## Abstract The hydroxyl proton chemical shifts of __tert__‐butyl alcohol, dissolved in acetone and in binary mixtures of acetone with cyclohexane, have been measured as functions of concentration at temperatures of 20, 35, 50 and 60 °C. Using both the equilibrium constant and the quasi‐lattice met
1H n.m.r. study of the self-association of acetone phenylhydrazone by hydrogen bonding
✍ Scribed by C. I. Stassinopoulou; J. Petrou
- Publisher
- John Wiley and Sons
- Year
- 1977
- Tongue
- English
- Weight
- 271 KB
- Volume
- 10
- Category
- Article
- ISSN
- 0749-1581
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
Proton magnetic resonance dilution studies of acetone phenylhydrazone were carried out in n‐heptane, carbon disulphide and hexachlorobutadiene solutions. Equilibrium constants and enthalpy values for the predominant self‐associated species are reported. Linear trimeric aggregates predominate in n‐heptane solutions. The monomeric units are associated by intermolecular hydrogen bonding of the NH proton to the iminic nitrogen. The enthalpy per hydrogen bond is 10.04 kJ (2.4 kcal). In carbon disulphide and hexachlorobutadiene solutions complexation of acetone phenylhydrazone with the solvent competes with self‐association.
📜 SIMILAR VOLUMES
## Abstract The carboxyl proton chemical shifts of trimethylacetic acid, which was dissolved in acetone and in binary mixtures of acetone and cyclohexane, have been measured as a function of concentration at temperatures of 0, +15, +30, +45 and +60 °C. The results obtained for the system studied, u
## Abstract The ^1^H n.m.r. spectra of eleven anilides of 6‐methyl‐picolinic acid __N__‐oxide in chloroform were obtained. The influence of temperature, concentration and substituents on the chemical shifts of the NH protons was investigated. The structure of the anilides is discussed.
## Abstract According to the density functional theory calculations, the X···H···N (XN, O) intramolecular bifurcated (three‐centered) hydrogen bond with one hydrogen donor and two hydrogen acceptors causes a significant decrease of the ^1h^__J__(N,H) and ^2h^__J__(N,N) coupling constants across th
## Abstract The self‐association of pyrimidine and its methylated derivatives was studied by measuring the concentration‐dependent changes in proton chemical shifts in deuterium oxide at 35°C. The data were analysed by a dimer model with two parameters. The equilibrium constants give an increasing