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dc.contributor.authorAkkurt, Mehmet
dc.contributor.authorSireci, Nihat
dc.contributor.authorDeniz, Selma
dc.contributor.authorKucukbay, Hasan
dc.contributor.authorBüyükgüngör, Orhan
dc.date.accessioned2020-06-21T14:55:12Z
dc.date.available2020-06-21T14:55:12Z
dc.date.issued2009
dc.identifier.issn1600-5368
dc.identifier.urihttps://doi.org/10.1107/S1600536809029626
dc.identifier.urihttps://hdl.handle.net/20.500.12712/18503
dc.descriptionKUCUKBAY, HASAN/0000-0002-7180-9486en_US
dc.descriptionWOS: 000268510800411en_US
dc.descriptionPubMed: 21583703en_US
dc.description.abstractThe title compound, C17H15N2O2+center dot Cl-center dot H2O, was synthesized from benzimidazole and furfryl chloride in dimethylformamide. The cationic benzimidazolium ring is connected to two furan rings via methylene bridges. The furan rings make dihedral angle of 79.09 (18)degrees with respect to each other, and make dihedral angles of 73.92 (12) and 72.58 (13)degrees with respect to the benzimidazole ring. O-H center dot center dot center dot Cl, C-H center dot center dot center dot O and C-H center dot center dot center dot Cl hydrogen bonds and C-H center dot center dot center dot pi interactions contribute to the stabilization of the crystal structure. Furthermore, there is a pi-pi interaction between adjacent five- and six-membered rings of the benzimidazole groups [centroid-centroid distance = 3.5305 (8) angstromen_US
dc.language.isoengen_US
dc.publisherWiley-Blackwellen_US
dc.relation.isversionof10.1107/S1600536809029626en_US
dc.rightsinfo:eu-repo/semantics/openAccessen_US
dc.title1,3-Difurfurylbenzimidazolium chloride monohydrateen_US
dc.typearticleen_US
dc.contributor.departmentOMÜen_US
dc.identifier.volume65en_US
dc.identifier.startpageO2037en_US
dc.identifier.endpageU4523en_US
dc.relation.journalActa Crystallographica Section E-Structure Reports Onlineen_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US


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