RESUMO
This work investigated the reaction kinetics of HNO3 with four Criegee intermediates (CIs): CH2OO, (CH3)2COO, methyl vinyl ketone oxide (MVKO), and methacrolein oxide (MACRO). Our results show that these reactions are extremely fast with rate coefficients of (1.51 ± 0.45) × 10-10, (3.54 ± 1.06) × 10-10, (3.93 ± 1.18) × 10-10, and (3.0 ± 1.0) × 10-10 cm3 s-1 for reactions of HNO3 with CH2OO, (CH3)2COO, syn-MVKO, and anti-MACRO, respectively. This is consistent with previous results for the reactions between CIs and carboxylic acids, but the rate coefficient of CH2OO + HNO3 in the literature [Foreman Angew. Chem. 2016, 128, 10575] was found to be overestimated by a factor of 3.6. In addition, we did not observe any significant pressure dependence in the HNO3 reactions with CH2OO and (CH3)2COO under 100-400 Torr. Our results indicate that in a dry area with severe NOx pollution, the reactions of CIs with HNO3 and their products may be worthy of attention, but these reactions may be insignificant under high-humidity conditions. However, CI reactions with HNO3 may not play an important role in the atmospheric removal processes of HNO3 because of the low concentrations of CIs.
RESUMO
Via intramolecular H atom transfer, 3-aminopropanol is more reactive toward Criegee intermediates, in comparison with amines or alcohols. Here we accessed the substituent effect of Criegee intermediates in their reactions with 3-aminopropanol. Through real-time monitoring the concentrations of two Criegee intermediates with their strong UV absorption at 340 nm, the experimental rate coefficients at 298 K (100-300 Torr) were determined to be (1.52 ± 0.08) × 10-11 and (1.44 ± 0.22) × 10-13 cm3 s-1 for the reactions of 3-aminopropanol with (CH3)2COO (acetone oxide) and CH2CHC(CH3)OO (methyl vinyl ketone oxide), respectively. Compared to our previous experimental value for the reaction with syn-CH3CHOO, (1.24 ± 0.13) × 10-11 cm3 s-1, we can see that the methyl substitution at the anti position has little effect on the reactivity while the vinyl substitution causes a drastic decrease in the reactivity. Our theoretical calculations based on CCSD(T)-F12 energies reproduce this 2-order-of-magnitude decrease in the rate coefficient caused by the vinyl substitution. Using the activation strain model, we found that the interaction of Criegee intermediates with 3-aminopropanol is weaker for the case of vinyl substitution. This effect can be further rationalized by the delocalization of the lowest unoccupied molecular orbital for the vinyl-substituted Criegee intermediates. These results would help us better estimate the impact of similar reactions like the reactions of Criegee intermediates with water vapor, some of which could be difficult to measure experimentally but can be important in the atmosphere. We also found that the B2PLYP-D3BJ/aug-cc-pVTZ calculation can reproduce the CCSD(T)-F12 reaction barrier energies within ca. 1 kcal mol-1, indicating that the use of the B2PLYP-D3BJ method is promising for future predictions of the reactions of larger Criegee intermediates.
