Os3(CO)9{μ3-η1-η1-η2-η2-C(SiMe3)C(Me)C(H)C(Fc)}, the second example of a cluster with the “face” coordination of the metallacyclopentadiene fragment and its conversion to the Os3(μ-H)(CO)8{μ3-η1-η1-η4-η1-C(SiMe3)C(Me)C(H)C(C5H3FeC5H5)} complex with theortho-metallated ferrocene moiety |
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| Authors: | A A Koridze A M Skeloumov F M Dolguskin A I Yanovsky Yu T Struckkov P V Petrovskii |
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| Institution: | 1. A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, 28 ul. Vavilova, 117813, Moscow, Russian Federation
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| Abstract: | Os3(μ-CO)(CO)9(μ3-Me3SiC2Me) alkyne complexes react with ferrocenylacetylene in hot benzene to form Os3(CO)9{μ3-η1-η1-η2-η2-C(SiMe3)C(Me)C(H)C(Fe)} and a small amount of the isomeric Os3(CO)9(μ-η1-η1-η4-C(SiMe3)C(Me)C(Fc)C(H)} complex. The structure of the major isomer was confirmed by X-ray structural analysis of the single crystal. Thermolysis of this complex in refluxing benzene affords the Os3(μ-H)(CO)8{μ3-η1-η1-η4-η1-C(SiMe3)C(Me)C(H)(C5H3FeC5H5)} complex with theortho-metallated ferrocene moiety. The spectral characteristics of clusters with the μ3-η1-η1-η2-η2 and μ-η1-η1-η4 coordinations of the metallacyclopentadiene fragment have been established, which made it possible to choose between the alternative modes of bonding of diene with the trimetallic core. |
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