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Polysulfobetaine-based diblock copolymer nano-objects via polymerization-induced self-assembly

机译:Polysulfobetaine-based diblock共聚物通过polymerization-induced nano-objects自组装

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摘要

A zwitterionic polysulfobetaine-based macromolecular chain transfer agent (PSBMA(38)) was prepared by reversible addition-fragmentation chain transfer (RAFT) solution polymerization of [2-(methacryloyloxy)-ethyl] dimethyl(3-sulfopropyl) ammonium hydroxide (SBMA) in an aqueous solution containing 0.5 M NaCl at 70 degrees C. This PSBMA(38) macro-CTA was then utilized for the RAFT aqueous dispersion polymerization of a water-miscible monomer, 2-hydroxypropyl methacrylate (HPMA). The growing PHPMA block became hydrophobic in situ, leading to polymerization-induced self-assembly. Systematic variation of the mean degree of polymerization of the PHPMA block and the copolymer concentration enabled access to pure phases of spheres, worms or vesicles, as judged by transmission electron microscopy and dynamic light scattering studies. A detailed phase diagram was constructed and the thermo-responsive behavior of selected PSBMA(38)-PHPMA(X) nanoparticles was investigated. Finally, the salt tolerance of PSBMA(38)-PHPMA(400) vesicles was compared to that of PGMA(71)-PHPMA(400) vesicles; the former vesicles exhibit much better colloidal stability in the presence of 1 M MgSO4.
机译:一个两性离子polysulfobetaine-based大分子链转移剂(PSBMA (38))是由可逆加成断裂链转移(筏)溶液聚合[2 - (methacryloyloxy) -ethyl]二甲基(3-sulfopropyl)氢氧化铵(SBMA)在水溶液中含有0.5 M氯化钠70度c这PSBMA macro-CTA当时(38)利用筏水分散体水溶性液体单体聚合,2-hydroxypropyl丙烯酸甲酯(HPMA)。原位PHPMA块变成了疏水性,领先polymerization-induced自组装。系统的平均程度的变化PHPMA块和聚合共聚物浓度启用访问纯粹阶段的球体,蠕虫或囊泡,判断通过透射电子显微镜和动态光散射研究。图构建和thermo-responsive的行为选择PSBMA (38) -PHPMA (X)纳米粒子被调查。PSBMA公差(38)-PHPMA(400)囊泡比PGMA (71) -PHPMA(400)囊泡;前囊泡具有更好的胶体稳定在1 M MgSO4面前。

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