Watching a hydroperoxyalkyl radical (•QOOH) dissociate

Author:

Hansen Anne S.1ORCID,Bhagde Trisha1ORCID,Moore Kevin B.2ORCID,Moberg Daniel R.2ORCID,Jasper Ahren W.2ORCID,Georgievskii Yuri2ORCID,Vansco Michael F.1ORCID,Klippenstein Stephen J.2ORCID,Lester Marsha I.1ORCID

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)

Subject

Multidisciplinary

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