9-alkenylcarbazoles - II.1H and13C NMR spectra of 9-vinylcarbazoles

V. D. Filimonov, V. A. Anfinogenov, N. E. Matyukov

Research output: Contribution to journalArticle

Abstract

The1H and13C NMR spectra of 9-vinylcarbazole and its 3-chloro, 3,6-dichloro, and 3-nitro derivatives were recorded and studied. It is shown that electron-acceptor substituents reduce the shielding of the β-carbon atom and the trans proton of the vinyl group. A good linear correlation between the chemical shifts of these nuclei and the Hammett σpara - constants with the ρ values (3.78 for13Cβ and 0.28 for1Htrans) is observed. It was established by comparison of the results with the1H and13C NMR spectral parameters for some of the vinyl compounds that the degree of conjugation of the p electrons of nitrogen with the π electrons of the double bond in 9-vinylcarbazoles is lower than in simple vinyl and vinyl phenyl ethers and vinyl acetate.

Original languageEnglish
Pages (from-to)1133-1136
Number of pages4
JournalChemistry of Heterocyclic Compounds
Volume12
Issue number10
DOIs
Publication statusPublished - Oct 1976

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Nuclear magnetic resonance
Vinyl Compounds
Electrons
Chemical shift
Shielding
Protons
Nitrogen
Carbon
Derivatives
Atoms
vinyl acetate
phenyl vinyl ether

ASJC Scopus subject areas

  • Organic Chemistry

Cite this

9-alkenylcarbazoles - II.1H and13C NMR spectra of 9-vinylcarbazoles. / Filimonov, V. D.; Anfinogenov, V. A.; Matyukov, N. E.

In: Chemistry of Heterocyclic Compounds, Vol. 12, No. 10, 10.1976, p. 1133-1136.

Research output: Contribution to journalArticle

Filimonov, V. D. ; Anfinogenov, V. A. ; Matyukov, N. E. / 9-alkenylcarbazoles - II.1H and13C NMR spectra of 9-vinylcarbazoles. In: Chemistry of Heterocyclic Compounds. 1976 ; Vol. 12, No. 10. pp. 1133-1136.
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