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Preparation and Characterization of Chiral Cyclosiloxane-Based Liquid-Crystalline Elastomers Bearing Menthyl Groups

机译:手性环硅氧烷的液晶弹性体的制备与表征轴承胶质基

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Chiral side-chain liquid-crystalline elastomers (LCEs) IP~IVP containig menthyl groups were synthesized by a one-step hydrosilylation reaction. The chemical structures and LC properties of the monomers and polymers were characterized by use of various experimental techniques. The effect of crosslinking mesogens on mesomorphic properties of the chiral LCEs was studied by swelling experiments. All the samples IP~IVP showed cholesteric mesophase when they were heated and cooled, proved by visual observation and X-ray measurements. The glass transition temperature (T_g) of elastomers increased slightly with increase of crosslinking mesogens in the polymer systems, but mesophase-isotropic phase transition temperature (Ti) decreased slightly, suggesting that the temperature range of mesophase became narrow with increase of crosslinking mesogens for all the elastomers. The maximum reflection bands shift slightly to long wavelength and become broad at the same temperature, indicating that the helical structure is partially disrupted because of both the constraint of chemical crosslinking agents and the different mesogenic units.
机译:通过一步氢化硅烷化反应合成手性侧链液晶弹性体(LCE)IP〜IVP容纳胶质基。通过使用各种实验技术,表征单体和聚合物的化学结构和LC性质。通过溶胀实验研究了交联蛋白质对手性LCE的中态性性质的影响。所有样品IVP〜IVP在加热和冷却时显示胆甾醇型中间相,通过视觉观察和X射线测量证明。弹性体的玻璃化转变温度(t_g)随着聚合物系统中的交联蛋白质的增加而略有增加,但是中间相 - 各向同性相转变温度(Ti)略微下降,表明中间相的温度范围与所有人的交联蛋白质增加变窄弹性体。最大反射带略微偏移到长波长并在相同温度下变宽,表明由于化学交联剂和不同介性单元的约束,螺旋结构部分被破坏。

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