手性固定相Chirex3001对安息香和联萘酚及其类似物的分子识别  

Molecular Recognition of Benzoin and Bi-β-naphthol Analogues by Chirex 3001-based Chiral Stationary Phase

作　　者：尤秀丽[1] 韩大雄[1] 翁文[2] 赵玉芬[1] 

机构地区：[1]厦门大学化学化工学院化学生物学福建省重点实验室,厦门361005 [2]漳州师范学院化学与环境科学系,漳州363000

出　　处：《化学学报》2008年第17期1974-1978,共5页Acta Chimica Sinica

基　　金：国家自然科学基金(No.20705031);福建省自然科学基金(No.U0750017)资助项目.

摘　　要：利用分子力学方法,建立了苯基甘氨酸型手性固定相Chirex3001的简化模型,并探讨了手性固定相Chirex3001与安息香和联萘酚及其类似物的识别机制.模拟结果表明,固定相主体与手性客体分子识别作用的推动力主要来自于它们之间的π-π堆积、氢键和范德华等作用.主体与(S)-构型的客体1～3结合能力强于(R)-构型的客体,而对于客体4～6,则是与(R)-构型的结合强于(S)-构型,这与高效液相色谱拆分实验结果相符.客体1～3对映体在Chirex3001柱上的分离因子分别为1.02,1.04和1.11,(R)-构型先被洗脱;客体4～6对映体的分离因子分别为1.23,1.26和1.09,(S)-构型先被洗脱.The simplified model of （R）-phenylglycine based chiral stationary phase （Chirex 3001） was built to investigate the process of chiral recognition of benzoin and bi-β-naphthol and their analogues by molecular mechanics methods. The results showed that the driving force of chiral recognition came from the π-π stacking, hydrogen bond and van der Waals interactions between the host and the guest molecule. The host preferred to bind with S-enantiomers of benzoin and its analogues 1-3, and preferred to bind with R-enantiomers of bi-β-naphthol and its analogues 4-6. This was consistent with the HPLC experimental results. The separation factors were 1.02, 1.04 and 1.11 respectively for compounds 1-3 when n-hexane/ 1,2-dichloroethane/ethanol （V ： V ： V=83.5 ： 15 ： 1.5） was used as mobile phase, and the R-enantiomers were eluted first. The separation factors were 1.23, 1.26 and 1.11 respectively when n-hexane/ chloroform/ethanol （V：V： V=78.5 ： 20 ： 1.5） was used as mobile phase, and the S-enantiomers were eluted first.

关 键 词：手性识别 分子力学 手性拆分 安息香 联萘酚 

分 类 号：O657.7[理学—分析化学]