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- W1971367266 abstract "Abstract Three new isomeric pyridine-containing diarylethenes with a benzofuran moiety were synthesized, and the structures of two diarylethenes were determined by single X-ray diffraction analysis. Their properties such as photochromism, acidchromism, fluorescence, as well as electrochemical properties, were investigated in detailed. The diarylethenes exhibited multi-addressable switching behavior by light and acid/base stimuli in solution and functioned as a remarkable fluorescent switch in both solution and poly(methyl methacrylate) films. Among these isomeric derivatives, the example with the nitrogen atom at the ortho -position of pyridine showed the largest absorption maxima, molar absorption coefficients, and cyclization quantum yield. The nitrogen atom position in the terminal pyridine unit could efficiently modulate the optical and electrochemical properties of the diarylethenes with a benzofuran moiety. The results suggested that the benzofuran moiety and the nitrogen atom position in the terminal pyridine unit played a vital role during the process of photoisomerization reaction for these isomeric diarylethenes." @default.
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- W1971367266 date "2013-12-01" @default.
- W1971367266 modified "2023-10-18" @default.
- W1971367266 title "Photochromism of new isomeric pyridine-containing diarylethenes with a benzofuran moiety" @default.
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- W1971367266 doi "https://doi.org/10.1016/j.dyepig.2013.06.036" @default.
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