Issue 91, 2020

Electrocatalytic oxidative Z/E isomerization of a stilbene favoured by the presence of an electroactive persistent radical

Abstract

A push–pull-functionalized stilbene has been prepared, with an electroactive perchlorotriphenylmethyl (PTM˙) radical and dimethylamine units as electron-withdrawing and -donating moieties, respectively, showing an electrocatalytic redox-induced ZE isomerization where the open-shell nature of PTM˙ plays a key role in the isomerization ocurrance.

Graphical abstract: Electrocatalytic oxidative Z/E isomerization of a stilbene favoured by the presence of an electroactive persistent radical

Supplementary files

Article information

Article type
Communication
Submitted
21 Jul 2020
Accepted
18 Oct 2020
First published
19 Oct 2020
This article is Open Access
Creative Commons BY-NC license

Chem. Commun., 2020,56, 14211-14214

Electrocatalytic oxidative Z/E isomerization of a stilbene favoured by the presence of an electroactive persistent radical

P. Mayorga-Burrezo, C. Sporer, J. A. de Sousa, N. Capra, K. Wurst, N. Crivillers, J. Veciana and C. Rovira, Chem. Commun., 2020, 56, 14211 DOI: 10.1039/D0CC04973E

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