Phototransformation of linuron and chlorbromuron in aqueous solution
✍ Scribed by Faure, Valérie; Boule, Pierre
- Publisher
- John Wiley and Sons
- Year
- 1997
- Tongue
- English
- Weight
- 231 KB
- Volume
- 51
- Category
- Article
- ISSN
- 1526-498X
No coin nor oath required. For personal study only.
✦ Synopsis
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 transformation is less speciÐc than with diuron. The orientation of the reaction depends on the wavelength : short wavelengths (254 nm) favour demethoxylation and photohydrolysis in the meta position whereas, with "black lightÏ, i.e. wavelengths longer than 330 nm, photohydrolysis in the para position is the main reaction observed.
📜 SIMILAR VOLUMES
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
The main photoproducts formed in an aqueous solution of napropamide irradiated in UV light are N,N-diethyl-2-(1-hydroxynaphthalen-2-yl)propionamide, N,N-diethyl-2-(4-hydroxynaphthalen-1-yl)propionamide and 1-naphthol. These account for c.60%, 15% and 10% of napropamide converted respectively. No inÑ
## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.