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流动相组成和温度对衍生化β-环糊精键合固定相拆分四种仲醇消旋体的影响
  • 期刊名称:化学学报
  • 时间:0
  • 页码:19-21
  • 语言:中文
  • 分类:O657.72[理学—分析化学;理学—化学] TQ455.4[化学工程—农药化工]
  • 作者机构:[1]西北大学化学系西北大学合成与天然功能分子化学教育部重点实验室,西安710069
  • 相关基金:国家自然科学基金(Nos.20575052,20875075)资助项目.
  • 相关项目:小分子药物与定向固定化受体的相互作用研究
作者: 卫引茂|
中文摘要:

采用3,5-二甲苯基异氰酸酯衍生化β-环糊精键合固定相,以正己烷-脂肪醇为流动相,研究了脂肪醇结构及其浓度、柱温对2-苯基环己醇、2-萘基环己醇、4-三氟甲基-2-苯基环己醇以及3-(1-羟乙基)香豆素等四种仲醇手性拆分行为的影响.当流动相中醇的摩尔浓度相同时,异构体容量因子随脂肪醇碳链的增长而减小;柱温升高,异构体容量因子减小,而分离因子增大.用溶质的计量置换保留模型(SDM—R)和热力学理论对此现象进行了解释.

英文摘要:

Four kinds of secondary alcohols, 2-phenylcyclohexanol, 2-(4-trifluoromethylphenyl)-cyclohexanol, 2-(2-naphthalenyl)-cyclohexanol and 3-(1-hydroxyethyl)coumarin, were directly resolved on N- (3,5-dimethylphenyl)carbamate-substituted 6-O-β-cyclodextin bonded silica stationary phase by a normalphase system with n-hexane-alcohol as a mobile phase. The influences of temperature, structure and concentration of the alcohol in the mobile phase on the separation of the four investigated solutes were investigated. It was found that the capacity factors for each diastereomer decreased either with increasing carbon number of alcohol or temperature while selectivity factor increased with temperature at the same molar concentration of alcohol, for which the reason was explained with a stoichiometric displacement model for retention and thermodynamic theory.

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