## Abstract Substituted phenol–trimethylamine __N__‐oxide (TMAO) systems were studied. The ^1^H chemical shift of the hydrogen‐bonded proton first increases with decreasing p__K__~a~ of the phenols and, after a sharp maximum, it then decreases. Thus, the shielding of the hydrogen‐bonded proton by t
FTIR and 13C NMR studies of hydrogen bonds and proton transfer in complexes of N-dodecyl-N,N-dimethylamine oxide with 26 phenols, carboxylic and mineral acids in solution.
✍ Scribed by Bogumil Brycki; Miroslaw Szafran
- Publisher
- Elsevier Science
- Year
- 1994
- Tongue
- English
- Weight
- 820 KB
- Volume
- 59
- Category
- Article
- ISSN
- 0167-7322
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