Reactions of the hexaruthenium cluster anions [Ru6C(CO)16]2- and...

Philip J. Bailey, Michael A. Beswick, Jack Lewis, Paul R. Raithby, M. Carmen Ramirez de Arellano

Research output: Contribution to journalArticlepeer-review

Abstract

Title full: Reactions of the hexaruthenium cluster anions [Ru6C(CO)16]2- and [Ru6(CO)18]2- with Au2{Ph2PCH2PPh2}Cl2 : crystal and molecular structures of Ru6C(CO)16Au2{Ph2PCH 2PPh2} and Ru5(CO)15Au2{Ph2PCH 2PPh2}. The reaction of the carbido dianion [Ru6C(CO)16]2- with Au2{Ph2PCH2PPh2}Cl2 , in dichloromethane, in the presence of TIPF6, affords the neutral cluster Ru6C(CO)16Au2{Ph2PCH2 PPh2} (1) in 90% yield. An X-ray analysis of 1 shows that the octahedral ruthenium core has remained intact, and that the two Au atoms of the chelating gold phosphine bridge two adjacent edges of one of the triangular faces of the Ru6 octahedron. In marked contrast, the reaction of the non-carbido dianion [Ru6(CO)18] 2- with Au2{Ph2PCH2PPh2}Cl2 under similar reaction conditions leads to the breakdown of the octahedral ruthenium core and the formation of Ru5(CO)15Au2{Ph2PCH2 PPh2} (2) in ca. 50% yield. The X-ray analysis of 2 shows that the ruthenium atoms adopt a trigonal bipyramidal framework with the Au atoms of the Au2{Ph2PCH2PPh2} ligand μ3- capping adjacent faces of the trigonal bipyramid in a manner not previously observed for mixed ruthenium-gold clusters.

Original languageEnglish
Pages (from-to)293-301
Number of pages9
JournalJournal of Organometallic Chemistry
Volume459
Issue number1-2
DOIs
Publication statusPublished - 19 Oct 1993

Funding

We are grateful to Johnson Matthey (M.A.B.) and the S.E.R.C. (P.J.B.) for funding and to the European Economic Communityf or a bursary( M.C.R. de A.).

FundersFunder number
European Economic Communityf
S.E.R.C.

    ASJC Scopus subject areas

    • Biochemistry
    • Physical and Theoretical Chemistry
    • Organic Chemistry
    • Inorganic Chemistry
    • Materials Chemistry

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