20
Views
30
CrossRef citations to date
0
Altmetric
Original Articles

Molecular Dynamics in Liquid Crystalline Side Chain Polymers

, &
Pages 1-13 | Received 15 Sep 1986, Published online: 13 Dec 2006
 

Abstract

The static and dynamic dielectric properties of two liquid crystalline side chain polymers, one with a polychloroacrylate and one with a polyacrylate backbone and mesogenic side groups based on phenylbenzoate cores have been studied. The substitution of the polar chloro group at the main chain was done in order to get more information about the role of the main chain in the molecular dynamic processes.

Dielectric permittivity measurements have been carried out with samples oriented in a magnetic field of 1.2 Tesla, in the frequency range 10 Hz to 10 MHz and a temperature range of – 50 °C to + 150 °C. A different behaviour is observed for the polyacrylate and the polychloroacrylate.

The polyacrylate shows well resolved δ- and α-relaxations. For the polychloroacrylate the α-relaxation is extremely broad on the temperature and frequency scale. The δ-relaxation is also unusually broad and sets in very near to the clearing point. The dipole strengths of the relaxations are different for the two compounds due to the chloro group. The broadening of the relaxation processes for the polychloroacrylate is explained by a rapid increase of the viscosity below the clearing point.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.