Comparison of separation performances of novel β-cyclodextrin-based chiral stationary phases in high-performance liquid chromatographic enantioseparation.
Comparison of separation performances of novel β-cyclodextrin-based chiral stationary phases in high-performance liquid chromatographic enantioseparation.
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DOI:
10.1016/j.jpba.2012.05.023
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发表时间:
2012-11
影响因子:
3.4
通讯作者:
G. Varga;G. Fodor;I. Ilisz;J. Szeman;J. Visy;L. Szente;A. Péter
中科院分区:
文献类型:
--
作者:
G. Varga;G. Fodor;I. Ilisz;J. Szeman;J. Visy;L. Szente;A. Péter
Three β-cyclodextrin-based chiral stationary phases were developed applying novel bonding chemistry. The separation performances of β-cyclodextrin, (R,S)-2-hydroxypropyl-β-cyclodextrin, and permethyl-β-cyclodextrin-based CSPs were compared in the resolution of structurally divergent analytes, such as coumarins, dansyl amino acids, and propionic acid derivatives. Separations were carried out in reversed phase mode applying 0.1% triethylammonium phosphate (pH 3.5)/MeOH mobile phase systems in different compositions. Of the three novel CSPs the permethyl-β-cyclodextrin bonded phase proved to be the most effective one for the enantioseparation of investigated analytes.