Skip to main content
Cerium-Catalyzed Hydrosilylation of Acrylates to Give α-Silyl Esters.
Title Cerium-Catalyzed Hydrosilylation of Acrylates to Give α-Silyl Esters.
Authors Pindwal, A.; Patnaik, S.; Everett, W.C.; Ellern, A.; Windus, T.L.; Sadow, A.D.
Journal Angew Chem Int Ed Engl
DOI 10.1002/anie.201610263
Abstract

The homoleptic organocerium complex Ce{C(SiHMe2 )3 }3 (1) reacts with B(C6 F5 )3 to produce the zwitterionic bis(alkyl) hydridoborato Ce{C(SiHMe2 )3 }2 HB(C6 F5 )3 (2). NMR and IR spectroscopy and X-ray crystallography indicate that each alkyl ligand contains two bridging Ce↼H-Si interactions in both 1 and 2. Compound 2 serves as a precatalyst for the hydrosilylation of acrylates to give α-silyl esters at room temperature with a turnover number of 2200.