Bielejewska Anna, Duszczyk Kazimiera, Kulig Katarzyna, Malawska Barbara, Miśkiewicz Magdalena, Leś Andrzej, Zukowski Janusz
Institute of Physical Chemistry, Polish Academy of Sciences, Kasprzaka 44/52, 01-224 Warsaw, Poland.
J Chromatogr A. 2007 Nov 30;1173(1-2):52-7. doi: 10.1016/j.chroma.2007.09.070. Epub 2007 Oct 7.
Chiral separations of a series of 15 pyrrolidin-2-ones on polysaccharide stationary phases in the HPLC system have been reported. Three stationary phases have been applied: Chiralpak AD, Chiralpak IA and Chiralcel OD. The changes of retention and enantioselectivity have been examined depending on the organic modifier (ethanol or 2-propanol). The addition of a small amount of water has also been studied. Amylose columns exhibit better enantioselectivity (higher alpha values) than cellulose ones. All compounds can be enantiomerically separated on a Chiralpak IA column with EtOH as the organic modifier. The separation of all compounds on a Chiralpak AD and Chiralcel OD columns required changes of mobile phase composition. Depending on the structure of the compounds, the type of stationary phase, as well as the composition of the mobile phase, different intermolecular interactions can play a key role in chiral discrimination.
已有报道在高效液相色谱系统中,一系列15种吡咯烷-2-酮在手性多糖固定相上的手性拆分情况。采用了三种固定相:Chiralpak AD、Chiralpak IA和Chiralcel OD。研究了保留和对映体选择性随有机改性剂(乙醇或2-丙醇)的变化情况。还研究了添加少量水的情况。直链淀粉柱表现出比纤维素柱更好的对映体选择性(更高的α值)。所有化合物都可以在以乙醇为有机改性剂的Chiralpak IA柱上实现对映体分离。在Chiralpak AD和Chiralcel OD柱上分离所有化合物需要改变流动相组成。根据化合物的结构、固定相类型以及流动相组成,不同的分子间相互作用在手性识别中可能起关键作用。