Bonding and Reactivity of a μ‐Hydrido Dicopper Cation

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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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