Stalcup A M, Chang S C, Armstrong D W, Pitha J
Department of Chemistry, University of Missouri-Rolla 65401.
J Chromatogr. 1990 Jul 27;513:181-94. doi: 10.1016/s0021-9673(01)89435-8.
(S)-2- and (R,S)-2-hydroxypropyl-beta-cyclodextrin have been bonded to silica gel and evaluated as stationary phases for reversed-phase liquid chromatography. Stationary phases also were prepared on two silicas having different pore sizes and surface areas. Dissimilarities were observed in enantiomeric selectivities between these columns and also between these and the native beta-cyclodextrin columns. With the exception of compounds 5 and 10, all other racemates reported here which have been successfully resolved on the new phases are enantiomers which have not been previously reported as separated on the beta-cyclodextrin stationary phase. In some cases, there were also differences in enantioselectivities observed between the (S)- and the (R,S)-hydroxypropyl-beta-cyclodextrin phases on the same silica. The results are discussed in terms of the retention mechanism and compared to results reported earlier for beta-cyclodextrin columns.
(S)-2-和(R,S)-2-羟丙基-β-环糊精已键合到硅胶上,并作为反相液相色谱的固定相进行了评估。还在两种具有不同孔径和表面积的硅胶上制备了固定相。在这些色谱柱之间以及它们与天然β-环糊精色谱柱之间观察到对映体选择性存在差异。除化合物5和10外,本文报道的所有其他已在新固定相上成功拆分的外消旋体都是对映体,以前尚未报道它们在β-环糊精固定相上能够分离。在某些情况下,在相同硅胶上的(S)-和(R,S)-羟丙基-β-环糊精固定相之间也观察到对映体选择性的差异。根据保留机理对结果进行了讨论,并与先前报道的β-环糊精色谱柱的结果进行了比较。