Computational and Experimental Investigation of Alkene Hydrogenation by a Pincer-Type [P2Si]Rh Complex: Alkane Release via Competitive σ-Bond Metathesis and Reductive Elimination
Author:
Affiliation:
1. Department of Chemistry, Carleton College, Northfield, Minnesota 55057, United States
2. Department of Chemistry, University of Portland, Portland, Oregon 97203, United States
Funder
Camille and Henry Dreyfus Foundation
Division of Chemistry
Publisher
American Chemical Society (ACS)
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.organomet.8b00922
Reference39 articles.
1. Mechanism of the chlorotris(triphenylphosphine) rhodium(I)-catalyzed hydrogenation of alkenes. The reaction of chlorodihydridotris(triphenyl-phosphine)rhodium(III) with cyclohexene
2. cHartwig, J. F. In Organotransition Metal Chemistry: From Bonding to Catalysis; University Science Books: Sausalito, CA, 2010; pp 575–665.
3. Mechanism of Asymmetric Hydrogenation Catalyzed by a Rhodium Complex of (S,S)-1,2-Bis(tert-butylmethylphosphino)ethane. Dihydride Mechanism of Asymmetric Hydrogenation
4. eFelgdus, S.; Landis, C. R. In Computational Modeling of Homogeneous Catalysis; Maseras, F., Lledos, A., Eds. Kluwer: Dordrecht, 2002; Vol. 25, pp 107–135.
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