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Enantioselective Separation on a Chiral Stationary Phase of Polysaccharide with 3,5-Dimethylphenylcarbamate Prepareded by ATRP

机译:通过ATRP制备的3,5-二甲基苯基氨基甲酸酯与多糖的手性固定相的对映选择性分离

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1.Introduction Polysaccharide derivatives coating onto silica matrices represents nowadays one of the most popular chiral stationary phases (CSPs) and these kinds of phases are commercially available [1-2]. However, the solubility of polysaccharide derivatives in a number of solvents limits the application range on the commercial chiral columns. This problem can be solved by chemically fixing polysaccharide derivatives onto silica matrices. Chemically bonded cellulose and amylose phenyicarbamate-based CSPs have been prepared by radical polymerization, radical co-polymerization reaction, and etc. By many researchers [3-5] On the one hand, atom transfer radical polymerization (ATRP) technique is very efficient for grafting from solid surfaces. Also, ATRP allows better control over the molecular weight and distribution of the target polymer, much attention has been paid to the use of this polymerization method in the synthesis of polymer brushes from a surface [6-7].
机译:1.引言如今,涂覆在硅胶基质上的多糖衍生物代表了最流行的手性固定相(CSP)之一,这些相可从市场上买到[1-2]。然而,多糖衍生物在多种溶剂中的溶解度限制了在商业手性柱上的应用范围。这个问题可以通过将多糖衍生物化学固定在二氧化硅基质上来解决。已通过自由基聚合,自由基共聚反应等方法制备了化学键合的纤维素和直链淀粉苯甲氨基甲酸酯基CSP。许多研究者[3-5]一方面,原子转移自由基聚合(ATRP)技术非常有效从固体表面接枝。同样,ATRP可以更好地控制目标聚合物的分子量和分布,在从表面合成聚合物刷的过程中已经非常关注这种聚合方法的使用[6-7]。

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