Interfacial crosslinking of self-assembled triblock copolymer nanoparticles via alkoxysilane hydrolysis and condensation

被引:7
作者
Teo, Guo Hui [1 ]
Zetterlund, Per B. [2 ]
Thickett, Stuart C. [1 ]
机构
[1] Univ Tasmania, Sch Nat Sci Chem, Hobart, Tas 7001, Australia
[2] Univ New South Wales, Sch Chem Engn, CAMD, Sydney, NSW 2052, Australia
关键词
polymerization-induced self-assembly; crosslinking; polymeric stabilizers; RAFT; CONTROLLED/LIVING RADICAL POLYMERIZATION; PERIPHERY RAFT POLYMERIZATION; LINKED MICELLES; DIBLOCK COPOLYMERS; DISPERSION POLYMERIZATION; MOLECULAR-WEIGHT; DRUG-DELIVERY; VESICLES; MORPHOLOGY; NANOCAPSULES;
D O I
10.1002/pola.29313
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
The use of amphiphilic triblock copolymers bearing a reactive alkoxysilane middle block as polymeric stabilizers is reported in this work. A series of poly(ethylene glycol) methyl ether methacrylate-b-(3-trimethoxysilyl)propyl methacrylate-b-benzyl methacrylate (PEGMA-b-MPS-b-BzMA) triblock copolymers were prepared by RAFT solution polymerization and polymerization-induced self-assembly (PISA), respectively, where the various block lengths and overall composition were varied. The copolymers prepared by solution polymerization were employed as oil-in-water stabilizers where upon application of a catalyst, the 3-(trimethoxysilyl)propyl methacrylate (MPS) block at the droplet interface was crosslinked to yield capsule-like structures. The effectiveness of interfacial crosslinking was validated by dynamic light scattering and electron microscopy. In situ self-assembly by the PISA method resulted in spherical nanoparticles of controllable size that were readily crosslinked by addition of base, with significant enhancement of colloidal stability. (c) 2018 Wiley Periodicals, Inc. J. Polym. Sci., Part A: Polym. Chem. 2019, 57, 1897-1907
引用
收藏
页码:1897 / 1907
页数:11
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