Reversible Control of Primary and Secondary Self-Assembly of Poly(4-allyloxystyrene)-Block-Polystyrene

E. Yoshida, S. Kuwayama
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引用次数: 1

Abstract

The reversible control of primary and secondary self-assemblies was attained using a poly(4-allyloxystyrene)- block-polystyrene diblock copolymer (PASt- 𝑏 -PSt) through variations in temperature. The copolymer showed no self-assembly in cyclohexane over 3 5 ∘ C and existed as a unimer with a 37.1 nm hydrodynamic diameter. When the temperature was lowered to 3 0 ∘ C , the copolymer formed micelles with 269.9 nm by the primary self-assembly. As the result of further lowering the temperature to 2 0 ∘ C , the secondary self-assembly of the micelles occurred to produce ca. 2975.9 nm aggregates. The aggregates were dissociated into unimers by increasing the temperature up to 4 0 ∘ C . The light scattering studies demonstrated that the thermoresponsivity of the copolymer showed good hysteresis throughout the variation in the temperature in the range between 20 and 4 0 ∘ C , based on the Marquadt analysis of the hydrodynamic diameter distribution. It was found that the primary and secondary self-assemblies of the copolymer were perfectly controlled by the temperature.
聚(4-烯丙氧基苯乙烯)-嵌段聚苯乙烯一、二次自组装的可逆控制
利用聚(4-烯丙氧基苯乙烯)-嵌段-聚苯乙烯二嵌段共聚物(PASt-𝑏- pst)通过温度变化实现了初级和次级自组装的可逆控制。该共聚物在3.5°C以上的环己烷中没有自组装,并以水动力直径为37.1 nm的一元聚合物存在。当温度降至30°C时,共聚物通过初级自组装形成269.9 nm的胶束。当温度进一步降低到20°C时,胶束的二次自组装产生了约2975.9纳米的聚集体。通过将温度升高到40°C,将聚集体分解成聚物。光散射研究表明,根据Marquadt对水动力直径分布的分析,共聚物的热响应性在20至40°C范围内的温度变化过程中表现出良好的滞后性。发现共聚物的一次和二次自组装完全受温度控制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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