Half-sandwich ruthenium(II)(eta(6)-p-cymene) complexes: Syntheses, characterization, transfer hydrogenation reactions, antioxidant and enzyme inhibitory activities

dc.authorscopusid56088739600
dc.authorscopusid35147160200
dc.authorscopusid15765751200
dc.authorscopusid30067583700
dc.contributor.authorBuldurun, Kenan
dc.contributor.authorTuran, Nevin
dc.contributor.authorMahmoudi, Ghodrat
dc.contributor.authorBursal, Ercan
dc.date.accessioned2022-09-04T10:26:49Z
dc.date.available2022-09-04T10:26:49Z
dc.date.issued2022
dc.departmentMeslek Yüksekokulları, Sağlık Hizmetleri Meslek Yüksekokulu, Tıbbi Hizmetler ve Teknikler Bölümüen_US
dc.departmentFakülteler, Sağlık Bilimleri Fakültesi, Hemşirelik Bölümüen_US
dc.departmentFakülteler, Fen-Edebiyat Fakültesi, Kimya Bölümüen_US
dc.departmentMeslek Yüksekokulları, Sağlık Hizmetleri Meslek Yüksekokulu, Tıbbi Hizmetler ve Teknikler Bölümüen_US
dc.departmentFakülteler, Sağlık Bilimleri Fakültesi, Hemşirelik Bölümüen_US
dc.departmentFakülteler, Fen-Edebiyat Fakültesi, Kimya Bölümüen_US
dc.description.abstractThe five new Ru(II)(eta(6)-p-cymene) complexes (1-5 ) were successfully synthesized, characterized by FT-IR, elemental analysis, electronic spectra, proton and carbon NMR, mass spectra and thermal analysis, and applied in the transfer hydrogenation of ketones. In addition, enzyme inhibitory and antioxidant activities of novel Ru(II)(eta(6)-p-cymene) complexes were evaluated using several in vitro methods. The stabilities of complexes were checked by UV-Vis. spectroscopy. The results of enzyme assays showed that novel Ru(II)(eta(6)-p-cymene) complexes had effective inhibitions against the tyrosinase and pancreatic lipase enzymes. The IC50 values of five different (1-5) for tyrosinase were found as 34.65 +/- 1.2 mu M, 31.51 +/- 1.7 mu M, 49.50 +/- 3.1 mu M, 19.25 +/- 0.9 mu M, and 63.01 +/- 3.3 mu M, respectively. Furthermore, ABTS, CUPRAC, DPPH, and FRAP in vitro methods were utilized to assess the antioxidant capabilities of the compounds. The powerful antioxidant potentials of the synthesized compounds were detected compared to the standards, such as BHA, BHT, ascorbic acid, and a-tocopherol. This study provides a valuable potential of the novel Ru(II)(eta(6)-p-cymene) complexes for pharmacological studies with further analytical experiments to explore their full properties. (C) 2022 Elsevier B.V. All rights reserved.en_US
dc.identifier.doi10.1016/j.molstruc.2022.133075
dc.identifier.issn0022-2860
dc.identifier.issn1872-8014
dc.identifier.orcid0000-0002-2462-7006
dc.identifier.scopus2-s2.0-85128303165
dc.identifier.scopusqualityQ1
dc.identifier.urihttps://doi.org/10.1016/j.molstruc.2022.133075
dc.identifier.urihttps://hdl.handle.net/20.500.12639/4597
dc.identifier.volume1262en_US
dc.identifier.wosWOS:000799270800009
dc.identifier.wosqualityQ2
dc.indekslendigikaynakWeb of Science
dc.indekslendigikaynakScopus
dc.institutionauthorBuldurun, Kenan
dc.institutionauthorBursal, Ercan
dc.institutionauthorTuran, Nevin
dc.language.isoen
dc.publisherElsevieren_US
dc.relation.ispartofJournal Of Molecular Structureen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectSpectroscopic methods; Schiff base; Antioxidant activities; Enzyme inhibitory; Transfer hydrogenation; Ru(II)(eta(6)-p-cymene) complexesen_US
dc.subjectRuthenium(Ii) Carbonyl-Complexes; Catalytic Transfer Hydrogenation; Base Ligands Synthesis; Schiff-Base; Structural-Characterization; Binding-Properties; Bearing; Ru(Ii); Oxidationen_US
dc.titleHalf-sandwich ruthenium(II)(eta(6)-p-cymene) complexes: Syntheses, characterization, transfer hydrogenation reactions, antioxidant and enzyme inhibitory activitiesen_US
dc.typeArticle

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