Abstract
Criegee intermediates (CIs), formed from the ozonolysis of alkenes, are highly reactive species with diverse reaction pathways, with important roles in atmospheric chemistry. This study focuses on the formation of accretion products through reactions of thermally stabilized CIs (sCIs) from the ozonolysis of three different terpenes (α-pinene, β-pinene, and β-caryophyllene) with malonic and oxalic acids. Our experimental results demonstrate that these reactions efficiently produce the expected accretion products, though with apparent variations in yields depending on the specific terpene and acid involved. To our knowledge, this is the first study to report direct gas-phase observations of expected adducts from several different terpene-derived sCIs and carboxylic acids, paving the way for a better understanding of the importance and atmospheric implications of these reactions, especially in terms of the aerosol-forming capabilities of these large product molecules.
| Original language | English |
|---|---|
| Journal | Atmospheric Chemistry and Physics |
| Volume | 25 |
| Issue number | 9 |
| Pages (from-to) | 4655-4664 |
| Number of pages | 10 |
| ISSN | 1680-7316 |
| DOIs | |
| Publication status | Published - 5 May 2025 |
| MoE publication type | A1 Journal article-refereed |
Fields of Science
- Conformer-dependent reactivity
- Secondary organic aerosol
- Beta-pinene
- Atmospheric chemistry
- Carboxylic-acids
- Kinetics
- Temperature
- Mechanism
- Isoprene
- Radicals
- 114 Physical sciences
- 116 Chemical sciences
- 1172 Environmental sciences