4.7 Article

Structural, spectral studies and antimicrobial activity of Zinc(II), Cadmium (II) and Nickel(II) complexes of 2-acetylbenzothiophene-3-thiosemicarba-zone and 2-acetylbenzothiophene-4-ethyl-3-thiosemicarbazone

Journal

INORGANIC CHEMISTRY COMMUNICATIONS
Volume 146, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.inoche.2022.110138

Keywords

Thiosemicarbazone complexes; Zinc(II); Cadmium(II); Nickel(II); Crystal structure; Antimicrobial

Funding

  1. Ministry of Higher Education Malaysia [UKM-ST-01-FRGS0022-2006, UKM-GUP-NBT-08-27-112]

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Zn(II), Cd(II) and Ni(II) complexes of 2-acetylbenzothiophene-3-thiosemicarbazone and 2-acetylbenzothio-phene-4-ethyl-3-thiosemicarbazone have been synthesized and characterized. The electronic structures of the ligands and complexes were studied using density functional theory. The Cd complexes showed strong inhibitory actions against certain bacteria, while the Ni complex showed strong activity against Staphylococcus aureus.
Zn(II), Cd(II) and Ni(II) complexes of 2-acetylbenzothiophene-3-thiosemicarbazone (HL1) and 2-acetylbenzothio-phene-4-ethyl-3-thiosemicarbazone (HL2) have been prepared. The new complexes [Zn(L1)2] (1), [Cd(L1)2] (2), [Ni(L1)2]0.0.5CH3CN (3), [Zn(L2)2] (4), [Cd(L2)2] (5) and [Ni(L2)2] (6) have been characterized by elemental analysis and spectroscopic methods. The crystal structures of 1, 3 and 4 are also reported. Density functional theory (DFT) computations have been conducted to study electronic structures of the ligands and complexes. The spectroscopic results obtained for the complexes indicated that the ligands coordinate in the thiole form and the X-ray crystal structures confirm the spectroscopic data. The crystal structures show that the ligands coordinate to the metal centers as a bidentate N, S-donors. The coordination geometry of the zinc complexes is distorted tetrahedral while that of the nickel complex is distorted square planar. In vitro tests of antibacterial activity show that the Cd complexes 2 and 5 have strong inhibitory actions, compared to Tobramycin, against G(+) Bacillus subtilis, while the Ni complex 3 showed strong activity against G(+) Staphylococcus aureus. In comparison to Nystatin, the cadmium complexes show strong activity against Aspergillus fumigatus and complexes 2 and 3 were effective against Aspergillus niger.

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