Issue 1, 1986

The reactivity of dinitrogen trioxide and of nitrosyl thiocyanate

Abstract

The reactions of dinitrogen trioxide as an electrophilic nitrosating agent with the azide ion and with m-chlorophenylhydrazine occur at rates close to the encounter limit. From the temperature variation of features in the kinetics of the reaction with azide ion it is calculated that ΔH for the formation of N2O3(aq) from 2HNO2(aq) is close to zero. Arguments are advanced to suggest that nitrosyl thiocyanate reacts with the azide ion and not with hydrazoic acid.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 2, 1986, 143-145

The reactivity of dinitrogen trioxide and of nitrosyl thiocyanate

A. M. M. Doherty, M. S. Garley, K. R. Howes and G. Stedman, J. Chem. Soc., Perkin Trans. 2, 1986, 143 DOI: 10.1039/P29860000143

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