Acid?base and cationic homoconjugation equilibria of substituted pyridine N-oxides in acetone
โ Scribed by Chmurzy?ski, Lech; Liwo, Adam
- Book ID
- 121374889
- Publisher
- Royal Society of Chemistry
- Year
- 1991
- Tongue
- English
- Weight
- 513 KB
- Volume
- 87
- Category
- Article
- ISSN
- 0956-5000
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๐ SIMILAR VOLUMES
## Based on potentiometrically determined cationic homoconjugation constants it has been found that in all the non-aqueous solvents studied the extent of cationic homoconjugation increases with the increasing basicity of pyridine N-oxide. The relationships between logarithms of cationic homoconjug
## Cationic heteroconjugation equilibria have been studied potentiometrically in systems containing substituted pyridine Noxides in a polar protophobic aprotic solvent, nitrobenzene. For comparison, systems with trimethylamine N-oxide, MesNO, representing aliphatic amine N-oxides, and pyridine, Py