Articles | Volume 15, issue 12
Atmos. Chem. Phys., 15, 6745–6765, 2015

Special issue: The Pan European Gas-Aerosols Climate Interaction Study...

Atmos. Chem. Phys., 15, 6745–6765, 2015

Research article 18 Jun 2015

Research article | 18 Jun 2015

Formation of highly oxidized multifunctional compounds: autoxidation of peroxy radicals formed in the ozonolysis of alkenes – deduced from structure–product relationships

T. F. Mentel1, M. Springer1, M. Ehn1,2, E. Kleist3, I. Pullinen1, T. Kurtén4, M. Rissanen2, A. Wahner1, and J. Wildt3 T. F. Mentel et al.
  • 1Institut für Energie- und Klimaforschung, IEK-8, Forschungszentrum Jülich, Jülich, Germany
  • 2Department of Physics, University of Helsinki, 00014 Helsinki, Finland
  • 3Institut für Bio- und Geowissenschaften, IBG-2, Forschungszentrum Jülich, Jülich, Germany
  • 4Department of Chemistry, University of Helsinki, 00014 Helsinki, Finland

Abstract. It has been postulated that secondary organic particulate matter plays a pivotal role in the early growth of newly formed particles in forest areas. The recently detected class of extremely low volatile organic compounds (ELVOC) provides the missing organic vapors and possibly contributes a significant fraction to atmospheric SOA (secondary organic aerosol). The sequential rearrangement of peroxy radicals and subsequent O2 addition results in ELVOC which are highly oxidized multifunctional molecules (HOM). Key for efficiency of such HOM in early particle growth is that their formation is induced by one attack of the oxidant (here O3), followed by an autoxidation process involving molecular oxygen. Similar mechanisms were recently observed and predicted by quantum mechanical calculations e.g., for isoprene. To assess the atmospheric importance and therewith the potential generality, it is crucial to understand the formation pathway of HOM.

To elucidate the formation path of HOM as well as necessary and sufficient structural prerequisites of their formation we studied homologous series of cycloalkenes in comparison to two monoterpenes. We were able to directly observe highly oxidized multifunctional peroxy radicals with 8 or 10 O atoms by an Atmospheric Pressure interface High Resolution Time of Flight Mass Spectrometer (APi-TOF-MS) equipped with a NO3-chemical ionization (CI) source. In the case of O3 acting as an oxidant, the starting peroxy radical is formed on the so-called vinylhydroperoxide path. HOM peroxy radicals and their termination reactions with other peroxy radicals, including dimerization, allowed for analyzing the observed mass spectra and narrowing down the likely formation path. As consequence, we propose that HOM are multifunctional percarboxylic acids, with carbonyl, hydroperoxy, or hydroxy groups arising from the termination steps. We figured that aldehyde groups facilitate the initial rearrangement steps. In simple molecules like cycloalkenes, autoxidation was limited to both terminal C atoms and two further C atoms in the respective α positions. In more complex molecules containing tertiary H atoms or small, constrained rings, even higher oxidation degrees were possible, either by simple H shift of the tertiary H atom or by initialization of complex ring-opening reactions.

Short summary
We studied a series of cycloalkenes and methyl-substituted alkenes in order to elucidate the structural pre-requisites and chemical pathways to the recently discovered class of highly oxidized molecules ELVOC (Ehn et al., Nature, 2014). ELVOC may totally change the view on (parts of) the mechanism of SOA formation. We present results which support recent observations of H shifts from C-H to peroxy radicals, highlighting the pivotal role of peroxyradicals in organic atmospheric chemistry.
Final-revised paper