Mono and dinuclear copper(II) naproxenato complexes containing 3-picoline and 4-picoline: Synthesis, structure, properties, catechol oxidase, and antimicrobial activities

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Mononuclear and dinuclear copper(II) complexes [Cu2(-nap) 4(3-pic)2] (1) and [Cu(nap)2(H 2O)(4-pic)2] (2) have been synthesized in the presence of 3-picoline and 4-picoline. Two complexes were characterized by FT-IR, UV-vis spectroscopic methods and their thermal stabilities were determined by TG/DTA/DTG techniques. The crystal structures of 1 and 2 were established by X-ray analysis. X-ray structure analysis has shown that copper(II) has a distorted square-pyramidal geometry. Naproxenate is a bridging ligand in 1 and monodentate in 2. Two complexes have shown catalytic activity on oxidation of 3,5-di-tert-butylcatechol to 3,5-di-tert-butylquinone exhibiting saturation kinetics at high substrate concentrations. The complexes were also screened for antimicrobial activity against pathogenic bacteria and fungi. The complexes exhibited antimicrobial activity against Entrococcus faecalis and Candida albicans. © 2014 Taylor & Francis.

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AlanDeğerDil
dc.contributor.authorCaglar, Sema
dc.contributor.authorAdiguzel, Ekrem
dc.contributor.authorSariboga, Bahtiyar
dc.contributor.authorTemel, Ersin
dc.contributor.authorBuyukgungor, Orhan
dc.date.accessioned2026-10-18T20:30:24.891740466Z
dc.date.available2026-10-18T20:30:24.891740466Z
dc.date.issued2014
dc.description.abstractMononuclear and dinuclear copper(II) complexes [Cu2(-nap) 4(3-pic)2] (1) and [Cu(nap)2(H 2O)(4-pic)2] (2) have been synthesized in the presence of 3-picoline and 4-picoline. Two complexes were characterized by FT-IR, UV-vis spectroscopic methods and their thermal stabilities were determined by TG/DTA/DTG techniques. The crystal structures of 1 and 2 were established by X-ray analysis. X-ray structure analysis has shown that copper(II) has a distorted square-pyramidal geometry. Naproxenate is a bridging ligand in 1 and monodentate in 2. Two complexes have shown catalytic activity on oxidation of 3,5-di-tert-butylcatechol to 3,5-di-tert-butylquinone exhibiting saturation kinetics at high substrate concentrations. The complexes were also screened for antimicrobial activity against pathogenic bacteria and fungi. The complexes exhibited antimicrobial activity against Entrococcus faecalis and Candida albicans. © 2014 Taylor & Francis.
dc.description.sponsorshipThis work was financially supported by the Erzincan University under project no. 110205.
dc.identifier.doi10.1080/00958972.2014.891198
dc.identifier.eissn1029-0389
dc.identifier.endpage683
dc.identifier.issn0095-8972
dc.identifier.issue4
dc.identifier.scopus2-s2.0-84899047985
dc.identifier.startpage670
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/15559
dc.identifier.volume67
dc.identifier.wosWOS:000333954500010
dc.language.isoen
dc.publisherTaylor and Francis Ltd.
dc.relation.ispartofJournal of Coordination Chemistry
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectAntimicrobial activity
dc.subjectCatechol oxidation
dc.subjectCopper(II) complex
dc.subjectNaproxen
dc.titleMono and dinuclear copper(II) naproxenato complexes containing 3-picoline and 4-picoline: Synthesis, structure, properties, catechol oxidase, and antimicrobial activities
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus19
rdl.citation.wos20
rdl.oa.statusgreen
rdl.source.indexSCOPUS
rdl.source.indexWOS
rdl.wos.indexScience Citation Index Expanded (SCI-EXPANDED)