Influences of Hydrogen Bonding and Peripheral Chain Length on Mesophase Structures of Mesogen-Jacketed Liquid Crystalline Polymers with Amide Side-Chain Linkages

被引:39
作者
Cheng, Yan-Hua [1 ,2 ]
Chen, Wen-Ping [2 ]
Shen, Zhihao [1 ]
Fan, Xing-He [1 ]
Zhu, Mei-Fang [2 ]
Zhou, Qi-Feng [1 ]
机构
[1] Peking Univ, Beijing Natl Lab Mol Sci, Key Lab Polymer Chem & Phys, Minist Educ,Coll Chem & Mol Engn, Beijing 100871, Peoples R China
[2] Donghua Univ, State Key Lab Modificat Chem Fibers & Polymer Mat, Shanghai 201620, Peoples R China
基金
中国国家自然科学基金;
关键词
INFRARED-SPECTROSCOPY; PHASE STRUCTURES; DESIGN; CORE; 1,3,4-OXADIAZOLE; BEHAVIOR; SCALES;
D O I
10.1021/ma102444t
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
A series of mesogen-jacketed liquid crystalline polymers, poly{2,5-bis-[(4-alkoxyphenyl)aminocarbonyl]styrene} (P-Cm, where m is the number of carbon atoms in the alkoxy groups, and m = 1, 4, 8, 12), with an amide core and flexible tails of varying lengths on the two ends in the side chain were designed and successfully synthesized via conventional radical polymerization. The mesophase structures of these polymers were dependent on the number of carbon atoms in the peripheral chains. Wide-angle X-ray diffraction and polarized light microscopy results revealed that the polymers with m >= 4 could form smectic A phases, while a columnar nematic phase could be formed for the polymer with methoxy end groups (P-C1). The hydrogen bonding among the side-chain amide groups might play an important role in forming and stabilizing these liquid crystalline phases, which was suggested by the results from variable-temperature FTIR and 2D IR analyses.
引用
收藏
页码:1429 / 1437
页数:9
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