Journal of Agricultural and Food Chemistry p. 814 - 821 (1994)
Update date:2022-08-02
Topics:
Durand, G.
Abad, J. L.
Sanchez-Baeza, F.
Messeguer, A.
Barcelo, D.
The photodegradation of fenitrothion was examined in a mixture of distilled water/methanol (5:1).The UV irradiation was carried out with a high-pressure Hg lamp during 7 h.For the identification of further breakdown products, fenitrooxon and carboxyfenitrothion were also irradiated under experimental conditions identical to those for fenitrothion.The identification of the breakdown products formed was carried out by gas chromatography-mass spectrometry (GC-MS) with electron impact (EI) and comparison with authentic standards synthesized in the laboratory.A total of 21 photoproducts of oxidation, isomerization, denitration, and solvolysis that may be of concern in environmental studies were unequivocally identified.Among them were formyldenitrofenitrothion, carbomethoxydenitrofenitrooxon. and hydroxymethyldenitrofenitrooxon.A proposed mechanism of the process is presented.Selected pathways for the photodegradation of fenitrothion were examined: (i) degradation through hydrolysis, with eventual remethylation; (ii) P=S to P=O oxidation; (iii) denitration; and (iv) oxidation of the methyl substituent through hydroxymethyl and formyl to give the corresponding carboxy derivatives.
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