Cooperative H2 activation at a nickel(0)–olefin centre

Catalytic olefin hydrogenation is ubiquitous in organic synthesis. In most proposed homogeneous catalytic cycles, reactive M–H bonds are generated either by oxidative addition of H₂ to a metal centre or by deprotonation of a non-classical metal dihydrogen (M–H₂) intermediate. Here we provide evidence for an alternative H₂-activation mechanism that instead involves direct ligand-to-ligand hydrogen transfer (LLHT) from a metal-bound H₂ molecule to a metal-coordinated olefin. An unusual pincer ligand that features two phosphine ligands and a central olefin supports the formation of a non-classical Ni–H₂ complex and the Ni(alkyl)(hydrido) product of LLHT, in rapid equilibrium with dissolved H₂. The usefulness of this cooperative H₂-activation mechanism for catalysis is demonstrated in the semihydrogenation of diphenylacetylene. Experimental and computational mechanistic investigations support the central role of LLHT for H₂ activation and catalytic semihydrogenation. The product distribution obtained is largely determined by the competition between (E)–(Z) isomerization and catalyst degradation by self-hydrogenation. (Figure presented.).