Methoxyphenols, which are emitted through biomass burning, are an important species in atmospheric chemistry. In the present study, temperature-dependent aqueous-phase OH radical reactions of six methoxyphenols and two related phenols have been investigated through laser flash photolysis and the density functional theory. The rate constants obtained were in a range of (1.1-1.9) × 10 L mol s with (3-MC) > (Cre) ≈ (Syr) ≈ (MEP) > (Res) > (3-MP) > (2-EP) ≈ (2-MP). We derived the parameters of these reactions from the obtained -dependent rate constants and found a mean Arrhenius activation energy of 16.9 kJ mol. The diffusion rate constants were calculated for each case and compared to the measured ones. Generally, the rate constants are found to be close to fully diffusion-controlled ( = (1.4-1.5) × 10 L mol s for all reactions). A structure-function relationship was established through the measurement result, which could be used for predicting unknown rate constants of other phenolic compounds. All of these findings are expected to enhance the predictive capabilities of models, such as the chemical aqueous-phase radical mechanism.
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