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Title: Formation and stability of gas-phase o-benzoquinone from oxidation of ortho-hydroxyphenyl: A combined neutral and distonic radical study

Journal Article · · Physical Chemistry Chemical Physics. PCCP
DOI:https://doi.org/10.1039/C5CP02953H· OSTI ID:1329619
 [1];  [2];  [3];  [3];  [3];  [4];  [4];  [5];  [1]
  1. Univ. of Wollongong, Wollongong (Australia)
  2. Lawrence Berkeley National Lab. (LBNL), Berkeley, CA (United States)
  3. Sandia National Lab. (SNL-CA), Livermore, CA (United States)
  4. Queensland Univ. of Technology, Brisbane (Australia)
  5. The Univ. of Melbourne, Melbourne (Australia)

Theo-hydroxyphenyl radical reacts with O2to formo-benzoquinone + OH and cyclopentadienone is assigned as a secondary product.

Research Organization:
Sandia National Lab. (SNL-CA), Livermore, CA (United States); Lawrence Berkeley National Laboratory (LBNL), Berkeley, CA (United States)
Sponsoring Organization:
USDOE Advanced Research Projects Agency - Energy (ARPA-E)
Grant/Contract Number:
AC04-94AL85000; AC02-05CH11231
OSTI ID:
1329619
Alternate ID(s):
OSTI ID: 1439984
Report Number(s):
SAND-2016-10073J; PPCPFQ; 648109
Journal Information:
Physical Chemistry Chemical Physics. PCCP, Vol. 18, Issue 6; ISSN 1463-9076
Publisher:
Royal Society of ChemistryCopyright Statement
Country of Publication:
United States
Language:
English
Citation Metrics:
Cited by: 24 works
Citation information provided by
Web of Science

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Cited By (2)

Product detection study of the gas-phase oxidation of methylphenyl radicals using synchrotron photoionisation mass spectrometry journal January 2019
Theoretical study of sensitive reactions in phenol decomposition journal January 2020

Figures / Tables (10)


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