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Palladium(II) complexes obtained from 3,4-bis(cyanamido)cyclobutane-1,2-dione dianion
Authors:Olivier Cortadellas  Brigitte Soula  Paul-Louis Fabre
Affiliation:a Laboratoire de Chimie Inorganique, EA 807, Université Paul Sabatier, 118 route de Narbonne, 31062 Toulouse, France
b Laboratoire de Chimie de Coordination, UPR CNRS 8241, 205 route de Narbonne, 31077 Toulouse, France
Abstract:Three palladium(II) complexes have been synthesized, using 3,4-bis(cyanamido) cyclobutane-1,2-dione dianion (3,4-bis(cyanamido)squarate or 3,4-NCNsq2−): [Pd(en)(3,4-NCNsq)] · 1.5H2O (1) (en=1,2-diaminoethane), [Pd(en)(3,4-(NC(O)NH2)sq)] · 0.5H2O (2) and K3Na[Pd2(3,4-(NCN)2sq)4] · 5H2O (3). Complex 1 has been characterized by elemental analysis, IR and 13C NMR spectroscopies. Complexes 2 and 3 have been characterized by single-crystal X-ray diffraction. In complex 2, the unusual hydration of the cyanamido ligand was observed, it proceeds in the coordination sphere of the palladium and leads to a chelating urea squarate ligand. Complex 3 is an anionic dinuclear complex containing four bridging cyanamido squarate ligands. In complexes 2 and 3, the 3,4-NCNsq2− ligand (hydrated or not) is, for the first time, coordinated to the metal atom by the two amido nitrogen atoms, either in a chelating mode (complex 2) or in a bridging mode giving a short Pd ? Pd distance of 2.8866(15) Å (complex 3). Electrochemical studies in acetonitrile and dmf solutions have been performed on complexes 1 and 3.
Keywords:Pseudo-oxocarbons   Cyanamido squarate   X-ray diffraction   Palladium(II) complexes   Hydration of nitriles   Electrochemistry
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