He Lijun, Zhang Wenzhu, Zhao Liang, Liu Xia, Jiang Shengxiang
Lanzhou Institute of Chemical Physics, Chinese Academy of Sciences, Tianshui Road 342, Lanzhou 73000, China.
J Chromatogr A. 2003 Jul 25;1007(1-2):39-45. doi: 10.1016/s0021-9673(03)00987-7.
The chromatographic behavior of ephedrines (norephedrine, ephedrine, pseudoephedrine and methylephedrine) on a C18 column was studied with different concentrations of 1-butyl-3-methylimidazolium tetrafluoroborate ionic liquids as the eluent at pH 3.0. The addition of ionic liquid has great effects on the separation of these basic compounds: decreasing band tailing, reducing band broadening, and improving resolution. The retention times of the analytes increase at first and then decrease with the increase in the concentration of ionic liquid. This effect may be attributed to the competition between imidazolium cations and the polar groups of the analytes for the silanol group on the alkylsilica surface, and also to the formation of weak bilayer electronic structure on the C18 column. Several ionic liquids with different alkyl substituents on the imidazolium cations or with different counterions as the eluents were compared.
在pH 3.0条件下,以不同浓度的1-丁基-3-甲基咪唑四氟硼酸盐离子液体为洗脱剂,研究了麻黄碱(去甲麻黄碱、麻黄碱、伪麻黄碱和甲基麻黄碱)在C18柱上的色谱行为。离子液体的加入对这些碱性化合物的分离有很大影响:减少拖尾、降低峰展宽并提高分离度。随着离子液体浓度的增加,分析物的保留时间先增加后减少。这种效应可能归因于咪唑阳离子与分析物的极性基团在烷基硅胶表面上对硅醇基团的竞争,也归因于在C18柱上形成弱双层电子结构。比较了几种咪唑阳离子上具有不同烷基取代基或具有不同抗衡离子作为洗脱剂的离子液体。