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The oxidation of widely-used herbicide metazachlor (MTZ) by hydroxyl radical (HO • ) in the gas and the aqueous phases was investigated in terms of mechanistic and kinetic behaviors using the M06-2X/6-311++G (3df, 3pd)//M06-2X/6-31 + G (d,p) level of theory over the temperature range 250-400 K. The formal hydrogen transfer, HO • -addition, and single electron transfer mechanisms were considered. The overall rate constants in the gas phase range from 8.40 × 10 10 to 8.31 × 10 9  M -1  s -1 at the temperature from 250 to 400 K, respectively, while the ones in the aqueous phase are close to diffusion-controlled rates, with diffusion-corrected rate constants being 1.31 × 10 9 to 1.27 × 10 9  M -1  s -1 . The formal hydrogen transfer mechanism is the most dominant in the gas phase, whereas the HO • -addition is the most favorable in the aqueous phase. The H-abstraction at two methyl groups and the HO • -addition to C11 and C12 atoms (pyrazole ring), C16 and C18 atoms (benzyl ring) are significant. The short lifetime in the environment, equal to only 4.16 h, requires more attention to this herbicide compound, whereas its lifetime in the aqueous condition varies sharply from half second to several thousand days depending on the HO • concentration. The ecotoxicity estimation of MTZ and its principal transformation products to aquatic organisms suggests that they are harmful or toxic substances. Moreover, the MTZ is a developmental toxicant and mutagenicity-positive, while its decomposed products are developmental toxicants with no mutagenic toxicity. Their bioaccumulation in aquatic organisms is negligible., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2022 Elsevier Ltd. All rights reserved.)

The reaction mechanisms of Br and I atoms with H 2 O 2 have been investigated using DFT and high-level ab initio calculations. The H-abstraction and OH-abstraction channels were highlighted. The geometries of the stationary points were optimized at the B3LYP/aug-cc-pVTZ level of theory, and the energetics were recalculated with the coupled cluster theory. Spin-orbit coupling for each halogenated species was also explicitly computed by employing the MRCI level of theory. Thermochemistry for HOBr and HOI has been revised and updated standard enthalpies of formation at 298 K for HOBr and HOI are the following: Δ f H° 298K (HOBr) = (-66.2 ± 4.6) kJ mol -1 and Δ f H° 298K (HOI) = (-66.8 ± 4.7) kJ mol -1 . The rate constants have been estimated using transition state theory (TST), canonical variational transition state theory (CVT), and CVT with small curvature tunneling (CVT/SCT) over a wide temperature range (250-2500 K). For the direct abstraction mechanism, the overall rate constant at 300 K was predicted to be 2.58 × 10 -16 and 7.42 × 10 -25 cm 3 molecule -1 s -1 for the Br + H 2 O 2 and I + H 2 O 2 reactions, respectively. The modified Arrhenius parameters have been estimated for the overall reactions: k Br+H2O2 (T) = 4.80 × 10 -26 T 4.31 exp(-5.51 (kJ mol -1 )/RT) and k I+H2O2 (T) = 3.41 × 10 -23 T 3.29 exp(-56.32 (kJ mol -1 )/RT).