C10H6+ (structure unspecified)


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.

Reactions leading to C10H6+ (ion structure unspecified)

Precursor AP (eV) Other Products Method Reference Comment
C10H6Cl4Fe14.6 ± 0.1?PIBarfuss, Emrich, et al., 1990 
C10H814.2 ± 0.1H2PIJochims, Rasekh, et al., 1992 
C10H814.7 ± 0.10H2EIVanBrunt and Wacks, 1964 
C10H815.60 ± 0.05H2PIJochims, Rasekh, et al., 1992 
C10H816.2 ± 0.15H2EIVanBrunt and Wacks, 1964 
C14H1018.2 ± 0.12C2H2EINatalis and Franklin, 1965 
C14H1020.8 ± 0.32C2H2EINounou, 1968 
C14H1020.9 ± 0.32C2H2EINatalis and Franklin, 1965 

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.

Barfuss, Emrich, et al., 1990
Barfuss, S.; Emrich, R.-H.; Hirschwald, W.; Dowben, P.A.; Boag, N.M., A mass spectrometric investigation of chloro-, bromo- and methyl-ferrocenes by electron and photon impact ionisation, J. Org. Chem., 1990, 391, 209. [all data]

Jochims, Rasekh, et al., 1992
Jochims, H.-W.; Rasekh, H.; Ruhl, E.; Baumgartel, H.; Leach, S., The photofragmentation of naphthalene and azulene monocations in the energy range 7-22 eV, Chem. Phys., 1992, 168, 159. [all data]

VanBrunt and Wacks, 1964
VanBrunt, R.J.; Wacks, M.E., Electron-impact studies of aromatic hydrocarbons. III. Azulene and naphthalene, J. Chem. Phys., 1964, 41, 3195. [all data]

Natalis and Franklin, 1965
Natalis, P.; Franklin, J.L., Ionization and dissociation of diphenyl and condensed ring aromatics by electron impact. I. Biphenyl, diphenylacetylene, and phenanthrene, J. Phys. Chem., 1965, 69, 2935. [all data]

Nounou, 1968
Nounou, P., Application of the quasi-equilibrium theory of, mass spectra to large aromatic molecules, Advan. Mass Spectrom., 1968, 4, 551. [all data]


Notes

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