Detection of radical species formed by the ozonolysis of α-pinene

Highly reactive free radical species have been subject of many toxicological in vivo and in vitro studies because of the oxidative cell damage they cause. Similar species have been postulated to be the key intermediates formed during many environmental chamber reactions and atmospheric oxidation of...

Full description

Saved in:
Bibliographic Details
Published inJournal of atmospheric chemistry Vol. 66; no. 3; pp. 137 - 155
Main Authors Pavlovic, Jelica, Hopke, Philip K.
Format Journal Article
LanguageEnglish
Published Dordrecht Springer Netherlands 01.07.2010
Springer
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:Highly reactive free radical species have been subject of many toxicological in vivo and in vitro studies because of the oxidative cell damage they cause. Similar species have been postulated to be the key intermediates formed during many environmental chamber reactions and atmospheric oxidation of organic species present in the troposphere. Thus, detection and characterization of these transient radical species are important steps in understanding the atmospheric chemistry and confirming the reaction pathways involved in secondary organic aerosol formation. Study of these species is particularly difficult because of their short life-times. To facilitate such studies, 5,5-dimethyl-1-pyrroline-N-oxide (DMPO) and diethyl-(2-methyl-1-oxido-3,4-dihydro-2H-pyrrol-2-yl) phosphonate (DEPMPO) nitrone spin traps were used to capture radicals formed from the α-pinene/ozone reaction. Electrospray ionization/tandem mass spectrometry (ESI/MS n ) was applied to elucidate their structures. Characteristic fragments with m/z 114, m/z 130 and m/z 148 with the DMPO trap, and m/z 236, m/z 252, and m/z 270 with the DEPMPO trap indicated the existence of alkyl, alkoxyl and peroxyl radicals, respectively.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0167-7764
1573-0662
DOI:10.1007/s10874-011-9197-y