Synthesis, Characterization, and Dft Calculation of Some New Pyrimidine Derivatives and Theoretical Studies on the Corrosion Inhibition Performance

dc.authorscopusid 8242109800
dc.authorscopusid 57992625200
dc.authorscopusid 57992625300
dc.authorscopusid 57191851849
dc.contributor.author Esvet, A.
dc.contributor.author Adem, R.
dc.contributor.author Cagla, A.
dc.contributor.author Ertan, S.
dc.date.accessioned 2025-05-10T16:53:56Z
dc.date.available 2025-05-10T16:53:56Z
dc.date.issued 2022
dc.department T.C. Van Yüzüncü Yıl Üniversitesi en_US
dc.department-temp Esvet A., Department of Chemistry, Faculty of Science, University of Van Yuzuncu Yil, Van, Turkey; Adem R., Department of Chemistry, Faculty of Science, University of Van Yuzuncu Yil, Van, Turkey; Cagla A., Faculty of Pharmacy, University of Inonu, Malatya, Turkey; Ertan S., Department of Chemistry, Ataturk University, Erzurum a, 25240, Turkey en_US
dc.description.abstract In this study, 5-benzoyl-6-phenyl-4-(4-(trifluoromethoxy) phenyl)-1,2,3,4-tetrahydroxypyrimidine (1); 5-benzoyl-6-phenyl-4-(4-(trifluoromethoxy) phenyl)-1,2,3,4-tetrahydrothioxypyrimidine (2) and 5-benzoyl-6-phenyl-4-(3,5-dimethoxy) phenyl)-1,2,3,4-tetrahydrothioxypyrimidine (3) compounds were prepared via Biginelli condensation reaction using Metal-organic framework (MIL-101) as an active catalyst. It was established to be an active heterogeneous catalyst for a three-component Biginelli condensation reaction with good yields (75-80 %). Moreover, the catalyst could easily be recovered and recycled without any significant loss of its catalytic activity. Also the compounds 5-benzoyl-6-phenyl-3-acetyl-4-(4-hydroxyphenyl)-1,2,3,4-tetrahydrothioxypyrimidine (4) and 5-benzoyl-6-phenyl-3-acetyl-4-(4-trifluoromethoxy)phenyl)-1,2,3,4-tetrahydrothioxypyrimidine (5) were obtained acetylation reaction. The structures were characterized on the basis of1H-NMR,13C-NMR, FT-IR, and elemental analysis. And also molecular characterizations of compound 4 were analyzed by X-ray crystal analysis. In addition, the corrosion inhibition activity of synthesized compounds was examined with theoretical calculation using DFT method at the level of B3LYP / 6-31G (d, p). © 2022, Iranian Institute of Research and Development in Chemical Industries. All rights reserved. en_US
dc.identifier.doi 10.30492/IJCCE.2021.521495.4479
dc.identifier.endpage 1656 en_US
dc.identifier.issn 1021-9986
dc.identifier.issue 5 en_US
dc.identifier.scopus 2-s2.0-85143363346
dc.identifier.scopusquality Q3
dc.identifier.startpage 1643 en_US
dc.identifier.uri https://doi.org/10.30492/IJCCE.2021.521495.4479
dc.identifier.uri https://hdl.handle.net/20.500.14720/2959
dc.identifier.volume 41 en_US
dc.identifier.wosquality Q3
dc.language.iso en en_US
dc.publisher Iranian Institute of Research and Development in Chemical Industries en_US
dc.relation.ispartof Iranian Journal of Chemistry and Chemical Engineering 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 Biginelli en_US
dc.subject Dft en_US
dc.subject Tetrahydropyrimidines en_US
dc.subject X-Ray Crystal Analysis en_US
dc.title Synthesis, Characterization, and Dft Calculation of Some New Pyrimidine Derivatives and Theoretical Studies on the Corrosion Inhibition Performance en_US
dc.type Article en_US
dspace.entity.type Publication

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