Synthesis of the tetraruthenium carbido cluster [Ru4(H) 2C(CO)12] via mixed ruthenium-gold carbido intermediates: X-ray crystal structures of [Ru4C(CO)12(AuPMe 2Ph)2], [Ru4C(CO)12(I)(AuPEt 3)], and [Ru4(H)C(CO)12(AuPPh3)]

Alan G. Cowie, Brian F.G. Johnson, Jack Lewis, Paul R. Raithby

Research output: Contribution to journalArticlepeer-review

Abstract

The action of CO on the pentanuclear carbido cluster [Ru 5C(CO)14(AuPR3)2] [PR3 = PEt3 (1), PPh3 (2), PMe2Ph (3)] (80 atm, 60°C) affords the tetranuclear carbido cluster [Ru4C(CO) 12(AuPR3)2] [PR3 = PEt3 (4), PPh3 (5), PMe2Ph (6)], which exhibits a carbide-centred, 'butterfly' Ru4C core with both the 'wing-tip' and 'hinge' Ru atoms bridged by AuPR3 groups; the 'hinge' bridging AuPR3 group may be replaced by reaction with I2 or Hl to give [Ru4C(CO)12(I)(AuPR3)] [PR3 = PEt3 (7), PPh3 (8)] and [Ru4(H)C(CO) 12(AuPR3)] [PR3 = PEt3 (9), PPh 3 (10)], respectively, and the subsequent reaction of (9) and (10) with [BH4]- removes the remaining AuPR3 group, acidification affording the tetraruthenium carbide [Ru4(H) 2C(CO)12] (11).

Original languageEnglish
Pages (from-to)1710-1712
Number of pages3
JournalJournal of the Chemical Society, Chemical Communications
Issue number24
DOIs
Publication statusPublished - 31 Dec 1984

ASJC Scopus subject areas

  • Molecular Medicine

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