Rachel E Lade, Kate A Livesey, Luc Vereecken, Robin J Shannon, Mark A Blitz, Paul W Seakins, Daniel Stone
{"title":"Kinetics of the Reaction Between the Criegee Intermediate CH<sub>2</sub>OO and NO<sub>2</sub>: Experimental Measurements and Comparison with Theory.","authors":"Rachel E Lade, Kate A Livesey, Luc Vereecken, Robin J Shannon, Mark A Blitz, Paul W Seakins, Daniel Stone","doi":"10.1021/acs.jpca.4c08203","DOIUrl":null,"url":null,"abstract":"<p><p>Kinetics of the gas phase reaction between the stabilized Criegee intermediate formaldehyde oxide (CH<sub>2</sub>OO) and nitrogen dioxide (NO<sub>2</sub>) have been measured using laser flash photolysis of CH<sub>2</sub>I<sub>2</sub>/O<sub>2</sub>/N<sub>2</sub>/NO<sub>2</sub> mixtures coupled with time-resolved broadband ultraviolet absorption spectroscopy. Experiments were performed in N<sub>2</sub> under pseudo-first-order conditions at temperatures between 242 and 353 K and pressures in the range 25 to 300 Torr. The kinetics of CH<sub>2</sub>OO + NO<sub>2</sub> are independent of pressure, with a mean rate coefficient of <i>k</i><sub>1</sub> = (1.24 ± 0.22) × 10<sup>-12</sup> cm<sup>3</sup> s<sup>-1</sup> at 298 K, where the uncertainty represents a combination of the 1σ statistical error and the systematic errors resulting from uncertainties in gas flow rates and in the concentration of NO<sub>2</sub>. Measurements indicate upper limits of <5% for production of NO<sub>3</sub> and <5% for production of NO, and further studies of product yields are warranted. In contrast to expectations from theory, the kinetics of CH<sub>2</sub>OO + NO<sub>2</sub> display a negative temperature dependence that can be described by <i>k</i><sub>1</sub> = (1.07 ± 0.02) × 10<sup>-12</sup> × (<i>T</i>/298)<sup>-(2.9±0.2)</sup> cm<sup>3</sup> s<sup>-1</sup>. Analysis using the Master Equation Solver for Multi-Energy well Reactions is able to reproduce a negative temperature dependence for the reaction if significant changes to barrier heights are made, but the overall agreement between the experiment and theory remains poor. This work highlights the challenges associated with calculations for systems with significant multi-reference character.</p>","PeriodicalId":59,"journal":{"name":"The Journal of Physical Chemistry A","volume":" ","pages":"2058-2066"},"PeriodicalIF":2.7000,"publicationDate":"2025-02-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11874013/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Journal of Physical Chemistry A","FirstCategoryId":"1","ListUrlMain":"https://doi.org/10.1021/acs.jpca.4c08203","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/2/12 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
Abstract
Kinetics of the gas phase reaction between the stabilized Criegee intermediate formaldehyde oxide (CH2OO) and nitrogen dioxide (NO2) have been measured using laser flash photolysis of CH2I2/O2/N2/NO2 mixtures coupled with time-resolved broadband ultraviolet absorption spectroscopy. Experiments were performed in N2 under pseudo-first-order conditions at temperatures between 242 and 353 K and pressures in the range 25 to 300 Torr. The kinetics of CH2OO + NO2 are independent of pressure, with a mean rate coefficient of k1 = (1.24 ± 0.22) × 10-12 cm3 s-1 at 298 K, where the uncertainty represents a combination of the 1σ statistical error and the systematic errors resulting from uncertainties in gas flow rates and in the concentration of NO2. Measurements indicate upper limits of <5% for production of NO3 and <5% for production of NO, and further studies of product yields are warranted. In contrast to expectations from theory, the kinetics of CH2OO + NO2 display a negative temperature dependence that can be described by k1 = (1.07 ± 0.02) × 10-12 × (T/298)-(2.9±0.2) cm3 s-1. Analysis using the Master Equation Solver for Multi-Energy well Reactions is able to reproduce a negative temperature dependence for the reaction if significant changes to barrier heights are made, but the overall agreement between the experiment and theory remains poor. This work highlights the challenges associated with calculations for systems with significant multi-reference character.
期刊介绍:
The Journal of Physical Chemistry A is devoted to reporting new and original experimental and theoretical basic research of interest to physical chemists, biophysical chemists, and chemical physicists.