In this study, right-handed dicinnamate isosorbide was synthesized via the esterification reaction betweefi optically active isosorbide and cinnamate. The chiral dopant was characterized by FT-IR, ^1H NMR, elemental a...In this study, right-handed dicinnamate isosorbide was synthesized via the esterification reaction betweefi optically active isosorbide and cinnamate. The chiral dopant was characterized by FT-IR, ^1H NMR, elemental analysis, SEM, UV absorption spectrum. After dissolving in a nematic liquid crystal mixture, the chiral dopant exhibited a temperature-dependent solubility in the chiral nematic liquid crystal mixture. Meanwhile, a relatively high value of helical twisting power of the polymerizable chiral dopant was determined. The results show that the chiral dopant has great potential in achieving a polymer stabilized chiral nematic liquid crystal film with a broad-band selective reflection. C 2009 Huai Yang. Published by Elsevier B.V. on behalf of Chinese Chemical Society. All rights reserved.展开更多
基金supported by the National Basic Research Program of China(No.2007CB613301)the National Natural Science Foundation(No.20674005)the Program of Beijing Municipal Science and Technology(No.Y0405004040121).
文摘In this study, right-handed dicinnamate isosorbide was synthesized via the esterification reaction betweefi optically active isosorbide and cinnamate. The chiral dopant was characterized by FT-IR, ^1H NMR, elemental analysis, SEM, UV absorption spectrum. After dissolving in a nematic liquid crystal mixture, the chiral dopant exhibited a temperature-dependent solubility in the chiral nematic liquid crystal mixture. Meanwhile, a relatively high value of helical twisting power of the polymerizable chiral dopant was determined. The results show that the chiral dopant has great potential in achieving a polymer stabilized chiral nematic liquid crystal film with a broad-band selective reflection. C 2009 Huai Yang. Published by Elsevier B.V. on behalf of Chinese Chemical Society. All rights reserved.
