Iridium Complexes as Hydrosilylation Catalysts
- UNCG Author/Contributor (non-UNCG co-authors, if there are any, appear on document)
- Terence "Terry" Nile, Professor (Creator)
- Institution
- The University of North Carolina at Greensboro (UNCG )
- Web Site: http://library.uncg.edu/
Abstract: Iridium complexes have been found to be active as catalysts for hydrosilylation reactions, especially for those involving 1,3-dienes and 1-alkynes. For ketones, iridium complexes show maximum activity if one molar equivalent (relative to iridium) of triphenylphosphine is added to the reaction mixture. Iridium complexes are also active catalysts for the hydrosilylation of a,ß-unsaturated ketones, although the regioselectivity differs from that obtained with rhodium complexes. Attempts at asymmetric hydrosilylation of keto compounds using iridium complexes resulted in extremely low enantiomeric excesses.
Iridium Complexes as Hydrosilylation Catalysts
PDF (Portable Document Format)
688 KB
Created on 4/19/2011
Views: 3958
Additional Information
- Publication
- Journal of Molecular Catalysis, 29, 55 (1985).
- Language: English
- Date: 1985
- Keywords
- Hydrosilylation reactions, ketones, iridium complexes, active catalysts, enantiomeric excesses