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 |