Benzo[g]quinoline


Reaction thermochemistry 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 by: Hussein Y. Afeefy, Joel F. Liebman, and Stephen E. Stein

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Individual Reactions

Benzo[g]isoquinoline dimer = 2Benzo[g]quinoline

By formula: C26H18N2 = 2C13H9N

Quantity Value Units Method Reference Comment
Δr-16.7kcal/molCmBendig, Buchwitz, et al., 1981liquid phase; solvent: Cyclohexane; Dimerization

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 by: Henry M. Rosenstock, Keith Draxl, Bruce W. Steiner, and John T. Herron

View reactions leading to C13H9N+ (ion structure unspecified)

Ionization energy determinations

IE (eV) Method Reference
7.6 ± 0.1CTSFarrell and Newton, 1966

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.

Bendig, Buchwitz, et al., 1981
Bendig, J.; Buchwitz, W.; Fischer, J.; Kreysig, D., Deactivation behavior of arenes and heteroarenes. XXXII. Effect of endo- and exocyclic substitution on the reversible dimerization behavior of anthracenes, J. Prakt. Chem., 1981, 323, 485-498. [all data]

Farrell and Newton, 1966
Farrell, P.G.; Newton, J., Ionization potentials of primary aromatic amines and aza-hydrocarbons, Tetrahedron Lett., 1966, 5517. [all data]


Notes

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