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Reference type: Journal
Authors: Gao BJ, Chen YX, Men JY
Article Title: Constructing chiral caves and efficiently separating enantiomers of glutamic acid with novel surface-imprinting technique.
Publication date: 2011
Journal: Journal of Chromatography A
Volume: 1218
Issue: (32)
Page numbers: 5441-5448.
DOI: 10.1016/j.chroma.2011.06.003
Alternative URL: http://www.sciencedirect.com/science/article/pii/S0021967311007977

Abstract: Dimethylaminoethyl methacrylate (DMAEMA) was first graft-polymerized onto the surfaces of micron-sized silica gel particles in the manner of "grafting from" in a solution polymerization system, obtaining the grafted particles PDMAEMA/SiO2. Then, the molecular imprinting towards the grafted PDMAEMA was conducted with one enantiomer of glutamic acid (Glu), l-Glu, as template molecule and with 2,2'-dichlorodiethylether (DCEE) as crosslinking agent by adopting the novel surface-molecular imprinting technique established by our research group, and the single enantiomer (l-Glu) molecule-imprinted material MIP-PDMAEMA/SiO2 was obtained. With another enantiomer of glutamic acid, d-Glu, as the contrast compound, the recognition property of MIP-PDMAEMA/SiO2 for l-Glu was investigated in depth with both static and dynamic methods, and its ability to separate l-Glu and d-Glu in the racemic solution was examined. The experiment results show that the surface-imprinted material MIP-PDMAEMA/SiO2 has fine recognition selectivity and binding affinity for l-Glu, whereas its ability to combine d-Glu is poor. The selectivity coefficient of MIP-PDMAEMA/SiO2 for l-Glu with respect to d-Glu is equal to 3.30, displaying an excellent chiral separation result. It is obvious that in this study, the substance separation at the molecular configuration level has been realized successfully
Template and target information: glutamic acid, Glu, l-Glu
Author keywords: glutamic acid, enantiomer separation, Recognition, Surface-molecular imprinting, Dimethylaminoethyl methacrylate, graft polymerization

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