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Voltammetry of organic ditellurides in protic media. mercury assisted chemical pre-reactions with catalytic effects

✍ Scribed by B. Nygård; Jiri Ludvik; S. Wendsjö


Publisher
Elsevier Science
Year
1996
Tongue
English
Weight
497 KB
Volume
41
Category
Article
ISSN
0013-4686

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✦ Synopsis


The different reduction mechanisms of two types of organic ditellurides have been studied in aqueous/ethanolic media by voltammetry of interest for a mercury assisted chemical pre-reaction as a first step in the electrode process. Bis carboxymethyl ditelluride, HOOC-CH,-TeTe-CH,-COOH (I) and diphenyl ditelluride Ph-TeTe-Ph (II) were model compounds. During the reduction of (I) on the mercury electrode a strong catalytic evolution of free tellurium (Te') is observed indicating a Te-C bond cleavage. Contrary to this, the reduction of diphenyl ditelluride proceeds as a mercury assisted cleavage of the Te-Te bond. The reduction pattern for the aromatic ditelluride is compared with the corresponding aromatic selenium and sulphur analogues.