A theoretical study of the electronic effect of the ligand bite angle on the hydrosilylation reaction of ketones by Cu(I) diphosphine complexes

Abstract

Diphosphine ligands are commonly used for the catalytic hydrosilylation of ketones using Cu(I) complexes. The electronic effect of the P–Cu–P bite angle has been investigated by a theoretical DFT study. An increase of the P–Cu–P bite angle induces a stronger phosphorus lone pair/Cu-H σ∗ orbital interaction due to a better overlap between these orbitals. This increase in overlap affects structural and electronic properties of the copper hydride catalyst. Increasing the bite angle leads to a decrease of the Cu-P distances and an increases of the Cu-H distances. From an electronic point of view, the effect of an increasing bite angle leads to a weakening of the σ Cu-H orbital, and an increase of the hydride population. The increased polarization of the hydride leads to an easier electron transfer from the σ Cu-H bond to the carbon of the ketone.