Abstract
A half-sandwich, coordinatively unsaturated N-heterocyclic carbene complex of iron with a metallacycle was found to cleave the Si–H bonds of hydrosilanes to give 16-electron iron–silyl complexes. The reactions of silyl complexes with H2 led to the formation of dihydride complexes, in which hydride ligands weakly interact with the silicon atom. The molecular structures of these new complexes have been determined by means of X-ray crystallography.
A half-sandwich, 16-electron iron complex with a cyclometalated N-heterocyclic carbene ligand was found to activate the Si–H bonds of hydrosilanes, thus giving rise to coordinatively unsaturated iron–silyl complexes. The silyl complexes interact with H2 to form 18-electron dihydride complexes.
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