4.2 Article

Contribution of steric repulsion to retention on an octaclecylsiloxane-bonded silica stationary phase in reversed-phase liquid chromatography

Journal

CHROMATOGRAPHIA
Volume 62, Issue 11-12, Pages 553-561

Publisher

SPRINGER HEIDELBERG
DOI: 10.1365/s10337-005-0654-0

Keywords

column liquid chromatography; salvation parameter model; ascentis C18; steric repulsion

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Plots of the retention factor against mobile phase composition were used to organize a varied group of solutes into three categories according to their retention mechanism on an octaclecylsilioxane-bonded silica stationary phase, Ascentis(TM) C18, with acetonitrile-water and methanol-water mobile phase compositions containing 10-70% (v/v) organic solvent. The solutes in category 1 could be fit to a general retention model, Eq. (1), and exhibited normal retention behavior for the full composition range. The solutes in category 2 exhibited normal retention behavior at high organic solvent compositions with a discontinuity at low organic solvent mobile phase compositions. The solutes in category 3 exhibited a pronounced step or plateau in the middle region of the retention plots with a retention mechanism similar to category 1 at mobile phase compositions after the discontinuity and a different retention mechanism before the discontinuity. Selecting solutes and appropriate composition ranges from the three categories where a single retention mechanism was operative allowed modeling of the experimental retention factors using the salvation parameter model. These models were then used to predict retention factors for solutes excluded from the models. The overwhelming number of residual values, here defined as the difference between experimental and model predicted retention factors for the excluded solutes, could be explained by contributions from steric repulsion. The latter defined as the inability of solutes to fully insert themselves into the solvated stationary phase because of their size or conformation. Steric repulsion resulted in a systematic reduction in retention compared with predicted values for the fully inserted solute. The bonding density of the stationary phase; the type and composition of the mobile phase; and the size, conformation, type and number of functional groups on the solute are shown to affect the contribution of steric repulsion to the retention mechanism.

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