## Abstract Bisβiminophosphoranes containing various types of linkers between two R~3~Pο£ΎN moieties were electrochemically oxidized at controlled potential __in situ__ in the electron spin resonance (ESR) cavity. For linkers constituted of phenylenes, conjugated phenylenes or merely a dicyanoethylen
ESR of cation radicals of phenothiazine derivatives
β Scribed by Ann G. Motten; Colin F. Chignell
- Publisher
- John Wiley and Sons
- Year
- 1985
- Tongue
- English
- Weight
- 650 KB
- Volume
- 23
- Category
- Article
- ISSN
- 0749-1581
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β¦ Synopsis
Phenothiazines are of interest as model heterocyclic compounds and also as pharmacological agents with a wide spectrum of biological activities. Cation radicals derived from six phenothiazine derivatives including phenothiazine, 2-chlorophenothiazine, promazine, chlorpromazine, promethazine and trimeprazine have been studied in aqueous solution by electron spin resonance. Their high-resolution electron spin resonance spectra have been fully analysed, and hyperfine splitting parameters have been compared with those obtained in other solvent systems where available. Previously undetected hyperfine splittings of about 0.2-0.4 G from y-protons on the alkyl chain were observed for promazine, promethazine and, possibly, chlorpromazine.
π SIMILAR VOLUMES
## Abstract Several deuteriated polycyclic aromatic radical cations were studied by ESR. Their hyperfine coupling constants are reported and mechanisms for their formation are proposed.