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Spectrochim Acta A Mol Biomol Spectrosc ; 133: 568-78, 2014 Dec 10.
Article in English | MEDLINE | ID: mdl-24992916

ABSTRACT

Schiff base complexes of Mn(II), Co(II), Ni(II), Cu(II), Cd(II), Hg(II) and U(VI)O2 with (E)-2-(1-(4-hydroxyphenyl)ethylidene)-N-(pyridin-2-yl)hydrazinecarbothioamide (H2PHAT) were synthesized and characterized by different physicochemical methods, elemental analysis, (UV-vis, IR and (1)H NMR spectra) and thermal analysis (TG and DTG) techniques. Spectral data showed that H2PHAT behaves as a NS bidentate ligand through both thione sulphur or thiol sulphur and the nitrogen of the pyridine ring or azomethine nitrogen, NSN tridentate ligand through both thione sulphur or thiol sulphur, the nitrogen of the pyridine ring and azomethine nitrogen. ESR spectrum data for Cu(II) solid complex confirms the square planar state is the most fitted one for the coordinated structure. The kinetic parameters were determined for each thermal degradation stage of the complexes using Coats-Redfern and Horowitz-Metzger methods. From modeling studies, the bond length, bond angle, HOMO, LUMO and dipole moment had been calculated to confirm the geometry of the ligand and their investigated complexes. The biological activity was tested against DNA showing that Cd(II), U(VI)O2, Ni(II) and Mn(II) complexes had powerful and complete degradation effect. Also, the ligand and its complexes were screened against Bacillus thuringiensis as Gram-positive bacteria and Pseudomonas aeuroginosa as Gram-negative bacteria using the inhibitory zone diameter.


Subject(s)
Anti-Bacterial Agents/chemistry , Coordination Complexes/chemistry , Thiosemicarbazones/chemistry , Anti-Bacterial Agents/chemical synthesis , Anti-Bacterial Agents/pharmacology , Bacteria/drug effects , Bacterial Infections/drug therapy , Coordination Complexes/chemical synthesis , Coordination Complexes/pharmacology , Differential Thermal Analysis , Humans , Metals, Heavy/chemical synthesis , Metals, Heavy/chemistry , Metals, Heavy/pharmacology , Models, Molecular , Spectrum Analysis , Thermogravimetry , Thiosemicarbazones/chemical synthesis , Thiosemicarbazones/pharmacology
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