Orbital - Vol. 7 No. 2 - April-June 2015
FULL PAPERS

Synthesis, Characterization and Biological Evaluation of Mononuclear Dichloro-bis[2-(2-chloro-6,7-substituted Quinolin-3-yl)-1H-benzo[d]imidazole]Co(II) Complexes

Minaxi S. Maru
Lab. No. 302, Discipline of Inorganic Materials and Catalysis, Central Salt and Marine Chemicals Research Institute, G. B. Marg, Waghawadi Road, Bhavnagar-364002, Gujarat, INDIA
Manish K. Shah
Department of Chemistry, Saurashtra University
Published June 25, 2015
Keywords
  • Co(II) complexes,
  • 1H-benzo[d]imidazoles,
  • antimicrobial activity,
  • antimycobacterial activity
How to Cite
(1)
Maru, M. S.; Shah, M. K. Synthesis, Characterization and Biological Evaluation of Mononuclear Dichloro-bis[2-(2-Chloro-6,7-Substituted Quinolin-3-Yl)-1H-benzo[d]imidazole]Co(II) Complexes. Orbital: Electron. J. Chem. 2015, 7, 108-121.

Abstract

A series of Co(II) complexes 3¢a-g of 2-(2-chloro-6,7-substituted quinolin-3-yl)-1H-benzo[d]imidazole ligands 3a-g were prepared and characterized by various spectroscopic and physico-chemical methods viz. FT-IR, ESI mass, 1H NMR, 13C NMR and UV-Visible spectroscopy, Thermogravimetric analysis, Magnetic susceptibility, Molar conductance and Elemental analysis. The 2-(2-chloro-6,7-substituted quinolin-3-yl)-1H-benzo[d]imidazole ligands 3a-g have been synthesized by cyclocondensation of benzene-1,2-diamine with 2-chloroquinoline-3-carbaldehydes by using ceric ammonium nitrate as a catalyst in presence of hydrogen peroxide as an oxidant. The structures of all ligands were confirmed by IR, Mass, UV-Visible, 1H NMR and 13C NMR spectroscopy. All ligands 3a-g and their Co(II) complexes 3¢a-g were screened for their in vitro antimicrobial activity using twofold serial dilution technique against standard MTCC strains of two Gram-positive Staphylococcus aureus and Streptococcus pyogenes, two Gram-negative Escherichia coli and Pseudomonas aeruginosa bacteria and three Candida albicansAspergillus niger and Aspergillus clavatus fungus in comparison with standard drugs. All ligands 3a-g and complexes 3¢a-g also evaluated for antimycobacterial activity against standard Mycobacterium tuberculosis H37Rv strain.

DOI: http://dx.doi.org/10.17807/orbital.v7i2.530