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Title: Direct observation of unimolecular decay of CH3CH2CHOO Criegee intermediates to OH radical products

Journal Article · · Journal of Chemical Physics
DOI:https://doi.org/10.1063/1.4958992· OSTI ID:1350088
 [1]; ORCiD logo [1];  [2];  [1]
  1. Univ. of Pennsylvania, Philadelphia, PA (United States). Dept. of Chemistry
  2. Argonne National Lab. (ANL), Argonne, IL (United States). Chemical Sciences and Engineering Division

The unimolecular decay of carbonyl oxide intermediates, known as Criegee intermediates, produced in alkene ozonolysis is a significant source of OH radicals in the troposphere. Here, the rate of appearance of OH radical products is examined directly in the time-domain for a prototypical alkyl-substituted Criegee intermediate, CH3CH2CHOO, following vibrational activation under collision-free conditions. Furthermore, complementary statistical Rice-Ramsperger-Kassel-Marcus calculations of the microcanonical unimolecular decay rate for CH3CH2CHOO are also carried out at energies in the vicinity of the barrier for 1,4 hydrogen atom transfer that leads to OH products. Tunneling through the barrier, derived from high level electronic structure calculations, contributes significantly to the decay rate. Infrared transitions of CH3CH2CHOO are identified in the CH stretch overtone region, which are detected by ultraviolet laser-induced fluorescence of the resultant OH products. The features observed are attributed to CH vibrational excitations and conformational forms utilizing insights from theory. Both experiment and theory yield unimolecular decay rates for CH3CH2CHOO of ca. 107 s-1, which are slower than those obtained for syn-CH3CHOO or (CH3)(2)COO reported previously at similar energies. Master equation modeling is also utilized to predict the thermal decay rate of CH3CH2CHOO under atmospheric conditions, giving a rate of 279 s-1 at 298 K.

Research Organization:
Argonne National Lab. (ANL), Argonne, IL (United States)
Sponsoring Organization:
USDOE Office of Science (SC), Basic Energy Sciences (BES). Chemical Sciences, Geosciences, and Biosciences Division; National Science Foundation (NSF)
Grant/Contract Number:
AC02-06CH11357; CHE-1362835
OSTI ID:
1350088
Alternate ID(s):
OSTI ID: 1273668
Journal Information:
Journal of Chemical Physics, Vol. 145, Issue 4; ISSN 0021-9606
Publisher:
American Institute of Physics (AIP)Copyright Statement
Country of Publication:
United States
Language:
English
Citation Metrics:
Cited by: 43 works
Citation information provided by
Web of Science

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Re-examining ammonia addition to the Criegee intermediate: converging to chemical accuracy journal January 2018
Effect of unsaturated substituents in the reaction of Criegee intermediates with water vapor journal January 2018
Kinetics of the reaction of the simplest Criegee intermediate with ammonia: a combination of experiment and theory journal January 2018
The addition of methanol to Criegee intermediates journal January 2019
Deep tunneling in the unimolecular decay of CH 3 CHOO Criegee intermediates to OH radical products journal December 2016
Conformational analysis of ethyl-substituted Criegee intermediate by FTMW spectroscopy journal December 2016
Tunneling effects in the unimolecular decay of (CH 3 ) 2 COO Criegee intermediates to OH radical products journal April 2017
Probing the conformational behavior of the doubly substituted methyl-ethyl Criegee intermediate by FTMW spectroscopy journal May 2017
Electronic spectroscopy of methyl vinyl ketone oxide: A four-carbon unsaturated Criegee intermediate from isoprene ozonolysis journal December 2018
Selective deuteration illuminates the importance of tunneling in the unimolecular decay of Criegee intermediates to hydroxyl radical products journal November 2017
Unimolecular decay dynamics of Criegee intermediates: Energy-resolved rates, thermal rates, and their atmospheric impact journal December 2019
Estimating the atmospheric concentration of Criegee intermediates and their possible interference in a FAGE-LIF instrument journal January 2017
The atmospheric impacts of monoterpene ozonolysis on global stabilised Criegee intermediate budgets and SO 2 oxidation: experiment, theory and modelling journal January 2018
Measurements of a potential interference with laser-induced fluorescence measurements of ambient OH from the ozonolysis of biogenic alkenes journal January 2018