## Abstract When a 1° or 2° alcohol solution of benzophenone and 2,4‐pyridinedicarbonitrile (**1**) is irradiated, the 2,4‐dicyanopyridinyl radical (**2**) is formed immediately. When the irradiation is performed in the cavity of an ESR spectrometer, the spectrum amplitude increases to a near stead
Formation and Structure of the Phosphoranyl Radical Derived from 1,2-Phenylene Phosphorochloridate: a Solid-State ESR Study
✍ Scribed by Maria Cattani-Lorente; Gérald Bernardinelli; Michel Geoffroy
- Publisher
- John Wiley and Sons
- Year
- 1987
- Tongue
- German
- Weight
- 442 KB
- Volume
- 70
- Category
- Article
- ISSN
- 0018-019X
No coin nor oath required. For personal study only.
✦ Synopsis
The crystal structure of 1,2-phenylene phosphorochloridate has been determined. X-Ray irradiation of these crystals, at low temperature, leads to the formation of a radical exhibiting hyperfine structure with P and CI nuclei. The corresponding ESR tensors are obtained, and they show that this radical is a phosphoranyl radical adopting a slightly distorded u* structure. The same species could be produced in frozen solution, its hyperfine tensors are, then, more in accordance with a trigonal-bipyramid structure. The effects of the host matrix on the stabilization of the structure of phosphoranyl are investigated.
📜 SIMILAR VOLUMES
## Benzimidazole -and benzotriazole-amino derivatives of prog2enoic acid were studied by 'H NMR spectroscopy in the liquid state and by "C NMR spectroscopy in the liquid and solid states. The spectra shows tautomerism of the benzimidazole and benzotriazole rings, E-2 isomerism of the double bond o