Abstract

We report the first examples of the carbide ligand in (Cy3P)2Cl2Ru≡C (RuC) developing into a μ3 ligand toward metal centers. Conventionally, sterics exclude this coordination mode, but Fe2(CO)9 and Co2(CO)8 expel bridging CO ligands upon reaction with RuC to form trimetallic (Cy3P)2Cl2Ru═CFe2(CO)8 (RuCFe2) and (Cy3P)2Cl2Ru═CCo2(CO)7 (RuCCo2) complexes. Thus, the proximity offered by metal-metal associations in bimetallic carbonyl complexes allows the formation of trinuclear carbide complexes as verified by NMR, Mössbauer, and X-ray spectroscopic techniques.

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