Azolium-based systems: application of an anion exchange resin (A- form) method and 1H NMR analysis of the charged-assisted (C<br>H)+·anion hydrogen bonds
| dc.contributor.author | Dinarès Milà, M. Immaculada | |
| dc.contributor.author | Mesquida Estévez, Ma. Neus | |
| dc.contributor.author | Ibáñez Jiménez, Anna | |
| dc.contributor.author | Alcalde Pais, Ma. Ermitas (María de las Ermitas) | |
| dc.date.accessioned | 2015-01-26T14:08:53Z | |
| dc.date.available | 2015-01-26T14:08:53Z | |
| dc.date.issued | 2013-08-18 | |
| dc.date.updated | 2015-01-26T14:08:53Z | |
| dc.description.abstract | The 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.extent | 18 p. | |
| dc.format.mimetype | application/pdf | |
| dc.identifier.idgrec | 627955 | |
| dc.identifier.issn | 1551-7012 | |
| dc.identifier.uri | https://hdl.handle.net/2445/61807 | |
| dc.language.iso | eng | |
| dc.publisher | Michigan Publishing | |
| dc.relation.isformatof | Reproducció del document publicat a: http://dx.doi.org/10.3998/ark.5550190.p008.203 | |
| dc.relation.ispartof | Arkivoc, 2013, vol. 2014, num. 2, p. 85-102 | |
| dc.relation.uri | http://dx.doi.org/10.3998/ark.5550190.p008.203 | |
| dc.rights | cc-by-nc (c) Dinarès Milà, M. Immaculada et al., 2013 | |
| dc.rights.accessRights | info:eu-repo/semantics/openAccess | |
| dc.rights.uri | http://creativecommons.org/licenses/by-nc/3.0/es | |
| dc.source | Articles publicats en revistes (Farmacologia, Toxicologia i Química Terapèutica) | |
| dc.subject.classification | Sals | |
| dc.subject.classification | Imidazoles | |
| dc.subject.classification | Resines de bescanvi iònic | |
| dc.subject.classification | Hidrogen | |
| dc.subject.classification | Solucions iòniques | |
| dc.subject.classification | Compostos heterocíclics | |
| dc.subject.other | Salts | |
| dc.subject.other | Imidazoles | |
| dc.subject.other | Ion exchange resins | |
| dc.subject.other | Hydrogen | |
| dc.subject.other | Ionic solutions | |
| dc.subject.other | Heterocyclic compounds | |
| dc.title | Azolium-based systems: application of an anion exchange resin (A- form) method and 1H NMR analysis of the charged-assisted (C<br>H)+·anion hydrogen bonds | eng |
| dc.type | info:eu-repo/semantics/article | |
| dc.type | info:eu-repo/semantics/publishedVersion |
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