Indene in a novel bonding mode in a carbonyl cluster: isolation, characterisation, and crystal and molecular structure of [HOs4(CO)9(C9H6)(C9H7)]

Hong Chen, Mariano Fajardo, Brian F.G. Johnson, Jack Lewis, Paul R. Raithby

Research output: Contribution to journalArticlepeer-review

Abstract

The reaction of [Os3(CO)12] with indene at 150°C under reflux affords the known compounds [H2Os3(CO)9(C9H6)] (2) and [Os4(CO)12(C9H6)] (3). When the reaction temperature is increased to 170°C, the yield of 2 is greatly reduced, and a new tetraosmium cluster [HOs4(CO)9(C9H6)(C9H7)] (1) is isolated. An X-ray diffraction study of 1 has shown that one face of the Os4 tetrahedron is capped by an indyne ligand coordinated in a μ32-- bonding mode, while the indenyl ligand (C9H7) is coordinated to a single Os atom in a η5 bonding mode through the five-membered ring.

Original languageEnglish
Pages (from-to)c16-c18
JournalJournal of Organometallic Chemistry
Volume389
Issue number1
DOIs
Publication statusPublished - 5 Jun 1990

Funding

Acknowledgements. We thank the Sino-British Friendship Scholarship Scheme for financial support (H.C.), the Comunidad Autonoma de Madrid for a grant and the Universidad de Alcala de Henares (Spain) for study leave (M-F.).

FundersFunder number
Universidad de Alcala de Henares
Comunidad Autónoma de Madrid

    ASJC Scopus subject areas

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

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