Structural Difference in the Core-forming Block Reshapes RAFT-mediated Polymerization-induced Self-assembly

IF 4.1 2区 化学 Q2 POLYMER SCIENCE
Yue-Xi Zhan, Li Zhang, Chun Feng, Jian-Bo Tan
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引用次数: 0

Abstract

Polymerization-induced self-assembly (PISA) has become one of the most versatile approaches for scalable preparation of linear block copolymer nanoparticles with various morphologies. However, the controlled introduction of branching into the core-forming block and the effect on the morphologies of block copolymer nanoparticles under PISA conditions have rarely been explored. Herein, a series of multifunctional macromolecular chain transfer agents (macro-CTAs) were first synthesized by a two-step green light-activated photoiniferter polymerization using two types of chain transfer monomers (CTMs). These macro-CTAs were then used to mediate reversible addition-fragmentation chain transfer (RAFT) dispersion polymerization of styrene (St) to prepare block copolymers with different core-forming block structures and the assemblies. The effect of the core-forming block structure on the morphology of block copolymer nanoparticles was investigated in detail. Transmission electron microscopy (TEM) analysis indicated that the brush-like core-forming block structure facilitated the formation of higher-order morphologies, while the branched core-forming block structure favored the formation of lower-order morphologies. Moreover, it was found that using macro-CTAs with a shorter length also promoted the formation of higher-order morphologies. Finally, structures of block copolymers and the assemblies were further controlled by changing the structure of macro-CTA or using a binary mixture of two different macro-CTAs. We expect that this work not only sheds light on the synthesis of block copolymer nanoparticles but also provide important mechanistic insights into PISA of nonlinear block copolymers.

核形成块的结构差异重塑了raft介导的聚合诱导的自组装
聚合诱导自组装(PISA)已成为制备具有各种形态的线性嵌段共聚物纳米粒子的最通用的方法之一。然而,在PISA条件下,控制引入分支进入成核块以及对嵌段共聚物纳米颗粒形貌的影响很少被探索。本文首次以两种链转移单体(CTMs)为原料,采用两步绿光活化光干扰素聚合法合成了一系列多功能大分子链转移剂(macro- cta)。然后,利用这些宏观cta介导苯乙烯(St)的可逆加成-破碎链转移(RAFT)分散聚合,制备了具有不同成核嵌段结构的嵌段共聚物。研究了成核嵌段结构对嵌段共聚物纳米颗粒形貌的影响。透射电镜(TEM)分析表明,电刷状成核块结构有利于高阶形貌的形成,而支状成核块结构有利于低阶形貌的形成。此外,使用较短长度的宏观cta也促进了高阶形貌的形成。最后,通过改变宏观cta的结构或使用两种不同的宏观cta的二元混合物来进一步控制嵌段共聚物及其组装体的结构。我们期望这项工作不仅能阐明嵌段共聚物纳米颗粒的合成,而且能为非线性嵌段共聚物的PISA提供重要的机理见解。
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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来源期刊
Chinese Journal of Polymer Science
Chinese Journal of Polymer Science 化学-高分子科学
CiteScore
7.10
自引率
11.60%
发文量
218
审稿时长
6.0 months
期刊介绍: Chinese Journal of Polymer Science (CJPS) is a monthly journal published in English and sponsored by the Chinese Chemical Society and the Institute of Chemistry, Chinese Academy of Sciences. CJPS is edited by a distinguished Editorial Board headed by Professor Qi-Feng Zhou and supported by an International Advisory Board in which many famous active polymer scientists all over the world are included. The journal was first published in 1983 under the title Polymer Communications and has the current name since 1985. CJPS is a peer-reviewed journal dedicated to the timely publication of original research ideas and results in the field of polymer science. The issues may carry regular papers, rapid communications and notes as well as feature articles. As a leading polymer journal in China published in English, CJPS reflects the new achievements obtained in various laboratories of China, CJPS also includes papers submitted by scientists of different countries and regions outside of China, reflecting the international nature of the journal.
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