Issue 19, 1991

Stereochemical effects in mass spectrometry: preferential formation of bromonium ions from trans-substituted 1,1′,2,2′-polyalkyl-2,2′-dibromodiethyl ethers

Abstract

The relative abundance of bromonium ions in the electron ionisation mass spectra of acyclic 1,1′,2,2′-polyalkyl-2,2′-dibromodiethyl ethers is enhanced by trans stereochemistry of the alkyl groups.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1991, 1346-1347

Stereochemical effects in mass spectrometry: preferential formation of bromonium ions from trans-substituted 1,1′,2,2′-polyalkyl-2,2′-dibromodiethyl ethers

R. D. Bowen, M. J. Harrison, D. Neill and S. E. Thomas, J. Chem. Soc., Chem. Commun., 1991, 1346 DOI: 10.1039/C39910001346

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