Liquid-crystal side-chain copolymers composed of a non-chiral mesogenic monomer and a chiral non-mesogenic monomer

J. M G Cowie, H. W. Hunter

Research output: Contribution to journalArticle

Abstract

A series of copolymers was prepared from a mesogenic monomer, 4-cyanobiphenyl-4-(6-acryloyloxy-hexyloxy) benzoate (1) and a chiral non-mesogenic monomer (S)-methyl(2-methyl-3-methacryloyloxy) propionate (2). The reactivity ratios for the copolymerization of the two monomers were found to be r1 = 0.15 and r2 = 3.00, indicating the greater tendency for the less bulky chiral monomer to be incorporated into the copolymer chains preferentially. Examination of the mesogenic behaviour showed that samples with compositions of mole fraction F2 = 0.6 exhibited a nematic phase which was stable over a temperature range of about 85°C. There was no evidence that the interaction of monomer 2 with mesogen 1 was strong enough to induce a chiral nematic phase in the copolymers. A crosslinked sample was also studied and it was observed that the alignment of the mesogenic phase was very sensitive to the application a uniaxial tensile force. © 1995.

Original languageEnglish
Pages (from-to)4147-4149
Number of pages3
JournalPolymer
Volume36
Issue number21
Publication statusPublished - 1995

Keywords

  • copolymerization
  • liquid crystal polymers
  • reactivity ratios

Fingerprint Dive into the research topics of 'Liquid-crystal side-chain copolymers composed of a non-chiral mesogenic monomer and a chiral non-mesogenic monomer'. Together they form a unique fingerprint.

  • Cite this