Transition-Metal Hydride Radical Cations
Author:
Affiliation:
1. Department of Chemistry, Columbia University, New York, New York 10027, United States
2. Pyrotechnics Technology and Prototyping Division, U.S. Army RDECOM-ARDEC, Picatinny Arsenal, New Jersey 07806, United States
Funder
Division of Chemistry
Office of Science
OFS Fitel
Boulder Scientific Company
Publisher
American Chemical Society (ACS)
Subject
General Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.chemrev.5b00532
Reference144 articles.
1. Hydrogen-Atom Transfer Reactions of Transition-Metal Hydrides
2. Hydrogenation of .alpha.-methylstyrene by hydridopentacarbonylmanganese (I). Evidence for a free-radical mechanism
3. The stoichiometric hydrogenation of 1,1-diphenylethylene with hydridocobalt tetracarbonyl; differences from the hydroformylation reaction
4. Reaction between hydridotetracarbonyl(trichlorosilyl)iron, HFe(CO)4SiCl3, and conjugated dienes. Evidence for a free radical mechanism
5. Mechanisms of the hydrometalation (insertion) and stoichiometric hydrogenation reactions of conjugated dienes effected by manganese pentacarbonyl hydride: processes involving the radical pair mechanism
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