Photochromism of diarylethene molecules and crystals

102Citations
Citations of this article
180Readers
Mendeley users who have this article in their library.

Abstract

Photochromism is defined as a reversible transformation of a chemical species between two isomers upon photoirradiation. Although vast numbers of photochromic molecules have been so far reported, photochromic molecules which exhibit thermally irreversible photochromic reactivity are limited to a few examples. The thermal irreversibility is an indispensable property for the application of photochromic molecules to optical memories and switches. We have developed a new class of photochromic molecules named "diarylethenes", which show the thermally irreversible photochromic reactivity. The well designed diarylethene derivatives provide outstanding photochromic performance: both isomers are thermally stable for more than 470,000 years, photoinduced coloration/decoloration can be repeated more than 105 cycles, the quantum yield of cyclization reaction is close to 1 (100%), and the response times of both coloration and decoloration are less than 10 ps. This review describes theoretical background of the photochromic reactions, color changes of the derivatives in solution as well as in the single crystalline phase, and application of the crystals to light-driven actuators. © 2010 The Japan Academy.

Cite

CITATION STYLE

APA

Irie, M. (2010, May). Photochromism of diarylethene molecules and crystals. Proceedings of the Japan Academy Series B: Physical and Biological Sciences. https://doi.org/10.2183/pjab.86.472

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free