## Abstract This paper presents a study of the chemical shift of the phenol hydroxyl group as a function of concentration and temperature in cyclohexane, methylcyclohexane and carbon tetrachloride solutions. The chemical shift of monomeric phenol has been found. For these solutions monomertrimer eq
A NMR study of phenol self-association. The quasi-chemical approximation
✍ Scribed by L. Kimtys; P. Mikulskis; N. N. Shape'ko
- Publisher
- John Wiley and Sons
- Year
- 1973
- Tongue
- English
- Weight
- 235 KB
- Volume
- 5
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
The NMR dilution chemical shifts of phenol in the cyclohexane, methylcyclohexane and carbon tetrachloride solutions at temperatures +10, +20, +40, +50, +60, +70 and +80°C have been interpreted applying the quasi‐chemical approximation. The interchange energies for the OH…O bonding and the chemical shifts of hydroxylic protons in associated phenol molecules have been determined and their temperature dependences studied.
The obtained results are in good accordance with the equilibrium calculation data.
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