Synthesis of high molecular weight comb block copolymers and their assembly into ordered morphologies in the solid state

被引:185
作者
Runge, M. Brett [1 ]
Bowden, Ned B. [1 ]
机构
[1] Univ Iowa, Dept Chem, Iowa City, IA 52242 USA
关键词
D O I
10.1021/ja072929q
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
This Article describes a simple two-step synthesis of comb block copolymers with molecular weights exceeding 1 000 000 g mol(-1) and their assembly into ordered morphologies in the solid state. This work is exciting because these polymers assembled into morphologies with domain sizes exceeding 100 nm and, in some examples, 200 nm without the use of additives. These materials reflected selected wavelengths of visible light, and these wavelengths could be affected by swelling with methylene chloride vapor. A comparison between the structures of comb block copolymers and linear block copolymers is presented with a discussion of important parameters affecting their assembly in the solid state. This Article will first describe the synthesis of comb block copolymers using ring opening metathesis polymerization and atom transfer radical polymerization and their subsequent characterization. The comb block copolymers, backbone polymers, and polystyrene arms were all characterized independent of each other and had low polydispersities. The comb block copolymers were assembled by dissolving in methylene chloride and allowing the solvent to evaporate. After thermal annealing, the polymers were characterized by scanning electron and optical microscopy. These polymers assembled into spherical, lamellar, and cylindrical arrays with domain sizes from 132 to 258 nm. This work extends the molecular architectures of polymers that can be assembled in the solid state, the molecular weights of block copolymers that were assembled, and the domain sizes that can be realized without the use of additives.
引用
收藏
页码:10551 / 10560
页数:10
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