高等学校化学学报

• 研究论文 • 上一篇    下一篇

巯基-烯点击反应制备手性多亚胺大环键合手性固定相用于高效液相色谱对映体分离

吴嘉蕾,俞力琴,谢生明,王帮进,章俊辉,袁黎明   

  1. 云南师范大学化学化工学院 云南省现代分离分析与物质转化重点实验室 
  • 收稿日期:2025-04-07 修回日期:2025-07-11 网络首发:2025-09-04 发布日期:2025-09-04
  • 通讯作者: 章俊辉 E-mail:zjh19861202@126.com
  • 基金资助:
    国家自然科学基金(批准号: 22064020, 22364022, 22174125)资助

Preparation of a Chiral Polyimine Macrocycle Bonded Chiral Stationary Phase via Thiol-Ene Click Reaction for Enantioseparation in High-Performance Liquid Chromatography

WU Jialei, YU Liqin, XIE Shengming, WANG Bangjin, ZHANG Junhui, YUAN Liming   

  1. Yunnan Key Laboratory of Modern Separation Analysis and Substance Transformation, College of Chemistry and Chemical Engineering, Yunnan Normal University
  • Received:2025-04-07 Revised:2025-07-11 Online First:2025-09-04 Published:2025-09-04
  • Contact: Jun-Hui Zhang E-mail:zjh19861202@126.com
  • Supported by:
    Supported by the National Natural Science Foundation of China (No. 22064020, 22364022, 22174125)

摘要: 本文以(S)-2,2'-二羟基-1,1'-联萘基-3,3'-二醛和1,2-苯二胺通过一步缩合反应合成了一种手性多亚胺大环(BINOL-CPM),将其修饰后利用巯基-烯点击反应键合到巯基硅胶表面制得了一种高效液相色谱手性固定相(CSP)。该CSP填充的色谱柱在正相(NP)和反相(RP)洗脱模式下均具有较好的手性拆分性能,有12种外消旋体在NP洗脱模式下实现了拆分,6种外消旋体在NP洗脱模式下实现了拆分。将该柱对这些外消旋体的拆分效果与两种常用的商品柱(Chiralpak AD-H和Chiralcel OD-H)进行了比较,NP洗脱模式下拆分的12种外消旋体中有1-(3-氟苯基)乙醇、1-苯乙醇、3-羟基-2-丁酮和1-(4-氟苯基)乙醇这4种外消旋体不能在Chiralpak AD-H柱上获得拆分,有1-(3-氟苯基)乙醇、3-羟基-2-丁酮和1-(4-氟苯基)乙醇这3种外消旋体不能在Chiralcel OD-H柱上获得拆分;RP洗脱模式下拆分的6种外消旋体中有1种(1-苯乙醇)不能在Chiralpak AD-H柱上获得拆分,一些手性化合物在该柱上的分离度(Rs)也高于其在这两种商品柱上的Rs。因此,该制备柱与这两种常用的商品柱之间具有良好的手性拆分互补性,可拆分它们不能拆分或不能很好拆分的一些手性化合物。此外,该柱还表现出优秀的拆分重现性和稳定性,在经历数百次进样使用后,对扁桃酸乙酯拆分的两个对映体色谱峰的保留时间(tR)和Rs与柱使用之初没有显著变化,其色谱峰的tR的相对标准偏差(RSD,n=5)小于0.49%,Rs的RSD(n = 5)小于2.88%。此外,该色谱柱的柱间重现性也较好,不同批次制备的柱对扁桃酸乙酯拆分的两个对映体色谱峰的tR和Rs的RSD(n=3)分别小于1.09%和5.75%。本研究表明BINOL-CPM是一种良好的HPLC手性分离材料,具有良好的研究意义和价值,也能为新型高效液相色谱CSP的研究提供参考。

关键词: 高效液相色谱, 手性分离, 手性固定相, 手性多亚胺大环

Abstract: In this study, a chiral polyimine macrocycle, BINOL-CPM, was synthesized via a one-step condensation of (S)-2,2'-dihydroxy-[1,1'-binaphthalene]-3,3'-dialdehyde and 1,2-phenylenediamine. After modification, it was bonded to the surface of thiolated silica via thiol-ene click reaction to fabricate a chiral stationary phase (CSP) for high-performance liquid chromatography (HPLC). The CSP-packed column exhibits good chiral separation performance in both normal-phase (NP) and reversed-phase (RP) elution modes, with 12 racemates resolved in the NP mode and 6 racemates resolved in the RP mode. The chiral separation performance of this column for these resolved racemates was compared with two commonly used commercial columns, Chiralpak AD-H and Chiralcel OD-H. Among the 12 racemates resolved in the NP mode, 4 racemates [1-(3-fluorophenyl)ethanol, 1-phenylethanol, 3-hydroxy-2-butanone, and 1-(4-fluorophenyl)ethanol] could not be resolved on the Chiralpak AD-H column, and 3 racemates [1-(3-fluorophenyl)ethanol, 3-hydroxy-2-butanone, and 1-(4-fluorophenyl)ethanol] could not be resolved on the Chiralcel OD-H column. Among the 6 racemates resolved in the RP mode, 1 racemates (1-phenylethanol) could not be resolved on the Chiralpak AD-H column. Moreover, the resolution values (Rs) of some racemates on this column was higher than that on the two commercial columns. Therefore, this prepared column demonstrates good complementarity in chiral separation with the two commonly used commercial columns, enabling the separation of some chiral compounds that cannot be resolved or not well be resolved by these two commercial columns. In addition, the column also demonstrates excellent reproducibility and stability in chiral separation. After hundreds of injections, the retention time (tR) and Rs of the two enantiomeric peaks for the separation of ethyl mandelate shows no significant changes compared to the initial use of the column. The relative standard deviation (RSD, n = 5) of tR for the chromatographic peaks of the two enantiomers was less than 0.49 %, and the RSD of Rs (n = 5) was less than 2.88 %. Moreover, the column-to-column reproducibility was also good, with the RSD (n = 3) of tR and Rs for the two enantiomeric peaks of ethyl mandelate separation on columns prepared from different batches being less than 1.09 % and 5.75 %, respectively. This study indicates that BINOL-CPM is a promising chiral separation material for HPLC and has good research significance and value. It also provides a reference for the development of novel HPLC CSP.

Key words: High-performance liquid chromatography, Chiral separation, Chiral stationary phase, Chiral polyimide macrocycle

中图分类号: 

TrendMD: