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A NMR study of trimethylacetic acid self-association

✍ Scribed by L. Kimtys


Publisher
John Wiley and Sons
Year
1975
Tongue
English
Weight
219 KB
Volume
7
Category
Article
ISSN
0749-1581

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✦ Synopsis


Abstract

The carboxyl proton chemical shifts of neat trimethylacetic acid and its solutions in cyclohexane have been measured as a function of temperature. Formation, at the melting point, of a carboxyl group satellite line on the low field side has been found. The intensity of this satellite line rises with decreasing temperature, whereas the intensity of the main line decreases. The chemical shifts of the monomer (Ξ΄~m~ = 4Β·9 Β± 0Β·6 ppm) and dimers, the equilibrium constants, enthalpy (Ξ”__H__ = βˆ’(11Β·3 Β± 0Β·6) kcal/mol) and entropy (Ξ”__S__ = βˆ’(13Β·5 Β± 0Β·7) cal/mol. degree) changes have been calculated using the concentration dependence of the chemical shifts of trimethylacetic acid in cyclohexane solutions at various temperatures. The chemical shift of the satellite line has been shown to correspond to the chemical shift of the cyclic dimers of the acid.


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