## 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
One- and Two-Dimensional 15N Exchange CP/MAS NMR Studies of the Structure and Electronic Properties of the Intermolecular N—H⋯N Hydrogen Bond in Imidazole Crystal
✍ Scribed by T. Ueda; H. Masui; N. Nakamura
- Publisher
- Elsevier Science
- Year
- 2001
- Tongue
- English
- Weight
- 128 KB
- Volume
- 20
- Category
- Article
- ISSN
- 0926-2040
No coin nor oath required. For personal study only.
✦ Synopsis
The hydrogen bond of the type N-H• • • N in imidazole crystal has been studied by oneand two-dimensional 15 N exchange CP/MAS NMR measurements as well as the powder NMR spectrum. The chemical shift anisotropies for -N and -N< were determined from the powder 1D spectrum. In 2D exchange CP/MAS NMR spectrum, the cross peaks between the 15 N main resonance peaks for -N and -N< were observed, implying that magnetization exchange between -N and -N< takes place. The 1D exchange CP/MAS NMR measurements determined the exchange rate of magnetization at 289 K to be 1.3 and 1.5 s -1 for -N and -N<, respectively. The proton-driven spin-diffusion model interprets the experimental values, and the exchange rate depends strongly on the RF power of the proton decoupling field, suggesting that the magnetization transfer between -N and -N< takes place by the 1 H-driven spin-diffusion mechanism.
📜 SIMILAR VOLUMES
A set of three aryl dimethyl pyrimidinones have been studied and their crystal structures described in terms of networks of C+H'''O and C+H'''N hydrogen bonds. Two of the three molecules in this study di4er in the replacement of a chloro group by a methyl group and obey the chloro+methyl exchange ru
## Abstract The ^15^N as well as ^13^C and ^1^H chemical shifts of eight __push–pull__ benzothiazolium iodides with various π‐conjugated chains between dimethylamino group and benzothiazolium moiety have been determined by NMR spectroscopy at the natural‐abundance level of all nuclei in DMSO‐__d__~
## Abstract The ^1^H, ^13^C and ^15^N NMR studies have shown that the __E__ and __Z__ isomers of pyrrole‐2‐carbaldehyde oxime adopt preferable conformation with the __syn__ orientation of the oxime group with respect to the pyrrole ring. The __syn__ conformation of __E__ and __Z__ isomers of pyrrol