| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 27057 | Journal of Photochemistry and Photobiology A: Chemistry | 2014 | 6 Pages |
•A novel diarylethene with a Schiff base unit was synthesized.•It could be transformed into a diarylethene with a benzoxazole moiety by NaOH and light.•Its multi-responsive photochromism could be effectively modulated by chemical and light stimuli.
A novel diarylethene with a Schiff base unit was successfully synthesized and its multi-responsive photochromism could be effectively modulated by chemical and light stimuli. By the stimulation of sodium hydroxide, the absorption maximum of its closed-ring isomer showed extraordinarily large redshift of 134 nm, accompanied with a notable color change from purple to green. Subsequent irradiation with 420 nm visible light further caused a dramatic change in its color from green to cyan due to the formation of the benzoxazole moiety. Moreover, the deprotonated open-ring isomer exhibited typical photochromism via the diarylethene intermediate with a benzoxazole unit.
Graphical abstractA novel diarylethene with a Schiff base unit was synthesized. It could be easily transformed into a diarylethene with a benzoxazole moiety by the stimulation of sodium hydroxide and photoirradiation. The structure transformation provided a new approach to construct a multi-responsive photochromic diarylethene system.Figure optionsDownload full-size imageDownload as PowerPoint slide
