## Abstract The ^1^H and ^19^F NMR spectra of fluorobenzene and 1,2‐difluorobenzene were measured in several pure solvents and in binary solvent mixtures to study the solvent dependence of ^1^H^19^F and ^19^F^19^F coupling constants. The solvents are distinctly divided into two groups on the basi
1H1H and 1H19F coupling constants of some styrene, benzaldehyde and benzylidene amine derivatives
✍ Scribed by Sirpa Suntioinen; Reino Laatikainen; Vladimir Král
- Publisher
- John Wiley and Sons
- Year
- 1994
- Tongue
- English
- Weight
- 372 KB
- Volume
- 32
- Category
- Article
- ISSN
- 0749-1581
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Five para‐fluorobenzene derivatives having a CHCR~2~ or a CHNR group were prepared and their ^1^H and ^19^F NMR spectra in acetone‐d~6~ were analysed. The ^6^J(H~α~,F) and ^4^J(H^α^,H) couplings of the nitrogen derivatives fall between those of the carbon and oxygen derivatives: the electronegativity of the side‐chain β‐atom seems to have a prominent role in the spin information transmission. The ^6^J(H^α^,F) and ^4^(H^α^,H) couplings indicate that the nitrogen derivatives are rigidly planar whereas the carbon derivatives are non‐planar.
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