This work was supported by GRL (2010-00353) and WCU program (R31-2008-000-10010-0) (W.N.) from the NRF, Korea, Grants-in-Aid (nos 20108010 and 23750014) (S.F. and K.O.) of the Global COE program from the JSPS (Japan), and RP-Grant 2010 (Y.Y.) of Ewha Womans University.
Communication
Photoelectrocatalysis to Improve Cycloreversion Quantum Yields of Photochromic Dithienylethene Compounds†
Article first published online: 13 NOV 2012
DOI: 10.1002/anie.201206256
Copyright © 2012 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
Issue

Angewandte Chemie International Edition
Volume 51, Issue 52, pages 13154–13158, December 21, 2012
Additional Information
How to Cite
Lee, S., You, Y., Ohkubo, K., Fukuzumi, S. and Nam, W. (2012), Photoelectrocatalysis to Improve Cycloreversion Quantum Yields of Photochromic Dithienylethene Compounds . Angew. Chem. Int. Ed., 51: 13154–13158. doi: 10.1002/anie.201206256
- †
Publication History
- Issue published online: 18 DEC 2012
- Article first published online: 13 NOV 2012
- Manuscript Received: 4 AUG 2012
Funded by
- GRL. Grant Number: 2010-00353
- WCU program. Grant Number: R31-2008-000-10010-0
- NRF, Korea. Grant Numbers: 20108010, 23750014
- JSPS
- Ewha Womans University
Keywords:
- electron transfer;
- photochemistry;
- photochromism
An open and shut case: Photoirradiation of the 9-mesityl-10-methylacridinium ion, which acts as a photoredox catalyst, evoked catalytic cycloreversion of the photochromic 1,2-dithienylethene (DTE) compounds with one order of magnitude enhancement in quantum yields. Mechanistic studies revealed that the back electron transfer and electron transfer from the neutral closed form of DTE compounds to the open-form radical cation are key steps.

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