Abstract

The triosmium nitrite carbonyl cluster [Os 3(μ-H)(CO) 10(μ-η 2-NO 2)] ( 1) was allowed to react with 1,1′-bis(diphenylphosphino)ferrocene (dppf) and N, N-dimethyl-1-[( S)-2-(diphenylphosphino)ferrocenyl]ethylamine (ppfa) in the presence of Me 3NO in CH 2Cl 2, and clusters [Os 3(μ-H)(CO) 8(μ-η 2-NO 2)(μ-dppf)] ( 2) and [Os 3(μ-H)(CO) 8(μ-η 2-NO 2)(μ-ppfa)] ( 3) were afforded in moderate yields. Clusters 2 and 3 were fully characterised by spectroscopic techniques and X-ray crystallography. The nitrite, hydride and the ferrocenyl phosphine ligands are all bridged across the same OsOs edge. The amine group of the ppfa ligand shows a preference to coordinate with the Os atom with a σ-bonded nitrite O atom. The redox properties of the nitrite complexes were investigated using cyclic voltammetry.

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