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Solute-solvent interactions in imidazolium camphorsulfonate ionic liquids.

Physical chemistry chemical physics : PCCP (2007-11-09)
Kaoru Nobuoka, Satoshi Kitaoka, Masashi Iio, Thomas Harran, Yuichi Ishikawa
RESUMEN

We directly observe the interaction between 1-butyl-3-methylimidazolium (bmim) or 1-butyl-2,3-dimethylimidazolium (bm(2)im) and the solute, ethyl acrylate (EA), which is the popular dienophile in the Diels-Alder reaction and an H-bonding acceptor, by using specially designed electrospray mass spectrometry. In imidazolium ionic liquids, cation-anion interactions are controlled by selecting the appropriate anion, and the naked C(2)-H of imidazolium, which loosely interacts with its counterion, can readily interact with an H-bonding acceptable solute. The ion-counterion (solvent-solvent) interaction affects the ion-solute (solvent-solute) interaction. This relation is one of the key criteria for selecting the cation-anion combination in tailoring ILs.

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Sigma-Aldrich
Ácido (1S)-(+)-10-alcanforsulfónico, 99%
Sigma-Aldrich
(1R)-(−)-10-Camphorsulfonic acid, 98%
Sigma-Aldrich
Camphor-10-sulfonic acid (β), 98%
Sigma-Aldrich
(+)-Camphor-10-sulfonic acid, purum, ≥98.0% (T)
Sigma-Aldrich
(−)-Camphor-10-sulfonic acid, purum, ≥98.0% (T)