PHDIWHEMISTRYOFCATIONRADICALSINSOIUl?IoN :EWYIO=OXI=m BYlXiEpHEN(JMIAzlNEC&TICNPALXCALu. %aboratiire d'Elec&mhimie Organiquz et Analytiqus (ERA CNFS 6751, DQarkmntde Rsdxerche Fondamntale, Centre d'Etu&sNucl&ires de Grencble, 85X 38O41Gren&le Cedsx (France) etkentre unimxsitake de Savoie, UERScience
Kinetics of dopamine oxidation by dialkylaminoalkylphenothiazine cation radicals
โ Scribed by Maria Rosa Gasco; Maria Eugenia Carlotti
- Publisher
- John Wiley and Sons
- Year
- 1979
- Tongue
- English
- Weight
- 378 KB
- Volume
- 68
- Category
- Article
- ISSN
- 0022-3549
No coin nor oath required. For personal study only.
โฆ Synopsis
The kinetics of dopamine oxidatinon dialkylaminoalkylphenothiazine cation radicals (with two- or three-carbon side chains) were investigated. The two-carbon side-chain derivatives have reaction rates higher than the three-carbon ones. For chlorpromazine and promazine, extrapolation of pH 1-6 data shows that reaction rates become very fast at physiological pH.
๐ SIMILAR VOLUMES
The structure of the gaseous long-lived radical cation generated upon electron ionization of trimethylphosphine oxide, (CH&PO, has been investigated by using ion-molecule reactions in a Fourier transform ion cyclotron resonance mass spectrometer. A radical cation with the connectivity of trimethylph
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