作者:Paul Kouwer、Wolter Jager、Wim Mijs、Stephen Picken
DOI:10.1080/15421400490435305
日期:2004.1
A series of novel mesogens have been prepared by a five-fold Sonogashira reaction of terminal acetylenes with a functionalized pentabromophenol. The corresponding side chain polymers were prepared by a polymer analogous substitution reaction. The mesogens differ in the nature of the substituents, linking five hexyl tails to the aromatic core, i.e. CH2, O, S, SO2 and CONH groups. A wide range of mesophases
通过末端乙炔与官能化五溴苯酚的五倍 Sonogashira 反应制备了一系列新型介晶。通过聚合物类似的取代反应制备相应的侧链聚合物。介晶的取代基性质不同,将五个己基尾部连接到芳香核,即 CH2、O、S、SO2 和 CONH 基团。已检测到范围广泛的中间相和相应的转变温度,从低熔点向列相到高度稳定的柱状相。广泛可变的相行为是根据特定的分子间相互作用来描述的。