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   <subfield code="a">UPLC a Powerful Tool for the Separation of Imidazolium Ionic Liquid Cations</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Asta Orentienė, Vilma Olšauskaitė, Vida Vičkačkaitė, Audrius Padarauskas]</subfield>
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   <subfield code="a">Ultra-performance liquid chromatography (UPLC) in reversed-phase (RP), ion pair (IP) and hydrophilic interaction chromatography (HILIC) has been investigated for the separation of imidazolium-based ionic liquid (IL) cations. Among the three stationary phases (i.e., C18, C8 and phenyl) studied under RP conditions the phenyl phase provided much stronger retention for the IL cations. Four acids (hydrochloric, methanesulfonic, perchloric and trifluoroacetic) as mobile phase additives were compared in light of their effects on the retention of IL cations. It was shown that the retention of all IL cations decreased upon acidification of the mobile phase, possibly due to suppression of residual silanol ionization. Very fast (~3min) and efficient RP-UPLC separation of six cations was achieved by gradient elution with acetonitrile-water mobile phase containing 2.5mmolL−1 perchloric acid. In IP-UPLC all solutes were well resolved in about 4min by gradient elution with acetonitrile-water mobile phase containing 1mmolL−1 sodium 1-octanesulfonate as ion pairing reagent. Finally, under HILIC conditions by using isocratic elution with acetonitrile-water (85:15, v/v) mobile phase containing 5mmol L−1 ammonium formate (pH 3.2) the separation time was reduced to less than 2min while maintaining excellent peak shapes and sufficient resolution. Compared to current LC systems UPLC allowed considerably faster separations with better peak shapes.</subfield>
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