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ClassificationCode:O652.6;TQ028.8
year,volume(issue):pagination: 2020,40(2):1-5

Abstract:
 Using vancomycin and 1,6-diisocyanatehexane as monomers, an enantioselective composite membrane was prepared by interfacial polymerization on a polyethersulfone support. After the composite membrane was mounted in a home-made device of membrane chromatography for high performance liquid chromatography, the enantioseparation of D,L-phenylglycine was carried outed by the chiral membrane chromatography. By optimizing the injection volume, the flow rate, the constituent of mobile phase, the size of the membrane, the layer numbers of the membrane, over 5.66 of separation factor (α) and 0.66 of resolution (Rs ) could be obtained, respectively. The advantage of the method is the ability to separate and prepare chiral compounds in an aqueous environment, which is rare in chromatographic chiral separation.

Funds:
国家自然科学基金地区项目“界面聚合手性高分子复合膜研究”(21365025)、国家自然科学基金重大研究计划项目“手性高分子固膜的精准结构调控和制备研究”(91856123)

AuthorIntro:
第一作者简介:艾萍(1962-),女,四川高县人,教授,从事手性分离研究,E-mail:aipdeyx@aliyun.com 通讯作者:E-mail:yuan_limingpd@126.com

Reference:
 [1] Wang L, Ghosh R. Feasibility study for the fractionation of the major human immunoglobulin G subclasses using hydrophobic interaction membrane chromatography [J]. Anal Chem, 2010, 82: 452-455.[2] Madadkar P, Umatheva U, Hale G,et al. Ultrafast separation and analysis of monoclonal antibody aggregates using membrane chromatography [J]. Anal Chem, 2017, 89: 4716-4720.
[3] 刘丛丛,裴洪昌,刘耀龙,等. 氨基苯并-15-冠-5接枝聚砜多孔膜填充膜色谱构建及锂同位素吸附分离性能研究[J].膜科学与技术,2018,38(4),14-22.
[4] Osada Y, Ohta F, Mizumoto A, et al. Specific permeation and adsorption of aqueous amino acids by plasma-polymerized membranes of d-camphor and l-menthol [J]. Journal of the Chemical Society of Japan, 1986, (7): 866-872.
[5] Yang M, Chu L, Wang H, et al. A thermoresponsive membrane for chiral resolution [J]. Adv Funct Mater, 2008, 18(4): 652-663.
[6] Xie R, Chu L Y, Deng J G. Membranes and membrane processes for chiral resolution [J]. Chem Soc Rev, 2008, 37(6): 1243-1263.
[7] Wang W J, Dong X L, Nan J P, et al.  A homochiral metal-organic framework membrane for enantioselective separation [J]. Chem Commun, 2012, 48(56): 7022-7024.
[8] Kang Z X, Xue M, Fan L L, et al.  “Single nickel source” in situ fabrication of a stable homochiral MOF membrane with chiral resolution properties [J]. Chem Commun, 2013, 49(90): 10569-10571.
[9] Meng C C, Chen Q B, Liu H L, et al.  Role of filled PLGA in improving enantioselectivity of Glu-GO/PLGA composite membranes [J]. J. Membr Sci, 2018, 555: 398-406.
[10] Higuchi A, Tamai M, Ko Y A, et al.  Polymeric membranes for chiral separation of pharmaceuticals and chemicals [J]. Polym Rev, 2010, 50(2):113-143.
[11] Yoshikawa M, Tharpa K, Dima S O. Molecularly imprinted membranes: past, present, and future [J]. Chem Rev, 2016, 116(19): 11500-11528.
[12] 艾萍,张紫恒,袁黎明. 金属-有机骨架材料[Zn2Camph2(dabco)].DMF.H2O作为手性选择剂的高分子膜及其应用研究[J].膜科学与技术, 2018, 38(5): 84-87.
[13] Yuan L M, Ma W, Xu M, et al. Optical resolution and mechanism using enantioselective membranes of cellulose, sodium alginate and hydroxypropyl-β-cyclodextrin [J]. Chirality, 2017, 29:

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