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R-1-苯基乙基氨基甲酸酯-β-环糊精键合手性固定相的制备与应用研究

Preparation and Application of R-1-Phenylethylcarbamoylated β-CD Bonded Chiral Stationary Phase

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【作者】 郭丽珍余光艳望丹妮谢飞云李杭燕林杰翁文

【Author】 Guo Li-zhen,Yu Guang-yan,Wang Dan-ni,Xie Fei-yun,Li Hang-yan,Lin Jie,Weng Wen(Department of Chemistry and Environmental Science,Zhangzhou Normal University,Zhangzhou,Fujian 363000,China)

【机构】 漳州师范学院化学与环境科学系

【摘要】 利用R-1-苯基乙基异氰酸酯对β-环糊精键合固定相进行衍生,合成了R-1-苯基乙基氨基甲酸酯-β-环糊精手性固定相,填充后在反相条件下考察其对氢化安息香、安息香和α-苯乙醇的手性拆分,探讨了流动相中乙腈含量、缓冲盐类型等对手性拆分的影响。氢化安息香获得了基线分离,分离因子可达1.214,安息香得到了部分分离,α-苯乙醇未能拆开。结合线性溶剂强度(LSS)模型和计量置换理论(SDM-R)对色谱保留机理进行了探讨,认为水分子和乙腈分子一起参与了溶质的置换。

【Abstract】 R-1-Phenylethylcarbamoylated β-CD bonded chiral stationary phase(CSP) was prepared from R-1-phenylethyl isocyanate and β-cyclodextrin bonded CSP.The obtained CSP was packed into stainless steel column by slurry method.Then enantioseparations of hydrobenzoin,benzoin and α-phenethyl alcohol were evaluated under the reverse mode.The effects of acetonitrile amount and buffer type on the retention and enantioseparation were investigated.Hydrobenzoin obtained baseline separation,and the separation factor could reach 1.214.Benzoin obtained partial enantioseparation,and α-phenethyl alcohol could not be separated wholly.Chromatographic retention mechanism was studied further with linear solvent strength(LSS) model and stoichiometric displacement method for retention(SDM-R).Water molecules and acetonitrile molecules were considered to participate in the displacing process of the solute.

【基金】 国家自然科学基金资助项目(20705031);福建省高校新世纪优秀人才支持计划资助项目(JK2011030)
  • 【文献出处】 福建分析测试 ,Fujian Analysis & Testing , 编辑部邮箱 ,2012年04期
  • 【分类号】O657.7
  • 【被引频次】1
  • 【下载频次】82
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