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Title: Comment on “A novel and facile decay path of Criegee intermediates by intramolecular insertion reactions via roaming transition states” [J. Chem. Phys. 142, 124312 (2015)]

Journal Article · · Journal of Chemical Physics
DOI:https://doi.org/10.1063/1.4934801· OSTI ID:1392423

In a recent article, Nguyen et al. report the discovery of a new decomposition pathway for small Criegee intermediates. Prior to this publication, the lowest known pathway for decomposition of Criegee intermediates involved ring closure to form a dioxirane followed by ring opening to make a methylenebisoxy biradical, which can then isomerize or decompose via a variety of pathways. The new pathway reported by Nguyen et al. involves the partial cleavage of the OO bond of the Criegee intermediate forming nascent H2CO and O(1D) fragments. The O(1D) fragment then orbits around the H2CO fragment in a manner reminiscent of roaming radical reactions and eventually inserts into one of the CH bonds of the H2CO fragment leading directly to formic acid. The authors report saddle point geometries for this pathway determined at a number of different levels of theory in which the distance between the oxygen atom and the formaldehyde varies from 2.0 Å to 3.5 Å depending on the level of theory. Density functional theory (DFT) calculations are found to give more compact, planar saddle point structures while coupled cluster, CCSD(T), and complete active space self consistent field, CASSCF, optimizations lead to looser saddle point structures in which the O atom orbits above the plane of the H2CO fragment.

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
Grant/Contract Number:
AC02-06CH11357
OSTI ID:
1392423
Journal Information:
Journal of Chemical Physics, Vol. 143, Issue 16; ISSN 0021-9606
Publisher:
American Institute of Physics (AIP)Copyright Statement
Country of Publication:
United States
Language:
English
Citation Metrics:
Cited by: 4 works
Citation information provided by
Web of Science

References (8)

A novel and facile decay path of Criegee intermediates by intramolecular insertion reactions via roaming transition states journal March 2015
Unimolecular Isomerizations and Oxygen Atom Loss in Formaldehyde and Acetaldehyde Carbonyl Oxides. A Theoretical Investigation journal January 1996
Mechanisms of gas-phase and liquid-phase ozonolysis journal November 1978
CASSCF and CAS+1+2 Studies on the Potential Energy Surface and the Rate Constants for the Reactions between CH 2 and O 2 journal March 2002
The Roaming Atom: Straying from the Reaction Path in Formaldehyde Decomposition journal November 2004
A CCSD (T) investigation of carbonyl oxide and dioxirane. Equilibrium geometries, dipole moments, infrared spectra, heats of formation and isomerization energies journal July 1993
Electronic structure and reactivity of dioxirane and carbonyl oxide journal August 1992
Temperature and Pressure-Dependent Rate Coefficients for the Reaction of Vinyl Radical with Molecular Oxygen journal February 2015

Cited By (1)

Water-catalyzed decomposition of the simplest Criegee intermediate CH2OO journal April 2016