Raju Nandhakumar - Academia.edu (original) (raw)

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Papers by Raju Nandhakumar

Research paper thumbnail of Synthesis, structure and in vitro biological activity of pyridoxal N(4)-substituted thiosemicarbazone cobalt(III) complexes

Cobalt(III) complexes containing pyridoxal N(4)-substituted thiosemicarbazone ligands with the co... more Cobalt(III) complexes containing pyridoxal N(4)-substituted thiosemicarbazone ligands with the composition [Co(HL 1À2 ÁCl)(HL 1À2 ÁH 2 O)] (1–2) have been synthesized from the reaction of [CoCl 2 (PPh 3) 2 ] and pyridoxal N-methyl-thiosemicarbazone hydrochloride (H 3 L 1 ÁCl)/pyridoxal N-phenyl-thiosemicarbazone hydrochloride (H 3 L 2 ÁCl). The richness of the coordination chemistry of this ligand is highlighted by the modulation of its charge from neutral (H 3 LÁCl) (L) to dianionic (HLÁCl) (L 2À) and monoanionic forms (HLÁH 2 O) (L À) and coordinated as tridentate binegative mode around cobalt(III) ion by forming neutral complex. The new complexes were characterized by various analytical and spectroscopic techniques (IR, electronic, 1 H NMR and ESI-Mass). The X-ray crystal structure of the complex 2, demonstrated distorted octahedral coordination geometry around the metal centre. Further, the investigation of effect of substitution (CH 3 or C 6 H 5) on terminal N(4)-nitrogen of thiosemicarbazone exhibited its influence on the potential binding and cleavage ability with DNA, BSA binding, free radical scavenging and cytotoxicity.

Research paper thumbnail of Synthesis, structure and in vitro biological activity of pyridoxal N(4)-substituted thiosemicarbazone cobalt(III) complexes

Cobalt(III) complexes containing pyridoxal N(4)-substituted thiosemicarbazone ligands with the co... more Cobalt(III) complexes containing pyridoxal N(4)-substituted thiosemicarbazone ligands with the composition [Co(HL 1À2 ÁCl)(HL 1À2 ÁH 2 O)] (1–2) have been synthesized from the reaction of [CoCl 2 (PPh 3) 2 ] and pyridoxal N-methyl-thiosemicarbazone hydrochloride (H 3 L 1 ÁCl)/pyridoxal N-phenyl-thiosemicarbazone hydrochloride (H 3 L 2 ÁCl). The richness of the coordination chemistry of this ligand is highlighted by the modulation of its charge from neutral (H 3 LÁCl) (L) to dianionic (HLÁCl) (L 2À) and monoanionic forms (HLÁH 2 O) (L À) and coordinated as tridentate binegative mode around cobalt(III) ion by forming neutral complex. The new complexes were characterized by various analytical and spectroscopic techniques (IR, electronic, 1 H NMR and ESI-Mass). The X-ray crystal structure of the complex 2, demonstrated distorted octahedral coordination geometry around the metal centre. Further, the investigation of effect of substitution (CH 3 or C 6 H 5) on terminal N(4)-nitrogen of thiosemicarbazone exhibited its influence on the potential binding and cleavage ability with DNA, BSA binding, free radical scavenging and cytotoxicity.

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