Bonding aspects of P-heterocyclic carbene transition metal complexes. A computational assessment

Abstract

Gradient-corrected (BP86) density-functional calculations were used to study the chemical bond between transition-metal complexes and N- and P-heterocyclic carbenes EHC (EHC = imidazolin-2-ylidene; 1,3-dimethylimidazolin-2-ylidene; 1,3-dihydro-1,3-diphosphol-2-ylidene; 1,3-dimethyl-1,3-diphosphol-2-ylidene). Forty two complexes of the type [M] ← EHC, [M] = CuCl, AgCl, AuCl, BeCl +, Cu +, Ag +, Au +, have been studied. Both electrostatic contributions as well as π-back-donation are of special importance for the [M] ← EHC bond. The metal–ligand bond strengths are comparable for NHC and PHC complexes. Whereas the former undergo stronger electrostatic interactions, the latter show a higher degree of π-bonding. When considering NHC and PHC as ligands for transition-metal-based catalysts, the results of the present study suggest that PHC both compete with NHC – in terms of metal-to-ligand bond strength – as well as complement NHC – in terms of the nature of the metal–ligand bond.