Issue 22, 2012

Oxidation of sulfides to sulfoxides mediated by ionic liquids

Abstract

A highly selective and efficient oxidation of sulfides to sulfoxides is presented. The reactions were carried out at room temperature in the absence of a catalyst in the ionic liquid [Bmim][BF4] (Bmim = 1-butyl-3-methylimidazolium) using aqueous H2O2 (35%) as oxidant. The products were obtained in high yields. Compared to the analogous reactions in organic solvents, this system can be recycled without significant loss of activity and selectivity. Additionally, the reaction mechanism was examined by IR, Raman and NMR spectroscopy. Based on these examinations, it appears that the crucial step during the oxidation procedure is the formation of a hydrogen bond between the ionic liquid and the oxidant.

Graphical abstract: Oxidation of sulfides to sulfoxides mediated by ionic liquids

Supplementary files

Article information

Article type
Paper
Submitted
29 Jun 2012
Accepted
11 Jul 2012
First published
12 Jul 2012

RSC Adv., 2012,2, 8416-8420

Oxidation of sulfides to sulfoxides mediated by ionic liquids

B. Zhang, M. Zhou, M. Cokoja, J. Mink, S. Zang and F. E. Kühn, RSC Adv., 2012, 2, 8416 DOI: 10.1039/C2RA21323K

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