Please use this identifier to cite or link to this item: https://dipositint.ub.edu/dspace/handle/2445/61807
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dc.contributor.authorDinarès Milà, M. Immaculada-
dc.contributor.authorMesquida Estévez, Ma. Neus-
dc.contributor.authorIbáñez Jiménez, Anna-
dc.contributor.authorAlcalde Pais, Ma. Ermitas (María de las Ermitas)-
dc.date.accessioned2015-01-26T14:08:53Z-
dc.date.available2015-01-26T14:08:53Z-
dc.date.issued2013-08-18-
dc.identifier.issn1551-7012-
dc.identifier.urihttps://hdl.handle.net/2445/61807-
dc.description.abstractThe counteranion exchange of quaternary 1,2,3-triazolium salts was examined using a simple method that permitted halide ions to be swap for a variety of anions using an anion exchange resin (A¯ form). The method was applied to 1,2,3-triazolium-based ionic liquids and the iodideto- anion exchange proceeded in excellent to quantitative yields, concomitantly removing halide impurities. Additionally, an anion exchange resin (N3¯ form) was used to obtain the benzyl azide from benzyl halide under mild reaction. Likewise, following a similar protocol, bis(azidomethyl)arenes were also synthesized in excellent yields. The results of a proton NMR spectroscopic study of simple azolium-based ion pairs are discussed, with attention focused on the significance of the charged-assisted (C<br>H)+···anion hydrogen bonds of simple azolium systems such as 1-butyl-3-methylimidazolium and 1-benzyl-3-methyl-1,2,3-triazolium salts.-
dc.format.extent18 p.-
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherMichigan Publishing-
dc.relation.isformatofReproducció del document publicat a: http://dx.doi.org/10.3998/ark.5550190.p008.203-
dc.relation.ispartofArkivoc, 2013, vol. 2014, num. 2, p. 85-102-
dc.relation.urihttp://dx.doi.org/10.3998/ark.5550190.p008.203-
dc.rightscc-by-nc (c) Dinarès Milà, M. Immaculada et al., 2013-
dc.rights.urihttp://creativecommons.org/licenses/by-nc/3.0/es-
dc.sourceArticles publicats en revistes (Farmacologia, Toxicologia i Química Terapèutica)-
dc.subject.classificationSals-
dc.subject.classificationImidazoles-
dc.subject.classificationResines de bescanvi iònic-
dc.subject.classificationHidrogen-
dc.subject.classificationSolucions iòniques-
dc.subject.classificationCompostos heterocíclics-
dc.subject.otherSalts-
dc.subject.otherImidazoles-
dc.subject.otherIon exchange resins-
dc.subject.otherHydrogen-
dc.subject.otherIonic solutions-
dc.subject.otherHeterocyclic compounds-
dc.titleAzolium-based systems: application of an anion exchange resin (A- form) method and 1H NMR analysis of the charged-assisted (C<br>H)+·anion hydrogen bondseng
dc.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/publishedVersion-
dc.identifier.idgrec627955-
dc.date.updated2015-01-26T14:08:53Z-
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess-
Appears in Collections:Articles publicats en revistes (Farmacologia, Toxicologia i Química Terapèutica)
Articles publicats en revistes (Nutrició, Ciències de l'Alimentació i Gastronomia)
Articles publicats en revistes (Psicologia Clínica i Psicobiologia)

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