The 'H and ''C NMR spectra of several fluorine-substituted polycyclic aromatic hydrocarbons in which fluorine projects into a bay region were studied. Both protons and carbons of the stericaUy opposed CH bond show anomalously large F-induced shifts and couplings to fluorine. The magnitudes of the co
13C19F spin–spin coupling in some monofluoro-substituted polycyclic aromatic hydrocarbons
✍ Scribed by P. E. Hansen; A. Berg; H. J. Jakobsen; A. P. Manzara; J. Michl
- Publisher
- John Wiley and Sons
- Year
- 1977
- Tongue
- English
- Weight
- 919 KB
- Volume
- 10
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
The determination and complete assignment of the ^13^C^19^F coupling constants and ^13^C chemical shifts for 15 monofluoro derivatives of nine polycyclic aromatic hydrocarbons are reported. Fluorine substitutent effects on the ^13^C chemical shifts are given and their regular behaviour, making comparisons between different compounds possible, is discussed. The numerical values of the ^13^C^19^F long range coupling constants are found, with a few exceptions, to decrease in an alternating manner along the periphery of the molecules. In several cases the signs of the coupling constants have been determined. It appears that the signs alternate, but additional evidence is required. The magnitudes of different types of coupling constants are discussed in terms of steric and electronic effects. CNDO/2 and INDO calculations of the ^13^C^19^F coupling constants in the fluoronaphthalenes have been performed using the ‘sum‐over‐states’ method with the aim of examining the orbital and spin–dipole contributions to the various couplings.
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