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Original Articles

Oxovanadium(IV) complexes based on S-alkyl-thiosemicarbazidato ligands. Synthesis, characterization, electrochemical, and antioxidant studies

, , , , , & show all
Pages 434-449 | Received 21 Jan 2015, Accepted 08 May 2015, Published online: 12 Jun 2015
 

Abstract

Reaction of VOSO4 with 2-hydroxy-napthaldeyde-S-R-thiosemicarbazones (R: methyl, ethyl, propyl or allyl) and salicyl aldehyde yielded five-coordinate oxovanadium(IV) complexes having a N1,N4-diarylidene-S-R-thiosemicarbazidato structures. The compounds were characterized by elemental analysis, magnetic measurements, electronic, infrared, 1H-NMR, and electron paramagnetic resonance (EPR) spectra. The X-band EPR signals were recorded from powder forms and also in solution. All the complexes have a single asymmetric line shape and theoretical fit studies prove the presence of axial symmetry around the paramagnetic vanadium ions. A computer simulation of the EPR spectrum of each complex was carried out to derive the related EPR parameters. Cyclic voltammograms of the complexes exhibited two metal-based reversible redox peaks around 500 and −800 mV corresponding to one electron oxidation/reduction of VIVO/VVO and VIVO/VIIIO, respectively. The reductive response in the 50–350 mV region was assigned to ligand reduction. Antioxidant activities of the compounds were determined with CUPric Reducing Antioxidant Capacity, 2,2-azino-bis-3-ethylbenzothiazoline-6-sulfonic acid, and 1,1-diphenyl-2-picrylhydrazyl assays. The test results indicated that the antioxidant capacity of the compounds increases with the carbon number of saturated hydrocarbon chain on sulfur atom.

GRAPHICAL ABSTRACT

Acknowledgements

The authors would like to thanks Prof. Yusuf Yerli for providing his laboratory conditions for EPR measurements.

Disclosure statement

No potential conflict of interest was reported by the authors.

Additional information

Funding

This present work was supported by the Research Fund of Istanbul University. Project No. BYP-12264 and BYP-16667.

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