## Abstract The chemical shifts of hydrogen bonded protons in complexes of 11 substituted pyridines with trifluoroacetic acid were examined, in five dry solvents of different activity, with respect to proton transfer and aggregation effects. The results were correlated with Δp__K__~__a__~, the Kirk
Nitrogen-15 nuclear magnetic resonance studies of hydrogen bonding and proton transfer in some pyridine trifluoroacetates in dichloromethane
✍ Scribed by Z. Dega-Szafran; M. Szafran; L. Stefaniak; C. Brevard; M. Bourdonneau
- Publisher
- John Wiley and Sons
- Year
- 1986
- Tongue
- English
- Weight
- 399 KB
- Volume
- 24
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
The "N NMR chemical shifts of ten substituted pyridines (B) and their complexes with trifluoroacetic acid (AHB) were measured at the natural abundance level in dichloromethane. The plot of the relative chemical shifts [A6("N) = G(AHB) -6(B)] against ApK, gives a titration curve which reflects a protometric eauilibrium AH -B $ A--* * HB+. These data were used to determine the constants of the transfer reaction (Kerp). A linear relationship holds between log Keap and ApK,. A6(15N) treated as a good hydrogen bond parameter. KEY WORDS I5N NMR spectroscopy Hydrogen bond Proton transfer Pyridines overall proton values can be
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