## Abstract The ^13^C and ^15^N CPMAS NMR spectra of 18 pyrazoles substituted at position 1 by dinitrophenyl and trinitrophenyl (picryl) groups have been recorded. To help in the assignments, some of these compounds were studied in DMSO‐__d__~6~ solution. Phenomena such as the conformation of the _
15N NMR chemical shifts of NH-pyrazoles in the solid state and in solution at low temperature
✍ Scribed by Francisco Aguilar-Parrilla; Ferdinand Männle; Hans-Heinrich Limbach; José Elguero; Nadine Jagerovic
- Publisher
- John Wiley and Sons
- Year
- 1994
- Tongue
- English
- Weight
- 332 KB
- Volume
- 32
- Category
- Article
- ISSN
- 0749-1581
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✦ Synopsis
Abstract
The ^15^N chemical shifts of thirteen NH‐pyrazoles in the solid state and of seven NH‐pyrazoles in [^2^H~8~] THF solution at 170–175 K (with frozen annular tautomerism) are reported. The solid‐state values are discussed using an additive model. The differences in chemical shifts between the solid state and solution are due to the different intermolecular hydrogen bonds present in the various environments.
📜 SIMILAR VOLUMES
## Abstract The proton transfer equilibrium in a series of double Schiff base derivatives of __trans__‐1,2‐diaminocyclohexane in solution and the solid state was studied by means of ^15^N NMR spectroscopy and analysis of the deuterium isotope effect on the chemical shifts Δ^15^N(D). The presence of
## Abstract The ^13^C [hexadeutero‐dimethylsulfoxide (DMSO‐__d__~6~), hexamethyl‐phosphoramide (HMPA)‐__d__~18~and solid‐state] and ^15^N (solid‐state) NMR spectra of six __C__‐aminobenzimidazoles have been recorded. The tautomerism of 4(7)‐aminobenzimidazoles and 5(6)‐aminobenzimidazoles has been
## Abstract Three __N__‐substituted pyrazoles and three __N__‐substituted indazoles [1‐(4‐nitrophenyl)‐3,5‐dimethylpyrazole (1), 1‐(2,4‐dinitrophenyl)‐3,5‐dimethylpyrazole (2), 1‐tosyl‐pyrazole (3), 1‐__p__‐chlorobenzoylindazole (4), 1‐tosylinda‐zole (5) and 2‐(2‐hydroxy‐2‐phenylethyl)‐indazole (6)
## Abstract Schiff base derivatives of 2‐hydroxynaphthylaldehyde were studied by means of ^13^C and ^15^N cross‐polarization magic angle spinning NMR spectroscopy and deuterium isotope effects on ^15^N chemical shifts, ΔN(D), in the solid state. ΔN(D) in the solid state provided evidenced for the p
## Abstract In this investigation we report a complete assignment of ^13^C, ^1^H and ^15^N solution and solid state chemical shifts of two bacterial photosynthetic pigments, bacteriochlorophyll (BChl) __a__ and bacteriopheophytin (BPheo) __a__. Uniform stable‐isotope labelling strategies were devel