Dissemin is shutting down on January 1st, 2025

Published in

Bulletin of the Academy of Sciences of the USSR Division of Chemical Science, 8(35), p. 1587-1591

DOI: 10.1007/bf00954591

Links

Tools

Export citation

Search in Google Scholar

Photolysis of p-azidoaniline in aprotic solvents

Journal article published in 1986 by E. A. Pritchina, N. P. Gritsan ORCID, N. M. Bazhin
This paper is available in a repository.
This paper is available in a repository.

Full text: Download

Green circle
Preprint: archiving allowed
Green circle
Postprint: archiving allowed
Red circle
Published version: archiving forbidden
Data provided by SHERPA/RoMEO

Abstract

1.The photolysis of p-azidoaniline in organic aprotic solvents was investigated in the absence of O2; the main product of photolysis at room temperature is 4,4'-diaminoazobenzene, but when samples irradiated at 77°K are thawed, the main products are 4,4'-diaminoazobenzene and p-phenylenediamine. The precursor of the end products is p-aminophenylnitrene in the triplet state.2.In the presence of O2, the main products of the photolysis of p-azidoaniline in aprotic solvents are p-nitroaniline and p-nitrosoaniline. The quantum and chemical yields of their formation were measured.3.p-aminophenylnitrene reacts with O2 to form an adduct; subsequently, a dimer is obtained, which breaks down to the end products.