Research Progress in Polypeptoids Prepared by Controlled Ring-Opening Polymerizations

被引：8
作者：
Ma, Anyao [1 ]
Yu, Xinyan [1 ]
Liao, Mingzhen [1 ]
Liu, Wenxiao [1 ]
Xuan, Sunting [1 ]
Zhang, Zhengbiao [1 ,2 ]
机构：
[1] Soochow Univ, Coll Chem Chem Engn & Mat Sci, Jiangsu Key Lab Adv Funct Polymer Design & Applic, State & Local Joint Engn Lab Novel Funct Polymer, Suzhou 215123, Peoples R China
[2] Soochow Univ, State Key Lab Radiat Med & Protect, Suzhou 215123, Peoples R China
来源：
MACROMOLECULAR RAPID COMMUNICATIONS | 2023年 / 44卷 / 01期
基金：
中国国家自然科学基金;
关键词：
biological applications; controlled ring-opening polymerizations; crystallization; polypeptoids; self-assembly; GLYCINE N-THIOCARBOXYANHYDRIDE; MEDIATED ZWITTERIONIC POLYMERIZATION; SEQUENCE-DEFINED PEPTOIDS; SIDE-CHAIN; INITIATED POLYMERIZATION; PEGYLATED POLYPEPTOIDS; DIBLOCK COPOLYPEPTOIDS; BLOCK-COPOLYMERS; CROSS-LINKING; CARBOXYANHYDRIDE;
D O I：
10.1002/marc.202200301
中图分类号：
O63 [高分子化学（高聚物）];
学科分类号：
070305 ; 080501 ; 081704 ;
摘要：
Polypeptoids, structural mimics of polypeptides, have attracted considerable attention due to their biocompatibility, proteolytic stability, thermal processability, good solubility, synthetic accessibility, and structural diversity. Polypeptoids have emerged as an interesting material in both polymer science and biological field. This review primarily discusses the research progress of polypeptoids prepared by controlled ring-opening polymerizations in the past decade, including synthetic strategies of monomers, polymerizations by different initiators, postfunctionalization, fundamental properties, crystallization-driven self-assembly, and potential biological applications.
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页数：18
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