| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1164561 | Analytica Chimica Acta | 2014 | 8 Pages |
•A new diamide-embedded octadecyl stationary phase was prepared.•Excellent hydrophobic and aromatic selectivity.•“Polymeric-C18” chromatographic behavior was found.•Superior shape and planarity selectivity over C18 towards isomeric PAHs.•Carbonyl group and adjacent double C18 chains impacted the retention substantially.
A novel branch-type diamide-embedded octadecyl stationary phase was prepared by facile amidation. The preparation of this new phase involves the synthesis of new bifunctional silane ligand and surface modification of spherical silica via anchoring of silane coupling agent. The obtained diamide-embedded octadecyl stationary phase demonstrated excellent hydrophobic selectivity, as well as enhanced shape and planarity selectivity in comparison to commercial polymeric and monomeric C18 phases, respectively, as revealed by the systematic investigation into its liquid chromatographic retention of isomeric polycyclic aromatic hydrocarbons. The applicability of this new stationary phase was further testified by the effective separation of isomeric compounds belong to different chemical classes, including chain isomers of alkylbenzenes, and positional isomers of substituted aromatics. An in-depth analysis of the separation mechanisms other than molecular shape recognition involved in the new stationary phase was performed using a linear solvation energy relationships model and compared with its monoamide and pure C18 counterparts correspondingly. The performance of the new stationary phase in quantitative analysis of phenols from real-world samples was also evaluated.
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