Azoxybenzene

• Formula: C₁₂H₁₀N₂O
• Molecular weight: 198.2206
• IUPAC Standard InChI: InChI=1S/C12H10N2O/c15-14(12-9-5-2-6-10-12)13-11-7-3-1-4-8-11/h1-10H Copy

  
• IUPAC Standard InChIKey: GAUZCKBSTZFWCT-UHFFFAOYSA-N Copy
• CAS Registry Number: 495-48-7
• Chemical structure:
  This structure is also available as a 2d Mol file
• Other names: Diazene, diphenyl-, 1-oxide; Azobenzene, oxide; Azoxybenzide; Diphenyldiazene N-oxide; Azossibenzene; Azoxybenzeen; Azoxybenzol; Benzene, azoxydi-; Fenazox; Fentoxan; Diazene, 1,2-diphenyl-, 1-oxide; NSC 1796
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• Information on this page:
  • Gas phase ion energetics data
  • References
  • Notes
• Other data available:
  • Gas phase thermochemistry data
  • Condensed phase thermochemistry data
  • Phase change data
  • IR Spectrum
  • Mass spectrum (electron ionization)
  • UV/Visible spectrum
  • Gas Chromatography
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Gas phase ion energetics data

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Data compiled as indicated in comments:
LL - Sharon G. Lias and Joel F. Liebman
LLK - Sharon G. Lias, Rhoda D. Levin, and Sherif A. Kafafi

Ionization energy determinations

References

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Data compilation copyright by the U.S. Secretary of Commerce on behalf of the U.S.A. All rights reserved.

Millefiori, Ciliberto, et al., 1981
Millefiori, S.; Ciliberto, E.; Millefiori, A.; Zerbo, M.A., Gas phase U. V. photoelectron investigation of azoxybenzene and 4,4'-di(n-alkoxy)azoxybenzenes, Spectromchim. Acta Part A, 1981, 37, 605. [all data]

Petrachenko, Vovna, et al., 1993
Petrachenko, N.E.; Vovna, V.I.; Furin, G.G., Photoelectron HeI spectra of fluorinated azo- and azoxy-benzenes, J. Fluorine Chem., 1993, 63, 85. [all data]

Furin, Petrachenko, et al., 1989
Furin, G.G.; Petrachenko, N.E.; Vovna, V.I., Photoelectron spectra of fluorine-containing azoxybenzenes, J. Org. Chem. USSR, 1989, 26, 1725, In original 1998. [all data]

Armen, Braunstein, et al., 1979
Armen, G.H.; Braunstein, C.; Weinstein, M.I.; Baker, A.D., Reaction of azoxyanisole with oxalyl chloride: Use of photoelectron spectroscopy in seeking new reactions, Tetrahedron Lett., 1979, 43, 4197. [all data]

Notes

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• Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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