摘要：

New nickel(II) complexes of general formula, [Ni(NNS)] (NNS= uninegatively charged tridentate ligands formed by condensation of 6-methyl-2-formylpyridine with S-methyl- and S-benzyldithiocarbazates) have been prepared and characterized by a variety of physico-chemical techniques. Magnetic and spectroscopic evidence support a distorted octahedral structure for these complexes. The crystal and molecular structure of the bis{S-methyl- -N-(6-methylpyrid-2-yl)methylenedithiocarbazato}nickel(II) complex has been determined by X-ray diffraction studies. The complex has a distorted octahedral structure with the ligands coordinated to the nickel(II) ion as uninegatively charged tridentate chelating agents via the pyridine nitrogen, the azomethine nitrogen and the mercaptide sulphur atoms. The distortion from the regular octahedral geometry is ascribed to the stereochemical limitations imposed by the planar tridentate ligands.

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