Abstract
Free radicals play an important role in many chemical and biological processes, but due to their highly reactive and short-lived nature, they evade most analytical techniques, limiting our understanding of their formation and reactivity. Spin trapping molecules can react with free radicals to form radical adducts with lifetimes long enough for analysis. Mass spectrometry is an attractive way to identify radical adducts, but due to their radical nature, they form untraditional oxidized [M]+ and reduced [M+2H]+ ions, which complicates the interpretation of mass spectrometry analysis. This work uses simplified mixtures of radicals generated in both water and dimethyl sulfoxide (DMSO) with spin trap 5-tert-butoxycarbonyl-5-methyl-1-pyrroline-N-oxide (BMPO), to elucidate the behavior of nitroxide spin traps in electrospray ionization (ESI) mass spectrometry (MS) interfaced with liquid chromatography (LC). This study proposes a disproportionation mechanism to explain the formation of the oxidized and reduced BMPO adducts detected by LC-ESI-MS and explores the formation of "di-adducts" through radical recombination. We finally present a framework for differentiating between the different types of ions using collision induced fragmentation mass spectra (MS/MS). This work offers a comprehensive investigation into the behavior of radical adducts in ESI-MS to streamline the identification of organic radicals and advance understanding of radical chemistry.
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