详细信息

Regulating the self-assembly of rigid 2D ribbon-like amphiphilic homopolymer via tailoring its holistic conformation    

文献类型:期刊文献

中文题名:Regulating the self-assembly of rigid 2D ribbon-like amphiphilic homopolymer via tailoring its holistic conformation

作者:Yumeng Gao[1];Weisheng Feng[1];Yao Sun[1];Yuan Yao[1];Liquan Wang[1];Shaoliang Lin[1]

机构:[1]Shanghai Key Laboratory of Advanced Polymeric Materials,Frontiers Science Center for Materiobiology and Dynamic Chemistry of Ministry of Education,School of Materials Science and Engineering,East China University of Science and Technology,Shanghai,200237,China

年份:2023

卷号:66

期号:8

起止页码:2339

中文期刊名:Science China Chemistry

外文期刊名:中国科学(化学英文版)

收录:CSTPCD;;Scopus;CSCD:【CSCD2023_2024】;PubMed;

基金:supported by the National Natural Science Foundation of China(52073094,52073092,52273291);the Projects of Shanghai Municipality(20ZR1415600)。

语种:英文

中文关键词:self-assembly;tunable conformation;rigid skeleton;two-dimensional nanoribbon;stimuli response

摘要:Amphiphilic rigid backbone polymers are traditionally seemed as one-dimensional(1D)rods and show distinct self-assembly behavior to flexible polymers,but they could hardly adapt morphology-tunable self-assembly by changing their holistic conformation upon external stimuli.In this study,we synthesized a series of amphiphilic homopolymers poly(acetylene azobenzene oligoethylene glycol)(P(AAzo-EGx))containing conjugated polyacetylene mainchain,azobenzene pendants and oligo ethylene glycol tails in each unit.This comb-like amphiphilic polymer could be treated as two-dimensional(2D)nanoribbons with tunable holistic conformation via meticulous tailoring intrastrand repulsion and interchainπ-πinteraction of azobenzene pendants by light,temperature,and solvent swelling.P(AAzo-EG_(2))could self-assemble into large vesicles in ambient,whereas transformed to supramolecular helix bundles(SHBs)at 65℃as well as depicted by dissipative particle dynamics(DPD)simulation,and then turned into grass leaf-like micelles upon sequential ultraviolet(UV)and blue light irradiation.The three assemblies featured different stacking mode of PAAzo skeletons although showed similar aggregate induce emission(AIE)effect.In this holistic macromolecular chain conformation-induced self-assembly and morphology transformation,temperature influenced the stacking of hydrophobic parts mainly by tuning the torsion of PAAzo skeleton.Certain amount of good solvent played a vital role by swelling of hydrophobic PAAzo skeleton,and helping the movement and rearrangement of azobenzene pendants and polyacetylene mainchains like a lubricant.The length and diameter of SHBs could be tuned by changing EGxtails.This work uncovered a facile strategy to tailor the self-assembly of rigid backbone polymers for fabrication of functional nanodevices.

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