Suppression of Side Chain Crystallization and Transformation of Monotropic Mesophases into Enantiotropic Mesophases by Copolymerization of the Parent Polymers' Monomer Pairs Containing Constitutional Isomeric Mesogenic Side Groups

Abstract

The synthesis and characterization of several copolymers based on the monomer pairs of 11-(4-methoxy-(4'-oxy)-alpha-methylstilbene)undecanyl methacrylate (4-11-MA) and 11-(4-oxy-(4'-methoxy)-alpha-methylstilbene)undecanyl methacrylate (4'-11-MA), 11-(4-methoxy-(4'-oxy)-alpha-methylstilbene)undecanyl acrylate (4-11-AC) and 11-(4-oxy-(4'-methoxy)-alpha-methylstilbene)undecanyl acrylate (4'11-AC), and 8-(4-methoxy-(4'-oxy)-alpha-methylstilbene(octyl acrylate (4-8-AC) nd 8-(4-methoxy-(4'-oxy)-alpha-methylstilbene(octyl acrylate (4-8-AC) and 8-(4-oxy-(4'methoxy)-alpha-methylstilbene)octyl acrylate (4-8'-AC) are described. In the case of polymers with poly-methacrylate backbones, the copolymerization of the two constitutional isomeric mesogenic monomers cancels the side chain crystallization tendency characteristic of their parent homopolymers. Subsequently, the copolymer presents a broader mesophase temperature range than any of the two parent homopolymers. In the case of polymers with polyacrylate backbones, copolymerization suppresses the tendency towards side chain crystallization and subsequently, transforms one or even two monotropic mesophases into enantiotropic mesophases.

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Document Details

Document Type
Technical Report
Publication Date
Dec 21, 1988
Accession Number
ADA209066

Entities

People

  • D. Tomazos
  • Virgil Percec

Organizations

  • Case Western Reserve University

Tags

DTIC Thesaurus Topics

  • Acrylates
  • Classification
  • Copolymerization
  • Crystallization
  • Crystals
  • Glass Transition Temperature
  • Liquid Chromatography
  • Liquid Crystals
  • Macromolecules
  • Military Research
  • Molecular Weight
  • Phase Diagrams
  • Phase Transformations
  • Polymers
  • Structural Isomers
  • Transition Temperature
  • Transitions

Fields of Study

  • Chemistry

Readers

  • Materials Science and Engineering.
  • Organic Chemistry

Technology Areas

  • Microelectronics