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Tert-butylbenzamidate diruthenium(II, III) compounds. Crystal structure of [Ru2(μ-HNOCC6H4-p-CMe3)4(OPPh3)2]BF4
Authors:M.C. Barral, R. Jim  nez-Aparicio, J.L. Priego, E.C. Royer, F.A. Urbanos, A. Monge,C. Ruí  z-Valero
Affiliation:

Departamento de Química Inorgánica, Facultad de Ciencias Químicas, Universidad Complutense, Ciudad Universitaria, 28040 Madrid, Spain

Instituto de Ciencias de los Materiales, sede D, C.S.I.C., Serrano 113, 28006 Madrid, Spain

Laboratorio de Rayos X, Facultad de Ciencias Químicas, Universidad Complutense, Ciudad Universitaria, 28040 Madrid, Spain

Abstract:The reaction between Ru2Cl(μ-O2CCH3)4 and molten p-tert-butylbenzamide led to the formation of Ru2Cl(μ-HNOCC6H4-p-CMe3)4. The polymeric structure of this insoluble compound was broken with AgBF4, in anhydrous thf, giving [Ru2(μ-HNOCC6 H4-p-CMe3)4(thf)2]BF4. The reaction of this cationic complex with OPPh3 gave [Ru2(μ-HNOCC6H4-p-CMe3)4(OPPh3)2]BF4. The compounds have been characterized by elemental analysis, spectroscopic data and magnetic measurements and the crystal structure of [Ru2(μ-HNOCC6H4-p-CMe3)4(OPPh3)2]BF4 was determined by X-ray crystallography. The asymmetric unit is composed of halves of two different crystallographically independent centrosymmetric cations. Each ruthenium(II,III) dimer is bonded to four bridging p-tert-butylbenzamidate ligands and to two axial triphenylphosphine oxide molecules. The Ru---Ru distances in the two dimeric cations of the unit cell are 2.281(2) and 2.280(2) Å. The compound has a non-polar 2 : 2 arrangement of the tert-butylbenzamidate ligands.
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