4.8 Article

Coacervate-Assisted Polymerization-Induced Self-Assembly of Chiral Alternating Copolymers into Hierarchical Bishell Capsules with Sub-5 nm Ultrathin Lamellae

期刊

SMALL METHODS
卷 -, 期 -, 页码 -

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/smtd.202300136

关键词

alternating copolymers; click chemistry; coacervates; multi-level structures; polymerization-induced self-assembly

向作者/读者索取更多资源

Hierarchical bishell capsules (BCs) with ultrathin lamellar phases have been prepared through a coacervate-assisted polymerization-induced self-assembly (CAPISA) method, which combines liquid-liquid phase separation (LLPS) with polymerization-induced self-assembly (PISA). The CAPISA method allows for the one-pot and scalable preparation of BCs in a bottom-up sequence, and the self-assembled structure and dynamic formation process of BCs have been revealed. CAPISA shows great potential in fabricating biomimetic polymer materials with higher structural complexity and sophisticated functions.
Hierarchical self-assembly of synthetic polymers in solution represents one of the sophisticated strategies to replicate the natural superstructures which lay the basis for their superb functions. However, it is still quite challenging to increase the degree of complexity of the as-prepared assemblies, especially in a large scale. Liquid-liquid phase separation (LLPS) widely exists in cells and is assumed to be responsible for the formation of many cellular organelles without membranes. Herein, through integrating LLPS with the polymerization-induced self-assembly (PISA), a coacervate-assisted PISA (CAPISA) methodology to realize the one-pot and scalable preparation of hierarchical bishell capsules (BCs) from nanosheets with ultrathin lamellae phase (sub-5 nm), microflakes, unishell capsules to final BCs in a bottom-up sequence is presented. Both the self-assembled structure and the dynamic formation process of BCs have been disclosed. Since CAPISA has combined the advantages of coacervates, click chemistry, interfacial reaction and PISA, it is believed that it will become a promising option to fabricate biomimetic polymer materials with higher structural complexity and more sophisticated functions.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.8
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据