Hydrosilylation of Olefins Catalyzed by Well-Defined Cationic Aluminum Complexes: Lewis Acid versus Insertion Mechanisms

Abstract

The cationic aluminum complex [NacNacAlH]+ (2; NacNac = CH{C(Me)N(2,6-Pri2C6H3)}2) can be easily generated from NacNacAlH2 by hydride abstraction and functions as a catalyst for the hydrosilylation of olefins and alkynes. Mechanistic studies suggest that, although olefin insertion into the Al–H bond is very facile, the catalysis does not proceed by an insertion/metathesis mechanism but likely by Lewis acid activation. Stoichiometric reactions of 2 with alkynes furnished unexpected products of C≡C addition across the NacNacAl moiety to give tripodal aluminum cations, which are also potent catalysts for the hydrosilylation of alkynes.