## Abstract The monomerβdimer equilibrium of retinoic acid in carbon tetrachloride was studied by ^1^H and ^13^C NMR spectroscopy. The dimer dissociation constant at 24Β°C was determined to be 0.38 mM from a fit of the changes in the carboxylic acid carbon chemical shift as a function of concentrati
1H and 13C NMR study of the adsorption of alcohols on charcoals with various pore structures
β Scribed by You-Ru Du; Han-Zhen Yuan; Dong-Hui Wu; Yu-Hua Kong
- Publisher
- John Wiley and Sons
- Year
- 1989
- Tongue
- English
- Weight
- 362 KB
- Volume
- 27
- Category
- Article
- ISSN
- 0749-1581
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β¦ Synopsis
A 'H NMR study of methyl, ethyl, n-propyl, isopropyl and allyl alcohols adsorbed on charcoals with various pore structures showed that the adsorption mechanism is by capillary condensation in pores with radii smaller than Mdi, and by mono-/multi-layer adsorption on the solid surface of pores with larger radii. This mechanism is identical with that of adsorbed hydrocarbons. The "C NMR parameters suggest that the adsorbed alcohols are preferentially oriented in the monolayer, with the methyl groups bonded to the solid surface. Longer chain alcohols are bent in capillaries with radii smaller than 10 di. The broadening of the "C resonances was partly eliminated in magic angle spinning experiments by using a spinning rate of 1.5-1.8 kHz.
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