Synthesis and Characterization of Novel Organocobaloximes as Potential Catecholase and Antimicrobial Activity Agents
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Tarih
2013
Dergi Başlığı
Dergi ISSN
Cilt Başlığı
Yayıncı
Wiley-V C H Verlag Gmbh
Erişim Hakkı
info:eu-repo/semantics/openAccess
Özet
An asymmetric, potentially bidentate dioxime ligand (H2L) was formed by condensation of 4-biphenylchloroglyoxime and napthyl-1-amine. Two equivalents of H2L were reacted with CoCl(2)6H(2)O under appropriate conditions with deprotonation of the dioxime ligand. A series of new organocobaloxime derivatives of the type [CoR(HL)(2)Py], [CoRL2PyB2F4], and [CoRL2Py(Cu(phen))(2)] (H2L=4-(napthyl-1-amino)biphenylglyoxime; phen=1,10-phenathroline; R=izopropyl and benzyl; Py=pyridine) were synthesized. The products were characterized by elemental analysis, molar conductance, FT-IR, H-1 NMR, and magnetic susceptibility measurements. Catecholase-like activity properties of all complexes were also studied. All complexes are catalysts for the oxidation of 3,5-di-tert-butylcatechol to 3,5-di-tert-butyl-1,2-benzoquinone in methanol. Antimicrobial activity studies of H2L and the six complexes were carried out on standard strains (human pathogenic) of bacteria (Staphylococcus aureus, methicillin-resistant S. aureus (MRSA), Bacillus cereus, Enterococcus faecalis, Streptococcus pneumoniae, Listeria monocytogenes, Bacillus subtilis, Escherichia coli, Pseudominas aeruginosa, Salmonella typhi) and the yeast Candida albicans. The compounds showed a significant inhibition of the growth of the Gram-positive bacteria tested. Among the tested microorganisms, S. aureus was the most sensitive strain, especially to H2L and its complexes.
Açıklama
Anahtar Kelimeler
Antimicrobial activity, Catecholase activity, Multinuclear, Organocobaloxime
Kaynak
Archiv Der Pharmazie
WoS Q Değeri
Q1
Scopus Q Değeri
Q1
Cilt
346
Sayı
10
