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Nickel(II) complexes of a thiosemicarbazone prepared from 2-Acetylpyridine
Authors:West  Douglas X  Scovill  John P  Silverton  J V  Bavoso  Alfonso
Institution:(1) Department of Chemistry, Illinois State University, 61761 Normal, IL, USA;(2) Division of Experimental Therapeutics, Walter Reed Army Institute of Research, 20307 Washington, DC;(3) Laboratory of Chemistry, National Heart, Lung, and Blood Institute, National Institutes of Health, 20892 Bethesda, MD;(4) Present address: Departimento di Chimica, Universita di Napoli, via Mezzocannone 4, 80134 Naples, Italy
Abstract:Summary The ligand 3-azabicyclo3.2.2]nonane-3-thiocarboxylic acid 2-1-(2-pyridinyl)ethylidene]hydrazide (HL), which is observed in an unusual tautomeric form in the solid state, and its selenium analogue (HLSe) have been used to prepare a series of nickel(II) complexes. Compounds of the general formula NiLX] (X=Cl, Br, NCS, N3, NO2 or NCSe) as well as Ni(LSe)Cl] have been found to be diamagnetic, planar complexes. A single crystal study of NiL(NCS)] shows the deprotonated ligand bound in a tridentate mannervia its pyridyl nitrogen, imine nitrogen and the thione sulphur atom with the nitrogen atom of the thiocyanato-ligand occupying the fourth coordination position. The solids prepared from the nickel(II) salts having tetrafluoroborate, nitrate and iodide ions approximate to octahedral symmetry and have neutral HL ligands coordinated in a bidentate fashionvia the pyridine and imine nitrogens with the remaining coordination sites being occupied by the anions or water molecules. The NiL2] solid is also octahedral with the two deprotonated ligands bonding as tridentate groupsvia the same atoms as in the NiLX] complexes.
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