Advertisement

Thermolysis of 2-(p-azidocinnamoyl)quinoline

  • M. F. Budyka
  • M. M. Kantor
  • A. P. Pleshkova
Brief Communications
  • 26 Downloads

Abstract

Mass spectrometry was used to study the thermolysis of 2-(p-azidocinnamoyl)quinoline and 4-azidochalcone at 160–230‡C. The primary thermolysis product of these azides is a nitrene. The reaction of this nitrene in the singlet state gives polymer products, while the triplet nitrene is reduced in the molten azide to give a primary amine and dimerized to give an azo compound.

Keywords

Polymer Nitrene Mass Spectrometry Azide Quinoline 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

Literature cited

  1. 1.
    S. Patai and Z. Rappoport (eds.), The Chemistry of Functional Groups. Supplement D, Wiley, Chichester (1983), pp. 1, 75.Google Scholar
  2. 2.
    S. V. Tsukerman, Ch. K. Shon, and V. F. Lavrushin, Zh. Obshch. Khim.,34, No. 9, 2881 (1964).Google Scholar

Copyright information

© Plenum Publishing Corporation 1990

Authors and Affiliations

  • M. F. Budyka
    • 1
  • M. M. Kantor
    • 1
  • A. P. Pleshkova
    • 1
  1. 1.N. N. Semenov Institute of Chemical PhysicsAcademy of Sciences of the USSR, Chernogolovka BranchUSSR

Personalised recommendations