Publication:
Synthesis, Spectral, X-Ray Diffraction and DFT Studies on 1-(2-methyl-2-propenyl)-3-(2,3,4,5,6-pentamethylbenzyl)benzimidazolium Chloride Hydrate

dc.authorscopusid57200152855
dc.authorscopusid57041198500
dc.authorscopusid8398877200
dc.authorscopusid6602553450
dc.authorscopusid7005334934
dc.contributor.authorŞahin, N.
dc.contributor.authorKılıç-Cıkla, I.
dc.contributor.authorÖzdemir, Nutullah
dc.contributor.authorGürbüz, N.
dc.contributor.authorÖzdemïr, İ.
dc.date.accessioned2020-06-21T13:12:23Z
dc.date.available2020-06-21T13:12:23Z
dc.date.issued2018
dc.departmentOndokuz Mayıs Üniversitesien_US
dc.department-temp[Şahin] Neslihan, Department of Basic Sciences, Cumhuriyet Üniversitesi, Sivas, Sivas, Turkey, Department of Chemistry, Inönü Üniversitesi, Malatya, Turkey, Catalysis Research and Application Center, Inönü Üniversitesi, Malatya, Turkey; [Kılıç-Cıkla] Işın, Department of General Secretary, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Özdemir] Namık, Department of Mathematics and Science Education, Ondokuz Mayis Üniversitesi, Samsun, Turkey; [Gürbüz] Nevin, Department of Chemistry, Inönü Üniversitesi, Malatya, Turkey, Catalysis Research and Application Center, Inönü Üniversitesi, Malatya, Turkey; [Özdemïr] İsmail, Department of Chemistry, Inönü Üniversitesi, Malatya, Turkey, Catalysis Research and Application Center, Inönü Üniversitesi, Malatya, Turkeyen_US
dc.description.abstractA new benzimidazole based N-heterocyclic carbene (NHC) salt (1) was synthesized by the reaction of benzimidazole precursor with alkyl halide. The structure of 1 was determined by elemental analysis, FT-IR, 1H NMR and 13C NMR spectroscopy tecniques and X-ray crystallography. The compound crystallized in the triclinic space group P-1 with two molecules in the unit cell. The optimization of 1 was firstly performed at B3LYP/6-311G++(d,p) level, then the theoretical spectral studies performed and compared with the experimental values. Besides the frontier molecular orbital energies and chemical reactivity analysis of 1, together with the electrostatic potential and molecular electrostatic potential analyses were performed at the same level of theory. © 2018, © 2018 Taylor & Francis Group, LLC.en_US
dc.identifier.doi10.1080/15421406.2018.1446692
dc.identifier.endpage123en_US
dc.identifier.issn1542-1406
dc.identifier.issn1563-5287
dc.identifier.issue1en_US
dc.identifier.scopus2-s2.0-85048861963
dc.identifier.scopusqualityQ4
dc.identifier.startpage109en_US
dc.identifier.urihttps://doi.org/10.1080/15421406.2018.1446692
dc.identifier.volume664en_US
dc.identifier.wosWOS:000436019400012
dc.identifier.wosqualityQ4
dc.language.isoenen_US
dc.publisherTaylor and Francis Inc. 325 Chestnut St, Suite 800 Philadelphia PA 19106en_US
dc.relation.ispartofMolecular Crystals and Liquid Crystalsen_US
dc.relation.journalMolecular Crystals and Liquid Crystalsen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subject1H and 13C NMRen_US
dc.subjectDFT Calculationsen_US
dc.subjectN-Heterocyclic Carbeneen_US
dc.subjectX-Ray Diffractionen_US
dc.titleSynthesis, Spectral, X-Ray Diffraction and DFT Studies on 1-(2-methyl-2-propenyl)-3-(2,3,4,5,6-pentamethylbenzyl)benzimidazolium Chloride Hydrateen_US
dc.typeArticleen_US
dspace.entity.typePublication

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