Premium
Synthesis and mesomorphic properties of side‐chain cholesteric liquid‐crystalline polymers containing menthyl groups
Author(s) -
Du BingGuang,
Hu JianShe,
Zhang BaoYan,
Xiao LinJiu,
Wei KeQi
Publication year - 2006
Publication title -
journal of applied polymer science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.575
H-Index - 166
eISSN - 1097-4628
pISSN - 0021-8995
DOI - 10.1002/app.23949
Subject(s) - thermotropic crystal , differential scanning calorimetry , mesophase , materials science , texture (cosmology) , polymer , monomer , thermal stability , thermogravimetric analysis , side chain , liquid crystal , polymer chemistry , fourier transform infrared spectroscopy , crystallography , glass transition , chemical engineering , organic chemistry , liquid crystalline , chemistry , composite material , thermodynamics , physics , optoelectronics , image (mathematics) , artificial intelligence , computer science , engineering
A series of new cholesteric liquid‐crystalline polysiloxanes ( P 1 – P 5 ) derived from menthyl groups were synthesized. The chemical structures of the monomers and polymers were characterized with Fourier transform infrared, 1 H‐NMR, 13 C‐NMR, and elemental analyses. The mesomorphic properties and thermal behavior were investigated with differential scanning calorimetry, polarizing optical microscopy, thermogravimetric analysis, and X‐ray diffraction measurements. The influence of the polymer structure on the thermal behavior was discussed. The monomer diosgeninyl 4‐allyloxybenzoate exhibited a typical cholesteric oily‐streak texture and a focal‐conic texture. Polymers P 1 – P 5 showed thermotropic liquid‐crystalline properties. P 1 displayed a smectic fan‐shaped texture, P 2 – P 5 showed a cholesteric Grandjean texture, and P 6 and P 7 did not show mesomorphic properties. The experimental results demonstrated that the glass‐transition temperature and the clearing temperature decreased, and the mesomorphic properties weakened with an increasing concentration of menthyl units. Moreover, P 1 – P 5 exhibited wide mesophase temperature ranges and high thermal stability. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102:5559–5565, 2006