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Synthesis, Characterization, Antioxidant Properties and Dft Calculation of Some New Pyrimidine Derivatives

dc.authorscopusid 8242109800
dc.authorscopusid 57193268077
dc.authorscopusid 55550270900
dc.authorscopusid 6602257873
dc.authorscopusid 57205305252
dc.authorscopusid 57194206876
dc.contributor.author Akbas, E.
dc.contributor.author Ergan, E.
dc.contributor.author Sahin, E.
dc.contributor.author Ekin, S.
dc.contributor.author Cakir, M.
dc.contributor.author Karakus, Y.
dc.date.accessioned 2025-05-10T17:01:55Z
dc.date.available 2025-05-10T17:01:55Z
dc.date.issued 2019
dc.department T.C. Van Yüzüncü Yıl Üniversitesi en_US
dc.department-temp Akbas E., Department of Chemistry, Faculty of Science, University of Van Yuzuncu Yil, Van, Turkey; Ergan E., Van Security Vocational School, University of Van Yuzuncu Yil, Van, Turkey; Sahin E., Department of Chemistry, Ataturk University, Erzurum, Turkey; Ekin S., Department of Chemistry, Faculty of Science, University of Van Yuzuncu Yil, Van, Turkey; Cakir M., Department of Chemistry, Faculty of Science, University of Van Yuzuncu Yil, Van, Turkey; Karakus Y., Department of Chemistry, Faculty of Science, University of Van Yuzuncu Yil, Van, Turkey en_US
dc.description.abstract In this study, 5-benzoyl-4-(4-(methylthio)phenyl)-6-phenyl-1,2,3,4-tetrahydro-2-thioxo (1), oxo (2) and imino (3) pyrimidine derivatives were prepared via Multicomponent Cyclocondensation Reactions (MCRs). The compounds thiazolo[3,2-a]pyrimidin-3(5H)-one (4) and thiazin-4(6H)-one (5) were obtained via the reaction of compound 1 with bromoacetic acid and 3-bromopropionic acid, respectively. Structures were determined by using FT-IR, 1H/13C NMR and elemental analyses. Also the compounds 4 and 5 were analyzed by X-ray single crystal analysis. All compounds were investigated as corrosion inhibitors using density functional theory (DFT) at the level of B3LYP/6-31G (d, p). According to the calculations, the compound 3 appears to be a good inhibitor for corrosion. On the other hand, total antioxidant properties were measured in vitro by DPPH•, ABTS•+ test, hemolysis of phenylhydrazine erythrocytes and metal chelating effect. The results were compared with standard antioxidants such as trolox and α-tocopherol. These data revealed that compounds 1, 2 and 5 are more active with respect to 3 and 4 in scavenging the radicals. © 2018, © 2018 Taylor & Francis Group, LLC. en_US
dc.description.sponsorship Van Yuzuncu Yil University of Turkey, (FYL-2017-5904) en_US
dc.identifier.doi 10.1080/10426507.2018.1550489
dc.identifier.endpage 802 en_US
dc.identifier.issn 1042-6507
dc.identifier.issue 8 en_US
dc.identifier.scopus 2-s2.0-85059461585
dc.identifier.scopusquality Q4
dc.identifier.startpage 796 en_US
dc.identifier.uri https://doi.org/10.1080/10426507.2018.1550489
dc.identifier.uri https://hdl.handle.net/20.500.14720/5329
dc.identifier.volume 194 en_US
dc.identifier.wosquality Q4
dc.language.iso en en_US
dc.publisher Taylor and Francis Ltd. en_US
dc.relation.ispartof Phosphorus, Sulfur and Silicon and the Related Elements en_US
dc.relation.publicationcategory Makale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanı en_US
dc.rights info:eu-repo/semantics/closedAccess en_US
dc.subject Antioxidant Properties en_US
dc.subject Corrosion en_US
dc.subject Dft en_US
dc.subject Mcrs en_US
dc.subject Pyrimidine en_US
dc.title Synthesis, Characterization, Antioxidant Properties and Dft Calculation of Some New Pyrimidine Derivatives en_US
dc.type Article en_US

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