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Hydrophobic energy estimation for giant vesicle formation by amphiphilic poly(methacrylic acid)-block-poly(alkyl methacrylate-random-mathacrylic acid) random block copolymers

机译:两亲性聚(甲基丙烯酸)-嵌段-聚(甲基丙烯酸烷基酯-无规-甲基丙烯酸)无规共聚物对大囊泡形成的疏水能估计

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摘要

The self-assembly induced by the photocontrolled/ living radical polymerization mediated by 4-methoxy-2,2,6,6-tetramethylpiperidine-1-oxyl was performed for amphiphilic poly(methacrylic acid)-block-poly(alkyl methacrylate-random-methacrylic acid) containing ethyl, n-propyl, and n-butyl methacrylates in order to control the morphology based on the hydrophobic-hydrophilic balance. The morphology transformation from films to spherical vesicles via the transition was well-controlled by adjusting the ratio of the alkyl methacrylate unit to the methacrylic acid in the hydrophobic random copolymer block. The copolymers formed the respective morphologies at different ratios dependent on the alkyl chain length of the methacrylates; the ratio for the formation of the respective morphologies decreased as the alkyl chain length increased. The hydrophobic energy estimation of these copolymers demonstrated that the respective morphologies had definite hydrophobic energies independent of the alkyl chain length, indicating that the morphologies were determined only by the hydrophobic magnitude of the random copolymer block.
机译:对于两亲性聚(甲基丙烯酸)-嵌段-聚(甲基丙烯酸烷基酯-无规-),进行了由4-甲氧基-2,2,6,6-四甲基哌啶-1-氧基介导的光控/活性自由基聚合诱导的自组装。 (甲基丙烯酸),以控制基于疏水-亲水平衡的形态,以控制甲基丙烯酸乙酯,正丙酯和正丁酯。通过调节疏水性无规共聚物嵌段中甲基丙烯酸烷基酯单元与甲基丙烯酸的比例,可以很好地控制从薄膜到球形囊泡通过过渡的形态转变。取决于甲基丙烯酸酯的烷基链长,共聚物以不同的比例形成各自的形态。随着烷基链长的增加,形成相应形态的比例降低。这些共聚物的疏水能估算结果表明,相应的形态具有独立于烷基链长的确定的疏水能,表明形态仅由无规共聚物嵌段的疏水量决定。

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