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1.新乡医学院三全学院 化学教研室, 河南 新乡 453003
2.广西壮族自治区环境保护科学研究院, 广西 南宁 530000
3.东北大学 理学院, 辽宁 沈阳 110004
[ "高利(1989-), 女, 河南濮阳人, 硕士, 讲师, 2012年于东北大学获得硕士学位, 主要从事高分子新型材料的合成与性能测试研究。E-mail:798731079@qq.com" ]
[ "田梅(1970-),女, 黑龙江镜泊湖人, 博士, 副教授, 2009年于东北大学获得博士学位, 主要从事功能液晶材料的研发工作. E-mail:tianmei613@sina.com." ]
收稿日期:2019-09-12,
修回日期:2019-11-07,
录用日期:2019-11-7,
纸质出版日期:2020-06-05
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高利, 郭璐璐, 陈新诗, 等. 室温显示胆甾相的侧链液晶聚合物的合成与表征[J]. 液晶与显示, 2020,35(6):524-530.
Li GAO, Lu-lu GUO, Xin-shi CHEN, et al. Synthesis and characterization of side chain liquid crystalline polymers displaying cholesteric phase at room temperature[J]. Chinese journal of liquid crystals and displays, 2020, 35(6): 524-530.
高利, 郭璐璐, 陈新诗, 等. 室温显示胆甾相的侧链液晶聚合物的合成与表征[J]. 液晶与显示, 2020,35(6):524-530. DOI: 10.3788/YJYXS20203506.0524.
Li GAO, Lu-lu GUO, Xin-shi CHEN, et al. Synthesis and characterization of side chain liquid crystalline polymers displaying cholesteric phase at room temperature[J]. Chinese journal of liquid crystals and displays, 2020, 35(6): 524-530. DOI: 10.3788/YJYXS20203506.0524.
将聚甲基含氢硅氧烷(PMHS)与向列相柔性单体11-(4'-(4-乙氧基苯甲酸)苯)十一烯酸酯(M
1
)和胆甾相单体烯丙氧基苯甲酸胆甾醇酯(M
2
)接枝共聚合成了聚合物P
1
~P
7
。利用红外光谱(FTIR)、氢谱(
1
H NMR)、差示扫描量热法(DSC)、偏光分析(POM)、X射线衍射分析(XRD)、热失重分析(TGA)、旋光分析等手段研究了单体和聚合物的结构和液晶性能。结果表明,除聚合物P
7
为向列型液晶聚合物外,P
1
~P
6
为胆甾型液晶聚合物,即向列相柔性单体M
1
的引入并未改变胆甾相,而且与柔软的硅氧烷主链共同作用起到了降低玻璃化温度(P
5
、P
6
在室温即出现液晶态)、拓宽液晶区间、稳定液晶相、降低成本的作用,有利于液晶聚合物的应用。
A series of liquid crystal (LC) polymers (P
1
~P
7
) were synthesized by grafting with nematic flexible monomer 4-(undec-10-enoyloxy) phenyl 4-ethoxybenzoate (M
1
) and cholesteric monomer cholesteryl allyloxybenzoate (M
2
) to polymethyl hydrosiloxane (PMHS). The chemical structures and properties of the monomers and copolymers were investigated by means of fourier transform infrared spectroscopy (FTIR)
nuclear magnetic resonance hydrogen spectrometer (
1
HNMR)
differential scanning calorimetry (DSC)
polarised optical microscopy (POM)
X-ray diffraction (XRD)
thermogravimetric analysis (TGA) and polarimeter. The analyses show that P
1
~P
6
are cholesteric LC polymers
except that P
7
is a nematic LC polymer. The introduction of nematic flexible monomer M
1
did not change the cholesteric phase. The introduction of M
1
together with the soft siloxane main chain play a role in reducing the glass transition temperature (P
5
and P
6
show LC state at room temperature)
widening the LC range
stabilizing the LC phase and reducing the cost
which is beneficial to the application of LC polymers.
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