Bicyclo[4.2.0]octa-1,3,5,7-tetraene


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:
B - John E. Bartmess
LLK - Sharon G. Lias, Rhoda D. Levin, and Sherif A. Kafafi

View reactions leading to C8H6+ (ion structure unspecified)

Electron affinity determinations

EA (eV) Method Reference Comment
0.321 ± 0.050IMRBBroadus and Kass, 2000Between phenanthrene, acetophenone; B

Ionization energy determinations

IE (eV) Method Reference Comment
7.5PEKoenig, Imre, et al., 1979LLK
7.87 ± 0.02PEKoenig, Imre, et al., 1979Vertical value; LLK

De-protonation reactions

C8H5- + Hydrogen cation = Bicyclo[4.2.0]octa-1,3,5,7-tetraene

By formula: C8H5- + H+ = C8H6

Quantity Value Units Method Reference Comment
Δr1608. ± 21.kJ/molG+TSBroadus and Kass, 2000, 2gas phase; between PhF, 1,3-diazine; B
Quantity Value Units Method Reference Comment
Δr1574. ± 21.kJ/molIMRBBroadus and Kass, 2000, 2gas phase; between PhF, 1,3-diazine; B

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.

Broadus and Kass, 2000
Broadus, K.M.; Kass, S.R., The electron as a protecting group. 2. Generation of benzocyclobutadiene radical anion in the gas phase and an experimental determination of the heat of formation of benzocyclobutadiene, J. Am. Chem. Soc., 2000, 122, 43, 10697-10703, https://doi.org/10.1021/ja002352b . [all data]

Koenig, Imre, et al., 1979
Koenig, T.; Imre, D.; Hoobler, J.A., He(I) photoelectron spectrum of benzocyclobutadiene, J. Am. Chem. Soc., 1979, 101, 6446. [all data]

Broadus and Kass, 2000, 2
Broadus, K.M.; Kass, S.R., Benzocyclobutadienyl anion: Formation and energetics of an antiaromatic molecule, J. Org. Chem., 2000, 65, 20, 6566-6571, https://doi.org/10.1021/jo000709o . [all data]


Notes

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