Crosslinked Polyesters

Abstract

According to the present invention, polyesters are formed in aqueous media by the formation of ester linkages via the intermolecular polycondensation between the acid and alcohol moieties of a single monomer. The preferred monomers are derivatives of tartaric acid, which has two carboxylic acid groups and two hydroxyl groups. Using the proper strategy, these groups can be used to propagate a chain reaction that leads to the formation of a desired polymer. The carboxyl groups are protected with an amine, such as dimethylamine, and the hydroxyl groups are O-alkylated with a haloalkanol. The resulting diamide is then hydrolyzed to deprotect the amido groups. Formation of quaternary ammonium intermediates during hydrolysis fosters the reaction of terminal hydroxyl groups to form an ester bond. Because the precursor monomer is bifunctional, possessing both hydroxyl and carboxyl groups, the esterification process propagates to give a highly crosslinked polymer. The haloalkanol which o-alkylates the monomers is chosen to impart the desired properties to the polymer.

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Document Details

Document Type
Technical Report
Publication Date
Mar 02, 2001
Accession Number
ADD019761

Entities

People

  • Alok Singh

Organizations

  • United States Department of the Navy

Tags

Communities of Interest

  • Advanced Electronics

DTIC Thesaurus Topics

  • Carboxylic Acids
  • Chain Reactions
  • Chemical Reactions
  • Chlorides
  • Dissociation
  • Films
  • Hydrolysis
  • Imines
  • Inventions
  • Materials
  • Molecules
  • Patent Applications
  • Polyesters
  • Polymeric Films
  • Polymers
  • Precursors
  • Self Assembly

Fields of Study

  • Chemistry

Readers

  • Organic Chemistry
  • Polymer Science and Technology