Role of structures with penta- and hexacoordinate silicon in the nucleophile-catalyzed hydrolysis of tetramethoxysilane

Abstract

The mechanism of the base catalyzed hydrolysis of tetramethoxysilane (TMOS), proposed earlier on the basis of experimental data, is assessed by theoretical methods, i.e. MP2 and B3LYP with 6-31G(d) and Dunning correlation-consistent basis sets. Models considered involve one and two hydrolyzing water molecules attacking (MeO)₄Si in the frontside position with a nucleophile (NH₃ and OH⁻) in the backside position. This approach allowed us to simulate uniformly the catalytic action of weak and strong bases. It was shown that the presence of a base in the backside position considerably lowers the activation barrier for hydrolysis. The inclusion of the additional water molecule which results in a substantial lowering of the barrier for uncatalyzed hydrolysis does not change noticeably the catalytic effect. In both one- and two-water molecules models the structure of the transition state in the presence of a nucleophile becomes nearly octahedral in which hexacoordinate silicon and four oxygens of the TMOS moiety have a planar arrangement