Influence of the mesophase structure on the β-relaxation in liquid crystalline poly(meth)acrylates

✍ Scribed by Andreas Schönhals; Dietmar Wolff; Jürgen Springer

• Publisher: John Wiley and Sons
• Year: 1996
• Tongue: English
• Weight: 566 KB
• Volume: 7
• Category: Article
• ISSN: 1042-7147
• DOI: 10.1002/(sici)1099-1581(199611)7:11<853::aid-pat593>3.0.co;2-5

✦ Synopsis

The dependence of the rotation of the mesogenic unit around its long axis (prelaxation) on the actual mesophase in liqid crystalline polymethac ylates and polyacrylates was studied by dielectric spectroscopy in the frequency range from 10-2Hz to 106Hz and in a temperature range from 170 K to 430 K. A s mesogenic units derivatives of (p-alkoxy-pheny1)-benzoate were used where different mesophases were achieved by small variation of the mesogenic structure, the spacer length and the tail group of the mesogenic unit. For all samples the temperature dependence of the relaxation rate of the p-relaxation can be described by an Arrhenius equation where both the pre-exponential factor and the activation energy increase significantly with the order of the mesophase. To characterize the structure X-ray measurements were also carried out. The mean lateral mesogenic distance was correlated directly with relaxational quantities.