Direct observation and kinetics of a hydroperoxyalkyl radical (QOOH)

Author:

Savee John D.1,Papajak Ewa1,Rotavera Brandon1,Huang Haifeng1,Eskola Arkke J.1,Welz Oliver1,Sheps Leonid1,Taatjes Craig A.1,Zádor Judit1,Osborn David L.1

Affiliation:

1. Combustion Research Facility, Mail Stop 9055, Sandia National Laboratories, Livermore, CA 94551-0969, USA.

Abstract

Catching a glimpse of the elusive QOOH It's straightforward to write down the net combustion reaction: Oxygen reacts with hydrocarbons to form water and carbon dioxide. The details of how all the bonds break and form in succession are a great deal more complicated. Savee et al. now report direct detection of a long-postulated piece of the puzzle, a so-called QOOH intermediate. This structure results from bound oxygen stripping a hydrogen atom from carbon, leaving a carbon-centered radical behind. The study explores the influence of the hydrocarbon's unsaturation on the stability of QOOH, which has implications for both combustion and tropospheric oxidation chemistry. Science , this issue p. 643

Funder

DOE

Lawrence Berkeley National Laboratory

Publisher

American Association for the Advancement of Science (AAAS)

Subject

Multidisciplinary

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