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Synthesis, characterization, electrochemical studies, and antibacterial activities of cobalt(III) complexes with Salpn-Tipe Schiff base ligands. Crystal structure of trans-[CoIII(L1)(Py)2]ClO4

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Abstract

The synthesis, characterization, spectroscopic and electrochemical properties of trans-[CoIII(L1)(Py)2]ClO4 (I) and trans-[CoIII(L2)(Py)2]ClO4 (II) complexes, where H2L1 = N,N′-bis(5-chloro-2-hydroxybenzylidene)-1,3-propylenediamine and H2L2 = N,N′-bis(5-bromo-2-hydroxybenzylidene)-1,3-propylenediamine, have been investigated. Both complexes have been characterized by elemental analysis, FT-IR, UV-Vis, and 1H NMR spectroscopy. The crystal structure of I has been determined by X-ray diffraction. The coordination geometry around cobalt(III) ion is best described as a distorted octahedron. The electrochemical studies of these complexes revealed that the first reduction process corresponding to Co(III/II) is electrochemically irreversible accompanied by dissociation of the axial Co-N(Py) bonds. The in vitro antimicrobial activity of the Schiff bse ligands and their corrsponding complexes have been tested against human pathogenic bacterias such as Staphylococcus aureus, Bacillus subtilis, Pseudomonas aeruginosa, and Escherichia coli. The cobalt(III) complexes showed lower antimicrobial activity than the free Schiff base ligands.

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Salehi, M., Kubicki, M., Dutkiewicz, G. et al. Synthesis, characterization, electrochemical studies, and antibacterial activities of cobalt(III) complexes with Salpn-Tipe Schiff base ligands. Crystal structure of trans-[CoIII(L1)(Py)2]ClO4 . Russ J Coord Chem 39, 716–722 (2013). https://doi.org/10.1134/S1070328413100084

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  • DOI: https://doi.org/10.1134/S1070328413100084

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