摘要
通过Mitsunobu反应合成了一系列手性液晶,收率63%～71%,并通过1 H NMR、MS、IR对其结构进行了表征。结合DSC和POM研究了目标化合物的介晶性。利用Cano's wedge法研究了目标化合物的扭曲力,发现随着手性中心邻近芳环上氟原子数的增多,手性液晶分子的扭曲力显著增大。实验结果表明,氟原子的引入影响了碳氧单键的自由旋转,导致手性液晶分子具有较少构象异构体,从而表现出大的扭曲力。
A series of chiral liquid crystals were synthesized through Mitsunobu reaction and the yields varied from 63% to 71%.The compounds were characterized by IR,1H NMR,MS.The mesomorphic property of objective compounds was investigated by DSC and POM.The helical twisting power（HTP） was determined by Cano＇s wedge method.It was found that HTP increased with the increase of the number of Fluorine atom attached to aromatic ring.The inducing of fluorine atom to aromatic ring influence the rotation of C—O bond,then chiral moleculer has small number of conformation and exhibits high HTP.
出处
《液晶与显示》
CAS
CSCD
北大核心
2011年第1期5-8,共4页
Chinese Journal of Liquid Crystals and Displays
基金
国防基础科研计划资助项目(No.C0920060318)
关键词
手性液晶
MITSUNOBU反应
扭曲力
构象异构体
chiral liquid crystals
Mitsunobu reaction
helical twisting power
conformational isomers
