Conducting Electronic Polymers by Non-Redox Processes

Abstract

Fully N-methylated polyaniline was obtained analytically pure by the oxidative polymerization of C6H5N(CH3)(H) with (NH4)2SO8 in 1.0M aqueous HC1. The resulting black-green polymer (sigma approx. .0001 S/cm) was shown by IR studies to have a similar backbone structure to parent polyaniline, and upon heating, lost HC1 and H2O, yielding a black-brown solid, sigma < 10 to the 8th S/cm) containing approx. 14% oxidized groups. Pseudo-protonic acid doping of emeraldine base with neat (CH3)2SO4 on the vacuum line yielded polymers whose extent of doping could be monitored continuously. The approx. 50% methylated emeraldine base (sigma approx. .01 S/cm) had XPauli approximately half that of 50% proton doped emeraldine base, consistent with the symmetry-breaking effect of the methyl groups. Emeraldine base prepared in air has been found to have an oxidation state as defined above of (1-y) approx.0.6 whereas when prepared under an inert atmosphere, (1-y) approx.0.4.

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Document Details

Document Type
Technical Report
Publication Date
Jun 30, 1988
Accession Number
ADA204408

Entities

People

  • Alan G. Macdiarmid

Organizations

  • University of Pennsylvania

Tags

Communities of Interest

  • Advanced Electronics

DTIC Thesaurus Topics

  • Biomedical And Dental Materials
  • Charge Carriers
  • Chemical Synthesis
  • Chemistry
  • Composite Materials
  • Conductive Polymers
  • Dielectric Permittivity
  • Infrared Spectra
  • Magnetic Fields
  • Materials
  • Materials Science
  • Polymer Chemistry
  • Polymeric Films
  • Semi-Flexible Rod Polymers
  • Spectra
  • Spectroscopy
  • Thin Films

Readers

  • Polymer Science and Technology

Technology Areas

  • Microelectronics