Abstract

The heteronuclear cluster RuOs 3(μ-H) 2(CO) 13 ( 1) reacted readily with a number of ditertiary phosphines under chemical activation with trimethylamine- N-oxide. The solid-state and solution structures of these derivatives have been examined. Six structural types have been characterized crystallographically, including one in which a phenyl group migrates from the ditertiary phosphine ligand to the metal framework. There are many more isomers present in solution, most of which are rapidly inter-converting via hydride migrations.

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