首页> 外文会议>International Conference on Smart Materials and Nanotechnology in Engineering >Synthesis and Self-assembly Behavior of Chiral Amphiphilic Diblock Copolymers Bearing L-phenylalanine1
【24h】

Synthesis and Self-assembly Behavior of Chiral Amphiphilic Diblock Copolymers Bearing L-phenylalanine1

机译:手性两亲二嵌段共聚物轴承L-苯丙胺1的合成及自组装行为

获取原文

摘要

Novel chiral amphiphilic diblock copolymers bearing L-phenylalanine was synthesized using a "click" reaction of N3-L-phenylalanine and MPEO-b-PGPE. The structure and composition of copolymers were characterized by 1H-NMR and elemental analysis. Additionally, the selfassembly behavior of these chiral copolymers was investigated in sodium dihydrogen phosphate buffer (pH 4.5): the CMC of copolymer MPEO-b-PGTP determined by the measurement of surface tension was 2.1 mg/mL; the size and morphology of the micelles were studied using TEM; the specific optical rotation ([α]25D) of the micellar solutions was also measured; the result indicated that the copolymers can form chiral micelles in sodium dihydrogen phosphate buffer (pH =4.5). In recent years, the synthesis, structure and properties of optically active polymer have been paid attention by scientists owing to its potential applications in chiral separation, asymmetric adsorption, chiral synthesis[1]. The amphiphilic block polymers bearing amino acid possess not only the characteristics of the conventional amphiphilic block copolymer, but also good optically activity and biocompatibility. So it can be employed as nanoreactors for asymmetrical catalysis and materials for drug delivery. But there have been few reports published on the synthesis of chiral amphiphilic copolymers bearing amino acid. Sutthira Sutthasupa reported the synthesis of amino acid-based norbornene block copolymer with ester and carboxyl groups as hydrophobic and hydrophilic units[2]. O'Reilly group synthesized the amino acid-based chiral amphiphilic block copolymers using RAFT technique, and elucidated its self-assembly into spherical micelles with optically active hydrophobic core[3]. In the present work, chiral amphiphilic diblock copolymers bearing L-phenylalanine (L-Phe) pendants poly(ethylene oxide)-b-poly (glycidyl triazolyl-Lphenylalanine) (MPEO-b-PGTP) have been synthesized by the modification of poly(ethylene oxide)-b-poly (propargyl glycidyl ether) (MPEO-b-PGPE) with L-phenylalanine.
机译:使用N3-L-苯丙氨酸和MPEO-B-PGPE的“点击”反应合成轴承L-苯丙氨酸的新型手性两亲二嵌段共聚物。共聚物的结构和组成特征在于1H-NMR和元素分析。另外,在二氢磷酸钠缓冲液(pH4.5)中研究了这些手性共聚物的自主结构行为:通过表面张力测量测定的共聚物MPEO-B-PGTP的CMC为2.1mg / ml;使用TEM研究胶束的大小和形态;还测量胶束溶液的特定光学旋转([α] 25d);结果表明,共聚物可以在二氢磷酸钠缓冲液(pH = 4.5)中形成手性胶束。近年来,由于其在手性分离,不对称吸附,手性合成中的潜在应用,科学家已经受到关注的合成,结构和性质。轴承氨基酸的两亲嵌段聚合物不仅具有常规两亲嵌段共聚物的特性,而且具有良好的光学活性和生物相容性。因此,它可以作为纳米反应器用于不对称催化和药物递送材料。但是关于携带氨基酸的手性两亲性共聚物的合成,已经发表了很少的报道。 Sutthira Sutthasupa报道了用酯和羧基作为疏水性和亲水单元合成氨基酸基降冰片烯共聚物[2]。 O'Reilly Group合成使用筏技术合成基于氨基酸的手性两亲嵌段共聚物,并用光学活性疏水芯阐明其自组装成球形胶束[3]。在本作的情况下,通过修饰聚合物(Poly)已经合成了轴承L-苯丙氨酸(L-PHE)坠子(L-PHE)侧链聚(环氧乙烷)-B-聚(缩水甘油酯三唑基 - 苯甲酰丙氨酸)(MPEO-B-PGTP)(MPEO-B-PGTP)的手性两亲二嵌段共聚物已经合成(环氧乙烷)-B-聚(炔丙基缩水甘油醚)(MPEO-B-PGPE)与L-苯丙氨酸。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号