Issue 43, 2010

Molecular mechanism of acid-triggered aryl–halide reductive elimination in well-defined aryl–CuIII–halide species

Abstract

Well-defined aryl–CuIIIhalide species undergo reductive elimination upon acid addition resulting in the formation of strong aryl–halide bonds. The computationally studied mechanism points towards ligand protonation as the rate-determining step, in agreement with previous experimental data.

Graphical abstract: Molecular mechanism of acid-triggered aryl–halide reductive elimination in well-defined aryl–CuIII–halide species

Supplementary files

Article information

Article type
Paper
Submitted
09 Apr 2010
Accepted
25 May 2010
First published
01 Oct 2010

Dalton Trans., 2010,39, 10458-10463

Molecular mechanism of acid-triggered aryl–halide reductive elimination in well-defined aryl–CuIIIhalide species

A. Casitas, A. Poater, M. Solà, S. S. Stahl, M. Costas and X. Ribas, Dalton Trans., 2010, 39, 10458 DOI: 10.1039/C0DT00284D

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