甲基丙烯酸缩水甘油酯
共聚物
高分子化学
聚合
单体
链式转移
水溶液
材料科学
甲基丙烯酸酯
化学工程
木筏
化学
自由基聚合
有机化学
聚合物
工程类
作者
Liam P. D. Ratcliffe,Anthony J. Ryan,Steven P. Armes
出处
期刊:Macromolecules
[American Chemical Society]
日期:2013-01-17
卷期号:46 (3): 769-777
被引量:111
摘要
We describe the facile atom-efficient synthesis of diblock copolymer nano-objects via a one-pot RAFT aqueous dispersion polymerization protocol starting from a water-immiscible methacrylic monomer. More specifically, an aqueous emulsion of glycidyl methacrylate (GlyMA) is quantitatively converted into a 10% w/w aqueous solution of glycerol monomethacrylate (GMA) at 80 °C in air within 9 h in deionized water. 1H NMR spectroscopy studies indicate no evidence for either methacrylic ester hydrolysis or polymerization during this ring-opening reaction. Kinetic analysis indicates that a significant rate acceleration occurs as the reaction mixture switches from a two-phase emulsion to a single aqueous phase. This observation is fully consistent with the GlyMA–GMA–water ternary phase diagram determined at 80 °C. The 10% w/w aqueous solution of GMA can be polymerized using RAFT chemistry to produce a near-monodisperse PGMA macromolecular chain-transfer agent (macro-CTA), which indicates that relatively little dimethacrylate impurity is produced during the conversion of GlyMA into GMA. This PGMA macro-CTA can be subsequently chain-extended using 2-hydroxypropyl methacrylate (HPMA) via a RAFT aqueous dispersion polymerization formulation. The resulting PGMA–PHPMA diblock copolymers can form well-defined spheres, worms, or vesicles depending on the relative block compositions, since this dictates the copolymer curvature and hence the self-assembly behavior. Bearing in mind that GMA is a relatively expensive specialty monomer and GlyMA is a commodity monomer, this appears to be a highly cost-effective, purely aqueous one-pot route to diblock copolymer nano-objects.
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