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Synthesis and investigation of mono- and binuclear cyano-bridged complexes of rhodium,ruthenium, and palladium
Authors:A. A. Bezrukova  V. S. Khandkarova  P. V. Petrovskii  A. Z. Rubezhov  Ya. S. Vygodskii  K. P. Butin  T. V. Magdesieva  G. A. Pirogova
Affiliation:(1) A. N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, 28 ul. Vavilova, 117813 Moscow, Russian Federation;(2) Department of Chemistry, M. V. Lomonosov Moscow State University, Vorob'evy Gory, 119899 Moscow, Russian Federation
Abstract:Binuclear RhIII and RuII complexes of the [M1-CN-M2]+BF4 (M1 and/or M2 are (eegr5-Cp)(eegr3-C3H5)Rh and (eegr6-C6H6)(eegr3-C3H5)Ru) type, heteronuclear organometallic compound (eegr5-Cp)(eegr3-C3H5)RhCNPd(eegr3-C3H5)Cl, and mononuclear RhIII and RuII complexes [(eegr3-C3H5)LM(MeCN)]+BF4 (M = Rh, L = eegr5-Cp; M = Ru, L = eegr6-C6H6) were synthesized. An electrochemical study of these compounds in solutions demonstrates that the bond between the bridged CN ligand and the metal atoms is rather strong, and there is no dissociation into mononuclear fragments in solutions. The kinetics of the reaction of [(eegr5-Cp)(eegr3-C3H5)Rh(MeCN)]+BF4 with halide ions was studied by electrochemical methods. The ligand exchange proceeds by a bimolecular dissociative-exchange mechanism.Translated fromIzvestiya Akademii Nauk. Seriya Khimicheskaya, No. 5, pp. 968–973, May, 1995.
Keywords:palladium, rhodium, ruthenium, binuclear complexes, synthesis  cyclopentadienyl, arenes, allyl, cyano-bridged ligands  electrochemistry  1H NMR spectra
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