Application of liquid chromatography/electrospray ionization tandem mass spectrometry for the elucidation of hydroxyl radical oxidation of metsulfuron methyl and related sulfonylurea pesticide products: evidence for the triazine skeleton scission

作者：Chahboune Rajae; Mountacer Hafida; Sarakha Mohamed^*

来源：Rapid Communications in Mass Spectrometry, 2015, 29(15): 1370-1380.

DOI：10.1002/rcm.7234

RationaleSulfonylureas are among the most important class of antidiabetic and herbicides. Solar light excitation and Advanced Oxidation Processes may result in the formation of a wide array of products owing to the relative complex structure. These products, that should be identified, may present a more toxic effect than the parent compound.
MethodsLiquid chromatography/electrospray ionization quadrupole time-of-flight mass spectrometry (LC/ESI-QTOFMS) with accurate mass determination emerges as a valuable technique for the precise elucidation of all possible byproducts. The hydroxyl radical was generated by excitation of the iron(III) aquacomplex [Fe(H2O)OH](2+) and hydrogen peroxide at pH3.5. Three different sulfonylureas were studied: metsulfuron methyl, cinosulfuron and thifensulfuron methyl.
ResultsSeveral products owing to the reactivity of hydroxyl radicals with sulfonylurea were obtained. They arise from scission of the sulfonylurea bridge, hydroxylation of the aromatic ring, demethylation of the methoxy group and more importantly and unequivocally from the rupture of the triazine skeleton. To reach such scission, a primary demethylation of the methoxy group on the triazine moiety seems to act as a precursor process. Such a process was observed with the three studied sulfonylurea compounds.
ConclusionsThe reported results demonstrated the usefulness of accurate mass measurements undertaken by LC/ESI-QTOFMS for structural elucidation of the unknown byproducts that were generated during hydroxyl radical reactions with some sulfonylureas. It has been possible herein to identify the structures of products arising from the opening of the recalcitrant triazine structure via hydrolysis processes in acidic solutions.

• 出版日期2015-8-15