“…The atmospheric chemistry of volatile organic sulfur compounds (VOSCs) plays an important role in the global biogeochemical sulfur cycles . Among the various atmospherically relevant VOSCs, dimethyl sulfide (DMS, CH 3 SCH 3 ) is one of the most important reduced-sulfur species that is mainly emitted into the atmosphere by marine bacteria through the enzymatic degradation of phytoplanktonic dimethylsulfoniopropionate (DMSP). , These emissions contribute to the global atmospheric sulfate aerosol between 19 to 42%, whose formation mainly involves the initial oxidation of DMS by its reaction with the principal oxidant hydroxyl radicals (·OH) in the atmosphere. − As the major sulfur-containing oxidation products from DMS, sulfuric acid (H 2 SO 4 ) and methanesulfonic acid (CH 3 SO 3 H) are important precursors to the formation of sulfate-containing aerosol particles and cloud condensation nuclei (CCN) that strongly influence the air quality, climate, and human health. , Therefore, the mechanism for the OH-initiated oxidation of DMS is of vital importance in understanding its atmospheric fate. , According to the recent model, the atmospheric oxidation of DMS by ·OH in an addition pathway proceeds by first formation of an addition reaction intermediate CH 3 S(·OH)CH 3 (Scheme ), which can be further oxidized by O 2 to form dimethyl sulfoxide (CH 3 S(O)CH 3 , DMSO). Alternatively, this intermediate can dissociate through homolytic C–S bond cleavage by releasing methyl radical (·CH 3 ) and methanesulfenic acid (CH 3 SOH, MSEA).…”