Transition metal-induced dehydrogenative coupling of zinc hydrides

摘要

The reaction of terminal zinc hydrides with palladium(0) species afforded an unprecedented [eta(2)-Zn2Pd] trimetallic complex through the reductive elimination of H-2. In contrast, the reaction of zinc hydrides with a nickel(0) reagent gave sigma-Zn-H coordination complexes with no direct Zn-Zn bonding. Computational studies indicated that an oxidative addition/reductive elimination process at the palladium center might be responsible for the formation of a covalent Zn-Zn bond.