Abstract
We examined the ability of TpxM (Tpx = hydrotris(pyrazolyl)borate ligand; M = Cu and Ag) and IPrMCl (IPr = 1,3-bis(diisopropylphenyl)imidazol-2-ylidene; M = Cu, Ag, Au) complexes as catalyst precursors for the cross-coupling of diazo compounds. Experimental data showed that the metal centre can be tuned with the appropriate selection of the ligand to yield either the homo- or hetero-coupling (cross-coupling) products. A computational study of the reaction mechanism allowed the rationalization of the experimental reactivity patterns, and the identification of the key reaction step controlling the selectivity: the initial reaction between the metallocarbene intermediate and one of the diazo compounds. © 2013 The Royal Society of Chemistry.
Original language | English |
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Pages (from-to) | 4132-4138 |
Journal | Journal of the Chemical Society. Dalton Transactions |
Volume | 42 |
Issue number | 2 |
DOIs | |
Publication status | Published - 18 Jan 2013 |