Selective abatement of electron-rich organic contaminants by trace complexed Mn(II)-catalyzed periodate via high-valent manganese-oxo species.

Mn(II) is among the most efficient catalysts for the periodate (PI)-based oxidation process. In-situ formed colloidal MnO simultaneously serves as the catalyst and oxidant during the degradation of organic contaminants by PI. Here, it is revealed that the complexation of Mn(II) by ethylene diamine tetraacetic acid (EDTA) further enhances the performance of PI-based oxidation in the selective degradation of organic contaminants. As evidenced by methyl phenyl sulfoxide probing, O-isotope labeling, and mass spectroscopy, EDTA complexation modulates the reaction pathway between Mn(II) and PI, triggering the generation of high-valent manganese-oxo (Mn-oxo) as the dominant reactive species. PI mediates the single-electron oxidation of Mn(II) to Mn(III), which is stabilized by EDTA complexation and then further oxidized by PI via the oxygen-atom transfer step, ultimately producing the Mn-oxo species. Ligands analogous to EDTA, namely, [S,S]-ethylenediaminedisuccinic acid and L-glutamic acid N,N-diacetic acid, also enhances the Mn(II)/PI process and favors Mn-oxo as the dominant species. This study demonstrates that functional ligands can tune the efficiency and reaction pathways of Mn(II)-catalyzed peroxide and peroxyacid-based oxidation processes.