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Isolation and characterization of charge-tagged phenylperoxyl radicals in the gas phase: direct evidence for products and pathways in low temperature benzene oxidation

Journal Article


Abstract


  • The phenylperoxyl radical has long been accepted as a critical intermediate in the oxidation of benzene and an archetype for arylperoxyl radicals in combustion and atmospheric chemistry. Despite being central to many contemporary mechanisms underpinning these chemistries, reports of the direct detection or isolation of phenylperoxyl radicals are rare and there is little experimental evidence connecting this intermediate with expected product channels. We have prepared and isolated two charge-tagged phenyl radical models in the gas phase [i.e., 4-(N,N,N-trimethylammonium)phenyl radical cation and 4-carboxylatophenyl radical anion] and observed their reactions with dioxygen by ion-trap mass spectrometry. Measured reaction rates show good agreement with prior reports for the neutral system (k2[(Me3N+)C6H4˙ + O2] = 2.8 × 10−11 cm3 molecule−1 s−1, Φ = 4.9%; k2[(−O2C)C6H4˙ + O2] = 5.4 × 10−11 cm3 molecule−1 s−1, Φ = 9.2%) and the resulting mass spectra provide unequivocal evidence for the formation of phenylperoxyl radicals. Collisional activation of isolated phenylperoxyl radicals reveals unimolecular decomposition by three pathways: (i) loss of dioxygen to reform the initial phenyl radical; (ii) loss of atomic oxygen yielding a phenoxyl radical; and (iii) ejection of the formyl radical to give cyclopentadienone. Stable isotope labeling confirms these assignments. Quantum chemical calculations for both charge-tagged and neutral phenylperoxyl radicals confirm that loss of formyl radical is accessible both thermodynamically and entropically and competitive with direct loss of both hydrogen atom and carbon dioxide.

Authors


  •   Kirk, Benjamin B. (external author)
  •   Harman, David G. (external author)
  •   Kenttamaa, Hilkka I. (external author)
  •   Trevitt, Adam J.
  •   Blanksby, Stephen J. (external author)

Publication Date


  • 2012

Citation


  • Kirk, B. B., Harman, D. G., Kenttamaa, H. I., Trevitt, A. J. & Blanksby, S. J. (2012). Isolation and characterization of charge-tagged phenylperoxyl radicals in the gas phase: direct evidence for products and pathways in low temperature benzene oxidation. Physical Chemistry Chemical Physics, 14 (48), 16719-16730.

Scopus Eid


  • 2-s2.0-84870197729

Ro Metadata Url


  • http://ro.uow.edu.au/smhpapers/511

Has Global Citation Frequency


Number Of Pages


  • 11

Start Page


  • 16719

End Page


  • 16730

Volume


  • 14

Issue


  • 48

Place Of Publication


  • United Kingdom

Abstract


  • The phenylperoxyl radical has long been accepted as a critical intermediate in the oxidation of benzene and an archetype for arylperoxyl radicals in combustion and atmospheric chemistry. Despite being central to many contemporary mechanisms underpinning these chemistries, reports of the direct detection or isolation of phenylperoxyl radicals are rare and there is little experimental evidence connecting this intermediate with expected product channels. We have prepared and isolated two charge-tagged phenyl radical models in the gas phase [i.e., 4-(N,N,N-trimethylammonium)phenyl radical cation and 4-carboxylatophenyl radical anion] and observed their reactions with dioxygen by ion-trap mass spectrometry. Measured reaction rates show good agreement with prior reports for the neutral system (k2[(Me3N+)C6H4˙ + O2] = 2.8 × 10−11 cm3 molecule−1 s−1, Φ = 4.9%; k2[(−O2C)C6H4˙ + O2] = 5.4 × 10−11 cm3 molecule−1 s−1, Φ = 9.2%) and the resulting mass spectra provide unequivocal evidence for the formation of phenylperoxyl radicals. Collisional activation of isolated phenylperoxyl radicals reveals unimolecular decomposition by three pathways: (i) loss of dioxygen to reform the initial phenyl radical; (ii) loss of atomic oxygen yielding a phenoxyl radical; and (iii) ejection of the formyl radical to give cyclopentadienone. Stable isotope labeling confirms these assignments. Quantum chemical calculations for both charge-tagged and neutral phenylperoxyl radicals confirm that loss of formyl radical is accessible both thermodynamically and entropically and competitive with direct loss of both hydrogen atom and carbon dioxide.

Authors


  •   Kirk, Benjamin B. (external author)
  •   Harman, David G. (external author)
  •   Kenttamaa, Hilkka I. (external author)
  •   Trevitt, Adam J.
  •   Blanksby, Stephen J. (external author)

Publication Date


  • 2012

Citation


  • Kirk, B. B., Harman, D. G., Kenttamaa, H. I., Trevitt, A. J. & Blanksby, S. J. (2012). Isolation and characterization of charge-tagged phenylperoxyl radicals in the gas phase: direct evidence for products and pathways in low temperature benzene oxidation. Physical Chemistry Chemical Physics, 14 (48), 16719-16730.

Scopus Eid


  • 2-s2.0-84870197729

Ro Metadata Url


  • http://ro.uow.edu.au/smhpapers/511

Has Global Citation Frequency


Number Of Pages


  • 11

Start Page


  • 16719

End Page


  • 16730

Volume


  • 14

Issue


  • 48

Place Of Publication


  • United Kingdom