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 μ3-η2-- 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 language | English |
---|---|
Pages (from-to) | c16-c18 |
Journal | Journal of Organometallic Chemistry |
Volume | 389 |
Issue number | 1 |
DOIs | |
Publication status | Published - 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.).
Funders | Funder 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