High-Nuclearity Ruthenium Carbonyl Cluster Chemistry. 2. Reaction of [Ru2(μ-H)(μ-NC5H4)2(CO)4(NC5H5)2][Ru10(μ-H)(μ6-C)(CO)24] with Triphenylphosphine: Stepwise Apical Substitution on a “Giant Tetrahedral” Cluster

Marie P. Cifuentes, Mark G. Humphrey*, Brian W. Skelton, Allan H. White

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

16 Citations (Scopus)

Abstract

The (hydrido)(carbido)decaruthenium cluster anion [Ru10(μ-H)(μ6-C)(CO)24]- reacts with triphenylphosphine in a stepwise manner to afford [Ru10(μ-H)(μ6-C)-(CO)24-xPPh3)]- (x = 1–4), with initial ligand displacement on the apical ruthenium associated with the hydride ligand and subsequent ligand substitution at the other apices; the location of the phosphine substituent of the monosubstituted cluster anion [Ru10(μ-H)(μ6-C)-(CO)23PPh3)]- has been confirmed by a single crystal X-ray diffraction study.

Original languageEnglish
Pages (from-to)1536-1538
Number of pages3
JournalOrganometallics
Volume14
Issue number3
DOIs
Publication statusPublished - Mar 1995

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