In this study, the salt (3) of 2-amino-5-chloropyridine (1) and 2,6-pyridinedicarboxylic acid (2) and the complexes of the salt (H1)x[M(2)2].nH2O, M = Fe (III), x = 1, n = 3 (4); M = Co(II), x = 2, n = 4 (5); M = Ni(II), x = 2, n = 5 (6); M = Cu(II), x = 2, n = 4 (7)} were synthesized. The structures of 3-7 were suggested by NMR, AAS, IR, UV, magnetic susceptibility and molar conductivity methods. As a result of spectroscopic analysis, it was observed that all metal complexes had an ionic and octahedral structure. All substances were susceptible to Candida albicans (yeast), Escherichia coli, Bacillus subtilis, Enterococcus faecalis, Pseudomonas aeruginosa, Listeria monocytogenes and Staphylococcus aureus bacteria were examined. Antimicrobial activity results were compared with Fluconazole, Ketoconazole, Chloramphenicol, Levofloxacin, Vancomycin and Cefepime. In the activity results, the best values were observed 3, 5 and 7 in S. aureus bacteria, 1 and 5 in E. coli bacteria, 1, 3 and 7 in P. aeruginoa bacteria, all compounds in L. monocytogenes bacteria, all compounds (except 4) in E. faecalis bacteria, 1 and 3-5 in B. subtilis bacteria and 3, 4 and 7 in C. albicans yeast.
2-Amino-5-chloropyridine 2,6-pyridinedicarboxylic acid salt metal complex antimicrobial activity.
Primary Language | English |
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Subjects | Transition Metal Chemistry |
Journal Section | Research Articles |
Authors | |
Publication Date | June 30, 2024 |
Submission Date | April 17, 2024 |
Acceptance Date | May 21, 2024 |
Published in Issue | Year 2024 |