Precise Synthesis and Surface Wettability of a Polymer with Liquid Crystalline Side Chains

被引:14
|
作者
Hirai, Tomoyasu [1 ]
Osumi, Shota [1 ]
Ogawa, Hirold [2 ]
Hayakawa, Teruaki [3 ]
Takahara, Atsushi [4 ,5 ]
Tanaka, Keiji [1 ,5 ]
机构
[1] Kyushu Univ, Dept Appl Chem, Fukuoka 8190395, Japan
[2] Japan Synchrotron Radiat Res Inst SPring 8, Harima, Hyogo 6795198, Japan
[3] Tokyo Inst Technol, Dept Organ & Polymer Mat, Tokyo 1528552, Japan
[4] Kyushu Univ, Inst Mat Chem & Engn, Fukuoka 8190395, Japan
[5] Kyushu Univ, Int Inst Carbon Neutral Energy Res WPI I2CNER, Fukuoka 8190395, Japan
关键词
ANIONIC-POLYMERIZATION; DESIGN; METHACRYLATE); COPOLYMERS; BEHAVIOR; FILMS; WATER; AIR;
D O I
10.1021/ma5010265
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
Well-defined poly(methacrylate)s with liquid crystal side chains, designated as PPHM, were synthesized by a living anionic polymerization method. Introducing a short-length alkyl chain at the end of the side chain, the solubility of the polymer was improved, resulting in higher molecular weight polymers. While the highest weight-average molecular weight (M-w) of PPHM was 68k, it exceeded 100k for a slight-polydisperse PPHM. Wide-angle X-ray diffraction (WAXD) revealed that PPHM formed a smectic A phase with 2.7 nm layer spacing and that the layer structure is present even in the glassy state at room temperature. Molecular aggregation states of PPHM in surface regions of films were characterized by sum-frequency generation, grazing-incidence WAXD, and contact angle measurements. The results show that the PPHM with a larger M-w formed a layer structure parallel to the film plane. Although low M-w PPHM also maintained a layer structure, the structure became more random within internal regions. The surface reorganization of PPHM with larger M-w was suppressed in comparison with smaller ones.
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页码:4901 / 4907
页数:7
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