Gas chromatography/mass spectrometry of paraquat UV-ozonation products

The chromatographic and mass spectral properties of 13 compounds isolated from the reaction of UV and ozone on paraquat are described. The products were extracted from the acidified reaction mixture and converted to TMS derivatives. The identified products were the diTMS ester of oxalic acid (m/z 234), the TMS ester of 4-picolinic acid (m/z 195), the diTMS ester of succinic acid (m/z 262), the diTMS derivative of N-formylglycine, 4,4'-bipyridyl (m/z 156), the triTMS derivative of malic acid (m/z 350), and the diTMS derivative of a hydroxy-4-picolinic acid. Structural features and tentative identification of some of the remaining compounds are discussed. The most prominent peak on the chromatogram has a probable molecular ion at m/z 219, isomeric to the diTMS derivative of glycine. The structures presented suggest that demethylation, ring oxidation and fragmentation of one or both rings of the bipyridinium di-cation occur during UV-ozonation of paraquat.