Reactions of Dimethylchloramine and Ammonia-Free Chloramine with Trialkylarsines and Phenarsazines

Academic Article

Abstract

  • The reactions of a series of trialkylarsines with chloramine and dimethylchloramine yield in every case examined the corresponding aminoarsonium chlorides. Chloramination of some 5,10-dihydrophenarsazines demonstrates that the preferred site for amination is the arsenic atom rather than the nitrogen atom. Some theoretical implications of these results are discussed. © 1972, American Chemical Society. All rights reserved.
  • Authors

    Digital Object Identifier (doi)

    Author List

  • Krannich LK; Sisler HH
  • Start Page

  • 1226
  • End Page

  • 1229
  • Volume

  • 11
  • Issue

  • 6