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dc.contributoren-US
dc.creatorMaharramov, Abel M.
dc.creatorDuruskari, Gulnara Sh.
dc.creatorMammadova, Gunay Z.
dc.creatorKhalilov, Ali N.
dc.creatorAslanova, Javahir M.
dc.creatorCisterna, Jonathan
dc.creatorCárdenas, Alejandro
dc.creatorBrito, Iván
dc.date2019-07-25
dc.date.accessioned2019-09-10T17:53:42Z
dc.date.available2019-09-10T17:53:42Z
dc.identifierhttp://www.jcchems.com/index.php/JCCHEMS/article/view/1211
dc.identifier.urihttps://revistaschilenas.uchile.cl/handle/2250/108742
dc.descriptionIn the cation of the title salt, the central thiazolidine ring adopts an envelope conformation. In the crystal N-H ··· Br hydrogen bonds link the components into a bi-dimensional network with the cations and anions stacked parallel to plane (101). The molecular structure shows several positional disorders over -CF3 and thiazolidine fragments and these were modeled. The weak intermolecular interactions in the crystal structure are mainly constituted by H ··· F, H ··· π and H ··· Br. Hirshfeld surface analysis were used to verify the contributions of the different intermolecular interactions.en-US
dc.formatapplication/pdf
dc.languageeng
dc.publisherSociedad Chilena de Químicaen-US
dc.relationhttp://www.jcchems.com/index.php/JCCHEMS/article/view/1211/314
dc.rightsCopyright (c) 2019 Journal of the Chilean Chemical Societyen-US
dc.rightshttp://creativecommons.org/licenses/by-nc-sa/4.0en-US
dc.sourceJournal of the Chilean Chemical Society; Vol 64, No 2 (2019): Journal of the Chilean Chemical Societyen-US
dc.source0717-9707
dc.subjecten-US
dc.titleCRYSTAL STRUCTURE AND HIRSHFELD SURFACE ANALYSIS OF (E)-5-PHENYL-3-((4- (TRIFLUOROMETHYL)BENZYLIDENE)AMINO)THIAZOLIDIN-2-IMINIUM BROMIDEen-US
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/publishedVersion
dc.typeen-US


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