Slow kinetics of phase transformation in a dipole-functionalized discotic liquid crystal

被引:5
|
作者
Elmahdy, Mahdy M. [1 ,2 ]
Mondeshki, Mihail [3 ]
Dou, Xi [3 ]
Butt, Hans-Juergen [3 ]
Spiess, Hans W. [3 ]
Muellen, Klaus [3 ]
Floudas, George [1 ,2 ]
机构
[1] FORTH BRI, Ioannina 45110, Greece
[2] Univ Ioannina, Dept Phys, GR-45110 Ioannina, Greece
[3] Max Planck Inst Polymer Res, D-55128 Mainz, Germany
来源
JOURNAL OF CHEMICAL PHYSICS | 2009年 / 131卷 / 11期
关键词
SOLID-STATE NMR; HEXA-PERI-HEXABENZOCORONENES; CHARGE-CARRIER MOBILITY; FUZZY SPIN MODEL; COLUMNAR HEXABENZOCORONENE; DIELECTRIC-SPECTROSCOPY; SIZE DEPENDENCE; RELAXATION-TIME; TEMPERATURE; PRESSURE;
D O I
10.1063/1.3225245
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The kinetics of phase transformation from the liquid crystalline mesophase to the crystalline phase has been studied in a model dipole-functionalized hexabenzocoronene derivative by x-ray diffraction, solid state NMR recoupling techniques, and dielectric spectroscopy. These probes revealed long-lived metastability and an intermediate state involving a change in the unit cell prior to crystallization. The barrier properties were dominant and amount to 1 and 2.5 eV, respectively, for the unit cell transformation and crystallization processes. These effects should be considered in the design of discotic liquid crystals for electronic applications. (C) 2009 American Institute of Physics. [doi: 10.1063/1.3225245]
引用
收藏
页数:9
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