Issue 34, 2015

1,2,4-Triazole-derived carbene complexes of gold: characterization, solid-state aggregation and ligand disproportionation

Abstract

Ligand redistribution reactions are well documented for silver(I) N-heterocyclic carbene (NHC) complexes of the type [AgX(NHC)] (X = halido ligand), but only two reports have been described in the literature for gold analogues of the general formula [AuX(NHC)]. In both cases, the NHCs in question were exceptionally strong donors. To probe the dependence of ligand redistribution processes on NHC donor strength, a model study was conducted using a weakly donating 1,2,4-triazolin-5-ylidene (tazy) ligand and different halido coligands. For [AuX(tazy)] (X = Cl, Br, OAc, tazy = 4-benzyl-1-methyl-1,2,4-triazolin-5-ylidene), no ligand redistribution was found, while a reversible disproportionation between [AuI(tazy)] in solution and [Au(tazy)2][AuI2] in the solid state was observed and studied by means of X-ray crystallography, NMR and UV-Vis spectroscopy, as well as DFT calculations.

Graphical abstract: 1,2,4-Triazole-derived carbene complexes of gold: characterization, solid-state aggregation and ligand disproportionation

Supplementary files

Article information

Article type
Paper
Submitted
17 Oct 2014
Accepted
20 Jan 2015
First published
20 Jan 2015
This article is Open Access
Creative Commons BY-NC license

Dalton Trans., 2015,44, 15157-15165

1,2,4-Triazole-derived carbene complexes of gold: characterization, solid-state aggregation and ligand disproportionation

S. Guo, J. C. Bernhammer and H. V. Huynh, Dalton Trans., 2015, 44, 15157 DOI: 10.1039/C4DT03201B

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