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A polymeric chiral surface functionality immobilized on uniformly sized macroporous polymer beads

机译:固定在大小均一的大孔聚合物微珠上的聚合物手性表面官能团

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Uniformly sized functionalized macroporous polymer beads were prepared by either a classical copolymerization method or recently reported in situ surface modification method utilizing chiral methacrylamide as a functional modifier. To evaluate conformational and/or specific differences in their surface chiral functionality, we applied chromatographic evaluation techniques. The prepared modified beads were utilized as chiral stationary phase in high-performance liquid chromatography (HPLC). Those prepared by the in situ surface modification method tended to show higher chiral recognition ability than those by the classical copolymerization method, even if the equivalent amount of the chiral functional group was involved within polymer beads. Detailed chromatographic studies exhibited the in situ surface modification method could lead to polymeric methacrylamide functionality on the surface within relatively large pore size regions of the macroporous polymer beads, while the classical copolymerization method tended to form less polymeric surface functionality. The difference in the chiral surface functionality on both of macroporous polymer beads afforded drastic change in chromatographic chiral recognition ability. Complete resolution of a drug, thalidomide could be achieved on the chiral stationary phase with the polymeric chiral surface functionality, while no resolution was found on that with the monomeric one even if the same chiral methacrylamide was used as a modifier to prepare the chiral stationary phases. (C) 1997 John Wiley & Sons, Inc.
机译:通过经典的共聚方法或最近报道的利用手性甲基丙烯酰胺作为功能性改性剂的原位表面改性方法来制备均一尺寸的功能化大孔聚合物珠。为了评估其表面手性功能的构象和/或特定差异,我们应用了色谱评估技术。制备的修饰珠在高效液相色谱(HPLC)中用作手性固定相。即使在聚合物珠粒中包含等量的手性官能团,通过原位表面改性方法制备的那些手征也倾向于比通过经典共聚方法获得的手征识别能力更高。详细的色谱研究表明,原位表面改性方法可能导致大孔聚合物珠粒的较大孔径区域内表面上的聚合甲基丙烯酰胺官能团,而经典的共聚方法则倾向于形成较少的聚合物表面官能团。两个大孔聚合物小珠上的手性表面官能度的差异使色谱的手性识别能力发生了巨大变化。可以完全拆分具有药物手性表面功能的手性固定相的沙利度胺,而即使使用相同的手性甲基丙烯酰胺作为改性剂制备手性固定相,也无法在单体型上实现拆分。 (C)1997年John Wiley&Sons,Inc.

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