Issue 11, 2012

Selective photoconversion of photochromic diarylethenes and their properties

Abstract

Selective photoconversions of photochromic diarylethene derivatives has been described using diarylethene derivative 1a as a model compound. Upon irradiation with 254 nm light, 1a undergoes photocyclization to yield the ring-closed isomer 1b in the absence of oxygen, or is transformed to the thiolactone derivative 1c in the presence of oxygen (in the air), respectively. It was found that 1b can be reversed back to 1a with visible light irradiation, the ring-opening and ring-closing photoswitch can be performed in the absence of oxygen. 1c is, however, photo-inactive and cannot be reversed back to 1a with UV or visible light irradiation. It was also found that 1c shows fluorescence whereas both 1a and 1b show no fluorescence.

Graphical abstract: Selective photoconversion of photochromic diarylethenes and their properties

Article information

Article type
Paper
Submitted
10 May 2012
Accepted
02 Aug 2012
First published
22 Aug 2012

New J. Chem., 2012,36, 2223-2227

Selective photoconversion of photochromic diarylethenes and their properties

H. Liu and Y. Chen, New J. Chem., 2012, 36, 2223 DOI: 10.1039/C2NJ40377C

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements