Issue 0, 1970

Radicals produced during γ-irradiation of 1-substituted 5-amino-tetrazoles

Abstract

The 1-methyl site of alkyl substituted 5-aminotetrazoles was found to be the most susceptible to γ-irradiation. The main paramagnetic radicals formed were identified as CH3· and R–CH2·(R = substittuted 5-aminotetrazole). With a 5-nitraminotetrazole claeavage of the nitramino N–N bond, yielding an NO2· radical, was the major interaction.

Article information

Article type
Paper

J. Chem. Soc. B, 1970, 378-380

Radicals produced during γ-irradiation of 1-substituted 5-amino-tetrazoles

R. N. Butler, R. C. Catton and M. C. R. Symons, J. Chem. Soc. B, 1970, 378 DOI: 10.1039/J29700000378

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements