Publication:
(E)-3-Chloro-N-((5-Nitrothiophen-2-yl)methylene)aniline: A Combined Crystallographic, Theoretical and Antimicrobial Activity Investigation

dc.authorscopusid14010761400
dc.authorscopusid8600292400
dc.authorscopusid54982667700
dc.authorscopusid7003281189
dc.authorscopusid55360859700
dc.contributor.authorYilmaz, I.
dc.contributor.authorKazak, C.
dc.contributor.authorGümüş, S.
dc.contributor.authorAģar, E.
dc.contributor.authorOrhan Ardali, Y.
dc.date.accessioned2020-06-21T14:17:28Z
dc.date.available2020-06-21T14:17:28Z
dc.date.issued2012
dc.departmentOndokuz Mayıs Üniversitesien_US
dc.department-temp[Yilmaz] Işil, Department of Physics, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Kazak] Canan, Department of Physics, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Gümüş] Sümeyye, Department of Chemistry, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Aģar] Erbil, Department of Chemistry, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Orhan Ardali] Yuksel-Yuksel-Yueksel, Department of Environmental Engineering, Ondokuz Mayis Üniversitesi, Samsun, Turkeyen_US
dc.description.abstractThe title molecule, (E)-3-chloro-N-((5-nitrothiophen-2-yl)methylene) aniline, (C<inf>11</inf>H<inf>7</inf>ClN<inf>2</inf>O<inf>2</inf>S), was synthesized and characterized by IR and single-crystal X-ray structure determination. The compound crystallizes in the monoclinic space group P2 <inf>1</inf>/c. In addition, the molecular geometry, vibrational frequencies and frontier molecular orbitals analysis of the title compound in the ground state have been calculated by using the PM3 semi-empirical, HF/6-31G(d) and B3LYP/6-31G(d) ab initio methods. The results of the optimized molecular structure are exhibited and compared with the experimental X-ray diffraction and the calculated results are show that the optimized geometry can well reproduce the crystal structure. The Schiff base compounds are very important in medicinal and pharmaceutical fields because of their wide spectrum of biological activities. Most of them show biological activities such as antimicrobial, antifungal as well as antitumor activity. Therefore, (C<inf>11</inf>H <inf>7</inf>ClN<inf>2</inf>O<inf>2</inf>S) was investigated for their antimicrobial activities, Gram-positive and Gram-negative bacteria. © 2012 Elsevier B.V. All rights reserved.en_US
dc.identifier.doi10.1016/j.saa.2012.06.032
dc.identifier.endpage428en_US
dc.identifier.issn1386-1425
dc.identifier.pmid22820045
dc.identifier.scopus2-s2.0-84866382455
dc.identifier.scopusqualityQ1
dc.identifier.startpage423en_US
dc.identifier.urihttps://doi.org/10.1016/j.saa.2012.06.032
dc.identifier.volume97en_US
dc.identifier.wosWOS:000310395800056
dc.identifier.wosqualityQ1
dc.language.isoenen_US
dc.publisherPergamon-Elsevier Science Ltden_US
dc.relation.ispartofSpectrochimica Acta Part A-Molecular and Biomolecular Spectroscopyen_US
dc.relation.journalSpectrochimica Acta Part A-Molecular and Biomolecular Spectroscopyen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectAntimicrobial Activityen_US
dc.subjectPM3en_US
dc.subjectQuantum Chemical Calculationsen_US
dc.subjectSchiff Baseen_US
dc.subjectVibrational Spectraen_US
dc.subjectX-Ray Diffractionen_US
dc.title(E)-3-Chloro-N-((5-Nitrothiophen-2-yl)methylene)aniline: A Combined Crystallographic, Theoretical and Antimicrobial Activity Investigationen_US
dc.typeArticleen_US
dspace.entity.typePublication

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