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Facile CH Bond Formation by Reductive Elimination at a Dinuclear Metal Site
Authors:Dr Richard D Adams  Dr Vitaly Rassolov  Yuen Onn Wong
Affiliation:Department of Chemistry and Biochemistry, University of South Carolina, JM Palms Ctr for GSR, Columbia, SC 29208 (USA)
Abstract:The electronically unsaturated dirhenium complex Re2(CO)8(µ‐AuPPh3)(µ‐Ph)] ( 1 ) was obtained from the reaction of Re2(CO)8{µ‐η2‐C(H)?C(H)nBu}(µ‐H)] with Au(PPh3)Ph]. The bridging {AuPPh3} group was replaced by a bridging hydrido ligand to yield the unsaturated dirhenium complex Re2(CO)8(µ‐H)(µ‐Ph)] ( 2 ) by reaction of 1 with HSnPh3. Compound 2 reductively eliminates benzene upon addition of NCMe at 25 °C. The electronic structure of 2 and the mechanism of the reductive elimination of the benzene molecule in its reaction with NCMe were investigated by DFT computational analyses.
Keywords:C  H bond formation  dinuclear metal site  reductive elimination  rhenium  unsaturated complexes
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