“…As illustrated in Figure c, DBT and 4,6-DMDBT showed similar reactivity, achieving complete conversion within 1.5 h, while the conversion rate of BT was lower, reaching 92% in 2 h. The reactivities decreased in the order of DBT > 4,6-DMDBT > BT, which was attributed to the difference of S electron density, for the oxidation of thiophene compounds follows the electrophilic addition principle . Besides, the steric effect of methyl groups may also impact the reaction, resulting in the conversion efficiency of 4,6-DMDBT to be slightly lower than that of DBT. , Furthermore, the reaction products were identified using gas chromatography-mass spectrometry (GC-MS), which were verified to be sulfones (Figure S6).…”