Issue 5, 2017, Issue in Progress

Switching of the π-electronic conjugations in the reduction of a dithienylethene-fused p-benzoquinone

Abstract

The electron accepting character of a dithienylethene-fused p-benzoquinone derivative is significantly reduced upon ring-closing isomerization. Visible light unlocks the π-electronic conjugation of the quinone so it can be utilized for a light-driven oxidation reaction.

Graphical abstract: Switching of the π-electronic conjugations in the reduction of a dithienylethene-fused p-benzoquinone

Supplementary files

Article information

Article type
Communication
Submitted
18 Nov 2016
Accepted
15 Dec 2016
First published
12 Jan 2017
This article is Open Access
Creative Commons BY license

RSC Adv., 2017,7, 2403-2406

Switching of the π-electronic conjugations in the reduction of a dithienylethene-fused p-benzoquinone

E. Saito, T. Ako, Y. Kobori and A. Tsuda, RSC Adv., 2017, 7, 2403 DOI: 10.1039/C6RA27001H

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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