Affiliation:
1. Department of Chemistry, University of Pennsylvania, Philadelphia, PA 19104, USA.
2. Chemical Sciences and Engineering Division, Argonne National Laboratory, Lemont, IL 60439, USA.
Abstract
Spectral fingerprint of stabilized •QOOH
Carbon-centered radicals containing the hydroperoxy group, commonly denoted as •QOOH, are elusive but are among the most critical intermediate species for kinetic modeling of hydrocarbon oxidation in various atmospheric and combustion processes. Their direct experimental observation is a long-standing challenge, with only one successful previous attempt. Using a combination of infrared activation spectroscopy and an ultraviolet laser–induced fluorescence detection method, Hansen
et al
. directly characterized the vibrational structure of a •QOOH intermediate in isobutane oxidation, collisionally stabilized and isolated, and followed its dissociative evolution under infrared activation with time and energy resolution. High-level electronic structure calculations revealed an important role of heavy-atom tunneling in this process. —YS
Funder
National Science Foundation
U.S. Department of Energy
Army Research Office
Carlsbergfondet
Independent Research Fund Denmark
Argonne-Sandia Consortium on High-Pressure 1194 Combustion Chemistry
Science and Engineering Discovery Environment
U.S. Department of Energy-Basic Energy Sciences
Molecular Structure and Dynamics program of the U.S. Army Research Office
U.S. Department of Energy- Basic Energy Sciences-Gas Phase Chemical Physics
Publisher
American Association for the Advancement of Science (AAAS)
Cited by
40 articles.
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