2015-01-26T14:08:53Z
2015-01-26T14:08:53Z
2013-08-18
2015-01-26T14:08:53Z
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.
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Sals; Imidazoles; Resines de bescanvi iònic; Hidrogen; Solucions iòniques; Compostos heterocíclics; Salts; Imidazoles; Ion exchange resins; Hydrogen; Ionic solutions; Heterocyclic compounds
Michigan Publishing
Reproducció del document publicat a: http://dx.doi.org/10.3998/ark.5550190.p008.203
Arkivoc, 2013, vol. 2014, num. 2, p. 85-102
http://dx.doi.org/10.3998/ark.5550190.p008.203
cc-by-nc (c) Dinarès Milà, M. Immaculada et al., 2013
http://creativecommons.org/licenses/by-nc/3.0/es