Polymerization-induced self-assembly via RAFT in emulsion: effect of Z-group on the nucleation step

被引:31
|
作者
Guimaraes, Thiago R. [1 ]
Bong, Y. Loong [1 ]
Thompson, Steven W. [1 ]
Moad, Graeme [2 ]
Perrier, Sebastien [3 ,4 ,5 ]
Zetterlund, Per B. [1 ]
机构
[1] Univ New South Wales, Sch Chem Engn, Ctr Adv Macromol Design CAMD, Sydney, NSW 2052, Australia
[2] CSIRO Mfg Flagship, Bag 10, Clayton, Vic 3169, Australia
[3] Univ Warwick, Dept Chem, Coventry CV4 7AL, W Midlands, England
[4] Univ Warwick, Warwick Med Sch, Coventry CV4 7AL, W Midlands, England
[5] Monash Univ, Fac Pharm & Pharmaceut Sci, 381 Royal Parade, Parkville, Vic 3052, Australia
基金
澳大利亚研究理事会;
关键词
RADICAL POLYMERIZATION; MINIEMULSION POLYMERIZATION; BLOCK-COPOLYMERS; STYRENE; EXPLOITATION; MORPHOLOGY; MECHANISM; KINETICS;
D O I
10.1039/d0py01311k
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Polymerization-induced self-assembly (PISA) has emerged as one of the most powerful and widely employed techniques for preparation of block copolymer and polymeric nanoparticles in dispersed systems. Its success relies on a rapid, easily scalable and straightforward process, associated with the ability to readily control nanoparticle morphology. In the present work, we have investigated the effect of the Z-group of RAFT agents ZC(=S)-SR on the nucleation step of aqueous RAFT PISA performed in environmentally friendly emulsion polymerization. Seven different poly(acrylic acid) (PAA) and poly(methacrylic acid) (PMAA) macroRAFTs were synthesized using RAFT agents containing Z-groups of different hydrophilicity. Slow polymerizations and incomplete chain extension reactions were observed for systems with the most hydrophilic Z-group, while the more hydrophobic Z groups led to higher polymerization rates and very successful chain extensions. A mechanism based on Z-group induced RAFT exit is proposed to rationalize this surprising behaviour, providing important information on the mechanistic understanding and optimization of PISA in emulsion.
引用
收藏
页码:122 / 133
页数:12
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