Formation of dihydroperoxide derivatives during the oxidation of cyclohexene and tetralin by dioxygen

G. Dombi, Ferenc Evanics, Károly Jáky, László J. Csányi

Research output: Contribution to journalArticle

1 Citation (Scopus)

Abstract

1H- and 13C-NMR investigations revealed that prolonged oxidation of unsubstituted cyclohexene and tetralin, containing symmetrical and weak allylic and benzylic CH bonds, results in the formation of both mono- and dihydroperoxo derivatives.

Original languageEnglish
Pages (from-to)241-244
Number of pages4
JournalReaction Kinetics and Catalysis Letters
Volume63
Issue number2
Publication statusPublished - 1998

Fingerprint

Nuclear magnetic resonance
methylidyne
Oxygen
Derivatives
Oxidation
nuclear magnetic resonance
oxidation
tetralin
cyclohexene

Keywords

  • H- and C-NMR detection of mono-and dihydro-peroxide formation
  • Liquid-phase oxidation

ASJC Scopus subject areas

  • Catalysis
  • Physical and Theoretical Chemistry

Cite this

Formation of dihydroperoxide derivatives during the oxidation of cyclohexene and tetralin by dioxygen. / Dombi, G.; Evanics, Ferenc; Jáky, Károly; Csányi, László J.

In: Reaction Kinetics and Catalysis Letters, Vol. 63, No. 2, 1998, p. 241-244.

Research output: Contribution to journalArticle

Dombi, G. ; Evanics, Ferenc ; Jáky, Károly ; Csányi, László J. / Formation of dihydroperoxide derivatives during the oxidation of cyclohexene and tetralin by dioxygen. In: Reaction Kinetics and Catalysis Letters. 1998 ; Vol. 63, No. 2. pp. 241-244.
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