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在不同溶剂中两亲性超支化多臂嵌段共聚物自组装的相图的耗散粒子动力学模拟研究。

A dissipative particle dynamics simulation study on phase diagrams for the self-assembly of amphiphilic hyperbranched multiarm copolymers in various solvents.

机构信息

School of Chemistry and Chemical Engineering, State Key Laboratory of Metal Matrix Composites, Shanghai Jiao Tong University, 800 Dongchuan Road, Shanghai 200240, P. R. China.

出版信息

Soft Matter. 2017 Sep 20;13(36):6178-6188. doi: 10.1039/c7sm01170a.

Abstract

Self-assembly of amphiphilic hyperbranched multiarm copolymers (HMCs) has shown great potential for preparing all kinds of delicate supramolecular structures in all scales and dimensions in solution. However, theoretical studies on the influencing factors for the self-assembly of HMCs have been greatly lagging behind. The phase diagram of HMCs in selective solvents is very necessary but has not been disclosed up to now. Here, the self-assembly of HMCs with different hydrophilic fractions in various solvents was studied systematically by using dissipative particle dynamics (DPD) simulations. Three morphological phase diagrams are constructed and a rich variety of morphologies, ranging from spherical micelles, worm-like micelles, membranes, vesicles, vesosomes, small micellar aggregates (SMAs), and aggregates of spherical and worm-like micelles to helical micelles, are obtained. In addition, both the self-assembly mechanisms and the dynamic processes for the formation of these self-assemblies have been systematically investigated. The simulation results are consistent with available experimental observations. Besides, several novel structures, like aggregates of spherical and worm-like micelles, vesosomes and helical micelles, are firstly discovered for HMC self-assembly. We believe the current work will extend the knowledge on the self-assembly of HMCs, especially on the control of supramolecular structures and on fabricating novel self-assemblies.

摘要

两亲性超支化多臂共聚物(HMCs)的自组装在溶液中制备各种精细的超分子结构方面具有很大的潜力,其在各种规模和维度上都可以实现。然而,关于 HMC 自组装影响因素的理论研究却严重滞后。HMC 在选择性溶剂中的相图非常必要,但迄今为止尚未公布。在此,我们通过耗散粒子动力学(DPD)模拟系统地研究了不同亲水区分数的 HMC 在各种溶剂中的自组装。构建了三个形态相图,并得到了丰富多样的形态,包括球形胶束、蠕虫状胶束、膜、囊泡、囊泡体、小胶束聚集体(SMAs)以及球形和蠕虫状胶束的聚集体和螺旋胶束。此外,还系统地研究了这些自组装体的形成的自组装机制和动态过程。模拟结果与现有的实验观察结果一致。此外,对于 HMC 自组装,我们首次发现了几种新颖的结构,如球形和蠕虫状胶束的聚集体、囊泡体和螺旋胶束。我们相信目前的工作将扩展对 HMC 自组装的认识,特别是对超分子结构的控制和新型自组装体的构建。

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