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Dynamic Control of Liquid-Crystalline Helical Structures with the Aid of Light- and Temperature-Driven MultiStable Chiral Materials

机译:借助光和温度驱动的多稳态手性材料对液晶螺旋结构的动态控制

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Light- and temperature-driven multistable chiral materials composed of a binaphthyl moiety as a twisting part and an azobenzene moiety as a photoresponsive part in a single component were investigated. It has been found that the materials show reversible change in a dihedral angle of the twisting part at various temperatures. In contrast, no change in the twisting angle of the materials during trans-cis photoisomerization was observed. Furthermore, the chiral compounds were dissolved in nematic (N) liquid crystals (LCs) to produce a chiral N phase with a helical structure. The mixture exhibited a dual molecular response to temperature and light. Helical pitch length of the chiral N LC decreased with increasing temperature because of a molecular twisting motion of the binaphthyl moiety, resulting in a stabilization of the LC helical structure. On the other hand, length of the helical pitch increased upon photoirradiation, and the resulting LC mixture was found to show photoswitching between chiral N and N phases upon trans-cis isomerization of the azobenzene moiety. The photoinduced deformation of the LC helical structure was derived from a bent shape of cis isomer of the azobenzene moiety in the chiral dopant. This dynamic modulation of the self-organizing helical structure was based on dual and selective molecular motions of the guest materials induced by external stimuli.
机译:对光和温度驱动的多稳态手性材料进行了研究,该材料由单一成分的联萘部分作为扭曲部分和偶氮苯部分作为光响应部分组成。已经发现,在各种温度下,材料在扭转部分的二面角上显示出可逆的变化。相反,在反式顺式光异构化过程中未观察到材料的扭转角的变化。此外,将手性化合物溶解在向列(N)液晶(LC)中以产生具有螺旋结构的手性N相。该混合物表现出对温度和光的双重分子响应。手性N LC的螺距长度随着温度的升高而降低,这是由于双萘基部分的分子扭转运动,导致了LC螺旋结构的稳定。另一方面,螺旋间距的长度在光辐照时增加,并且发现所得的LC混合物在偶氮苯部分的反式-顺式异构化后显示出手性N相和N相之间的光转换。 LC螺旋结构的光诱导变形源自手性掺杂剂中偶氮苯部分的顺式异构体的弯曲形状。自组织螺旋结构的这种动态调节是基于外部刺激引起的客体材料的双重和选择性分子运动。

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