胆甾型侧链液晶共聚物的研究

合成并表征了两个胆甾型液晶烯类单位以及它们分别与辛烯－１，二氧化硫进行自由基共聚合得到的一系列不同组成的胆甾型侧链液晶三元共聚砜。研究结果表明：该共聚砜的两个液晶热转变温度均随其中辛烯－１单体单元组份含量的增加而降低。     

用于电响应红外反射窗的液晶聚合物薄膜特性研究

提出了一种红外反射器件,通过载体液晶在电场下的转向控制胆甾型液晶聚合物粒子在器件中的排布方向,实现红外反射与透射之间切换.其中,胆甾型液晶聚合物粒子是实现红外反射关键.介绍了胆甾型液晶聚合物薄膜的制备方法,并采用超声波破碎的方法制备液晶粒子.研究了液晶混合物中不同比例的交联剂液晶1对液晶聚合物薄膜脆性和反射波段的影响,发现当液晶1占100%时,液晶聚合物薄膜的脆性最大,且其清亮点最高,并且薄膜的反射波段随着液晶1比例的增加而向短波方向偏移.同时,研究了薄膜厚度对液晶聚合物粒子的影响,发现液晶薄膜厚度越小,制备的液晶聚合物粒子越小且越均匀,其制成的器件电驱动性更好.该研究有利于帮助电响应红外反射窗的性能优化.     

具有双螺旋结构胆甾相液晶聚合物复合材料研究进展

胆甾相液晶(Ch-LC)的特征螺旋结构使其具有选择性反射和圆二向色性的光学性质,其反射强度被限制在自然光(非偏振光)的 50%。若Ch-LC聚合物复合体系中同时具有左右双螺旋结构,那么Ch-LC的反射强度将超过非偏振光50%的上限,从而可制备具有高反射通量的Ch-LC薄膜。具备这种特性的反射器件在无偏振片反射式显示器和需要智能控制太阳光的建筑、汽车、温室等领域具有潜在的应用前景。本文结合作者在该领域的研究工作,综述了近年来可同时反射左右旋圆偏振光的胆甾相液晶聚合物薄膜材料研究进展,并对该类材料未来的发展提出了展望。     

磁场对乙基纤维素胆甾型液晶相的影响

高分子胆甾型液晶相是一个在高分子和液晶领域都引起广泛兴趣的课题,不仅因为自然界中的多种生物大分子,如纤维素,多肽,DNA等可以形成胆甾型液晶相;而且由于胆甾相具有特殊的螺旋结构(如图1所示),能产生一些特殊的光学性能,如强烈的旋光性,圆二色性和选择性反射光性能等;并带来相应的应用,正是由于高分子胆甾相材料的性能和应用,使得高分子胆甾相液晶的相态转变和结构变化也一直倍受关注。     

Synthesis and thermal properties of side-chain liquid crystalline polyethers with racemic and chiral backbone

Racemic and chiral [(4-cyano-4′-biphenyl)oxy] and [(4-methoxy-4′-biphenyl)oxy]methyloxiranes were prepared from racemic epichlorohydrin or racemic and chiral glycidols and polymerized in dimethylsulfoxide (DMSO) with Bu^tOK as the initiator system. Initial phase identifications were made by differential scanning calorimetry (DSC) and optical microscopy techniques and confirmed by X-ray diffraction measurements. Upon heating, all the monomers show only a crystal–isotropic phase transition. The racemic and chiral [(4-cyano-4′-biphenyl)oxy]methyloxiranes exhibit a nematic and a cholesteric monotropic phase, respectively. Methoxybiphenyl substituted polyethers are crystalline and insoluble in virtually all common solvents. Cyanobiphenyl substituted polyethers are soluble under the same experimental conditions and show enantiotropic liquid crystalline properties. The racemic polymer exhibits a nematic phase, while the optically active polymer forms a cholesteric phase.     

Phase and optical behaviours of chiral-azo liquid crystal polymethylsiloxanes with isosorbide units

ABSTRACT

In this study, we synthesised two series of cholesteric liquid crystal polymers CPQ and CPZ series. First, we prepared four different monomers ML₁ containing a cholesteryl group, ML₂ containing a cyano group, ML₃ containing a phenolic hydroxyl group and ML₄ containing isosorbide with azo groups. With the polymethylsiloxanes as the main chain, CPQ series were then synthesised by copolymerisation among the monomers ML₁, ML₂ and ML₃ and CPZ series were synthesised by esterification between the CPQ series and the monomer ML₄. ¹HNMR and FT-IR spectra confirmed the chemical structures of all the monomers and polymers. The mesomorphic behaviours and thermal properties were investigated by TGA, DSC, POM and XRD. Both the CPQ and CPZ series exhibited excellent thermal stability and reversible phase transitions, as well as interesting Grandjean textures under POM. CPZ series showed higher optical activity than CPQ series due to the introduction of the isosorbide group and the azo group, which could tune the pitch to make Bragg selective reflection appear more easily. UV–Vis spectra investigated the photoresponse behaviours of CPZ series thoroughly.     

Synthesis and characterization of two series of pressure-sensitive cholesteric liquid crystal elastomers with optical properties

ABSTRACT

We synthesized two series of cholesteric liquid-crystal elastomers by hydrosilylation among monomers MA containing a cholesteryl group, MB (MC) containing a phenolic hydroxyl group and MD as the crosslinker. The chemical structures of all the monomers and LCEs were confirmed by ¹H NMR and FT-IR. We explored the mesomorphic properties and phase behaviours by TGA, DSC, POM, and XRD. All the LCEs presented elasticity, reversible phase transition, and high thermal stability. For two series of LCEs, the glass transition temperature increased slowly, and the isotropic transition temperature increased obviously. PA-I-PA-V and PB-I-PB-IV displayed selective reflection and colourful Grandjean texture, but PA-VI, PB-V, and PB-VI needed external pressure to show them.