Non-aqueous capillary electrophoresis in acetonitrile using ionic-liquid buffer electrolytes

Citation
M. Vaher et al., Non-aqueous capillary electrophoresis in acetonitrile using ionic-liquid buffer electrolytes, CHROMATOGR, 53, 2001, pp. S302-S306
Citations number
14
Categorie Soggetti
Chemistry & Analysis","Spectroscopy /Instrumentation/Analytical Sciences
Journal title
CHROMATOGRAPHIA
ISSN journal
00095893 → ACNP
Volume
53
Year of publication
2001
Part
2
Supplement
S
Pages
S302 - S306
Database
ISI
SICI code
0009-5893(2001)53:<S302:NCEIAU>2.0.ZU;2-E
Abstract
The use of non-aqueous solvents in analysis has become a distinct field of interest in capillary electrophoresis (CE), and is designated to here as 'n on-aqueous capillary electrophoresis (NACE)". Organic solvents are of inter est in capillary elect ro-separations because they extend the range of appl ication of CE techniques to more hydrophobic species, addressing one of the main limitations, of this method. Changing the buffer electrolyte composition alters mobility in different wa ys, which include alteration of the ionic charge due to acid dissociation, alteration of the effective size of the ion by complexation and alteration of its mobility due to interaction with buffer additives. The dialkylimidazolium-based, liquid organic salts ("ionic liquids") are us ed as buffer electrolytes in this study. Their properties are governed by s trong, proton donor-acceptor and orientation interactions. A selected appli cation of separations of water-insoluble dyes in acetonitrile that were pre viously not accessible using conventional CE methodology are discussed. Ani onic part of ionic liquid changes the general electrophoretic mobility of t he system as well as the concentration of ionic liquid. Separation of analy tes is achieved because of dissociation of analytes in the presence of ioni c liquids in the separating medium. The migration order of analytes is base d on differences in the effective charge-hydrodynamic radius ratio of the a nalytes.