Organophosphazenes. XIV. Para Substituted Aryl and Mixed Para Substituted Aryl/Phenyl Fluorocyclotriphosphazene Derivatives.

Abstract

The reactions of aryl lithium reagents containing electron donating substituents in the para position with hexafluorocyclotriphosphazene, P3N3F6, have been examined. These reactions yield the appropriate monoaryl pentafluorocyclotriphosphazenes in moderate yields. The monoaryl phosphazenes are converted to the geminally substituted mixed aryl/phenyl derivatives by the Friedel-Crafts reaction. The infrared and nmr spectroscopic data along with the mass spectrometry data are discussed in terms of perturbations of the aryl system by both the phosphazene and electron donor substituents.

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Document Details

Document Type
Technical Report
Publication Date
Jan 15, 1980
Accession Number
ADA080091

Entities

People

  • Christopher W. Allen
  • George E. Brunst
  • Michael E. Perlman

Organizations

  • University of Vermont

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Communities of Interest

  • Advanced Electronics
  • Air Platforms
  • Ground and Sea Platforms
  • Weapons Technologies

DTIC Thesaurus Topics

  • Alkanes
  • Chemical Synthesis
  • Chemistry
  • Electron Donors
  • Electrons
  • Engineering
  • Mass Spectra
  • Mass Spectrometry
  • Materials
  • Military Research
  • Mixing
  • New York
  • Sodium Compounds
  • Spectra
  • Spectrometry
  • Spectroscopy
  • United States

Fields of Study

  • Chemistry

Readers

  • Organic Chemistry

Technology Areas

  • Microelectronics