| Literature DB >> 17649993 |
Andrew J Roering1, Samantha N MacMillan, Joseph M Tanski, Rory Waterman.
Abstract
Triamidoamine-supported zirconium complexes catalyze the heterodehydrocoupling of primary phosphines with silane and germanes. In this catalysis, P-Si or P-Ge products are observed exclusively with no competitive P-P bond formation. Phosphido complexes (N3N)ZrPHR (N3N = N(CH2CH2NSiMe3)33-, R = Ph, 2; Cy, 3) were observed to be the catalyst resting state, and complex 2 was structurally characterized.Entities:
Year: 2007 PMID: 17649993 DOI: 10.1021/ic7013144
Source DB: PubMed Journal: Inorg Chem ISSN: 0020-1669 Impact factor: 5.165