Synthesis, spectral characterization, in vitro antibacterial, antifungal and cytotoxic activities of Co(II), Ni(II) and Cu(II) complexes with 1,2,4-triazole Schiff bases
A series of metal complexes of cobalt(II), nickel(II) and copper(II) have been synthesized with newly synthesized biologically active 1,2,4-triazole Schiff bases derived from the condensation of 3-substituted-4-amino-5-mercapto-1,2,4-triazole and 8-formyl-7-hydroxy-4-methylcoumarin, which have been...
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Veröffentlicht in: | European journal of medicinal chemistry 2008-12, Vol.43 (12), p.2639-2649 |
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Sprache: | eng |
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Zusammenfassung: | A series of metal complexes of cobalt(II), nickel(II) and copper(II) have been synthesized with newly synthesized biologically active 1,2,4-triazole Schiff bases derived from the condensation of 3-substituted-4-amino-5-mercapto-1,2,4-triazole and 8-formyl-7-hydroxy-4-methylcoumarin, which have been characterized by elemental analyses, spectroscopic measurements (IR, UV–vis, fluorescence, ESR), magnetic measurements and thermal studies. Electrochemical study of the complexes is also reported. All the complexes are soluble to limited extent in common organic solvents but soluble to larger extent in DMF and DMSO and are non-electrolytes in DMF and DMSO. All these Schiff bases and their complexes have also been screened for their antibacterial (
Escherichia coli,
Staphylococcus aureus,
Streptococcus pyogenes,
Pseudomonas aeruginosa and
Salmonella typhi) and antifungal activities (
Aspergillus niger,
Aspergillus flavus and
Cladosporium) by MIC method. The brine shrimp bioassay was also carried out to study their in vitro cytotoxic properties.
[Display omitted] A series of Co(II), Ni(II) and Cu(II) complexes have been synthesized with 3-substituted-4-amino(8-formyl-7-hydroxy-4-methylcoumarin)-5-mercapto-1,2,4-triazole Schiff bases. The octahedral structures of the Co(II), Ni(II) and Cu(II) complexes have been proposed on the basis of various physico-chemical techniques. All these ligands and their complexes have been screened for their in vitro antibacterial (
Escherichia coli,
Staphylococcus aureus,
Streptococcus pyogenes,
Pseudomonas aeruginosa and
Salmonella typhi), antifungal (
Aspergillus niger,
Aspergillus flavus and
Cladosporium) and cytotoxic activities. |
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ISSN: | 0223-5234 1768-3254 |
DOI: | 10.1016/j.ejmech.2008.02.013 |