Electron‐impact induced rearrangements of substituted biphenyls

Research output: Contribution to journalArticle

16 Scopus citations

Abstract

The electron‐impact induced rearrangements of halobiphenyls show substituent equilibration in the molecular ion for the chloro, bromo and iodo isomers. The above halo compounds as well as the fluoro, methyl and methoxybiphenyls all show considerable H/D randomization in the molecular ion or some subsequent decomposition ion.

Original languageEnglish (US)
Pages (from-to)1221-1226
Number of pages6
JournalOrganic Mass Spectrometry
Volume5
Issue number10
DOIs
StatePublished - Oct 1971

ASJC Scopus subject areas

  • Biochemistry
  • Molecular Medicine
  • Instrumentation

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