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NMR-studien an chinonanilen. Der einfluss paraständiger substituenten im phenylring auf die thermische isomerisierung

  • University of Tübingen

Research output: Contribution to journalArticlepeer-review

48 Scopus citations

Abstract

Owing to isomerization at the CN double bond the NMR spectra of quinone aniles are temperature dependent. The free enthalpy of activation of the isomerization (ΔG) is correlated to the Hammett σp-constants of the para substituents of the benzene ring: A large σp-value corresponds to a small ΔG value. This leads to the conclusion that the isomerization implies an inversion of the nitrogen atom.

Original languageGerman
Pages (from-to)3723-3732
Number of pages10
JournalTetrahedron
Volume23
Issue number9
DOIs
StatePublished - 1967
Externally publishedYes

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