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Femtosecond infrared studies of ligand rearrangement reactions: silyl hydride products from Group 6 carbonyls

The ultrafast dynamics of the SiH bond activation reaction by the Group 6 d 6 organometallic compounds M(CO) 5 (M=Cr, Mo, and W) have been studied in neat tri-substituted silanes under ambient conditions. The ultrafast spectral evolutions of the CO stretching bands were monitored following UV photo...

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Bibliographic Details
Published in:Journal of organometallic chemistry 2000-02, Vol.596 (1), p.183-192
Main Authors: Kotz, K.T, Yang, H, Snee, P.T, Payne, C.K, Harris, C.B
Format: Article
Language:English
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Summary:The ultrafast dynamics of the SiH bond activation reaction by the Group 6 d 6 organometallic compounds M(CO) 5 (M=Cr, Mo, and W) have been studied in neat tri-substituted silanes under ambient conditions. The ultrafast spectral evolutions of the CO stretching bands were monitored following UV photolysis using femtosecond pump–probe spectroscopic methods. It was found that the coordinatively unsaturated species, which is formed following CO photolysis from the parent molecule, is quickly solvated (
ISSN:0022-328X
1872-8561
DOI:10.1016/S0022-328X(99)00676-2