Issue 39, 2021

Disulfide metathesis via sulfur⋯iodine interaction and photoswitchability

Abstract

The idea of constitutional dynamic chemistry (CDC) and dynamic combinatorial chemistry (DCC) is widespread in the literature using the chemistry of disulfides. The synthesis of unsymmetrical diaryl disulfides is challenging due to the presence of a weak S–S bond. We report herein the synthesis of unsymmetrical diaryl disulfides from two symmetrical disulfides via a cross-metathesis reaction which was controlled by a weak sulfur⋯iodine (S⋯I) interaction. The unsymmetrical disulfides were stable in acetonitrile solution in the presence of N-iodosuccinimide (NIS), and found to be reversibly photoswitchable to the symmetrical disulfides under visible light irradiation.

Graphical abstract: Disulfide metathesis via sulfur⋯iodine interaction and photoswitchability

Supplementary files

Article information

Article type
Paper
Submitted
11 Aug 2021
Accepted
10 Sep 2021
First published
10 Sep 2021

Org. Biomol. Chem., 2021,19, 8539-8543

Disulfide metathesis via sulfur⋯iodine interaction and photoswitchability

A. Mathuri, M. Pramanik, A. Parida and P. Mal, Org. Biomol. Chem., 2021, 19, 8539 DOI: 10.1039/D1OB01581H

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