ISSN:
0894-3230
Keywords:
Chemistry
;
Theoretical, Physical and Computational Chemistry
Source:
Wiley InterScience Backfile Collection 1832-2000
Topics:
Chemistry and Pharmacology
,
Physics
Notes:
The 15N NMR chemical shifts of eight substituted pyridine N-oxides (B) and their complexes (AHB) with methanol and dichloroacetic and trifluoromethanesulfonic acids were measured in chloroform-d at the natural abundance level. The measured chemical shifts are strongly affected by substituents, hydrogen bond strength and protonation. The plot of the relative chemical shifts, Δδ(15N) = δ(AHB) - δ(B), against ΔpKa gives a titration curve that reflects the variation of the hydrogen bond strength and the proton moves from the acid to the N-oxide. According to previous IR data, in the complexes from the inversion region (ΔpKa = 1·26), the proton is either delocalized (B…H…A) or more likely the lifetime is so short (≤10-13 s) that the method does not recognize the B…H-A and B+H…A- species. Protonation of pyridine N-oxides shifts the nitrogen signal ca 50 ppm to lower frequencies compared with the ca 123 ppm for pyridines.
Additional Material:
3 Ill.
Type of Medium:
Electronic Resource
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