JOURNAL ARTICLE

Photochromism of Diarylethene Maleimide Derivatives

Tadatsugu YamaguchiMasatsugu MatsuoMasahiro Irie

Year: 2005 Journal:   Bulletin of the Chemical Society of Japan Vol: 78 (6)Pages: 1145-1148   Publisher: Oxford University Press

Abstract

Abstract Diarylmaleimide derivatives having an indole ring, N-cyanomethyl-2-[2-methoxy-1-benzothiophen-3-yl]-3-[2-methyl-1-octadecylindol-3-yl]maleimide or N-cyanomethyl-2-[2-ethoxy-1-benzothiophen-3-yl]-3-[2-methyl-1-octadecylindol-3-yl]maleimide, were synthesized in an attempt to shift the photosensitive wavelength longer such that it becomes longer than 450 nm. The derivatives underwent the photocyclization reaction upon irradiation with 450–550 nm light in hexane solution and the photogenerated closed-ring isomers returned to the initial open-ring isomers upon irradiation with light longer than 600 nm.

Keywords:
Photochromism Chemistry Diarylethene Maleimide Photochemistry Organic chemistry

Metrics

11
Cited By
0.97
FWCI (Field Weighted Citation Impact)
16
Refs
0.73
Citation Normalized Percentile
Is in top 1%
Is in top 10%

Citation History

Topics

Photochromic and Fluorescence Chemistry
Physical Sciences →  Materials Science →  Materials Chemistry
Photoreceptor and optogenetics research
Life Sciences →  Neuroscience →  Cellular and Molecular Neuroscience
Synthesis of Indole Derivatives
Physical Sciences →  Chemistry →  Organic Chemistry

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