Issue 89, 2016

Redox interactions of Au(iii) with carboxylated dithiafulvenes and tetrathiafulvalene analogues in polar organic media

Abstract

The redox interactions between HAuCl4 and a series of π-conjugated organic donors, namely carboxylated dithiafulvenes and tetrathiafulvalene vinylogues, were investigated. Interestingly, the dithiafulvene derivative with two carboxylic groups showed the ability to directly induce the formation of Au(0) nanoparticles in dipolar aprotic solvents such as DMF and DMSO.

Graphical abstract: Redox interactions of Au(iii) with carboxylated dithiafulvenes and tetrathiafulvalene analogues in polar organic media

Supplementary files

Article information

Article type
Communication
Submitted
26 Sep 2016
Accepted
11 Oct 2016
First published
11 Oct 2016

Chem. Commun., 2016,52, 13101-13104

Redox interactions of Au(III) with carboxylated dithiafulvenes and tetrathiafulvalene analogues in polar organic media

H. Adows and Y. Zhao, Chem. Commun., 2016, 52, 13101 DOI: 10.1039/C6CC07769B

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