Syntheses, Characterization, and Antimicrobial Screening of N‐(benzothiazol‐2‐yl)benzenesulphonamide and its Cu(I), Ni(II), Mn(II), Co(II), and Zn(II) Complexes
N‐(benzothiazol‐2‐yl)benzenesulphonamide (BS2ABT) was synthesized by the condensation (by refluxing) of 2‐aminobenzothiazole and benzenesulphonylchloride in acetone at 140ºC. The resulting crude precipitates were recrystallized from dimethylformamide (DMF). Five metal complexes of copper(I), nickel(...
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Veröffentlicht in: | E-journal of chemistry 2012-01, Vol.9 (4), p.2354-2370 |
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Sprache: | eng |
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Zusammenfassung: | N‐(benzothiazol‐2‐yl)benzenesulphonamide (BS2ABT) was synthesized by the condensation (by refluxing) of 2‐aminobenzothiazole and benzenesulphonylchloride in acetone at 140ºC. The resulting crude precipitates were recrystallized from dimethylformamide (DMF). Five metal complexes of copper(I), nickel(II), manganese(II), cobalt(II) and zinc(II) of the ligands were synthesized. The compounds were characterized using magnetic susceptibility measurements, UV/VIS spectrophotometry, infra red, proton and
13
C nmr spectroscopies. The antimicrobial tests of the ligands and its metal complexes were carried out on both multi‐resistant bacterial strains isolated under clinical conditions and cultured species using agar‐well diffusion method. The multi‐resistant bacterial strains used were
Escherichia coli, Proteus
species,
Pseudomonas aeroginosa and Staphylococcus aureus
which were isolated from dogs. The culture species were
Pseudomonas aeruginosa
(ATCC 27853),
Escherichia Coli
(ATCC 25922)
Staphylococcus aureus
(ATCC 25923), and the fungi,
Candida krusei
(ATCC 6258) and
Candida albicans
(ATCC 90028). The tests were both
in vitro
and
in vivo
. Thus the Inhibition Zone Diameter (IZD), the Minimum Inhibitory Concentration (MIC), and the Lethal and Effective Concentrations (LC
50
and EC
50
) were determined. The antimicrobial activities of the compounds were compared with those of Ciprofloxacin and trimethoprim‐sulphamethoxazole as antibacterial agents and Fluconazole as an antifungal drug. All the compounds showed varying activities against the cultured typed bacteria and fungi used. However, they were less active than the standard drugs used except Fluconazole which did not show any activity against
Candida krusei
(ATCC 6258) but most of the compounds synthesized were very active against it. The Lethal Concentration (LC
50
) ranged from 26.25±4.9‐1833.88±186.92 ppm. These are within the permissible concentrations. |
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ISSN: | 2090-9063 0973-4945 2090-9071 2090-9810 |
DOI: | 10.1155/2012/496541 |