Polymerization-Induced Self-Assembly Process for All-Styrenic Nano-objects Using the Living Anionic Polymerization Mechanism

Polymerization-Induced Self-Assembly Process for All-Styrenic Nano-objects Using the Living Anionic Polymerization Mechanism
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利用活性阴离子聚合机制的全苯乙烯纳米物体的聚合诱导自组装过程

DOI:
10.1039/d0py00296h
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发表时间:
2020
期刊:
影响因子:
4.6
通讯作者:
Guowei Wang
Guowei Wang
中科院分区:
化学2区
文献类型:
--
作者:
Chengcheng Zhou;Jian Wang;Peng Zhou;Guowei Wang

文献摘要

相似文献

本文报道了活性阴离子聚合机理与聚合诱导自组装(比萨)过程的结合,以及基于活性阴离子聚合的全苯乙烯嵌段共聚物聚(对叔丁基苯乙烯)-b-聚苯乙烯(PtBS-b-PS)的自组装比萨。首先,通过良好控制的分子量(MW)和窄的分子量分布(Mw/Mn < 1.10),成功地证实了所述双比萨的实用性和可控性。随后,研究了PtBS和PS链段的分子量、目标分子量比Mn、PS/Mn、PtBS和重量固含量等关键因素对形态演变的影响,并绘制了相图。
We report the combination of the living anionic polymerization (LAP) mechanism with the polymerization-induced self-assembly (PISA) process, and the all-styrenic diblock copolymer poly(p-tert-butylstyrene)-b-polystyrene (PtBS-b-PS) based LAP PISA. Firstly, the practicability and controllability of the LAP PISA were successfully confirmed by the well-controlled molecular weight (MW) and narrow molecular weight distribution (Mw/Mn < 1.10). Subsequently, the effect of key factors, including the MWs of PtBS and PS segments, targeted MW ratio Mn,PS/Mn,PtBS, and weight solids content, on the morphological evolution was investigated, and the phase diagram was finally presented.