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Synthesis and characterization of the [Ru(η5-C5Me4CF3)(CO)2]2 and Ru6(μ3-H)(η2-μ4-CO)2(μ-CO)(CO)12(η5-C5Me4CF3) complexes
Authors:Z. A. Kerzina  M. I. Rybinskaya  F. M. Dolgushin  A. I. Yanovsky  P. V. Petrovskii  E. Kolehmainen
Affiliation:(1) A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, 28 ul. Vavilova, 117813 Moscow, Russian Federation;(2) Department of Chemistry, University of Jyvaskyla, P.O. Box 35 FIN-40351, Jyvaskula, Finland
Abstract:The reaction of Ru3(CO)12 with tetramethyltrifluoromethylcyclopentadiene at various ratios of the reagents was studied. Refluxing of Ru3(CO)12 with a sixfold excess of tetramethyltrifluoromethylcyclopentadiene in octane in an inert atmosphere gave a complex, which is, according to X-ray diffraction data, a dimer,trans-[Ru(η5-C5Me4CF3)(CO)2]2. The reaction under the same conditions but starting from Ru3(CO)12 and C5Me4CF3H in 2∶1 molar ratio gave a hexaruthenium cluster [Ru63-H)(η24-CO)2(μ-CO)(Co)125-C5Me4CF2)], which was characterized by IR as well as1H,13C, and19F NMR spectroscopy. According to X-ray diffraction data, an Ru4 tetrahedron, in which two edges are bound by additional “briding” Ru atoms, constitutes the frame of this compound. This complex has one (η5-C5Me4CF3) ligand, as well as one (μ3-H) and two (η24-CO) groups. Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 3, pp. 507–512, March, 1998.
Keywords:hexaruthenium cluster  pentamethylcyclopentadiene  tetramethyltrifluoromethylcyclopentadiene  synthesis  X-ray diffraction study  IR spectra   1H   13C  and19F NMR spectra
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