Issue 2, 2014

Dehydrogenative coupling of aromatic thiols with Et3SiH catalysed by N-heterocyclic carbene nickel complexes

Abstract

A series of new tetramethylcyclopentadienyl-functionalised N-heterocyclic carbene ligands with different wingtip substituents have been prepared and characterised. These ligands have been successfully coordinated to nickel affording complexes of the general type (Cp*-NHCR)NiX (X = Cl, I). These well-defined nickel complexes selectively catalysed the coupling of aromatic thiols with Et3SiH to give the corresponding silylthioethers (RSSiEt3). The nickel complexes bearing ethyl, iso-butyl, and n-butyl wingtips displayed comparable catalytic efficiency, while the nickel complex bearing a methyl substituent on the wingtip was the worst performing catalyst.

Graphical abstract: Dehydrogenative coupling of aromatic thiols with Et3SiH catalysed by N-heterocyclic carbene nickel complexes

Supplementary files

Article information

Article type
Paper
Submitted
29 Jul 2013
Accepted
01 Oct 2013
First published
02 Oct 2013

Dalton Trans., 2014,43, 853-858

Dehydrogenative coupling of aromatic thiols with Et3SiH catalysed by N-heterocyclic carbene nickel complexes

L. Postigo, R. Lopes and B. Royo, Dalton Trans., 2014, 43, 853 DOI: 10.1039/C3DT52052H

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