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New heteroleptic Cu(II) complexes of chrysin with 2,2-bipyridine and substituted 1,10-phenanthrolines: synthesis, characterization, thermal stability and antioxidant activity

dc.contributor.buuauthorGençkal, Hasene Mutlu
dc.contributor.departmentFen Edebiyat Fakültesi
dc.contributor.departmentKimya Bölümü
dc.contributor.orcid0000-0002-0026-7755
dc.contributor.researcheridAAH-2888-2021
dc.contributor.scopusid57212275330
dc.date.accessioned2023-10-09T11:10:11Z
dc.date.available2023-10-09T11:10:11Z
dc.date.issued2020-06-05
dc.description.abstractIn this study, the new heteroleptic Cu(II) complexes of chrysin were synthesized by using 2,2ꞌ–bipyridine and substituted 1,10–phenanthroline (1,10–phenanthroline, 4,7–dimethyl–1,10–phenanthroline or bathophenanthroline) co–ligands. The characterization of the obtained heteroleptic Cu(II) complexes were carried out by elemental analysis, ESI–MS, UV–visible and infrared spectral analyses, thermal analysis, magnetic susceptibility and molar conductivity measurements. In these complexes, chrysin, 2,2ꞌ–bipyridine, or substituted 1,10–phenanthrolines and Cu(II) ion were found in a ratio of 1: 1: 1. In addition, the resulting data supported square plane geometry for Cu(II) complexes. According to the results obtained, the proposed compositions are as follows: [Cu(chrH–1)(bpy)]ClO4·H2O (1, chrH = chrysin, bpy = 2,2′–bipyridine), [Cu(chrH–1)(phen)]ClO4.1.5H2O (2, phen = 1,10–phenanthroline), [Cu(chrH–1)(dmphen)]ClO4 (3, dmphen = 4,7–dimethyl–1,10–phenanthroline) and [Cu(chrH–1)(Bphen)]ClO4 (4, Bphen = Bathophenanthroline). Total phenolic contents and antioxidant capacities of Complexes 1–4 were measured by the Folin–Ciocalteu and ABTS (2,2′–azino–bis (3–ethylbenzothiazoline–6–sulfonic acid)) methods, respectively. According to the results, Complex 4 has the highest antioxidant capacity.
dc.identifier.citationGençkal H. M. (2020). "New heteroleptic Cu(II) complexes of chrysin with 2,2-bipyridine and substituted 1,10-phenanthrolines: synthesis, characterization, thermal stability and antioxidant activity". Journal of Molecular Structure,1209.
dc.identifier.doi10.1016/j.molstruc.2020.127917
dc.identifier.issn00222860
dc.identifier.issn1872-8014
dc.identifier.scopus2-s2.0-85080069585
dc.identifier.urihttps://doi.org/10.1016/j.molstruc.2020.127917
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S0022286020302416
dc.identifier.urihttp://hdl.handle.net/11452/34260
dc.identifier.volume1209
dc.identifier.wos000522727600028
dc.indexed.wosSCIE
dc.language.isoen
dc.publisherElsevier
dc.relation.journalJournal of Molecular Structure
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi
dc.rightsinfo:eu-repo/semantics/closedAccess
dc.subjectAntioxidants
dc.subjectFlavonoids
dc.subjectMagnetic susceptibility
dc.subjectSpectrum analysis
dc.subjectSynthesis (chemical)
dc.subjectThermoanalysis
dc.subjectBathophenanthroline
dc.subjectBipyridines
dc.subjectChrysin
dc.subjectCu complexes
dc.subjectPhenanthrolines
dc.subjectCopper compounds
dc.subjectChemistry
dc.subjectCu(II) complexes
dc.subjectChrysin
dc.subjectBathophenanthroline
dc.subject4,7-dimethyl-1,10-phenanthroline
dc.subject2,2-bipyridine
dc.subject1,10-phenanthroline
dc.subjectAntitumor activities
dc.subjectPhysicochemical properties
dc.subjectCopper(II) complexes
dc.subjectMetal complexes
dc.subjectII complexes
dc.subjectQuercetin
dc.subjectZN(II)
dc.subjectDNA
dc.subject2,2'-Bipyridine
dc.subjectFlavonoids
dc.subject.scopusTaxifolin; Morin; Complex
dc.subject.wosChemistry, physical
dc.titleNew heteroleptic Cu(II) complexes of chrysin with 2,2-bipyridine and substituted 1,10-phenanthrolines: synthesis, characterization, thermal stability and antioxidant activity
dc.typeArticle
dc.wos.quartileQ3
dspace.entity.typePublication
local.contributor.departmentFen Edebiyat Fakültesi/Kimya Bölümü
local.indexed.atScopus
local.indexed.atWOS

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