Issue 3, 1969

Nitramines and nitramides. Part XIV. Application of nuclear magnetic resonance spectra to the problem of isomerism in ON-dialkylnitramines, with some observations on ON-dialkylnitrosohydroxylamines

Abstract

1 H Nuclear magnetic resonance spectra provide evidence for the existence of ON-dialkylnitramines (RH:NO2R′) in geometrically isomeric forms, which do not appear to be readily interconvertible. The spectra of some isomeric dialkyl nitrosohydroxylamines [RN(NO)OR′ and RN(O):NOR′] suggest for the structure RN(NO)OR′ an easier interconversion of conformers than is observed in N-nitrosodialkylamines. No signs of rotational isomerism were observed at 35° in the alkoxyurethanes which were prepared as intermediates.

Article information

Article type
Paper

J. Chem. Soc. C, 1969, 397-400

Nitramines and nitramides. Part XIV. Application of nuclear magnetic resonance spectra to the problem of isomerism in ON-dialkylnitramines, with some observations on ON-dialkylnitrosohydroxylamines

Alex. H. Lamberton and H. M. Yusuf, J. Chem. Soc. C, 1969, 397 DOI: 10.1039/J39690000397

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