caption stringlengths 1 1.54k | caption_summary stringlengths 2 202 | image_features sequencelengths 512 512 | text_features sequencelengths 512 512 |
|---|---|---|---|
EBSD inverse-pole maps of SLM from cross-section vertical to the build direction. | ['EBSD', 'inverse-pole maps', 'SLM'] | [
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Electron backscatter diffraction (EBSD) inverse-pole maps of HIP and CR. | ['EBSD', 'inverse-pole maps'] | [
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A bright-field transmission electron microscopy (TEM) image of HIP sample. | ['TEM', 'microscopy', 'HIP'] | [
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Morphology of HEA raw powder. | ['morphology', 'HEA', 'raw powder'] | [
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A bright-field transmission electron microscopy (TEM) image of CR sample. | ['TEM', 'bright-field', 'CR sample'] | [
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EBSD inverse-pole maps of SLM from cross-section parallel to the build direction. | ['EBSD', 'inverse-pole maps', 'SLM'] | [
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Electron backscatter diffraction (EBSD) inverse-pole maps of HIP and CR. | ['EBSD', 'inverse-pole maps'] | [
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A schematic of three different kinds of processing routes. | ['processing routes', 'schematic', 'materials'] | [
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The initial step is a Wittig reaction, which is followed by a one-pot transesterification and desilylation. The terminal alkyne product is subjected to a Sonogashira reaction, furnishing the molecular wire with thioacetate end groups. The last step is a Knoevenagel condensation. Me, methyl; Et, ethyl; Pr, propyl; Bu, butyl; Ac, acetyl; Ph, phenyl; THF, tetrahydrofuran; rt, room temperature. | ['Chemical reactions', 'Wittig reaction', 'Transesterification and desilylation', 'Sonogashira reaction', 'Knoevenagel condensation'] | [
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"The respective differences in the reduced pair-distribution functions obtained by subtracting the r(...TRUNCATED) | ['pair-distribution functions', 'reference pattern', 'temperature'] | [0.021635334938764572,0.036660633981227875,0.04399430379271507,-0.01028273906558752,0.03650242090225(...TRUNCATED) | [-0.012989181093871593,0.0667819157242775,0.017539067193865776,0.005173197481781244,0.03951716050505(...TRUNCATED) |
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