Nucleophilic addition via metal–metal bond cleavage in an osmium–antimony cluster

Abstract

The room-temperature reaction of a number of two-electron nucleophiles with the osmium–antimony cluster [Os₃(µ-H)(CO)₁₀(µ-SbPh₂)] 1 gave adducts [Os₃H(CO)₁₀(µ-SbPh₂)L] 2 (L = PPh₃ a, AsPh₃ b, SbPh₃ c or CO d), in which the antimony-bridged Os–Os bond has been cleaved in order to accommodate the incoming ligand. X-Ray crystallographic studies on 2b and 2c confirmed that the ligands L occupied an equatorial site of the Os₃Sb framework, while NMR studies indicated that the clusters 2a–2c existed as isomeric mixtures, which probably differ in the arrangements of the ligand L relative to the antimony vertex. The reaction leading to the formation of 2b, which was carried out at elevated temperature, also led to decarbonylation to a substituted analogue of 1 in which the ligand L was on the unbridged osmium.