| Abstract: | The neutral complex TcOCl(hdc)] (1) (hdc?=?S-methyl-β-N-(2-hydroxyphenylethylidene)dithiocarbazate) was prepared by reaction of (n-Bu4N)TcOCl4] with an equimolar amount of H2hdc in ethanol/dichloromethane at room temperature. With a fourfold mol excess of H2hdc in methanol/acetone, the ‘3?+?2’ complex TcO(hdc)(adc)] (2) (adc?=?S-methyl-β-N-(prop-2-ylidene)dithiocarbazate) was isolated. Adc was formed by ketone exchange between solvent acetone and the hydroxyacetophenone fragment of hdc. Compounds 1 and 2 were characterized by infrared spectroscopy, 1H NMR spectrometry, elemental analysis and single-crystal X-ray crystallography. Complex 1 has square-pyramidal geometry with the SNO-donor atoms of the tridentate chelate hdc and chloride forming a square plane, with the oxo oxygen atom in the apical position. Complex 2 has a distorted octahedral geometry, with an S2N2 donor set in the equatorial plane and the oxo and phenolate oxygen atoms in trans apical positions. |
