Issue 0, 1968

Electron-impact studies. Part XXI. The mass spectra of sulphonamides and sulphonyl chlorides: the formation of C–O and C–N bonds upon electron impact

Abstract

The mass spectra of a series of arenesulphonamides and some representative sulphonyl chlorides are reported and discussed. The sulphonyl chlorides and the primary arenesulphonamides have prominent rearrangement ions in their spectra owing to loss of the elements of SO2 from the molecular ions, whereas the sulphonamido-groups of N-alkyl and dihydrophenanthrenesulphonamides are not involved in skeletal-rearrangement processes. Fragmentation modes have been established by high resolution measurements and metastable ions.

Article information

Article type
Paper

J. Chem. Soc. B, 1968, 15-21

Electron-impact studies. Part XXI. The mass spectra of sulphonamides and sulphonyl chlorides: the formation of C–O and C–N bonds upon electron impact

E. Dynesen, S.-O. Lawesson, G. Schroll, J. H. Bowie and R. G. Cooks, J. Chem. Soc. B, 1968, 15 DOI: 10.1039/J29680000015

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