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Ceria-Catalyzed Hydrolytic Cleavage of Sulfonamides.

Jiri HenychMartin Št AstnýSylvie KříženeckáJan ČundrleJakub TolaszTereza DuškováMartin KormundaJakub EdererStepan StehlikPetr RyšánekViktorie NeubertováPavel Janoš
Published in: Inorganic chemistry (2024)
Nanoceria is a promising nanomaterial for the catalytic hydrolysis of a wide variety of substances. In this study, it was experimentally demonstrated for the first time that CeO 2 nanostructures show extraordinary reactivity toward sulfonamide drugs (sulfadimethoxine, sulfamerazine, and sulfapyridine) in aqueous solution without any illumination, activation, or pH adjustment. Hydrolytic cleavage of various bonds, including S-N, C-N, and C-S, was proposed as the main reaction mechanism and was indicated by the formation of various reaction products, namely, sulfanilic acid, sulfanilamide, and aniline, which were identified by HPLC-DAD, LC-MS/MS, and NMR spectroscopy. The kinetics and efficiency of the ceria-catalyzed hydrolytic cleavage were dependent on the structure of the sulfonamide molecule and physicochemical properties of Nanoceria prepared by three different precipitation methods. However, in general, all three ceria samples were able to cleave SA drugs tested, proving the robust and unique surface reactivity toward these compounds inherent to cerium dioxide. The demonstrated reactivity of CeO 2 to molecules containing sulfonamide or even sulfonyl (and similar) functional groups may be significant for both heterogeneous catalysis and environmentally important degradation reactions.
Keyphrases
  • aqueous solution
  • ms ms
  • dna binding
  • simultaneous determination
  • room temperature
  • transcription factor
  • high performance liquid chromatography
  • drug induced
  • anaerobic digestion