Efficient hydrosilylation of imines using catalysts based on iridium(iii) metallacycles

Abstract

Ir(III) metallacycles were applied as catalysts for the hydrosilylation of various ketimines and aldimines with sodium tetrakis[(3,5-trifluoromethyl)phenyl]borate, NaBArF₂₄, as an additive. By using a slight excess of the organosilane reagent, the reactions proceeded rapidly and efficiently, at low catalyst loadings and at room temperature. Several examples of cationic Ir(III) catalysts could be synthesised, characterized and tested. In situ-generated catalysts proved to be more active as compared to isolated ones and species with non-coordinating BArF₂₄ counterion gave the highest catalytic activities.