Publication:
Experimental Studies of Schiff Base (E)-4 Phenol Compound With Various Spectroscopic Methods

dc.authorscopusid57212141572
dc.authorscopusid35567972100
dc.authorscopusid23392062100
dc.authorscopusid57212151490
dc.authorscopusid7003281189
dc.authorscopusid7004106981
dc.authorscopusid7004106981
dc.authorwosidNarcis, Duteanu/H-8765-2019
dc.authorwosidÇiçek, Candan/Abh-1161-2021
dc.contributor.authorGuezel, E.
dc.contributor.authorCoruh, U.
dc.contributor.authorDuteanu, N.
dc.contributor.authorCicek, C.
dc.contributor.authorAgar, E.
dc.contributor.authorVazquez Lopez, E. M.
dc.contributor.authorYavuz, M.
dc.contributor.authorIDGüzel, Enis/0000-0001-8068-2934
dc.date.accessioned2025-12-11T01:03:02Z
dc.date.issued2024
dc.departmentOndokuz Mayıs Üniversitesien_US
dc.department-temp[Guezel, E.; Coruh, U.; Yavuz, M.] Ondokuz Mayis Univ, Fac Sci, Dept Phys, Samsun, Turkiye; [Cicek, C.; Agar, E.] Ondokuz Mayis Univ, Fac Sci, Dept Chem, Samsun, Turkiye; [Vazquez Lopez, E. M.] Univ Vigo, Dept Inorgan Chem, Vigo 36200, Galicia, Spain; [Duteanu, N.] Univ Politehn Timisoara, Dept Ind Chem & Environm Engn, Timisoara, Romaniaen_US
dc.descriptionGüzel, Enis/0000-0001-8068-2934en_US
dc.description.abstractSchiff-based compounds, which represent an important class in the field of organic compounds, form the basis of this research article. This research article aims to investigate the synthesized compound (E)-4-methoxy-2-(((2-phenoxyphenyl) imino) methyl) phenol using experimental methods. FTIR, UV-Vis, 13C and 1H nuclear magnetic resonance (NMR) spectroscopy and X-ray diffraction methods were used to elucidate the structural properties of the compound synthesized at the end of chemical processes. The structure solution was carried out from the data obtained as a result of X-ray analysis. According to these results, one of the two compounds in the asymmetric cell completed their formation in the enol-imine form and the other in the keto-amine form. This structural situation, which is rare in the literature, was supported and explained by FTIR, 13C and 1H NMR spectroscopy studies. According to the results obtained as a result of UV-Vis spectroscopy, the structure revealed that the enol-imine form was dominant. The reasons for this situation were explained.en_US
dc.description.woscitationindexScience Citation Index Expanded
dc.identifier.doi10.1134/S0022476624110076
dc.identifier.endpage2197en_US
dc.identifier.issn0022-4766
dc.identifier.issn1573-8779
dc.identifier.issue11en_US
dc.identifier.scopus2-s2.0-85217167297
dc.identifier.scopusqualityQ4
dc.identifier.startpage2187en_US
dc.identifier.urihttps://doi.org/10.1134/S0022476624110076
dc.identifier.urihttps://hdl.handle.net/20.500.12712/40939
dc.identifier.volume65en_US
dc.identifier.wosWOS:001376818100004
dc.identifier.wosqualityQ4
dc.language.isoenen_US
dc.publisherPleiades Publishing Ltden_US
dc.relation.ispartofJournal of Structural Chemistryen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectX-Ray Diffractionen_US
dc.subjectUV-Visen_US
dc.subjectNMRen_US
dc.subjectSchiff Baseen_US
dc.titleExperimental Studies of Schiff Base (E)-4 Phenol Compound With Various Spectroscopic Methodsen_US
dc.typeArticleen_US
dspace.entity.typePublication

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