Abstract
The vibrational (conventional and far infrared), 1H n.m.r. and electronic spectra together with the room temperature magnetic susceptibility and molar conductivity measurements are reported and discussed for the complexes [Ni(PPKTE-H)X]2, [Ni(LPKTE-H)]2X2 and [M(L-H)Cl2.H2O], where L = phenyl-2-picolylketone-hydrazone-S-methyl dithiocarboxylate (PPKTE) or phenyl-2-(2,6-lutidyl)ketone-hydrazone-S-methyl dithiocarboxylate (LPKTE), X = Cl−, Br− or I− and M = Cr3+, Mn3+ or Fe3+. The prementioned data suggest trigonal bipyramidal structure for [Ni(PPKTE-H)X]2, square-planar structure for [Ni(LPKTE-H)]2X2 and octahedral structure for [M(L-H)Cl2.H2O]. The ligating properties of these complexes towards pyridine are also reported. The ligand field parameters for some of these complexes are given and used to interpret the nature of bonding.