Issue 17, 2012

Hydrotris(3-mesitylpyrazolyl)borato-copper(i) alkyne complexes: synthesis, structural characterization and rationalization of their activities as alkyne cyclopropenation catalysts

Abstract

The use of the bulky hydrotris(3-mesitylpyrazolyl)borate anionic ligand has allowed the synthesis of stable TpMsCu(alkyne) complexes (alkyne = 1-hexyne, 1, phenylacetylene, 2, and ethyl propiolate, 3). The spectroscopic and structural features of these compounds and their relative reactivity have been examined, indicating the existence of a low π back-bonding from the copper(I) centre to the alkyne. Ligand exchange experiments have shown that terminal alkyne adducts are more stable than internal alkyne analogues. In good accordance with this, the previously reported alkyne cyclopropenation reaction catalysed by the TpxCu complexes can be rationalized and correlated with their relative stability.

Graphical abstract: Hydrotris(3-mesitylpyrazolyl)borato-copper(i) alkyne complexes: synthesis, structural characterization and rationalization of their activities as alkyne cyclopropenation catalysts

Supplementary files

Article information

Article type
Paper
Submitted
16 Oct 2011
Accepted
16 Jan 2012
First published
02 Mar 2012

Dalton Trans., 2012,41, 5319-5325

Hydrotris(3-mesitylpyrazolyl)borato-copper(I) alkyne complexes: synthesis, structural characterization and rationalization of their activities as alkyne cyclopropenation catalysts

C. Martín, M. Sierra, E. Alvarez, T. R. Belderrain and P. J. Pérez, Dalton Trans., 2012, 41, 5319 DOI: 10.1039/C2DT11951J

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