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J Agric Food Chem ; 53(13): 5347-52, 2005 Jun 29.
Artículo en Inglés | MEDLINE | ID: mdl-15969517

RESUMEN

The abiotic degradation of iodosulfuron-methyl-ester was investigated under both alkaline and acidic pH conditions in the dark, and results showed it to be a rather stable molecule in neutral or slightly alkaline environments. Photochemical reactions were studied using a high-pressure mercury arc lamp, and results showed that direct phototransformation is possible under normal environmental conditions (lambda > 290 nm). High-performance liquid chromatography (HPLC-UV and HPLC-MS) analyses were used to identify the degradates and to study the kinetics of photodecomposition and hydrolysis. Five main products of iodosulfuron-methyl-ester degradation were tentatively identified, and one of them (4-methoxy-6-methyl-1,3,5-triazin-2-amine) was confirmed using an authentic standard. Among the phototransformation mechanisms, photosubstitution of the iodide atom by a hydroxyl group, photodissociation of the N-S bond, and photoassisted hydrolysis were observed. The quantum efficiencies (multiwavelength quantum yield) of the photodegradation under different conditions were determined, and values of 0.054 +/- 0.02 (pH 9.6), 0.08 +/- 0.02 (pH 7), and 0.044 +/- 0.008 (pH 5.3) were obtained.


Asunto(s)
Ésteres/química , Soluciones , Sulfonamidas/química , Cromatografía Líquida de Alta Presión , Concentración de Iones de Hidrógeno , Hidrólisis , Cinética , Espectrometría de Masas , Metilación , Fotoquímica , Espectrometría de Fluorescencia , Espectrofotometría , Agua
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