A 5, 13807-13816 (2017)."
3070,O=C1C2=C(C=CC=C2)C(/C1=C/C(S3)=CC4=C3C(CCCCCC)=C(S4)C(S5)=CC6=C5C(SC(C7=C(CCCCCC)C(SC(/C=C8C(C(C=CC=C9)=C9C\8=O)=O)=C%10)=C%10S7)=C%11)=C%11[Si]6(CCCCCCCC)CCCCCCCC)=O,DINTTDTS,,,0.98,14.25,65,9.08,"	Yang L, et al. New Wide Band Gap Donor for Efficient Fullerene-Free All-Small-Molecule Organic Solar Cells. J Am Chem Soc 139, 1958-1966 (2017)."
3071,CC1(C)C(C=C2C([O-])=C(C3=C(O)C=C(N4CCC5=C4C=CC6=C5C=CC=C6)C=C3O)C2=O)=[N+](CCCC)C7=C1C8=C(C=C7)C=CC=C8,USQ-BI,,,0.79,8.98,39.5,2.79,"	Chen X, et al. Dithienosilole-based small molecule donors for efficient all-small-molecule organic solar cells. Dyes and Pigments 158, 445-450 (2018)."
3072,CC1(C)C(C=C2C([O-])=C(C3=C(O)C=C(N4CCC5=C4C=CC=C5)C=C3O)C2=O)=[N+](CCCC)C6=C1C7=C(C=C6)C=CC=C7,ASQ-5,,,0.73,15.64,47,5.35,"	Chen Y, et al. Synthesis of 3H-Benzo[e]indoline and Its Application to Small-Molecule Organic Solar Cells. Chemistry 24, 8747-8750 (2018)."
3073,[H]C1=C(C2=C3C=C(C4=CC(CCCCCCCC)=C(C5=CC=C(C6=C(CCCCCCCC)C=C(/C=C(\C#N)C(=O)CC(CC)CCCC)S6)S5)S4)SC3=C(C3=CC=C(CC(CC)CCCC)S3)C3=C2SC(C2=CC(CCCCCCCC)=C(C4=CC=C(C5=C(CCCCCCCC)C=C(/C=C(\C#N)C(=O)CC(CC)CCCC)S5)S4)S2)=C3)SC(CC(CC)CCCC)=C1,BTEC,,,0.81,11.03,48,4.29,"	Chen Y, et al. Synthesis of 3H-Benzo[e]indoline and Its Application to Small-Molecule Organic Solar Cells. Chemistry 24, 8747-8750 (2018)."
3074,CCCCCCCCC1=C(C2=CC=C(C3=C(CCCCCCCC)C=C(C4=CC5=C(S4)C(C4=C(F)C=C(CC(CC)CCCC)S4)=C4C=C(C6=CC(CCCCCCCC)=C(C7=CC=C(C8=C(CCCCCCCC)C=C(/C=C(\C#N)C(=O)CC(CC)CCCC)S8)S7)S6)SC4=C5C4=CC(F)=C(CC(CC)CCCC)S4)S3)S2)SC(/C=C(\C#N)C(=O)CC(CC)CCCC)=C1,BTEC-F,,,0.804,21.71,60.95,10.64,"J. Ge, L. Xie, R. Peng, B. Fanady, J. Huang, W. Song, T. Yan, W. Zhang, Z. Ge, 13.34 % Efficiency Non-Fullerene All-Small-Molecule Organic Solar Cells Enabled by Modulating the Crystallinity of Donors via a Fluorination Strategy. Angewandte Chemie International Edition. 59, 2808¨C2815 (2020)."
3075,CCCCCCCCC1=C(C2=CC=C(C3=C(CCCCCCCC)C=C(C4=CC5=C(S4)C(C4=C(F)C(F)=C(CC(CC)CCCC)S4)=C4C=C(C6=CC(CCCCCCCC)=C(C7=CC=C(C8=C(CCCCCCCC)C=C(/C=C(\C#N)C(=O)CC(CC)CCCC)S8)S7)S6)SC4=C5C4=C(F)C(F)=C(CC(CC)CCCC)S4)S3)S2)SC(/C=C(\C#N)C(=O)CC(CC)CCCC)=C1,BTEC-2F,,,0.87,21.21,61.35,11.33,"J. Ge, L. Xie, R. Peng, B. Fanady, J. Huang, W. Song, T. Yan, W. Zhang, Z. Ge, 13.34 % Efficiency Non-Fullerene All-Small-Molecule Organic Solar Cells Enabled by Modulating the Crystallinity of Donors via a Fluorination Strategy. Angewandte Chemie International Edition. 59, 2808¨C2815 (2020)."
3076,CCCCC(CC)COC1=CC(C2=CC=C(C3=CC4=C(C5=CC=C(CC(CC)CCCC)S5)C5=C(C=C(/C=C6/SC(=S)NC6=O)S5)C(C5=CC=C(CC(CC)CCCC)S5)=C4S3)S2)=C(OCC(CC)CCCC)C=C1C1=CC=C(C2=CC3=C(C4=CC=C(CC(CC)CCCC)S4)C4=C(C=C(/C=C5\SC(=S)NC5=O)S4)C(C4=CC=C(CC(CC)CCCC)S4)=C3S2)S1,P2TBR,,,0.854,21.55,72.35,13.34,"J. Ge, L. Xie, R. Peng, B. Fanady, J. Huang, W. Song, T. Yan, W. Zhang, Z. Ge, 13.34 % Efficiency Non-Fullerene All-Small-Molecule Organic Solar Cells Enabled by Modulating the Crystallinity of Donors via a Fluorination Strategy. Angewandte Chemie International Edition. 59, 2808¨C2815 (2020)."
3077,CCCCCCC1=C(C2=CC(CCCC)=C(C3=CC=C(/C=C/SC(=S)NCCCCC)S3)S2)SC(C2=CC3=C(S2)C(C2=CC(Cl)=C(CC(CC)CCCC)S2)=C2C=C(C4=CC(CCCC)=C(C5=CC(CCCCCC)=C(C6=CC=C(/C=C7/SC(=S)N(CCCCCC)C7=O)S6)S5)S4)SC2=C3C2=CC(Cl)=C(CC(CC)CCC)S2)=C1,BTR-Cl,,,0.94,17.5,70.1,11.5,"X. Li, Y. Wang, Q. Zhu, X. Guo, W. Ma, X. Ou, M. Zhang, Y. Li, A small molecule donor containing a non-fused ring core for all-small-molecule organic solar cells with high efficiency over 11%. J. Mater. Chem. A. 7, 3682¨C3690 (2019)."
3078,CCCCCCC1=C(CC(CC)CCCC)SC(C2=C3C=C(C4=CC(CCCC)=C(C5=CC(CCCCCC)=C(C6=CC=C(/C=C7/SC(=S)N(CCCCCC)C7=O)S6)S5)S4)SC3=C(C3=CC(CCCCCC)=C(CC(CC)CCC)S3)C3=C2SC(C2=CC(CCCCCC)=C(C4=CC(CCCC)=C(C5=CC=C(/C=C/SC(=S)NCCCCC)S5)S4)S2)=C3)=C1,BTR,,,0.86,24.17,0.655,13.61,"H. Chen, D. Hu, Q. Yang, J. Gao, J. Fu, K. Yang, H. He, S. Chen, Z. Kan, T. Duan, C. Yang, J. Ouyang, Z. Xiao, K. Sun, S. Lu, All-Small-Molecule Organic Solar Cells with an Ordered Liquid Crystalline Donor. Joule. 3, 3034¨C3047 (2019)."
3079,CCCCCCCCC1=C(C2=CC=C(C3=C(CCCCCCCC)C=C(C4=CC5=C(C6=CC=C(CC(CC)CCCC)S6)C6=C(C=C([C@H]7CC(CCCCCCCC)=C(C8=CC=C(C9=C(CCCCCCCC)C=C(/C=C%10\SC(=S)N(CC(=O)OCC(CC)CCCC)C%10=O)S9)S8)S7)S6)C(C6=CC=C(CC(CC)CCCC)S6)=C5N4)S3)S2)SC(/C=C2\SC(=S)N(CC(=O)OCC(CC)CCCC)C2=O)=C1,BDT-RO,,,0.85,22.25,0.564,10.67,"H. Chen, D. Hu, Q. Yang, J. Gao, J. Fu, K. Yang, H. He, S. Chen, Z. Kan, T. Duan, C. Yang, J. Ouyang, Z. Xiao, K. Sun, S. Lu, All-Small-Molecule Organic Solar Cells with an Ordered Liquid Crystalline Donor. Joule. 3, 3034¨C3047 (2019)."
3080,[H]C1=C(CC(CC)CCCC)SC(C2=C3C=C(C4=CC(CCCCCC)=C(C5=CC(CCCCCC)=C(C6=CC=C(/C=C7\SC(=S)N(CCCCCC)C7=O)S6)S5)S4)SC3=C(C3=CC([H])=C(CC(CC)CCCCC)S3)C3=C2SC(C2=CC(CCCCCC)=C(C4=CC(CCCCCC)=C(C5=CC=C(/C=C6\SC(=S)N(C)C6=O)S5)S4)S2)=C3)=C1,FYSM-H,,,0.88,15.37,66.56,8.85,"T. Duan, H. Tang, R.-Z. Liang, J. Lv, Z. Kan, R. Singh, M. Kumar, Z. Xiao, S. Lu, F. Laquai, Terminal group engineering for small-molecule donors boosts the performance of nonfullerene organic solar cells. J. Mater. Chem. A. 7, 2541¨C2546 (2019)."
3081,CCCCCCNC(=O)/C(S)=C\C1CC=C(C2=C(CCCCCC)C=C(C3=C(CCCCCC)C=C(C4=CC5=C(CC6=CC(F)=C(C(CC)CCCC)C(F)=C6)C6=C(C=C(C7=CC(CCCCCC)=C(C8=CC(CCCCCC)=C(C9=CC=C(/C=C%10/SC(=S)N(CCCCCC)C%10=O)S9)S8)S7)S6)C(C6=CC(F)=C(C(C)CCCC)C(F)=C6)=C5S4)S3)S2)S1,s35,,,0.81,22.2,0.608,10.9,"W. Su, Y. Wang, Z. Yin, Q. Fan, X. Guo, L. Yu, Y. Li, L. Hou, M. Zhang, Q. Peng, Y. Li, E. Wang, 13.4 % Efficiency from All-Small-Molecule Organic Solar Cells Based on a Crystalline Donor with Chlorine and Trialkylsilyl Substitutions. ChemSusChem. 14, 3535¨C3543 (2021)."
3082,CCCCCCCCCCCCOC(=O)C1=C(C2=CC=C(C3=C(C(=O)OCCCCCCCCCCCC)C=C(C4=CC5=C(C6=CC=C(CC(CC)CCCC)S6)C6=C(C=C(C7=CC(C(=O)OCCCCCCCCCCCC)C(C8=CC=C(C9=C(C(=O)OCCCCCCCCCCCC)C=C(/C=C%10\SC(=S)N(CCCC)C%10=O)S9)S8)S7)S6)C(C6=CC=C(CC(CC)CCC)S6)=C5S4)S3)S2)SC(/C=C2\SC(=S)N(CCCCCC)C2=O)=C1,BER6,,,0.85,22.54,62.35,11.95,"Q. Wang, S. Lei, M. Luo, J. Liang, D. Zhou, L. Zhang, J. Chen, Introducing Siloxane-Terminated Side Chains in Small Molecular Donors for All-Small-Molecule Organic Solar Cells: Modulated Molecular Orientation and Enhanced Efficiency. ACS Appl. Mater. Interfaces. 13, 36080¨C36088 (2021)."
3083,CCCCCCCCCCCCOC(=O)C1=C(C2=CC=C(C3=C(C(=O)OCCCCCCCCCCCC)C=C(C4=CC5=C(C6=CC=C(CC(CC)CCCC)S6)C6=C(C=C(C7=CC(C(=O)OCCCCCCCCCCCC)C(C8=CC=C(C9=C(C(=O)OCCCCCCCCCCCC)C=C(/C=C(\C#N)C(=O)OCC(CC)CCCC)S9)S8)S7)S6)C(C6=CC=C(CC(CC)CCC)S6)=C5S4)S3)S2)SC(/C=C(\C#N)C(=O)OCC(CC)CCCC)=C1,BECN,,,0.97,14.86,0.63,9.03,"J. Zhao, X. Yu, M. Zhu, H. Xia, W. Tang, W. Peng, J. Guo, C. Qian, B. Zhang, Y. Liu, H. Tan, W. Zhu, Wide-Band Gap Small-Molecule Donors with Diester-Terthiophene Bridged Units for High-Efficiency All-Small-Molecule Organic Solar Cells. ACS Appl. Energy Mater. 4, 5868¨C5876 (2021)."
3084,CCCCCCCCOC(=O)/C(C#N)=C\C1=CC=C(C2=C(C(CC)CCCC)C=C(C3=C(C(CC)CCCC)C=C(C4=CC5=C(S4)C(C4=CC(Cl)=C(CC(CC)CCCC)S4)=C4C=C(C6=CC(C(CC)CCCC)=C(C7=CC(C(CC)CCCC)=C(C8=CC=C(/C=C(/C#N)C(=O)OCCCCCCCC)S8)S7)S6)SC4=C5C4=CC(Cl)=C(CC(CC)CCCC)S4)S3)S2)S1,BT-RO-Cl,,,0.96,11.1,0.51,5.52,"J. Zhao, X. Yu, M. Zhu, H. Xia, W. Tang, W. Peng, J. Guo, C. Qian, B. Zhang, Y. Liu, H. Tan, W. Zhu, Wide-Band Gap Small-Molecule Donors with Diester-Terthiophene Bridged Units for High-Efficiency All-Small-Molecule Organic Solar Cells. ACS Appl. Energy Mater. 4, 5868¨C5876 (2021)."
3085,CCCCC(CC)COC(=O)/C(C#N)=C\C1=CC=C(C2=C(C(CC)CCCC)C=C(C3=C(C(CC)CCCC)C=C(C4=CC5=C(S4)C(C4=CC(Cl)=C(CC(CC)CCCC)S4)=C4C=C(C6=CC(C(CC)CCCC)=C(C7=CC(C(CC)CCCC)=C(C8=CC=C(/C=C(/C#N)C(=O)OCC(CC)CCCC)S8)S7)S6)SC4=C5C4=CC(Cl)=C(CC(CC)CCCC)S4)S3)S2)S1,BT-Reh-Cl,,,0.87,22.5,0.69,13.35,"H. Chen, H. Tang, D. Hu, Y. Xiao, J. Fu, J. Lv, Q. Yu, Z. Xiao, X. Lu, H. Hu, S. Lu, Design of All-Small-Molecule Organic Solar Cells Approaching 14% Efficiency via Isometric Terminal Alkyl Chain Engineering. Energies. 14, 2505 (2021)."
3086,CCCCCCCCC1=C(C2=CC=C(/C=C3/SC(=S)N(C(CC)CCCC)C3=O)S2)SC(C2=CC3=C(S2)C2=C(S3)C(C3=CC=C(SCC(CCCCCC)CCCCCCCC)C=C3)=C3C4=C(C=C(C5=CC(CCCCCCCC)=C(C6=CC=C(/C=C7/SC(=S)N(CCCCCC)C7=O)S6)S5)S4)SC3=C2C2=C=C=C(SCC(CCCCCC)CCCCCCCC)C=C2)=C1,P-PHS,,,0.87,22.93,0.7,13.9,"H. Chen, H. Tang, D. Hu, Y. Xiao, J. Fu, J. Lv, Q. Yu, Z. Xiao, X. Lu, H. Hu, S. Lu, Design of All-Small-Molecule Organic Solar Cells Approaching 14% Efficiency via Isometric Terminal Alkyl Chain Engineering. Energies. 14, 2505 (2021)."
3087,CCCCCCCCC1=C(C2=CC=C(/C=C3/SC(=S)N(C(CC)CCCC)C3=O)S2)SC(C2=CC3=C(S2)C2=C(S3)C(C3=CC=CC(SCC(CCCCCC)CCCCCCCC)=C3)=C3C4=C(C=C(C5=CC(CCCCCCCC)=C(C6=CC=C(/C=C7/SC(=S)N(CCCCCC)C7=O)S6)S5)S4)SC3=C2C2=CC=CC(SCC(CCCCCC)CCCCCCCC)=C2)=C1,M-PHS,,,0.88,21.6,0.626,11.4,"L. Zhang, X. Zhu, D. Deng, Z. Wang, Z. Zhang, Y. Li, J. Zhang, K. Lv, L. Liu, X. Zhang, H. Zhou, H. Ade, Z. Wei, High Miscibility Compatible with Ordered Molecular Packing Enables an Excellent Efficiency of 16.2% in All-small-molecule Organic Solar Cells. Advanced Materials. n/a, 2106316."
3088,CCCC/C(=C/C1=CC=C(C2=C3SC(C4=CC(CC(CC)CCCC)=C(C5=CC=C(C6=C(CC(CC)CCCC)C=C(/C=C(\C#N)C(=O)OCC(CC)CCCC)S6)S5)S4)=CC3=C(C3=CC=C(CC(CC)CCCC)S3)C3=C2C=C(C2=CC(CC(CC)CCCC)=C(C4=CC=C(C5=C(CC(CC)CCCC)C=C(/C=C(\C#N)C(=O)OCC(CC)CCCC)S5)S4)S2)S3)S1)CC,SM1-EH,,,0.84,25.4,0.756,15.9,"L. Zhang, X. Zhu, D. Deng, Z. Wang, Z. Zhang, Y. Li, J. Zhang, K. Lv, L. Liu, X. Zhang, H. Zhou, H. Ade, Z. Wei, High Miscibility Compatible with Ordered Molecular Packing Enables an Excellent Efficiency of 16.2% in All-small-molecule Organic Solar Cells. Advanced Materials. n/a, 2106316."
3089,CCCCCCCCOC(=O)/C(C#N)=C/C1=CC(CCCCCCCC)=C(C2=CC=C(C3=C(CCCCCCCC)C=C(C4=CC5=C(S4)C(C4=CC=C(CCCCCCCC)S4)=C4C=C(C6=CC(CCCCCCCC)=C(C7=CC=C(C8=C(CCCCCCCC)C=C(/C=C(\C#N)C(=O)OCCCCCCCC)S8)S7)S6)SC4=C5C4=CC=C(CCCCCCCC)S4)S3)S2)S1,SM1-Oct,,,0.819,20.32,0.506,8.42,"K. Shi, B. Qiu, C. Zhu, J. Yao, X. Xia, J. Zhang, L. Meng, S. Huang, X. Lu, Y. Wan, Z.-G. Zhang, Y. Li, Effects of Alkyl Side Chains of Small Molecule Donors on Morphology and the Photovoltaic Property of All-Small-Molecule Solar Cells. ACS Appl. Mater. Interfaces. 13, 54237¨C54245 (2021)."
3090,CCCCC(CC)CC1=CC=C(C2=C3C=C(C4=CC5=C(S4)C(C4=CC=C(CC(CC)CCCC)S4)=C4C=C(C6=CC(C(CC)CCCC)=C(C7=CC=C(/C=C8/SC(=S)N(CC(CC)CCCC)C8=O)S7)S6)SC4=C5C4=CC=C(CC(CC)CCCC)S4)SC3=C(C3=CC=C(CC(CC)CCCC)S3)C3=C2SC(C2=CC4=C(C5=CC=C(CC(CC)CCCC)S5)C5=C(C=C(C6=CC(C(CC)CCCC)=C(C7=CC=C(/C=C8/SC(=S)N(C(CC)CCCC)C8=O)S7)S6)S5)C(C5=CC=C(CC(CC)CCCC)S5)=C4S2)=C3)S1,3BDT-4,,,0.766,22.39,0.684,11.73,"K. Shi, B. Qiu, C. Zhu, J. Yao, X. Xia, J. Zhang, L. Meng, S. Huang, X. Lu, Y. Wan, Z.-G. Zhang, Y. Li, Effects of Alkyl Side Chains of Small Molecule Donors on Morphology and the Photovoltaic Property of All-Small-Molecule Solar Cells. ACS Appl. Mater. Interfaces. 13, 54237¨C54245 (2021)."
3091,CCCCCCCCC1=C(C2=CC=C(/C=C(\C#N)C(=O)OCC(CC)CCCC)S2)SC(C2=CC3=C(C4=CC=C(CC(CC)CCCC)S4)C4=C(C=C(C5=CC6=C(C7=CC=C(CC(CC)CCCC)S7)C7=C(C=C(C8=CC9=C(C%10=CC=C(CC(CC)CCCC)S%10)C%10=C(C=C(C%11CC(CCCCCCCC)=C(C%12=CC=C(/C=C(\C#N)C(=O)OCC(CC)CCCC)S%12)S%11)S%10)C(C%10=CC=C(CC(CC)CCCC)S%10)=C9S8)S7)C(C7=CC=C(CC(CC)CCCC)S7)=C6S5)S4)C(C4=CC=C(CC(CC)CCCC)S4)=C3S2)=C1,3BDT-5,,,0.829,17,0.413,5.82,"D. Yang, K. Yu, J. Xu, J. Zhang, J. Zhang, J. Gao, W. Song, D. Li, Z. Chen, Z. Ge, Achieving 10% efficiency in non-fullerene all-small-molecule organic solar cells without extra treatments. J. Mater. Chem. A. 9, 10427¨C10436 (2021)."
3092,CCCCC(CC)CC1=CC=C(C2=C3C=C(/C=C4\SC(=S)N(CC)C4=O)SC3=C(C3=CC=C(CC(CC)CCCC)S3)C3=C2SC(C2=CC4=C(C5=CC(Cl)=C(CC(CC)CCCC)S5)C5=C(C=C(C6=CC7=C(C8=CC=C(CC(CC)CCCC)S8)C8=C(C=C(/C=C9\SC(=S)N(CC)C9=O)S8)C(C8=CC=C(CC(CC)CCCC)S8)=C7S6)S5)C(C5=CC(Cl)=C(CC(CC)CCCC)S5)=C4S2)=C3)S1,DRTB-CT,,,0.84,21.3,0.581,10.4,"D. Yang, K. Yu, J. Xu, J. Zhang, J. Zhang, J. Gao, W. Song, D. Li, Z. Chen, Z. Ge, Achieving 10% efficiency in non-fullerene all-small-molecule organic solar cells without extra treatments. J. Mater. Chem. A. 9, 10427¨C10436 (2021)."
3093,CCCCCCCCC1=C(C2=CC=C(C3=C(CCCCCCCC)C=C(C4=CC5=C(S4)C(C4=CC(F)=C(SCC(CC)CCCC)S4)=C4C6=C(C=C(C7=CC(CCCCCCCC)=C(C8=CC=C(C9=C(CCCCCCCC)C=C(/C=C%10\OC(=S)N(CCCC)C%10=O)S9)S8)S7)S6)SC4=C5C4=CC(F)=C(SCC(CC)CCCC)S4)S3)S2)OC(/C=C2\CC(=S)N(CCCC)C2=O)=C1,TBD-S2,,,1.057,15.07,0.568,9.05,"N. Qiu, Z. Xu, X. Chen, Z. Guo, X. Wang, Y. Song, Z. Xu, X. Wan, Improving the performances of all-small-molecule organic solar cells by fine-tuning halogen substituents of donor molecule. Organic Electronics. 99, 106340 (2021)."
3094,[H]C1=C(C2=CC(F)=C(C3=C([H])C(CC(CC)CCCC)=C(/C=C4/SC(=S)N(CC)C4=O)S3)C=C2F)SC(C2=CC3=C(S2)C(C2=CC=C(C(CC)CCCC)S2)=C2C=C(C4=C(C(CC)CCCC)C([H])=C(C5=CC(F)=C(C6=C([H])C(C(CC)CCCC)=C(/C=C7/SC(=S)N(CC)C7=O)S6)C=C5F)S4)SC2=C3C2=CC=C(C(CC)CCCC)S2)=C1C(CC)CCCC,BTBR-2F,,,0.85,22.3,0.69,13.1,"X. Wang, D. Huang, J. Han, L. Hu, C. Xiao, Z. Li, R. Yang, Backbone Engineering with Asymmetric Core to Finely Tune Phase Separation for High-Performance All-Small-Molecule Organic Solar Cells. ACS Appl. Mater. Interfaces. 13, 11108¨C11116 (2021)."
3095,CCCCC(CC)CSC1=C(F)C=C(C2=C3C=C(C4=CC(C(CC)CCCC)=C(C5=CC(C(CC)CCCC)=C(C6=CC=C(/C=C7\SC(=S)N(CCCC)C7=O)S6)S5)S4)SC3=C(C3=CC(F)=C(SCC(CC)CCCC)S3)C3=C2SC(C2=CC(C(CC)CCCC)=C(C4=CC=C(C5=CC=C(/C=C6\SC(=S)N(CCCC)C6=O)S5)S4)S2)=C3)S1,B3T-T,,,0.859,27.46,74.11,17.38,"L. Xu, W. Tao, H. Liu, J. Ning, M. Huang, B. Zhao, X. Lu, S. Tan, Achieving 17.38% efficiency of ternary organic solar cells enabled by a large-bandgap donor with noncovalent conformational locking. J. Mater. Chem. A. 9, 11734¨C11740 (2021)."
3096,CCCCC(CC)CSC1=CC=C(C2=C3C=C(C4=CC(C(CC)CCCC)=C(C5=CC(C(CC)CCCC)=C(C6=CC=C(/C=C7\SC(=S)N(CCCC)C7=O)S6)S5)S4)SC3=C(C3=CC=C(SCC(CC)CCCC)C=C3)C3=C2SC(C2=CC(C(CC)CCCC)=C(C4=CC=C(C5=CC=C(/C=C6\SC(=S)N(CCCC)C6=O)S5)S4)S2)=C3)C=C1,B3T-P,,,0.865,21.8,0.583,11,"C. An, Y. Qin, T. Zhang, Q. Lv, J. Qin, S. Zhang, C. He, H. Ade, J. Hou, Optimization of active layer morphology by small-molecule donor design enables over 15% efficiency in small-molecule organic solar cells. J. Mater. Chem. A. 9, 13653¨C13660 (2021)."
3097,CCCCC(CC)C1=C(/C=C2\SC(=S)N(CCCC)C2=O)SC(C2=NC3=C(N=C(C4=CC(C(CC)CCCC)=C(C5=CC6=C(S5)C(C5=CC(C7CCCCC7)=C(C(CC)CCCC)S5)=C5C=C(C7=C(C(CC)CCCC)C=C(C8=NC9=C(N=C(C%10=CC(C(CC)CCCC)=C(/C=C%11\SC(=S)N(CCCC)C%11=O)S%10)S9)S8)S7)SC5=C6C5=CC(C6CCCCC6)=C(C(CC)CCCC)S5)S4)S3)S2)=C1,BTTZR,,,0.813,25.6,0.717,14.9,"C. An, Y. Qin, T. Zhang, Q. Lv, J. Qin, S. Zhang, C. He, H. Ade, J. Hou, Optimization of active layer morphology by small-molecule donor design enables over 15% efficiency in small-molecule organic solar cells. J. Mater. Chem. A. 9, 13653¨C13660 (2021)."
3098,CCCCC(CC)CSC1=C(F)C=C(C2=C3SC4=C(SC(C5=CC(C(CC)CCCC)=C(C6=CC(C(CC)CCCC)=C(C7=CC=C(/C=C8\SC(=S)N(C(CC)CCCC)C8=O)S7)S6)S5)=C4)C3=C(C3=CC(F)=C(SCC(CC)CCCC)S3)C3=C2C=C(C2=CC(C(CC)CCCC)=C(C4=CC(C(CC)CCCC)=C(C5=CC=C(/C=C6\SC(=S)N(C(CC)CCCC)C6=O)S5)S4)S2)O3)S1,FBD-S3,,,0.88,23.2,0.68,13.9,"Y. Wang, Y. Wang, L. Zhu, H. Liu, J. Fang, X. Guo, F. Liu, Z. Tang, M. Zhang, Y. Li, A novel wide-bandgap small molecule donor for high efficiency all-small-molecule organic solar cells with small non-radiative energy losses. Energy Environ. Sci. 13, 1309¨C1317 (2020)."
3099,CCCCC(CC)CSC1=C(F)C=C(C2=C3SC4=C(SC(C5=CC(C(CC)CCCC)=C(C6=CC(C(CC)CCCC)=C(C7=CC=C(/C=C8\SC(=S)N(C(CC)CCCC)C8=O)S7)S6)S5)=C4)C3=C(C3=CC(F)=C(SCC(CC)CCCC)S3)C3=C2C=C(C2=CC(C(CC)CCCC)=C(C4=CC(C(CC)CCCC)=C(C5=CC=C(/C=C6\SC(=S)N(C(CC)CCCC)C6=O)S5)S4)S2)S3)S1,TBD-S4,,,0.849,21.77,0.6774,12.53,"X. Wang, J. Wang, J. Han, D. Huang, P. Wang, L. Zhou, C. Yang, X. Bao, R. Yang, Over 15% efficiency all-small-molecule organic solar cells enabled by a C-shaped small molecule donor with tailorable asymmetric backbone. Nano Energy. 81, 105612 (2021)."
3100,CCCCC(CC)CC1=CC=C(C2=C3C=C(/C=C4\SC(=S)N(CC)C4=O)SC3=C(C3=CC=C(CC(CC)CCCC)S3)C3=C2SC(C2=CC4=C(C5=CC(F)=C(CC(CC)CCCC)S5)C5=C(C=C(C6=CC7=C(C8=CC=C(CC(CC)CCCC)S8)C8=C(C=C(/C=C9\SC(=S)N(CC)C9=O)S8)C(C8=CC=C(CC(CC)CCCC)S8)=C7S6)S5)C(C5=CC(F)=C(CC(CC)CCCC)N5)=C4S2)=C3)S1,DRTB-FT,,,0.854,24.53,0.721,15.1,"X. Wang, J. Wang, J. Han, D. Huang, P. Wang, L. Zhou, C. Yang, X. Bao, R. Yang, Over 15% efficiency all-small-molecule organic solar cells enabled by a C-shaped small molecule donor with tailorable asymmetric backbone. Nano Energy. 81, 105612 (2021)."
3101,CCCCC(CC)CSC1=C(Cl)C=C(C2=C3SC4=C(SC(C5=CC(CC(CC)CCCC)=C(C6=CC=C(/C=C7/SC(=S)N(CC(CC)CCCC)C7=O)S6)S5)=C4)C3=C(C3=CC(Cl)=C(SCC(CC)CCCC)S3)C3=C2C2=C(C=C(C4=CC(C(CC)CCCC)=C(C5=CC=C(/C=C6/SC(=S)N(C(CC)CCCC)C6=O)S5)S4)S2)S3)S1,ZR1-S-CL,,,0.969,17.24,0.64,10.76,"C. Liu, N. Qiu, Y. Sun, X. Ke, H. Zhang, C. Li, X. Wan, Y. Chen, All-Small-Molecule Organic Solar Cells Based on a Fluorinated Small Molecule Donor With High Open-Circuit Voltage of 1.07 V. Frontiers in Chemistry. 8, 329 (2020)."
3102,CCCCC(CC)CC1=CC=C(C2=C3C=C(C4=CC(CC(CC)CCCC)=C(C5=CC=C(C6=C(CC(CC)CCCC)C=C(/C=C7\SC(=S)N(C)C7=O)S6)S5)S4)SC3=C(C3=CC=C(CC(CC)CCCC)S3)C3=C2SC(C2=CC(CC(CC)CCCC)=C(C4=CC=C(C5=C(CC(CC)CCCC)C=C(/C=C6\SC(=S)N(CC)C6=O)S5)S4)S2)=C3)S1,BDTT-TR,,,0.885,19.78,0.688,12.02,"R. Zhou, C. Yang, W. Zou, M. Abdullah Adil, H. Li, M. Lv, Z. Huang, M. Lv, J. Zhang, K. Lu, Z. Wei, Combining chlorination and sulfuration strategies for high-performance all-small-molecule organic solar cells. Journal of Energy Chemistry. 52, 228¨C233 (2021)."
3103,CCCCC(CC)COC(=O)/C(C#N)=C/C1=CC(C)=C(C2=CC=C(C3=C(CC(CC)CCCC)C=C(C4=CC5=C(C6=CC=C(CC(CC)CCCC)S6)C6=C(C=C(C7=CC(CC(CC)CCCC)=C(C8=CC=C(C9=C(CC(CC)CCCC)C=C(/C=C(\C#N)C(=O)OCC(CC)CCCC)S9)S8)S7)S6)C(C6=CC=C(CC(CC)CCCC)S6)=C5S4)S3)S2)S1,SM1,,,0.774,24.5,0.726,13.76,"R. Sun, Y. Wu, J. Guo, Z. Luo, C. Yang, J. Min, High-efficiency all-small-molecule organic solar cells based on an organic molecule donor with an asymmetric thieno[2,3-f] benzofuran unit. Sci. China Chem. 63, 1246¨C1255 (2020)."
3104,CCCCC(CC)COC(=O)/C(C#N)=C/C1=CC(C)=C(C2=CC=C(C3=C(CC(CC)CCCC)C=C(C4=CC5=C(C6=CC=C(CC(CC)CCCC)S6)C6=C(C=C(C7=CC(CC(CC)CCCC)=C(C8=CC=C(C9=C(CC(CC)CCCC)C=C(/C=C(\C#N)C(=O)OCC(CC)CCCC)S9)S8)S7)S6)C(C6=CC=C(SC(CC)CCCC)S6)=C5S4)S3)S2)S1,SM1-S,,,0.805,23.59,0.67,12.72,"B. Qiu, Z. Chen, S. Qin, J. Yao, W. Huang, L. Meng, H. Zhu, Y. (Michael) Yang, Z.-G. Zhang, Y. Li, Highly Efficient All-Small-Molecule Organic Solar Cells with Appropriate Active Layer Morphology by Side Chain Engineering of Donor Molecules and Thermal Annealing. Advanced Materials. 32, 1908373 (2020)."
3105,CCCCC(CC)COC(=O)/C(C#N)=C/C1=CC(C)=C(C2=CC=C(C3=C(CC(CC)CCCC)C=C(C4=CC5=C(C6=CC(F)=C(CC(CC)CCCC)S6)C6=C(C=C(C7=CC(CC(CC)CCCC)=C(C8=CC=C(C9=C(CC(CC)CCCC)C=C(/C=C(\C#N)C(=O)OCC(CC)CCCC)S9)S8)S7)S6)C(C6=CC(F)=C(CC(CC)CCCC)S6)=C5S4)S3)S2)S1,SM1-F,,,0.825,23.23,0.677,12.94,"B. Qiu, Z. Chen, S. Qin, J. Yao, W. Huang, L. Meng, H. Zhu, Y. (Michael) Yang, Z.-G. Zhang, Y. Li, Highly Efficient All-Small-Molecule Organic Solar Cells with Appropriate Active Layer Morphology by Side Chain Engineering of Donor Molecules and Thermal Annealing. Advanced Materials. 32, 1908373 (2020)."
3106,CCCCC(CC)CNC1=C(Cl)C=C(C2=C3SC(C4=C(C(CC)CCCC)C5=C(C=C(C6=C(C(CC)CCCC)C=C(/C=C7\OC(=S)N(CC(CC)CCCC)C7=O)S6)S5)S4)=CC3=C(C3=CC(Cl)=C(SCC(CC)CCCC)S3)C3=C2C=C(C2=C(C(CC)CCCC)C4=C(C=C(C5=C(C(CC)CCCC)C=C(/C=C6\OC(=S)C(CC(CC)CCCC)C6=O)S5)S4)S2)S3)S1,BSCL-C2,,,0.866,23.25,0.699,14.07,"B. Qiu, Z. Chen, S. Qin, J. Yao, W. Huang, L. Meng, H. Zhu, Y. (Michael) Yang, Z.-G. Zhang, Y. Li, Highly Efficient All-Small-Molecule Organic Solar Cells with Appropriate Active Layer Morphology by Side Chain Engineering of Donor Molecules and Thermal Annealing. Advanced Materials. 32, 1908373 (2020)."
3107,CCCCCCCN1C(=O)/C(=C/C2=CC(C(CC)CCCC)=C(C3=CC4=C(S3)C(C(CC)CCCC)=C(C3=CC5=C(S3)C(C3=CC(Cl)=C(SCC(CC)CCCC)S3)=C3C=C(C6=C(C(CC)CCCC)C7=C(C=C(C8=C(C(CC)CCCC)C=C(/C=C9\SC(=S)N(CCCCCCC)C9=O)S8)S7)S6)SC3=C5C3=CC(Cl)=C(SCC(CC)CCCC)S3)S4)S2)SC1=S,BSCL,,,0.865,20.1,0.713,12.4,"Q. Wu, D. Deng, R. Zhou, J. Zhang, W. Zou, L. Liu, S. Wu, K. Lu, Z. Wei, Modulation of Donor Alkyl Terminal Chains with the Shifting Branching Point Leads to the Optimized Morphology and Efficient All-Small-Molecule Organic Solar Cells. ACS Appl. Mater. Interfaces. 12, 25100¨C25107 (2020)."
3108,CCCCCCCC(CC1=C(F)C=C(C2=C3SC(C4=C(CCCCCC)C5=C(C=C(C6=C(CCCCCC)C=C(/C=C(\C#N)C(=O)OCC(CC)CCCC)S6)S5)S4)=CC3=C(C3=CC(F)=C(CC(CCCCCC)CC(CC)CCCC)S3)C3=C2C=C(C2=C(CCCCCC)C4=C(C=C(C5=C(CCCCCC)C=C(/C=C(\C#N)C(=O)OCC(CC)CCCC)S5)S4)S2)S3)S1)CC(CC)CCCC,BDTF-CA,,,0.865,21.5,0.7,13.03,"Z. Zhang, Q. Wu, D. Deng, S. Wu, R. Sun, J. Min, J. Zhang, Z. Wei, The post-treatment effects on open circuit voltages and device performances in a high efficiency all-small-molecule organic solar cell. J. Mater. Chem. C. 8, 15385¨C15392 (2020)."
3109,CCCCCCC1=C(C2=CC(CCCCCC)=C(C3=CC=C(/C=C4\OC(=S)N(CCCC)C4=O)S3)S2)SC(C2=CC3=C(S2)C(C2=CC=C(SCC(CC)CCCC)C=C2)=C2C=C(C4=CC(CCCCCC)=C(C5=CC(CCCCCC)=C(C6=CC=C(/C=C7\SC(=S)N(CCCC)C7=O)S6)S5)S4)SC2=C3C2=CC=C(SCC(CC)CCCC)C=C2)=C1,B1,,,0.94,16.69,0.58,9.11,"Q. Wu, D. Deng, J. Zhang, W. Zou, Y. Yang, Z. Wang, H. Li, R. Zhou, K. Lu, Z. Wei, Fluorination-substitution effect on all-small-molecule organic solar cells. Sci. China Chem. 62, 837¨C844 (2019)."
3110,CCCCCCC(CCCC)CC1=CC=C(C2=C3SC4=C(SC(C5=CC(CC(CC)CCCC)=C(C6=CC=C(/C=C7/SC(=S)N(CCCCCC)C7=O)S6)S5)=C4)C3=C(C3=CC=C(CC(CCCC)CCCCCC)S3)C3=C2C2=C(C=C(C4=CC(CC(CC)CCCC)=C(C5=CC=C(/C=C6/SC(=S)N(CCCCCC)C6=O)S5)S4)S2)S3)S1,ZR1,,,0.83,25.27,0.73,15.3,"J. Qin, C. An, J. Zhang, K. Ma, Y. Yang, T. Zhang, S. Li, K. Xian, Y. Cui, Y. Tang, W. Ma, H. Yao, S. Zhang, B. Xu, C. He, J. Hou, 15.3% efficiency all-small-molecule organic solar cells enabled by symmetric phenyl substitution. Sci. China Mater. 63, 1142¨C1150 (2020)."
3111,CCCCCCC1=C(C2=CC(CCCCCC)=C(C3=CC=C(/C=C4/SC(=S)N(C(CC)CCCC)C4=O)S3)S2)SC(C2=CC3=C(C4=CC(F)=C(SCC(CC)CCCC)S4)C4SC(C5=CC(CCCCCC)=C(C6=CC(CCCCCC)=C(C7=CC=C(/C=C8/SC(=S)N(C(CC)CCCC)C8=O)S7)S6)S5)=CC4C(C4=CC(F)=C(SC(CC)CCCC)S4)=C3S2)=C1,BSFTR,,,0.861,24.34,68.44,14.34,"R. Zhou, Z. Jiang, C. Yang, J. Yu, J. Feng, M. A. Adil, D. Deng, W. Zou, J. Zhang, K. Lu, W. Ma, F. Gao, Z. Wei, All-small-molecule organic solar cells with over 14% efficiency by optimizing hierarchical morphologies. Nat Commun. 10, 5393 (2019)."
3112,CCCCC(CC)CC1=C(C2=CC(CC(CC)CCCC)=C(C3=CC(CC(CC)CCCC)=C(C4=C(F)C(Cl)=C(C5=C(CC(CC)CCCC)C=C(C6=C(CC(CC)CCCC)C=C(C7=C(CC(CC)CCCC)C=C(/C=C8\SC(=C(C#N)C#N)N(CC)C8=O)S7)S6)S5)S4)S3)S2)SC(/C=C2\SC(=C(C#N)C#N)N(CC)C2=O)=C1,2CL7T,,,0.85,23.16,0.7,13.69,"Q. Yue, H. Wu, Z. Zhou, M. Zhang, F. Liu, X. Zhu, 13.7% Efficiency Small-Molecule Solar Cells Enabled by a Combination of Material and Morphology Optimization. Advanced Materials. 31, 1904283 (2019)."
3113,[H]C1=C(C2=CC=C(/C=C3\C(=O)C4=CC=CC(F)=C4C3=O)[Se]2)SC2=C1SC(C1=CC3=C(S1)C(C1=CC=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)S1)=C1C=C(C4=C(CCCCCC)C5=C(S4)C([H])=C(C4=CC=C(/C=C6\C(=O)C7C=CC=C(F)C7C6=O)[Se]4)S5)SC1=C3C1=CC=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)S1)=C2CCCCCC,SE-1,,,0.83,19.69,0.68,11.19,"T. Duan, J. Gao, T. Xu, Z. Kan, W. Chen, R. Singh, G. P. Kini, C. Zhong, D. Yu, Z. Xiao, Z. Xiao, S. Lu, Simple organic donors based on halogenated oligothiophenes for all small molecule solar cells with efficiency over 11%. J. Mater. Chem. A. 8, 5843¨C5847 (2020)."
3114,[H]C1=C(C2=CC3=C(S2)C(C2=CC=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)S2)=C2C=C(C4=C([H])C5=C(S4)C(CCCCCC)=C(C4=CC=C(/C=C6\C(=O)C7C=CC=C(F)C7C6=O)[Se]4)S5)SC2=C3C2=CC=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)S2)SC2=C1SC(C1=CC=C(/C=C3\C(=O)C4=CC=CC(F)=C4C3=O)[Se]1)=C2CCCCCC,SE-2,,,0.84,18.6,0.599,9.4,"Y. Li, D. Deng, R. Sun, S. Wu, L. Zhang, Z. Zhang, J. Zhang, J. Min, G. Zhao, Z. Wei, Efficient charge generation and low open circuit voltage loss enable a PCE of 10.3% in small molecule donor and polymer acceptor organic solar cells. J. Mater. Chem. C (2021), doi:10.1039/D1TC04428A."
3115,CCCCCCCCC1=C(C2=CC=C(/C=C3/SC(=S)N(CCCCCC)C3=O)S2)CC(C2=CC3=C(S2)C2=C(C4=CC=C(CC(CCCCCCCC)CCCCCCCC)S4)C4=C(C5=C(C=C(C6=CC(CCCCCCCC)=C(C7=CC=C(/C=C8/SC(=S)N(CCCCCC)C8=O)S7)S6)S5)S4)C(C4=CC=C(CC(CCCCCCCC)CCCCCCCC)S4)=C2S3)=C1,ZR2-C1,,,0.87,19.42,0.612,10.3,"Y. Li, D. Deng, R. Sun, S. Wu, L. Zhang, Z. Zhang, J. Zhang, J. Min, G. Zhao, Z. Wei, Efficient charge generation and low open circuit voltage loss enable a PCE of 10.3% in small molecule donor and polymer acceptor organic solar cells. J. Mater. Chem. C (2021), doi:10.1039/D1TC04428A."
3116,CCCCCCCCC1=C(C2=CC=C(/C=C3/SC(=S)N(CCCCCC)C3=O)S2)SC(C2=CC3=C(S2)C2=C(S3)C(C3=CC=C(CCC(CCCCCCCC)CCCCCCCC)S3)=C3C4=C(C=C(C5=CC(CCCCCCCC)=C(C6=CC=C(/C=C7/SC(=S)N(CCCCCC)C7=O)S6)S5)S4)SC3=C2C2=CC=C(CCC(CCCCCCCC)CCCCCCCC)S2)=C1,ZR2-C2,,,0.848,21.35,0.6512,11.79,"R. Zhou, Z. Jiang, Y. Shi, Q. Wu, C. Yang, J. Zhang, K. Lu, Z. Wei, Moving Alkyl-Chain Branching Point Induced a Hierarchical Morphology for Efficient All-Small-Molecule Organic Solar Cells. Advanced Functional Materials. 30, 2005426 (2020)."
3117,CCCCCCCCC1=C(C2=CC=C(/C=C3/SC(=S)N(CCCCCC)C3=O)S2)CC(C2=CC3=C(S2)C2=C(C4=CC=C(CCCC(CCCCCCCC)CCCCCCCC)S4)C4=C(C5=C(C=C(C6=CC(CCCCCCCC)=C(C7=CC=C(/C=C8/SC(=S)N(CCCCCC)C8=O)S7)S6)S5)S4)C(C4=CC=C(CCCC(CCCCCCCC)CCCCCCCC)S4)=C2S3)=C1,ZR2-C3,,,0.852,23.03,0.6543,12.84,"R. Zhou, Z. Jiang, Y. Shi, Q. Wu, C. Yang, J. Zhang, K. Lu, Z. Wei, Moving Alkyl-Chain Branching Point Induced a Hierarchical Morphology for Efficient All-Small-Molecule Organic Solar Cells. Advanced Functional Materials. 30, 2005426 (2020)."
3118,CCCCCCCCC(CCCCCC)CN1N=C2C(=N1)C(C1=CC=C(C3=CC4=C(C5=CC(Cl)=C(CC(CC)CCCC)S5)C5=C(C=C(C6=CC=C(C7=C(F)C(F)=C(C8=CC=C(/C=C(\C#N)C(=O)OCC(CC)CCCC)S8)C8=NN(CC(CC)CCCC)N=C87)S6)S5)C(C5=CC(Cl)=C(CC(CC)CCCC)S5)=C4S3)S1)=C(F)C(F)=C2C1=CC=C(/C=C(\C#N)C(=O)OCC(CC)CCCC)S1,H13,,,0.854,24.69,0.7,14.78,"R. Zhou, Z. Jiang, Y. Shi, Q. Wu, C. Yang, J. Zhang, K. Lu, Z. Wei, Moving Alkyl-Chain Branching Point Induced a Hierarchical Morphology for Efficient All-Small-Molecule Organic Solar Cells. Advanced Functional Materials. 30, 2005426 (2020)."
3119,CCCCCCCCC(CCCCCC)CN1N=C2C(=N1)C(C1=CC=C(C3=CC4=C(C5=CC(Cl)=C(CC(CC)CCCC)S5)C5=C(C=C(C6=CC=C(C7=C(F)C(F)=C(C8=CC=C(/C=C(\C#N)C(=O)OCC(CC)CCCC)S8)C8=NN(CC(CC)CCCC)N=C87)S6)S5)C(C5=CC(Cl)=C(CC(CC)CCCC)S5)=C4S3)S1)=C(F)C(F)=C2C1=CC=C(/C=C(\C#N)C(=O)OCC(CC)CCCC)S1,H14,,,0.939,17.3,0.632,10.1,"H. Bin, I. Angunawela, B. Qiu, F. J. M. Colberts, M. Li, M. J. Dyson, M. M. Wienk, H. Ade, Y. Li, R. A. J. Janssen, Precise Control of Phase Separation Enables 12% Efficiency in All Small Molecule Solar Cells. Advanced Energy Materials. 10, 2001589 (2020)."
3120,CCCCCCC1=C(/C=C2/SC(=S)NC2=O)SC(C2=C(CCCCCC)C3=C(C=C(C4=CC5=C(C6=CC(CCCCCC)=C(CC(CC)CCC)S6)C6=C(C=C(C7=CC8=C(S7)C(CCCCC)=C(C7=CC(CCCCC)=C(/C=C9/SC(=S)N(CCCCCC)C9=O)S7)S8)S6)C(C6=CC(CCCCCC)=C(CC(CC)CCC)S6)=C5S4)S3)S2)=C1.O,BOHTR,,,0.943,18.3,0.7,12,"H. Bin, I. Angunawela, B. Qiu, F. J. M. Colberts, M. Li, M. J. Dyson, M. M. Wienk, H. Ade, Y. Li, R. A. J. Janssen, Precise Control of Phase Separation Enables 12% Efficiency in All Small Molecule Solar Cells. Advanced Energy Materials. 10, 2001589 (2020)."
3121,CCCCCCC1=C(CC(CC)CCC)SC(C2=C3C=C(C4=C(CCCCCC)C5=C(C=C(C6=C(CCCCCC)C=C(/C=C7/SC(=S)NC7=O)S6)S5)S4)SC3=C(C3=CC(CCCCCC)=C(CC(CC)CCC)S3)C3=C2SC(C2=C(CCCCCC)C4=C(C=C(C5=C(CCCCCC)C=C(/C=C6/SC(=S)N(CCCCCC)C6=O)S5)S4)S2)=C3)=C1.O,BIHTR,,,0.83,23.1,0.56,10.8,"X. Dong, K. Yang, H. Tang, D. Hu, S. Chen, J. Zhang, Z. Kan, T. Duan, C. Hu, X. Dai, Z. Xiao, K. Sun, S. Lu, Improving Molecular Planarity by Changing Alky Chain Position Enables 12.3% Efficiency All©\Small©\Molecule Organic Solar Cells with Enhanced Carrier Lifetime and Reduced Recombination. Sol. RRL. 4, 1900326 (2020)."
3122,CCCCCCC1=C(C2=CC(CCCCCC)=C(C3=CC=C(/C=C(\C#N)C(=O)OCC(CC)CCCC)S3)S2)SC(C2=CC3=C(S2)C(C2=C(F)C(F)=C(CC(CC)CCCC)S2)=C2C=C(C4=CC(CCCCC)=C(C5=CC(CCCC)=C(C6=CC=C(/C=C(\C#N)C(=O)OCC(CC)CCCC)S6)S5)S4)SC2=C3C2=C(F)C(F)=C(CC(CC)CCCC)S2)=C1,BT-2F,,,0.84,21.5,0.68,12.3,"X. Dong, K. Yang, H. Tang, D. Hu, S. Chen, J. Zhang, Z. Kan, T. Duan, C. Hu, X. Dai, Z. Xiao, K. Sun, S. Lu, Improving Molecular Planarity by Changing Alky Chain Position Enables 12.3% Efficiency All©\Small©\Molecule Organic Solar Cells with Enhanced Carrier Lifetime and Reduced Recombination. Sol. RRL. 4, 1900326 (2020)."
3123,CCCCCCCC1=C(C2=CC=C(C3=C(CCCCCC)C=C(C4=CC5=C(S4)C4=C(S5)C(C5=CC=C(CCCCCC)S5)=C5C6=C(C=C(C7=CC(CCCCCC)=C(C8=CC=C(C9=C(CCCCCC)C=C(/C=C(\C#N)C(=O)OCC(CC)CCCC)S9)S8)S7)S6)SC5=C4C4=CC=C(CCCCCC)S4)S3)S2)SC(/C=C(\CC#N)C(=O)OC(CC)CCCC)=C1,SM-DTBDT,,,0.853,22.38,0.72,13.8,"J. Gao, J. Ge, R. Peng, C. Liu, L. Cao, D. Zhang, B. Fanady, L. Hong, E. Zhou, Z. Ge, Over 14% efficiency nonfullerene all-small-molecule organic solar cells enabled by improving the ordering of molecular donors via side-chain engineering. J. Mater. Chem. A. 8, 7405¨C7411 (2020)."
3124,CCCCCCCC1=C(C2=CC=C(C3=C(CCCCCC)C=C(C4=CC5=C(S4)C4=C(S5)C(C5=CC=C(C(CC)CCCC)S5)=C5C6=C(C=C(C7=CC(CCCCCC)=C(C8=CC=C(C9=C(CCCCCC)C=C(/C=C(\C#N)C(=O)OCC(CC)CCCC)S9)S8)S7)S6)SC5=C4C4=CC=C(C(CC)CCCC)S4)S3)S2)SC(/C=C(\CC#N)C(=O)OC(CC)CCCC)=C1,SM-BDT,,,0.81,24.55,0.63,12.45,"S. Li, Q. Ma, B. Qiu, L. Meng, J. Zhang, Y. Wu, Z. Zhang, Z.-G. Zhang, Y. Li, Effects of the Center Units of Small©\Molecule Donors on the Morphology, Photovoltaic Performance, and Device Stability of All©\Small©\Molecule Organic Solar Cells. Sol. RRL. 5, 2100515 (2021)."
3125,CCCCCCCCSC1=CC=C(C2=C3C=C(C4=CC(CCCCCCCC)=C(C5=CC=C(C6=C(CCCCCCCC)C=C(/C=C(\C#N)C(=O)OC(CC)CCCC)S6)S5)S4)SC3=C(C3=CC=C(SCCCCCCCC)S3)C3=C2SC(C2=CC(CCCCCCCC)=C(C4=CC=C(C5=C(CCCCCCCC)C=C(/C=C(\C#N)C(=O)OC(CC)CCCC)S5)S4)S2)=C3)S1,SM8,,,0.84,21.63,0.588,10.68,"S. Li, Q. Ma, B. Qiu, L. Meng, J. Zhang, Y. Wu, Z. Zhang, Z.-G. Zhang, Y. Li, Effects of the Center Units of Small©\Molecule Donors on the Morphology, Photovoltaic Performance, and Device Stability of All©\Small©\Molecule Organic Solar Cells. Sol. RRL. 5, 2100515 (2021)."
3126,CCCCCCCCCCCCSC1=CC=C(C2=C3C=C(C4=CC(CCCCCCCC)=C(C5=CC=C(C6=C(CCCCCCCC)C=C(/C=C(\C#N)C(=O)OC(CC)CCCC)S6)S5)S4)SC3=C(C3=CC=C(SCCCCCCCCCCCC)S3)C3=C2SC(C2=CC(CCCCCCCC)=C(C4=CC=C(C5=C(CCCCCCCC)C=C(/C=C(\C#N)C(=O)OC(CC)CCCC)S5)S4)S2)=C3)S1,SM12,,,0.851,21.23,0.7256,13.1,"J. Guo, K. Hu, B. Qiu, J. Zhang, D. Yang, L. Zhou, S. Li, L. Meng, Z. Zhang, Y. Li, Fine-Tuning Miscibility and ¦Ð¨C¦Ð Stacking by Alkylthio Side Chains of Donor Molecules Enables High-Performance All-Small-Molecule Organic Solar Cells. ACS Appl. Mater. Interfaces. 13, 36033¨C36043 (2021)."
3127,CCCCCCC1=C(C(CC)CCCC)SC(C2=C3C=C(C4=C(CC(C)C)C=C(C5=NC6=C(N=C(C7=CC(CC(CC)CCCC)=C(/C=C8\SC(=S)N(CCCC)C8=O)S7)S6)S5)S4)SC3=C(C3=CC(CCCCCC)=C(C(CC)CCCC)S3)C3=C2SC(C2=C(CC(CC)CCCC)C=C(C4=NC5=C(N=C(C6=CC(CC(CC)CCCCC)=C(/C=C7\SC(=S)N(CCC)C7=O)S6)S5)S4)S2)=C3)=C1,SL1,,,0.837,19.2,0.659,10.5,"J. Guo, K. Hu, B. Qiu, J. Zhang, D. Yang, L. Zhou, S. Li, L. Meng, Z. Zhang, Y. Li, Fine-Tuning Miscibility and ¦Ð¨C¦Ð Stacking by Alkylthio Side Chains of Donor Molecules Enables High-Performance All-Small-Molecule Organic Solar Cells. ACS Appl. Mater. Interfaces. 13, 36033¨C36043 (2021)."
3128,CCCCCC(CC)CC1=C(/C=C2\SC(=S)N(CCC)C2=O)SC(C2=NC3=C(N=C(C4=CC(CC(CC)CCCC)=C(C5=CC6=C(S5)C(C5=CC=C(C(CC)CCCC)S5)=C5C=C(C7=C(CC(C)C)C=C(C8=NC9=C(N=C(C%10=CC(CC(CC)CCCC)=C(/C=C%11\SC(=S)N(CCCC)C%11=O)S%10)S9)S8)S7)SC5=C6C5=CC=C(C(CC)CCCC)S5)S4)S3)S2)=C1,SL2,,,0.88,23.2,0.68,13.9,"Y. Wang, Q. Fan, Y. Wang, J. Fang, Q. Liu, L. Zhu, J. Qiu, X. Guo, F. Liu, W. Su, M. Zhang, Modulating Crystallinity and Miscibility via Side-chain Variation Enable High Performance All-Small-Molecule Organic Solar Cells. Chinese Journal of Chemistry. 39, 2147¨C2153 (2021)."
3129,CCCCCCCCC1=C(C(CC)CCCC)SC(C2=C3C=C(C4=C(CC(C)C)C=C(C5=NC6=C(N=C(C7=CC(CC(CC)CCCC)=C(/C=C8\SC(=S)N(CCCC)C8=O)S7)S6)S5)S4)SC3=C(C3=CC(CCCCCCCC)=C(C(CC)CCCC)S3)C3=C2SC(C2=C(CC(CC)CCCC)C=C(C4=NC5=C(N=C(C6=CC(CC(CC)CCCCC)=C(/C=C7\SC(=S)N(CCC)C7=O)S6)S5)S4)S2)=C3)=C1,SL3,,,0.89,21.6,0.6,11.5,"Y. Wang, Q. Fan, Y. Wang, J. Fang, Q. Liu, L. Zhu, J. Qiu, X. Guo, F. Liu, W. Su, M. Zhang, Modulating Crystallinity and Miscibility via Side-chain Variation Enable High Performance All-Small-Molecule Organic Solar Cells. Chinese Journal of Chemistry. 39, 2147¨C2153 (2021)."
3130,CCCCCCC1=C(CCCCCC)SC(C2=C3C=C(C4=C(CC(C)C)C=C(C5=NC6=C(N=C(C7=CC(CC(CC)CCCC)=C(/C=C8\SC(=S)N(CCCC)C8=O)S7)S6)S5)S4)SC3=C(C3=CC(CCCCCC)=C(CCCCCC)S3)C3=C2SC(C2=C(CC(CC)CCCC)C=C(C4=NC5=C(N=C(C6=CC(CC(CC)CCCCC)=C(/C=C7\SC(=S)N(CCC)C7=O)S6)S5)S4)S2)=C3)=C1,SL4,,,0.88,21.6,0.67,12.7,"Y. Wang, Q. Fan, Y. Wang, J. Fang, Q. Liu, L. Zhu, J. Qiu, X. Guo, F. Liu, W. Su, M. Zhang, Modulating Crystallinity and Miscibility via Side-chain Variation Enable High Performance All-Small-Molecule Organic Solar Cells. Chinese Journal of Chemistry. 39, 2147¨C2153 (2021)."
3131,CCCCCCCCC1=C(C2=CC=C(C3=C(CCCCCCCC)C=C(C4=CC5=C(O4)C(C4=CC=C(CC(CC)CCCC)S4)=C4C=C(C6=CC(CCCCCCCC)=C(C7=CC=C(C8=C(CCCCCCCC)C=C(/C=C9\SC(=S)N(CC)C9=O)S8)S7)S6)SC4=C5C4=CC=C(CC(CC)CCCC)S4)S3)S2)SC(/C=C2\SC(=S)N(CC)C2=O)=C1,TBFT-TR,,,0.87,23,0.62,12.4,"Y. Wang, Q. Fan, Y. Wang, J. Fang, Q. Liu, L. Zhu, J. Qiu, X. Guo, F. Liu, W. Su, M. Zhang, Modulating Crystallinity and Miscibility via Side-chain Variation Enable High Performance All-Small-Molecule Organic Solar Cells. Chinese Journal of Chemistry. 39, 2147¨C2153 (2021)."
3132,CCCCC(CC)C1=CC=C(C2=C3C=C(/C=C4\SC(=S)N(CC)C4=O)SC3=C(C3=CC=C(C(CC)CCCC)S3)C3=C2SC(C2=C(C(CC)CCCC)C4=C(S2)C(C(CCC)CCCC)=C(C2=CC5=C(S2)C(C2=CC=C(C(CC)CCCC)S2)=C2C=C(/C=C6\SC(=S)N(CC)C6=O)SC2=C5C2=CC=C(C(CC)CCCC)S2)S4)=C3)S1,DRTT-R,,,0.784,24.59,0.7278,14.03,"R. Sun, Y. Wu, J. Guo, Z. Luo, C. Yang, J. Min, High-efficiency all-small-molecule organic solar cells based on an organic molecule donor with an asymmetric thieno[2,3-f] benzofuran unit. Sci. China Chem. 63, 1246¨C1255 (2020)."
3133,CCCCC(CC)CC1=CSC(C2=CC=C(C3=CC(CC(CC)CCCC)=C(C4=CC5=C(C6=CC(F)=C(CC(CC)CCCC)S6)C6=C(C=CS6)C(C6=CC(F)=C(CC(CC)CCCC)S6)=C5S4)S3)C3=NSN=C23)=C1,W2-CA,,,0.95,15.72,0.626,10.4,"X. Cheng, M. Li, Z. Guo, J. Yu, G. Lu, L. Bu, L. Ye, H. Ade, Y. Chen, Y. Geng, ¡°Twisted¡± conjugated molecules as donor materials for efficient all-small-molecule organic solar cells processed with tetrahydrofuran. J. Mater. Chem. A. 7, 23008¨C23018 (2019)."
3134,CCCCC(CC)CC1=CSC(C2=CC=C(C3=CC(CC(CC)CCCC)=C(C4=CC5=C(C6=CC(F)=C(CC(CC)CCCC)S6)C6=C(C=CS6)C(C6=CC(F)=C(CC(CC)CCCC)S6)=C5S4)S3)C3N=NSC23)=C1,W2-Reh,,,0.83,25.19,76.8,16.06,"Q. Wang, X. Zhang, Y. Miao, X. Jiang, X. Wang, Z. Zhang, Z. Lv, T. Liu, B. Zou, H. Xu, R. Yang, Y. Kan, Y. Sun, K. Gao, Synergy Effect of Symmetry-Breaking and End-Group Engineering Enables 16.06% Efficiency for All-Small-Molecule Organic Solar Cells, ACS Materials Lett. 6 (2024) 713¨C719. https://doi.org/10.1021/acsmaterialslett.3c01500."
3135,CCCCCCCCC1=C(C2=CC=C(C3=C(CCCCCCCC)C=C(C4=NC5=C(S4)C(C4=CC=C(CC(CC)CCCC)S4)=C4N=C(C6=CC(CCCCCCCC)=C(C7=CC=C(C8=C(CCCCCCCC)C=C(/C=C(/C#N)C(=O)OCC(CC)CCCC)S8)S7)S6)SC4=C5C4=CC=C(CC(CC)CCCC)S4)S3)S2)SC(/C=C(/C#N)C(=O)OCC(CC)CCCC)=C1,BBTSM-1,,,0.826,25.31,74.8,15.63,"Q. Wang, X. Zhang, Y. Miao, X. Jiang, X. Wang, Z. Zhang, Z. Lv, T. Liu, B. Zou, H. Xu, R. Yang, Y. Kan, Y. Sun, K. Gao, Synergy Effect of Symmetry-Breaking and End-Group Engineering Enables 16.06% Efficiency for All-Small-Molecule Organic Solar Cells, ACS Materials Lett. 6 (2024) 713¨C719. https://doi.org/10.1021/acsmaterialslett.3c01500."
3136,CCCCCCCCC1=C(C2=CC(CCCCCCCC)=C(C3=CC(CCCCCCCC)=C(C4=NC(Cl)=C(C5=C(CCCCCCCC)C=C(C6=C(CCCCCCCC)C=C(C7=C(CCCCCCCC)C=C(/C=C8/SC(=C(C#N)C#N)N(C(C)C)C8=O)S7)S6)S5)S4)S3)S2)SC(/C=C2/SC(=C(C#N)C#N)N(CC)C2=O)=C1,Tz6T-iP,,,0.87,21.6,63,11.8," D. Han, S. Wen, F. Bi, C. Shang, X. Ding, A. Saparbaev, E. Zakhidov, V. Kuvondikov, C. Yang, M. Sun, Small molecular donor materials based on electron withdrawing benzobisthiazole core unit enable an efficiency of 11.8% for organic solar cells, Chemical Engineering Journal 463 (2023) 142400. https://doi.org/10.1016/j.cej.2023.142400."
3137,CCCCCCCCC1=C(C2=CC(CCCCCCCC)=C(C3=CC(CCCCCCCC)=C(C4=NC(Cl)=C(C5=C(CCCCCCCC)C=C(C6=C(CCCCCCCC)C=C(C7=C(CCCCCCCC)C=C(/C=C8/SC(=C(C#N)C#N)N(CCC)C8=O)S7)S6)S5)S4)S3)S2)SC(/C=C2/SC(=C(C#N)C#N)N(CCC)C2=O)=C1,Tz6T-P,,,849.1,25.55,72.49,15.7," Q. Chen, Y. Li, D. Hu, S. Lu, Z. Xiao, Branched Terminal Alkyl Chain Enabling 15.7% Efficiency Oligothiophene Donor, Solar RRL 8 (2024) 2300802. https://doi.org/10.1002/solr.202300802."
3138,CCCCCCCCC1=C(C2=CC=C(/C=C3\SC(=S)N(CC)C3=O)S2)SC(C2=CC3=C(S2)C2=C(S3)C(C3=CC(SCC(CCCCCC)CCCCCCCC)=CC=C3)=C3C4=C(C=C(C5=CC(CCCCCCCC)=C(C6=CC=C(/C=C7\SC(=S)N(CC)C7=O)S6)S5)S4)SC3=C2C2=CC(SCC(CCCCCC)CCCCCCCC)=CC=C2)=C1,MPhS-C2,,,876.1,24.83,67.4,14.7," Q. Chen, Y. Li, D. Hu, S. Lu, Z. Xiao, Branched Terminal Alkyl Chain Enabling 15.7% Efficiency Oligothiophene Donor, Solar RRL 8 (2024) 2300802. https://doi.org/10.1002/solr.202300802."
3139,CCCCCCCCC1=C(C2=CC=C(/C=C3\SC(=S)N(CC4=CC=CC=C4)C3=O)S2)SC(C2=CC3=C(S2)C2=C(S3)C(C3=CC(SCC(CCCCCC)CCCCCCCC)=CC=C3)=C3C4=C(C=C(C5=CC(CCCCCCCC)=C(C6=CC=C(/C=C7\SC(=S)N(CC8=CC=CC=C8)C7=O)S6)S5)S4)SC3=C2C2=CC(SCC(CCCCCC)CCCCCCCC)=CC=C2)=C1,MPhS-Ph,,,0.867,24.42,74.08,15.67," X. Ma, C. Wang, D. Deng, H. Zhang, L. Zhang, J. Zhang, Y. Yang, Z. Wei, Small Molecule Donors Design Rules for Non-Halogen Solvent Fabricated Organic Solar Cells, Small n/a (n.d.) 2309042. https://doi.org/10.1002/smll.202309042."
3140,CCCCCCCCC1=C(C2=CC=C(C3=C(CCCCCCCC)C=C(C4=CC5=C(S4)C(C4=CC(Cl)=C(CC(CC)CCCC)S4)=C4C=C(C6=CC(CCCCCCCC)=C(C7=CC=C(C8=C(CCCCCCCC)C=C(/C=C9/SC(=S)N(CC)C9=O)S8)[Se]7)S6)SC4=C5C4=CC(Cl)=C(CC(CC)CCCC)S4)S3)[Se]2)SC(/C=C2/SC(=S)N(CCCCCCC)C2=O)=C1,CBTSeEHR,,,0.859,23.63,72.75,14.77," X. Ma, C. Wang, D. Deng, H. Zhang, L. Zhang, J. Zhang, Y. Yang, Z. Wei, Small Molecule Donors Design Rules for Non-Halogen Solvent Fabricated Organic Solar Cells, Small n/a (n.d.) 2309042. https://doi.org/10.1002/smll.202309042."
3141,CCCCCCCCC1=C(C2=CC=C(C3=C(CCCCCCCC)C=C(C4=CC5=C(S4)C(C4=CC(Cl)=C(CC(CC)CCCC)S4)=C4C=C(C6=CC(CCCCCCCC)=C(C7=CC=C(C8=C(CCCCCCCC)C=C(/C=C9/SC(=S)N(CC)C9=O)S8)S7)S6)SC4=C5C4=CC=C(CC(CC)CCCC)S4)S3)S2)SC(/C=C2/SC(=S)N(CC)C2=O)=C1,BTEHR-CTb,,,0.881,18.76,0.732,12.1," C. Liu, Z. Wu, N. Qiu, C. Li, Y. Lu, Selenophene-containing benzodithiophene based donors with different alkyl chains in terminal groups for high-performance all-small-molecule organic solar cells, New J. Chem. 47 (2023) 2840¨C2846. https://doi.org/10.1039/D2NJ06222D."
3142,CCCCCCCCC1=C(C2=CC=C(C3=C(CCCCCCCC)C=C(C4=CC5=C(S4)C(C4=CC(Cl)=C(CC(CC)CCCC)S4)=C4C=C(C6=CC(CCCCCCCC)=C(C7=CC=C(C8=C(CCCCCCCC)C=C(/C=C9/SC(=S)N(CC(CC)CCCC)C9=O)S8)[Se]7)S6)SC4=C5C4=CC(Cl)=C(CC(CC)CCCC)S4)S3)[Se]2)SC(/C=C2/SC(=S)N(CC(CC)CCCC)C2=O)=C1,CBTSeHR,,,0.908,17.43,0.685,10.84," C. Liu, Z. Wu, N. Qiu, C. Li, Y. Lu, Selenophene-containing benzodithiophene based donors with different alkyl chains in terminal groups for high-performance all-small-molecule organic solar cells, New J. Chem. 47 (2023) 2840¨C2846. https://doi.org/10.1039/D2NJ06222D."
3143,CCN(CC)C1=CC=C2C=C(C(/C=C/C=C/C3=CC=C(N(C)C)C=C3)=C(C#N)C#N)C(=O)OC2=C1,C3-CN,,,0.871,15.28,0.698,9.3," C. Liu, Z. Wu, N. Qiu, C. Li, Y. Lu, Selenophene-containing benzodithiophene based donors with different alkyl chains in terminal groups for high-performance all-small-molecule organic solar cells, New J. Chem. 47 (2023) 2840¨C2846. https://doi.org/10.1039/D2NJ06222D."
3144,CCN(CC)C1=CC=C2C=C(C(=O)/C=C/C=C/C3=CC=C(N(C)C)C=C3)C(=O)OC2=C1,C3,,,1.05,20.54,0.68,14.62?," R. Pradhan, K. Khandelwal, S.J. Panda, C.S. Purohit, B.P. Bag, R. Singhal, W. Liu, X. Zhu, G.D. Sharma, A. Mishra, Achieving High-Efficiency in Binary Organic Solar Cells by the Structural Fine-Tuning of Coumarin-Based Donor, Solar RRL 7 (2023) 2300032. https://doi.org/10.1002/solr.202300032."
3145,CCCCCCC1=C(C2=CC(CCCCCC)=C(C3=CC=C(/C=C4\SC(=S)N(CC(CC)CCCC)C4=O)S3)S2)SC(C2=CC3=C(C4=C(F)C(F)=C(CC(CC)CCCC)S4)C4=C(C=C(C5=CC(CCCCCC)=C(C6=CC(CCCCCC)=C(C7=CCC(/C=C8\SC(=S)N(CC(CC)CCCC)C8=O)S7)S6)S5)S4)C(C4=C(F)C(F)=C(CC(CC)CCCC)S4)=C3S2)=C1,SM-REH ,,,0.96,18.41,0.62,10.85," R. Pradhan, K. Khandelwal, S.J. Panda, C.S. Purohit, B.P. Bag, R. Singhal, W. Liu, X. Zhu, G.D. Sharma, A. Mishra, Achieving High-Efficiency in Binary Organic Solar Cells by the Structural Fine-Tuning of Coumarin-Based Donor, Solar RRL 7 (2023) 2300032. https://doi.org/10.1002/solr.202300032."
3146,CCCCCCC1=C(C2=CC(CC(CC)CCCC)=C(C3=CC=C(/C=C4\SC(=S)N(CC(CC)CCCC)C4=O)S3)S2)SC(C2=CC3=C(S2)C(C2=C(F)C(F)=C(CC(CC)CCCC)S2)=C2C=C(C4=CC(CCCCCC)=C(C5=CC(CC(CC)CCCC)=C(C6=CC=C(/C=C7\SC(=S)N(CC(CC)CCCC)C7=O)S6)S5)S4)SC2=C3C2=C(F)C(F)=C(CC(CC)CCCC)S2)=C1,SM-EH-R ,,,0.85,25.42,72.4,15.6," J. Ge, Z. Chen, Q. Ye, L. Xie, W. Song, Y. Guo, J. Zhang, X. Tong, J. Zhang, E. Zhou, Z. Wei, Z. Ge, Modulation of Molecular Stacking via Tuning 2-Ethylhexyl Alkyl Chain Enables Improved Efficiency for All-Small-Molecule Organic Solar Cells, ACS Appl. Mater. Interfaces 15 (2023) 10803¨C10811. https://doi.org/10.1021/acsami.3c00167."
3147,CCCCCCC1=C(C2=CC(CCCCCC)=C(C3=CC=C(/C=C4\SC(=S)N(CCCCCC)C4=O)S3)S2)SC(C2=CC3=C(C4=C(F)C(F)=C(CC(CC)CCCC)S4)C4=C(C=C(C5=CC(CCCCCC)=C(C6=CC(CCCCCC)=C(C7=CCC(/C=C8\SC(=S)N(CCCCCC)C8=O)S7)S6)S5)S4)C(C4=C(F)C(F)=C(CC(CC)CCCC)S4)=C3S2)=C1,SM-R ,,,0.85,23.73,71.3,14.4," J. Ge, Z. Chen, Q. Ye, L. Xie, W. Song, Y. Guo, J. Zhang, X. Tong, J. Zhang, E. Zhou, Z. Wei, Z. Ge, Modulation of Molecular Stacking via Tuning 2-Ethylhexyl Alkyl Chain Enables Improved Efficiency for All-Small-Molecule Organic Solar Cells, ACS Appl. Mater. Interfaces 15 (2023) 10803¨C10811. https://doi.org/10.1021/acsami.3c00167."
3148,CCCCCCC1=C(C2=CC(CC(CC)CCCC)=C(C3=CC=C(/C=C4\SC(=S)N(CCCCCC)C4=O)S3)S2)SC(C2=CC3=C(S2)C(C2=C(F)C(F)=C(CC(CC)CCCC)S2)=C2C=C(C4=CC(CCCCCC)=C(C5=CC(CC(CC)CCCC)=C(C6=CC=C(/C=C7\SC(=S)N(CCCCCC)C7=O)S6)S5)S4)SC2=C3C2=C(F)C(F)=C(CC(CC)CCCC)S2)=C1,SM-EH-R ,,,0.86,24.64,66.2,14," J. Ge, Z. Chen, Q. Ye, L. Xie, W. Song, Y. Guo, J. Zhang, X. Tong, J. Zhang, E. Zhou, Z. Wei, Z. Ge, Modulation of Molecular Stacking via Tuning 2-Ethylhexyl Alkyl Chain Enables Improved Efficiency for All-Small-Molecule Organic Solar Cells, ACS Appl. Mater. Interfaces 15 (2023) 10803¨C10811. https://doi.org/10.1021/acsami.3c00167."
3149,CCCCC(CC)CC1=CC=C(C2=C3C=C(/C=C4\SC(=S)N(CC)C4=O)SC3=C(C3=CC=C(CC(CC)CCCC)[Se]3)C3=C2SC(C2=C(C4=CC=C(CC(CC)CCCC)[Se]4)C4=C(C2)C(C2=CC=C(CC(CC)CCCC)[Se]2)=C(C2=CC5=C(S2)C(C2=CC=C(CC(CC)CCCC)[Se]2)=C2C=C(/C=C6\SC(=S)N(CC)C6=O)SC2=C5C2=CC=C(CC(CC)CCCC)[Se]2)S4)=C3)[Se]1,DRTT-6Se,,,0.85,21.96,63.4,11.9," J. Ge, Z. Chen, Q. Ye, L. Xie, W. Song, Y. Guo, J. Zhang, X. Tong, J. Zhang, E. Zhou, Z. Wei, Z. Ge, Modulation of Molecular Stacking via Tuning 2-Ethylhexyl Alkyl Chain Enables Improved Efficiency for All-Small-Molecule Organic Solar Cells, ACS Appl. Mater. Interfaces 15 (2023) 10803¨C10811. https://doi.org/10.1021/acsami.3c00167."
3150,CCCCC(CC)CC1=CC=C(C2=C3C=C(/C=C4\SC(=S)N(CC)C4=O)SC3=C(C3=CC=C(CC(CC)CCCC)S3)C3=C2SC(C2=C(C4=CC=C(CC(CC)CCCC)[Se]4)C4=C(C2)C(C2=CC=C(CC(CC)CCCC)[Se]2)=C(C2=CC5=C(S2)C(C2=CC=C(CC(CC)CCCC)S2)=C2C=C(/C=C6\SC(=S)N(CC)C6=O)SC2=C5C2=CC=C(CC(CC)CCCC)S2)S4)=C3)S1,DRTT-2Se,,,0.85,25.29,69.9,15.03," X. Cheng, Z. Liang, S. Liang, X. Zhang, J. Xu, Y. Xu, W. Ni, M. Li, Y. Geng, ¡°Twisted¡± small molecule donors with enhanced intermolecular interactions in the condensed phase towards efficient and thick-film all-small-molecule organic solar cells, J. Mater. Chem. A 11 (2023) 13984¨C13993. https://doi.org/10.1039/D3TA01893H."
3151,CCCCC(CC)CC1=CC=C(C2=C3C=C(/C=C4\SC(=S)N(CC)C4=O)SC3=C(C3=CC=C(CC(CC)CCCC)S3)C3=C2SC(C2=C(C4=CC=C(CC(CC)CCCC)S4)C4=C(C2)C(C2=CC=C(CC(CC)CCCC)S2)=C(C2=CC5=C(S2)C(C2=CC=C(CC(CC)CCCC)S2)=C2C=C(/C=C6\SC(=S)N(CC)C6=O)SC2=C5C2=CC=C(CC(CC)CCCC)S2)S4)=C3)S1,DRTT-T,,,0.85,25.18,68.8,14.79," X. Cheng, Z. Liang, S. Liang, X. Zhang, J. Xu, Y. Xu, W. Ni, M. Li, Y. Geng, ¡°Twisted¡± small molecule donors with enhanced intermolecular interactions in the condensed phase towards efficient and thick-film all-small-molecule organic solar cells, J. Mater. Chem. A 11 (2023) 13984¨C13993. https://doi.org/10.1039/D3TA01893H."
3152,CCCCCCC1=C(C2=CC(CCCCCC)=C(C3=CC=C(/C=C4\SC(=S)N(CCCCCC)C4=O)S3)S2)SC(C2=CC3=C(S2)C(C2=CC=C(SCC(CC)CCCC)C(F)=C2)=C2C=C(C4=CC(CCCCCC)=C(C5=CC(CCCCCC)=C(C6=CC=C(/C=C7\SC(=S)N(CCCCCC)C7=O)S6)S5)S4)SC2=C3C2=CC=C(CCCCCCC3CCCC3)S2)=C1,As-TCp,,,0.85,24.85,62.9,13.37," X. Cheng, Z. Liang, S. Liang, X. Zhang, J. Xu, Y. Xu, W. Ni, M. Li, Y. Geng, ¡°Twisted¡± small molecule donors with enhanced intermolecular interactions in the condensed phase towards efficient and thick-film all-small-molecule organic solar cells, J. Mater. Chem. A 11 (2023) 13984¨C13993. https://doi.org/10.1039/D3TA01893H."
3153,CCCCCCC1=C(C2=CC(CCCCCC)=C(C3=CC=C(/C=C4\SC(=S)N(CCCCCC)C4=O)S3)S2)SC(C2=CC3=C(S2)C(C2=CC(Cl)=C(CCCCCCC4CCCC4)S2)=C2C=C(C4=CC(CCCCCC)=C(C5=CC(CCCCCC)=C(C6=CC=C(/C=C7\SC(=S)N(CCCCCC)C7=O)S6)S5)S4)SC2=C3C2=CC(Cl)=C(CCCCCCC3CCCC3)S2)=C1,S-TCp,,,0.873,24.45,74.9,16.46," X. Wang, Z. Li, X. Zheng, C. Xiao, T. Hu, Y. Liao, R. Yang, High-Efficiency All-Small-Molecule Organic Solar Cells Based on New Molecule Donors with Conjugated Symmetric/Asymmetric Hybrid Cyclopentyl-Hexyl Side Chains, Advanced Functional Materials 33 (2023) 2300323. https://doi.org/10.1002/adfm.202300323."
3154,CCCCCCC1=C(C2=CC(CCCCCC)=C(C3=CC=C(/C=C4\SC(=S)N(CCCCCC)C4=O)S3)S2)SC(C2=CC3=C(S2)C(C2=CC=C(SCC(CC)CCCC)C(F)=C2)=C2C=C(C4=CC(CCCCCC)=C(C5=CC(CCCCCC)=C(C6=CC=C(/C=C7\SC(=S)N(CCCCCC)C7=O)S6)S5)S4)SC2=C3C2=CC=C(SCC(CC)CCCC)C(F)=C2)=C1,S-BF,,,0.87,23.88,73.83,15.77?," X. Wang, Z. Li, X. Zheng, C. Xiao, T. Hu, Y. Liao, R. Yang, High-Efficiency All-Small-Molecule Organic Solar Cells Based on New Molecule Donors with Conjugated Symmetric/Asymmetric Hybrid Cyclopentyl-Hexyl Side Chains, Advanced Functional Materials 33 (2023) 2300323. https://doi.org/10.1002/adfm.202300323."
3155,CCCCCCC1=C(C2=CC(CCCCCC)=C(C3=CC=C(/C=C4\SC(=S)N(CCC)C4=O)S3)S2)SC(C2=CC3=C(S2)C(C2=CC=C(SCC(CC)CCCC)C=C2)=C2C=C(C4=CC(CCCCCC)=C(C5=CC(CCCCCC)=C(C6=CC=C(/C=C7\SC(=S)N(C(C)CC)C7=O)S6)S5)S4)SC2=C3C2=CC=C(SCC(CC)CCCC)C=C2)=C1,SM-s-Bu,,,0.868,22.91,69.39,14.92?," X. Wang, Z. Li, X. Zheng, C. Xiao, T. Hu, Y. Liao, R. Yang, High-Efficiency All-Small-Molecule Organic Solar Cells Based on New Molecule Donors with Conjugated Symmetric/Asymmetric Hybrid Cyclopentyl-Hexyl Side Chains, Advanced Functional Materials 33 (2023) 2300323. https://doi.org/10.1002/adfm.202300323."
3156,CCCCCCC1=C(C2=CC(CCCCCC)=C(C3=CC=C(/C=C4\SC(=S)N(CCCC)C4=O)S3)S2)SC(C2=CC3=C(S2)C(C2=CC=C(SCC(CC)CCCC)C=C2)=C2C=C(C4=CC(CCCCCC)=C(C5=CC(CCCCCC)=C(C6=CC=C(/C=C7\SC(=S)N(CCCC)C7=O)S6)S5)S4)SC2=C3C2=CC=C(SCC(CC)CCCC)C=C2)=C1,SM-n-Bu,,,0.841,25.18,74.34,16.06," H.-F. Zhi, M. Jiang, H. Zhang, Q. An, H.-R. Bai, M.H. Jee, H.Y. Woo, D. Li, X. Huang, J.-L. Wang, Isomeric Small Molecule Donor with Terminal Branching Position Directly Attached to the Backbone Enables Efficient All-Small-Molecule Organic Solar Cells with Excellent Stability, Advanced Functional Materials 33 (2023) 2300878. https://doi.org/10.1002/adfm.202300878."
3157,CCCCCCCCC1=C(C2=CC=C(C3=C(CCCCCCCC)C=C(C4=CC5=C(S4)C(C4=CC(Cl)=C(CC(CC)CCCC)S4)=C4C=C(C6=CC(CCCCCCCC)=C(C7=CC=C(C8=C(CCCCCCCC)C=C(/C=C9\SC(=S)N(CC(CC)CCCC)C9=O)S8)S7)S6)SC4=C5C4=CC(Cl)=C(CC(CC)CCCC)S4)S3)S2)SC(/C=C2\SC(=S)N(CC(CC)CCCC)C2=O)=C1,BTEHR-CT,,,0.83,24.75,72.12,15.12," H.-F. Zhi, M. Jiang, H. Zhang, Q. An, H.-R. Bai, M.H. Jee, H.Y. Woo, D. Li, X. Huang, J.-L. Wang, Isomeric Small Molecule Donor with Terminal Branching Position Directly Attached to the Backbone Enables Efficient All-Small-Molecule Organic Solar Cells with Excellent Stability, Advanced Functional Materials 33 (2023) 2300878. https://doi.org/10.1002/adfm.202300878."
3158,CCCCCCCCC1=C(C2=CC=C(C3=C(CCCCCCCC)C=C(C4=CC5=C(S4)C(OCC(CCCCCC)CCCCCCCC)=C4C=C(C6=CC(CCCCCCCC)=C(C7=CC=C(C8=C(CCCCCCCC)C=C(/C=C9\SC(=S)N(CC(CC)CCCC)C9=O)S8)S7)S6)SC4=C5C4=CC=C(SCC(CC)CCCC)S4)S3)S2)SC(/C=C2\SC(=S)N(CC(CC)CCCC)C2=O)=C1,a-BTR-H4,,,0.946,17.05,0.69,11.13," C. Liu, L. Liu, N. Qiu, X. Wan, C. Li, Y. Lu, A novel chlorinated small molecule donor for efficient binary and ternary all-small-molecule organic solar cells, Organic Electronics 106 (2022) 106532. https://doi.org/10.1016/j.orgel.2022.106532."
3159,CCCCCCC1=C(C2=CC(CCCCCC)=C(C3=CC=C(/C=C4/SC(=S)N(CC(CC)CCCC)C4=O)S3)S2)SC(C2=CC3=C(S2)C(C2=CN=C(SCC(CC)CCCC)S2)=C2C=C(C4=CC(CCCCCC)=C(C5=CC(CCCCCC)=C(C6=CC=C(/C=C7/SC(=S)N(CC(CC)CCCC)C7=O)S6)S5)S4)SC2=C3C2=CN=C(SCC(CC)CCCC)S2)=C1,SW2,,,0.815,24.8,53.5,11.36," Y. Zhao, Z. Huang, X. Kang, J. Yu, M. Ding, D. Liu, G. Lu, X. Bao, L. Yu, M. Sun, End Group Effect of Asymmetric Benzodithiophene-Based Donor with Liquid-Crystal State for Small-Molecule Binary Solar Cell, Small 19 (2023) 2205244. https://doi.org/10.1002/smll.202205244."
3160,CCCCCCC1=C(C2=CC(CCCCCC)=C(C3=CC=C(/C=C4/SC(=S)N(CC(C)CC)C4=O)S3)S2)SC(C2=CC3=C(S2)C(C2=CC=C(SCC(CC)CCCC)S2)=C2C=C(C4=CC(CCCCCC)=C(C5=CC(CCCCCC)=C(C6=CC=C(/C=C7/SC(=S)N(CC(CC)CCCC)C7=O)S6)S5)S4)SC2=C3C2=CC=C(SCC(CC)CCCC)S2)=C1,SW1,,,0.835,74,25.1,15.51," S. Wu, W. Feng, L. Meng, Z. Zhang, X. Si, Y. Chen, X. Wan, C. Li, Z. Yao, Y. Chen, 15.51 % efficiency all-small-molecule organic solar cells achieved by symmetric thiazolyl substitution, Nano Energy 103 (2022) 107801. https://doi.org/10.1016/j.nanoen.2022.107801."
3161,CCCCOC(=O)/C(C#N)=C/C1=CC2=C(S1)C(C1=CC=C(CC(CC)CCCC)S1)=C1C=C(C3=CC4=C(S3)C(C3=CC=C(CC(CC)CCCC)S3)=C3C=C(C5=CC6=C(S5)C(C5=CC=C(CC(CC)CCCC)S5)=C5C=C(/C=C(\C#N)C(=O)OCCCC)SC5=C6C5=CC=C(CC(CC)CCCC)S5)SC3=C4C3=CC=C(CC(CC)CCCC)S3)SC1=C2C1=CC=C(CC(CC)CCCC)S1,TBCA-C4,,,0.806,63.8,25.09,12.9," S. Wu, W. Feng, L. Meng, Z. Zhang, X. Si, Y. Chen, X. Wan, C. Li, Z. Yao, Y. Chen, 15.51 % efficiency all-small-molecule organic solar cells achieved by symmetric thiazolyl substitution, Nano Energy 103 (2022) 107801. https://doi.org/10.1016/j.nanoen.2022.107801."
3162,CCCCCCCCCCC1=CC=C(C2(C3=CC=C(CCCCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(S3)C3=C(C=C(/C=C5C(=O)C6=C(C=C(F)C(F)=C6)C5=C(C#N)C#N)S3)S2)C(C2=CC=C(CCCCCCCCCC)C=C2)(C2=CC=C(CCCCCCCCCC)C=C2)C2=C4SC3=C2SC2=C3SC(/C=C3C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)=C2)C=C1,2F-C10,,,19.92,0.804,0.6482,9.96,"F. Zhao, D. He, J. Xin, S. Dai, H. Xue, L. Jiang, Z. Wei, W. Ma, X. Zhan, Y. Li, C. Wang, Modulating morphology via side-chain engineering of fused ring electron acceptors for high performance organic solar cells, Sci. China Chem. 62 (2019) 790¨C796. https://doi.org/10.1007/s11426-019-9453-7."
3163,CCCCCCCCC(C)N1C2=C(SC(/C=C3C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)=C2)C2=C1C1=C(S2)C2=C(SC3=C2N(C(CCCCCCCC)CCCCCCCC)C2=C3SC(/C=C3C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)=C2)C2=C1SC1=C2N(C(CCCCCCCC)CCCCCCCC)C2=C1SC(/C=C1C(=O)C3=C(C=C(F)C(F)=C3)C1=C(C#N)C#N)=C2,BTDTP-C8C9-6F,-5.68,-4.01,14.9,0.89,0.7498,9.95,"W. Wang, R. An, T. Wang, H. Li, J. Zhang, H. Tian, X. Wu, H. Tong, L. Wang, Nitrogen-Bridged Star-Shaped Fused-Ring Electron Acceptors for Organic Solar Cells, Giant. (2022) 100093. https://doi.org/10.1016/j.giant.2022.100093."
3164,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(C=C(/C=C5C(=O)C6=C(C=CC=C6)C5=C(C#N)C#N)S2)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC3=C2SC(/C=C2C(=O)C4=C(C=C(F)C(F)=C4)C2=C(C#N)C#N)=C3)C=C1,ITIC-4F,-5.74,-4.15,17.6,0.83,0.677,9.91,"T.J. Aldrich, M. Matta, W. Zhu, S.M. Swick, C.L. Stern, G.C. Schatz, A. Facchetti, F.S. Melkonyan, T.J. Marks, Fluorination Effects on Indacenodithienothiophene Acceptor Packing and Electronic Structure, End-Group Redistribution, and Solar Cell Photovoltaic Response, J. Am. Chem. Soc. 141 (2019) 3274¨C3287. https://doi.org/10.1021/jacs.8b13653."
3165,CCCCCCC1(CCCCCC)C2=CC3=C(C=C2C2=C1C=C(/C=C1C(=O)C4=CC=CC=C4C1=C(C#N)C#N)S2)C(CCCCCC)(CCCCCC)C1=C3C=C2C(=C1)C1=C(C=C(/C=C3C(=O)C4=C(C=CC=C4)C3=C(C#N)C#N)S1)C2(CCCCCC)CCCCCC,FTIC-C6C6,-5.6,-3.81,16.03,0.91,0.6317,9.91,"Z. Zhang, M. Li, Y. Liu, J. Zhang, S. Feng, X. Xu, J. Song, Z. Bo, Simultaneous enhancement of the molecular planarity and the solubility of non-fullerene acceptors: effect of aliphatic side-chain substitution on the photovoltaic performance, J. Mater. Chem. A. 5 (2017) 7776¨C7783. https://doi.org/10.1039/C7TA02141K."
3166,O=C(C(C=C(Cl)C(Cl)=C1)=C1C/2=C(C#N)/C#N)C2=C/C3=CC(C4(CCCCCCCC)CCCCCCCC)=C(S3)C5=C4C=C(C(C=C(C(CCCCCCCC)(CCCCCCCC)C6=C7SC(/C=C8C(C(C=C(Cl)C(Cl)=C9)=C9C8=C(C#N)C#N)=O)=C6)C7=C%10)=C%10C%11(CCCCCCCC)CCCCCCCC)C%11=C5,F-2CL,-5.5,-3.86,15.97,0.906,0.684,9.89,"Y. Wang, Y. Wang, B. Kan, X. Ke, X. Wan, C. Li, Y. Chen, High-Performance All-Small-Molecule Solar Cells Based on a New Type of Small Molecule Acceptors with Chlorinated End Groups, Adv. Energy Mater. 8 (2018) 1802021. https://doi.org/10.1002/aenm.201802021."
3167,CCCCC(CC)CC1(CC(CC)CCCC)C2=C(SC(/C=C3C(=O)C4=CC(F)=C(F)C=C4C3=C(C#N)C#N)=C2)C2=C1C=C(C1=CC=C(C3=CC4C(S3)C3=C(C=C(/C=C5C(=O)C6=CC(F)=C(F)C=C6C5=C(C#N)C#N)S3)C4(CC(CC)CCCC)CC(CC)CCCC)N=N1)S2,NOCIC,,,16.22,0.907,0.67,9.89,"J. Gao, Y. Li, S. Li, X. Xia, X. Lu, M. Shi, H. Chen, Non-fullerene acceptors with nitrogen-containing six-membered heterocycle cores for the applications in organic solar cells, Sol. Energy Mater. Sol. Cells. 225 (2021) 111046. https://doi.org/10.1016/j.solmat.2021.111046."
3168,CCCCCC1=CC=C(C2(C3=CC=C(CCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(S3)C3=C(C=C(/C=C5C(=O)C6=C(C=C(F)C(F)=C6)C5=C(C#N)C#N)S3)S2)C(C2=CC=C(CCCCC)C=C2)(C2=CC=C(CCCCC)C=C2)C2=C4SC3=C2SC2=C3SC(/C=C3C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)=C2)C=C1,2F-C5,,,19.63,0.77,0.673,9.87,"F. Zhao, D. He, J. Xin, S. Dai, H. Xue, L. Jiang, Z. Wei, W. Ma, X. Zhan, Y. Li, C. Wang, Modulating morphology via side-chain engineering of fused ring electron acceptors for high performance organic solar cells, Sci. China Chem. 62 (2019) 790¨C796. https://doi.org/10.1007/s11426-019-9453-7."
3169,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(C=C(/C=C5C(=O)C6=CC=CC=C6C5=C(C#N)C#N)S2)S3)N(CC(CC)CCCC)C2=CC3=C(C=C24)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C3SC3=C2SC(/C=C2C(=O)C4=CC=CC=C4C2=C(C#N)C#N)=C3)C=C1,CZTT-IC ,-5.54,-3.97,17.26,0.97,0.5897,9.87,"H. Wang, Z. Zhang, J. Yu, X. Liu, S. Qu, S. Guang, W. Tang, Nonacyclic carbazole-based non-fullerene acceptors enable over 12% efficiency with enhanced stability for organic solar cells, J. Mater. Chem. A. 7 (2019) 21903¨C21910. https://doi.org/10.1039/C9TA08573D."
3170,CCCCC(CC)CC1(CC(CC)CCCC)C2=C(SC(/C=C3C(=O)C4=C(C=CC(F)=C4)C3=C(C#N)C#N)=C2)C2=C1C=C(C1=C(F)C(F)=C(C3=CC4=C(S3)C3=C(C=C(/C=C5C(=O)C6=C(C=C(F)C(F)=C6)C5=C(C#N)C#N)S3)C4(CC(CC)CCCC)CC(CC)CCCC)S1)S2,HF-TCIC,-5.43,-3.83,20.04,0.76,0.65,9.86,"R. Qin, W. Yang, S. Li, T.-K. Lau, Z. Yu, Z. Liu, M. Shi, X. Lu, C.-Z. Li, H. Chen, Enhanced intramolecular charge transfer of unfused electron acceptors for efficient organic solar cells, Mater. Chem. Front. 3 (2019) 513¨C519. https://doi.org/10.1039/C8QM00609A."
3171,CCCCCCCCC(CCCCCCCC)N1C2=CC(C3=CC=C(/C=C4C(=O)C5=CC(Br)=CC=C5C4=C(C#N)C#N)S3)=CC=C2C2=CC=C(C3=CC=C(/C=C4C(=O)C5=CC(Br)=CC=C5C4=C(C#N)C#N)S3)C=C21,C8IDT-Br,-5.73,-3.86,15.66,0.97,0.6481,9.85,"L. Zhang, S. Tu, W. Wang, Q. Ling, Brominated Small-Molecule Acceptors with a Simple Non-fused Framework for Efficient Organic Solar Cells, ACS Appl. Energy Mater. 4 (2021) 4805¨C4814. https://doi.org/10.1021/acsaem.1c00369."
3172,CCCCC(CC)CC1(CC(CC)CCCC)C2=C(SC(/C=C3C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)=C2)C2=C1C=C(C1=CC=C(C3=CC4=C(S3)C3=C(C=C(/C=C5C(=O)C6=C(C=C(F)C(F)=C6)C5=C(C#N)C#N)S3)C4(CC(CC)CCCC)CC(CC)CCCC)C3=NSN=C13)S2,BT-IC4F,-5.89,-4.27,21.4,0.69,0.664,9.83,"Y. Wang, Z. Liu, X. Cui, C. Wang, H. Lu, Y. Liu, Z. Fei, Z. Ma, Z. Bo, Small molecule acceptors with a ladder-like core for high-performance organic solar cells with low non-radiative energy losses, J. Mater. Chem. A. 8 (2020) 12495¨C12501. https://doi.org/10.1039/D0TA03683H."
3173,CCCCCCOC1=C(C2=CC3=C(S2)C2=C(C=C(/C=C4C(=O)C5=C(C=C(F)C(F)=C5)C4=C(C#N)C#N)S2)C3(CC(CC)CCCC)CC(CC)CCCC)SC(C2=CC3=C(S2)C2=C(C=C(/C=C4C(=O)C5=C(C=C(F)C(F)=C5)C4=C(C#N)C#N)S2)C3(CC(CC)CCCC)CC(CC)CCCC)=C1OCCCCCC,C6OT-4F,-5.36,-4.03,21.5,0.761,0.6001,9.83,"D. Luo, Y. Zhang, L. Li, C. Shan, Q. Liu, Z. Wang, W.C.H. Choy, A.K.K. Kyaw, Near-infrared non-fused ring acceptors with light absorption up to 1000?nm for efficient and low-energy loss organic solar cells, Mater. Today Energy. 24 (2022) 100938. https://doi.org/10.1016/j.mtener.2021.100938."
3174,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C=C(C2=C5C(F)=C(C(=O)OCC(CC)CCCC)SC5=C(/C=C5C(=O)C6=C(C=CC=C6)C5=C(C#N)C#N)S2)O3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC(C3=C4C(F)=C(C(=O)OCC(CC)CCCC)SC4=C(/C=C4C(=O)C5=C(C=CC=C5)C4=C(C#N)C#N)S3)=C2)C=C1,T1,-5.42,-3.91,20.95,0.72,0.65,9.82,"F.-X. Chen, J.-Q. Xu, Z.-X. Liu, M. Chen, R. Xia, Y. Yang, T.-K. Lau, Y. Zhang, X. Lu, H.-L. Yip, A.K.-Y. Jen, H. Chen, C.-Z. Li, Near-Infrared Electron Acceptors with Fluorinated Regioisomeric Backbone for Highly Efficient Polymer Solar Cells, Adv. Mater. 30 (2018) 1803769. https://doi.org/10.1002/adma.201803769."
3175,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=C(SC(/C=C4C(=O)C5=C(C=CC(C)=C5)C4=C(C#N)C#N)=C3)C3=C2C2=C(S3)C(C3=CC4=C(C=C(CC(CC)CCCC)S4)S3)=C3C(=C2C2=CC4=C(C=C(CC(CC)CCCC)S4)S2)SC2=C3C(C3=CC=C(CCCCCC)C=C3)(C3=CC=CC(CCCCCC)=C3)C3=C2SC(/C=C2C(=O)C4=C(C=CC(C)=C4)C2=C(C#N)C#N)=C3)C=C1,BTT-MIC,-5.55,-3.76,15.9,1.027,0.6151,9.82,"Y. Jia, Y. Zhang, W. Jiang, B. Su, C. Liu, E. Zhu, G. Che, A fused-ring non-fullerene acceptor based on a benzo[1,2-b:4,5-b¡ä]dithiophene central core with a thieno[3,2-b]thiophene side-chain for highly efficient organic solar cells, J. Mater. Chem. A. 7 (2019) 10905¨C10911. https://doi.org/10.1039/C9TA01888C."
3176,C#CC(CCCC)CN1C(=O)C2=C(C3=CC4=C(S3)C3=C(C=C(/C=C5C(=O)C6=C(C=C7C=CC=CC7=C6)C5=C(C#N)C#N)S3)C4(CC(CC)CCCC)CC(CC)CCCC)SC(C3=CC4=C(S3)C3=C(C=C(/C=C5C(=O)C6=C(C=C7C=CC=CC7=C6)C5=C(C#N)C#N)S3)C4(CC(CC)CCCC)CC(CC)CCCC)=C2C1=O,TPDCNC ,-5.37,-3.83,17.4,0.8,0.704,9.8,"S.-Z. Geng, W.-T. Yang, J. Gao, S.-X. Li, M.-M. Shi, T.-K. Lau, X.-H. Lu, C.-Z. Li, H.-Z. Chen, Non-fullerene Acceptors with a Thieno[3,4-c]pyrrole-4,6-dione (TPD) Core for Efficient Organic Solar Cells, Chin. J. Polym. Sci. 37 (2019) 1005¨C1014. https://doi.org/10.1007/s10118-019-2309-x."
3177,O=C1N(CCCCCC)/C(S/C1=C/C2=CC=C(C3=CC4=C(C=C3)N(CC(CC)CCCC)C5=C4C=C(N(CC(CC)CCCC)C6=C7C=C(C8=CC=C(/C=C9S/C(N(CCCCCC)C/9=O)=C(C#N)C#N)C%10=NSN=C8%10)C=C6)C7=C5)C%11=NSN=C2%11)=C(C#N)/C#N,ICz-RdCN2,-5.58,-3.98,15.58,1.01,0.62,9.76,"Suman, A. Siddiqui, M.L. Keshtov, G.D. Sharma, S.P. Singh, New indolo carbazole-based non-fullerene n-type semiconductors for organic solar cell applications, J. Mater. Chem. C. 7 (2019) 543¨C552. https://doi.org/10.1039/C8TC05318A."
3178,O=C(C(C=CC=C1)=C1C/2=C(C#N)C#N)C2=C/C(S3)=CC4=C3C5=C(C4(C6=CC=C(CCCCCC)C=C6)C7=CC=C(CCCCCC)C=C7)C8=CC9=C(C(C(C%10=CC=C(CCCCCC)C=C%10)(C%11=CC=C(CCCCCC)C=C%11)C%12=C%13SC(/C=C%14C(C(C=CC=C%15)=C%15C\%14=C(C#N)/C#N)=O)=C%12)=C%13S9)C=C8S5,BDCPDT-IC,-5.41,-3.87,16.84,0.84,0.69,9.73,"S.-L. Chang, F.-Y. Cao, W.-C. Huang, P.-K. Huang, C.-S. Hsu, Y.-J. Cheng, Highly Efficient Inverted D:A1:A2 Ternary Blend Organic Photovoltaics Combining a Ladder-type Non-Fullerene Acceptor and a Fullerene Acceptor, ACS Appl. Mater. Interfaces. 9 (2017) 24797¨C24803. https://doi.org/10.1021/acsami.7b06650."
3179,CCCCCCCCCCC(CCCCCCCC)CC1=C(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)SC(C2=CC(C(C)C)=C3C=CC4=C(C5=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(/C=C6C(=O)C7=C(C=C(F)C(F)=C7)C6=C(C#N)C#N)S5)C=C(C(C)C)C5=C4C3=C2C=C5)=C1,Py-2F,-5.58,-3.62,15.44,0.92,0.6822,9.73,"H. Li, J. Chen, L. Yi, J. Cao, M. Xiao, W. Zhuang, J. Li, R. Xia, J. Yu, Z. Tang, Easily synthesized pyrene-based nonfullerene acceptors for efficient organic solar cells, Synth. Met. 281 (2021) 116904. https://doi.org/10.1016/j.synthmet.2021.116904."
3180,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(C=C(/C=C/C=C5/C(=O)C6=C(C=CC=C6)C5=C(C#N)C#N)S2)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC3=C2SC(/C=C/C=C2/C(=O)C4=C(C=CC(F)=C4)C2=C(C#N)C#N)=C3)C=C1,lTVflC,-5.56,-4.01,19.73,0.84,0.5867,9.72,"X. Li, H. Huang, H. Bin, Z. Peng, C. Zhu, L. Xue, Z.-G. Zhang, Z. Zhang, H. Ade, Y. Li, Synthesis and Photovoltaic Properties of a Series of Narrow Bandgap Organic Semiconductor Acceptors with Their Absorption Edge Reaching 900 nm, Chem. Mater. 29 (2017) 10130¨C10138. https://doi.org/10.1021/acs.chemmater.7b03928."
3181,CCCCCCCCC1(CCCCCCCC)C2=CC(C3=CC=C(/C=C4C(=O)C5=CC(Br)=CC=C5C4=C(C#N)C#N)S3)=CC=C2C2=CC=C(C3=CC=C(/C=C4C(=O)C5=CC(Br)=CC=C5C4=C(C#N)C#N)S3)C=C21,F8IDT-Br,-5.82,-3.87,14.6,0.98,0.6776,9.7,"L. Zhang, S. Tu, W. Wang, Q. Ling, Brominated Small-Molecule Acceptors with a Simple Non-fused Framework for Efficient Organic Solar Cells, ACS Appl. Energy Mater. 4 (2021) 4805¨C4814. https://doi.org/10.1021/acsaem.1c00369."
3182,CCCCCCOC1=CC=C(C2(C3=CC=C(OCCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(C=C(/C=C5/C(=O)C6=C(C=CC=C6)C5=C(C#N)C#N)S2)S3)C(C2=CC=C(OCCCCCC)C=C2)(C2=CC=C(OCCCCCC)C=C2)C2=C4SC3=C2SC(/C=C2/C(=O)C4=C(C=CC=C4)C2=C(C#N)C#N)=C3)C=C1,POIT-IC,-5.57,-3.92,16.1,1.04,0.601,9.7,"Q. Fan, W. Su, M. Zhang, J. Wu, Y. Jiang, X. Guo, F. Liu, T.P. Russell, M. Zhang, Y. Li, Synergistic Effects of Side-Chain Engineering and Fluorination on Small Molecule Acceptors to Simultaneously Broaden Spectral Response and Minimize Voltage Loss for 13.8% Efficiency Organic Solar Cells, Sol. RRL. 3 (2019) 1900169. https://doi.org/10.1002/solr.201900169."
3183,CCCCCCCCOC1=CC=CC(OCCCCCCCC)=C1C1=C(C2=CC=C(/C=C3/C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)S2)SC(C2=CC(OCC(CC)CCCC)=C(C3=CC(C4=C(OCCCCCCCC)C=CC=C4OCCCCCCCC)=C(C4=CC=C(/C=C5/C(=O)C6=CC(F)=C(F)C=C6C5=C(C#N)C#N)S4)S3)C=C2OCC(CC)CCCC)=C1,PhO4T-1,-5.53,-3.94,20.71,0.859,0.5446,9.69,"C. Li, X. Zhang, N. Yu, X. Gu, L. Qin, Y. Wei, X. Liu, J. Zhang, Z. Wei, Z. Tang, Q. Shi, H. Huang, Simple Nonfused-Ring Electron Acceptors with Noncovalently Conformational Locks for Low-Cost and High-Performance Organic Solar Cells Enabled by End-Group Engineering, Adv. Funct. Mater. 32 (2022) 2108861. https://doi.org/10.1002/adfm.202108861."
3184,CCCCCCCCC1(C)C2=C(C=C3C(=C2)C2=C(C=C(/C=C4C(=O)C5=C(C=CC(C)=C5)C4=C(C#N)C#N)S2)C3(CCCCCCCC)CCCCCCCC)C2=C1C=C(/C=C1C(=O)C3=C(C=C(C)C=C3)C1=C(C#N)C#N)S2,IDT-2O,-5.73,-3.85,15.64,0.86,0.723,9.68,"S. Feng, C. Zhang, Y. Liu, Z. Bi, Z. Zhang, X. Xu, W. Ma, Z. Bo, Fused-Ring Acceptors with Asymmetric Side Chains for High-Performance Thick-Film Organic Solar Cells, Adv. Mater. 29 (2017) 1703527. https://doi.org/10.1002/adma.201703527."
3185,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=C([Se]C(/C=C4C(=O)C5=C(C=CC=C5)C4=C(C#N)C#N)=C3)C3=C2C2=C(S3)C3=C(S2)C2=C(C=C(/C=C4C(=O)C5=C(C=CC=C5)C4=C(C#N)C#N)[Se]2)C3(C2=CC=C(CCCCCC)C=C2)C2=CC=C(CCCCCC)C=C2)C=C1,STIC,-5.2,-3.91,19.96,0.77,0.63,9.68,"X. Liao, X. Shi, M. Zhang, K. Gao, L. Zuo, F. Liu, Y. Chen, A.K.-Y. Jen, Fused selenophene-thieno[3,2-b]thiophene¨Cselenophene (ST)-based narrow-bandgap electron acceptor for efficient organic solar cells with small voltage loss, Chem. Commun. 55 (2019) 8258¨C8261. https://doi.org/10.1039/C9CC03585K."
3186,CCCCCCCCC1(CCCCCCCC)C2=CC3=C(C=C2C2=C1C=C(/C=C1C(=O)C4=C(C=CC(C)=C4)C1=C(C#N)C#N)S2)C(CCCCCCCC)(CCCCCCCC)C1=C3SC(/C=C2C(=O)C3=C(C=C(C)C=C3)C2=C(C#N)C#N)=C1,IDT-2O,-5.72,-3.85,15.7,0.86,0.716,9.65,"C. Zhang, S. Feng, Y. Liu, S. Ming, H. Lu, D. Ma, X. Xu, Y. Wu, Z. Bo, High efficiency ternary polymer solar cells based on a fused pentacyclic electron acceptor, J. Mater. Chem. A. 6 (2018) 6854¨C6859. https://doi.org/10.1039/C8TA00944A."
3187,CCCCC(CC)CCC1(CC(CC)CCCC)C2=C(SC(/C=C3C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)=C2)C2=C1C=C(C1=C(OCC(CC)CCCC)C(OCC(CC)CCCC)=C(C3=CC4=C(S3)C3=C(C=C(/C=C5C(=O)C6=C(C=C(F)C(F)=C6)C5=C(C#N)C#N)S3)C4(CC(CC)CCCC)CC(CC)CCCC)C3=NSN=C31)S2,BCDT-4F,-5.46,-3.86,18.28,0.8,0.66,9.65,"C. He, Y. Li, S. Li, Z.-P. Yu, Y. Li, X. Lu, M. Shi, C.-Z. Li, H. Chen, Near-Infrared Electron Acceptors with Unfused Architecture for Efficient Organic Solar Cells, ACS Appl. Mater. Interfaces. 12 (2020) 16700¨C16706. https://doi.org/10.1021/acsami.0c00837."
3188,O=C(C(C=CC=C1)=C1C/2=C(C#N)C#N)C2=C/C3=CC(N(C(CCCCCCCC)CCCCCCCC)C4=C5SC6=C4SC7=C6N(C(CCCCCCCC)CCCCCCCC)C8=C7SC(/C=C9C(C(C=CC=C%10)=C%10C9=C(C#N)C#N)=O)=C8)=C5S3,SN61C,-5.38,-3.93,16.5,0.88,0.66,9.6,"C. Huang, X. Liao, K. Gao, L. Zuo, F. Lin, X. Shi, C.-Z. Li, H. Liu, X. Li, F. Liu, Y. Chen, H. Chen, A.K.-Y. Jen, Highly Efficient Organic Solar Cells Based on S,N-Heteroacene Non-Fullerene Acceptors, Chem. Mater. 30 (2018) 5429¨C5434. https://doi.org/10.1021/acs.chemmater.8b02276."
3189,O=C(C1=C(C)SC(C)=C1C/2=C(C#N)C#N)C2=C/C3=CC4=C(S3)C5=C(C6=C(C7=CC=C(CC(CC)CCCC)S7)C8=C(C9=C(S8)C(SC(/C=C%10C(C%11=C(C)SC(C)=C%11C\%10=C(C#N)/C#N)=O)=C%12)=C%12C9(C%13=CC=C(CCCCCC)C=C%13)C%14=CC=C(CCCCCC)C=C%14)C(C%15=CC=C(CC(CC)CCCC)S%15)=C6S5)C4(C%16=CC=C(CCCCCC)C=C%16)C%17=CC=C(CCCCCC)C=C%17,BTTIC-4M,-5.55,-3.79,15.67,0.968,0.637,9.6,"W. Gao, T. Liu, Z. Luo, L. Zhang, R. Ming, C. Zhong, W. Ma, H. Yan, C. Yang, Regulating exciton bonding energy and bulk heterojunction morphology in organic solar cells via methyl-functionalized non-fullerene acceptors, J. Mater. Chem. A. 7 (2019) 6809¨C6817. https://doi.org/10.1039/C9TA00597H."
3190,O=C(C(C=CC=C1)=C1C/2=C(C#N)/C#N)C2=C/C(C(OCCCCCC)=C3)=CC(OCCCCCC)=C3C4=CC5=C(C6=CC(C7(C8=CC=C(CCCCCC)C=C8)C9=CC=C(CCCCCC)C=C9)=C(C%10=C7C=C(C%11=C(OCCCCCC)C=C(/C=C%12C(C(C=CC=C%13)=C%13C\%12=C(C#N)C#N)=O)C(OCCCCCC)=C%11)S%10)C=C6C5(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15)S4,IDT-BOC6,-5.51,-3.78,17.52,1.01,0.54,9.6,"Y. Liu, Z. Zhang, S. Feng, M. Li, L. Wu, R. Hou, X. Xu, X. Chen, Z. Bo, Exploiting Noncovalently Conformational Locking as a Design Strategy for High Performance Fused-Ring Electron Acceptor Used in Polymer Solar Cells, J. Am. Chem. Soc. 139 (2017) 3356¨C3359. https://doi.org/10.1021/jacs.7b00566."
3191,CCCCCCCCC1(CCCCCCCC)C2=CC3=C(C=C2C2=C1C=C(/C=C1C(=O)C4=CC=CC=C4C1=C(C#N)C#N)S2)C(CCCCCCCC)(CCCCCCCC)C1=C3C=C2C(=C1)C1=C(C=C(/C=C3C(=O)C4=CC=CC=C4C3=C(C#N)C#N)S1)C2(CCCCCCCC)CCCCCCCC,F-H,-5.42,-3.79,15.02,0.94,0.67,9.59,"Y. Wang, Y. Zhang, N. Qiu, H. Feng, H. Gao, B. Kan, Y. Ma, C. Li, X. Wan, Y. Chen, A Halogenation Strategy for over 12% Efficiency Nonfullerene Organic Solar Cells, Adv. Energy Mater. 8 (2018) 1702870. https://doi.org/10.1002/aenm.201702870."
3192,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(OCC(CC)CCCC)C5=C(C=C4C(OCC(CC)CCCC)=C3C3=C2C2=C(C=C(/C=C4C(=O)C6=C(Cl)SC=C6C4=C(C#N)C#N)S2)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C5SC3=C2SC(/C=C2C(=O)C4=C(Cl)SC=C4C2=C(C#N)C#N)=C3)C=C1,NITT-ThCl,-5.71,-4.1,16.3,0.97,0.6062,9.58,"R. Ming, G. Li, C. Xu, Z. Luo, W. Ning, C. Zhong, X. Liu, C. Ye, F. Zhang, C. Yang, Naphthalene-fused octacyclic electron-donating central core constructs non-fullerene acceptors for organic solar cells, Chem. Eng. J. 425 (2021) 130618. https://doi.org/10.1016/j.cej.2021.130618."
3193,CCCCCCCCC1(CCCCCCCC)C2=CC3=C(C=C2C2=CC4=C(C=C21)C1=C(S4)C2=C(C=C(/C=C4C(=O)C5=C(C=C(F)C(F)=C5)C4=C(C#N)C#N)S2)C1(C1=CC=C(CCCCCC)C=C1)C1=CC=C(CCCCCC)C=C1)SC1=C3C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C1SC(/C=C1C(=O)C3=C(C=C(F)C(F)=C3)C1=C(C#N)C#N)=C2,DTFT9-FIC,-5.49,-4.01,19.01,0.86,0.5861,9.58,"F.-Y. Cao, P.-K. Huang, Y.-C. Su, W.-C. Huang, S.-L. Chang, K.-E. Hung, Y.-J. Cheng, Forced coplanarity of dithienofluorene-based non-fullerene acceptors to achieve high-efficiency organic solar cells, J. Mater. Chem. A. 7 (2019) 17947¨C17953. https://doi.org/10.1039/C9TA05116C."
3194,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=C(SC4=C3SC(/C=C3C(=O)C5=C(C=C(F)C(F)=C5)C3=C(C#N)C#N)=C4)C3=C2C2=C(S3)C3=C(S2)C2=C(C4=C(C=C(/C=C5C(=O)C6=C(C=C(F)C(F)=C6)C5=C(C#N)C#N)S4)S2)C3(C2=CC=C(CCCCCC)C=C2)C2=CC=C(CCCCCC)C=C2)C=C1,F8IC,-5.47,-4.06,23.3,0.65,0.634,9.55,"G. Cai, P. Xue, Z. Chen, T. Li, K. Liu, W. Ma, J. Lian, P. Zeng, Y. Wang, R.P.S. Han, X. Zhan, High-Performance Mid-Bandgap Fused-Pyrene Electron Acceptor, Chem. Mater. 31 (2019) 6484¨C6490. https://doi.org/10.1021/acs.chemmater.8b04668."
3195,CCCCCCCCC1=C(/C=C2C(=O)C3=C(C=CC=C3)C2=C(C#N)C#N)SC2=C1C(CCCCCCCC)(CCCCCCCC)OC1=CC3=C(C=C12)C(CCCCCCCC)(CCCCCCCC)C1=C3C=C2OC(CCCCCCCC)(CCCCCCCC)C3=C(SC(/C=C4C(=O)C5=C(C=CC=C5)C4=C(C#N)C#N)=C3CCCCCCCC)C2=C1,FOR-1N,-5.7,-3.67,15.38,1.071,0.5798,9.55,"S. Wu, L. Meng, Z. Zhang, M. Li, Y. Yang, J. Wang, H. Chen, C. Jiang, X. Wan, C. Li, Z. Yao, Y. Chen, Molecular optimization of incorporating pyran fused acceptor¨Cdonor¨Cacceptor type acceptors enables over 15% efficiency in organic solar cells, J. Mater. Chem. C. 10 (2022) 1977¨C1983. https://doi.org/10.1039/D1TC05779K."
3196,O=C1N(C(CCCCCC)CCCCCC)C(C2=C(C1C=C3[Se]4)C5=C3C(C4=CC6C(N(C(CCCCCC)CCCCCC)C7=O)=O)=C(C6=C7C=C8C9=CC=C(S9)C%10=C(C%11=CC=C(C%12=CC%13=C%14C%15=C%16C%17=C%18C(C=CC(C(N(C(CCCCCC)CCCCCC)C%19=O)=O)=C%18C%19C=C%17[Se]C%16=CC%14C(N(C(CCCCCC)CCCCCC)C%13=O)=O)=C%15%12)S%11)C(C=C(C%20=CC%21=C%22C%23=C%24C%25=C%26C(C=CC(C(N(C(CCCCCC)CCCCCC)C%27=O)=O)=C%26C%27C=C%25[Se]C%24=CC%22C(N(C(CCCCCC)CCCCCC)C%21=O)=O)=C%23%20)S%28)=C%28C%29=C%10C=C(C%30=CC%31=C%32C%33=C%34C%35=C%36C(C=CC(C(N(C(CCCCCC)CCCCCC)C%37=O)=O)=C%36C%37C=C%35[Se]C%34=CC%32C(N(C(CCCCCC)CCCCCC)C%31=O)=O)=C%33%30)S%29)C8=C5C=C2)=O,BPT-Se1,-5.85,-3.81,10.287,1.059,0.732,9.54,"Z. Luo, T. Liu, Z. Chen, Y. Xiao, G. Zhang, L. Huo, C. Zhong, X. Lu, H. Yan, Y. Sun, C. Yang, Isomerization of Perylene Diimide Based Acceptors Enabling High-Performance Nonfullerene Organic Solar Cells with Excellent Fill Factor, Adv. Sci. 6 (2019) 1802065. https://doi.org/10.1002/advs.201802065."
3197,CCCCCCCCCCCCCCCCN1C2=CC3=C(C=C2C2=C1C=C1C(=C2)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C1SC1=C2SC(/C=C2C(=O)C4=C(C=C(F)C(F)=C4)C2=C(C#N)C#N)=C1)C(C1=CC=C(CCCCCC)C=C1)(C1=CC=C(CCCCCC)C=C1)C1=C3SC2=C1SC(/C=C1C(=O)C3=C(C=C(F)C(F)=C3)C1=C(C#N)C#N)=C2,4TC-4F-C16,-5.53,-3.96,16.12,0.91,0.65,9.53,"J. Ouyang, B. Zhang, G. Zeng, J. Zhang, X. Zhao, X. Yang, Improving Efficiency of Organic Solar Cells by Restricting the Rotation of Side Chain on Small Molecule Acceptor, Sol. RRL. 4 (2020) 2000359. https://doi.org/10.1002/solr.202000359."
3198,CCCCCCCCC(CCCC)COC1=C(OCC(CCCC)CCCCCCCC)C(C2=CC3=C(S2)C2=C(CC(/C=C4C(=O)C5=C(C=C(Cl)C(Cl)=C5)C4=C(C#N)C#N)S2)C3(CCCCCC)CCCCCC)=C2N=CC=NC2=C1C1=CC2=C(S1)C1=C(C=C(/C=C3C(=O)C4=C(C=C(Cl)C(Cl)=C4)C3=C(C#N)C#N)S1)C2(CCCCCC)CCCCCC.Cl,QCIC4,-5.49,-3.9,19.16,0.78,0.638,9.53,"S. Ye, S. Chen, S. Li, Y. Pan, X. Xia, W. Fu, L. Zuo, X. Lu, M. Shi, H. Chen, Synergistic Effects of Chlorination and Branched Alkyl Side Chain on the Photovoltaic Properties of Simple Non-Fullerene Acceptors with Quinoxaline as the Core, ChemSusChem. 14 (2021) 3599¨C3606. https://doi.org/10.1002/cssc.202100689."
3199,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=C(SC(/C=C4C(=O)C5=C(C=CC(F)=C5)C4=C(C#N)C#N)=C3)C3=C2C2=C(OCC(CC)CCCC)C4=C(C(OCC(CC)CCCC)=C2S3)C2=C(S4)C3=C(C=C(CC4C(=O)C5=C(C=C(F)C=C5)C4=C(C#N)C#N)S3)C2(C2=CC=C(CCCCCC)C=C2)C2=CC=C(CCCCCC)C=C2)C=C1,BT-SFIC,-5.46,-4.04,18.46,0.77,0.67,9.52,"Y. Li, W. Su, F. Wu, Z. Xu, Y.-K. Wang, M. Zhang, Z.-Q. Jiang, L.-S. Liao, Near-infrared non-fullerene acceptors based on dithienyl[1,2-b:4,5-b¡¯]benzodithiophene core for high performance PTB7-Th-based polymer solar cells, Org. Electron. 65 (2019) 63¨C69. https://doi.org/10.1016/j.orgel.2018.10.042."
3200,CCN(C/1=O)C(SC1=C/C2=CC=C(C(S3)=CC4=C3C(C5=CC=C(C(CC(CC)CCCC)(CC(CC)CCCC)C6=C7SC(C8=CC=C(/C=C9SC(N(CC)C9=O)=S)C%10=NSN=C8%10)=C6)C7=C5C=C%11)=C%11C4(CC(CC)CCCC)CC(CC)CCCC)C%12=NSN=C2%12)=S,DTNR,-5.67,-3.75,15.72,1.08,0.56,9.51,"Y. Ma, M. Zhang, Y. Tang, W. Ma, Q. Zheng, Angular-Shaped Dithienonaphthalene-Based Nonfullerene Acceptor for High-Performance Polymer Solar Cells with Large Open-Circuit Voltages and Minimal Energy Losses, Chem. Mater. 29 (2017) 9775¨C9785. https://doi.org/10.1021/acs.chemmater.7b03770."
3201,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(C=C(/C=C5C(=O)C6=CC(F)=CC=C6C5=C(C#N)C#N)S2)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC3=C2SC(/C=C2C(=O)C4=CC(F)=CC=C4C2=C(C#N)C#N)=C3)C=C1,Cl-ITIC,-5.7,-4.14,15.6,0.94,0.65,9.5,"F. Yang, C. Li, W. Lai, A. Zhang, H. Huang, W. Li, Halogenated conjugated molecules for ambipolar field-effect transistors and non-fullerene organic solar cells, Mater. Chem. Front. 1 (2017) 1389¨C1395. https://doi.org/10.1039/C7QM00025A."
3202,CCCCCCC(CCCCCC)N1C(=O)C2=CC=C3C4=C(C=CC(=C24)C1=O)C1=C2C4=C(C=C1)C(=O)N(C(CCCCCC)CCCCCC)C(=O)C4=CC(C1=CC=C4C(=C1)C1(C5=CC=CC=C5C5=CC=CC=C51)C1=C4C=CC(C4=CC5=C6C(=CC=C7C8=CC=C9C(=O)N(C(CCCCCC)CCCCCC)C(=O)C%10=C9C8=C(C=C%10)C4=C76)C(=O)N(C(CCCCCC)CCCCCC)C5=O)=C1)=C32,SF-PDI2,-5.99,-3.62,13.27,1.11,0.643,9.5,"J. Liu, S. Chen, D. Qian, B. Gautam, G. Yang, J. Zhao, J. Bergqvist, F. Zhang, W. Ma, H. Ade, O. Ingan?s, K. Gundogdu, F. Gao, H. Yan, Fast charge separation in a non-fullerene organic solar cell with a small driving force, Nat. Energy. 1 (2016) 1¨C7. https://doi.org/10.1038/nenergy.2016.89."
3203,CCCCCCCCC1(CCCCCCCC)C2=C(SC(/C=C3C(=O)C4=C(C=C(Cl)C(Cl)=C4)C3=C(C#N)C#N)=C2)C2=C1C=C(C1=CC3=C(S1)C1=CC4=C(C=C1C3(C1=CC=C(CCCCCC)C=C1)C1=CC=C(CCCCCC)C=C1)C1=C(C=C(C3=CC5=C(S3)C3=C(C=C(/C=C6C(=O)C7=C(C=C(Cl)C(Cl)=C7)C6=C(C#N)C#N)S3)C5(CCCCCCCC)CCCCCCCC)S1)C4(C1=CC=C(CCCCCC)C=C1)C1=CC=C(CCCCCC)C=C1)S2,IDTC-4Cl ,-5.5,-3.79,19.19,0.822,0.602,9.5,"Y.-Q.-Q. Yi, H. Feng, X. Ke, J. Yan, M. Chang, X. Wan, C. Li, Y. Chen, A cyclopentadithiophene-bridged small molecule acceptor with near-infrared light absorption for efficient organic solar cells, J. Mater. Chem. C. 7 (2019) 4013¨C4019. https://doi.org/10.1039/C9TC00162J."
3204,CCCCCCCCC1=CC=C(C2(C3=CC=C(CCCCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C=C(/C=C2C(=O)C5=C(C=CC=C5)C2=C(C#N)C#N)S3)N(C(CCCCCCCC)CCCCCCCC)C2=CC3=C(C=C24)C(C2=CC=C(CCCCCCCC)C=C2)(C2=CC=C(CCCCCCCC)C=C2)C2=C3SC(/C=C3C(=O)C4=C(C=CC=C4)C3=C(C#N)C#N)=C2)C=C1,DTC(4Ph)-IC,-5.75,-3.67,14.27,0.97,0.6782,9.48,"J. Yuan, Y. Zhang, L. Zhou, G. Zhang, H.-L. Yip, T.-K. Lau, X. Lu, C. Zhu, H. Peng, P.A. Johnson, M. Leclerc, Y. Cao, J. Ulanski, Y. Li, Y. Zou, Single-Junction Organic Solar Cell with over 15% Efficiency Using Fused-Ring Acceptor with Electron-Deficient Core, Joule. 3 (2019) 1140¨C1151. https://doi.org/10.1016/j.joule.2019.01.004."
3205,O=C(C(C=CC=C1)=C1C/2=C(C#N)/C#N)C2=C/C(S3)=CC4=C3C5=CC6=C(C=C5C4(C7=CC=C(CCCCCCCC)C=C7)C8=CC=C(CCCCCCCC)C=C8)C9=CC%10=C(C(SC(/C=C%11C(C(C=CC=C%12)=C%12C\%11=C(C#N)C#N)=O)=C%13)=C%13C%10(C%14=CC=C(CCCCCCCC)C=C%14)C%15=CC=C(CCCCCCCC)C=C%15)C=C9N6C(CCCCCCCC)CCCCCCCC,DTCCIC-C17,-5.46,-3.65,14.27,0.97,0.67,9.48,"Y.-T. Hsiao, C.-H. Li, S.-L. Chang, S. Heo, K. Tajima, Y.-J. Cheng, C.-S. Hsu, Haptacyclic Carbazole-Based Ladder-Type Nonfullerene Acceptor with Side-Chain Optimization for Efficient Organic Photovoltaics, ACS Appl. Mater. Interfaces. 9 (2017) 42035¨C42042. https://doi.org/10.1021/acsami.7b12612."
3206,CCCCC(CC)CC1=CC=C(C2=C3C=C(C4=CC5=C(S4)C4=C(C=C(/C=C6C(=O)C7=C(C=C(F)C(F)=C7)C6=C(C#N)C#N)S4)C5(CC(CC)CCCC)CC(CC)CCCC)SC3=C(C3=CC=C(CC(CC)CCCC)S3)C3=C2SC(C2=CC4=C(S2)C2=C(C=C(/C=C5C(=O)C6=C(C=C(F)C(F)=C6)C5=C(C#N)C#N)S2)C4(CC(CC)CCCC)CC(CC)CCCC)=C3)S1,BDTC-4F,-5.59,-3.88,19.04,0.868,0.572,9.46,"Y. Wang, S. Liu, H. Gao, L. Wang, W. Wang, B. Zhao, H. Wu, C. Gao, Synergistic halogenation of backbone and end group for high-performance non-fused acceptors based organic solar cells, Dyes Pigments. (2022) 110178. https://doi.org/10.1016/j.dyepig.2022.110178."
3207,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C=C(C2=C5C(F)=C(C(=O)OCC(CC)CCCC)SC5=C(/C=C5C(=O)C6=C(C=C(F)C(F)=C6)C5=C(C#N)C#N)S2)O3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC(C3=C4C(F)=C(C(=O)OCC(CC)CCCC)SC4=C(/C=C4C(=O)C5=C(C=CC(F)=C5)C4=C(C#N)C#N)S3)=C2)C=C1,T3,-5.31,-4,22,0.61,0.7,9.43,"F.-X. Chen, J.-Q. Xu, Z.-X. Liu, M. Chen, R. Xia, Y. Yang, T.-K. Lau, Y. Zhang, X. Lu, H.-L. Yip, A.K.-Y. Jen, H. Chen, C.-Z. Li, Near-Infrared Electron Acceptors with Fluorinated Regioisomeric Backbone for Highly Efficient Polymer Solar Cells, Adv. Mater. 30 (2018) 1803769. https://doi.org/10.1002/adma.201803769."
3208,CCCCCCCCC1(CCCCCCCC)C2=CC3=CC4=C(C=C3C=C2C2=C1C=C(/C=C1C(=O)C3=C(C=CC=C3)C1=C(C#N)C#N)S2)C(CCCCCCCC)(CCCCCCCC)C1=C4SC(/C=C2C(=O)C3=C(C=CC=C3)C2=C(C#N)C#N)=C1,NDIC,-5.71,-3.88,15.1,0.9,0.696,9.43,"Z. Zhang, X. Cui, M. Li, Y. Liu, D. Li, P. Jiang, Z. Bo, Nonfullerene acceptors comprising a naphthalene core for high efficiency organic solar cells, RSC Adv. 9 (2019) 39163¨C39169. https://doi.org/10.1039/C9RA08092A."
3209,CCCCCCC1(CCCCCC)C2=CC3=C(C=C2C2=C1C=C(/C=C1C(=O)C4=C(C=C(F)C(F)=C4)C1=C(C#N)C#N)S2)C(CCCCCC)(CCCCCC)C1=C3SC(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)=C1,IDIC-4F,-5.76,-3.93,16.83,0.86,0.652,9.43,"Z. Li, R. Liang, J. Wang, B. Na, H. Liu, Solution-Processable All-Small-Molecules for High-Performance Nonfullerene Organic Solar Cells with High Crystallinity Acceptor, J. Phys. Chem. C. 123 (2019) 28021¨C28026. https://doi.org/10.1021/acs.jpcc.9b06773."
3210,CCCCCCCCCCCCCCCCC1(CCCCCCCCCCCCCCCC)C2=CC3=C(C=C2C2=C1C=C(/C=C1C(=O)C4=C(C=C(F)C(F)=C4)C1=C(C#N)C#N)S2)C(CCCCCCCCCCCCCCCC)(CCCCCCCCCCCCCCCC)C1=C3SC(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)=C1,IDTC16-4F,-5.54,-3.79,7.1,0.899,0.7148,9.42,"H. Lin, M.A. Adil, Q. Zhang, J. Zhang, Q. Wang, Small-molecule acceptors with long alkyl chains for high-performance as-cast nonfullerene organic solar cells, Org. Electron. 93 (2021) 106167. https://doi.org/10.1016/j.orgel.2021.106167."
3211,CCCCCCC1=CC=C(C2(C3=CC=C(C)C=C3)C3=CC4=C(C=C3C3=C2C=C(/C=C2C(=O)C5=C(C=CC(F)=C5)C2=C(C#N)C#N)S3)C2(C3=C(C=CC=C3)OC3=C2C=CC=C3)C2=C4C=C3C(=C2)C2=C(C=C(/C=C4C(=O)C5=C(C=CC(F)=C5)C4=C(C#N)C#N)S2)C3(C2=CC=C(CCCCCC)C=C2)C2=CC=C(CCCCCC)C=C2)C=C1,TSFX-2F,-5.82,-3.94,15.27,0.89,0.693,9.42,"D. Yang, Q. Ma, X. Li, S. Chen, J. Zhang, C. Yang, L. Meng, Y. Li, Two new A-D-A type small molecule acceptors based on C2v-symmetric dithienocyclopentaspiro[fluorene-9,9¡ä-xanthene] core for polymer solar cells, Org. Electron. 92 (2021) 106120. https://doi.org/10.1016/j.orgel.2021.106120."
3212,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=C(C=C4C(=C3)C3=C(C5=C(S3)C3SC(/C=C6C(=O)C7=C(C)SC=C7C6=C(C#N)C#N)=CC3S5)C4(C3=CC=C(CCCCCC)C=C3)C3=CC=C(CCCCCC)C=C3)C3=C2C=C(/C=C2CC4=C(C)SC=C4C2=C(C#N)C#N)S3)C=C1,MELC1,-5.59,-3.89,15.94,0.889,0.6645,9.42,"X. Ma, M. Luo, W. Gao, J. Yuan, Q. An, M. Zhang, Z. Hu, J. Gao, J. Wang, Y. Zou, C. Yang, F. Zhang, Achieving 14.11% efficiency of ternary polymer solar cells by simultaneously optimizing photon harvesting and exciton distribution, J. Mater. Chem. A. 7 (2019) 7843¨C7851. https://doi.org/10.1039/C9TA01497G."
3213,CCCCCCCCC1(CCCCCCCC)C2=CC3=C(C=C2C2=C1C=C(/C=C1C(=O)C4=C(C=CC=C4)C1=C(C#N)C#N)S2)C(CCCCCCCC)(CCCCCCCC)C1=C3SC(C2=C3C(F)=C(C(=O)OCC(CC)CCCC)SC3=C(/C=C3C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)S2)=C1,ICIF2F,-5.45,-4.02,19.3,0.79,0.614,9.42,"Y. Zhang, Y. Wang, Z. Xie, T. Shan, L. Zhu, F. Liu, H. Zhong, Preparation of non-fullerene acceptors with a multi-asymmetric configuration in a one-pot reaction for organic solar cells, J. Mater. Chem. C. 8 (2020) 17229¨C17236. https://doi.org/10.1039/D0TC04749J."
3214,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=C(C=C4C(=C3)C3=C(C5=C(C=C(/C=C6C(=O)C7=C(C=CC=C7)C6=C(C#N)C#N)S5)S3)C4(C3=CC=C(CCCCCC)C=C3)C3=CC=C(CCCCCC)C=C3)C3=C2C=C(/C=C2C(=O)C4=C(C=CC=C4)C2=C(C#N)C#N)S3)C=C1,T-TT,-5.54,-3.37,15.99,0.97,0.606,9.41,"S. Liu, B. Zhao, Z. Cong, Q. Cheng, W. Wang, H. Pan, J. Liu, H. Wu, C. Gao, Influences of the terminal groups on the performances of asymmetric small molecule acceptors-based polymer solar cells, Dyes Pigments. 178 (2020) 108388. https://doi.org/10.1016/j.dyepig.2020.108388."
3215,CCCCCCCCOC1=CC(C2=CC3=C(S2)C2=C(C=C(/C=C4C(=O)C5=CC=CC=C5C4=C(C#N)C#N)S2)C3(CC(CC)CCCC)CC(CC)CCCC)=C(OCCCCCCCC)C=C1C1=CC2=C(S1)C1=C(C=C(/C=C3C(=O)C4=CC=CC=C4C3=C(C#N)C#N)S1)C2(CC(CC)CCCC)CC(CC)CCCC,DOC8-IC,,,17.74,0.92,0.5765,9.41,"H. Huang, Q. Guo, S. Feng, C. Zhang, Z. Bi, W. Xue, J. Yang, J. Song, C. Li, X. Xu, Z. Tang, W. Ma, Z. Bo, Noncovalently fused-ring electron acceptors with near-infrared absorption for high-performance organic solar cells, Nat. Commun. 10 (2019) 3038. https://doi.org/10.1038/s41467-019-11001-6."
3216,CCCCCCCCOC1=CC(C2=CC3=C(S2)C2=C(C=C(/C=C4C(=O)C5=C(C=CC=C5)C4=C(C#N)C#N)S2)C3(CC(CC)CCCC)CC(CC)CCCC)=C(OCCCCCCCC)C=C1C1=CC2=C(S1)C1=C(C=C(/C=C3C(=O)C4=C(C=CC=C4)C3=C(C#N)C#N)S1)C2(CC(CC)CCCC)CC(CC)CCCC,DOC8-IC,,,17.74,0.92,0.5765,9.41,"H. Huang, Q. Guo, S. Feng, C. Zhang, Z. Bi, W. Xue, J. Yang, J. Song, C. Li, X. Xu, Z. Tang, W. Ma, Z. Bo, Noncovalently fused-ring electron acceptors with near-infrared absorption for high-performance organic solar cells, Nat. Commun. 10 (2019) 3038. https://doi.org/10.1038/s41467-019-11001-6."
3217,CCCCCCCCC1=C(C2=C3C(=O)N(CC(CC)CCCC)C(=O)C3=C(C3=CC=C(C4=C5C(=O)N(CC(CC)CCCC)C(=O)C5=C(C5=C(CCCCCCCC)C=C(/C=C6/SC(=C(C#N)C#N)N(CC)C6C)S5)S4)C4=NSN=C34)S2)SC(/C=C2/SC(=C(C#N)C#N)N(CC)C2=O)=C1,BPTCN,-5.38,-3.66,23.65,0.72,0.55,9.41,"D. Luo, M. Zhang, J.-B. Li, Z. Xiao, F. Liu, L. Ding, X.-H. Zhu, Enhanced efficiency and stability of nonfullerene ternary polymer solar cells based on a spontaneously assembled active layer: the role of a high mobility small molecular electron acceptor, J. Mater. Chem. C. 8 (2020) 6196¨C6202. https://doi.org/10.1039/D0TC00225A."
3218,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(C=C(/C=C5C(=O)C6=CC(Br)=CC=C6C5=C(C#N)C#N)S2)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC3=C2SC(/C=C2C(=O)C4=CC(Br)=CC=C4C2=C(C#N)C#N)=C3)C=C1,Br-ITIC,-5.73,-4.2,15.4,0.93,0.66,9.4,"F. Yang, C. Li, W. Lai, A. Zhang, H. Huang, W. Li, Halogenated conjugated molecules for ambipolar field-effect transistors and non-fullerene organic solar cells, Mater. Chem. Front. 1 (2017) 1389¨C1395. https://doi.org/10.1039/C7QM00025A."
3219,CCCCCCCCC1(CCCCCCCC)C2=CC3=C(C=C2C2=C1C=C(C1=C(F)C(F)=C(/C=C4SC(=S)N(CC)C4=O)C4=NSN=C41)S2)C(CCCCCCCC)(CCCCCCCC)C1=C3SC(C2=C(F)C(F)=C(/C=C3SC(=S)N(CC)C3=O)C3=NSN=C32)=C1,O-FFBR,-5.59,-3.95,17,0.94,0.59,9.4,"M. Chen, Y. Nian, Z. Hu, L. Zhang, Alkyl side chain engineering for difluorinated benzothiadiazole flanked non-fullerene acceptors toward efficient polymer solar cells, J. Mater. Sci. Mater. Electron. 32 (2021) 219¨C231. https://doi.org/10.1007/s10854-020-04757-x."
3220,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=C(SC4=C3SC(/C=C3C(=O)C5=CC=CC=C5C3=C(C#N)C#N)=C4)C3=C2C2=C(S3)C3=C(S2)C2=C(C4=C(C=C(/C=C5C(=O)C6=CC=CC=C6C5=C(C#N)C#N)S4)S2)C3(C2=CC=C(CCCCCC)C=C2)C2=CC=C(CCCCCC)C=C2)C=C1,IXIC,-5.13,-3.78,19.9,0.84,0.566,9.4,"Y. Chen, T. Liu, H. Hu, T. Ma, J.Y.L. Lai, J. Zhang, H. Ade, H. Yan, Modulation of End Groups for Low-Bandgap Nonfullerene Acceptors Enabling High-Performance Organic Solar Cells, Adv. Energy Mater. 8 (2018) 1801203. https://doi.org/10.1002/aenm.201801203."
3221,CCCCCCCCC(CCCCCCCC)N1C2=CC3=C(C=C2C2=C1C=C1C(=C2)C(CCCCCCCC)(CCCCCCCC)C2=C1SC(/C=C1C(=O)C4=C(C=CC=C4)C1=C(C#N)C#N)=C2)C(CCCCCCCC)(CCCCCCCC)C1=C3SC(/C=C2C(=O)C3=C(C=CC=C3)C2=C(C#N)C#N)=C1,DTC(4R)-IC,-5.69,-3.63,16.44,0.94,0.62,9.39,"T.-W. Chen, Y.-T. Hsiao, Y.-W. Lin, C.-C. Chang, W.-T. Chuang, Y. Li, C.-S. Hsu, Fluorinated heptacyclic carbazole-based ladder-type acceptors with aliphatic side chains for efficient fullerene-free organic solar cells, Mater. Chem. Front. 3 (2019) 829¨C835. https://doi.org/10.1039/C9QM00005D."
3222,CCCCC(CC)CC1(CC(CC)CCCC)C2=C(SC(/C=C3C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)=C2)C2=C1C=C(C1=CC=C(C3=CC4=C(S3)C3=C(C=C(/C=C5/C(=O)C6=C(C=C(F)C(F)=C6)C5=C(C#N)C#N)S3)C4(CC(CC)CCCC)CC(CC)CCCC)C3=NSN=C13)S2,WHC-2,-5.49,-4.1,21.34,0.75,0.57,9.37,"MD.W. Hussain, H.J. Shin, B.R. Lee, M. Ak, S.-J. Ko, J. Lee, H. Choi, Design of Nonfused Nonfullerene Acceptors Based on Pyrido- or Benzothiadiazole Cores for Organic Solar Cells, ACS Appl. Energy Mater. (2022). https://doi.org/10.1021/acsaem.1c03741."
3223,CCCCCCCCC1(CCCCCCCC)C2=CC3=C(C=C2C2=C1C=C(C1=C4C(F)=C(C(=O)OCC(CC)CCCC)SC4=C(/C=C4C(=O)C5=CC(F)=C(F)C=C5C4=C(C#N)C#N)S1)S2)C(CCCCCCCC)(CCCCCCCC)C1=C3SC(C2=C3C(F)=C(C(=O)OCC(CC)CCCC)SC3=C(/C=C3C(=O)C4=CC=CC=C4C3=C(C#N)C#N)S2)=C1,6-IFIC,-5.34,-4.02,22.35,0.69,0.614,9.35,"Y. Zhang, Y. Wang, T. Shan, Q. Wei, Y.X. Xu, H. Zhong, Non-Fullerene Acceptors with an Optical Response over 1000 nm toward Efficient Organic Solar Cells, ACS Appl. Mater. Interfaces. 13 (2021) 51279¨C51288. https://doi.org/10.1021/acsami.1c13404."
3224,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C=C(/C=C2C(=O)C5=C(C=CC=C5)C2=C(C#N)C#N)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC3=C2SC(/C=C2C(=O)C4=C(C=CC=C4)C2=C(C#N)C#N)=C3)C=C1,A201,-5.69,-3.93,13.15,0.88,0.6715,9.31,"W. Zhai, A. Tang, B. Xiao, X. Wang, F. Chen, E. Zhou, A small molecular electron acceptor based on asymmetric hexacyclic core of thieno[1,2-b]indaceno[5,6-b¡ä]thienothiophene for efficient fullerene-free polymer solar cells, Sci. Bull. 63 (2018) 845¨C852. https://doi.org/10.1016/j.scib.2018.05.025."
3225,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C=C(/C=C2C(=O)C5=CC=C(C6=CC=CS6)C=C5C2=C(C#N)C#N)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC(/C=C3C(=O)C4=C(C=CC(C5=CC=CS5)=C4)C3=C(C#N)C#N)=C2)C=C1,IDT-IC-T,-5.72,-3.91,15.73,0.85,0.7,9.3,"S. Feng, D. Ma, L. Wu, Y. Liu, C. Zhang, X. Xu, X. Chen, S. Yan, Z. Bo, Enhance the performance of polymer solar cells via extension of the flanking end groups of fused ring acceptors, Sci. China Chem. 61 (2018) 1320¨C1327. https://doi.org/10.1007/s11426-018-9252-9."
3226,CCCCC(CC)CC1(CC(CC)CCCC)C2=C(SC(/C=C3C(=O)C4=C(C=CC=C4)C3=C(C#N)C#N)=C2)C2=C1C=C(C1=CC=C(C3=CC4=C(S3)C3=C(C=C(/C=C5C(=O)C6=C(C=CC=C6)C5=C(C#N)C#N)S3)C4(CC(CC)CCCC)CC(CC)CCCC)C3=NSN=C13)S2,BTCIC,-5.53,-4,18.6,0.79,0.63,9.3,"S. Pang, X. Zhou, S. Zhang, H. Tang, S. Dhakal, X. Gu, C. Duan, F. Huang, Y. Cao, Nonfused Nonfullerene Acceptors with an A¨CD¨CA¡ä¨CD¨CA Framework and a Benzothiadiazole Core for High-Performance Organic Solar Cells, ACS Appl. Mater. Interfaces. 12 (2020) 16531¨C16540. https://doi.org/10.1021/acsami.0c01850."
3227,CCCCCCCCC1(CCCCCCCC)C2=CC3=C(C=C2C2=C1C=C(C1=C(OC(CC)CCCC)C=C(/C=C4C(=O)C5=CC(F)=C(F)C=C5C4=C(C#N)C#N)S1)S2)C(CCCCCCCC)(CCCCCCCC)C1=C3SC(C2=C(OCC(CC)CCCC)C=C(/C=C3C(=O)C4=CC(F)=C(F)C=C4C3=C(C#N)C#N)S2)=C1,o-IO2,-5.41,-4.21,21.8,0.68,0.63,9.3,"J. Lee, S. Song, J. Huang, Z. Du, H. Lee, Z. Zhu, S.-J. Ko, T.-Q. Nguyen, J.Y. Kim, K. Cho, G.C. Bazan, Bandgap Tailored Nonfullerene Acceptors for Low-Energy-Loss Near-Infrared Organic Photovoltaics, ACS Mater. Lett. 2 (2020) 395¨C402. https://doi.org/10.1021/acsmaterialslett.9b00512."
3228,CCCCC(CC)CC1=CC=C(C2=C3C=C(C4=CC5=C(S4)C4=C(C=C(/C=C6C(=O)C7=C(C=C(Cl)C(Cl)=C7)C6=C(C#N)C#N)S4)C5(CC(CC)CCCC)CC(CC)CCCC)SC3=C(C3=CC=C(CC(CC)CCCC)S3)C3=C2SC(C2=CC4=C(S2)C2=C(C=C(/C=C5C(=O)C6=C(C=C(Cl)C(Cl)=C6)C5=C(C#N)C#N)S2)C4(CC(CC)CCCC)CC(CC)CCCC)=C3)S1,BDTC-4Cl,-5.41,-3.88,19.21,0.87,0.556,9.3,"Y. Wang, S. Liu, H. Gao, L. Wang, W. Wang, B. Zhao, H. Wu, C. Gao, Synergistic halogenation of backbone and end group for high-performance non-fused acceptors based organic solar cells, Dyes Pigments. (2022) 110178. https://doi.org/10.1016/j.dyepig.2022.110178."
3229,O=C(C1=CSC=C1C/2=C(C#N)C#N)C2=C/C3=CC4=C(C5=CC(C6(C7=CC=C(CCCCCC)C=C7)C8=CC=C(CCCCCC)C=C8)=C(C9=C6C(SC(/C=C%10C(C%11=CSC=C%11C\%10=C(C#N)C#N)=O)=C%12)=C%12S9)C=C5C4(C%13=CC=C(CCCCCC)C=C%13)C%14=CC=C(CCCCCC)C=C%14)S3,IDT6CN1:1,-5.68,-3.97,15.14,0.83,0.737,9.27,"W. Gao, M. Zhang, T. Liu, R. Ming, Q. An, K. Wu, D. Xie, Z. Luo, C. Zhong, F. Liu, F. Zhang, H. Yan, C. Yang, Asymmetrical Ladder-Type Donor-Induced Polar Small Molecule Acceptor to Promote Fill Factors Approaching 77% for High-Performance Nonfullerene Polymer Solar Cells, Adv. Mater. 30 (2018) 1800052. https://doi.org/10.1002/adma.201800052."
3230,O=C(C(C=CC=C1)=C1C/2=C(C#N)C#N)C2=C/C=C/C3=CC4=C(C5=C(C4(C6=CC=C(CCCCCC)C=C6)C7=CC=C(CCCCCC)C=C7)C=C(C8=C9C=C(/C=C/C=C%10C(C(C=CC=C%11)=C%11C\%10=C(C#N)/C#N)=O)S8)C(C9(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)=C5)S3,SJ-IC,-5.61,-3.94,16.99,0.83,0.6595,9.27,"X. Li, T. Yan, H. Bin, G. Han, L. Xue, F. Liu, Y. Yi, Z.-G. Zhang, T.P. Russell, Y. Li, Insertion of double bond ¦Ð-bridges of A¨CD¨CA acceptors for high performance near-infrared polymer solar cells, J. Mater. Chem. A. 5 (2017) 22588¨C22597. https://doi.org/10.1039/C7TA07049G."
3231,CCCCCCCCC(CCCCCC)CN1C2=C(SC(/C=C3C(=O)C4=C(C=CC(F)=C4)C3=C(C#N)C#N)=C2)C2=C1C1=C(OCCCCCC)C3=C(C(OCCCCCC)=C1S2)C1=C(S3)C2=C(C=C(/C=C3C(=O)C4=C(C=C(F)C=C4)C3=C(C#N)C#N)S2)N1CC(CCCCCC)CCCCCCCC,SNC6C8¨CF,-5.48,-3.93,16.74,0.89,0.621,9.25,"Y. Xin, J. Liang, Y. Zhong, T. Liang, C. Zhang, X. He, Achieving additive-free organic solar cells by modulating the side-chain length of non-fullerene small molecule acceptors, Dyes Pigments. 195 (2021) 109661. https://doi.org/10.1016/j.dyepig.2021.109661."
3232,O=C(C(C=C(Cl)C(Cl)=C1)=C1C/2=C(C#N)C#N)C2=C/C3=CC4=C(C5=C(C4(C6=CC=C(CCCCCC)C=C6)C7=CC=C(CCCCCC)C=C7)C=C(C8=C9C=C(/C=C%10C(C(C=C(Cl)C(Cl)=C%11)=C%11C\%10=C(C#N)/C#N)=O)S8)C(C9(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)=C5)S3,IDIC-4CI,-5.78,-4.02,16.21,0.83,0.6869,9.24,"C. Zhang, S. Feng, Y. Liu, S. Ming, H. Lu, D. Ma, X. Xu, Y. Wu, Z. Bo, High efficiency ternary polymer solar cells based on a fused pentacyclic electron acceptor, J. Mater. Chem. A. 6 (2018) 6854¨C6859. https://doi.org/10.1039/C8TA00944A."
3233,CCCCC(CC)CC1(CC(CC)CCCC)C2=C(SC(/C=C3C(=O)C4=CC(F)=C(F)C=C4C3=C(C#N)C#N)=C2)C2=C1C=C(C1=C(C)/C(=C(C3=CC=CC=C3)C3=C(C)C(C4=CC5=C(S4)C4=C(C=C(/C=C6C(=O)C7=CC(F)=C(F)C=C7C6=C(C#N)C#N)S4)C5(CC(CC)CCCC)CC(CC)CCCC)=C(C)N3B(F)F)N=C1C)S2,tMBCIC,-5.45,-3.42,16.21,0.954,0.5961,9.22,"X. Song, Y. Xu, X. Tao, X. Gao, Y. Wu, R. Yu, Y. He, Y. Tao, BODIPY Cored A?D?A¡¯?D?A Type Nonfused-Ring Electron Acceptor for Efficient Polymer Solar Cells, Macromol. Rapid Commun. n/a (n.d.) 2100828. https://doi.org/10.1002/marc.202100828."
3234,O=C(C(C=C(C=CC=C1)C1=C2)=C2C/3=C(C#N)C#N)C3=C/C4=CC(C(C5=CC=C(OCC(CCCCCC)CCCC)C=C5)(C6=CC=C(OCC(CCCCCC)CCCC)C=C6)C7=C8C=CC9=C7C=CC%10=C9C(C%11=CC=C(OCC(CCCC)CCCCCC)C=C%11)(C%12=CC=C(OCC(CCCCCC)CCCC)C=C%12)C%13=C%10SC(/C=C%14C(C(C=C(C=CC=C%15)C%15=C%16)=C%16C\%14=C(C#N)/C#N)=O)=C%13)=C8S4,IHIC1,-5.47,-3.75,14.3,0.95,0.679,9.21,"J. Zhu, Y. Wu, J. Rech, J. Wang, K. Liu, T. Li, Y. Lin, W. Ma, W. You, X. Zhan, Enhancing the performance of a fused-ring electron acceptor via extending benzene to naphthalene, J. Mater. Chem. C. 6 (2017) 66¨C71. https://doi.org/10.1039/C7TC04520D."
3235,O=C(C(C=CC=C1)=C1C/2=C(C#N)C#N)C2=C/C3=CC=C(C4=CC(OC(C5=CC=C(CCCCCC)C=C5)(C6=CC=C(CCCCCC)C=C6)C7=CC8=C(C=C97)C(C%10=CC=C(CCCCCC)C=C%10)(C%11=CC=C(CCCCCC)C=C%11)OC%12=C8SC(C%13=CC=C(/C=C%14C(C(C=CC=C%15)=C%15C\%14=C(C#N)/C#N)=O)S%13)=C%12)=C9S4)S3,Ph-DTDP-TIC,-5.33,-3.89,17.31,0.89,0.5961,9.21,"M. Li, M. Yu, L. Yang, N. Yu, Y. Zhou, L. Hu, Z. Ma, C. Qin, R. Qin, J. Song, Using fullerene as the third component to boosting the photovoltaic performances of pyran acceptor, Dyes Pigments. 197 (2022) 109933. https://doi.org/10.1016/j.dyepig.2021.109933."
3236,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(C=C(/C=C5C(=O)C6=C(C=C(C)S6)C5=C(C#N)C#N)S2)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC3=C2SC(/C=C2C(=O)C4=C(C=C(Cl)S4)C2=C(C#N)C#N)=C3)C=C1,ITCC-M,-5.35,-3.69,17,1.01,0.588,9.2,"J. Cai, X. Zhang, C. Guo, Y. Zhuang, L. Wang, D. Li, D. Liu, T. Wang, Asymmetric and Halogenated Fused-Ring Electron Acceptor for Efficient Organic Solar Cells, Adv. Funct. Mater. 31 (2021) 2102189. https://doi.org/10.1002/adfm.202102189."
3237,CCCCCCCCC1(CCCCCCCC)C2=C(C=C3C(=C2)C2=C(C=C(/C=C4C(=O)C5=CC=CC=C5C4=C(C#N)C#N)S2)C3(CCCCCC)CCCCCC)C2=C1C=C1C(=C2)C(CCCCCC)(CCCCCC)C2=C1SC(/C=C1C(=O)C3=C(C=CC=C3)C1=C(C#N)C#N)=C2,FTIC-C8C6,-5.62,-3.83,16.1,0.92,0.6773,9.18,"Z. Zhang, M. Li, Y. Liu, J. Zhang, S. Feng, X. Xu, J. Song, Z. Bo, Simultaneous enhancement of the molecular planarity and the solubility of non-fullerene acceptors: effect of aliphatic side-chain substitution on the photovoltaic performance, J. Mater. Chem. A. 5 (2017) 7776¨C7783. https://doi.org/10.1039/C7TA02141K."
3238,CCCCCCC1=C(C#CC2=CC=C(C3=C4C(=O)N(CC(CC)CCCC)C(C5=CC=C(C#CC6=C(CCCCCC)C(CCCCCC)=C(/C=C7SC(=C(C#N)C#N)N(CC)C7=O)S6)S5)=C4C(=O)N3CC(CC)CCCC)S2)SC(/C=C2SC(=C(C#N)C#N)N(CC)C2=O)=C1CCCCCC,MPU3,-5.61,-3.74,13.72,0.98,0.67,9.14,"M. Privado, P. de la Cruz, S. Biswas, R. Singhal, G.D. Sharma, F. Langa, A non-fullerene all small molecule solar cell constructed with a diketopyrrolopyrrole-based acceptor having a power conversion efficiency higher than 9% and an energy loss of 0.54 eV, J. Mater. Chem. A. 6 (2018) 11714¨C11724. https://doi.org/10.1039/C8TA02633E."
3239,CCCCCCC1=CC=C(C2=C3SC4=C(C3=C(C3=CC=C(CCCCCC)C=C3)C3=C2C2=C(S3)C3=C(C=C(/C=C5C(=O)C6=C(C)SC=C6C5=C(C#N)C#N)S3)C2(C2=CC=C(CCCCCC)C=C2)C2=CC=C(CCCCCC)C=C2)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC(/C=C3C(=O)C4=C(C)SC=C4C3=C(C#N)C#N)=C2)C=C1,BTTIC-Ph,-5.48,-3.78,16.47,0.93,0.597,9.14,"T. Liu, W. Gao, Y. Wang, T. Yang, R. Ma, G. Zhang, C. Zhong, W. Ma, H. Yan, C. Yang, Unconjugated Side-Chain Engineering Enables Small Molecular Acceptors for Highly Efficient Non-Fullerene Organic Solar Cells: Insights into the Fine-Tuning of Acceptor Properties and Micromorphology, Adv. Funct. Mater. 29 (2019) 1902155. https://doi.org/10.1002/adfm.201902155."
3240,FC1=C(C2=CC=C(/C=C3C(N(CCCCCCCC)/C(S3)=C(C#N)C#N)=O)S2)C4=NSN=C4C(C(S5)=CC6=C5C7=CC(C8(C9=CC=C(CCCCCC)C=C9)C%10=CC=C(CCCCCC)C=C%10)=C(C=C7C6(C%11=CC=C(CCCCCC)C=C%11)C%12=CC=C(CCCCCC)C=C%12)C%13=C8C=C(C%14=CC(F)=C(C%15=CC=C(/C=C%16C(N(CCCCCCCC)/C(S\%16)=C(C#N)C#N)=O)S%15)C%17=NSN=C%14%17)S%13)=C1,IDT-FBTR,-5.47,-3.65,15.18,1.02,0.5755,9.14,"Y. Yang, J. Wang, H. Xu, X. Zhan, X. Chen, Nonfullerene Acceptor with ¡°Donor¨CAcceptor Combined ¦Ð-Bridge¡± for Organic Photovoltaics with Large Open-Circuit Voltage, ACS Appl. Mater. Interfaces. 10 (2018) 18984¨C18992. https://doi.org/10.1021/acsami.8b04541."
3241,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(C=C(/C=C5C(=O)C6=C(C=C(F)C(F)=C6)C5=C(C#N)C#N)S2)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC3=C2SC(C2=C(C#N)C(C#N)=C(C4=CC5=C(S4)C4=C(S5)C5=CC6=C(C=C5C4(C4=CC=C(CCCCCC)C=C4)C4=CC=C(CCCCCC)C=C4)C4=C(C5=C(C=C(/C=C7C(=O)C8=C(C=C(F)C(F)=C8)C7=C(C#N)C#N)S5)S4)C6(C4=CC=C(CCCCCC)C=C4)C4=CC=C(CCCCCC)C=C4)C4=NSN=C42)=C3)C=C1,CNDTBT-IDTT-FINCN,-5.56,-3.98,17.06,0.82,0.65,9.13,"H.S. Kim, C.E. Song, J.-W. Ha, S. Lee, S. Rasool, H.K. Lee, W.S. Shin, D.-H. Hwang, Synthesis of ITIC Derivatives with Extended ¦Ð-Conjugation as Non-Fullerene Acceptors for Organic Solar Cells, ACS Appl. Mater. Interfaces. 11 (2019) 47121¨C47130. https://doi.org/10.1021/acsami.9b15247."
3242,O=C(C(C=CC=C1)=C1C/2=C(C#N)C#N)C2=C/C3=CC4=C(S3)C5=C(C6=C(C7=CC=C(CC(CC)CCCC)S7)C(S8)=C(C9=C8C(SC(/C=C%10C(C(C=CC=C%11)=C%11C\%10=C(C#N)/C#N)=O)=C%12)=C%12C9(C%13=CC=CC=C%13)C%14=CC=CC=C%14)C(C%15=CC=C(CC(CC)CCCC)S%15)=C6S5)C4(C%16=CC=C(CCCCCC)C=C%16)C%17=CC=C(CCCCCC)C=C%17,ITIC2,-5.43,-3.8,17.01,0.9444,0.569,9.13,"J. Wang, W. Wang, X. Wang, Y. Wu, Q. Zhang, C. Yan, W. Ma, W. You, X. Zhan, Enhancing Performance of Nonfullerene Acceptors via Side-Chain Conjugation Strategy, Adv. Mater. 29 (2017) 1702125. https://doi.org/10.1002/adma.201702125."
3243,O=C(C(C=CC=C1)=C1C/2=C(C#N)C#N)C2=C/C3=CC(C(C4=CC=C(CCCCCC)C=C4)(C5=CC=C(CCCCCC)C=C5)OC6=C7SC8=C6SC9=C8OC(C%10=CC=C(CCCCCC)C=C%10)(C%11=CC=C(CCCCCC)C=C%11)C%12=C9SC(/C=C%13C(C(C=CC=C%14)=C%14C\%13=C(C#N)/C#N)=O)=C%12)=C7S3,COi6FIC,-5.6,-3.93,19.38,0.75,0.626,9.12,"T. Li, H. Zhang, Z. Xiao, J.J. Rech, H. Niu, W. You, L. Ding, A carbon¨Coxygen-bridged hexacyclic ladder-type building block for low-bandgap nonfullerene acceptors, Mater. Chem. Front. 2 (2018) 700¨C703. https://doi.org/10.1039/C8QM00004B."
3244,CCCCCCC(CCCC)COC1=CC=C(C2(C3=CC=C(OCC(CCCC)CCCCCC)C=C3)C3=C(SC(CC4C(=O)C5=C(C=CC=C5)C4=C(C#N)C#N)=C3)C3=CC=C4C(=C32)C=CC2=C4C(C3=CC=C(OCC(CCCC)CCCCCC)C=C3)(C3=CC=C(OCC(CCCC)CCCCCC)C=C3)C3=C2SC(CC2C(=O)C4=C(C=CC=C4)C2=C(C#N)C#N)=C3)C=C1,O-NTIC,-5.51,-367,13.31,0.978,0.699,9.1,"H. Feng, Y.-Q.-Q. Yi, X. Ke, Y. Zhang, X. Wan, C. Li, Y. Chen, Synergistic Modifications of Side Chains and End Groups in Small Molecular Acceptors for High Efficient Non-Fullerene Organic Solar Cells, Sol. RRL. 2 (2018) 1800053. https://doi.org/10.1002/solr.201800053."
3245,CCCCCCC1(CCCCCC)C2=CC3=C(C=C2C2=C1C=C(C1=C(F)C(F)=C(/C=C4SC(=S)N(CC)C4=O)C4=NSN=C41)S2)C(CCCCCC)(CCCCCC)C1=C3SC(C2=C(F)C(F)=C(/C=C3SC(=S)N(CC)C3=O)C3=NSN=C32)=C1,H-FFBR,-5.54,-3.93,16.9,0.94,0.57,9.1,"M. Chen, Y. Nian, Z. Hu, L. Zhang, Alkyl side chain engineering for difluorinated benzothiadiazole flanked non-fullerene acceptors toward efficient polymer solar cells, J. Mater. Sci. Mater. Electron. 32 (2021) 219¨C231. https://doi.org/10.1007/s10854-020-04757-x."
3246,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(C=C(CC5C(=O)C6=C(C=C(Cl)C(Cl)=C6)C5=C(C#N)C#N)S2)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC3=C2SC(/C=C2C(=O)C4=C(C=C(Cl)C(Cl)=C4)C2=C(C#N)C#N)=C3)C=C1,ITIC-Cl4,-5.5,-3.9,21.5,0.74,0.57,9.1,"A. Laventure, G.C. Welch, A tetrachlorinated molecular non-fullerene acceptor for high performance near-IR absorbing organic solar cells, J. Mater. Chem. C. 6 (2018) 9060¨C9064. https://doi.org/10.1039/C8TC02701C."
3247,CCCCC(CC)CC1(CC(CC)CCCC)C2=C(SC(/C=C3C(=O)C4=CC5=CC(F)=C(F)C=C5C=C4C3=C(C#N)C#N)=C2)C2=C1C=C(C1=C(F)C(F)=C(C3=CC4=C(S3)C3=C(C=C(/C=C5C(=O)C6=CC7=CC(F)=C(F)C=C7C=C6C5=C(C#N)C#N)S3)C4(CC(CC)CCCC)CC(CC)CCCC)C(F)=C1)S2,OF¨CPCIC,-5.66,-3.86,13.76,0.91,0.7337,9.09,"S. Li, L. Zhan, W. Zhao, S. Zhang, B. Ali, Z. Fu, T.-K. Lau, X. Lu, M. Shi, C.-Z. Li, J. Hou, H. Chen, Revealing the effects of molecular packing on the performances of polymer solar cells based on A¨CD¨CC¨CD¨CA type non-fullerene acceptors, J. Mater. Chem. A. 6 (2018) 12132¨C12141. https://doi.org/10.1039/C8TA03753A."
3248,CCCCCCCCC1=C(/C=C2C(=O)C3=CC(F)=C(F)C=C3C2=C(C#N)C#N)SC(C2=CC(CC(CC)CCCC)=C(C3=C(CC(CC)CCCC)C=C(C4=CC(CCCCCCCC)=C(/C=C5C(=O)C6=CC(F)=C(F)C=C6C5=C(C#N)C#N)S4)S3)S2)=C1,4T-2,-5.85,-4.02,15.68,0.82,0.7032,9.09,"Y. Zhou, M. Li, H. Lu, H. Jin, X. Wang, Y. Zhang, S. Shen, Z. Ma, J. Song, Z. Bo, High-Efficiency Organic Solar Cells Based on a Low-Cost Fully Non-Fused Electron Acceptor, Adv. Funct. Mater. 31 (2021) 2101742. https://doi.org/10.1002/adfm.202101742."
3249,CCCCCCCCCCCCCCCCC1(CCCCCCCCCCCCCCCC)C2=CC3=C(C=C2C2=C1C=C(/C=C1C(=O)C4=CSC=C4C1=C(C#N)C#N)S2)C(CCCCCCCCCCCCCCCC)(CCCCCCCCCCCCCCCC)C1=C3SC(/C=C2C(=O)C3=CSC=C3C2=C(C#N)C#N)=C1,IDTC16-Th,-5.55,-3.71,13.1,0.998,0.6959,9.09,"H. Lin, M.A. Adil, Q. Zhang, J. Zhang, Q. Wang, Small-molecule acceptors with long alkyl chains for high-performance as-cast nonfullerene organic solar cells, Org. Electron. 93 (2021) 106167. https://doi.org/10.1016/j.orgel.2021.106167."
3250,CCCCC(CC)COC1=C(OCC(CC)CCCC)C(C2=CC3=C(S2)C2=C(CC(/C=C4C(=O)C5=C(C=C(F)C(F)=C5)C4=C(C#N)C#N)S2)C3(CC(CC)CCCC)CC(CC)CCCC)=C2N=CC=NC2=C1C1=CC2=C(S1)C1=C(C=C(/C=C3C(=O)C4=C(C=C(Cl)C(Cl)=C4)C3=C(C#N)C#N)S1)C2(CC(CC)CCCC)CC(CC)CCCC.Cl,QCIC2,-5.52,-3.84,18.65,0.807,0.6603,9.09,"S. Ye, S. Chen, S. Li, Y. Pan, X. Xia, W. Fu, L. Zuo, X. Lu, M. Shi, H. Chen, Synergistic Effects of Chlorination and Branched Alkyl Side Chain on the Photovoltaic Properties of Simple Non-Fullerene Acceptors with Quinoxaline as the Core, ChemSusChem. 14 (2021) 3599¨C3606. https://doi.org/10.1002/cssc.202100689."
3251,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=C(SC(/C=C4C(=O)C5=C(C=C(F)C(F)=C5)C4=C(C#N)C#N)=C3)C3=C2C2=C(S3)C(C3=CC=C(CC(CC)CCCC)S3)=C3C(=C2C2=CC=C(CC(CC)CCCC)S2)SC2=C3C(C3=CC=C(CCCCCC)C=C3)(C3=CC=C(CCCCCC)C=C3)C3=C2SC(/C=C2C(=O)C4=C(C=C(F)C(F)=C4)C2=C(C#N)C#N)=C3)C=C1,BDTThIT-4F,-5.57,-3.92,17.52,0.746,0.708,9.08,"M. Zhang, Z. Xiao, W. Gao, Q. Liu, K. Jin, W. Wang, Y. Mi, Q. An, X. Ma, X. Liu, C. Yang, L. Ding, F. Zhang, Over 13% Efficiency Ternary Nonfullerene Polymer Solar Cells with Tilted Up Absorption Edge by Incorporating a Medium Bandgap Acceptor, Adv. Energy Mater. 8 (2018) 1801968. https://doi.org/10.1002/aenm.201801968."
3252,O=C(C1=C2C(C3=C(SC(C4=CC5=C(C6=CC(C7(C8=CC=C(CCCCCC)C=C8)C9=CC=C(CCCCCC)C=C9)=C(C%10=C7C=C(C%11=CC%12=C(C(N(CC(CC)CCCC)C%13=O)=O)C%14=C%13C=CC(C(N(CC(CC)CCCC)C%15=O)=O)=C%14C%15=C%12S%11)S%10)C=C6C5(C%16=CC=C(CCCCCC)C=C%16)C%17=CC=C(CCCCCC)C=C%17)S4)=C%18)C%18=C2%19)=C(C(N(CC(CC)CCCC)C3=O)=O)C=C1)N(CC(CC)CCCC)C%19=O,IDT-NTI-2EH,-5.4,-3.9,14.43,0.92,0.69,9.07,"J. Hamonnet, M. Nakano, K. Nakano, H. Sugino, K. Takimiya, K. Tajima, Bis(naphthothiophene diimide)indacenodithiophenes as Acceptors for Organic Photovoltaics, Chem. Mater. 29 (2017) 9618¨C9622. https://doi.org/10.1021/acs.chemmater.7b03733."
3253,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)S3)C3=CC4=C(C=C3C3=C2C2=C(C=C(/C=C5C(=O)C6=C(C=CC(F)=C6)C5=C(C#N)C#N)S2)S3)C(C2=CC=C(CCCCCC)S2)(C2=CC=C(CCCCCC)S2)C2=C4SC3=C2SC(/C=C2C(=O)C4=C(C=C(F)C(F)=C4)C2=C(C#N)C#N)=C3)S1,ITIC-Th2,-5.75,-4.07,17.19,0.751,0.7007,9.06,"Z. Li, S. Dai, J. Xin, L. Zhang, Y. Wu, J. Rech, F. Zhao, T. Li, K. Liu, Q. Liu, W. Ma, W. You, C. Wang, X. Zhan, Enhancing the performance of the electron acceptor ITIC-Th via tailoring its end groups, Mater. Chem. Front. 2 (2018) 537¨C543. https://doi.org/10.1039/C7QM00547D."
3254,CCN(C/1=O)C(SC1=C/C2=C(F)C(F)=C(C(S3)=CC4=C3C5=CC(C6(C7=CC=C(CCCCCC)C=C7)C8=CC=C(CCCCCC)C=C8)=C(C=C5C4(C9=CC=C(CCCCCC)C=C9)C%10=CC=C(CCCCCC)C=C%10)C%11=C6C=C(C%12=C(F)C(F)=C(/C=C%13SC(N(CC)C\%13=O)=S)C%14=NSN=C%12%14)S%11)C%15=NSN=C2%15)=S,IffBR,-5.71,-3.77,14.52,0.908,0.6747,9.06,"W. Zhong, J. Cui, B. Fan, L. Ying, Y. Wang, X. Wang, G. Zhang, X.-F. Jiang, F. Huang, Y. Cao, Enhanced Photovoltaic Performance of Ternary Polymer Solar Cells by Incorporation of a Narrow-Bandgap Nonfullerene Acceptor, Chem. Mater. 29 (2017) 8177¨C8186. https://doi.org/10.1021/acs.chemmater.7b02228."
3255,O=C(C(C=C(F)C(F)=C1)=C1C/2=C(C#N)C#N)C2=C/C3=CC(C4(C5=CC=C(CCCCCC)C=C5)C6=CC=C(CCCCCC)C=C6)=C(S3)C7=C4C8=CC(CCCCCCCCCCCC)=C(C(SC9=C%10C(C%11=CC=C(CCCCCC)C=C%11)(C%12=CC=C(CCCCCC)C=C%12)C%13=C9SC(/C=C%14C(C(C=C(F)C(F)=C%15)=C%15C\%14=C(C#N)/C#N)=O)=C%13)=C%10C=C%16CCCCCCCCCCCC)C%16=C8S7,DTNIC8,-5.91,-3.92,12.92,0.96,0.7284,9.03,"Y. Ma, M. Zhang, Y. Yan, J. Xin, T. Wang, W. Ma, C. Tang, Q. Zheng, Ladder-Type Dithienonaphthalene-Based Small-Molecule Acceptors for Efficient Nonfullerene Organic Solar Cells, Chem. Mater. 29 (2017) 7942¨C7952. https://doi.org/10.1021/acs.chemmater.7b02887."
3256,O=C(C1=CSC=C1C/2=C(C#N)C#N)C2=C/C3=CC4=C(S3)C5=C(C6=C(C5(C7=CC=C(CCCCCC)[Se]7)C8=CC=C(CCCCCC)[Se]8)C=C(C9=C%10C(SC(/C=C%11C(C%12=CSC=C%12C\%11=C(C#N)/C#N)=O)=C%13)=C%13S9)C(C%10(C%14=CC=C(CCCCCC)[Se]%14)C%15=CC=C(CCCCCC)[Se]%15)=C6)S4,ITCPTC-Se,-5.65,4,15.2,0.87,0.683,9.02,"W. Gao, Q. An, R. Ming, D. Xie, K. Wu, Z. Luo, Y. Zou, F. Zhang, C. Yang, Side Group Engineering of Small Molecular Acceptors for High-Performance Fullerene-Free Polymer Solar Cells: Thiophene Being Superior to Selenophene, Adv. Funct. Mater. 27 (2017) 1702194. https://doi.org/10.1002/adfm.201702194."
3257,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C=C(C2=C(OCC(CC)CCCC)C=C(CC5C(=O)C6=CC(F)=CC=C6C5=C(C#N)C#N)S2)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC(C3=C(OCC(CC)CCCC)C=C(/C=C4C(=O)C5=CC=C(F)C=C5C4=C(C#N)C#N)S3)=C2)C=C1,IOTIC-2F,-5.34,-4.06,20.7,0.779,0.56,9,"J. Lee, S.-J. Ko, M. Seifrid, H. Lee, C. McDowell, B.R. Luginbuhl, A. Karki, K. Cho, T.-Q. Nguyen, G.C. Bazan, Design of Nonfullerene Acceptors with Near-Infrared Light Absorption Capabilities, Adv. Energy Mater. 8 (2018) 1801209. https://doi.org/10.1002/aenm.201801209."
3258,CCCCCCCCCCCC1=C(/C=C2C(=O)C3=C(C=C4C=CC=CC4=C3)C2=C(C#N)C#N)SC2=C1SC1=C2N(CC(CC)CCCC)C2=C1C1=NSN=C1C1=C2N(CC(CC)CCCC)C2=C1SC1=C2SC(/C=C2C(=O)C3=C(C=C4C=C(F)C(F)=CC4=C3)C2=C(C#N)C#N)=C1CCCCCCCCCCC,BT-L4F,-5.57,-4,21.2,0.84,0.513,9,"G. Li, X. Zhang, L.O. Jones, J.M. Alzola, S. Mukherjee, L. Feng, W. Zhu, C.L. Stern, W. Huang, J. Yu, V.K. Sangwan, D.M. DeLongchamp, K.L. Kohlstedt, M.R. Wasielewski, M.C. Hersam, G.C. Schatz, A. Facchetti, T.J. Marks, Systematic Merging of Nonfullerene Acceptor ¦Ð-Extension and Tetrafluorination Strategies Affords Polymer Solar Cells with >16% Efficiency, J. Am. Chem. Soc. 143 (2021) 6123¨C6139. https://doi.org/10.1021/jacs.1c00211."
3259,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C=C(/C=C2C(=O)C5=C(C=C6C=CC=CC6=C5)C2=C(C#N)C#N)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC(/C=C3C(=O)C4=C(C=C5C=CC=CC5=C4)C3=C(C#N)C#N)=C2)C=C1,IDT-N,-5.84,-3.95,15.88,0.79,0.7191,8.99,"R. Li, G. Liu, R. Xie, Z. Wang, X. Yang, K. An, W. Zhong, X.-F. Jiang, L. Ying, F. Huang, Y. Cao, Introducing cyclic alkyl chains into small-molecule acceptors for efficient polymer solar cells, J. Mater. Chem. C. 6 (2018) 7046¨C7053. https://doi.org/10.1039/C8TC01780H."
3260,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=CC5=C(C=C4C=C3C3=C2C2=C(S3)C3=C(C=C(/C=C4C(=O)C6=C(C=C(F)C(F)=C6)C4=C(C#N)C#N)S3)S2)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C5SC3=C2SC2=C3SC(/C=C3C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)=C2)C=C1,FTIC1,-5.53,-4.03,13.8,0.943,0.685,8.98,"B. Lu, Z. Zhang, B. Jia, G. Cai, J. Zhu, X. Lu, X. Zhan, Y. Yao, Precise Synthesis of Fused Decacyclic Electron Acceptor Isomers for Organic Solar Cells, Sol. RRL. 5 (2021) 2100163. https://doi.org/10.1002/solr.202100163."
3261,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(S3)C3=C(S2)C2=C5C6=C3C=C3C(=O)N(C(CCCCC)CCCCC)C(=O)C7=CC(F)=C(C8=C(F)C=C9C(=O)N(C(CCCCC)CCCCC)C(=O)C(=C2)C9=C85)C6=C73)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC3=C2SC2=C3C3=C4C5=C2C=C2C(=O)N(C(CCCCC)CCCCC)C(=O)C6=CC(F)=C(C7=C4C4=C(C=C7F)C(=O)N(C(CCCCC)CCCCC)C(=O)C4=C3)C5=C62)C=C1,F-2PDI-4F,-5.55,-3.81,13.42,1,0.668,8.96,"Y. Wang, H. Zhong, Y. Hong, T. Shan, K. Ding, L. Zhu, F. Liu, H. Wei, C. Yu, H. Zhong, Tailoring the molecular geometry of polyfluoride perylene diimide acceptors towards efficient organic solar cells, J. Mater. Chem. C. 8 (2020) 8224¨C8233. https://doi.org/10.1039/D0TC01707H."
3262,CCCCCCC(CCCC)CC1(CC(CCCC)CCCCCC)C2=C(SC(CC3C(=O)C4=CC=CC=C4C3=C(C#N)C#N)=C2)C2=C1C=C(C1=CC3=C(S1)C1=C(C=C(C4=CC5=C(S4)C4=C(C=C(CC6C(=O)C7=C(C=CC=C7)C6=C(C#N)C#N)S4)C5(CC(CCCC)CCCCCC)CC(CCCC)CCCCCC)S1)C1=NSN=C13)S2,BTCD-IC,-5.42,-3.82,16.15,0.89,0.64,8.96,"Z. Liu, Q. Mao, J. Wang, F. Wu, D. Zhou, Y. Cheng, S. Huang, B. Huang, C. Yang, L. Chen, Exploiting Novel Unfused-Ring Acceptor for Efficient Organic Solar Cells with Record Open-Circuit Voltage and Fill Factor, ChemSusChem. n/a (n.d.) e202102563. https://doi.org/10.1002/cssc.202102563."
3263,CCCCCCCCC(CCCCCCCC)N1C2=C(SC3=C2SC(/C=C2C(=O)C4=C(C=C(F)C(F)=C4)C2=C(C#N)C#N)=C3)C2=C1C1=C(C=C(/C=C3C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)S1)S2,DTP-C17-4F,-5.59,-4.16,21.17,0.691,0.611,8.94,"X. Chen, H. Liu, L. Xia, T. Hayat, A. Alsaedi, Z. Tan, A pentacyclic S,N-heteroacene based electron acceptor with strong near-infrared absorption for efficient organic solar cells, Chem. Commun. 55 (2019) 7057¨C7060. https://doi.org/10.1039/C9CC03536B."
3264,CCCCCCC(CCCC)N1C(=O)C2=CC=C3C4=C(C=CC(=C24)C1=O)C1=CC=C2C(=O)N(C(CCCC)CCCCCC)C(=O)C4=C2C1=C3C(C1=NC(C2=CC3=C5C(=CC=C6C7=CC=C8C(=O)N(C(CCCC)CCCCCC)C(=O)C9=C8C7=C(C=C9)C2=C65)C(=O)N(C(CCCC)CCCCCC)C3=O)=NC(C2=CC3=C5C(=CC=C6C7=CC=C8C(=O)N(C(CCCC)CCCCCC)C(=O)C9=C8C7=C(C=C9)C2=C65)C(=O)N(C(CCCC)CCCCCC)C3=O)=N1)=C4,Ta-PDI,-6.03,-3.81,17.1,0.78,0.685,8.91,"Y. Duan, X. Xu, H. Yan, W. Wu, Z. Li, Q. Peng, Pronounced Effects of a Triazine Core on Photovoltaic Performance¨CEfficient Organic Solar Cells Enabled by a PDI Trimer-Based Small Molecular Acceptor, Adv. Mater. 29 (2017) 1605115. https://doi.org/10.1002/adma.201605115."
3265,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=C(SC(/C=C4C(=O)C5=C(C=CC=C5)C4=C(C#N)C#N)=C3)C3=C2C2=C(S3)C3=C(S2)C2=C(C=C(/C=C4C(=O)C5=C(C=CC=C5)C4=C(C#N)C#N)S2)C32C3=CC=C(CCCCCC)C=C3C3=C2C=CC(CCCCCC)=C3)C=C1,4TIC,-5.56,-4.03,17.3,0.78,0.66,8.91,"X. Liao, H. Pei, H. Zhao, Y. Cui, L. Li, X. Shi, P. Zhu, W. Ma, Y. Chen, A.K.-Y. Jen, The synergistic effects of central core size and end group engineering on performance of narrow bandgap nonfullerene acceptors, Chem. Eng. J. 435 (2022) 135020. https://doi.org/10.1016/j.cej.2022.135020."
3266,CCCCCCCCC1(CCCCCCCC)C2=C(C=C3C(=C2)C2=C(C=C(/C=C4C(=O)C5=CC=CC=C5C4=C(C#N)C#N)S2)C3(C2=CC=C(CCCCCC)C=C2)C2=CC=C(CCCCCC)C=C2)C2=C1C1=C(S2)C2=C(C=C3C(=C2)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C3SC(/C=C3C(=O)C4=CC=CC=C4C3=C(C#N)C#N)=C2)C1(CCCCCCCC)CCCCCCCC,IDIDTT ,-5.5,-3.84,14.03,0.99,0.6413,8.91,"R. Hou, M. Li, J. Wang, Z. Bi, S. Feng, X. Xu, W. Ma, Z. Bo, Nonfullerene acceptors with a novel nonacyclic core for high-performance polymer solar cells, J. Mater. Chem. C. 7 (2019) 3335¨C3341. https://doi.org/10.1039/C8TC06245E."
3267,CCCCCCCCC1=CC=C(C2(C3=CC=C(CCCCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(S3)C3=C(C=C(/C=C5C(=O)C6=C(C=CC=C6)C5=C(C#N)C#N)S3)S2)C(C2=CC=C(CCCCCCCC)C=C2)(C2=CC=C(CCCCCCCC)C=C2)C2=C4SC3=C2SC2=C3SC(/C=C3C(=O)C4=C(C=CC=C4)C3=C(C#N)C#N)=C2)C=C1,3TP3T-IC,-5.55,-3.88,13,1.05,0.656,8.9,"J. Song, C. Li, L. Zhu, J. Guo, J. Xu, X. Zhang, K. Weng, K. Zhang, J. Min, X. Hao, Y. Zhang, F. Liu, Y. Sun, Ternary Organic Solar Cells with Efficiency >16.5% Based on Two Compatible Nonfullerene Acceptors, Adv. Mater. 31 (2019) 1905645. https://doi.org/10.1002/adma.201905645."
3268,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(C=C(/C=C5C(=O)C6=CC(I)=CC=C6C5=C(C#N)C#N)S2)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC3=C2SC(/C=C2C(=O)C4=CC(I)=CC=C4C2=C(C#N)C#N)=C3)C=C1,I-ITIC,-5.68,-4.14,14.5,0.95,0.65,8.9,"F. Yang, C. Li, W. Lai, A. Zhang, H. Huang, W. Li, Halogenated conjugated molecules for ambipolar field-effect transistors and non-fullerene organic solar cells, Mater. Chem. Front. 1 (2017) 1389¨C1395. https://doi.org/10.1039/C7QM00025A."
3269,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)S3)C3=CC4=C(C=C3C3=C2C2=C(C=C(/C=C5C(=O)C6=C(C=CC=C6)C5=C(C#N)C#N)S2)S3)C(C2=CC=C(CCCCCC)S2)(C2=CC=C(CCCCCC)S2)C2=C4SC3=C2SC(/C=C2C(=O)C4=C(C=CC=C4)C2=C(C#N)C#N)=C3)S1,ITIC-TH,-5.66,-3.93,15.84,0.915,0.6126,8.88,"F. Zhao, S. Dai, Y. Wu, Q. Zhang, J. Wang, L. Jiang, Q. Ling, Z. Wei, W. Ma, W. You, C. Wang, X. Zhan, Single-Junction Binary-Blend Nonfullerene Polymer Solar Cells with 12.1% Efficiency, Adv. Mater. 29 (2017) 1700144. https://doi.org/10.1002/adma.201700144."
3270,O=C(C(C=CC=C1)=C1C/2=C(C#N)C#N)C2=C/C3=CC4=C(S3)C5=C(C6=CC(C7(C8=CC=C(CCCCCC)S8)C9=CC=C(CCCCCC)S9)=C(C%10=C7C(SC(/C=C%11C(C(C=CC=C%12)=C%12C\%11=C(C#N)C#N)=O)=C%13)=C%13S%10)C=C6C5(C%14=CC=C(CCCCCC)S%14)C%15=CC=C(CCCCCC)S%15)S4,ITIC-Th,-5.66,-3.93,15.84,0.915,0.6126,8.88,"Z. Li, S. Dai, J. Xin, L. Zhang, Y. Wu, J. Rech, F. Zhao, T. Li, K. Liu, Q. Liu, W. Ma, W. You, C. Wang, X. Zhan, Enhancing the performance of the electron acceptor ITIC-Th via tailoring its end groups, Mater. Chem. Front. 2 (2018) 537¨C543. https://doi.org/10.1039/C7QM00547D."
3271,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=C(SC(/C=C4C(=O)C5=C(C)SC=C5C4=C(C#N)C#N)=C3)C3=C2C2=C(S3)C3=C(S2)C2=C(C4=C(C=C(/C=C5C(=O)C6=C(C)SC=C6C5=C(C#N)C#N)S4)S2)C3(C2=CC=C(CCCCCC)C=C2)C2=CC=C(CCCCCC)C=C2)C=C1,T7Me,-5.45,-3.93,17.12,0.89,0.5879,8.87,"R. Ming, J. Wang, W. Gao, M. Zhang, J. Gao, W. Ning, Z. Luo, X. Liu, C. Zhong, F. Zhang, C. Yang, Fused-Ring Core Engineering for Small Molecule Acceptors Enable High-Performance Nonfullerene Polymer Solar Cells, Small Methods. 3 (2019) 1900280. https://doi.org/10.1002/smtd.201900280."
3272,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=C(SC(C4=CC=C(/C=C5C(=O)C6=CC(F)=C(F)C=C6C5=C(C#N)C#N)S4)=C3OCC(CC)CCCC)C3=C2C2=C(S3)C3=C(S2)C2=C(C(OCC(CC)CCCC)=C(C4=CC=C(/C=C5C(=O)C6=C(C=C(F)C(F)=C6)C5=C(C#N)C#N)S4)S2)C3(C2=CC=C(CCCCCC)C=C2)C2=CC=C(CCCCCC)C=C2)C=C1,4TO-T-4F,-5.3,-3.85,20.4,0.75,0.5805,8.87,"D. Liu, T. Wang, X. Ke, N. Zheng, Z. Chang, Z. Xie, Y. Liu, Ultra-narrow bandgap non-fullerene acceptors for organic solar cells with low energy loss, Mater. Chem. Front. 3 (2019) 2157¨C2163. https://doi.org/10.1039/C9QM00505F."
3273,CCCCCCOC1=C(/C=C2C(=O)C3=C(C=CC=C3)C2=C(C#N)C#N)SC(C2=CC3=C(S2)C2=CC4=C(C=C2C3(C2=CC=C(CCCCCC)C=C2)C2=CC=C(CCCCCC)C=C2)C2=C(C=C(C3=C(OCCCCCC)C(OCCCCCC)=C(/C=C5C(=O)C6=C(C=CC=C6)C5=C(C#N)C#N)S3)S2)C4(C2=CC=C(CCCCCC)C=C2)C2=CC=C(CCCCCC)C=C2)=C1OCCCCCC,TOIC,,,15.73,1.024,0.551,8.87,"Y. Liu, C. Zhang, D. Hao, Z. Zhang, L. Wu, M. Li, S. Feng, X. Xu, F. Liu, X. Chen, Z. Bo, Enhancing the Performance of Organic Solar Cells by Hierarchically Supramolecular Self-Assembly of Fused-Ring Electron Acceptors, Chem. Mater. 30 (2018) 4307¨C4312. https://doi.org/10.1021/acs.chemmater.8b01319."
3274,O=C1N(C(CCCCC)CCCCC)C(C2=C(C1C=C3[Se]4)C5=C3C(C4=CC6C(N(C(CCCCC)CCCCC)C7=O)=O)=C(C6=C7C=C8C9=CC%10C%11=C(C(N(C(CCCCC)CCCCC)C%10=O)=O)C=CC%12=C%13C(C%14=C%15C=C%13C%16=CC%17=C%18C%19=C%20C%21=C%22C(C=CC(C(N(C(CCCCC)CCCCC)C%23=O)=O)=C%22C%23C=C%21[Se]C%20=CC%18C(N(C(CCCCC)CCCCC)C%17=O)=O)=C%19%16)=C(C=CC%14C(N(C(CCCCC)CCCCC)C%15=O)=O)C9=C%12%11)C8=C5C=C2)=O,Tri-PDI-Se,-5.94,-3.86,17.15,0.77,0.668,8.82,"Y. Duan, X. Xu, Y. Li, Z. Li, Q. Peng, Chalcogen-Atom-Annulated Perylene Diimide Trimers for Highly Efficient Nonfullerene Polymer Solar Cells, Macromol. Rapid Commun. 38 (2017) 1700405. https://doi.org/10.1002/marc.201700405."
3275,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C=C(C2=CC=C(/C=C5SC(=S)N(CC)C5=O)C5=NSN=C25)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC(C3=CC=C(/C=C4SC(=S)N(CC)C4=O)C4=NSN=C34)=C2)C=C1,IDT-BT-R2,-5.31,-3.7,13.57,1.04,0.6264,8.82,"L.-M. Tang, J. Xiao, W.-Y. Bai, Q.-Y. Li, H.-C. Wang, M.-S. Miao, H.-L. Yip, Y.-X. Xu, End-chain effects of non-fullerene acceptors on polymer solar cells, Org. Electron. 64 (2019) 1¨C6. https://doi.org/10.1016/j.orgel.2018.10.005."
3276,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(C=C(/C=C5C(=O)C6=CC(F)=CC=C6C5=C(C#N)C#N)S2)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC3=C2SC(/C=C2C(=O)C4=CC(F)=CC=C4C2=C(C#N)C#N)=C3)C=C1,F-ITIC,-5.65,-4.09,14.1,0.94,0.66,8.8,"F. Yang, C. Li, W. Lai, A. Zhang, H. Huang, W. Li, Halogenated conjugated molecules for ambipolar field-effect transistors and non-fullerene organic solar cells, Mater. Chem. Front. 1 (2017) 1389¨C1395. https://doi.org/10.1039/C7QM00025A."
3277,CCCCCCCCC1(CCCCCCCC)C2=C(C=CC(C3=CC=C(/C=C4C(=O)C5=CSC=C5C4=C(C#N)C#N)S3)=C2)C2=C1C=C(C1=CC=C(/C=C3C(=O)C4=CSC=C4C3=C(C#N)C#N)S1)C=C2,DTC-T-F,-5.48,-3.83,17.46,0.78,0.646,8.8,"J. Liao, P. Zheng, Z. Cai, S. Shen, G. Xu, H. Zhao, Y. Xu, Construction of simple and low-cost acceptors for efficient non-fullerene organic solar cells, Org. Electron. 89 (2021) 106026. https://doi.org/10.1016/j.orgel.2020.106026."
3278,CCCCCCCCC(CCCCCC)CN1C(=O)C2=C(C3=CC4=C(S3)C3=C(C=C(/C=C5C(=O)C6=C(C=C(F)C(F)=C6)C5=C(C#N)C#N)S3)C4(CC(CC)CCCC)CC(CC)CCCC)SC(C3=CC4=C(S3)C3=C(C=C(/C=C5C(=O)C6=C(C=C(F)C(F)=C6)C5=C(C#N)C#N)S3)C4(CC(CC)CCCC)CC(CC)CCCC)=C2C1=O,TCIC2F,-5.59,-3.89,19.1,0.713,0.646,8.8,"Y. Li, H. Fu, Z. Wu, X. Wu, M. Wang, H. Qin, F. Lin, H.Y. Woo, A.K.-Y. Jen, Regulating the Aggregation of Unfused Non-Fullerene Acceptors via Molecular Engineering towards Efficient Polymer Solar Cells, ChemSusChem. 14 (2021) 3579¨C3589. https://doi.org/10.1002/cssc.202100746."
3279,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(C=C(/C=C5C(=O)C6=CC=CC=C6C5=C(C#N)C#N)S2)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC3=C2SC(/C=C2C(=O)C4=CC=CC=C4C2=C(C#N)C#N)=C3)C=C1,ITIC-C6,-5.7,-4,15.6,0.87,0.65,8.77,"T.J. Aldrich, S.M. Swick, F.S. Melkonyan, T.J. Marks, Enhancing Indacenodithiophene Acceptor Crystallinity via Substituent Manipulation Increases Organic Solar Cell Efficiency, Chem. Mater. 29 (2017) 10294¨C10298. https://doi.org/10.1021/acs.chemmater.7b04616."
3280,CCCCCCC(CCCC)CC1=C(C2=NC3=C(N=C(C4=C(CC(CCCC)CCCCCC)C=C(C5=CC=C(C=C(C#N)C#N)C6=NSN=C56)S4)S3)S2)SC(C2=CC=C(C=C(C#N)C#N)C3=NSN=C23)=C1,TTZ1,-5.7,-3.86,15.43,0.9,0.6318,8.77,"W. Peng, G. Zhang, L. Shao, C. Ma, B. Zhang, W. Chi, Q. Peng, W. Zhu, Simple-structured small molecule acceptors constructed by a weakly electron-deficient thiazolothiazole core for high-efficiency non-fullerene organic solar cells, J. Mater. Chem. A. 6 (2018) 24267¨C24276. https://doi.org/10.1039/C8TA09370A."
3281,CCN1C(/C(S/C1=C(C#N)/C#N)=C/C2=CC=C(C(S3)=CC(CC(CCCC)CCCCCC)=C3C4=NC5=C(N=C(C6=C(CC(CCCC)CCCCCC)C=C(C7=CC=C(/C=C(C(N/8CC)=O)SC8=C(C#N)C#N)C9=NSN=C79)S6)S5)S4)C%10=NSN=C2%10)=O,TTz2,-5.5,-3.8,15.43,0.9,0.63,8.77,"W. Peng, G. Zhang, L. Shao, C. Ma, B. Zhang, W. Chi, Q. Peng, W. Zhu, Simple-structured small molecule acceptors constructed by a weakly electron-deficient thiazolothiazole core for high-efficiency non-fullerene organic solar cells, J. Mater. Chem. A. 6 (2018) 24267¨C24276. https://doi.org/10.1039/C8TA09370A."
3282,CCCCC(CC)CC1(CC(CC)CCCC)C2=CC=C3C(=C2C2=C1C=C(/C=C1C(=O)C4=C(CCC(F)=C4)C1=C(C#N)C#N)S2)C=CC1=C3C2=C(C=C(/C=C3C(=O)C4=C(C=CC(F)=C4)C3=C(C#N)C#N)S2)C1(CC(CC)CCCC)CC(CC)CCCC,DTNIF,-5.82,-3.92,13.26,0.9,0.7277,8.73,"M. Zhang, Y. Ma, Q. Zheng, Dithienonaphthalene-Based Non-fullerene Acceptors With Different Bandgaps for Organic Solar Cells, Front. Chem. 6 (2018). https://www.frontiersin.org/article/10.3389/fchem.2018.00427 (accessed March 7, 2022)."
3283,CCCCC(CC)CC1(CC(CC)CCCC)C2=C(C=CC(C3=CC=C(/C=C4C(=O)C5=CC=CC=C5C4=C(C#N)C#N)S3)=C2)C2=C1C1=C(C=C(C3=CC=C(/C=C4C(=O)C5=CC=CC=C5C4=C(C#N)C#N)S3)C=C1)C2(CC(CC)CCCC)CC(CC)CCCC,YITI-0F,-5.59,-3.86,13.3,0.978,0.6718,8.73,"Q. Yue, Z. Zhou, S. Xu, J. Zhang, X. Zhu, Design and synthesis of medium-bandgap small-molecule electron acceptors for efficient tandem solar cells, J. Mater. Chem. A. 6 (2018) 13588¨C13592. https://doi.org/10.1039/C8TA04405H."
3284,O=C(C(C=CC=C1)=C1C/2=C(C#N)C#N)C2=C/C3=CC4=C(C5=CC(C6(CCCCCC)CCCCCC)=C(C7=C6C=C(/C=C8C(C(C=CC=C9)=C9C8=C(C#N)C#N)=O)S7)C=C5C4(CCCCCC)CCCCCC)S3,IC-C6IDT-IC,-5.69,-3.91,15.05,0.89,0.63,8.71,"Y. Lin, Q. He, F. Zhao, L. Huo, J. Mai, X. Lu, C.-J. Su, T. Li, J. Wang, J. Zhu, Y. Sun, C. Wang, X. Zhan, A Facile Planar Fused-Ring Electron Acceptor for As-Cast Polymer Solar Cells with 8.71% Efficiency, J. Am. Chem. Soc. 138 (2016) 2973¨C2976. https://doi.org/10.1021/jacs.6b00853."
3285,O=C(N(CC)/C(S/1)=C(C#N)C#N)C1=C/C2=CN=C(C3=CC4=C(C5=C(C4(C6=CC=C(CCCCCC)C=C6)C7=CC=C(CCCCCC)C=C7)C=C(C8=C9C=C(C%10=NC=C(/C=C%11C(N(CC)/C(S\%11)=C(C#N)C#N)=O)S%10)S8)C(C9(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)=C5)S3)S2,IDTzCR1:1,-5.67,-3.77,13.8,1.04,0.607,8.71,"P. Ye, Y. Chen, J. Wu, X. Wu, S. Yu, W. Xing, Q. Liu, X. Jia, A. Peng, H. Huang, Wide bandgap small molecular acceptors for low energy loss organic solar cells, J. Mater. Chem. C. 5 (2017) 12591¨C12596. https://doi.org/10.1039/C7TC04669C."
3286,O=C(N(CC)C(S/1)=S)C1=C/C2=CC=C(C3=CC4=C(C5=CC=C(C6=CC=C(C7=CC=C(/C=C8C(N(CC)C(S8)=S)=O)C9=NSN=C79)S6)C=C5C4(C%10=CC=C(CCCCCC)C=C%10)C%11=CC=C(CCCCCC)C=C%11)S3)C%12=NSN=C2%12,TIDT-R2,-5.25,-3.65,13.1,1.04,0.639,8.7,"S. Feng, C. Zhang, Z. Bi, Y. Liu, P. Jiang, S. Ming, X. Xu, W. Ma, Z. Bo, Controlling Molecular Packing and Orientation via Constructing a Ladder-Type Electron Acceptor with Asymmetric Substituents for Thick-Film Nonfullerene Solar Cells, ACS Appl. Mater. Interfaces. 11 (2019) 3098¨C3106. https://doi.org/10.1021/acsami.8b19596."
3287,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=C(SC(/C=C4C(=O)C5=C(C=CC=C5)C4=C(C#N)C#N)=C3)C3=C2C2=C(O3)C(C3=CC=C(CC(CC)CCCC)S3)=C3C(=C2C2=CC=C(CC(CC)CCCC)S2)OC2=C3C(C3=CC=C(CCCCCC)C=C3)(C3=CC=C(CCCCCC)C=C3)C3=C2SC(/C=C2C(=O)C4=C(C=CC=C4)C2=C(C#N)C#N)=C3)C=C1,BFHIC,-5.61,-3.83,15.9,0.97,0.558,8.7,"K. Wang, J. Chen, J. Hu, X. Guo, M. Zhang, Y. Li, A small molecule acceptor with a heptacyclic benzodi(thienocyclopentafuran) central unit achieving 13.4% efficiency in polymer solar cells with low energy loss, J. Mater. Chem. C. 9 (2021) 2744¨C2751. https://doi.org/10.1039/D0TC05539E."
3288,CCCCCCCCCCC1(CCCCCCCCCC)C2=C(C=CC(C3=C(F)C=C(C#CC4=CC=C5C(=O)N(CC(CC)CCCC)C(=O)C6=CC=CC4=C65)C4=NSN=C43)=C2)C2C=CC(C3=C(F)C=C(C#CC4=CC=C5C(=O)N(CC(CC)CCCC)C(=O)C6=CCCC4=C56)C4=NSN=C43)=CC21,BYG-1,-5.89,-3.4,12.95,1.08,0.62,8.67,"H. Chen, D. Hu, Q. Yang, J. Gao, J. Fu, K. Yang, H. He, S. Chen, Z. Kan, T. Duan, C. Yang, J. Ouyang, Z. Xiao, K. Sun, S. Lu, All-Small-Molecule Organic Solar Cells with an Ordered Liquid Crystalline Donor, Joule. 3 (2019) 3034¨C3047. https://doi.org/10.1016/j.joule.2019.09.009."
3289,CCCCC(CC)CC1(CC(CC)CCCC)C2=C(SC(/C=C3C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)=C2)C2=C1C=C(C1=CC=C(C3=CC4=C(S3)C3=C(C=C(/C=C5C(=O)C6=C(C=C(Cl)C(Cl)=C6)C5=C(C#N)C#N)S3)C4(CC(CC)CCCC)CC(CC)CCCC)C3=NSN=C13)S2,BT-CL,-5.5,-3.74,17.85,0.79,0.6105,8.65,"B.-S. Lu, Y. Zhang, T.-Y. Hu, Y.-F. Ma, Y.-N. Zhu, D.-W. Liu, Z.-Q. Zhang, E. Wang, W. Ma, H.-L. Zhang, Non-fullerene acceptors based on multiple non-covalent interactions for low cost and air stable organic solar cells, Org. Electron. 93 (2021) 106132. https://doi.org/10.1016/j.orgel.2021.106132."
3290,CCCCC(CC)CC1(CC(CC)CCCC)C2=CC3=C(C=C2C2=C1C=C(C1=CC=C(/C=C4C(=O)C5=C(C=CC=C5)C4=C(C#N)C#N)[Se]1)S2)C(CC(CC)CCCC)(CC(CC)CCCC)C1=C3SC(C2=CC=C(/C=C3C(=O)C4=C(C=CC=C4)C3=C(C#N)C#N)[Se]2)=C1,IDT2SeC2C4,-5.3,-3.91,16.91,0.88,0.585,8.65,"X. Zhang, Q. Wang, Z. Liang, M. Li, Y. Geng, Low-bandgap non-fullerene acceptors based on selenophene ¦Ð spacer and alkylated indaceno[1,2-b:5,6-b¡ä]dithiophene for organic solar cells, Org. Electron. 69 (2019) 200¨C207. https://doi.org/10.1016/j.orgel.2019.03.038."
3291,CCCCCCC1(CCCCCC)C2=C(C=C(/C=C3C(=O)C4=C(C=CC(F)=C4)C3=C(C#N)C#N)S2)C2=C(OC)C3=C(C4=C(SC(/C=C5C(=O)C6=C(C=C(F)C=C6)C5=C(C#N)C#N)=C4)C3(CCCCCC)CCCCCC)C(OC)=C21,Y-MODF,-5.81,-3.9,12.3,0.984,0.7155,8.63,"H. Huang, X. Li, S. Chen, B. Qiu, J. Du, L. Meng, Z. Zhang, C. Yang, Y. Li, Enhanced performance of ternary organic solar cells with a wide bandgap acceptor as the third component, J. Mater. Chem. A. 7 (2019) 27423¨C27431. https://doi.org/10.1039/C9TA09268D."
3292,CCCCC(CC)CC1=C(F)C=C(C2=C3C=C(C4=CC5=C(S4)C4=C(C=C(/C=C6C(=O)C7=C(C=C(F)C(F)=C7)C6=C(C#N)C#N)S4)C5(CC(CC)CCCC)CC(CC)CCCC)SC3=C(C3=CC(F)=C(CC(CC)CCCC)S3)C3=C2SC(C2=CC4=C(S2)C2=C(C=C(/C=C5C(=O)C6=C(C=C(F)C(F)=C6)C5=C(C#N)C#N)S2)C4(CC(CC)CCCC)CC(CC)CCCC)=C3)S1,F-BDTC-4F,-5.54,-3.89,16.93,0.862,0.591,8.62,"Y. Wang, S. Liu, H. Gao, L. Wang, W. Wang, B. Zhao, H. Wu, C. Gao, Synergistic halogenation of backbone and end group for high-performance non-fused acceptors based organic solar cells, Dyes Pigments. (2022) 110178. https://doi.org/10.1016/j.dyepig.2022.110178."
3293,O=C(C(C=CC=C1)=C1C/2=C(C#N)C#N)C2=C/C3=CC(CC(CC)CCCC)=C(C4=CC5=C(C6=CC(C7(C8=CC=C(CCCCCC)C=C8)C9=CC=C(CCCCCC)C=C9)=C(C%10=C7C=C(C%11=C(CC(CC)CCCC)C=C(/C=C%12C(C(C=CC=C%13)=C%13C\%12=C(C#N)/C#N)=O)S%11)[Se]%10)C=C6C5(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15)[Se]4)S3,ID-Se-IC,-5.45,-3.79,15.2,0.91,0.62,8.6,"Y. Li, L. Zhong, F.-P. Wu, Y. Yuan, H.-J. Bin, Z.-Q. Jiang, Z. Zhang, Z.-G. Zhang, Y. Li, L.-S. Liao, Non-fullerene polymer solar cells based on a selenophene-containing fused-ring acceptor with photovoltaic performance of 8.6%, Energy Environ. Sci. 9 (2016) 3429¨C3435. https://doi.org/10.1039/C6EE00315J."
3294,CCCCC(CC)COC1=C(OCC(CC)CCCC)C(C2=CC3=C(S2)C2=C(CC(/C=C4C(=O)C5=C(C=C(F)C(F)=C5)C4=C(C#N)C#N)S2)C3(CC(CC)CCCC)CC(CC)CCCC)=C2N=CC=NC2=C1C1=CC2=C(S1)C1=C(C=C(/C=C3C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)S1)C2(CC(CC)CCCC)CC(CC)CCCC,QCIC1,-5.53,-3.8,18.81,0.822,0.555,8.58,"S. Ye, S. Chen, S. Li, Y. Pan, X. Xia, W. Fu, L. Zuo, X. Lu, M. Shi, H. Chen, Synergistic Effects of Chlorination and Branched Alkyl Side Chain on the Photovoltaic Properties of Simple Non-Fullerene Acceptors with Quinoxaline as the Core, ChemSusChem. 14 (2021) 3599¨C3606. https://doi.org/10.1002/cssc.202100689."
3295,CCCCCCCCC1(CCCCCCCC)C2=CC3=C(C=C2C2=C1C=C1C(=C2)C(CCCCCCCC)(CCCCCCCC)C2=C1SC(/C=C1C(=O)C4=C(C=CC=C4)C1=C(C#N)C#N)=C2)C(CCCCCCCC)(CCCCCCCC)C1=C3C=C2C(=C1)C1=C(C=C(/C=C3C(=O)C4=C(C=CC=C4)C3=C(C#N)C#N)S1)C2(CCCCCCCC)CCCCCCCC,TfIF-IC-C8,-5.63,-3.8,13.21,0.97,0.667,8.57,"J. Jia, G. Liu, T. Jia, Z. Wang, K. Lin, Y. Li, F. Huang, Y. Cao, Fused nonacyclic electron acceptors with additional alkyl side chains for efficient polymer solar cells, Org. Electron. 68 (2019) 151¨C158. https://doi.org/10.1016/j.orgel.2019.01.052."
3296,CCCCCCCCC(CCCCCCCC)N1C2=C(SC(/C=C3C(=O)C4=C(C=C(Cl)C(Cl)=C4)C3=C(C#N)C#N)=C2)C2=C1C=C(C1=C(OC(CC)CCCC)C=C(C3=CC(CCCCCC)=C(/C=C4C(=O)C5=CC(Cl)=C(Cl)C=C5C4=C(C#N)C#N)S3)C(OC(CC)CCCC)=C1)S2,DBT-EH,-5.62,-3.97,18.95,0.83,0.543,8.54,"J. Cao, H. Wang, L. Yang, F. Du, J. Yu, W. Tang, Chlorinated unfused acceptor enabling 13.57% efficiency and 73.39% fill factor organic solar cells via fine-tuning alkoxyl chains on benzene core, Chem. Eng. J. 427 (2022) 131828. https://doi.org/10.1016/j.cej.2021.131828."
3297,O=C(C(C=CC=C1)=C1C/2=C(C#N)C#N)C2=C/C3=CN=C(C4=CC5=C(C6=C(C5(C7=CC=C(CCCCCC)C=C7)C8=CC=C(CCCCCC)C=C8)C=C(C9=C%10C=C(C%11=NC=C(/C=C%12C(C(C=CC=C%13)=C%13C\%12=C(C#N)/C#N)=O)S%11)S9)C(C%10(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15)=C6)S4)S3,IDT-Tz1:1,-5.62,-3.96,13.67,0.88,0.708,8.52,"S. Yu, Y. Chen, L. Yang, P. Ye, J. Wu, J. Yu, S. Zhang, Y. Gao, H. Huang, Significant enhancement of photovoltaic performance through introducing S?N conformational locks, J. Mater. Chem. A. 5 (2017) 21674¨C21678. https://doi.org/10.1039/C7TA05774A."
3298,CCCCC(CC)CC1(CC(CC)CCCC)C2=C(SC(/C=C3C(=O)C4=C(C=C(Cl)C(Cl)=C4)C3=C(C#N)C#N)=C2)C2=C1C=C(C1=CC(F)=C(C3=CC4=C(S3)C3=C(C=C(/C=C5C(=O)C6=C(C=C(Cl)C(Cl)=C6)C5=C(C#N)C#N)S3)C4(CC(CC)CCCC)CC(CC)CCCC)C=C1F)S2,HC-PCIC,-5.54,-3.87,17.53,0.73,0.6908,8.52,"S. Li, L. Zhan, C. Sun, H. Zhu, G. Zhou, W. Yang, M. Shi, C.-Z. Li, J. Hou, Y. Li, H. Chen, Highly Efficient Fullerene-Free Organic Solar Cells Operate at Near Zero Highest Occupied Molecular Orbital Offsets, J. Am. Chem. Soc. 141 (2019) 3073¨C3082. https://doi.org/10.1021/jacs.8b12126."
3299,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(S3)C(CCCCCC)=C(C=C3C(=O)N(CC)C(=S)N(CC)C3=O)S2)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC3=C2SC(C=C2C(=O)N(CC)C(=S)N(CC)C2=O)=C3)C=C1,C6-IDTT-T,-5.71,-3.78,14.42,1.052,0.561,8.51,"T. Xia, C. Li, H.S. Ryu, X. Sun, H.Y. Woo, Y. Sun, Asymmetrically Alkyl-Substituted Wide-Bandgap Nonfullerene Acceptor for Organic Solar Cells, Sol. RRL. 4 (2020) 2000061. https://doi.org/10.1002/solr.202000061."
3300,O=C(C(C=CC=C1)=C1C/2=C(C#N)C#N)C2=C/C3=CC4=C(S3)C5=C(C6=CC(C7(C8=CC=C(COCCOC)C=C8)C9=CC=C(COCCOC)C=C9)=C(C%10=C7C(SC(/C=C%11C(C(C=CC=C%12)=C%12C\%11=C(C#N)/C#N)=O)=C%13)=C%13S%10)C=C6C5(C%14=CC=C(COCCOC)C=C%14)C%15=CC=C(COCCOC)C=C%15)S4,ITIC-OE,-5.67,-4.04,14.8,0.85,0.67,8.5,"X. Liu, B. Xie, C. Duan, Z. Wang, B. Fan, K. Zhang, B. Lin, F.J.M. Colberts, W. Ma, R.A.J. Janssen, F. Huang, Y. Cao, A high dielectric constant non-fullerene acceptor for efficient bulk-heterojunction organic solar cells, J. Mater. Chem. A. 6 (2018) 395¨C403. https://doi.org/10.1039/C7TA10136H."
3301,O=C(C(C=CC=C1)=C1C/2=C(C#N)C#N)C2=C/C3=CC4=C(S3)C5=C(C6=CC(C7(C8=CC=C(COCCOC)C=C8)C9=CC=C(COCCOC)C=C9)=C(C%10=C7C(SC(/C=C%11C(C(C=CC=C%12)=C%12C\%11=C(C#N)/C#N)=O)=C%13)=C%13S%10)C=C6C5(C%14=CC=C(COCCOC)C=C%14)C%15=CC=C(COCCOC)C=C%15)S4,CI-ITIC,-5.67,-4.03,14.8,0.85,0.67,8.5,"X. Liu, B. Xie, C. Duan, Z. Wang, B. Fan, K. Zhang, B. Lin, F.J.M. Colberts, W. Ma, R.A.J. Janssen, F. Huang, Y. Cao, A high dielectric constant non-fullerene acceptor for efficient bulk-heterojunction organic solar cells, J. Mater. Chem. A. 6 (2018) 395¨C403. https://doi.org/10.1039/C7TA10136H."
3302,CCCCCCCCCCC(CCCCCC)N1N=C2C(=N1)C(C1=CC3=C(S1)C1=C(C=C(/C=C4C(=O)C5=C(C=CC=C5)C4=C(C#N)C#N)S1)C3(CC(CC)CCCC)CC(CC)CCCC)=C(F)C(F)=C2C1=CC2=C(S1)C1=C(C=C(/C=C3C(=O)C4=C(C=CC=C4)C3=C(C#N)C#N)S1)C2(CC(CC)CCCC)CC(CC)CCCC,BTC6-0F,-5.47,-3.71,17.99,0.87,0.542,8.49,"J. Huang, C.-Y. Gao, X.-H. Fan, X. Zhu, L.-M. Yang, A¨CD¨CC¨CD¨CA type non-fullerene acceptors based on the benzotriazole (BTA) unfused core for organic solar cells, New J. Chem. 45 (2021) 12802¨C12807. https://doi.org/10.1039/D1NJ01978C."
3303,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C=C(/C=C2C(=O)C5=C(C=CC(F)=C5)C2=C(C#N)C#N)S3)C2(C3=C(C=CC=C3)OC3=C2C=CC=C3)C2=C4C=C3C(=C2)C2=C(C=C(/C=C4C(=O)C5=C(C=CC(F)=C5)C4=C(C#N)C#N)S2)C3(C2=CC=C(CCCCCC)C=C2)C2=CC=C(CCCCCC)C=C2)C=C1,TSFX-4F,-5.82,-4.04,15.48,0.83,0.6616,8.47,"D. Yang, Q. Ma, X. Li, S. Chen, J. Zhang, C. Yang, L. Meng, Y. Li, Two new A-D-A type small molecule acceptors based on C2v-symmetric dithienocyclopentaspiro[fluorene-9,9¡ä-xanthene] core for polymer solar cells, Org. Electron. 92 (2021) 106120. https://doi.org/10.1016/j.orgel.2021.106120."
3304,O=C1N(C(CCC)CCC)C(C2=C(C1C=C3)C4=C3C(C=CC5C(N(C(CCC)CCC)C6=O)=O)=C(C5=C6C(C(S7)=CC8=C7C(C9=CC=C(C%10=CC%11=C(C=CC(C(N(C(CCC)CCC)C%12=O)=O)=C%13C%12C=C%14)C%13=C%14C(C=CC%15C(N%16C(CCC)CCC)=O)=C%11C%15=C%10C%16=O)S9)=C(C=C(C(C(C(N%17C(CCC)CCC)=O)=C%18C(C=CC%19=C%18%20)C%17=O)=CC%20=C%21C=CC%22=C%23C(C=CC%19=C%23%21)C(N(C%22=O)C(CCC)CCC)=O)S%24)C%24=C8C%25=CC=C(C(C(C(N%26C(CCC)CCC)=O)=C%27C(C=CC%28=C%27%29)C%26=O)=CC%29=C%30C=CC%31=C%32C(C=CC%28=C%32%30)C(N(C%31=O)C(CCC)CCC)=O)S%25)=C%33)C%33=C4C=C2)=O,TPB,-5.71,-3.89,17.9,0.79,0.58,8.47,"Q. Wu, D. Zhao, A.M. Schneider, W. Chen, L. Yu, Covalently Bound Clusters of Alpha-Substituted PDI¡ªRival Electron Acceptors to Fullerene for Organic Solar Cells, J. Am. Chem. Soc. 138 (2016) 7248¨C7251. https://doi.org/10.1021/jacs.6b03562."
3305,O=C1C2=C(C=C(Cl)C(Cl)=C2)C(/C1=C/C3=CC(C(C4=CC=C(OCC(CC)CCCC)C=C4)(C5=CC=C(OCC(CC)CCCC)C=C5)C6=C7C=CC(C6=C8)=CC9=C8C=CC%10=C9C(C%11=CC=C(OCC(CC)CCCC)C=C%11)(C%12=CC=C(OCC(CC)CCCC)C=C%12)C%13=C%10SC(/C=C%14/C(C(C=C(Cl)C(Cl)=C%15)=C%15C%14=O)=C(C#N)/C#N)=C%13)=C7S3)=C(C#N)C#N,FPIC,-5.75,-3.97,15.3,0.755,0.731,8.45,"G. Cai, P. Xue, Z. Chen, T. Li, K. Liu, W. Ma, J. Lian, P. Zeng, Y. Wang, R.P.S. Han, X. Zhan, High-Performance Mid-Bandgap Fused-Pyrene Electron Acceptor, Chem. Mater. 31 (2019) 6484¨C6490. https://doi.org/10.1021/acs.chemmater.8b04668."
3306,CCCCC(CC)CC1(CC(CC)CCCC)C2=C(SC(/C=C3C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)=C2)C2=C1C=C(C1=C(F)C(F)=C(C3=CC4=C(S3)C3=C(C=C(/C=C5C(=O)C6=C(C=C(F)C(F)=C6)C5=C(C#N)C#N)S3)C4(CC(CC)CCCC)CC(CC)CCCC)C3=NSN=C31)S2,BT2F-IC4F,-5.98,-4.31,19.43,0.67,0.647,8.45,"Y. Wang, Z. Liu, X. Cui, C. Wang, H. Lu, Y. Liu, Z. Fei, Z. Ma, Z. Bo, Small molecule acceptors with a ladder-like core for high-performance organic solar cells with low non-radiative energy losses, J. Mater. Chem. A. 8 (2020) 12495¨C12501. https://doi.org/10.1039/D0TA03683H."
3307,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C=C(C2=C(OCC(CC)CCCC)C(/C=C/C=C5C(=O)C6=C(C=C(F)C(F)=C6)C5=C(C#N)C#N)=CS2)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC(C3=C(OCC(CC)CCCC)C(/C=C/C=C4C(=O)C5=C(C=C(F)C(F)=C5)C4=C(C#N)C#N)=CS3)=C2)C=C1,i-V-4F,-5.49,-3.55,19.56,0.751,0.574,8.44,"B. Zhao, W. Wang, Z. Cong, L. Wang, H. Wu, S. Liu, C. Gao, Efficient and Stable Nonfullerene Polymer Solar Cell Enabled by a Narrow-Bandgap, Nonplanar, Small-Molecule Acceptor with an Extended Main Chain, ACS Appl. Energy Mater. 4 (2021) 4119¨C4128. https://doi.org/10.1021/acsaem.1c00467."
3308,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)OC3=C(SC4=C3SC3=C4OC(C4=CC=C(CCCCCC)C=C4)(C4=CC=C(CCCCCC)C=C4)C4=C3SC(/C=C3C(=O)C5=C(C=CC=C5)C3=C(C#N)C#N)=C4)C3=C2C=C(/C=C2C(=O)C4=C(C=CC=C4)C2=C(C#N)C#N)S3)C=C1,COi6IC,-5.57,-3.86,17.45,0.82,0.59,8.43,"T. Li, H. Zhang, Z. Xiao, J.J. Rech, H. Niu, W. You, L. Ding, A carbon¨Coxygen-bridged hexacyclic ladder-type building block for low-bandgap nonfullerene acceptors, Mater. Chem. Front. 2 (2018) 700¨C703. https://doi.org/10.1039/C8QM00004B."
3309,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=C(C=C4SC(/C=C5C(=O)C6=C(C=C(F)C(F)=C6)C5=C(C#N)C#N)=CC4=C3)C3=C2C2=C(S3)C3=C(S2)C2=C(C=C4C=C(/C=C5C(=O)C6=C(C=C(F)C(F)=C6)C5=C(C#N)C#N)SC4=C2)C3(C2=CC=C(CCCCCC)C=C2)C2=CC=C(CCCCCC)C=C2)C=C1,IHBT-2F,-5.46,-4.18,18.2,0.699,0.662,8.42,"Y. Xu, H. Jiang, T.-K. Lau, J. Zhu, J. Wang, X. Lu, X. Zhan, Y. Lin, Fused thienobenzene-thienothiophene electron acceptors for organic solar cells, J. Energy Chem. 37 (2019) 58¨C65. https://doi.org/10.1016/j.jechem.2018.12.002."
3310,CCCCCCCCC1(CCCCCCCC)C2=CC3=C(C=C2C2=C1C=C(/C=C1C(=O)C4=C(C=C(F)C=C4)C1=C(C#N)C#N)S2)C(CCCCCCCC)(CCCCCCCC)C1=C3SC(/C=C2C(=O)C3=C(C=CC(F)=C3)C2=C(C#N)C#N)=C1,IDIC8-F,-5.51,-3.82,15.21,0.864,0.641,8.42,"C. Liu, N. Qiu, Y. Sun, X. Ke, H. Zhang, C. Li, X. Wan, Y. Chen, All-Small-Molecule Organic Solar Cells Based on a Fluorinated Small Molecule Donor With High Open-Circuit Voltage of 1.07 V, Front. Chem. 8 (2020) 329. https://doi.org/10.3389/fchem.2020.00329."
3311,CCCCCCSC1=C(SCCCCCC)S/C(S1)=C/C2=CC=C(C3=CC4=C(C=C3)C(C=CC(C5=CC=C(/C=C6SC(SCCCCCC)=C(SCCCCCC)S6)C7=NSN=C57)=C8)=C8C4(CCCCCCCCCC)CCCCCCCCCC)C9=NSN=C29,BAF-4CN,-5.71,-3.55,15.52,0.77,0.707,8.4,"Suman, V. Gupta, A. Bagui, S.P. Singh, Molecular Engineering of Highly Efficient Small Molecule Nonfullerene Acceptor for Organic Solar Cells, Adv. Funct. Mater. 27 (2017) 1603820. https://doi.org/10.1002/adfm.201603820."
3312,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=C(C=CC(C4=CC=C(C5=CC=C(/C=C6/SC(=S)N(CC)C6O)C6=NSN=C56)S4)=C3)C3=C2C=C(C2=CC=C(/C=C4/SC(=S)N(CC)C4=O)C4=NSN=C24)S3)C=C1,TIDT-BT-R2,-5.25,-3.65,13.1,1.04,0.639,8.4,"W. Bai, X. Xu, Q. Li, Y. Xu, Q. Peng, Efficient Nonfullerene Polymer Solar Cells Enabled by Small-Molecular Acceptors with a Decreased Fused-Ring Core, Small Methods. 2 (2018) 1700373. https://doi.org/10.1002/smtd.201700373."
3313,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(C=C(C5=CC=C(C=C(C#N)C#N)C6=NSN=C56)S2)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC3=C2SC(C2=CC=C(C=C(C#N)C#N)C4=NSN=C24)=C3)C=C1,IDTTBM,,,15.5,0.83,0.63,8.4,"M.A. Alamoudi, J.I. Khan, Y. Firdaus, K. Wang, D. Andrienko, P.M. Beaujuge, F. Laquai, Impact of Nonfullerene Acceptor Core Structure on the Photophysics and Efficiency of Polymer Solar Cells, ACS Energy Lett. 3 (2018) 802¨C811. https://doi.org/10.1021/acsenergylett.8b00045."
3314,O=C(C(C=CC=C1)=C1C/2=C(C#N)C#N)C2=C/C3=CC(C(OC)=O)=C(C4=CC5=C(C6=CC(C7(C8=CC=C(CCCCCC)C=C8)C9=CC=C(CCCCCC)C=C9)=C(C%10=C7C=C(C%11=C(C(OC)=O)C=C(/C=C%12C(C(C=CC=C%13)=C%13C\%12=C(C#N)/C#N)=O)S%11)S%10)C=C6C5(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15)S4)S3,6(IDT-3MT)1:1,-5.68,-4.16,14.43,0.95,0.613,8.4,"S.H. Park, G.E. Park, S. Choi, Y.U. Kim, S.Y. Park, C.G. Park, M.J. Cho, D.H. Choi, Effect of a methyl thiophene-3-carboxylate bridge in an indacenodithiophene-based acceptor¨Cdonor¨Cacceptor-type molecule on the performance of non-fullerene polymer solar cells, J. Mater. Chem. C. 6 (2018) 7549¨C7556. https://doi.org/10.1039/C8TC01508B."
3315,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C=C(C2=CC=C(/C=C5SC(=S)N(COF)C5=O)C5=NSN=C25)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC(C3=CC=C(/C=C4SC(=S)N(COC)C4=O)C4=NSN=C34)=C2)C=C1,IDT-BT-RO,-5.33,-3.74,13.46,0.89,0.6103,8.4,"L.-M. Tang, J. Xiao, W.-Y. Bai, Q.-Y. Li, H.-C. Wang, M.-S. Miao, H.-L. Yip, Y.-X. Xu, End-chain effects of non-fullerene acceptors on polymer solar cells, Org. Electron. 64 (2019) 1¨C6. https://doi.org/10.1016/j.orgel.2018.10.005."
3316,CCCCC(CC)CC1=C2C(=O)C3=C(C4=CC5=C(S4)C4=C(C=C(/C=C6C(=O)C7=C(C=C(F)C(F)=C7)C6=C(C#N)C#N)S4)C5(CC(CC)CCCC)CC(CC)CCCC)SC(C4=CC5=C(S4)C4=C(C=C(/C=C6C(=O)C7=C(C=C(F)C(F)=C7)C6=C(C#N)C#N)S4)C5(CC(CC)CCCC)CC(CC)CCCC)=C3C(=O)C2=C(CC(CC)CCCC)S1,BDDEH-4F ,-5.57,-3.94,18.58,0.89,0.5067,8.39,"Z. Wu, Y. Chen, L. Zhang, D. Yuan, R. Qiu, S. Deng, H. Liu, Z. Zhang, J. Chen, A ligand-free direct heteroarylation approach for benzodithiophenedione-based simple small molecular acceptors toward high efficiency polymer solar cells, J. Mater. Chem. A. 9 (2021) 3314¨C3321. https://doi.org/10.1039/D0TA12288B."
3317,CCCCC(CC)CC1(CC(CC)CCCC)C2=C(SC(/C=C3C(=O)C4=CC5=CC(F)=C(F)C=C5C=C4C3=C(C#N)C#N)=C2)C2=C1C=C(C1=C(F)C(OC)=C(C3=CC4=C(S3)C3=C(C=C(/C=C5C(=O)C6=CC7=CC(F)=C(F)C=C7C=C6C5=C(C#N)C#N)S3)C4(CC(CC)CCCC)CC(CC)CCCC)C(F)=C1OC)S2,HFO¨CPCIC ,-5.5,-3.81,12.62,0.93,0.7099,8.36,"S. Li, L. Zhan, W. Zhao, S. Zhang, B. Ali, Z. Fu, T.-K. Lau, X. Lu, M. Shi, C.-Z. Li, J. Hou, H. Chen, Revealing the effects of molecular packing on the performances of polymer solar cells based on A¨CD¨CC¨CD¨CA type non-fullerene acceptors, J. Mater. Chem. A. 6 (2018) 12132¨C12141. https://doi.org/10.1039/C8TA03753A."
3318,CCCCCCCCC1=C(/C=C2C(=O)C3=CSC=C3C2=C(C#N)C#N)SC2=C1SC(C1=CC3=C(C=C1)C1=C(C4=C(S1)C(CCCCCCCC)=C(/C=C1C(=O)C5=CSC=C5C1=C(C#N)C#N)S4)C3(C1=CC=C(CCCCCC)C=C1)C1=CC=C(CC3=CC=C4C=C5C=CC(C)=CC5=CC4=C3)C=C1)=C2,ITOTC,-5.66,-3.87,15.1,0.94,0.5882,8.35,"M. Zhang, Y. Ma, Q. Zheng, Asymmetric indenothienothiophene-based unfused core for A-D-A type nonfullerene acceptors, Dyes Pigments. 180 (2020) 108495. https://doi.org/10.1016/j.dyepig.2020.108495."
3319,CCCCCCCCC(CCCCCC)COC1=CC(C2=CC3=C(S2)C2=C(C=C(/C=C4C(=O)C5=CC(F)=C(F)C=C5C4=C(C#N)C#N)S2)N3C(CCCCCCCC)CCCCCCCC)=C(OCC(CCCCCC)CCCCCCCC)C=C1C1=CC2=C(S1)C1=C(C=C(/C=C3C(=O)C4=CC(F)=C(F)C=C4C3=C(C#N)C#N)S1)N2C(CCCCCCCC)CCCCCCCC,DBD-4F,-5.55,-3.74,15.92,0.88,0.5952,8.34,"J. Cao, S. Qu, L. Yang, H. Wang, F. Du, J. Yu, W. Tang, Asymmetric simple unfused acceptor enabling over 12% efficiency organic solar cells, Chem. Eng. J. 412 (2021) 128770. https://doi.org/10.1016/j.cej.2021.128770."
3320,CCCCCCCCC1=CC2=C(/C=C3C(=O)C4=C(C=CC=C4)C3=C(C#N)C#N)SC(C3=CC=C4C(=C3)C(CCCCCCCC)(CCCCCCCC)C3=C4C=CC(C4=C5SC(CCCCCCCC)=CC5=C(/C=C5C(=O)C6=C(C=CC=C6)C5=C(C#N)C#N)S4)=C3)=C2S1,NFTI,-5.46,-3.77,16.22,0.898,0.57,8.34,"H. Fan, T. Vergote, S. Xu, S. Chen, C. Yang, X. Zhu, A thieno[3,4-b]thiophene linker enables a low-bandgap fluorene-cored molecular acceptor for efficient non-fullerene solar cells, Mater. Chem. Front. 2 (2018) 760¨C767. https://doi.org/10.1039/C7QM00585G."
3321,CCCCCCCCC1=CC=C(C2(C3=CC=C(CCCCCCCC)C=C3)C3=C(SC(/C=C4C(=O)C5=C(C=CC=C5)C4=C(C#N)C#N)=C3)C3=C2C2=C(C=C3)C3=C(S2)C2=C(S3)C3=C(C=C2)C2=C(C=C(/C=C4C(=O)C5=C(C=CC=C5)C4=C(C#N)C#N)S2)C3(C2=CC=C(CCCCCCCC)C=C2)C2=CC=C(CCCCCCCC)C=C2)C=C1,DBTIC,-5.45,-3.73,11.18,0.93,0.625,8.33,"Y. Wang, M. Chang, X. Ke, X. Wan, G. Yang, A new medium-bandgap fused-[1]benzothieno[3,2-b][1]benzo-thiophene (BTBT) nonfullerene acceptor for organic solar cells with high open-circuit voltage, Polymer. 185 (2019) 121976. https://doi.org/10.1016/j.polymer.2019.121976."
3322,CCCCCCCCCCCC1=C(/C=C2C(=O)C3=CC(OC(C)=O)=CC=C3C2=C(C#N)C#N)SC2=C1SC1=C2N(CC(CC)CCCC)C2=C1C1=NSN=C1C1=C2N(CC(CC)CCCC)C2=C1SC1=C2SC(/C=C2C(=O)C3=CC=C(OC(C)=O)C=C3C2=C(C#N)C#N)=C1CCCCCCCCCCC,BTIC-OCOMe,,,15.55,0.95,0.562,8.32,"H. Lai, L. Liu, N. Zheng, L. Han, F. He, Push or Pull Electrons: Acetoxy and Carbomethoxy-Substituted Isomerisms in Organic Solar Cell Acceptors, J. Phys. Chem. Lett. 12 (2021) 4666¨C4673. https://doi.org/10.1021/acs.jpclett.1c01077."
3323,CCCCCCC1=CC=C(C2(C3=CC=C(C)C=C3)C3=C(SC(/C=C4C(=O)C5=C(C=CC=C5)C4=C(C#N)C#N)=C3)C3=C2C2=CC4=C(C=C2S3)C2=C(S4)C3=C(C=C(/C=C4C(=O)C5=C(C=CC=C5)C4=C(C#N)C#N)S3)C2(C2=CC=C(CCCCCC)C=C2)C2=CC(CCCCCC)=CC=C2)C=C1,ITIC1,-5.48,-3.84,16.06,0.922,0.562,8.32,"J. Wang, W. Wang, X. Wang, Y. Wu, Q. Zhang, C. Yan, W. Ma, W. You, X. Zhan, Enhancing Performance of Nonfullerene Acceptors via Side-Chain Conjugation Strategy, Adv. Mater. 29 (2017) 1702125. https://doi.org/10.1002/adma.201702125."
3324,O=C1N(C(CC)CC)C(C2=C(C1C=C3)C4=C3C(C=CC5C(N(C(CC)CC)C6=O)=O)=C(C5=C6C=C7)C7=C4C=C2C8=CC9=C%10C(C%11=C%12C=C%10)=C(C=CC%11C(N(C(CC)CC)C%12=O)=O)C%13=C9C(C%14C=C%13)=C8C(N(C(CC)CC)C%14=O)=O)=O,oo-2PDI,-6.15,-3.9,18.79,0.799,0.553,8.3,"H. Wang, L. Chen, Y. Xiao, A simple molecular structure of ortho-derived perylene diimide diploid for non-fullerene organic solar cells with efficiency over 8%, J. Mater. Chem. A. 5 (2017) 22288¨C22296. https://doi.org/10.1039/C7TA06804B."
3325,CCCCC(CC)CC1(CC(CC)CCCC)C2=C(SC(/C=C3C(=O)C4=C(C=C(OC)C(F)=C4)C3=C(C#N)C#N)=C2)C2=C1C=C(C1=CC(F)=C(C3=CC4=C(S3)C3=C(C=C(/C=C5C(=O)C6=C(C=C(OC)C(F)=C6)C5=C(C#N)C#N)S3)C4(CC(CC)CCCC)CC(CC)CCCC)C=C1F)S2,FO-PCIC,-5.49,-3.75,15.02,0.9,0.6112,8.29,"S. Li, L. Zhan, C. Sun, H. Zhu, G. Zhou, W. Yang, M. Shi, C.-Z. Li, J. Hou, Y. Li, H. Chen, Highly Efficient Fullerene-Free Organic Solar Cells Operate at Near Zero Highest Occupied Molecular Orbital Offsets, J. Am. Chem. Soc. 141 (2019) 3073¨C3082. https://doi.org/10.1021/jacs.8b12126."
3326,O=C1N(C(CCCCCC)CCCCCC)C(C2=C(C1C=C3S4)C5=C3C(C4=CC6C(N(C(CCCCCC)CCCCCC)C7=O)=O)=C(C6=C7C=C8CC9=CC%10=C(C%11=CC=C(C%12=CC%13=C%14C%15=C%16C%17=C%18C(C=CC(C(N(C(CCCCCC)CCCCCC)C%19=O)=O)=C%18C%19C=C%17SC%16=CC%14C(N(C(CCCCCC)CCCCCC)C%13=O)=O)=C%15%12)S%11)C%20=C(C=C(CC%21=CC(C(N(C(CCCCCC)CCCCCC)C%22=O)=O)=C(C%22C=C%23S%24)C%25=C%23C(C%24=CC%26C(N(C(CCCCCC)CCCCCC)C%27=O)=O)=C(C%26=C%27C=C%28)C%28=C%25%21)S%20)C(C%29=CC=C(CC%30=CC%31=C%32C%33=C%34C%35=C%36C(C=CC(C(N(C(CCCCCC)CCCCCC)C%37=O)=O)=C%36C%37C=C%35SC%34=CC%32C(N(C(CCCCCC)CCCCCC)C%31=O)=O)=C%33%30)S%29)=C%10S9)C8=C5C=C2)=O,BPT-S,-6.08,-3.79,11.94,1.02,0.681,8.28,"Z. Luo, T. Liu, W. Cheng, K. Wu, D. Xie, L. Huo, Y. Sun, C. Yang, A three-dimensional thiophene-annulated perylene bisimide as a fullerene-free acceptor for a high performance polymer solar cell with the highest PCE of 8.28% and a VOC over 1.0 V, J. Mater. Chem. C. 6 (2018) 1136¨C1142. https://doi.org/10.1039/C7TC05261H."
3327,CCCCCCC(CCCC)CC1(CC(CCCC)CCCCCC)C2=C(SC(/C=C3C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)=C2)C2=C1C=C(C1=CC3=C(S1)C1=C(C=C(C4=CC5=C(S4)C4=C(C=C(/C=C6C(=O)C7=C(C=C(F)C(F)=C7)C6=C(C#N)C#N)S4)C5(CC(CCCC)CCCCCC)CC(CCCC)CCCCCC)S1)C1=C3C=C(C(=O)C(CCCC)CCCCCC)S1)S2,BTTBo-4F ,-5.56,-3.85,15.04,0.85,0.6461,8.27,"S. Ma, Q. Huang, Y. Liang, H. Tang, Y. Chen, J. Zhang, K. Zhang, F. Huang, Y. Cao, Non-fullerene electron acceptors with benzotrithiophene with ¦Ð-extension terminal groups for the development of high-efficiency organic solar cells, J. Mater. Chem. C. 9 (2021) 13896¨C13903. https://doi.org/10.1039/D1TC03259C."
3328,CCCCC(CC)COC1=C(/C=C2C(=O)C3=CC(F)=C(F)C=C3C2=C(C#N)C#N)SC(C2=CC(CC(CC)CCCC)=C(C3=C(CC(CC)CCCC)C=C(C4=CC(OCC(CC)CCCC)=C(/C=C5C(=O)C6=CC(F)=C(F)C=C6C5=C(C#N)C#N)S4)S3)S2)=C1,4T-4,-5.85,-3.86,14.27,0.94,0.6182,8.27,"Y. Zhou, M. Li, H. Lu, H. Jin, X. Wang, Y. Zhang, S. Shen, Z. Ma, J. Song, Z. Bo, High-Efficiency Organic Solar Cells Based on a Low-Cost Fully Non-Fused Electron Acceptor, Adv. Funct. Mater. 31 (2021) 2101742. https://doi.org/10.1002/adfm.202101742."
3329,CCCCC(CC)CC1(CC(CC)CCCC)C2=C(SC(/C=C3C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)=C2)C2=C1C=C(C1=CC=C(C3=CC4=C(S3)C3=C(C=C(/C=C5C(=O)C6=C(C=C(F)C(F)=C6)C5=C(C#N)C#N)S3)C4(CC(CC)CCCC)CC(CC)CCCC)C3=NSN=C13)S2,BT-F,-5.45,-3.68,16.99,0.82,0.593,8.26,"B.-S. Lu, Y. Zhang, T.-Y. Hu, Y.-F. Ma, Y.-N. Zhu, D.-W. Liu, Z.-Q. Zhang, E. Wang, W. Ma, H.-L. Zhang, Non-fullerene acceptors based on multiple non-covalent interactions for low cost and air stable organic solar cells, Org. Electron. 93 (2021) 106132. https://doi.org/10.1016/j.orgel.2021.106132."
3330,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C=C(C2=C(OCC(CC)CCCC)C(/C=C5C(=O)C6=C(C=CC=C6)C5=C(C#N)C#N)=CS2)[Se]3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4[Se]C(C3=C(OCC(CC)CCCC)C(/C=C4C(=O)C5=C(C=CC=C5)C4=C(C#N)C#N)=CS3)=C2)C=C1,i-IDSe,-5.41,-3.71,14.39,0.98,0.586,8.26,"W. Wang, B. Zhao, Z. Liang, Z. Cong, L. Wang, H. Wu, N. Zheng, C. Gao, Achieving Efficient Polymer Solar Cells Based on Near-Infrared Absorptive Backbone Twisted Nonfullerene Acceptors through a Synergistic Strategy of an Indacenodiselenophene Fused-Ring Core and a Chlorinated Terminal Group, ACS Appl. Energy Mater. 5 (2022) 1322¨C1330. https://doi.org/10.1021/acsaem.1c03817."
3331,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)OC3=C(SC4=C3SC3=C4OC(C4=CC=C(CCCCCC)C=C4)(C4=CC=C(CCCCCC)C=C4)C4=C3SC(/C=C3C(=O)C5=C(C=C(F)C(F)=C5)C3=C(C#N)C#N)=C4)C3=C2C=C(/C=C2C(=O)C4=C(C=C(F)C(F)=C4)C2=C(C#N)C#N)S3)C=C1,COi6DFIC,5.64,-4.04,20.98,0.67,0.589,8.25,"T. Li, H. Zhang, Z. Xiao, J.J. Rech, H. Niu, W. You, L. Ding, A carbon¨Coxygen-bridged hexacyclic ladder-type building block for low-bandgap nonfullerene acceptors, Mater. Chem. Front. 2 (2018) 700¨C703. https://doi.org/10.1039/C8QM00004B."
3332,CCCCC(CC)CC1(CC(CC)CCCC)C2=C(SC(/C=C3C(=O)C4=C(C=CC=C4)C3=C(C#N)C#N)=C2)C2=C1C=C(C1=C(F)C(F)=C(C3=CC4=C(S3)C3=C(C=C(/C=C5C(=O)C6=C(C=CC=C6)C5=C(C#N)C#N)S3)C4(CC(CC)CCCC)CC(CC)CCCC)S1)S2,DF-TCIC ,-5.37,-3.76,16.39,0.86,0.58,8.23,"R. Qin, W. Yang, S. Li, T.-K. Lau, Z. Yu, Z. Liu, M. Shi, X. Lu, C.-Z. Li, H. Chen, Enhanced intramolecular charge transfer of unfused electron acceptors for efficient organic solar cells, Mater. Chem. Front. 3 (2019) 513¨C519. https://doi.org/10.1039/C8QM00609A."
3333,CCCCCCCCOC(=O)C1=CC2=C(C3=CC4=C(S3)C3=CC5=C(C=C3C4(C3=CC=CC(CCCCCC)=C3)C3=CC=CC(CCCCCC)=C3)C3=C(C=C(C4=C6C=C(C(=O)OCCCCCCCC)SC6=C(/C=C6SC(=C(C#N)C#N)N(CC)C6=O)S4)S3)C5(C3=CC=CC(CCCCCC)=C3)C3=CC(CCCCCC)=CC=C3)SC(/C=C3SC(=C(C#N)C#N)N(CC)C3=O)=C2S1,ATT-6,-5.48,-3.66,14.66,0.96,0.5937,8.22,"J. Zhang, F. Liu, S. Chen, C. Yang, X. Zhu, D. Zhu, High-Performance Polymer Solar Cells Achieved by Introducing Side-Chain Heteroatom on Small-Molecule Electron Acceptor, Macromol. Rapid Commun. 40 (2019) 1800393. https://doi.org/10.1002/marc.201800393."
3334,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C=C(C2=CC=C(/C=C5/SC(=S)N(CC)C5=O)C5=NSN=C25)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC(C3=CC=C(/C=C4/SC(=S)N(CC)C4=O)C4=NSN=C34)=C2)C=C1,IDT-BT-R,-5.3,-3.56,13.6,1.02,0.591,8.2,"Q.-Y. Li, J. Xiao, L.-M. Tang, H.-C. Wang, Z. Chen, Z. Yang, H.-L. Yip, Y.-X. Xu, Thermally stable high performance non-fullerene polymer solar cells with low energy loss by using ladder-type small molecule acceptors, Org. Electron. 44 (2017) 217¨C224. https://doi.org/10.1016/j.orgel.2017.02.008."
3335,CCCCCCOC1=C(C2=CC=C(/C=C3SC(=S)N(CC)C3=O)S2)C2=NSN=C2C(C2=CC=C(/C=C3SC(=S)N(CC)C3=O)S2)=C1OCCCCCC,BTDT2R,-5.61,-3.73,13.52,1.06,0.57,8.19,"J. Ahn, S. Oh, H. Lee, S. Lee, C.E. Song, H.K. Lee, S.K. Lee, W.-W. So, S.-J. Moon, E. Lim, W.S. Shin, J.-C. Lee, Simple and Versatile Non-Fullerene Acceptor Based on Benzothiadiazole and Rhodanine for Organic Solar Cells, ACS Appl. Mater. Interfaces. 11 (2019) 30098¨C30107. https://doi.org/10.1021/acsami.9b09256."
3336,CCCCCCC1(CCCCCC)C2=CC3=C(C=C2C2=C1C=C(/C=C1C(=O)C4=C(C=CC=C4)C1=C(C#N)C#N)S2)C(CCCCCC)(CCCCCC)C1C=C(C2=CC4=C(S2)C2=CC5=C(C=C2C4(CCCCCC)CCCCCC)C2SC(/C=C4C(=O)C6=C(C=CC=C6)C4=C(C#N)C#N)=CC2C5(CCCCCC)CCCCCC)SC31,IDT2-IC,-5.28,-3.91,13.23,0.94,0.6571,8.18,"Z. Shao, Z. Zhu, H. Tan, X. Yu, J. Yu, W. Zhu, An A-D-D-A-type small-molecule electron acceptor with chlorine substitution for high-efficiency polymer solar cells, Org. Electron. 99 (2021) 106329. https://doi.org/10.1016/j.orgel.2021.106329."
3337,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(C=C(C5=CC=C(/C=C6SC(=C(C#N)C#N)N(CCCCCC)C6=O)C6=NSN=C56)S2)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC3=C2SC(C2=CC=C(/C=C4SC(=C(C#N)C#N)N(CCCCCC)C4=O)C4=NSN=C24)=C3)C=C1,ITBTR-C6,-5.3,-3.71,15.72,0.89,0.5783,8.18,"J. Qu, Z. Mu, H. Lai, H. Chen, T. Liu, S. Zhang, W. Chen, F. He, Alkyl Chain End Group Engineering of Small Molecule Acceptors for Non-Fullerene Organic Solar Cells, ACS Appl. Energy Mater. 1 (2018) 4724¨C4730. https://doi.org/10.1021/acsaem.8b00851."
3338,CCCCC(CC)CC1(CC(CC)CCCC)C2=C(SC(C3=CC=C(/C=C4SC(=S)N(CC)C4=O)C4=NSN=C34)=C2)C2=C1C=C(C1=CC=C(/C=C3SC(=S)N(CC)C3=O)C3=NSN=C13)S2,SSBR ,-5.44,-3.72,15.91,0.92,0.5583,8.16,"C. Tang, S.-C. Chen, Y. Tang, W. Ma, Q. Zheng, Cyclopentadithiophene-cored non-fullerene acceptors for efficient polymer solar cells with superior stability, Sol. Energy. 174 (2018) 991¨C998. https://doi.org/10.1016/j.solener.2018.09.077."
3339,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C=C(C2=CC=C(/C=C5SC(=C(C#N)C#N)N(CC)C5=O)C5=NSN=C25)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC(C3=CC=C(/C=C4SC(=C(C#N)C#N)N(CC)C4=O)C4=NSN=C34)=C2)C=C1,IDT-4CN,-5.45,-3.95,14.66,0.91,0.609,8.13,"L. Yang, W. Gu, Y. Yang, L. Hong, X. Zhang, Y. Xiao, X. Wu, A. Peng, H. Huang, A Highly Planar Nonfullerene Acceptor with Multiple Noncovalent Conformational Locks for Efficient Organic Solar Cells, Small Methods. 2 (2018) 1700330. https://doi.org/10.1002/smtd.201700330."
3340,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=C(SC(/C=C4C(=O)C5=C(C=CC(OC)=C5)C4=C(C#N)C#N)=C3)C3=CC=C4C(=C32)C=CC2=C4C(C3=CC=C(CCCCCC)C=C3)(C3=CC=C(CCCCCC)C=C3)C3=C2SC(/C=C2C(=O)C4=C(C=CC(O)=C4)C2=C(C#N)C#N)=C3)C=C1,NTIC-OMe,-5.53,-3.7,12.97,0.962,0.651,8.12,"Y.-Q.-Q. Yi, H. Feng, M. Chang, H. Zhang, X. Wan, C. Li, Y. Chen, New small-molecule acceptors based on hexacyclic naphthalene(cyclopentadithiophene) for efficient non-fullerene organic solar cells, J. Mater. Chem. A. 5 (2017) 17204¨C17210. https://doi.org/10.1039/C7TA05809H."
3341,CCCCCCCCC1(CCCCCCCC)C2=CC3=C(C=C2C2=C1C=C1C(=C2)C(CCCCCCCC)(CCCCCCCC)C2=C1SC(/C=C1C(=O)C4=C(C=CC=C4)C1=C(C#N)C#N)=C2)C(CCCCCCCC)(CCCCCCCC)C1=C3SC(/C=C2C(=O)C3=C(C=C(Cl)C=C3)C2=C(C#N)C#N)=C1,F-1CL,-5.46,-3.75,13.07,0.975,0.637,8.12,"Y. Wang, Y. Wang, B. Kan, X. Ke, X. Wan, C. Li, Y. Chen, High-Performance All-Small-Molecule Solar Cells Based on a New Type of Small Molecule Acceptors with Chlorinated End Groups, Adv. Energy Mater. 8 (2018) 1802021. https://doi.org/10.1002/aenm.201802021."
3342,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=C(SC(/C=C4C(=O)C5=C(C=C(F)C(F)=C5)C4=C(C#N)C#N)=C3)C3=C2C2=CC4=C(C=C2S3)C2=C(S4)C3=C(C=C(/C=C4C(=O)C5=C(C=CC(F)=C5)C4=C(C#N)C#N)S3)C2(C2=CC=C(CCCCCC)C=C2)C2=CC=C(CCCCCC)C=C2)C=C1,BDCPDT-FIC,-5.52,-4,19.12,0.7,0.6067,8.12,"S.-L. Chang, F.-Y. Cao, W.-C. Huang, P.-K. Huang, K.-H. Huang, C.-S. Hsu, Y.-J. Cheng, New Thieno[3,2-b]thiophene-Based Acceptor: Tuning Acceptor Strength of Ladder-Type N-Type Materials to Simultaneously Achieve Enhanced Voc and Jsc of Nonfullerene Solar Cells, ACS Energy Lett. 3 (2018) 1722¨C1729. https://doi.org/10.1021/acsenergylett.8b00563."
3343,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=C(SC(/C=C4C(=O)C5=C(C=C(F)C(F)=C5)C4=C(C#N)C#N)=C3)C3=C2C2=C4SC5=C(C4=C4SC6=C(C4=C2S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C6SC(/C=C3C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)=C2)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C5SC(/C=C3C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)=C2)C=C1,BTCDT-ICF,-5.83,-3.98,16.93,0.73,0.656,8.11,"X. Wu, W. Wang, H. Hang, H. Li, Y. Chen, Q. Xu, H. Tong, L. Wang, Star-Shaped Fused-Ring Electron Acceptors with a C3h-Symmetric and Electron-Rich Benzotri(cyclopentadithiophene) Core for Efficient Nonfullerene Organic Solar Cells, ACS Appl. Mater. Interfaces. 11 (2019) 28115¨C28124. https://doi.org/10.1021/acsami.9b08017."
3344,CCCCCCCCN1N=C2C(/C=C3SC(=C(C#N)C#N)N(CC)C3=O)=CC=C(C3=CC4=C(S3)C3=CC5=C(C=C3C4(C3=CC=C(CCCCCC)C=C3)C3=CC=C(CCCCCC)C=C3)C3=C(C=C(C4=CC=C(/C=C6/SC(=C(C#N)C#N)N(CC)C6=O)C6=NN(CCCCCCCC)N=C46)S3)C5(C3=CC=C(CCCCCC)C=C3)C3=CC=C(CCCCCC)C=C3)C2=N1,BTA3,-5.59,-3.7,10.89,1.21,0.565,8.1,"N. An, Y. Cai, H. Wu, A. Tang, K. Zhang, X. Hao, Z. Ma, Q. Guo, H.S. Ryu, H.Y. Woo, Y. Sun, E. Zhou, Solution-Processed Organic Solar Cells with High Open-Circuit Voltage of 1.3 V and Low Non-Radiative Voltage Loss of 0.16 V, Adv. Mater. 32 (2020) 2002122. https://doi.org/10.1002/adma.202002122."
3345,CCCCCCCCC1(CCCCCCCC)C2=CC3=C(C=C2C2=C1C=C(/C=C1C(=O)C4=C(C=CC(C)=C4)C1=C(C#N)C#N)S2)C(CCCCCCCC)(CCCCCCCC)C1=C3SC(/C=C2C(=O)C3=C(C=CC=C3)C2=C(C#N)C#N)=C1,IDIC8-H,-5.52,-3.76,13.44,0.952,0.625,8,"C. Liu, N. Qiu, Y. Sun, X. Ke, H. Zhang, C. Li, X. Wan, Y. Chen, All-Small-Molecule Organic Solar Cells Based on a Fluorinated Small Molecule Donor With High Open-Circuit Voltage of 1.07 V, Front. Chem. 8 (2020) 329. https://doi.org/10.3389/fchem.2020.00329."
3346,O=C(C(C=CC=C1)=C1C/2=C(C#N)/C#N)C2=C/C3=CC=C(C4=CC5=C(C6=C(C5(CC(CC)CCCC)CC(CC)CCCC)C=C(C7=CC=C(C8=CC=C(/C=C9C(C(C=CC=C%10)=C%10C9=C(C#N)C#N)=O)S8)S7)C=C6)S4)S3.CCCCCC.CCCCCC,ITDI,-5.89,-4.18,13.94,0.94,0.5978,8,"Z. Kang, S.-C. Chen, Y. Ma, J. Wang, Q. Zheng, Push¨CPull Type Non-Fullerene Acceptors for Polymer Solar Cells: Effect of the Donor Core, ACS Appl. Mater. Interfaces. 9 (2017) 24771¨C24777. https://doi.org/10.1021/acsami.7b05417."
3347,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(C=C(/C=C5C(=O)C6=CC(F)=CC=C6C5=C(C#N)C#N)S2)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC3=C2SC(/C=C2C(=O)C4=C(C=CC(F)=C4)C2=C(C#N)C#N)=C3)C=C1,ITIC3,-5.54,-3.9,17,0.758,0.619,7.98,"T. Li, S. Dai, Z. Ke, L. Yang, J. Wang, C. Yan, W. Ma, X. Zhan, Fused Tris(thienothiophene)-Based Electron Acceptor with Strong Near-Infrared Absorption for High-Performance As-Cast Solar Cells, Adv. Mater. 30 (2018) 1705969. https://doi.org/10.1002/adma.201705969."
3348,CCCCCCCCC1=CC=C(C2(C3=CC=C(CCCCCCCC)C=C3)C3=CC(C4=CC=C(C5=C(CC(CC)CCCC)C=C(/C=C6C(=O)C7=CSC=C7C6=C(C#N)C#N)S5)S4)=CC=C3C3=C2C=C(C2=C(CC(CC)CCCC)C=C(/C=C4C(=O)C5=CSC=C5C4=C(C#N)C#N)S2)S3)C=C1,IOTC,-5.7,-4.01,15.04,0.95,0.5552,7.94,"Z. Kang, Y. Ma, Q. Zheng, Asymmetric indenothiophene-based nonfullerene acceptors for binary- and ternary-blend polymer solar cells, Dyes Pigments. 170 (2019) 107555. https://doi.org/10.1016/j.dyepig.2019.107555."
3349,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C=C(C2=CC5=C(S2)/C(=C(C)C#N)C2=CC(F)=C(F)C=C25)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC(C3=CC4=C(S3)C(=C(C#N)C#N)C3=CC(F)=C(F)C=C34)=C2)C=C1,Q1-4F,-5.54,-3.99,15.63,0.73,0.69,7.93,"Q.-Q. Zhang, Y. Li, D. Wang, Z. Chen, Y. Li, S. Li, H. Zhu, X. Lu, H. Chen, C.-Z. Li, Intrinsically Chemo- and Thermostable Electron Acceptors for Efficient Organic Solar Cells, Bull. Chem. Soc. Jpn. 94 (2021) 183¨C190. https://doi.org/10.1246/bcsj.20200231."
3350,O=C(C(C=CC=C1)=C1C/2=C(C#N)C#N)C2=C/C3=CC=C(C4=CC5=C(C=C4)C(C=CC(C6=CC=C(/C=C7C(C(C=CC=C8)=C8C7=C(C#N)/C#N)=O)S6)=C9)=C9C5(CCCCCCCC)CCCCCCCC)S3,DICTF1:1.4,-5.67,-3.79,16.33,0.85,0.55,7.93,"M. Li, Y. Liu, W. Ni, F. Liu, H. Feng, Y. Zhang, T. Liu, H. Zhang, X. Wan, B. Kan, Q. Zhang, T.P. Russell, Y. Chen, A simple small molecule as an acceptor for fullerene-free organic solar cells with efficiency near 8%, J. Mater. Chem. A. 4 (2016) 10409¨C10413. https://doi.org/10.1039/C6TA04358E."
3351,CCCCCCC(CCCCCC)N1C(=O)C2=CC=C3C4=CC=C5C(=O)N(C(CCCCCC)CCCCCC)C(=O)C6=CC7=C(C8=C(C=C(C1=O)C2=C38)C1=C7C2=C(S1)C1=C(SC3=C7C=C8C(=O)N(C(CCCCCC)CCCCCC)C(=O)C9=CC=C%10C%11=CC=C%12C(=O)N(C(CCCCCC)CCCCCC)C(=O)C%13=CC(=C31)C(=C7C%10=C98)C%11=C%12%13)C1=C2SC2=C3C=C7C(=O)N(C(CCCCCC)CCCCCC)C(=O)C8=CC=C9C%10=CC=C%11C(=O)N(C(CCCCCC)CCCCCC)C(=O)C%12=CC(=C21)C(=C3C9=C87)C%10=C%11%12)C4=C56,FBT-PDI3,,,12.1,1.11,0.59,7.9,"H. Hu, Y. Li, J. Zhang, Z. Peng, L. Ma, J. Xin, J. Huang, T. Ma, K. Jiang, G. Zhang, W. Ma, H. Ade, H. Yan, Effect of Ring-Fusion on Miscibility and Domain Purity: Key Factors Determining the Performance of PDI-Based Nonfullerene Organic Solar Cells, Adv. Energy Mater. 8 (2018) 1800234. https://doi.org/10.1002/aenm.201800234."
3352,CCCCCCC1=CC=C(C2=NC3=C(N=C2C2=CC=C(CCCCCC)C=C2)C(C2=CC4=C(S2)C2=C(C=C(/C=C5C(=O)C6=C(C=CC=C6)C5=C(C#N)C#N)S2)C4(CC(CC)CCCC)CC(CC)CCCC)=C(F)C(F)=C3C2=CC3=C(S2)C2=C(C=C(/C=C4C(=O)C5=C(C=CC=C5)C4=C(C#N)C#N)S2)C3(CC(CC)CCCC)CC(CC)CCCC)C=C1,QOC6-4H,-5.59,-3.8,16.19,0.862,0.5664,7.9,"J. Huang, S. Li, J. Qin, L. Xu, X. Zhu, L.-M. Yang, Facile Modification of a Noncovalently Fused-Ring Electron Acceptor Enables Efficient Organic Solar Cells, ACS Appl. Mater. Interfaces. 13 (2021) 45806¨C45814. https://doi.org/10.1021/acsami.1c11412."
3353,CCCCCCCCN1C(=O)/C(=C/C2=CC=C(C3=CC4=C(S3)C3=C(S4)C4=CC5=C(C=C4C3(C3=CC=C(CCCCCC)C=C3)C3=CC=C(CCCCCC)C=C3)C3=C(C4=C(C=C(C6=CC=C(/C=C7SC(=C(C#N)C#N)N(CCCCCCCC)C7=O)C7=NSN=C67)S4)S3)C5(C3=CC=C(CCCCCC)C=C3)C3=CC=C(CCCCCC)C=C3)C3=NSN=C23)SC1=C(C#N)C#N,ITBTR-C8,-5.28,-3.7,14.74,0.9,0.5847,7.85,"J. Qu, Z. Mu, H. Lai, H. Chen, T. Liu, S. Zhang, W. Chen, F. He, Alkyl Chain End Group Engineering of Small Molecule Acceptors for Non-Fullerene Organic Solar Cells, ACS Appl. Energy Mater. 1 (2018) 4724¨C4730. https://doi.org/10.1021/acsaem.8b00851."
3354,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C=C(/C=C2C(=O)C5=C(C=C(F)C(F)=C5)C2=C(C#N)C#N)O3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4OC(/C=C3C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)=C2)C=C1,IDF-4F,-5.83,-4.27,17.49,0.736,0.61,7.81,"E. He, X. Wang, Y. Lu, Y. Yin, F. Guo, S. Gao, Z. He, L. Zhao, Y. Cao, Y. Zhang, Indacenodifuran-Based Non-Fullerene Electron Acceptors for Efficient Polymer Solar Cells, ACS Appl. Energy Mater. 3 (2020) 6133¨C6138. https://doi.org/10.1021/acsaem.0c01247."
3355,CCCCCCN1C(=O)/C(=CC2=CC=C(C3=CC=C(C4=CC5=C(C=C4)C4=C(C=C(C6=CC=C(C7=CC=C(/C=C8/SC(=C(C#N)C#N)N(CCCCCC)C8=O)O7)C7=NSN=C67)C=C4)C5(CC(CC)CCCC)CC(CC)CCCC)C4=NSN=C34)O2)SC1=C(C#N)C#N,FRdCN2,-5.88,-3.81,16,0.934,0.719,7.8,"Suman, A. Bagui, A. Garg, B. Tyagi, V. Gupta, S.P. Singh, A fluorene-core-based electron acceptor for fullerene-free BHJ organic solar cells¡ªtowards power conversion efficiencies over 10%, Chem. Commun. 54 (2018) 4001¨C4004. https://doi.org/10.1039/C7CC08440D."
3356,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=C(SC(/C=C4C(=O)C5=C(C=CC(C)=C5)C4=C(C#N)C#N)=C3)C3=CC=C4C(=C32)C=CC2=C4C(C3=CC=C(CCCCCC)C=C3)(C3=CC=C(CCCCCC)C=C3)C3=C2SC(/C=C2C(=O)C4=C(C=CC=C4)C2=C(C#N)C#N)=C3)C=C1,NTIC-Me,-5.53,-3.73,12.5,0.961,0.649,7.8,"Y.-Q.-Q. Yi, H. Feng, M. Chang, H. Zhang, X. Wan, C. Li, Y. Chen, New small-molecule acceptors based on hexacyclic naphthalene(cyclopentadithiophene) for efficient non-fullerene organic solar cells, J. Mater. Chem. A. 5 (2017) 17204¨C17210. https://doi.org/10.1039/C7TA05809H."
3357,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C=C(/C=C2C(=O)C5=C(C=CC=C5)C2=C(C#N)C#N)O3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4OC(/C=C3C(=O)C4=C(C=CC=C4)C3=C(C#N)C#N)=C2)C=C1,IDF-IC,-5.75,-4.13,14.55,0.905,0.59,7.8,"E. He, X. Wang, Y. Lu, Y. Yin, F. Guo, S. Gao, Z. He, L. Zhao, Y. Cao, Y. Zhang, Indacenodifuran-Based Non-Fullerene Electron Acceptors for Efficient Polymer Solar Cells, ACS Appl. Energy Mater. 3 (2020) 6133¨C6138. https://doi.org/10.1021/acsaem.0c01247."
3358,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(C=C(/C=C5C(=O)C6=C(C=C(F)C(F)=C6)C5=C(C#N)C#N)S2)S3)C(C2=CC=C(C)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC3=C2SC(/C=C2C(=O)C4=C(C=C(F)C(F)=C4)C2=C(C#N)C#N)=C3)C=C1,F7IC,-5.74,-4.01,18.3,0.741,0.575,7.8,"S. Dai, Y. Xiao, P. Xue, J. James Rech, K. Liu, Z. Li, X. Lu, W. You, X. Zhan, Effect of Core Size on Performance of Fused-Ring Electron Acceptors, Chem. Mater. 30 (2018) 5390¨C5396. https://doi.org/10.1021/acs.chemmater.8b02222."
3359,O=C1N(C(CCCCCC)CCCCCC)C(C2=C(C1C=C3[Se]4)C5=C3C(C4=CC6C(N(C(CCCCCC)CCCCCC)C7=O)=O)=C(C6=C7C=C8C(S9)=CC=C9C%10=C%11C(C=C(C%12=CC%13=C%14C%15=C%16C%17=C%18C(C=CC(C(N(C(CCCCCC)CCCCCC)C%19=O)=O)=C%18C%19C=C%17[Se]C%16=CC%14C(N(C(CCCCCC)CCCCCC)C%13=O)=O)=C%15%12)S%11)=C(C%20=CC=C(C%21=CC%22=C%23C%24=C%25C%26=C%27C(C=CC(C(N(C(CCCCCC)CCCCCC)C%28=O)=O)=C%27C%28C=C%26[Se]C%25=CC%23C(N(C(CCCCCC)CCCCCC)C%22=O)=O)=C%24%21)S%20)C%29=C%10C=C(C%30=CC(C(N(C(CCCCCC)CCCCCC)C%31=O)=O)=C(C%31C=C%32[Se]%33)C%34=C%32C(C%33=CC%35C(N(C(CCCCCC)CCCCCC)C%36=O)=O)=C(C%35=C%36C=C%37)C%37=C%34%30)S%29)C8=C5C=C2)=O,BPT-Se,-5.92,-3.85,11.1,1.039,0.675,7.78,"Z. Luo, T. Liu, Z. Chen, Y. Xiao, G. Zhang, L. Huo, C. Zhong, X. Lu, H. Yan, Y. Sun, C. Yang, Isomerization of Perylene Diimide Based Acceptors Enabling High-Performance Nonfullerene Organic Solar Cells with Excellent Fill Factor, Adv. Sci. 6 (2019) 1802065. https://doi.org/10.1002/advs.201802065."
3360,O=C(C(C=CC=C1)=C1C/2=C(C#N)C#N)C2=C/C3=CC4=C(S3)C(SC5=C6SC7=C5C(C8=CC=C(CCCCCC)C=C8)(C9=CC=C(CCCCCC)C=C9)C%10=C7SC(/C=C%11C(C(C=CC=C%12)=C%12C\%11=C(C#N)/C#N)=O)=C%10)=C6C4(C%13=CC=C(CCCCCC)C=C%13)C%14=CC=C(CCCCCC)C=C%14,IHIC,-5.45,-3.93,17.1,0.744,0.609,7.77,"W. Wang, C. Yan, T.-K. Lau, J. Wang, K. Liu, Y. Fan, X. Lu, X. Zhan, Fused Hexacyclic Nonfullerene Acceptor with Strong Near-Infrared Absorption for Semitransparent Organic Solar Cells with 9.77% Efficiency, Adv. Mater. 29 (2017) 1701308. https://doi.org/10.1002/adma.201701308."
3361,CCCCC(CC)CC1(CC(CC)CCCC)C2=C(SC(/C=C3C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)=C2)C2=C1C=C(C1=C(OC)C(OC)=C(C3=CC4=C(S3)C3=C(C=C(/C=C5C(=O)C6=C(C=C(F)C(F)=C6)C5=C(C#N)C#N)S3)C4(CC(CC)CCCC)CC(CC)CCCC)C3=NSN=C31)S2,BOC-4F,-5.4,-3.78,14.41,0.88,0.6126,7.76,"H. Yu, Z. Qi, X. Li, Z. Wang, W. Zhou, H. Ade, H. Yan, K. Chen, Modulating Energy Level on an A-D-A¡ä-D-A-Type Unfused Acceptor by a Benzothiadiazole Core Enables Organic Solar Cells with Simple Procedure and High Performance, Sol. RRL. 4 (2020) 2000421. https://doi.org/10.1002/solr.202000421."
3362,CCCCCCCCC1(CCCCCCCC)C2=CC3=C(C=C2C2=C1C=C(C1=CC=C(/C=C4SC(=S)N(CC)C4=O)C4=NON=C14)S2)C(CCCCCCCC)(CCCCCCCC)C1=C3SC(C2=CC=C(/C=C3SC(=S)N(CC)C3=O)C3=NON=C23)=C1,IDTBOR,-5.49,-3.93,15.98,0.89,0.5467,7.74,"Y. Nian, F. Pan, S. Li, H. Jiang, S. Feng, L. Zhang, Y. Cao, J. Chen, Benzoxadiazole and Benzoselenadiazole as ¦Ð-Bridges in Nonfullerene Acceptors for Efficient Polymer Solar Cells, Asian J. Org. Chem. 7 (2018) 2285¨C2293. https://doi.org/10.1002/ajoc.201800389."
3363,CCCCCCCCC1(CCCCCCCC)C2=CC(C3=CC=C(/C=C4SC(=S)N(CC)C4=O)C4=NSN=C34)=CC=C2C2=CC3=C(C=C21)C1=C(C=C(C2=CC=C(/C=C4SC(=S)N(CC)C4=O)C4=NSN=C24)C=C1)C3(CCCCCCCC)CCCCCCCC,IDFBR,,,14.4,0.82,0.64,7.7,"D. Baran, R.S. Ashraf, D.A. Hanifi, M. Abdelsamie, N. Gasparini, J.A. R?hr, S. Holliday, A. Wadsworth, S. Lockett, M. Neophytou, C.J.M. Emmott, J. Nelson, C.J. Brabec, A. Amassian, A. Salleo, T. Kirchartz, J.R. Durrant, I. McCulloch, Reducing the efficiency¨Cstability¨Ccost gap of organic photovoltaics with highly efficient and stable small molecule acceptor ternary solar cells, Nat. Mater. 16 (2017) 363¨C369. https://doi.org/10.1038/nmat4797."
3364,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(S3)C3=C(C=C(/C=C5C(=O)C6=C(C=CC=C6)C5=C(C#N)C#N)S3)S2)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC3=C2SC2=C3SC(CC3C(=O)C4=C(C=CC=C4)C3=C(C#N)C#N)=C2)C=C1,INIC,-5.45,-3.88,13.51,0.957,0.579,7.7,"S. Dai, F. Zhao, Q. Zhang, T.-K. Lau, T. Li, K. Liu, Q. Ling, C. Wang, X. Lu, W. You, X. Zhan, Fused Nonacyclic Electron Acceptors for Efficient Polymer Solar Cells, J. Am. Chem. Soc. 139 (2017) 1336¨C1343. https://doi.org/10.1021/jacs.6b12755."
3365,CCCCCCCCCCCC1=C(/C=C2C(=O)C3=CSC=C3C2=C(C#N)C#N)SC2=C1SC1=C2C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CC3=CC=C4C=C5C=CC(C)=CC5=CC4=C3)C=C2)C2=C1C=CC(C1=CC3=C(S1)C(CCCCCCCC)=C(/C=C1C(=O)C4=CSC=C4C1=C(C#N)C#N)S3)=C2,ITUTC,-5.66,-3.85,14.54,0.94,0.5637,7.68,"M. Zhang, Y. Ma, Q. Zheng, Asymmetric indenothienothiophene-based unfused core for A-D-A type nonfullerene acceptors, Dyes Pigments. 180 (2020) 108495. https://doi.org/10.1016/j.dyepig.2020.108495."
3366,CCCCCC(CCCCC)N1C(=O)C2=CC3=C4C5=C(C=CC(=C25)C1=O)C1=C2C5=C(C=C1)C(=O)N(C(CCCCC)CCCCC)C(=O)C5=CC(=C24)C1=C3C2=CC3=C4C(=CC5=C6C7=C(C=C8C(=O)N(C(CCCCC)CCCCC)C(=O)C9=C8C7=C(C1=C9)C2=C46)C1=C5SC2=C1SC1=C2C2=CC4=C5C(=CC6=C7C8=C(C=C9C(=O)N(C(CCCCC)CCCCC)C(=O)C%10=C9C8=C(C1=C%10)C2=C57)C1=C6C2=CC5=C6C(=CC=C7C8=CC=C9C(=O)N(C(CCCCC)CCCCC)C(=O)C%10=C9C8=C(C1=C%10)C2=C76)C(=O)N(C(CCCCC)CCCCC)C5=O)C(=O)N(C(CCCCC)CCCCC)C4=O)C(=O)N(C(CCCCC)CCCCC)C3=O,FTT-FDI,-6,-4.01,16.5,0.822,0.564,7.66,"Y. Yin, W. Zhang, Z. Zheng, Z. Ge, Y. Liu, F. Guo, S. Gao, L. Zhao, Y. Zhang, Integrated linker-regulation and ring-fusion engineering for efficient additive-free non-fullerene organic solar cells, J. Mater. Chem. C. 8 (2020) 12516¨C12526. https://doi.org/10.1039/D0TC02499F."
3367,O=C1N(C(CCCCC)CCCCC)C(C2=C(C1C=C3[Se]4)C5=C3C(C4=CC6C(N(C(CCCCC)CCCCC)C7=O)=O)=C(C6=C7C=C8C9=CC=C(/C(C%10=CC=C(C%11=CC%12=C%13C%14=C%15C%16=C%17C(C=CC(C(N(C(CCCCC)CCCCC)C%18=O)=O)=C%17C%18C=C%16[Se]C%15=CC%13C(N(C(CCCCC)CCCCC)C%12=O)=O)=C%14%11)C=C%10)=C(C%19=CC=C(C%20=CC%21=C%22C%23=C%24C%25=C%26C(C=CC(C(N(C(CCCCC)CCCCC)C%27=O)=O)=C%26C%27C=C%25[Se]C%24=CC%22C(N(C(CCCCC)CCCCC)C%21=O)=O)=C%23%20)C=C%19)C%28=CC=C(C%29=CC%30=C%31C%32=C%33C%34=C%35C(C=CC(C(N(C(CCCCC)CCCCC)C%36=O)=O)=C%35C%36C=C%34[Se]C%33=CC%31C(N(C(CCCCC)CCCCC)C%30=O)=O)=C%32%29)C=C%28)C=C9)C8=C5C=C2)=O,TPE-PDI4-Se,-5.89,-3.81,10.287,1.051,0.688,7.63,"G. Li, S. Wang, T. Liu, P. Hao, Z. Liu, F. Li, L.-M. Yang, Y. Zhang, D. Li, S. Yang, J. Zhao, J. Li, H. Yan, B. Tang, Non-fullerene acceptor engineering with three-dimensional thiophene/selenophene-annulated perylene diimides for high performance polymer solar cells, J. Mater. Chem. C. 6 (2018) 12601¨C12607. https://doi.org/10.1039/C8TC04926B."
3368,CCCCC(CC)COC1=C(C2=CC3=C(S2)C2=C(C=C(/C=C4C(=O)C5=C(C=C(F)C(F)=C5)C4=C(C#N)C#N)S2)C3(CC(CC)CCCC)CC(CC)CCCC)SC2=C1SC(C1=CC3=C(S1)C1=C(C=C(/C=C4C(=O)C5=C(C=C(F)C(F)=C5)C4=C(C#N)C#N)S1)C3(CC(CC)CCCC)CC(CC)CCCC)=C2OCC(CC)CCCC,TTDTC-4F,-5.21,-3.75,22.1,0.56,0.601,7.62,"Z. Liang, X. Cheng, Y. Jiang, J. Yu, X. Xu, Z. Peng, L. Bu, Y. Zhang, Z. Tang, M. Li, L. Ye, Y. Geng, P3HT-Based Organic Solar Cells with a Photoresponse to 1000 nm Enabled by Narrow Band Gap Nonfullerene Acceptors with High HOMO Levels, ACS Appl. Mater. Interfaces. 13 (2021) 61487¨C61495. https://doi.org/10.1021/acsami.1c21089."
3369,CCCCC(CC)COC(=O)C1=C(C2=CC3=C(S2)C2=C(C=C(C4=C(C(=O)OCC(CC)CCCC)C=C(/C=C5C(=O)C6=CC(F)=C(F)C=C6C5=C(C#N)C#N)S4)S2)C3(CC(CC)CCCC)CC(CC)CCCC)SC(/C=C2C(=O)C3=CC(F)=C(F)C=C3C2=C(C#N)C#N)=C1,CETIC-4F,-5.47,-4.13,19.1,0.65,0.61,7.61,"J. Vollbrecht, J. Lee, S.-J. Ko, V.V. Brus, A. Karki, W. Le, M. Seifrid, M.J. Ford, K. Cho, G.C. Bazan, T.-Q. Nguyen, Design of narrow bandgap non-fullerene acceptors for photovoltaic applications and investigation of non-geminate recombination dynamics, J. Mater. Chem. C. 8 (2020) 15175¨C15182. https://doi.org/10.1039/D0TC02136A."
3370,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C=C(C2=CC=C(/C=C5SC(=S)N(CC(F)(F)F)C5=O)C5=NSN=C25)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC(C3=CC=C(/C=C4SC(=S)N(CC(F)(F)F)C4=O)C4=NSN=C34)=C2)C=C1,IDT-BT-RF3,-5.35,-3.78,14.47,1.02,0.5888,7.59,"L.-M. Tang, J. Xiao, W.-Y. Bai, Q.-Y. Li, H.-C. Wang, M.-S. Miao, H.-L. Yip, Y.-X. Xu, End-chain effects of non-fullerene acceptors on polymer solar cells, Org. Electron. 64 (2019) 1¨C6. https://doi.org/10.1016/j.orgel.2018.10.005."
3371,CCCCC(CC)COC1=CC=CC(C2(C3=CC=CC(OCC(CC)CCCC)=C3)C3=CC4=C(C=C3C3=C2C2=C(C=C(/C=C5C(=O)C6=CSC(SC)=C6C5=C(C#N)C#N)S2)S3)C(C2=CC=CC(OCC(CC)CCCC)=C2)(C2=CC(OCC(CC)CCCC)=CC=C2)C2=C4SC3=C2SC(/C=C2C(=O)C4=C(SC)SC=C4C2=C(C#N)C#N)=C3)=C1,IT-SM,-5.51,-3.97,15.15,0.84,0.59,7.55,"S. Jeong, H. Je, J.H. Lee, S.H. Lee, S.-Y. Jang, K. Park, H. Kang, S.-K. Kwon, Y.-H. Kim, K. Lee, Molecular engineering of non-fullerene acceptors based on thiophene-fused end groups for fullerene-free organic solar cells, Dyes Pigments. 198 (2022) 109987. https://doi.org/10.1016/j.dyepig.2021.109987."
3372,CCCCCCCCC(CCCCCC)COC1=C(C2=CC3=C(S2)C2=C(C=C(/C=C4C(=O)C5=C(C=C(F)C(F)=C5)C4=C(C#N)C#N)S2)C3(CC(CC)CCCC)CC(CC)CCCC)C2=NSN=C2C(C2=CC3=C(S2)C2=C(C=C(/C=C4C(=O)C5=C(C=C(F)C(F)=C5)C4=C(C#N)C#N)S2)C3(CC(CC)CCCC)CC(CC)CCCC)=C1OCC(CCCCCC)CCCCCCCC,BTOC6C8-IC4F,-5.52,-3.92,17.02,0.8,0.5544,7.55,"Y. Shi, J. Pan, H. Zhang, C. Yang, Z. Zhang, D. Deng, J. Zhang, K. Lu, Z. Wei, The substituents on the intermediate electron-deficient groups in small molecular acceptors result appropriate morphologies for organic solar cells, Org. Electron. 93 (2021) 106133. https://doi.org/10.1016/j.orgel.2021.106133."
3373,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C=C(C2=C(C(=O)OCC(CC)CCCC)C=C(/C=C5C(=O)C6=C(C=C(F)C(F)=C6)C5=C(C#N)C#N)S2)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC(C3=C(C(=O)OCC(CC)CCCC)C=C(/C=C4C(=O)C5=C(C=C(F)C(F)=C5)C4=C(C#N)C#N)S3)=C2)C=C1,IDT-3EsT-2IC2F,-5.38,-3.93,14.68,0.886,0.58,7.54,"T.B. Raju, H.W. Cho, P. Gopikrishna, Y. Lee, J.Y. Kim, B. Kim, Positional Effect of the 2-Ethylhexyl Carboxylate Side Chain on the Thiophene ¦Ð-Bridge of Nonfullerene Acceptors for Efficient Organic Solar Cells, ACS Appl. Energy Mater. 4 (2021) 11675¨C11683. https://doi.org/10.1021/acsaem.1c02403."
3374,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C=C(/C=C2C(=O)C5=CC=C(C6=CC=CC=C6)C=C5C2=C(C#N)C#N)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC(/C=C3C(=O)C4=C(C=CC(C5=CC=CC=C5)=C4)C3=C(C#N)C#N)=C2)C=C1,IDT-IC-B,-5.75,-3.92,13.5,0.86,0.65,7.53,"S. Feng, D. Ma, L. Wu, Y. Liu, C. Zhang, X. Xu, X. Chen, S. Yan, Z. Bo, Enhance the performance of polymer solar cells via extension of the flanking end groups of fused ring acceptors, Sci. China Chem. 61 (2018) 1320¨C1327. https://doi.org/10.1007/s11426-018-9252-9."
3375,CCCCCCCCC1(CCCCCCCC)C2=C(C=CC(C3=CC=C(/C=C4C(=O)C5=CSC=C5C4=C(C#N)C#N)O3)=C2)C2=C1C=C(C1=CC=C(/C=C3C(=O)C4=CSC=C4C3=C(C#N)C#N)O1)C=C2,DTC-F-F,-5.51,-3.83,16.01,0.84,0.56,7.53,"J. Liao, P. Zheng, Z. Cai, S. Shen, G. Xu, H. Zhao, Y. Xu, Construction of simple and low-cost acceptors for efficient non-fullerene organic solar cells, Org. Electron. 89 (2021) 106026. https://doi.org/10.1016/j.orgel.2020.106026."
3376,O=C1C2=C(C=CC=C2)/C(C1CC3=CC4=C(S3)C5=CC6=CC7=C(C(SC(CC8/C(C(C=CC=C9)=C9C8=O)=C(C#N)C#N)=C%10)=C%10C7(CCCCCCCC)CCCCCCCC)C=C6C=C5C4(CCCCCCCC)CCCCCCCC)=C(C#N)/C#N,NCFIC,-5.43,-3.94,15.19,0.88,0.563,7.52,"F.-Y. Cao, W.-C. Huang, S.-L. Chang, Y.-J. Cheng, Angular-Shaped 4,9-Dialkylnaphthodithiophene-Based Octacyclic Ladder-Type Non-Fullerene Acceptors for High Efficiency Ternary-Blend Organic Photovoltaics, Chem. Mater. 30 (2018) 4968¨C4977. https://doi.org/10.1021/acs.chemmater.8b01089."
3377,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(S3)C(CCCCCC)=C(/C=C3/C(=O)N(CC)C(=S)N(CC)C3O)S2)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC3=C2SC(C=C2C(=O)N(CC)C(=S)N(CC)C2=O)=C3CCCCCC)C=C1,2C6-IDTT-T,-5.74,-3.72,13.32,1.069,0.528,7.52,"T. Xia, C. Li, H.S. Ryu, X. Sun, H.Y. Woo, Y. Sun, Asymmetrically Alkyl-Substituted Wide-Bandgap Nonfullerene Acceptor for Organic Solar Cells, Sol. RRL. 4 (2020) 2000061. https://doi.org/10.1002/solr.202000061."
3378,CCCCCC(CCCCC)N1C(=O)C2=CC=C3C4=CC=C5C(=O)N(C(CCCCC)CCCCC)C(=O)C6=C5C4=C4C(=C6)C5=C6C7=CC8=C9C(=CC=C%10C%11=CC=C%12C(=O)N(C(CCCCC)CCCCC)C(=O)C%13=C%12C%11=C(C(=C%13)C6=C6C%11=CC%12=C%13C(=CC=C%14C%15=CC=C%16C(=O)N(C(CCCCC)CCCCC)C(=O)C%17=C%16C%15=C(C(=C%17)C6=C5C5=CC(=C2C3=C54)C1=O)C%11=C%14%13)C(=O)N(C(CCCCC)CCCCC)C%12=O)C7=C%109)C(=O)N(C(CCCCC)CCCCC)C8=O,PDI4,-5.85,-3.81,10.6,1.14,0.63,7.5,"X. Liu, X. Du, J. Wang, C. Duan, X. Tang, T. Heumueller, G. Liu, Y. Li, Z. Wang, J. Wang, F. Liu, N. Li, C.J. Brabec, F. Huang, Y. Cao, Efficient Organic Solar Cells with Extremely High Open-Circuit Voltages and Low Voltage Losses by Suppressing Nonradiative Recombination Losses, Adv. Energy Mater. 8 (2018) 1801699. https://doi.org/10.1002/aenm.201801699."
3379,CCCCCCCCC1(CCCCCCCC)C2=CC3=C(C=C2C2=C1C=C(C1=C4OCCOC4=C(/C=C4C(=O)C5=C(C=C(F)C(F)=C5)C4=C(C#N)C#N)S1)C=C2)C(CCCCCCCC)(CCCCCCCC)C1=C3C=CC(C2=C3OCCOC3=C(/C=C3C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)S2)=C1,IFL-ED-4F,-5.71,-3.84,13.64,0.94,0.5824,7.5,"S.J. Jeon, Y.H. Kim, I.N. Kim, N.G. Yang, J.H. Yun, D.K. Moon, Utilizing 3,4-ethylenedioxythiophene (EDOT)-bridged non-fullerene acceptors for efficient organic solar cells, J. Energy Chem. 65 (2022) 194¨C204. https://doi.org/10.1016/j.jechem.2021.05.032."
3380,O=C(C(C=CC=C1)=C1C/2=C(C#N)C#N)C2=C/C(S3)=CC4=C3C5=C(C4(C6=CC=C(CCCCCC)C=C6)C7=CC=C(CCCCCC)C=C7)C=C8C(C=C(C(C9=CC=C(CCCCCC)C=C9)(C%10=CC=C(CCCCCC)C=C%10)C%11=C%12SC(/C=C%13C(C(C=CC=C%14)=C%14C\%13=C(C#N)/C#N)=O)=C%11)C%12=C8)=C5,NTIC,-5.58,-3.76,13.55,0.926,0.608,7.43,"Y.-Q.-Q. Yi, H. Feng, M. Chang, H. Zhang, X. Wan, C. Li, Y. Chen, New small-molecule acceptors based on hexacyclic naphthalene(cyclopentadithiophene) for efficient non-fullerene organic solar cells, J. Mater. Chem. A. 5 (2017) 17204¨C17210. https://doi.org/10.1039/C7TA05809H."
3381,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C=C(C2=C(C(=O)OCC(CC)CCCC)C=C(/C=C5C(=O)C6=C(C=CC=C6)C5=C(C#N)C#N)S2)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC(C3=C(C(=O)OCC(CC)CCCC)C=C(/C=C4C(=O)C5=C(C=CC=C5)C4=C(C#N)C#N)S3)=C2)C=C1,IDT-3EsT,-5.38,-3.85,13.49,0.985,0.56,7.43,"T.B. Raju, H.W. Cho, P. Gopikrishna, Y. Lee, J.Y. Kim, B. Kim, Positional Effect of the 2-Ethylhexyl Carboxylate Side Chain on the Thiophene ¦Ð-Bridge of Nonfullerene Acceptors for Efficient Organic Solar Cells, ACS Appl. Energy Mater. 4 (2021) 11675¨C11683. https://doi.org/10.1021/acsaem.1c02403."
3382,O=C(C(C=C(F)C(F)=C1)=C1C/2=C(C#N)C#N)C2=C/C3=CC(OCC(CC)CCCC)=C(C4=CC(C5(CC(CC)CCCC)CC(CC)CCCC)=C(S4)C6=C5C=C(C7=C(OCC(CC)CCCC)C=C(/C=C8C(C(C=C(F)C(F)=C9)=C9C8=C(C#N)/C#N)=O)S7)S6)S3,COTIC-4F,-5.26,-4.16,20.3,0.56,0.563,7.4,"J. Lee, S.-J. Ko, M. Seifrid, H. Lee, B.R. Luginbuhl, A. Karki, M. Ford, K. Rosenthal, K. Cho, T.-Q. Nguyen, G.C. Bazan, Bandgap Narrowing in Non-Fullerene Acceptors: Single Atom Substitution Leads to High Optoelectronic Response Beyond 1000 nm, Adv. Energy Mater. 8 (2018) 1801212. https://doi.org/10.1002/aenm.201801212."
3383,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=C(SC(C4=CC=C(/C=C5C(=O)C6=CC(F)=C(F)C=C6C5=C(C#N)C#N)[Se]4)=C3OCC(CC)CCCC)C3=C2C2=C(S3)C3=C(S2)C2=C(C(OCC(CC)CCCC)=C(C4=CC=C(/C=C5C(=O)C6=C(C=C(F)C(F)=C6)C5=C(C#N)C#N)[Se]4)S2)C3(C2=CC=C(CCCCCC)C=C2)C2=CC=C(CCCCCC)C=C2)C=C1,4TO-Se-4F,-5.29,-3.85,19.13,0.7,0.5548,7.4,"D. Liu, T. Wang, X. Ke, N. Zheng, Z. Chang, Z. Xie, Y. Liu, Ultra-narrow bandgap non-fullerene acceptors for organic solar cells with low energy loss, Mater. Chem. Front. 3 (2019) 2157¨C2163. https://doi.org/10.1039/C9QM00505F."
3384,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C=C(/C=C2C(=O)C5=CSC=C5C2=C(C#N)C#N)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC(/C=C3C(=O)C4=CSC=C4C3=C(C#N)C#N)=C2)C=C1,IDTCN,-5.91,-3.94,13.9,0.98,0.54,7.4,"Z. Luo, C. Sun, S. Chen, Z.-G. Zhang, K. Wu, B. Qiu, C. Yang, Y. Li, C. Yang, Side-Chain Impact on Molecular Orientation of Organic Semiconductor Acceptors: High Performance Nonfullerene Polymer Solar Cells with Thick Active Layer over 400 nm, Adv. Energy Mater. 8 (2018) 1800856. https://doi.org/10.1002/aenm.201800856."
3385,CCCCC(CC)CC1=CC=C(C2(C3=CC=C(CC(CC)CCCC)C=C3)C3=CC(C4=CC=C(C5=C(CC(CC)CCCC)C=C(/C=C6C(=O)C7=CSC=C7C6=C(C#N)C#N)S5)S4)=CC=C3C3=C2C=C(C2=C(CC(CC)CCCC)C=C(/C=C4C(=O)C5=CSC=C5C4=C(C#N)C#N)S2)S3)C=C1,IETC,-5.72,-4,14.53,0.96,0.5321,7.4,"Z. Kang, Y. Ma, Q. Zheng, Asymmetric indenothiophene-based nonfullerene acceptors for binary- and ternary-blend polymer solar cells, Dyes Pigments. 170 (2019) 107555. https://doi.org/10.1016/j.dyepig.2019.107555."
3386,O=C(C(C=CC=C1)=C1C/2=C(C#N)C#N)C2=C/C3=CC4=C(C5=CC(C6(C7=CC=C(CCCCCC)C=C7)C8=CC=C(CCCCCC)C=C8)=C(C9=C6C=C(/C=C%10C(C(C=CC=C%11)=C%11C\%10=C(C#N)C#N)=O)S9)C=C5C4(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)S3,IC-C1IDT-IC,-5.91,-3.83,13.39,0.92,0.6,7.39,"Y. Lin, Q. He, F. Zhao, L. Huo, J. Mai, X. Lu, C.-J. Su, T. Li, J. Wang, J. Zhu, Y. Sun, C. Wang, X. Zhan, A Facile Planar Fused-Ring Electron Acceptor for As-Cast Polymer Solar Cells with 8.71% Efficiency, J. Am. Chem. Soc. 138 (2016) 2973¨C2976. https://doi.org/10.1021/jacs.6b00853."
3387,CCCCCCOC1=C2C3=C(C4=C(C=C(/C=C5C(=O)C6=C(C=CC=C6)C5=C(C#N)C#N)S4)S3)C(C3=CC=C(CCCCCC)C=C3)(C3=CC=C(CCCCCC)C=C3)C3=CC(OCCCCCC)=C4C5=C(C6=C(C=C(/C=C7C(=O)C8=C(C=CC=C8)C7=C(C#N)C#N)S6)S5)C(C5=CC=C(CCCCCC)C=C5)(C5=CC=C(CCCCCC)C=C5)C(=C1)C4=C32,PTT-IC,-5.51,-3.78,12.58,0.99,0.59,7.39,"S. Du, N. Yao, S. Liu, Y. Xu, J. Cao, W. Zhuang, J. Yu, N. Wang, D. Yu, F. Zhang, E. Wang, Nonfullerene acceptors from thieno[3,2-b]thiophene-fused naphthalene donor core with six-member-ring connection for efficient organic solar cells, Dyes Pigments. 185 (2021) 108892. https://doi.org/10.1016/j.dyepig.2020.108892."
3388,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)OC3=CC4=C(C=C3C3=C2C=C(C2=CC=C(/C=C5C(=O)C6=C(C=CC=C6)C5=C(C#N)C#N)S2)S3)OC(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC(C3=CC=C(/C=C4C(=O)C5=C(C=CC=C5)C4=C(C#N)C#N)S3)=C2)C=C1,PTTIC,-5.48,-4.04,14.27,0.93,0.5549,7.35,"Z. Liu, X. Zhang, P. Ren, Y. Wu, D. Zeng, X. Duan, X. Gao, P. Cai, Pyran-bridged A-D-A type small molecular acceptors for organic solar cells, Sol. Energy. 183 (2019) 463¨C468. https://doi.org/10.1016/j.solener.2019.03.046."
3389,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(C=C(/C=C/C=C5/C(=O)C6=C(C=CC=C6)C5=C(C#N)C#N)S2)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC3=C2SC(/C=C/C=C2/C(=O)C4=C(C=CC=C4)C2=C(C#N)C#N)=C3)C=C1,ITVIV,-5.46,-3.97,14.47,0.89,0.5764,7.34,"X. Li, H. Huang, H. Bin, Z. Peng, C. Zhu, L. Xue, Z.-G. Zhang, Z. Zhang, H. Ade, Y. Li, Synthesis and Photovoltaic Properties of a Series of Narrow Bandgap Organic Semiconductor Acceptors with Their Absorption Edge Reaching 900 nm, Chem. Mater. 29 (2017) 10130¨C10138. https://doi.org/10.1021/acs.chemmater.7b03928."
3390,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(C=C(C5=CC=C(/C=C6SC(=C(C#N)C#N)N(CC)C6=O)C6=NSN=C56)S2)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC3=C2SC(C2=CC=C(/C=C4SC(=C(C#N)C#N)N(CCCC)C4=O)C4=NSN=C24)=C3)C=C1,ITBTR-C4,-5.3,-3.71,14.75,0.9,0.5415,7.33,"J. Qu, Z. Mu, H. Lai, H. Chen, T. Liu, S. Zhang, W. Chen, F. He, Alkyl Chain End Group Engineering of Small Molecule Acceptors for Non-Fullerene Organic Solar Cells, ACS Appl. Energy Mater. 1 (2018) 4724¨C4730. https://doi.org/10.1021/acsaem.8b00851."
3391,CCCCC(CC)CC1(CC(CC)CCCC)C2=C(SC(/C=C3C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)=C2)C2=C1C=C(C1=C(F)C(F)=C(C3=CC4=C(S3)C3=C(C=C(/C=C5C(=O)C6=C(C=C(F)C(F)=C6)C5=C(C#N)C#N)S3)C4(CC(CC)CCCC)CC(CC)CCCC)C3=NSN=C31)S2,BTCPDTF,-5.64,-3.92,15.29,0.71,0.68,7.32,"N. Yoon, J.-Y. Jeong, S. Oh, C.E. Song, H.K. Lee, W.S. Shin, J.-C. Lee, S.-J. Moon, S.K. Lee, Effects of Electron-Donating and Electron-Accepting Substitution on Photovoltaic Performance in Benzothiadiazole-Based A¨CD¨CA¡ä¨CD¨CA-Type Small-Molecule Acceptor Solar Cells, ACS Appl. Energy Mater. 3 (2020) 12327¨C12337. https://doi.org/10.1021/acsaem.0c02083."
3392,CCCCCCC1(CCCCCC)C2=C(SC(/C=C3C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)=C2)C2=C1C1=C(C=C2)C2=C(C=C1)C1=C(C=C(/C=C3C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)S1)C2(CCCCCC)CCCCCC,IHIC2,-5.69,-3.86,15.6,0.774,0.605,7.3,"J. Zhu, Z. Ke, Q. Zhang, J. Wang, S. Dai, Y. Wu, Y. Xu, Y. Lin, W. Ma, W. You, X. Zhan, Naphthodithiophene-Based Nonfullerene Acceptor for High-Performance Organic Photovoltaics: Effect of Extended Conjugation, Adv. Mater. 30 (2018) 1704713. https://doi.org/10.1002/adma.201704713."
3393,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(C=C(/C=C5C(=O)C6=C(C=C(F)C(F)=C6)C5=C(C#N)C#N)S2)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC3=C2SC(C2=C(F)C(F)=C(C4=CC5=C(S4)C4=C(S5)C5=CC6=C(C=C5C4(C4=CC=C(CCCCCC)C=C4)C4=CC=C(CCCCCC)C=C4)C4=C(C5=C(C=C(/C=C7C(=O)C8=C(C=C(F)C(F)=C8)C7=C(C#N)C#N)S5)S4)C6(C4=CC=C(CCCCCC)C=C4)C4=CC=C(CCCCCC)C=C4)C4=NSN=C42)=C3)C=C1,FDTBT-IDTT-FINCN,-5.46,-3.92,13.56,0.86,0.62,7.27,"H.S. Kim, C.E. Song, J.-W. Ha, S. Lee, S. Rasool, H.K. Lee, W.S. Shin, D.-H. Hwang, Synthesis of ITIC Derivatives with Extended ¦Ð-Conjugation as Non-Fullerene Acceptors for Organic Solar Cells, ACS Appl. Mater. Interfaces. 11 (2019) 47121¨C47130. https://doi.org/10.1021/acsami.9b15247."
3394,CCCCCCCCCCCC1=C(/C=C2/C3=C(C=CC=C3)C3=C2N=C(C#N)C(C#N)=N3)SC2=C1SC1=C2N(CC(CC)CCCC)C2=C1C1=NSN=C1C1=C2N(CC(CC)CCCC)C2=C1SC1=C2SC(/C=C2/C3=C(C=CC=C3)C3=C2N=C(C#N)C(C#N)=N3)=C1CCCCCCCCCCC,IPC-BEH-IPC,-5.38,-3.67,15.22,0.967,0.4937,7.26,"P. Gopikrishna, H. Choi, D.H. Kim, J.H. Hwang, Y. Lee, H. Jung, G. Yu, T.B. Raju, E. Lee, Y. Lee, S. Cho, B. Kim, Impact of symmetry-breaking of non-fullerene acceptors for efficient and stable organic solar cells, Chem. Sci. 12 (2021) 14083¨C14097. https://doi.org/10.1039/D1SC04153C."
3395,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=C(SC(/C=C4C(=O)C5=C(C=CC=C5)C4=C(C#N)C#N)=C3)C3=C2C2=C(S3)C3=C(S2)C2=C(C=C(/C=C4C(=O)C5=C(C=C(F)C(F)=C5)C4=C(C#N)C#N)S2)C32C3=CC=C(CCCCCC)C=C3C3=C2C=CC(CCCCCC)=C3)C=C1,4TIC-4F,-5.6,-4.21,17.7,0.63,0.65,7.25,"X. Liao, H. Pei, H. Zhao, Y. Cui, L. Li, X. Shi, P. Zhu, W. Ma, Y. Chen, A.K.-Y. Jen, The synergistic effects of central core size and end group engineering on performance of narrow bandgap nonfullerene acceptors, Chem. Eng. J. 435 (2022) 135020. https://doi.org/10.1016/j.cej.2022.135020."
3396,CCCCC(CC)CC1(CC(CC)CCCC)C2=C(SC(/C=C3C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)=C2)C2=C1C=C(C1=CC=C(C3=CC4=C(S3)C3=C(C=C(/C=C5C(=O)C6=C(C=C(F)C(F)=C6)C5=C(C#N)C#N)S3)C4(CC(CC)CCCC)CC(CC)CCCC)C3=NSN=C13)S2,BTCPDT,-5.54,-3.95,15.7,0.69,0.67,7.22,"N. Yoon, J.-Y. Jeong, S. Oh, C.E. Song, H.K. Lee, W.S. Shin, J.-C. Lee, S.-J. Moon, S.K. Lee, Effects of Electron-Donating and Electron-Accepting Substitution on Photovoltaic Performance in Benzothiadiazole-Based A¨CD¨CA¡ä¨CD¨CA-Type Small-Molecule Acceptor Solar Cells, ACS Appl. Energy Mater. 3 (2020) 12327¨C12337. https://doi.org/10.1021/acsaem.0c02083."
3397,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C=C(C2=C(SCC(CC)CCCC)C=C(/C=C5C(=O)C6=C(C=C(F)C(F)=C6)C5=C(C#N)C#N)S2)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC(C3=C(SCC(CC)CCCC)C=C(/C=C4C(=O)C5=C(C=C(F)C(F)=C5)C4=C(C#N)C#N)S3)=C2)C=C1,IEICS-4F,,,9.83,1.72,0.61,7.2,"S. Chen, H. Yao, B. Hu, G. Zhang, L. Arunagiri, L.-K. Ma, J. Huang, J. Zhang, Z. Zhu, F. Bai, W. Ma, H. Yan, A Nonfullerene Semitransparent Tandem Organic Solar Cell with 10.5% Power Conversion Efficiency, Adv. Energy Mater. 8 (2018) 1800529. https://doi.org/10.1002/aenm.201800529."
3398,CCCCCC(CCCCC)N1C(=O)C2=CC3=C4C5=C(C=CC(=C25)C1=O)C1=C2C5=C(C=C1)C(=O)N(C(CCCCC)CCCCC)C(=O)C5=CC(=C24)C1=C3C2=CC3=C4C(=CC=C5C6=C(C7=CC8=C(C=C(C9=CC%10=C%11C(=CC%12=C%13C%14=C(C=C%15C(=O)N(C(CCCCC)CCCCC)C(=O)C%16=C%15C%14=C(C=C%16)C9=C%11%13)C9=C%12C%11=CC%12=C%13C(=CC=C%14C%15=CC=C%16C(=O)N(C(CCCCC)CCCCC)C(=O)C%17=C%16C%15=C(C9=C%17)C%11=C%14%13)C(=O)N(C(CCCCC)CCCCC)C%12=O)C(=O)N(C(CCCCC)CCCCC)C%10=O)S8)S7)C=C7C(=O)N(C(CCCCC)CCCCC)C(=O)C8=C7C6=C(C1=C8)C2=C54)C(=O)N(C(CCCCC)CCCCC)C3=O,TT-FDI,-5.91,-4.06,14.4,0.791,0.629,7.17,"Y. Yin, W. Zhang, Z. Zheng, Z. Ge, Y. Liu, F. Guo, S. Gao, L. Zhao, Y. Zhang, Integrated linker-regulation and ring-fusion engineering for efficient additive-free non-fullerene organic solar cells, J. Mater. Chem. C. 8 (2020) 12516¨C12526. https://doi.org/10.1039/D0TC02499F."
3399,O=C1N(CC(CCCCC)CCCCC)C(C2=C(C1C=C3)C4=C3C(C=CC5C(N(CC(CCCCC)CCCCC)C6=O)=O)=C(C5=C6C=C7C8=C9C%10=CC%11C%12=C(C(N(CC(CCCCC)CCCCC)C%11=O)=O)C=C%13C%14=C%15C(C%16=C%17C=C%15C%13%18C%19=CC%20=C%21C%22=C(C%23=CC%21C(N(CC(CCCCC)CCCCC)C%20=O)=O)C%24=C%25C(C%18=CC(C(N(CC(CCCCC)CCCCC)C%26=O)=O)=C%25C%26C=C%24C%27=C%23C%28=CC%29=C%30C%31=C(C=CC%30C(N(CC(CCCCC)CCCCC)C%29=O)=O)C%32=C%33C(C%27=CC(C(N(CC(CCCCC)CCCCC)C%34=O)=O)=C%33C%34C=C%32)=C%31%28)=C%22%19)=C(C8=CC%16C(N(CC(CCCCC)CCCCC)C%17=O)=O)C%10=C%14%12)C7=C4C9=C2)=O,SNTP,-6.13,-3.95,15.22,0.77,0.6,7.17,"G. Gao, N. Liang, H. Geng, W. Jiang, H. Fu, J. Feng, J. Hou, X. Feng, Z. Wang, Spiro-Fused Perylene Diimide Arrays, J. Am. Chem. Soc. 139 (2017) 15914¨C15920. https://doi.org/10.1021/jacs.7b09140."
3400,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(C=C(/C=C5C(=O)C6=C(C=C(Cl)C(Cl)=C6)C5=C(C#N)C#N)S2)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC3=C2SC(/C=C2C(=O)C4=C(C=C(Cl)C(Cl)=C4)C2=C(C#N)C#N)=C3)C=C1,IDTT-4CL,-5.49,-3.91,18.34,0.61,0.643,7.16,"J. Zhang, Y. Li, Z. Peng, F. Bai, L.-K. Ma, H. Ade, Z. Li, H. Yan, Near-infrared electron acceptors with fused nonacyclic molecular backbones for nonfullerene organic solar cells, Mater. Chem. Front. 4 (2020) 1729¨C1738. https://doi.org/10.1039/C9QM00754G."
3401,CCCCCCCCN1N=C2C(/C=C3SC(=C(C#N)C#N)N(CC)C3=O)=CC=C(C3=CC4=C(S3)C3=C(S4)C4=CC5=C(C=C4C3(C3=CC=C(CCCCCC)C=C3)C3=CC=C(CCCCCC)C=C3)C3=C(C4=C(C=C(C6=CC=C(/C=C7SC(=C(C#N)C#N)N(CC)C7=O)C7=NN(CCCCCCCC)N=C67)S4)S3)C5(C3=CC=C(CCCCCC)C=C3)C3=CC=C(CCCCCC)C=C3)C2=N1,BTA13,-5.34,-3.62,9.95,1.23,0.5842,7.16,"Q. Guo, F. Li, J. Li, Y. Xiao, K. Zuo, A. Tang, B. Zhang, E. Zhou, Modulating the middle and end-capped units of A2-A1-D-A1-A2 type non-fullerene acceptors for high VOC organic solar cells, Org. Electron. 95 (2021) 106195. https://doi.org/10.1016/j.orgel.2021.106195."
3402,CCCCC(CC)CC1(CC(CC)CCCC)C2=CC=C3C(=C2C2=C1C=C(C1=CC=C(/C=C4C(=O)C5=C(C=CC(F)=C5)C4=C(C#N)C#N)S1)S2)C=CC1=C3C2=C(C=C(C3=CC=C(/C=C4C(=O)C5=C(C=CC(F)=C5)C4=C(C#N)C#N)S3)S2)C1(CC(CC)CCCC)CC(CC)CCCC,DTNSF,-5.52,-4,14.49,0.92,0.5462,7.15,"M. Zhang, Y. Ma, Q. Zheng, Dithienonaphthalene-Based Non-fullerene Acceptors With Different Bandgaps for Organic Solar Cells, Front. Chem. 6 (2018). https://www.frontiersin.org/article/10.3389/fchem.2018.00427 (accessed March 7, 2022)."
3403,CCCCCCCCCCC1(CCCCCCCCCC)C2=C(C=CC(C3=CC=C(C#CC4=CC=C5C(=O)N(CC(CC)CCCC)C(=O)C6=CC=CC4=C65)C4=NSN=C34)=C2)C2C=CC(C3=CC=C(C#CC4=CC=C5C(=O)N(CC(CC)CCCC)C(=O)C6=CCCC4=C56)C4=NSN=C34)=CC21,BYG-2,-5.84,-3.39,11.84,1.02,0.59,7.12,"H. Chen, D. Hu, Q. Yang, J. Gao, J. Fu, K. Yang, H. He, S. Chen, Z. Kan, T. Duan, C. Yang, J. Ouyang, Z. Xiao, K. Sun, S. Lu, All-Small-Molecule Organic Solar Cells with an Ordered Liquid Crystalline Donor, Joule. 3 (2019) 3034¨C3047. https://doi.org/10.1016/j.joule.2019.09.009."
3404,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C=C(C2=C(SCC(CC)CCCC)C=C(/C=C5C(=O)C6=C(C=C(F)C(F)=C6)C5=C(C#N)C#N)S2)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC(/C=C3C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)=C2)C=C1,PIST-4F,-5.65,-4.03,13.2,0.84,0.64,7.1,"J. Lin, Q. Guo, Q. Liu, J. Lv, H. Liang, Y. Wang, L. Zhu, F. Liu, X. Guo, M. Zhang, A Noncovalently Fused-Ring Asymmetric Electron Acceptor Enables Efficient Organic Solar Cells, Chin. J. Chem. 39 (2021) 2685¨C2691. https://doi.org/10.1002/cjoc.202100323."
3405,O=C(C(C=C(F)C(F)=C1)=C1C/2=C(C#N)C#N)C2=C/C3=CC(C(C4=CC=C(CCCCCC)C=C4)(C5=CC=C(CCCCCC)C=C5)C6=C7SC8=C6SC9=C8C(C%10=CC=C(CCCCCC)C=C%10)(C%11=CC=C(CCCCCC)C=C%11)C%12=C9SC(/C=C%13C(C(C=C(F)C(F)=C%14)=C%14C\%13=C(C#N)/C#N)=O)=C%12)=C7S3,F6IC,-5.66,-4.02,18.07,0.611,0.64,7.1,"S. Dai, T. Li, W. Wang, Y. Xiao, T.-K. Lau, Z. Li, K. Liu, X. Lu, X. Zhan, Enhancing the Performance of Polymer Solar Cells via Core Engineering of NIR-Absorbing Electron Acceptors, Adv. Mater. 30 (2018) 1706571. https://doi.org/10.1002/adma.201706571."
3406,CCCCCC(CCCCC)N1C(=O)C2=CC3=C4C5=C(C=C6C(=O)N(C(CCCCC)CCCCC)C(=O)C7=C6C5=C5C(=C7)C6=C7C8=CC9=C%10C(=CC%11=C%12C%13=C(C=C%14C(=O)N(C(CCCCC)CCCCC)C(=O)C%15=C%14C%13=C(C(=C%15)C7=C7C%13=CC%14=C%15C(=CC%16=C%17C%18=C(C=C%19C(=O)N(C(CCCCC)CCCCC)C(=O)C%20=C%19C%18=C(C(=C%20)C7=C6C6=CC(=C2C4=C65)C1=O)C%13=C%17%15)[Se]%16)C(=O)N(C(CCCCC)CCCCC)C%14=O)C8=C%12%10)[Se]%11)C(=O)N(C(CCCCC)CCCCC)C9=O)[Se]3,PDI6,-5.83,-3.73,9.5,1.17,0.63,7.1,"X. Liu, X. Du, J. Wang, C. Duan, X. Tang, T. Heumueller, G. Liu, Y. Li, Z. Wang, J. Wang, F. Liu, N. Li, C.J. Brabec, F. Huang, Y. Cao, Efficient Organic Solar Cells with Extremely High Open-Circuit Voltages and Low Voltage Losses by Suppressing Nonradiative Recombination Losses, Adv. Energy Mater. 8 (2018) 1801699. https://doi.org/10.1002/aenm.201801699."
3407,CCCCCCCCC1(CCCCCCCC)C2=CC3=C(C=C2C2=C1C=C(C=C1C(=O)N(CC)C(=S)N(CC)C1=O)S2)C(CCCCCCCC)(CCCCCCCC)C1=C3SC(C=C2C(=O)N(CC)C(=S)N(CC)C2=O)=C1,IDTA ,-5.88,-3.9,12.2,0.99,0.6,7.1,"Y. Firdaus, Q. He, Y. Lin, F.A.A. Nugroho, V.M.L. Corre, E. Yengel, A.H. Balawi, A. Seitkhan, F. Laquai, C. Langhammer, F. Liu, M. Heeney, T.D. Anthopoulos, Novel wide-bandgap non-fullerene acceptors for efficient tandem organic solar cells, J. Mater. Chem. A. 8 (2020) 1164¨C1175. https://doi.org/10.1039/C9TA11752K."
3408,CCCCCCCCC1(C)C2=C(SC(/C=C3C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)=C2)C2=C1C=C(C1=C3C(=O)C4=C(CC(CC)CCCC)SC(CC(CC)CCCC)=C4C(=O)C3=C(C3=CC4=C(S3)C3=C(C=C(/C=C5C(=O)C6=C(C=C(F)C(F)=C6)C5=C(C#N)C#N)S3)C4(CCCCCCCC)CCCCCCCC)S1)S2,BCPDT-1,-5.36,-3.85,16.03,0.75,0.578,7.1,"Q. Wang, K. Huang, Y. Zhang, L. Ye, W. Ni, M. Li, Y. Geng, Near-infrared absorbing non-fullerene acceptors with unfused D-A-D core for efficient organic solar cells, Org. Electron. 92 (2021) 106131. https://doi.org/10.1016/j.orgel.2021.106131."
3409,CCCCC(CC)COC1=C2C=C(/C=C3/C(=O)C4=CC(F)=C(F)C=C4C3=C(C#N)C#N)SC2=C(OCC(CC)CCCC)C2=C1SC1=C2N(CC(CC)CCCC)C2=C1C1=NSN=C1C1=C2N(CC(CC)CCCC)C2=C1SC1=C(OCC(CC)CCCC)C3=C(SC(/C=C4/C(=O)C5=CC(F)=C(F)C=C5C4=C(C#N)C#N)=C3)C(OCC(CC)CCCC)=C12,X94FIC,-5.58,-4.17,14.67,0.73,0.661,7.08,"J. Xiao, T. Yan, T. Lei, Y. Li, Y. Han, L. cao, W. Song, S. Tan, Z. Ge, Organic solar cells based on non-fullerene acceptors of nine fused-ring by modifying end groups, Org. Electron. 81 (2020) 105662. https://doi.org/10.1016/j.orgel.2020.105662."
3410,CCCCC(CC)CC1(CC(CC)CCCC)C2=C(SC(/C=C3C(=O)C4=C(C=C(Cl)C(Cl)=C4)C3=C(C#N)C#N)=C2)C2=C1C=C(C1=CC3=C(S1)C1=C(C=C(/C=C4CC5=C(C=C(Cl)C(Cl)=C5)C4=C(/C)C#N)S1)C3(CC(CC)CCCC)CC(CC)CCCC)S2,CPDT-4Cl-2EH,-5.3,-3.87,19.04,0.72,0.5171,7.08,"K. Wang, H. Wei, Z. Li, S. Lu, Near-infrared small molecule acceptors based on 4H-cyclopenta[1,2-b:5,4-b¡¯]dithiophene units for organic solar cells, Dyes Pigments. 196 (2021) 109801. https://doi.org/10.1016/j.dyepig.2021.109801."
3411,CCCCCCOC1=C2C3=C(C=C(/C=C4C(=O)C5=C(C=C(F)C(F)=C5)C4=C(C#N)C#N)S3)C(C3=CC=C(CCCCCC)C=C3)(C3=CC=C(CCCCCC)C=C3)C3=CC(OCCCCCC)=C4C5=C(C=C(/C=C6C(=O)C7=C(C=C(F)C(F)=C7)C6=C(C#N)C#N)S5)C(C5=CC=C(CCCCCC)C=C5)(C5=CC=C(CCCCCC)C=C5)C(=C1)C4=C32,PDT,-5.52,-3.9,13.48,0.97,0.54,7.07,"P. Jiang, H. Lu, Q.-Q. Jia, S. Feng, C. Li, H.-B. Li, Z. Bo, Dihydropyreno[1,2-b:6,7-b¡ä]dithiophene based electron acceptors for high efficiency as-cast organic solar cells, J. Mater. Chem. A. 7 (2019) 5943¨C5948. https://doi.org/10.1039/C9TA00614A."
3412,CCCCCCC(CCCC)CC1=C2C(=O)C3=C(C4=CC5=C(S4)C4=C(C=C(/C=C6C(=O)C7=C(C=C(F)C(F)=C7)C6=C(C#N)C#N)S4)C5(CC(CC)CCCC)CC(CC)CCCC)SC(C4=CC5=C(S4)C4=C(C=C(/C=C6C(=O)C7=C(C=C(F)C(F)=C7)C6=C(C#N)C#N)S4)C5(CC(CC)CCCC)CC(CC)CCCC)=C3C(=O)C2=C(CC(CCCC)CCCCCC)S1,BDDBO-4F ,-5.56,-3.93,16.38,0.91,0.474,7.07,"Z. Wu, Y. Chen, L. Zhang, D. Yuan, R. Qiu, S. Deng, H. Liu, Z. Zhang, J. Chen, A ligand-free direct heteroarylation approach for benzodithiophenedione-based simple small molecular acceptors toward high efficiency polymer solar cells, J. Mater. Chem. A. 9 (2021) 3314¨C3321. https://doi.org/10.1039/D0TA12288B."
3413,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C=C(/C=C2C(=O)C5=C(C=CC=C5)C2=C(C#N)C#N)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC(/C=C3C(=O)C4=C(C=CC=C4)C3=C(C#N)C#N)=C2)C=C1,IDIC1,-5.51,-3.81,13.5,0.894,0.581,7.05,"J. Zhu, Y. Wu, J. Rech, J. Wang, K. Liu, T. Li, Y. Lin, W. Ma, W. You, X. Zhan, Enhancing the performance of a fused-ring electron acceptor via extending benzene to naphthalene, J. Mater. Chem. C. 6 (2017) 66¨C71. https://doi.org/10.1039/C7TC04520D."
3414,CCCCCCC1=C(C2=CC=C3C(=C2)N(CCCCCC)C2=C3N(CCCCCC)C3=C2C=CC(C2=C(CCCCCC)C=C(C4=C(CCCCCC)C=C(CC5C(=O)C6=C(C=CC=C6)C5=O)S4)S2)=C3)SC(C2=C(CCCCCC)C=C(C=C3C(=O)C4=C(C=CC=C4)C3=O)S2)=C1,DINI-IND,-5.12,-3.12,12.18,0.85,0.68,7.04,"J. Sim, H. Lee, K. Song, S. Biswas, A. Sharma, G.D. Sharma, J. Ko, Solution processed bulk heterojunction solar cells based on A¨CD¨CA small molecules with a dihydroindoloindole (DINI) central donor and different acceptor end groups, J. Mater. Chem. C. 4 (2016) 3508¨C3516. https://doi.org/10.1039/C6TC00323K."
3415,CCCCCCCCC(CCCCCC)COC1=CC(C2=CC(C3=CC=C(CCCCCC)C=C3)=C(/C=C3C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)S2)=C(OCC(CCCCCC)CCCCCCCC)C=C1C1=CC(C2=CC=C(CCCCCC)C=C2)=C(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)S1,PTB4F,-5.87,-3.89,14.55,0.94,0.5148,7.04,"T.-J. Wen, Z.-X. Liu, Z. Chen, J. Zhou, Z. Shen, Y. Xiao, X. Lu, Z. Xie, H. Zhu, C.-Z. Li, H. Chen, Simple Non-Fused Electron Acceptors Leading to Efficient Organic Photovoltaics, Angew. Chem. Int. Ed. 60 (2021) 12964¨C12970. https://doi.org/10.1002/anie.202101867."
3416,CCCCCCC(CCC)CC1(CC(CCC)CCCCCC)C2=C(SC(/C=C3C(=O)C4=C(C=C(Cl)C(Cl)=C4)C3=C(C#N)C#N)=C2)C2=C1C=C(C1=CC3=C(S1)C1=C(C=C(C4=CC5=C(S4)C4=C(C=C(/C=C6C(=O)C7=C(C=C(Cl)C(Cl)=C7)C6=C(C#N)C#N)S4)C5(CC(CCC)CCCCCC)CC(CCC)CCCCCC)S1)C1=NSN=C13)S2,DTBCIC-CL,-5.55,-3.71,12.38,1.01,0.5586,7.02,"Y. Tang, H. Feng, Y. Liang, H. Tang, Z. Du, J. Xu, F. Huang, Y. Cao, Dithienobenzothiadiazole-Bridged Nonfullerene Electron Acceptors for Efficient Organic Solar Cells, ACS Appl. Polym. Mater. (2021). https://doi.org/10.1021/acsapm.1c01406."
3417,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C=C(C2=C5C(F)=C(C(=O)OCC(CC)CCCC)SC5=C(/C=C5C(=O)C6=C(C=C(F)C=C6)C5=C(C#N)C#N)S2)O3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC(C3=C4C(F)=C(C(=O)OCC(CC)CCCC)SC4=C(/C=C4C(=O)C5=C(C=C(F)C=C5)C4=C(C#N)C#N)S3)=C2)C=C1,T4,-5.36,-4.01,18.57,0.61,0.62,7.01,"F.-X. Chen, J.-Q. Xu, Z.-X. Liu, M. Chen, R. Xia, Y. Yang, T.-K. Lau, Y. Zhang, X. Lu, H.-L. Yip, A.K.-Y. Jen, H. Chen, C.-Z. Li, Near-Infrared Electron Acceptors with Fluorinated Regioisomeric Backbone for Highly Efficient Polymer Solar Cells, Adv. Mater. 30 (2018) 1803769. https://doi.org/10.1002/adma.201803769."
3418,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(S3)C3=C(S2)C2=C5C6=C3C=C3C(=O)N(C(CCCCC)CCCCC)C(=O)C7=CC(F)=C(C8=C(F)C=C9C(=O)N(C(CCCCC)CCCCC)C(=O)C(=C2)C9=C85)C6=C73)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC3=C2SC2=C3C3=C4C5=C(C=CC6=C5C(=C3)C(=O)N(C(CCCCC)CCCCC)C6=O)C3=CC=C5C(=O)N(C(CCCCC)CCCCC)C(=O)C6=CC2=C4C3=C56)C=C1,F-2PDI,-5.52,-3.76,11.23,1.03,0.604,6.99,"Y. Wang, H. Zhong, Y. Hong, T. Shan, K. Ding, L. Zhu, F. Liu, H. Wei, C. Yu, H. Zhong, Tailoring the molecular geometry of polyfluoride perylene diimide acceptors towards efficient organic solar cells, J. Mater. Chem. C. 8 (2020) 8224¨C8233. https://doi.org/10.1039/D0TC01707H."
3419,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(C=C(C5=CC=C(/C=C6SC(=C(C#N)C#N)N(CC)C6=O)C6=NSN=C56)S2)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC3=C2SC(C2=CC=C(/C=C4SC(=C(C#N)C#N)N(CC)C4=O)C4=NSN=C24)=C3)C=C1,ITBTR-C2,-5.3,-3.7,13.38,0.89,0.5842,6.96,"J. Qu, Z. Mu, H. Lai, H. Chen, T. Liu, S. Zhang, W. Chen, F. He, Alkyl Chain End Group Engineering of Small Molecule Acceptors for Non-Fullerene Organic Solar Cells, ACS Appl. Energy Mater. 1 (2018) 4724¨C4730. https://doi.org/10.1021/acsaem.8b00851."
3420,CCCCCCCCC1(CCCCCCCC)C2=CC3=C(C=C2C2=C1C=C(C1=CC=C(/C=C4SC(=S)N(CC)C4=O)C4=N[Se]N=C14)S2)C(CCCCCCCC)(CCCCCCCC)C1=C3SC(C2=CC=C(/C=C3SC(=S)N(CC)C3=O)C3=NON=C23)=C1,IDTBSR,-5.41,-3.88,13.95,0.95,0.5238,6.95,"Y. Nian, F. Pan, S. Li, H. Jiang, S. Feng, L. Zhang, Y. Cao, J. Chen, Benzoxadiazole and Benzoselenadiazole as ¦Ð-Bridges in Nonfullerene Acceptors for Efficient Polymer Solar Cells, Asian J. Org. Chem. 7 (2018) 2285¨C2293. https://doi.org/10.1002/ajoc.201800389."
3421,O=C(C(C=CC=C1)=C1C/2=C(C#N)/C#N)C2=C/C3=CC(CCCCCC)=C(C4=CC(CCCCCC)=C(C5=CC(N6C(CCCCCCCC)CCCCCCCC)=C(S5)C7=C6C=C(C8=C(CCCCCC)C=C(C9=C(CCCCCC)C=C(/C=C%10C(C(C=CC=C%11)=C%11C\%10=C(C#N)C#N)=O)S9)S8)S7)S4)S3,DCI-2,-5.24,-4.05,13.771,0.8,0.63,6.94,"A. Mishra, M.L. Keshtov, A. Looser, R. Singhal, M. Stolte, F. W¨¹rthner, P. B?uerle, G.D. Sharma, Unprecedented low energy losses in organic solar cells with high external quantum efficiencies by employing non-fullerene electron acceptors, J. Mater. Chem. A. 5 (2017) 14887¨C14897. https://doi.org/10.1039/C7TA04703G."
3422,CCCCCCCCC1(CCCCCCCC)C2=NC3=C(N=C2C2=C1C=C1C(=C2)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C1SC(/C=C1C(=O)C4=C(C=C(F)C(F)=C4)C1=C(C#N)C#N)=C2)C(CCCCCCCC)(CCCCCCCC)C1=C3C=C2C(=C1)C1=C(C=C(/C=C3C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)S1)C2(C1=CC=C(CCCCCC)C=C1)C1=CC=C(CCCCCC)C=C1,IPY-T-ICF,-5.67,-3.51,14.29,0.79,0.612,6.92,"L. Chen, M. Zeng, X. Tang, C. Weng, S. Tan, P. Shen, Development of A¨CDA¡äD¨CA Small-Molecular Acceptors Based on a 6,12-Dihydro-diindolo[1,2-b:10,20-e]pyrazine Unit for Efficient As-Cast Polymer Solar Cells, J. Phys. Chem. C. 124 (2020) 21366¨C21377. https://doi.org/10.1021/acs.jpcc.0c07557."
3423,CCCCCCC(C)N1C(=O)C2=CC3=C4C5=C(C=CC(=C25)C1=O)C1=C2C5=C(C=C1)C(=O)N(C(CCCCCC)CCCCCC)C(=O)C5=CC(=C24)C1=C3C2=CC3=C4C(=CC(C5=CC=C(/C(=C/C6=CC=C(C7=C8C9=CC=C%10C(=O)N(C(CCCCCC)CCCCCC)C(=O)C%11=C%10C9=C9C(=C%11)C%10=C(C%11=CC%12=C(C(=C7)C(=O)N(C(CCCCCC)CCCCCC)C%12=O)C8=C%119)C7=C8C9=C(C=CC%11=C9C(=C7)C(=O)N(C(CCCCCC)CCCCCC)C%11=O)C7=C9C%11=C(C=C7)C(=O)N(C(CCCCCC)CCCCCC)C(=O)C%11=CC%10=C98)C=C6)C6=CC=C(C7=C8C9=CC=C%10C(=O)N(C(CCCCCC)CCCCCC)C(=O)C%11=C%10C9=C9C(=C%11)C%10=C(C%11=CC%12=C(C(=C7)C(=O)N(C(CCCCCC)CCCCCC)C%12=O)C8=C%119)C7=C8C9=C(C=CC%11=C9C(=C7)C(=O)N(C(CCCCCC)CCCCCC)C%11=O)C7=C9C%11=C(C=C7)C(=O)N(C(CCCCCC)CCCCCC)C(=O)C%11=CC%10=C98)C=C6)C=C5)=C5C6=CC=C7C(=O)N(C(CCCCCC)CCCCCC)C(=O)C8=C7C6=C(C1=C8)C2=C45)C(=O)N(C(CCCCCC)CCCCCC)C3=O,TriPE-3PDI2,-6,-3.94,15.2,0.789,0.5758,6.91,"K. Xu, J. Hu, K. Lu, M. Wu, H. Lu, J. Yi, D. Wu, J. Xia, Tetraphenylethylene vs triphenylethylene core-based perylene diimide acceptor for non-fullerene organic solar cells, Dyes Pigments. 184 (2021) 108813. https://doi.org/10.1016/j.dyepig.2020.108813."
3424,CCCCCCC1=CC(C2=CC3=C(S2)C2=C(C=C(/C=C4C(=O)C5=CC=CC=C5C4=C(C#N)C#N)S2)C3(CC(CC)CCCC)CC(CC)CCCC)=C(CCCCCC)C=C1C1=CC2=C(S1)C1=C(C=C(/C=C3C(=O)C4=CC=CC=C4C3=C(C#N)C#N)S1)C2(CC(CC)CCCC)CC(CC)CCCC,DC6-IC,,,11.19,0.99,0.6221,6.87,"H. Huang, Q. Guo, S. Feng, C. Zhang, Z. Bi, W. Xue, J. Yang, J. Song, C. Li, X. Xu, Z. Tang, W. Ma, Z. Bo, Noncovalently fused-ring electron acceptors with near-infrared absorption for high-performance organic solar cells, Nat. Commun. 10 (2019) 3038. https://doi.org/10.1038/s41467-019-11001-6."
3425,CCCCC(CC)COC1=CC(C2=CC3=C(S2)C2=C(C=C(/C=C4C(=O)C5=C(C=CC=C5)C4=C(C#N)C#N)S2)C3(CC(CC)CCCC)CC(CC)CCCC)=C(OCC(CC)CCCC)C=C1C1=CC2=C(S1)C1=C(C=C(/C=C3C(=O)C4=C(C=CC=C4)C3=C(C#N)C#N)S1)C2(CC(CC)CCCC)CC(CC)CCCC,DOC2C6-IC,,,11.19,0.99,0.6221,6.87,"H. Huang, Q. Guo, S. Feng, C. Zhang, Z. Bi, W. Xue, J. Yang, J. Song, C. Li, X. Xu, Z. Tang, W. Ma, Z. Bo, Noncovalently fused-ring electron acceptors with near-infrared absorption for high-performance organic solar cells, Nat. Commun. 10 (2019) 3038. https://doi.org/10.1038/s41467-019-11001-6."
3426,CCCCCCCCCCCCC1=CC2=C(SC3=C2C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C3SC(/C=C3C(=O)C4=C(C=CC=C4)C3=C(C#N)N=O)=C2)C2=C1C1=C(C=C2CCCCCCCCCCCC)C2=C(S1)C1=C(C=C(/C=C3C(=O)C4=C(C=CC=C4)C3=C(C#N)C#N)S1)C2(C1=CC=C(CCCCCC)C=C1)C1=CC=C(CCCCCC)C=C1,NCIC,-5.37,-3.73,12.69,1,0.62,6.84,"F.-Y. Cao, W.-C. Huang, S.-L. Chang, Y.-J. Cheng, Angular-Shaped 4,9-Dialkylnaphthodithiophene-Based Octacyclic Ladder-Type Non-Fullerene Acceptors for High Efficiency Ternary-Blend Organic Photovoltaics, Chem. Mater. 30 (2018) 4968¨C4977. https://doi.org/10.1021/acs.chemmater.8b01089."
3427,CCCCCCCCC1(CCCCCCCC)C2=CC(C3=CC4=C5C(=CC6=C7C8=C9C(=CC=C%10C(=O)N(C(CCCCC)CCCCC)C(=O)C(=C%109)C=C8C8=C6C6=CC9=C%10C(=CC=C%11C%12=C%13C%14=C(C=C%12)C(=O)N(C(C)CCCCC)C(=O)C%14=CC8=C%13C6=C%11%10)C(=O)N(C(CCCCC)CCCCC)C9=O)C3=C57)C(=O)N(C(CCCCC)CCCCC)C4=O)=CC=C2C2=C1C=C(C1=C3C4=C5C6=C(C=C4)C(=O)N(C(CCCCC)CCCCC)C(=O)C6=CC4=C5C5=C3C3=C(C=C5C5=C4C4=CC6=C7C(=CC=C8C9=C%10C%11=C(C=C9)C(=O)N(C(CCCCC)CCCCC)C(=O)C%11=CC5=C%10C4=C87)C(=O)N(C(CCCCC)CCCCC)C6=O)C(=O)N(C(CCCCC)CCCCC)C(=O)C3=C1)C=C2,F2PDI-I,-5.75,-3.81,11.32,0.9,0.6655,6.82,"H. Wang, M. Li, J. Song, C. Li, Z. Bo, Extended ¦Ð-conjugated perylene diimide dimers toward efficient organic solar cells, Dyes Pigments. 183 (2020) 108736. https://doi.org/10.1016/j.dyepig.2020.108736."
3428,CCCCCC(CCCCC)N1C(=O)C2=CC3=C4C5=C(C=C6C(=O)N(C(CCCCC)CCCCC)C(=O)C7=C6C5=C(C(C5=C6C8=CC=C9C(=O)N(C(CCCCC)CCCCC)C(=O)C%10=C9C8=C(C(C8=C9C%11=CC=C%12C(=O)N(C(CCCCC)CCCCC)C(=O)C%13=C%12C%11=C%11C(=C%13)SC%12=CC%13=C(C(=C8)C(=O)N(C(CCCCC)CCCCC)C%13=O)C9=C%12%11)=C%10)C8=C6C6=C(C=C8)C(=O)N(C(CCCCC)CCCCC)C(=O)C6=C5)=C7)C5=C4C2=C(C=C5)C1=O)S3,Tri-PDI-S,-5.88,-3.84,15.85,0.74,0.581,6.81,"Y. Duan, X. Xu, Y. Li, Z. Li, Q. Peng, Chalcogen-Atom-Annulated Perylene Diimide Trimers for Highly Efficient Nonfullerene Polymer Solar Cells, Macromol. Rapid Commun. 38 (2017) 1700405. https://doi.org/10.1002/marc.201700405."
3429,CCCCCCCCC1(CCCCCCCC)C2=CC3=C(C=C2C2=C1C=C1C(=C2)C(CC(CCCC)CCCCCC)(CC(CCCC)CCCCCC)C2=C1SC(/C=C1C(=O)C4=C(C=CC=C4)C1=C(C#N)C#N)=C2)C(CCCCCCCC)(CCCCCCCC)C1=C3C=C2C(=C1)C1=C(C=C(/C=C3C(=O)C4=C(C=CC=C4)C3=C(C#N)C#N)S1)C2(CC(CCCC)CCCCCC)CC(CCCC)CCCCCC,TfIF-IC-C4C8,-5.55,-3.73,11.56,1.02,0.5797,6.81,"J. Jia, G. Liu, T. Jia, Z. Wang, K. Lin, Y. Li, F. Huang, Y. Cao, Fused nonacyclic electron acceptors with additional alkyl side chains for efficient polymer solar cells, Org. Electron. 68 (2019) 151¨C158. https://doi.org/10.1016/j.orgel.2019.01.052."
3430,CCCCCCCCC1=CC=C(C2(C3=CC=C(CCCCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C=C(C2=CC=C5C(=C2)C(CCCCCCCC)(CCCCCCCC)C2=C5SC(/C=C5C(=O)C6=CC(F)=C(F)C=C6C5=C(C#N)C#N)=C2)S3)C(C2=CC=C(CCCCCCCC)C=C2)(C2=CC=C(CCCCCCCC)C=C2)C2=C4SC(C3=CC=C4C(=C3)C(CCCCCCCC)(CCCCCCCC)C3=C4SC(/C=C4C(=O)C5=CC(F)=C(F)C=C5C4=C(C#N)C#N)=C3)=C2)C=C1,BITIC-C8F4,-5.5,-3.9,14.01,1,0.4859,6.81,"Y.A. Avalos-Quiroz, O. Bardagot, Y. Kervella, C. Auma?tre, L. Cabau, A. Rivaton, O. Margeat, C. Videlot-Ackermann, U. Vongsaysy, J. Ackermann, R. Demadrille, Non-Fullerene Acceptors with an Extended ¦Ð-Conjugated Core: Third Components in Ternary Blends for High-Efficiency, Post-Treatment-Free Organic Solar Cells, ChemSusChem. 14 (2021) 3502¨C3510. https://doi.org/10.1002/cssc.202101005."
3431,CCCCCCCCCCCC1=C(/C=C2C(=O)C3=C(C=C4C=CC=CC4=C3)C2=C(C#N)C#N)SC2=C1SC1=C2N(CC(CC)CCCC)C2=C1C1=NSN=C1C1=C2N(CC(CC)CCCC)C2=C1SC1=C2SC(/C=C2C(=O)C3=C(C=C4C=CC=CC4=C3)C2=C(C#N)C#N)=C1C,BT-LIC,-5.42,-3.84,15,0.72,0.635,6.8,"G. Li, X. Zhang, L.O. Jones, J.M. Alzola, S. Mukherjee, L. Feng, W. Zhu, C.L. Stern, W. Huang, J. Yu, V.K. Sangwan, D.M. DeLongchamp, K.L. Kohlstedt, M.R. Wasielewski, M.C. Hersam, G.C. Schatz, A. Facchetti, T.J. Marks, Systematic Merging of Nonfullerene Acceptor ¦Ð-Extension and Tetrafluorination Strategies Affords Polymer Solar Cells with >16% Efficiency, J. Am. Chem. Soc. 143 (2021) 6123¨C6139. https://doi.org/10.1021/jacs.1c00211."
3432,O=C(C(C=CC=C1)=C1C/2=C(C#N)C#N)C2=C/C3=CC4=C(S3)C5=C(C6=CC(C7(C8=CC=C(CCCCCC)C=C8)C9=CC=C(CCCCCC)C=C9)=C(C%10=C7C(SC(/C=C%11C(C(C=CC=C%12)=C%12C\%11=C(C#N)C#N)=O)=C%13)=C%13S%10)C=C6C5(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15)S4,ITIC,-5.48,-3.83,14.21,0.81,0.591,6.8,"Y. Lin, J. Wang, Z.-G. Zhang, H. Bai, Y. Li, D. Zhu, X. Zhan, An Electron Acceptor Challenging Fullerenes for Efficient Polymer Solar Cells, Adv. Mater. 27 (2015) 1170¨C1174. https://doi.org/10.1002/adma.201404317."
3433,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C=C(C2=CC=C(/C=C5SC(=S)N(N6CCCCC6)C5=O)C5=NSN=C25)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC(C3=CC=C(/C=C4SC(=S)N(C5CCCCC5)C4=O)C4=NSN=C34)=C2)C=C1,IDT-BT-RN,-5.26,-3.62,11.6,1.1,0.5229,6.78,"L.-M. Tang, J. Xiao, W.-Y. Bai, Q.-Y. Li, H.-C. Wang, M.-S. Miao, H.-L. Yip, Y.-X. Xu, End-chain effects of non-fullerene acceptors on polymer solar cells, Org. Electron. 64 (2019) 1¨C6. https://doi.org/10.1016/j.orgel.2018.10.005."
3434,CCCCCCCCC1(CCCCCCCC)C2=CC3=C(C=C2C2=C1C=C1C(=C2)C(CC(CC)CCCC)(CC(CC)CCCC)C2=C1SC(/C=C1C(=O)C4=C(C=CC=C4)C1=C(C#N)C#N)=C2)C(CCCCCCCC)(CCCCCCCC)C1=C3C=C2C(=C1)C1=C(C=C(/C=C3C(=O)C4=C(C=CC=C4)C3=C(C#N)C#N)S1)C2(CC(CC)CCCC)CC(CC)CCCC,TfIF-IC-C2C6,-5.68,-3.82,12.34,0.9,0.6094,6.75,"J. Jia, G. Liu, T. Jia, Z. Wang, K. Lin, Y. Li, F. Huang, Y. Cao, Fused nonacyclic electron acceptors with additional alkyl side chains for efficient polymer solar cells, Org. Electron. 68 (2019) 151¨C158. https://doi.org/10.1016/j.orgel.2019.01.052."
3435,CCCCCC(CCCCC)N1C(=O)C2=CC3=C4C5=C(C=CC(=C25)C1=O)C1=C2C5=C(C=C1)C(=O)N(C(CCCCC)CCCCC)C(=O)C5=CC(=C24)C1=C3C2=CC3=C4C(=CC5=C6C7=C(C=C8C(=O)N(C(CCCCC)CCCCC)C(=O)C9=C8C7=C(C1=C9)C2=C46)C1=C5SC2=C1C1=CC4=C5C(=CC6=C7C8=C(C=C9C(=O)N(C(CCCCC)CCCCC)C(=O)C%10=C9C8=C(C2=C%10)C1=C57)C1=C6C2=CC5=C6C(=CC=C7C8=CC=C9C(=O)N(C(CCCCC)CCCCC)C(=O)C%10=C9C8=C(C1=C%10)C2=C76)C(=O)N(C(CCCCC)CCCCC)C5=O)C(=O)N(C(CCCCC)CCCCC)C4=O)C(=O)N(C(CCCCC)CCCCC)C3=O,FT-FDI,-6.04,-4.04,14.4,0.805,0.582,6.75,"Y. Yin, W. Zhang, Z. Zheng, Z. Ge, Y. Liu, F. Guo, S. Gao, L. Zhao, Y. Zhang, Integrated linker-regulation and ring-fusion engineering for efficient additive-free non-fullerene organic solar cells, J. Mater. Chem. C. 8 (2020) 12516¨C12526. https://doi.org/10.1039/D0TC02499F."
3436,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=C(SC(/C=C4C(=O)C5=C(C=CC=C5)C4=C(C)C#N)=C3)C3=C2C2=CC4=C(C=C2S3)C2=C(S4)C3=C(C=C(/C=C4C(=O)C5=C(C=CC=C5)C4=C(C#N)C#N)S3)C2(C2=CC=C(CCCCCC)C=C2)C2=CC=C(CCCCCC)C=C2)C=C1,NFBDT,-5.43,-3.88,14.59,0.8,0.56,6.74,"Y. Zhang, B. Kan, Y. Sun, Y. Wang, R. Xia, X. Ke, Y.-Q.-Q. Yi, C. Li, H.-L. Yip, X. Wan, Y. Cao, Y. Chen, Nonfullerene Tandem Organic Solar Cells with High Performance of 14.11%, Adv. Mater. 30 (2018) 1707508. https://doi.org/10.1002/adma.201707508."
3437,CCCCCCCCCCCCCCCCN1C2=C(SC(/C=C3C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)=C2)C2=C1C1=C(S2)C2=C(SC3=C2N(C)C2=C3SC(/C=C3C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)=C2)C2=C1SC1=C2N(CCCCCCCCCCCCCCCC)C2=C1SC(/C=C1C(=O)C3=C(C=C(F)C(F)=C3)C1=C(C#N)C#N)=C2,BTDTP-C16-6F,-5.67,-3.98,13.17,0.94,0.5439,6.74,"W. Wang, R. An, T. Wang, H. Li, J. Zhang, H. Tian, X. Wu, H. Tong, L. Wang, Nitrogen-Bridged Star-Shaped Fused-Ring Electron Acceptors for Organic Solar Cells, Giant. (2022) 100093. https://doi.org/10.1016/j.giant.2022.100093."
3438,CCCCCCCCC1=CC=C(C2(C3=CC=C(CCCCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C=C(C2=CC=C5C(=C2)C(CCCCCCCC)(CCCCCCCC)C2=C5SC(/C=C5C(=O)C6=CC(F)=C(F)C=C6C5=C(C#N)C#N)=C2)S3)C(C2=CC=C(CCCCCCCC)C=C2)(C2=CC=C(CCCCCCCC)C=C2)C2=C4SC(C3=CC=C4C(=C3)C(CCCCCCCC)(CCCCCCCC)C3=C4SC(/C=C4C(=O)C5=CC=CC=C5C4=C(C#N)C#N)=C3)=C2)C=C1,BITIC-C8,-5.4,-3.9,13.12,0.98,0.5192,6.73,"Y.A. Avalos-Quiroz, O. Bardagot, Y. Kervella, C. Auma?tre, L. Cabau, A. Rivaton, O. Margeat, C. Videlot-Ackermann, U. Vongsaysy, J. Ackermann, R. Demadrille, Non-Fullerene Acceptors with an Extended ¦Ð-Conjugated Core: Third Components in Ternary Blends for High-Efficiency, Post-Treatment-Free Organic Solar Cells, ChemSusChem. 14 (2021) 3502¨C3510. https://doi.org/10.1002/cssc.202101005."
3439,CCCCC(CC)CC1(CC(CC)CCCC)C2=C(SC(C3=C(OC(CC)CCCC)C=C(/C=C4C(=O)C5=CC(F)=C(F)C=C5C4=C(C#N)C#N)S3)=C2)C2=C1C=C(C1=C(OC(CC)CCCC)C=C(/C=C3C(=O)C4=CC(F)=C(F)C=C4C3=C(C#N)C#N)S1)S2,COTIC-4F,-5.22,-4.14,20.2,0.56,0.59,6.66,"J. Vollbrecht, J. Lee, S.-J. Ko, V.V. Brus, A. Karki, W. Le, M. Seifrid, M.J. Ford, K. Cho, G.C. Bazan, T.-Q. Nguyen, Design of narrow bandgap non-fullerene acceptors for photovoltaic applications and investigation of non-geminate recombination dynamics, J. Mater. Chem. C. 8 (2020) 15175¨C15182. https://doi.org/10.1039/D0TC02136A."
3440,CCCCC(CC)CC1(CC(CC)CCCC)C2=C(C=CC(C3=CC=C(/C=C4C(=O)C5=CC(F)=CC=C5C4=C(C#N)C#N)S3)=C2)C2=C1C1=C(C=C(C3=CC=C(/C=C4C(=O)C5=CC(F)=C(F)C=C5C4=C(C#N)C#N)S3)C=C1)C2(CC(CC)CCCC)CC(CC)CCCC,YITI-4F,-5.61,-3.93,14.41,0.825,0.5589,6.64,"Q. Yue, Z. Zhou, S. Xu, J. Zhang, X. Zhu, Design and synthesis of medium-bandgap small-molecule electron acceptors for efficient tandem solar cells, J. Mater. Chem. A. 6 (2018) 13588¨C13592. https://doi.org/10.1039/C8TA04405H."
3441,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=C(SC4=C3SC(/C=C3C(=O)C5=CC(Cl)=C(Cl)C=C5C3=C(C#N)C#N)=C4)C3=C2C2=C(C=C(/C=C4C(=O)C5=CC(Cl)=C(Cl)C=C5C4=C(C#N)C#N)S2)S3)C=C1,CC5,-5.75,-4.09,17.09,0.65,0.597,6.63,"C. Jiao, Z. Guo, B. Sun, Y. Yi, L. Meng, X. Wan, M. Zhang, H. Zhang, C. Li, Y. Chen, An acceptor¨Cdonor¨Cacceptor type non-fullerene acceptor with an asymmetric backbone for high performance organic solar cells, J. Mater. Chem. C. 8 (2020) 6293¨C6298. https://doi.org/10.1039/D0TC00981D."
3442,CCCCCCCCC(CCCCCC)COC1=CC(C2=CC(OCCCCCC)=C(/C=C3C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)S2)=C(OCC(CCCCCC)CCCCCCCC)C=C1C1=CC(OCCCCCC)=C(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)S1,PTICO,-5.48,-3.66,12.6,1.01,0.52,6.62,"Z.-P. Yu, Z.-X. Liu, F.-X. Chen, R. Qin, T.-K. Lau, J.-L. Yin, X. Kong, X. Lu, M. Shi, C.-Z. Li, H. Chen, Simple non-fused electron acceptors for efficient and stable organic solar cells, Nat. Commun. 10 (2019) 2152. https://doi.org/10.1038/s41467-019-10098-z."
3443,CCCCC(CC)CC1(CC(CC)CCCC)C2=C(SC(/C=C3/C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)=C2)C2=C1C=C(C1=CN=C(C3=CC4=C(S3)C3=C(C=C(/C=C5C(=O)C6=C(C=C(F)C(F)=C6)C5=C(C#N)C#N)S3)C4(CC(CC)CCCC)CC(CC)CCCC)C3=NSN=C13)S2,WHC-1,-5.64,-4.29,17.83,0.69,0.54,6.61,"MD.W. Hussain, H.J. Shin, B.R. Lee, M. Ak, S.-J. Ko, J. Lee, H. Choi, Design of Nonfused Nonfullerene Acceptors Based on Pyrido- or Benzothiadiazole Cores for Organic Solar Cells, ACS Appl. Energy Mater. (2022). https://doi.org/10.1021/acsaem.1c03741."
3444,CCCCCCCCCCCOCC1=C(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)SC2=C1SC1=C2N(CC(CC)CCCC)C2=C1C1=NSN=C1C1=C2N(CC(CC)CCCC)C2=C1SC1=C2SC(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)=C1OCCCCCCCCCCC,Y6-2O,-5.73,-3.76,13.3,0.92,0.535,6.6,"Y. Chen, F. Bai, Z. Peng, L. Zhu, J. Zhang, X. Zou, Y. Qin, H.K. Kim, J. Yuan, L.-K. Ma, J. Zhang, H. Yu, P.C.Y. Chow, F. Huang, Y. Zou, H. Ade, F. Liu, H. Yan, Asymmetric Alkoxy and Alkyl Substitution on Nonfullerene Acceptors Enabling High-Performance Organic Solar Cells, Adv. Energy Mater. 11 (2021) 2003141. https://doi.org/10.1002/aenm.202003141."
3445,CCCCC(CC)COC1=C(C2=C(OCC(CC)CCCC)C(OCC(CC)CCCC)=C(C3=C(OCC(CC)CCCC)C=C(/C=C4C(=O)C5=CC(F)=C(F)C=C5C4=C(C#N)C#N)S3)S2)SC(/C=C2C(=O)C3=CC(F)=C(F)C=C3C2=C(C#N)C#N)=C1,AOT3,-5.37,-3.95,17.63,0.62,0.59,6.59,"Z. Yao, Y. Li, S. Li, J. Xiang, X. Xia, X. Lu, M. Shi, H. Chen, Conformation Locking of Simple Nonfused Electron Acceptors Via Multiple Intramolecular Noncovalent Bonds to Improve the Performances of Organic Solar Cells, ACS Appl. Energy Mater. 4 (2021) 819¨C827. https://doi.org/10.1021/acsaem.0c02719."
3446,CCCCC(CC)CC1=C2C(=O)C3=C(C4=CC5=C(S4)C4=C(C=C(/C=C6C(=O)C7=C(C=C(F)C(F)=C7)C6=C(C#N)C#N)S4)C5(CC(CC)CCCC)CC(CC)CCCC)SC(C4=CC5=C(S4)C4=C(C=C(/C=C6C(=O)C7=C(C=C(F)C(F)=C7)C6=C(C#N)C#N)S4)C5(CC(CC)CCCC)CC(CC)CCCC)=C3C(=O)C2=C(CC(CC)CCCC)S1,BDC-4F-C8,-5.66,-3.73,19.5,0.728,0.464,6.58,"D. Luo, X. Lai, N. Zheng, C. Duan, Z. Wang, K. Wang, A.K.K. Kyaw, High-performance and low-energy loss organic solar cells with non-fused ring acceptor by alkyl chain engineering, Chem. Eng. J. 420 (2021) 129768. https://doi.org/10.1016/j.cej.2021.129768."
3447,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=C(C=CC(C4=CC=C(C5=CC=C(C=C(C#N)C#N)C6=NSN=C56)S4)=C3)C3=C2C=C(C2=CC=C(C=C(C#N)C#N)C4=NSN=C24)S3)C=C1,PhITBD,-5.74,-3.69,14.07,0.757,0.62,6.57,"Y.U. Kim, G.E. Park, S. Choi, D.H. Lee, M.J. Cho, D.H. Choi, A new n-type semiconducting molecule with an asymmetric indenothiophene core for a high-performing non-fullerene type organic solar cell, J. Mater. Chem. C. 5 (2017) 7182¨C7190. https://doi.org/10.1039/C7TC00706J."
3448,CCCCCCCCN1N=C2C(/C=C3/SC(=C(C#N)C#N)N(CC)C3=O)=CC=C(C3=CC4=C(S3)C3=CC5=C(C=C3C4(C3=CC=C(OCCCCCC)C=C3)C3=CC=C(OCCCCCC)C=C3)C3=C(C=C(C4=CC=C(/C=C6/SC(=C(C#N)C#N)N(CC)C6=O)C6=NN(CCCCCCCC)N=C46)S3)C5(C3=CC=C(OCCCCCC)C=C3)C3=CC=C(OCCCCCC)C=C3)C2=N1,BTA43,-5.44,-3.47,10.84,0.89,0.68,6.56,"B. Xiao, M. Du, X. Wang, Z. Xiao, G. Li, A. Tang, L. Ding, Y. Geng, X. Sun, E. Zhou, Effects of Oxygen Atoms Introduced at Different Positions of Non-Fullerene Acceptors in the Performance of Organic Solar Cells with Poly(3-hexylthiophene), ACS Appl. Mater. Interfaces. 12 (2020) 1094¨C1102. https://doi.org/10.1021/acsami.9b16662."
3449,CCCCCCCCOCCCCCCC1(CCCCCCOO)C2=CC(C3=CC4=C5C(=CC6=C7C8=C9C(=CC=C%10C(=O)N(C(CCCCC)CCCCC)C(=O)C(=C%109)C=C8C8=C6C6=CC9=C%10C(=CC=C%11C%12=C%13C%14=C(C=C%12)C(=O)N(C(CCCCC)CCCCC)C(=O)C%14=CC8=C%13C6=C%11%10)C(=O)N(C(CCCCC)CCCCC)C9=O)C3=C57)C(=O)N(C(CCCCC)CCCCC)C4=O)=CC=C2C2=C1C=C(C1=C3C4=C5C6=C(C=C4)C(=O)N(C(CCCCC)CCCCC)C(=O)C6=CC4=C5C5=C3C3=C(C=C5C5=C4C4=CC6=C7C(=CC=C8C9=C%10C%11=C(C=C9)C(=O)N(C(CCCCC)CCCCC)C(=O)C%11=CC5=C%10C4=C87)C(=O)N(C(CCCCC)CCCCC)C6=O)C(=O)N(C(CCCCC)CCCCC)C(=O)C3=C1)C=C2,F2PDI-II ,-5.78,-3.77,11.56,0.9,0.628,6.56,"H. Wang, M. Li, J. Song, C. Li, Z. Bo, Extended ¦Ð-conjugated perylene diimide dimers toward efficient organic solar cells, Dyes Pigments. 183 (2020) 108736. https://doi.org/10.1016/j.dyepig.2020.108736."
3450,CCCCCCC1=C(/C=C2C(=O)C3=C(Cl)SC=C3C2=C(C#N)C#N)SC2=C1N(CC(CC)CCCC)C1=C2C2=NSN=C2C2=C1N(CC(CC)CCCC)C1=C2SC(/C=C2C(=O)C3=C(Cl)SC=C3C2=C(C#N)C#N)=C1CCCCCC,BTTCN-Cl,-5.63,-4.01,13.15,0.9,0.5546,6.56,"R. Ming, J. Gao, W. Gao, W. Ning, Z. Luo, F. Zhang, C. Yang, Benzo[c][1,2,5]thiadiazole-fused pentacyclic small molecule acceptors for organic solar cells, Dyes Pigments. 185 (2021) 108970. https://doi.org/10.1016/j.dyepig.2020.108970."
3451,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=C(SC(/C=C4C(=O)C5=C(C=CC(O)=C5)C4=C(C#N)C#N)=C3)C3=CC=C4C(=C32)C=CC2=C4C(C3=CC=C(CCCCCC)C=C3)(C3=CC=C(CCCCCC)C=C3)C3=C2SC(/C=C2C(=O)C4=C(C=CC(F)=C4)C2=C(C#N)C#N)=C3)C=C1,NTIC-F,-5.52,-3.77,13.61,0.811,0.589,6.5,"Y.-Q.-Q. Yi, H. Feng, M. Chang, H. Zhang, X. Wan, C. Li, Y. Chen, New small-molecule acceptors based on hexacyclic naphthalene(cyclopentadithiophene) for efficient non-fullerene organic solar cells, J. Mater. Chem. A. 5 (2017) 17204¨C17210. https://doi.org/10.1039/C7TA05809H."
3452,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C=C2C=C(/C=C5C(=O)C6=C(C=C(F)C(F)=C6)C5=C(C#N)C#N)SC2=C3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4C=C3SC(/C=C4C(=O)C5=C(C=C(F)C(F)=C5)C4=C(C#N)C#N)=CC3=C2)C=C1,IDBT-2F,-5.72,-4.19,14.3,0.708,0.642,6.49,"Y. Xu, H. Jiang, T.-K. Lau, J. Zhu, J. Wang, X. Lu, X. Zhan, Y. Lin, Fused thienobenzene-thienothiophene electron acceptors for organic solar cells, J. Energy Chem. 37 (2019) 58¨C65. https://doi.org/10.1016/j.jechem.2018.12.002."
3453,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(C=C(C5=C(OC)C(OC)=C(/C=C6C(=O)C7=C(C=CC=C7)C6=C(C#N)C#N)S5)S2)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC3=C2SC(C2=C(OC)C(OC)=C(/C=C4C(=O)C5=C(C=CC=C5)C4=C(C#N)C#N)S2)=C3)C=C1,IDTT2OT,-5.06,-3.15,12.3,0.93,0.567,6.46,"I.N. Kim, S.J. Jeon, Y.H. Kim, H.S. Lee, Y.W. Han, N.G. Yang, D.H. Hong, C.H. Jung, D.K. Moon, Synthesis of 3,4-dimethoxythiophene spacer-based non-fullerene acceptors for efficient organic solar cells, Synth. Met. 280 (2021) 116880. https://doi.org/10.1016/j.synthmet.2021.116880."
3454,CCCCCCCCCCCC1=C(/C=C2C(=O)C3=C(C=CC=C3)C2=C(C#N)C#N)SC2=C1SC(C1=CC3=C(C=C1)C1=C(C4=C(S1)C(CCCCCCCCCCC)=C(/C=C1C(=O)C5=CC=CC=C5C1=C(C#N)C#N)S4)C3(C1=CC=C(CCCCCC)C=C1)C1=CC=C(CC3=CC=C4C=C5C=CC(C)=CC5=CC4=C3)C=C1)=C2,ITUIC,-5.65,-3.83,13.64,0.97,0.4858,6.45,"M. Zhang, Y. Ma, Q. Zheng, Asymmetric indenothienothiophene-based unfused core for A-D-A type nonfullerene acceptors, Dyes Pigments. 180 (2020) 108495. https://doi.org/10.1016/j.dyepig.2020.108495."
3455,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C=C(/C=C2C(=O)C5=C(C=CC(C)=C5)C2=C(C#N)C#N)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC(/C=C3C(=O)C4=C(C=C(C)C=C4)C3=C(C#N)C#N)=C2)C=C1,IDT-2B,-5.8,-3.84,13.3,0.89,0.539,6.42,"S. Feng, C. Zhang, Y. Liu, Z. Bi, Z. Zhang, X. Xu, W. Ma, Z. Bo, Fused-Ring Acceptors with Asymmetric Side Chains for High-Performance Thick-Film Organic Solar Cells, Adv. Mater. 29 (2017) 1703527. https://doi.org/10.1002/adma.201703527."
3456,CCCCCCC1(CCCCCC)C2=CC3=C(C=C2C2=C1C=C(/C=C1C(=O)C4=C(C=C(F)C(F)=C4)C1=C(C#N)C#N)S2)C(CCCCCC)(CCCCCC)C1=C3SC(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)=C1,ID-4F,-5.75,-4.06,13.5,0.73,0.65,6.4,"Q. Guo, J. Lin, H. Liu, X. Dong, X. Guo, L. Ye, Z. Ma, Z. Tang, H. Ade, M. Zhang, Y. Li, Asymmetrically noncovalently fused-ring acceptor for high-efficiency organic solar cells with reduced voltage loss and excellent thermal stability, Nano Energy. 74 (2020) 104861. https://doi.org/10.1016/j.nanoen.2020.104861."
3457,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(C=C(/C=C5C(=O)C6=CC=CC=C6C5=C(C#N)C#N)S2)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC3=C2SC(/C=C2C(=O)C4=CC=CC=C4C2=C(C#N)C#N)=C3)C=C1,H-ITIC,-5.61,-4.02,10.6,1.04,0.58,6.4,"F. Yang, C. Li, W. Lai, A. Zhang, H. Huang, W. Li, Halogenated conjugated molecules for ambipolar field-effect transistors and non-fullerene organic solar cells, Mater. Chem. Front. 1 (2017) 1389¨C1395. https://doi.org/10.1039/C7QM00025A."
3458,CCCCC(CC)CC1(CC(CC)CCCC)C2=C(C=CC(C3=CC=C(C4=CC=C(/C=C5/SC(=S)N(CC)C5=O)O4)C4=NSN=C34)=C2)C2=C1C=C(C1=CC=C(C3=CC=C(/C=C4/SC(=S)N(CC)C4=O)O3)C3=NSN=C13)C=C2,FRD2,-5.67,-3.58,13.3,0.835,0.578,6.4,"Suman, A. Bagui, R. Datt, V. Gupta, S.P. Singh, A simple fluorene core-based non-fullerene acceptor for high performance organic solar cells, Chem. Commun. 53 (2017) 12790¨C12793. https://doi.org/10.1039/C7CC08237A."
3459,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C=C(/C=C2C(=O)C5=CC(F)=C(F)C=C5C2=C(C#N)C#N)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC(C3=C(F)C=C(C4=CC5=C(S4)C4=CC6=C(C=C4C5(C4=CC=C(CCCCCC)C=C4)C4=CC=C(CCCCCC)C=C4)C4=C(C=C(/C=C5C(=O)C7=C(C=C(F)C(F)=C7)C5=C(C#N)C#N)S4)C6(C4=CC=C(CCCCCC)C=C4)C4=CC=C(CCCCCC)C=C4)C(F)=C3)=C2)C=C1,DFB-dIDT,-5.53,-3.87,15.57,0.86,0.4856,6.37,"M. Zhang, M. Zeng, H. Chen, L. Li, B. Zhao, S. Tan, A2-D-A1-D-A2-type small molecule acceptors incorporated with electron-deficient core for non-fullerene organic solar cells, Sol. Energy. 197 (2020) 511¨C518. https://doi.org/10.1016/j.solener.2020.01.032."
3460,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=C(C=C4C(=C3)C3SC(C5=CC=C(/C=C6C(=O)C7=C(C=CC=C7)C6=C(C#N)C#N)S5)=CC3C4(C3=CC=C(CCCCCC)C=C3)C3=CC=C(CCCCCC)C=C3)C3=C2C=C(C2=CC=C(/C=C4C(=O)C5=C(C=CC=C5)C4=C(C#N)C#N)S2)S3)C=C1,IDT-T,-5.57,-4.01,11.21,0.952,0.5962,6.36,"S.H. Park, G.E. Park, S. Choi, Y.U. Kim, S.Y. Park, C.G. Park, M.J. Cho, D.H. Choi, Effect of a methyl thiophene-3-carboxylate bridge in an indacenodithiophene-based acceptor¨Cdonor¨Cacceptor-type molecule on the performance of non-fullerene polymer solar cells, J. Mater. Chem. C. 6 (2018) 7549¨C7556. https://doi.org/10.1039/C8TC01508B."
3461,CCCCCCCCC1(CCCCCCCC)C2=CC(C3=CC=C(/C=C4C(=O)C5=C(C=CC=C5)C4=C(C#N)C#N)S3)=CC=C2C2=CC3=C(C=C21)C1=C(C=C(C2=CC=C(/C=C4C(=O)C5=C(C=CC=C5)C4=C(C#N)C#N)S2)C=C1)C3(CCCCCCCC)CCCCCCCC,IFTIC,-5.42,-3.85,12.71,0.92,0.542,6.33,"J. Zhang, B. Zhao, Y. Mi, H. Liu, Z. Guo, G. Bie, W. Wei, C. Gao, Z. An, A new wide bandgap small molecular acceptor based on indenofluorene derivatives for fullerene-free organic solar cells, Dyes Pigments. 140 (2017) 261¨C268. https://doi.org/10.1016/j.dyepig.2017.01.039."
3462,CCCCCCCCN1N=C2C(/C=C3/SC(=C(C#N)C#N)N(CC)C3=O)=CC=C(C3=CC4=C(S3)C3=CC5=C(C=C3C(C3=CC=C(CCCCCC)C=C3)(C3=CC=C(CCCCCC)C=C3)O4)C3=C(C=C(C4=CC=C(/C=C6/SC(=C(C#N)C#N)N(CC)C6=O)C6=NN(CCCCCCCC)N=C46)S3)OC5(C3=CC=C(CCCCCC)C=C3)C3=CC=C(CCCCCC)C=C3)C2=N1,BTA53,-5.48,-3.58,11.57,0.88,0.62,6.31,"B. Xiao, M. Du, X. Wang, Z. Xiao, G. Li, A. Tang, L. Ding, Y. Geng, X. Sun, E. Zhou, Effects of Oxygen Atoms Introduced at Different Positions of Non-Fullerene Acceptors in the Performance of Organic Solar Cells with Poly(3-hexylthiophene), ACS Appl. Mater. Interfaces. 12 (2020) 1094¨C1102. https://doi.org/10.1021/acsami.9b16662."
3463,CCCCCCCCC1(CCCCCCCC)C2=CC3=C(C=C2C2=C1C=C(/C=C1C(=O)C4=C(C=CC(C)=C4)C1=C(C#N)C#N)S2)C(CCCCCCCC)(CCCCCCCC)C1=C3SC(/C=C2C(=O)C3=C(C=CC(C)=C3)C2=C(C#N)C#N)=C1,IDIC8-M,-5.51,-3.72,10.36,1.002,0.607,6.31,"C. Liu, N. Qiu, Y. Sun, X. Ke, H. Zhang, C. Li, X. Wan, Y. Chen, All-Small-Molecule Organic Solar Cells Based on a Fluorinated Small Molecule Donor With High Open-Circuit Voltage of 1.07 V, Front. Chem. 8 (2020) 329. https://doi.org/10.3389/fchem.2020.00329."
3464,O=C(C(C=CC=C1)=C1C/2=C(C#N)/C#N)C2=C/C(S3)=CC4=C3C5=C(N4CC(CC)CCCC)C6=C(C(SC(/C=C7C(C(C=CC=C8)=C8C7=C(C#N)C#N)=O)=C9)=C9N6CC(CC)CCCC)C%10=NN(CC(CC)CCCC)N=C5%10,BZIC,-5.42,-3.88,12.67,0.84,0.59,6.3,"L. Feng, J. Yuan, Z. Zhang, H. Peng, Z.-G. Zhang, S. Xu, Y. Liu, Y. Li, Y. Zou, Thieno[3,2-b]pyrrolo-Fused Pentacyclic Benzotriazole-Based Acceptor for Efficient Organic Photovoltaics, ACS Appl. Mater. Interfaces. 9 (2017) 31985¨C31992. https://doi.org/10.1021/acsami.7b10995."
3465,CCCCC(CC)COC1=C2C=C(/C=C3/C(=O)C4=CC=CC=C4C3=C(C#N)C#N)SC2=C(OCC(CC)CCCC)C2=C1SC1=C2N(CC(CC)CCCC)C2=C1C1=NSN=C1C1=C2N(CC(CC)CCCC)C2=C1SC1=C(OCC(CC)CCCC)C3=C(SC(/C=C4/C(=O)C5=CC=CC=C5C4=C(C#N)C#N)=C3)C(OCC(CC)CCCC)=C12,X9IC,-5.53,-4.06,11.4,0.86,0.639,6.29,"J. Xiao, T. Yan, T. Lei, Y. Li, Y. Han, L. cao, W. Song, S. Tan, Z. Ge, Organic solar cells based on non-fullerene acceptors of nine fused-ring by modifying end groups, Org. Electron. 81 (2020) 105662. https://doi.org/10.1016/j.orgel.2020.105662."
3466,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C=C(/C=C2C(=O)C5=C(C=CC=C5)C2=C(C#N)C#N)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC(/C=C3C(=O)C4=C(C=CC=C4)C3=C(C#N)C#N)=C2)C=C1,ITIC-2T,-5.61,-3.93,13.56,0.92,0.502,6.26,"Q. Zhu, D. Liu, Z. Lu, C. Gu, K. Zhang, X. Bao, Q. Li, R. Yang, Length evolution of fused-ring electron acceptors toward optimal blend morphology in polymer solar cells incorporating asymmetric benzodithiophene-based donors, J. Mater. Chem. A. 7 (2019) 4823¨C4828. https://doi.org/10.1039/C8TA11363G."
3467,CCCCCCCCN1C2=C(C=C3C(=C2)C2=C(C=C(C4=CC=C(/C=C5C(=O)C6=C(C=CC=C6)C5=C(C#N)C#N)S4)S2)C3(C2=CC=C(C)C=C2)C2=CC=C(CCCCCC)C=C2)C2=C1C=C1C(=C2)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C1SC(C1=CC=C(/C=C3C(=O)C4=C(C=CC=C4)C3=C(C#N)C#N)S1)=C2,CDTCN,-5.39,-3.8,11.26,0.96,0.5758,6.23,"J. Wei, Q. Tu, Q. Zheng, Heteroheptacene-cored semiconducting molecules for non-fullerene organic solar cells, Dyes Pigments. 144 (2017) 133¨C141. https://doi.org/10.1016/j.dyepig.2017.05.026."
3468,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C=C(/C=C2C(=O)C5=CC(F)=C(F)C=C5C2=C(C#N)C#N)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC(C3=CC4=C(S3)C(C3=CC=C(CC(CC)CCCC)S3)=C3C=C(C5=CC6=C(S5)C5=CC7=C(C=C5C6(C5=CC=C(CCCCCC)C=C5)C5=CC=C(CCCCCC)C=C5)C5=C(C=C(/C=C6/C(=O)C8=CC(F)=C(F)C=C8C6=C(C#N)C#N)S5)C7(C5=CC=C(CCCCCC)C=C5)C5=CC=C(CCCCCC)C=C5)SC3=C4C3=CC=C(CC(CC)CCCC)S3)=C2)C=C1,BDT(IDT-IC-2F)2,-5.51,-3.97,13.6,0.83,0.55,6.21,"J. Zhu, X. Zheng, H. Tan, H. Tan, J. Yang, J. Yu, W. Zhu, Small molecule acceptors with indacenodithiophene¨Cbenzodithiophene¨Cindacenodithiophene as donating cores for solution-processed non-fullerene solar cells, Chem. Phys. Lett. 726 (2019) 7¨C12. https://doi.org/10.1016/j.cplett.2019.04.024."
3469,CCCCCCCCN1C(=O)/C(=C/C2=CC=C(C3=CC=C(C4=CC=C(/C=C5SC(=S)N(CCCCCCCC)C5=O)S4)C4=NSN=C34)S2)SC1=S,TBTT-ORH,-5.74,-3.6,14.99,0.92,0.45,6.21,"T. Lee, C.E. Song, S.K. Lee, W.S. Shin, E. Lim, Alkyl-Side-Chain Engineering of Nonfused Nonfullerene Acceptors with Simultaneously Improved Material Solubility and Device Performance for Organic Solar Cells, ACS Omega. 6 (2021) 4562¨C4573. https://doi.org/10.1021/acsomega.0c04495."
3470,O=C1N(C(CCCCC)CCCCC)C(C2=C(C1C=C3)C4=C3C(C=CC5C(N(C(CCCCC)CCCCC)C6=O)=O)=C(C5=C6C=C7)C7=C4C(C8=CC9=C(C=C8)C%10=CC=C(C%11=CC(C(N(C(CCCCC)CCCCC)C%12=O)=O)=C(C%12C=C%13)C%14=C%13C(C=CC%15C(N(C(CCCCC)CCCCC)C%16=O)=O)=C(C%15=C%16C=C%17)C%17=C%14%11)C=C%10C9%18C%19=CC=CC=C%19C%20=C%18C=CC=C%20)=C2)=O,SFPDI,-5.71,-3.69,8.9,1.23,0.56,6.2,"X. Liu, X. Du, J. Wang, C. Duan, X. Tang, T. Heumueller, G. Liu, Y. Li, Z. Wang, J. Wang, F. Liu, N. Li, C.J. Brabec, F. Huang, Y. Cao, Efficient Organic Solar Cells with Extremely High Open-Circuit Voltages and Low Voltage Losses by Suppressing Nonradiative Recombination Losses, Adv. Energy Mater. 8 (2018) 1801699. https://doi.org/10.1002/aenm.201801699."
3471,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=C(SC4=C3SC3=C4SC(/C=C4C(=O)C5=CC=CC=C5C4=C(C#N)C#N)=C3)C3=C2C2=C(S3)C3=C(S2)C2=C(C4=C(S2)C2=C(C=C(/C=C5C(=O)C6=C(C=CC=C6)C5=C(C#N)C#N)S2)S4)C3(C2=CC=C(CCCCCC)C=C2)C2=CC=C(CCCCCC)C=C2)C=C1,8TIC,-5.3,-3.72,13.1,0.86,0.55,6.2,"X. Liao, H. Pei, H. Zhao, Y. Cui, L. Li, X. Shi, P. Zhu, W. Ma, Y. Chen, A.K.-Y. Jen, The synergistic effects of central core size and end group engineering on performance of narrow bandgap nonfullerene acceptors, Chem. Eng. J. 435 (2022) 135020. https://doi.org/10.1016/j.cej.2022.135020."
3472,CCCCCCCCC1(CCCCCCCC)C2=NC3=C(N=C2C2=C1C=C1C(=C2)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C1SC(/C=C1C(=O)C4=C(C=C(F)C(F)=C4)C1=C(C#N)C#N)=C2)C(CCCCCCCC)(CCCCCCCC)C1=C3C=C2C(=C1)C1=C(C=C(/C=C3C(=O)C4=C(C=CC=C4)C3=C(C#N)C#N)S1)C2(C1=CC=C(CCCCCC)C=C1)C1=CC=C(CCCCCC)C=C1,IPY-T-IC,-5.64,-3.48,13.08,0.91,0.523,6.19,"L. Chen, M. Zeng, X. Tang, C. Weng, S. Tan, P. Shen, Development of A¨CDA¡äD¨CA Small-Molecular Acceptors Based on a 6,12-Dihydro-diindolo[1,2-b:10,20-e]pyrazine Unit for Efficient As-Cast Polymer Solar Cells, J. Phys. Chem. C. 124 (2020) 21366¨C21377. https://doi.org/10.1021/acs.jpcc.0c07557."
3473,CCCCC(CC)COC1=C(C2=CC3=C(S2)C2=C(C=C(/C=C4C(=O)C5=C(C=CC=C5)C4=C(C#N)C#N)S2)C3(CC(CC)CCCC)CC(CC)CCCC)SC2=C1SC(C1=CC3=C(S1)C1=C(C=C(/C=C4C(=O)C5=C(C=C(F)C=C5)C4=C(C#N)C#N)S1)C3(CC(CC)CCCC)CC(CC)CCCC)=C2OCC(CC)CCCC,TTDTC-2F,-5.17,-3.73,15.8,0.6,0.613,6.18,"Z. Liang, X. Cheng, Y. Jiang, J. Yu, X. Xu, Z. Peng, L. Bu, Y. Zhang, Z. Tang, M. Li, L. Ye, Y. Geng, P3HT-Based Organic Solar Cells with a Photoresponse to 1000 nm Enabled by Narrow Band Gap Nonfullerene Acceptors with High HOMO Levels, ACS Appl. Mater. Interfaces. 13 (2021) 61487¨C61495. https://doi.org/10.1021/acsami.1c21089."
3474,CCCCC(CC)CC1=C(C2=CC3=C(S2)C2=C(C=C(C4=C(CC(CC)CCCC)C=C(C=C5C(=O)C6=C(C=CC=C6)C5=O)S4)S2)C32C3=C(C=CC(C(C)(C)C)=C3)C3=C2C=C(C(C)(C)C)C=C3)SC(C=C2C(=O)C3=C(C=CC=C3)C2=O)=C1,STFTYT,-5.26,-3.77,12.54,0.97,0.508,6.17,"J. Wang, W. Wang, X. Dong, G. Wang, Z.-G. Zhang, Y. Li, P. Shen, STFTYT: A simple and broadly absorbing small molecule for efficient organic solar cells with a very low energy loss, Org. Electron. 57 (2018) 45¨C52. https://doi.org/10.1016/j.orgel.2018.02.039."
3475,CCCCCCC1=C(C2=CC=C3C(=C2)N(CCCCCC)C2=C3N(CCCCCC)C3=C2C=CC(C2=C(CCCCCC)C=C(C4=C(CCCCCC)C=C(C=C(C#N)C#N)S4)S2)=C3)SC(C2=C(CCCCCC)C=C(C=C(C#N)C#N)S2)=C1,DINI-DCV,-5.14,-3.11,11.74,0.86,0.61,6.16,"J. Sim, H. Lee, K. Song, S. Biswas, A. Sharma, G.D. Sharma, J. Ko, Solution processed bulk heterojunction solar cells based on A¨CD¨CA small molecules with a dihydroindoloindole (DINI) central donor and different acceptor end groups, J. Mater. Chem. C. 4 (2016) 3508¨C3516. https://doi.org/10.1039/C6TC00323K."
3476,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C=C(/C=C2C(=O)C5=C(C=CC=C5)C2=C(C#N)C#N)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC(/C=C3C(=O)C4=C(C=CC=C4)C3=C(C#N)C#N)=C2)C=C1,IDT-IC,-5.86,-4.01,11.94,0.88,0.579,6.11,"R. Li, G. Liu, R. Xie, Z. Wang, X. Yang, K. An, W. Zhong, X.-F. Jiang, L. Ying, F. Huang, Y. Cao, Introducing cyclic alkyl chains into small-molecule acceptors for efficient polymer solar cells, J. Mater. Chem. C. 6 (2018) 7046¨C7053. https://doi.org/10.1039/C8TC01780H."
3477,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)CC3)C3=CC4=C(C=C3C3=C2C=C(C2=CC=C(/C=C5/SC(=C(C#N)C#N)N(CC)C5=O)S2)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC(C3=CC=C(/C=C4/SC(=C(C#N)C#N)N(C)C4=O)S3)=C2)C=C1,IDTCR,-5.46,-3.67,11.01,1.11,0.499,6.1,"P. Ye, Y. Chen, J. Wu, X. Wu, S. Yu, W. Xing, Q. Liu, X. Jia, A. Peng, H. Huang, Wide bandgap small molecular acceptors for low energy loss organic solar cells, J. Mater. Chem. C. 5 (2017) 12591¨C12596. https://doi.org/10.1039/C7TC04669C."
3478,CCC(CCCC)CN1C(C(C2=C1C3=CC=C(C4=CC5=C(C=C4)C6=CC=C(C7=CC=C(C8=C9C(C(N8CC(CC)CCCC)=O)=C(C%10=CC=C(C%11=CC=CC=C%11)S%10)N(CC(CC)CCCC)C9=O)S7)C=C6C%125C%13=C(C=CC(C%14=CC=C(C%15=C%16C(C(N%15CC(CC)CCCC)=O)=C(C%17=CC=C(C%18=CC=CC=C%18)S%17)N(CC(CC)CCCC)C%16=O)S%14)=C%13)C%19=CC=C(C%20=CC=C(C%21=C%22C(C(N%21CC(CC)CCCC)=O)=C(C%23=CC=C(C%24=CC=CC=C%24)S%23)N(CC(CC)CCCC)C%22=O)S%20)C=C%19%12)S3)=C(C%25=CC=C(C%26=CC=CC=C%26)S%25)N(CC(CC)CCCC)C2=O)=O,P3,-5.6,-3.5,9.03,1.11,0.54,6.09,"W. Liu, S. Li, J. Huang, S. Yang, J. Chen, L. Zuo, M. Shi, X. Zhan, C.-Z. Li, H. Chen, Nonfullerene Tandem Organic Solar Cells with High Open-Circuit Voltage of 1.97 V, Adv. Mater. 28 (2016) 9729¨C9734. https://doi.org/10.1002/adma.201603518."
3479,CCCCCCCCC1(CCCCCCCC)C2=CC3=C(C=C2C2=C1C=C1C(=C2)C(CCCCCCCC)(CCCCCCCC)C2=C1C=C1C(=C2)C2=C(C=C(/C=C4C(=O)C5=C(C=CC=C5)C4=C(C#N)C#N)S2)C1(C1=CC=C(CCCCCC)C=C1)C1=CC=C(CCCCCC)C=C1)C(C1=CC=C(CCCCCC)C=C1)(C1=CC=C(CCCCCC)C=C1)C1=C3SC(/C=C2C(=O)C3=C(C=CC=C3)C2=C(C#N)C#N)=C1,DTIF-IC,-5.47,-3.86,13.99,0.95,0.528,6.09,"W. Guo, H. Liu, J. Zhang, Z. Yang, Y. Niu, Y. Mi, Y. Liu, X. Song, Z. Wu, A small molecular acceptor based on dithienocyclopentaindenefluorene core for efficient fullerene-free polymer solar cells, Synth. Met. 272 (2021) 116667. https://doi.org/10.1016/j.synthmet.2020.116667."
3480,CCCCCCCCC1(CCCCCCCC)C2=CC3=C(C=C2C2=C1C=C(C1=CC=C(/C=C4/SC(=O)N(CC)C4=O)C4=NSN=C14)S2)C(CCCCCCCC)(CCCCCCCC)C1=C3SC(C2=CC=C(/C=C3/SC(=O)N(CC)C3=O)C3=NSN=C23)=C1,BT2B,-5.41,-3.56,10.02,0.92,0.66,6.08,"B. Xiao, A. Tang, L. Cheng, J. Zhang, Z. Wei, Q. Zeng, E. Zhou, Non-Fullerene Acceptors With A2 = A1-D-A1 = A2 Skeleton Containing Benzothiadiazole and Thiazolidine-2,4-Dione for High-Performance P3HT-Based Organic Solar Cells, Sol. RRL. 1 (2017) 1700166. https://doi.org/10.1002/solr.201700166."
3481,CCN(C/1=O)C(SC1=CC2=CC=C(C3=CC4=C(C5=C(C4(CCCCCCCC)CCCCCCCC)C=C(C6=C7C=C(C8=CC=C(/C=C9SC(N(CC)C/9=O)=S)C%10=NSN=C8%10)S6)C(C7(CCCCCCCC)CCCCCCCC)=C5)S3)C%11=NSN=C2%11)=S,IDTBR,-5.45,-3.9,12.55,0.72,0.67,6.05,"N. Gasparini, M. Salvador, S. Strohm, T. Heumueller, I. Levchuk, A. Wadsworth, J.H. Bannock, J.C. de Mello, H.-J. Egelhaaf, D. Baran, I. McCulloch, C.J. Brabec, Burn-in Free Nonfullerene-Based Organic Solar Cells, Adv. Energy Mater. 7 (2017) 1700770. https://doi.org/10.1002/aenm.201700770."
3482,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C=C(C2=CC5=C(S2)/C(=C(C)C#N)C2=CC=CC=C25)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC(C3=CC4=C(S3)C(=C(C#N)C#N)C3=CC=C(F)C=C34)=C2)C=C1,Q1-2F,-5.43,-3.9,12.4,0.76,0.64,6.05,"Q.-Q. Zhang, Y. Li, D. Wang, Z. Chen, Y. Li, S. Li, H. Zhu, X. Lu, H. Chen, C.-Z. Li, Intrinsically Chemo- and Thermostable Electron Acceptors for Efficient Organic Solar Cells, Bull. Chem. Soc. Jpn. 94 (2021) 183¨C190. https://doi.org/10.1246/bcsj.20200231."
3483,CCCCC(CC)CC1(CC(CC)CCCC)C2=C(SC(/C=C3C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)=C2)C2=C1C=C(C1=C3OCCCOC3=C(C3=CC4=C(S3)C3=C(C=C(/C=C5C(=O)C6=C(C=C(F)C(F)=C6)C5=C(C#N)C#N)S3)C4(CC(CC)CCCC)CC(CC)CCCC)S1)S2,PDOT-4F,-5.3,-4.05,15.61,0.696,0.5541,6.02,"D. Luo, Y. Zhang, L. Li, C. Shan, Q. Liu, Z. Wang, W.C.H. Choy, A.K.K. Kyaw, Near-infrared non-fused ring acceptors with light absorption up to 1000?nm for efficient and low-energy loss organic solar cells, Mater. Today Energy. 24 (2022) 100938. https://doi.org/10.1016/j.mtener.2021.100938."
3484,O=C(C(C=CC=C1)=C1C/2=C(C#N)/C#N)C2=C/C(S3)=CC4=C3C5=CC6=C(C=C5C4(C7=CC=C(OCCCCCCCC)C=C7)C8=CC=C(OCCCCCCCC)C=C8)C9=CC%10=C(C(SC(/C=C%11C(C(C=CC=C%12)=C%12C\%11=C(C#N)C#N)=O)=C%13)=C%13C%10(C%14=CC=C(OCCCCCCCC)C=C%14)C%15=CC=C(OCCCCCCCC)C=C%15)C=C9N6CCCCCCCC,DTCC-IC,-5.5,-3.87,11.23,0.95,0.562,6,"Q. Cao, W. Xiong, H. Chen, G. Cai, G. Wang, L. Zheng, Y. Sun, Design, synthesis, and structural characterization of the first dithienocyclopentacarbazole-based n-type organic semiconductor and its application in non-fullerene polymer solar cells, J. Mater. Chem. A. 5 (2017) 7451¨C7461. https://doi.org/10.1039/C7TA01143A."
3485,O=C(N1C2=C(C(C)C)C=CC=C2C(C)C)C3=C4C5=C(C=C3)C(C6=C7C=CCC6=C5C=CC4C1=O)=CC=C7C8=CC=C(C(C=CC(C9=CC=C%10C%11=C9C=CCC%11=C%12C%13=C%10C=CC(C(N(C%14=C(C(C)C)C=CC=C%14C(C)C)C%15=O)=O)=C%13C%15C=C%12)=C%16)=C%16C%17(CCCCCCCC)CCCCCCCC)C%17=C8,PMI-F-PMI,-5.31,-3.34,7.2,1.3,0.635,6,"Y. Zhang, X. Guo, B. Guo, W. Su, M. Zhang, Y. Li, Nonfullerene Polymer Solar Cells based on a Perylene Monoimide Acceptor with a High Open-Circuit Voltage of 1.3 V, Adv. Funct. Mater. 27 (2017) 1603892. https://doi.org/10.1002/adfm.201603892."
3486,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=C(SC4=C3SC(/C=C3C(=O)C5=C(C)SC=C5C3=C(C#N)C#N)=C4)C3=C2C2=C(S3)C3=C(S2)C2=C(C4=C(C=C(/C=C5CC6=C(C)SC=C6C5=C(C#N)C#N)S4)S2)C3(C2=CC=C(CCCCCC)C=C2)C2=CC=C(CCCCCC)C=C2)C=C1,T8Me,-5.39,-3.89,10.54,0.9,0.6421,5.97,"R. Ming, J. Wang, W. Gao, M. Zhang, J. Gao, W. Ning, Z. Luo, X. Liu, C. Zhong, F. Zhang, C. Yang, Fused-Ring Core Engineering for Small Molecule Acceptors Enable High-Performance Nonfullerene Polymer Solar Cells, Small Methods. 3 (2019) 1900280. https://doi.org/10.1002/smtd.201900280."
3487,CCCCCCC(CCCC)CN1C(=O)/C(=C/C2=CC=C(C3=CC=C(C4=CC=C(/C=C5SC(=S)N(CC(CCCC)CCCCC)C5=O)S4)C4=NSN=C34)S2)SC1=S,TBTT-BORH,-5.76,-3.58,13.3,1.02,0.44,5.97,"T. Lee, C.E. Song, S.K. Lee, W.S. Shin, E. Lim, Alkyl-Side-Chain Engineering of Nonfused Nonfullerene Acceptors with Simultaneously Improved Material Solubility and Device Performance for Organic Solar Cells, ACS Omega. 6 (2021) 4562¨C4573. https://doi.org/10.1021/acsomega.0c04495."
3488,CCCCC(CC)CC1(CC(CC)CCCC)C2=C(SC(/C=C3C(=O)C4=CC5=CC=CC=C5C=C4C3=C(C#N)C#N)=C2)C2=C1C=C(C1=CC(F)=C(C3=CC4=C(S3)C3=C(C=C(/C=C5C(=O)C6=CC7=CC=CC=C7C=C6C5=C(C#N)C#N)S3)C4(CC(CC)CCCC)CC(CC)CCCC)C=C1F)S2,DF-PCNC,-5.42,-3.81,14.36,0.9,0.4498,5.94,"N. Wang, L. Zhan, S. Li, M. Shi, T.-K. Lau, X. Lu, R. Shikler, C.-Z. Li, H. Chen, Enhancement of intra- and inter-molecular ¦Ð-conjugated effects for a non-fullerene acceptor to achieve high-efficiency organic solar cells with an extended photoresponse range and optimized morphology, Mater. Chem. Front. 2 (2018) 2006¨C2012. https://doi.org/10.1039/C8QM00318A."
3489,CCCCCCCCC1(CCCCCCCC)C2=CC3=C(C=C2C2=C1C=C1C(=C2)C(CCCCCCCC)(CCCCCCCC)C2=C1SC(/C=C1C(=O)C4=C(C=CC=C4)C1=C(C#N)C#N)=C2)C(CCCCCCCC)(CCCCCCCC)C1=C3C=C2C(=C1)C1=C(C=C(/C=C3C(=O)C4=C(C=CC=C4)C3=C(C#N)C#N)S1)C2(CCCCCCCC)CCCCCCCC,TfIF-IC,-5.51,-3.77,10.8,1.01,0.54,5.9,"G. Liu, J. Jia, K. Zhang, X. Jia, Q. Yin, W. Zhong, L. Li, F. Huang, Y. Cao, 15% Efficiency Tandem Organic Solar Cell Based on a Novel Highly Efficient Wide-Bandgap Nonfullerene Acceptor with Low Energy Loss, Adv. Energy Mater. 9 (2019) 1803657. https://doi.org/10.1002/aenm.201803657."
3490,CCCCCCCCOC(=O)C1=CC2=C(C3=CC4=C(S3)C3=C(C=C5C(=C3)C(C3=CC=C(CCCCCC)C=C3)(C3=CC=C(CCCCCC)C=C3)C3=C5SC(C5=C6C=C(C(O)OCCCCCCCC)SC6=C(/C=C6SC(=S)N(CC)C6=O)S5)=C3)C4(C3=CC=C(CCCCCC)C=C3)C3=CC=C(CCCCCC)C=C3)SC(/C=C3SC(=S)N(CC)C3=O)=C2S1,ATT-3,-5.32,-3.4,10.81,0.927,0.59,5.89,"F. Liu, J. Zhang, Z. Zhou, J. Zhang, Z. Wei, X. Zhu, Poly(3-hexylthiophene)-based non-fullerene solar cells achieve high photovoltaic performance with small energy loss, J. Mater. Chem. A. 5 (2017) 16573¨C16579. https://doi.org/10.1039/C7TA05108E."
3491,CCCCCCCCCCCCCCCCC1(CCCCCCCCCCCCCCCC)C2=CC3=C(C=C2C2=C1C=C(/C=C1C(=O)C4=C(C=CC=C4)C1=C(C#N)C#N)S2)C(CCCCCCCCCCCCCCCC)(CCCCCCCCCCCCCCCC)C1=C3SC(/C=C2C(=O)C3=C(C=CC=C3)C2=C(C#N)C#N)=C1,IDTC16-IC,-5.52,-3.68,9.87,1.046,0.5698,5.89,"H. Lin, M.A. Adil, Q. Zhang, J. Zhang, Q. Wang, Small-molecule acceptors with long alkyl chains for high-performance as-cast nonfullerene organic solar cells, Org. Electron. 93 (2021) 106167. https://doi.org/10.1016/j.orgel.2021.106167."
3492,CCCCCCCCC(CCCCCC)CN1N=C2C(=N1)C(C1=CC3=C(S1)C1=C(C=C(/C=C4C(=O)C5=C(C=C(F)C(F)=C5)C4=C(C#N)C#N)S1)C3(CC(CC)CCCC)CC(CC)CCCC)=C(F)C(F)=C2C1=CC2=C(S1)C1=C(C=C(/C=C3C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)S1)C2(CC(CC)CCCC)CC(CC)CCCC,TR2F-IC4F,-5.57,-3.94,17.95,0.77,0.4263,5.89,"Y. Shi, J. Pan, H. Zhang, C. Yang, Z. Zhang, D. Deng, J. Zhang, K. Lu, Z. Wei, The substituents on the intermediate electron-deficient groups in small molecular acceptors result appropriate morphologies for organic solar cells, Org. Electron. 93 (2021) 106133. https://doi.org/10.1016/j.orgel.2021.106133."
3493,CCCCC(CC)CN1C(=O)C2=C(C3=CC=C(/C=C4SC(=C(C#N)C#N)N(CC)C4=O)[Se]3)N(CC(CC)CCCC)C(=O)C2=C1C1=CC=C(/C=C2SC(=C(C#N)C#N)N(CC)C2=O)[Se]1,MPU5,-5.75,-4,11.48,0.98,0.536,5.86,"M. Privado, P. de la Cruz, P. Malhotra, G.D. Sharma, F. Langa, Influence of the dipole moment on the photovoltaic performance of polymer solar cells employing non-fullerene small molecule acceptor, Sol. Energy. 221 (2021) 393¨C401. https://doi.org/10.1016/j.solener.2021.04.049."
3494,CCCCC(CC)COC1=CC=CC(/C(C2=CC=CC(OCC(CC)CCCC)=C2)=C2/C3=CC4=C(C=C3C3=C2C=C(/C=C2C(=O)C5=C(C=CC=C5)C2=C(C#N)C#N)S3)/C(=C(C2=CC=CC(OCC(CC)CCCC)=C2)C2=CC(OCC(CC)CCCC)=CC=C2)C2=C4SC(/C=C3C(=O)C4=C(C=CC=C4)C3=C(C#N)C#N)=C2)=C1,m-IDTV-PhIC,-5.63,-3.78,11.58,0.99,0.5091,5.85,"J. Liang, P. Yin, T. Zheng, G. Wang, X. Zeng, C. Cui, P. Shen, Conjugated side-chain optimization of indacenodithiophene-based nonfullerene acceptors for efficient polymer solar cells, J. Mater. Chem. C. 7 (2019) 10028¨C10038. https://doi.org/10.1039/C9TC02237F."
3495,CCCCCCCCC1(CCCCCCCC)C2=CC(C3=C4N=C(C5=CC=CC=C5)C(C5=CC=CC=C5)=NC4=C(/C=C4/SC(=S)N(CC)C4=O)S3)=CC=C2C2=CC=C(C3=C4N=C(C5=CC=CC=C5)C(C5=CC=CC=C5)=NC4=C(/C=C4/SC(=S)N(CC)C4=O)S3)C=C21,TP21,-5.46,-3.61,10.92,1.05,0.51,5.81,"J. Li, J. Yang, J. Hu, Y. Chen, B. Xiao, E. Zhou, The first thieno[3,4-b]pyrazine based small molecular acceptor with a linear A2¨CA1¨CD¨CA1¨CA2 skeleton for fullerene-free organic solar cells with a high Voc of 1.05 V, Chem. Commun. 54 (2018) 10770¨C10773. https://doi.org/10.1039/C8CC06198J."
3496,CCCCCCCCOC1=C(C2=CC3=C(S2)C2=C(C=C(/C=C4C(=O)C5=C(C=C(F)C(F)=C5)C4=C(C#N)C#N)S2)C3(CC(CC)CCCC)CC(CC)CCCC)C2=NSN=C2C(C2=CC3=C(S2)C2=C(C=C(/C=C4C(=O)C5=C(C=C(F)C(F)=C5)C4=C(C#N)C#N)S2)C3(CC(CC)CCCC)CC(CC)CCCC)=C1OCCCCCCCC,BTOC8-IC4F ,-5.48,-3.96,18.1,0.77,0.4166,5.81,"Y. Shi, J. Pan, H. Zhang, C. Yang, Z. Zhang, D. Deng, J. Zhang, K. Lu, Z. Wei, The substituents on the intermediate electron-deficient groups in small molecular acceptors result appropriate morphologies for organic solar cells, Org. Electron. 93 (2021) 106133. https://doi.org/10.1016/j.orgel.2021.106133."
3497,CCCCCCC1=CC=C(OC2=C(C3=C(C4=CC=C(CCCCCC)C=C4)C=C4C(=C3)C(C3=CC=C(CCCCCC)C=C3)(C3=CC=C(CCCCCC)C=C3)OC3=C4SC(/C=C4/C(=O)C5=C(C=CC=C5)C4=C(C#N)C#N)=C3)SC(/C=C3/C(=O)C4=C(C=CC=C4)C3=C(C#N)C#N)=C2)C=C1,i-PTIC,-5.41,-3.86,11.04,0.83,0.645,5.8,"J. Li, Y. Wu, X. Zhang, D. Zeng, Y. Luo, X. Duan, X. Gao, P. Cai, Q. Zhang, J. Zhang, Z. Liu, A new fluorinated pyran-bridged A-D-A type small molecular acceptor for organic solar cells, Dyes Pigments. 175 (2020) 108165. https://doi.org/10.1016/j.dyepig.2019.108165."
3498,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(C=C(/C=C5C(=O)C6=C(C=CC=C6)C5=C(C#N)C#N)S2)[Se]3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4[Se]C3=C2SC(/C=C2C(=O)C4=C(C=CC=C4)C2=C(C#N)C#N)=C3)C=C1,SeTIC,-5.55,-3.9,14.21,0.96,0.43,5.8,"J.-L. Wang, K.-K. Liu, L. Hong, G.-Y. Ge, C. Zhang, J. Hou, Selenopheno[3,2-b]thiophene-Based Narrow-Bandgap Nonfullerene Acceptor Enabling 13.3% Efficiency for Organic Solar Cells with Thickness-Insensitive Feature, ACS Energy Lett. 3 (2018) 2967¨C2976. https://doi.org/10.1021/acsenergylett.8b01808."
3499,CCCCCCCCN1N=C2C(C=C(C#N)C#N)=CC=C(C3=CC4=C(S3)C3=CC5=C(C=C3C4(C3=CC=C(CCCCCC)C=C3)C3=CC=C(CCCCCC)C=C3)C3=C(C=C(C4=CC=C(C=C(C#N)C#N)C6=NN(CCCCCCCC)N=C46)S3)C5(C3=CC=C(CCCCCC)C=C3)C3=CC=C(CCCCCC)C=C3)C2=N1,BTA7,-5.56,-3.66,9.74,1.13,0.5254,5.78,"Q. Guo, F. Li, J. Li, Y. Xiao, K. Zuo, A. Tang, B. Zhang, E. Zhou, Modulating the middle and end-capped units of A2-A1-D-A1-A2 type non-fullerene acceptors for high VOC organic solar cells, Org. Electron. 95 (2021) 106195. https://doi.org/10.1016/j.orgel.2021.106195."
3500,CCCCCCCCC1(CCCCCCCC)C2=CC3=C(C=C2C2=C1C=C(C1=C(CC(CC)CCCC)C=C(/C=C4C(=O)C5=C(C=C6C=CC=CC6=C5)C4=C(C#N)C#N)S1)S2)C(CCCCCCCC)(CCCCCCCC)C1=C3SC(C2=C(CC(CC)CCCC)C=C(/C=C3C(=O)C4=C(C=C5C=CC=CC5=C4)C3=C(C#N)C#N)S2)=C1,IDT-TN,-5.42,-4.03,13.22,0.967,0.4517,5.77,"R. Li, G. Liu, B. Fan, X. Du, X. Tang, N. Li, L. Ying, C.J. Brabec, F. Huang, Y. Cao, Non-fullerene acceptors end-capped with an extended conjugation group for efficient polymer solar cells, Org. Electron. 59 (2018) 366¨C373. https://doi.org/10.1016/j.orgel.2018.05.050."
3501,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)CC3)C3=CC4=C(C=C3C3=C2C2=C(C=C(C5=CC(OC)=C(C=C(C#N)C#N)C=C5OC)S2)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC3C=C(C4=CC(OC)=C(C=C(C#N)C#N)C=C4OC)SC23)C=C1,IDTT-BO-MN,,,10.15,0.93,0.6134,5.75,"A. Irfan, A. Mahmood, A.G. Al-Sehemi, F. Ahmad, Experimental and theoretical study of planar small molecule acceptor for organic solar cells, J. Mol. Struct. 1196 (2019) 169¨C175. https://doi.org/10.1016/j.molstruc.2019.06.035."
3502,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=C(C=CC(C4=CC=C(C5=CC=C(C=C(C#N)C#N)C6=NSN=C56)S4)=C3)C3=C2C=C(C2=CC=C(C=C(C#N)C#N)C4=NSN=C24)S3)C=C1,Me-ITBD,-5.74,-3.95,11.1,0.89,0.58,5.75,"C.H. Jeong, Y.U. Kim, C.G. Park, S. Choi, M.J. Cho, D.H. Choi, Improved performance of non-fullerene polymer solar cells by simple structural change of asymmetric acceptor based on indenothiophene, Synth. Met. 246 (2018) 164¨C171. https://doi.org/10.1016/j.synthmet.2018.10.014."
3503,CCCCCCCCN1C(=O)/C(=C/C2=C3SC(C(F)(F)F)=CC3=C(C3=CC4=C(S3)C3=CC5=C(C=C3C4(C3=CC=C(CCCCCC)C=C3)C3=CC=C(CCCCCC)C=C3)C3=C(C=C(C4=C6C=C(C(F)(F)F)SC6=C(/C=C6SC(=C(C#N)C#N)N(CCCCCCCC)C6=O)S4)S3)C5(C3=CC=C(CCCCCC)C=C3)C3=CC=C(CCCCCC)C=C3)S2)SC1=C(C#N)C#N,ATT-8,-5.46,-3.71,12.95,0.93,0.4748,5.72,"P. Wang, H. Fan, X. Zhu, A 2-(trifluoromethyl)thieno[3,4-b]thiophene-based small-molecule electron acceptor for polymer solar cell application, Dyes Pigments. 155 (2018) 179¨C185. https://doi.org/10.1016/j.dyepig.2018.03.032."
3504,CCCCCC(CCCCC)N1C(=O)C2=CC=C3C4=C5C6=C(C=C4)C(=O)N(C(CCCCC)CCCCC)C(=O)C6=CC4=C5C5=C(C=C(C1=O)C2=C35)C1=C4SC2=C1C1=C3C4=C2CC2C(=O)N(C(CCCCC)CCCCC)C(=O)C5=CC=C(C6=CC=C7C(=O)N(C(CCCCC)CCCCC)C(=O)C(=C1)C7=C63)C4=C52,FPDI-T,-5.98,-3.77,11.76,0.94,0.51,5.69,"H. Zhong, C.-H. Wu, C.-Z. Li, J. Carpenter, C.-C. Chueh, J.-Y. Chen, H. Ade, A.K.-Y. Jen, Rigidifying Nonplanar Perylene Diimides by Ring Fusion Toward Geometry-Tunable Acceptors for High-Performance Fullerene-Free Solar Cells, Adv. Mater. 28 (2016) 951¨C958. https://doi.org/10.1002/adma.201504120."
3505,CCCCCCC1=CC=C(OC2=C(C3=C(C4=CC=C(CCCCCC)C=C4)C=C4C(=C3)C(C3=CC=C(CCCCCC)C=C3)(C3=CC=C(CCCCCC)C=C3)OC3=C4SC(/C=C4/C(=O)C5=C(C=C(F)C(F)=C5)C4=C(C#N)C#N)=C3)SC(/C=C3/C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)=C2)C=C1,i-PTIC-F,-5.66,-4.18,14.56,0.63,0.62,5.68,"J. Li, Y. Wu, X. Zhang, D. Zeng, Y. Luo, X. Duan, X. Gao, P. Cai, Q. Zhang, J. Zhang, Z. Liu, A new fluorinated pyran-bridged A-D-A type small molecular acceptor for organic solar cells, Dyes Pigments. 175 (2020) 108165. https://doi.org/10.1016/j.dyepig.2019.108165."
3506,CCCCCCCCCCCCCCCCN1C2=C(SC(/C=C3C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)=C2)C2=C1C1=C(OCC(CC)CCCC)C3=C(C(OCC(CC)CCCC)=C1S2)C1=C(S3)C2=C(C=C(/C=C3C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)S2)N1CCCCCCCCCCCCCCCC,M32,-5.59,-3.84,11.34,0.96,0.5196,5.67,"Y. Ma, M. Zhang, S. Wan, P. Yin, P. Wang, D. Cai, F. Liu, Q. Zheng, Efficient Organic Solar Cells from Molecular Orientation Control of M-Series Acceptors, Joule. 5 (2021) 197¨C209. https://doi.org/10.1016/j.joule.2020.11.006."
3507,CCCCCCCCC1(CCCCCCCC)C2=CC3=C(C=C2C2=C1C=C(/C=C1C(=O)C4=C(C=CC=C4)C1=C(C#N)C#N)S2)C(CCCCCCCC)(CCCCCCCC)C1=C3C=CC(C2=CC=C(/C=C3C(=O)C4=C(C=CC=C4)C3=C(C#N)C#N)S2)=C1,DICTF,-5.67,-3.79,10.3,0.93,0.59,5.65,"N. Qiu, H. Zhang, X. Wan, C. Li, X. Ke, H. Feng, B. Kan, H. Zhang, Q. Zhang, Y. Lu, Y. Chen, A New Nonfullerene Electron Acceptor with a Ladder Type Backbone for High-Performance Organic Solar Cells, Adv. Mater. 29 (2017) 1604964. https://doi.org/10.1002/adma.201604964."
3508,CCCCCCC(CCCCCC)N1C(=O)C2=CC=C3C4=CC=C5C(=O)N(C(CCCCCC)CCCCCC)C(=O)C6=CC(C7=CC=C(C8=C9SC(C%10=C%11C%12=CC=C%13C(=O)N(C(CCCCCC)CCCCCC)C(=O)C%14=CC=C(C%15=CC=C%16C(=O)N(C(CCCCCC)CCCCCC)C(=O)C(=C%10)C%16=C%15%11)C%12=C%14%13)=CC9=C(C9=CC=C(C%10=C%11C%12=CC=C%13C(=O)N(C(CCCCCC)CCCCCC)C(=O)C%14=C%13C%12=C(C=C%14)C%12=C%11C%11=C(C=C%12)C(=O)N(C(CCCCCC)CCCCCC)C(=O)C%11=C%10)S9)C9=C8C=C(C8=C%10C%11=CC=C%12C(=O)N(C(CCCCCC)CCCCCC)C(=O)C%13=C%12C%11=C(C=C%13)C%11=CC=C%12C(=O)N(C(CCCCCC)CCCCCC)C(=O)C(=C8)C%12=C%11%10)S9)S7)=C(C7=CC=C(C1=O)C2=C37)C4=C56,BDT-PDI4,,,10.5,1.02,0.518,5.6,"H. Hu, Y. Li, J. Zhang, Z. Peng, L. Ma, J. Xin, J. Huang, T. Ma, K. Jiang, G. Zhang, W. Ma, H. Ade, H. Yan, Effect of Ring-Fusion on Miscibility and Domain Purity: Key Factors Determining the Performance of PDI-Based Nonfullerene Organic Solar Cells, Adv. Energy Mater. 8 (2018) 1800234. https://doi.org/10.1002/aenm.201800234."
3509,CCCCCCCCC1(CCCCCCCC)C2=CC3=C(C=C2C2=C1C=C(C1=CC=C(C#N)C4=NSN=C14)S2)C(CCCCCCCC)(CCCCCCCC)C1=C3SC(C2=CC=C(C#N)C3=NSN=C23)=C1,IDT-C8-BC,-5.39,-3.5,9.21,1.11,0.501,5.6,"J. Zhang, J. Lv, X. Dong, T. Xu, X. Dai, T. Duan, Z. Kan, P. Liu, S. Lu, Cyano-functionalized small-molecule acceptors for high-efficiency wide-bandgap organic solar cells, J. Mater. Chem. C. 8 (2020) 9195¨C9200. https://doi.org/10.1039/D0TC02061C."
3510,CCCCCCCCOC1=C(C2=CC3=C(S2)C2=C(C=C(/C=C4C(=O)C5=C(C=C(F)C(F)=C5)C4=C(C#N)C#N)S2)N3C(CCCCCCCC)CCCCCCCC)C2=NSN=C2C(C2=CC3C(S2)C2=C(C=C(/C=C4C(=O)C5=C(C=C(F)C(F)=C5)C4=C(C#N)C#N)S2)N3C(CCCCCCCC)CCCCCCCC)=C1OCCCCCCCC,DBTD-4F,-5.51,-3.9,12.91,0.81,0.5302,5.55,"J. Cao, S. Qu, L. Yang, H. Wang, F. Du, J. Yu, W. Tang, Asymmetric simple unfused acceptor enabling over 12% efficiency organic solar cells, Chem. Eng. J. 412 (2021) 128770. https://doi.org/10.1016/j.cej.2021.128770."
3511,CCCCCCCCC1=C(/C=C2C(=O)C3=CC(F)=C(F)C=C3C2=C(C#N)C#N)SC(C2=CC(CCCCCCCC)=C(C3=C(CCCCCCCC)C=C(C4=CC(CCCCCCCC)=C(/C=C5C(=O)C6=CC(F)=C(F)C=C6C5=C(C#N)C#N)S4)S3)S2)=C1,4T-1,-5.71,-4.09,12.7,0.84,0.5171,5.53,"Y. Zhou, M. Li, H. Lu, H. Jin, X. Wang, Y. Zhang, S. Shen, Z. Ma, J. Song, Z. Bo, High-Efficiency Organic Solar Cells Based on a Low-Cost Fully Non-Fused Electron Acceptor, Adv. Funct. Mater. 31 (2021) 2101742. https://doi.org/10.1002/adfm.202101742."
3512,CCCCCCCCCCC1(CCCCCCCCCC)C2=C(C=CC(C3=CC=C(C=C4SC(SCCCCCC)=C(SCCCCCC)S4)C4=NSN=C34)=C2)C2=C1C=C(C1=CC=C(C=C3SC(SCCCCCC)=C(SCCCCCC)S3)C3=NSN=C13)C=C2,BAF-2HDT,-5.7,-3.6,13.69,0.76,0.53,5.51,"Suman, A. Bagui, V. Gupta, K.K. Maurya, S.P. Singh, High-Performance Non-Fullerene Acceptor Derived from Diathiafulvalene Wings for Solution-Processed Organic Photovoltaics, J. Phys. Chem. C. 120 (2016) 24615¨C24622. https://doi.org/10.1021/acs.jpcc.6b07778."
3513,CCCCCC(CCCCC)N1C(=O)C2=CC3=C4C5=C(C=CC(=C25)C1=O)C1=C2C5=C(C=C1)C(=O)N(C(CCCCC)CCCCC)C(=O)C5=CC(=C24)C1=C3C2=CC3=C4C(=CC=C5C6=C(C7=CC=C(C8=CC9=C%10C(=CC%11=C%12C%13=C(C=C%14C(=O)N(C(CCCCC)CCCCC)C(=O)C%15=C%14C%13=C(C=C%15)C8=C%10%12)C8=C%11C%10=CC%11=C%12C(=CC=C%13C%14=CC=C%15C(=O)N(C(CCCCC)CCCCC)C(=O)C%16=C%15C%14=C(C8=C%16)C%10=C%13%12)C(=O)N(C(CCCCC)CCCCC)C%11=O)C(=O)N(C(CCCCC)CCCCC)C9=O)S7)C=C7C(=O)N(C(CCCCC)CCCCC)C(=O)C8=C7C6=C(C1=C8)C2=C54)C(=O)N(C(CCCCC)CCCCC)C3=O,T-FDI,-5.98,-4.09,13.4,0.78,0.53,5.5,"Y. Yin, W. Zhang, Z. Zheng, Z. Ge, Y. Liu, F. Guo, S. Gao, L. Zhao, Y. Zhang, Integrated linker-regulation and ring-fusion engineering for efficient additive-free non-fullerene organic solar cells, J. Mater. Chem. C. 8 (2020) 12516¨C12526. https://doi.org/10.1039/D0TC02499F."
3514,CCCCCCCN1C(=O)/C(=CC2=CC=C(C3=CC4=C(S3)C3=CC5=C(C=C3C4(C3=CC=C(CCCCCC)C=C3)C3=CC=C(CCCCCC)C=C3)C3=C(C=C(C4=CC=C(/C=C6/SC(=C(C#N)C#N)N(CCCCCCC)C6=O)C6=NSN=C46)S3)C5(C3=CC=C(CCCCCC)C=C3)C3=CC=C(CCCCCC)C=C3)C3=NSN=C23)SC1=C(C#N)C#N,IDTBT-R-CN,-5.38,-3.67,12.4,0.88,0.501,5.5,"Q.-Y. Li, J. Xiao, L.-M. Tang, H.-C. Wang, Z. Chen, Z. Yang, H.-L. Yip, Y.-X. Xu, Thermally stable high performance non-fullerene polymer solar cells with low energy loss by using ladder-type small molecule acceptors, Org. Electron. 44 (2017) 217¨C224. https://doi.org/10.1016/j.orgel.2017.02.008."
3515,CCCCCCCCC1(CCCCCCCC)C2=CC3=C(C=C2C2=C1C=C1C(=C2)C(CCCCCCCC)(CCCCCCCC)C2=C1SC(/C=C1C(=O)C4=C(C=CC=C4)C1=C(C#N)C#N)=C2)C(CCCCCCCC)(CCCCCCCC)C1=C3SC(/C=C2C(=O)C3=C(C=CC=C3)C2=C(C#N)C#N)=C1,F-0CL,-5.43,-3.71,9.64,1.09,0.523,5.49,"Y. Wang, Y. Wang, B. Kan, X. Ke, X. Wan, C. Li, Y. Chen, High-Performance All-Small-Molecule Solar Cells Based on a New Type of Small Molecule Acceptors with Chlorinated End Groups, Adv. Energy Mater. 8 (2018) 1802021. https://doi.org/10.1002/aenm.201802021."
3516,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C=C(C2=CC(C(=O)OCC(CC)CCCC)=C(/C=C5C(=O)C6=C(C=C(F)C(F)=C6)C5=C(C#N)C#N)S2)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC(C3=CC(C(=O)OCC(CC)CCCC)=C(/C=C4C(=O)C5=C(C=C(F)C(F)=C5)C4=C(C#N)C#N)S3)=C2)C=C1,IDT-4EsT-2IC2F,-5.35,-3.95,13.02,0.745,0.56,5.45,"T.B. Raju, H.W. Cho, P. Gopikrishna, Y. Lee, J.Y. Kim, B. Kim, Positional Effect of the 2-Ethylhexyl Carboxylate Side Chain on the Thiophene ¦Ð-Bridge of Nonfullerene Acceptors for Efficient Organic Solar Cells, ACS Appl. Energy Mater. 4 (2021) 11675¨C11683. https://doi.org/10.1021/acsaem.1c02403."
3517,CCCCCCCCC1(CCCCCCCC)C2=CC3=C(C=C2C2=CC4=C(C=C(C5=C(CC(CC)CCCC)C=C(/C=C6C(=O)C7=C(C=C(F)C(F)=C7)C6=C(C#N)C#N)S5)S4)C=C21)SC(C1=C(CC(C)CC)C=C(/C=C2C(=O)C4=C(C=C(F)C(F)=C4)C2=C(C#N)C#N)S1)=C3,DTFT5-FIC ,-5.52,-3.87,11.64,0.9,0.5204,5.45,"F.-Y. Cao, P.-K. Huang, Y.-C. Su, W.-C. Huang, S.-L. Chang, K.-E. Hung, Y.-J. Cheng, Forced coplanarity of dithienofluorene-based non-fullerene acceptors to achieve high-efficiency organic solar cells, J. Mater. Chem. A. 7 (2019) 17947¨C17953. https://doi.org/10.1039/C9TA05116C."
3518,CCCCC(CC)COC1=CC=CC(C2(C3=CC=CC(OCC(CC)CCCC)=C3)C3=CC4=C(C=C3C3=C2C2=C(C=C(/C=C5C(=O)C6=C(SC)SC(SC)=C6C5=C(C#N)C#N)S2)S3)C(C2=CC=CC(OCC(CC)CCCC)=C2)(C2=CC(OCC(CC)CCCC)=CC=C2)C2=C4SC3=C2SC(/C=C2C(=O)C4=C(SC)SC(SC)=C4C2=C(C#N)C#N)=C3)=C1,IT-DSM,-5.58,-3.99,12.54,0.88,0.49,5.41,"S. Jeong, H. Je, J.H. Lee, S.H. Lee, S.-Y. Jang, K. Park, H. Kang, S.-K. Kwon, Y.-H. Kim, K. Lee, Molecular engineering of non-fullerene acceptors based on thiophene-fused end groups for fullerene-free organic solar cells, Dyes Pigments. 198 (2022) 109987. https://doi.org/10.1016/j.dyepig.2021.109987."
3519,CCCCCCCCC1(CCCCCCCC)C2=CC(C3=CC4=C5C(=CC=C6C7=C8C(=CC=C9C(=O)N(C(CCCCC)CCCCC)C(=O)C(=C98)C=C7)C3=C65)C(=O)N(C(CCCCC)CCCCC)C4=O)=CC=C2C2=C1C=C(C1=C3C4=C5C(=CC=C6C(=O)N(C(CCCCC)CCCCC)C(=O)C(=C65)C=C4)C4=C3C3=C(C=C4)C(=O)N(C(CCCCC)CCCCC)C(=O)C3=C1)C=C2,FPDI-I,-5.82,-3.47,10.17,0.93,0.5698,5.39,"H. Wang, M. Li, J. Song, C. Li, Z. Bo, Extended ¦Ð-conjugated perylene diimide dimers toward efficient organic solar cells, Dyes Pigments. 183 (2020) 108736. https://doi.org/10.1016/j.dyepig.2020.108736."
3520,CCCCCCCCOC1=CC=C(C2(C3=CC=C(OCCCCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C=C(C2=CC=C(/C=C5SC(=S)N(CC)C5=O)C5=NSN=C25)S3)C(C2=CC=C(OCCCCCCCC)C=C2)(C2=CC=C(OCCCCCCCC)C=C2)C2=C4SC(C3=CC=C(/C=C4SC(=S)N(CC)C4=O)C4=NSN=C34)=C2)C=C1,I-IDTBTRH,-5.42,-3.68,8.81,0.86,0.71,5.38,"H. Huang, B. Xiao, C. Huang, J. Zhang, S. Liu, N. Fu, B. Zhao, T. Qin, E. Zhou, W. Huang, Enhanced open circuit voltage of small molecule acceptors containing angular-shaped indacenodithiophene units for P3HT-based organic solar cells, J. Mater. Chem. C. 6 (2018) 12347¨C12354. https://doi.org/10.1039/C8TC04608E."
3521,CCCCC(CC)CC1(CC(CC)CCCC)C2=C(SC(C3=CC(F)=C(C4=CC5=C(S4)C4=C(C=C(C6=CC=C(/C=C7SC(=S)N(CC)C7=O)C7=NSN=C67)S4)C5(CC(CC)CCCC)CC(CC)CCCC)C=C3F)=C2)C2=C1C=C(C1=CC=C(/C=C3SC(=S)N(CC)C3O)C3=NSN=C13)S2,DFPCBR,-5.12,-3.59,10.39,0.8,0.6439,5.34,"N. Wang, W. Yang, S. Li, M. Shi, T.-K. Lau, X. Lu, R. Shikler, C.-Z. Li, H. Chen, A non-fullerene acceptor enables efficient P3HT-based organic solar cells with small voltage loss and thickness insensitivity, Chin. Chem. Lett. 30 (2019) 1277¨C1281. https://doi.org/10.1016/j.cclet.2019.01.010."
3522,CCCCC(CC)CN1C(=O)C2=CC=C3C4=C(C=CC(=C24)C1=O)C1=C2C4=C(C=C1)C(=O)N(CC(CC)CCCC)C(=O)C4=CC(C1=CC4=C(C=C1)C1=C(C=C(C5=C6C7=CC=C8C(=O)N(CC(CC)CCCC)C(=O)C9=C8C7=C(C=C9)C7=C6C6=C(C=C7)C(=O)N(CC(CC)CCCC)C(=O)C6=C5)C=C1)C41C4=C(C=CC(C5=C6C7=CC=C8C(=O)N(CC(CC)CCCC)C(=O)C9=C8C7=C(C=C9)C7=C6C6=C(C=C7)C(=O)N(CC(CC)CCCC)C(=O)C6=C5)=C4)C4=C1C=C(C1=C5C6=CC=C7C(=O)N(CC(CC)CCCC)C(=O)C8=C7C6=C(C=C8)C6=C5C5=C(C=C6)C(=O)N(CC(CC)CCCC)C(=O)C5=C1)C=C4)=C32,SBF-PDI4,-6.24,-4.11,13.08,0.85,0.48,5.34,"J. Yi, Y. Wang, Q. Luo, Y. Lin, H. Tan, H. Wang, C.-Q. Ma, A 9,9¡ä-spirobi[9H-fluorene]-cored perylenediimide derivative and its application in organic solar cells as a non-fullerene acceptor, Chem. Commun. 52 (2016) 1649¨C1652. https://doi.org/10.1039/C5CC08484A."
3523,O=C(N(CC)/C(S/1)=C(C#N)C#N)C1=CC2=C(OC)C(OC)=C(C3=CC4=C(C5=C(C4(C6=CC=C(CCCCCC)C=C6)C7=CC=C(CCCCCC)C=C7)C=C(C8=C9C=C(C%10=C(OC)C(OC)=C(/C=C%11C(N(CC)/C(S/%11)=C(C#N)C#N)=O)C%12=NN(CCCCCCCC)N=C%10%12)S8)C(C9(C%13=CC=C(CCCCCC)C=C%13)C%14=CC=C(CCCCCC)C=C%14)=C5)S3)C%15=NN(CCCCCCCC)N=C2%15,BTA103,-5.37,-3.61,8.56,0.94,0.66,5.31,"Q. Zhang, B. Xiao, M. Du, G. Li, A. Tang, E. Zhou, A2¨CA1¨CD¨CA1¨CA2 type non-fullerene acceptors based on methoxy substituted benzotriazole with three different end-capped groups for P3HT-based organic solar cells, J. Mater. Chem. C. 6 (2018) 10902¨C10909. https://doi.org/10.1039/C8TC03963A."
3524,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=C(SC(/C=C4C(=O)C5=C(C=CC=C5)C4=C(C#N)C#N)=C3)C3=C2C2=C4SC5=C(C4=C4SC6=C(C4=C2S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C6SC(/C=C3C(=O)C4=C(C=CC=C4)C3=C(C#N)C#N)=C2)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C5SC(/C=C3C(=O)C4=C(C=CC=C4)C3=C(C#N)C#N)=C2)C=C1,BTCDT-IC,-5.75,-3.87,9.75,0.92,0.59,5.3,"X. Wu, W. Wang, H. Hang, H. Li, Y. Chen, Q. Xu, H. Tong, L. Wang, Star-Shaped Fused-Ring Electron Acceptors with a C3h-Symmetric and Electron-Rich Benzotri(cyclopentadithiophene) Core for Efficient Nonfullerene Organic Solar Cells, ACS Appl. Mater. Interfaces. 11 (2019) 28115¨C28124. https://doi.org/10.1021/acsami.9b08017."
3525,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C=C(/C=C2C(=O)C5=C(C=C(F)C(F)=C5)C2=C(C#N)C#N)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC(/C=C3C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)=C2)C=C1,F5IC,-5.82,-4.05,14.49,0.703,0.52,5.3,"S. Dai, Y. Xiao, P. Xue, J. James Rech, K. Liu, Z. Li, X. Lu, W. You, X. Zhan, Effect of Core Size on Performance of Fused-Ring Electron Acceptors, Chem. Mater. 30 (2018) 5390¨C5396. https://doi.org/10.1021/acs.chemmater.8b02222."
3526,CCCCC(CC)CC1=CC=C(C2(C3=CC=C(CC(CC)CCCC)C=C3)C3=CC(C4=CC=C(C5=C(CC(CC)CCCC)C=C(/C=C6C(=O)C7=C(C=CC=C7)C6=C(C#N)C#N)S5)S4)=CC=C3C3=C2C=C(C2=C(CC(CC)CCCC)C=C(/C=C4C(=O)C5=CC=CC=C5C4=C(C#N)C#N)S2)S3)C=C1,IEPC,-5.72,-3.96,11.55,1,0.4554,5.26,"Z. Kang, Y. Ma, Q. Zheng, Asymmetric indenothiophene-based nonfullerene acceptors for binary- and ternary-blend polymer solar cells, Dyes Pigments. 170 (2019) 107555. https://doi.org/10.1016/j.dyepig.2019.107555."
3527,CCCCCCC1=C(C2=CC=C3C(=C2)N(CCCCCC)C2=C3N(CCCCCC)C3=C2C=CC(C2=C(CCCCC)C=C(C4=C(CCCCCC)C=C(CC5SC(=S)N(C)C5=O)S4)S2)=C3)SC(C2=C(CCCCCC)C=C(/C=C3/SC(=S)N(CC)C3=O)S2)=C1,DINI-Rho,-5.08,-3.06,11.08,0.82,0.58,5.23,"J. Sim, H. Lee, K. Song, S. Biswas, A. Sharma, G.D. Sharma, J. Ko, Solution processed bulk heterojunction solar cells based on A¨CD¨CA small molecules with a dihydroindoloindole (DINI) central donor and different acceptor end groups, J. Mater. Chem. C. 4 (2016) 3508¨C3516. https://doi.org/10.1039/C6TC00323K."
3528,CCCCCCC(CCCCCC)N1C(=O)C2=CC=C3C4=CC=C5C(=O)N(C(CCCCCC)CCCCCC)C(=O)C6=CC(C7=CC8=C(S7)C7=C(SC(C9=C%10C%11=CC=C%12C(=O)N(C(CCCCCC)CCCCCC)C(=O)C%13=CC=C(C%14=CC=C%15C(=O)N(C(CCCCCC)CCCCCC)C(=O)C(=C9)C%15=C%14%10)C%11=C%13%12)=C7)C7=C8SC(C8=C9C%10=CC=C%11C(=O)N(C(CCCCCC)CCCCCC)C(=O)C%12=CC=C(C%13=CC=C%14C(=O)N(C(CCCCCC)CCCCCC)C(=O)C(=C8)C%14=C%139)C%10=C%12%11)=C7)=C(C7=CC=C(C1=O)C2=C37)C4=C56,BT-PDI3,,,10,1,0.528,5.2,"H. Hu, Y. Li, J. Zhang, Z. Peng, L. Ma, J. Xin, J. Huang, T. Ma, K. Jiang, G. Zhang, W. Ma, H. Ade, H. Yan, Effect of Ring-Fusion on Miscibility and Domain Purity: Key Factors Determining the Performance of PDI-Based Nonfullerene Organic Solar Cells, Adv. Energy Mater. 8 (2018) 1800234. https://doi.org/10.1002/aenm.201800234."
3529,CCCCCCCCN1N=C2C(C=C(C#N)C#N)=CC=C(C3=CC4=C(S3)C3=C(S4)C4=CC5=C(C=C4C3(C3=CC=C(CCCCCC)C=C3)C3=CC=C(CCCCCC)C=C3)C3=C(C4=C(C=C(C6=CC=C(C=C(C#N)C#N)C7=NN(CCCCCCCC)N=C67)S4)S3)C5(C3=CC=C(CCCCCC)C=C3)C3=CC=C(CCCCCC)C=C3)C2=N1,BTA17,-5.41,-3.69,7.08,1.09,0.6717,5.18,"Q. Guo, F. Li, J. Li, Y. Xiao, K. Zuo, A. Tang, B. Zhang, E. Zhou, Modulating the middle and end-capped units of A2-A1-D-A1-A2 type non-fullerene acceptors for high VOC organic solar cells, Org. Electron. 95 (2021) 106195. https://doi.org/10.1016/j.orgel.2021.106195."
3530,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C=C(/C=C2C(=O)C5=C(C=C(F)C(F)=C5)C2=C(C#N)C#N)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC(/C=C3C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)=C2)C=C1,IDIC-4F,-5.79,-4.11,13.13,0.64,0.6156,5.17,"H. Tan, X. Zheng, J. Zhu, J. Yu, W. Zhu, An A¨CD¨CD¨CA-type non-fullerene small-molecule acceptor with strong near-infrared absorption for high performance polymer solar cells, J. Mater. Chem. C. 7 (2019) 13301¨C13306. https://doi.org/10.1039/C9TC04898G."
3531,CCCCCCC(CCCC)N1C(=O)C2=CC=C3C4=C(C=CC(=C24)C1=O)C1=CC=C2C(=O)N(C(CCCC)CCCCCC)C(=O)C4=C2C1=C3C(C1=NC(C2=CC3=C5C(=CC=C6C7=CC=C8C(=O)N(C(CCCC)CCCCCC)C(=O)C9=C8C7=C(C=C9)C2=C65)C(=O)N(C(CCCC)CCCCCC)C3=O)=CC(C2=CC3=C5C(=CC=C6C7=CC=C8C(=O)N(C(CCCC)CCCCCC)C(=O)C9=C8C7=C(C=C9)C2=C65)C(=O)N(C(CCCC)CCCCCC)C3=O)=C1)=C4,Ph-PDI,-6.02,-3.78,11.91,0.85,0.549,5.15,"Y. Duan, X. Xu, H. Yan, W. Wu, Z. Li, Q. Peng, Pronounced Effects of a Triazine Core on Photovoltaic Performance¨CEfficient Organic Solar Cells Enabled by a PDI Trimer-Based Small Molecular Acceptor, Adv. Mater. 29 (2017) 1605115. https://doi.org/10.1002/adma.201605115."
3532,CCCCCCCCCCC(CCCCCCCC)CC1=C(/C=C2C(=O)C3=C(C=CC=C3)C2=C(C#N)C#N)SC(C2=CC(C(C)C)=C3C=CC4=C(C5=CC(CC(CCCCCCCC)CCCCCCCCCC)=C(/C=C6C(=O)C7=C(C=CC=C7)C6=C(C#N)C#N)S5)C=C(C(C)C)C5=C4C3=C2C=C5)=C1,Py-2H,-5.67,-3.46,10.64,1.01,0.4781,5.13,"H. Li, J. Chen, L. Yi, J. Cao, M. Xiao, W. Zhuang, J. Li, R. Xia, J. Yu, Z. Tang, Easily synthesized pyrene-based nonfullerene acceptors for efficient organic solar cells, Synth. Met. 281 (2021) 116904. https://doi.org/10.1016/j.synthmet.2021.116904."
3533,CCCCCCOC1=CC=C(C2(C3=CC=C(OCCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C=C(/C=C2C(=O)C5=C(C=CC=C5)C2=C(C#N)C#N)S3)C(C2=CC=C(OCCCCCC)C=C2)(C2=CC=C(OCCCCCC)C=C2)C2=C4SC(/C=C3C(=O)C4=C(C=CC=C4)C3=C(C#N)C#N)=C2)C=C1,IDT-PhIC,-5.67,-3.89,9.99,0.93,0.5466,5.11,"J. Liang, P. Yin, T. Zheng, G. Wang, X. Zeng, C. Cui, P. Shen, Conjugated side-chain optimization of indacenodithiophene-based nonfullerene acceptors for efficient polymer solar cells, J. Mater. Chem. C. 7 (2019) 10028¨C10038. https://doi.org/10.1039/C9TC02237F."
3534,CCCCCCCCC1(CCCCCCCC)C2=C(C=CC(C3=CC=C(C=C(C#N)C#N)C4=NSN=C34)=C2)C2=C1C=C(C1=CC=C(C=C(C#N)C#N)C3=NSN=C13)C=C2,FBM,-6.14,-4.03,11.2,0.88,0.51,5.1,"K. Wang, Y. Firdaus, M. Babics, F. Cruciani, Q. Saleem, A. El Labban, M.A. Alamoudi, T. Marszalek, W. Pisula, F. Laquai, P.M. Beaujuge, ¦Ð-Bridge-Independent 2-(Benzo[c][1,2,5]thiadiazol-4-ylmethylene)malononitrile-Substituted Nonfullerene Acceptors for Efficient Bulk Heterojunction Solar Cells, Chem. Mater. 28 (2016) 2200¨C2208. https://doi.org/10.1021/acs.chemmater.6b00131."
3535,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)OC3=CC4=C(C=C3C3=C2C=C(C2=CC=C(/C=C5/C(=O)N(CC)SC5=S)C5=NSN=C25)S3)OC(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC(C3=CC=C(/C=C4C(=O)N(CC)SC4=S)C4=NSN=C34)=C2)C=C1,PTBT-R,-5.59,-3.7,10.38,0.97,0.5013,5.06,"Z. Liu, X. Zhang, P. Ren, Y. Wu, D. Zeng, X. Duan, X. Gao, P. Cai, Pyran-bridged A-D-A type small molecular acceptors for organic solar cells, Sol. Energy. 183 (2019) 463¨C468. https://doi.org/10.1016/j.solener.2019.03.046."
3536,CCCCCCCCCCCC1=C(C=C2C(=O)N(CC)C(=S)N(CC)C2=O)SC2=C1SC1=C2N(CC(CC)CCCC)C2=C1C1=NSN=C1C1=C2N(CC(CC)CCCC)C2=C1SC1=C2SC(C=C2C(=O)N(CC)C(=S)N(CC)C2=O)=C1CCCCCCCCCCC,Y-T,-5.42,-3.7,9.21,1.19,0.4615,5.06,"Y. Yin, L. Zhan, M. Liu, C. Yang, F. Guo, Y. Liu, S. Gao, L. Zhao, H. Chen, Y. Zhang, Boosting photovoltaic performance of ternary organic solar cells by integrating a multi-functional guest acceptor, Nano Energy. 90 (2021) 106538. https://doi.org/10.1016/j.nanoen.2021.106538."
3537,CCCCCCCC(CCCCCC)N1C(=O)C2=CC=C3C(=O)N(C(CCCCCC)CCCCCCC)C(=O)C4=C3C2=C(C1=O)C1=C4SC(C2=CC3=C(S2)C2=CC4=C(C=C2C3(C2=CC=C(CCCCCC)C=C2)C2=CC=C(CCCCCC)C=C2)C2=C(C=C(C3=CC5=C(S3)C3=C6C(=CC=C7C(=O)N(C(CCCCCC)CCCCCCC)C(=O)C5=C76)C(=O)N(C(CCCCCC)CCCCCCC)C3=O)S2)C4(C2=CC=C(CCCCCC)C=C2)C2=CC=C(CCCCCC)C=C2)=C1,IDT-NTI-1HH,-5.4,-3.8,8.07,1.01,0.59,5.05,"J. Hamonnet, M. Nakano, K. Nakano, H. Sugino, K. Takimiya, K. Tajima, Bis(naphthothiophene diimide)indacenodithiophenes as Acceptors for Organic Photovoltaics, Chem. Mater. 29 (2017) 9618¨C9622. https://doi.org/10.1021/acs.chemmater.7b03733."
3538,CCCCCCCCOCCCCCCC1(CCCCCCOCCCCCCCC)C2=CC(C3=CC4=C5C(=CC=C6C7=C8C(=CC=C9C(=O)N(C(CCCCC)CCCCC)C(=O)C(=C98)C=C7)C3=C65)C(=O)N(C(CCCCC)CCCCC)C4=O)=CC=C2C2=C1C=C(C1=C3C4=C5C(=CC=C6C(=O)N(C(CCCCC)CCCCC)C(=O)C(=C65)C=C4)C4=C3C3=C(C=C4)C(=O)N(C(CCCCC)CCCCC)C(=O)C3=C1)C=C2,FPDI-II,-5.84,-3.6,9.76,0.94,0.5472,5.04,"H. Wang, M. Li, J. Song, C. Li, Z. Bo, Extended ¦Ð-conjugated perylene diimide dimers toward efficient organic solar cells, Dyes Pigments. 183 (2020) 108736. https://doi.org/10.1016/j.dyepig.2020.108736."
3539,CCCCCCCCC1=C(/C=C2C(=O)C3=C(C=CC=C3)C2=C(C#N)C#N)SC2=C1SC1=C2C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C1SC1=C2SC2=C1C(C1=CC=C(CCCCCC)C=C1)(C1=CC=C(CCCCCC)C=C1)C1=C2SC(/C=C2C(=O)C3=C(C=CC=C3)C2=C(C#N)C#N)=C1CCCCCCCC,5T-2C8-IN,-5.48,-3.79,10.24,0.965,0.51,5.04,"H. Gao, X. Wan, Z. Xuan, W. Ma, J. Xin, C. Li, Y. Chen, Finely modulated asymmetric nonfullerene acceptors enabling simultaneously improved voltage and current for efficient organic solar cells, J. Mater. Chem. C. 10 (2022) 2742¨C2748. https://doi.org/10.1039/D1TC03793E."
3540,CCC(CC)N1C(=O)C2=CC=C3C4=C5C6=C(C=C4)C(=O)N(C(CC)CC)C(=O)C6=CC(C4=C6C7=C8C(=CC=C9C(=O)N(C(CC)CC)C(=O)C(=C98)C=C7)C7=C6C6=C(C=C7)C(=O)N(C(CC)CC)C(=O)C6=C4)=C5C4=C3C2=C(C=C4)C1=O,BB-2PDI,-6.21,-3.92,12.96,0.791,0.492,5.03,"H. Wang, L. Chen, Y. Xiao, A simple molecular structure of ortho-derived perylene diimide diploid for non-fullerene organic solar cells with efficiency over 8%, J. Mater. Chem. A. 5 (2017) 22288¨C22296. https://doi.org/10.1039/C7TA06804B."
3541,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C=C(C2=NC=C(/C=C5/SC(=S)N(CC)C5=O)S2)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC(C3=NC=C(/C=C4/SC(=S)N(CC)C4=O)S3)=C2)C=C1,P-IDTzR,-5.31,-3.42,9,1.02,0.546,5.01,"P. Ye, Y. Chen, J. Wu, X. Wu, Y. Xu, Z. Li, S. Hong, M. Sun, A. Peng, H. Huang, Combination of noncovalent conformational locks and side chain engineering to tune the crystallinity of nonfullerene acceptors for high-performance P3HT based organic solar cells, Mater. Chem. Front. 3 (2018) 64¨C69. https://doi.org/10.1039/C8QM00461G."
3542,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=C(C=C4C(=C3)C3=C(C=C(C5=CC=C(C#N)C6=NSN=C56)S3)C43C4=CC=C(CCCCCC)C=C4C4=C3C=CC(CCCCCC)=C4)C3=C2C=C(C2=CC=C(C#N)C4=NSN=C24)S3)C=C1,IDT-BC,-5.5,-3.57,8.76,1.14,0.542,5,"J. Zhang, J. Lv, X. Dong, T. Xu, X. Dai, T. Duan, Z. Kan, P. Liu, S. Lu, Cyano-functionalized small-molecule acceptors for high-efficiency wide-bandgap organic solar cells, J. Mater. Chem. C. 8 (2020) 9195¨C9200. https://doi.org/10.1039/D0TC02061C."
3543,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=C(C=CC(C4=CC=C(C5=CC=C(/C=C6/SC(=S)N(CCCCCC)C6O)C6=NSN=C56)S4)=C3)C3=C2C=C(C2=CC=C(/C=C4/SC(=S)N(CCCCCC)C4=O)C4=NCN=C24)S3)C=C1,TIDT-BT-R6,-5.28,-3.67,10.3,1.03,0.523,5,"W. Bai, X. Xu, Q. Li, Y. Xu, Q. Peng, Efficient Nonfullerene Polymer Solar Cells Enabled by Small-Molecular Acceptors with a Decreased Fused-Ring Core, Small Methods. 2 (2018) 1700373. https://doi.org/10.1002/smtd.201700373."
3544,CCCCCCC(C)CN1C(=O)C2=CC=C3C(=O)N(CC(CCCCCC)CCCCCC)C(=O)C4=C3C2=C(C1=O)C1=C4SC(C2=CC=C3C(=C2)C2(C4=C3C=CC(C3=CC5=C(S3)C3=C6C(=CC=C7C(=O)N(CC(CCCCCC)CCCCCC)C(=O)C5=C76)C(=O)N(CC(CCCCCC)CCCCCC)C3=O)=C4)C3=C(C=CC=C3)C3=C2C=CC=C3)=C1,SF-NTI-1HH,-5.88,-3.85,11.2,0.89,0.51,5,"J. Hamonnet, M. Nakano, A. Takahara, K. Takimiya, Tuning the absorption range of naphthothiophene diimide-based acceptors for organic solar cells, Dyes Pigments. 171 (2019) 107691. https://doi.org/10.1016/j.dyepig.2019.107691."
3545,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C=C(/C=C2C(=O)C5=CC=CC=C5C2=C(C#N)C#N)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC(C3=CC4=C(S3)C(C3=CC=C(CC(CC)CCCC)S3)=C3C=C(C5=CC6=C(S5)C5=CC7=C(C=C5C6(C5=CC=C(CCCCCC)C=C5)C5=CC=C(CCCCCC)C=C5)C5=C(C=C(/C=C6/C(=O)C8=CC=CC=C8C6=C(C#N)C#N)S5)C7(C5=CC=C(CCCCCC)C=C5)C5=CC=C(CCCCCC)C=C5)SC3=C4C3=CC=C(CC(CC)CCCC)S3)=C2)C=C1,BDT(IDT-IC)2,-5.53,-3.96,10.97,0.89,0.5102,4.98,"J. Zhu, X. Zheng, H. Tan, H. Tan, J. Yang, J. Yu, W. Zhu, Small molecule acceptors with indacenodithiophene¨Cbenzodithiophene¨Cindacenodithiophene as donating cores for solution-processed non-fullerene solar cells, Chem. Phys. Lett. 726 (2019) 7¨C12. https://doi.org/10.1016/j.cplett.2019.04.024."
3546,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C=C(C2=CC=C(/C=C5/SC(=O)N(CC)C5=O)C5=NSN=C25)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC(C3=CC=C(/C=C4/SC(=O)N(CC)C4=O)C4=NSN=C34)=C2)C=C1,BT2B,-5.5,-3.53,7.59,0.97,0.67,4.93,"B. Xiao, A. Tang, L. Cheng, J. Zhang, Z. Wei, Q. Zeng, E. Zhou, Non-Fullerene Acceptors With A2 = A1-D-A1 = A2 Skeleton Containing Benzothiadiazole and Thiazolidine-2,4-Dione for High-Performance P3HT-Based Organic Solar Cells, Sol. RRL. 1 (2017) 1700166. https://doi.org/10.1002/solr.201700166."
3547,CCCCCCCCN1C2=C(C=CC(C3=CC=C(/C=C4SC(=S)N(CC)C4=O)C4=NSN=C34)=C2)C2=C1C=C(C1=CC=C(/C=C3SC(=S)N(CC)C3=O)C3=NSN=C13)C=C2,CzC8,-5.72,-3.74,11.24,0.98,0.45,4.91,"D. Ma, S. Feng, J. Zhang, C. Kou, X. Gong, Q. Li, X. Xu, S. Yan, Z. Bo, Non-fullerene small molecular acceptors with a carbazole core for organic solar cells with high open-circuit voltage, Dyes Pigments. 146 (2017) 293¨C299. https://doi.org/10.1016/j.dyepig.2017.07.014."
3548,CCCCCCCCC(CCCCCCCC)N1C2=C(SC(C3=C(CCCCCC)C=C(C4=C(CCCCCC)C=C(/C=C5C(=O)N(CCCC)C(=O)C(C#N)=C5C)S4)S3)=C2)C2=C1C=C(C1=C(CCCCCC)C=C(C3=C(CCCCCC)C=C(/C=C4C(=O)N(CCCC)C(=O)C(C#N)=C4C)S3)S1)S2,PY1,-5.27,-4,10.53,0.83,0.56,4.89,"A. Mishra, M.L. Keshtov, A. Looser, R. Singhal, M. Stolte, F. W¨¹rthner, P. B?uerle, G.D. Sharma, Unprecedented low energy losses in organic solar cells with high external quantum efficiencies by employing non-fullerene electron acceptors, J. Mater. Chem. A. 5 (2017) 14887¨C14897. https://doi.org/10.1039/C7TA04703G."
3549,CCCCCCCCC1=CC=C(C2(C3=CC=C(CCCCCCCC)C=C3)C3=CC(C4=CC=C(C5=C(CC(CC)CCCC)C=C(/C=C6C(=O)C7=C(C=CC=C7)C6=C(C#N)C#N)S5)S4)=CC=C3C3=C2C=C(C2=C(CC(CC)CCCC)C=C(/C=C4C(=O)C5=CC=CC=C5C4=C(C#N)C#N)S2)S3)C=C1,IOPC,-5.71,-3.95,10.69,1.01,0.449,4.86,"Z. Kang, Y. Ma, Q. Zheng, Asymmetric indenothiophene-based nonfullerene acceptors for binary- and ternary-blend polymer solar cells, Dyes Pigments. 170 (2019) 107555. https://doi.org/10.1016/j.dyepig.2019.107555."
3550,CCCCCCCCC1(CCCCCCCC)C2=CC3=C(C=C2C2=C1C=C(C1=CC=C(/C=C4/SC(=S)N(CC)C4=O)C4=C1N=C(C1=CC=CC=C1)C(C1=CC=CC=C1)=N4)S2)C(CCCCCCCC)(CCCCCCCC)C1=C3SC(C2=CC=C(/C=C3/SC(=S)N(CC)C3=O)C3=C2N=C(C2=CC=CC=C2)C(C2=CC=CC=C2)=N3)=C1,Qx1b,-5.35,-3.66,7.34,0.95,0.69,4.81,"B. Xiao, A. Tang, J. Yang, A. Mahmood, X. Sun, E. Zhou, Quinoxaline-Containing Nonfullerene Small-Molecule Acceptors with a Linear A2-A1-D-A1-A2 Skeleton for Poly(3-hexylthiophene)-Based Organic Solar Cells, ACS Appl. Mater. Interfaces. 10 (2018) 10254¨C10261. https://doi.org/10.1021/acsami.8b00216."
3551,CCCCC(CC)CC1(CC(CC)CCCC)C2=C(C=CC(C3=CC=C(/C=C4/C(=C(C#N)C#N)C5=C(C=CC=C5)C4O)S3)=C2)C2=C1C=C(C1=CCC(/C=C3C(=O)C4=C(C=CC=C4)C3C(C#N)C#N)S1)C=C2,DICTiF ,-5.55,-3.62,10.12,0.98,0.51,4.81,"H. Zhang, Y. Liu, Y. Sun, M. Li, W. Ni, Q. Zhang, X. Wan, Y. Chen, A simple small molecule as the acceptor for fullerene-free organic solar cells, Sci. China Chem. 60 (2017) 366¨C369. https://doi.org/10.1007/s11426-016-0417-9."
3552,CCN1C(=O)/C(=C/C2=CC=C(C3=CC=C4C(=C3)C3(C5=C4C=CC(C4=CC=C(/C=C6SC(=S)N(CC)C6=O)C6=NSN=C46)=C5)C4=C(C=CC(C5=CC=C(/C=C6SC(=S)N(CC)C6=O)C6=NSN=C56)=C4)C4=C3C=C(C3=CC=C(/C=C5SC(=S)N(CC)C5=O)C5=NSN=C35)C=C4)C3=NSN=C23)SC1=S,SF(BR)4,-5.78,-3.73,11.5,0.93,0.43,4.61,"H. Tan, Y. Long, J. Zhang, J. Zhu, J. Yang, J. Yu, W. Zhu, Spirobifluorene-cored wide bandgap non-fullerene small molecular acceptor with 3D structure for organic solar cells, Dyes Pigments. 162 (2019) 797¨C801. https://doi.org/10.1016/j.dyepig.2018.11.016."
3553,CCCCCCCCC1(CCCCCCCC)C2=C(SC(C3=CC=C(C=C(C#N)C#N)C4=NSN=C34)=C2)C2=C1C=C(C1=CC=C(C=C(C#N)C#N)C3=NSN=C13)S2,CDTBM,-5.79,-3.9,11.7,0.68,0.53,4.6,"K. Wang, Y. Firdaus, M. Babics, F. Cruciani, Q. Saleem, A. El Labban, M.A. Alamoudi, T. Marszalek, W. Pisula, F. Laquai, P.M. Beaujuge, ¦Ð-Bridge-Independent 2-(Benzo[c][1,2,5]thiadiazol-4-ylmethylene)malononitrile-Substituted Nonfullerene Acceptors for Efficient Bulk Heterojunction Solar Cells, Chem. Mater. 28 (2016) 2200¨C2208. https://doi.org/10.1021/acs.chemmater.6b00131."
3554,O=C1/C(=C/C2=CC=C(C3=CC=C(/C=C4SC(=S)N(CCCC5CCCCC5)C4=O)S3)S2)SC(=S)C1CCCC1CCCCC1,T2-Cy6PRH,-5.67,-3.62,11.04,1.03,0.4,4.6,"S. Hong, C.E. Song, D.H. Ryu, S.K. Lee, W.S. Shin, E. Lim, Cyclohexyl-substituted non-fullerene small-molecule acceptors for organic solar cells, New J. Chem. 45 (2021) 10373¨C10382. https://doi.org/10.1039/D0NJ04240D."
3555,CCCCC(CC)COC1=C(C2=CC3=C(S2)C2=C(C=C(/C=C4C(=O)C5=C(C=CC=C5)C4=C(C#N)C#N)S2)C3(CC(CC)CCCC)CC(CC)CCCC)SC2=C1SC(C1=CC3=C(S1)C1=C(C=C(/C=C4C(=O)C5=C(C=CC=C5)C4=C(C#N)C#N)S1)C3(CC(CC)CCCC)CC(CC)CCCC)=C2OCC(CC)CCCC,TTDTC-0F,-5.1,-3.69,9.9,0.69,0.638,4.55,"Z. Liang, X. Cheng, Y. Jiang, J. Yu, X. Xu, Z. Peng, L. Bu, Y. Zhang, Z. Tang, M. Li, L. Ye, Y. Geng, P3HT-Based Organic Solar Cells with a Photoresponse to 1000 nm Enabled by Narrow Band Gap Nonfullerene Acceptors with High HOMO Levels, ACS Appl. Mater. Interfaces. 13 (2021) 61487¨C61495. https://doi.org/10.1021/acsami.1c21089."
3556,CCCCCCCCN1N=C2C(/C=C3SC(=O)N(CC)C3=O)=CC=C(C3=CC4=C(S3)C3=CC5=C(C=C3C4(C3=CC=C(CCCCCC)C=C3)C3=CC=C(CCCCCC)C=C3)C3=C(C=C(C4=CC=C(/C=C6SC(=O)N(CC)C6=O)C6=NN(CCCCCCCC)N=C46)S3)C5(C3=CC=C(CCCCCC)C=C3)C3=CC=C(CCCCCC)C=C3)C2=N1,BTA2,-5.43,-3.38,6.15,1.22,0.6,4.5,"B. Xiao, A. Tang, J. Yang, Z. Wei, E. Zhou, P3HT-Based Photovoltaic Cells with a High Voc of 1.22 V by Using a Benzotriazole-Containing Nonfullerene Acceptor End-Capped with Thiazolidine-2,4-dione, ACS Macro Lett. 6 (2017) 410¨C414. https://doi.org/10.1021/acsmacrolett.7b00097."
3557,CCCCC(CC)CC1(CC(CC)CCCC)C2=C(SC(/C=C3C(=O)C4=CC(F)=C(F)C=C4C3=C(C#N)C#N)=C2)C2=C1C=C(C1=CC3=C(S1)C1=C(C=C(/C=C4C(=O)C5=CC(F)=C(F)C=C5C4=C(C#N)C#N)S1)C3(CC(CC)CCCC)CC(CC)CCCC)S2,bCIC,-5.23,-3.4,11.88,0.739,0.5093,4.47,"X. Song, Y. Xu, X. Tao, X. Gao, Y. Wu, R. Yu, Y. He, Y. Tao, BODIPY Cored A?D?A¡¯?D?A Type Nonfused-Ring Electron Acceptor for Efficient Polymer Solar Cells, Macromol. Rapid Commun. n/a (n.d.) 2100828. https://doi.org/10.1002/marc.202100828."
3558,O=C(C(C=CC=C1)=C1C/2=C(C#N)C#N)C2=C/C(S3)=CC(C3=C4)=CC5=C4C6=CC7=C(C=C6C5(C8=CC=C(CCCCCC)C=C8)C9=CC=C(CCCCCC)C=C9)C%10=CC%11=C(C=C(/C=C%12C(C(C=CC=C%13)=C%13C\%12=C(C#N)/C#N)=O)S%11)C=C%10C7(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15,NIBDT,-5.87,-3.91,11.45,0.831,0.467,4.45,"P. Wang, H. Fan, C. Zhang, X. Zhu, A large-bandgap small-molecule electron acceptor utilizing a new indacenodibenzothiophene core for organic solar cells, Mater. Chem. Front. 2 (2017) 136¨C142. https://doi.org/10.1039/C7QM00403F."
3559,CCCCCCC(C)N1C(=O)C2=CC3=C4C5=C(C=CC(=C25)C1=O)C1=C2C5=C(C=C1)C(=O)N(C(CCCCCC)CCCCCC)C(=O)C5=CC(=C24)C1=C3C2=CC3=C4C(=CC(C5=CC=C(/C(C6=CC=C(C7=C8C9=CC=C%10C(=O)N(C(CCCCCC)CCCCCC)C(=O)C%11=C%10C9=C9C(=C%11)C%10=C(C%11=CC%12=C(C(=C7)C(=O)N(C(CCCCCC)CCCCCC)C%12=O)C8=C%119)C7=C8C9=C(C=CC%11=C9C(=C7)C(=O)N(C(CCCCCC)CCCCCC)C%11=O)C7=C9C%11=C(C=C7)C(=O)N(C(CCCCCC)CCCCCC)C(=O)C%11=CC%10=C98)C=C6)=C(/C6=CC=C(C7=C8C9=CC=C%10C(=O)N(C(CCCCCC)CCCCCC)C(=O)C%11=C%10C9=C9C(=C%11)C%10=C(C%11=CC%12=C(C(=C7)C(=O)N(C(CCCCCC)CCCCCC)C%12=O)C8=C%119)C7=C8C9=C(C=CC%11=C9C(=C7)C(=O)N(C(CCCCCC)CCCCCC)C%11=O)C7=C9C%11=C(C=C7)C(=O)N(C(CCCCCC)CCCCCC)C(=O)C%11=CC%10=C98)C=C6)C6=CC=C(C7C=C8C(=O)N(C(CCCCCC)CCCCCC)C(=O)C9=C8C8=C%10C(=C9)C9=C(C%11=CC%12=C%13C(=CC=C(C%13=C%11%10)C87)C(=O)N(C(CCCCCC)CCCCCC)C%12=O)C7=C8C%10=C(C=CC%11=C%10C(=C7)C(=O)N(C(CCCCCC)CCCCCC)C%11=O)C7=C%10C%11=C(C=C7)C(=O)N(C(CCCCCC)CCCCCC)C(=O)C%11=CC9=C%108)C=C6)C=C5)=C5C6=CC=C7C(=O)N(C(CCCCCC)CCCCCC)C(=O)C8=C7C6=C(C1=C8)C2=C45)C(=O)N(C(CCCCCC)CCCCCC)C3=O,TPE-4PDI2,-5.91,-3.84,13.41,0.774,0.4298,4.45,"K. Xu, J. Hu, K. Lu, M. Wu, H. Lu, J. Yi, D. Wu, J. Xia, Tetraphenylethylene vs triphenylethylene core-based perylene diimide acceptor for non-fullerene organic solar cells, Dyes Pigments. 184 (2021) 108813. https://doi.org/10.1016/j.dyepig.2020.108813."
3560,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(C=C(/C=C5/C(=O)C6=C(C=CC=C6)S5(=O)=O)S2)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC3=C2SC(/C=C2C(=O)C4=C(C=CC=C4)C2=C(C#N)C#N)=C3)C=C1,ITBTD-IC,-5.47,-3.78,10.53,0.97,0.42,4.34,"S. Baik, D.W. Kim, H.-S. Kang, S.H. Hong, S. Park, B.-K. An, S.Y. Park, ITIC derivative acceptors for ternary organic solar cells: fine-tuning of absorption bands, LUMO energy levels, and cascade charge transfer, Sustain. Energy Fuels. 6 (2021) 110¨C120. https://doi.org/10.1039/D1SE01429C."
3561,CCCCCCCCC(CCCCCC)CN1C(=O)C2=CC=C3C4=C(C=CC(=C24)C1=O)C1=C2C4=C(C=C1)C(=O)N(CC(CCCCCC)CCCCCCCC)C(=O)C4=CC(C1=CC(F)=C(/C=C/C4=C(C#N)C=C(C5=C6C7=CC=C8C(=O)N(CC(CCCCCC)CCCCCCCC)C(=O)C9=C8C7=C(C=C9)C7=C6C6=C(C=C7)C(=O)N(CC(CCCCCC)CCCCCCCC)C(=O)C6=C5)S4)S1)=C32,PDI-CNTVT-PDI,-6.01,-3.89,10.16,0.71,0.6,4.32,"H.S. Kim, H.J. Park, S.K. Lee, W.S. Shin, C.E. Song, D.-H. Hwang, Effects of the core unit on perylene-diimide-based molecular acceptors in fullerene-free organic solar cells, Org. Electron. 71 (2019) 238¨C245. https://doi.org/10.1016/j.orgel.2019.05.029."
3562,CCCCCCCCN1C2=C(SC(/C=C3C(=O)C4=CC=CC=C4C3=C(C#N)C#N)=C2)C2=C1C1=C(S2)C2=CC3=C(C=C2C1(C1=CC=C(CCCCCC)C=C1)C1=CC=C(CCCCCC)C=C1)C1=C(C2=C(S1)C1=C(C=C(/C=C4C(=O)C5=CC=CC=C5C4=C(C#N)C#N)S1)N2CCCCCCCC)C3(C1=CC=C(CCCCCC)C=C1)C1=CC=C(CCCCCC)C=C1,INPIC,-5.36,-3.82,8.55,0.96,0.525,4.31,"J. Sun, X. Ma, Z. Zhang, J. Yu, J. Zhou, X. Yin, L. Yang, R. Geng, R. Zhu, F. Zhang, W. Tang, Dithieno[3,2-b:2¡ä,3¡ä-d]pyrrol Fused Nonfullerene Acceptors Enabling Over 13% Efficiency for Organic Solar Cells, Adv. Mater. 30 (2018) 1707150. https://doi.org/10.1002/adma.201707150."
3563,CCCCCCCCC1=C(C2=C(F)C(F)=C(C3=C(CCCCCCCC)C(F)=C(C4=C(CCCCCCCC)C(F)=C(C=C(C#N)C#N)S4)S3)S2)SC(C2=C(CCCCCCCC)C(F)=C(C=C(C#N)C#N)S2)=C1F,D5T6F-M,,,8.7,1.05,0.469,4.3,"T. Duan, M. Babics, A. Seitkhan, Y. Firdaus, R.-Z. Liang, F. Cruciani, S. Liu, S. Lopatin, P.M. Beaujuge, F-Substituted oligothiophenes serve as nonfullerene acceptors in polymer solar cells with open-circuit voltages >1 V, J. Mater. Chem. A. 6 (2018) 9368¨C9372. https://doi.org/10.1039/C8TA02781A."
3564,CC1=CC(C)=C(B(C2=CC=C(N(C3=CC=C(C4=CC=C(C5=CC=C(C6=CC=C(N(C7=CC=C(B(C8=C(C)C=C(C)C=C8C)C8=C(C)C=C(C)C=C8C)C=C7)C7=CC=C(/C(C8=CC=CN8B(F)F)=C8C=CC=N8)C=C7)C=C6)S5)S4)C=C3)C3=CC=C(/C(C4=CC=CN4B(F)F)=C4C=CC=N4)C=C3)C=C2)C2=C(C)C=C(C)C=C2C)C=C1,BDY,-5.52,-3.84,10.52,0.67,0.61,4.28,"S.K. Sarkar, L.J. Kang, U.K. Pandey, C.K. Luscombe, P. Thilagar, Triarylborane-BODIPY conjugate: An efficient non-fullerene electron acceptor for bulk heterojunction organic solar cell, Sol. Energy. 230 (2021) 242¨C249. https://doi.org/10.1016/j.solener.2021.10.048."
3565,CC1=CC(C)=C(B(C2=CC=C(N(C3=CC=C(C4=CC=C(C5=CC=C(C6=CC=C(N(C7=CC=C(B(C8=C(C)C=C(C)C=C8C)C8=C(C)C=C(C)C=C8C)C=C7)C7=CC=C(/C(C8=CC=CN8B(F)F)=C8C=CC=N8)C=C7)C=C6)S5)S4)C=C3)C3=CC=C(/C(C4=CC=CN4B(F)F)=C4C=CC=N4)C=C3)C=C2)C2=C(C)C=CC=C2C)C=C1,BDY,-5.52,-3.84,10.52,0.67,0.61,4.28,"S.K. Sarkar, L.J. Kang, U.K. Pandey, C.K. Luscombe, P. Thilagar, Triarylborane-BODIPY conjugate: An efficient non-fullerene electron acceptor for bulk heterojunction organic solar cell, Sol. Energy. 230 (2021) 242¨C249. https://doi.org/10.1016/j.solener.2021.10.048."
3566,CCCCCCCCC(CCCCCC)CN1C(=O)C2=C(C3=CC=C(C4=CC=C(C5=C6C(=O)N(CCCCCCCC)C(=O)C6=C(C6=CC=C(C7=CC8=C(S7)C(C7=CC=C(C(CC)CCCC)S7)=C7C=C(C9=CC=C(C%10=C%11C(=O)N(CCCCCCCC)C(=O)C%11=C(C%11=CC=C(C%12=CC=C(C%13=C%14C(=O)N(CC(CCCCCC)CCCCCCCC)C(C%15=CC=C(C%16=CC=CC=C%16)S%15)=C%14C(=O)N%13CC(CCCCCC)CCCCCCCC)S%12)S%11)S%10)S9)SC7=C8C7=CC=C(C(CC)CCCC)S7)S6)S5)S4)S3)N(CC(CCCCCC)CCCCCCCC)C(=O)C2=C1C1=CC=C(C2=CC=CC=C2)S1,BDTT(TPD-DPP)2,-5.68,-3.64,10.83,0.77,0.509,4.25,"Q. Tao, L. Duan, W. Xiong, G. Huang, P. Wang, H. Tan, Y. Wang, R. Yang, W. Zhu, D(A-A¡ä)2 architecture: An efficient strategy to improve photovoltaic performance of small molecules for solution-processed organic solar cells, Dyes Pigments. 133 (2016) 153¨C160. https://doi.org/10.1016/j.dyepig.2016.05.033."
3567,CCCCCCOC1=C2SC3=C(C2=C(OCCCCCC)C2=C1C1=C(S2)C2=C(C=C(/C=C4C(=O)C5=C(C=C(F)C=C5)C4=C(C#N)C#N)S2)N1CC(CC)CCCC)N(CC(CC)CCCC)C1=C3SC(/C=C2C(=O)C3=C(C=CC(F)=C3)C2=C(C#N)C#N)=C1,SNC2C4¨CF,-5.41,-4,10.63,0.85,0.47,4.25,"Y. Xin, J. Liang, Y. Zhong, T. Liang, C. Zhang, X. He, Achieving additive-free organic solar cells by modulating the side-chain length of non-fullerene small molecule acceptors, Dyes Pigments. 195 (2021) 109661. https://doi.org/10.1016/j.dyepig.2021.109661."
3568,C#C/C=C/C(CCCCCC)CN1C(=O)C2=C(C3=CC=C(C4=CC5=C(S4)C4=C(C=C(C6=CC=C(C7=C8C(=O)N(CC(CCCC)CCCCCC)C(C9=CC=C(C=C(C#N)C#N)S9)=C8C(=O)N7CC(CCCC)CCCCCC)S6)S4)C54C5=C(SC(C6=CC=C(C7=C8C(=O)N(CC(CCCC)CCCCCC)C(C9=CC=C(C=C(C#N)C#N)S9)=C8C(=O)N7CC(CCCC)CCCCCC)S6)=C5)C5=C4C=C(C4=CC=C(C6=C7C(=O)N(CC(CCCC)CCCCCC)C(C8=CC=C(C=C(C#N)C#N)S8)=C7C(=O)N6CC(CCCC)CCCCCC)S4)S5)S3)N(CC(CCCC)CCCCCC)C(=O)C2=C1C1=CC=C(C=C(C#N)C#N)S1,SCPDT-4DPPDCV,-5.31,-3.89,11.69,0.697,0.516,4.2,"P. Sun, H. Sun, X. Li, Y. Wang, H. Shan, J. Xu, C. Zhang, Z. Xu, Z.-K. Chen, W. Huang, Three dimensional multi-arm acceptors based on diketopyrrolopyrrole with (hetero)aromatic cores for non-fullerene organic solar cells without additional treatment, Dyes Pigments. 139 (2017) 412¨C419. https://doi.org/10.1016/j.dyepig.2016.11.049."
3569,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C=C(C2=CC=C(/C=C5/S/C(=C(/C#N)C(=O)OC)N(CC)C5=O)C5=NSN=C25)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC(C3=CC=C(/C=C4/S/C(=C(/C#N)C(=O)OCC)N(CC)C4=O)C4=NSN=C34)=C2)C=C1,IDT-CA,-5.59,-3.64,7.77,0.84,0.64,4.19,"R. Liu, Z. Du, S. Wen, Y. Wu, D. Zhu, R. Yang, Energy levels modulation of small molecule acceptors for polymer solar cells, Synth. Met. 235 (2018) 131¨C135. https://doi.org/10.1016/j.synthmet.2017.12.005."
3570,CCN(C/1=O)C(SC1=CC2=CC=C(C3=CC4=C(C=C3)C(C=CC(C5=CC=C(/C=C6SC(N(CC)C/6=O)=S)C7=NSN=C57)=C8)=C8C4(CCCCCCCC)CCCCCCCC)C9=NSN=C29)=S,FBR,-5.7,-3.57,7.95,0.82,0.63,4.11,"S. Holliday, R.S. Ashraf, C.B. Nielsen, M. Kirkus, J.A. R?hr, C.-H. Tan, E. Collado-Fregoso, A.-C. Knall, J.R. Durrant, J. Nelson, I. McCulloch, A Rhodanine Flanked Nonfullerene Acceptor for Solution-Processed Organic Photovoltaics, J. Am. Chem. Soc. 137 (2015) 898¨C904. https://doi.org/10.1021/ja5110602."
3571,CCCCCCCCC(CCCCCCCC)N1C2=C(C=CC(C3=CC=C(C=C(C#N)C#N)C4=NSN=C34)=C2)C2=C1C=C(C1=CC=C(C=C(C#N)C#N)C3=NSN=C13)C=C2,CBM,-6.1,-3.64,9.4,0.89,0.48,4.1,"K. Wang, Y. Firdaus, M. Babics, F. Cruciani, Q. Saleem, A. El Labban, M.A. Alamoudi, T. Marszalek, W. Pisula, F. Laquai, P.M. Beaujuge, ¦Ð-Bridge-Independent 2-(Benzo[c][1,2,5]thiadiazol-4-ylmethylene)malononitrile-Substituted Nonfullerene Acceptors for Efficient Bulk Heterojunction Solar Cells, Chem. Mater. 28 (2016) 2200¨C2208. https://doi.org/10.1021/acs.chemmater.6b00131."
3572,CCCCCCCCC(CCCCCC)COC1=CC(C2=CC=C(/C=C3C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)S2)=C(OCC(CCCCCC)CCCCCCCC)C=C1C1=CC=C(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)S1,PTICH,-5.59,-3.8,8.22,0.92,0.54,4.08,"Z.-P. Yu, Z.-X. Liu, F.-X. Chen, R. Qin, T.-K. Lau, J.-L. Yin, X. Kong, X. Lu, M. Shi, C.-Z. Li, H. Chen, Simple non-fused electron acceptors for efficient and stable organic solar cells, Nat. Commun. 10 (2019) 2152. https://doi.org/10.1038/s41467-019-10098-z."
3573,CCCCOC1=C(C2=CC=C(B(C3=CC=C(C4=C(OCCCC)C=C(/C=C5C(=O)C6=C(C=CC=C6)C5=C(C#N)C#N)S4)S3)C3=C(C(C)(C)C)C=C(C(C)(C)C)C=C3C(C)(C)C)S2)SC(/C=C2C(=O)C3=C(C=CC=C3)C2=C(C#N)C#N)=C1,B-bo,-5.63,-3.97,10.27,0.84,0.472,4.07,"Y. Yu, B. Meng, F. J?kle, J. Liu, L. Wang, Molecular Acceptors Based on a Triarylborane Core Unit for Organic Solar Cells, Chem. ¨C Eur. J. 26 (2020) 873¨C880. https://doi.org/10.1002/chem.201904178."
3574,CCCCC(CC)COC1=C(/C=C2C(=O)C3=CC(F)=C(F)C=C3C2=C(C#N)C#N)SC(C2=C(OCC(CC)CCCC)C(OCC(CC)CCCC)=C(C3=C(OCC(CC)CCCC)C=C(/C=C4C(=O)C5=CC(F)=C(F)C=C5C4=C(C#N)C#N)S3)S2)=C1,AOT2,-5.39,-3.9,10.5,0.7,0.54,4.06,"Z. Yao, Y. Li, S. Li, J. Xiang, X. Xia, X. Lu, M. Shi, H. Chen, Conformation Locking of Simple Nonfused Electron Acceptors Via Multiple Intramolecular Noncovalent Bonds to Improve the Performances of Organic Solar Cells, ACS Appl. Energy Mater. 4 (2021) 819¨C827. https://doi.org/10.1021/acsaem.0c02719."
3575,CCCCC(CC)CN1C(=O)C2=CC(OCCOC)=C3C4=C5C6=C(C=C4)C(=O)N(CC(CC)CCCC)C(=O)C6=CC(C4=CC=C(C6=CC7=C8C(=CC=C9C%10=C%11C(=CC=C%12C(=O)N(CC(CC)CCCC)C(=O)C(=C%12%11)C=C%10OCCOC)C6C98)C(=O)N(CC(CC)CCCC)C7=O)S4)=C5C4=C3C2=C(C=C4)C1=O,Bis-PDI-T-EG,-5.65,-3.84,8.86,0.85,0.541,4.03,"X. Zhang, Z. Lu, L. Ye, C. Zhan, J. Hou, S. Zhang, B. Jiang, Y. Zhao, J. Huang, S. Zhang, Y. Liu, Q. Shi, Y. Liu, J. Yao, A Potential Perylene Diimide Dimer-Based Acceptor Material for Highly Efficient Solution-Processed Non-Fullerene Organic Solar Cells with 4.03% Efficiency, Adv. Mater. 25 (2013) 5791¨C5797. https://doi.org/10.1002/adma.201300897."
3576,C#C/C=C/C(CCCCCC)CN1C(=O)C2=C(C3=CC=C(C4=CC=C(C(C5=CC=C(C6=CC=C(C7=C8C(=O)N(CC(CCCC)CCCCCC)C(C9=CC=C(C=C(C#N)C#N)S9)=C8C(=O)N7CC(CCCC)CCCCCC)S6)C=C5)=C(C5=CC=C(C6=CC=C(C7=C8C(=O)N(CC(CCCC)CCCCCC)C(C9=CC=C(C=C(C#N)C#N)S9)=C8C(=O)N7CC(CCCC)CCCCCC)S6)C=C5)C5=CC=C(C6=CC=C(C7=C8C(=O)N(CC(CCCC)CCCCCC)C(C9=CC=C(C=C(C#N)C#N)S9)=C8C(=O)N7CC(CCCC)CCCCCC)S6)C=C5)C=C4)S3)N(CC(CCCC)CCCCCC)C(=O)C2=C1C1=CC=C(C=C(C#N)C#N)S1,TPE-4DPPDCV,-5.4,-3.81,9.89,0.753,0.538,4.01,"P. Sun, H. Sun, X. Li, Y. Wang, H. Shan, J. Xu, C. Zhang, Z. Xu, Z.-K. Chen, W. Huang, Three dimensional multi-arm acceptors based on diketopyrrolopyrrole with (hetero)aromatic cores for non-fullerene organic solar cells without additional treatment, Dyes Pigments. 139 (2017) 412¨C419. https://doi.org/10.1016/j.dyepig.2016.11.049."
3577,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(S3)C3=C(C=C(/C=C5C(=O)C6=C(C=CC=C6)C5=C(C#N)C#N)S3)N2CC(CCCC)CCCCCC)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC3=C2N(CC(CCCC)CCCCCC)C2=C3SC(/C=C3C(=O)C4=C(C=CC=C4)C3=C(C#N)C#N)=C2)C=C1,IPIC,-5.12,-3.12,7.16,0.95,0.586,3.98,"R. Geng, X. Song, H. Feng, J. Yu, M. Zhang, N. Gasparini, Z. Zhang, F. Liu, D. Baran, W. Tang, Nonfullerene Acceptor for Organic Solar Cells with Chlorination on Dithieno[3,2-b:2¡ä,3¡ä-d]pyrrol Fused-Ring, ACS Energy Lett. 4 (2019) 763¨C770. https://doi.org/10.1021/acsenergylett.9b00147."
3578,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C=C(C2=CC=C(C=C(C#N)C#N)C5=NSN=C25)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC(C3=CC=C(C=C(C#N)C#N)C4=NSN=C34)=C2)C=C1,IDT-2BM,-5.56,-3.65,9.29,0.826,0.52,3.97,"Y.U. Kim, G.E. Park, S. Choi, D.H. Lee, M.J. Cho, D.H. Choi, A new n-type semiconducting molecule with an asymmetric indenothiophene core for a high-performing non-fullerene type organic solar cell, J. Mater. Chem. C. 5 (2017) 7182¨C7190. https://doi.org/10.1039/C7TC00706J."
3579,CCCCCCC(CCCC)CN1C(=O)C2=C(C3=CC=C(C4=CC=C5C(=C4)C4(C6=CC(C7=CC=C(C8=C9C(=O)N(CC(CCCC)CCCCCC)C(C%10=CC=C(C=C(C#N)C#N)S%10)=C9C(=O)N8CC(CCCC)CCCCCC)S7)=CC=C6C6=C4C=C(C4=CC=C(C7=C8C(=O)N(CC(CCCC)CCCCCC)C(C9=CC=C(C=C(C#N)C#N)S9)=C8C(=O)N7CC(CCCC)CCCCCC)S4)C=C6)C4=C5C=CC(C5=CC=C(C6=C7C(=O)N(CC(CCCC)CCCCCC)C(C8=CC=C(C=C(C#N)C#N)S8)=C7C(=O)N6CC(CCCC)CCCCCC)S5)=C4)S3)N(CC(CCCC)CCCCCC)C(=O)C2=C1C1=CC=C(C=C(C#N)C#N)S1,SBF-4DPPDCV,-5.48,-3.86,10.71,0.74,0.4869,3.85,"P. Sun, X. Li, Y. Wang, H. Shan, J. Xu, C. Liu, C. Zhang, F. Chen, Z. Xu, Z. Chen, W. Huang, Diketopyrrolopyrrole-based acceptors with multi-arms for organic solar cells, RSC Adv. 8 (2018) 25031¨C25039. https://doi.org/10.1039/C8RA03792B."
3580,CCCCCCC1COC2=C(C3=CC4=C(S3)C3=C(C=C(/C=C5C(=O)C6=C(C=C(F)C(F)=C6)C5=C(C#N)C#N)S3)C4(CC(CC)CCCC)CC(CC)CCCC)SC(C3=CC4=C(S3)C3=C(C=C(/C=C5C(=O)C6=C(C=C(F)C(F)=C6)C5=C(C#N)C#N)S3)C4(CC(CC)CCCC)CC(CC)CCCC)=C2O1,C6EDOT-4F,-5.27,-4.08,11.3,0.671,0.502,3.81,"D. Luo, Y. Zhang, L. Li, C. Shan, Q. Liu, Z. Wang, W.C.H. Choy, A.K.K. Kyaw, Near-infrared non-fused ring acceptors with light absorption up to 1000?nm for efficient and low-energy loss organic solar cells, Mater. Today Energy. 24 (2022) 100938. https://doi.org/10.1016/j.mtener.2021.100938."
3581,CCCCC1=C(C2=CC=C(B(C3=CC=C(C4=C(CCCC)C=C(/C=C5C(=O)C6=C(C=CC=C6)C5=C(C#N)C#N)S4)S3)C3=C(C(C)(C)C)C=C(C(C)(C)C)C=C3C(C)(C)C)S2)SC(/C=C2C(=O)C3=C(C=CC=C3)C2=C(C#N)C#N)=C1,B-b,-5.87,-3.91,10.3,0.87,0.418,3.75,"Y. Yu, B. Meng, F. J?kle, J. Liu, L. Wang, Molecular Acceptors Based on a Triarylborane Core Unit for Organic Solar Cells, Chem. ¨C Eur. J. 26 (2020) 873¨C880. https://doi.org/10.1002/chem.201904178."
3582,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(C=C(/C=C5/C(=O)C6=C(C=CC(F)=C6)S5(=O)=O)S2)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC3=C2SC(/C=C2C(=O)C4=C(C=CC(F)=C4)S2(=O)=O)=C3)C=C1,ITBTDF,-5.5,-3.69,8.67,1.06,0.41,3.73,"S. Baik, D.W. Kim, H.-S. Kang, S.H. Hong, S. Park, B.-K. An, S.Y. Park, ITIC derivative acceptors for ternary organic solar cells: fine-tuning of absorption bands, LUMO energy levels, and cascade charge transfer, Sustain. Energy Fuels. 6 (2021) 110¨C120. https://doi.org/10.1039/D1SE01429C."
3583,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C=C(C2=CC=C(/C=C5/SC(=S)N(CC)C5=O)C5=C2N=C(C2=CC=CC=C2)C(C2=CC=CC=C2)=N5)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC(C3=CC=C(/C=C4/SC(=S)N(CC)C4=O)C4=C3N=C(C3=CC=CC=C3)C(C3=CC=CC=C3)=N4)=C2)C=C1,Qx1,-5.42,-3.6,6.02,1,0.67,3.7,"B. Xiao, A. Tang, J. Yang, A. Mahmood, X. Sun, E. Zhou, Quinoxaline-Containing Nonfullerene Small-Molecule Acceptors with a Linear A2-A1-D-A1-A2 Skeleton for Poly(3-hexylthiophene)-Based Organic Solar Cells, ACS Appl. Mater. Interfaces. 10 (2018) 10254¨C10261. https://doi.org/10.1021/acsami.8b00216."
3584,CCCCC(CC)CC1(CC(CC)CCCC)C2=C(SC(/C=C3C(=O)C4=C(C=C(C)C(C)=C4)C3=C(C#N)C#N)=C2)C2=C1C=C(C1=CC3=C(S1)C1=C(C=C(/C=C4CC5=C(C=C(C)C(C)=C5)C4=C(/C)C#N)S1)C3(CC(CC)CCCC)CC(CC)CCCC)S2,CPDT-Me-2Eh,-5.18,-3.73,9.29,0.85,0.464,3.68,"K. Wang, H. Wei, Z. Li, S. Lu, Near-infrared small molecule acceptors based on 4H-cyclopenta[1,2-b:5,4-b¡¯]dithiophene units for organic solar cells, Dyes Pigments. 196 (2021) 109801. https://doi.org/10.1016/j.dyepig.2021.109801."
3585,CCCCCCCCN1N=C2C(=N1)C(C1=CC3=C(S1)C1=CC4=C(C=C1C3(C1=CC=C(CCCCCC)C=C1)C1=CC=C(CCCCCC)C=C1)C1=C(C=C(C3=C(OC)C(OC)=C(/C=C5SC(=S)N(CC)C5=O)C5=NN(CCCCCCCC)N=C53)S1)C4(C1=CC=C(CCCCCC)C=C1)C1=CC=C(CCCCCC)C=C1)=C(OC)C(OC)=C2/C=C1SC(=O)N(CC)C1=O,BTA101,-5.41,-3.55,5.33,1.19,0.56,3.55,"Q. Zhang, B. Xiao, M. Du, G. Li, A. Tang, E. Zhou, A2¨CA1¨CD¨CA1¨CA2 type non-fullerene acceptors based on methoxy substituted benzotriazole with three different end-capped groups for P3HT-based organic solar cells, J. Mater. Chem. C. 6 (2018) 10902¨C10909. https://doi.org/10.1039/C8TC03963A."
3586,CCCCCCC1(C)C2=CC3=C(C=C2C2=C1C=C(C1=NC=C(/C=C4/SC(=S)N(CC)C4=O)S1)S2)C(CCCCCC)(CCCCCC)C1=C3SC(C2=NC=C(/C=C3/SC(=S)N(CC)C3=O)S2)=C1,H-IDTzR,-5.31,-3.44,6.67,1.04,0.525,3.53,"P. Ye, Y. Chen, J. Wu, X. Wu, Y. Xu, Z. Li, S. Hong, M. Sun, A. Peng, H. Huang, Combination of noncovalent conformational locks and side chain engineering to tune the crystallinity of nonfullerene acceptors for high-performance P3HT based organic solar cells, Mater. Chem. Front. 3 (2018) 64¨C69. https://doi.org/10.1039/C8QM00461G."
3587,CCCCCCC1(CCCCCC)C2=C(SC(/C=C3C(=O)C4=C(C=CC=C4)C3=C(C#N)C#N)=C2)C2=C1C=C(C1=CC3=C(S1)C1=C(C=C(/C=C4C(=O)C5=C(C=CC=C5)C4=C(C#N)C#N)S1)C3(CCCCCC)CCCCCC)S2,2CIC,-5.35,-3.83,10.97,0.75,0.43,3.53,"J. Cao, S. Liu, W. Hu, Y. Xu, W. Zhou, Y. Zeng, J. Yu, Z. Tang, Small-molecule acceptors based on 4H-cyclopenta[1,2-b:5,4-b¡ä]dithiophene units with near-infrared absorption for nonfullerene polymer solar cells, Synth. Met. 240 (2018) 15¨C20. https://doi.org/10.1016/j.synthmet.2018.03.011."
3588,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C=C(/C=C2C(=O)C5=CC(F)=C(F)C=C5C2=C(C#N)C#N)S3)N(N2C3=C(C=C5C(=C3)C3=C(C=C(/C=C6/C(=O)C7=CC(F)=C(F)C=C7C6=C(C#N)C#N)S3)C5(C3=CC=C(CCCCCC)C=C3)C3=CC=C(CCCCCC)C=C3)C3=C2C=C2C(=C3)C(C3=CC=C(CCCCCC)C=C3)(C3=CC=C(CCCCCC)C=C3)C3=C2SC(/C=C2/C(=O)C5=CC(F)=C(F)C=C5C2=C(C#N)C#N)=C3)C2=C4C=C3C(=C2)C2=C(C=C(/C=C4C(=O)C5=CC(F)=C(F)C=C5C4=C(C#N)C#N)S2)C3(C2=CC=C(CCCCCC)C=C2)C2=CC=C(CCCCCC)C=C2)C=C1,99CZ-8F,-5.79,-3.88,7.2,0.96,0.512,3.5,"C. Jiang, X. Huang, B. Sun, Y. Li, M. Gao, L. Ye, H. Ade, S.R. Forrest, J. Fan, A 3D nonfullerene electron acceptor with a 9,9¡ä-bicarbazole backbone for high-efficiency organic solar cells, Org. Electron. 84 (2020) 105784. https://doi.org/10.1016/j.orgel.2020.105784."
3589,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C=C(C2=CC=C(/C=C5SC(=S)N(CC)C5=O)C5=NCN=C25)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC(C3=CC=C(/C=C4SC(=S)N(CC)C4=O)C4=NSN=C34)=C2)C=C1,IDT-2BR,-5.52,-3.69,5.99,0.84,0.694,3.49,"Y. Wu, H. Bai, Z. Wang, P. Cheng, S. Zhu, Y. Wang, W. Ma, X. Zhan, A planar electron acceptor for efficient polymer solar cells, Energy Environ. Sci. 8 (2015) 3215¨C3221. https://doi.org/10.1039/C5EE02477C."
3590,CCCCCCCCC1=CC=C(C2(C3=CC=C(CCCCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C=C(C2=CC=C5C(=C2)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C5SC(/C=C5C(=O)C6=CC=CC=C6C5=C(C#N)C#N)=C2)S3)C(C2=CC=C(CCCCCCCC)C=C2)(C2=CC=C(CCCCCCCC)C=C2)C2=C4SC(C3=CC=C4C(=C3)C(C3=CC=C(CCCCCC)C=C3)(C3=CC=C(CCCCCC)C=C3)C3=C4SC(/C=C4C(=O)C5=CC=CC=C5C4=C(C#N)C#N)=C3)=C2)C=C1,BITIC-PhC6,-5.5,-3.8,7.14,1.08,0.4519,3.48,"Y.A. Avalos-Quiroz, O. Bardagot, Y. Kervella, C. Auma?tre, L. Cabau, A. Rivaton, O. Margeat, C. Videlot-Ackermann, U. Vongsaysy, J. Ackermann, R. Demadrille, Non-Fullerene Acceptors with an Extended ¦Ð-Conjugated Core: Third Components in Ternary Blends for High-Efficiency, Post-Treatment-Free Organic Solar Cells, ChemSusChem. 14 (2021) 3502¨C3510. https://doi.org/10.1002/cssc.202101005."
3591,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(C=C(/C=C(C#N)C5=NC6=C(C=CC(Cl)=C6)O5)S2)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC3=C2SC(/C=C(C#N)C2=NC4=C(C=CC=C4)O2)=C3)C=C1,IDTT-BOACl,-5.44,-3.62,8.07,1.16,0.369,3.45,"Y. Zhao, X. Tang, J. Cao, P. Huang, C. Weng, P. Shen, Balancing the Voc-Jsc trade-off in polymer solar cells based on 2-(benzoxazol-2-yl)-acetonitrile end-capped small-molecule acceptors through asymmetry and halogenation of end groups, Org. Electron. 102 (2022) 106446. https://doi.org/10.1016/j.orgel.2022.106446."
3592,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C=C(C2=CC=C(/C=C5/SC(=C(C#N)C#N)N(CC)C5=O)C5=NSN=C25)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC(C3=CC=C(/C=C4/SC(=C(C#N)C#N)N(CC)C4=O)C4=NSN=C34)=C2)C=C1,IDT-RCN,-5.62,-3.75,7.92,0.69,0.63,3.42,"R. Liu, Z. Du, S. Wen, Y. Wu, D. Zhu, R. Yang, Energy levels modulation of small molecule acceptors for polymer solar cells, Synth. Met. 235 (2018) 131¨C135. https://doi.org/10.1016/j.synthmet.2017.12.005."
3593,CCCCC(CC)CC1(CC(CC)CCCC)C2=C(SC(C3=CC=C(/C=C4SC(=C(C#N)C#N)N(CC)C4=O)C4=NSN=C34)=C2)C2=C1C=C(C1=CC=C(/C=C3SC(=C(C#N)C#N)N(CC)C3=O)C3=NSN=C13)S2,SSBRC,-5.47,-3.84,8.56,0.77,0.5026,3.32,"C. Tang, S.-C. Chen, Y. Tang, W. Ma, Q. Zheng, Cyclopentadithiophene-cored non-fullerene acceptors for efficient polymer solar cells with superior stability, Sol. Energy. 174 (2018) 991¨C998. https://doi.org/10.1016/j.solener.2018.09.077."
3594,CCCCOC1=C2C3=CC=C4C(=O)N(CC(CC)CCC)C(=O)C5=C4C3=C(C(C3=CC=C(N(C4=CC=C(C6=CC7=C8C(=CC=C9C%10=C(OCCC)C=C%11C(=O)N(CC(CC)CCC)C(=O)C%12=CC=C(C6=C98)C%10=C%12%11)C(=O)N(CC(CC)CCC)C7=O)C=C4)C4=CC=C(C6=CC7=C8C(=CC=C9C%10=C(OCCCC)C=C%11C(=O)N(CC(CC)CCCC)C(=O)C%12=CC=C(C6=C98)C%10=C%12%11)C(=O)N(CC(CC)CCCC)C7=O)C=C4)C=C3)=C5)C3=CC=C4C(=O)N(CC(CC)CCCC)C(=O)C(=C1)C4=C32,S(TPA-PDI),-5.4,-3.7,11.92,0.88,0.336,3.32,"Y. Lin, Y. Wang, J. Wang, J. Hou, Y. Li, D. Zhu, X. Zhan, A Star-Shaped Perylene Diimide Electron Acceptor for High-Performance Organic Solar Cells, Adv. Mater. 26 (2014) 5137¨C5142. https://doi.org/10.1002/adma.201400525."
3595,CCCCC(CC)COC1=C(/C=C2C(=O)C3=CC(F)=C(F)C=C3C2=C(C#N)C#N)SC(C2=C(OCC(CC)CCCC)C(OCC(CC)CCCC)=C(C3=CC(OCC(CC)CCCC)=C(/C=C4C(=O)C5=CC(F)=C(F)C=C5C4=C(C#N)C#N)S3)S2)=C1,AOT1,-5.52,-3.88,7.31,0.74,0.6,3.31,"Z. Yao, Y. Li, S. Li, J. Xiang, X. Xia, X. Lu, M. Shi, H. Chen, Conformation Locking of Simple Nonfused Electron Acceptors Via Multiple Intramolecular Noncovalent Bonds to Improve the Performances of Organic Solar Cells, ACS Appl. Energy Mater. 4 (2021) 819¨C827. https://doi.org/10.1021/acsaem.0c02719."
3596,CCCCCCCCC(CCCCCC)CN1C2=C(C=CC(C3=CC=C(/C=C4SC(=S)N(CC)C4=O)C4=NSN=C34)=C2)C2=C1C=C(C1=CC=C(/C=C3SC(=S)N(CC)C3=O)C3=NSN=C13)C=C2,CzC6C8,-5.79,-3.79,8.24,0.99,0.41,3.3,"D. Ma, S. Feng, J. Zhang, C. Kou, X. Gong, Q. Li, X. Xu, S. Yan, Z. Bo, Non-fullerene small molecular acceptors with a carbazole core for organic solar cells with high open-circuit voltage, Dyes Pigments. 146 (2017) 293¨C299. https://doi.org/10.1016/j.dyepig.2017.07.014."
3597,CCCCCCCCN1N=C2C(/C=C3/SC(=S)N(CC)C3=O)=CC=C(C3=CC4=C(C=C3)C3=C(C=C(C5=CC=C(/C=C6/SC(=S)N(CC)C6=O)C6=NN(CCCCCCCC)N=C56)C=C3)C43C4=C(C=CC=C4)C4=C3C=CC=C4)C2=N1,BTA21,-5.61,-3.04,5.45,1.02,0.43,3.28,"X. Wen, B. Xiao, A. Tang, J. Hu, C. Yang, E. Zhou, Wide Band Gap Non-Fullerene Small Molecular Acceptors Containing Spirobifluorene and Benzotriazole with Three Different End-Capped Groups for P3HT-Based Organic Solar Cells, Chin. J. Chem. 36 (2018) 392¨C398. https://doi.org/10.1002/cjoc.201700792."
3598,CCCCCCCCC1=C(C2=CC3=C(OCC(CC)CCCC)C4=C(C(OCC(CC)CCCC)=C3S2)C2=C(S4)C3=C(C4=C(C5=NSN=C53)C3=C(C5=C(OCC(CC)CCCC)C6=C(C=C(C7=C(CCCCCCCC)C=C(/C=C8/C(=O)C9=CC(F)=C(F)C=C9C8=C(C#N)C#N)S7)S6)C(OCC(CC)CCCC)=C5S3)N4CC(CC)CCCC)N2CC(CC)CCCC)SC(/C=C2C(=O)C3=CC(F)=C(F)C=C3C2=C(C#N)C#N)=C1,X9T4FIC,-5.51,-4.1,7.01,0.85,0.541,3.22,"J. Xiao, T. Yan, T. Lei, Y. Li, Y. Han, L. cao, W. Song, S. Tan, Z. Ge, Organic solar cells based on non-fullerene acceptors of nine fused-ring by modifying end groups, Org. Electron. 81 (2020) 105662. https://doi.org/10.1016/j.orgel.2020.105662."
3599,CCCCCCC1(CCCCCC)C2=C(SC(/C=C3C(=O)C4=CC=CC=C4C3=C(C#N)C#N)=C2)C2=C1C=CC1=C2C=CC2=C1C1=C(C=C(/C=C3C(=O)C4=CC=CC=C4C3=C(C#N)C#N)S1)C2(CCCCCC)CCCCCC,DTNIC6,-5.87,-3.92,6.49,0.98,0.51,3.22,"Y. Ma, M. Zhang, Y. Yan, J. Xin, T. Wang, W. Ma, C. Tang, Q. Zheng, Ladder-Type Dithienonaphthalene-Based Small-Molecule Acceptors for Efficient Nonfullerene Organic Solar Cells, Chem. Mater. 29 (2017) 7942¨C7952. https://doi.org/10.1021/acs.chemmater.7b02887."
3600,CCCCCC(CCCCC)N1C(=O)C2=CC=C3C4=C5C6=C(C=C4)C(=O)N(C(CCCCC)CCCCC)C(=O)C6=CC4=C5C5=C(C=C(C1=O)C2=C35)C1=C4OC2=C1C1=C3C4=C2CC2C(=O)N(C(CCCCC)CCCCC)C(=O)C5=CC=C(C6=CC=C7C(=O)N(C(CCCCC)CCCCC)C(=O)C(=C1)C7=C63)C4=C52,FPDI-F,-6.1,-3.43,8.71,0.92,0.4,3.2,"H. Zhong, C.-H. Wu, C.-Z. Li, J. Carpenter, C.-C. Chueh, J.-Y. Chen, H. Ade, A.K.-Y. Jen, Rigidifying Nonplanar Perylene Diimides by Ring Fusion Toward Geometry-Tunable Acceptors for High-Performance Fullerene-Free Solar Cells, Adv. Mater. 28 (2016) 951¨C958. https://doi.org/10.1002/adma.201504120."
3601,CCCCC(CC)CN1C(=O)C2=C(C3=CC=CS3)N(CC(CC)CCCC)C(=O)C2=C1C1=CC=C(C#CC2=CC3=C4N=C5C6=C(C=C(C#CC7=CC=C(C8=C9C(=O)N(CC(CC)CCCC)C(C%10=CC=CS%10)=C9C(=O)N8CC(CC)CCCC)S7)C=C6)/C6=N/C7=N/C(=NC(=C3C=C2)N4B(OC2=CC=C(C(C)(C)C)C=C2)N56)C2=C7C=CC(C#CC3=CC=C(C4=C5C(=O)N(CC(CC)CCCC)C(C6=CC=CS6)=C5C(=O)N4CC(CC)CCCC)S3)=C2)C1,C1-OPh 1,-5.74,-3.79,6.42,1.17,0.4216,3.17,"M.J. ¨¢lvaro-Martins, J.G. S¨¢nchez, G. Lavarda, D. Molina, J. Pallar¨¨s, T. Torres, L.F. Marsal, ¨¢. Sastre-Santos, Subphthalocyanine-Diketopyrrolopyrrole Conjugates: 3D Star-Shaped Systems as Non-Fullerene Acceptors in Polymer Solar Cells with High Open-Circuit Voltage, ChemPlusChem. 86 (2021) 1366¨C1373. https://doi.org/10.1002/cplu.202100103."
3602,CCCCCCC(C)N1C(=O)C2=CC3=C(C=C2C1=O)C1=CC=C(C2=C(CC(CC)CCCC)C=C(C4=C(F)C5=C(C6=NSN=C64)C(F)=C(C4=CC(CC(CC)CCCC)=C(C6=CC=C7C8=C(C=C9C(=O)N(C(C)CCCCCC)C(=O)C9=C8)C8=CC=CC6=C87)S4)C4=NSN=C45)S2)C2=C1C3=CC=C2,FNTz-Teh-FA,-6.17,-3.55,5.81,0.89,0.6,3.12,"S. Chatterjee, Y. Ie, T. Seo, T. Moriyama, G.-J.A.H. Wetzelaer, P.W.M. Blom, Y. Aso, Fluorinated naphtho[1,2-c:5,6-c¡¯]bis[1,2,5]thiadiazole-containing ¦Ð-conjugated compound: synthesis, properties, and acceptor applications in organic solar cells, NPG Asia Mater. 10 (2018) 1016¨C1028. https://doi.org/10.1038/s41427-018-0088-4."
3603,CC(C)(C)C1=CC(C(C)(C)C)=C(B(C2=CC=C(C3=CC=C(/C=C4C(=O)C5=C(C=CC=C5)C4=C(C#N)C#N)S3)S2)C2=CC=C(C3=CC=C(/C=C4C(=O)C5=C(C=CC=C5)C4=C(C#N)C#N)S3)S2)C(C(C)(C)C)=C1,B-H,-5.92,-3.97,8.97,0.8,0.435,3.12,"Y. Yu, B. Meng, F. J?kle, J. Liu, L. Wang, Molecular Acceptors Based on a Triarylborane Core Unit for Organic Solar Cells, Chem. ¨C Eur. J. 26 (2020) 873¨C880. https://doi.org/10.1002/chem.201904178."
3604,CCCCC(CC)CN1C(=O)C2=C3C(=C(C4=CC=C(/C=C5SC(=S)N(CC)C5=O)S4)C=C4C(=O)N(CC(CC)CCCC)C(=O)C(=C43)C(C3=CC=C(/C=C4SC(=S)N(CC)C4=O)S3)=C2)C1=O,NDI-TR,-5.81,-3.95,7.01,0.64,0.69,3.07,"M.J. Sung, M. Huang, S.H. Moon, T.H. Lee, S.Y. Park, J.Y. Kim, S.-K. Kwon, H. Choi, Y.-H. Kim, Naphthalene diimide-based small molecule acceptors for fullerene-free organic solar cells, Sol. Energy. 150 (2017) 90¨C95. https://doi.org/10.1016/j.solener.2017.03.090."
3605,CCCCC(CC)CC1(CC(CC)CCCC)C2=C(C=CC=C2)C2=C1C=C1C(=C2)C2=C3C(=CC=C2)C2=C4C(=CC=CC4=C13)C1=CC3=C(C=C12)C(CC(CC)CCCC)(CC(CC)CCCC)C1=C3C=CC=C1,DIR-2EH,-5.38,-3.3,4.29,1.22,0.582,3.05,"H.-Y. Chen, J. Golder, S.-C. Yeh, C.-W. Lin, C.-T. Chen, C.-T. Chen, Diindeno[1,2-g:1¡ä,2¡ä-s]rubicene: all-carbon non-fullerene electron acceptor for efficient bulk-heterojunction organic solar cells with high open-circuit voltage, RSC Adv. 5 (2014) 3381¨C3385. https://doi.org/10.1039/C4RA12505C."
3606,CCCCCCCCN1N=C2C(/C=C3SC(=O)N(CC)C3=O)=CC=C(C3=CC4=C(S3)C3=CC5=C(C=C3C4(C3=CC=C(CCCCCC)C=C3)C3=CC=C(CCCCCC)C=C3)C3=C(C=C(C4=CC=C(/C=C6SC(=O)N(CC)C6=S)C6=NN(CCCCCCCC)N=C46)S3)C5(C3=CC=C(CCCCCC)C=C3)C3=CC=C(CCCCCC)C=C3)C2=N1,BTA1,-5.46,-3.59,5.21,1.24,0.4671,3.02,"A. Tang, B. Xiao, Y. Wang, F. Gao, K. Tajima, H. Bin, Z.-G. Zhang, Y. Li, Z. Wei, E. Zhou, Simultaneously Achieved High Open-Circuit Voltage and Efficient Charge Generation by Fine-Tuning Charge-Transfer Driving Force in Nonfullerene Polymer Solar Cells, Adv. Funct. Mater. 28 (2018) 1704507. https://doi.org/10.1002/adfm.201704507."
3607,CCCCCCOC1=C(/C=C(C#N)C2=CC=C(C3=CC=C4C(=O)N(CC(CC)CCCC)C(=O)C5=C4C3=CC=C5)S2)C=CC2=C(OCCCCCC)C(/C=C(C#N)C3=CC=C(C4=CC=C5C(=O)N(CC(CC)CCCC)C(=O)C6=C5C4=CC=C6)S3)=CC=C21,NIDCSN ,-5.73,-3.08,5.44,1.08,0.55,3.01,"O.K. Kwon, J.-H. Park, S.Y. Park, An efficient nonfullerene acceptor for all-small-molecule solar cells with versatile processability in environmentally benign solvents, Org. Electron. 30 (2016) 105¨C111. https://doi.org/10.1016/j.orgel.2015.12.017."
3608,CCCCCCCCC(CCCCCC)CN1C2=C(SC(/C=C3C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)=C2)C2=C1C=C(C1=C3C(=O)C4=C(CC(CC)CCCC)SC(CC(CC)CCCC)=C4C(=O)C3=C(C3=CC4=C(S3)C3=C(C=C(/C=C5C(=O)C6=C(C=C(F)C(F)=C6)C5=C(C#N)C#N)S3)N4CC(CCCCCC)CCCCCCCC)S1)S2,BDIC2F,-5.55,-3.85,9.9,0.799,0.379,3.01,"Y. Li, H. Fu, Z. Wu, X. Wu, M. Wang, H. Qin, F. Lin, H.Y. Woo, A.K.-Y. Jen, Regulating the Aggregation of Unfused Non-Fullerene Acceptors via Molecular Engineering towards Efficient Polymer Solar Cells, ChemSusChem. 14 (2021) 3579¨C3589. https://doi.org/10.1002/cssc.202100746."
3609,CCCCCCOC(=O)/C(C#N)=C/C1=CC(CCCCCC)=C(C2=CC(CCCCCC)=C(C3=CC=C4C(=C3)N(CCCCCC)C3=C4N(CCCCCC)C4=C3C=CC(C3=C(CCCCCC)C=C(C5=C(CCCCCC)C=C(/C=C(C#N)C(=O)OCCCCCC)S5)S3)=C4)S2)S1,DINI-CA,-4.96,-2.92,7.3,0.75,0.54,2.95,"J. Sim, H. Lee, K. Song, S. Biswas, A. Sharma, G.D. Sharma, J. Ko, Solution processed bulk heterojunction solar cells based on A¨CD¨CA small molecules with a dihydroindoloindole (DINI) central donor and different acceptor end groups, J. Mater. Chem. C. 4 (2016) 3508¨C3516. https://doi.org/10.1039/C6TC00323K."
3610,CCCCCCCCC1(CCCCCCCC)C2=CC3=C(C=C2C2=C1C=C(C1=C(CC(CC)CCCC)C=C(/C=C4C(=O)C5=C(C=C6C=CC=CC6=C5)C4=C(C#N)C#N)S1)C=C2)C(CCCCCCCC)(CCCCCCCC)C1=C3C=CC(C2=C(CC(CC)CCCC)C=C(/C=C3C(=O)C4=C(C=C5C=CC=CC5=C4)C3=C(C#N)C#N)S2)=C1,IF-TN,-5.8,-3.93,7.02,1.006,0.4095,2.89,"R. Li, G. Liu, B. Fan, X. Du, X. Tang, N. Li, L. Ying, C.J. Brabec, F. Huang, Y. Cao, Non-fullerene acceptors end-capped with an extended conjugation group for efficient polymer solar cells, Org. Electron. 59 (2018) 366¨C373. https://doi.org/10.1016/j.orgel.2018.05.050."
3611,CCCCCCCCC1(CCCCCCCC)C2=C(C=CC(C3=C(CCCCCC)C=C(/C=C4C(=O)C5=C(C=CC=C5)C4=C(C#N)C#N)S3)=C2)C2=C1C=C(C1=C(CCCCCC)C=C(/C=C3C(=O)C4=C(C=CC=C4)C3=C(C#N)C#N)S1)C=C2,DCF2HT,-5.67,-3.72,9.29,0.97,0.3212,2.89,"Y. Liu, H. Zhang, Y. Sun, X. Wan, Y. Chen, A-D-A-type small molecular acceptor with one hexyl-substituted thiophene as ¦Ð bridge for fullerene-free organic solar cells, Sci. China Mater. 60 (2017) 49¨C56. https://doi.org/10.1007/s40843-016-5155-2."
3612,CCCCC(CC)COC1=C2C3=C(OCC(CC)CCCC)C=CC4=C3C3=C(C5=NN(CC(CC)CCCC)N=C5C5=C3C2=C(C=C1)C1=C5SC(C2=CC=C(C3=C5C(=O)N(CC(CC)CCCC)C(C6=CC=CS6)=C5C(=O)N3CC(CC)CCCC)S2)=C1)C1=C4C=C(C2=CC=C(C3=C4C(=O)N(CC(CC)CCCC)C(C5=CC=CS5)=C4C(=O)N3CC(CC)CCCC)S2)S1,BTrP-DPP,-5.24,-3.24,9.44,0.69,0.443,2.88,"Z. Chen, J. Li, M. Li, C. Chen, S. Xu, X. Tang, L. Chen, R. Chen, W. Huang, Synthesis and Application of Perylene-Embedded Benzoazoles for Small-Molecule Organic Solar Cells, Org. Lett. 20 (2018) 6376¨C6379. https://doi.org/10.1021/acs.orglett.8b02650."
3613,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(C=C(/C=C5C(=O)C6=C(C=CC=C6)C5=C(/C#N)C5=CC(F)=CC(F)=C5)S2)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC3=C2SC(/C=C2C(=O)C4=C(C=CC=C4)C2=C(/C#N)C2=CC(F)=CC(F)=C2)=C3)C=C1,ITIF,-5.6,-3.78,7.78,0.958,0.382,2.85,"R. Lv, D. Chen, X. Liao, L. Chen, Y. Chen, A Terminally Tetrafluorinated Nonfullerene Acceptor for Well-Performing Alloy Ternary Solar Cells, Adv. Funct. Mater. 29 (2019) 1805872. https://doi.org/10.1002/adfm.201805872."
3614,CCCCCCC(CCCC)CC1=C(C2=CC=C3C(=C2)N(CC(CCCC)CCCCCC)C(=O)/C3=C2/C(=O)N(CC(CCCC)CCCCCC)C3=C2C=CC(C2=C(CC(CCCC)CCCCCC)C=C(/C=C4C(=O)C5=C(C=CC=C5)C4=C(C#N)C#N)S2)=C3)SC(/C=C2C(=O)C3=C(C=CC=C3)C2=C(C#N)C#N)=C1,IID-IC,-5.99,-3.95,6.36,0.83,0.53,2.82,"J. Miao, B. Meng, J. Liu, L. Wang, An A¨CD¨CA¡ä¨CD¨CA type small molecule acceptor with a broad absorption spectrum for organic solar cells, Chem. Commun. 54 (2018) 303¨C306. https://doi.org/10.1039/C7CC08497H."
3615,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C=C(C2=CC5=C(S2)/C(=C(C)C#N)C2=CC=CC=C25)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC(C3=CC4=C(S3)C(=C(C#N)C#N)C3=CC=CC=C34)=C2)C=C1,Q1-0F,-5.4,-3.78,7.2,0.89,0.44,2.75,"Q.-Q. Zhang, Y. Li, D. Wang, Z. Chen, Y. Li, S. Li, H. Zhu, X. Lu, H. Chen, C.-Z. Li, Intrinsically Chemo- and Thermostable Electron Acceptors for Efficient Organic Solar Cells, Bull. Chem. Soc. Jpn. 94 (2021) 183¨C190. https://doi.org/10.1246/bcsj.20200231."
3616,CCCCCCCCC(CCCCCCCC)N1C2=C(C=CC(C3=CC=C(/C=C4C(=O)C5=CSC=C5C4=C(C#N)C#N)O3)=C2)C2=C1C=C(C1=CC=C(/C=C3C(=O)C4=CSC=C4C3=C(C#N)C#N)S1)C=C2,DTC-F-C,-5.66,-3.94,8.94,0.74,0.408,2.7,"J. Liao, P. Zheng, Z. Cai, S. Shen, G. Xu, H. Zhao, Y. Xu, Construction of simple and low-cost acceptors for efficient non-fullerene organic solar cells, Org. Electron. 89 (2021) 106026. https://doi.org/10.1016/j.orgel.2020.106026."
3617,CCCCCCC1=C(C2=CC3=C(C=C2)N(CC(CCCC)CCCCCC)C2=CC4=C(C=C2C3=C(C#N)C#N)N(CC(CCCC)CCCCCC)C2=CC=C(C3=C(CCCCCC)C=C(/C=C5/SC(=S)N(CC)C5=O)S3)C=C2C4=C(C#N)C#N)SC(/C=C2SC(=S)N(CC)C2=O)=C1,CN-QA-RH,-5.4,-3.7,6.46,0.92,0.45,2.66,"T. Yang, Y. Liu, J. Qiu, H. Zhang, F. Li, Y. Wang, Quinacridone-based small molecule acceptor as a third component in ternary organic solar cells, Chem. Eng. J. 432 (2022) 134405. https://doi.org/10.1016/j.cej.2021.134405."
3618,CCCCC(CC)COC1=CC(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)=C(OCC(CC)CCCC)C=C1C1=CC2=C(S1)C1=C(C=C(C3=CC(OCC(CC)CCCC)=C(/C=C4C(=O)C5=C(C=C(F)C(F)=C5)C4=C(C#N)C#N)C=C3OCC(CC)CCCC)S1)C2(CC(CC)CCCC)CC(CC)CCCC,DTP-BO-4F,-5.63,-3.86,6.49,0.84,0.488,2.65,"Y. Zhou, M. Li, N. Yu, S. Shen, J. Song, Z. Ma, Z. Bo, Simple Tricyclic-Based A-¦Ð-D-¦Ð-A-Type Nonfullerene Acceptors for High-Efficiency Organic Solar Cells, ACS Appl. Mater. Interfaces. 14 (2022) 6039¨C6047. https://doi.org/10.1021/acsami.1c22520."
3619,CCCCCCN1C(=O)C2=CC=CC3=C2C(=CC=C3C#CC2=CC=C3C(=O)N(CCCCCC)C(=O)C4=CC=CC2=C43)C1=O,NI-A-C6,-6.04,-3.48,4.71,1.06,0.56,2.63,"J. Zhang, H. Xiao, X. Zhang, Y. Wu, G. Li, C. Li, X. Chen, W. Ma, Z. Bo, 1,8-Naphthalimide-based nonfullerene acceptors for wide optical band gap polymer solar cells with an ultrathin active layer thickness of 35 nm, J. Mater. Chem. C. 4 (2016) 5656¨C5663. https://doi.org/10.1039/C6TC01438K."
3620,CCCCCCOC1=CC(OCCCCCC)=CC(C2=C(C3=C(C4=CC(OCCCCCC)=CC(OCCCCCC)=C4)C=C(C4=CC=C(/C=C5C(=O)C6=C(C=C(F)C(F)=C6)C5=C(C#N)C#N)S4)S3)SC(C3=CC=C(/C=C4C(=O)C5=CC(F)=C(F)C=C5C4=C(C#N)C#N)S3)=C2)=C1,m-4TB-2F,-5.68,-4,7.9,0.84,0.4,2.63,"Y.-N. Chen, M. Li, Y. Wang, J. Wang, M. Zhang, Y. Zhou, J. Yang, Y. Liu, F. Liu, Z. Tang, Q. Bao, Z. Bo, A Fully Non-fused Ring Acceptor with Planar Backbone and Near-IR Absorption for High Performance Polymer Solar Cells, Angew. Chem. Int. Ed. 59 (2020) 22714¨C22720. https://doi.org/10.1002/anie.202010856."
3621,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(C=C(/C=C5/C(=C(C#N)C#N)C6=C(C=CC=C6)S5=O)S2)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC3=C2SC(/C=C2/C(=C(C#N)C#N)C4=C(C=CC=C4)S2(=O)=O)=C3)C=C1,ITIC-ICS,-5.48,-4.02,9.26,0.75,0.37,2.54,"S. Baik, D.W. Kim, H.-S. Kang, S.H. Hong, S. Park, B.-K. An, S.Y. Park, ITIC derivative acceptors for ternary organic solar cells: fine-tuning of absorption bands, LUMO energy levels, and cascade charge transfer, Sustain. Energy Fuels. 6 (2021) 110¨C120. https://doi.org/10.1039/D1SE01429C."
3622,CCN(C/1=O)C(SC1=C/C2=CC=C(C3=CC(C4=C(C5(C6=CC=C(CCCCCCCC)C=C6)C7=CC=C(CCCCCCCC)C=C7)C=C(C8=C9SC(C%10=CC=C(/C=C%11SC(N(CC)C\%11=O)=S)C%12=NSN=C%10%12)=C8)C(C9(C%13=CC=C(OCCCCCCCC)C=C%13)C%14=CC=C(CCCCCCCC)C=C%14)=C4)=C5S3)C%15=NSN=C2%15)=S,A-IDTBTRH,-5.63,-3.59,5,0.92,0.55,2.53,"H. Huang, B. Xiao, C. Huang, J. Zhang, S. Liu, N. Fu, B. Zhao, T. Qin, E. Zhou, W. Huang, Enhanced open circuit voltage of small molecule acceptors containing angular-shaped indacenodithiophene units for P3HT-based organic solar cells, J. Mater. Chem. C. 6 (2018) 12347¨C12354. https://doi.org/10.1039/C8TC04608E."
3623,CCCCC(CC)COC1=C2C=C(/C=C3SC(=C(C#N)C#N)N(CC)C3=O)SC2=C(OCC(CC)CCCC)C2=C1SC1=C2N(CC(CC)CCCC)C2=C1C1=NSN=C1C1=C2N(CC(CC)CCCC)C2=C1SC1=C(OCC(CC)CCCC)C3=C(SC(/C=C4SC(=C(C#N)C#N)N(CC)C4=O)=C3)C(OCC(CC)CCCC)=C12,X9Rd,-5.51,-3.8,6.7,1.08,0.341,2.48,"J. Xiao, T. Yan, T. Lei, Y. Li, Y. Han, L. cao, W. Song, S. Tan, Z. Ge, Organic solar cells based on non-fullerene acceptors of nine fused-ring by modifying end groups, Org. Electron. 81 (2020) 105662. https://doi.org/10.1016/j.orgel.2020.105662."
3624,CCCCCCCCC1=CC=C(C2(C3=CC=C(CCCCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C=C(C2=CC=C5C(=C2)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C5SC(/C=C5C(=O)C6=CC(F)=C(F)C=C6C5=C(C#N)C#N)=C2)S3)C(C2=CC=C(CCCCCCCC)C=C2)(C2=CC=C(CCCCCCCC)C=C2)C2=C4SC(C3=CC=C4C(=C3)C(C3=CC=C(CCCCCC)C=C3)(C3=CC=C(CCCCCC)C=C3)C3=C4SC(/C=C4C(=O)C5=CC(F)=C(F)C=C5C4=C(C#N)C#N)=C3)=C2)C=C1,BITIC-PhC6F4,-5.4,-3.8,5.44,1.1,0.4117,2.46,"Y.A. Avalos-Quiroz, O. Bardagot, Y. Kervella, C. Auma?tre, L. Cabau, A. Rivaton, O. Margeat, C. Videlot-Ackermann, U. Vongsaysy, J. Ackermann, R. Demadrille, Non-Fullerene Acceptors with an Extended ¦Ð-Conjugated Core: Third Components in Ternary Blends for High-Efficiency, Post-Treatment-Free Organic Solar Cells, ChemSusChem. 14 (2021) 3502¨C3510. https://doi.org/10.1002/cssc.202101005."
3625,CCCCC(CC)COC1=C2C3=C(OCC(CC)CCCC)C=CC4=C3C3=C(C5=NSN=C5C5=C3C2=C(C=C1)C1=C5SC(C2=CC=C(C3=C5C(=O)N(CC(CC)CCCC)C(C6=CC=CS6)=C5C(=O)N3CC(CC)CCCC)S2)=C1)C1=C4C=C(C2=CC=C(C3=C4C(=O)N(CC(CC)CCCC)C(C5=CC=CS5)=C4C(=O)N3CC(CC)CCCC)S2)S1,BThP¨CDPP,-5.3,-3.37,7.37,0.63,0.527,2.45,"Z. Chen, J. Li, M. Li, C. Chen, S. Xu, X. Tang, L. Chen, R. Chen, W. Huang, Synthesis and Application of Perylene-Embedded Benzoazoles for Small-Molecule Organic Solar Cells, Org. Lett. 20 (2018) 6376¨C6379. https://doi.org/10.1021/acs.orglett.8b02650."
3626,CCCCCCCCC(CCCCCC)CN1C(=O)C2=CC=C3C4=C(C=CC(=C24)C1=O)C1=C2C4=C(C=C1)C(=O)N(CC(CCCCCC)CCCCCCCC)C(=O)C4=CC(C1=CC(F)=C(/C=C/C4=C(F)C=C(C5=C6C7=CC=C8C(=O)N(CC(CCCCCC)CCCCCCCC)C(=O)C9=C8C7=C(C=C9)C7=C6C6=C(C=C7)C(=O)N(CC(CCCCCC)CCCCCCCC)C(=O)C6=C5)S4)S1)=C32,PDI-FTVT-PDI,-5.65,-3.82,7.19,0.75,0.46,2.45,"H.S. Kim, H.J. Park, S.K. Lee, W.S. Shin, C.E. Song, D.-H. Hwang, Effects of the core unit on perylene-diimide-based molecular acceptors in fullerene-free organic solar cells, Org. Electron. 71 (2019) 238¨C245. https://doi.org/10.1016/j.orgel.2019.05.029."
3627,CCCCCCCCC(CCCCCC)CN1C(=O)C2=C(C3=CC=C(C4=CC=C(C5=C6C(=O)N(CCCCCCCC)C(=O)C6=C(C6=CC=C(C7=CC8=C(S7)C(OCC(CC)CCCC)=C7C=C(C9=CC=C(C%10=C%11C(=O)N(CCCCCCCC)C(=O)C%11=C(C%11=CC=C(C%12=CC=C(C%13=C%14C(=O)N(CC(CCCCCC)CCCCCCCC)C(C%15=CC=C(C%16=CC=CC=C%16)S%15)=C%14C(=O)N%13CC(CCCCCC)CCCCCCCC)S%12)S%11)S%10)S9)SC7=C8OCC(CC)CCCC)S6)S5)S4)S3)N(CC(CCCCCC)CCCCCCCC)C(=O)C2=C1C1=CC=C(C2=CC=CC=C2)S1,BDT(TPD-DPP)2,-5.67,-3.63,5.69,0.78,0.545,2.41,"Q. Tao, L. Duan, W. Xiong, G. Huang, P. Wang, H. Tan, Y. Wang, R. Yang, W. Zhu, D(A-A¡ä)2 architecture: An efficient strategy to improve photovoltaic performance of small molecules for solution-processed organic solar cells, Dyes Pigments. 133 (2016) 153¨C160. https://doi.org/10.1016/j.dyepig.2016.05.033."
3628,CCCCC(CC)CN1C(=O)C(C#N)=C(C)/C(=CC2=CC3=C(C=C(C4=CC=C(N(C5=CC=CC=C5)C5=CC=CC=C5)C=C4)S3)S2)C1=O,1,-5.4,-3.7,5.44,0.83,0.53,2.39,"A. Gupta, A. Ali, M. Gao, Th.B. Singh, A. Bilic, S.E. Watkins, U. Bach, R.A. Evans, Small molecules containing rigidified thiophenes and a cyanopyridone acceptor unit for solution-processable bulk-heterojunction solar cells, Dyes Pigments. 119 (2015) 122¨C132. https://doi.org/10.1016/j.dyepig.2015.03.028."
3629,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(C=C(/C=C5/C(=C(C#N)C#N)C6=C(C=CC=C6)S5(=O)=O)S2)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC3=C2SC(/C=C2/C(=C(C#N)C#N)C4=C(C=CC=C4)S2(=O)=O)=C3)C=C1,ITICS,-5.53,-4.03,9.42,0.71,0.36,2.39,"S. Baik, D.W. Kim, H.-S. Kang, S.H. Hong, S. Park, B.-K. An, S.Y. Park, ITIC derivative acceptors for ternary organic solar cells: fine-tuning of absorption bands, LUMO energy levels, and cascade charge transfer, Sustain. Energy Fuels. 6 (2021) 110¨C120. https://doi.org/10.1039/D1SE01429C."
3630,CCCCCCCCC(CCCCCCCC)CN1C2=CC3=C(C=C2C2=C1C=C1C(=C2)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C1SC1=C2SC(/C=C2C(=O)C4=C(C=C(F)C(F)=C4)C2=C(C#N)C#N)=C1)C(C1=CC=C(CCCCCC)C=C1)(C1=CC=C(CCCCCC)C=C1)C1=C3SC2=C1SC(/C=C1C(=O)C3=C(C=C(F)C(F)=C3)C1=C(C#N)C#N)=C2,4TC-4F-C6C8,-5.59,-4,6.75,0.84,0.42,2.38,"J. Ouyang, B. Zhang, G. Zeng, J. Zhang, X. Zhao, X. Yang, Improving Efficiency of Organic Solar Cells by Restricting the Rotation of Side Chain on Small Molecule Acceptor, Sol. RRL. 4 (2020) 2000359. https://doi.org/10.1002/solr.202000359."
3631,CCCCCCCCC(CCCCCC)CN1C(=O)C2=CC=C3C4=C(C=CC(=C24)C1=O)C1=C3C(C2=CC=CC=C2C)=C2C3=C4C(=CC=C3)C=CC=C4C2=C1C1=C(C)C=CC=C1,AFI3,-5.99,-3.52,5.21,0.96,0.47,2.37,"L. Ding, C.-Y. Yang, Y.-Q. Zheng, J.-Y. Wang, J. Pei, Z. Su, Acenaphtho[1, 2-k]fluoranthene-Fused Diimide Derivatives: An Investigation of the Relationship Between Molecular Structure and Device Performance, Asian J. Org. Chem. 6 (2017) 1231¨C1234. https://doi.org/10.1002/ajoc.201700203."
3632,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(C=C(/C=C5/C(=O)C6=C(C=CC=C6)S5(=O)=O)S2)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC3=C2SC(/C=C2C(=O)C4=C(C=CC(F)=C4)S2(=O)=O)=C3)C=C1,ITBTD,-5.48,-3.63,5.99,1.11,0.37,2.36,"S. Baik, D.W. Kim, H.-S. Kang, S.H. Hong, S. Park, B.-K. An, S.Y. Park, ITIC derivative acceptors for ternary organic solar cells: fine-tuning of absorption bands, LUMO energy levels, and cascade charge transfer, Sustain. Energy Fuels. 6 (2021) 110¨C120. https://doi.org/10.1039/D1SE01429C."
3633,CCCCCCCCN1C(=O)C2=CC=CC3=C2C(=CC=C3C#CC2=CC=C3C(=O)N(CCCCCC)C(=O)C4=CC=CC2=C43)C1=O,NI-A-C8,-6.02,-3.47,4.43,1.07,0.55,2.35,"J. Zhang, H. Xiao, X. Zhang, Y. Wu, G. Li, C. Li, X. Chen, W. Ma, Z. Bo, 1,8-Naphthalimide-based nonfullerene acceptors for wide optical band gap polymer solar cells with an ultrathin active layer thickness of 35 nm, J. Mater. Chem. C. 4 (2016) 5656¨C5663. https://doi.org/10.1039/C6TC01438K."
3634,CCCCCCCCC(CCCCCC)CN1C(=O)C2=CC=C3C4=C(C=CC(=C24)C1=O)C1=C2C4=C(C=C1)C(=O)N(CC(CCCCCC)CCCCCCCC)C(=O)C4=CC(C1=CC=C(/C=C/C4=CC=C(C5=C6C7=CC=C8C(=O)N(CC(CCCCCC)CCCCCCCC)C(=O)C9=C8C7=C(C=C9)C7=C6C6=C(C=C7)C(=O)N(CC(CCCCCC)CCCCCCCC)C(=O)C6=C5)S4)S1)=C32,PDI-TVT-PDI,-5.57,-3.71,6.91,0.81,0.42,2.33,"H.S. Kim, H.J. Park, S.K. Lee, W.S. Shin, C.E. Song, D.-H. Hwang, Effects of the core unit on perylene-diimide-based molecular acceptors in fullerene-free organic solar cells, Org. Electron. 71 (2019) 238¨C245. https://doi.org/10.1016/j.orgel.2019.05.029."
3635,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=C(C=C4C(=C3)C3SC(C5=C(CCCCCC)C=C(/C=C6C(=O)C7=C(C=CC=C7)C6=C(C#N)C#N)C(CCCCCC)=C5)CC3C4(C3=CC=C(CCCCCC)C=C3)C3=CC=C(CCCCCC)C=C3)C3SC(C4=C(CCCCCC)C=C(/C=C5C(=O)C6=C(C=CC=C6)C5=C(C#N)C#N)C(CCCCCC)=C4)=CC32)C=C1,,-5.55,-3.82,5.63,0.92,0.44,2.3,"Y. Liu, Z. Zhang, S. Feng, M. Li, L. Wu, R. Hou, X. Xu, X. Chen, Z. Bo, Exploiting Noncovalently Conformational Locking as a Design Strategy for High Performance Fused-Ring Electron Acceptor Used in Polymer Solar Cells, J. Am. Chem. Soc. 139 (2017) 3356¨C3359. https://doi.org/10.1021/jacs.7b00566."
3636,CCCCC(CC)CN1C(=O)C(C#N)=C(C)/C(=CC2=CC=C(C3=CC=C(C4=CC=C(N(C5=CC=CC=C5)C5=CC=CC=C5)C=C4)S3)S2)C1=O,R1,-5.4,-3.85,6.77,0.872,0.38,2.25,"A. Gupta, A. Ali, M. Gao, Th.B. Singh, A. Bilic, S.E. Watkins, U. Bach, R.A. Evans, Small molecules containing rigidified thiophenes and a cyanopyridone acceptor unit for solution-processable bulk-heterojunction solar cells, Dyes Pigments. 119 (2015) 122¨C132. https://doi.org/10.1016/j.dyepig.2015.03.028."
3637,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C=C(/C=C2/C(=O)C5=CC=CC=C5C2=C(C#N)C#N)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC(/C=C3/C(=O)C4=C(C=CC=C4)C3=C(C#N)C#N)=C2)C=C1,IDT-4,-5.86,-4,7.23,0.54,0.5653,2.21,"N. Terenti, G.-I. Giurgi, L. Szolga, I. Stroia, A. Terec, I. Grosu, A.P. Cri?an, Effect of the Terminal Acceptor Unit on the Performance of Non-Fullerene Indacenodithiophene Acceptors in Organic Solar Cells, Molecules. 27 (2022) 1229. https://doi.org/10.3390/molecules27041229."
3638,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C=C(/C=C2C(=O)C5=C(C=C(F)C(F)=C5)C2=C(C#N)C#N)S3)C2=C3C(=C5C(=C2N4CC(CC)CCCC)C2=C(C=C4C(=C2)C2=C(C=C(/C=C6C(=O)C7=C(C=C(F)C(F)=C7)C6=C(C#N)C#N)S2)C4(C2=CC=C(CCCCCC)C=C2)C2=CC=C(CCCCCC)C=C2)N5CC(CC)CCCC)C2=C(C=C4C(=C2)C2=C(C=C(/C=C5C(=O)C6=C(C=C(F)C(F)=C6)C5=C(C#N)C#N)S2)C4(C2=CC=C(CCCCCC)C=C2)C2=CC=C(CCCCCC)C=C2)N3CC(CC)CCCC)C=C1,TF1,-5.38,-3.92,4.76,0.951,0.4889,2.21,"X. Liao, Q. Xie, Y. Guo, Q. He, Z. Chen, N. Yu, P. Zhu, Y. Cui, Z. Ma, X. Xu, H. Zhu, Y. Chen, Inhibiting excessive molecular aggregation to achieve highly efficient and stabilized organic solar cells by introducing a star-shaped nitrogen heterocyclic-ring acceptor, Energy Environ. Sci. 15 (2022) 384¨C394. https://doi.org/10.1039/D1EE02858H."
3639,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C=C(C2=C5OCCCOC5=C(/C=C5C(=O)C6=C(C=C(F)C(F)=C6)C5=C(C#N)C#N)S2)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC(/C=C3OCCCOC3=C/C=C3C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)=C2)C=C1,IDT-PDOT,-5.39,-3.77,5.26,0.85,0.489,2.18,"P. Jiang, S. Ming, Q.-Q. Jia, Y. Liu, H. Lu, M. Li, X. Xu, H.-B. Li, Z. Bo, The influence of the ¦Ð-bridging unit of fused-ring acceptors on the performance of organic solar cells, J. Mater. Chem. A. 6 (2018) 21335¨C21340. https://doi.org/10.1039/C8TA08410F."
3640,CC1=C(/C=C2C(N(CCCCCC)/C(S2)=C(C#N)/C#N)=O)SC(C3=CC4=C(C5=CC(C6(C7=CC=C(CCCCCC)S7)C8=CC=C(CCCCCC)S8)=C(C9=C6C=C(C%10=CC(CC(CC)CCCC)=C(/C=C%11C(N(CCCCCC)/C(S\%11)=C(C#N)C#N)=O)S%10)S9)C=C5C4(C%12=CC=C(CCCCCC)S%12)C%13=CC=C(CCCCCC)S%13)S3)=C1,IT-M1:0.2:0.8,-5.4,-3.62,4.97,1.165,0.367,2.16,"W. Jiang, R. Yu, Z. Liu, R. Peng, D. Mi, L. Hong, Q. Wei, J. Hou, Y. Kuang, Z. Ge, Ternary Nonfullerene Polymer Solar Cells with 12.16% Efficiency by Introducing One Acceptor with Cascading Energy Level and Complementary Absorption, Adv. Mater. 30 (2018) 1703005. https://doi.org/10.1002/adma.201703005."
3641,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(C=C(/C=C(C#N)C5=NC6=C(C=CC=C6)O5)S2)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC3=C2SC(/C=C(C#N)C2=NC4=C(C=CC=C4)O2)=C3)C=C1,IDTT-BOA,-5.41,-3.41,4.95,1.19,0.366,2.16,"Y. Zhao, X. Tang, J. Cao, P. Huang, C. Weng, P. Shen, Balancing the Voc-Jsc trade-off in polymer solar cells based on 2-(benzoxazol-2-yl)-acetonitrile end-capped small-molecule acceptors through asymmetry and halogenation of end groups, Org. Electron. 102 (2022) 106446. https://doi.org/10.1016/j.orgel.2022.106446."
3642,CCCCC(CC)CN1C(=O)C(C#N)=C(C)/C(=CC2=CC3=C(I2)C2=C(C=C(C4=CC=C(N(C5=CC=CC=C5)C5=CC=CC=C5)C=C4)B2)N3CC(CC)CCCC)C1=O,2,-5.4,-3.9,7.33,0.81,0.36,2.14,"A. Gupta, A. Ali, M. Gao, Th.B. Singh, A. Bilic, S.E. Watkins, U. Bach, R.A. Evans, Small molecules containing rigidified thiophenes and a cyanopyridone acceptor unit for solution-processable bulk-heterojunction solar cells, Dyes Pigments. 119 (2015) 122¨C132. https://doi.org/10.1016/j.dyepig.2015.03.028."
3643,CCCCC(CC)CN1C(=O)C2=CC=CC3=C2C(=CC=C3C2=CC=C(C3=C4C(=O)N(CC(CC)CCCC)C(=O)C4=C(C4=CC=C(C5=CC=C6C(=O)N(CC(CC)CCCC)C(=O)C7=CC=CC5=C76)S4)C4=NSN=C43)S2)C1=O,BIBT-NI,-6.06,-3.78,6.14,0.77,0.442,2.1,"L. Lan, B. Zhao, J. Zhang, Y. Li, Y. Liu, Y. Mai, B. Liao, C. Gao, A naphthalimide end capped imide-fused benzothiadiazole based small molecule acceptor for organic solar cells, New J. Chem. 43 (2019) 3565¨C3571. https://doi.org/10.1039/C8NJ04896G."
3644,CCCCC(CC)CC1=CC=C(C(C2=CC=C(CC(CC)CCCC)S2)=C2C3=CC4=C(C=C3C3=C2N=C(C2=C5C6=CC=C7C(=O)N(CC(CC)CCCC)C(=O)C8=CC=C(C9=CC=C%10C(=O)N(CC(CC)CCCC)C(=O)C(=C2)C%10=C95)C6=C87)S3)C(=C(C2=CC=C(CC(CC)CCCC)S2)C2=CC=C(CC(CC)CCCC)S2)C2N=C(C3=C5C6=CC=C7C(=O)N(CC(CC)CCCC)C(=O)C8=CC=C(C9=CC=C%10C(=O)N(CC(CC)CCCC)C(=O)C(=C3)C%10=C95)C6=C87)SC42)S1,TVIDTzPDI,-5.5,-3.86,6.88,0.76,0.4,2.09,"Z.-F. Chang, Y. Cai, K.-K. Liu, X.-X. Song, J.-J. Liu, X. Liu, Y. Sun, R. bo Zhang, J.-L. Wang, Rational design of two-dimensional PDI-based small molecular acceptor from extended indacenodithiazole core for organic solar cells, Dyes Pigments. 147 (2017) 31¨C39. https://doi.org/10.1016/j.dyepig.2017.07.060."
3645,CCCCCCCCC(CCC)CN1C2=C(SC(/C=C3C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)=C2)C2=C1C1=C(C3=NSN=C32)C2=C(C=C(/C=C3C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)S2)N1CC(CCC)CCCCCCCC,L1,-5.68,-3.79,7.44,0.69,0.4027,2.07,"Z. Zhang, D. Li, H. Zhang, X. Ma, Y.-N. Chen, A. Zhang, X. Xu, Y. Liu, Z. Ma, Z. Bo, An asymmetric A¨CDA¡äD¨C¦Ð-A type non-fullerene acceptor for high-performance organic solar cells, J. Mater. Chem. C. 10 (2022) 2792¨C2799. https://doi.org/10.1039/D1TC04425G."
3646,CCCCCCC(CCCC)CC1=C(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)SC2=C1SC1=C2N(CC(CC)CCCC)C2=C1C1=NSN=C1C1=C2N(CC(CC)CCCC)C2=C1SC1=C2SC(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)=C1CC(CCCC)CCCCCC,L8-BO,-5.68,-3.9,25.72,0.87,0.815,18.32,"C. Li, J. Zhou, J. Song, J. Xu, H. Zhang, X. Zhang, J. Guo, L. Zhu, D. Wei, G. Han, J. Min, Y. Zhang, Z. Xie, Y. Yi, H. Yan, F. Gao, F. Liu, Y. Sun, Non-fullerene acceptors with branched side chains and improved molecular packing to exceed 18% efficiency in organic solar cells, Nat. Energy. 6 (2021) 605¨C613. https://doi.org/10.1038/s41560-021-00820-x."
3647,CCCCCCCCCCCC1=C(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)SC2=C1SC1=C2N(CC(CC)CCCC)C2=C1C1=NSN=C1C1=C2N(CC(CCCCCC)CCCCCCCC)C2=C1SC1=C2SC(/C=C2C(=O)C3=C(C=CC(F)=C3)C2=C(C#N)C#N)=C1CCCCCCCCCCC,EH-HD-4F,-5.69,-4.04,27.5,0.84,0.793,18.3,"S. Chen, L. Feng, T. Jia, J. Jing, Z. Hu, K. Zhang, F. Huang, High-performance polymer solar cells with efficiency over 18% enabled by asymmetric side chain engineering of non-fullerene acceptors, Sci. China Chem. 64 (2021) 1192¨C1199. https://doi.org/10.1007/s11426-021-1013-0."
3648,CCCCC(CC)CC1=CC=CC(C2=C(/C=C3C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)SC3=C2SC2=C3N(CC(CC)CCCC)C3=C2C2=NSN=C2C2=C3N(CC(CC)CCCC)C3=C2SC2=C3SC(/C=C3C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)=C2C2=CC=CC(CC(CC)CCCC)=C2)=C1,BTP-4F-P2EH,-5.65,-3.87,25.85,0.88,0.8008,17.96,"J. Zhang, F. Bai, I. Angunawela, X. Xu, S. Luo, C. Li, G. Chai, H. Yu, Y. Chen, H. Hu, Z. Ma, H. Ade, H. Yan, Alkyl-Chain Branching of Non-Fullerene Acceptors Flanking Conjugated Side Groups toward Highly Efficient Organic Solar Cells, Adv. Energy Mater. 11 (2021) 2102596. https://doi.org/10.1002/aenm.202102596."
3649,CCCCCCCCC(CCCCCC)CN1C2=C(SC3=C2SC(/C=C2C(=O)C4=CC(F)=C(F)C=C4C2=C(C#N)C#N)=C3CCCCC)C2=C1C1=C(C3=NSN=C32)C2=C(C3=C(S2)C(CCCCC)=C(/C=C2CC4=CC(F)=C(F)C=C4C2=C(C#N)C#N)S3)N1CC(CCCCCC)CCCCCCCC,BTP-4F-C5-16,-5.73,-3.93,27.36,0.841,0.7754,17.84,"L. Wang, C. Guo, X. Zhang, S. Cheng, D. Li, J. Cai, C. Chen, Y. Fu, J. Zhou, H. Qin, D. Liu, T. Wang, Alkyl Chain Tuning of Non-fullerene Electron Acceptors toward 18.2% Efficiency Binary Organic Solar Cells, Chem. Mater. 33 (2021) 8854¨C8862. https://doi.org/10.1021/acs.chemmater.1c03104."
3650,CCCCCCCCCC1=C(/C=C2C(=O)C3=C(C=C(Cl)C(Cl)=C3)C2=C(C#N)C#N)SC2=C1SC1=C2N(CC(CCCC)CCCCCC)C2=C1C1=NSN=C1C1=C2N(CC(CCCC)CCCCCC)C2=C1SC1=C2SC(/C=C2C(=O)C3=C(C=C(Cl)C(Cl)=C3)C2=C(C#N)C#N)=C1CCCCCCCCC,BTP-eC9,,,26.2,0.829,0.735,17.8,"Y. Cui, H. Yao, J. Zhang, K. Xian, T. Zhang, L. Hong, Y. Wang, Y. Xu, K. Ma, C. An, C. He, Z. Wei, F. Gao, J. Hou, Single-Junction Organic Photovoltaic Cells with Approaching 18% Efficiency, Adv. Mater. 32 (2020) 1908205. https://doi.org/10.1002/adma.201908205."
3651,CCCCCCC1=CC=CC(C2=C(/C=C3C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)SC3=C2SC2=C3N(CC(CC)CCCC)C3=C2C2=NSN=C2C2=C3N(CC(CC)CCCC)C3=C2SC2=C3SC(/C=C3C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)=C2C2=CC(CCCCCC)=CC=C2)=C1,m-BTP-PhC6,-5.59,-3.86,25.3,0.883,0.793,17.7,"G. Chai, Y. Chang, J. Zhang, X. Xu, L. Yu, X. Zou, X. Li, Y. Chen, S. Luo, B. Liu, F. Bai, Z. Luo, H. Yu, J. Liang, T. Liu, K.S. Wong, H. Zhou, Q. Peng, H. Yan, Fine-tuning of side-chain orientations on nonfullerene acceptors enables organic solar cells with 17.7% efficiency, Energy Environ. Sci. 14 (2021) 3469¨C3479. https://doi.org/10.1039/D0EE03506H."
3652,CCCCCCCCCCCC1=C(/C=C2C(=O)C3=C(C=C(Cl)C=C3)C2=C(C#N)C#N)SC2=C1SC1=C2N(CC(CCCC)CCCCCC)C2=C1C1=NSN=C1C1=C2N(CC(CCCC)CCCCCC)C2=C1SC1=C2SC(/C=C2C(=O)C3=C(C=C4C=C(Cl)SC4=C3)C2=C(C#N)C#N)=C1CCCCCCCCCCC,BTP-T-3Cl,-5.56,-3.99,26.02,0.893,0.7579,17.61,"Y. Pan, X. Zheng, J. Guo, Z. Chen, S. Li, C. He, S. Ye, X. Xia, S. Wang, X. Lu, H. Zhu, J. Min, L. Zuo, M. Shi, H. Chen, A New End Group on Nonfullerene Acceptors Endows Efficient Organic Solar Cells with Low Energy Losses, Adv. Funct. Mater. 32 (2022) 2108614. https://doi.org/10.1002/adfm.202108614."
3653,CCCCCCCCCCCC1=C(C=C2C(=O)C3=C(Br)SC(Br)=C3C2=O)SC2=C1SC1=C2N(CC(CC)CCCC)C2=C1C1=NSN=C1C1=C2N(CC(CC)CCCC)C2=C1SC1=C2SC(C=C2C(=O)C3=C(Br)SC(Br)=C3C2=O)=C1CCCCCCCCCCC,BTIC-EH-2ThBr,-5.47,-3.69,26.39,0.853,0.779,17.54,"C. Cao, H. Lai, H. Chen, Y. Zhu, M. Pu, N. Zheng, F. He, Over 17.5% efficiency ternary organic solar cells with enhanced photon utilization via a medium band gap non-fullerene acceptor, J. Mater. Chem. A. 9 (2021) 16418¨C16426. https://doi.org/10.1039/D1TA04454K."
3654,CCCCCCCCCCCC1=C(/C=C2C(=O)C3=C(C=C(F)C(Cl)=C3)C2=C(C#N)C#N)SC2=C1SC1=C2N(CC(CCCC)CCCCCC)C2=C1C1=NSN=C1C1=C2N(CC(CCCC)CCCCCC)C2=C1SC1=C2SC(/C=C2C(=O)C3=C(C=C(F)C(Cl)=C3)C2=C(C#N)C#N)=C1CCCCCCCCCCC.F,"Y-BO-FCl,",-5.74,-4.03,26.45,0.85,0.7792,17.52,"L. Wang, Q. An, L. Yan, H.-R. Bai, M. Jiang, A. Mahmood, C. Yang, H. Zhi, J.-L. Wang, Non-fullerene acceptors with hetero-dihalogenated terminals induce significant difference in single crystallography and enable binary organic solar cells with 17.5% efficiency, Energy Environ. Sci. 15 (2022) 320¨C333. https://doi.org/10.1039/D1EE01832A."
3655,CCCCCCCCC(CCCCCC)CC1=C(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)SC2=C1SC1=C2N(CC(CC)CCCC)C2=C1C1=NSN=C1C1=C2N(CC(CC)CCCC)C2=C1SC1=C2SC(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)=C1CC(CCCCCC)CCCCCCCC,L8-HD,-5.71,-3.9,25.08,0.88,0.788,17.39,"C. Li, J. Zhou, J. Song, J. Xu, H. Zhang, X. Zhang, J. Guo, L. Zhu, D. Wei, G. Han, J. Min, Y. Zhang, Z. Xie, Y. Yi, H. Yan, F. Gao, F. Liu, Y. Sun, Non-fullerene acceptors with branched side chains and improved molecular packing to exceed 18% efficiency in organic solar cells, Nat. Energy. 6 (2021) 605¨C613. https://doi.org/10.1038/s41560-021-00820-x."
3656,CCCCCCCCCCCC1=C(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)SC2=C1SC1=C2N(CC(C)C)C2=C1C1=NSN=C1C1=C2N(CC(CCCCCCCC)CCCCCCCCCC)C2=C1SC1=C2SC(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)=C1CCCCCCCCCCC,Bu-OD-4F,-5.68,-4.01,27,0.85,0.767,17.37,"S. Chen, L. Feng, T. Jia, J. Jing, Z. Hu, K. Zhang, F. Huang, High-performance polymer solar cells with efficiency over 18% enabled by asymmetric side chain engineering of non-fullerene acceptors, Sci. China Chem. 64 (2021) 1192¨C1199. https://doi.org/10.1007/s11426-021-1013-0."
3657,CCCCC(CC)CCC1=CC=CC(C2=C(/C=C3C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)SC3=C2SC2=C3N(CC(CC)CCCC)C3=C2C2=NSN=C2C2=C3N(CC(CC)CCCC)C3=C2SC2=C3SC(/C=C3C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)=C2C2=CC=CC(CCC(CC)CCCC)=C2)=C1,BTP-4F-P3EH,-5.66,-3.89,26.11,0.861,0.7813,17.29,"J. Zhang, F. Bai, I. Angunawela, X. Xu, S. Luo, C. Li, G. Chai, H. Yu, Y. Chen, H. Hu, Z. Ma, H. Ade, H. Yan, Alkyl-Chain Branching of Non-Fullerene Acceptors Flanking Conjugated Side Groups toward Highly Efficient Organic Solar Cells, Adv. Energy Mater. 11 (2021) 2102596. https://doi.org/10.1002/aenm.202102596."
3658,CCCCCCCCC(CCCCCC)CN1C2=C(SC3=C2SC(/C=C2C(=O)C4=CC(F)=C(F)C=C4C2=C(C#N)C#N)=C3CCCCCC)C2=C1C1=C(C3=NSN=C32)C2=C(C3=C(S2)C(CCCCCC)=C(/C=C2CC4=CC(F)=C(F)C=C4C2=C(C#N)C#N)S3)N1CC(CCCCCC)CCCCCCCC,BTP-4F-C6-16,-5.72,-3.92,26.61,0.843,0.7691,17.26,"L. Wang, C. Guo, X. Zhang, S. Cheng, D. Li, J. Cai, C. Chen, Y. Fu, J. Zhou, H. Qin, D. Liu, T. Wang, Alkyl Chain Tuning of Non-fullerene Electron Acceptors toward 18.2% Efficiency Binary Organic Solar Cells, Chem. Mater. 33 (2021) 8854¨C8862. https://doi.org/10.1021/acs.chemmater.1c03104."
3659,CCCCCCCCCCCC1=C(/C=C2C(=O)C3=C(C=C(Cl)C(Cl)=C3)C2=C(C#N)C#N)SC2=C1SC1=C2N(CC(CCCC)CCCCCC)C2=C1C1=NSN=C1C1=C2N(CC(CCCC)CCCCCC)C2=C1SC1=C2SC(/C=C2C(=O)C3=C(C=C(Cl)C(Cl)=C3)C2=C(C#N)C#N)=C1CCCCCCCCCCC,BTP-4Cl-BO,-5.62,-4.05,26.74,0.844,0.7619,17.2,"Y. Pan, X. Zheng, J. Guo, Z. Chen, S. Li, C. He, S. Ye, X. Xia, S. Wang, X. Lu, H. Zhu, J. Min, L. Zuo, M. Shi, H. Chen, A New End Group on Nonfullerene Acceptors Endows Efficient Organic Solar Cells with Low Energy Losses, Adv. Funct. Mater. 32 (2022) 2108614. https://doi.org/10.1002/adfm.202108614."
3660,CCCCCCC1=C(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)SC2=C1SC1=C2N(CC(CC)CCCC)C2=C1C1=NN(CC(C)C)N=C1C1=C2N(CC(CC)CCC)C2=C1SC1=C2SC(/C=C2/C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)=C1CCCCCC,BTA-C5,-5.66,-4,26.51,0.847,0.7619,17.11,"H. Chen, X. Xia, J. Yuan, Q. Wei, W. Liu, Z. Li, C. Zhu, X. Wang, H. Guan, X. Lu, Y. Li, Y. Zou, Compatibility between Solubility and Enhanced Crystallinity of Benzotriazole-Based Small Molecular Acceptors with Less Bulky Alkyl Chains for Organic Solar Cells, ACS Appl. Mater. Interfaces. 13 (2021) 36053¨C36061. https://doi.org/10.1021/acsami.1c07254."
3661,CCCCCCCCCCCOC1=C(/C=C2C(=O)C3=C(C=C(Cl)C(Cl)=C3)C2=C(C#N)C#N)SC2=C1OC1=C2N(CC(CCCC)CCCCCCC)C2=C1C1=NSN=C1C1=C2N(CC(CCCC)CCCCCC)C2=C1SC1=C2SC(/C=C2C(=O)C3=C(C=C(Cl)C(Cl)=C3)C2=C(C#N)C#N)=C1CCCCCCCCCCC,BTP1O-4Cl-C12,-5.84,-3.9,23.8,0.91,0.788,17.1,"Y. Chen, R. Ma, T. Liu, Y. Xiao, H.K. Kim, J. Zhang, C. Ma, H. Sun, F. Bai, X. Guo, K.S. Wong, X. Lu, H. Yan, Side-Chain Engineering on Y-Series Acceptors with Chlorinated End Groups Enables High-Performance Organic Solar Cells, Adv. Energy Mater. 11 (2021) 2003777. https://doi.org/10.1002/aenm.202003777."
3662,CCCCCCC1=CC=C(C2=C(/C=C3C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)SC3=C2SC2=C3N(CC(CC)CCCC)C3=C2C2=NSN=C2C2=C3N(CC(CC)CCCC)C3=C2SC2=C3SC(/C=C3C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)=C2C2=CC=C(CCCCCC)C=C2)C=C1,n-BTP-PhC6,-5.59,-3.85,24.7,0.888,0.779,17.1,"G. Chai, Y. Chang, J. Zhang, X. Xu, L. Yu, X. Zou, X. Li, Y. Chen, S. Luo, B. Liu, F. Bai, Z. Luo, H. Yu, J. Liang, T. Liu, K.S. Wong, H. Zhou, Q. Peng, H. Yan, Fine-tuning of side-chain orientations on nonfullerene acceptors enables organic solar cells with 17.7% efficiency, Energy Environ. Sci. 14 (2021) 3469¨C3479. https://doi.org/10.1039/D0EE03506H."
3663,CCCCCCCCCCCC1=C(/C=C2C(=O)C3=C(Cl)SC=C3C2=C(C#N)C#N)SC2=C1SC1=C2N(CC(CC)CCCC)C2=C1C1=NSN=C1C1=C2N(CC(CC)CCCC)C2=C1SC1=C2SC(/C=C2C(=O)C3=CSC(Cl)=C3C2=C(C#N)C#N)=C1CCCCCCCCCCC,BTP-2ThCl,-5.83,-3.81,25.38,0.869,0.774,17.06,"Z. Luo, R. Ma, T. Liu, J. Yu, Y. Xiao, R. Sun, G. Xie, J. Yuan, Y. Chen, K. Chen, G. Chai, H. Sun, J. Min, J. Zhang, Y. Zou, C. Yang, X. Lu, F. Gao, H. Yan, Fine-Tuning Energy Levels via Asymmetric End Groups Enables Polymer Solar Cells with Efficiencies over 17%, Joule. 4 (2020) 1236¨C1247. https://doi.org/10.1016/j.joule.2020.03.023."
3664,CCCCCCCCCCCC1=C(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)SC2=C1SC1=C2N(CC(CCCC)CCCCCC)C2=C1C1=NSN=C1C1=C2N(CC(CCCC)CCCCCC)C2=C1SC1=C2SC(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)=C1CCCCCCCCCCC,Bo-4F,-5.7,-4.01,26.2,0.84,0.766,17.06,"S. Chen, L. Feng, T. Jia, J. Jing, Z. Hu, K. Zhang, F. Huang, High-performance polymer solar cells with efficiency over 18% enabled by asymmetric side chain engineering of non-fullerene acceptors, Sci. China Chem. 64 (2021) 1192¨C1199. https://doi.org/10.1007/s11426-021-1013-0."
3665,CCCCCCC1=C(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)[Se]C2=C1SC1=C2N(CC(CCCC)CCCCCC)C2=C1C1=NNN=C1C1=C2N(CC(CCCC)CCCCCC)C2=C1SC1=C2[Se]C(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)=C1CC1=CC=C2C=C3C=CC(C)=CC3=CC2=C1,mBzS-4F,-5.6,-3.9,27.72,0.804,0.7635,17.02,"F. Qi, K. Jiang, F. Lin, Z. Wu, H. Zhang, W. Gao, Y. Li, Z. Cai, H.Y. Woo, Z. Zhu, A.K.-Y. Jen, Over 17% Efficiency Binary Organic Solar Cells with Photoresponses Reaching 1000 nm Enabled by Selenophene-Fused Nonfullerene Acceptors, ACS Energy Lett. 6 (2021) 9¨C15. https://doi.org/10.1021/acsenergylett.0c02230."
3666,CCCCCCCCCCCC1=C(/C=C2C(=O)C3=C(C=C(Cl)C(Cl)=C3)C2=C(C#N)C#N)SC2=C1SC1=C2N(CC(CCCC)CCCCCCCC)C2=C1C1=NSN=C1C1=C2N(CC(CCCC)CCCCCCCC)C2=C1SC1=C2SC(/C=C2C(=O)C3=C(C=C(Cl)C(Cl)=C3)C2=C(C#N)C#N)=C1CCCCCCCCCCC,BTP-4Cl-12,,,25.6,0.858,0.776,17,"Y. Cui, H. Yao, L. Hong, T. Zhang, Y. Tang, B. Lin, K. Xian, B. Gao, C. An, P. Bi, W. Ma, J. Hou, Organic photovoltaic cell with 17% efficiency and superior processability, Natl. Sci. Rev. 7 (2020) 1239¨C1246. https://doi.org/10.1093/nsr/nwz200."
3667,CCCCCCC1=CC=CC(C2=C(/C=C3C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)SC3=C2SC2=C3N(CC(CC)CCCC)C3=C2C2=NSN=C2C2=C3N(CC(CC)CCCC)C3=C2SC2=C3SC(/C=C3C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)=C2C2=CC=CC(CCCCCC)=C2)=C1,BTP-4F-PC6,-5.65,-3.9,25.08,0.855,0.8033,16.86,"J. Zhang, F. Bai, I. Angunawela, X. Xu, S. Luo, C. Li, G. Chai, H. Yu, Y. Chen, H. Hu, Z. Ma, H. Ade, H. Yan, Alkyl-Chain Branching of Non-Fullerene Acceptors Flanking Conjugated Side Groups toward Highly Efficient Organic Solar Cells, Adv. Energy Mater. 11 (2021) 2102596. https://doi.org/10.1002/aenm.202102596."
3668,CCCCCCCCCCCC1=C(C=C2C(=O)C3=C(Br)SC(Br)=C3C2=O)SC2=C1SC1=C2N(CC(CCCC)CCCCCC)C2=C1C1=NSN=C1C1=C2N(CC(CCCC)CCCCCC)C2=C1SC1=C2SC(C=C2C(=O)C3=C(Br)SC(Br)=C3C2=O)=C1CCCCCCCCCCC,BTIC-BO-2ThBr,-5.48,-3.71,26.02,0.851,0.761,16.86,"C. Cao, H. Lai, H. Chen, Y. Zhu, M. Pu, N. Zheng, F. He, Over 17.5% efficiency ternary organic solar cells with enhanced photon utilization via a medium band gap non-fullerene acceptor, J. Mater. Chem. A. 9 (2021) 16418¨C16426. https://doi.org/10.1039/D1TA04454K."
3669,CCCCCCCCC1=C(/C=C2C(=O)C3=C(C=C(Cl)C(Cl)=C3)C2=C(C#N)C#N)SC2=C1SC1=C2N(CC(CC)CCCC)C2=C1C1=NN(CC(CC)CCCC)N=C1C1=C2N(CC(CC)CCCC)C2=C1SC1=C2SC(/C=C2C(=O)C3=C(C=C4C(=C3)C3=C4C4C=CC3C4)C2=C(C#N)C#N)=C1CCCCCCCC,LL3,-5.48,-3.78,26.97,0.86,0.7227,16.82,"H. Lu, H. Jin, H. Huang, W. Liu, Z. Tang, J. Zhang, Z. Bo, High-Efficiency Organic Solar Cells Based on Asymmetric Acceptors Bearing One 3D Shape-Persistent Terminal Group, Adv. Funct. Mater. 31 (2021) 2103445. https://doi.org/10.1002/adfm.202103445."
3670,CCCCCCCCC(CCCCCC)CN1C2=C(SC3=C2SC(/C=C2C(=O)C4=CC(F)=C(F)C=C4C2=C(C#N)C#N)=C3CCCCCCC)C2=C1C1=C(C3=NSN=C32)C2=C(C3=C(S2)C(CCCCCCC)=C(/C=C2CC4=CC(F)=C(F)C=C4C2=C(C#N)C#N)S3)N1CC(CCCCCC)CCCCCCCC,BTP-4F-C7-16,-5.72,-3.92,26.3,0.848,0.7541,16.81,"L. Wang, C. Guo, X. Zhang, S. Cheng, D. Li, J. Cai, C. Chen, Y. Fu, J. Zhou, H. Qin, D. Liu, T. Wang, Alkyl Chain Tuning of Non-fullerene Electron Acceptors toward 18.2% Efficiency Binary Organic Solar Cells, Chem. Mater. 33 (2021) 8854¨C8862. https://doi.org/10.1021/acs.chemmater.1c03104."
3671,CCCCCCCCC1=C(/C=C2C(=O)C3=CC(F)=C(F)C=C3C2=C(C#N)C#N)SC2=C1SC1=C2N(CC(CCCCCC)CCCCCCCC)C2=C1C1=NSN=C1C1=C2N(CC(CCCCCC)CCCCCCCC)C2=C1SC1=C2SC(/C=C2CC3=CC(F)=C(F)C=C3C2=C(C#N)C#N)=C1CCCCCCCC,BTP-4F-C8-16,-5.71,-3.91,26.14,0.851,0.7534,16.76,"L. Wang, C. Guo, X. Zhang, S. Cheng, D. Li, J. Cai, C. Chen, Y. Fu, J. Zhou, H. Qin, D. Liu, T. Wang, Alkyl Chain Tuning of Non-fullerene Electron Acceptors toward 18.2% Efficiency Binary Organic Solar Cells, Chem. Mater. 33 (2021) 8854¨C8862. https://doi.org/10.1021/acs.chemmater.1c03104."
3672,CCCCC(CC)CN1C2=C(SC3=C2SC(/C=C2C(=O)C4=C(C=C(F)C(F)=C4)C2=C(C#N)C#N)=C3CCCCCC2=CC=CC=C2)C2=C1C1=C(C3=NSN=C32)C2=C(C3=C(S2)C(CCCCCC2=CC=CC=C2)=C(/C=C2C(=O)C4=C(C=C(F)C(F)=C4)C2=C(C#N)C#N)S3)N1CC(CC)CCCC,BTP-C6Ph,-5.6,-3.94,25,0.865,0.77,16.7,"G. Chai, Y. Chang, Z. Peng, Y. Jia, X. Zou, D. Yu, H. Yu, Y. Chen, P.C.Y. Chow, K.S. Wong, J. Zhang, H. Ade, L. Yang, C. Zhan, Enhanced hindrance from phenyl outer side chains on nonfullerene acceptor enables unprecedented simultaneous enhancement in organic solar cell performances with 16.7% efficiency, Nano Energy. 76 (2020) 105087. https://doi.org/10.1016/j.nanoen.2020.105087."
3673,CCCCCCCCC(CCCCCC)CN1C2=C(SC(/C=C3C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)=C2)C2=C1C1=C(OCC(CC)CCCC)C3=C(C(OCC(CC)CCCC)=C1S2)C1=C(S3)C2=C(C=C(/C=C3C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)S2)N1CC(CCCCCC)CCCCCCCC,M3,-5.6,-3.85,24.03,0.92,0.7622,16.66,"Y. Ma, M. Zhang, S. Wan, P. Yin, P. Wang, D. Cai, F. Liu, Q. Zheng, Efficient Organic Solar Cells from Molecular Orientation Control of M-Series Acceptors, Joule. 5 (2021) 197¨C209. https://doi.org/10.1016/j.joule.2020.11.006."
3674,CCCCCCCCCCCC1=C(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)SC2=C1SC1=C2N(CC(CC)CCCC)C2=C1C1=NC=CN=C1C1=C2N(CC(CC)CCCC)C2=C1SC1=C2SC(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)=C1CCCCCCCCCCC,AQX-2,-5.62,-3.88,25.38,0.86,0.7625,16.64,"Z. Zhou, W. Liu, G. Zhou, M. Zhang, D. Qian, J. Zhang, S. Chen, S. Xu, C. Yang, F. Gao, H. Zhu, F. Liu, X. Zhu, Subtle Molecular Tailoring Induces Significant Morphology Optimization Enabling over 16% Efficiency Organic Solar Cells with Efficient Charge Generation, Adv. Mater. 32 (2020) 1906324. https://doi.org/10.1002/adma.201906324."
3675,CCCCCCCCCC1=C(/C=C2C(=O)C3=C(C=C4C=CC(F)=CC4=C3)C2=C(C#N)C#N)SC2=C1SC1=C2N(CC(CCCC)CCCCCC)C2=C1C1=NSN=C1C1=C2N(CC(CCCC)CCCCCC)C2=C1SC1=C2SC(/C=C2C(=O)C3=C(C=C4C=C(F)C(F)=CC4=C3)C2=C(C#N)C#N)=C1CCCCCCCCC,BTP-C9-N4F,-5.51,-4.02,26.3,0.85,0.757,16.6,"Y. Shi, J. Pan, J. Yu, J. Zhang, F. Gao, K. Lu, Z. Wei, Optimizing the Charge Carrier and Light Management of Nonfullerene Acceptors for Efficient Organic Solar Cells with Small Nonradiative Energy Losses, Sol. RRL. 5 (2021) 2100008. https://doi.org/10.1002/solr.202100008."
3676,CCCCCCC1=C(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)SC2=C1SC1=C2N(CC(CC)CCCC)C2=C1C1=NN(CCCCCC)N=C1C1=C2N(CC(CC)CCC)C2=C1SC1=C2SC(/C=C2/C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)=C1CCCCCC,BTA-C8,-5.66,-3.96,26.18,0.837,0.7567,16.59,"H. Chen, X. Xia, J. Yuan, Q. Wei, W. Liu, Z. Li, C. Zhu, X. Wang, H. Guan, X. Lu, Y. Li, Y. Zou, Compatibility between Solubility and Enhanced Crystallinity of Benzotriazole-Based Small Molecular Acceptors with Less Bulky Alkyl Chains for Organic Solar Cells, ACS Appl. Mater. Interfaces. 13 (2021) 36053¨C36061. https://doi.org/10.1021/acsami.1c07254."
3677,CCCCCCCCCCCC1=C(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)SC2=C1SC1=C2N(CC(CC)CCCC)C2=C1C1=NN(CC(CC)CCCC)N=C1C1=C2N(CC(CC)CCCC)C2=C1SC1=C2SC(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)=C1CCCCCCCCCCC,Y11,,,26.74,0.833,0.7433,16.54,"S. Liu, J. Yuan, W. Deng, M. Luo, Y. Xie, Q. Liang, Y. Zou, Z. He, H. Wu, Y. Cao, High-efficiency organic solar cells with low non-radiative recombination loss and low energetic disorder, Nat. Photonics. 14 (2020) 300¨C305. https://doi.org/10.1038/s41566-019-0573-5."
3678,CCCCCCCCCCCC1=C(/C=C2C(=O)C3=C(C=C(Cl)C(Cl)=C3)C2=C(C#N)C#N)SC2=C1SC1=C2N(CCC(CC)CCCC)C2=C1C1=NSN=C1C1=C2N(CCC(CC)CCCC)C2=C1SC1=C2SC(/C=C2C(=O)C3=C(C=C(Cl)C(Cl)=C3)C2=C(C#N)C#N)=C1CCCCCCCCCCC,N3-4CL,-563,-3.98,25.901,0.852,0.749,16.532,"H. Yu, R. Ma, Y. Xiao, J. Zhang, T. Liu, Z. Luo, Y. Chen, F. Bai, X. Lu, H. Yan, H. Lin, Improved organic solar cell efficiency based on the regulation of an alkyl chain on chlorinated non-fullerene acceptors, Mater. Chem. Front. 4 (2020) 2428¨C2434. https://doi.org/10.1039/D0QM00151A."
3679,CCCCCCCCCCCC1=C(/C=C2C(=O)C3=C(C=C(Cl)C(Cl)=C3)C2=C(C#N)C#N)SC2=C1SC1=C2N(CC(CC)CCCC)C2=C1C1=NSN=C1C1=C2N(CC(CC)CCCC)C2=C1SC1=C2SC(/C=C2C(=O)C3=C(C=C(Cl)C(Cl)=C3)C2=C(C#N)C#N)=C1CCCCCCCCCCC,BTP-4Cl,-5.68,-4.12,25.4,0.867,0.75,16.5,"Y. Cui, H. Yao, J. Zhang, T. Zhang, Y. Wang, L. Hong, K. Xian, B. Xu, S. Zhang, J. Peng, Z. Wei, F. Gao, J. Hou, Over 16% efficiency organic photovoltaic cells enabled by a chlorinated acceptor with increased open-circuit voltages, Nat. Commun. 10 (2019) 2515. https://doi.org/10.1038/s41467-019-10351-5."
3680,CCCCCCCCCCC(CCCCCCCC)CN1C2=C(SC3=C2SC(/C=C2C(=O)C4=C(C=C(F)C(F)=C4)C2=C(C#N)C#N)=C3CCCCCCCCC)C2=C1C1=C(C3=NSN=C32)C2=C(C3=C(S2)C(CCCCCCCCC)=C(/C=C2C(=O)C4=C(C=C(F)C(F)=C4)C2=C(C#N)C#N)S3)N1CC(CCCCCCCC)CCCCCCCCCC,BTP-4F¨CC9-20,-5.7,-3.9,16.5,0.86,0.742,16.5,"S. Cheng, L. Wang, C. Guo, D. Li, J. Cai, W. Miao, B. Du, P. Wang, D. Liu, T. Wang, Reduced miscibility between highly compatible non-fullerene acceptor and donor enables efficient ternary organic solar cells, Polymer. 236 (2021) 124322. https://doi.org/10.1016/j.polymer.2021.124322."
3681,CCCCCCCCCCCC1=C(/C=C2C(=O)C3=C(C=C(F)C(Cl)=C3)C2=C(C#N)C#N)SC2=C1SC1=C2N(CC(CCCC)CCCCCC)C2=C1C1=NSN=C1C1=C2N(CC(CCCC)CCCCCC)C2=C1SC1=C2SC(/C=C2C(=O)C3=C(C=C(F)C(Br)=C3)C2=C(C#N)C#N)=C1CCCCCCCCCCC.F,Y-BO-FBr ,-5.73,-4.03,25.83,0.85,0.7502,16.47,"L. Wang, Q. An, L. Yan, H.-R. Bai, M. Jiang, A. Mahmood, C. Yang, H. Zhi, J.-L. Wang, Non-fullerene acceptors with hetero-dihalogenated terminals induce significant difference in single crystallography and enable binary organic solar cells with 17.5% efficiency, Energy Environ. Sci. 15 (2022) 320¨C333. https://doi.org/10.1039/D1EE01832A."
3682,CCCCCCCCCCCOC1=C(/C=C2C(=O)C3=C(C=C(Cl)C(Cl)=C3)C2=C(C#N)C#N)SC2=C1OC1=C2N(CC(CCC)CCCCC)C2=C1C1=NSN=C1C1=C2N(CC(CCC)CCCCC)C2=C1SC1=C2SC(/C=C2C(=O)C3=C(C=C(Cl)C(Cl)=C3)C2=C(C#N)C#N)=C1OCCCCCCCCCCC,BTP1O-4Cl-C10,-5.81,-3.9,23.42,0.9,0.776,16.4,"Y. Chen, R. Ma, T. Liu, Y. Xiao, H.K. Kim, J. Zhang, C. Ma, H. Sun, F. Bai, X. Guo, K.S. Wong, X. Lu, H. Yan, Side-Chain Engineering on Y-Series Acceptors with Chlorinated End Groups Enables High-Performance Organic Solar Cells, Adv. Energy Mater. 11 (2021) 2003777. https://doi.org/10.1002/aenm.202003777."
3683,CCCCCCCCCCCC1=C(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)SC2=C1SC1=C2N(CC(CCCC)CCCCCC)C2=C1C1=NSN=C1C1=C2N(CC(CCCC)CCCCCC)C2=C1SC1=C2SC(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)=C1CCCCCCCCC,Y7-BO,-5.7,-4.1,26.7,0.84,0.731,16.4,"S. Cheng, L. Wang, C. Guo, D. Li, J. Cai, W. Miao, B. Du, P. Wang, D. Liu, T. Wang, Reduced miscibility between highly compatible non-fullerene acceptor and donor enables efficient ternary organic solar cells, Polymer. 236 (2021) 124322. https://doi.org/10.1016/j.polymer.2021.124322."
3684,CCCCCCCCCCCC1=C(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)SC2=C1SC1=C2N(CC(CC)CCCC)C2=C1C1=NSN=C1C1=C2N(CC(CC)CCCC)C2=C1SC1=C2SC(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)=C1CCCCCCCCCCC,BTP-4F,-5.85,-3.82,25.19,0.841,0.773,16.37,"Z. Luo, R. Ma, T. Liu, J. Yu, Y. Xiao, R. Sun, G. Xie, J. Yuan, Y. Chen, K. Chen, G. Chai, H. Sun, J. Min, J. Zhang, Y. Zou, C. Yang, X. Lu, F. Gao, H. Yan, Fine-Tuning Energy Levels via Asymmetric End Groups Enables Polymer Solar Cells with Efficiencies over 17%, Joule. 4 (2020) 1236¨C1247. https://doi.org/10.1016/j.joule.2020.03.023."
3685,CCCCCCCCCCCC1=C(C=C2C(=O)C3=C(C2=O)C(Cl)=C(Cl)C(Cl)=C3Cl)SC2=C1SC1=C2N(CC(CC)CCCC)C2=C1C1=NSN=C1C1=C2N(CC(CC)CCCC)C2=C1SC1=C2SC(/C=C2C(=O)C3=C(C=C(Cl)C(Cl)=C3)C2=C(C#N)C#N)=C1CCCCCCCCCCC,BTP-S2,-5.65,-4.1,24.07,0.945,0.7202,16.37,"S. Li, L. Zhan, Y. Jin, G. Zhou, T.-K. Lau, R. Qin, M. Shi, C.-Z. Li, H. Zhu, X. Lu, F. Zhang, H. Chen, Asymmetric Electron Acceptors for High-Efficiency and Low-Energy-Loss Organic Photovoltaics, Adv. Mater. 32 (2020) 2001160. https://doi.org/10.1002/adma.202001160."
3686,CCCCCCCCCCCC1=C(/C=C2C(=O)C3=C(C=C(Cl)C(Cl)=C3)C2=C(C#N)C#N)SC2=C1OC1=C2N(CC(CCCC)CCCCCCC)C2=C1C1=NSN=C1C1=C2N(CC(CCCC)CCCCCC)C2=C1SC1=C2SC(/C=C2C(=O)C3=C(C=C(Cl)C(Cl)=C3)C2=C(C#N)C#N)=C1CCCCCCCCCCC,BTP-4Cl-C12,-5.81,-3.95,25.73,0.85,0.746,16.3,"Y. Chen, R. Ma, T. Liu, Y. Xiao, H.K. Kim, J. Zhang, C. Ma, H. Sun, F. Bai, X. Guo, K.S. Wong, X. Lu, H. Yan, Side-Chain Engineering on Y-Series Acceptors with Chlorinated End Groups Enables High-Performance Organic Solar Cells, Adv. Energy Mater. 11 (2021) 2003777. https://doi.org/10.1002/aenm.202003777."
3687,CCCCCCCCCCCC1=C(/C=C2C(=O)C3=C(C=C(Cl)C(Cl)=C3)C2=C(C#N)C#N)SC2=C1SC1=C2N(CC(CC)CCCC)C2=C1C1=NSN=C1C1=C2N(CC(CC)CCCC)C2=C1SC1=C2SC(/C=C2C(=O)C3=C(C=C(Cl)C(Cl)=C3)C2=C(C#N)C#N)=C1CCCCCCCCCCC,BTP-4Cl-8,,,25.2,0.872,0.743,16.3,"Y. Cui, H. Yao, L. Hong, T. Zhang, Y. Tang, B. Lin, K. Xian, B. Gao, C. An, P. Bi, W. Ma, J. Hou, Organic photovoltaic cell with 17% efficiency and superior processability, Natl. Sci. Rev. 7 (2020) 1239¨C1246. https://doi.org/10.1093/nsr/nwz200."
3688,CCCCCCCCCCC(CCCCCCCC)CC1=C(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)SC2=C1SC1=C2N(CC(CC)CCCC)C2=C1C1=NSN=C1C1=C2N(CC(CC)CCCC)C2=C1SC1=C2SC(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)=C1CC(CCCCCCCC)CCCCCCCCCC,L8-OD,-5.71,-3.91,24.57,0.89,0.746,16.26,"C. Li, J. Zhou, J. Song, J. Xu, H. Zhang, X. Zhang, J. Guo, L. Zhu, D. Wei, G. Han, J. Min, Y. Zhang, Z. Xie, Y. Yi, H. Yan, F. Gao, F. Liu, Y. Sun, Non-fullerene acceptors with branched side chains and improved molecular packing to exceed 18% efficiency in organic solar cells, Nat. Energy. 6 (2021) 605¨C613. https://doi.org/10.1038/s41560-021-00820-x."
3689,CCCCCCC1=C(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)SC2=C1SC1=C2N(CC(CC)CCCC)C2=C1C1=NN(CCCC)N=C1C1=C2N(CC(CC)CCC)C2=C1SC1=C2SC(/C=C2/C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)=C1CCCCCC,BTA-C6,-5.65,-3.97,25.2,0.851,0.7568,16.23,"H. Chen, X. Xia, J. Yuan, Q. Wei, W. Liu, Z. Li, C. Zhu, X. Wang, H. Guan, X. Lu, Y. Li, Y. Zou, Compatibility between Solubility and Enhanced Crystallinity of Benzotriazole-Based Small Molecular Acceptors with Less Bulky Alkyl Chains for Organic Solar Cells, ACS Appl. Mater. Interfaces. 13 (2021) 36053¨C36061. https://doi.org/10.1021/acsami.1c07254."
3690,CCCCCCC1=C(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)SC2=C1SC1=C2N(CC(CC)CCCC)C2=C1C1=NN(C)N=C1C1=C2N(CC(CC)CCC)C2=C1SC1=C2SC(/C=C2/C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)=C1CCCCCC,BTA-C1,-5.64,-3.99,24.75,0.844,0.7762,16.21,"H. Chen, X. Xia, J. Yuan, Q. Wei, W. Liu, Z. Li, C. Zhu, X. Wang, H. Guan, X. Lu, Y. Li, Y. Zou, Compatibility between Solubility and Enhanced Crystallinity of Benzotriazole-Based Small Molecular Acceptors with Less Bulky Alkyl Chains for Organic Solar Cells, ACS Appl. Mater. Interfaces. 13 (2021) 36053¨C36061. https://doi.org/10.1021/acsami.1c07254."
3691,CCCCCCCCCCCC1=C(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)SC2=C1SC1=C2N(CC(CCCC)CCCCCC)C2=C1C1=NSN=C1C1=C2N(CC(CCCC)CCCCCC)C2=C1SC1=C2SC(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)=C1CCCCCCCCCCC,Y6-BO,-5.68,-4.38,26.6,0.81,0.755,16.2,"T. Jiang, G. Zhang, R. Xia, J. Huang, X. Li, M. Wang, H.-L. Yip, Y. Cao, Semitransparent organic solar cells based on all-low-bandgap donor and acceptor materials and their performance potential, Mater. Today Energy. 21 (2021) 100807. https://doi.org/10.1016/j.mtener.2021.100807."
3692,CCCCCCCCCC1=C(/C=C2C(=O)C3=C(C=CC(F)=C3)C2=C(C#N)C#N)SC2=C1SC1=C2N(CC(CCCC)CCCCCC)C2=C1C1=NSN=C1C1=C2N(CC(CCCC)CCCCCC)C2=C1SC1=C2SC(/C=C2C(=O)C3=C(C=CC(F)=C3)C2=C(C#N)C#N)=C1CCCCCCCCC,BTP-F,-5.55,-3.86,24.05,0.9,0.75,16.2,"Y. Li, Y. Cai, Y. Xie, J. Song, H. Wu, Z. Tang, J. Zhang, F. Huang, Y. Sun, A facile strategy for third-component selection in non-fullerene acceptor-based ternary organic solar cells, Energy Environ. Sci. 14 (2021) 5009¨C5016. https://doi.org/10.1039/D1EE01864G."
3693,CCCCCCCCCCCOCC1=C(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)SC2=C1SC1=C2N(CC(CC)CCCC)C2=C1C1=NSN=C1C1=C2N(CC(CC)CCCC)C2=C1SC1=C2SC(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)=C1C,Y6-1O,-5.71,-3.84,23.6,0.89,0.783,16.1,"Y. Chen, F. Bai, Z. Peng, L. Zhu, J. Zhang, X. Zou, Y. Qin, H.K. Kim, J. Yuan, L.-K. Ma, J. Zhang, H. Yu, P.C.Y. Chow, F. Huang, Y. Zou, H. Ade, F. Liu, H. Yan, Asymmetric Alkoxy and Alkyl Substitution on Nonfullerene Acceptors Enabling High-Performance Organic Solar Cells, Adv. Energy Mater. 11 (2021) 2003141. https://doi.org/10.1002/aenm.202003141."
3694,CCCCCCCCCCCC1=C(/C=C2C(=O)C3=C(C=C(Cl)C(Cl)=C3)C2=C(C#N)C#N)SC2=C1SC1=C2N(CC(CC)CCCC)C2=C1C1=NSN=C1C1=C2N(CC(CC)CCCC)C2=C1SC1=C2SC(/C=C2C(=O)C3=C(C=C(Cl)C(Cl)=C3)C2=C(C#N)C#N)=C1CCCCCCCCCCC,Y6-4CL,-5.65,-4,25.849,0.839,0.741,16.061,"H. Yu, R. Ma, Y. Xiao, J. Zhang, T. Liu, Z. Luo, Y. Chen, F. Bai, X. Lu, H. Yan, H. Lin, Improved organic solar cell efficiency based on the regulation of an alkyl chain on chlorinated non-fullerene acceptors, Mater. Chem. Front. 4 (2020) 2428¨C2434. https://doi.org/10.1039/D0QM00151A."
3695,CCCCCCC1=C(C2=C(/C=C3C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)SC3=C2SC2=C3N(CC(CC)CCCC)C3=C2C2=NSN=C2C2=C3N(CC(CC)CCCC)C3=C2SC2=C3SC(/C=C3C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)=C2C2=C(CCCCCC)C=CC=C2)C=CC=C1,o-BTP-PhC6,-5.53,-3.76,22.8,0.923,0.762,16,"G. Chai, Y. Chang, J. Zhang, X. Xu, L. Yu, X. Zou, X. Li, Y. Chen, S. Luo, B. Liu, F. Bai, Z. Luo, H. Yu, J. Liang, T. Liu, K.S. Wong, H. Zhou, Q. Peng, H. Yan, Fine-tuning of side-chain orientations on nonfullerene acceptors enables organic solar cells with 17.7% efficiency, Energy Environ. Sci. 14 (2021) 3469¨C3479. https://doi.org/10.1039/D0EE03506H."
3696,CCCCCCCCCCCC1=C(/C=C2C(=O)C3=C(C=C4C=C(F)C(F)=CC4=C3)C2=C(C#N)C#N)SC2=C1SC1=C2N(CC(CCCC)CCCCCC)C2=C1C1=NSN=C1C1=C2N(CC(CCCC)CCCCCC)C2=C1SC1=C2SC(/C=C2C(=O)C3=C(C=C4C=C(F)C(F)=CC4=C3)C2=C(C#N)C#N)=C1CCCCCCCCCCC,BT-BO-L4F,-5.58,-3.98,27.8,0.83,0.695,16,"G. Li, X. Zhang, L.O. Jones, J.M. Alzola, S. Mukherjee, L. Feng, W. Zhu, C.L. Stern, W. Huang, J. Yu, V.K. Sangwan, D.M. DeLongchamp, K.L. Kohlstedt, M.R. Wasielewski, M.C. Hersam, G.C. Schatz, A. Facchetti, T.J. Marks, Systematic Merging of Nonfullerene Acceptor ¦Ð-Extension and Tetrafluorination Strategies Affords Polymer Solar Cells with >16% Efficiency, J. Am. Chem. Soc. 143 (2021) 6123¨C6139. https://doi.org/10.1021/jacs.1c00211."
3697,CCCCCCCCCCCC1=C(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)SC2=C1SC1=C2N(CCC(CC)CCCC)C2=C1C1=NSN=C1C1=C2N(CCC(CC)CCCCC)C2=C1SC1=C2SC(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)=C1CCCCCCCCCCC,N3,,,25.81,0.837,0.739,15.98,"K. Jiang, Q. Wei, J.Y.L. Lai, Z. Peng, H.K. Kim, J. Yuan, L. Ye, H. Ade, Y. Zou, H. Yan, Alkyl Chain Tuning of Small Molecule Acceptors for Efficient Organic Solar Cells, Joule. 3 (2019) 3020¨C3033. https://doi.org/10.1016/j.joule.2019.09.010."
3698,CCCCCCC1=C(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)[Se]C2=C1SC1=C2N(CC(CCCC)CCCCCC)C2=C1C1=NN(CC(CC)CCCC)N=C1C1=C2N(CC(CCCC)CCCCCC)C2=C1SC1=C2[Se]C(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)=C1CC1=CC=C2C=C3C=CC(C)=CC3=CC2=C1,EHBzS-4F,-5.61,-3.86,27.58,0.825,0.7007,15.94,"F. Qi, K. Jiang, F. Lin, Z. Wu, H. Zhang, W. Gao, Y. Li, Z. Cai, H.Y. Woo, Z. Zhu, A.K.-Y. Jen, Over 17% Efficiency Binary Organic Solar Cells with Photoresponses Reaching 1000 nm Enabled by Selenophene-Fused Nonfullerene Acceptors, ACS Energy Lett. 6 (2021) 9¨C15. https://doi.org/10.1021/acsenergylett.0c02230."
3699,CCCCCCCCCC1=C(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)SC2=C1SC1=C2N(CC(CCCC)CCCCCC)C2=C1C1=NSN=C1C1=C2N(CC(CCCC)CCCCCC)C2=C1SC1=C2SC(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)=C1CCCCCCCCC,BTP-C9-IC4F,-5.66,-4.03,25.7,0.82,0.757,15.9,"Y. Shi, J. Pan, J. Yu, J. Zhang, F. Gao, K. Lu, Z. Wei, Optimizing the Charge Carrier and Light Management of Nonfullerene Acceptors for Efficient Organic Solar Cells with Small Nonradiative Energy Losses, Sol. RRL. 5 (2021) 2100008. https://doi.org/10.1002/solr.202100008."
3700,O=C(C(C=C(F)C(F)=C1)=C1C/2=C(C#N)/C#N)C2=C/C3=C(CCCCCCCCCCC)C(S4)=C(S3)C5=C4C6=C(N5CC(CC)CCCC)C7=C(C(SC8=C9SC(/C=C%10C(C(C=C(F)C(F)=C%11)=C%11C\%10=C(C#N)C#N)=O)=C8CCCCCCCCCCC)=C9N7CC(CC)CCCC)C%12=NSN=C6%12,Y6,-5.65,-4.1,25.3,0.83,0.748,15.7,"K. Jiang, Q. Wei, J.Y.L. Lai, Z. Peng, H.K. Kim, J. Yuan, L. Ye, H. Ade, Y. Zou, H. Yan, Alkyl Chain Tuning of Small Molecule Acceptors for Efficient Organic Solar Cells, Joule. 3 (2019) 3020¨C3033. https://doi.org/10.1016/j.joule.2019.09.010."
3701,CCCCCCCCCCCOC1=C(/C=C2C(=O)C3=C(C=C(Cl)C(Cl)=C3)C2=C(C#N)C#N)SC2=C1OC1=C2N(CC(CCCC)CCCCCCC)C2=C1C1=NSN=C1C1=C2N(CC(CCCC)CCCCCC)C2=C1SC1=C2SC(/C=C2C(=O)C3=C(C=C(Cl)C(Cl)=C3)C2=C(C#N)C#N)=C1OCCCCCCCCCCC,BTP2O-4Cl-C12,-5.85,-3.79,21.14,0.96,0.772,15.6,"Y. Chen, R. Ma, T. Liu, Y. Xiao, H.K. Kim, J. Zhang, C. Ma, H. Sun, F. Bai, X. Guo, K.S. Wong, X. Lu, H. Yan, Side-Chain Engineering on Y-Series Acceptors with Chlorinated End Groups Enables High-Performance Organic Solar Cells, Adv. Energy Mater. 11 (2021) 2003777. https://doi.org/10.1002/aenm.202003777."
3702,CCCCCCCCCCCC1=C(/C=C2C(=O)C3=C(C=C(Cl)C(Cl)=C3)C2=C(C#N)C#N)SC2=C1SC1=C2N(CC(CCCCCC)CCCCCCCCCC)C2=C1C1=NSN=C1C1=C2N(CC(CCCCCC)CCCCCCCCCC)C2=C1SC1=C2SC(/C=C2C(=O)C3=C(C=C(Cl)C(Cl)=C3)C2=C(C#N)C#N)=C1CCCCCCCCCCC,BTP-4Cl-16,,,24.2,0.862,0.748,15.6,"Y. Cui, H. Yao, L. Hong, T. Zhang, Y. Tang, B. Lin, K. Xian, B. Gao, C. An, P. Bi, W. Ma, J. Hou, Organic photovoltaic cell with 17% efficiency and superior processability, Natl. Sci. Rev. 7 (2020) 1239¨C1246. https://doi.org/10.1093/nsr/nwz200."
3703,CCCCCCCCCCCC1=C(/C=C2C(=O)C3=C(C=CC(C(F)(F)F)=C3)C2=C(C#N)C#N)SC2=C1SC1=C2N(CC(CC)CCCC)C2=C1C1=NSN=C1C1=C2N(CC(CC)CCCC)C2=C1SC1=C2SC(/C=C2C(=O)C3=C(C=CC(C(F)(F)F)=C3)C2=C(C#N)C#N)=C1CCCCCCCCCCC,BTIC-CF3,-5.45,-3.96,25.19,0.85,0.7282,15.59,"H. Lai, Q. Zhao, Z. Chen, H. Chen, P. Chao, Y. Zhu, Y. Lang, N. Zhen, D. Mo, Y. Zhang, F. He, Trifluoromethylation Enables a 3D Interpenetrated Low-Band-Gap Acceptor for Efficient Organic Solar Cells, Joule. 4 (2020) 688¨C700. https://doi.org/10.1016/j.joule.2020.02.004."
3704,CCCCCCC1=CC=C(C2=C(/C=C3C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)SC3=C2SC2=C3N(CC(CC)CCCC)C3=C2C2=NSN=C2C2=C3N(CC(CC)CCCC)C3=C2SC2=C3SC(/C=C3C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)=C2C2=CC=C(CCCCCC)C=C2)C=C1,BTP-PhC6,-5.58,-3.85,24.3,0.839,0.762,15.5,"G. Chai, Y. Chang, Z. Peng, Y. Jia, X. Zou, D. Yu, H. Yu, Y. Chen, P.C.Y. Chow, K.S. Wong, J. Zhang, H. Ade, L. Yang, C. Zhan, Enhanced hindrance from phenyl outer side chains on nonfullerene acceptor enables unprecedented simultaneous enhancement in organic solar cell performances with 16.7% efficiency, Nano Energy. 76 (2020) 105087. https://doi.org/10.1016/j.nanoen.2020.105087."
3705,CCCCCCCCCC1=C(/C=C2C(=O)C3=C(C=C4C=C(F)C=CC4=C3)C2=C(C#N)C#N)SC2=C1SC1=C2N(CC(CCCC)CCCCCC)C2=C1C1=NSN=C1C1=C2N(CC(CCCC)CCCCCC)C2=C1SC1=C2SC(/C=C2C(=O)C3=C(C=C4C=C(F)C=CC4=C3)C2=C(C#N)C#N)=C1CCCCCCCCC,BTP-C9-N2F,-5.46,-3.96,24.4,0.89,0.723,15.5,"Y. Shi, J. Pan, J. Yu, J. Zhang, F. Gao, K. Lu, Z. Wei, Optimizing the Charge Carrier and Light Management of Nonfullerene Acceptors for Efficient Organic Solar Cells with Small Nonradiative Energy Losses, Sol. RRL. 5 (2021) 2100008. https://doi.org/10.1002/solr.202100008."
3706,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(C=C(/C=C5C(=O)C6=C(C=C(F)C(F)=C6)C5=C(C#N)C#N)S2)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC3=C2SC(/C=C2C(=O)C4=C(C=C(F)C(F)=C4)C2=C(C#N)C#N)=C3)C=C1,IT-4F,-5.66,-4.19,21.2,0.92,0.785,15.3,"J. Wu, Q. Fan, M. Xiong, Q. Wang, K. Chen, H. Liu, M. Gao, L. Ye, X. Guo, J. Fang, Q. Guo, W. Su, Z. Ma, Z. Tang, E. Wang, H. Ade, M. Zhang, Carboxylate substituted pyrazine: A simple and low-cost building block for novel wide bandgap polymer donor enables 15.3% efficiency in organic solar cells, Nano Energy. 82 (2021) 105679. https://doi.org/10.1016/j.nanoen.2020.105679."
3707,CCCCCCCCCCCC1=C(/C=C2C(=O)C3=C(C=CC(Br)=C3)C2=C(C#N)C#N)SC2=C1SC1=C2N(CC(CC)CCCC)C2=C1C1=NSN=C1C1=C2N(CC(CC)CCCC)C2=C1SC1=C2SC(/C=C2C(=O)C3=C(C=C(Br)C=C3)C2=C(C#N)C#N)=C1CCCCCCCCCCC,ZB,-5.69,-4.14,26.38,0.9,0.6416,15.23,"M. Zhang, M. Zeng, L. Ye, S. Tan, B. Zhao, H.S. Ryu, H.Y. Woo, Y. Sun, Effects of monohalogenated terminal units of non-fullerene acceptors on molecular aggregation and photovoltaic performance, Sol. Energy. 208 (2020) 866¨C872. https://doi.org/10.1016/j.solener.2020.07.100."
3708,CCCCCCCCCCCC1=C(/C=C2C(=O)C3=C(C=C4SC(Br)=CC4=C3)C2=C(C#N)C#N)SC2=C1SC1=C2N(CC(CCCC)CCCCCC)C2=C1C1=NSN=C1C1=C2N(CC(CCCC)CCCCCC)C2=C1SC1=C2SC(/C=C2C(=O)C3=C(C=C4SC(Br)=CC4=C3)C2=C(C#N)C#N)=C1CCCCCCCCCCC,BTTPC-Br,-5.54,-3.88,24.71,0.86,0.71,15.22,"R. Qin, D. Wang, G. Zhou, Z.-P. Yu, S. Li, Y. Li, Z.-X. Liu, H. Zhu, M. Shi, X. Lu, C.-Z. Li, H. Chen, Tuning terminal aromatics of electron acceptors to achieve high-efficiency organic solar cells, J. Mater. Chem. A. 7 (2019) 27632¨C27639. https://doi.org/10.1039/C9TA11285E."
3709,CCCCCCCCCCCC1=C(C=C2C(=O)C3=C(C2=O)C(Cl)=C(Cl)C(Cl)=C3Cl)SC2=C1SC1=C2N(CC(CC)CCCC)C2=C1C1=NSN=C1C1=C2N(CC(CC)CCCC)C2=C1SC1=C2SC(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)=C1CCCCCCCCCCC,BTP-S1,-5.55,-4.01,22.39,0.934,0.7269,15.21,"S. Li, L. Zhan, Y. Jin, G. Zhou, T.-K. Lau, R. Qin, M. Shi, C.-Z. Li, H. Zhu, X. Lu, F. Zhang, H. Chen, Asymmetric Electron Acceptors for High-Efficiency and Low-Energy-Loss Organic Photovoltaics, Adv. Mater. 32 (2020) 2001160. https://doi.org/10.1002/adma.202001160."
3710,CCCCC(CC)CC1=C(C2=CC(C3=C(C(C)C)C=C(C(C)C)C=C3C(C)C)=C(C3=C(C4=C(C(C)C)C=C(C(C)C)C=C4C(C)C)C=C(C4=C(CC(CC)CCCC)C=C(/C=C5C(=O)C6=C(C=C(F)C(F)=C6)C5=C(C#N)C#N)S4)S3)S2)SC(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)=C1,A4T-16,-5.67,-3.96,21.8,0.876,0.798,15.2,"L. Ma, S. Zhang, J. Zhu, J. Wang, J. Ren, J. Zhang, J. Hou, Completely non-fused electron acceptor with 3D-interpenetrated crystalline structure enables efficient and stable organic solar cell, Nat. Commun. 12 (2021) 5093. https://doi.org/10.1038/s41467-021-25394-w."
3711,CCCCCCCCC1=C(/C=C2C(=O)C3=C(C=CC(F)=C3)C2=C(C#N)C#N)SC2=C1C(CCCCCCCC)(CCCCCCCC)OC1=CC3=C(C=C12)C(CCCCCCCC)(CCCCCCCC)C1=C3C=C2OC(CCCCCCCC)(CCCCCCCC)C3=C(SC(/C=C4C(=O)C5=C(C=C(F)C(F)=C5)C4=C(C#N)C#N)=C3CCCCCCCC)C2=C1,FOR-2F,-5.76,-3.76,21.25,0.969,0.7374,15.18,"S. Wu, L. Meng, Z. Zhang, M. Li, Y. Yang, J. Wang, H. Chen, C. Jiang, X. Wan, C. Li, Z. Yao, Y. Chen, Molecular optimization of incorporating pyran fused acceptor¨Cdonor¨Cacceptor type acceptors enables over 15% efficiency in organic solar cells, J. Mater. Chem. C. 10 (2022) 1977¨C1983. https://doi.org/10.1039/D1TC05779K."
3712,CCCCCCCCCCCC1=C(/C=C2C(=O)C3=C(C=C4C(=C3)C3=C4C4C=CC3C4)C2=C(C#N)C#N)SC2=C1SC1=C2N(CC(CC)CCCC)C2=C1C1=NSN=C1C1=C2N(CC(CC)CCCC)C2=C1SC1=C2SC(/C=C2C(=O)C3=C(C=C(Cl)C(Cl)=C3)C2=C(C#N)C#N)=C1CCCCCCCC,LL4,-5.56,-3.82,26.05,0.82,0.7087,15.18,"H. Lu, H. Jin, H. Huang, W. Liu, Z. Tang, J. Zhang, Z. Bo, High-Efficiency Organic Solar Cells Based on Asymmetric Acceptors Bearing One 3D Shape-Persistent Terminal Group, Adv. Funct. Mater. 31 (2021) 2103445. https://doi.org/10.1002/adfm.202103445."
3713,CCCCCCCCCCCC1=C(/C=C2C(=O)C3=C(C=CC(F)=C3)C2=C(C#N)C#N)SC2=C1SC1=C2N(CC(CC)CCCC)C2=C1C1=NSN=C1C1=C2N(CC(CC)CCCC)C2=C1SC1=C2SC(/C=C2C(=O)C3=C(C=CC(F)=C3)C2=C(C#N)C#N)=C1CCCCCCCCCCC,Y6-F,,,23.61,0.871,0.737,15.17,"Y. Li, Y. Cai, Y. Xie, J. Song, H. Wu, Z. Tang, J. Zhang, F. Huang, Y. Sun, A facile strategy for third-component selection in non-fullerene acceptor-based ternary organic solar cells, Energy Environ. Sci. 14 (2021) 5009¨C5016. https://doi.org/10.1039/D1EE01864G."
3714,CCCCCCC(CCCC)CC1=C(/C=C2C(=O)C3=C(C=CC(F)=C3)C2=C(C#N)C#N)SC2=C1SC1=C2N(CC(CC)CCCC)C2=C1C1=NSN=C1C1=C2N(CC(CC)CCCC)C2=C1SC1=C2SC(/C=C2C(=O)C3=C(C=CC(F)=C3)C2=C(C#N)C#N)=C1CC(CCCC)CCCCCC,L8-BO-F,,,22.45,0.932,0.716,14.94,"Y. Li, Y. Cai, Y. Xie, J. Song, H. Wu, Z. Tang, J. Zhang, F. Huang, Y. Sun, A facile strategy for third-component selection in non-fullerene acceptor-based ternary organic solar cells, Energy Environ. Sci. 14 (2021) 5009¨C5016. https://doi.org/10.1039/D1EE01864G."
3715,CCCCCCCC1=C(/C=C2C(=O)C3=C(C=C(Cl)C(Cl)=C3)C2=C(C#N)C#N)SC2=C1SC1=C2N(CC(CCCC)CCCCCC)C2=C1C1=NSN=C1C1=C2N(CC(CCCC)CCCCCC)C2=C1SC1=C2SC(/C=C2C(=O)C3=C(C=C(Cl)C(Cl)=C3)C2=C(C#N)C#N)=C1CCCCCCC,BTP-eC7,,,24.1,0.847,0.811,14.9,"Y. Cui, H. Yao, J. Zhang, K. Xian, T. Zhang, L. Hong, Y. Wang, Y. Xu, K. Ma, C. An, C. He, Z. Wei, F. Gao, J. Hou, Single-Junction Organic Photovoltaic Cells with Approaching 18% Efficiency, Adv. Mater. 32 (2020) 1908205. https://doi.org/10.1002/adma.201908205."
3716,CCCCCCCCCCCC1=C(/C=C2C(=O)C3=C(C=C4C=C(F)C=CC4=C3)C2=C(C#N)C#N)SC2=C1SC1=C2N(CC(CCCC)CCCCCC)C2=C1C1=NSN=C1C1=C2N(CC(CCCC)CCCCCC)C2=C1SC1=C2SC(/C=C2C(=O)C3=C(C=C4C=C(F)C=CC4=C3)C2=C(C#N)C#N)=C1CCCCCCCCCCC,BTP-C11-N2F,-5.47,-3.96,23.7,0.9,0.701,14.9,"Y. Shi, J. Pan, J. Yu, J. Zhang, F. Gao, K. Lu, Z. Wei, Optimizing the Charge Carrier and Light Management of Nonfullerene Acceptors for Efficient Organic Solar Cells with Small Nonradiative Energy Losses, Sol. RRL. 5 (2021) 2100008. https://doi.org/10.1002/solr.202100008."
3717,CCCCCCCCCCCC1=C(/C=C2C(=O)C3=C(C=C4C=C(Cl)SC4=C3)C2=C(C#N)C#N)SC2=C1SC1=C2N(CC(CCCC)CCCCCC)C2=C1C1=NSN=C1C1=C2N(CC(CCCC)CCCCCC)C2=C1SC1=C2SC(/C=C2C(=O)C3=C(C=C4C=C(Cl)SC4=C3)C2=C(C#N)C#N)=C1CCCCCCCCCCC,BTP-T-2Cl,-5.52,-3.93,22.32,0.936,0.7159,14.89,"Y. Pan, X. Zheng, J. Guo, Z. Chen, S. Li, C. He, S. Ye, X. Xia, S. Wang, X. Lu, H. Zhu, J. Min, L. Zuo, M. Shi, H. Chen, A New End Group on Nonfullerene Acceptors Endows Efficient Organic Solar Cells with Low Energy Losses, Adv. Funct. Mater. 32 (2022) 2108614. https://doi.org/10.1002/adfm.202108614."
3718,CCCCCCCCC1=C(/C=C2C(=O)C3=C(C=C(Cl)C(Cl)=C3)C2=C(C#N)C#N)SC2=C1N(CC(CCCC)CCCCCC)C1=C2C2=NCN=C2C2=C1N(CC(CCCC)CCCCCC)C1=C2SC2=C1N(CC(CC)CCCC)C1=C2SC(/C=C2C(=O)C3=C(C=C(Cl)C(Cl)=C3)C2=C(C#N)C#N)=C1,PTIC-4CL,-5.68,-3.91,23.3,0.86,0.7389,14.81,"Z. Xia, J. Zhang, X. Gao, W. Song, J. Ge, L. Xie, X. Zhang, Z. Liu, Z. Ge, Fine-Tuning the Dipole Moment of Asymmetric Non-Fullerene Acceptors Enabling Efficient and Stable Organic Solar Cells, ACS Appl. Mater. Interfaces. 13 (2021) 23983¨C23992. https://doi.org/10.1021/acsami.1c02652."
3719,CCCCCCCCCCCC1=C(/C=C2C(=O)C3=C(C=C(Cl)C(Cl)=C3)C2=C(C#N)C#N)SC2=C1SC1=C2N(CC(CC)CCCC)C2=C1C1=NSN=C1C1=C2N(CC(CC)CCCC)C2=C1SC1=C2SC(/C=C2C(=O)C3=C(C=C4C(=C3)C3=C4C4C=CC3C4)C2=C(C#N)C#N)=C1CCCCCCCCCCC,LL2,-5.58,-3.88,24.24,0.84,0.7267,14.75,"H. Lu, H. Jin, H. Huang, W. Liu, Z. Tang, J. Zhang, Z. Bo, High-Efficiency Organic Solar Cells Based on Asymmetric Acceptors Bearing One 3D Shape-Persistent Terminal Group, Adv. Funct. Mater. 31 (2021) 2103445. https://doi.org/10.1002/adfm.202103445."
3720,CCCCCCCCCCCC1=C(/C=C2C(=O)C3=C(C=CC(Cl)=C3)C2=C(C#N)C#N)SC2=C1SC1=C2N(CC(CC)CCCC)C2=C1C1=NSN=C1C1=C2N(CC(CC)CCCC)C2=C1SC1=C2SC(/C=C2C(=O)C3=C(C=C(Cl)C=C3)C2=C(C#N)C#N)=C1CCCCCCCCCCC,ZC,-5.69,-4.12,25.11,0.9,0.6509,14.71,"M. Zhang, M. Zeng, L. Ye, S. Tan, B. Zhao, H.S. Ryu, H.Y. Woo, Y. Sun, Effects of monohalogenated terminal units of non-fullerene acceptors on molecular aggregation and photovoltaic performance, Sol. Energy. 208 (2020) 866¨C872. https://doi.org/10.1016/j.solener.2020.07.100."
3721,CCCCCCCCCCCOC1=C(/C=C2C(=O)C3=C(C=C(Cl)C(Cl)=C3)C2=C(C#N)C#N)SC2=C1OC1=C2N(CC(CC)CCCC)C2=C1C1=NSN=C1C1=C2N(CC(CC)CCCC)C2=C1SC1=C2SC(/C=C2C(=O)C3=C(C=C(Cl)C(Cl)=C3)C2=C(C#N)C#N)=C1OCCCCCCCCCCC,BTP1O-4Cl-C8,-5.83,-3.9,23.37,0.9,0.699,14.7,"Y. Chen, R. Ma, T. Liu, Y. Xiao, H.K. Kim, J. Zhang, C. Ma, H. Sun, F. Bai, X. Guo, K.S. Wong, X. Lu, H. Yan, Side-Chain Engineering on Y-Series Acceptors with Chlorinated End Groups Enables High-Performance Organic Solar Cells, Adv. Energy Mater. 11 (2021) 2003777. https://doi.org/10.1002/aenm.202003777."
3722,CCCCCCCCC1=C(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)SC2=C1SC(C1=C(N(C3=CC=C(CCCC)C=C3)C3=CC=C(CCCC)C=C3)C3=C(S1)C(N(C1=CC=C(CCCC)C=C1)C1=CC=C(CCCC)C=C1)=C(C1=CC4=C(S1)C(CCCCCCCC)=C(/C=C1C(=O)C5=C(C=C(F)C(F)=C5)C1=C(C#N)C#N)S4)S3)=C2,2BTh-2F,-5.55,-3.98,24.02,0.84,0.7214,14.53,"X. Wang, H. Lu, Y. Liu, A. Zhang, N. Yu, H. Wang, S. Li, Y. Zhou, X. Xu, Z. Tang, Z. Bo, Simple Nonfused Ring Electron Acceptors with 3D Network Packing Structure Boosting the Efficiency of Organic Solar Cells to 15.44%, Adv. Energy Mater. 11 (2021) 2102591. https://doi.org/10.1002/aenm.202102591."
3723,CCCCC(CC)COC1=CC(C2=CC3=C(S2)C2=C(C=C(/C=C4/C(=O)C5=CC6=CC=C(F)C=C6C=C5C4=C(C#N)C#N)S2)C3(CC(CC)CCC)CC(CC)CCCC)=C(OCC(CC)CCCC)C=C1C1=CC2=C(S1)C1=C(C=C(/C=C3/C(=O)C4=C(C=C5C=C(F)C=CC5=C4)C3=C(C#N)C#N)S1)C2(CC(CC)CC)CC(CC)CCC,BN-2F,-5.39,-3.99,25.25,0.813,0.7078,14.53,"X. Zhang, L. Qin, J. Yu, Y. Li, Y. Wei, X. Liu, X. Lu, F. Gao, H. Huang, High-Performance Noncovalently Fused-Ring Electron Acceptors for Organic Solar Cells Enabled by Noncovalent Intramolecular Interactions and End-Group Engineering, Angew. Chem. Int. Ed. 60 (2021) 12475¨C12481. https://doi.org/10.1002/anie.202100390."
3724,CCCCCCCCCCCC1=C(/C=C2C(=O)C3=C(C=C4SC=CC4=C3)C2=C(C#N)C#N)SC2=C1SC1=C2N(CC(CCCC)CCCCCC)C2=C1C1=NSN=C1C1=C2N(CC(CCCC)CCCCCC)C2=C1SC1=C2SC(/C=C2C(=O)C3=C(C=C4SC(Br)=CC4=C3)C2=C(C#N)C#N)=C1CCCCCCCCCCC,BTTPC,-5.47,-3.78,22.25,0.89,0.73,14.51,"R. Qin, D. Wang, G. Zhou, Z.-P. Yu, S. Li, Y. Li, Z.-X. Liu, H. Zhu, M. Shi, X. Lu, C.-Z. Li, H. Chen, Tuning terminal aromatics of electron acceptors to achieve high-efficiency organic solar cells, J. Mater. Chem. A. 7 (2019) 27632¨C27639. https://doi.org/10.1039/C9TA11285E."
3725,CCCCCCCCCCCC1=C(/C=C2C(=O)C3=CC(F)=C(F)C=C3C2=C(C#N)C#N)SC2=C1SC1=C2N(CC(CC)CCCC)C2=C1C1=NSN=C1C1=C2N(CC(CC)CCCC)C2=C1SC1=C2SC(/C=C2C(=O)C3=CSC(Cl)=C3C2=C(C#N)C#N)=C1CCCCCCCCCCC,BTP-2F-ThCl,-5.8,-3.8,23.46,0.885,0.698,14.49,"Z. Luo, R. Ma, T. Liu, J. Yu, Y. Xiao, R. Sun, G. Xie, J. Yuan, Y. Chen, K. Chen, G. Chai, H. Sun, J. Min, J. Zhang, Y. Zou, C. Yang, X. Lu, F. Gao, H. Yan, Fine-Tuning Energy Levels via Asymmetric End Groups Enables Polymer Solar Cells with Efficiencies over 17%, Joule. 4 (2020) 1236¨C1247. https://doi.org/10.1016/j.joule.2020.03.023."
3726,CCCCCCCCC1=C(/C=C2C(=O)C3=C(C=C(Cl)C(Cl)=C3)C2=C(C#N)C#N)SC2=C1SC1=C2N(CC(CC)CCCC)C2=C1C1=NSN=C1C1=C2N(CC(CC)CCCC)C2=C1SC(/C=C1C(=O)C3=C(C=C(Cl)C(Cl)=C3)C1=C(C#N)C#N)=C2CCCCCCCC,TB-4CL,-5.81,-3.94,23.2,0.836,0.7456,14.45,"Z. Xia, J. Zhang, X. Gao, W. Song, J. Ge, L. Xie, X. Zhang, Z. Liu, Z. Ge, Fine-Tuning the Dipole Moment of Asymmetric Non-Fullerene Acceptors Enabling Efficient and Stable Organic Solar Cells, ACS Appl. Mater. Interfaces. 13 (2021) 23983¨C23992. https://doi.org/10.1021/acsami.1c02652."
3727,CCCCC(CC)CN1N=C2C(=N1)C1=C(C3=C2C2=C(C4=C(C=C(/C=C5C(=O)C6=C(C=C(F)C(F)=C6)C5=C(C#N)C#N)S4)S2)N3CC(CC)CCCC)N(CC(CC)CCCC)C2=C1SC1=C2SC(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)=C1,Y1-4F,-5.56,-4.11,25.2,0.83,0.683,14.4,"R. Wang, J. Yuan, R. Wang, G. Han, T. Huang, W. Huang, J. Xue, H.-C. Wang, C. Zhang, C. Zhu, P. Cheng, D. Meng, Y. Yi, K.-H. Wei, Y. Zou, Y. Yang, Rational Tuning of Molecular Interaction and Energy Level Alignment Enables High-Performance Organic Photovoltaics, Adv. Mater. 31 (2019) 1904215. https://doi.org/10.1002/adma.201904215."
3728,CCCCCCCCC1=C(/C=C2C(=O)C3=C(C=C(Cl)C(Cl)=C3)C2=C(C#N)C#N)SC2=C1SC1=C2N(CC(CC)CCCC)C2=C1C1=NN(CC(CC)CCCC)N=C1C1=C2N(CC(CC)CCCC)C2=C1SC1=C2SC(/C=C2C(=O)C3=C(C=C(Cl)C(Cl)=C3)C2=C(C#N)C#N)=C1CCCCCCCC,LL3-2CL,-5.53,-3.92,26.96,0.79,0.677,14.4,"H. Lu, H. Jin, H. Huang, W. Liu, Z. Tang, J. Zhang, Z. Bo, High-Efficiency Organic Solar Cells Based on Asymmetric Acceptors Bearing One 3D Shape-Persistent Terminal Group, Adv. Funct. Mater. 31 (2021) 2103445. https://doi.org/10.1002/adfm.202103445."
3729,CCCCCCCCCCCC1=C(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)SC2=C1SC1=C2N(CCCC(CC)CCCC)C2=C1C1=NSN=C1C1=C2N(CCCC(CC)CCCC)C2=C1SC1=C2SC(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)=C1CCCCCCCCCCC,N4,,,25.01,0.819,0.699,14.31,"K. Jiang, Q. Wei, J.Y.L. Lai, Z. Peng, H.K. Kim, J. Yuan, L. Ye, H. Ade, Y. Zou, H. Yan, Alkyl Chain Tuning of Small Molecule Acceptors for Efficient Organic Solar Cells, Joule. 3 (2019) 3020¨C3033. https://doi.org/10.1016/j.joule.2019.09.010."
3730,CCCCCCCCCCCC1=C(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)SC2=C1SC1=C2N(CCCCCCCC)C2=C1C1=NSN=C1C1=C2N(CCCC(CC)CCCC)C2=C1SC1=C2SC(/C=C2C(=O)C3=C(C=C(F)C=C3)C2=C(C#N)C#N)=C1CCCCCCCCCCC,N4,,,25.01,0.819,0.699,14.31,"K. Jiang, Q. Wei, J.Y.L. Lai, Z. Peng, H.K. Kim, J. Yuan, L. Ye, H. Ade, Y. Zou, H. Yan, Alkyl Chain Tuning of Small Molecule Acceptors for Efficient Organic Solar Cells, Joule. 3 (2019) 3020¨C3033. https://doi.org/10.1016/j.joule.2019.09.010."
3731,CCCCCCC1(CCCCCC)C2=CC3=C(C=C2C2=C1C=C(C1=C(SCC(CC)CCCC)C=C(/C=C4C(=O)C5=C(C=C(F)C(F)=C5)C4=C(C#N)C#N)S1)S2)C(CCCCCC)(CCCCCC)C1=C3SC(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)=C1,IDST-4F,-5.59,-4.01,24.9,0.82,0.7,14.3,"Q. Guo, J. Lin, H. Liu, X. Dong, X. Guo, L. Ye, Z. Ma, Z. Tang, H. Ade, M. Zhang, Y. Li, Asymmetrically noncovalently fused-ring acceptor for high-efficiency organic solar cells with reduced voltage loss and excellent thermal stability, Nano Energy. 74 (2020) 104861. https://doi.org/10.1016/j.nanoen.2020.104861."
3732,CCCCCCCCCCCC1=C(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)SC2=C1SC1=C2N(CC(CC)CCCC)C2=C1C1=NSN=C1C1=C2N(CC(CC)CCCC)C2=C1N(C)C1=C2SC(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)=C1CCCCCCCCCCC,SN,-5.51,,25.14,0.82,0.689,14.3,"W. Liu, S. Sun, L. Zhou, Y. Cui, W. Zhang, J. Hou, F. Liu, S. Xu, X. Zhu, Design of Near-Infrared Nonfullerene Acceptor with Ultralow Nonradiative Voltage Loss for High-Performance Semitransparent Ternary Organic Solar Cells, Angew. Chem. Int. Ed. n/a (n.d.) e202116111. https://doi.org/10.1002/anie.202116111."
3733,CCCCCCCCCCCC1=C(/C=C2C(=O)C3=C(C=CC(F)=C3)C2=C(C#N)C#N)SC2=C1SC1=C2N(CC(CC)CCCC)C2=C1C1=NN(CC(CC)CCCC)N=C1C1=C2N(CC(CC)CCCC)C2=C1SC1=C2SC(/C=C2C(=O)C3=C(C=C(F)C=C3)C2=C(C#N)C#N)=C1CCCCCCCCCCC,Y14,-5.56,-4.01,25.2,0.798,0.7087,14.25,"M. Luo, C. Zhao, J. Yuan, J. Hai, F. Cai, Y. Hu, H. Peng, Y. Bai, Z. Tan, Y. Zou, Semitransparent solar cells with over 12% efficiency based on a new low bandgap fluorinated small molecule acceptor, Mater. Chem. Front. 3 (2019) 2483¨C2490. https://doi.org/10.1039/C9QM00499H."
3734,CCCCCCCCCCCC1=C(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)SC2=C1SC1=C2N(CC(CCCC)CCCCCC)C2=C1C1=NSN=C1C1=C2N(CC(CCCC)CCCCCC)C2=C1SC1=C2SC(/C=C/C=C2C(=O)C3=CC(F)=C(F)C=C3C2=C(C#N)C#N)=C1CCCCCCCCCCC,BTP-1V-2F,-5.64,-3.92,24.75,0.8,0.72,14.24,"J. Hai, W. Zhao, S. Luo, H. Yu, H. Chen, Z. Lu, L. Li, Y. Zou, H. Yan, Vinylene ¦Ð-bridge: A simple building block for ultra-narrow bandgap nonfullerene acceptors enable 14.2% efficiency in binary organic solar cells, Dyes Pigments. 188 (2021) 109171. https://doi.org/10.1016/j.dyepig.2021.109171."
3735,CCCCCCCCCCCC1=C(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)SC2=C1SC1=C2N(CC(CCCC)CCCCCC)C2=C1C1=NNN=C1C1=C2N(CC(CCCC)CCCCCC)C2=C1SC1=C2SC(/C=C/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)=C1CCCCCCCCCCC,BTP-Se,-5.64,-4.04,28.66,0.711,0.697,14.2,"Y. Song, Z. Zhong, L. Li, X. Liu, J. Huang, H. Wu, M. Li, Z. Lu, J. Yu, J. Hai, Fused-heterocycle engineering on asymmetric non-fullerene acceptors enables organic solar cells approaching 29?mA/cm2 short-circuit current density, Chem. Eng. J. 430 (2022) 132830. https://doi.org/10.1016/j.cej.2021.132830."
3736,CCCCCCCCCCCC1=C(/C=C2C(=O)C3=C(C=C(Cl)C(Cl)=C3)C2=C(C#N)C#N)SC2=C1SC1=C2N(CC(CC)CCCC)C2=C1C1=NN(CC(CC)CCCC)N=C1C1=C2N(CC(CC)CCCC)C2=C1SC1=C2SC(/C=C2C(=O)C3=C(C=C(Cl)C(Cl)=C3)C2=C(C#N)C#N)=C1CCCCCCCCCCC,Y15,-5.56,-3.93,23.79,0.884,0.6849,14.13,"M. Luo, C. Zhu, J. Yuan, L. Zhou, M.L. Keshtov, D.Y. Godovsky, Y. Zou, A chlorinated non-fullerene acceptor for efficient polymer solar cells, Chin. Chem. Lett. 30 (2019) 2343¨C2346. https://doi.org/10.1016/j.cclet.2019.07.023."
3737,O=C(C(C=CC(C)=C1)=C1C/2=C(C#N)/C#N)C2=C/C(S3)=CC4=C3C5=CC6=C(C=C5C4(CCCCCCCC)CCCCCCCC)C7=CC8=C(C(SC(/C=C9C(C(C=C(C)C=C%10)=C%10C9=C(C#N)C#N)=O)=C%11)=C%11C8(CCCCCCCC)CCCCCCCC)C=C7C6(CCCCCCCC)CCCCCCCC,F-M,-5.42,-3.7,11.72,1.71,0.7,14.11,"Y. Zhang, B. Kan, Y. Sun, Y. Wang, R. Xia, X. Ke, Y.-Q.-Q. Yi, C. Li, H.-L. Yip, X. Wan, Y. Cao, Y. Chen, Nonfullerene Tandem Organic Solar Cells with High Performance of 14.11%, Adv. Mater. 30 (2018) 1707508. https://doi.org/10.1002/adma.201707508."
3738,O=C(C(C=C(Cl)C(Cl)=C1)=C1C/2=C(C#N)C#N)C2=C/C(S3)=CC4=C3C5=C(C4(C6=CC=C(CCCCCC)C=C6)C7=CC=C(CCCCCC)C=C7)C8=C(CCCCCCCC)C9=C(C(C(C%10=CC=C(CCCCCC)C=C%10)(C%11=CC=C(CCCCCC)C=C%11)C%12=C%13SC(/C=C%14C(C(C=C(Cl)C(Cl)=C%15)=C%15C\%14=C(C#N)/C#N)=O)=C%12)=C%13S9)C(CCCCCCCC)=C8S5,NCBDT-4CI,-5.6,-4.02,22.35,0.851,0.743,14.1,"B. Kan, H. Feng, H. Yao, M. Chang, X. Wan, C. Li, J. Hou, Y. Chen, A chlorinated low-bandgap small-molecule acceptor for organic solar cells with 14.1% efficiency and low energy loss, Sci. China Chem. 61 (2018) 1307¨C1313. https://doi.org/10.1007/s11426-018-9334-9."
3739,CCCCC(CC)CC1=CC=C(C2(C3=CC=C(CC(CC)CCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(C=C(/C=C5C(=O)C6=C(C=C7C=CC=CC7=C6)C5=C(C#N)C#N)S2)S3)C(C2=CC=C(CC(CC)CCCC)C=C2)(C2=CC=C(CC(CC)CCCC)C=C2)C2=C4SC3=C2SC(/C=C2C(=O)C4=C(C=C5C=CC=CC5=C4)C2=C(C#N)C#N)=C3)C=C1,IDTT8-N,-5.67,-3.98,20.9,0.94,0.72,14.1,"J. Wu, Q. Liu, L. Ye, X. Guo, Q. Fan, J. Lv, M. Zhang, W.-Y. Wong, New Electron Acceptor with End-Extended Conjugation for High-Performance Polymer Solar Cells, Energy Fuels. 35 (2021) 19061¨C19068. https://doi.org/10.1021/acs.energyfuels.1c02470."
3740,O=C(C(C=CC=C1)=C1C/2=C(C#N)/C#N)C2=C/C3=C(CCCCCCCCCCC)C(S4)=C(S3)C5=C4C6=C(N5CC(CC)CCCC)C7=C(C(SC8=C9SC(/C=C%10C(C(C=CC=C%11)=C%11C\%10=C(C#N)C#N)=O)=C8CCCCCCCCCCC)=C9N7CC(CC)CCCC)C%12=NSN=C6%12,Y5,-5.55,-3.87,22.8,0.88,0.702,14.1,"J. Yuan, Y. Zhang, L. Zhou, C. Zhang, T.-K. Lau, G. Zhang, X. Lu, H.-L. Yip, S.K. So, S. Beaupr¨¦, M. Mainville, P.A. Johnson, M. Leclerc, H. Chen, H. Peng, Y. Li, Y. Zou, Fused Benzothiadiazole: A Building Block for n-Type Organic Acceptor to Achieve High-Performance Organic Solar Cells, Adv. Mater. 31 (2019) 1807577. https://doi.org/10.1002/adma.201807577."
3741,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=C(C)C4=C(C(C)=C3C3=C2C2=C(C=C(/C=C5C(=O)C6=CC(F)=C(F)C=C6C5=C(C#N)C#N)S2)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC3=C2SC(/C=C2C(=O)C4=CC(F)=C(F)C=C4C2=C(C#N)C#N)=C3)C=C1,IM-4F,-5.7,-4.11,21.91,0.879,0.731,14.08,"H. Wang, Z. Zhang, J. Yu, X. Liu, W. Tang, High mobility acceptor as third component enabling high-performance large area and thick active layer ternary solar cells, Chem. Eng. J. 418 (2021) 129539. https://doi.org/10.1016/j.cej.2021.129539."
3742,CCCCCCCCCCCCC(CCCCCCCCCC)CC1=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C2=C(SC3=C2SC2=C3C(CC(CCCCCCCCCC)CCCCCCCCCCCC)=C(CC(CCCCCCCCCC)CCCCCCCCCCCC)C3=C2SC(/C=C2C(=O)C4=C(C=CC=C4)C2=C(C#N)C#N)=C3)C2=C1C=C(/C=C1C(=O)C3=CC=CC=C3C1=C(C#N)C#N)S2,DBTBT-IC,-5.77,-3.85,22.78,0.87,0.71,14.07,"M.L. Keshtov, I.O. Konstantinov, S.A. Kuklin, Y. Zou, A. Agrawal, F.C. Chen, G.D. Sharma, Binary and Ternary Polymer Solar Cells Based on a Wide Bandgap D-A Copolymer Donor and Two Nonfullerene Acceptors with Complementary Absorption Spectral, ChemSusChem. 14 (2021) 4731¨C4740. https://doi.org/10.1002/cssc.202101407."
3743,CCCCCCCCCCC(CCCC)COC1=C(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)SC(C2=CC3=C(S2)C2=C(C4=C(C5=NSN=C52)C2=C(C=C(/C=C5C(=O)C6=C(C=C(F)C(F)=C6)C5=C(C#N)C#N)S2)N4CC(CCC)CCCCCCCC)N3CC(CCC)CCCCCCCC)=C1,L2,-5.56,-3.88,24.01,0.82,0.7173,14.06,"Z. Zhang, D. Li, H. Zhang, X. Ma, Y.-N. Chen, A. Zhang, X. Xu, Y. Liu, Z. Ma, Z. Bo, An asymmetric A¨CDA¡äD¨C¦Ð-A type non-fullerene acceptor for high-performance organic solar cells, J. Mater. Chem. C. 10 (2022) 2792¨C2799. https://doi.org/10.1039/D1TC04425G."
3744,O=C(C(C=CC=C1)=C1C/2=C(C#N)C#N)C2=C/C3=CC4=C(C5=CC(C6(CCCCC7=CC=CC=C7)CCCCC8CC=CC=C8)=C(C9=C6C=C(/C=C%10C(C(C=CC=C%11)=C%11C\%10=C(C#N)C#N)=O)S9)C=C5C4(CCCCC%12=CC=CC=C%12)CCCCC%13=CC=CC=C%13)S3,IDICC4Ph,-5.7,-3.93,19.06,0.941,0.7832,14.04,"Y. Li, N. Zheng, L. Yu, S. Wen, C. Gao, M. Sun, R. Yang, A Simple Phenyl Group Introduced at the Tail of Alkyl Side Chains of Small Molecular Acceptors: New Strategy to Balance the Crystallinity of Acceptors and Miscibility of Bulk Heterojunction Enabling Highly Efficient Organic Solar Cells, Adv. Mater. 31 (2019) 1807832. https://doi.org/10.1002/adma.201807832."
3745,CCCCCCCCN1C2=C(SC(/C=C3C(=O)C4=CC(F)=CC=C4C3=C(C#N)C#N)=C2)C2=C1C1=C(S2)C2=C(C=C3C(=C2)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C3SC(/C=C3C(=O)C4=C(C=CC(F)=C4)C3=C(C#N)C#N)=C2)C1(C1=CC=C(CCCCCC)C=C1)C1=CC=C(CCCCCC)C=C1,IPT-2F,-5.51,-3.96,22.4,0.86,0.724,14,"L. Yang, X. Song, J. Yu, H. Wang, Z. Zhang, R. Geng, J. Cao, D. Baran, W. Tang, Tuning of the conformation of asymmetric nonfullerene acceptors for efficient organic solar cells, J. Mater. Chem. A. 7 (2019) 22279¨C22286. https://doi.org/10.1039/C9TA07634D."
3746,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=C(SC(/C=C4C(=O)C5=C(C=C(F)C(F)=C5)C4=C(C#N)C#N)=C3)C3=C2C2=C(S3)C(C3=CC=C(CC(CC)CCCC)C=C3)=C3C(=C2C2=CC=C(CC(CC)CCCC)C=C2)SC2=C3C(C3=CC=C(CCCCCC)C=C3)(C3=CC=C(CCCCCC)C=C3)C3=C2SC(/C=C2C(=O)C4=C(C=C(F)C(F)=C4)C2=C(C#N)C#N)=C3)C=C1,BP-4F,-5.63,-3.9,21.6,0.9,0.72,13.9,"Q. Guo, X. Zhu, X. Dong, Q. Zhu, J. Fang, X. Guo, W. Ma, M. Zhang, Y. Li, A non-fullerene acceptor based on alkylphenyl substituted benzodithiophene for high efficiency polymer solar cells with a small voltage loss and excellent stability, J. Mater. Chem. A. 7 (2019) 24366¨C24373. https://doi.org/10.1039/C9TA08636F."
3747,O=C(C(C=C(F)C(F)=C1)=C1C/2=C(C#N)C#N)C2=C/C(S3)=CC4=C3C5=CC(C(CCCCCCCCCC)(CCCCCCCCCC)C6C7C(CCCCCCCCCC)(CCCCCCCCCC)C8=C6C=C(CC9=C%10SC(/C=C%11C(C(C=C(F)C(F)=C%12)=C%12C\%11=C(C#N)/C#N)=O)=C9)C%10=C8)=C7C=C5C4,ZITI-m,-5.65,-3.81,21.49,0.87,0.73,13.85,"J. Zhang, W. Liu, S. Chen, S. Xu, C. Yang, X. Zhu, One-pot synthesis of electron-acceptor composite enables efficient fullerene-free ternary organic solar cells, J. Mater. Chem. A. 6 (2018) 22519¨C22525. https://doi.org/10.1039/C8TA08961B."
3748,O=C(C(C=C(F)C=C1)=C1C/2=C(C#N)C#N)C2=C/C3=CC4=C(S3)C5=C(C6=CC(C7(C8=CC=C(CCCCCC)C=C8)C9=CC=C(CCCCCC)C=C9)=C(C%10=C7C(SC(/C=C%11C(C(C=C(F)C(F)=C%12)=C%12C\%11=C(C#N)C#N)=O)=C%13)=C%13S%10)C=C6C5(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15)S4,IT-3F,-5.39,-3.37,20.02,0.9,0.733,13.83,"B. Gao, H. Yao, J. Hou, R. Yu, L. Hong, Y. Xu, J. Hou, Multi-component non-fullerene acceptors with tunable bandgap structures for efficient organic solar cells, J. Mater. Chem. A. 6 (2018) 23644¨C23649. https://doi.org/10.1039/C8TA09830A."
3749,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C=C(/C=C2C(=O)C5=C(C=C(F)C(F)=C5)C2=C(C#N)C#N)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC(/C=C3C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)=C2)C=C1,PI-4F,-5.8,-4.06,21.9,0.87,0.72,13.8,"J. Lin, Q. Guo, Q. Liu, J. Lv, H. Liang, Y. Wang, L. Zhu, F. Liu, X. Guo, M. Zhang, A Noncovalently Fused-Ring Asymmetric Electron Acceptor Enables Efficient Organic Solar Cells, Chin. J. Chem. 39 (2021) 2685¨C2691. https://doi.org/10.1002/cjoc.202100323."
3750,CCCCC(CC)COC1=C(C2=CC3=C(S2)C2=C(C=C(/C=C4C(=O)C5=C(C=C(F)C(F)=C5)C4=C(C#N)C#N)S2)C3(CC(CC)CCCC)CC(CC)CCCC)C2=NN(CC(CC)CCCC)N=C2C(C2=CC3=C(S2)C2=C(C=C(/C=C4C(=O)C5=C(C=C(F)C(F)=C5)C4=C(C#N)C#N)S2)C3(CC(CC)CCCC)CC(CC)CCCC)=C1OCC(CC)CCCC,BTzO-4F,-5.45,-3.88,23.58,0.839,0.6973,13.8,"X. Liu, Y. Wei, X. Zhang, L. Qin, Z. Wei, H. Huang, An A-D-A¡ä-D-A type unfused nonfullerene acceptor for organic solar cells with approaching 14% efficiency, Sci. China Chem. 64 (2021) 228¨C231. https://doi.org/10.1007/s11426-020-9868-8."
3751,CCCCCCCCC1=C(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)SC2=C1SC(C1=C(N(C3=CC=C(CCCC)C=C3)C3=CC=C(CCCC)C=C3)C3=C(S1)C(N(C1=CC=C(CCCC)C=C1)C1=CC=C(CCCC)C=C1)=C(C1=CC4=C(S1)C(CCCCCCCC)=C(/C=C1C(=O)C5=C(C=C(F)C(F)=C5)C1=C(C#N)C#N)S4)S3)=C2,2BTH-2F,-5.55,-3.98,23.61,0.9,0.723,13.76,"X. Wang, H. Lu, Y. Liu, A. Zhang, N. Yu, H. Wang, S. Li, Y. Zhou, X. Xu, Z. Tang, Z. Bo, Simple Nonfused Ring Electron Acceptors with 3D Network Packing Structure Boosting the Efficiency of Organic Solar Cells to 15.44%, Adv. Energy Mater. 11 (2021) 2102591. https://doi.org/10.1002/aenm.202102591."
3752,CCCCCCCCOC1=CC=CC(OCCCCCCCC)=C1C1=C(C2=CC=C(/C=C3C(=O)C4=C(C=C5C=C(Cl)C(Cl)=CC5=C4)C3=C(C#N)C#N)S2)SC(C2=CC(OCC(CC)CCCC)=C(C3=CC(C4=C(OCCCCCCCC)C=CC=C4OCCCCCCCC)=C(C4=CC=C(/C=C5C(=O)C6=C(C=C7C=C(Cl)C(Cl)=CC7=C6)C5=C(C#N)C#N)S4)S3)C=C2OCC(CC)CCCC)=C1,,-5.58,-4.09,23.03,0.839,0.7121,13.76,"C. Li, X. Zhang, N. Yu, X. Gu, L. Qin, Y. Wei, X. Liu, J. Zhang, Z. Wei, Z. Tang, Q. Shi, H. Huang, Simple Nonfused-Ring Electron Acceptors with Noncovalently Conformational Locks for Low-Cost and High-Performance Organic Solar Cells Enabled by End-Group Engineering, Adv. Funct. Mater. 32 (2022) 2108861. https://doi.org/10.1002/adfm.202108861."
3753,CCCCCCCCOC1=CC=CC(OCCCCCCCC)=C1C1=C(C2=CC=C(/C=C3/C(=O)C4=C(C=C5C=C(Cl)C(Cl)=CC5=C4)C3=C(C#N)C#N)S2)SC(C2=CC(OCC(CC)CCCC)=C(C3=CC(C4=C(OCCCCCCCC)C=CC=C4OCCCCCCCC)=C(C4=CC=C(/C=C5/C(=O)C6=CC7=C(C=CC(Cl)=C7)C=C6C5=C(C#N)C#N)S4)S3)C=C2OCC(CC)CCCC)=C1,PhO4T-3,-5.58,-4.09,23.03,0.839,0.7121,13.76,"C. Li, X. Zhang, N. Yu, X. Gu, L. Qin, Y. Wei, X. Liu, J. Zhang, Z. Wei, Z. Tang, Q. Shi, H. Huang, Simple Nonfused-Ring Electron Acceptors with Noncovalently Conformational Locks for Low-Cost and High-Performance Organic Solar Cells Enabled by End-Group Engineering, Adv. Funct. Mater. 32 (2022) 2108861. https://doi.org/10.1002/adfm.202108861."
3754,CCCCCCCCCCC(CCCC)CN1C2=C(SC3=C2CC(/C=C2C(=O)C4=C(C=C(F)C(F)=C4)C2=C(C#N)C#N)=C3CCCCCC)C2=C1C1=C(C3=NSN=C32)C2=C(C3=C(S2)C(CCCCCC)=C(/C=C2C(=O)C4=C(C=C(F)C(F)=C4)C2=C(C#N)C#N)S3)N1CC(CCC)CCCCCCCCCC,Y6-eC6-HD,-5.61,-3.94,21.17,0.87,0.7446,13.74,"Y. Qi, H. Chen, X. Wang, Q. Wei, D. Li, Y. Li, L. Jiang, G. Chen, Y. Zou, Modifying side chain of non-fullerene acceptors to obtain efficient organic solar cells with high fill factor, Chem. Phys. 546 (2021) 111172. https://doi.org/10.1016/j.chemphys.2021.111172."
3755,N#CC(C#N)=C1C2=C(C=CC=C2)C(=O)/C1=CC1=CC2=C(S1)C1=CC3=C(C=C1C2(CCCCC1=CC=CC=C1)CCCCC1=CC=CC=C1)C1=C(C=C(/C=C2C(=O)C4=C(C=CC=C4)C2=C(C#N)C#N)S1)C3(CCCCC1=CC=CC=C1)CCCCC1=CC=CC=C1,IDIC-C4Ph,-5.7,-3.93,19.06,0.941,0.7832,13.72,"Y. Li, N. Zheng, L. Yu, S. Wen, C. Gao, M. Sun, R. Yang, A Simple Phenyl Group Introduced at the Tail of Alkyl Side Chains of Small Molecular Acceptors: New Strategy to Balance the Crystallinity of Acceptors and Miscibility of Bulk Heterojunction Enabling Highly Efficient Organic Solar Cells, Adv. Mater. 31 (2019) 1807832. https://doi.org/10.1002/adma.201807832."
3756,CCCCCCC1=CC=C2C(=C1)C1=C(C=CC(CCCCCC)=C1)C21C2=CC3=C(C=C2C2=C1C=C(C1=C(SCC(CC)CCCC)C(/C=C4C(=O)C5=C(C=C(F)C(F)=C5)C4=C(C#N)C#N)=CS1)S2)C1(C2=CC=C(CCCCCC)C=C2C2=C1C=CC(CCCCCC)=C2)C1=C3SC(C2=C(SCC(CC)CCCC)C(/C=C3C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)=CS2)=C1,IE4F-S,-5.54,-3.89,22.88,0.868,0.691,13.72,"Y. Zou, Y. Dong, C. Sun, Y. Wu, H. Yang, C. Cui, Y. Li, High-Performance Polymer Solar Cells with Minimal Energy Loss Enabled by a Main-Chain-Twisted Nonfullerene Acceptor, Chem. Mater. 31 (2019) 4222¨C4227. https://doi.org/10.1021/acs.chemmater.9b01175."
3757,O=C(C(C=C(F)C(F)=C1)=C1C/2=C(C#N)C#N)C2=C/C3=CC4=C(S3)C5=C(C6=CC(C7(C8=CC=C(CCCCCC)C=C8)C9=CC=C(CCCCCC)C=C9)=C(C%10=C7C(SC(/C=C%11C(C(C=C(F)C(F)=C%12)=C%12C\%11=C(C#N)C#N)=O)=C%13)=C%13S%10)C=C6C5(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15)S4,IT-4F,-5.67,-4.15,20.38,0.87,0.77,13.7,"W. Zhao, S. Li, H. Yao, S. Zhang, Y. Zhang, B. Yang, J. Hou, Molecular Optimization Enables over 13% Efficiency in Organic Solar Cells, J. Am. Chem. Soc. 139 (2017) 7148¨C7151. https://doi.org/10.1021/jacs.7b02677."
3758,CCCCCCCCC1=CC=C(C2(C3=CC=C(CCCCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(S3)C3=C(C=C(/C=C5C(=O)C6=C(C=C(F)C(F)=C6)C5=C(C#N)C#N)S3)S2)C(C2=CC=C(CCCCCCCC)C=C2)(C2=CC=C(CCCCCCCC)C=C2)C2=C4SC3=C2SC2=C3SC(/C=C3C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)=C2)C=C1,3TP3T-4F,-5.66,-4.02,20.3,0.92,0.739,13.7,"J. Song, C. Li, L. Zhu, J. Guo, J. Xu, X. Zhang, K. Weng, K. Zhang, J. Min, X. Hao, Y. Zhang, F. Liu, Y. Sun, Ternary Organic Solar Cells with Efficiency >16.5% Based on Two Compatible Nonfullerene Acceptors, Adv. Mater. 31 (2019) 1905645. https://doi.org/10.1002/adma.201905645."
3759,CCCCCCCCCCCC1=C(/C=C2C(=O)C3=C(C=C(F)C(Br)=C3)C2=C(C#N)C#N)SC2=C1SC1=C2N(CC(CCCC)CCCCCC)C2=C1C1=NSN=C1C1=C2N(CC(CCCC)CCCCCC)C2=C1SC1=C2SC(/C=C2C(=O)C3=C(C=C(Cl)C(Br)=C3)C2=C(C#N)C#N)=C1CCCCCCCCCCC.F,Y-BO-ClBr,-5.72,-4.02,22.09,0.86,0.7162,13.61,"L. Wang, Q. An, L. Yan, H.-R. Bai, M. Jiang, A. Mahmood, C. Yang, H. Zhi, J.-L. Wang, Non-fullerene acceptors with hetero-dihalogenated terminals induce significant difference in single crystallography and enable binary organic solar cells with 17.5% efficiency, Energy Environ. Sci. 15 (2022) 320¨C333. https://doi.org/10.1039/D1EE01832A."
3760,CCCCCCCCCCCC1=C(/C=C2C(=O)C3=C(C=CC(F)=C3)C2=C(C#N)C#N)SC2=C1SC1=C2N(CC(CC)CCCC)C2=C1C1=NSN=C1C1=C2N(CC(CC)CCCC)C2=C1SC1=C2SC(/C=C2C(=O)C3=C(C=CC(F)=C3)C2=C(C#N)C#N)=C1CCCCCCCCCCC,BTIC-F,-5.42,-3.9,21.41,0.92,0.6909,13.61,"H. Lai, Q. Zhao, Z. Chen, H. Chen, P. Chao, Y. Zhu, Y. Lang, N. Zhen, D. Mo, Y. Zhang, F. He, Trifluoromethylation Enables a 3D Interpenetrated Low-Band-Gap Acceptor for Efficient Organic Solar Cells, Joule. 4 (2020) 688¨C700. https://doi.org/10.1016/j.joule.2020.02.004."
3761,O=C(C(C=CC=C1)=C1C/2=C(C#N)C#N)C2=C/C(S3)=CC4=C3C5=C(C4(C6=CC=C(CCCCCC)C=C6)C7=CC=C(CCCCCC)C=C7)C8=CC9=C(C(C(C%10=CC=C(CCCCCC)C=C%10)(C%11=CC=C(CCCCCC)C=C%11)C%12=C%13SC(/C=C%14C(C(C=CC=C%15)=C%15C\%14=C(C#N)/C#N)=O)=C%12)C%13S9)C=C8S5,IDCIC,-5.19,-3.72,21.98,0.87,0.7103,13.58,"D. He, F. Zhao, J. Xin, J.J. Rech, Z. Wei, W. Ma, W. You, B. Li, L. Jiang, Y. Li, C. Wang, A Fused Ring Electron Acceptor with Decacyclic Core Enables over 13.5% Efficiency for Organic Solar Cells, Adv. Energy Mater. 8 (2018) 1802050. https://doi.org/10.1002/aenm.201802050."
3762,CCCCCCCCC(CCCCCCCC)COC1=CC(C2=CC3=C(S2)C2=C(C=C(/C=C4C(=O)C5=C(C=C(Cl)C(Cl)=C5)C4=C(C#N)C#N)S2)N3C(CCCCCCCC)CCCCCCCC)=C(OCC(CCCCCCCC)CCCCCCCC)C=C1C1=CC(CCCCCC)=C(/C=C2C(=O)C3=CC(Cl)=C(Cl)C=C3C2=C(C#N)C#N)S1,DBT-HD,-5.63,-3.95,21.75,0.85,0.7339,13.54,"J. Cao, H. Wang, L. Yang, F. Du, J. Yu, W. Tang, Chlorinated unfused acceptor enabling 13.57% efficiency and 73.39% fill factor organic solar cells via fine-tuning alkoxyl chains on benzene core, Chem. Eng. J. 427 (2022) 131828. https://doi.org/10.1016/j.cej.2021.131828."
3763,CCCCCCCCCCCC1=C(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)SC2=C1SC1=C2N(CCCCCCCC)C2=C1C1N=C(C3=CC=C(C(F)(F)F)C=C3)C(C3=CC=C(C(F)(F)F)C=C3)=NC1C1=C2N(CCCCCCCC)C2=C1SC1=C2SC(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)=C1CCCCCCCCCCC,TFQ-F,-5.67,-3.91,23.7,0.857,0.665,13.51,"B. Sun, Y. Chen, Y. Huang, Y. Li, J. Fan, Fused-ring acceptors based on quinoxaline unit for highly efficient single-junction organic solar cells with low charge recombination, Org. Electron. 98 (2021) 106282. https://doi.org/10.1016/j.orgel.2021.106282."
3764,O=C(C(C=C(Cl)C(Cl)=C1)=C1C/2=C(C#N)C#N)C2=C/C3=CC4=C(S3)C5=C(C6=CC(C7(C8=CC=C(CCCCCC)C=C8)C9=CC=C(CCCCCC)C=C9)=C(C%10=C7C(SC(/C=C%11C(C(C=C(Cl)C(Cl)=C%12)=C%12C\%11=C(C#N)C#N)=O)=C%13)=C%13S%10)C=C6C5(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15)S4,ITIC-4CI,-5.75,-4.09,22.67,0.79,0.752,13.45,"H. Zhang, H. Yao, J. Hou, J. Zhu, J. Zhang, W. Li, R. Yu, B. Gao, S. Zhang, J. Hou, Over 14% Efficiency in Organic Solar Cells Enabled by Chlorinated Nonfullerene Small-Molecule Acceptors, Adv. Mater. 30 (2018) 1800613. https://doi.org/10.1002/adma.201800613."
3765,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=C(SC(/C=C4C(=O)C5=C(C)SC=C5C4=C(C#N)C#N)=C3)C3=C2C2=C(S3)C(C3=CC4=C(C=C(CC(CC)CCCC)S4)S3)=C3C(=C2C2=CC4=C(C=C(CC(CC)CCCC)S4)S2)SC2=C3C(C3=CC=C(CCCCCC)C=C3)(C3=CC=C(CCCCCC)C=C3)C3=C2SC(/C=C2C(=O)C4=C(C)SC=C4C2=C(C#N)C#N)=C3)C=C1,BTTIC-TT,-5.54,-3.9,19.61,0.924,0.742,13.44,"T. Liu, W. Gao, Y. Wang, T. Yang, R. Ma, G. Zhang, C. Zhong, W. Ma, H. Yan, C. Yang, Unconjugated Side-Chain Engineering Enables Small Molecular Acceptors for Highly Efficient Non-Fullerene Organic Solar Cells: Insights into the Fine-Tuning of Acceptor Properties and Micromorphology, Adv. Funct. Mater. 29 (2019) 1902155. https://doi.org/10.1002/adfm.201902155."
3766,CCC1(CC)C2=C(C=CC(/C=C/C3=CC(C)=C(/C(C4=C(C)C=C(C)C=C4C)=C4N=C(/C=C/C5=CC=C(N(C)C)C=C5)C=C4C)N3B(F)F)=C2)C2=C1C1=C(C3=C2C(CC)(CC)C2=C3C=CC(/C=C/C3=CC(C)=C(/C(C4=C(C)C=C(C)C=C4C)=C4N=C(/C=C/C5=CC=C(N(C)C)C=C5)C=C4C)N3B(F)F)=C2)C(CC)(CC)C2=C1C=CC(/C=C/C1=CC(C)=C(/C(C3=C(C)C=C(C)C=C3C)=C3N=C(/C=C/C4=CC=C(N(C)C)C=C4)C=C3C)N1B(F)F)=C2,3a,-5.4,-3.96,19.92,1.02,0.66,13.41,"P. Li, F. Wu, Y. Fang, H. Dahiya, M.L. Keshtov, H. Xu, A. Agrawal, G.D. Sharma, Truxene ¦Ð-Expanded BODIPY Star-Shaped Molecules as Acceptors for Non-Fullerene Solar Cells with over 13% Efficiency, ACS Appl. Energy Mater. (2022). https://doi.org/10.1021/acsaem.1c03781."
3767,O=C(C(C=C(Cl)C(Cl)=C1)=C1C/2=C(C#N)C#N)C2=C/C(S3)=CC4=C3C5=C(N4CC(CCCC)CCCCCC)C6=C(C7=CC(C8(C9=CC=C(CCCCCC)C=C9)C%10=CC=C(CCCCCC)C=C%10)=C(C%11=C8C(N(CC(CCCC)CCCCCC)C%12=C%13SC(/C=C%14C(C(C=C(Cl)C(Cl)=C%15)=C%15C\%14=C(C#N)/C#N)=O)=C%12)=C%13S%11)C=C7C6(C%16=CC=C(CCCCCC)C=C%16)C%17=CC=C(CCCCCC)C=C%17)S5,IPIC-4CL,-5.51,-3.95,22.2,0.813,0.74,13.4,"R. Geng, X. Song, H. Feng, J. Yu, M. Zhang, N. Gasparini, Z. Zhang, F. Liu, D. Baran, W. Tang, Nonfullerene Acceptor for Organic Solar Cells with Chlorination on Dithieno[3,2-b:2¡ä,3¡ä-d]pyrrol Fused-Ring, ACS Energy Lett. 4 (2019) 763¨C770. https://doi.org/10.1021/acsenergylett.9b00147."
3768,CCCCCCOC1=CC=C(C2(C3=CC=C(OCCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(C=C(/C=C5/C(=O)C6=C(C=C(F)C(F)=C6)C5=C(C#N)C#N)S2)S3)C(C2=CC=C(OCCCCCC)C=C2)(C2=CC=C(OCCCCCC)C=C2)C2=C4SC3=C2SC(/C=C2/C(=O)C4=C(C=CC(F)=C4)C2=C(C#N)C#N)=C3)C=C1,POIT-IC4F,-5.65,-4.07,20.9,0.91,0.726,13.4,"Q. Fan, W. Su, M. Zhang, J. Wu, Y. Jiang, X. Guo, F. Liu, T.P. Russell, M. Zhang, Y. Li, Synergistic Effects of Side-Chain Engineering and Fluorination on Small Molecule Acceptors to Simultaneously Broaden Spectral Response and Minimize Voltage Loss for 13.8% Efficiency Organic Solar Cells, Sol. RRL. 3 (2019) 1900169. https://doi.org/10.1002/solr.201900169."
3769,CCCCCCOC1=CC=C(C2(C3=CC=C(OCCCCCC)C=C3)C3=C(SC(CC4C(=O)C5=C(C=C(F)C(F)=C5)C4=C(C#N)C#N)=C3)C3=C2C2=C(OCCCCCC)C=C4C(=C2S3)C=C(OCCCCCC)C2=C4SC3=C2C(C2=CC=C(OCCCCCC)C=C2)(C2=CC=C(OCCCCCC)C=C2)C2=C3SC(/C=C3C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)=C2)C=C1,IOIC5,-5.65,-4.19,20.5,0.922,0.705,13.4,"J. Zhu, Y. Xiao, C. Zhang, B. Jia, H. Lu, J. Wang, X. Lu, Z. Li, X. Zhan, Effects of alkoxylation position on fused-ring electron acceptors, J. Mater. Chem. C. 8 (2020) 15128¨C15134. https://doi.org/10.1039/D0TC02158J."
3770,O=C1C2=CSC=C2C(/C1=C/C(S3)=CC4=C3C(N5CC(CC)CCCC)=C(S4)C6=C5C(N(CC(CC)CCCC)C7=C8SC9=C7SC(/C=C%10/C(C%11=CSC=C%11C%10=O)=C(C#N)C#N)=C9)=C8C%12=NN(CC(CC)CCCC)N=C6%12)=C(C#N)/C#N,Y2,-5.43,-4.04,23.56,0.82,0.694,13.4,"J. Yuan, T. Huang, P. Cheng, Y. Zou, H. Zhang, J.L. Yang, S.-Y. Chang, Z. Zhang, W. Huang, R. Wang, D. Meng, F. Gao, Y. Yang, Enabling low voltage losses and high photocurrent in fullerene-free organic photovoltaics, Nat. Commun. 10 (2019) 570. https://doi.org/10.1038/s41467-019-08386-9."
3771,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=C(SC(/C=C4C(=O)C5=C(C=C(F)C(F)=C5)C4=C(C#N)C#N)=C3)C3=C2C2=C(O3)C(C3=CC=C(CC(CC)CCCC)S3)=C3C(=C2C2=CC=C(CC(CC)CCCC)S2)OC2=C3C(C3=CC=C(CCCCCC)C=C3)(C3=CC=C(CCCCCC)C=C3)C3=C2SC(/C=C2C(=O)C4=C(C=CC(F)=C4)C2=C(C#N)C#N)=C3)C=C1,BFHIC-4F,-5.63,-3.99,22.8,0.87,0.677,13.4,"K. Wang, J. Chen, J. Hu, X. Guo, M. Zhang, Y. Li, A small molecule acceptor with a heptacyclic benzodi(thienocyclopentafuran) central unit achieving 13.4% efficiency in polymer solar cells with low energy loss, J. Mater. Chem. C. 9 (2021) 2744¨C2751. https://doi.org/10.1039/D0TC05539E."
3772,CCCCCCC1=CC=C(CC2(CC3=CC=CC=C3)C3=CC4=C(C=C3C3=C2C2=C(C=C(/C=C5C(=O)C6=C(C=C(F)C(F)=C6)C5=C(C#N)C#N)S2)S3)C(CC2=CC=C(CCCCCC)C=C2)(CC2=CC=C(CCCCCC)C=C2)C2=C4SC3=C2SC(/C=C2C(=O)C4=C(C=C(F)C(F)=C4)C2=C(C#N)C#N)=C3)C=C1,IT-BnC6-4F,-5.7,-4.16,20.99,0.87,0.729,13.36,"Y. Man, L. Ye, Y. Cai, X. Sun, Y. Sun, Benzyl side-chain engineering of non-fullerene acceptors for efficient organic solar cells, Dyes Pigments. 195 (2021) 109706. https://doi.org/10.1016/j.dyepig.2021.109706."
3773,CCCCCCCCC1=CC=C(C2(C3=CC=C(CCCCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(S3)C(CCCCCCCC)=C(/C=C3C(=O)C5=C(C=C(F)C(F)=C5)C3=C(C#N)C#N)S2)N(C(CCCCCCCC)CCCCCCCC)C2=C4C=C3C(=C2)C2=C(C4=C(S2)C(CCCCCCCC)=C(/C=C2C(=O)C5=C(C=C(F)C(F)=C5)C2=C(C#N)C#N)S4)C3(C2=CC=C(CCCCCCCC)C=C2)C2=CC=C(CCCCCCCC)C=C2)C=C1,DTTC-4F-C8,-5.63,-3.9,19.19,0.98,0.7079,13.36,"V.K. Karapala, T.-W. Chen, K.-J. Ma, P.-L. Lu, Y.-J. Su, W.-D. Fu, H.-M. Shih, S.-J. Lu, T.-Y. Lee, C.-F. Chang, J.-T. Chen, C.-S. Hsu, Exploring Ternary Organic Solar Cells for the Improved Efficiency of 16.5% with the Compatible Nonacyclic Carbazole-Based Nonfullerene Acceptors as the Third Component, ACS Appl. Energy Mater. 4 (2021) 2847¨C2855. https://doi.org/10.1021/acsaem.1c00149."
3774,CCCCCCCCCCCC1=C(/C=C2C(=O)C3=C(C=CC(F)=C3)C2=C(C#N)C#N)SC2=C1SC1=C2N(CC(CC)CCCC)C2=C1C1=NSN=C1C1=C2N(CC(CC)CCCC)C2=C1SC1=C2SC(/C=C2C(=O)C3=C(C=C(F)C=C3)C2=C(C#N)C#N)=C1CCCCCCCCCCC,Z5,-5.67,-4.09,24.25,0.89,0.6188,13.36,"M. Zhang, M. Zeng, L. Ye, S. Tan, B. Zhao, H.S. Ryu, H.Y. Woo, Y. Sun, Effects of monohalogenated terminal units of non-fullerene acceptors on molecular aggregation and photovoltaic performance, Sol. Energy. 208 (2020) 866¨C872. https://doi.org/10.1016/j.solener.2020.07.100."
3775,CCCCC(CC)CN1C(=O)C2=C(C3=CC4=C(S3)C3=C(C=C(/C=C5C(=O)C6=C(C=C(F)C(F)=C6)C5=C(C#N)C#N)S3)C4(CC(CC)CCCC)CC(CC)CCCC)SC(C3=CC4=C(S3)C3=C(C=C(/C=C5C(=O)C6=C(C=C(F)C(F)=C6)C5=C(C#N)C#N)S3)C4(CC(CC)CCCC)CC(CC)CCCC)=C2C1=O,TPDC-4F,-5.83,-3.99,22.19,0.852,0.706,13.35,"D. Luo, L. Li, Y. Shi, J. Zhang, K. Wang, X. Guo, A.K.K. Kyaw, Electron-deficient diketone unit engineering for non-fused ring acceptors enabling over 13% efficiency in organic solar cells, J. Mater. Chem. A. 9 (2021) 14948¨C14957. https://doi.org/10.1039/D1TA03643B."
3776,O=C(C(C=C(Cl)C(Cl)=C1)=C1C/2=C(C#N)/C#N)C2=C/C3=CC4=C(S3)C5=C(C6=C(C5(C7=CC=C(CCCCCC)C=C7)C8=CC=C(CCCCCC)C=C8)C=C(C9=C%10C(SC(/C=C%11C(C(C=C(Cl)C(Cl)=C%12)=C%12C\%11=C(C#N)C#N)=O)=C%13)=C%13[Se]9)C(C%10(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15)=C6)[Se]4,SeTIC4CI,-5.65,-4.08,22.92,0.78,0.75,13.32,"J.-L. Wang, K.-K. Liu, L. Hong, G.-Y. Ge, C. Zhang, J. Hou, Selenopheno[3,2-b]thiophene-Based Narrow-Bandgap Nonfullerene Acceptor Enabling 13.3% Efficiency for Organic Solar Cells with Thickness-Insensitive Feature, ACS Energy Lett. 3 (2018) 2967¨C2976. https://doi.org/10.1021/acsenergylett.8b01808."
3777,CCCCCCC1=C(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)SC2=C1N(CC(CC)CCCC)C1=C2C2=NN(CC(CC)CCCC)N=C2C2=C1N(CC(CC)CCCC)C1=C2SC(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)=C1CCCCCC,Y26,-5.58,-4.03,21.42,0.86,0.723,13.32,"J. Song, F. Cai, C. Zhu, H. Chen, Q. Wei, D. Li, C. Zhang, R. Zhang, J. Yuan, H. Peng, S.K. So, Y. Zou, Over 13% Efficient Organic Solar Cells Based on Low-Cost Pentacyclic A-DA¡äD-A-Type Nonfullerene Acceptor, Sol. RRL. 5 (2021) 2100281. https://doi.org/10.1002/solr.202100281."
3778,CCCCCCCCCCCC1=C(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)SC2=C1SC1=C2N(CC(CC)CCCC)C2=C1C1=NC(C)=C(C)N=C1C1=C2N(CC(CC)CCCC)C2=C1SC1=C2SC(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)=C1CCCCCCCCCCC,AQx-1,-5.59,-3.85,22.18,0.89,0.6714,13.31,"Z. Zhou, W. Liu, G. Zhou, M. Zhang, D. Qian, J. Zhang, S. Chen, S. Xu, C. Yang, F. Gao, H. Zhu, F. Liu, X. Zhu, Subtle Molecular Tailoring Induces Significant Morphology Optimization Enabling over 16% Efficiency Organic Solar Cells with Efficient Charge Generation, Adv. Mater. 32 (2020) 1906324. https://doi.org/10.1002/adma.201906324."
3779,CCCCCCCCC1(CCCCCCCC)OC2=C(SC(/C=C3C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)=C2)C2=CC3=C(C=C21)C1=C(C=C2C(=C1)C(CCCCCCCC)(CCCCCCCC)OC1=C2SC(/C=C2C(=O)C4=C(C=C(F)C(F)=C4)C2=C(C#N)C#N)=C1)C3(CCCCCCCC)CCCCCCCC,FCO-2F,-5.37,-3.78,20.9,0.884,0.723,13.3,"X. Ke, L. Meng, X. Wan, Y. Sun, Z. Guo, S. Wu, H. Zhang, C. Li, Y. Chen, An oxygen heterocycle-fused fluorene based non-fullerene acceptor for high efficiency organic solar cells, Mater. Chem. Front. 4 (2020) 3594¨C3601. https://doi.org/10.1039/D0QM00287A."
3780,CCCCCCCCCCCC1=C(/C=C2C(=O)C3=C(C=C(Cl)C(Cl)=C3)C2=C(C#N)C#N)SC2=C1OC1=C2N(CC(CC)CCCC)C2=C1C1=C(N=C3C(=O)N(CC(CC)CCCC)C(=O)C3=N1)C1=C2N(CC(CC)CCCC)C2=C1SC1=C2SC(/C=C2C(=O)C3=C(C=C(Cl)C(Cl)=C3)C2=C(C#N)C#N)=C1CCCCCCCCCCC,QIP-4Cl,-5.77,-3.89,19.62,0.94,0.7211,13.3,"C. Zhu, K. An, W. Zhong, Z. Li, Y. Qian, X. Su, L. Ying, Design and synthesis of non-fullerene acceptors based on a quinoxalineimide moiety as the central building block for organic solar cells, Chem. Commun. 56 (2020) 4700¨C4703. https://doi.org/10.1039/D0CC00896F."
3781,CCCCC(C)CC1(CC(CC)CCCC)C2=C(SC(/C=C3C(=O)C4=C(C=CC=C4)C3=C(C#N)C#N)=C2)C2=C1C=C(C1=C3C(=O)N(CC(CC)CCCC)C(=O)C3=C(C3=CC4=C(S3)C3=C(C=C(/C=C5C(=O)C6=C(C=CC=C6)C5=C(C#N)C#N)S3)C4(CC(CC)CCCC)CC(CC)CCCC)S1)S2,TPDC-4F,-5.83,-3.99,22.19,0.852,0.706,13.3,"D. Luo, L. Li, Y. Shi, J. Zhang, K. Wang, X. Guo, A.K.K. Kyaw, Electron-deficient diketone unit engineering for non-fused ring acceptors enabling over 13% efficiency in organic solar cells, J. Mater. Chem. A. 9 (2021) 14948¨C14957. https://doi.org/10.1039/D1TA03643B."
3782,CCCCCCCCCCCC1=C(/C=C2C(=O)C3=C(C=C(Cl)C(Cl)=C3)C2=C(C#N)C#N)SC2=C1SC1=C2N(CCCCCCCC)C2=C1C1N=C(C3=CC=C(C(F)(F)F)C=C3)C(C3=CC=C(C(F)(F)F)C=C3)=NC1C1=C2N(CCCCCCCC)C2=C1SC1=C2SC(/C=C2C(=O)C3=C(C=C(Cl)C(Cl)=C3)C2=C(C#N)C#N)=C1CCCCCCCCCCC,TFQ-Cl,-5.64,-4.11,25.1,0.837,0.6299,13.28,"B. Sun, Y. Chen, Y. Huang, Y. Li, J. Fan, Fused-ring acceptors based on quinoxaline unit for highly efficient single-junction organic solar cells with low charge recombination, Org. Electron. 98 (2021) 106282. https://doi.org/10.1016/j.orgel.2021.106282."
3783,O=C(C(C=C(F)C(F)=C1)=C1C/2=C(C#N)C#N)C2=C/C3=CC=C(C4=CC(C5(C6=CC=C(CCCCCC)C=C6)C7=CC=C(CCCCCC)C=C7)=C(S4)C8=C(OCCCCCC)C=C9C%10=C(C(SC(C%11=CC=C(/C=C%12C(C(C=C(F)C(F)=C%13)=C%13C\%12=C(C#N)/C#N)=O)S%11)=C%14)=C%14C9(C%15=CC=C(CCCCCC)C=C%15)C%16=CC=C(CCCCCC)C=C%16)C(OCCCCCC)=CC5=C%108)S3.C,AT-4CI,-5.71,-3.89,19.52,0.90196,0.755,13.27,"H. Feng, Y.-Q.-Q. Yi, X. Ke, J. Yan, Y. Zhang, X. Wan, C. Li, N. Zheng, Z. Xie, Y. Chen, New Anthracene-Fused Nonfullerene Acceptors for High-Efficiency Organic Solar Cells: Energy Level Modulations Enabling Match of Donor and Acceptor, Adv. Energy Mater. 9 (2019) 1803541. https://doi.org/10.1002/aenm.201803541."
3784,CCCCC(CC)COC1=CC(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)=C(OCC(CC)CCCC)C=C1C1=CC2=C(S1)C1SC(C3=CC(OCC(CC)CCCC)=C(/C=C4C(=O)C5=C(C=C(F)C(F)=C5)C4=C(C#N)C#N)C=C3OCC(CC)CCCC)=CC1C2(CC(CC)CCCC)CC(CC)CCCC,DTC-BO-4F,-5.59,-3.83,22.77,0.83,0.7022,13.26,"Y. Zhou, M. Li, N. Yu, S. Shen, J. Song, Z. Ma, Z. Bo, Simple Tricyclic-Based A-¦Ð-D-¦Ð-A-Type Nonfullerene Acceptors for High-Efficiency Organic Solar Cells, ACS Appl. Mater. Interfaces. 14 (2022) 6039¨C6047. https://doi.org/10.1021/acsami.1c22520."
3785,O=C(C(C=C(F)C(C)=C1)=C1C/2=C(C#N)C#N)C2=C/C3=CC4=C(S3)C5=C(C6=CC(C7(C8=CC=C(CCCCCC)C=C8)C9=CC=C(CCCCCC)C=C9)=C(C%10=C7C(SC(/C=C%11C(C(C=C(F)C(C)=C%12)=C%12C\%11=C(C#N)C#N)=O)=C%13)=C%13S%10)C=C6C5(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15)S4,ITCF1:1,-5.59,-3.95,18.48,0.91,0.788,13.25,"M. Hao, T. Liu, Y. Xiao, L.-K. Ma, G. Zhang, C. Zhong, Z. Chen, Z. Luo, X. Lu, H. Yan, L. Wang, C. Yang, Achieving Balanced Charge Transport and Favorable Blend Morphology in Non-Fullerene Solar Cells via Acceptor End Group Modification, Chem. Mater. 31 (2019) 1752¨C1760. https://doi.org/10.1021/acs.chemmater.8b05327."
3786,CCCCCCCCCCCC1=C(/C=C2C(=O)C3=CC(C(=O)OC)=CC=C3C2=C(C#N)C#N)SC2=C1SC1=C2N(CC(CC)CCCC)C2=C1C1=NSN=C1C1=C2N(CC(CC)CCCC)C2=C1SC1=C2SC(/C=C2C(=O)C3=CC=C(C(=O)OC)C=C3C2=C(C#N)C#N)=C1CCCCCCCCCCC,BTIC-COOMe,,,22.13,0.9,0.6671,13.25,"H. Lai, L. Liu, N. Zheng, L. Han, F. He, Push or Pull Electrons: Acetoxy and Carbomethoxy-Substituted Isomerisms in Organic Solar Cell Acceptors, J. Phys. Chem. Lett. 12 (2021) 4666¨C4673. https://doi.org/10.1021/acs.jpclett.1c01077."
3787,CCCCC(CC)COC1=CC(C2=CC3=C(S2)C2=C(C=C(/C=C4C(=O)C5=C(C=C(F)C=C5)C4=C(C#N)C#N)S2)C3(CC(CC)CCCC)CC(CC)CCCC)=C(OCC(CC)CCCC)C=C1C1=CC2=C(S1)C1=C(C=C(/C=C3C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)S1)C2(CC(CC)CCCC)CC(CC)CCCC.F,DOC2C6-2F,,,21.35,0.85,0.7315,13.24,"H. Huang, Q. Guo, S. Feng, C. Zhang, Z. Bi, W. Xue, J. Yang, J. Song, C. Li, X. Xu, Z. Tang, W. Ma, Z. Bo, Noncovalently fused-ring electron acceptors with near-infrared absorption for high-performance organic solar cells, Nat. Commun. 10 (2019) 3038. https://doi.org/10.1038/s41467-019-11001-6."
3788,CCCCC(CC)COC1=CC(C2=CC3=C(S2)C2=C(C=C(/C=C4C(=O)C5=CC(F)=C(F)C=C5C4=C(C#N)C#N)S2)C3(CC(CC)CCCC)CC(CC)CCCC)=C(OCC(CC)CCCC)C=C1C1=CC2=C(S1)C1=C(C=C(/C=C3C(=O)C4=CC(F)=C(F)C=C4C3=C(C#N)C#N)S1)C2(CC(CC)CCCC)CC(CC)CCCC,DOC2C6-2F,-5.49,-3.83,21.35,0.85,0.731,13.24,"H. Huang, Q. Guo, S. Feng, C. Zhang, Z. Bi, W. Xue, J. Yang, J. Song, C. Li, X. Xu, Z. Tang, W. Ma, Z. Bo, Noncovalently fused-ring electron acceptors with near-infrared absorption for high-performance organic solar cells, Nat. Commun. 10 (2019) 3038. https://doi.org/10.1038/s41467-019-11001-6."
3789,CCCCC(CC)COC1=C(C2=CC3=C(S2)C2=C(C=C(/C=C4C(=O)C5=CC=CC=C5C4=C(C#N)C#N)S2)C3(CC(CC)CCCC)CC(CC)CCCC)C2=NN(CC(CC)CCCC)N=C2C(C2=CC3=C(S2)C2=C(C=C(/C=C4C(=O)C5=CC=CC=C5C4=C(C#N)C#N)S2)C3(CC(CC)CCCC)CC(CC)CCCC)=C1OCC(CC)CCCC,NOCA-5,-5.43,-3.83,21.35,0.85,0.731,13.24,"X. Zhang, C. Li, L. Qin, H. Chen, J. Yu, Y. Wei, X. Liu, J. Zhang, Z. Wei, F. Gao, Q. Peng, H. Huang, Side-Chain Engineering for Enhancing the Molecular Rigidity and Photovoltaic Performance of Noncovalently Fused-Ring Electron Acceptors, Angew. Chem. Int. Ed. 60 (2021) 17720¨C17725. https://doi.org/10.1002/anie.202106753."
3790,O=C(C(C=CC(F)=C1)=C1C/2=C(C#N)C#N)C2=C/C(S3)=CC4=C3C5=CC(C(CCCCCCCCCC)(CCCCCCCCCC)C6C7C(CCCCCCCCCC)(CCCCCCCCCC)C8=C6C=C(CC9=C%10SC(/C=C%11C(C(C=CC(F)=C%12)=C%12C\%11=C(C#N)/C#N)=O)=C9)C%10=C8)=C7C=C5C4,ZITI,-5.59,-3.74,20.37,0.93,0.69,13.24,"W. Liu, J. Zhang, Z. Zhou, D. Zhang, Y. Zhang, S. Xu, X. Zhu, Design of a New Fused-Ring Electron Acceptor with Excellent Compatibility to Wide-Bandgap Polymer Donors for High-Performance Organic Photovoltaics, Adv. Mater. 30 (2018) 1800403. https://doi.org/10.1002/adma.201800403."
3791,CCCCC(CC)COC1=CC(C2=CC3=C(S2)C2=C(C=C(/C=C4/C(=O)C5=CC6=CC(F)=C(F)C=C6C=C5C4=C(C#N)C#N)S2)C3(CC(CC)CCC)CC(CC)CCCC)=C(OCC(CC)CCCC)C=C1C1=CC2=C(S1)C1=C(C=C(/C=C3/C(=O)C4=C(C=C5C=C(F)C(F)=CC5=C4)C3=C(C#N)C#N)S1)C2(CC(CC)CC)CC(CC)CCC,BN-4F,-5.44,-4.06,25.76,0.792,0.6491,13.24,"X. Zhang, L. Qin, J. Yu, Y. Li, Y. Wei, X. Liu, X. Lu, F. Gao, H. Huang, High-Performance Noncovalently Fused-Ring Electron Acceptors for Organic Solar Cells Enabled by Noncovalent Intramolecular Interactions and End-Group Engineering, Angew. Chem. Int. Ed. 60 (2021) 12475¨C12481. https://doi.org/10.1002/anie.202100390."
3792,O=C(N(CC)C(N(CC)C/1=O)=S)C1=C/C2=CC3=C(S2)C(C(C4=CC=C(CCCCCC)C=C4)(C5=CC=C(CCCCCC)C=C5)C6=C7SC8=C6SC9=C8C(C%10=CC=C(CCCCCC)C=C%10)(C%11=CC=C(CCCCCC)C=C%11)C%12=C9SC%13=C%12SC(/C=C%14C(N(CC)C(N(CC)C\%14=O)=S)=O)=C%13)=C7S3,6TBA,-5.24,-3.78,10.7,1.69,0.73,13.2,"L. Zuo, X. Shi, S.B. Jo, Y. Liu, F. Lin, A.K.-Y. Jen, Tackling Energy Loss for High-Efficiency Organic Solar Cells with Integrated Multiple Strategies, Adv. Mater. 30 (2018) 1706816. https://doi.org/10.1002/adma.201706816."
3793,O=C(C(C=C(F)C(F)=C1)=C1C/2=C(C#N)C#N)C2=C/C3=CC(N(C(CCCCCCCC)CCCCCCCC)C4=C5SC6=C4SC7=C6N(C(CCCCCCCC)CCCCCCCC)C8=C7SC(/C=C9C(C(C=C(F)C(F)=C%10)=C%10C9=C(C#N)C#N)=O)=C8)=C5S3,SN61C-4F,-5.52,-4.11,23.2,0.78,0.73,13.2,"C. Huang, X. Liao, K. Gao, L. Zuo, F. Lin, X. Shi, C.-Z. Li, H. Liu, X. Li, F. Liu, Y. Chen, H. Chen, A.K.-Y. Jen, Highly Efficient Organic Solar Cells Based on S,N-Heteroacene Non-Fullerene Acceptors, Chem. Mater. 30 (2018) 5429¨C5434. https://doi.org/10.1021/acs.chemmater.8b02276."
3794,O=C(C(C=CC=C1)=C1C/2=C(C#N)C#N)C2=CC3=CC4=C(S3)C5=C(C6=CC(C7(CCCCCCCC)CCCCCCCC)=C(C8=C7C(SC(/C=C9C(C(C=CC=C%10)=C%10C/9=C(C#N)/C#N)=O)=C%11)=C%11S8)C=C6C5(CCCCCCCC)CCCCCCCC)S4,C8-ITIC,-5.63,-3.91,19.6,0.94,0.72,13.2,"Z. Fei, F.D. Eisner, X. Jiao, M. Azzouzi, J.A. R?hr, Y. Han, M. Shahid, A.S.R. Chesman, C.D. Easton, C.R. McNeill, T.D. Anthopoulos, J. Nelson, M. Heeney, An Alkylated Indacenodithieno[3,2-b]thiophene-Based Nonfullerene Acceptor with High Crystallinity Exhibiting Single Junction Solar Cell Efficiencies Greater than 13% with Low Voltage Losses, Adv. Mater. 30 (2018) 1705209. https://doi.org/10.1002/adma.201705209."
3795,CCCCCCCCOC1=C2SC3=C(C2=C(CCCCCCCC)C2=C1C1=C(S2)C2=C(C=C(/C=C4C(=O)C5=C(C=C(Cl)C(Cl)=C5)C4=C(C#N)C#N)S2)C1(C1=CC=C(CCCCCC)C=C1)C1=CC=C(CCCCCC)C=C1)C(C1=CC=C(CCCCCC)C=C1)(C1=CC=C(CCCCCC)C=C1)C1=C3SC(/C=C2C(=O)C3=C(C=C(Cl)C(Cl)=C3)C2=C(C#N)C#N)=C1,COBDT-4Cl,-5.57,-3.98,21.6,0.86,0.7,13.2,"B. Kan, X. Chen, K. Gao, M. Zhang, F. Lin, X. Peng, F. Liu, A.K.-Y. Jen, Asymmetrical side-chain engineering of small-molecule acceptors enable high-performance nonfullerene organic solar cells, Nano Energy. 67 (2020) 104209. https://doi.org/10.1016/j.nanoen.2019.104209."
3796,O=C(C(C=C(F)C(F)=C1)=C1C/2=C(C#N)C#N)C2=C/C3=CC(SCC(CC)CCCC)=C(C4=CC5=C(C6=CC(C7(C8=CC=C(CCCCCC)C=C8)C9=CC=C(CCCCCC)C=C9)=C(C%10=C7C=C(C%11=C(SCC(CC)CCCC)C=C(/C=C%12C(C(C=C(F)C(F)=C%13)=C%13C\%12=C(C#N)/C#N)=O)S%11)S%10)C=C6C5(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15)S4)S3,ACS8,-5.54,-4.05,25.3,0.75,0.693,13.2,"J. Chen, G. Li, Q. Zhu, X. Guo, Q. Fan, W. Ma, M. Zhang, Highly efficient near-infrared and semitransparent polymer solar cells based on an ultra-narrow bandgap nonfullerene acceptor, J. Mater. Chem. A. 7 (2019) 3745¨C3751. https://doi.org/10.1039/C8TA11484F."
3797,O=C(C1=C(C)SC=C1C/2=C(C#N)C#N)C2=C/C(S3)=CC4=C3C5=C(C4(C6=CC=C(CCCCCC)C=C6)C7=CC=C(CCCCCC)C=C7)C8=C(C9=CC=C(CC(CC)CCCC)S9)C%10=C(C(C(C%11=CC=C(CCCCCC)C=C%11)(C%12=CC=C(CCCCCC)C=C%12)C%13=C%14SC(/C=C%15/C(C%16=CSC(C)=C%16C%15=O)=C(C#N)C#N)=C%13)=C%14S%10)C(C%17=CC=C(CC(CC)CCCC)S%17)=C8S5,BTTIC,-5.59,-3.86,19.52,0.904,0.747,13.18,"W. Gao, T. Liu, R. Ming, Z. Luo, K. Wu, L. Zhang, J. Xin, D. Xie, G. Zhang, W. Ma, H. Yan, C. Yang, Near-Infrared Small Molecule Acceptor Enabled High-Performance Nonfullerene Polymer Solar Cells with Over 13% Efficiency, Adv. Funct. Mater. 28 (2018) 1803128. https://doi.org/10.1002/adfm.201803128."
3798,CCCCC(CC)CC1(CC(CC)CCCC)C2=C(C=C3CC4=C(SC(/C=C5C(=O)C6=C(C=C(F)C(F)=C6)C5=C(C#N)C#N)=C4)C3=C2)C2=C1C1=C(C=C3C(=C1)CC1=C3SC(/C=C3C(=O)C4=C(C=CC(F)=C4)C3=C(C#N)C#N)=C1)C2(CC(CC)CCCC)CC(CC)CCCC,ZITI-4F,-5.66,-3.81,21.3,0.85,0.7276,13.18,"J. Zhang, W. Liu, S. Chen, S. Xu, C. Yang, X. Zhu, One-pot synthesis of electron-acceptor composite enables efficient fullerene-free ternary organic solar cells, J. Mater. Chem. A. 6 (2018) 22519¨C22525. https://doi.org/10.1039/C8TA08961B."
3799,O=C(C(C=C(F)C(F)=C1)=C1C/2=C(C#N)C#N)C2=CC3=CSC(C4=CC5=C(C6=CC(C7(C8=CC=C(CCCCCC)C=C8)C9=CC=C(CCCCCC)C=C9)=C(C%10=C7C=C(C%11=C(OCC(CC)CCCC)C(/C=C%12C(C(C=C(F)C(F)=C%13)=C%13C/%12=C(C#N)C#N)=O)=CS%11)S%10)C=C6C5(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15)S4)=C3OCC(CC)CCCC,I-IEICO-4F,,,22.86,0.849,0.679,13.18,"W. Wang, B. Zhao, Z. Cong, Y. Xie, H. Wu, Q. Liang, S. Liu, F. Liu, C. Gao, H. Wu, Y. Cao, Nonfullerene Polymer Solar Cells Based on a Main-Chain Twisted Low-Bandgap Acceptor with Power Conversion Efficiency of 13.2%, ACS Energy Lett. (2018). https://doi.org/10.1021/acsenergylett.8b00627."
3800,CCCCCCCCCC1=C(/C=C2C(=O)C3=C(C=C(Cl)C(Cl)=C3)C2=C(C#N)C#N)SC2=C1SC1=C2C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=CC3=C(C=C21)N(C(CCCCCCCC)CCCCCCCC)C1=C3C=C2C(=C1)C1=C(C3=C(S1)C(CCCCCCCCC)=C(/C=C1C(=O)C4=C(C=C(Cl)C(Cl)=C4)C1=C(C#N)C#N)S3)C2(C1=CC=C(CCCCCC)C=C1)C1=CC=C(CCCCCC)C=C1,DTTC-4Cl-C9,-5.65,-3.95,20.5,0.95,0.6723,13.17,"V.K. Karapala, T.-W. Chen, K.-J. Ma, P.-L. Lu, Y.-J. Su, W.-D. Fu, H.-M. Shih, S.-J. Lu, T.-Y. Lee, C.-F. Chang, J.-T. Chen, C.-S. Hsu, Exploring Ternary Organic Solar Cells for the Improved Efficiency of 16.5% with the Compatible Nonacyclic Carbazole-Based Nonfullerene Acceptors as the Third Component, ACS Appl. Energy Mater. 4 (2021) 2847¨C2855. https://doi.org/10.1021/acsaem.1c00149."
3801,O=C(C(C=C(Cl)C=C1)=C1C/2=C(C#N)C#N)C2=C/C3=CC4=C(S3)C5=C(C6=CC(C7(C8=CC=C(CCCCCC)C=C8)C9=CC=C(CCCCCC)C=C9)=C(C%10=C7C(SC(/C=C%11C(C(C=CC(Cl)=C%12)=C%12C\%11=C(C#N)C#N)=O)=C%13)=C%13S%10)C=C6C5(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15)S4,ITIC-2CI,-5.68,-3.99,19.08,0.922,0.748,13.16,"H. Zhang, H. Yao, J. Hou, J. Zhu, J. Zhang, W. Li, R. Yu, B. Gao, S. Zhang, J. Hou, Over 14% Efficiency in Organic Solar Cells Enabled by Chlorinated Nonfullerene Small-Molecule Acceptors, Adv. Mater. 30 (2018) 1800613. https://doi.org/10.1002/adma.201800613."
3802,CCCCCCCCCCCC1=C(/C=C2C(=O)C3=C(C=CC(Cl)=C3)C2=C(C#N)C#N)SC2=C1SC1=C2N(CC(CC)CCCC)C2=C1C1=NSN=C1C1=C2N(CC(CC)CCCC)C2=C1SC1=C2SC(/C=C2C(=O)C3=C(C=CC(Cl)=C3)C2=C(C#N)C#N)=C1CCCCCCCCCCC,BTIC-Cl,-5.42,-3.91,21.35,0.88,0.697,13.16,"H. Lai, Q. Zhao, Z. Chen, H. Chen, P. Chao, Y. Zhu, Y. Lang, N. Zhen, D. Mo, Y. Zhang, F. He, Trifluoromethylation Enables a 3D Interpenetrated Low-Band-Gap Acceptor for Efficient Organic Solar Cells, Joule. 4 (2020) 688¨C700. https://doi.org/10.1016/j.joule.2020.02.004."
3803,CCCCCCCCC1=CC=C(C2(C3=CC=C(CCCCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C=C(/C=C2C(=O)C5=C(C=C(F)C(F)=C5)C2=C(C#N)C#N)S3)N(C(CCCCCCCC)CCCCCCCC)C2=CC3=C(C=C24)C(C2=CC=C(CCCCCCCC)C=C2)(C2=CC=C(CCCCCCCC)C=C2)C2=C3SC(/C=C3C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)=C2)C=C1,DTC(4Ph)-4FIC,-5.8,-3.94,18.29,0.95,0.757,13.15,"J. Yuan, Y. Zhang, L. Zhou, G. Zhang, H.-L. Yip, T.-K. Lau, X. Lu, C. Zhu, H. Peng, P.A. Johnson, M. Leclerc, Y. Cao, J. Ulanski, Y. Li, Y. Zou, Single-Junction Organic Solar Cell with over 15% Efficiency Using Fused-Ring Acceptor with Electron-Deficient Core, Joule. 3 (2019) 1140¨C1151. https://doi.org/10.1016/j.joule.2019.01.004."
3804,O=C(C1=C(C)SC=C1C/2=C(C#N)C#N)C2=C/C3=CC4=C(S3)C5=C(C6=C(C7=CC=C(CC(CC)CCCC)S7)C8=C(C9=C(S8)C(SC(/C=C%10C(C%11=C(C)SC=C%11C\%10=C(C#N)/C#N)=O)=C%12)=C%12C9(C%13=CC=C(CCCCCC)C=C%13)C%14=CC=C(CCCCCC)C=C%14)C(C%15=CC=C(CC(CC)CCCC)S%15)=C6S5)C4(C%16=CC=C(CCCCCC)C=C%16)C%17=CC=C(CCCCCC)C=C%17,BTTIC-2M,-5.6,-3.86,19.39,0.9,0.753,13.15,"W. Gao, T. Liu, Z. Luo, L. Zhang, R. Ming, C. Zhong, W. Ma, H. Yan, C. Yang, Regulating exciton bonding energy and bulk heterojunction morphology in organic solar cells via methyl-functionalized non-fullerene acceptors, J. Mater. Chem. A. 7 (2019) 6809¨C6817. https://doi.org/10.1039/C9TA00597H."
3805,CCCCC(CC)CC1(CC(CC)CCCC)C2=C(C=C3CC4=C(SC(/C=C5C(=O)C6=C(C=C(F)C(F)=C6)C5=C(C#N)C#N)=C4)C3=C2)C2=C1C1=C(C=C3C(=C1)CC1=C3SC(/C=C3C(=O)C4=C(C=CC(F)=C4)C3=C(C#N)C#N)=C1)C2(CC(CC)CCCC)CC(CC)CCCC,ZITI-3F,-5.64,-3.76,20.67,0.9,0.7153,13.15,"J. Zhang, W. Liu, S. Chen, S. Xu, C. Yang, X. Zhu, One-pot synthesis of electron-acceptor composite enables efficient fullerene-free ternary organic solar cells, J. Mater. Chem. A. 6 (2018) 22519¨C22525. https://doi.org/10.1039/C8TA08961B."
3806,CCCCCCC1=C(SC(/C=C2S/C(N(C2=O)CC)=C(C#N)C#N)=C1CCCCCC)C#CC3=CC=C(S3)C4=C5C(N(C(C6=CC=C(S6)C#CC7=C(C(CCCCCC)=C(S7)/C=C8S/C(N(C8=O)CC)=C(C#N)C#N)CCCCCC)=C5C(N4CC(CCCC)CC)=O)CC(CCCC)CC)=O,MPU6,-5.54,-3.7,20.38,1.04,0.62,13.14,"M. Privado, H. Dahiya, P. de la Cruz, M.L. Keshtov, F. Langa, G.D. Sharma, A ternary organic solar cell with 15.6% efficiency containing a new DPP-based acceptor, J. Mater. Chem. C. 9 (2021) 16272¨C16281. https://doi.org/10.1039/D1TC02241E."
3807,O=C(C(C=C(F)C(F)=C1)=C1C/2=C(C#N)C#N)C2=C/C(S3)=CC4=C3C5=C(N4CCCCCCCC)C6=C(C7=CC(C8(C9=CC=C(CCCCCC)C=C9)C%10=CC=C(CCCCCC)C=C%10)=C(C%11=C8C(N(CCCCCCCC)C%12=C%13SC(/C=C%14C(C(C=C(F)C(F)=C%15)=C%15C\%14=C(C#N)/C#N)=O)=C%12)=C%13S%11)C=C7C6(C%16=CC=C(CCCCCC)C=C%16)C%17=CC=C(CCCCCC)C=C%17)S5,INPIC-4F,-5.42,-3.94,21.61,0.85,0.715,13.13,"J. Sun, X. Ma, Z. Zhang, J. Yu, J. Zhou, X. Yin, L. Yang, R. Geng, R. Zhu, F. Zhang, W. Tang, Dithieno[3,2-b:2¡ä,3¡ä-d]pyrrol Fused Nonfullerene Acceptors Enabling Over 13% Efficiency for Organic Solar Cells, Adv. Mater. 30 (2018) 1707150. https://doi.org/10.1002/adma.201707150."
3808,CCCCCCCCC1=C(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)SC2=C1SC1=C2C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C1SC1=C2SC2=C1C(C1=CC=C(CCCCCC)C=C1)(C1=CC=C(CCCCCC)C=C1)C1=C2SC(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)=C1CCCCCCCC,5T-OFIC-,-5.51,-3.86,24.32,0.792,0.682,13.12,"L. Meng, H.-H. Gao, S. Wu, Y. Sun, X. Wan, Y. Yang, J. Wang, Z. Guo, H. Chen, C. Li, Y. Chen, Structural optimization of acceptor molecules guided by a semi-empirical model for organic solar cells with efficiency over 15%, Sci. China Mater. 64 (2021) 2388¨C2396. https://doi.org/10.1007/s40843-020-1651-5."
3809,O=C(C(C=C(F)C(F)=C1)=C1C/2=C(C#N)/C#N)C2=C/C3=CC(C4(CCCCCCCC)CCCCCCCC)=C(S3)C5=C4C=C(C(C=C6C(C(C=C7C(CCCCCCCC)(CCCCCCCC)C8=C(C7=C9)SC(/C=C%10C(C(C=C(F)C(F)=C%11)=C%11C\%10=C(C#N)C#N)=O)=C8)=C9C6(CCCCCCCC)CCCCCCCC)=C%12)=C%12C%13(CCCCCCCC)CCCCCCCC)C%13=C5,TflF-4FIC,-5.71,-3.96,17.6,0.98,0.76,13.1,"G. Liu, J. Jia, K. Zhang, X. Jia, Q. Yin, W. Zhong, L. Li, F. Huang, Y. Cao, 15% Efficiency Tandem Organic Solar Cell Based on a Novel Highly Efficient Wide-Bandgap Nonfullerene Acceptor with Low Energy Loss, Adv. Energy Mater. 9 (2019) 1803657. https://doi.org/10.1002/aenm.201803657."
3810,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=C(SC(/C=C4/C(=O)C5=CSC=C5C4=C(C#N)C#N)=C3)C3=C2C2=C(S3)C(C3=CC(F)=C(SC(CC)CCCC)S3)=C3C(=C2C2=C(F)C=C(SC(CC)CCCC)S2)SC2=C3C(C3=CC=C(CCCCCC)C=C3)(C3=CC=C(CCCCCC)C=C3)C3=C2SC(/C=C2/C(=O)C4=CSC=C4C2=C(C#N)C#N)=C3)C=C1,BDTSF-IC,-5.58,-3.93,20.36,0.9,0.7148,13.1,"Y. Zhang, Y. Cho, L. Zhong, Y. Wang, B. Huang, Z. Yuan, C. Yang, Y. Chen, Y. Li, Two-Dimension Conjugated Acceptors Based on Benzodi(cyclopentadithiophene) Core with Thiophene-Fused Ending Group for Efficient Polymer Solar Cells, Sol. RRL. 4 (2020) 2000071. https://doi.org/10.1002/solr.202000071."
3811,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(C=C(/C=C5C(=O)C6=C(C=C(F)C(F)=C6)C5=C(C#N)C#N)S2)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC3=C2SC(/C=C2C(=O)C4=C(C=C(C)S4)C2=C(C#N)C#N)=C3)C=C1,IDTT-Cl-2F,-5.42,-3.92,19.2,0.96,0.711,13.1,"J. Cai, X. Zhang, C. Guo, Y. Zhuang, L. Wang, D. Li, D. Liu, T. Wang, Asymmetric and Halogenated Fused-Ring Electron Acceptor for Efficient Organic Solar Cells, Adv. Funct. Mater. 31 (2021) 2102189. https://doi.org/10.1002/adfm.202102189."
3812,O=C(C(C=C(F)C(F)=C1)=C1C/2=C(C#N)C#N)C2=C/C3=CC4=C(S3)C(C(C5=CC=C(CCCCCC)C=C5)(C6=CC=C(CCCCCC)C=C6)OC7=C8SC9=C7SC%10=C9OC(C%11=CC=C(CCCCCC)C=C%11)(C%12=CC=C(CCCCCC)C=C%12)C%13=C%10SC%14=C%13SC(/C=C%15C(C(C=C(F)C(F)=C%16)=C%16C\%15=C(C#N)/C#N)=O)=C%14)=C8S4,O6F-4F,-5.71,-3.96,16.8,0.98,0.69,13.1,"B. Wang, Y. Fu, Q. Yang, J. Wu, H. Liu, H. Tang, Z. Xie, High-efficiency ternary nonfullerene organic solar cells fabricated with a near infrared acceptor enhancing exciton utilization and extending absorption, J. Mater. Chem. C. 7 (2019) 10498¨C10506. https://doi.org/10.1039/C9TC03534F."
3813,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C=C(C2=C(OC(CC)CCCC)C=C(/C=C5C(=O)C6=CC(F)=C(F)C=C6C5=C(C#N)C#N)S2)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC(C3=C(OCC(CC)CCCC)C=C(/C=C4C(=O)C5=CC(F)=C(F)C=C5C4=C(C#N)C#N)S3)=C2)C=C1,o-IO1,-5.44,-4.15,26.3,0.74,0.67,13.1,"J. Lee, S. Song, J. Huang, Z. Du, H. Lee, Z. Zhu, S.-J. Ko, T.-Q. Nguyen, J.Y. Kim, K. Cho, G.C. Bazan, Bandgap Tailored Nonfullerene Acceptors for Low-Energy-Loss Near-Infrared Organic Photovoltaics, ACS Mater. Lett. 2 (2020) 395¨C402. https://doi.org/10.1021/acsmaterialslett.9b00512."
3814,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(C=C(/C=C5C(=O)C6=C(C=C(F)C(F)=C6)C5=C(C#N)C#N)[Se]2)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC3=C2[Se]C(/C=C2C(=O)C4=C(C=C(F)C(F)=C4)C2=C(C#N)C#N)=C3)C=C1,SRID-4F,,,20.21,0.846,0.752,13.05,"F. Lin, L. Zuo, K. Gao, M. Zhang, S.B. Jo, F. Liu, A.K.-Y. Jen, Regio-Specific Selenium Substitution in Non-Fullerene Acceptors for Efficient Organic Solar Cells, Chem. Mater. 31 (2019) 6770¨C6778. https://doi.org/10.1021/acs.chemmater.9b01242."
3815,CCCCCCCCC(C)N1C2=CC3=C(C=C2C2=C1C=C1C(=C2)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C1SC1=C2SC(/C=C2C(=O)C4=C(C=C(F)C(F)=C4)C2=C(C#N)C#N)=C1)C(C1=CC=C(CCCCCC)C=C1)(C1=CC=C(CCCCCC)C=C1)C1=C3SC2=C1SC(/C=C1C(=O)C3=C(C=C(F)C(F)=C3)C1=C(C#N)C#N)=C2,4TCIC-4F,-5.53,-3.95,18.98,0.94,0.73,13.02,"J. Ouyang, G. Zeng, Y. Xin, X. Zhao, X. Yang, A Novel Carbazole-Based Nonfullerene Acceptor for High-Efficiency Polymer Solar Cells, Sol. RRL. 4 (2020) 1900417. https://doi.org/10.1002/solr.201900417."
3816,CCCCCCCCC1=C(/C=C2C(=O)C3=C(C=C(Cl)C(Cl)=C3)C2=C(C#N)C#N)SC2=C1SC1=C2C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C1SC1=C2SC2=C1C(C1=CC=C(CCCCCC)C=C1)(C1=CC=C(CCCCCC)C=C1)C1=C2SC(/C=C2C(=O)C3=C(C=C(Cl)C(Cl)=C3)C2=C(C#N)C#N)=C1CCCCCCCC,5T-2C8-2Cl,-5.57,-3.9,24.97,0.802,0.65,13.02,"H. Gao, X. Wan, Z. Xuan, W. Ma, J. Xin, C. Li, Y. Chen, Finely modulated asymmetric nonfullerene acceptors enabling simultaneously improved voltage and current for efficient organic solar cells, J. Mater. Chem. C. 10 (2022) 2742¨C2748. https://doi.org/10.1039/D1TC03793E."
3817,CCCCC(CC)CN1N=C2C(=N1)C1=C(C3=C2C2=C(C4=C(C=C(/C=C5C(=O)C6=C(C=CC=C6)C5=C(C#N)C#N)S4)S2)N3CC(CC)CCCC)N(CC(CC)CCCC)C2=C1SC1=C2SC(/C=C2C(=O)C3=C(C=CC=C3)C2=C(C#N)C#N)=C1,Y1,-5.45,-3.95,21.4,0.88,0.695,13,"R. Wang, J. Yuan, R. Wang, G. Han, T. Huang, W. Huang, J. Xue, H.-C. Wang, C. Zhang, C. Zhu, P. Cheng, D. Meng, Y. Yi, K.-H. Wei, Y. Zou, Y. Yang, Rational Tuning of Molecular Interaction and Energy Level Alignment Enables High-Performance Organic Photovoltaics, Adv. Mater. 31 (2019) 1904215. https://doi.org/10.1002/adma.201904215."
3818,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C=C(/C=C2C(=O)C5=C(C=C(F)C(F)=C5)C2=C(C#N)C#N)S3)N(CCCCCC)C2=C4SC3=C2C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C3SC(/C=C3C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)=C2)C=C1,TIT-2FIC,-5.46,-3.98,20.69,0.905,0.6942,13,"L. Xie, Y. Zhang, W. Zhuang, S.Y. Jeong, Q. Bian, H. Li, J. Cao, W. Liu, H. Tan, H.Y. Woo, J. Zhang, E. Wang, Low-bandgap nonfullerene acceptor based on thieno[3,2-b]indole core for highly efficient binary and ternary organic solar cells, Chem. Eng. J. 427 (2022) 131674. https://doi.org/10.1016/j.cej.2021.131674."
3819,O=C1C2=C(C=CC=C2)C(/C1=C/C3=C(CCCCCC)C(S4)=C(S3)C5=C4C6=C(N5CC(CC)CCCC)C7=C(C(SC8=C9SC(/C=C%10/C(C(C=CC=C%11)=C%11C%10=O)=C(C#N)C#N)=C8CCCCCC)=C9N7CC(CC)CCCC)C%12=NN(CC(CC)CCCC)N=C6%12)=C(C#N)/C#N,Y16,-5.25,-3.66,21.33,0.914,0.6669,13,"X. Ma, M. Luo, W. Gao, J. Yuan, Q. An, M. Zhang, Z. Hu, J. Gao, J. Wang, Y. Zou, C. Yang, F. Zhang, Achieving 14.11% efficiency of ternary polymer solar cells by simultaneously optimizing photon harvesting and exciton distribution, J. Mater. Chem. A. 7 (2019) 7843¨C7851. https://doi.org/10.1039/C9TA01497G."
3820,CCCCCCCCCCCC1=C(/C=C2C(=O)C3=C(C=CC4=CC=CC=C43)C2=C(C#N)C#N)SC2=C1SC1=C2N(CC(CC)CCCC)C2=C1C1=NSN=C1C1=C2N(CC(CC)CCCC)C2=C1SC1=C2SC(/C=C2C(=O)C3=C(C=CC4=C3C=CC=C4)C2=C(C#N)C#N)=C1CCCCCCCCCCC,BT-BIC,-5.46,-3.73,24.1,0.85,0.616,13,"G. Li, X. Zhang, L.O. Jones, J.M. Alzola, S. Mukherjee, L. Feng, W. Zhu, C.L. Stern, W. Huang, J. Yu, V.K. Sangwan, D.M. DeLongchamp, K.L. Kohlstedt, M.R. Wasielewski, M.C. Hersam, G.C. Schatz, A. Facchetti, T.J. Marks, Systematic Merging of Nonfullerene Acceptor ¦Ð-Extension and Tetrafluorination Strategies Affords Polymer Solar Cells with >16% Efficiency, J. Am. Chem. Soc. 143 (2021) 6123¨C6139. https://doi.org/10.1021/jacs.1c00211."
3821,CCCCCCCCCCCC1=C(/C=C2C(=O)C3=C(C=C(Cl)C(Cl)=C3)C2=C(C#N)C#N)SC2=C1SC1=C2N(CC(CC)CCCC)C2=C1C1=NSN=C1C1=C2N(CC(CC)CCCC)C2=C1SC1=C2SC(/C=C2C(=O)C3=C(C=C(Cl)C(Cl)=C3)C2=C(C#N)C#N)=C1CCCCCCCCCCC,LL2-2CL,-5.64,-4.02,26.66,0.72,0.671,12.95,"H. Lu, H. Jin, H. Huang, W. Liu, Z. Tang, J. Zhang, Z. Bo, High-Efficiency Organic Solar Cells Based on Asymmetric Acceptors Bearing One 3D Shape-Persistent Terminal Group, Adv. Funct. Mater. 31 (2021) 2103445. https://doi.org/10.1002/adfm.202103445."
3822,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(C=C(/C=C5C(=O)C6=CC=CC=C6C5=C(C#N)C#N)S2)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC3=C2SC(/C=C2C(=O)C4=C(C=C(Br)C(Br)=C4)C2=C(C#N)C#N)=C3)C=C1,IT-2Br,-5.72,-4.15,21.98,0.845,0.6953,12.92,"Y. Liu, Y. Zhao, S. Lu, K. Zhu, Q. Wang, X. Kang, L. Yu, S. Dai, M. Sun, Effects of brominated terminal groups on the performance of fused-ring electron acceptors in organic solar cells, Dyes Pigments. 194 (2021) 109652. https://doi.org/10.1016/j.dyepig.2021.109652."
3823,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=C(SC(/C=C4C(=O)C5=C(C)SC=C5C4=C(C#N)C#N)=C3)C3=C2C2=C(S3)C(C3=CC=C(CC(CC)CCCC)S3)=C3C(=C2C2=CC=C(CC(CC)CCCC)S2)SC2=C3C(C3=CC=C(CCCCCC)C=C3)(C3=CC=C(CCCCCC)C=C3)C3=C2SC(/C=C2C(=O)C4=C(C)SC=C4C2=C(C#N)C#N)=C3)C=C1,BTTIC-Th,-5.49,-3.9,19.45,0.902,0.736,12.91,"T. Liu, W. Gao, Y. Wang, T. Yang, R. Ma, G. Zhang, C. Zhong, W. Ma, H. Yan, C. Yang, Unconjugated Side-Chain Engineering Enables Small Molecular Acceptors for Highly Efficient Non-Fullerene Organic Solar Cells: Insights into the Fine-Tuning of Acceptor Properties and Micromorphology, Adv. Funct. Mater. 29 (2019) 1902155. https://doi.org/10.1002/adfm.201902155."
3824,CCCCCCOC1=C(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)SC(C2=CC3=C(S2)C2=CC4=C(C=C2C3(C2=CC=C(CCCCCC)C=C2)C2=CC=C(CCCCCC)C=C2)C2=C(C=C(C3=CC(OCCCCCC)=C(/C=C5C(=O)C6=C(C=C(F)C(F)=C6)C5=C(C#N)C#N)S3)S2)C4(C2=CC=C(CCCCCC)C=C2)C2=CC=C(CCCCCC)C=C2)=C1,IDTCN-O,-5.54,-3.8,19.96,0.91,0.732,12.91,"Y. Liu, M. Li, J. Yang, W. Xue, S. Feng, J. Song, Z. Tang, W. Ma, Z. Bo, High-Efficiency As-Cast Organic Solar Cells Based on Acceptors with Steric Hindrance Induced Planar Terminal Group, Adv. Energy Mater. 9 (2019) 1901280. https://doi.org/10.1002/aenm.201901280."
3825,CCCCCCCCCCCN1C2=C(SC3=C2SC(/C=C2C(=O)C4=C(C=C(F)C(F)=C4)C2=C(C#N)C#N)=C3CC(CC)CCCC)C2=C1C1=C(C3=NSN=C32)C2=C(C3=C(S2)C(CC(CC)CCCC)=C(/C=C2C(=O)C4=C(C=C(F)C(F)=C4)C2=C(C#N)C#N)S3)N1CC[C@H](C)CCCCCCCC,N-C11,,,21.47,0.852,0.706,12.91,"K. Jiang, Q. Wei, J.Y.L. Lai, Z. Peng, H.K. Kim, J. Yuan, L. Ye, H. Ade, Y. Zou, H. Yan, Alkyl Chain Tuning of Small Molecule Acceptors for Efficient Organic Solar Cells, Joule. 3 (2019) 3020¨C3033. https://doi.org/10.1016/j.joule.2019.09.010."
3826,CCCCCCCCCCCN1C2=C(SC3=C2SC(/C=C2C(=O)C4=C(C=C(F)C(F)=C4)C2=C(C#N)C#N)=C3CC(CC)CCCC)C2=C1C1=C(C3=NSN=C32)C2=C(C3=C(S2)C(CC(CC)CCCC)=C(/C=C2C(=O)C4=C(C=C(F)C(F)=C4)C2=C(C#N)C#N)S3)N1CCCCCCCCCCC,N-C11,,,21.47,0.852,0.706,12.91,"K. Jiang, Q. Wei, J.Y.L. Lai, Z. Peng, H.K. Kim, J. Yuan, L. Ye, H. Ade, Y. Zou, H. Yan, Alkyl Chain Tuning of Small Molecule Acceptors for Efficient Organic Solar Cells, Joule. 3 (2019) 3020¨C3033. https://doi.org/10.1016/j.joule.2019.09.010."
3827,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=C(SC(/C=C4C(=O)C5=CC(F)=CC=C5C4=C(C#N)C#N)=C3)C3=C2C2=C(S3)C(C3=CC=C(CC(CC)CCCC)S3)=C3C(=C2C2=CC(Cl)=C(CC(CC)CCCC)S2)SC2=C3C(C3=CC=C(CCCCCC)C=C3)(C3=CC=C(CCCCCC)C=C3)C3=C2SC(/C=C2C(=O)C4=CC(F)=CC=C4C2=C(C#N)C#N)=C3)C=C1,BTC-2,-5.64,-3.91,2.3,0.92,0.693,12.9,"G. Li, J. Wu, J. Fang, X. Guo, L. Zhu, F. Liu, M. Zhang, Y. Li, A Non-Fullerene Acceptor with Chlorinated Thienyl Conjugated Side Chains for High-Performance Polymer Solar Cells via Toluene Processing, Chin. J. Chem. 38 (2020) 697¨C702. https://doi.org/10.1002/cjoc.201900495."
3828,CCCCCCCCC1=C(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)SC(C2=C(N(C3=CC=C(CCCC)C=C3)C3=CC=C(CCCC)C=C3)C3=C(S2)C(N(C2=CC=C(CCCC)C=C2)C2=CC=C(CCCC)C=C2)=C(C2=CC4=C(S2)C(CCCCCCCC)=C(/C=C2C(=O)C5=C(C=C(F)C(F)=C5)C2=C(C#N)C#N)S4)S3)=C1,BTh-Th-2F,-5.58,-3.96,23.59,0.81,0.6714,12.87,"X. Wang, H. Lu, Y. Liu, A. Zhang, N. Yu, H. Wang, S. Li, Y. Zhou, X. Xu, Z. Tang, Z. Bo, Simple Nonfused Ring Electron Acceptors with 3D Network Packing Structure Boosting the Efficiency of Organic Solar Cells to 15.44%, Adv. Energy Mater. 11 (2021) 2102591. https://doi.org/10.1002/aenm.202102591."
3829,O=C1C2=C(C=C3C(C=CC=C3)=C2)C(/C1=C/C4=CC(C(C5=CC=C(OCC(CC)CCCC)C=C5)(C6=CC=C(OCC(CC)CCCC)C=C6)C7=C8C=CC(C7=C9)=CC%10=C9C=CC%11=C%10C(C%12=CC=C(OCC(CC)CCCC)C=C%12)(C%13=CC=C(OCC(CC)CCCC)C=C%13)C%14=C%11SC(/C=C%15/C(C(C=C%16C(C=CC=C%16)=C%17)=C%17C%15=O)=C(C#N)/C#N)=C%14)=C8S4)=C(C#N)C#N,IOIC3,-5.38,-3.84,22.6,0.77,0.741,12.8,"J. Zhu, Y. Xiao, J. Wang, K. Liu, H. Jiang, Y. Lin, X. Lu, X. Zhan, Alkoxy-Induced Near-Infrared Sensitive Electron Acceptor for High-Performance Organic Solar Cells, Chem. Mater. 30 (2018) 4150¨C4156. https://doi.org/10.1021/acs.chemmater.8b01677."
3830,O=C(C(C=C1C(C=CC=C1)=C2)=C2C/3=C(C#N)C#N)C3=C/C(S4)=CC5=C4C6=C(C5(C7=CC=C(CCCCCC)C=C7)C8=CC=C(CCCCCC)C=C8)C9=C(CCCCCCCC)C%10=C(C(C(C%11=CC=C(CCCCCC)C=C%11)(C%12=CC=C(CCCCCC)C=C%12)C%13=C%14SC(/C=C%15C(C(C=C%16C(C=CC=C%16)=C%17)=C%17C\%15=C(C#N)/C#N)=O)=C%13)=C%14S%10)C(CCCCCCCC)=C9S6,NNBDT,-5.46,-3.94,19.89,0.887,0.72,12.8,"B. Kan, Y.-Q.-Q. Yi, X. Wan, H. Feng, X. Ke, Y. Wang, C. Li, Y. Chen, Ternary Organic Solar Cells With 12.8% Efficiency Using Two Nonfullerene Acceptors With Complementary Absorptions, Adv. Energy Mater. 8 (2018) 1800424. https://doi.org/10.1002/aenm.201800424."
3831,O=C(C(C=CC=C1)=C1C/2=C(C#N)C#N)C2=C/C3=CC(OCC(CC)CCCC)=C(C4=CC5=C(C6=CC(C7(C8=CC=C(CCCCCC)C=C8)C9=CC=C(CCCCCC)C=C9)=C(C%10=C7C=C(C%11=C(OCC(CC)CCCC)C=C(/C=C%12C(C(C=CC=C%13)=C%13C\%12=C(C#N)/C#N)=O)S%11)S%10)C=C6C5(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15)S4)S3,IEICO,-5.32,-3.95,11.51,1.71,0.66,12.8,"Y. Qin, Y. Chen, Y. Cui, S. Zhang, H. Yao, J. Huang, W. Li, Z. Zheng, J. Hou, Achieving 12.8% Efficiency by Simultaneously Improving Open-Circuit Voltage and Short-Circuit Current Density in Tandem Organic Solar Cells, Adv. Mater. 29 (2017) 1606340. https://doi.org/10.1002/adma.201606340."
3832,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C=C(C2=C(OC)C(OC)=C(/C=C5C(=O)C6=C(C=C(F)C(F)=C6)C5=C(C#N)C#N)S2)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC(C3=C(OC)C(OC)=C(/C=C4C(=O)C5=C(C=C(F)C(F)=C5)C4=C(C#N)C#N)S3)=C2)C=C1,IEICF-DMOT,-5.49,-3.85,22.14,0.87,0.6753,12.79,"Y. Chang, X. Zhang, Y. Tang, M. Gupta, D. Su, J. Liang, D. Yan, K. Li, X. Guo, W. Ma, H. Yan, C. Zhan, 14%-efficiency fullerene-free ternary solar cell enabled by designing a short side-chain substituted small-molecule acceptor, Nano Energy. 64 (2019) 103934. https://doi.org/10.1016/j.nanoen.2019.103934."
3833,CCCCCCCCC(CCCCCC)COC1=CC(C2=CC(C3=CC=C(CCCCCC)C=C3)=C(/C=C3C(=O)C4=C(C=C(Cl)C(Cl)=C4)C3=C(C#N)C#N)S2)=C(OCC(CCCCCC)CCCCCCCC)C=C1C1=CC(C2=CC=C(CCCCCC)C=C2)=C(/C=C2C(=O)C3=C(C=C(Cl)C(Cl)=C3)C2=C(C#N)C#N)S1,PTB4Cl,-5.91,-3.93,19.01,0.93,0.7217,12.76,"T.-J. Wen, Z.-X. Liu, Z. Chen, J. Zhou, Z. Shen, Y. Xiao, X. Lu, Z. Xie, H. Zhu, C.-Z. Li, H. Chen, Simple Non-Fused Electron Acceptors Leading to Efficient Organic Photovoltaics, Angew. Chem. Int. Ed. 60 (2021) 12964¨C12970. https://doi.org/10.1002/anie.202101867."
3834,O=C1C2=C(C(/C1=C/C3=C4C(SC(CCCCCCCC)=C4)=C(S3)C5=CC6=C(C(C(CC(CCCC)CC)(C7=C8C=CC(C9=C%10SC(CCCCCCCC)=CC%10=C(S9)/C=C%11/C(C%12=C(C%11=O)C=C(F)C(F)=C%12)=C(C#N)C#N)=C7)CC(CCCC)CC)C8C6(CC(CCCC)CC)CC(CCCC)CC)C=C5)=C(C#N)C#N)C=C(F)C(F)=C2,NITI,-5.68,-3.84,20.67,0.86,0.71,12.74,"S. jie Xu, Z. Zhou, W. Liu, Z. Zhang, F. Liu, H. Yan, X. Zhu, A Twisted Thieno[3,4-b]thiophene-Based Electron Acceptor Featuring a 14-¦Ð-Electron Indenoindene Core for High-Performance Organic Photovoltaics, Adv. Mater. 29 (2017) 1704510. https://doi.org/10.1002/adma.201704510."
3835,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=C(C=C4C(=C3)C3=C(C5=C(C=C(/C=C6C(=O)C7=CC(F)=CC=C7C6=C(C#N)C#N)S5)S3)C4(C3=CC=C(CCCCCC)C=C3)C3=CC=C(CCCCCC)C=C3)C3=C2C=C(C2=CC=C(/C=C4C(=O)C5=CC=C(F)C=C5C4=C(C#N)C#N)S2)S3)C=C1,TTPT-T-2F,-5.6,-4,18.5,0.915,0.751,12.71,"X. Li, C. Li, L. Ye, K. Weng, H. Fu, H.S. Ryu, D. Wei, X. Sun, H.Y. Woo, Y. Sun, Asymmetric A¨CD¨C¦Ð¨CA-type nonfullerene small molecule acceptors for efficient organic solar cells, J. Mater. Chem. A. 7 (2019) 19348¨C19354. https://doi.org/10.1039/C9TA06476A."
3836,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(C=C(/C=C5C(=O)C6=C(C=C(F)C(F)=C6)C5=C(C#N)N=O)S2)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC3=C2SC2=C3C(C3=CC=C(CCCCCC)C=C3)(C3=CC=C(CCCCCC)C=C3)C3=C2C=C2C(=C3)C3=C(C4=C(C=C(/C=C5C(=O)C6=C(C=C(F)C(F)=C6)C5C(C#N)C#N)S4)S3)C2(C2=CC=C(CCCCCC)C=C2)C2=CC=C(CCCCCC)C=C2)C=C1,LC81,-5.49,-3.97,19.84,0.875,0.732,12.71,"T. Xia, C. Li, H.S. Ryu, J. Guo, J. Min, H.Y. Woo, Y. Sun, Efficient Fused-Ring Extension of A¨CD¨CA-Type Non-Fullerene Acceptors by a Symmetric Replicating Core Unit Strategy, Chem. ¨C Eur. J. 26 (2020) 12411¨C12417. https://doi.org/10.1002/chem.202000889."
3837,CCCCCCC(CCC)CC1(CC(CCC)CCCCCC)C2=C(SC(/C=C3C(=O)C4=C(C=CC=C4)C3=C(C#N)C#N)=C2)C2=C1C=C(C1=CC3=C(S1)C1=C(C=C(C4=CC5=C(S4)C4=C(C=C(/C=C6C(=O)C7=C(C=CC=C7)C6=C(C#N)C#N)S4)C5(CC(CCC)CCCCCC)CC(CCC)CCCCCC)S1)C1=NSN=C13)S2,DTBCIC,-5.62,-3.87,20.4,0.89,0.6939,12.71,"Y. Tang, H. Feng, Y. Liang, H. Tang, Z. Du, J. Xu, F. Huang, Y. Cao, Dithienobenzothiadiazole-Bridged Nonfullerene Electron Acceptors for Efficient Organic Solar Cells, ACS Appl. Polym. Mater. (2021). https://doi.org/10.1021/acsapm.1c01406."
3838,CCCCCCCCCCCC1=C(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)SC2=C1SC1=C2N(CC(C)CCCC)C2=C1C1=NSN=C1C1=C2N(CC(CC)CCCC)C2=C1SC1=C2SC(/C=C2/C3=C(C=CC=C3)C3=C2N=C(C#N)C(C#N)=N3)=C1CCCCCCCCCCC,IPC-BEH-IC2F,-5.55,-3.9,22.29,0.852,0.6683,12.7,"P. Gopikrishna, H. Choi, D.H. Kim, J.H. Hwang, Y. Lee, H. Jung, G. Yu, T.B. Raju, E. Lee, Y. Lee, S. Cho, B. Kim, Impact of symmetry-breaking of non-fullerene acceptors for efficient and stable organic solar cells, Chem. Sci. 12 (2021) 14083¨C14097. https://doi.org/10.1039/D1SC04153C."
3839,O=C(C(C=C(F)C(F)=C1)=C1C/2=C(C#N)C#N)C2=C/C3=CC=C(C4=C(OCCCCCCCC)C5=C(C6=CC(C7(C8=CC=C(CCCCCC)C=C8)C9=CC=C(CCCCCC)C=C9)=C(C%10=C7C(OCCCCCCCC)=C(C%11=CC=C(/C=C%12C(C(C=C(F)C(F)=C%13)=C%13C\%12=C(C#N)/C#N)=O)S%11)S%10)C=C6C5(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15)S4)S3,IDTO-T-4F,-5.49,-3.88,20.12,0.864,0.727,12.62,"D. Liu, B. Kan, X. Ke, N. Zheng, Z. Xie, D. Lu, Y. Liu, Extended Conjugation Length of Nonfullerene Acceptors with Improved Planarity via Noncovalent Interactions for High-Performance Organic Solar Cells, Adv. Energy Mater. 8 (2018) 1801618. https://doi.org/10.1002/aenm.201801618."
3840,O=C(C(C=CC=C1)=C1C/2=C(C#N)C#N)C2=C/C3=CC(C(C4=CC=C(CCCCCC)C=C4)(C5=CC=C(CCCCCC)C=C5)C6=C7SC8=C6SC9=C8C(C%10=CC=C(CCCCCC)C=C%10)(C%11=CC=C(CCCCCC)C=C%11)C%12=C9SC(/C=C%13C(C(C=CC=C%14)=C%14C\%13=C(C#N)/C#N)=O)=C%12)=C7S3,ITIC,-5.28,-3.87,10.62,1.65,0.71,12.62,"X. Shi, L. Zuo, S.B. Jo, K. Gao, F. Lin, F. Liu, A.K.-Y. Jen, Design of a Highly Crystalline Low-Band Gap Fused-Ring Electron Acceptor for High-Efficiency Solar Cells with Low Energy Loss, Chem. Mater. 29 (2017) 8369¨C8376. https://doi.org/10.1021/acs.chemmater.7b02853."
3841,CCCCCCCCC(CCCCCCCC)N1C2=C(SC(/C=C3C(=O)C4=C(C=C(Cl)C(Cl)=C4)C3=C(C#N)C#N)=C2)C2=C1C=C(C1=C(OC(CCCC)CCCCCC)C=C(C3=CC(CCCCCC)=C(/C=C4C(=O)C5=CC(Cl)=C(Cl)C=C5C4=C(C#N)C#N)S3)C(OC(CCCC)CCCCCC)=C1)S2,DBT-BO,-5.62,-3.97,21.12,0.84,0.7096,12.59,"J. Cao, H. Wang, L. Yang, F. Du, J. Yu, W. Tang, Chlorinated unfused acceptor enabling 13.57% efficiency and 73.39% fill factor organic solar cells via fine-tuning alkoxyl chains on benzene core, Chem. Eng. J. 427 (2022) 131828. https://doi.org/10.1016/j.cej.2021.131828."
3842,CCCCCCCCC1=C(/C=C2C(=O)C3=C(C=CC(F)=C3)C2=C(C#N)C#N)SC2=C1C(CCCCCCCC)(CCCCCCCC)OC1=CC3=C(C=C12)C(CCCCCCCC)(CCCCCCCC)C1=C3C=C2OC(CCCCCCCC)(CCCCCCCC)C3=C(SC(/C=C4C(=O)C5=C(C=CC(F)=C5)C4=C(C#N)C#N)=C3CCCCCCCC)C2=C1,FOR-1F,-5.73,-3.73,18.65,1.02,0.6621,12.59,"S. Wu, L. Meng, Z. Zhang, M. Li, Y. Yang, J. Wang, H. Chen, C. Jiang, X. Wan, C. Li, Z. Yao, Y. Chen, Molecular optimization of incorporating pyran fused acceptor¨Cdonor¨Cacceptor type acceptors enables over 15% efficiency in organic solar cells, J. Mater. Chem. C. 10 (2022) 1977¨C1983. https://doi.org/10.1039/D1TC05779K."
3843,CCCCCCCCC1(CCCCCCCC)C2=CC3=C(C=C2C2=C1C=C(/C=C1C(=O)C4=CC(F)=C(F)C=C4C1=C(C#N)C#N)S2)C(CCCCCCCC)(CCCCCCCC)C1=C3SC2=C1C1=C3C4=C2C=C2C(=O)N(C(CCCCC)CCCCC)C(=O)C5=CC6=C(C7=C(C=C8C(=O)N(C(CCCCC)CCCCC)C(=O)C(=C1)C8=C73)C1=C6C3=C(S1)C1=C(C=C6C(=C1)C(CCCCCCCC)(CCCCCCCC)C1=C6SC(/C=C6C(=O)C7=CC(F)=C(F)C=C7C6=C(C#N)C#N)=C1)C3(CCCCCCCC)CCCCCCCC)C4=C25,PDFC,-5.57,-3.85,15.93,0.97,0.813,12.56,"K. Ding, T. Shan, J. Xu, M. Li, Y. Wang, Y. Zhang, Z. Xie, Z. Ma, F. Liu, H. Zhong, A perylene diimide-containing acceptor enables high fill factor in organic solar cells, Chem. Commun. 56 (2020) 11433¨C11436. https://doi.org/10.1039/D0CC04297H."
3844,CCCCCCCCCCCC1=C(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)SC2=C1SC1=C2N(CC(CCCC)CCCCCC)C2=C1C1=NSN=C1C1=C2N(CC(CCCC)CCCCCC)C2=C1SC1=C2SC(/C=C/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)=C1CCCCCCCCCCC,BTP-S,-5.66,-4.03,26.5,0.711,0.6665,12.56,"Y. Song, Z. Zhong, L. Li, X. Liu, J. Huang, H. Wu, M. Li, Z. Lu, J. Yu, J. Hai, Fused-heterocycle engineering on asymmetric non-fullerene acceptors enables organic solar cells approaching 29?mA/cm2 short-circuit current density, Chem. Eng. J. 430 (2022) 132830. https://doi.org/10.1016/j.cej.2021.132830."
3845,O=C(C1=C(C)SC=C1C/2=C(C#N)C#N)C2=C/C3=CC4=C(S3)C5=C(C6=CC(C7(C8=CC=C(CCCCCC)C=C8)C9=CC=C(CCCCCC)C=C9)=C(C%10=C7C(SC(/C=C%11C(C%12=C(C)SC=C%12C\%11=C(C#N)/C#N)=O)=C%13)=C%13S%10)C=C6C5(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15)S4,MeIC,-5.57,-3.92,18.41,0.918,0.742,12.54,"Z. Luo, H. Bin, T. Liu, Z.-G. Zhang, Y. Yang, C. Zhong, B. Qiu, G. Li, W. Gao, D. Xie, K. Wu, Y. Sun, F. Liu, Y. Li, C. Yang, Fine-Tuning of Molecular Packing and Energy Level through Methyl Substitution Enabling Excellent Small Molecule Acceptors for Nonfullerene Polymer Solar Cells with Efficiency up to 12.54%, Adv. Mater. 30 (2018) 1706124. https://doi.org/10.1002/adma.201706124."
3846,O=C(C1=C/2C=C(F)C(F)=C1)C(CC3=CC4=C(S3)C5=C(C6=CC(C7(C8=CC(CCCCCC)=CC=C8)C9=CC=CC(CCCCCC)=C9)=C(C%10=C7C(SC(/C=C%11C(C(C=C(F)C(F)=C%12)=C%12C\%11=C(C#N)/C#N)=O)=C%13)=C%13S%10)C=C6C5(C%14=CC(CCCCCC)=CC=C%14)C%15=CC=CC(CCCCCC)=C%15)S4)C2=C(C#N)C#N,m-ITIC-4F,-5.73,-4.02,19.76,0.902,0.703,12.53,"X. Li, J. Yao, I. Angunawela, C. Sun, L. Xue, A. Liebman-Pelaez, C. Zhu, C. Yang, Z.-G. Zhang, H. Ade, Y. Li, Improvement of Photovoltaic Performance of Polymer Solar Cells by Rational Molecular Optimization of Organic Molecule Acceptors, Adv. Energy Mater. 8 (2018) 1800815. https://doi.org/10.1002/aenm.201800815."
3847,CCCCCCC1(CCCCCC)C2=CC3=C(C=C2C2=C1C=C(/C=C1C(=O)C4=C(C=C(Cl)C=C4)C1=C(C#N)C#N)S2)C(CCCCCC)(CCCCCC)C1C=C(C2=CC4=C(S2)C2=CC5=C(C=C2C4(CCCCCC)CCCCCC)C2SC(/C=C4C(=O)C6=C(C=C(Cl)C(Cl)=C6)C4=C(C#N)C#N)=CC2C5(CCCCCC)CCCCCC)SC31,IDT2-IC-4Cl.,-5.34,-3.95,22.22,0.84,0.6981,12.53,"Z. Shao, Z. Zhu, H. Tan, X. Yu, J. Yu, W. Zhu, An A-D-D-A-type small-molecule electron acceptor with chlorine substitution for high-efficiency polymer solar cells, Org. Electron. 99 (2021) 106329. https://doi.org/10.1016/j.orgel.2021.106329."
3848,O=C(C1=C/2C=CC(F)=C1)C(CC3=CC4=C(S3)C5=C(C6=CC(C7(C8=CC(CCCCCC)=CC=C8)C9=CC=CC(CCCCCC)=C9)=C(C%10=C7C(SC(/C=C%11C(C(C=C(F)C=C%12)=C%12C\%11=C(C#N)/C#N)=O)=C%13)=C%13S%10)C=C6C5(C%14=CC(CCCCCC)=CC=C%14)C%15=CC=CC(CCCCCC)=C%15)S4)C2=C(C#N)C#N,m-ITIC-2F,-5.73,-3.95,18.98,0.955,0.691,12.53,"X. Li, J. Yao, I. Angunawela, C. Sun, L. Xue, A. Liebman-Pelaez, C. Zhu, C. Yang, Z.-G. Zhang, H. Ade, Y. Li, Improvement of Photovoltaic Performance of Polymer Solar Cells by Rational Molecular Optimization of Organic Molecule Acceptors, Adv. Energy Mater. 8 (2018) 1800815. https://doi.org/10.1002/aenm.201800815."
3849,CCCCCCCCCCCC1=C(/C=C2C(=O)C3=C(C=C(Cl)C(Cl)=C3)C2=C(C#N)C#N)SC2=C1SC1=C2N(CC(CCCC)CCCCCC)C2=C1C1=NSN=C1C1=C2N(CC(CCCC)CCCCCC)C2=C1SC1=C2N(CC(CC)CCCC)C2=C1SC(/C=C1C(=O)C3=C(C=C(Cl)C(Cl)=C3)C1=C(C#N)C#N)=C2,PT2IC-4CL,-5.6,-3.9,20.7,0.834,0.7237,12.51,"Z. Xia, J. Zhang, X. Gao, W. Song, J. Ge, L. Xie, X. Zhang, Z. Liu, Z. Ge, Fine-Tuning the Dipole Moment of Asymmetric Non-Fullerene Acceptors Enabling Efficient and Stable Organic Solar Cells, ACS Appl. Mater. Interfaces. 13 (2021) 23983¨C23992. https://doi.org/10.1021/acsami.1c02652."
3850,O=C(C1=CSC=C1C/2=C(C#N)C#N)C2=C/C3=CC4=C(S3)C5=C(C6=CC7=C(C8=C(S7)C(SC(/C=C9C(C%10=CSC=C%10C9=C(C#N)/C#N)=O)=C%11)=C%11C8(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)C=C6S5)C4(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15,ITIC5,-5.48,-3.95,18.48,0.897,0.755,12.5,"C. Yan, W. Wang, T.-K. Lau, K. Li, J. Wang, K. Liu, X. Lu, X. Zhan, Enhancing the performance of non-fullerene organic solar cells via end group engineering of fused-ring electron acceptors, J. Mater. Chem. A. 6 (2018) 16638¨C16644. https://doi.org/10.1039/C8TA05800H."
3851,O=C(C(C=CC(C#CC1=CC=CC=C1)=C2)=C2C/3=C(C#N)C#N)C3=C/C4=CC5=C(S4)C6=C(C7=CC(C8(C9=CC=C(CC(CC)CCCCCC)S9)C%10=CC=C(CC(CC)CCCCCC)S%10)=C(C%11=C8C(SC(/C=C%12C(C(C=C(C#CC%13=CC=CC=C%13)C=C%14)=C%14C\%12=C(C#N)C#N)=O)=C%15)=C%15S%11)C=C7C6(C%16=CC=C(CC(CC)CCCCCC)S%16)C%17=CC=C(CC(CC)CCCCCC)S%17)S5,ITPN,-5.69,-3.91,17.5,0.986,0.73,12.5,"R. Yu, H. Yao, L. Hong, Y. Xu, B. Gao, J. Zhu, Y. Zu, J. Hou, Enhancing the Photovoltaic Performance of Nonfullerene Acceptors via Conjugated Rotatable End Groups, Adv. Energy Mater. 8 (2018) 1802131. https://doi.org/10.1002/aenm.201802131."
3852,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C=C(/C=C2C(=O)C5=C(C=C(Cl)C(Cl)=C5)C2=C(C#N)C#N)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC(C3=C(F)C(F)=C(C4=CC5=C(S4)C4=C(C=C6C(=C4)C(C4=CC=C(CCCCCC)C=C4)(C4=CC=C(CCCCCC)C=C4)C4=C6SC(/C=C6C(=O)C7=C(C=C(Cl)C(Cl)=C7)C6=C(C#N)C#N)=C4)C5(C4=CC=C(CCCCCC)C=C4)C4=CC=C(CCCCCC)C=C4)C4=NSN=C43)=C2)C=C1,BT2FIDT-4Cl,-5.7,-3.88,18.1,0.97,0.715,12.5,"C. Zhang, X. Song, K.-K. Liu, M. Zhang, J. Qu, C. Yang, G.-Z. Yuan, A. Mahmood, F. Liu, F. He, D. Baran, J.-L. Wang, Electron-Deficient and Quinoid Central Unit Engineering for Unfused Ring-Based A1¨CD¨CA2¨CD¨CA1-Type Acceptor Enables High Performance Nonfullerene Polymer Solar Cells with High Voc and PCE Simultaneously, Small. 16 (2020) 1907681. https://doi.org/10.1002/smll.201907681."
3853,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=C(C=C4C(=C3)C3=C(C5=C(S3)C3=C(C=C(/C=C6C(=O)C7=C(C=C(Cl)C(Cl)=C7)C6=C(C#N)C#N)S3)C(CCCCCC)(CCCCCC)O5)C4(C3=CC=C(C)C=C3)C3=CC=C(C)C=C3)C3=C2C2=C(S3)C3=C(C=C(/C=C4C(=O)C5=C(C=C(Cl)C(Cl)=C5)C4=C(C#N)C#N)S3)C(C)(C)O2)C=C1,ITOT-4Cl,-5.49,-3.9,22.89,0.775,0.705,12.5,"X. Ke, L. Meng, X. Wan, Y. Cai, H.-H. Gao, Y.-Q.-Q. Yi, Z. Guo, H. Zhang, C. Li, Y. Chen, A nonfullerene acceptor incorporating a dithienopyran fused backbone for organic solar cells with efficiency over 14%, Nano Energy. 75 (2020) 104988. https://doi.org/10.1016/j.nanoen.2020.104988."
3854,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=C(SC(/C=C4C(=O)C5=C(C=CC(F)=C5)C4=C(C#N)C#N)=C3)C3=C2C2=C(S3)C(C3=CC4=C(C=C(CC(CC)CCCC)S4)S3)=C3C(=C2C2=CC4=C(C=C(CC(CC)CCCC)S4)S2)SC2=C3C(C3=CC=C(CCCCCC)C=C3)(C3=CC=CC(CCCCCC)=C3)C3=C2SC(/C=C2C(=O)C4=C(C=CC(F)=C4)C2=C(C#N)C#N)=C3)C=C1,BTT-FIC,-5.64,-3.87,18.54,0.953,0.7163,12.46,"Y. Jia, Y. Zhang, W. Jiang, B. Su, C. Liu, E. Zhu, G. Che, A fused-ring non-fullerene acceptor based on a benzo[1,2-b:4,5-b¡ä]dithiophene central core with a thieno[3,2-b]thiophene side-chain for highly efficient organic solar cells, J. Mater. Chem. A. 7 (2019) 10905¨C10911. https://doi.org/10.1039/C9TA01888C."
3855,O=C(C(C(C)=CC=C1)=C1C/2=C(C#N)C#N)C2=C/C3=CC(S4)=C(S3)C5=C4C6=C(C7=CC(C8(C9=CC=C(CCCCCC)C=C9)C%10=CC=C(CCCCCC)C=C%10)=C(C%11=C8C(SC(/C=C%12C(C%13=C(C(C)=CC=C%13)C\%12=C(C#N)C#N)=O)=C%14)=C%14S%11)C=C7C6(C%15=CC=C(CCCCCC)C=C%15)C%16=CC=C(CCCCCC)C=C%16)S5,IDT8CN-M,-5.54,-3.91,17.11,0.92,0.789,12.43,"W. Gao, T. Liu, C. Zhong, G. Zhang, Y. Zhang, R. Ming, L. Zhang, J. Xin, K. Wu, Y. Guo, W. Ma, H. Yan, Y. Liu, C. Yang, Asymmetrical Small Molecule Acceptor Enabling Nonfullerene Polymer Solar Cell with Fill Factor Approaching 79%, ACS Energy Lett. 3 (2018) 1760¨C1768. https://doi.org/10.1021/acsenergylett.8b00825."
3856,CCCCCCCCC1=C(/C=C2C(=O)C3=C(C=C(Cl)C(Cl)=C3)C2=C(C#N)C#N)SC2=C1SC1=C2C(C2=CC=C(CC(CC)CCCC)C=C2)(C2=CC=C(CC(CC)CCCC)C=C2)C2=C1SC1=C2SC2=C1C(C1=CC=C(CC(CC)CCCC)C=C1)(C1=CC=C(CC(CC)CCCC)C=C1)C1=C2SC2=C1SC(/C=C1C(=O)C3=C(C=C(Cl)C(Cl)=C3)C1=C(C#N)C#N)=C2CCCCCCCC,3TT-OCIC,-5.22,-3.91,26.49,0.68,0.69,12.43,"H.-H. Gao, Y. Sun, Y. Cai, X. Wan, L. Meng, X. Ke, S. Li, Y. Zhang, R. Xia, N. Zheng, Z. Xie, C. Li, M. Zhang, H.-L. Yip, Y. Cao, Y. Chen, Achieving Both Enhanced Voltage and Current through Fine-Tuning Molecular Backbone and Morphology Control in Organic Solar Cells, Adv. Energy Mater. 9 (2019) 1901024. https://doi.org/10.1002/aenm.201901024."
3857,CCCCCCCCC1=C(/C=C2C(=O)C3=C(C=C(Cl)C(Cl)=C3)C2=C(C#N)C#N)SC2=C1SC1=C2C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C1PC1=C2OC2C3=C(C4=C(S3)C(CCCCCCCC)=C(CC3C(=O)C5=C(C=C(Cl)C(Cl)=C5)C3=C(C#N)C#N)S4)C(C3=CC=C(CCCCCC)C=C3)(C3=CC=C(CCCCCC)C=C3)C12,6T-2C8-2Cl,-5.56,-3.95,24.4,0.785,0.65,12.43,"H. Gao, X. Wan, Z. Xuan, W. Ma, J. Xin, C. Li, Y. Chen, Finely modulated asymmetric nonfullerene acceptors enabling simultaneously improved voltage and current for efficient organic solar cells, J. Mater. Chem. C. 10 (2022) 2742¨C2748. https://doi.org/10.1039/D1TC03793E."
3858,O=C(C1=C(C)SC=C1C/2=C(C#N)C#N)C2=C/C3=CC4=C(C5=C(C4(C6=CC=C(CCCCCC)S6)C7=CC=C(CCCCCC)S7)C=C(C8=C9C(SC(/C=C%10C(C%11=C(C)SC=C%11C\%10=C(C#N)C#N)=O)=C%12)=C%12S8)C(C9(C%13=CC=C(CCCCCC)S%13)C%14=CC=C(CCCCCC)S%14)=C5)S3,IDT6CN-TM,-5.7,-3.96,17.4,0.953,0.747,12.4,"W. Gao, F. Wu, T. Liu, G. Zhang, Z. Chen, C. Zhong, L. Zhu, F. Liu, H. Yan, C. Yang, Multifunctional asymmetrical molecules for high-performance perovskite and organic solar cells, J. Mater. Chem. A. 7 (2019) 2412¨C2420. https://doi.org/10.1039/C8TA10975C."
3859,CCCCCCCCC1(CCCCCCCC)C2=CC3=C(C=C2C2=C1C1=C(C=C(/C=C4C(=O)C5=C(C=C(Cl)S5)C4=C(C#N)C#N)S1)S2)C(CCCCCCCC)(CCCCCCCC)C1=C3SC2=C1SC(/C=C1C(=O)C3=C(C=C(Cl)S3)C1=C(C#N)C#N)=C2,C8-ITCC-Cl,-5.5,-3.93,17.9,0.95,0.73,12.4,"J. Zhang, Y. Li, H. Hu, G. Zhang, H. Ade, H. Yan, Chlorinated Thiophene End Groups for Highly Crystalline Alkylated Non-Fullerene Acceptors toward Efficient Organic Solar Cells, Chem. Mater. 31 (2019) 6672¨C6676. https://doi.org/10.1021/acs.chemmater.9b00980."
3860,CCCCC(CC)CC1=C2C(=O)C3=C(C4=CC5=C(S4)C4=C(C=C(/C=C6C(=O)C7=C(C=C(F)C(F)=C7)C6=C(C#N)C#N)S4)C5(CC(CC)CCCC)CC(CC)CCCC)SC(C4=CC5=C(S4)C4=C(C=C(/C=C6C(=O)C7=C(C=C(F)C(F)=C7)C6=C(C#N)C#N)S4)C5(CC(CC)CCCC)CC(CC)CCCC)=C3C(=O)C2=C(CC(CC)CCCC)S1,BCIC2F,-5.54,-3.87,22.1,0.792,0.71,12.4,"Y. Li, H. Fu, Z. Wu, X. Wu, M. Wang, H. Qin, F. Lin, H.Y. Woo, A.K.-Y. Jen, Regulating the Aggregation of Unfused Non-Fullerene Acceptors via Molecular Engineering towards Efficient Polymer Solar Cells, ChemSusChem. 14 (2021) 3579¨C3589. https://doi.org/10.1002/cssc.202100746."
3861,CCCCCCCCOC1=C2SC3=C(C2=C(OCCCCCCCC)C2=C1C1=C(S2)C2=C(C4=C(C=C(/C=C5C(=O)C6=C(C=C(F)C=C6)C5=C(C#N)C#N)S4)S2)C1(C1=CC=C(CCCCCC)C=C1)C1=CC=C(CCCCCC)C=C1)C(C1=CC=C(CCCCCC)C=C1)(C1=CC=C(CCCCCC)C=C1)C1=C3SC2=C1SC(/C=C1/C(=O)C3=CC(F)=CC=C3C1=C(C#N)C#N)=C2,OBTT-2F,-5.3,-3.97,20.83,0.828,0.575,12.36,"Y. Sun, H.-H. Gao, Y.-Q.-Q. Yi, X. Wan, H. Feng, X. Ke, Y. Zhang, J. Yan, C. Li, Y. Chen, Fluorination-modulated end units for high-performance non-fullerene acceptors based organic solar cells, Sci. China Mater. 62 (2019) 1210¨C1217. https://doi.org/10.1007/s40843-019-9415-2."
3862,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(C=C(/C=C5C(=O)C6=C(C=C(F)C(F)=C6)C5=C(C#N)C#N)S2)[Se]3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4[Se]C3=C2SC(/C=C2C(=O)C4=C(C=C(F)C(F)=C4)C2=C(C#N)C#N)=C3)C=C1,TRID-4F,,,18.45,0.89,0.75,12.33,"F. Lin, L. Zuo, K. Gao, M. Zhang, S.B. Jo, F. Liu, A.K.-Y. Jen, Regio-Specific Selenium Substitution in Non-Fullerene Acceptors for Efficient Organic Solar Cells, Chem. Mater. 31 (2019) 6770¨C6778. https://doi.org/10.1021/acs.chemmater.9b01242."
3863,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(C=C(/C=C5C(=O)C6=C(C=C(F)C(F)=C6)C5=C(C#N)C#N)N2CCCCCC)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC3=C2N(CCCCCC)C(/C=C2C(=O)C4=C(C=C(F)C(F)=C4)C2=C(C#N)C#N)=C3)C=C1,PTBTP-4F,-5.57,-4.11,20.74,0.862,0.6902,12.33,"J. Zhu, Z. Zhang, Y. Lv, A. Lan, H. Lu, H. Do, F. Chen, Organic solar cells based on non-fullerene acceptors containing thiophene [3,2-b] pyrrole, Org. Electron. (2022) 106461. https://doi.org/10.1016/j.orgel.2022.106461."
3864,CCCCCCC1=CC=C(C2=NC3=C(N=C2C2=CC=C(CCCCCC)C=C2)C(C2=CC4=C(S2)C2=C(C=C(/C=C5C(=O)C6=C(C=C(Cl)C(Cl)=C6)C5=C(C#N)C#N)S2)C4(CC(CC)CCCC)CC(CC)CCCC)=C(F)C(F)=C3C2=CC3=C(S2)C2=C(C=C(/C=C4C(=O)C5=C(C=CC(Cl)=C5)C4=C(C#N)C#N)S2)C3(CC(CC)CCCC)CC(CC)CCCC)C=C1,QOC6-4CL,-5.62,-3.87,22.91,0.782,0.69001,12.32,"J. Huang, S. Li, J. Qin, L. Xu, X. Zhu, L.-M. Yang, Facile Modification of a Noncovalently Fused-Ring Electron Acceptor Enables Efficient Organic Solar Cells, ACS Appl. Mater. Interfaces. 13 (2021) 45806¨C45814. https://doi.org/10.1021/acsami.1c11412."
3865,CCCCCCC1=CC=C(C2(C3=CC=C(C)C=C3)C3=CC4=C(OCC(CC)CCCC)C5=C(C=C4C(OCC(CC)CCCC)=C3C3=C2C2=C(C=C(/C=C4C(=O)C6=C(C=C(F)C(F)=C6)C4=C(C#N)C#N)S2)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C5SC3=C2SC(/C=C2C(=O)C4=C(C=C(F)C(F)=C4)C2=C(C#N)C#N)=C3)C=C1,NITT-BF,-5.75,-4.15,18.08,0.94,0.7238,12.3,"R. Ming, G. Li, C. Xu, Z. Luo, W. Ning, C. Zhong, X. Liu, C. Ye, F. Zhang, C. Yang, Naphthalene-fused octacyclic electron-donating central core constructs non-fullerene acceptors for organic solar cells, Chem. Eng. J. 425 (2021) 130618. https://doi.org/10.1016/j.cej.2021.130618."
3866,O=C(C(C=C(F)C(F)=C1)=C1C/2=C(C#N)C#N)C2=C/C3=CC4=C(S3)C5=C(S4)C(C(C6=CC=C(CCCCCC)C=C6)(C7=CC=C(CCCCCC)C=C7)C8=C9SC%10=C8SC%11=C%10C(C%12=CC=C(CCCCCC)C=C%12)(C%13=CC=C(CCCCCC)C=C%13)C%14=C%11SC%15=C%14SC%16=C%15SC(/C=C%17C(C(C=C(F)C(F)=C%18)=C%18C\%17=C(C#N)/C#N)=O)=C%16)=C9S5,F10IC,-5.26,-396,25.61,0.67,0.715,12.3,"S. Dai, T. Li, W. Wang, Y. Xiao, T.-K. Lau, Z. Li, K. Liu, X. Lu, X. Zhan, Enhancing the Performance of Polymer Solar Cells via Core Engineering of NIR-Absorbing Electron Acceptors, Adv. Mater. 30 (2018) 1706571. https://doi.org/10.1002/adma.201706571."
3867,O=C(C(C=C(F)C(F)=C1)=C1C/2=C(C#N)C#N)C2=C/C3=CC(C4(C5=CC=C(CCCCCC)C=C5)C6=CC=C(CCCCCC)C=C6)=C(S3)C7=C4C8=C(CCCCCC)C=C(C(SC9=C%10C(C%11=CC=C(CCCCCC)C=C%11)(C%12=CC=C(CCCCCC)C=C%12)C%13=C9SC(/C=C%14C(C(C=C(F)C(F)=C%15)=C%15C\%14=C(C#N)/C#N)=O)=C%13)=C%10C(CCCCCC)=C%16)C%16=C8S7,IOIC2,-5.41,-3.78,19.7,0.9,0.693,12.3,"J. Zhu, Z. Ke, Q. Zhang, J. Wang, S. Dai, Y. Wu, Y. Xu, Y. Lin, W. Ma, W. You, X. Zhan, Naphthodithiophene-Based Nonfullerene Acceptor for High-Performance Organic Photovoltaics: Effect of Extended Conjugation, Adv. Mater. 30 (2018) 1704713. https://doi.org/10.1002/adma.201704713."
3868,CCCCCCCCN1C2=C(SC(/C=C3C(=O)C4=CC(F)=CC=C4C3=C(C#N)C#N)=C2)C2=C1C1=C(S2)C2=C(C=C3C(=C2)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C3SC3=C2SC2=C3SC(/C=C3C(=O)C4=C(C=CC(F)=C4)C3=C(C#N)C#N)=C2)C1(C1=CC=C(CCCCCC)C=C1)C1=CC=C(CCCCCC)C=C1,IPTTT-2F,-5.4,-4.07,20,0.894,0.693,12.3,"L. Yang, X. Song, J. Yu, H. Wang, Z. Zhang, R. Geng, J. Cao, D. Baran, W. Tang, Tuning of the conformation of asymmetric nonfullerene acceptors for efficient organic solar cells, J. Mater. Chem. A. 7 (2019) 22279¨C22286. https://doi.org/10.1039/C9TA07634D."
3869,CCCCCCCCOC1=C2SC3=C(C2=C(C2=CC=C(CCCCCC)C=C2)C2=C1C1=C(S2)C2=C(C=C(/C=C4C(=O)C5=C(C=C(Cl)C(Cl)=C5)C4=C(C#N)C#N)S2)C1(C1=CC=C(CCCCCC)C=C1)C1=CC=C(CCCCCC)C=C1)C(C1=CC=C(CCCCCC)C=C1)(C1=CC=C(CCCCCC)C=C1)C1=C3SC(/C=C2C(=O)C3=C(C=C(Cl)C(Cl)=C3)C2=C(C#N)C#N)=C1,POBDT-4Cl,-5.58,-3.97,20.7,0.87,0.67,12.3,"B. Kan, X. Chen, K. Gao, M. Zhang, F. Lin, X. Peng, F. Liu, A.K.-Y. Jen, Asymmetrical side-chain engineering of small-molecule acceptors enable high-performance nonfullerene organic solar cells, Nano Energy. 67 (2020) 104209. https://doi.org/10.1016/j.nanoen.2019.104209."
3870,O=C(C(C=CC(F)=C1)=C1C/2=C(C#N)C#N)C2=C/C3=CC(S4)=C(S3)C5=C4C6=C(C7=CC(C8(C9=CC=C(CCCCCC)C=C9)C%10=CC=C(CCCCCC)C=C%10)=C(C%11=C8C=C(/C=C%12C(C(C=C(F)C=C%13)=C%13C\%12=C(C#N)/C#N)=O)[Se]%11)C=C7C6(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15)S5,TPTTT-2F,-5.66,-3.97,18.02,0.895,0.759,12.24,"C. Li, T. Xia, J. Song, H. Fu, H.S. Ryu, K. Weng, L. Ye, H.Y. Woo, Y. Sun, Asymmetric selenophene-based non-fullerene acceptors for high-performance organic solar cells, J. Mater. Chem. A. 7 (2019) 1435¨C1441. https://doi.org/10.1039/C8TA11197A."
3871,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(C=C(/C=C5C(=O)C6=C(C=C7C=CC=CC7=C6)C5=C(C#N)C#N)S2)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC3=C2SC(/C=C2C(=O)C4=C(C=C5C=CC=CC5=C4)C2=C(C#N)C#N)=C3)C=C1,IDTN,-5.77,-3.97,16.58,0.946,0.78,12.2,"J. Wu, Q. Liu, L. Ye, X. Guo, Q. Fan, J. Lv, M. Zhang, W.-Y. Wong, New Electron Acceptor with End-Extended Conjugation for High-Performance Polymer Solar Cells, Energy Fuels. 35 (2021) 19061¨C19068. https://doi.org/10.1021/acs.energyfuels.1c02470."
3872,O=C(C1=CSC=C1C/2=C(C#N)C#N)C2=C/C3=CC4=C(C5=CC(C6(CCCCCC)CCCCCC)=C(C7=C6C=C(/C=C8C(C9=CSC=C9C8=C(C#N)/C#N)=O)S7)C=C5C4(CCCCCC)CCCCCC)S3,IDTPC1:1,-5.84,-3.98,17.5,0.93,0.746,12.2,"Z. Luo, C. Sun, S. Chen, Z.-G. Zhang, K. Wu, B. Qiu, C. Yang, Y. Li, C. Yang, Side-Chain Impact on Molecular Orientation of Organic Semiconductor Acceptors: High Performance Nonfullerene Polymer Solar Cells with Thick Active Layer over 400 nm, Adv. Energy Mater. 8 (2018) 1800856. https://doi.org/10.1002/aenm.201800856."
3873,O=C(C1=CSC=C1C/2=C(C#N)C#N)C2=C/C3=CC4=C(C5=CC(C6(CCCCCC)CCCCCC)=C(C7=C6C=C(/C=C8C(C9=CSC=C9C8=C(C#N)/C#N)=O)S7)C=C5C4(CCCCCC)CCCCCC)S3,IDTPC,-5.84,-3.98,17.5,0.93,0.746,12.2,"Z. Luo, C. Sun, S. Chen, Z.-G. Zhang, K. Wu, B. Qiu, C. Yang, Y. Li, C. Yang, Side-Chain Impact on Molecular Orientation of Organic Semiconductor Acceptors: High Performance Nonfullerene Polymer Solar Cells with Thick Active Layer over 400 nm, Adv. Energy Mater. 8 (2018) 1800856. https://doi.org/10.1002/aenm.201800856."
3874,CC(C=C1)=CC=C1C2(C3=CC=C(CCCCCC)C=C3)C4=CC(C5=C6C=C(/C=C7C(N(CC)C(N(CC)C/7=O)=S)=O)S5)=C(C6(C8=CC=C(CCCCCC)C=C8)C9=CC=C(CCCCCC)C=C9)C=C4C%10=C2C=C(/C=C%11C(N(CC)C(N(CC)C/%11=O)=S)=O)S%10,ITIC:IDT-T,-5.73,-3.59,17.9,0.935,0.731,12.2,"L. Xiao, B. He, Q. Hu, L. Maserati, Y. Zhao, B. Yang, M.A. Kolaczkowski, C.L. Anderson, N.J. Borys, L.M. Klivansky, T.L. Chen, A.M. Schwartzberg, T.P. Russell, Y. Cao, X. Peng, Y. Liu, Multiple Roles of a Non-fullerene Acceptor Contribute Synergistically for High-Efficiency Ternary Organic Photovoltaics, Joule. 2 (2018) 2154¨C2166. https://doi.org/10.1016/j.joule.2018.08.002."
3875,O=C(C(C=C(Cl)C=C1)=C1C/2=C(C#N)C#N)C2=C/C3=CC4=C(S3)C(C(C5=CC=C(CCCCCC)C=C5)(C6=CC=C(CCCCCC)C=C6)C7=C8SC9=C7SC%10=C9C(C%11=CC=C(CCCCCC)C=C%11)(C%12=CC=C(CCCCCC)C=C%12)C%13=C%10SC%14=C%13SC(/C=C%15C(C(C=C(Cl)C=C%16)=C%16C\%15=C(C#N)/C#N)=O)=C%14)=C8S4,IXIC-2Cl,-5.2,-3.9,23.6,0.73,0.709,12.2,"Y. Chen, T. Liu, H. Hu, T. Ma, J.Y.L. Lai, J. Zhang, H. Ade, H. Yan, Modulation of End Groups for Low-Bandgap Nonfullerene Acceptors Enabling High-Performance Organic Solar Cells, Adv. Energy Mater. 8 (2018) 1801203. https://doi.org/10.1002/aenm.201801203."
3876,O=C(C(C=C(F)C(F)=C1)=C1C/2=C(C#N)C#N)C2=C/C3=C(OCCCCCC)C(OCCCCCC)=C(C4=CC5=C(C6=CC(C7(C8=CC=C(CCCCCC)C=C8)C9=CC=C(CCCCCC)C=C9)=C(C%10=C7C=C(C%11=C(OCCCCCC)C(OCCCCCC)=C(/C=C%12C(C(C=C(F)C(F)=C%13)=C%13C\%12=C(C#N)/C#N)=O)S%11)S%10)C=C6C5(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15)S4)S3,ITOIC-2F,-5.57,-3.87,21.04,0.897,0.645,12.17,"Y. Liu, C. Zhang, D. Hao, Z. Zhang, L. Wu, M. Li, S. Feng, X. Xu, F. Liu, X. Chen, Z. Bo, Enhancing the Performance of Organic Solar Cells by Hierarchically Supramolecular Self-Assembly of Fused-Ring Electron Acceptors, Chem. Mater. 30 (2018) 4307¨C4312. https://doi.org/10.1021/acs.chemmater.8b01319."
3877,O=C(C(C=C(F)C(F)=C1)=C1C/2=C(C#N)C#N)C2=C/C3=CC(S4)=C(S3)C5=C4C(SC6=C7SC8=C6OC(C9=CC=C(CCCCCC)C=C9)(C%10=CC=C(CCCCCC)C=C%10)C%11=C8SC%12=C%11SC(/C=C%13C(C(C=C(F)C(F)=C%14)=C%14C\%13=C(C#N)/C#N)=O)=C%12)=C7OC5(C%15=CC=C(CCCCCC)C=C%15)C%16=CC=C(CCCCCC)C=C%16,COi8DFIC,-5.5,-3.88,26.12,0.68,0.682,12.16,"Z. Xiao, X. Jia, L. Ding, Ternary organic solar cells offer 14% power conversion efficiency, Sci. Bull. 62 (2017) 1562¨C1564. https://doi.org/10.1016/j.scib.2017.11.003."
3878,CCCCCCCCC(CCCCCC)COC1=CC(/C=C/C2=CC3=C(C=C(/C=C4C(=O)C5=CC(F)=C(F)C=C5C4=C(C#N)C#N)S3)N2C(CCCCCCCC)CCCCCCCC)=C(OCC(CCCCCC)CCCCCCCC)C=C1C1=CC(CCCCCC)=C(/C=C2C(=O)C3=CC(F)=C(F)C=C3C2=C(C#N)C#N)S1,DBT-4F,-5.67,-3.87,19.65,0.88,0.7024,12.14,"J. Cao, S. Qu, L. Yang, H. Wang, F. Du, J. Yu, W. Tang, Asymmetric simple unfused acceptor enabling over 12% efficiency organic solar cells, Chem. Eng. J. 412 (2021) 128770. https://doi.org/10.1016/j.cej.2021.128770."
3879,CCCCCCCCCCCC1=C(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)SC2=C1OC1=C2N(CC(CC)CCCC)C2=C1C1=C(N=C3C(=O)N(CC(CC)CCCC)C(=O)C3=N1)C1=C2N(CC(CC)CCCC)C2=C1SC1=C2SC(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)=C1CCCCCCCCCCC,QIP-4F,-5.75,-3.86,18.27,0.94,0.7053,12.12,"C. Zhu, K. An, W. Zhong, Z. Li, Y. Qian, X. Su, L. Ying, Design and synthesis of non-fullerene acceptors based on a quinoxalineimide moiety as the central building block for organic solar cells, Chem. Commun. 56 (2020) 4700¨C4703. https://doi.org/10.1039/D0CC00896F."
3880,O=C(C(C=C(F)C=C1)=C1C/2=C(C#N)C#N)C2=C/C3=CC4=C(S3)C5=C(C6=CC(C7(C8=CC=C(CCCCCC)S8)C9=CC=C(CCCCCC)S9)=C(C%10=C7C(SC(/C=C%11C(C(C=CC(F)=C%12)=C%12C\%11=C(C#N)C#N)=O)=C%13)=C%13S%10)C=C6C5(C%14=CC=C(CCCCCC)S%14)C%15=CC=C(CCCCCC)S%15)S4,ITIC-Th1,-5.74,-4.01,19.33,0.849,0.737,12.1,"F. Zhao, S. Dai, Y. Wu, Q. Zhang, J. Wang, L. Jiang, Q. Ling, Z. Wei, W. Ma, W. You, C. Wang, X. Zhan, Single-Junction Binary-Blend Nonfullerene Polymer Solar Cells with 12.1% Efficiency, Adv. Mater. 29 (2017) 1700144. https://doi.org/10.1002/adma.201700144."
3881,CCCCC(CC)COC1=C2SC3=C(C2=C(OCC(CC)CCCC)C2=C1C1=C(S2)C2=C(C=C(/C=C4C(=O)C5=C(C=CC=C5)C4=C(C#N)C#N)S2)N1CC(CC)CCCC)N(CC(CC)CCCC)C1=C3SC(/C=C2C(=O)C3=C(C=CC=C3)C2=C(C#N)C#N)=C1,BDTIC,-5.3,-3.85,20,0.88,0.68,12.1,"Z. Chen, S.-S. Ma, K. Zhang, Z.-C. Hu, Q.-W. Yin, F. Huang, Y. Cao, A Near-infrared Non-fullerene Acceptor with Thienopyrrole-expanded Benzo[1,2-b:4,5-b¡ä]dithiophene Core for Polymer Solar Cells, Chin. J. Polym. Sci. 39 (2021) 35¨C42. https://doi.org/10.1007/s10118-020-2440-8."
3882,CCCCC(CC)CCC1(CC(CC)CCCC)C2=C(SC(/C=C3C(=O)C4=C(C=C(Cl)C(Cl)=C4)C3=C(C#N)C#N)=C2)C2=C1C=C(C1=C(OCC(CC)CCCC)C(OCC(CC)CCCC)=C(C3=CC4=C(S3)C3=C(C=C(/C=C5C(=O)C6=C(C=C(Cl)C(Cl)=C6)C5=C(C#N)C#N)S3)C4(CC(CC)CCCC)CC(CC)CCCC)C3=NSN=C31)S2,BCDT-4Cl,-5.47,-3.88,23.77,0.76,0.67,12.1,"C. He, Y. Li, S. Li, Z.-P. Yu, Y. Li, X. Lu, M. Shi, C.-Z. Li, H. Chen, Near-Infrared Electron Acceptors with Unfused Architecture for Efficient Organic Solar Cells, ACS Appl. Mater. Interfaces. 12 (2020) 16700¨C16706. https://doi.org/10.1021/acsami.0c00837."
3883,CCCCCCCCN1C2=C(SC(/C=C3C(=O)C4=CC(F)=C(F)C=C4C3=C(C#N)C#N)=C2)C2=C1C1=C(S2)C2=CC3=C(C=C2C1(C1=CC(OCCCCCC)=CC=C1)C1=CC(OCCCCCC)=CC=C1)C1=C(C2=C(S1)C1=C(C=C(/C=C4C(=O)C5=CC(F)=C(F)C=C5C4=C(C#N)C#N)S1)N2CCCCCCCC)C3(C1=CC=CC(OCCCCCC)=C1)C1=CC(OCCCCCC)=CC=C1,m-INPOIC,-5.41,-3.97,21.3,0.85,0.669,12.1,"H. Feng, X. Song, Z. Zhang, R. Geng, J. Yu, L. Yang, D. Baran, W. Tang, Molecular Orientation Unified Nonfullerene Acceptor Enabling 14% Efficiency As-Cast Organic Solar Cells, Adv. Funct. Mater. 29 (2019) 1903269. https://doi.org/10.1002/adfm.201903269."
3884,CCCCCCCCCCCC1=C(/C=C/C=C2C(=O)C3=C(C=CC(F)=C3)C2=C(C#N)C#N)SC2=C1SC1=C2N(CC(CC)CCCC)C2=C1C1=NSN=C1C1=C2N(CC(CC)CCCC)C2=C1SC1=C2SC(/C=C/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)=C1CCCCCCCCCCC,BTPV-4F,-5.67,-3.89,28.3,0.65,0.659,12.1,"Z. Jia, S. Qin, L. Meng, Q. Ma, I. Angunawela, J. Zhang, X. Li, Y. He, W. Lai, N. Li, H. Ade, C.J. Brabec, Y. Li, High performance tandem organic solar cells via a strongly infrared-absorbing narrow bandgap acceptor, Nat. Commun. 12 (2021) 178. https://doi.org/10.1038/s41467-020-20431-6."
3885,CCCCCCCCCCCC1=C(/C=C2C(=O)C3=CC4=CC=CC=C4C=C3C2=C(C#N)C#N)SC2=C1SC1=C2N(CC(CCCC)CCCCCC)C2=C1C1=NSN=C1C1=C2N(CC(CCCC)CCCCCC)C2=C1SC1=C2SC(/C=C2C(=O)C3=C(C=C4C=CC=CC4=C3)C2=C(C#N)C#N)=C1CCCCCCCCCCC,BTP-C4C6-N,-5.5,-3.9,20.7,0.94,0.621,12.1,"J. Pan, Y. Shi, J. Yu, H. Zhang, Y. Liu, J. Zhang, F. Gao, X. Yu, K. Lu, Z. Wei, ¦Ð-Extended Nonfullerene Acceptors for Efficient Organic Solar Cells with a High Open-Circuit Voltage of 0.94 V and a Low Energy Loss of 0.49 eV, ACS Appl. Mater. Interfaces. 13 (2021) 22531¨C22539. https://doi.org/10.1021/acsami.1c04273."
3886,O=C(C1=C(C)SC=C1C/2=C(C#N)C#N)C2=CC3=CC4=C(S3)C5=C(C6=CC(C7(C8=CC=CC(CCCCCC)=C8)C9=CC(CCCCCC)=CC=C9)=C(C%10=C7C(SC(/C=C%11C(C%12=C(C)SC=C%12C/%11=CC#N)=O)=C%13)=C%13S%10)C=C6C5(C%14=CC(CCCCCC)=CC=C%14)C%15=CC=CC(CCCCCC)=C%15)S4,m-MeIC,-5.54,-3.9,18.45,0.919,0.692,12.08,"Z. Luo, G. Li, W. Gao, K. Wu, Z.-G. Zhang, B. Qiu, H. Bin, L. Xue, F. Liu, Y. Li, C. Yang, A universal nonfullerene electron acceptor matching with different band-gap polymer donors for high-performance polymer solar cells, J. Mater. Chem. A. 6 (2018) 6874¨C6881. https://doi.org/10.1039/C7TA11339K."
3887,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(C=C(/C=C5C(=O)C6=C(C=C(OC)C(OC)=C6)C5=C(C#N)C#N)S2)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC3=C2SC(/C=C2C(=O)C4=C(C=CC=C4)C2=C(C#N)C#N)=C3)C=C1,a-IT-2OM,-5.61,-3.92,18.11,0.93,0.7152,12.07,"M. Li, Y. Zhou, J. Zhang, J. Song, Z. Bo, Tuning the dipole moments of nonfullerene acceptors with an asymmetric terminal strategy for highly efficient organic solar cells, J. Mater. Chem. A. 7 (2019) 8889¨C8896. https://doi.org/10.1039/C8TA12530A."
3888,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(C=C(/C=C5C(=O)C6=CC(F)=C(F)C=C6C5=C(C#N)C#N)S2)S3)N(CC(CC)CCCC)C2=CC3=C(C=C24)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C3SC3=C2SC(/C=C2C(=O)C4=CC=CC=C4C2=C(C#N)C#N)=C3)C=C1,CZTT-4F,-5.61,-4.11,19.73,0.94,0.6506,12.07,"H. Wang, Z. Zhang, J. Yu, X. Liu, S. Qu, S. Guang, W. Tang, Nonacyclic carbazole-based non-fullerene acceptors enable over 12% efficiency with enhanced stability for organic solar cells, J. Mater. Chem. A. 7 (2019) 21903¨C21910. https://doi.org/10.1039/C9TA08573D."
3889,CCCCCCCCC(CCCCCCCC)CN1C2=CC3=C(C=C2C2=C1C=C1C(=C2)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C1SC1=C2SC(/C=C2C(=O)C4=C(C=C(F)C(F)=C4)C2=C(C#N)C#N)=C1)C(C1=CC=C(CCCCCC)C=C1)(C1=CC=C(CCCCCC)C=C1)C1=C3SC2=C1SC(/C=C1C(=O)C3=C(C=C(F)C(F)=C3)C1=C(C#N)C#N)=C2,4TC-4F-C8C8,-5.6,-3.96,18.61,0.9,0.72,12.06,"J. Ouyang, B. Zhang, G. Zeng, J. Zhang, X. Zhao, X. Yang, Improving Efficiency of Organic Solar Cells by Restricting the Rotation of Side Chain on Small Molecule Acceptor, Sol. RRL. 4 (2020) 2000359. https://doi.org/10.1002/solr.202000359."
3890,O=C(C(C(Cl)=CC=C1)=C1C/2=C(C#N)/C#N)C2=C/C(S3)=CC4=C3C5=CC6=C(C=C5C4(CCCCCCCC)CCCCCCCC)C7=CC8=C(C(SC(/C=C9C(C(C=CC(Br)=C%10)=C%10C9=C(C#N)C#N)=O)=C%11)=C%11C8(CCCCCCCC)CCCCCCCC)C=C7C6(CCCCCCCC)CCCCCCCC,F-Br,-5.62,-4.06,18.22,0.87,0.76,12.05,"Y. Wang, Y. Zhang, N. Qiu, H. Feng, H. Gao, B. Kan, Y. Ma, C. Li, X. Wan, Y. Chen, A Halogenation Strategy for over 12% Efficiency Nonfullerene Organic Solar Cells, Adv. Energy Mater. 8 (2018) 1702870. https://doi.org/10.1002/aenm.201702870."
3891,CC.O=C(C(C=CC=C1)=C1C/2=C(C#N)C#N)C2=C/C3=CC4=C(S3)C5=C(C6=CC(C7(C8=CC=C(CCCCCC)C=C8)C9=CC=C(CCCCCC)C=C9)=C(C%10=C7C(SC(/C=C%11C(C(C=CC=C%12)=C%12C\%11=C(C#N)/C#N)=O)=C%13)=C%13S%10)C=C6C5(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15)S4.CC,IT-M,-5.58,-3.98,17.4,0.94,0.735,12.05,"S. Li, L. Ye, W. Zhao, S. Zhang, S. Mukherjee, H. Ade, J. Hou, Energy-Level Modulation of Small-Molecule Electron Acceptors to Achieve over 12% Efficiency in Polymer Solar Cells, Adv. Mater. 28 (2016) 9423¨C9429. https://doi.org/10.1002/adma.201602776."
3892,CCCCC(CC)CC1(CC(CC)CCCC)C2=C(SC(/C=C3C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)=C2)C2=C1C=C(C1=C(F)C(F)=C(C3=CC4=C(S3)C3=C(C=C(/C=C5C(=O)C6=C(C=C(F)C(F)=C6)C5=C(C#N)C#N)S3)C4(CC(CC)CCCC)CC(CC)CCCC)C3=NCN=C31)S2,BFC-4F,-5.54,-3.82,20.5,0.81,0.7235,12.05,"H. Yu, Z. Qi, X. Li, Z. Wang, W. Zhou, H. Ade, H. Yan, K. Chen, Modulating Energy Level on an A-D-A¡ä-D-A-Type Unfused Acceptor by a Benzothiadiazole Core Enables Organic Solar Cells with Simple Procedure and High Performance, Sol. RRL. 4 (2020) 2000421. https://doi.org/10.1002/solr.202000421."
3893,O=C(C1=C(C=C(F)C(F)=C1)C/2=C(C#N)/C#N)C2=C/C3=CC4=C(S3)C5=C(C6=C(C5(C7=CC=C(CCCCCC)C=C7)C8=CC=C(CCCCCC)C=C8)C=C(C9=C%10C%11=C(C(SC(/C=C%12C(C%13=C(C=C(F)C(F)=C%13)C\%12=C(C#N)C#N)=O)=C%14)=C%14S%11)S9)C(C%10(C%15=CC=C(CCCCCC)C=C%15)C%16=CC=C(CCCCCC)C=C%16)=C6)S4,TTPTTT-4F,-5.69,-4.12,19.36,0.863,0.721,12.05,"J. Song, C. Li, L. Ye, C. Koh, Y. Cai, D. Wei, H.Y. Woo, Y. Sun, Extension of indacenodithiophene backbone conjugation enables efficient asymmetric A¨CD¨CA type non-fullerene acceptors, J. Mater. Chem. A. 6 (2018) 18847¨C18852. https://doi.org/10.1039/C8TA07334A."
3894,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(C=C(/C=C5C(=O)C6=C(C=CC(Br)=C6)C5=C(C#N)C#N)S2)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC3=C2SC(/C=C2C(=O)C4=C(C=CC(Br)=C4)C2=C(C#N)C#N)=C3)C=C1,ITIC-2Br-¦Ã,-5.54,-3.9,19.01,0.89,0.7121,12.05,"J. Qu, D. Li, H. Wang, J. Zhou, N. Zheng, H. Lai, T. Liu, Z. Xie, F. He, Bromination of the Small-Molecule Acceptor with Fixed Position for High-Performance Solar Cells, Chem. Mater. 31 (2019) 8044¨C8051. https://doi.org/10.1021/acs.chemmater.9b02501."
3895,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C=C(C2=C(OCC(CC)CCCC)C(/C=C5C(=O)C6=C(C=C(Cl)C(Cl)=C6)C5=C(C#N)C#N)=CS2)[Se]3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4[Se]C(C3=C(OCC(CC)CCCC)C(/C=C4C(=O)C5=C(C=C(Cl)C(Cl)=C5)C4=C(C#N)C#N)=CS3)=C2)C=C1,i-IDSe-4Cl,-5.46,-3.78,20.27,0.86,0.69,12.05,"W. Wang, B. Zhao, Z. Liang, Z. Cong, L. Wang, H. Wu, N. Zheng, C. Gao, Achieving Efficient Polymer Solar Cells Based on Near-Infrared Absorptive Backbone Twisted Nonfullerene Acceptors through a Synergistic Strategy of an Indacenodiselenophene Fused-Ring Core and a Chlorinated Terminal Group, ACS Appl. Energy Mater. 5 (2022) 1322¨C1330. https://doi.org/10.1021/acsaem.1c03817."
3896,CCCCC(CC)CN1C(=O)C2=C(SC(C3=CC4=C(S3)C3=C(C=C(/C=C5C(=O)C6=C(C=C(F)C(F)=C6)C5=C(C#N)C#N)S3)C4(CC(CC)CCCC)CC(CC)CCCC)=C2)C2=C(C=C(C3=CC4=C(S3)C3=C(C=C(/C=C5C(=O)C6=C(C=C(F)C(F)=C6)C5=C(C#N)C#N)S3)C4(CC(CC)CCCC)CC(CC)CCCC)S2)C1=O,BTIC-4F,-5.71,-3.95,20.5,0.894,0.657,12.04,"D. Luo, L. Li, Y. Shi, J. Zhang, K. Wang, X. Guo, A.K.K. Kyaw, Electron-deficient diketone unit engineering for non-fused ring acceptors enabling over 13% efficiency in organic solar cells, J. Mater. Chem. A. 9 (2021) 14948¨C14957. https://doi.org/10.1039/D1TA03643B."
3897,O=C(C(C=C(F)C=C1)=C1C/2=C(C#N)C#N)C2=C/C3=CC(S4)=C(S3)C5=C4C6=C(C7=CC(C8(C9=CC=C(CCCCCC)C=C9)C%10=CC=C(CCCCCC)C=C%10)=C(C%11=C8C=C(/C=C%12C(C(C=C(F)C=C%13)=C%13C\%12=C(C#N)/C#N)=O)S%11)C=C7C6(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15)S5,TPTTT-2F,-5.69,-4.01,17.63,0.916,0.745,12.03,"J. Song, C. Li, L. Ye, C. Koh, Y. Cai, D. Wei, H.Y. Woo, Y. Sun, Extension of indacenodithiophene backbone conjugation enables efficient asymmetric A¨CD¨CA type non-fullerene acceptors, J. Mater. Chem. A. 6 (2018) 18847¨C18852. https://doi.org/10.1039/C8TA07334A."
3898,CCCCCCCCC1=C(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)SC2=C1SC1=C2C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C1SC1=C2SC2=C1C(C1=CC=C(CCCCCC)C=C1)(C1=CC=C(CCCCCC)C=C1)C1=C2SC2=C1SC(/C=C1C(=O)C3=C(C=C(F)C(F)=C3)C1=C(C#N)C#N)=C2CCCCCCCC,6T-OFIC-,-5.47,-3.89,22.5,0.779,0.686,12.02,"L. Meng, H.-H. Gao, S. Wu, Y. Sun, X. Wan, Y. Yang, J. Wang, Z. Guo, H. Chen, C. Li, Y. Chen, Structural optimization of acceptor molecules guided by a semi-empirical model for organic solar cells with efficiency over 15%, Sci. China Mater. 64 (2021) 2388¨C2396. https://doi.org/10.1007/s40843-020-1651-5."
3899,O=C(C(C=C(F)C(F)=C1)=C1C/2=C(C#N)/C#N)C2=C/C3=CC4=C(S3)C5=C(C6=C(C5(C7=CC=C(CCCCCC)C=C7)C8=CC=C(CCCCCC)C=C8)C=C(C9=C%10C(SC(/C=C%11C(C%12=CSC=C%12C\%11=C(C#N)/C#N)=O)=C%13)=C%13S9)C(C%10(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15)=C6)S4,IDTT-2F-Th,-5.78,-4.02,17.82,0.912,0.739,12.01,"L. Ye, Y. Xie, Y. Xiao, J. Song, C. Li, H. Fu, K. Weng, X. Lu, S. Tan, Y. Sun, Asymmetric fused-ring electron acceptor with two distinct terminal groups for efficient organic solar cells, J. Mater. Chem. A. 7 (2019) 8055¨C8060. https://doi.org/10.1039/C9TA01285K."
3900,O=C(C(C=C(F)C=C1)=C1C/2=C(C#N)C#N)C2=C/C3=CC4=C(S3)C(C(C5=CC=C(CCCCCC)C=C5)(C6=CC=C(CCCCCC)C=C6)C7=C8SC9=C7SC%10=C9C(C%11=CC=C(CCCCCC)C=C%11)(C%12=CC=C(CCCCCC)C=C%12)C%13=C%10SC%14=C%13SC(/C=C%15C(C(C(F)=CC=C%16)=C%16C\%15=C(C#N)/C#N)=O)=C%14)=C8S4,FOIC,-5.36,-3.92,24,0.743,0.671,12,"T. Li, S. Dai, Z. Ke, L. Yang, J. Wang, C. Yan, W. Ma, X. Zhan, Fused Tris(thienothiophene)-Based Electron Acceptor with Strong Near-Infrared Absorption for High-Performance As-Cast Solar Cells, Adv. Mater. 30 (2018) 1705969. https://doi.org/10.1002/adma.201705969."
3901,CCCCCCC1(CCCCCC)C2=CC3=C(C=C2C2=C1C=C(C1=C4C=C(C(=O)OCC(CC)CCCC)SC4=C(/C=C4SC(=C(C#N)C#N)N(CC)C4=O)S1)S2)C(CCCCCC)(CCCCCC)C1=C3SC(C2=C3C=C(C(=O)OCC(CC)CCCC)SC3=C(/C=C3SC(=C(C#N)C#N)N(CC)C3=O)S2)=C1,ATT-5,-5.41,-3.6,18.86,0.93,0.71,11.97,"F. Liu, J. Zhang, Y. Wang, S. Chen, Z. Zhou, C. Yang, F. Gao, X. Zhu, Modulating Structure Ordering via Side-Chain Engineering of Thieno[3,4-b]thiophene-Based Electron Acceptors for Efficient Organic Solar Cells with Reduced Energy Losses, ACS Appl. Mater. Interfaces. 11 (2019) 35193¨C35200. https://doi.org/10.1021/acsami.9b10641."
3902,CCCCCCCCC1=C(/C=C2C(=O)C3=C(C=C(Cl)C(Cl)=C3)C2=C(C#N)C#N)SC2=C1SC1=C2N(CC(CC)CCCC)C2=C1C1=NSN=C1C1=C2N(CC(CC)CCCC)C2=C1SC1=C2SC(/C=C2C(=O)C3=C(C=C(Cl)C(Cl)=C3)C2=C(C#N)C#N)=C1CCCCCCCC,LL4-2CL,-5.56,-3.99,25.36,0.71,0.7087,11.97,"H. Lu, H. Jin, H. Huang, W. Liu, Z. Tang, J. Zhang, Z. Bo, High-Efficiency Organic Solar Cells Based on Asymmetric Acceptors Bearing One 3D Shape-Persistent Terminal Group, Adv. Funct. Mater. 31 (2021) 2103445. https://doi.org/10.1002/adfm.202103445."
3903,CCCCCCCCCCCC1=C(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)SC2=C1SC1=C2N(CC(CCCC)CCCCCC)C2=C1C1=NN(CC(CC)CCCC)N=C1C1=C2N(CC(CCCC)CCCCCC)C2=C1SC1=C2SC(/C=C/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)=C1CCCCCCCCCCC,BTP-N,-5.63,-3.98,24.87,0.748,0.6435,11.97,"Y. Song, Z. Zhong, L. Li, X. Liu, J. Huang, H. Wu, M. Li, Z. Lu, J. Yu, J. Hai, Fused-heterocycle engineering on asymmetric non-fullerene acceptors enables organic solar cells approaching 29?mA/cm2 short-circuit current density, Chem. Eng. J. 430 (2022) 132830. https://doi.org/10.1016/j.cej.2021.132830."
3904,CCCCC(CC)CC1=CC=C(C2(C3=CC=C(CC(CC)CCCC)C=C3)C3=C(SC4=C3SC(/C=C3C(=O)C5=C(C=C(F)C(F)=C5)C3=C(C#N)C#N)=C4)C3=C2C2=C(S3)C3=C(S2)C2=C(C4=C(C=C(/C=C5C(=O)C6=C(C=C(F)C(F)=C6)C5=C(C#N)C#N)S4)S2)C3(C2=CC=C(CC(CC)CCCC)C=C2)C2=CC=C(CC(CC)CCCC)C=C2)C=C1,3TT-FIC,-5.42,-4.17,25.89,0.662,0.712,11.96,"H.-H. Gao, Y. Sun, X. Wan, X. Ke, H. Feng, B. Kan, Y. Wang, Y. Zhang, C. Li, Y. Chen, A New Nonfullerene Acceptor with Near Infrared Absorption for High Performance Ternary-Blend Organic Solar Cells with Efficiency over 13%, Adv. Sci. 5 (2018) 1800307. https://doi.org/10.1002/advs.201800307."
3905,CCCCC(CC)CC1=CC=C(C2(C3=CC=C(CC(CC)CCCC)C=C3)C3=C(SC4=C3SC(/C=C3C(=O)C5=C(C=C(Cl)C(Cl)=C5)C3=C(C#N)C#N)=C4)C3=C2C2=C(S3)C3=C(S2)C2=C(C4=C(C=C(/C=C5C(=O)C6=C(C=C(Cl)C(Cl)=C6)C5=C(C#N)C#N)S4)S2)C3(C2=CC=C(CC(CC)CCCC)C=C2)C2=CC=C(CC(CC)CCCC)C=C2)C=C1,3TT-CIC,-5.24,-3.95,26.67,0.65,0.69,11.96,"H.-H. Gao, Y. Sun, Y. Cai, X. Wan, L. Meng, X. Ke, S. Li, Y. Zhang, R. Xia, N. Zheng, Z. Xie, C. Li, M. Zhang, H.-L. Yip, Y. Cao, Y. Chen, Achieving Both Enhanced Voltage and Current through Fine-Tuning Molecular Backbone and Morphology Control in Organic Solar Cells, Adv. Energy Mater. 9 (2019) 1901024. https://doi.org/10.1002/aenm.201901024."
3906,CCCCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(S3)C3=C(C=C(/C=C5C(=O)C6=C(C=C(F)C(F)=C6)C5=C(C#N)C#N)S3)S2)C(C2=CC=C(CCCCCCCC)C=C2)(C2=CC=C(CCCCCCCC)C=C2)C2=C4SC3=C2SC2=C3SC(/C=C3C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)=C2)C=C1,2F-C8,,,21.27,0.802,0.7196,11.95,"F. Zhao, D. He, J. Xin, S. Dai, H. Xue, L. Jiang, Z. Wei, W. Ma, X. Zhan, Y. Li, C. Wang, Modulating morphology via side-chain engineering of fused ring electron acceptors for high performance organic solar cells, Sci. China Chem. 62 (2019) 790¨C796. https://doi.org/10.1007/s11426-019-9453-7."
3907,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=C(SC(/C=C4C(=O)C5=C(C)SC=C5C4=C(C#N)C#N)=C3)C3=C2C2=C(S3)C3=C(S2)C2=C(C=C(/C=C4C(=O)C5=C(C)SC=C5C4=C(C#N)C#N)S2)C3(C2=CC=C(CCCCCC)C=C2)C2=CC=C(CCCCCC)C=C2)C=C1,T6Me,-5.5,-3.94,21.33,0.87,0.6513,11.94,"R. Ming, J. Wang, W. Gao, M. Zhang, J. Gao, W. Ning, Z. Luo, X. Liu, C. Zhong, F. Zhang, C. Yang, Fused-Ring Core Engineering for Small Molecule Acceptors Enable High-Performance Nonfullerene Polymer Solar Cells, Small Methods. 3 (2019) 1900280. https://doi.org/10.1002/smtd.201900280."
3908,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(C=C(/C=C5C(=O)C6=C(C=C(Br)C(Br)=C6)C5=C(C#N)C#N)[Se]2)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC3=C2[Se]C(/C=C2C(=O)C4=C(C=C(Br)C(Br)=C4)C2=C(C#N)C#N)=C3)C=C1,TSeIC4Br,-5.69,-3.97,21.27,0.77,0.724,11.92,"C. Zhang, T. Liu, J.-L. Wang, K.-K. Liu, C. Yang, H.-J. Zhang, R. Ma, H. Yan, Tetrabromination versus Tetrachlorination: A Molecular Terminal Engineering of Nonfluorinated Acceptors to Control Aggregation for Highly Efficient Polymer Solar Cells with Increased Voc and Higher Jsc Simultaneously, Sol. RRL. 4 (2020) 2000212. https://doi.org/10.1002/solr.202000212."
3909,CCCCCCCCOC1=CC=CC(OCCCCCCCC)=C1C1=C(C2=CC=C(/C=C3/C(=O)C4=C(C=C(Cl)C(Cl)=C4)C3=C(C#N)C#N)S2)SC(C2=CC(OCC(CC)CCCC)=C(C3=CC(C4=C(OCCCCCCCC)C=CC=C4OCCCCCCCC)=C(C4=CC=C(/C=C5/C(=O)C6=CC(Cl)=C(Cl)C=C6C5=C(C#N)C#N)S4)S3)C=C2OCC(CC)CCCC)=C1,PhO4T-2,-5.62,-4.07,21.49,0.841,0.6591,11.91,"C. Li, X. Zhang, N. Yu, X. Gu, L. Qin, Y. Wei, X. Liu, J. Zhang, Z. Wei, Z. Tang, Q. Shi, H. Huang, Simple Nonfused-Ring Electron Acceptors with Noncovalently Conformational Locks for Low-Cost and High-Performance Organic Solar Cells Enabled by End-Group Engineering, Adv. Funct. Mater. 32 (2022) 2108861. https://doi.org/10.1002/adfm.202108861."
3910,O=C(C(C=C(F)C(F)=C1)=C1C/2=C(C#N)C#N)C2=C/C3=CC4=C(S3)C(C(C5=CC=C(CCCCCC)C=C5)(C6=CC=C(CCCCCC)C=C6)C7=C8C=C9C=CC%10=C(C9=C7C=C%11)C%11=CC%12=C%10C(C%13=CC=C(CCCCCC)C=C%13)(C%14=CC=C(CCCCCC)C=C%14)C%15=C%12SC%16=C%15SC(/C=C%17C(C(C=C(F)C(F)=C%18)=C%18C\%17=C(C#N)/C#N)=O)=C%16)=C8S4,IHIC-N,-5.57,-3.8,21.3,0.785,0.708,11.9,"J. Zhang, C. Yan, W. Wang, Y. Xiao, X. Lu, S. Barlow, T.C. Parker, X. Zhan, S.R. Marder, Panchromatic Ternary Photovoltaic Cells Using a Nonfullerene Acceptor Synthesized Using C¨CH Functionalization, Chem. Mater. 30 (2018) 309¨C313. https://doi.org/10.1021/acs.chemmater.7b04499."
3911,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(C=C(/C=C5C(=O)C6=C(C=C(F)C(F)=C6)C5=C(C#N)C#N)S2)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC3=C2SC(/C=C2C(=O)C4=C(C=C(Br)S4)C2=C(C#N)C#N)=C3)C=C1,IDTT-Br-2F,-5.79,-3.99,18.4,0.94,0.687,11.9,"J. Cai, C. Guo, L. Wang, Y. Fu, C. Chen, D. Li, D. Liu, T. Wang, An asymmetry strategy to reduce excessive aggregation of brominated non-fullerene acceptors for enhanced efficiency of organic solar cells, Org. Electron. 100 (2022) 106357. https://doi.org/10.1016/j.orgel.2021.106357."
3912,CCCCCCOC1=CC=C(C2(C3=CC=C(OCCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(C=C(/C=C5/C(=O)C6=C(C=CC(F)=C6)C5=C(C#N)C#N)S2)S3)C(C2=CC=C(OCCCCCC)C=C2)(C2=CC=C(OCCCCCC)C=C2)C2=C4SC3=C2SC(/C=C2/C(=O)C4=C(C=CC(F)=C4)C2=C(C#N)C#N)=C3)C=C1,POIT-IC2F,-5.6,-3.98,18.6,0.97,0.685,11.9,"Q. Fan, W. Su, M. Zhang, J. Wu, Y. Jiang, X. Guo, F. Liu, T.P. Russell, M. Zhang, Y. Li, Synergistic Effects of Side-Chain Engineering and Fluorination on Small Molecule Acceptors to Simultaneously Broaden Spectral Response and Minimize Voltage Loss for 13.8% Efficiency Organic Solar Cells, Sol. RRL. 3 (2019) 1900169. https://doi.org/10.1002/solr.201900169."
3913,CCCCCCCCCCCC1=C(/C=C2C(=O)C3=C(C=C4C=CC=CC4=C3)C2=C(C#N)C#N)SC2=C1SC1=C2N(CC(CCCC)CCCCCC)C2=C1C1=NSN=C1C1=C2N(CC(CCCCCC)CCCCCCCC)C2=C1SC1=C2SC(/C=C2C(=O)C3=CC4=CC=CC=C4C=C3C2=C(C#N)C#N)=C1CCCCCCCCCCC,BTP-C6C8-N,-5.5,-3.88,20.2,0.95,0.62,11.9,"J. Pan, Y. Shi, J. Yu, H. Zhang, Y. Liu, J. Zhang, F. Gao, X. Yu, K. Lu, Z. Wei, ¦Ð-Extended Nonfullerene Acceptors for Efficient Organic Solar Cells with a High Open-Circuit Voltage of 0.94 V and a Low Energy Loss of 0.49 eV, ACS Appl. Mater. Interfaces. 13 (2021) 22531¨C22539. https://doi.org/10.1021/acsami.1c04273."
3914,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(S3)C3=C(C=C(/C=C5C(=O)C6=C(C=C(Cl)C(Cl)=C6)C5=C(C#N)C#N)S3)C2(CCC)CCC)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC3=C2C(CCC)(CCC)C2=C3SC(/C=C3C(=O)C4=C(C=C(Cl)C(Cl)=C4)C3=C(C#N)C#N)=C2)C=C1,CPDT-4CL,-5.32,-3.78,23.24,0.74,0.691,11.88,"J. Zhang, Y. Li, Z. Peng, F. Bai, L.-K. Ma, H. Ade, Z. Li, H. Yan, Near-infrared electron acceptors with fused nonacyclic molecular backbones for nonfullerene organic solar cells, Mater. Chem. Front. 4 (2020) 1729¨C1738. https://doi.org/10.1039/C9QM00754G."
3915,O=C(C1=CSC=C1C/2=C(C#N)C#N)C2=C/C3=CC4=C(S3)C5=C(C6=C(C7=CC=C(CC(CC)CCCC)S7)C8=C(C9=C(S8)C(SC(/C=C%10C(C%11=CSC=C%11C\%10=C(C#N)/C#N)=O)=C%12)=C%12C9(C%13=CC=C(CCCCCC)C=C%13)C%14=CC=C(CCCCCC)C=C%14)C(C%15=CC=C(CC(CC)CCCC)S%15)=C6S5)C4(C%16=CC=C(CCCCCC)C=C%16)C%17=CC=C(CCCCCC)C=C%17,BTTIC-0M,-5.62,-3.89,18.95,0.86,0.729,11.87,"W. Gao, T. Liu, Z. Luo, L. Zhang, R. Ming, C. Zhong, W. Ma, H. Yan, C. Yang, Regulating exciton bonding energy and bulk heterojunction morphology in organic solar cells via methyl-functionalized non-fullerene acceptors, J. Mater. Chem. A. 7 (2019) 6809¨C6817. https://doi.org/10.1039/C9TA00597H."
3916,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=C(SC(/C=C4C(=O)C5=C(C=CC(C)=C5)C4=C(C#N)C#N)=C3)C3=C2C2=C(S3)C(C3=CC=C(C(CC)CCCC)S3)=C3C(=C2C2=CC=C(C(CC)CCCC)S2)SC2=C3C(C3=CC=C(CCCCCC)C=C3)(C3=CC=C(CCCCCC)C=C3)C3=C2SC(/C=C2C(=O)C4=C(C=C(C)C=C4)C2=C(C#N)C#N)=C3)C=C1,BDTThIT-M,-5.35,-3.82,18.03,0.942,0.714,11.87,"Q. An, W. Gao, F. Zhang, J. Wang, M. Zhang, K. Wu, X. Ma, Z. Hu, C. Jiao, C. Yang, Energy level modulation of non-fullerene acceptors enables efficient organic solar cells with small energy loss, J. Mater. Chem. A. 6 (2018) 2468¨C2475. https://doi.org/10.1039/C7TA10763C."
3917,CCCCOC1=C(C2=CC3=C(S2)C2=C(C=C(/C=C4C(=O)C5=C(C=C(F)C(F)=C5)C4=C(C#N)C#N)S2)C3(CC(CC)CCCC)CC(CC)CCCC)C2=NSN=C2C(C2=CC3=C(S2)C2=C(C=C(/C=C4C(=O)C5=C(C=C(F)C(F)=C5)C4=C(C#N)C#N)S2)C3(CC(CC)CCCC)CC(CC)CCCC)=C1OC,BTCPDTO4,-5.52,-3.9,21.21,0.78,0.71,11.85,"N. Yoon, J.-Y. Jeong, S. Oh, C.E. Song, H.K. Lee, W.S. Shin, J.-C. Lee, S.-J. Moon, S.K. Lee, Effects of Electron-Donating and Electron-Accepting Substitution on Photovoltaic Performance in Benzothiadiazole-Based A¨CD¨CA¡ä¨CD¨CA-Type Small-Molecule Acceptor Solar Cells, ACS Appl. Energy Mater. 3 (2020) 12327¨C12337. https://doi.org/10.1021/acsaem.0c02083."
3918,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(C=C(/C=C5C(=O)C6=CC(Br)=CC=C6C5=C(C#N)C#N)S2)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC3=C2SC(/C=C2C(=O)C4=C(C=CC(Br)=C4)C2=C(C#N)C#N)=C3)C=C1,m-ITBr,-5.68,-4.12,20.12,0.938,0.6278,11.84,"Y. Liu, Y. Zhao, S. Lu, K. Zhu, Q. Wang, X. Kang, L. Yu, S. Dai, M. Sun, Effects of brominated terminal groups on the performance of fused-ring electron acceptors in organic solar cells, Dyes Pigments. 194 (2021) 109652. https://doi.org/10.1016/j.dyepig.2021.109652."
3919,O=C(C1=CSC=C1C/2=C(C#N)C#N)C2=C/C3=CC4=C(S3)C5=C(C6=CC(C7(C8=CC=C(CCCCCC)C=C8)C9=CC=C(CCCCCC)C=C9)=C(C%10=C7C(SC(/C=C%11C(C%12=CSC=C%12C\%11=C(C#N)/C#N)=O)=C%13)=C%13S%10)C=C6C5(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15)S4,PBT1-E,-5.62,-3.96,16.5,0.95,0.751,11.8,"D. Xie, T. Liu, W. Gao, C. Zhong, L. Huo, Z. Luo, K. Wu, W. Xiong, F. Liu, Y. Sun, C. Yang, A Novel Thiophene-Fused Ending Group Enabling an Excellent Small Molecule Acceptor for High-Performance Fullerene-Free Polymer Solar Cells with 11.8% Efficiency, Sol. RRL. 1 (2017) 1700044. https://doi.org/10.1002/solr.201700044."
3920,CCCCCCCCCCC(CCCCCCCC)CN1C2=C(SC3=C2C2=NN(CC(CC)CCCC)N=C2C2=C3SC(/C=C3C(=O)C4=C(C=C(Cl)C(Cl)=C4)C3=C(C#N)C#N)=C2)C2=C1C1=C(C3=NSN=C32)C2=C(C3=C(S2)C2=C(C=C(/C=C4C(=O)C5=C(C=C(Cl)C(Cl)=C5)C4=C(C#N)C#N)S2)C2=NN(CC(CC)CCCC)N=C23)N1CC(CCCCCCCC)CCCCCCCCCC,MS-4CL,5.68,-3.99,20.3,0.81,0.712,11.79,"S. Ma, H. Feng, X. Liu, Z. Hu, X. Yang, Y. Liang, J. Zhang, F. Huang, Y. Cao, Dodecacyclic-Fused Electron Acceptors with Multiple Electron-Deficient Units for Efficient Organic Solar Cells, ChemSusChem. 14 (2021) 3544¨C3552. https://doi.org/10.1002/cssc.202100592."
3921,O=C(C(C=CC=C1)=C1C/2=C(C#N)C#N)C2=C/C3=CC4=C(S3)C5=C(C6=CC(C7(C8=CC(CCCCCC)=CC=C8)C9=CC=CC(CCCCCC)=C9)=C(C%10=C7C(SC(/C=C%11C(C(C=CC=C%12)=C%12C\%11=C(C#N)C#N)=O)=C%13)=C%13S%10)C=C6C5(C%14=CC(CCCCCC)=CC=C%14)C%15=CC=CC(CCCCCC)=C%15)S4,m-ITIC,-5.52,-3.82,18.31,0.91,0.705,11.77,"Y. Yang, Z.-G. Zhang, H. Bin, S. Chen, L. Gao, L. Xue, C. Yang, Y. Li, Side-Chain Isomerization on an n-type Organic Semiconductor ITIC Acceptor Makes 11.77% High Efficiency Polymer Solar Cells, J. Am. Chem. Soc. 138 (2016) 15011¨C15018. https://doi.org/10.1021/jacs.6b09110."
3922,CCCCCCC1=C(/C=C2C(=O)C3=C(C=CC=C3)C2=C(C#N)C#N)SC2=C1SC1=C2N(CCC(C)CCCC(C)C)C2=C1C1=NN(CC(CC)CCCC)N=C1C1=C2N(CCC(C)CCCC(C)C)C2=C1SC1=C2SC(CC2C(=O)C3=C(C=CC=C3)C2=C(C#N)C#N)=C1CCCCCC,Y18-DMO,-5.63,-3.93,18.56,0.96,0.66,11.76,"M.L. Keshtov, I.O. Konstantinov, S.A. Kuklin, Y. Zou, A. Agrawal, F.C. Chen, G.D. Sharma, Binary and Ternary Polymer Solar Cells Based on a Wide Bandgap D-A Copolymer Donor and Two Nonfullerene Acceptors with Complementary Absorption Spectral, ChemSusChem. 14 (2021) 4731¨C4740. https://doi.org/10.1002/cssc.202101407."
3923,CCCCCCCCCCC(CCCCCCCC)CN1C2=C(SC3=C2C2=NN(CC(CC)CCCC)N=C2C2=C3SC(/C=C3C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)=C2)C2=C1C1=C(C3=NSN=C32)C2=C(C3=C(S2)C2=C(C=C(/C=C4C(=O)C5=C(C=C(F)C(F)=C5)C4=C(C#N)C#N)S2)C2=NN(CC(CC)CCCC)N=C23)N1CC(CCCCCCCC)CCCCCCCCCC,MS-4F,-5.63,-3.91,19.61,0.85,0.7059,11.75,"S. Ma, H. Feng, X. Liu, Z. Hu, X. Yang, Y. Liang, J. Zhang, F. Huang, Y. Cao, Dodecacyclic-Fused Electron Acceptors with Multiple Electron-Deficient Units for Efficient Organic Solar Cells, ChemSusChem. 14 (2021) 3544¨C3552. https://doi.org/10.1002/cssc.202100592."
3924,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C=C(C2=CC(CCCCCC)=C(/C=C5C(=O)C6=C(C=C(F)C(F)=C6)C5=C(C#N)C#N)S2)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC(C3=CC(CCCCCC)=C(/C=C4C(=O)C5=C(C=C(F)C(F)=C5)C4=C(C#N)C#N)S3)=C2)C=C1,IDTCN-C,-5.59,-3.92,20.33,0.84,0.696,11.75,"Y. Liu, M. Li, J. Yang, W. Xue, S. Feng, J. Song, Z. Tang, W. Ma, Z. Bo, High-Efficiency As-Cast Organic Solar Cells Based on Acceptors with Steric Hindrance Induced Planar Terminal Group, Adv. Energy Mater. 9 (2019) 1901280. https://doi.org/10.1002/aenm.201901280."
3925,CCC1(CC)C2=C(C=CC(/C=C/C3=CC(C)=C(/C(C4=C(C)C=C(C)C=C4C)=C4N=C(/C=C/C5=CC=C(N(C6=CC=CC=C6)C6=CC=CC=C6)C=C5)C=C4C)N3B(F)F)=C2)C2=C1C1=C(C3=C2C(CC)(CC)C2=C3C=CC(/C=C/C3=CC(C)=C(/C(C4=C(C)C=C(C)C=C4C)=C4N=C(/C=C/C5=CC=C(N(C6=CC=CC=C6)C6=CC=CC=C6)C=C5)C=C4C)N3B(F)F)=C2)C(CC)(CC)C2=C1C=CC(/C=C/C1=CC(C)=C(/C(C3=C(C)C=C(C)C=C3C)=C3N=C(/C=C/C4=CC=C(N(C5=CC=CC=C5)C5=CC=CC=C5)C=C4)C=C3C)N1B(F)F)=C2,3b,-5.52,-3.94,18.34,1.05,0.61,11.75,"P. Li, F. Wu, Y. Fang, H. Dahiya, M.L. Keshtov, H. Xu, A. Agrawal, G.D. Sharma, Truxene ¦Ð-Expanded BODIPY Star-Shaped Molecules as Acceptors for Non-Fullerene Solar Cells with over 13% Efficiency, ACS Appl. Energy Mater. (2022). https://doi.org/10.1021/acsaem.1c03781."
3926,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC=C4C(=C3C3=C2C2=C(S3)C3=C(C=C(/C=C5C(=O)C6=C(C=C(F)C(F)=C6)C5=C(C#N)C#N)S3)S2)C=CC2=C4C3=C(C4=C(S3)C3=C(C=C(/C=C5C(=O)C6=C(C=C(F)C(F)=C6)C5=C(C#N)C#N)S3)S4)C2(C2=CC=C(CCCCCC)C=C2)C2=CC=C(CC3=CC=C4C=C5C=CC(C)=CC5=CC4=C3)C=C2)C=C1,FTIC2,-5.51,-4.02,17.2,0.947,0.713,11.7,"B. Lu, Z. Zhang, B. Jia, G. Cai, J. Zhu, X. Lu, X. Zhan, Y. Yao, Precise Synthesis of Fused Decacyclic Electron Acceptor Isomers for Organic Solar Cells, Sol. RRL. 5 (2021) 2100163. https://doi.org/10.1002/solr.202100163."
3927,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(C=C(/C=C5C(=O)C6=C(SC=C6Br)C5=C(C#N)C#N)S2)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC3=C2SC(/C=C2C(=O)C4=C(SC=C4Br)C2=C(C#N)C#N)=C3)C=C1,ITC-2Br1,-5.7,-3.95,16.6,1.01,0.7,11.7,"M. Guo, H. Chen, Z. Luo, Y. Zhu, F. He, C. Yang, Ternary organic solar cells with PCEs of up to 16.6% by two complementary acceptors working in alloy-like model, Org. Electron. 91 (2021) 106085. https://doi.org/10.1016/j.orgel.2021.106085."
3928,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(S3)C3=C(C=C(/C=C5C(=O)C6=C(C=C(F)C(F)=C6)C5=C(C#N)C#N)S3)N2CC(CC)CCCC)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC3=C2N(CC(CC)CCCC)C2=C3SC(/C=C3C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)=C2)C=C1,INPIC-EH,-5.48,-3.99,20.7,0.837,0.684,11.7,"H. Feng, X. Song, M. Zhang, J. Yu, Z. Zhang, R. Geng, L. Yang, F. Liu, D. Baran, W. Tang, Side chain engineering on dithieno[3,2-b:2,3-d]pyrrol fused electron acceptors for efficient organic solar cells, Mater. Chem. Front. 3 (2019) 702¨C708. https://doi.org/10.1039/C8QM00669E."
3929,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C=C(C2=C(OCC(CC)CCCC)C(/C=C5C(=O)C6=C(C=C(F)C(F)=C6)C5=C(C#N)C#N)=CS2)[Se]3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4[Se]C(C3=C(OCC(CC)CCCC)C(/C=C4C(=O)C5=C(C=C(F)C(F)=C5)C4=C(C#N)C#N)=CS3)=C2)C=C1,i-IDSe-4F,-5.48,-3.78,19.48,0.86,0.694,11.66,"W. Wang, B. Zhao, Z. Liang, Z. Cong, L. Wang, H. Wu, N. Zheng, C. Gao, Achieving Efficient Polymer Solar Cells Based on Near-Infrared Absorptive Backbone Twisted Nonfullerene Acceptors through a Synergistic Strategy of an Indacenodiselenophene Fused-Ring Core and a Chlorinated Terminal Group, ACS Appl. Energy Mater. 5 (2022) 1322¨C1330. https://doi.org/10.1021/acsaem.1c03817."
3930,CCCCCCC(CCC)CC1(CC(CCC)CCCCCC)C2=C(SC(/C=C3C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)=C2)C2=C1C=C(C1=CC3=C(S1)C1=C(C=C(C4=CC5=C(S4)C4=C(C=C(/C=C6C(=O)C7=C(C=C(F)C(F)=C7)C6=C(C#N)C#N)S4)C5(CC(CCC)CCCCCC)CC(CCC)CCCCCC)S1)C1=NSN=C13)S2,DTBCIC-F,-5.59,-3.82,19.15,0.91,0.6785,11.66,"Y. Tang, H. Feng, Y. Liang, H. Tang, Z. Du, J. Xu, F. Huang, Y. Cao, Dithienobenzothiadiazole-Bridged Nonfullerene Electron Acceptors for Efficient Organic Solar Cells, ACS Appl. Polym. Mater. (2021). https://doi.org/10.1021/acsapm.1c01406."
3931,CCCCCCCCCCCC1=C(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)SC2=C1SC1=C2N(CCCCCCC2=CC=CC=C2)C2=C1C1=NSN=C1C1=C2N(CCCCCCC2=CC=CC=C2)C2=C1SC1=C2SC(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)=C1CCCCCCCCCCC,Y6-phC6,-5.74,-4.04,21.8,0.803,0.673,11.66,"L. Yi, S. Dai, R. Sun, W. Wang, Y. Wu, X. Jiao, C. Zhang, J. Min, Alkyl chain engineering of non-fullerene small molecule acceptors for solution-processable organic solar cells, Org. Electron. 87 (2020) 105963. https://doi.org/10.1016/j.orgel.2020.105963."
3932,O=C(C(C=CC(F)=C1)=C1C/2=C(C#N)C#N)C2=C/C(S3)=CC4=C3C5=C(C4(C6=CC=C(CCCCCC)C=C6)C7=CC=C(CCCCCC)C=C7)C8=C(CCCCCCCC)C9=C(C(C(C%10=CC=C(CCCCCC)C=C%10)(C%11=CC=C(CCCCCC)C=C%11)C%12=C%13SC(/C=C%14C(C(C=CC(F)=C%15)=C%15C\%14=C(C#N)/C#N)=O)=C%12)=C%13S9)C(CCCCCCCC)=C8S5,NCBDT,-5.36,-3.89,19.73,0.835,0.702,11.62,"B. Kan, J. Zhang, F. Liu, X. Wan, C. Li, X. Ke, Y. Wang, H. Feng, Y. Zhang, G. Long, R.H. Friend, A.A. Bakulin, Y. Chen, Fine-Tuning the Energy Levels of a Nonfullerene Small-Molecule Acceptor to Achieve a High Short-Circuit Current and a Power Conversion Efficiency over 12% in Organic Solar Cells, Adv. Mater. 30 (2018) 1704904. https://doi.org/10.1002/adma.201704904."
3933,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=C(SC4=C3SC(/C=C3C(=O)C5=C(C=C(F)C(F)=C5)C3=C(C#N)C#N)=C4)C3=C2C2=C(S3)C3=C(S2)C2=C(C4=C(C=C(/C=C5C(=O)C6=CC(F)=C(F)C=C6C5=C(C#N)C#N)S4)S2)C32C3=CC=C(CCCCCC)C=C3C3=C2C=CC(CCCCCC)=C3)C=C1.F,6TIC-4F,-5.45,-4.14,24.4,0.67,0.71,11.61,"X. Liao, H. Pei, H. Zhao, Y. Cui, L. Li, X. Shi, P. Zhu, W. Ma, Y. Chen, A.K.-Y. Jen, The synergistic effects of central core size and end group engineering on performance of narrow bandgap nonfullerene acceptors, Chem. Eng. J. 435 (2022) 135020. https://doi.org/10.1016/j.cej.2022.135020."
3934,O=C(C(C=CC(OC)=C1)=C1C/2=C(C#N)C#N)C2=C/C3=CC4=C(S3)C5=C(C6=CC(C7(C8=CC=C(CCCCCC)C=C8)C9=CC=C(CCCCCC)C=C9)=C(C%10=C7C(SC(/C=C%11C(C(C=CC(OC)=C%12)=C%12C\%11=C(C#N)/C#N)=O)=C%13)=C%13S%10)C=C6C5(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15)S4,IT-O1,-5.48,-3.95,17.35,0.93,0.72,11.6,"J. Zhu, S. Li, X. Liu, H. Yao, F. Wang, S. Zhang, M. Sun, J. Hou, Subtle side-chain tuning on terminal groups of small molecule electron acceptors for efficient fullerene-free polymer solar cells, J. Mater. Chem. A. 5 (2017) 15175¨C15182. https://doi.org/10.1039/C7TA04431C."
3935,O=C(C(C=CC=C1)=C1C/2=C(C#N)C#N)C2=C/C3=CC(OCCCCCC)=C(C4=CC5=C(S4)C6=C(C7=CC(C8(C9=CC=C(CCCCCC)S9)C%10=CC=C(CCCCCC)S%10)=C(C%11=C8C(SC(C%12=C(OCCCCCC)C=C(/C=C%13C(C(C=CC=C%14)=C%14C\%13=C(C#N)/C#N)=O)S%12)=C%15)=C%15S%11)C=C7C6(C%16=CC=C(CCCCCC)S%16)C%17=CC=C(CCCCCC)S%17)S5)S3,IDT-2S,-5.35,-3.91,18.5,0.85,0.719,11.6,"P. Cheng, J. Wang, Q. Zhang, W. Huang, J. Zhu, R. Wang, S.-Y. Chang, P. Sun, L. Meng, H. Zhao, H.-W. Cheng, T. Huang, Y. Liu, C. Wang, C. Zhu, W. You, X. Zhan, Y. Yang, Unique Energy Alignments of a Ternary Material System toward High-Performance Organic Photovoltaics, Adv. Mater. 30 (2018) 1801501. https://doi.org/10.1002/adma.201801501."
3936,CCCCCCC(CCCC)CC1(CC(CCCC)CCCCCC)C2=C(SC(/C=C3C(=O)C4=C(C=C5C=C(F)C(F)=CC5=C4)C3=C(C#N)C#N)=C2)C2=C1C=C(C1=CC3=C(S1)C1=C(C=C(C4=CC5=C(S4)C4=C(C=C(/C=C6C(=O)C7=C(C=C8C=C(F)C(F)=CC8=C7)C6=C(C#N)C#N)S4)C5(CC(CCCC)CCCCCC)CC(CCCC)CCCCCC)S1)C1=C3C=C(C(=O)C(CCCC)CCCCCC)S1)S2,BTTBo-4FN,-5.48,-3.86,19.56,0.84,0.7047,11.6,"S. Ma, Q. Huang, Y. Liang, H. Tang, Y. Chen, J. Zhang, K. Zhang, F. Huang, Y. Cao, Non-fullerene electron acceptors with benzotrithiophene with ¦Ð-extension terminal groups for the development of high-efficiency organic solar cells, J. Mater. Chem. C. 9 (2021) 13896¨C13903. https://doi.org/10.1039/D1TC03259C."
3937,O=C(C(C=C(C)C=C1)=C1C/2=C(C#N)C#N)C2=CC3=CC4=C(S3)C5=C(C6=CC(C7(C8=CC(OCCCCCC)=CC=C8)C9=CC=CC(OCCCCCC)=C9)=C(C%10=C7C(SC(/C=C%11C(C(C=CC(C)=C%12)=C%12C/%11=C(C#N)C#N)=O)=C%13)=C%13S%10)C=C6C5(C%14=CC(OCCCCCC)=CC=C%14)C%15=CC=CC(OCCCCCC)=C%15)S4,MOIT-M,-5.61,-3.89,17.5,0.96,0.688,11.6,"W. Su, Q. Fan, X. Guo, J. Chen, Y. Wang, X. Wang, P. Dai, C. Ye, X. Bao, W. Ma, M. Zhang, Y. Li, Significant enhancement of the photovoltaic performance of organic small molecule acceptors via side-chain engineering, J. Mater. Chem. A. 6 (2018) 7988¨C7996. https://doi.org/10.1039/C8TA01509K."
3938,CCN(C/1=O)C(SC1=C/C2=CC=C(C(S3)=CC4=C3C5=CC(C6(CCCCCCCC)CCCCCCCC)=C(C=C5C4(CCCCCCCC)CCCCCCCC)C7=C6C=C(C8=CC=C(/C=C9SC(N(CC)C9=O)=S)C%10=NSN=C8%10)S7)C%11=NSN=C2%11)=S,O-IDTBR,-5.47,-3.42,16.26,1.08,0.64,11.6,"S. Chen, Y. Liu, L. Zhang, P.C.Y. Chow, Z. Wang, G. Zhang, W. Ma, H. Yan, A Wide-Bandgap Donor Polymer for Highly Efficient Non-fullerene Organic Solar Cells with a Small Voltage Loss, J. Am. Chem. Soc. 139 (2017) 6298¨C6301. https://doi.org/10.1021/jacs.7b01606."
3939,CCCCCCCCOC1=C2SC3=C(C2=C(OCCCCCCCC)C2=C1C1=C(S2)C2=C(C4=C(C=C(/C=C5C(=O)C6=C(C=C(F)C=C6)C5=C(C#N)C#N)S4)S2)C1(C1=CC=C(CCCCCC)C=C1)C1=CC=C(CCCCCC)C=C1)C(C1=CC=C(CCCCCC)C=C1)(C1=CC=C(CCCCCC)C=C1)C1=C3SC2=C1SC(/C=C1/C(=O)C3=CC(F)=C(F)C=C3C1=C(C#N)C#N)=C2,OBTT-4F,-5.39,-4.01,21.67,0.772,0.691,11.55,"Y. Sun, H.-H. Gao, Y.-Q.-Q. Yi, X. Wan, H. Feng, X. Ke, Y. Zhang, J. Yan, C. Li, Y. Chen, Fluorination-modulated end units for high-performance non-fullerene acceptors based organic solar cells, Sci. China Mater. 62 (2019) 1210¨C1217. https://doi.org/10.1007/s40843-019-9415-2."
3940,CCCCCCCCC1(CCCCCCCC)C2=CC3=C(C=C2C2=C1C1=C(C=C(/C=C4C(=O)C5=C(C=C(F)C(F)=C5)C4=C(C#N)C#N)S1)S2)C(CCCCCCCC)(CCCCCCCC)C1=C3SC2=C1SC(/C=C1C(=O)C3=C(C=C(F)C(F)=C3)C1=C(C#N)C#N)=C2,C8-SF,-5.53,-4.05,20.03,0.787,0.7315,11.53,"H. Huang, X. Li, S. Chen, B. Qiu, J. Du, L. Meng, Z. Zhang, C. Yang, Y. Li, Enhanced performance of ternary organic solar cells with a wide bandgap acceptor as the third component, J. Mater. Chem. A. 7 (2019) 27423¨C27431. https://doi.org/10.1039/C9TA09268D."
3941,CCCCCCCCC1=C(/C=C2C(=O)C3=C(C=CC(Cl)=C3)C2=C(C#N)C#N)SC2=C1SC1=C2C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C1SC1=C2SC2=C1C(C1=CC=C(CCCCCC)C=C1)(C1=CC=C(CCCCCC)C=C1)C1=C2SC(/C=C2C(=O)C3=C(C=CC(Cl)=C3)C2=C(C#N)C#N)=C1CCCCCCCC,5T-2C8-Cl ,-5.52,-3.83,20.86,0.864,0.64,11.53,"H. Gao, X. Wan, Z. Xuan, W. Ma, J. Xin, C. Li, Y. Chen, Finely modulated asymmetric nonfullerene acceptors enabling simultaneously improved voltage and current for efficient organic solar cells, J. Mater. Chem. C. 10 (2022) 2742¨C2748. https://doi.org/10.1039/D1TC03793E."
3942,CCCCCCCCC1(CCCCCCCC)C2=CC3=C(C=C2C2=C1C=C(/C=C1C(=O)C4=C(C=CC(Br)=C4)C1=C(C#N)C#N)C2)C(CCCCCCCC)(CCCCCCCC)C1=C3C=C2C(=C1)C1=C(C=C(/C=C3C(=O)C4=C(C=CC(Br)=C4)C3=C(C#N)C#N)S1)C2(CCCCCCCC)CCCCCCCC,F-Br,-5.73,-3.88,18.05,0.862,0.74,11.52,"X. Ke, L. Meng, X. Wan, Y. Cai, H.-H. Gao, Y.-Q.-Q. Yi, Z. Guo, H. Zhang, C. Li, Y. Chen, A nonfullerene acceptor incorporating a dithienopyran fused backbone for organic solar cells with efficiency over 14%, Nano Energy. 75 (2020) 104988. https://doi.org/10.1016/j.nanoen.2020.104988."
3943,CCCCCCC1=CC=C(C2(C3=CC=C(C)C=C3)C3=C(SC4=C3SC(/C=C3C(=O)C5=C(C=C(Cl)C(Cl)=C5)C3=C(C#N)C#N)=C4)C3=C2C2=C(CCCCCC)C4=C(C=C(/C=C5C(=O)C6=C(C=C(Cl)C(Cl)=C6)C5=C(C#N)C#N)S4)C(CCCCCC)=C2S3)C=C1,CC10,-5.72,-4.07,22.64,0.775,0.657,11.52,"C. Jiao, Z. Guo, B. Sun, Y. Yi, L. Meng, X. Wan, M. Zhang, H. Zhang, C. Li, Y. Chen, An acceptor¨Cdonor¨Cacceptor type non-fullerene acceptor with an asymmetric backbone for high performance organic solar cells, J. Mater. Chem. C. 8 (2020) 6293¨C6298. https://doi.org/10.1039/D0TC00981D."
3944,O=C(C(C=C(F)C(F)=C1)=C1C/2=C(C#N)C#N)C2=C/C(S3)=CC4=C3C5=C(S4)C6=C(C7=CC(C8(C9=CC=C(CCCCCC)C=C9)C%10=CC=C(CCCCCC)C=C%10)=C(C%11=C8C(SC%12=C%13SC(/C=C%14C(C(C=C(F)C(F)=C%15)=C%15C\%14=C(C#N)/C#N)=O)=C%12)=C%13S%11)C=C7C6(C%16=CC=C(CCCCCC)C=C%16)C%17=CC=C(CCCCCC)C=C%17)S5,INIC3,-5.52,-4.02,19.44,0.857,0.674,11.5,"S. Dai, F. Zhao, Q. Zhang, T.-K. Lau, T. Li, K. Liu, Q. Ling, C. Wang, X. Lu, W. You, X. Zhan, Fused Nonacyclic Electron Acceptors for Efficient Polymer Solar Cells, J. Am. Chem. Soc. 139 (2017) 1336¨C1343. https://doi.org/10.1021/jacs.6b12755."
3945,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(C=C(/C=C5C(=O)C6=C(C=C(F)C(F)=C6)C5=C(C#N)C#N)S2)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC3=C2SC(/C=C2C(=O)C4=C(C=C(C)S4)C2=C(C#N)C#N)=C3)C=C1,IDTT-M-2F,-5.4,-3.87,17.3,0.99,0.668,11.5,"J. Cai, X. Zhang, C. Guo, Y. Zhuang, L. Wang, D. Li, D. Liu, T. Wang, Asymmetric and Halogenated Fused-Ring Electron Acceptor for Efficient Organic Solar Cells, Adv. Funct. Mater. 31 (2021) 2102189. https://doi.org/10.1002/adfm.202102189."
3946,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=C(SC(/C=C4C(=O)C5=C(C=C(F)C(F)=C5)C4=C(C#N)C#N)=C3)C3=C2C2=C(S3)C3=C(C(OCC(CC)CCCC)=C2)C2=C(C=C3OCC(CC)CCCC)C3=C(S2)C2=C(C=C(/C=C4C(=O)C5=C(C=C(F)C(F)=C5)C4=C(C#N)C#N)S2)C3(C2=CC=C(CCCCCC)C=C2)C2=CC=C(CCCCCC)C=C2)C=C1,NTO-4F,-5.61,-3.88,19.1,0.99,0.61,11.5,"X. Dong, Q. Guo, Q. Liu, L. Zhu, X. Guo, F. Liu, M. Zhang, A naphthodithiophene-based nonfullerene acceptor for high-performance polymer solar cells with a small energy loss, J. Mater. Chem. C. 8 (2020) 6513¨C6520. https://doi.org/10.1039/D0TC00270D."
3947,FC1=CC(C2=CC3=C(C(SC(/C=C4C(C(C=C(F)C(F)=C5)=C5C4=C(C#N)C#N)=O)=C6)=C6C3(CC(CC)CCCC)CC(CC)CCCC)S2)=C(F)C=C1C7=CC(C8(CC(CC)CCCC)CC(CC)CCCC)=C(S7)C9=C8C=C(/C=C%10C(C(C=C(F)C(F)=C%11)=C%11C\%10=C(C#N)C#N)=O)S9,HF-PCIC,-5.53,-3.83,17.81,0.91,0.7077,11.49,"S. Li, L. Zhan, W. Zhao, S. Zhang, B. Ali, Z. Fu, T.-K. Lau, X. Lu, M. Shi, C.-Z. Li, J. Hou, H. Chen, Revealing the effects of molecular packing on the performances of polymer solar cells based on A¨CD¨CC¨CD¨CA type non-fullerene acceptors, J. Mater. Chem. A. 6 (2018) 12132¨C12141. https://doi.org/10.1039/C8TA03753A."
3948,CCCCCCCCC1=C(C2=CC3=C(S2)C2=C(C=C(/C=C4C(=O)C5=C(C=C(F)C(F)=C5)C4=C(C#N)C#N)S2)C3(CC(CC)CCCC)CC(CC)CCCC)C2=NSN=C2C(C2=CC3=C(S2)C2=C(C=C(/C=C4C(=O)C5=C(C=C(F)C(F)=C5)C4=C(C#N)C#N)S2)C3(CC(CC)CCCC)CC(CC)CCCC)=C1CCCCCCCC,BTOR-IC4F,-5.92,-4.23,20.57,0.8,0.696,11.48,"Y. Wang, Z. Liu, X. Cui, C. Wang, H. Lu, Y. Liu, Z. Fei, Z. Ma, Z. Bo, Small molecule acceptors with a ladder-like core for high-performance organic solar cells with low non-radiative energy losses, J. Mater. Chem. A. 8 (2020) 12495¨C12501. https://doi.org/10.1039/D0TA03683H."
3949,CCCCCCCCC1(CCCCCCCC)C2=CC3=C(C=C2C2=C1C=C(/C=C1C(=O)C4=CC(F)=CC=C4C1=C(C#N)C#N)S2)C(CCCCCCCC)(CCCCCCCC)C1=C3C=C2C(=C1)C1=C(C=C(/C=C3C(=O)C4=CC(F)=CC=C4C3=C(C#N)C#N)S1)C2(CCCCCCCC)CCCCCCCC,F-CL,-5.62,-4.04,17.61,0.87,0.75,11.47,"Y. Wang, Y. Zhang, N. Qiu, H. Feng, H. Gao, B. Kan, Y. Ma, C. Li, X. Wan, Y. Chen, A Halogenation Strategy for over 12% Efficiency Nonfullerene Organic Solar Cells, Adv. Energy Mater. 8 (2018) 1702870. https://doi.org/10.1002/aenm.201702870."
3950,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(C=C(/C=C5C(=O)C6=C(C=C(F)C(F)=C6F)C5=C(C#N)C#N)S2)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC3=C2SC(/C=C2C(=O)C4=C(C=C(F)C(F)=C4F)C2=C(C#N)C#N)=C3)C=C1,ITIC-6F,-5.78,-4.16,21.2,0.81,0.667,11.41,"T.J. Aldrich, M. Matta, W. Zhu, S.M. Swick, C.L. Stern, G.C. Schatz, A. Facchetti, F.S. Melkonyan, T.J. Marks, Fluorination Effects on Indacenodithienothiophene Acceptor Packing and Electronic Structure, End-Group Redistribution, and Solar Cell Photovoltaic Response, J. Am. Chem. Soc. 141 (2019) 3274¨C3287. https://doi.org/10.1021/jacs.8b13653."
3951,O=C(C(SC=C1)=C1C/2=C(C#N)C#N)C2=C/C3=CC4=C(S3)C5=C(C6=CC(C7(C8=CC=C(CCCCCC)C=C8)C9=CC=C(CCCCCC)C=C9)=C(C%10=C7C(SC(/C=C%11C(C(SC=C%12)=C%12C\%11=C(C#N)/C#N)=O)=C%13)=C%13S%10)C=C6C5(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15)S4,ITCC,-5.47,-3.76,15.9,1.01,0.71,11.4,"H. Yao, L. Ye, J. Hou, B. Jang, G. Han, Y. Cui, G.M. Su, C. Wang, B. Gao, R. Yu, H. Zhang, Y. Yi, H.Y. Woo, H. Ade, J. Hou, Achieving Highly Efficient Nonfullerene Organic Solar Cells with Improved Intermolecular Interaction and Open-Circuit Voltage, Adv. Mater. 29 (2017) 1700254. https://doi.org/10.1002/adma.201700254."
3952,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(S3)C3=C(C=C(/C=C5C(=O)C6=C(C=C(F)C(F)=C6)C5=C(C#N)C#N)S3)S2)C(C2=CC=C(C)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC3=C2SC2=C3SC(/C=C3C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)=C2)C=C1,F9IC,-5.52,-3.97,19.72,0.856,0.677,11.4,"S. Dai, Y. Xiao, P. Xue, J. James Rech, K. Liu, Z. Li, X. Lu, W. You, X. Zhan, Effect of Core Size on Performance of Fused-Ring Electron Acceptors, Chem. Mater. 30 (2018) 5390¨C5396. https://doi.org/10.1021/acs.chemmater.8b02222."
3953,CCCCCCCCN1C2=C(SC(/C=C3C(=O)C4=CC(F)=CC=C4C3=C(C#N)C#N)=C2)C2=C1C1=C(S2)C2=C(C=C3C(=C2)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C3SC3=C2SC=C3/C=C2C(=O)C3=C(C=CC(F)=C3)C2=C(C#N)C#N)C1(C1=CC=C(CCCCCC)C=C1)C1=CC=C(CCCCCC)C=C1,IPTT-2F,-5.46,-4.04,19.7,0.874,0.662,11.4,"L. Yang, X. Song, J. Yu, H. Wang, Z. Zhang, R. Geng, J. Cao, D. Baran, W. Tang, Tuning of the conformation of asymmetric nonfullerene acceptors for efficient organic solar cells, J. Mater. Chem. A. 7 (2019) 22279¨C22286. https://doi.org/10.1039/C9TA07634D."
3954,CCCCCCC(CCCC)CC1(CC(CCCC)CCCCCC)C2=C(SC(CC3C(=O)C4=CC(F)=C(F)C=C4C3=C(C#N)C#N)=C2)C2=C1C=C(C1=CC3=C(S1)C1=C(C=C(C4=CC5=C(S4)C4=C(C=C(CC6C(=O)C7=C(C=C(F)C(F)=C7)C6=C(C#N)C#N)S4)C5(CC(CCCC)CCCCCC)CC(CCCC)CCCCCC)S1)C1=NSN=C13)S2,BTCD-2FIC,-5.48,-3.9,18.24,0.85,0.73,11.32,"Z. Liu, Q. Mao, J. Wang, F. Wu, D. Zhou, Y. Cheng, S. Huang, B. Huang, C. Yang, L. Chen, Exploiting Novel Unfused-Ring Acceptor for Efficient Organic Solar Cells with Record Open-Circuit Voltage and Fill Factor, ChemSusChem. n/a (n.d.) e202102563. https://doi.org/10.1002/cssc.202102563."
3955,O=C(C(C=C(F)C(F)=C1)=C1C/2=C(C#N)/C#N)C2=C/C3=CC4=C(C5=CC(C6(C7=CC=CC(CCCCCC)=C7)C8=CC(CCCCCC)=CC=C8)=C(C9=C6C%10=C(C%11=C(C%12=CC(C%13(C%14=CC=CC(CCCCCC)=C%14)C%15=CC(CCCCCC)=CC=C%15)=C(C%16=C%13C=C(/C=C%17C(C(C=C(F)C(F)=C%18)=C%18C\%17=C(C#N)C#N)=O)S%16)C=C%12C%11(C%19=CC(CCCCCC)=CC=C%19)C%20=CC=CC(CCCCCC)=C%20)S%10)S9)C=C5C4(C%21=CC(CCCCCC)=CC=C%21)C%22=CC=CC(CCCCCC)=C%22)S3,m-IDTIDT-FIC,-5.47,-3.94,18.01,0.92,0.683,11.32,"F. Wu, L. Zhong, H. Hu, Y. Li, Z. Zhang, Y. Li, Z.-G. Zhang, H. Ade, Z.-Q. Jiang, L.-S. Liao, A decacyclic indacenodithiophene-based non-fullerene electron acceptor with meta-alkyl-phenyl substitutions for polymer solar cells, J. Mater. Chem. A. 7 (2019) 4063¨C4071. https://doi.org/10.1039/C8TA11972D."
3956,O=C(C(C=C(F)C(F)=C1)=C1C/2=C(C#N)C#N)C2=C/C3=C4C(OCCO4)=C(C5=CC6=C(C7=CC(C8(C9=CC=C(CCCCCC)C=C9)C%10=CC=C(CCCCCC)C=C%10)=C(C%11=C8C=C(C%12=C(OCCO%13)C%13=C(/C=C%14C(C(C=C(F)C(F)=C%15)=C%15C\%14=C(C#N)/C#N)=O)S%12)S%11)C=C7C6(C%16=CC=C(CCCCCC)C=C%16)C%17=CC=C(CCCCCC)C=C%17)S5)S3,IDT-EDOT,-5.43,-3.8,21.34,0.86,0.62,11.32,"P. Jiang, S. Ming, Q.-Q. Jia, Y. Liu, H. Lu, M. Li, X. Xu, H.-B. Li, Z. Bo, The influence of the ¦Ð-bridging unit of fused-ring acceptors on the performance of organic solar cells, J. Mater. Chem. A. 6 (2018) 21335¨C21340. https://doi.org/10.1039/C8TA08410F."
3957,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(C=C(/C=C5C(=O)C6=C(C=C(Cl)S6)C5=C(C#N)C#N)S2)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC3=C2SC(/C=C2C(=O)C4=C(C=C(Cl)S4)C2=C(C#N)C#N)=C3)C=C1,ITCC-Cl,-5.4,-3.78,16.7,1.04,0.657,11.3,"J. Cai, X. Zhang, C. Guo, Y. Zhuang, L. Wang, D. Li, D. Liu, T. Wang, Asymmetric and Halogenated Fused-Ring Electron Acceptor for Efficient Organic Solar Cells, Adv. Funct. Mater. 31 (2021) 2102189. https://doi.org/10.1002/adfm.202102189."
3958,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=C(SC(/C=C4C(=O)C5=CC(F)=CC=C5C4=C(C#N)C#N)=C3)C3=C2C2=C(S3)C(C3=CC=C(CC(CC)CCCC)S3)=C3C(=C2C2=CC=C(CC(CC)CCCC)S2)SC2=C3C(C3=CC=C(CCCCCC)C=C3)(C3=CC=C(CCCCCC)C=C3)C3=C2SC(/C=C2C(=O)C4=CC(F)=CC=C4C2=C(C#N)C#N)=C3)C=C1,BTH-2F,-5.59,-3.91,19.5,0.92,0.631,11.3,"G. Li, J. Wu, J. Fang, X. Guo, L. Zhu, F. Liu, M. Zhang, Y. Li, A Non-Fullerene Acceptor with Chlorinated Thienyl Conjugated Side Chains for High-Performance Polymer Solar Cells via Toluene Processing, Chin. J. Chem. 38 (2020) 697¨C702. https://doi.org/10.1002/cjoc.201900495."
3959,O=C(C(C=C(F)C(F)=C1)=C1C/2=C(C#N)C#N)C2=C/C3=CC(C(C4=CC=C(CCCCCC)C=C4)(C5=CC=C(CCCCCC)C=C5)C6=CC7=C(C=C86)C(CCCCCCCC)(CCCCCCCC)C9=C7SC%10=C9C(CCCCCCCC)(CCCCCCCC)C(C=C%11%12)=C%10C=C%11C(C%13=CC=C(CCCCCC)C=C%13)(C%14=CC=C(CCCCCC)C=C%14)C%15=C%12SC(/C=C%16C(C(C=C(F)C(F)=C%17)=C%17C\%16=C(C#N)/C#N)=O)=C%15)C8S3,IDIDTT-2F,-5.51,-3.96,19.79,0.92,0.6185,11.29,"R. Hou, M. Li, J. Wang, Z. Bi, S. Feng, X. Xu, W. Ma, Z. Bo, Nonfullerene acceptors with a novel nonacyclic core for high-performance polymer solar cells, J. Mater. Chem. C. 7 (2019) 3335¨C3341. https://doi.org/10.1039/C8TC06245E."
3960,CCCCCCCC1(CCCCCC)C2=C(SC(/C=C3C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)=C2)C2=C1C=C(C1=C3C(=O)C4=C(CC(CC)CCCC)SC(CC(CC)CCCC)=C4C(=O)C3=C(C3=CC4=C(S3)C3=C(C=C(/C=C5C(=O)C6=C(C=C(F)C(F)=C6)C5=C(C#N)C#N)S3)C4(CCCCCC)CCCCCC)S1)S2,BDC-4F-C6,-5.72,-3.76,22.31,0.785,0.643,11.25,"D. Luo, X. Lai, N. Zheng, C. Duan, Z. Wang, K. Wang, A.K.K. Kyaw, High-performance and low-energy loss organic solar cells with non-fused ring acceptor by alkyl chain engineering, Chem. Eng. J. 420 (2021) 129768. https://doi.org/10.1016/j.cej.2021.129768."
3961,CCCCCCCCC1(CCCCCCCC)C2=CC3=C(C=C2C2=C1C=C1C(=C2)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C1SC1=C2SC(/C=C2C(=O)C4=C(C=C(F)C(F)=C4)C2=C(C#N)C#N)=C1)C(C1=CC=C(CCCCCC)C=C1)(C1=CC=C(CCCCCC)C=C1)C1=C3SC2=C1SC(/C=C1C(=O)C3=C(C=C(F)C(F)=C3)C1=C(C#N)C#N)=C2,4TFIC-4F,-5.66,-3.98,16.56,0.93,0.73,11.24,"J. Ouyang, G. Zeng, Y. Xin, X. Zhao, X. Yang, A Novel Carbazole-Based Nonfullerene Acceptor for High-Efficiency Polymer Solar Cells, Sol. RRL. 4 (2020) 1900417. https://doi.org/10.1002/solr.201900417."
3962,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(C=C(/C=C5C(=O)C6=CSC=C6C5=C(C#N)C#N)S2)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC3=C2SC(/C=C2C(=O)C4=CSC=C4C2=C(C#N)C#N)=C3)C=C1,ITCPTC,-5.62,-3.96,17.71,0.877,0.723,11.23,"Z. Luo, H. Bin, T. Liu, Z.-G. Zhang, Y. Yang, C. Zhong, B. Qiu, G. Li, W. Gao, D. Xie, K. Wu, Y. Sun, F. Liu, Y. Li, C. Yang, Fine-Tuning of Molecular Packing and Energy Level through Methyl Substitution Enabling Excellent Small Molecule Acceptors for Nonfullerene Polymer Solar Cells with Efficiency up to 12.54%, Adv. Mater. 30 (2018) 1706124. https://doi.org/10.1002/adma.201706124."
3963,CCCCCCCCCCC(CCCCCC)N1N=C2C(=N1)C(C1=CC3=C(S1)C1=C(C=C(/C=C4C(=O)C5=C(C=C(F)C(F)=C5)C4=C(C#N)C#N)S1)C3(CC(CC)CCCC)CC(CC)CCCC)=C(F)C(F)=C2C1=CC2=C(S1)C1=C(C=C(/C=C3C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)S1)C2(CC(CC)CCCC)CC(CC)CCCC,BTC6-4F,-5.56,-3.86,19.81,0.79,0.7165,11.23,"J. Huang, C.-Y. Gao, X.-H. Fan, X. Zhu, L.-M. Yang, A¨CD¨CC¨CD¨CA type non-fullerene acceptors based on the benzotriazole (BTA) unfused core for organic solar cells, New J. Chem. 45 (2021) 12802¨C12807. https://doi.org/10.1039/D1NJ01978C."
3964,CCCCCCCCCCCC1=C(/C=CC=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)SC2=C1SC1=C2N(CC(CCCC)CCCCCC)C2=C1C1=NSN=C1C1=C2N(CC(CCCC)CCCCCC)C2=C1SC1=C2SC(/C=C/C=C2C(=O)C3=CC(F)=C(F)C=C3C2=C(C#N)C#N)=C1CCCCCCCCCCC,BTP-2V-2F,-5.53,-3.71,26.5,0.66,0.64,11.22,"J. Hai, W. Zhao, S. Luo, H. Yu, H. Chen, Z. Lu, L. Li, Y. Zou, H. Yan, Vinylene ¦Ð-bridge: A simple building block for ultra-narrow bandgap nonfullerene acceptors enable 14.2% efficiency in binary organic solar cells, Dyes Pigments. 188 (2021) 109171. https://doi.org/10.1016/j.dyepig.2021.109171."
3965,O=C(C(C=CC(C)=C1)=C1C/2=C(C#N)C#N)C2=C/C3=CC4=C(C5=CC(C6(C7=CC=C(CCCCCC)C=C7)C8=CC=C(CCCCCC)C=C8)=C(C9=C6C(SC(/C=C%10C(C%11=C(C=CC(C)=C%11)C\%10=C(C#N)C#N)=O)=C%12)=C%12S9)C=C5C4(C%13=CC=C(CCCCCC)C=C%13)C%14=CC=C(CCCCCC)C=C%14)S3,IDT6CN-M1:1,-5.6,-3.87,16.02,0.91,0.768,11.2,"W. Gao, T. Liu, C. Zhong, G. Zhang, Y. Zhang, R. Ming, L. Zhang, J. Xin, K. Wu, Y. Guo, W. Ma, H. Yan, Y. Liu, C. Yang, Asymmetrical Small Molecule Acceptor Enabling Nonfullerene Polymer Solar Cell with Fill Factor Approaching 79%, ACS Energy Lett. 3 (2018) 1760¨C1768. https://doi.org/10.1021/acsenergylett.8b00825."
3966,O=C(C(C=CC(F)=C1)=C1C/2=C(C#N)C#N)C2=C/C=C/C3=CC4=C(C5=C(C4(C6=CC=C(CCCCCC)C=C6)C7=CC=C(CCCCCC)C=C7)C=C(C8=C9C=C(/C=C/C=C%10C(C(C=C(F)C=C%11)=C%11C\%10=C(C#N)/C#N)=O)S8)C(C9(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)=C5)S3,ITC6-2F,-5.73,-3.81,17.83,0.861,0.728,11.2,"C. Zhang, S. Ming, H. Wu, X. Wang, H. Huang, W. Xue, X. Xu, Z. Tang, W. Ma, Z. Bo, High-efficiency ternary nonfullerene organic solar cells with record long-term thermal stability, J. Mater. Chem. A. 8 (2020) 22907¨C22917. https://doi.org/10.1039/D0TA07887E."
3967,O=C(C(C=C1C(C=CC=C1)=C2)=C2C/3=C(C#N)/C#N)C3=C/C(S4)=CC5=C4C6=CC7=C(C=C6C5(CCCCCCCC)CCCCCCCC)C8=CC9=C(C(SC(/C=C%10C(C(C=C(C=CC=C%11)C%11=C%12)=C%12C\%10=C(C#N)C#N)=O)=C%13)=C%13C9(CCCCCCCC)CCCCCCCC)C=C8C7(CCCCCCCC)CCCCCCCC,FDNCTF,-5.42,-3.73,16.3,0.93,0.725,11.2,"B. Kan, Y.-Q.-Q. Yi, X. Wan, H. Feng, X. Ke, Y. Wang, C. Li, Y. Chen, Ternary Organic Solar Cells With 12.8% Efficiency Using Two Nonfullerene Acceptors With Complementary Absorptions, Adv. Energy Mater. 8 (2018) 1800424. https://doi.org/10.1002/aenm.201800424."
3968,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=C(SC4=C3SC(/C=C3C(=O)C5=CC(Cl)=CC=C5C3=C(C#N)C#N)=C4)C3=C2C2=C(S3)C3=C(S2)C2=C(C4=C(C=C(/C=C5C(=O)C6=CC(Cl)=C(Cl)C=C6C5=C(C#N)C#N)S4)S2)C3(C2=CC=C(CCCCCC)C=C2)C2=CC=C(CCCCCC)C=C2)C=C1,IXIC-4CL,-5.2,-3.95,22.1,0.69,0.712,11.2,"Y. Chen, T. Liu, H. Hu, T. Ma, J.Y.L. Lai, J. Zhang, H. Ade, H. Yan, Modulation of End Groups for Low-Bandgap Nonfullerene Acceptors Enabling High-Performance Organic Solar Cells, Adv. Energy Mater. 8 (2018) 1801203. https://doi.org/10.1002/aenm.201801203."
3969,CC(C=C1)=CC=C1N(C2=CC=C(C)C=C2)C(C=C3)=CC=C3C4=CC=C(/C=C(C#N)/C#N)C5=NSN=C45,BT-CIC,-5.49,-4.09,22.5,0.07,0.71,11.2,"X. Che, Y. Li, Y. Qu, S.R. Forrest, High fabrication yield organic tandem photovoltaics combining vacuum- and solution-processed subcells with 15% efficiency, Nat. Energy. 3 (2018) 422¨C427. https://doi.org/10.1038/s41560-018-0134-z."
3970,O=C(C1=C/2C=CC=C1)C(CC3=CC4=C(S3)C5=C(C6=CC(C7(CCCCCCCCCCCCCCCC)CCCCCCCCCCCCCCCC)=C(C8=C7C(SC(/C=C9C(C(C=CC=C%10)=C%10C9=C(C#N)/C#N)=O)=C%11)=C%11S8)C=C6C5(CCCCCCCCCCCCCCCC)CCCCCCCCCCCCCCCC)S4)C2=C(C#N)C#N,IDTTIC,-5.68,-3.89,17.3,0.919,0.704,11.2,"X. Song, N. Gasparini, M.M. Nahid, H. Chen, S.M. Macphee, W. Zhang, V. Norman, C. Zhu, D. Bryant, H. Ade, I. McCulloch, D. Baran, A Highly Crystalline Fused-Ring n-Type Small Molecule for Non-Fullerene Acceptor Based Organic Solar Cells and Field-Effect Transistors, Adv. Funct. Mater. 28 (2018) 1802895. https://doi.org/10.1002/adfm.201802895."
3971,CCCCCCC1=CC=C(C2=C3SC4=C(C3=C(C3=CC=C(CCCCCC)C=C3)C3=C2C2=C(S3)C3=C(C=C(/C=C5C(=O)C6=C(C=C(Cl)C(Cl)=C6)C5=C(C#N)C#N)S3)C2(C2=CC=C(CCCCCC)C=C2)C2=CC=C(CCCCCC)C=C2)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC(/C=C3C(=O)C4=C(C=C(Cl)C(Cl)=C4)C3=C(C#N)C#N)=C2)C=C1,DPBDT-4Cl,-5.62,-3.94,18.7,0.89,0.65,11.2,"B. Kan, X. Chen, K. Gao, M. Zhang, F. Lin, X. Peng, F. Liu, A.K.-Y. Jen, Asymmetrical side-chain engineering of small-molecule acceptors enable high-performance nonfullerene organic solar cells, Nano Energy. 67 (2020) 104209. https://doi.org/10.1016/j.nanoen.2019.104209."
3972,O=C(C(C=C(F)C(F)=C1)=C1C/2=C(C#N)C#N)C2=C/C3=CC(C4(C5=CC=C(CCCCCC)C=C5)C6=CC=C(CCCCCC)C=C6)=C(S3)C7=C4C8=C(S7)C9=C(C%10=CC(C%11(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)=C(C%14=C%11C(SC%15=C%16C(C%17=CC=C(CCCCCC)C=C%17)(C%18=CC=C(CCCCCC)C=C%18)C%19=C%15SC(/C=C%20C(C(C=C(F)C(F)=C%21)=C%21C\%20=C(C#N)/C#N)=O)=C%19)=C%16S%14)C=C%10C9(C%22=CC=C(CCCCCC)C=C%22)C%23=CC=C(CCCCCC)C=C%23)S8,IUIC,-5.45,-3.87,21.74,0.796,0.649,11.2,"B. Jia, S. Dai, Z. Ke, C. Yan, W. Ma, X. Zhan, Breaking 10% Efficiency in Semitransparent Solar Cells with Fused-Undecacyclic Electron Acceptor, Chem. Mater. 30 (2018) 239¨C245. https://doi.org/10.1021/acs.chemmater.7b04251."
3973,O=C(C(C=CC(F)=C1)=C1C/2=C(C#N)/C#N)C2=C/C(S3)=CC4=C3C5=C(C(CC(CC)CCCC)(CC(CC)CCCC)O4)C=C6C(C(CC(CC)CCCC)(CC(CC)CCCC)OC7=C6SC(/C=C8C(C(C(F)=CC=C9)=C9C8=C(C#N)C#N)=O)=C7)=C5,NBDTP-Fout,-5.45,-4,21.87,0.798,0.6437,11.2,"H. Wu, H. Fan, S. Xu, L. Ye, Y. Guo, Y. Yi, H. Ade, X. Zhu, Isomery-Dependent Miscibility Enables High-Performance All-Small-Molecule Solar Cells, Small. 15 (2019) 1804271. https://doi.org/10.1002/smll.201804271."
3974,O=C(C(C(C)=CC=C1)=C1C/2=C(C#N)C#N)C2=C/C3=CC4=C(S3)C5=C(C6=CC(C7(C8=CC=C(CCCCCC)C=C8)CCCCCCCC)C(C9=C7C(SC(/C=C%10C(C(C=CC(C)=C%11)=C%11C\%10=C(C#N)/C#N)=O)=C%12)=C%12S9)C=C6C5(C%13=CC=C(CCCCCC)C=C%13)CCCCCCCC)S4,IDTT-OB1:1,-5.59,-3.88,16.41,0.91,0.74,11.19,"S. Feng, C. Zhang, Z. Bi, Y. Liu, P. Jiang, S. Ming, X. Xu, W. Ma, Z. Bo, Controlling Molecular Packing and Orientation via Constructing a Ladder-Type Electron Acceptor with Asymmetric Substituents for Thick-Film Nonfullerene Solar Cells, ACS Appl. Mater. Interfaces. 11 (2019) 3098¨C3106. https://doi.org/10.1021/acsami.8b19596."
3975,O=C(C(C=C(F)C(F)=C1)=C1C/2=C(C#N)C#N)C2=C/C3=CC=C(C4=CC5=C(C6=CC(C7(C8=CC=C(CCCCCC)C=C8)C9=CC=C(CCCCCC)C=C9)=C(C%10=C7C=C(C%11=CC=C(/C=C%12C(C(C=C(F)C(F)=C%13)=C%13C\%12=C(C#N)/C#N)=O)[Se]%11)S%10)C=C6C5(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15)S4)[Se]3,2Se-4F,-5.51,-4,21.49,0.79,0.659,11.19,"Z. Liang, M. Li, X. Zhang, Q. Wang, Y. Jiang, H. Tian, Y. Geng, Near-infrared absorbing non-fullerene acceptors with selenophene as ¦Ð bridges for efficient organic solar cells, J. Mater. Chem. A. 6 (2018) 8059¨C8067. https://doi.org/10.1039/C8TA00783G."
3976,CCCCCCCCC1=CC=C(C2(C3=CC=C(CCCCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(C=C(C5=CC=C(/C=C6/C(=O)C7=C(C=CC=C7)C6=C(C#N)C#N)C6=NSN=C56)S2)S3)C(C2=CC=C(CCCCCCCC)C=C2)(C2=CC=C(CCCCCCCC)C=C2)C2=C4SC3=C2SC(C2=CC=C(/C=C4C(=O)C5=C(C=CC=C5)C4=C(C#N)C#N)C4=NSN=C24)=C3)C=C1,IT-BT-ICN,-5.59,-4.08,17.54,0.87,0.7323,11.14,"S. Shome, H.J. Shin, J. Yang, B. Park, S.-J. Ko, J. Lee, H. Choi, Microwave-Assisted Synthesis of Non-Fullerene Acceptors and Their Photovoltaic Studies for High-Performance Organic Solar Cells, ACS Appl. Energy Mater. 4 (2021) 9816¨C9826. https://doi.org/10.1021/acsaem.1c01872."
3977,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(C=C(/C=C5C(=O)C6=C(C=C(F)C=C6)C5=C(C#N)C#N)N2CCCCCC)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC3=C2N(CCCCCC)C(/C=C2C(=O)C4=C(C=C(F)C=C4)C2=C(C#N)C#N)=C3)C=C1,PTBTP-2F,-5.56,-4.09,17.89,0.907,0.6866,11.14,"J. Zhu, Z. Zhang, Y. Lv, A. Lan, H. Lu, H. Do, F. Chen, Organic solar cells based on non-fullerene acceptors containing thiophene [3,2-b] pyrrole, Org. Electron. (2022) 106461. https://doi.org/10.1016/j.orgel.2022.106461."
3978,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(C=C(/C=C5C(=O)C6=CC=CC=C6C5=C(C#N)C#N)S2)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC3=C2SC(/C=C2C(=O)C4=C(C=CC=C4)C2=C(C#N)C#N)=C3)C=C1,o-ITBr,-5.62,-4.09,19.68,0.945,0.5994,11.14,"Y. Liu, Y. Zhao, S. Lu, K. Zhu, Q. Wang, X. Kang, L. Yu, S. Dai, M. Sun, Effects of brominated terminal groups on the performance of fused-ring electron acceptors in organic solar cells, Dyes Pigments. 194 (2021) 109652. https://doi.org/10.1016/j.dyepig.2021.109652."
3979,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(C=C(/C=C5C(=O)C6=C(C=C(Cl)C(Cl)=C6)C5=C(C#N)C#N)[Se]2)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC3=C2[Se]C(/C=C2C(=O)C4=C(C=C(Cl)C(Cl)=C4)C2=C(C#N)C#N)=C3)C=C1,TSeIC4Cl,-5.75,-3.99,20.92,0.74,0.717,11.13,"C. Zhang, T. Liu, J.-L. Wang, K.-K. Liu, C. Yang, H.-J. Zhang, R. Ma, H. Yan, Tetrabromination versus Tetrachlorination: A Molecular Terminal Engineering of Nonfluorinated Acceptors to Control Aggregation for Highly Efficient Polymer Solar Cells with Increased Voc and Higher Jsc Simultaneously, Sol. RRL. 4 (2020) 2000212. https://doi.org/10.1002/solr.202000212."
3980,O=C(C(C=CC=C1)=C1C/2=C(C#N)/C#N)C2=C/C(S3)=CC4=C3C5=CC6=C(C=C5C4(CCCCCCCC)CCCCCCCC)C7=CC8=C(C(SC(/C=C9C(C(C=CC=C%10)=C%10C9=C(C#N)C#N)=O)=C%11)=C%11C8(CCCCCCCC)CCCCCCCC)C=C7C6(CCCCCC)CCCCCC,FTIC-C6C8,-5.64,-4.01,18.55,0.93,0.6472,11.12,"Z. Zhang, M. Li, Y. Liu, J. Zhang, S. Feng, X. Xu, J. Song, Z. Bo, Simultaneous enhancement of the molecular planarity and the solubility of non-fullerene acceptors: effect of aliphatic side-chain substitution on the photovoltaic performance, J. Mater. Chem. A. 5 (2017) 7776¨C7783. https://doi.org/10.1039/C7TA02141K."
3981,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(S3)C3=C(C=C(/C=C5C(=O)C6=C(C=C(F)C(F)=C6)C5=C(C#N)C#N)S3)N2CC(CCCC)CCCCCC)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC3=C2N(CC(CCCC)CCCCCC)C2=C3SC(/C=C3C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)=C2)C=C1,IPIC-4F,-5.25,-3.27,19.8,0.835,0.671,11.1,"R. Geng, X. Song, H. Feng, J. Yu, M. Zhang, N. Gasparini, Z. Zhang, F. Liu, D. Baran, W. Tang, Nonfullerene Acceptor for Organic Solar Cells with Chlorination on Dithieno[3,2-b:2¡ä,3¡ä-d]pyrrol Fused-Ring, ACS Energy Lett. 4 (2019) 763¨C770. https://doi.org/10.1021/acsenergylett.9b00147."
3982,CCCCCCC1=CC(C2=CC3=C(S2)C2=C(C=C(/C=C4C(=O)C5=C(C=CC=C5)C4=C(C#N)C#N)S2)C3(CC(CC)CCCC)CC(CC)CCCC)=C(CCCCCC)C=C1C1=CC2=C(S1)C1=C(C=C(/C=C3C(=O)C4=C(C=CC=C4)C3=C(C#N)C#N)S1)C2(CC(CC)CCCC)CC(CC)CCCC,DC6-IC,,,18.85,0.93,0.6333,11.1,"H. Huang, Q. Guo, S. Feng, C. Zhang, Z. Bi, W. Xue, J. Yang, J. Song, C. Li, X. Xu, Z. Tang, W. Ma, Z. Bo, Noncovalently fused-ring electron acceptors with near-infrared absorption for high-performance organic solar cells, Nat. Commun. 10 (2019) 3038. https://doi.org/10.1038/s41467-019-11001-6."
3983,O=C(C(C=CC=C1)=C1C/2=C(C#N)C#N)C2=C/C3=CC4=C(S3)C(C(C5=CC=C(CCCCCC)C=C5)(C6=CC=C(CCCCCC)C=C6)C7=C8SC9=C7SC%10=C9C(C%11=CC=C(CCCCCC)C=C%11)(C%12=CC=C(CCCCCC)C=C%12)C%13=C%10SC%14=C%13SC(/C=C%15C(C(C=CC=C%16)=C%16C\%15=C(C#N)/C#N)=O)=C%14)=C8S4,6TIC,-5.21,-3.83,20.11,0.83,0.6616,11.07,"X. Shi, J. Chen, K. Gao, L. Zuo, Z. Yao, F. Liu, J. Tang, A.K.-Y. Jen, Terthieno[3,2-b]Thiophene (6T) Based Low Bandgap Fused-Ring Electron Acceptor for Highly Efficient Solar Cells with a High Short-Circuit Current Density and Low Open-Circuit Voltage Loss, Adv. Energy Mater. 8 (2018) 1702831. https://doi.org/10.1002/aenm.201702831."
3984,CCCCCCCCCCCC1=C(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)SC2=C1SC1=C2N(CC(C)CCCC)C2=C1C1=NSN=C1C1=C2N(CC(CC)CCCC)C2=C1SC1=C2SC(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)=C1CCCCCCCCCCC,IC2F-BEH-IC2F,-5.66,-4.02,23.64,0.704,0.6638,11.05,"P. Gopikrishna, H. Choi, D.H. Kim, J.H. Hwang, Y. Lee, H. Jung, G. Yu, T.B. Raju, E. Lee, Y. Lee, S. Cho, B. Kim, Impact of symmetry-breaking of non-fullerene acceptors for efficient and stable organic solar cells, Chem. Sci. 12 (2021) 14083¨C14097. https://doi.org/10.1039/D1SC04153C."
3985,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C=C(/C=C2C(=O)C5=C(C=CC=C5)C2=C(C#N)C#N)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC3=C2SC(/C=C2C(=O)C4=C(C=CC=C4)C2=C(C#N)C#N)=C3)C=C1,ITIC-3T,-5.54,-3.93,17.51,0.924,0.681,11.02,"Q. Zhu, D. Liu, Z. Lu, C. Gu, K. Zhang, X. Bao, Q. Li, R. Yang, Length evolution of fused-ring electron acceptors toward optimal blend morphology in polymer solar cells incorporating asymmetric benzodithiophene-based donors, J. Mater. Chem. A. 7 (2019) 4823¨C4828. https://doi.org/10.1039/C8TA11363G."
3986,O=C(C(C=CC=C1)=C1C/2=C(C#N)/C#N)C2=C/C3=CC(C4(C5=CC=C(CCCCCC)C=C5)C6=CC=C(CCCCCC)C=C6)=C(S3)C7=C4C8=C(OCC(CC)CCCC)C(SC9=C%10C(C%11=CC=C(CCCCCC)C=C%11)(C%12=CC=C(CCCCCC)C=C%12)C%13=C9SC(/C=C%14C(C(C=CC=C%15)=C%15C\%14=C(C#N)C#N)=O)=C%13)=C%10C(OCC(CC)CCCC)=C8S7,PDT-T1,-5.43,-3.97,18.88,0.88,0.663,11.02,"P. Jiang, H. Lu, Q.-Q. Jia, S. Feng, C. Li, H.-B. Li, Z. Bo, Dihydropyreno[1,2-b:6,7-b¡ä]dithiophene based electron acceptors for high efficiency as-cast organic solar cells, J. Mater. Chem. A. 7 (2019) 5943¨C5948. https://doi.org/10.1039/C9TA00614A."
3987,O=C(C(C=C(F)C(F)=C1)=C1C/2=C(C#N)C#N)C2=C/C3=CC(C(C4=CC=C(CCCCCC)C=C4)(C5=CC=C(CCCCCC)C=C5)C6=C7SC8=C6C(OCCCCCC)=CC9=C8C=C(OCCCCCC)C%10=C9SC%11=C%10C(C%12=CC=C(CCCCCC)C=C%12)(C%13=CC=C(CCCCCC)C=C%13)C%14=C%11SC(/C=C%15C(C(C=C(F)C(F)=C%16)=C%16C\%15=C(C#N)/C#N)=O)=C%14)=C7S3,O-NTNC,-5.54,-3.78,15.98,0.942,0.734,11,"H. Feng, Y.-Q.-Q. Yi, X. Ke, Y. Zhang, X. Wan, C. Li, Y. Chen, Synergistic Modifications of Side Chains and End Groups in Small Molecular Acceptors for High Efficient Non-Fullerene Organic Solar Cells, Sol. RRL. 2 (2018) 1800053. https://doi.org/10.1002/solr.201800053."
3988,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=C(SC(/C=C4C(=O)C5=C(C=CC(C)=C5)C4=C(C#N)C#N)=C3)C3=C2C2=C(S3)C(C3=CC=C(C(CC)CCCC)S3)=C3C(=C2)SC2=C3C(C3=CC=C(CCCCCC)C=C3)(C3=CC=C(CCCCCC)C=C3)C3=C2SC(/C=C2C(=O)C4=C(C=C(C)C=C4)C2=C(C#N)C#N)=C3)C=C1,BDTIT-M,-5.4,-3.85,17.56,0.903,0.713,11,"Q. An, W. Gao, F. Zhang, J. Wang, M. Zhang, K. Wu, X. Ma, Z. Hu, C. Jiao, C. Yang, Energy level modulation of non-fullerene acceptors enables efficient organic solar cells with small energy loss, J. Mater. Chem. A. 6 (2018) 2468¨C2475. https://doi.org/10.1039/C7TA10763C."
3989,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=C(SC4=C3SC(/C=C3C(=O)C5=C(C=C(F)C(F)=C5)C3=C(C#N)C#N)=C4)C3=C2C2=C(S3)C3=C(S2)C2=C(C4=C(S2)C2=C(S4)C4=C(C5=C(C=C(/C=C6C(=O)C7=C(C=C(F)C(F)=C7)C6=C(C#N)C#N)S5)S4)C2(C2=CC=CC=C2)C2=CC=CC=C2)C3(C2=CC=C(CCCCCC)C=C2)C2=CC=C(CCCCCC)C=C2)C=C1,FUIC,-5.31,-4.06,23.3,0.692,0.689,11,"T. Li, L. Yang, Y. Xiao, K. Liu, J. Wang, X. Lu, X. Zhan, Facile synthesis of high-performance nonfullerene acceptor isomers via a one stone two birds strategy, J. Mater. Chem. A. 7 (2019) 20667¨C20674. https://doi.org/10.1039/C9TA07917C."
3990,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(C=C(/C=C5C(=O)C6=C(C=C(Cl)C(Cl)=C6)C5=C(C#N)C#N)S2)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC3=C2SC(/C=C/C2=C(F)C(F)=C(/C=C/C4=CC5=C(S4)C4=C(S5)C5=CC6=C(C=C5C4(C4=CC=C(CCCCCC)C=C4)C4=CC=C(CCCCCC)C=C4)C4=C(C5=C(C=C(/C=C7C(=O)C8=C(C=C(Cl)C(Cl)=C8)C7=C(C#N)C#N)S5)S4)C6(C4=CC=C(CCCCCC)C=C4)C4=CC=C(CCCCCC)C=C4)C(F)=C2F)=C3)C=C1,FB-2IDTT-4Cl,-5.48,-3.86,20.3,0.84,0.648,11,"C.-M. Hsieh, M.-R. Chuang, Y. Yamada, C.-J. Su, Y.J. Chang, M. Murata, U.-S. Jeng, S.-C. Chuang, p-Tetrafluorophenylene Divinylene-Bridged Nonfullerene Acceptors as Binary Components or Additives for High-Efficiency Organic Solar Cells, ACS Appl. Mater. Interfaces. 13 (2021) 61473¨C61486. https://doi.org/10.1021/acsami.1c19943."
3991,CCCCCCCCC1=C(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)SC(C2=C(N(C3=CC=C(CCCC)C=C3)C3=CC=C(CCCC)C=C3)C3=C(S2)C(N(C2=CC=C(CCCC)C=C2)C2=CC=C(CCCC)C=C2)=C(C2=CC(CCCCCCCC)=C(/C=C4C(=O)C5=C(C=C(F)C(F)=C5)C4=C(C#N)C#N)S2)S3)=C1,2Th-2F,-5.55,-3.95,21.62,0.79,0.643,11,"X. Wang, H. Lu, Y. Liu, A. Zhang, N. Yu, H. Wang, S. Li, Y. Zhou, X. Xu, Z. Tang, Z. Bo, Simple Nonfused Ring Electron Acceptors with 3D Network Packing Structure Boosting the Efficiency of Organic Solar Cells to 15.44%, Adv. Energy Mater. 11 (2021) 2102591. https://doi.org/10.1002/aenm.202102591."
3992,CCCCCCCCC1(CCCCCCCC)C2=CC3=C(C=C2C2=C1C=C(/C=C1C(=O)C4=C(C=C(F)C(F)=C4)C1=C(C#N)C#N)S2)C(CCCCCCCC)(CCCCCCCC)C1=C3SC(C2=C3C(F)=C(C(=O)OCC(CC)CCCC)SC3=C(/C=C3C(=O)C4=C(C=CC=C4)C3=C(C#N)C#N)S2)=C1,2FIFIC,-5.45,-3.97,22.4,0.8,0.615,11,"Y. Zhang, Y. Wang, Z. Xie, T. Shan, L. Zhu, F. Liu, H. Zhong, Preparation of non-fullerene acceptors with a multi-asymmetric configuration in a one-pot reaction for organic solar cells, J. Mater. Chem. C. 8 (2020) 17229¨C17236. https://doi.org/10.1039/D0TC04749J."
3993,CCCCC(CC)COC1=CC(C2=CC3=C(S2)C2=C(C=C(/C=C4/C(=O)C5=CC6=CC=CC=C6C=C5C4=C(C#N)C#N)S2)C3(CC(CC)CCC)CC(CC)CCCC)=C(OCC(CC)CCCC)C=C1C1=CC2=C(S1)C1=C(C=C(/C=C3/C(=O)C4=C(C=C5C=CC=CC5=C4)C3=C(C#N)C#N)S1)C2(CC(CC)CC)CC(CC)CCC,BN-0F,-5.35,-3.94,21.91,0.835,0.601,11,"X. Zhang, L. Qin, J. Yu, Y. Li, Y. Wei, X. Liu, X. Lu, F. Gao, H. Huang, High-Performance Noncovalently Fused-Ring Electron Acceptors for Organic Solar Cells Enabled by Noncovalent Intramolecular Interactions and End-Group Engineering, Angew. Chem. Int. Ed. 60 (2021) 12475¨C12481. https://doi.org/10.1002/anie.202100390."
3994,CCCCCCCCC1(CCCCCCCC)C2=C(SC3=C2SC(/C=C2C(=O)C4=C(C=CC=C4)C2=C(C#N)C#N)=C3)C2=C1C1=C(C=C(/C=C3C(=O)C4=C(C=CC=C4)C3=C(C#N)C#N)S1)S2,CDTTIC,-5.62,-3.98,24.9,0.78,0.56,11,"Q. He, M. Shahid, J. Wu, X. Jiao, F.D. Eisner, T. Hodsden, Z. Fei, T.D. Anthopoulos, C.R. McNeill, J.R. Durrant, M. Heeney, Fused Cyclopentadithienothiophene Acceptor Enables Ultrahigh Short-Circuit Current and High Efficiency >11% in As-Cast Organic Solar Cells, Adv. Funct. Mater. 29 (2019) 1904956. https://doi.org/10.1002/adfm.201904956."
3995,O=C(C1=C(C)SC=C1C/2=C(C#N)C#N)C2=C/C(S3)=CC4=C3C5=C(C4(C6=CC=C(CCCCCC)C=C6)C7=CC=C(CCCCCC)C=C7)C8=C(OCC(CC)CCCC)C9=C(C(C(C%10=CC=C(CCCCCC)C=C%10)(C%11=CC=C(CCCCCC)C=C%11)C%12=C%13SC(/C=C%14/C(C%15=CSC(C)=C%15C%14=O)=C(C#N)C#N)=C%12)=C%13S9)C(OCC(CC)CCCC)=C8S5,BTOIC,-5.42,-3.93,18.6,0.862,0.684,10.96,"W. Gao, T. Liu, R. Ming, Z. Luo, K. Wu, L. Zhang, J. Xin, D. Xie, G. Zhang, W. Ma, H. Yan, C. Yang, Near-Infrared Small Molecule Acceptor Enabled High-Performance Nonfullerene Polymer Solar Cells with Over 13% Efficiency, Adv. Funct. Mater. 28 (2018) 1803128. https://doi.org/10.1002/adfm.201803128."
3996,CCCCCCCCOC(=O)C1=CC2=C(C3=CC4=C(S3)C3=CC5=C(C=C3C4(CCCCCC)CCCCCC)C3=C(C=C(C4=C6C=C(C(=O)OCCCCCCCC)SC6=C(/C=C6SC(=C(C#N)C#N)N(CC)C6=O)S4)S3)C5(CCCCCC)CCCCCC)SC(/C=C3SC(=C(C#N)C#N)N(CC)C3=O)=C2S1,ATT-4,-5.41,-3.62,17.31,0.93,0.7,10.92,"F. Liu, J. Zhang, Y. Wang, S. Chen, Z. Zhou, C. Yang, F. Gao, X. Zhu, Modulating Structure Ordering via Side-Chain Engineering of Thieno[3,4-b]thiophene-Based Electron Acceptors for Efficient Organic Solar Cells with Reduced Energy Losses, ACS Appl. Mater. Interfaces. 11 (2019) 35193¨C35200. https://doi.org/10.1021/acsami.9b10641."
3997,CCCCCCCCCCCC1=C(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)SC2=C1SC1=C2N(CCCCCCOC2=CC=CC=C2)C2=C1C1=NSN=C1C1=C2N(CCCCCCOC2=CC=CC=C2)C2=C1SC1=C2SC(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)=C1CCCCCCCCCCC,Y6-phOC6,-5.75,-4.05,21.31,0.844,0.616,10.92,"L. Yi, S. Dai, R. Sun, W. Wang, Y. Wu, X. Jiao, C. Zhang, J. Min, Alkyl chain engineering of non-fullerene small molecule acceptors for solution-processable organic solar cells, Org. Electron. 87 (2020) 105963. https://doi.org/10.1016/j.orgel.2020.105963."
3998,O=C(C(C=C(F)C(F)=C1)=C1C/2=C(C#N)C#N)C2=C/C(S3)=CC4=C3C(C5(C6=CC=C(CCCCCC)C=C6)C7=CC=C(CCCCCC)C=C7)=C(S4)C8=C5C9=C(CCCCCC)C=C(C(SC%10=C%11C(C%12=CC=C(CCCCCC)C=C%12)(C%13=CC=C(CCCCCC)C=C%13)C%14=C%10SC%15=C%14SC(/C=C%16C(C(C=C(F)C(F)=C%17)=C%17C\%16=C(C#N)/C#N)=O)=C%15)=C%11C(CCCCCC)=C%18)C%18=C9S8,AT-NC,-5.44,-3.8,17.11,0.919,0.694,10.91,"H. Feng, Y.-Q.-Q. Yi, X. Ke, J. Yan, Y. Zhang, X. Wan, C. Li, N. Zheng, Z. Xie, Y. Chen, New Anthracene-Fused Nonfullerene Acceptors for High-Efficiency Organic Solar Cells: Energy Level Modulations Enabling Match of Donor and Acceptor, Adv. Energy Mater. 9 (2019) 1803541. https://doi.org/10.1002/aenm.201803541."
3999,O=C(C(C=C(F)C=C1)=C1C/2=C(C#N)C#N)C2=C/C3=CC4=C(C5=CC(C6(C7=CC=C(CCCCCC)C=C7)C8=CC=C(CCCCCC)C=C8)=C(C9=C6C(SC(/C=C%10C(C(C=C(F)C=C%11)=C%11C\%10=C(C#N)C#N)=O)=C%12)=C%12S9)C=C5C4(C%13=CC=C(CCCCCC)C=C%13)C%14=CC=C(CCCCCC)C=C%14)[Se]3,SePTT-2F,-5.71,-4,17.51,0.83,0.75,10.9,"C. Li, T. Xia, J. Song, H. Fu, H.S. Ryu, K. Weng, L. Ye, H.Y. Woo, Y. Sun, Asymmetric selenophene-based non-fullerene acceptors for high-performance organic solar cells, J. Mater. Chem. A. 7 (2019) 1435¨C1441. https://doi.org/10.1039/C8TA11197A."
4000,CCCCCCCCC1(CCCCCCCC)C2=CC3=C(C=C2C2=C1C1=C(C=C(/C=C4C(=O)C5=C(CCC=C5)C4=C(C#N)C#N)S1)S2)C(CCCCCCCC)(CCCCCCCC)C1=C3SC2=C1SC(/C=C1C(=O)C3=C(CCC=C3)C1=C(C#N)C#N)=C2,O-ITIC,-5.71,-4.15,16.8,0.97,0.687,10.9,"L. Guo, Z. Xu, X. Jiao, Q. Ruan, X. Xie, B. Xiao, Q. Li, Y.-P. Cai, S. Liu, Compatible Acceptors Mediate Morphology and Charge Generation, Transpration, Extraction, and Energy Loss in Efficient Ternary Polymer Solar Cells, ACS Appl. Energy Mater. 4 (2021) 10187¨C10196. https://doi.org/10.1021/acsaem.1c02067."
4001,O=C(C(C=CC=C1)=C1C/2=C(C#N)C#N)C2=C/C(S3)=CC4=C3C5=C(C4(C6=CC=C(CCCCCC)C=C6)C7=CC=C(CCCCCC)C=C7)C8=CC9=C(C(C(C%10=CC=C(CCCCCC)C=C%10)(C%11=CC=C(CCCCCC)C=C%11)C%12=C%13SC(/C=C%14C(C(C=CC=C%15)=C%15C\%14=C(C#N)/C#N)=O)=C%12)=C%13S9)C=C8S5,BDT-IC1,-5.51,-3.9,17.7,0.93,0.684,10.9,"Y. Li, L. Zhong, J.-D. Lin, F.-P. Wu, H.-J. Bin, Z. Zhang, L. Xu, Z.-Q. Jiang, Z.-G. Zhang, F. Liu, T.P. Russell, Y. Li, L.-S. Liao, S.R. Forrest, Isomeric Effects of Solution Processed Ladder-Type Non-Fullerene Electron Acceptors, Sol. RRL. 1 (2017) 1700107. https://doi.org/10.1002/solr.201700107."
4002,O=C(C(C=C(F)C(F)=C1)=C1C/2=C(C#N)C#N)C2=C/C3=CC4=C(S3)C(C(C5=CC=C(CCCCCC)C=C5)(C6=CC=C(CCCCCC)C=C6)C7=C8SC9=C7SC%10=C9C(C%11=CC=C(CCCCCC)C=C%11)(C%12=CC=C(CCCCCC)C=C%12)C%13=C%10SC%14=C%13SC(/C=C%15C(C(C=C(F)C(F)=C%16)=C%16C\%15=C(C#N)/C#N)=O)=C%14)=C8S4,F10IC,-5.43,-4,25.12,0.64,0.676,10.9,"S. Dai, T. Li, W. Wang, Y. Xiao, T.-K. Lau, Z. Li, K. Liu, X. Lu, X. Zhan, Enhancing the Performance of Polymer Solar Cells via Core Engineering of NIR-Absorbing Electron Acceptors, Adv. Mater. 30 (2018) 1706571. https://doi.org/10.1002/adma.201706571."
4003,O=C(C(C=CC(C#CC)=C1)=C1C/2=C(C#N)C#N)C2=C/C3=CC4=C(S3)C5=C(C6=CC(C7(C8=CC=C(CCCCCC)C=C8)C9=CC=C(CCCCCC)C=C9)=C(C%10=C7C(SC(/C=C%11C(C(C=C(C#CC)C=C%12)=C%12C\%11=C(C#N)/C#N)=O)=C%13)=C%13S%10)C=C6C5(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15)S4,ITEN,-5.63,-3.9,16.5,0.989,0.67,10.9,"R. Yu, H. Yao, L. Hong, Y. Xu, B. Gao, J. Zhu, Y. Zu, J. Hou, Enhancing the Photovoltaic Performance of Nonfullerene Acceptors via Conjugated Rotatable End Groups, Adv. Energy Mater. 8 (2018) 1802131. https://doi.org/10.1002/aenm.201802131."
4004,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(S3)C3=C(C=C(/C=C5C(=O)C6=C(C=C(F)C(F)=C6)C5=C(C#N)C#N)S3)N2CC(CC)CCCC)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC3=C2N(CC(CCCC)CCCCCC)C2=C3SC(/C=C3C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)=C2)C=C1,INPIC-BO,-5.47,-3.97,20,0.839,0.668,10.9,"H. Feng, X. Song, M. Zhang, J. Yu, Z. Zhang, R. Geng, L. Yang, F. Liu, D. Baran, W. Tang, Side chain engineering on dithieno[3,2-b:2,3-d]pyrrol fused electron acceptors for efficient organic solar cells, Mater. Chem. Front. 3 (2019) 702¨C708. https://doi.org/10.1039/C8QM00669E."
4005,O=C(C(C=C(F)C(F)=C1)=C1C/2=C(C#N)C#N)C2=C/C3=CC(OCC(CC)CCCC)=C(C4=CC5=C(C6=C(C5(C7=CC=C(CCCCCC)C=C7)C8=CC=C(CCCCCC)C=C8)C=C(C9=C%10C=C(C%11=C(OCC(CC)CCCC)C=C(/C=C%12C(C(C=C(F)C(F)=C%13)=C%13C\%12=C(C#N)/C#N)=O)S%11)S9)C(C%10(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15)=C6)S4)S3,IEICO-4F,-5.44,-4.19,25.3,0.731,0.589,10.9,"H. Yao, Y. Cui, R. Yu, B. Gao, H. Zhang, J. Hou, Design, Synthesis, and Photovoltaic Characterization of a Small Molecular Acceptor with an Ultra-Narrow Band Gap, Angew. Chem. Int. Ed. 56 (2017) 3045¨C3049. https://doi.org/10.1002/anie.201610944."
4006,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)S3)C3=C(C=C4C(=C3)C3=C(C5=C(C=C(/C=C6C(=O)C7=C(C=C(F)C(F)=C7)C6=C(C#N)C#N)S5)S3)C4(C3=CC=C(CCCCCC)S3)C3=CC=C(CCCCCC)S3)C3=C2C=C(/C=C2C(=O)C4=C(C=C(F)C(F)=C4)C2=C(C#N)C#N)S3)S1,IDT6CN-4F,-5.73,-4.12,22.23,1.065,0.8,10.88,"W. Gao, F. Wu, T. Liu, G. Zhang, Z. Chen, C. Zhong, L. Zhu, F. Liu, H. Yan, C. Yang, Multifunctional asymmetrical molecules for high-performance perovskite and organic solar cells, J. Mater. Chem. A. 7 (2019) 2412¨C2420. https://doi.org/10.1039/C8TA10975C."
4007,O=C(C(C=CC=C1)=C1C/2=C(C#N)C#N)C2=C/C3=C(CCCCCC)C4=C(S3)C5=C(C6=CC(C7(C8=CC=C(CCCCCC)C=C8)C9=CC=C(CCCCCC)C=C9)=C(C%10=C7C(SC(/C=C%11C(C(C=CC=C%12)=C%12C\%11=C(C#N)C#N)=O)=C%13CCCCCC)=C%13S%10)C=C6C5(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15)S4,ITC6-IC,-5.73,-3.92,16.24,0.938,0.7115,10.87,"C. Zhang, S. Ming, H. Wu, X. Wang, H. Huang, W. Xue, X. Xu, Z. Tang, W. Ma, Z. Bo, High-efficiency ternary nonfullerene organic solar cells with record long-term thermal stability, J. Mater. Chem. A. 8 (2020) 22907¨C22917. https://doi.org/10.1039/D0TA07887E."
4008,CCCCCCCCC1(CCCCCCCC)C2=CC3=C(C=C2C2=C1C=C(/C=C1C(=O)C4=CC(F)=CC=C4C1=C(C#N)C#N)S2)C(CCCCCCCC)(CCCCCCCC)C1=C3C=C2C(=C1)C1=C(C=C(/C=C3C(=O)C4=CC(F)=CC=C4C3=C(C#N)C#N)S1)C2(CCCCCCCC)CCCCCCCC,F-F,-5.72,-4.13,17.36,0.88,0.71,10.85,"Y. Wang, Y. Zhang, N. Qiu, H. Feng, H. Gao, B. Kan, Y. Ma, C. Li, X. Wan, Y. Chen, A Halogenation Strategy for over 12% Efficiency Nonfullerene Organic Solar Cells, Adv. Energy Mater. 8 (2018) 1702870. https://doi.org/10.1002/aenm.201702870."
4009,CCCCCCCCC1(CCCCCCCC)C2=CC3=C(C=C2C2=C1C=C(C1=C4C(F)=C(C(=O)OCC(CC)CCCC)SC4=C(/C=C4C(=O)C5=CC(F)=C(F)C=C5C4=C(C#N)C#N)S1)S2)C(CCCCCCCC)(CCCCCCCC)C1=C3SC(C2=C3C(F)=C(C(=O)OCC(CC)CCCC)SC3=C(/C=C3C(=O)C4=CC(F)=CC=C4C3=C(C#N)C#N)S2)=C1,6-IF2F,-5.38,-4.07,24.69,0.65,0.678,10.82,"Y. Zhang, Y. Wang, T. Shan, Q. Wei, Y.X. Xu, H. Zhong, Non-Fullerene Acceptors with an Optical Response over 1000 nm toward Efficient Organic Solar Cells, ACS Appl. Mater. Interfaces. 13 (2021) 51279¨C51288. https://doi.org/10.1021/acsami.1c13404."
4010,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(C=C(/C=C5C(=O)C6=C(C=CC=C6)C5=C(C#N)C#N)S2)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC3=C2SC(/C=C2C(=O)C4=C(C=CC(C)=C4)C2=C(C#N)C#N)=C3)C=C1,IT-M,-5.58,-3.98,17.05,0.937,0.681,10.81,"W. Jiang, R. Yu, Z. Liu, R. Peng, D. Mi, L. Hong, Q. Wei, J. Hou, Y. Kuang, Z. Ge, Ternary Nonfullerene Polymer Solar Cells with 12.16% Efficiency by Introducing One Acceptor with Cascading Energy Level and Complementary Absorption, Adv. Mater. 30 (2018) 1703005. https://doi.org/10.1002/adma.201703005."
4011,CCCCCCSC1=C(C2=CC3=C(S2)C2=C(S3)C3=CC4=C(C=C3C2(C2=CC=C(CCCCCC)S2)C2=CC=C(CCCCCC)S2)C2=C(C3=C(C=C(C5=C(SCCCCCC)C=C(/C=C6C(=O)C7=CC=CC=C7C6=C(C#N)C#N)S5)S3)S2)C4(C2=CC=C(CCCCCC)S2)C2=CC=C(CCCCCC)S2)SC(/C=C2C(=O)C3=CC=CC=C3C2=C(C#N)C#N)=C1,ITIC-Th-S,,,17.8,0.85,0.712,10.8,"P. Cheng, J. Wang, Q. Zhang, W. Huang, J. Zhu, R. Wang, S.-Y. Chang, P. Sun, L. Meng, H. Zhao, H.-W. Cheng, T. Huang, Y. Liu, C. Wang, C. Zhu, W. You, X. Zhan, Y. Yang, Unique Energy Alignments of a Ternary Material System toward High-Performance Organic Photovoltaics, Adv. Mater. 30 (2018) 1801501. https://doi.org/10.1002/adma.201801501."
4012,CCCCCCCCC1(CCCCCCCC)C2=CC3=C(C=C2C2=C1C=C(C1=C(CC(CC)CCCC)C=C(/C=C4C(=O)C5=CC(F)=C(F)C=C5C4=C(C#N)C#N)S1)S2)C(CCCCCCCC)(CCCCCCCC)C1=C3SC(C2=C(OCC(CC)CCCC)C=C(/C=C3C(=O)C4=CC(F)=C(F)C=C4C3=C(C#N)C#N)S2)=C1,p-IO2,-5.44,-4.19,23,0.7,0.67,10.8,"J. Lee, S. Song, J. Huang, Z. Du, H. Lee, Z. Zhu, S.-J. Ko, T.-Q. Nguyen, J.Y. Kim, K. Cho, G.C. Bazan, Bandgap Tailored Nonfullerene Acceptors for Low-Energy-Loss Near-Infrared Organic Photovoltaics, ACS Mater. Lett. 2 (2020) 395¨C402. https://doi.org/10.1021/acsmaterialslett.9b00512."
4013,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(S3)C3=C(C=C(/C=C5C(=O)C6=C(C=CC=C6)C5=C(C#N)C#N)S3)S2)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC3=C2SC2=C3SC(CC3C(=O)C4=C(C=CC(F)=C4)C3=C(C#N)C#N)=C2)C=C1,INIC2,-5.52,-3.98,17.56,0.903,0.668,10.8,"S. Dai, F. Zhao, Q. Zhang, T.-K. Lau, T. Li, K. Liu, Q. Ling, C. Wang, X. Lu, W. You, X. Zhan, Fused Nonacyclic Electron Acceptors for Efficient Polymer Solar Cells, J. Am. Chem. Soc. 139 (2017) 1336¨C1343. https://doi.org/10.1021/jacs.6b12755."
4014,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C=C(C2=C(CC(CC)CCCC)C=C(/C=C5C(=O)C6=CC(F)=C(F)C=C6C5=C(C#N)C#N)S2)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC(C3=C(OCC(CC)CCCC)C=C(/C=C4C(=O)C5=CC(F)=C(F)C=C5C4=C(C#N)C#N)S3)=C2)C=C1,p-IO1,-5.46,-4.13,22.3,0.78,0.62,10.8,"J. Lee, S. Song, J. Huang, Z. Du, H. Lee, Z. Zhu, S.-J. Ko, T.-Q. Nguyen, J.Y. Kim, K. Cho, G.C. Bazan, Bandgap Tailored Nonfullerene Acceptors for Low-Energy-Loss Near-Infrared Organic Photovoltaics, ACS Mater. Lett. 2 (2020) 395¨C402. https://doi.org/10.1021/acsmaterialslett.9b00512."
4015,CCCCCCCCN1N=C2C(/C=C3/SC(=C(C#N)C#N)N(CC)C3=O)=CC(F)=C(C3=CC4=C(O3)C3=CC5=C(C=C3C4(C3=CC=C(CCCCCC)C=C3)C3=CC=C(CCCCCC)C=C3)C3=C(C=C(C4=C(F)C=C(/C=C6/SC(=C(C#N)C#N)N(CC)C6=O)C6=NN(CCCCCCCC)N=C64)S3)C5(C3=CC=C(CCCCCC)C=C3)C3=CC=C(CCCCCC)C=C3)C2=N1,BTA3-CL,-5.7,-3.9,13.65,1.09,0.7228,10.75,"T. Dai, Q. Nie, P. Lei, B. Zhang, J. Zhou, A. Tang, H. Wang, Q. Zeng, E. Zhou, Effects of Halogenation on the Benzotriazole Unit of Non-Fullerene Acceptors in Organic Solar Cells with High Voltages, ACS Appl. Mater. Interfaces. 13 (2021) 58994¨C59005. https://doi.org/10.1021/acsami.1c14317."
4016,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C=C(C2=CC=C(/C=C5C(=O)C6=CC(F)=CC=C6C5=C(C#N)C#N)S2)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC(C3=CC=C(/C=C4C(=O)C5=CC=C(F)C=C5C4=C(C#N)C#N)S3)=C2)C=C1,T-TPT-T-2F,-5.5,-3.99,17.63,0.933,0.671,10.71,"X. Li, C. Li, L. Ye, K. Weng, H. Fu, H.S. Ryu, D. Wei, X. Sun, H.Y. Woo, Y. Sun, Asymmetric A¨CD¨C¦Ð¨CA-type nonfullerene small molecule acceptors for efficient organic solar cells, J. Mater. Chem. A. 7 (2019) 19348¨C19354. https://doi.org/10.1039/C9TA06476A."
4017,CCCCCCOC1=C2SC3=C(C2=C(OCCCCCC)C2=C1C1=C(S2)C2=C(C=C(/C=C4C(=O)C5=C(C=C(F)C=C5)C4=C(C#N)C#N)S2)N1CC(CCCC)CCCCCC)N(CC(CCCC)CCCCCC)C1=C3SC(/C=C2C(=O)C3=C(C=CC(F)=C3)C2=C(C#N)C#N)=C1,SNC4C6¨CF,-5.5,-3.94,19.1,0.86,0.652,10.71,"Y. Xin, J. Liang, Y. Zhong, T. Liang, C. Zhang, X. He, Achieving additive-free organic solar cells by modulating the side-chain length of non-fullerene small molecule acceptors, Dyes Pigments. 195 (2021) 109661. https://doi.org/10.1016/j.dyepig.2021.109661."
4018,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(S3)C3=C(C=C(/C=C5C(=O)C6=C(C=C(F)C(F)=C6)C5=C(C#N)C#N)S3)S2)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC3=C2SC2=C3SC(/C=C3C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)=C2)C=C1,2F-C6,,,20.97,0.786,0.6836,10.7,"F. Zhao, D. He, J. Xin, S. Dai, H. Xue, L. Jiang, Z. Wei, W. Ma, X. Zhan, Y. Li, C. Wang, Modulating morphology via side-chain engineering of fused ring electron acceptors for high performance organic solar cells, Sci. China Chem. 62 (2019) 790¨C796. https://doi.org/10.1007/s11426-019-9453-7."
4019,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)S3)C3=CC4=C(C=C3C3=C2C2=C(C=C(/C=C5C(=O)C6=C(C=C(OC)C=C6)C5=C(C#N)C#N)S2)S3)C(C2=CC=C(CCCCCC)S2)(C2=CC=C(CCCCCC)S2)C2=C4SC3=C2SC(/C=C2C(=O)C4=C(C=C(OC)C=C4)C2=C(C#N)C#N)=C3)S1,ITIC-Th3,-5.67,-3.73,16.34,0.962,0.6833,10.7,"Z. Li, S. Dai, J. Xin, L. Zhang, Y. Wu, J. Rech, F. Zhao, T. Li, K. Liu, Q. Liu, W. Ma, W. You, C. Wang, X. Zhan, Enhancing the performance of the electron acceptor ITIC-Th via tailoring its end groups, Mater. Chem. Front. 2 (2018) 537¨C543. https://doi.org/10.1039/C7QM00547D."
4020,CCCCCCOC1=CC=C(C2(C3=CC=C(OCCCCCC)C=C3)C3=C(SC(CC4C(=O)C5=C(C=C(F)C(F)=C5)C4=C(C#N)C#N)=C3)C3=C2C2=C(OCCCCCC)C=C4C(=C2S3)C=C(CCCCCC)C2=C4SC3=C2C(C2=CC=C(OCCCCCC)C=C2)(C2=CC=C(OCCCCCC)C=C2)C2=C3SC(/C=C3C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)=C2)C=C1,IOIC4,-5.7,-4.17,17,0.966,0.651,10.7,"J. Zhu, Y. Xiao, C. Zhang, B. Jia, H. Lu, J. Wang, X. Lu, Z. Li, X. Zhan, Effects of alkoxylation position on fused-ring electron acceptors, J. Mater. Chem. C. 8 (2020) 15128¨C15134. https://doi.org/10.1039/D0TC02158J."
4021,O=C(C(C=C(C)C=C1)=C1C/2=C(C#N)C#N)C2=C/C3=CC4=C(C5=CC(C6(CCCCCCCC)CCCCCCCC)=C(C7=C6C=C(/C=C8C(C(C=C(C)C=C9)=C9C8=C(C#N)/C#N)=O)S7)C=C5C4(CCCCCCCC)CCCCCCCC)S3,IDT-2O,-5.72,-3.85,16.8,0.87,0.72,10.67,"R. Li, G. Liu, R. Xie, Z. Wang, X. Yang, K. An, W. Zhong, X.-F. Jiang, L. Ying, F. Huang, Y. Cao, Introducing cyclic alkyl chains into small-molecule acceptors for efficient polymer solar cells, J. Mater. Chem. C. 6 (2018) 7046¨C7053. https://doi.org/10.1039/C8TC01780H."
4022,O=C(C(C=C(F)C(F)=C1)=C1C/2=C(C#N)C#N)C2=C/C3=CC=C(C4=C(OCCCCCCCC)C5=C(C6=CC(C7(C8=CC=C(CCCCCC)C=C8)C9=CC=C(CCCCCC)C=C9)=C(C%10=C7C(OCCCCCCCC)=C(C%11=CC=C(/C=C%12C(C(C=C(F)C(F)=C%13)=C%13C\%12=C(C#N)/C#N)=O)[Se]%11)S%10)C=C6C5(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15)S4)[Se]3,IDTO-Se-4F,-5.48,-3.9,18.55,0.831,0.692,10.67,"D. Liu, B. Kan, X. Ke, N. Zheng, Z. Xie, D. Lu, Y. Liu, Extended Conjugation Length of Nonfullerene Acceptors with Improved Planarity via Noncovalent Interactions for High-Performance Organic Solar Cells, Adv. Energy Mater. 8 (2018) 1801618. https://doi.org/10.1002/aenm.201801618."
4023,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C=C(C2=C5OCC(CCCCCC)(CCCCCC)COC5=C(/C=C5C(=O)C6=CC(F)=C(F)C=C6C5=C(C#N)C#N)S2)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC(C3=C4OCC(CCCCCC)(CCCCCC)COC4=C(/C=C4C(=O)C5=CC(F)=C(F)C=C5C4=C(C#N)C#N)S3)=C2)C=C1,IDT-PDOT-C6,-5.47,-3.8,18.94,0.903,0.6225,10.67,"C. Zhang, S. Ming, H. Wu, X. Wang, H. Huang, W. Xue, X. Xu, Z. Tang, W. Ma, Z. Bo, High-efficiency ternary nonfullerene organic solar cells with record long-term thermal stability, J. Mater. Chem. A. 8 (2020) 22907¨C22917. https://doi.org/10.1039/D0TA07887E."
4024,CCCCCCOC1=C(/C=C2C(=O)C3=C(C=C(F)C=C3)C2=C(C#N)C#N)SC(C2=CC3=C(S2)C2=CC4=C(C=C2C3(C2=CC=C(CCCCCC)C=C2)C2=CC=C(CCCCCC)C=C2)C2=C(C=C(C3=C(OCCCCCC)C(OCCCCCC)=C(/C=C5C(=O)C6=C(C=C(F)C=C6)C5=C(C#N)C#N)S3)S2)C4(C2=CC=C(CCCCCC)C=C2)C2=CC=C(CCCCCC)C=C2)=C1OCCCCCC,TOIC-F,,,18.6,0.946,0.605,10.65,"Y. Liu, C. Zhang, D. Hao, Z. Zhang, L. Wu, M. Li, S. Feng, X. Xu, F. Liu, X. Chen, Z. Bo, Enhancing the Performance of Organic Solar Cells by Hierarchically Supramolecular Self-Assembly of Fused-Ring Electron Acceptors, Chem. Mater. 30 (2018) 4307¨C4312. https://doi.org/10.1021/acs.chemmater.8b01319."
4025,CCCCCCCCC(CCCCCCCC)N1C2=CC3=C(C=C2C2=C1C=C1C(=C2)C(CCCCCCCC)(CCCCCCCC)C2=C1SC(/C=C1C(=O)C4=C(C=C(F)C(F)=C4)C1=C(C#N)C#N)=C2)C(CCCCCCCC)(CCCCCCCC)C1=C3SC(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)=C1,DTC(4R)-4FIC,-5.79,-3.99,18.92,0.82,0.7022,10.62,"T.-W. Chen, Y.-T. Hsiao, Y.-W. Lin, C.-C. Chang, W.-T. Chuang, Y. Li, C.-S. Hsu, Fluorinated heptacyclic carbazole-based ladder-type acceptors with aliphatic side chains for efficient fullerene-free organic solar cells, Mater. Chem. Front. 3 (2019) 829¨C835. https://doi.org/10.1039/C9QM00005D."
4026,O=C(C1=CSC=C1C/2=C(C#N)C#N)C2=C/C3=CC4=C(S3)C5=C(C6=C(C5(C7=CC=C(CCCCCC)S7)C8=CC=C(CCCCCC)S8)C=C(C9=C%10C(SC(/C=C%11C(C%12=CSC=C%12C\%11=C(C#N)/C#N)=O)=C%13)=C%13S9)C(C%10(C%14=CC=C(CCCCCC)S%14)C%15=CC=C(CCCCCC)S%15)=C6)S4,ITCPTC-Th,-5.68,-4.03,17.05,0.86,0.727,10.61,"W. Gao, Q. An, R. Ming, D. Xie, K. Wu, Z. Luo, Y. Zou, F. Zhang, C. Yang, Side Group Engineering of Small Molecular Acceptors for High-Performance Fullerene-Free Polymer Solar Cells: Thiophene Being Superior to Selenophene, Adv. Funct. Mater. 27 (2017) 1702194. https://doi.org/10.1002/adfm.201702194."
4027,O=C1C2=C(C=CC=C2)/C(C1CC3=CC(C4(C5=CC=C(CCCCCC)C=C5)C6=CC=C(CCCCCC)C=C6)=C(C7=C4C(S8)=C(S7)C9=C8C(SC(CC%10/C(C(C=CC=C%11)=C%11C%10=O)=C(C#N)C#N)=C%12)=C%12C9(C%13=CC=C(CCCCCC)C=C%13)C%14=CC=C(CCCCCC)C=C%14)S3)=C(C#N)/C#N,IHIC,-5.45,-3.93,19.4,0.752,0.725,10.6,"J. Zhang, C. Yan, W. Wang, Y. Xiao, X. Lu, S. Barlow, T.C. Parker, X. Zhan, S.R. Marder, Panchromatic Ternary Photovoltaic Cells Using a Nonfullerene Acceptor Synthesized Using C¨CH Functionalization, Chem. Mater. 30 (2018) 309¨C313. https://doi.org/10.1021/acs.chemmater.7b04499."
4028,CCCCCCCCN1C2=C(SC(/C=C3C(=O)C4=CC(F)=C(F)C=C4C3=C(C#N)C#N)=C2)C2=C1C1=C(S2)C2=CC3=C(C=C2C1(C1=CC=C(OCCCCCC)C=C1)C1=CC=C(OCCCCCC)C=C1)C1=C(C2=C(S1)C1=C(C=C(/C=C4C(=O)C5=CC(F)=C(F)C=C5C4=C(C#N)C#N)S1)N2CCCCCCCC)C3(C1=CC=C(OCCCCCC)C=C1)C1=CC=C(OCCCCCC)C=C1,p-INPOIC,-5.38,-4,19,0.846,0.661,10.6,"H. Feng, X. Song, Z. Zhang, R. Geng, J. Yu, L. Yang, D. Baran, W. Tang, Molecular Orientation Unified Nonfullerene Acceptor Enabling 14% Efficiency As-Cast Organic Solar Cells, Adv. Funct. Mater. 29 (2019) 1903269. https://doi.org/10.1002/adfm.201903269."
4029,O=C1N(C(C2=C3C1C=CC(C4=C5C6C7=CC8=C5C(C=C4)C(N(C8=O)C(CCCCCC)CCCCCC)=O)=C3C6C(C9=C7SC(C%10=C(C%11=CC%12=C(S%11)C%13=CC%14=C(C(C=C%15)C(N(C%14=O)C(CCCCCC)CCCCCC)=O)C(C%16%13)=C%15C%17=C%18C%16=C%12CC(C(N%19C(CCCCCC)CCCCCC)=O)=C%18C(C=C%17)C%19=O)C=C(C%20=CC%21=C(S%20)C%22=CC%23=C(C(C=C%24)C(N(C%23=O)C(CCCCCC)CCCCCC)=O)C(C%25%22)=C%24C%26=C%27C%25C%21=CC(C(N%28C(CCCCCC)CCCCCC)=O)=C%27C(C=C%26)C%28=O)C(C%29=CC%30=C(S%29)C%31=CC%32=C(C(C=C%33)C(N(C%32=O)C(CCCCCC)CCCCCC)=O)C(C%34%31)=C%33C%35=C%36C%34C%30=CC(C(N%37C(CCCCCC)CCCCCC)=O)=C%36C(C=C%35)C%37=O)=C%10)=C9)=C2)=O)C(CCCCCC)CCCCCC,FTTB-PDI4,-,-,13.9,1.13,0.66,10.6,"H. Hu, Y. Li, J. Zhang, Z. Peng, L. Ma, J. Xin, J. Huang, T. Ma, K. Jiang, G. Zhang, W. Ma, H. Ade, H. Yan, Effect of Ring-Fusion on Miscibility and Domain Purity: Key Factors Determining the Performance of PDI-Based Nonfullerene Organic Solar Cells, Adv. Energy Mater. 8 (2018) 1800234. https://doi.org/10.1002/aenm.201800234."
4030,O=C1C2=C(C(/C1=C/C3=C4C(SC(CCCCCCCC)=C4)=C(S3)C5=CC6=C(C(C(CC(CCCC)CC)(C7=C8C=CC(C9=C%10SC(CCCCCCCC)=CC%10=C(S9)/C=C%11/C(C%12=C(C%11=O)C=C(F)C(F)=C%12)=C(C#N)C#N)=C7)CC(CCCC)CC)C8C6(CC(CCCC)CC)CC(CCCC)CC)C=C5)=C(C#N)C#N)C=C(F)C(F)=C2,FTTB-PDI4,-5.74,-3.58,13.89,1.13,0.659,10.58,"J. Zhang, Y. Li, J. Huang, H. Hu, G. Zhang, T. Ma, P.C.Y. Chow, H. Ade, D. Pan, H. Yan, Ring-Fusion of Perylene Diimide Acceptor Enabling Efficient Nonfullerene Organic Solar Cells with a Small Voltage Loss, J. Am. Chem. Soc. 139 (2017) 16092¨C16095. https://doi.org/10.1021/jacs.7b09998."
4031,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=C(C=C4C(=C3)C3=C(C5=C(C=C(/C=C6C(=O)C7=CSC=C7C6=C(C#N)C#N)S5)S3)C4(C3=CC=C(CCCCCC)C=C3)C3=CC=C(CCCCCC)C=C3)C3=C2C=C2C(=C3)C(C3=CC=C(CCCCCC)C=C3)(C3=CC=C(CCCCCC)C=C3)C3=C2SC2=C3SC(/C=C3C(=O)C4=CSC=C4C3=C(C#N)C#N)=C2)C=C1,FTTCN,-5.54,-3.95,15.89,0.9,0.7382,10.56,"R. Ming, M. Zhang, W. Gao, W. Ning, Z. Luo, C. Zhong, F. Zhang, C. Yang, Fluorene-fused ladder-type non-fullerene small molecule acceptors for high-performance polymer solar cells, Mater. Chem. Front. 3 (2019) 709¨C715. https://doi.org/10.1039/C9QM00013E."
4032,O=C(C1=C(C)SC(C)=C1C/2=C(C#N)C#N)C2=C/C3=CC4=C(S3)C5=C(C6=CC(C7(C8=CC=C(CCCCCC)C=C8)C9=CC=C(CCCCCC)C=C9)=C(C%10=C7C(SC(/C=C%11C(C%12=C(C)SC(C)=C%12C\%11=C(C#N)/C#N)=O)=C%13)=C%13S%10)C=C6C5(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15)S4,ITCT-DM,-5.48,-3.9,17.4,0.904,0.65,10.56,"D. Yan, W. Liu, J. Yao, C. Zhan, Fused-Ring Nonfullerene Acceptor Forming Interpenetrating J-Architecture for Fullerene-Free Polymer Solar Cells, Adv. Energy Mater. 8 (2018) 1800204. https://doi.org/10.1002/aenm.201800204."
4033,CCCCCCCCC(CCCC)COC1=C(OCC(CCCC)CCCCCCCC)C(C2=CC3=C(S2)C2=C(CC(/C=C4C(=O)C5=C(C=C(Cl)C(Cl)=C5)C4=C(C#N)C#N)S2)C3(CC(CC)CCCC)CC(CC)CCCC)=C2N=CC=NC2=C1C1=CC2=C(S1)C1=C(C=C(/C=C3C(=O)C4=C(C=C(Cl)C(Cl)=C4)C3=C(C#N)C#N)S1)C2(CC(CC)CCCC)CC(CC)CCCC.Cl,QCIC3,-5.53,-3.89,19.39,0.816,0.669,10.55,"S. Ye, S. Chen, S. Li, Y. Pan, X. Xia, W. Fu, L. Zuo, X. Lu, M. Shi, H. Chen, Synergistic Effects of Chlorination and Branched Alkyl Side Chain on the Photovoltaic Properties of Simple Non-Fullerene Acceptors with Quinoxaline as the Core, ChemSusChem. 14 (2021) 3599¨C3606. https://doi.org/10.1002/cssc.202100689."
4034,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(C=C(/C=C5C(=O)C6=CC=C(F)C=C6C5=C(C#N)C#N)S2)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC3=C2SC(/C=C2C(=O)C4=CC=C(F)C=C4C2=C(C#N)C#N)=C3)C=C1,IT-2F,-5.67,-4.02,16.5,0.902,0.708,10.54,"X. Li, C. Li, L. Ye, K. Weng, H. Fu, H.S. Ryu, D. Wei, X. Sun, H.Y. Woo, Y. Sun, Asymmetric A¨CD¨C¦Ð¨CA-type nonfullerene small molecule acceptors for efficient organic solar cells, J. Mater. Chem. A. 7 (2019) 19348¨C19354. https://doi.org/10.1039/C9TA06476A."
4035,O=C1C2=C(C=C(F)C(F)=C2)C(/C1=CC=CC3=CC4=C(S3)C5=C(C6=CC(C7(C8=CC=C(CCCCCC)C=C8)C9=CC=C(CCCCCC)C=C9)=C(C%10=C7C(SC(/C=C/C=C%11C(C(C=C(F)C(F)=C%12)=C%12C%11=O)=C(C#N)/C#N)=C%13)=C%13S%10)C=C6C5(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15)S4)=C(C#N)C#N,lTVfflC,-5.58,-4.04,20.6,0.81,0.6318,10.54,"X. Li, H. Huang, H. Bin, Z. Peng, C. Zhu, L. Xue, Z.-G. Zhang, Z. Zhang, H. Ade, Y. Li, Synthesis and Photovoltaic Properties of a Series of Narrow Bandgap Organic Semiconductor Acceptors with Their Absorption Edge Reaching 900 nm, Chem. Mater. 29 (2017) 10130¨C10138. https://doi.org/10.1021/acs.chemmater.7b03928."
4036,CCCCCCOC1=CC(C2=CC3=C(S2)C2=C(C=C(/C=C4C(=O)C5=CC=CC=C5C4=C(C#N)C#N)S2)C3(CC(CC)CCCC)CC(CC)CCCC)=C(OCCCCCC)C=C1C1=CC2=C(S1)C1=C(C=C(/C=C3C(=O)C4=CC=CC=C4C3=C(C#N)C#N)S1)C2(CC(CC)CCCC)CC(CC)CCCC,DOC6-IC,,,19.21,0.91,0.6011,10.52,"H. Huang, Q. Guo, S. Feng, C. Zhang, Z. Bi, W. Xue, J. Yang, J. Song, C. Li, X. Xu, Z. Tang, W. Ma, Z. Bo, Noncovalently fused-ring electron acceptors with near-infrared absorption for high-performance organic solar cells, Nat. Commun. 10 (2019) 3038. https://doi.org/10.1038/s41467-019-11001-6."
4037,CCCCCCOC1=CC(C2=CC3=C(S2)C2=C(C=C(/C=C4C(=O)C5=C(C=CC=C5)C4=C(C#N)C#N)S2)C3(CC(CC)CCCC)CC(CC)CCCC)=C(OCCCCCC)C=C1C1=CC2=C(S1)C1=C(C=C(/C=C3C(=O)C4=C(C=CC=C4)C3=C(C#N)C#N)S1)C2(CC(CC)CCCC)CC(CC)CCCC,DOC6-IC,,,19.21,0.91,0.6011,10.52,"H. Huang, Q. Guo, S. Feng, C. Zhang, Z. Bi, W. Xue, J. Yang, J. Song, C. Li, X. Xu, Z. Tang, W. Ma, Z. Bo, Noncovalently fused-ring electron acceptors with near-infrared absorption for high-performance organic solar cells, Nat. Commun. 10 (2019) 3038. https://doi.org/10.1038/s41467-019-11001-6."
4038,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=C(SC(/C=C4/C(=O)C5=CSC=C5C4=C(C#N)C#N)=C3)C3=C2C2=C(S3)C(C3=CC=C(C(CC)CCCC)S3)=C3C(=C2C2=CC=C(C(CC)CCCC)S2)SC2=C3C(C3=CC=C(CCCCCC)C=C3)(C3=CC=C(CCCCCC)C=C3)C3=C2SC(/C=C2/C(=O)C4=CSC=C4C2=C(C#N)C#N)=C3)C=C1,BDTCH-IC,-5.51,-3.89,17.11,0.96,0.636,10.51,"Y. Zhang, Y. Cho, L. Zhong, Y. Wang, B. Huang, Z. Yuan, C. Yang, Y. Chen, Y. Li, Two-Dimension Conjugated Acceptors Based on Benzodi(cyclopentadithiophene) Core with Thiophene-Fused Ending Group for Efficient Polymer Solar Cells, Sol. RRL. 4 (2020) 2000071. https://doi.org/10.1002/solr.202000071."
4039,O=C(C(C=CC=C1)=C1C/2=C(C#N)C#N)C2=C/C3=CC4=C(C5=CC(C6(C7=CC=C(CCCCCC)C=C7)C8=CC=C(CCCCCC)C=C8)=C(C9=C6C(SC(/C=C%10C(C(C=CC=C%11)=C%11C\%10=C(C#N)C#N)=O)=C%12)=C%12S9)C=C5C4(C%13=CC=C(CCCCCC)C=C%13)C%14=CC=C(CCCCCC)C=C%14)S3,TPTT-C1,-5.78,-3.95,15.6,0.96,0.7,10.5,"C. Li, Y. Xie, B. Fan, G. Han, Y. Yi, Y. Sun, A nonfullerene acceptor utilizing a novel asymmetric multifused-ring core unit for highly efficient organic solar cells, J. Mater. Chem. C. 6 (2018) 4873¨C4877. https://doi.org/10.1039/C8TC01229F."
4040,O=C(C(C=CC=C1)=C1C/2=C(C#N)C#N)C2=C/C(S3)=CC4=C3C5=C(C4(C6=CC=C(CCCCCC)C=C6)C7=CC=C(CCCCCC)C=C7)C8=CC9=C(C(C(C%10=CC=C(CCCCCC)C=C%10)(C%11=CC=C(CCCCCC)C=C%11)C%12=C%13SC(/C=C%14C(C(C=CC=C%15)=C%15C\%14=C(C#N)/C#N)=O)=C%12)=C%13S9)C=C8S5,BT-IC,-5.32,-3.85,17.75,0.9,0.657,10.5,"Y. Li, L. Zhong, B. Gautam, H.-J. Bin, J.-D. Lin, F.-P. Wu, Z. Zhang, Z.-Q. Jiang, Z.-G. Zhang, K. Gundogdu, Y. Li, L.-S. Liao, A near-infrared non-fullerene electron acceptor for high performance polymer solar cells, Energy Environ. Sci. 10 (2017) 1610¨C1620. https://doi.org/10.1039/C7EE00844A."
4041,O=C(C(C=C(F)C(F)=C1)=C1C/2=C(C#N)C#N)C2=C/C3=CC(SCC(CC)CCCC)=C(C4=CC5=C(C6=CC(C7(C8=CC=C(CCCCCC)C=C8)C9=CC=C(CCCCCC)C=C9)=C(C%10=C7C=C(C%11=C(SCC(CC)CCCC)C=C(/C=C%12C(C(C=C(F)C(F)=C%13)=C%13C\%12=C(C#N)/C#N)=O)S%11)S%10)C=C6C5(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15)S4)S3,IEICS4F,-5.43,-4.08,9.62,1.73,0.63,10.5,"S. Chen, H. Yao, B. Hu, G. Zhang, L. Arunagiri, L.-K. Ma, J. Huang, J. Zhang, Z. Zhu, F. Bai, W. Ma, H. Yan, A Nonfullerene Semitransparent Tandem Organic Solar Cell with 10.5% Power Conversion Efficiency, Adv. Energy Mater. 8 (2018) 1800529. https://doi.org/10.1002/aenm.201800529."
4042,CCCCCCCCC1(CCCCCCCC)C2=CC3=C(C=C2C2=C1C1=C(C=C(/C=C4C(=O)C5=C(C=CS5)C4=C(C#N)C#N)S1)S2)C(CCCCCCCC)(CCCCCCCC)C1=C3SC2=C1SC(/C=C1C(=O)C3=C(C=CS3)C1=C(C#N)C#N)=C2,C8-ITCC,-5.45,-3.85,16.1,1.04,0.63,10.5,"J. Zhang, Y. Li, H. Hu, G. Zhang, H. Ade, H. Yan, Chlorinated Thiophene End Groups for Highly Crystalline Alkylated Non-Fullerene Acceptors toward Efficient Organic Solar Cells, Chem. Mater. 31 (2019) 6672¨C6676. https://doi.org/10.1021/acs.chemmater.9b00980."
4043,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(S3)C3=C(C=C(/C=C5C(=O)C6=C(C=C(Cl)C(Cl)=C6)C5=C(C#N)C#N)S3)OC2(CCC)CCC)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC3=C2C(CCC)(CCC)OC2=C3SC(/C=C3C(=O)C4=C(C=C(Cl)C(Cl)=C4)C3=C(C#N)C#N)=C2)C=C1,DTPR-4CL,-5.35,-3.85,24.97,0.68,0.618,10.49,"J. Zhang, Y. Li, Z. Peng, F. Bai, L.-K. Ma, H. Ade, Z. Li, H. Yan, Near-infrared electron acceptors with fused nonacyclic molecular backbones for nonfullerene organic solar cells, Mater. Chem. Front. 4 (2020) 1729¨C1738. https://doi.org/10.1039/C9QM00754G."
4044,O=C(C(C=C(F)C(F)=C1)=C1C/2=C(C#N)C#N)C2=C/C=C/C3=CC4=C(C5=C(C4(C6=CC=C(CCCCCC)C=C6)C7=CC=C(CCCCCC)C=C7)C=C(C8=C9C=C(/C=C/C=C%10C(C(C=C(F)C(F)=C%11)=C%11C\%10=C(C#N)/C#N)=O)S8)C(C9(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)=C5)S3,ITC6-4F,-5.74,-3.84,18.55,0.776,0.7318,10.48,"C. Zhang, S. Ming, H. Wu, X. Wang, H. Huang, W. Xue, X. Xu, Z. Tang, W. Ma, Z. Bo, High-efficiency ternary nonfullerene organic solar cells with record long-term thermal stability, J. Mater. Chem. A. 8 (2020) 22907¨C22917. https://doi.org/10.1039/D0TA07887E."
4045,CCCCCCCCN1N=C2C(/C=C3/SC(=C(C#N)C#N)N(CC)C3=O)=CC=C(C3=CC4=C(O3)C3=CC5=C(C=C3C4(C3=CC=C(CCCCCC)C=C3)C3=CC=C(CCCCCC)C=C3)C3=C(C=C(C4=C(F)C=C(/C=C6/SC(=C(C#N)C#N)N(CC)C6=O)C6=NN(CCCCCCCC)N=C64)S3)C5(C3=CC=C(CCCCCC)C=C3)C3=CC=C(CCCCCC)C=C3)C2=N1,BTA3-F,-5.67,-3.85,12.81,1.13,0.7237,10.48,"T. Dai, Q. Nie, P. Lei, B. Zhang, J. Zhou, A. Tang, H. Wang, Q. Zeng, E. Zhou, Effects of Halogenation on the Benzotriazole Unit of Non-Fullerene Acceptors in Organic Solar Cells with High Voltages, ACS Appl. Mater. Interfaces. 13 (2021) 58994¨C59005. https://doi.org/10.1021/acsami.1c14317."
4046,CCCCC(CC)CC1=C2C(=O)C3=C(C4=CC5=C(S4)C4=C(C=C(/C=C6C(=O)C7=C(C=C(F)C(F)=C7)C6=C(C#N)C#N)S4)C5(CC(CC)CCCC)CC(CC)CCCC)SC(C4=CC5=C(S4)C4=C(C=C(/C=C6C(=O)C7=C(C=C(F)C(F)=C7)C6=C(C#N)C#N)S4)C5(CC(CC)CCCC)CC(CC)CCCC)=C3C(=O)C2=C(CC(CC)CCCC)S1,BCPDT-2,-5.4,-3.79,19.01,0.81,0.67,10.46,"Q. Wang, K. Huang, Y. Zhang, L. Ye, W. Ni, M. Li, Y. Geng, Near-infrared absorbing non-fullerene acceptors with unfused D-A-D core for efficient organic solar cells, Org. Electron. 92 (2021) 106131. https://doi.org/10.1016/j.orgel.2021.106131."
4047,CCCCCCCCCCCCC(CCCCCCCCCC)CN1C2=C(SC3=C2SC(/C=C2C(=O)C4=C(C=C(F)C(F)=C4)C2=C(C#N)C#N)=C3CCCCCCCCCCC)C2=C1C1=C(C3=NSN=C32)C2=C(C3=C(S2)C(CCCCCCCCCCC)=C(/C=C2C(=O)C4=C(C=C(F)C(F)=C4)C2=C(C#N)C#N)S3)N1CC(CCCCCCCCCC)CCCCCCCCCCCC,Y6-DT-4F,-5.67,-4.04,22.16,0.862,0.5471,10.45,"X. Liu, Z. Liang, S. Du, X. Niu, J. Tong, C. Yang, X. Lu, X. Bao, L. Yan, J. Li, Y. Xia, Two Compatible Acceptors as an Alloy Model with a Halogen-Free Solvent for Efficient Ternary Polymer Solar Cells, ACS Appl. Mater. Interfaces. (2022). https://doi.org/10.1021/acsami.1c23332."
4048,CCCCCCCCC1(CCCCCCCC)C2=CC3=C(C=C2C2=C1C=C(/C=C1C(=O)C4=C(C=C(F)C(F)=C4)C1=C(C#N)C#N)S2)C(CCCCCCCC)(CCCCCCCC)C1=C3SC(C2=CC=C(/C=C3SC(=S)N(CC)C3=O)C3=NSN=C23)=C1,IDTBF,-5.64,-3.8,16.98,0.94,0.6514,10.43,"T. Duan, L. Hou, J. Fu, Z. Kan, Q. Yang, Q. Chen, C. Zhong, Z. Xiao, D. Yu, S. Lu, An asymmetric end-capping strategy enables a new non-fullerene acceptor for organic solar cells with efficiency over 10%, Chem. Commun. 56 (2020) 6531¨C6534. https://doi.org/10.1039/D0CC01739F."
4049,O=C(C(SC=C1)=C1C/2=C(C#N)C#N)C2=C/C3=CC4=C(S3)C5=C(C6=CC(C7(C8=CC=C(CCCCCC)C=C8)C9=CC=C(CCCCCC)C=C9)=C(C%10=C7C(SC(/C=C%11C(C(SC=C%12)=C%12C\%11=C(C#N)/C#N)=O)=C%13)=C%13S%10)C=C6C5(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15)S4,ITCT,-5.62,-3.92,15.13,0.95,0.72,10.42,"J. Sun, Z. Zhang, X. Yin, J. Zhou, L. Yang, R. Geng, F. Zhang, R. Zhu, J. Yu, W. Tang, High performance non-fullerene polymer solar cells based on PTB7-Th as the electron donor with 10.42% efficiency, J. Mater. Chem. A. 6 (2018) 2549¨C2554. https://doi.org/10.1039/C7TA10391C."
4050,O=C(C(C(F)=CC=C1)=C1C/2=C(C#N)C#N)C2=C/C(S3)=CC4=C3C5=C(C4(C6=CC=C(CCCCCC)C=C6)C7=CC=C(CCCCCC)C=C7)C8=C(CCCCCCCC)C9=C(C(C(C%10=CC=C(CCCCCC)C=C%10)(C%11=CC=C(CCCCCC)C=C%11)C%12=C%13SC(/C=C%14C(C(C=CC=C%15F)=C%15C\%14=C(C#N)/C#N)=O)=C%12)=C%13S9)C(CCCCCCCC)=C8S5,NFBDT,-5.4,-3.83,17.85,0.87,0.67,10.42,"B. Kan, H. Feng, X. Wan, F. Liu, X. Ke, Y. Wang, Y. Wang, H. Zhang, C. Li, J. Hou, Y. Chen, Small-Molecule Acceptor Based on the Heptacyclic Benzodi(cyclopentadithiophene) Unit for Highly Efficient Nonfullerene Organic Solar Cells, J. Am. Chem. Soc. 139 (2017) 4929¨C4934. https://doi.org/10.1021/jacs.7b01170."
4051,O=C(C1=CSC=C1C/2=C(C#N)C#N)C2=C/C3=CC4=C(C5=CC(C6(C7=CC=C(CCCCCC)S7)C8=CC=C(CCCCCC)S8)=C(C9=C6C(SC(/C=C%10C(C%11=CSC=C%11C\%10=C(C#N)C#N)=O)=C%12)=C%12S9)C=C5C4(C%13=CC=C(CCCCCC)S%13)C%14=CC=C(CCCCCC)S%14)S3,IDT6CN-Th1:1,-5.71,-4.01,16.75,0.81,0.767,10.41,"W. Gao, M. Zhang, T. Liu, R. Ming, Q. An, K. Wu, D. Xie, Z. Luo, C. Zhong, F. Liu, F. Zhang, H. Yan, C. Yang, Asymmetrical Ladder-Type Donor-Induced Polar Small Molecule Acceptor to Promote Fill Factors Approaching 77% for High-Performance Nonfullerene Polymer Solar Cells, Adv. Mater. 30 (2018) 1800052. https://doi.org/10.1002/adma.201800052."
4052,CCCCC(CC)CN1N=C2C(=N1)C1=C(C3=C2C2=C(C=C(/C=C4C(=O)C5=C(C=C(F)C(F)=C5)C4=C(C#N)C#N)S2)N3CC(CC)CCCC)N(CC(CC)CCCC)C2=C1SC(/C=C1C(=O)C3=C(C=C(F)C(F)=C3)C1=C(C#N)C#N)=C2,Y25,-5.49,-4.06,18.41,0.84,0.6638,10.41,"J. Song, F. Cai, C. Zhu, H. Chen, Q. Wei, D. Li, C. Zhang, R. Zhang, J. Yuan, H. Peng, S.K. So, Y. Zou, Over 13% Efficient Organic Solar Cells Based on Low-Cost Pentacyclic A-DA¡äD-A-Type Nonfullerene Acceptor, Sol. RRL. 5 (2021) 2100281. https://doi.org/10.1002/solr.202100281."
4053,O=C(C(C=CC=C1)=C1C/2=C(C#N)/C#N)C2=C/C3=CC(C4(C5=CC=C(OCCCCCC)C=C5)C6=CC=C(OCCCCCC)C=C6)=C(S3)C7=C4C=C(C(C=C(C(C8=CC=C(OCCCCCC)C=C8)(C9=CC=C(OCCCCCC)C=C9)C%10=C%11SC(/C=C%12C(C(C=CC=C%13)=C%13C\%12=C(C#N)C#N)=O)=C%10)C%11=C%14)=C%14C%15(CCCCCCCC)CCCCCCCC)C%15=C7,DTCFOIC,-5.63,-3.93,18.56,0.88,0.641,10.41,"P. Yin, T. Zheng, Y. Wu, G. Liu, Z.-G. Zhang, C. Cui, Y. Li, P. Shen, Achieving efficient thick active layer and large area ternary polymer solar cells by incorporating a new fused heptacyclic non-fullerene acceptor, J. Mater. Chem. A. 6 (2018) 20313¨C20326. https://doi.org/10.1039/C8TA06836D."
4054,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=C(SC4=C3SC3=C4SC(/C=C4C(=O)C5=CC(F)=C(F)C=C5C4=C(C#N)C#N)=C3)C3=C2C2=C(S3)C3=C(S2)C2=C(C4=C(S2)C2=C(C=C(/C=C5C(=O)C6=C(C=C(F)C(F)=C6)C5=C(C#N)C#N)S2)S4)C3(C2=CC=C(CCCCCC)C=C2)C2=CC=C(CCCCCC)C=C2)C=C1,8TIC-4F,-5.36,-3.88,21,0.75,0.66,10.4,"X. Liao, H. Pei, H. Zhao, Y. Cui, L. Li, X. Shi, P. Zhu, W. Ma, Y. Chen, A.K.-Y. Jen, The synergistic effects of central core size and end group engineering on performance of narrow bandgap nonfullerene acceptors, Chem. Eng. J. 435 (2022) 135020. https://doi.org/10.1016/j.cej.2022.135020."
4055,CCCCCCOC1=C2C3=C(C4=C(C=C(/C=C5C(=O)C6=C(C=C(F)C(F)=C6)C5=C(C#N)C#N)S4)S3)C(C3=CC=C(CCCCCC)C=C3)(C3=CC=C(CCCCCC)C=C3)C3=CC(OCCCCCC)=C4C5=C(C6=C(C=C(/C=C7C(=O)C8=C(C=C(F)C(F)=C8)C7=C(C#N)C#N)S6)S5)C(C5=CC=C(CCCCCC)C=C5)(C5=CC=C(CCCCCC)C=C5)C(=C1)C4=C32,PTT-2FIC,-5.54,-3.87,18.26,0.87,0.65,10.4,"S. Du, N. Yao, S. Liu, Y. Xu, J. Cao, W. Zhuang, J. Yu, N. Wang, D. Yu, F. Zhang, E. Wang, Nonfullerene acceptors from thieno[3,2-b]thiophene-fused naphthalene donor core with six-member-ring connection for efficient organic solar cells, Dyes Pigments. 185 (2021) 108892. https://doi.org/10.1016/j.dyepig.2020.108892."
4056,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(C=C(/C=C5C(=O)C6=C(C=C(Br)S6)C5=C(C#N)C#N)S2)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC3=C2SC(/C=C2C(=O)C4=C(C=C(Br)S4)C2=C(C#N)C#N)=C3)C=C1,ITCC-Br,-5.74,-3.91,16.2,0.99,0.649,10.4,"J. Cai, C. Guo, L. Wang, Y. Fu, C. Chen, D. Li, D. Liu, T. Wang, An asymmetry strategy to reduce excessive aggregation of brominated non-fullerene acceptors for enhanced efficiency of organic solar cells, Org. Electron. 100 (2022) 106357. https://doi.org/10.1016/j.orgel.2021.106357."
4057,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(C=C(C5=C(OC)C(OC)=C(/C=C6C(=O)C7=C(C=C(F)C(F)=C7)C6=C(C#N)C#N)S5)S2)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC3=C2SC(C2=C(OC)C(OC)=C(/C=C4C(=O)C5=C(C=C(F)C(F)=C5)C4=C(C#N)C#N)S2)=C3)C=C1,IDTT2OT-4F,-5.15,-3.29,19.3,0.86,0.624,10.4,"I.N. Kim, S.J. Jeon, Y.H. Kim, H.S. Lee, Y.W. Han, N.G. Yang, D.H. Hong, C.H. Jung, D.K. Moon, Synthesis of 3,4-dimethoxythiophene spacer-based non-fullerene acceptors for efficient organic solar cells, Synth. Met. 280 (2021) 116880. https://doi.org/10.1016/j.synthmet.2021.116880."
4058,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C=C(/C=C2C(=O)C5=C(C=C(Cl)C(Cl)=C5)C2=C(C#N)C#N)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC(C3=C(F)C(F)=C(C4=CC5=C(S4)C4=C(C=C6C(=C4)C(C4=CC=C(CCCCCC)C=C4)(C4=CC=C(CCCCCC)C=C4)C4=C6SC(/C=C6C(=O)C7=C(C=C(Cl)C(Cl)=C7)C6=C(C#N)C#N)=C4)C5(C4=CC=C(CCCCCC)C=C4)C4=CC=C(CCCCCC)C=C4)C4=NON=C43)=C2)C=C1,BO2FIDT-4Cl,-5.73,-3.89,16.1,0.96,0.613,10.4,"C. Zhang, X. Song, K.-K. Liu, M. Zhang, J. Qu, C. Yang, G.-Z. Yuan, A. Mahmood, F. Liu, F. He, D. Baran, J.-L. Wang, Electron-Deficient and Quinoid Central Unit Engineering for Unfused Ring-Based A1¨CD¨CA2¨CD¨CA1-Type Acceptor Enables High Performance Nonfullerene Polymer Solar Cells with High Voc and PCE Simultaneously, Small. 16 (2020) 1907681. https://doi.org/10.1002/smll.201907681."
4059,CCCCCCC(CCCC)C1=C(C2=CC(C3=C(C)C=C(C)C=C3C)=C(C3=C(C4=C(C)C=C(C)C=C4C)C=C(C4=C(C(CCCC)CCCCCC)C=C(/C=C5C(=O)C6=C(C=C(F)C(F)=C6)C5=C(C#N)C#N)S4)S3)S2)SC(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)=C1,A4T-23,-5.63,-3.98,21,0.87,0.568,10.4,"L. Ma, S. Zhang, J. Zhu, J. Wang, J. Ren, J. Zhang, J. Hou, Completely non-fused electron acceptor with 3D-interpenetrated crystalline structure enables efficient and stable organic solar cell, Nat. Commun. 12 (2021) 5093. https://doi.org/10.1038/s41467-021-25394-w."
4060,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C=C(C2=C5OCCOC5=C(/C=C5C(=O)C6=C(C=C(F)C(F)=C6)C5=C(C#N)C#N)S2)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC(C3=C4OCCOC4=C(/C=C4C(=O)C5=C(C=C(F)C(F)=C5)C4=C(C#N)C#N)S3)=C2)C=C1,IDT-ED-4F,-5.38,-3.88,22.14,0.88,0.5304,10.4,"S.J. Jeon, Y.H. Kim, I.N. Kim, N.G. Yang, J.H. Yun, D.K. Moon, Utilizing 3,4-ethylenedioxythiophene (EDOT)-bridged non-fullerene acceptors for efficient organic solar cells, J. Energy Chem. 65 (2022) 194¨C204. https://doi.org/10.1016/j.jechem.2021.05.032."
4061,CCCCCCCCCCCC1=C(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)SC2=C1SC1=C2N(CCCCCCCC)C2=C1C1=NSN=C1C1=C2N(CCCCCCCC)C2=C1SC1=C2SC(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)=C1CCCCCCCCCCC,Y6-nC8,-5.71,-4.08,19.07,0.863,0.631,10.38,"L. Yi, S. Dai, R. Sun, W. Wang, Y. Wu, X. Jiao, C. Zhang, J. Min, Alkyl chain engineering of non-fullerene small molecule acceptors for solution-processable organic solar cells, Org. Electron. 87 (2020) 105963. https://doi.org/10.1016/j.orgel.2020.105963."
4062,CCCCCCOC1=C(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)SC(C2=CC3=C(S2)C2=C(C=C4C(=C2)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC(C4=CC(SCCCCCC)=C(/C=C5C(=O)C6=C(C=C(F)C(F)=C6)C5=C(C#N)C#N)S4)=C2)C3(C2=CC=C(CCCCCC)C=C2)C2=CC=C(CCCCCC)C=C2)=C1,IDTCN-S,-5.57,-3.9,19.04,0.85,0.657,10.34,"Y. Liu, M. Li, J. Yang, W. Xue, S. Feng, J. Song, Z. Tang, W. Ma, Z. Bo, High-Efficiency As-Cast Organic Solar Cells Based on Acceptors with Steric Hindrance Induced Planar Terminal Group, Adv. Energy Mater. 9 (2019) 1901280. https://doi.org/10.1002/aenm.201901280."
4063,CCCCC(CC)CC1(CC(CC)CCCC)C2=C(SC(/C=C3C(=O)C4=CC(F)=C(F)C=C4C3=C(C#N)C#N)=C2)C2=C1C=C(C1=NC=C(C3=CC4C(S3)C3=C(C=C(/C=C5C(=O)C6=CC(F)=C(F)C=C6C5=C(C#N)C#N)S3)C4(CC(CC)CCCC)CC(CC)CCCC)N=C1)S2,NCIC,,,17.53,0.879,0.667,10.32,"J. Gao, Y. Li, S. Li, X. Xia, X. Lu, M. Shi, H. Chen, Non-fullerene acceptors with nitrogen-containing six-membered heterocycle cores for the applications in organic solar cells, Sol. Energy Mater. Sol. Cells. 225 (2021) 111046. https://doi.org/10.1016/j.solmat.2021.111046."
4064,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=C(CC4=C3SC3=C4C4(C5=CC=C(CCCCCC)C=C5C5=C4C=CC(CCCCCC)=C5)C4=C3SC3=C4SC(/C=C4C(=O)C5=CC=CC=C5C4=C(C#N)C#N)=C3)C3=C2C2=C(C=C(/C=C4C(=O)C5=C(C=CC=C5)C4=C(C#N)C#N)S2)S3)C=C1,6TIC,-5.42,-3.91,19.6,0.81,0.65,10.32,"X. Liao, H. Pei, H. Zhao, Y. Cui, L. Li, X. Shi, P. Zhu, W. Ma, Y. Chen, A.K.-Y. Jen, The synergistic effects of central core size and end group engineering on performance of narrow bandgap nonfullerene acceptors, Chem. Eng. J. 435 (2022) 135020. https://doi.org/10.1016/j.cej.2022.135020."
4065,CCCCC(CC)CC1(CC(CC)CCCC)C2=CC3=C(C=C2C2=C1C=C(C1=CC=C(/C=C4C(=O)C5=C(C=C(F)C(F)=C5)C4=C(C#N)C#N)[Se]1)S2)C(CC(CC)CCCC)(CC(CC)CCCC)C1=C3SC(C2=CC=C(/C=C3C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)[Se]2)=C1,IDT2SeC2C4-4F,-5.4,-4.08,21.81,0.77,0.618,10.32,"X. Zhang, Q. Wang, Z. Liang, M. Li, Y. Geng, Low-bandgap non-fullerene acceptors based on selenophene ¦Ð spacer and alkylated indaceno[1,2-b:5,6-b¡ä]dithiophene for organic solar cells, Org. Electron. 69 (2019) 200¨C207. https://doi.org/10.1016/j.orgel.2019.03.038."
4066,CCCCCCCCCCCC1=C(/C=C2C(=O)C3=CC4=CC=CC=C4C=C3C2=C(C#N)C#N)SC2=C1SC1=C2N(CC(CC)CCCC)C2=C1C1=NSN=C1C1=C2N(CC(CC)CCCC)C2=C1SC1=C2SC(/C=C2C(=O)C3=C(C=C4C=CC=CC4=C3)C2=C(C#N)C#N)=C1CCCCCCCCCCC,BTP-C2C4-N,-5.49,-3.9,18.2,0.93,0.571,10.3,"J. Pan, Y. Shi, J. Yu, H. Zhang, Y. Liu, J. Zhang, F. Gao, X. Yu, K. Lu, Z. Wei, ¦Ð-Extended Nonfullerene Acceptors for Efficient Organic Solar Cells with a High Open-Circuit Voltage of 0.94 V and a Low Energy Loss of 0.49 eV, ACS Appl. Mater. Interfaces. 13 (2021) 22531¨C22539. https://doi.org/10.1021/acsami.1c04273."
4067,O=C(C1=C(SC2=C1SC=C2)C/3=C(C#N)C#N)C3=C/C4=CC5=C(S4)C6=C(C7=CC8=C(C9=C(S8)C(SC(/C=C%10C(C%11=C(SC%12=C%11SC=C%12)C\%10=C(C#N)/C#N)=O)=C%13)=C%13C9(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15)C=C7S6)C5(C%16=CC=C(CCCCCC)C=C%16)C%17=CC=C(CCCCCC)C=C%17,BDCPDT-TTC,-5.38,-3.78,17.72,0.94,0.6178,10.29,"S.-L. Chang, F.-Y. Cao, W.-C. Huang, P.-K. Huang, K.-H. Huang, C.-S. Hsu, Y.-J. Cheng, New Thieno[3,2-b]thiophene-Based Acceptor: Tuning Acceptor Strength of Ladder-Type N-Type Materials to Simultaneously Achieve Enhanced Voc and Jsc of Nonfullerene Solar Cells, ACS Energy Lett. 3 (2018) 1722¨C1729. https://doi.org/10.1021/acsenergylett.8b00563."
4068,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(C=C(/C=C5C(=O)C6=C(C=C(F)C(F)=C6)C5=C(C#N)C#N)S2)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC3=C2SC(/C=C2C(=O)C4=C(C=CC=C4)C2=C(C#N)C#N)=C3)C=C1,a-IT-2F,-5.67,-4.07,19.06,0.78,0.6884,10.28,"M. Li, Y. Zhou, J. Zhang, J. Song, Z. Bo, Tuning the dipole moments of nonfullerene acceptors with an asymmetric terminal strategy for highly efficient organic solar cells, J. Mater. Chem. A. 7 (2019) 8889¨C8896. https://doi.org/10.1039/C8TA12530A."
4069,CCCCCCCCC(CCCCCC)COC1=CC(C2=CC(CCCCCC)=C(/C=C3C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)S2)=C(OCC(CCCCCC)CCCCCCCC)C=C1C1=CC(CCCCCC)=C(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)S1,PTIC,-5.59,-3.81,16.73,0.93,0.66,10.27,"Z.-P. Yu, Z.-X. Liu, F.-X. Chen, R. Qin, T.-K. Lau, J.-L. Yin, X. Kong, X. Lu, M. Shi, C.-Z. Li, H. Chen, Simple non-fused electron acceptors for efficient and stable organic solar cells, Nat. Commun. 10 (2019) 2152. https://doi.org/10.1038/s41467-019-10098-z."
4070,CCCCCCOC1=C2SC3=C(C2=C(OCCCCCC)C2=C1C1=C(S2)C2=C(C=C(/C=C4C(=O)C5=C(C=CC=C5)C4=C(C#N)C#N)S2)C1(C1=CC=C(CCCCCC)C=C1)C1=CC=C(CCCCCC)C=C1)C(C1=CC=C(CCCCCC)C=C1)(C1=CC=C(CCCCCC)C=C1)C1=C3SC(/C=C2C(=O)C3=C(C=CC=C3)C2=C(C)C#N)=C1,NOBDT,-5.26,-3.89,19.16,0.77,0.7,10.26,"Y. Zhang, B. Kan, Y. Sun, Y. Wang, R. Xia, X. Ke, Y.-Q.-Q. Yi, C. Li, H.-L. Yip, X. Wan, Y. Cao, Y. Chen, Nonfullerene Tandem Organic Solar Cells with High Performance of 14.11%, Adv. Mater. 30 (2018) 1707508. https://doi.org/10.1002/adma.201707508."
4071,CCCCCCOC1=CC=CC(OCCCCCC)=C1C1=C(C2=C(C3=C(OCCCCCC)C=CC=C3OCCCCCC)C=C(C3=CC=C(/C=C4C(=O)C5=C(C=C(F)C(F)=C5)C4=C(C#N)C#N)S3)S2)SC(C2=CC=C(/C=C3C(=O)C4=CC(F)=C(F)C=C4C3=C(C#N)C#N)S2)=C1,o-4TB-2F,-5.63,-4,20.48,0.76,0.657,10.26,"Y.-N. Chen, M. Li, Y. Wang, J. Wang, M. Zhang, Y. Zhou, J. Yang, Y. Liu, F. Liu, Z. Tang, Q. Bao, Z. Bo, A Fully Non-fused Ring Acceptor with Planar Backbone and Near-IR Absorption for High Performance Polymer Solar Cells, Angew. Chem. Int. Ed. 59 (2020) 22714¨C22720. https://doi.org/10.1002/anie.202010856."
4072,CCN(C/1=O)/C(SC1=C/C2=CC=C(C3=CC4=C(C=C3)C5=CC=C(C6=CC=C(/C=C7S/C(N(CC)C7=O)=C(C#N)C#N)C8=NSN=C68)C=C5C49C%10=CC=C(OCCCCCCCC)C=C%10C%11=C9C=CC(OCCCCCCCC)=C%11)C%12=NSN=C2%12)=C(C#N)/C#N,SFBRCN1,-5.93,-3.86,17.25,0.9,0.65,10.26,"X. Xu, Z. Bi, W. Ma, Z. Wang, W.C.H. Choy, W. Wu, G. Zhang, Y. Li, Q. Peng, Highly Efficient Ternary-Blend Polymer Solar Cells Enabled by a Nonfullerene Acceptor and Two Polymer Donors with a Broad Composition Tolerance, Adv. Mater. 29 (2017) 1704271. https://doi.org/10.1002/adma.201704271."
4073,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C=C(C2=C(OCC(CC)CCCC)C(/C=C5C(=O)C6=C(C=CC=C6)C5=C(C#N)C#N)=CS2)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC(C3=C(OCC(CC)CCCC)C(/C=C4C(=O)C5=C(C=CC=C5)C4=C(C#N)C#N)=CS3)=C2)C=C1,i-IEICO,-5.31,-3.68,18.76,0.96,0.582,10.26,"Z. Cong, B. Zhao, Z. Chen, W. Wang, H. Wu, J. Liu, J. Wang, L. Wang, W. Ma, C. Gao, Efficient Polymer Solar Cells Having High Open-Circuit Voltage and Low Energy Loss Enabled by a Main-Chain Twisted Small Molecular Acceptor, ACS Appl. Mater. Interfaces. 11 (2019) 16795¨C16803. https://doi.org/10.1021/acsami.9b03499."
4074,CCCCCCC1(CCCCCC)C2=CC3=C(C=C2C2=C1C=C(/C=C1C(=O)C4=C(C=C(Cl)C(Cl)=C4)C1=C(C#N)C#N)S2)C(CCCCCC)(CCCCCC)C1=C3SC(/C=C2C(=O)C3=C(C=C(Cl)C(Cl)=C3)C2=C(C#N)C#N)=C1,ID-4Cl,-5.81,-4.01,17.87,0.767,0.7426,10.25,"X. Li, H. Meng, F. Shen, D. Su, S. Huo, J. Shan, J. Huang, C. Zhan, Semitransparent fullerene-free polymer solar cell with 44% AVT and 7% efficiency based on a new chlorinated small molecule acceptor, Dyes Pigments. 166 (2019) 196¨C202. https://doi.org/10.1016/j.dyepig.2019.03.024."
4075,O=C(C(C=CC=C1)=C1C/2=C(C#N)C#N)C2=C/C3=CC4=C(S3)C5=C(C6=CC(C7(C8=CC=C(CCCCCCCCC)C=C8)C9=CC=C(CCCCCCCCC)C=C9)=C(C%10=C7C(SC(/C=C%11C(C(C=CC=C%12)=C%12C\%11=C(C#N)/C#N)=O)=C%13)=C%13S%10)C=C6C5(C%14=CC=C(CCCCCCCCC)C=C%14)C%15=CC=C(CCCCCCCCC)C=C%15)S4,ITIC-9,-5.78,-3.97,14.55,0.99,0.666,10.24,"T.J. Aldrich, S.M. Swick, F.S. Melkonyan, T.J. Marks, Enhancing Indacenodithiophene Acceptor Crystallinity via Substituent Manipulation Increases Organic Solar Cell Efficiency, Chem. Mater. 29 (2017) 10294¨C10298. https://doi.org/10.1021/acs.chemmater.7b04616."
4076,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=C(C=C4C(=C3)C3=C(C5=C(C=C(/C=C6C(=O)C7=C(C=C(F)C(F)=C7)C6=C(C#N)C#N)S5)S3)C4(C3=CC=C(CCCCCC)C=C3)C3=CC=C(CCCCCC)C=C3)C3=C2C=C(/C=C2C(=O)C4=C(C=C(F)C(F)=C4)C2=C(C#N)C#N)S3)C=C1,T-TT-4F,-5.68,-3.53,18.6,0.856,0.643,10.23,"S. Liu, B. Zhao, Z. Cong, Q. Cheng, W. Wang, H. Pan, J. Liu, H. Wu, C. Gao, Influences of the terminal groups on the performances of asymmetric small molecule acceptors-based polymer solar cells, Dyes Pigments. 178 (2020) 108388. https://doi.org/10.1016/j.dyepig.2020.108388."
4077,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C=C(/C=C2C(=O)C5=C(C=C6CCCCC6=C5)C2=C(C#N)C#N)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC(/C=C3C(=O)C4=C(C=C5CCCCC5=C4)C3=C(C#N)C#N)=C2)C=C1,IDT-HN,-5.92,-3.86,14.43,0.93,0.7641,10.22,"R. Li, G. Liu, R. Xie, Z. Wang, X. Yang, K. An, W. Zhong, X.-F. Jiang, L. Ying, F. Huang, Y. Cao, Introducing cyclic alkyl chains into small-molecule acceptors for efficient polymer solar cells, J. Mater. Chem. C. 6 (2018) 7046¨C7053. https://doi.org/10.1039/C8TC01780H."
4078,O=C(C(C=CC=C1)=C1C/2=C(C#N)C#N)C2=C/C3=CC4=C(C5=CC(C6(C7=CC=C(CCCCCC)C=C7)C8=CC=C(CCCCCC)C=C8)=C(C9=C6C=C(/C=C%10C(C(C=CC=C%11)=C%11C\%10=C(C#N)C#N)=O)S9)C=C5C4(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)S3,IDT-,-5.92,-3.86,14.43,0.93,0.76,10.22,"S. Li, L. Ye, W. Zhao, X. Liu, J. Zhu, H. Ade, J. Hou, Design of a New Small-Molecule Electron Acceptor Enables Efficient Polymer Solar Cells with High Fill Factor, Adv. Mater. 29 (2017) 1704051. https://doi.org/10.1002/adma.201704051."
4079,CCCCCCCCC1(CCCCCCCC)C2=CC3=C(C=C2C2=C1C=C(C1=C4C(F)=C(C(=O)OCC(CC)CCCC)SC4=C(/C=C4C(=O)C5=CC(F)=C(F)C=C5C4=C(C#N)C#N)S1)S2)C(CCCCCCCC)(CCCCCCCC)C1=C3SC(C2=C3C(F)=C(C(=O)OCC(CC)CCCC)SC3=C(/C=C3C(=O)C4=CC(F)=C(F)C=C4C3=C(C#N)C#N)S2)=C1,6-IF4F,-5.42,-4.14,25.21,0.59,0.679,10.22,"Y. Zhang, Y. Wang, T. Shan, Q. Wei, Y.X. Xu, H. Zhong, Non-Fullerene Acceptors with an Optical Response over 1000 nm toward Efficient Organic Solar Cells, ACS Appl. Mater. Interfaces. 13 (2021) 51279¨C51288. https://doi.org/10.1021/acsami.1c13404."
4080,O=C(C(C=C(F)C(F)=C1)=C1C/2=C(C#N)C#N)C2=C/C(S3)=CC4=C3C=C(C5=C(OCCCCCCCC)C6=C(C7=CC(C8(C9=CC=C(CCCCCC)C=C9)C%10=CC=C(CCCCCC)C=C%10)=C(C%11=C8C(OCCCCCCCC)=C(C%12=CC%13=C(C=C(/C=C%14C(C(C=C(F)C(F)=C%15)=C%15C\%14=C(C#N)/C#N)=O)S%13)S%12)S%11)C=C7C6(C%16=CC=C(CCCCCC)C=C%16)C%17=CC=C(CCCCCC)C=C%17)S5)S4,IDTO-TT-4F,-5.39,-3.89,17.21,0.856,0.694,10.21,"D. Liu, B. Kan, X. Ke, N. Zheng, Z. Xie, D. Lu, Y. Liu, Extended Conjugation Length of Nonfullerene Acceptors with Improved Planarity via Noncovalent Interactions for High-Performance Organic Solar Cells, Adv. Energy Mater. 8 (2018) 1801618. https://doi.org/10.1002/aenm.201801618."
4081,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(C=C(/C=C5C(=O)C6=C(C=C(F)C(F)=C6F)C5=C(C#N)C#N)S2)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC3=C2SC(/C=C2C(=O)C4=C(C=C(F)C(F)=C4F)C2=C(C#N)C#N)=C3)C=C1,ITIC-3F,-5.73,-4.12,17.8,0.89,0.641,10.21,"T.J. Aldrich, M. Matta, W. Zhu, S.M. Swick, C.L. Stern, G.C. Schatz, A. Facchetti, F.S. Melkonyan, T.J. Marks, Fluorination Effects on Indacenodithienothiophene Acceptor Packing and Electronic Structure, End-Group Redistribution, and Solar Cell Photovoltaic Response, J. Am. Chem. Soc. 141 (2019) 3274¨C3287. https://doi.org/10.1021/jacs.8b13653."
4082,O=C(C(C=C(F)C(F)=C1)=C1C/2=C(C#N)/C#N)C2=C/C(S3)=CC4=C3C5=C6C7=C8C9=C%10C(C%11=CC=C%10C7=CC=C6C4(C%12=CC=C(CCCCCC)C=C%12)C%13=CC=C(CCCCCC)C=C%13)=C(C(SC(/C=C%14C(C(C=C(F)C(F)=C%15)=C%15C\%14=C(C#N)C#N)=O)=C%16)=C%16C%11(C%17=CC=C(CCCCCC)C=C%17)C%18=CC=C(CCCCCC)C=C%18)C=C9N(CC(CCCCCC)CCCCCCCC)C8=C5,DTPC-DFIC,-5.31,-4.1,21.92,0.76,0.613,10.21,"Z. Yao, X. Liao, K. Gao, F. Lin, X. Xu, X. Shi, L. Zuo, F. Liu, Y. Chen, A.K.-Y. Jen, Dithienopicenocarbazole-Based Acceptors for Efficient Organic Solar Cells with Optoelectronic Response Over 1000 nm and an Extremely Low Energy Loss, J. Am. Chem. Soc. 140 (2018) 2054¨C2057. https://doi.org/10.1021/jacs.7b13239."
4083,CCCCCCCCC1(CCCCCCCC)C2=CC3=C(C=C2C2=C1C1=C(C=C(C=C4C(=O)N(CC)C(=S)N(CC)C4=O)S1)S2)C(CCCCCCCC)(CCCCCCCC)C1=C3SC2=C1SC(C=C1C(=O)N(CC)C(=S)N(CC)C1=O)=C2,IDTTA,-5.81,-3.97,14.9,0.98,0.69,10.2,"Y. Firdaus, Q. He, Y. Lin, F.A.A. Nugroho, V.M.L. Corre, E. Yengel, A.H. Balawi, A. Seitkhan, F. Laquai, C. Langhammer, F. Liu, M. Heeney, T.D. Anthopoulos, Novel wide-bandgap non-fullerene acceptors for efficient tandem organic solar cells, J. Mater. Chem. A. 8 (2020) 1164¨C1175. https://doi.org/10.1039/C9TA11752K."
4084,CCCCC(CC)CC1(CC(CC)CCCC)C2=C(SC(/C=C3C(=O)C4=C(C=C(Cl)C(Cl)=C4)C3=C(C#N)C#N)=C2)C2=C1C=C(C1=CC=C(C3=CC4=C(S3)C3=C(C=C(/C=C5C(=O)C6=C(C=C(Cl)C(Cl)=C6)C5=C(C#N)C#N)S3)C4(CC(CC)CCCC)CC(CC)CCCC)C3=NSN=C13)S2,BTCIC-4CL,-5.64,-4.12,23.2,0.63,0.69,10.2,"S. Pang, X. Zhou, S. Zhang, H. Tang, S. Dhakal, X. Gu, C. Duan, F. Huang, Y. Cao, Nonfused Nonfullerene Acceptors with an A¨CD¨CA¡ä¨CD¨CA Framework and a Benzothiadiazole Core for High-Performance Organic Solar Cells, ACS Appl. Mater. Interfaces. 12 (2020) 16531¨C16540. https://doi.org/10.1021/acsami.0c01850."
4085,CCCCCCCCOC1=C2SC3=C(C2=C(OCCCCCCCC)C2=C1C1=C(S2)C2=C(C4=C(C=C(/C=C5C(=O)C6=C(C=CC=C6)C5=C(C#N)C#N)S4)S2)C1(C1=CC=C(CCCCCC)C=C1)C1=CC=C(CCCCCC)C=C1)C(C1=CC=C(CCCCCC)C=C1)(C1=CC=C(CCCCCC)C=C1)C1=C3SC2=C1SC(/C=C1/C(=O)C3=CC=CC=C3C1=C(C#N)C#N)=C2,OBTT-0F,-5.27,-3.87,16.86,0.889,0.679,10.2,"Y. Sun, H.-H. Gao, Y.-Q.-Q. Yi, X. Wan, H. Feng, X. Ke, Y. Zhang, J. Yan, C. Li, Y. Chen, Fluorination-modulated end units for high-performance non-fullerene acceptors based organic solar cells, Sci. China Mater. 62 (2019) 1210¨C1217. https://doi.org/10.1007/s40843-019-9415-2."
4086,CCCCCCCCC1=CC=C(C2(C3=CC=C(C)C=C3)C3=CC4=C(C=C3C3=C2C2=C(C=C(C5=CC=C(C=C(C#N)C#N)C6=NSN=C56)S2)S3)C(C2=CC=C(CCCCCCCC)C=C2)(C2=CC=C(CCCCCCCC)C=C2)C2=C4SC3=C2SC(C2=CC=C(C=C(C#N)C#N)C4=NSN=C24)=C3)C=C1,IT-BT-CN,-5.53,-3.96,16.38,1,0.6247,10.2,"S. Shome, H.J. Shin, J. Yang, B. Park, S.-J. Ko, J. Lee, H. Choi, Microwave-Assisted Synthesis of Non-Fullerene Acceptors and Their Photovoltaic Studies for High-Performance Organic Solar Cells, ACS Appl. Energy Mater. 4 (2021) 9816¨C9826. https://doi.org/10.1021/acsaem.1c01872."
4087,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(C=C(/C=C5C(=O)C6=C(C=C(Cl)C(Cl)=C6)C5=C(C#N)C#N)S2)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC3=C2SC(/C=C(C#N)C2=NC4=C(C=CC(Cl)=C4)O2)=C3)C=C1,ICCl-IDTT-BOACl,-5.48,-3.73,18.37,0.99,0.561,10.2,"Y. Zhao, X. Tang, J. Cao, P. Huang, C. Weng, P. Shen, Balancing the Voc-Jsc trade-off in polymer solar cells based on 2-(benzoxazol-2-yl)-acetonitrile end-capped small-molecule acceptors through asymmetry and halogenation of end groups, Org. Electron. 102 (2022) 106446. https://doi.org/10.1016/j.orgel.2022.106446."
4088,CCCCC(CC)CC1=C(/C=C2C(=O)C3=CC(F)=C(F)C=C3C2=C(C#N)C#N)SC(C2=CC(CC(CC)CCCC)=C(C3=C(CC(CC)CCCC)C=C(C4=CC(CC(CC)CCCC)=C(/C=C5C(=O)C6=CC(F)=C(F)C=C6C5=C(C#N)C#N)S4)S3)S2)=C1,4T-3,-5.86,-3.98,17.27,0.81,0.7245,10.15,"Y. Zhou, M. Li, H. Lu, H. Jin, X. Wang, Y. Zhang, S. Shen, Z. Ma, J. Song, Z. Bo, High-Efficiency Organic Solar Cells Based on a Low-Cost Fully Non-Fused Electron Acceptor, Adv. Funct. Mater. 31 (2021) 2101742. https://doi.org/10.1002/adfm.202101742."
4089,FC1=CC(C2=CC3=C(C(SC(/C=C4C(C(C=CC=C5)=C5C4=C(C#N)C#N)=O)=C6)=C6C3(CC(CC)CCCC)CC(CC)CCCC)S2)=C(F)C=C1C7=CC(C8(CC(CC)CCCC)CC(CC)CCCC)=C(S7)C9=C8C=C(/C=C%10C(C(C=CC=C%11)=C%11C\%10=C(C#N)C#N)=O)S9,DF-PCIC,-5.49,-3.77,15.66,0.91,0.7,10.14,"N. Wang, L. Zhan, S. Li, M. Shi, T.-K. Lau, X. Lu, R. Shikler, C.-Z. Li, H. Chen, Enhancement of intra- and inter-molecular ¦Ð-conjugated effects for a non-fullerene acceptor to achieve high-efficiency organic solar cells with an extended photoresponse range and optimized morphology, Mater. Chem. Front. 2 (2018) 2006¨C2012. https://doi.org/10.1039/C8QM00318A."
4090,CCCCC(CC)CC1=C(F)C=C(C2=C3C=C(C4=CC5=C(S4)C4=C(C=C(/C=C6C(=O)C7=C(C=C(Cl)C(Cl)=C7)C6=C(C#N)C#N)S4)C5(CC(CC)CCCC)CC(CC)CCCC)SC3=C(C3=CC(F)=C(CC(CC)CCCC)S3)C3=C2SC(C2=CC4=C(S2)C2=C(C=C(/C=C5C(=O)C6=C(C=C(Cl)C(Cl)=C6)C5=C(C#N)C#N)S2)C4(CC(CC)CCCC)CC(CC)CCCC)=C3)S1,F-BDTC-Cl,-5.59,-3.9,19.16,0.841,0.628,10.13,"Y. Wang, S. Liu, H. Gao, L. Wang, W. Wang, B. Zhao, H. Wu, C. Gao, Synergistic halogenation of backbone and end group for high-performance non-fused acceptors based organic solar cells, Dyes Pigments. (2022) 110178. https://doi.org/10.1016/j.dyepig.2022.110178."
4091,O=C(C(C(C)=CC=C1)=C1C/2=C(C#N)C#N)C2=C/C3=CC4=C(C5=CC(C6(CCCCCCCC)C7=CC=C(CCCCCC)C=C7)=C(C8=C6C=C(/C=C9C(C(C=CC(C)=C%10)=C%10C9=C(C#N)C#N)=O)S8)C=C5C4(CCCCCCCC)C%11=CC=C(CCCCCC)C=C%11)S3,IDT-OB1:1,-5.77,-3.87,16.18,0.88,0.71,10.12,"S. Feng, C. Zhang, Y. Liu, Z. Bi, Z. Zhang, X. Xu, W. Ma, Z. Bo, Fused-Ring Acceptors with Asymmetric Side Chains for High-Performance Thick-Film Organic Solar Cells, Adv. Mater. 29 (2017) 1703527. https://doi.org/10.1002/adma.201703527."
4092,CCCCC(CC)CN1C(=O)C2=C(C3=CC4=C(S3)C3=C(C=C(/C=C5C(=O)C6=C(C=CC=C6)C5=C(C#N)C#N)S3)C4(CC(CC)CCCC)CC(CC)CCCC)SC(C3=CC4=C(S3)C3=C(C=C(/C=C5C(=O)C6=C(C=CC=C6)C5=C(C#N)C#N)S3)C4(CC(CC)CCCC)CC(CC)CCCC)=C2C1=O,TPDCIC,-5.38,-3.78,18.16,0.83,0.6714,10.12,"S.-Z. Geng, W.-T. Yang, J. Gao, S.-X. Li, M.-M. Shi, T.-K. Lau, X.-H. Lu, C.-Z. Li, H.-Z. Chen, Non-fullerene Acceptors with a Thieno[3,4-c]pyrrole-4,6-dione (TPD) Core for Efficient Organic Solar Cells, Chin. J. Polym. Sci. 37 (2019) 1005¨C1014. https://doi.org/10.1007/s10118-019-2309-x."
4093,CCCCCCCCOC(=O)C1=CC2=C(C3=CC4=C(S3)C3=C(C=C5C(=C3)C(C3=CC=CC(OCCCCCC)=C3)(C3=CC=CC(OCCCCCC)=C3)C3=C5SC(C5=C6C=C(C(=O)OCO)SC6=C(/C=C6SC(=C(C#N)C#N)N(CC)C6=O)S5)=C3)C4(C3=CC=CC(OCCCCCC)=C3)C3=CC(OCCCCCC)=CC=C3)SC(/C=C3SC(=C(C#N)C#N)N(CC)C3=O)=C2S1,ATT-7,-5.45,-3.61,15.99,0.97,0.6667,10.12,"J. Zhang, F. Liu, S. Chen, C. Yang, X. Zhu, D. Zhu, High-Performance Polymer Solar Cells Achieved by Introducing Side-Chain Heteroatom on Small-Molecule Electron Acceptor, Macromol. Rapid Commun. 40 (2019) 1800393. https://doi.org/10.1002/marc.201800393."
4094,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C=C(/C=C2C(=O)C5=CC(F)=C(F)C=C5C2=C(C#N)C#N)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC(C3=CC=C(C4=CC5=C(S4)C4=CC6=C(C=C4C5(C4=CC=C(CCCCCC)C=C4)C4=CC=C(CCCCCC)C=C4)C4=C(C=C(/C=C5C(=O)C7=C(C=C(F)C(F)=C7)C5=C(C#N)C#N)S4)C6(C4=CC=C(CCCCCC)C=C4)C4=CC=C(CCCCCC)C=C4)C4=NSN=C34)=C2)C=C1,BT-dIDT,-5.34,-3.87,18.59,0.87,0.6461,10.12,"M. Zhang, M. Zeng, H. Chen, L. Li, B. Zhao, S. Tan, A2-D-A1-D-A2-type small molecule acceptors incorporated with electron-deficient core for non-fullerene organic solar cells, Sol. Energy. 197 (2020) 511¨C518. https://doi.org/10.1016/j.solener.2020.01.032."
4095,O=C1C2=C(C=CS2)C(/C1=C/C(S3)=CC4=C3C5=CC(OC(CC(CC)CCCC)(CC(CC)CCCC)C6=C7SC(/C=C8/C(C(C=CS9)=C9C8=O)=C(C#N)C#N)=C6)=C7C=C5OC4(CC(CC)CCCC)CC(CC)CCCC)=C(C#N)/C#N,NBDTP,-5.66,-3.79,16.12,0.942,0.665,10.1,"H. Wu, H. Fan, S. Xu, C. Zhang, S. Chen, C. Yang, D. Chen, F. Liu, X. Zhu, A Designed Ladder-Type Heteroarene Benzodi(Thienopyran) for High-Performance Fullerene-Free Organic Solar Cells, Sol. RRL. 1 (2017) 1700165. https://doi.org/10.1002/solr.201700165."
4096,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C=C(C2=C5C(F)=C(C(=O)OCC(CC)CCCC)SC5=C(/C=C5C(=O)C6=C(C=CC(F)=C6)C5=C(C#N)C#N)S2)O3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC(C3=C4C(F)=C(C(=O)OCC(CC)CCCC)SC4=C(/C=C4C(=O)C5=C(C=CC(F)=C5)C4=C(C#N)C#N)S3)=C2)C=C1,T2,-5.34,-3.96,22.65,0.67,0.66,10.1,"F.-X. Chen, J.-Q. Xu, Z.-X. Liu, M. Chen, R. Xia, Y. Yang, T.-K. Lau, Y. Zhang, X. Lu, H.-L. Yip, A.K.-Y. Jen, H. Chen, C.-Z. Li, Near-Infrared Electron Acceptors with Fluorinated Regioisomeric Backbone for Highly Efficient Polymer Solar Cells, Adv. Mater. 30 (2018) 1803769. https://doi.org/10.1002/adma.201803769."
4097,O=C(C(C=CC=C1)=C1C/2=C(C#N)C#N)C2=C/C3=CC=C(C4=CC(C5(CCCCCCCC)CCCCCCCC)=C(C=C4)C6=C5C(C(CCCCCCCC)(CCCCCCCC)C7=C8C=CC(C9=CC=C(/C=C%10C(C(C=CC=C%11)=C%11C\%10=C(C#N)/C#N)=O)S9)=C7)=C8S6)S3,IDIDT-C8,-5.5,-3.86,15.81,0.97,0.6588,10.1,"R. Hou, M. Li, S. Feng, Y. Liu, L. Wu, Z. Bi, X. Xu, W. Ma, Z. Bo, Fused pentacyclic electron acceptors with four cis-arranged alkyl side chains for efficient polymer solar cells, J. Mater. Chem. A. 6 (2018) 3724¨C3729. https://doi.org/10.1039/C7TA10026D."
4098,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=C(C=C4C(=C3)C3=C(C5=C(C=C(/C=C6C(=O)C7=C(C=C(Cl)C(Cl)=C7)C6=C(C#N)C#N)S5)S3)C4(C3=CC=C(CCCCCC)C=C3)C3=CC=C(CCCCCC)C=C3)C3=C2C=C(/C=C2C(=O)C4=C(C=C(F)C(F)=C4)C2=C(C#N)C#N)S3)C=C1,T-TT-4CL,-5.73,-3.61,18.92,0.811,0.65,10.1,"S. Liu, B. Zhao, Z. Cong, Q. Cheng, W. Wang, H. Pan, J. Liu, H. Wu, C. Gao, Influences of the terminal groups on the performances of asymmetric small molecule acceptors-based polymer solar cells, Dyes Pigments. 178 (2020) 108388. https://doi.org/10.1016/j.dyepig.2020.108388."
4099,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=C(SC(/C=C4C(=O)C5=C(C=C(F)C(F)=C5)C4=C(C#N)C#N)=C3)C3=C2C2=C(OCC(CC)CCCC)C4=C(C(OCC(CC)CCCC)=C2S3)C2=C(S4)C3=C(C=C(CC4C(=O)C5=C(C=C(F)C=C5)C4=C(C#N)C#N)S3)C2(C2=CC=C(CCCCCC)C=C2)C2=CC=C(CCCCCC)C=C2)C=C1,BT-FIC,-5.48,-4.1,21.28,0.73,0.65,10.1,"Y. Li, W. Su, F. Wu, Z. Xu, Y.-K. Wang, M. Zhang, Z.-Q. Jiang, L.-S. Liao, Near-infrared non-fullerene acceptors based on dithienyl[1,2-b:4,5-b¡¯]benzodithiophene core for high performance PTB7-Th-based polymer solar cells, Org. Electron. 65 (2019) 63¨C69. https://doi.org/10.1016/j.orgel.2018.10.042."
4100,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(S3)C3=C(C=C(/C=C5C(=O)C6=C(C=CC=C6F)C5=C(C#N)C#N)S3)S2)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC3=C2SC2=C3SC(CC3C(=O)C4=C(C=CC=C4)C3=C(C#N)C#N)=C2)C=C1,INIC1,-5.54,-3.97,16.63,0.929,0.643,10.1,"S. Dai, F. Zhao, Q. Zhang, T.-K. Lau, T. Li, K. Liu, Q. Ling, C. Wang, X. Lu, W. You, X. Zhan, Fused Nonacyclic Electron Acceptors for Efficient Polymer Solar Cells, J. Am. Chem. Soc. 139 (2017) 1336¨C1343. https://doi.org/10.1021/jacs.6b12755."
4101,CCCCCCCCCCC(CCCCCC)N1N=C2C(=N1)C(C1=CC3=C(S1)C1=C(C=C(/C=C4C(=O)C5=C(C=CC(F)=C5)C4=C(C#N)C#N)S1)C3(CC(CC)CCCC)CC(CC)CCCC)=C(F)C(F)=C2C1=CC2=C(S1)C1=C(C=C(/C=C3C(=O)C4=C(C=CC(F)=C4)C3=C(C#N)C#N)S1)C2(CC(CC)CCCC)CC(CC)CCCC,BTC6-2F,-5.52,-3.8,19.32,0.81,0.6414,10.1,"J. Huang, C.-Y. Gao, X.-H. Fan, X. Zhu, L.-M. Yang, A¨CD¨CC¨CD¨CA type non-fullerene acceptors based on the benzotriazole (BTA) unfused core for organic solar cells, New J. Chem. 45 (2021) 12802¨C12807. https://doi.org/10.1039/D1NJ01978C."
4102,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=C(C=C4C(=C3)C3=C(C5=C(C=C(/C=C6C(=O)C7=C(C)SC=C7C6=C(C#N)C#N)S5)S3)C4(C3=CC=C(CCCCCC)C=C3)C3=CC=C(CCCCCC)C=C3)C3=C2C=C2C(=C3)C(C3=CC=C(CCCCCC)C=C3)(C3=CC=C(CCCCCC)C=C3)C3=C2SC2=C3SC(/C=C3C(=O)C4=C(C)SC=C4C3=C(C#N)C#N)=C2)C=C1,FTTCN-M,-5.53,-3.91,15.19,0.93,0.7137,10.08,"R. Ming, M. Zhang, W. Gao, W. Ning, Z. Luo, C. Zhong, F. Zhang, C. Yang, Fluorene-fused ladder-type non-fullerene small molecule acceptors for high-performance polymer solar cells, Mater. Chem. Front. 3 (2019) 709¨C715. https://doi.org/10.1039/C9QM00013E."
4103,CCN(C/1=O)/C(SC1=C/C2=C(CC(C(OCCCCCCCC)=O)=C3)C3=C(C4=CC5=C(C(C=C(C(C6=CC=C(CCCCCC)C=C6)(C7=CC=C(CCCCCC)C=C7)C8=C9SC(C%10=C%11C(CC(C(OCCCCCCCC)=O)=C%11)=C(/C=C%12S/C(N(CC)C\%12=O)=C(C#N)/C#N)S%10)=C8)C9=C%13)=C%13C5(C%14=CC=C(CCCCCC)C=C%14)C%15=CC=C(CCCCCC)C=C%15)S4)S2)=C(C#N)C#N,ATT-1,-5.5,-3.63,16.48,0.87,0.7,10.07,"F. Liu, Z. Zhou, C. Zhang, T. Vergote, H. Fan, F. Liu, X. Zhu, A Thieno[3,4-b]thiophene-Based Non-fullerene Electron Acceptor for High-Performance Bulk-Heterojunction Organic Solar Cells, J. Am. Chem. Soc. 138 (2016) 15523¨C15526. https://doi.org/10.1021/jacs.6b08523."
4104,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C=C(/C=C2C(=O)C5=C(C=C(F)C(F)=C5)C2=C(C#N)C#N)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC(C3=CC4=C(S3)C3=CC5=C(C=C3C4(C3=CC=C(CCCCCC)C=C3)C3=CC=C(CCCCCC)C=C3)C3=C(C=C(/C=C4C(=O)C6=C(C=C(F)C(F)=C6)C4=C(C#N)C#N)S3)C5(C3=CC=C(CCCCCC)C=C3)C3=CC=C(CCCCCC)C=C3)=C2)C=C1,IDT2-DFIC,-5.39,-3.97,16.06,0.91,0.6922,10.06,"H. Tan, X. Zheng, J. Zhu, J. Yu, W. Zhu, An A¨CD¨CD¨CA-type non-fullerene small-molecule acceptor with strong near-infrared absorption for high performance polymer solar cells, J. Mater. Chem. C. 7 (2019) 13301¨C13306. https://doi.org/10.1039/C9TC04898G."
4105,O=C(C(C=CC=C1)=C1C/2=C(C#N)/C#N)C2=C/C(S3)=CC4=C3C5=CC6=C(C=C5C4(CCCCCCCC)CCCCCCCC)C7=CC8=C(C(SC(/C=C9C(C(C=CC=C%10)=C%10C9=C(C#N)C#N)=O)=C%11)=C%11C8(CCCCCCCC)CCCCCCCC)C=C7C6(CCCCCCCC)CCCCCCCC,FDICTF,-5.43,-3.71,15.81,0.94,0.66,10.06,"N. Qiu, H. Zhang, X. Wan, C. Li, X. Ke, H. Feng, B. Kan, H. Zhang, Q. Zhang, Y. Lu, Y. Chen, A New Nonfullerene Electron Acceptor with a Ladder Type Backbone for High-Performance Organic Solar Cells, Adv. Mater. 29 (2017) 1604964. https://doi.org/10.1002/adma.201604964."
4106,CCCCC(CC)CC1(CC(CC)CCCC)C2=C(C=CC(C3=CC=C(/C=C4C(=O)C5=CC=CC=C5C4=C(C#N)C#N)S3)=C2)C2=C1C1=C(C=C(C3=CC=C(/C=C4C(=O)C5=CC(F)=CC=C5C4=C(C#N)C#N)S3)C=C1)C2(CC(CC)CCCC)CC(CC)CCCC,YITI-2F,-5.6,-3.92,15.54,0.928,0.6969,10.05,"Q. Yue, Z. Zhou, S. Xu, J. Zhang, X. Zhu, Design and synthesis of medium-bandgap small-molecule electron acceptors for efficient tandem solar cells, J. Mater. Chem. A. 6 (2018) 13588¨C13592. https://doi.org/10.1039/C8TA04405H."
4107,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(C=C(C5=C(OC)C(OC)=C(/C=C6C(=O)C7=C(C=C(F)C=C7)C6=C(C#N)C#N)S5)S2)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC3=C2SC(C2=C(OC)C(OC)=C(/C=C4C(=O)C5=C(C=CC(F)=C5)C4=C(C#N)C#N)S2)=C3)C=C1,IDTT2OT-2F,-5.12,-3.23,17.5,0.88,0.651,10.04,"I.N. Kim, S.J. Jeon, Y.H. Kim, H.S. Lee, Y.W. Han, N.G. Yang, D.H. Hong, C.H. Jung, D.K. Moon, Synthesis of 3,4-dimethoxythiophene spacer-based non-fullerene acceptors for efficient organic solar cells, Synth. Met. 280 (2021) 116880. https://doi.org/10.1016/j.synthmet.2021.116880."
4108,CCCCCCC1=C(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)SC2=C1N(CC(CC)CCCC)C1=C2C2=NSN=C2C2=C1N(CC(CC)CCCC)C1=C2SC(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)=C1CCCCCC,BTT-4F ,-5.71,-4.02,17.08,0.88,0.6668,10.03,"R. Ming, J. Gao, W. Gao, W. Ning, Z. Luo, F. Zhang, C. Yang, Benzo[c][1,2,5]thiadiazole-fused pentacyclic small molecule acceptors for organic solar cells, Dyes Pigments. 185 (2021) 108970. https://doi.org/10.1016/j.dyepig.2020.108970."
4109,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(C=C(/C=C5C(=O)C6=C(C=CC=C6)C5=C(C#N)C#N)S2)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC3=C2SC(/C=C2C(=O)C4=C(C=C(F)C(F)=C4)C2=C(C#N)C#N)=C3)C=C1,ITIC-2F,-5.76,-4.07,16.7,0.91,0.656,10.03,"T.J. Aldrich, M. Matta, W. Zhu, S.M. Swick, C.L. Stern, G.C. Schatz, A. Facchetti, F.S. Melkonyan, T.J. Marks, Fluorination Effects on Indacenodithienothiophene Acceptor Packing and Electronic Structure, End-Group Redistribution, and Solar Cell Photovoltaic Response, J. Am. Chem. Soc. 141 (2019) 3274¨C3287. https://doi.org/10.1021/jacs.8b13653."
4110,CCCCCCC1(CCCCCC)C2=CC3=C(C=C2C2=C1C=C(/C=C1C(=O)C4=C(C=CC=C4)C1=C(C#N)C#N)S2)C(CCCCCC)(CCCCCC)C1=C3CC(/C=C2C(=O)C3=C(C=CC=C3)C2=C(C#N)C#N)=C1,IDIC,,,16.6,0.85,0.71,10,"P. Cheng, J. Wang, Q. Zhang, W. Huang, J. Zhu, R. Wang, S.-Y. Chang, P. Sun, L. Meng, H. Zhao, H.-W. Cheng, T. Huang, Y. Liu, C. Wang, C. Zhu, W. You, X. Zhan, Y. Yang, Unique Energy Alignments of a Ternary Material System toward High-Performance Organic Photovoltaics, Adv. Mater. 30 (2018) 1801501. https://doi.org/10.1002/adma.201801501."
4111,CCCCC(CC)CC1(CC(CC)CCCC)C2=CC3=C(C=C2C2=C1C=C(C1=CC=C(/C=C4C(=O)C5=C(C=C(F)C(F)=C5)C4=C(C#N)C#N)[Se]1)S2)C(CC(CC)CCCC)(CC(CC)CCCC)C1=C3SC(C2=CC=C(/C=C3C(=O)C4=C(C=C(F)C=C4)C3=C(C#N)C#N)[Se]2)=C1,IDT2SeC2C4-2F,-5.37,-3.99,18.9,0.81,0.652,10,"X. Zhang, Q. Wang, Z. Liang, M. Li, Y. Geng, Low-bandgap non-fullerene acceptors based on selenophene ¦Ð spacer and alkylated indaceno[1,2-b:5,6-b¡ä]dithiophene for organic solar cells, Org. Electron. 69 (2019) 200¨C207. https://doi.org/10.1016/j.orgel.2019.03.038."
4112,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=C(SC4=C3SC=C4/C=C3C(=O)C4=C(C=C(F)C(F)=C4)C3=C(C#N)C#N)C3=C2C2=C(S3)C3=C(S2)C2=C(C4=C(S2)C2=C(S4)C4=C(C5=C(S4)C(/C=C4C(=O)C6=C(C=C(F)C(F)=C6)C4=C(C#N)C#N)=CS5)C2(C2=CC=CC=C2)C2=CC=CC=C2)C3(C2=CC=C(CCCCCC)C=C2)C2=CC=C(CCCCCC)C=C2)C=C1,I-FUIC,-5.31,-3.99,20.2,0.779,0.634,10,"T. Li, L. Yang, Y. Xiao, K. Liu, J. Wang, X. Lu, X. Zhan, Facile synthesis of high-performance nonfullerene acceptor isomers via a one stone two birds strategy, J. Mater. Chem. A. 7 (2019) 20667¨C20674. https://doi.org/10.1039/C9TA07917C."
4113,CCCCCCCCCCCCN1C(=O)C2=CC=CC3=C2C(=CC=C3C2=CC=C(C3=CC=C4C(=O)N(CCCCCCCCCCCC)C(=O)C5=CC=CC3=C54)S2)C1=O,NI-T-NI,-6.07,-3.53,2.91,1.3,0.53,1.91,"X. Zhang, J. Zhang, H. Lu, J. Wu, G. Li, C. Li, S. Li, Z. Bo, A 1,8-naphthalimide based small molecular acceptor for polymer solar cells with high open circuit voltage, J. Mater. Chem. C. 3 (2015) 6979¨C6985. https://doi.org/10.1039/C5TC01148E."
4114,CCCCCCCCN1N=C2C(/C=C3/SC(=C(C#N)C#N)N(CC)C3=O)=CC=C(C3=CC4=C(C=C3)C3=C(C=C(C5=CC=C(/C=C6/SC(=C(C#N)C#N)N(CC)C6=O)C6=NN(CCCCCCCC)N=C56)C=C3)C43C4=C(C=CC=C4)C4=C3C=CC=C4)C2=N1,BTA23,-5.79,-3.24,3.98,0.9,0.52,1.86,"X. Wen, B. Xiao, A. Tang, J. Hu, C. Yang, E. Zhou, Wide Band Gap Non-Fullerene Small Molecular Acceptors Containing Spirobifluorene and Benzotriazole with Three Different End-Capped Groups for P3HT-Based Organic Solar Cells, Chin. J. Chem. 36 (2018) 392¨C398. https://doi.org/10.1002/cjoc.201700792."
4115,CCCCC(CC)COC(=O)/C(C#N)=C/C1=CC=C(C2=CC=C(C3=C4OCCOC4=C(C4=CC=C(C5=CC=C(/C=C(C#N)C(=O)OCC(CC)CCCC)S5)S4)S3)S2)S1,SAM-72,-5.46,-3.41,4.13,0.74,0.6108,1.85,"N.A. Mica, S. a. J. Almahmoud, L.K. Jagadamma, G. Cooke, I.D.W. Samuel, An investigation of the role acceptor side chains play in the processibility and efficiency of organic solar cells fabricated from small molecular donors featuring 3,4-ethylenedioxythiophene cores, RSC Adv. 8 (2018) 39231¨C39240. https://doi.org/10.1039/C8RA07034B."
4116,CCCCCCCCCCC(CCCC)COC1=C(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)SC(C2=CC3=C(S2)C2=C(C4=C(C5=NSN=C52)C2=C(C=C(C5=CC(OCC(CCCC)CCCCCCCCCC)=C(/C=C6C(=O)C7=C(C=C(F)C(F)=C7)C6=C(C#N)C#N)S5)S2)N4CC(CCC)CCCCCCCC)N3CC(CCC)CCCCCCCC)=C1,L3,-5.38,-3.87,4.07,0.91,0.4083,1.78,"Z. Zhang, D. Li, H. Zhang, X. Ma, Y.-N. Chen, A. Zhang, X. Xu, Y. Liu, Z. Ma, Z. Bo, An asymmetric A¨CDA¡äD¨C¦Ð-A type non-fullerene acceptor for high-performance organic solar cells, J. Mater. Chem. C. 10 (2022) 2792¨C2799. https://doi.org/10.1039/D1TC04425G."
4117,CCCCC(CC)COC1=CC=C(C(C2=CC=C(OCC(CC)CCCC)C=C2)=C2C3=CC4=C(C=C3C3=C2C=C(/C=C2C(=O)C5=C(C=CC=C5)C2=C(C#N)C#N)S3)C(=C(C2=CC=C(OCC(CC)CCCC)C=C2)C2=CC=C(OCC(CC)CCCC)C=C2)C2=C4SC(/C=C3C(=O)C4=C(C=CC=C4)C3=C(C#N)C#N)=C2)C=C1,IDTV-PhIC,-5.52,-3.84,4.93,0.98,0.3664,1.77,"J. Liang, P. Yin, T. Zheng, G. Wang, X. Zeng, C. Cui, P. Shen, Conjugated side-chain optimization of indacenodithiophene-based nonfullerene acceptors for efficient polymer solar cells, J. Mater. Chem. C. 7 (2019) 10028¨C10038. https://doi.org/10.1039/C9TC02237F."
4118,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C=C(/C=C2SC(=S)N(CC)C2=O)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC(/C=C3SC(=S)N(CC)C3=O)=C2)C=C1,IDT-2,-5.68,-3.6,3.91,0.97,0.4556,1.74,"N. Terenti, G.-I. Giurgi, L. Szolga, I. Stroia, A. Terec, I. Grosu, A.P. Cri?an, Effect of the Terminal Acceptor Unit on the Performance of Non-Fullerene Indacenodithiophene Acceptors in Organic Solar Cells, Molecules. 27 (2022) 1229. https://doi.org/10.3390/molecules27041229."
4119,CCC(CC)N1C(=O)C2=CC=C3C4=C5C(=CC(C6=CC7=C8C(=CC=C9C%10=C%11C(=CC=C%12C(=O)N(C(CC)CC)C(=O)C(=C%12%11)C=C%10)C6=C98)C(=O)N(C(CC)CC)C7=O)=C6C(=O)N(C(CC)CC)C(=O)C(=C65)C=C4)C4=C3C2=C(C=C4)C1=O,BO-2PDI,-6.09,-3.99,6.37,0.693,0.389,1.71,"H. Wang, L. Chen, Y. Xiao, A simple molecular structure of ortho-derived perylene diimide diploid for non-fullerene organic solar cells with efficiency over 8%, J. Mater. Chem. A. 5 (2017) 22288¨C22296. https://doi.org/10.1039/C7TA06804B."
4120,CCCCCCCCC1=C(C2=C(F)C(F)=C(C3=C(CCCCCCCC)C(F)=C(C4=C(CCCCCCCC)C(F)=C(C5=C(CCCCCCCC)C(F)=C(C=C(C#N)C#N)S5)S4)S3)S2)SC(C2=C(CCCCCCCC)C(F)=C(C3=C(CCCCCCCC)C(F)=C(C=C(C#N)C#N)S3)S2)=C1F,D7T8F-M,,,4.4,1.11,0.345,1.7,"T. Duan, M. Babics, A. Seitkhan, Y. Firdaus, R.-Z. Liang, F. Cruciani, S. Liu, S. Lopatin, P.M. Beaujuge, F-Substituted oligothiophenes serve as nonfullerene acceptors in polymer solar cells with open-circuit voltages >1 V, J. Mater. Chem. A. 6 (2018) 9368¨C9372. https://doi.org/10.1039/C8TA02781A."
4121,CCCCCCCCCCCCN1C(=O)C2=CC=CC3=C2C(=CC=C3C2=CC=C(C#CC3=CC=C(C4=C5C=CC=C6C(=O)N(CCCCCCCCCCCC)C(=O)C(=C65)C=C4)S3)S2)C1=O,NI-TAT-NI-C12,-5.83,-3.39,3.71,1.22,0.36,1.68,"R. Hou, S. Feng, X. Gong, Y. Liu, J. Zhang, C. Li, Z. Bo, Side chain effect of nonfullerene acceptors on the photovoltaic performance of wide band gap polymer solar cells, Synth. Met. 220 (2016) 578¨C584. https://doi.org/10.1016/j.synthmet.2016.07.015."
4122,CCCCCCCCC(CCCCCC)CN1C(=O)C2=CC=C3C4=C(C=CC(=C24)C1=O)C1=C3C(C2=CC=CS2)=C2C3=C4C(=CC=C3)C=CC=C4C2=C1C1=CC=CS1,AFI2,-6.03,-3.55,3.4,0.81,0.6,1.64,"L. Ding, C.-Y. Yang, Y.-Q. Zheng, J.-Y. Wang, J. Pei, Z. Su, Acenaphtho[1, 2-k]fluoranthene-Fused Diimide Derivatives: An Investigation of the Relationship Between Molecular Structure and Device Performance, Asian J. Org. Chem. 6 (2017) 1231¨C1234. https://doi.org/10.1002/ajoc.201700203."
4123,CCCCCCCCC1=C(C2=CC=C(CCCCCC)S2)SC(C2=CC=C(C3=CC(CCCCCCCC)=C(C4=CC(CC(CC)CCCC)=C(C5=NC6=C(N=C(C7=C(CC(CC)CCCC)C=C(C8=C(CCCCCCCC)C=C(C9=CC=C(C%10=CC(CCCCCCCC)=C(C%11=CC=C(CCCCCC)S%11)S%10)C%10=NSN=C9%10)S8)S7)S6)S5)S4)S3)C3=NSN=C23)=C1,DTTz-DTBTT,-5.05,-3.07,5.11,0.66,0.483,1.64,"Y. Chen, Z. Du, W. Chen, S. Wen, L. Sun, Q. Liu, M. Sun, R. Yang, New small molecules with thiazolothiazole and benzothiadiazole acceptors for solution-processed organic solar cells, New J. Chem. 38 (2014) 1559¨C1564. https://doi.org/10.1039/C3NJ01457F."
4124,CCCCCCCCC(CCCCCCCC)N1C2=C(C=CC(C3=CC=C(C=C4C(=O)N(C)C(=O)N(C)C4=O)S3)=C2)C2=C1C=C(C1=CC=C(C=C3C(=O)N(C)C(=O)N(C)C3=O)S1)C=C2,Cz-BAR,-5.63,-3.51,3.06,0.88,0.58,1.57,"E. Lim, Two A-D-A-type Non-Fullerene Small Molecule Acceptors Based on 1,3-Dimethylbarbituric Acid for OPVs, Bull. Korean Chem. Soc. 38 (2017) 285¨C288. https://doi.org/10.1002/bkcs.11071."
4125,CCCCCCC(CCCC)C1=C(C2=CC(C3=CC=CC=C3)=C(C3=C(C4=CC=CC=C4)C=C(C4=C(C(CCCC)CCCCCC)C=C(/C=C5C(=O)C6=C(C=C(F)C(F)=C6)C5=C(C#N)C#N)S4)S3)S2)SC(/C=C2C(=O)C3=C(C=C(F)C(F)=C3)C2=C(C#N)C#N)=C1,A4T-21,-5.89,-3.92,5.55,0.936,0.303,1.57,"L. Ma, S. Zhang, J. Zhu, J. Wang, J. Ren, J. Zhang, J. Hou, Completely non-fused electron acceptor with 3D-interpenetrated crystalline structure enables efficient and stable organic solar cell, Nat. Commun. 12 (2021) 5093. https://doi.org/10.1038/s41467-021-25394-w."
4126,CCCCC(CC)CC1=CC=C(C(C2=CC=C(CC(CC)CCCC)S2)=C2C3=CC4=C(C=C3C3=C2C=C(C2=C5C6=CC=C7C(=O)N(CC(CC)CCCC)C(=O)C8=CC=C(C9=CC=C%10C(=O)N(CC(CC)CCCC)C(=O)C(=C2)C%10=C95)C6=C87)S3)C(=C(C2=CC=C(CC(CC)CCCC)S2)C2=CC=C(CC(CC)CCCC)S2)C2C=C(C3=C5C6=CC=C7C(=O)N(CC(CC)CCCC)C(=O)C8=CC=C(C9=CC=C%10C(=O)N(CC(CC)CCCC)C(=O)C(=C3)C%10=C95)C6=C87)SC42)S1,TVIDTPDI,-5.48,-3.85,4.96,0.79,0.38,1.5,"Z.-F. Chang, Y. Cai, K.-K. Liu, X.-X. Song, J.-J. Liu, X. Liu, Y. Sun, R. bo Zhang, J.-L. Wang, Rational design of two-dimensional PDI-based small molecular acceptor from extended indacenodithiazole core for organic solar cells, Dyes Pigments. 147 (2017) 31¨C39. https://doi.org/10.1016/j.dyepig.2017.07.060."
4127,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(C=CS2)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC3=C2SC(C2=C4OCCOC4=C(/C=C4C(=O)C5=C(C=C(F)C(F)=C5)C4=C(C#N)C#N)S2)=C3)C=C1,IDTT-ED-2F,-5.47,-3.81,5.1,0.91,0.3175,1.5,"S.J. Jeon, Y.H. Kim, I.N. Kim, N.G. Yang, J.H. Yun, D.K. Moon, Utilizing 3,4-ethylenedioxythiophene (EDOT)-bridged non-fullerene acceptors for efficient organic solar cells, J. Energy Chem. 65 (2022) 194¨C204. https://doi.org/10.1016/j.jechem.2021.05.032."
4128,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C=C(C2=CC=C(C5=C6C(=O)N(CC(CC)CCCC)C(C7=CC=C(/C=C8/SC(=S)N(CC)C8=O)S7)=C6C(=O)N5CC(CC)CCCC)S2)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC(C3=CC=C(C4=C5C(=O)N(CC(CC)CCCC)C(C6=CC=C(/C=C7/SC(=S)N(CC)C7=O)S6)=C5C(=O)N4CC(CC)CCCC)S3)=C2)C=C1,IDT-DPP-R,-5.39,-3.55,4.07,0.65,0.544,1.42,"T. Li, J. Wang, H. Chen, P. Cheng, S. Huang, Y. Lin, H. Yu, X. Zhan, Nonfullerene acceptor with strong near-infrared absorption for polymer solar cells, Dyes Pigments. 137 (2017) 553¨C559. https://doi.org/10.1016/j.dyepig.2016.11.005."
4129,COCCOCCOCCOC1=CC=C(C2(C3=CC=C(OCCOCCOCCOC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(C=C(/C=C5C(=O)C6=C(C=CC=C6)C5=C(C#N)C#N)S2)S3)C(C2=CC=C(OCCOCCOCCOC)C=C2)(C2=CC=C(OCCOCCOCCOC)C=C2)C2=C4SC3=C2SC(/C=C2C(=O)C4=C(C=CC=C4)C2=C(C#N)C#N)=C3)C=C1,ITIC©\OEG,-5.39,-3.99,3.56,0.9,0.49,1.42,"B. Jang, C. Lee, Y.W. Lee, D. Kim, M.A. Uddin, F.S. Kim, B.J. Kim, H.Y. Woo, A High Dielectric N-Type Small Molecular Acceptor Containing Oligoethyleneglycol Side-Chains for Organic Solar Cells, Chin. J. Chem. 36 (2018) 199¨C205. https://doi.org/10.1002/cjoc.201700629."
4130,O=C(C(C=C(F)C=C1)=C1C/2=C(C#N)C#N)C2=C/C3=CC(OCC(CC)CCCC)=C(C4=CC5=C(S4)C6=C(C7=CC(C8(C9=CC=C(CCCCCC)C=C9)C%10=CC=C(CCCCCC)C=C%10)=C(C%11=C8C(SC(C%12=C(OCC(CC)CCCC)C=C(/C=C%13C(C(C=C(F)C=C%14)=C%14C\%13=C(C#N)/C#N)=O)S%12)=C%15)=C%15S%11)C=C7C6(C%16=CC=C(CCCCCC)C=C%16)C%17=CC=C(CCCCCC)C=C%17)S5)S3,ITOTIC-2F,-5.22,-4.11,3.4,0.794,0.53,1.4,"J. Lee, S.-J. Ko, M. Seifrid, H. Lee, C. McDowell, B.R. Luginbuhl, A. Karki, K. Cho, T.-Q. Nguyen, G.C. Bazan, Design of Nonfullerene Acceptors with Near-Infrared Light Absorption Capabilities, Adv. Energy Mater. 8 (2018) 1801209. https://doi.org/10.1002/aenm.201801209."
4131,CC#CC1=C2N=C3C=C4CC5(CC4=CC3=NC2=C(C#CC)C2=NSN=C21)CC1=CC2=NC3=C(C#CC)C4=NSN=C4C(C#CC)=C3N=C2C=C1C5,4,,,5.1,0.7,0.3856,1.39,"L. Ahrens, Y.J. Hofstetter, B. Celik, J.F. Butscher, F. Rominger, J. Freudenberg, Y. Vaynzof, U.H.F. Bunz, Dimeric Phenazinothiadiazole Acceptors in Bulk Heterojunction Solar Cells, Org. Mater. 03 (2021) 168¨C173. https://doi.org/10.1055/s-0041-1726459."
4132,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(C=C(/C=C5/C(=O)C6=C(C=CC=C6)S5(=O)=O)S2)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC3=C2SC(/C=C2/C(=C(C#N)C#N)C4=C(C=CC=C4)S2(=O)=O)=C3)C=C1,ITBTD-ICS,-5.49,3.99,5.23,0.77,0.34,1.37,"S. Baik, D.W. Kim, H.-S. Kang, S.H. Hong, S. Park, B.-K. An, S.Y. Park, ITIC derivative acceptors for ternary organic solar cells: fine-tuning of absorption bands, LUMO energy levels, and cascade charge transfer, Sustain. Energy Fuels. 6 (2021) 110¨C120. https://doi.org/10.1039/D1SE01429C."
4133,CC#CCC1=C2N=C3C=C4C(=CC3=NC2=C(C#CC)C2=NSN=C21)C1(C)CCC4(C)C2=CC3=NC4=C(C#CC)C5=NSN=C5C(C#CC)=C4N=C3C=C21,3,,,4.62,0.73,0.3844,1.29,"L. Ahrens, Y.J. Hofstetter, B. Celik, J.F. Butscher, F. Rominger, J. Freudenberg, Y. Vaynzof, U.H.F. Bunz, Dimeric Phenazinothiadiazole Acceptors in Bulk Heterojunction Solar Cells, Org. Mater. 03 (2021) 168¨C173. https://doi.org/10.1055/s-0041-1726459."
4134,CCCCCCCCC1(CCCCCCCC)C2=C(C=CC(C3=CC=C(C=C4C(=O)N(C)C(=O)N(C)C4=O)S3)=C2)C2=C1C=C(C1=CC=C(C=C3C(=O)N(C)C(=O)N(C)C3=O)S1)C=C2,Flu-BAR,-5.81,-3.53,2.49,0.9,0.57,1.28,"E. Lim, Two A-D-A-type Non-Fullerene Small Molecule Acceptors Based on 1,3-Dimethylbarbituric Acid for OPVs, Bull. Korean Chem. Soc. 38 (2017) 285¨C288. https://doi.org/10.1002/bkcs.11071."
4135,CC#CC1=C2N=C3C=C4C(=CC3=NC2=C(C#CC)C2=NSN=C21)C1(CC4(C)C)CC(C)(C)C2=CC3=NC4=C(C#CC)C5=NSN=C5C(C#CC)=C4N=C3C=C21,B,,,4.85,0.7,0.3782,1.28,"L. Ahrens, Y.J. Hofstetter, B. Celik, J.F. Butscher, F. Rominger, J. Freudenberg, Y. Vaynzof, U.H.F. Bunz, Dimeric Phenazinothiadiazole Acceptors in Bulk Heterojunction Solar Cells, Org. Mater. 03 (2021) 168¨C173. https://doi.org/10.1055/s-0041-1726459."
4136,CCCCCCCCC(CCCCCC)CN1C(=O)C2=C(C3=CC=C(C4=CC5=C(S4)C(OCC(CC)CCCC)=C4C=C(C6=CC=C(C7=C8C(=O)N(CC(CCCCCC)CCCCCCCC)C(C9=CC=C(C%10=CC=CC=C%10)S9)=C8C(O)N7CC(CCCCCC)CCCCCCCC)S6)SC4=C5OCC(CC)CCCC)S3)N(CC(CCCCCC)CCCCCCCC)C(=O)C2=C1C1=CC=C(C2=CC=CC=C2)S1,BDT(DPP)2,-5.62,-3.47,3.2,0.81,0.492,1.26,"Q. Tao, L. Duan, W. Xiong, G. Huang, P. Wang, H. Tan, Y. Wang, R. Yang, W. Zhu, D(A-A¡ä)2 architecture: An efficient strategy to improve photovoltaic performance of small molecules for solution-processed organic solar cells, Dyes Pigments. 133 (2016) 153¨C160. https://doi.org/10.1016/j.dyepig.2016.05.033."
4137,CCCCCCC1=C(SC(/C(C2=CC=CN2B(F)F)=C3C=CC=N3)=C1)C4=CC5=C(C(C6=CC=C(S6)CC(CCCC)CC)=C7C=C(SC7=C5C8=CC=C(S8)CC(CCCC)CC)C9=C(C=C(S9)/C(C%10=CC=CN%10B(F)F)=C%11C=CC=N\%11)CCCCCC)S4,BDP-BDT,-5.4,-3.79,3.09,0.65,0.6,1.21,"A.M. Poe, A.M.D. Pelle, A.V. Subrahmanyam, W. White, G. Wantz, S. Thayumanavan, Small molecule BODIPY dyes as non-fullerene acceptors in bulk heterojunction organic photovoltaics, Chem. Commun. 50 (2014) 2913¨C2915. https://doi.org/10.1039/C3CC49648A."
4138,CCCCCCCCN1N=C2C(/C=C/C3C(C#N)C(=C(C#N)C#N)OC3(C)C)=CC=C(C3=CC4=C(S3)C3=CC5=C(C=C3C4(C3=CC=C(CCCCCC)C=C3)C3=CC=C(CCCCCC)C=C3)C3=C(C=C(C4=CC=C(/C=C/C6C(C#N)C(=C(C#N)C#N)OC6(C)C)C6=NN(CCCCCCCC)N=C46)S3)C5(C3=CC=C(CCCCCC)C=C3)C3=CC=C(CCCCCC)C=C3)C2=N1,BTA703,-5.48,-3.61,3.56,0.85,0.4,1.21,"B. Xiao, Y. Geng, A. Tang, X. Wang, Y. Chen, Q. Zeng, E. Zhou, Controlling the Cyano-Containing A2 Segments in A2-A1-D-A1-A2 Type Non-Fullerene Acceptors to Combine with a Benzotriazole-Based p-Type Polymer: ¡°Same-Acceptor-Strategy¡± for High VOC Organic Solar Cells, Sol. RRL. 3 (2019) 1800332. https://doi.org/10.1002/solr.201800332."
4139,CCCCCCC1=C(C2=CC3=C(S2)C2=C(C=C(C4=C(CCCCCC)C=C(/C(C5=CC=CN5B(F)F)=C5C=CC=N5)S4)S2)C3(CC(CC)CCCC)CC(CC)CCCC)SC(/C(C2=CC=CN2B(F)F)=C2C=CC=N2)=C1,BDP-CPDT,-5.12,-3.82,3.28,0.6,0.61,1.2,"A.M. Poe, A.M.D. Pelle, A.V. Subrahmanyam, W. White, G. Wantz, S. Thayumanavan, Small molecule BODIPY dyes as non-fullerene acceptors in bulk heterojunction organic photovoltaics, Chem. Commun. 50 (2014) 2913¨C2915. https://doi.org/10.1039/C3CC49648A."
4140,CCCCCCCCC1(CCCCCCCC)C2=CC(C3=CC=C(C4=C5C(=O)N(CC(CC)CCCC)C(C6=CC=CS6)=C5C(=O)N4CC(CC)CCCC)S3)=CC=C2C2=C1C=C(C1=CC=C(C3=C4C(=O)N(CC(CC)CCCC)C(C5=CC=CS5)=C4C(=O)N3CC(CC)CCCC)S1)C=C2,DPP1,-5.3,-3.5,2.42,1.1,0.45,1.2,"H. Patil, W.X. Zu, A. Gupta, V. Chellappan, A. Bilic, P. Sonar, A. Rananaware, S.V. Bhosale, S.V. Bhosale, A non-fullerene electron acceptor based on fluorene and diketopyrrolopyrrole building blocks for solution-processable organic solar cells with an impressive open-circuit voltage, Phys. Chem. Chem. Phys. 16 (2014) 23837¨C23842. https://doi.org/10.1039/C4CP03727H."
4141,CCCCCCC(CCCC)CN1C(=O)C2=C(C3=CC=C(C4=CC5=C(C=C4)C4=C(C=C(C6=CC=C(C7=C8C(=O)N(CC(CCCC)CCCCCC)C(C9=CC=CS9)=C8C(=O)N7CC(CCCC)CCCCCC)S6)C=C4)C5=O)S3)N(CC(CCCC)CCCCCC)C(=O)C2=C1C1=CC=CS1,DPP-FN-DPP,-5.56,-3.81,3.2,0.97,0.372,1.2,"T.T. Do, K. Rundel, Q. Gu, E. Gann, S. Manzhos, K. Feron, J. Bell, C.R. McNeill, P. Sonar, 9-Fluorenone and 9,10-anthraquinone potential fused aromatic building blocks to synthesize electron acceptors for organic solar cells, New J. Chem. 41 (2017) 2899¨C2909. https://doi.org/10.1039/C6NJ03938C."
4142,CCCCCCCCN1N=C2C(=N1)C(C1=CC3=C(S1)C1=CC4=C(C=C1C3(C1=CC=C(CCCCCC)C=C1)C1=CC=C(CCCCCC)C=C1)C1=C(C=C(C3=C(OC)C(OC)=C(/C=C5SC(=O)N(CC)C5=O)C5=NN(CCCCCCCC)N=C53)S1)C4(C1=CC=C(CCCCCC)C=C1)C1=CC=C(CCCCCC)C=C1)=C(OC)C(OC)=C2/C=C1SC(=O)N(CC)C1=O,BTA100,-5.32,-3.23,1.65,1.34,0.47,1.04,"Q. Zhang, B. Xiao, M. Du, G. Li, A. Tang, E. Zhou, A2¨CA1¨CD¨CA1¨CA2 type non-fullerene acceptors based on methoxy substituted benzotriazole with three different end-capped groups for P3HT-based organic solar cells, J. Mater. Chem. C. 6 (2018) 10902¨C10909. https://doi.org/10.1039/C8TC03963A."
4143,CCCCC(CC)CN1C(=O)C2=CC=C(C#CC3=CC=C(C4=C(F)C=C(C5=CC=C(C#CC6=CC7=C(C=C6)C(=O)N(CC(CC)CCCC)C7=O)S5)C5=NSN=C54)S3)C=C2C1=O,(PIAT)2dfBT,-5.57,-3.22,6.55,0.64,0.25,1.04,"X. He, L. Yin, Y. Li, Efficient design and structural modifications for tuning the photoelectric properties of small-molecule acceptors in organic solar cells, New J. Chem. 43 (2019) 6577¨C6586. https://doi.org/10.1039/C9NJ00600A."
4144,CCCCCCCCCCCCN1C(=O)C2=CC=C3C4=C(C=CC(=C24)C1=O)C1=C3C(C2=CC=CS2)=C2C3=C4C(=CC=C3)C=CC=C4C2=C1C1=CC=CC1,AFI1,-6.03,-3.55,2.65,0.71,0.55,1.03,"L. Ding, C.-Y. Yang, Y.-Q. Zheng, J.-Y. Wang, J. Pei, Z. Su, Acenaphtho[1, 2-k]fluoranthene-Fused Diimide Derivatives: An Investigation of the Relationship Between Molecular Structure and Device Performance, Asian J. Org. Chem. 6 (2017) 1231¨C1234. https://doi.org/10.1002/ajoc.201700203."
4145,CCCCCCC(C)N1C(=O)C2=CC3=C(C=C2C1=O)C1=CC=C(C2=C(CC(CC)CCCC)C=C(C4=CC5=C(C=C(C6=CC(CC(CC)CCCC)=C(C7=CC=C8C9=C(C=C%10C(=O)N(C(C)CCCCCC)C(=O)C%10=C9)C9=CC=CC7=C98)S6)C6=NSN=C65)C5=NSN=C45)S2)C2=C1C3=CC=C2,NTz-Teh-FA,-6.06,-3.38,2.13,0.95,0.53,1.02,"S. Chatterjee, Y. Ie, T. Seo, T. Moriyama, G.-J.A.H. Wetzelaer, P.W.M. Blom, Y. Aso, Fluorinated naphtho[1,2-c:5,6-c¡¯]bis[1,2,5]thiadiazole-containing ¦Ð-conjugated compound: synthesis, properties, and acceptor applications in organic solar cells, NPG Asia Mater. 10 (2018) 1016¨C1028. https://doi.org/10.1038/s41427-018-0088-4."
4146,CCCCC(CC)CN1C(=O)C2=C3C(=C(C4=CC=C(C5=C6C(=O)N(CC(CC)CCCC)C(C7=CC=CS7)=C6C(=O)N5CC(CC)CCCC)S4)C=C4C(=O)N(CC(CC)CCCC)C(=O)C(=C43)C(C3=CC=C(C4=C5C(=O)N(CC(CC)CCCC)C(C6=CC=CS6)=C5C(=O)N4CC(CC)CCCC)S3)=C2)C1=O,HP1,-4.92,-3.46,2.15,1.05,0.45,1.02,"H. Patil, A. Gupta, A. Bilic, S.V. Bhosale, S.V. Bhosale, A solution-processable electron acceptor based on diketopyrrolopyrrole and naphthalenediimide motifs for organic solar cells, Tetrahedron Lett. 55 (2014) 4430¨C4432. https://doi.org/10.1016/j.tetlet.2014.06.017."
4147,CCCCC(CC)CN1C(=O)C2=C(C3=CC=CS3)N(CC(CC)CCCC)C(=O)C2=C1C1=CC=C(C#CC2=CC3=C4N=C5C6=C(C=C(C#CC7=CC=C(C8=C9C(=O)N(CC(CC)CCCC)C(C%10=CC=CS%10)=C9C(=O)N8CC(CC)CCCC)S7)C=C6)/C6=N/C7=N/C(=NC(=C3C=C2)N4B(Cl)N56)C2=C7C=CC(C#CC3=CC=C(C4=C5C(=O)N(CC(CC)CCCC)C(C6=CC=CS6)=C5C(=O)N4CC(CC)CCCC)S3)=C2)C1,C1-Cl 3,-5.41,-3.37,3.04,0.93,0.3572,1.01,"M.J. ¨¢lvaro-Martins, J.G. S¨¢nchez, G. Lavarda, D. Molina, J. Pallar¨¨s, T. Torres, L.F. Marsal, ¨¢. Sastre-Santos, Subphthalocyanine-Diketopyrrolopyrrole Conjugates: 3D Star-Shaped Systems as Non-Fullerene Acceptors in Polymer Solar Cells with High Open-Circuit Voltage, ChemPlusChem. 86 (2021) 1366¨C1373. https://doi.org/10.1002/cplu.202100103."
4148,CCCCCCC(CCCC)CN1C(=O)C2=C(C3=CC=C(C4=CC=C5C(=C4)C4(C6=CC=CC=C6C6=C4C=CC=C6)C4=C5C=CC(C5=CC=C(C6=C7C(=O)N(CC(CCCC)CCCCCC)C(C8=CC=C(C=C(C#N)C#N)S8)=C7C(=O)N6CC(CCCC)CCCCCC)S5)=C4)S3)N(CC(CCCC)CCCCCC)C(=O)C2=C1C1=CC=C(C=C(C#N)C#N)S1,SBF-2DPPDCV,-5.46,-3.85,3.22,0.74,0.4137,0.98,"P. Sun, X. Li, Y. Wang, H. Shan, J. Xu, C. Liu, C. Zhang, F. Chen, Z. Xu, Z. Chen, W. Huang, Diketopyrrolopyrrole-based acceptors with multi-arms for organic solar cells, RSC Adv. 8 (2018) 25031¨C25039. https://doi.org/10.1039/C8RA03792B."
4149,CCCCC(CC)CC1(CC(CC)CCCC)C2=C(SC(C3=CC=C(/C=C4C(=O)C5=C(C=CC=C5)C4=C(C#N)C#N)S3)=C2)C2=C1C=C(C1=CC=C(/C=C3C(=O)C4=C(C=CC=C4)C3=C(C#N)C#N)S1)S2,CDTDI,-5.75,-4.26,3.91,0.87,0.2677,0.97,"Z. Kang, S.-C. Chen, Y. Ma, J. Wang, Q. Zheng, Push¨CPull Type Non-Fullerene Acceptors for Polymer Solar Cells: Effect of the Donor Core, ACS Appl. Mater. Interfaces. 9 (2017) 24771¨C24777. https://doi.org/10.1021/acsami.7b05417."
4150,CCCCCCCCCCC(CCCCCC)CN1C(=O)C2=C(C3=CC=C(C#C/C(C4=C(C)C=C(C)N4B(F)F)=C4/N=C(C)C=C4C)S3)N(CC(CCCCCC)CCCCCCCCCC)C(=O)C2=C1C1=CC=C(C#C/C(C2=C(C)C=C(C)N2B(F)F)=C2/N=C(C)C=C2C)S1,DPP(E-BODIPY)2,-5.36,-3.79,3.36,0.526,0.546,0.888,"W. Liu, J. Yao, C. Zhan, A Novel BODIPY-Based Low-Band-Gap Small-Molecule Acceptor for Efficient Non-fullerene Polymer Solar Cells, Chin. J. Chem. 35 (2017) 1813¨C1823. https://doi.org/10.1002/cjoc.201700542."
4151,CCCCCC1(CCCCC)C2=C(SC(C3=CC=C(C=C(C#N)C#N)C4=NSN=C34)=C2)C2=C1C=C(C1=CC=C(C=C(C#N)C#N)C3=NSN=C13)S2,CBD,-5.42,-3.84,2.93,0.78,0.3758,0.86,"Q. Yue, S. Liu, S. Xu, G. Liu, Y. Jiang, Y. Wang, X. Zhu, Vacuum-deposited organic solar cells utilizing a low-bandgap non-fullerene acceptor, J. Mater. Chem. C. 10 (2022) 2569¨C2574. https://doi.org/10.1039/D1TC03954G."
4152,CCCCCCC1=C(C2=CC3=C(S2)C2=C(C=C(C4=C(CCCCCC)C=C(/C(C5=CC=CN5B(F)F)=C5C=CC=N5)S4)S2)N3CC(CC)CCCC)SC(/C(C2=CC=CN2B(F)F)=C2C=CC=N2)=C1,BDP-DTP,-5.14,-3.74,2.18,0.6,0.65,0.84,"A.M. Poe, A.M.D. Pelle, A.V. Subrahmanyam, W. White, G. Wantz, S. Thayumanavan, Small molecule BODIPY dyes as non-fullerene acceptors in bulk heterojunction organic photovoltaics, Chem. Commun. 50 (2014) 2913¨C2915. https://doi.org/10.1039/C3CC49648A."
4153,CCCCCCCCN1C(=O)C2=CC=CC3=C2C(=CC=C3C2=CC=C(C#CC3=CC=C(C4=C5C=CC=C6C(=O)N(CCCCCCCC)C(=O)C(=C65)C=C4)S3)S2)C1=O,NI-TAT-NI-C8,-5.84,-3.41,2.16,1.24,0.3,0.82,"R. Hou, S. Feng, X. Gong, Y. Liu, J. Zhang, C. Li, Z. Bo, Side chain effect of nonfullerene acceptors on the photovoltaic performance of wide band gap polymer solar cells, Synth. Met. 220 (2016) 578¨C584. https://doi.org/10.1016/j.synthmet.2016.07.015."
4154,CCCCC(CC)CN1C(=O)C2=CC=C3C4=NC5=C(N=C4C4=C3C2=C(C=C4)C1=O)C(C1=CC=CS1)=C1C(=O)N(CC(CC)CCCC)C(=O)C1=C5C1=CC=CS1,AQI-T2 ,-5.55,-3.64,2.04,0.86,0.4398,0.77,"L. Lan, Z. Chen, L. Ying, F. Huang, Y. Cao, Acenaphtho[1,2-b]quinoxaline diimides derivative as a potential small molecule non-fullerene acceptor for organic solar cells, Org. Electron. 30 (2016) 176¨C181. https://doi.org/10.1016/j.orgel.2015.12.022."
4155,CCCCCCCCC(CCCCCC)CN1C(=O)C2=C(C3=CC=C(C4=CC5=C(S4)C(C4=CC=C(C(CC)CCCC)S4)=C4C=C(C6=CC=C(C7=C8C(=O)N(CC(CCCCCC)CCCCCCCC)C(C9=CC=C(C%10=CC=CC=C%10)S9)=C8C(O)N7CC(CCCCCC)CCCCCCCC)S6)SC4=C5C4=CC=C(C(CC)CCCC)S4)S3)N(CC(CCCCCC)CCCCCCCC)C(=O)C2=C1C1=CC=C(C2=CC=CC=C2)S1,BDTT(DPP)2,-5.68,-3.46,2.83,0.78,0.349,0.77,"Q. Tao, L. Duan, W. Xiong, G. Huang, P. Wang, H. Tan, Y. Wang, R. Yang, W. Zhu, D(A-A¡ä)2 architecture: An efficient strategy to improve photovoltaic performance of small molecules for solution-processed organic solar cells, Dyes Pigments. 133 (2016) 153¨C160. https://doi.org/10.1016/j.dyepig.2016.05.033."
4156,CCCCCCCCC(CCCCCCCC)N1C2=C(C=CC(C3=CC=C(/C=C4C(=O)C5=CSC=C5C4=C(C#N)C#N)S3)=C2)C2=C1C=C(C1=CC=C(/C=C3C(=O)C4=CSC=C4C3=C(C#N)C#N)S1)C=C2,DTC-T-C,-5.68,-4.09,2.88,0.69,0.358,0.71,"J. Liao, P. Zheng, Z. Cai, S. Shen, G. Xu, H. Zhao, Y. Xu, Construction of simple and low-cost acceptors for efficient non-fullerene organic solar cells, Org. Electron. 89 (2021) 106026. https://doi.org/10.1016/j.orgel.2020.106026."
4157,CCCCCCC(CCCC)CN1C(=O)C2=C(C3=CC=C(C4=CC5=C(C=C4)C(=O)C4=C(C=CC(C6=CC=C(C7=C8C(=O)N(CC(CCCC)CCCCCC)C(C9=CC=CS9)=C8C(=O)N7CC(CCCC)CCCCCC)S6)=C4)C5=O)S3)N(CC(CCCC)CCCCCC)C(=O)C2=C1C1=CC=CS1,DPP-ANQ-DPP,-5.7,-3.99,2,0.85,0.387,0.7,"T.T. Do, K. Rundel, Q. Gu, E. Gann, S. Manzhos, K. Feron, J. Bell, C.R. McNeill, P. Sonar, 9-Fluorenone and 9,10-anthraquinone potential fused aromatic building blocks to synthesize electron acceptors for organic solar cells, New J. Chem. 41 (2017) 2899¨C2909. https://doi.org/10.1039/C6NJ03938C."
4158,CCCCC(CC)CN1C(=O)C2=CC=C(C#CC3=CC=C(C4=CC=C(C5=CC=C(C#CC6=CC7=C(C=C6)C(=O)N(CC(CC)CCCC)C7=O)S5)C5=NSN=C45)S3)C=C2C1=O,(PIAT)2fBT,-5.51,-3.2,3.03,1.01,0.23,0.7,"X. He, L. Yin, Y. Li, Efficient design and structural modifications for tuning the photoelectric properties of small-molecule acceptors in organic solar cells, New J. Chem. 43 (2019) 6577¨C6586. https://doi.org/10.1039/C9NJ00600A."
4159,CCCCCCCCC1=C(C2=CC=C(C3=C(CCCCCCCC)C=C(C4=CC5=C6C(=C(C7=CC(CCCCCCCC)=C(C8=CC=C(C9=C(CCCCCCCC)C=C(/C=C%10/SC(=S)N(CC)C%10=O)S9)S8)S7)C=C7C(=O)N(CC(CC)CCCC)C(=O)C4=C76)C(=O)N(CC(CC)CCCC)C5=O)S3)S2)SC(/C=C2/SC(=S)N(CC)C2=O)=C1,NDI-TTR,-5.6,-3.95,2.24,0.78,0.38,0.67,"M.J. Sung, M. Huang, S.H. Moon, T.H. Lee, S.Y. Park, J.Y. Kim, S.-K. Kwon, H. Choi, Y.-H. Kim, Naphthalene diimide-based small molecule acceptors for fullerene-free organic solar cells, Sol. Energy. 150 (2017) 90¨C95. https://doi.org/10.1016/j.solener.2017.03.090."
4160,CCCCCCCCN1N=C2C(C=C(C#N)C#N)=CC=C(C3=CC4=C(C=C3)C3=C(C=C(C5=CC=C(C=C(C#N)C#N)C6=NN(CCCCCCCC)N=C56)C=C3)C43C4=C(C=CC=C4)C4=C3C=CC=C4)C2=N1,BTA27,-5.94,-3.3,2.89,0.6,0.36,0.62,"X. Wen, B. Xiao, A. Tang, J. Hu, C. Yang, E. Zhou, Wide Band Gap Non-Fullerene Small Molecular Acceptors Containing Spirobifluorene and Benzotriazole with Three Different End-Capped Groups for P3HT-Based Organic Solar Cells, Chin. J. Chem. 36 (2018) 392¨C398. https://doi.org/10.1002/cjoc.201700792."
4161,CCCCC(CC)CC1=CC=C(C(C2=CC=C(CC(CC)CCCC)S2)=C2C3=CC4=C(C=C3C3=C2C=C(/C=C2C(=O)C5=C(C=CC=C5)C2=C(C#N)C#N)S3)C(=C(C2=CC=C(CC(CC)CCCC)S2)C2=CC=C(CC(CC)CCCC)S2)C2=C4SC(/C=C3C(=O)C4=C(C=CC=C4)C3=C(C#N)C#N)=C2)S1,IDTV-ThIC,-5.43,-3.72,2.06,0.91,0.3326,0.62,"J. Liang, P. Yin, T. Zheng, G. Wang, X. Zeng, C. Cui, P. Shen, Conjugated side-chain optimization of indacenodithiophene-based nonfullerene acceptors for efficient polymer solar cells, J. Mater. Chem. C. 7 (2019) 10028¨C10038. https://doi.org/10.1039/C9TC02237F."
4162,CCCCCCCCN1C2=C(SC(C3=C(CCCCCC)C=C(C=C(C#N)C#N)S3)=C2)C2=C1C=C(C1=C(CCCCCC)C=C(C=C(C#N)C#N)S1)S2,DTPy(THDCV)2,-5.55,-3.77,2.6,0.78,0.32,0.56,"J. Wu, Y. Ma, N. Wu, Y. Lin, J. Lin, L. Wang, C.-Q. Ma, 2,2-Dicyanovinyl-end-capped oligothiophenes as electron acceptor in solution processed bulk-heterojunction organic solar cells, Org. Electron. 23 (2015) 28¨C38. https://doi.org/10.1016/j.orgel.2015.04.003."
4163,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C=C(C=C(C#N)C#N)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC(C=C(C#N)C#N)=C2)C=C1,IDT-1,-5.85,-3.85,1.76,0.67,0.4632,0.55,"N. Terenti, G.-I. Giurgi, L. Szolga, I. Stroia, A. Terec, I. Grosu, A.P. Cri?an, Effect of the Terminal Acceptor Unit on the Performance of Non-Fullerene Indacenodithiophene Acceptors in Organic Solar Cells, Molecules. 27 (2022) 1229. https://doi.org/10.3390/molecules27041229."
4164,CCCCC(CC)CN1C(=O)C2=CC=C(C#CC3=CC=C(C4=CC=C(C5=CC=C(C#CC6=CC7=C(C=C6)C(=O)N(CC(CC)CCCC)C7=O)S5)C5=NSN=C45)S3)C=C2C1=O,(PIAT)2BT,-5.47,-3.15,2.96,0.81,0.21,0.51,"X. He, L. Yin, Y. Li, Efficient design and structural modifications for tuning the photoelectric properties of small-molecule acceptors in organic solar cells, New J. Chem. 43 (2019) 6577¨C6586. https://doi.org/10.1039/C9NJ00600A."
4165,CCCCCCCCN1C(=O)C2=C(C3=CC=C(C4=CC=C5C(=O)N(C(CC)CC)C(=O)C5=C4)S3)C=CC(C3=CC=C(C4=CC5C(=O)N(C(CC)CC)C(=O)C5C=C4)S3)=C2C1=O,M2,-5.92,-2.98,1.7,0.92,0.31,0.5,"A.D. Hendsbee, S.M. McAfee, J.-P. Sun, T.M. McCormick, I.G. Hill, G.C. Welch, Phthalimide-based ¦Ð-conjugated small molecules with tailored electronic energy levels for use as acceptors in organic solar cells, J. Mater. Chem. C. 3 (2015) 8904¨C8915. https://doi.org/10.1039/C5TC01877C."
4166,CCC(CC)N1C(=O)C2=CC=C(C3=CC=C(C4=CC=C(C5=CC6C(=O)N(C(CC)CC)C(=O)C6C=C5)S4)S3)C=C2C1=O,M1,-5.6,-3.03,1.2,1.23,0.32,0.46,"A.D. Hendsbee, S.M. McAfee, J.-P. Sun, T.M. McCormick, I.G. Hill, G.C. Welch, Phthalimide-based ¦Ð-conjugated small molecules with tailored electronic energy levels for use as acceptors in organic solar cells, J. Mater. Chem. C. 3 (2015) 8904¨C8915. https://doi.org/10.1039/C5TC01877C."
4167,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=C(C=CC(C4=CC=C(C5=CC=C(C=C(C#N)C#N)C6=NSN=C56)S4)=C3)C3=C2C=C(C2=CC=C(C=C(C#N)C#N)C4=NSN=C24)S3)C=C1,PhITBD,-5.69,-3.99,1.86,0.82,0.29,0.44,"C.H. Jeong, Y.U. Kim, C.G. Park, S. Choi, M.J. Cho, D.H. Choi, Improved performance of non-fullerene polymer solar cells by simple structural change of asymmetric acceptor based on indenothiophene, Synth. Met. 246 (2018) 164¨C171. https://doi.org/10.1016/j.synthmet.2018.10.014."
4168,CCCCCCCCN1C(=O)C2=C(C3=CC=C(C4=CC5C(=O)N(C(CC)CC)C(=O)C5C=C4)S3)N(CCCCCCCC)C(=O)C2=C1C1=CC=C(C2=CC=C3C(=O)N(C(CC)CC)C(=O)C3=C2)S1,M3,-5.23,-3.44,1.4,0.81,0.33,0.37,"A.D. Hendsbee, S.M. McAfee, J.-P. Sun, T.M. McCormick, I.G. Hill, G.C. Welch, Phthalimide-based ¦Ð-conjugated small molecules with tailored electronic energy levels for use as acceptors in organic solar cells, J. Mater. Chem. C. 3 (2015) 8904¨C8915. https://doi.org/10.1039/C5TC01877C."
4169,CCCCC(CC)CN1C(=O)C2=C(C3=CC=C(C=O)S3)N(CC(CC)CCCC)C(=O)C2=C1C1=CC=C(C=O)S1,DPP¨CTA1,-5.9,-4.09,1.93,0.52,0.31,0.31,"B.P. Karsten, J.C. Bijleveld, R.A.J. Janssen, Diketopyrrolopyrroles as Acceptor Materials in Organic Photovoltaics, Macromol. Rapid Commun. 31 (2010) 1554¨C1559. https://doi.org/10.1002/marc.201000133."
4170,CCCCCCC1=CC=C(C2(C3=CC=C(CCCCCC)C=C3)C3=CC4=C(C=C3C3=C2C=C(/C=C2SC(SCC)=NC2=O)S3)C(C2=CC=C(CCCCCC)C=C2)(C2=CC=C(CCCCCC)C=C2)C2=C4SC(/C=C3SC(SCC)=NC3=O)=C2)C=C1,IDT-3,-5.66,-3.62,0.89,0.79,0.4131,0.29,"N. Terenti, G.-I. Giurgi, L. Szolga, I. Stroia, A. Terec, I. Grosu, A.P. Cri?an, Effect of the Terminal Acceptor Unit on the Performance of Non-Fullerene Indacenodithiophene Acceptors in Organic Solar Cells, Molecules. 27 (2022) 1229. https://doi.org/10.3390/molecules27041229."
4171,C#CC(CCCC)CC1(CC(CC)CCCC)C2=C(SC(C3=C(CCCCCC)C=C(C=C(C#N)C#N)S3)=C2)C2=C1C=C(C1=C(CCCCCC)C=C(C=C(C#N)C#N)S1)S2,DTCP(THDCV)2,-5.62,-3.74,1.76,0.58,0.31,0.27,"J. Wu, Y. Ma, N. Wu, Y. Lin, J. Lin, L. Wang, C.-Q. Ma, 2,2-Dicyanovinyl-end-capped oligothiophenes as electron acceptor in solution processed bulk-heterojunction organic solar cells, Org. Electron. 23 (2015) 28¨C38. https://doi.org/10.1016/j.orgel.2015.04.003."
4172,CCCCCCC1(CCCCCC)C2=C(SC(/C=C3C(=O)C4=C(C=CC=C4)C3=C(C#N)C#N)=C2)C2=C1C=C(/C=C1C(=O)C3=C(C=CC=C3)C1=C(C#N)C#N)S2,1CIC,-5.82,-3.99,1.05,0.6,0.4133,0.26,"J. Cao, S. Liu, W. Hu, Y. Xu, W. Zhou, Y. Zeng, J. Yu, Z. Tang, Small-molecule acceptors based on 4H-cyclopenta[1,2-b:5,4-b¡ä]dithiophene units with near-infrared absorption for nonfullerene polymer solar cells, Synth. Met. 240 (2018) 15¨C20. https://doi.org/10.1016/j.synthmet.2018.03.011."
4173,CCCCCCC(CCCC)CN1C(=O)C2=C(C3=CC=C(C4=CC5=C(C=C4)C4=CC=CC=C4C54C5=CC=CC=C5C5=C4C=CC=C5)S3)N(CC(CCCC)CCCCCC)C(=O)C2=C1C1=CC=C(C=C(C#N)C#N)S1,SBF-1DPPDCV,-5.52,-3.89,1.09,0.74,0.3152,0.26,"P. Sun, X. Li, Y. Wang, H. Shan, J. Xu, C. Liu, C. Zhang, F. Chen, Z. Xu, Z. Chen, W. Huang, Diketopyrrolopyrrole-based acceptors with multi-arms for organic solar cells, RSC Adv. 8 (2018) 25031¨C25039. https://doi.org/10.1039/C8RA03792B."
4174,CCC1(CC)C2=C(C=CC=C2)C2=C1C=C(C1=CC3=C(C=C1)C1=C(C=C(C4=CC5=C(C=C4)C4=C(C=CC=C4)C5(CC)CC)C=C1)C3=C1C3=C(C=CC(C4=CC5=C(C=C4)C4=C(C=CC=C4)C5(CC)CC)=C3)C3=C1C=C(C1=CC4=C(C=C1)C1=C(C=CC=C1)C4(CC)CC)C=C3)C=C2,TFBF,-5.81,-3.49,1.2,0.7,0.3,0.26,"O.Y. Park, H.U. Kim, J.-H. Kim, J.B. Park, J. Kwak, W.S. Shin, S.C. Yoon, D.-H. Hwang, Tetrafluorene-9,9¡ä-bifluorenylidene as a non-fullerene type electron acceptor for P3HT-based bulk-heterojunction polymer solar cells, Sol. Energy Mater. Sol. Cells. 116 (2013) 275¨C282. https://doi.org/10.1016/j.solmat.2013.05.008."
4175,CCCCCCCCC(CCCCCC)CN1C(=O)C2=CC=CC3=C(C4=CC=C(C#CC5=CC=C(C6=CC=C7C(=O)N(C(CCCCCC)CCCCCCCC)C(=O)C8=CC=CC6=C87)S5)S4)C=CC(=C23)C1=O,NI-TAT-NI-C16,-5.95,-3.49,0.9,1.2,0.9,0.24,"R. Hou, S. Feng, X. Gong, Y. Liu, J. Zhang, C. Li, Z. Bo, Side chain effect of nonfullerene acceptors on the photovoltaic performance of wide band gap polymer solar cells, Synth. Met. 220 (2016) 578¨C584. https://doi.org/10.1016/j.synthmet.2016.07.015."
4176,CCCCCCCCC1=C(C2=CC=C(C3=C4C(=O)N(CC(CC)CCCC)C(C5=CC=C(C6=C(CCCCCCCC)C=C(C=O)S6)S5)=C4C(=O)N3CC(CC)CCCC)S2)SC=C1,DPP¨CT2,-5.39,-3.68,0.87,0.85,0.32,0.24,"B.P. Karsten, J.C. Bijleveld, R.A.J. Janssen, Diketopyrrolopyrroles as Acceptor Materials in Organic Photovoltaics, Macromol. Rapid Commun. 31 (2010) 1554¨C1559. https://doi.org/10.1002/marc.201000133."
4177,CCC(CC)N1C(=O)C2=CC=C(C3=CC=C(C4=C(F)C(F)=C(C5=CC=C(C6=CC7C(=O)N(C(CC)CC)C(=O)C7C=C6)S5)C5=NSN=C54)S3)C=C2C1=O,M7,-5.66,-3.29,0.84,0.94,0.28,0.22,"A.D. Hendsbee, S.M. McAfee, J.-P. Sun, T.M. McCormick, I.G. Hill, G.C. Welch, Phthalimide-based ¦Ð-conjugated small molecules with tailored electronic energy levels for use as acceptors in organic solar cells, J. Mater. Chem. C. 3 (2015) 8904¨C8915. https://doi.org/10.1039/C5TC01877C."
4178,CCCCC(CC)CN1C(=O)C2=C(C3=CC=CS3)N(CC(CC)CCCC)C(=O)C2=C1C1=CC=CS1,DPP¨CT1,-5.55,-3.59,0.79,0.85,0.25,0.17,"B.P. Karsten, J.C. Bijleveld, R.A.J. Janssen, Diketopyrrolopyrroles as Acceptor Materials in Organic Photovoltaics, Macromol. Rapid Commun. 31 (2010) 1554¨C1559. https://doi.org/10.1002/marc.201000133."
4179,CCCCCCCCC1=C(C2=CC=C(C3=C4C(=O)N(CC(CC)CCCC)C(C5=CC=C(C6=C(CCCCCCCC)C=C(CO)S6)S5)=C4C(=O)N3CC(CC)CCCC)S2)SC(CO)=C1,DPP¨CTA2,-5.54,-3.94,0.86,0.6,0.29,0.15,"B.P. Karsten, J.C. Bijleveld, R.A.J. Janssen, Diketopyrrolopyrroles as Acceptor Materials in Organic Photovoltaics, Macromol. Rapid Commun. 31 (2010) 1554¨C1559. https://doi.org/10.1002/marc.201000133."
4180,CCCCCCCCN1N=C2C(/C=C3SC(=S)N(CC)C3=O)=CC=C(C3=CC4=C(S3)C3=C(S4)C4=CC5=C(C=C4C3(C3=CC=C(CCCCCC)C=C3)C3=CC=C(CCCCCC)C=C3)C3=C(C4=C(C=C(C6=CC=C(/C=C7SC(=S)N(CC)C7=O)C7=NN(CCCCCCCC)N=C67)S4)S3)C5(C3=CC=C(CCCCCC)C=C3)C3=CC=C(CCCCCC)C=C3)C2=N1,BTA11,-5.29,-3.53,0.43,1.2,0.2592,0.13,"Q. Guo, F. Li, J. Li, Y. Xiao, K. Zuo, A. Tang, B. Zhang, E. Zhou, Modulating the middle and end-capped units of A2-A1-D-A1-A2 type non-fullerene acceptors for high VOC organic solar cells, Org. Electron. 95 (2021) 106195. https://doi.org/10.1016/j.orgel.2021.106195."
4181,CCCC1=CC=C(C2(C3=CC=C(CCC)C=C3)C3=CC4=C(C=C3C3=C2C2=C(C=C(/C=C5C(=O)C6=CC=CC=C6C5=C(C#N)C#N)S2)S3)C(C2=CC=C(CCC)C=C2)(C2=CC=C(CCC)C=C2)C2=C4SC3=C2SC(/C=C2C(=O)C4=CC=CC=C4C2=C(C#N)C#N)=C3)C=C1,ITIC-C3,-5.86,-4.05,0.7,0.31,0.291,0.12,"T.J. Aldrich, S.M. Swick, F.S. Melkonyan, T.J. Marks, Enhancing Indacenodithiophene Acceptor Crystallinity via Substituent Manipulation Increases Organic Solar Cell Efficiency, Chem. Mater. 29 (2017) 10294¨C10298. https://doi.org/10.1021/acs.chemmater.7b04616."
4182,CCCCN1C(=O)C2=CC=CC3=C2C(=CC=C3C#CC2=CC=C3C(=O)N(CCCC)C(=O)C4=CC=CC2=C43)C1=O,NI-A-C4,-6.05,-3.54,1.34,1.09,0.1,0.11,"J. Zhang, H. Xiao, X. Zhang, Y. Wu, G. Li, C. Li, X. Chen, W. Ma, Z. Bo, 1,8-Naphthalimide-based nonfullerene acceptors for wide optical band gap polymer solar cells with an ultrathin active layer thickness of 35 nm, J. Mater. Chem. C. 4 (2016) 5656¨C5663. https://doi.org/10.1039/C6TC01438K."
4183,CCCCCCCCN1C(=O)C2=C(C3=CC=C(C4=CC=C5C(=O)N(CC(CC)CCCC)C(=O)C5=C4)S3)N(CCCCCCCC)C(=O)C2=C1C1=CC=C(C#CC2=CC=C3C4=CC=C(C#CC5=CC=C(C6=C7C(=O)N(CCCCCCCC)C(C8=CC=C(C9=CC%10=C(C=C9)C(=O)N(CC(CC)CCCC)C%10=O)S8)=C7C(=O)N6CCCCCCCC)S5)C=C4C(CCCCCCCC)(CCCCCCCC)C3=C2)S1,FADPPPI,-4.99,-3.05,0.57,0.76,0.23,0.1,"X. He, L. Yin, Y. Li, Efficient design and structural modifications for tuning the photoelectric properties of small-molecule acceptors in organic solar cells, New J. Chem. 43 (2019) 6577¨C6586. https://doi.org/10.1039/C9NJ00600A."
4184,CCCCCCCCN1N=C2C(/C=C/C3=CC=C(C#N)C=C3)=CC=C(C3=CC4=C(S3)C3=CC5=C(C=C3C4(C3=CC=C(CCCCCC)C=C3)C3=CC=C(CCCCCC)C=C3)C3=C(C=C(C4=CC=C(/C=C/C6=CC=C(C#N)C=C6)C6=NN(CCCCCCCC)N=C46)S3)C5(C3=CC=C(CCCCCC)C=C3)C3=CC=C(CCCCCC)C=C3)C2=N1,BTA701,-4.93,-2.67,0.21,1.32,0.25,0.07,"B. Xiao, Y. Geng, A. Tang, X. Wang, Y. Chen, Q. Zeng, E. Zhou, Controlling the Cyano-Containing A2 Segments in A2-A1-D-A1-A2 Type Non-Fullerene Acceptors to Combine with a Benzotriazole-Based p-Type Polymer: ¡°Same-Acceptor-Strategy¡± for High VOC Organic Solar Cells, Sol. RRL. 3 (2019) 1800332. https://doi.org/10.1002/solr.201800332."
4185,CCC(CC)N1C(=O)C2=CC=C(C3=CC=C(C4=C5C(=O)N(C(CC)CC)C(=O)C6=CC(C7=CC=C(C8=CC9C(=O)N(C(CC)CC)C(=O)C9C=C8)S7)=C7C(=O)N(C(CC)CC)C(=O)C(=C4)C7=C65)S3)C=C2C1=O,M5,-5.92,-3.82,0.29,0.49,0.39,0.056,"A.D. Hendsbee, S.M. McAfee, J.-P. Sun, T.M. McCormick, I.G. Hill, G.C. Welch, Phthalimide-based ¦Ð-conjugated small molecules with tailored electronic energy levels for use as acceptors in organic solar cells, J. Mater. Chem. C. 3 (2015) 8904¨C8915. https://doi.org/10.1039/C5TC01877C."
4186,CCC(CC)N1C(=O)C2=CC=C(C3=CC=C(C4=CC5=C6C(=CC=C7C8=C(C9=CC=C(C%10=CC%11C(=O)N(C(CC)CC)C(=O)C%11C=C%10)S9)C=C9C(=O)N(C(CC)CC)C(=O)C%10=CC=C(C4=C76)C8=C%109)C(=O)N(C(CC)CC)C5=O)S3)C=C2C1=O,M6,-5.69,-3.9,0.23,0.78,0.3,0.054,"A.D. Hendsbee, S.M. McAfee, J.-P. Sun, T.M. McCormick, I.G. Hill, G.C. Welch, Phthalimide-based ¦Ð-conjugated small molecules with tailored electronic energy levels for use as acceptors in organic solar cells, J. Mater. Chem. C. 3 (2015) 8904¨C8915. https://doi.org/10.1039/C5TC01877C."
4187,CCCCCCCCN1C(=O)/C(=C2C(=O)N(CCCCCCCC)C3C=C(C4=CC=C(C5=CC6C(=O)N(C(CC)CC)C(=O)C6C=C5)S4)C=CC23)C2=CC=C(C3=CSC(C4=CC=C5C(=O)N(C(CC)CC)C(=O)C5=C4)=C3)C=C21,M4,-5.47,-3.64,0.15,0.63,0.28,0.027,"A.D. Hendsbee, S.M. McAfee, J.-P. Sun, T.M. McCormick, I.G. Hill, G.C. Welch, Phthalimide-based ¦Ð-conjugated small molecules with tailored electronic energy levels for use as acceptors in organic solar cells, J. Mater. Chem. C. 3 (2015) 8904¨C8915. https://doi.org/10.1039/C5TC01877C."
4188,CCCCCCCCN1C(=O)C2=C(C3=CC=C(C#CC4=CC5=C(C=C4)C(=O)N(CC(CC)CCCC)C5=O)S3)N(CCCCCCCC)C(=O)C2=C1C1=CC=C(C#CC2=CC=C3C(=O)N(CC(CC)CCCC)C(=O)C3=C2)S1,(PIAT)2DPP,-5.2,-3.21,0.13,0.48,0.24,0.02,"X. He, L. Yin, Y. Li, Efficient design and structural modifications for tuning the photoelectric properties of small-molecule acceptors in organic solar cells, New J. Chem. 43 (2019) 6577¨C6586. https://doi.org/10.1039/C9NJ00600A."