Bonding and reactivity of a μ-hydrido dicopper cation
Chelsea M Wyss1, Brandon K Tate, John Bacsa
1School of Chemistry and Biochemistry, Georgia Institute of Technology, Atlanta, GA 30332 (USA).
Abstract:
A bent dicopper-hydride cation that has an N-heterocyclic carbene supporting ligand has a Cu-H-Cu angle of 122° in the solid state. Density functional theory suggests an open three-centered metal-hydrogen interaction. The hydride reacts readily with methanol and with carbon dioxide; insertion of phenylacetylene affords a gem-dicopper vinyl complex.
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