The main photoproducts initially formed in the phototransformation of linuron and chlorbromuron in aqueous solution result from photohydrolysis, i.e. hydroxylation with release of halide ion, and from elimination of a methoxy group. Reductive debromination was also observed with chlorbromuron. The t
Phototransformation of Dichlorophen in Aqueous Phase
β Scribed by Mansfield, Elka; Richard, Claire
- Publisher
- John Wiley and Sons
- Year
- 1996
- Tongue
- English
- Weight
- 313 KB
- Volume
- 48
- Category
- Article
- ISSN
- 1526-498X
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β¦ Synopsis
The photolysis of dichlorophen (DCP) in acidic medium yields 4chloro-4-hydroxy-2,2'-methylenediphenol (I) in the absence of oxygen and a benzoquinone-like derivative (11) in oxygenated solution. At pH = 9, DCP is in monoanionic form, and three products, I, I1 and 4-chloro-2,2'-methylenediphenol (111) are detected after irradiation of deoxygenated solutions of DCP. Formation of 111 is also observed in acidic or neutral solutions containing a low percentage of isopropanol. These results can be explained by the formation of a carbene after HCI elimination and reaction of this intermediate with water, oxygen, alcohol, anionic form of I or DCP.
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