Synthesis of Conjugated Polymers with Alternating Aromatic and Quinonoid Sequences Via Elimination on Precursors.

Abstract

An elimination reaction for the formation of conjugated polymers from polymer precursors containing alternating sp superscript 3 carbon atom and conjugatged segments in the main chain is described. The resulting conjugated polymers with alternating aromatic and quinonoid sequences are inaccessible by conventional polymerization processes. The Pi-electron conjugation extension process is exemplified by reactions performed on poly(5,5',alpha-bithiophenediyl p acetoxybenzylidene) at 23 C and followed by electronic and infrared spectra. The semiconductor band gap narrowed from an initial value of 1.53 ev for the precursor polymer to about 0.83 ev for the conjugated derivative. Further evidence for the sp superscript 3 to sp superscript 2 carbon atom conversion by the elimination process is provided by infrared data.

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Document Details

Document Type
Technical Report
Publication Date
Aug 14, 1986
Accession Number
ADA171331

Entities

People

  • Samson A. Jenekhe

Organizations

  • Honeywell International, Inc.

Tags

Communities of Interest

  • Materials and Manufacturing Processes

DTIC Thesaurus Topics

  • Absorption
  • Absorption Spectra
  • Aromatic Hydrocarbons
  • Band Gaps
  • Conjugated Polymers
  • Elimination
  • Elimination Reactions
  • Energy Bands
  • Infrared Spectra
  • Macromolecules
  • Minnesota
  • Monitoring
  • Optical Absorption
  • Physical Sciences
  • Polymers
  • Spectra
  • United States

Fields of Study

  • Chemistry

Readers

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

Technology Areas

  • Microelectronics