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dc.contributor.authorGÜVELİ, Şükriye
dc.date.accessioned2021-03-04T12:45:11Z
dc.date.available2021-03-04T12:45:11Z
dc.date.issued2020
dc.identifier.citationGÜVELİ Ş., "Nickel(II)-PPh3 complexes of substituted benzophenone thiosemicarbazones: Electrochemistry, structural analysis, and antioxidant properties", JOURNAL OF COORDINATION CHEMISTRY, cilt.73, sa.1, ss.137-153, 2020
dc.identifier.issn0095-8972
dc.identifier.otherav_78e62a67-3dab-4a6e-a8a9-a0673ca259fe
dc.identifier.othervv_1032021
dc.identifier.urihttp://hdl.handle.net/20.500.12627/82900
dc.identifier.urihttps://doi.org/10.1080/00958972.2020.1711888
dc.description.abstractNew mixed ligand complexes of nickel(II) were synthesized by using dibasic H/5-bromo-/5-chloro-/4-hydroxy-2-hydroxybenzophenone-thiosemicarbazones (L1-4H2) and [Ni(PPh3)(2)Cl-2]. The ligands and complexes were characterized by cyclic voltammetry, infrared, H-1 and P-31 NMR spectroscopy techniques. Crystallographic analyses of the 5-bromo-substituted (2) and 5-chloro-substituted (3) complexes as representatives were performed and so confirmed the ONS chelate structure and presence of PPh3 as co-ligand in the complexes. To reveal the antioxidant properties of the compounds, TEAC values (by CUPRAC method) were determined along with free radical-scavenging activity (by DPPH method). The compounds bearing 4-hydroxy substituent, (LH2)-H-4 and complex 4 were the most effective compounds. The relationship between structure and antioxidant capacity in the context of benzophenone substituents and nickel(II) center was evaluated. Electrochemical results revealed that all complexes displayed metal-centered and ligand-centered redox processes. The antioxidant capacities of complexes were well correlated to electrochemical parameters.
dc.language.isoeng
dc.subjectTemel Bilimler (SCI)
dc.subjectTemel Bilimler
dc.subjectKİMYA, İNORGANİK VE NÜKLEER
dc.subjectKimya
dc.subjectİnorganik Kimya
dc.titleNickel(II)-PPh3 complexes of substituted benzophenone thiosemicarbazones: Electrochemistry, structural analysis, and antioxidant properties
dc.typeMakale
dc.relation.journalJOURNAL OF COORDINATION CHEMISTRY
dc.contributor.departmentİstanbul Üniversitesi-Cerrahpaşa , Mühendislik Fakültesi , Kimya Bölümü
dc.identifier.volume73
dc.identifier.issue1
dc.identifier.startpage137
dc.identifier.endpage153
dc.contributor.firstauthorID2275953


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