Publication:
Two New Benzamides: Synthesis, Spectroscopic Characterization, X-Ray Diffraction, and Electronic Structure Analyses

dc.authorscopusid8415734200
dc.authorscopusid7003931071
dc.authorscopusid46462159400
dc.authorscopusid8328133400
dc.authorscopusid36039473500
dc.authorscopusid6701793097
dc.contributor.authorKo̧sar, B.K.
dc.contributor.authorÇakmak, S.
dc.contributor.authorYakan, H.
dc.contributor.authorOdaba̧soǧlu, M.
dc.contributor.authorBüyuk̈güngör, O.
dc.contributor.authorKütük, H.
dc.date.accessioned2020-06-21T12:18:13Z
dc.date.available2020-06-21T12:18:13Z
dc.date.issued2020
dc.departmentOndokuz Mayıs Üniversitesien_US
dc.department-temp[Ko̧sar] Başak, Department of Mathematics and Science Education, Sinop Üniversitesi, Sinop, Turkey; [Çakmak] Şükriye, Environmental Health Programme, Sinop Üniversitesi, Sinop, Turkey; [Yakan] Hasan, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Odaba̧soǧlu] Mustafà, Chemical Technology Program, Pamukkale Üniversitesi, Denizli, Denizli, Turkey; [Büyuk̈güngör] Orhan, Department of Physics, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Kütük] Halil, Ondokuz Mayis Üniversitesi, Samsun, Turkeyen_US
dc.description.abstractThis work includes the syntheses, molecular and electronic structure analyses of two novel secondary amide compounds 3-acetoxy-2-methyl-N-(2-methoxyphenyl)benzamide, 1 and 3-acetoxy-2-methyl-N-(3-methylphenyl)benzamide, 2. The title compounds were characterized by X-ray single crystal diffraction, FT-IR, 1H NMR and 13C NMR techniques and quantum chemical calculations were used for the investigations on electronic structure. X-ray diffraction analyses show that both compounds 1 and 2 crystallized in the triclinic system with space group P-1. While the characteristic amide bands were observed in IR and NMR spectra, crystallographic studies indicate that the supramolecular structures were stabilized by intramolecular and intermolecular hydrogen bonds and C–H … π interactions for both compounds. Beside the experimental studies, natural bond orbital and molecular electrostatic potential analyses were carried out to understand the intramolecular charge transfers and hydrogen bonding behaviors of compounds. © 2019 Elsevier B.V.en_US
dc.identifier.doi10.1016/j.molstruc.2019.127314
dc.identifier.issn0022-2860
dc.identifier.scopus2-s2.0-85075872045
dc.identifier.scopusqualityQ1
dc.identifier.urihttps://doi.org/10.1016/j.molstruc.2019.127314
dc.identifier.volume1203en_US
dc.identifier.wosWOS:000504448700008
dc.identifier.wosqualityQ2
dc.language.isoenen_US
dc.publisherElsevier B.V.en_US
dc.relation.ispartofJournal of Molecular Structureen_US
dc.relation.journalJournal of Molecular Structureen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectElectronic Structureen_US
dc.subjectNon-Covalent Interactionsen_US
dc.subjectSecondary Amidesen_US
dc.subjectSpectroscopic Techniquesen_US
dc.subjectX-Ray Diffractionen_US
dc.titleTwo New Benzamides: Synthesis, Spectroscopic Characterization, X-Ray Diffraction, and Electronic Structure Analysesen_US
dc.typeArticleen_US
dspace.entity.typePublication

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