Dissemin is shutting down on January 1st, 2025

Published in

American Association for the Advancement of Science, Science, 6555(373), p. 679-682, 2021

DOI: 10.1126/science.abj0412

Links

Tools

Export citation

Search in Google Scholar

Watching a hydroperoxyalkyl radical (•QOOH) dissociate

This paper was not found in any repository, but could be made available legally by the author.
This paper was not found in any repository, but could be made available legally by the author.

Full text: Unavailable

Green circle
Preprint: archiving allowed
Green circle
Postprint: archiving allowed
Red circle
Published version: archiving forbidden
Data provided by SHERPA/RoMEO

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