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Photoinduced orientation in photoreactive hydrogen-bonding liquid crystalline polymers and liquid crystal alignment on the resultant films

机译:光反应性氢键键合液晶聚合物中的光致取向和所得膜上的液晶取向

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摘要

The photoinduced orientation in polymethacrylate, which has a hexamethylene spacer group terminated with a 4-oxycinnamic acid in its side chain (P6CAM), is explored using linearly polarized ultraviolet (LPUV) light irradiation. Because of the hydrogen- (H-) bonding among the cinnamic acid groups, P6CAM exhibits a liquid crystalline phase, and the axis-selective photoreaction of the cinnamic acid moiety generates the optical anisotropy of the film. When the exposed film is annealed or a virgin film is exposed to LPUV light at elevated temperatures, molecular reorientation both perpendicular and parallel to the polarization (E) of LPUV light is achieved, and the generated birefringence is 0.15. The orientation behavior of the film is determined by polarization UV and FTIR spectroscopies. Furthermore, the molecular orientation is erased by annealing at elevated temperature, while reexposing to LPUV light reorganizes the orientation. Finally, homogeneous alignment control of low-molecular liquid crystals on P6CAM films is demonstrated both perpendicular and parallel to E by adjusting the exposure energy.
机译:使用线偏振紫外线(LPUV)光线探索了聚甲基丙烯酸酯中的光诱导取向,该甲基丙烯酸酯的侧链具有一个以4-氧肉桂酸为末端的六亚甲基间隔基团(P6CAM)。由于肉桂酸基团之间的氢-(H-)键,P6CAM呈现液晶相,并且肉桂酸部分的轴选择性光反应产生了薄膜的光学各向异性。当将暴露的薄膜退火或在高温下将原始薄膜暴露于LPUV光时,可获得与LPUV光的偏振(E)垂直和平行的分子重新定向,并且产生的双折射为0.15。膜的取向行为由偏振UV和FTIR光谱学确定。此外,通过在高温下退火消除了分子取向,而再次暴露于LPUV光则重新组织了取向。最后,通过调节曝光能量,证明了垂直和平行于E的P6CAM膜上低分子液晶的均匀取向控制。

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