Identification of different products obtained by electrochemical and photochemical reduction of the herbicide metamitron
β Scribed by Carlos Olmedo; Luis Deban; Enrique Barrado; Yolanda Castrillejo; Luis Herrero
- Publisher
- Elsevier Science
- Year
- 1994
- Tongue
- English
- Weight
- 391 KB
- Volume
- 39
- Category
- Article
- ISSN
- 0013-4686
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β¦ Synopsis
The electrochemical reduction of the herbicide Metamitron (4-amino_4,5dihydro-3-methyl& phenyl-1,2,4-triazin-5-one) has been carried out at different pHs using a mercury pool cathode. The iinal product of these reductions depends both on the electrolysis potential and on the pH. All processes are irreversible and the reductions of the C-N and the N-NH, (pH > 3) or N-NH: bond @H < 3) are inferred.
An aqueous solution of Metamitron is also degraded by sunlight leading to 4,5dihydro-3-methyl&phenyl-1,2,4-triazin-5-one (deaminometamitron). This reaction can be monitored polarographically.
π SIMILAR VOLUMES
Unsymmetrical disulphides and trisulphides were obtained after electrochemical reduction of 1,2-dithiole-3-thiones in N,N dimethylformamide as by-products in addition to the major symmetrical disulphide. In a previous paper', we reported the electrochemical reduction of 1,2-dithiole-3-thiones