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Updated: Apr 28, 2026

Synthesis and Purification of Iodoaziridines Involving Quantitative Selection of the Optimal Stationary Phase for Chromatography
Published on: May 16, 2014
Novel imidazolium-embedded and imidazolium-spaced octadecyl stationary phases for reversed phase liquid
Mingliang Zhang1, Jia Chen2, Tongnian Gu2
1Key Laboratory of Chemistry of Northwestern Plant Resources and Key Laboratory for Natural Medicine of Gansu Province, Lanzhou Institute of Chemical Physics, Chinese Academy of Sciences, Lanzhou 730000, China; University of Chinese Academy of Sciences, Chinese Academy of Sciences, Beijing 100049, China.
Abstract:
Two new stationary phases modified by alkylimidazoliums were prepared for the first time and characterized. One of the new phases was obtained via monomeric immobilization of octadecylimidazole to γ-chloropropyltrimethoxysilane modified silica to form polar-embedded phase; the other one was prepared by co-immobilization of two silane coupling agents (γ-chloropropyltrichlorosilane and octadecyltrichlorosilane) to silica, followed by quaternization of methylimidazole to form polar-spaced phase. This study was intended to compare the retention characteristics of these two stationary phases using linear solvation energy relationships model, as well as to examine the difference in selectivity by eluting alkylbenzenes, alkylnaphthalenes, condensed-ring and phenylene polynuclear aromatic hydrocarbons on both phases. Different effects of distributions of polar functional group and octadecyl chain were found to impact the chromatographic properties.
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