POLYPHENYLENESULFONES BY FRIEDEL-CRAFTS TYPE POLYCONDENSATIONS

Abstract

Homocondensation of benzenesulfonylchloride and cocondensation of aromatic disulfonylchlorides with diphenyl, diphenylether and diphenylcarbonate under Friedel-Crafts conditions resulted in polymers with inherent viscosities up to 0.11 and molecular weights probably in the range of 3000-4000. The polymers are low melting, tan to black powders, soluble in dimethylformamide and tetrahydrofuran. TGA indicates a wide molecular weight distribution. The sulfur content is lower than expected for a 1:1 copolymer; under the reaction conditions used, homocondensation of the aromatic hydrocarbon component could have occurred, according to a cationic oxidative mechanism. It is also possible (and known) that the aromatic disulfonylchlorides, under pyrolysis conditions, condense with evolution of sulfurdioxide and hydrogen chloride. At least 50 percent of the sulfur content of the polymers is present in the form of pending sulfonylchloride (in one case: sulfonic acid) groups. The polymers can be considered as copolyphenylenes-polyphenylene sulfones with pending sulfonlychloride groups.

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Document Details

Document Type
Technical Report
Publication Date
Jun 01, 1966
Accession Number
AD0800375

Entities

People

  • Gerhard F. Ehlers
  • Robert L. Buchenauer

Organizations

  • Air Force Research Laboratory

Tags

DTIC Thesaurus Topics

  • Abstracts
  • Acids
  • Air Force
  • Alcohols
  • Aromatic Compounds
  • Aromatic Hydrocarbons
  • Chlorides
  • Cyclic Hydrocarbons
  • Governments
  • Gunpowder
  • Hydrocarbons
  • Hydrogen
  • Materials
  • Materials Laboratories
  • Molecular Weight
  • Polymers
  • Sulfonic Acids

Fields of Study

  • Chemistry

Readers

  • Organic Chemistry
  • Polymer Science and Engineering.
  • Polymer Science and Technology

Technology Areas

  • Microelectronics