Acta Chimica Sinica ›› 2011, Vol. 69 ›› Issue (14): 1705-1714. Previous Articles     Next Articles

Full Papers

采用新型分子表面印迹技术构建手性空穴实现对氨基酸对映体识别拆分的研究

陈迎鑫,高保娇*,姜桂明,张瑞霞   

  1. (中北大学化工系 太原 030051)
  • 投稿日期:2010-11-25 修回日期:2011-02-20 发布日期:2011-03-17
  • 通讯作者: 高保娇 E-mail:gaobaojiao@126.com
  • 基金资助:

    山西省自然科学基金资助项目

Constituting Chiral Caves by Using Novel Surface-Molecular Imprinting Technique and Realizating Chiral Separation of Enantiomers of Amino Acid

CHEN Ying-Xin, GAO Bao-Jiao, JIANG Gui-Ming, ZHANG Rui-Xia   

  1. (Department of Chemical Engineering, North University of China, Taiyuan 030051)
  • Received:2010-11-25 Revised:2011-02-20 Published:2011-03-17
  • Contact: Bao-jiao GAO E-mail:gaobaojiao@126.com

Dimethylaminoethyl methacrylate (DMAEMA) was grafted on micron-sized silica gel particles in a manner of “graft from” in a solution polymerization system by right of the mediation action of the coupling agent 3-methacryloxypropyl trimethoxysilane (MPS), obtaining the grafted functional particles PDMAEMA/SiO2. Then, the molecular imprinting towards the grafted PDMAEMA was performed with L-Asp that is one enantiomer of aspartic acid (Asp) as template molecule and dichloroether as crosslinking agent by using the novel surface-molecular imprinting technique established by our research group, and the L-Asp molecule-imprinted material MIP-PDMAEMA/SiO2 was prepared. Both static and dynamic methods were adopted to study the recognition property of MIP-PDMAEMA/SiO2 particles for L-Asp with respect to another enantiomer of aspartic acid, D-Asp, and the separation ability towards L-Asp and D-Asp in the raceme. The experiment results show that MIP-PDMAEMA/SiO2 particles possess obvious recognition selectivity and fine binding affinity for L-Asp, and the selectivity coefficient is equal to 3.24. Besides, MIP-PDMAEMA/SiO2 particles have excellent elution property, and with a diluted aqueous solution of NaOH as the eluent, the desorption ratios of L-Asp reach 99.73% in 13 BV.

Key words: aspartic acid, enantiomer separation, sueface-molecular imprinting, dimethylaminoethyl methacrylate, graft polymerization, molecular recognition

CLC Number: