Electrochemical reaction properties of platinum(I1) aryl isocyanide complexes were investigated to determine preparative conditions of electroreduction and to analyse formation mechanisms of low-valent di-and tri-platinum complexes. Polarographic and chronoamperometric measurements were carried out
Electrode reactions of nitroxide radicals at platinum in acetonitrile
β Scribed by M. Tsunaga; C. Iwakura; H. Tamura
- Publisher
- Elsevier Science
- Year
- 1973
- Tongue
- English
- Weight
- 359 KB
- Volume
- 18
- Category
- Article
- ISSN
- 0013-4686
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β¦ Synopsis
Electrode reactions of 2,2,6,6-tetramethylpiperidinenitroxide (TMPNO) and di-tertbutytnitroxide (DTBNO) at platinum in acetonitrile solution were investigated by means of linear sweep voltammetry and controlled potential coulometry. In the case of TMPNO, the voltammetric results were satisfied with diagnostic criteria for reversible charge transfer, and those of esr and coulometry led to one electron transfer. In the case of DTBNO, the coulometric results in which apparent number of electron was l/3 times the real one led to a mechanism with interesting series of reactions. This was also confirmed by CW-.
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The adsorption of acetonitrile and reduction of adsorbed molecules at platinized platinum electrode were studied by potentiodynamic and radiometric techniques. During acetonitrile adsorption the reversibly and irreversibly adsorbed species are formed. One electron reduction process occurs in the pot
Electrode reaction of 2,2,6,6-tetramethylpiperidine-nitroxide (TMPNO) cation at platinum in acetonitrile containing anhydrous hydrogep chloride was investigated by means of linear sweep voltammetry, electric conductivity measurement and esr spectrum, TMPNO cation is reversibly reduced to TMPNO radic
The cathodic behavior ofacetonitrile at a platinum electrode is strongly dependent on the cation of the supporting electrolyte, and contamination by moisture. Mixtures of supporting electrolytes can give anomalous effects under certain conditions; the results are consistent with the formation of hyd