## Abstract Anodic oxidation of hexamethylbenzene (**1**) in acetonitrile with Bu~4~NBF~4~ as electrolyte at a platinum anode at +1.7 V (versus Ag/0.01 M Ag^+^) gives mainly 1,3‐bis(acetamidomethyl)‐2,4,5,6‐tetramethylbenzene (**6**). The mechanism of this electrochemical difunctionalisation of a h
Voltammetric studies on anodic oxidation of silver
✍ Scribed by V. Lǎzǎrescu; O. Radovici; M. Vass
- Publisher
- Elsevier Science
- Year
- 1985
- Tongue
- English
- Weight
- 205 KB
- Volume
- 30
- Category
- Article
- ISSN
- 0013-4686
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✦ Synopsis
Although extensively studied[l-1 11, the anodic oxidation of silver in alkaline solutions is not completely understood. The well-defined oxides, Ag(I) oxide and a higher oxide formulated as Ag(I)Ag(III)O,, are generally recognixed[ 1-I 1 J_ However, as the cyclic voltammetry studies show[4,5,10,12, 131, there are another two anodic processes occurring before the formation of these oxides: a minor one, usually ignored (considered an artifact due to the method of metal fabricationC4, 53 or associated with carbonate impurities[lO]) and a more important one which, for various reasons, was assigned as AgOH[4] or Ag,O[S, 9] formation, Hads desorption[l] or silver dissolution[lO, 111. Recent investigations on the potentiodynarnic behaviour of Ag/aAl,OJ in alkaline solutions[ 141 have shown, however, that the minor peak represents a process which also takes place on a catalyst surface, not only on the mechanically worked surfaces as it had been supposed[4,5]. On the other hand, the invariance of this peak on changes of the carbonate concentrations reported by Droog et aZ.[12] contradicts the earlier suggestions. The anodic oxidation of silver in alkaline solutions
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Ag,O and AgO formed by potentiostatic oxidation of silver in O.lN KOH have been chemically analysed for the mean valency of silver ion. The anodic oxide formation proceeds in two stages and the silver ion in the oxide changes from Ag+ to Ag2+ at a transition potential. The reduction of AgO at consta
A silver electrode prepared by electrolytic deposition on a platinum wire was oxidized anodically in alkaline solution at constant cd. The impedance change and the potential change after opening the circuit in the course of anodic oxidation were observed and analysed. In the anodic oxidation, crysta
The formation and the oxidation of silver sulphate have been examined at constant potential on silver electrodes . Nuclei of the oxide are formed rapidly and grow in two dimensions in the silver sulphate . The deduced rate constants show that the slow stage of the reaction is AgI +OHaas -\* AgO I H-