## Abstract The effect of introduction of fluorinated groups (CH~2~F, CHF~2~, CF~3~, C~2~F~5~, OCF~3~, SCF~3~) on the ^13^C NMR chemical shifts in cyclohexanes is examined. The two main effects are caused by location at the Ξ± and Ξ³ carbon positions. Comparison of the various data allowed the calcul
Influence of the spatial position of a trifluoromethyl group on the 13C chemical shifts in the cyclohexane series
β Scribed by Yvan Carcenac; Patrick Diter; Claude Wakselman; Marc Tordeux
- Publisher
- John Wiley and Sons
- Year
- 2006
- Tongue
- English
- Weight
- 210 KB
- Volume
- 44
- Category
- Article
- ISSN
- 0749-1581
- DOI
- 10.1002/mrc.1804
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β¦ Synopsis
Abstract
The influence of the introduction of a trifluoromethyl group on the ^13^C chemical shifts in cyclohexane was examined. The two main effects observed are located at the Ξ± and Ξ³ positions relative to the carbon bearing the fluorine atoms. By comparison of the collected data it was possible to calculate the increments corresponding to the substitution of a hydrogen atom by a CF~3~ group at axial or equatorial positions on the cyclohexane ring. Copyright Β© 2006 John Wiley & Sons, Ltd.
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