Criegee intermediates are important atmospheric oxidants, formed via the reaction of ozone with volatile alkenes emitted into the troposphere. Small Criegee intermediates (e.g., CHOO and CHCHOO) are highly reactive, and their removal via unimolecular decay or bimolecular chemistry dominates their atmospheric lifetimes. As the molecular complexity of Criegee intermediates increases, their electronic absorption spectra show a bathochromic shift within the solar spectrum relevant to the troposphere. In these cases, solar photolysis may become a competitive contributor to their atmospheric removal. In this article, we report the conformer-dependent simulated electronic absorption spectra of two four-carbon-centered Criegee intermediates, methyl vinyl ketone oxide (MVK-oxide) and methacrolein oxide (MACR-oxide). Both MVK-oxide and MACR-oxide contain four low-energy conformers, which are convoluted in the experimentally measured spectra. Here, we deconvolute each conformer and estimate contributions from each of the four conformers to the experimentally measured spectra. We also estimate the photolysis rates and predict that solar photolysis should be a more competitive removal process for MVK-oxide and MACR-oxide (cf. CHOO and CHCHOO).

Download full-text PDF

Source
http://dx.doi.org/10.1021/acs.jpca.1c08381DOI Listing

Publication Analysis

Top Keywords

criegee intermediates
16
electronic absorption
12
absorption spectra
12
photolysis rates
8
methyl vinyl
8
vinyl ketone
8
ketone oxide
8
methacrolein oxide
8
choo chchoo
8
solar photolysis
8

Similar Publications

Dioxiranes and their heavier chalcogen analogs have long been recognized as pivotal reagents and intermediates in synthetic chemistry, while trioxetanes have largely remained theoretical constructs. In this work, we present the synthesis of neutral, isoelectronic aluminum/chalcogen analogs of dioxiranes and trioxetanes, specifically aluminadiselenirane, aluminaditellurirane, aluminatriselenetane, aluminatritelluretane, and a mixed Se/Te analog of aluminatrichalcogenetane. These compounds, featuring strained AlCh2 and AlCh3 ring (Ch = Se, Te), exhibit significant polarization between the aluminum and chalcogen components.

View Article and Find Full Text PDF

The present work employs the CCSD(T)/CBS//M06-2X/aug-cc-pVTZ level of theory to investigate the effect of a water monomer (WM) and dimer (WD) on the oxidation of nitrous acid (HONO) by the Criegee intermediate (CHOO). The present work suggests that similar to an uncatalyzed path, a water catalyzed reaction can also proceed two paths, , the oxygen atom transfer (OAT) and the hydrogen atom transfer (HAT) path. In addition, here also, the HAT path dominates over the OAT path.

View Article and Find Full Text PDF

Computational Study of the 1,3-Dipolar Cycloaddition between Criegee Intermediates and Linalool: Atmospheric Implications.

J Phys Chem A

January 2025

Centro de Bioinformática, Simulación y Modelado (CBSM), Departamento de Bioinformática, Facultad de Ingeniería, Universidad de Talca, Talca 3465548, Chile.

In this research, we investigated the essential role of biogenic volatile organic compound emissions in regulating tropospheric ozone levels, atmospheric chemistry, and climate dynamics. We explored linalool ozonolysis and secondary organic aerosol formation mechanisms, providing key insights into atmospheric processes. Computational techniques, such as density functional theory calculations and molecular dynamics simulations, were employed for the analysis.

View Article and Find Full Text PDF

Fenton-like reactions between organic peroxides and transition-metal ions in the atmospheric aqueous phase have profound impacts on the chemistry, composition, and health effects of aerosols. However, the kinetics, mechanisms, and key influencing factors of such reactions remain poorly understood. In this study, we synthesized a series of monoterpene-derived α-acyloxyalkyl hydroperoxides (AAHPs), an important class of organic peroxides formed from Criegee intermediates during the ozonolysis of alkenes, and investigated their Fenton-like reactions with iron ions in the aqueous phase.

View Article and Find Full Text PDF

Unraveling the Meaning of Effective Uptake Coefficients in Multiphase and Aerosol Chemistry.

Acc Chem Res

January 2025

Chemical Sciences Division, Lawrence Berkeley National Laboratory, Berkeley, California 94720, United States.

ConspectusReactions of gas phase molecules with surfaces play key roles in atmospheric and environmental chemistry. Reactive uptake coefficients (γ), the fraction of gas-surface collisions that yield a reaction, are used to quantify the kinetics in these heterogeneous and multiphase systems. Unlike rate coefficients for homogeneous gas- or liquid-phase reactions, uptake coefficients are system- and observation-dependent quantities that depend upon a multitude of underlying elementary steps.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!