Abstract
Hydrophilic interaction chromatography (HILIC) could be characterized as a complex chromatographic system that involves multiple mechanisms. These are partitioning as well as polar and ionic interactions. Among several HILIC columns, ZIC-HILIC can be used to separate small organic ionic compounds. The presence of both positive and negative charge on the stationary phase may facilitate separations of both anionic and cationic analytes. Based on the Partial Least Squares methodology, an attempt to clarify the mechanism on this column revealed that the forces dominating are mainly determined by structural features. Consequently, the physicochemical properties which are related to the analytes’ structure may heighten or attenuate the process. Ionic interactions are stronger for analytes containing moieties with basic properties since the interaction with the sulfonyl group is facilitated. The partition mechanism is prevailing for those analytes that are not sufficiently ionized at the experimental conditions (mobile phase pH 3 and 6.5) and for analytes that can create halogen bonds. Moreover, the stagnant water layer on the silica bed enhances the retention of water soluble compounds due to the increased hydrophilic interactions.
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