Bicyclo[4.2.0]octa-1,3,5-triene


Gas phase 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

Quantity Value Units Method Reference Comment
Δfgas199.4 ± 0.9kJ/molCcbRoth, Biermann, et al., 1978 

Condensed phase 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

Quantity Value Units Method Reference Comment
Δfliquid155.7 ± 0.9kJ/molCcbRoth, Biermann, et al., 1978 
Quantity Value Units Method Reference Comment
Δcliquid-4447.0 ± 0.9kJ/molCcbRoth, Biermann, et al., 1978Corresponding Δfliquid = 155.6 kJ/mol (simple calculation by NIST; no Washburn corrections)

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

o-Xylylene = Bicyclo[4.2.0]octa-1,3,5-triene

By formula: C8H8 = C8H8

Quantity Value Units Method Reference Comment
Δr-54.8kJ/molKinRoth and Scholz, 1981gas phase
Δr-44.2 ± 1.9kJ/molCmRoth, Biermann, et al., 1978liquid phase

C8H8N2O = Nitrous oxide + Bicyclo[4.2.0]octa-1,3,5-triene

By formula: C8H8N2O = N2O + C8H8

Quantity Value Units Method Reference Comment
Δr-41.2 ± 0.54kJ/molKinOth, Olsen, et al., 1977liquid phase; solvent: THF; At 413 K

3Hydrogen + Bicyclo[4.2.0]octa-1,3,5-triene = Bicyclo[4.2.0]octane

By formula: 3H2 + C8H8 = C8H14

Quantity Value Units Method Reference Comment
Δr-210.5 ± 0.1kJ/molChydTurner, Goebel, et al., 1968liquid phase; solvent: Acetic acid

Bicyclo[4.2.0]octa-1,3,5-triene = o-Xylylene

By formula: C8H8 = C8H8

Quantity Value Units Method Reference Comment
Δr46.4 ± 0.8kJ/molEqkRoth, Ebbrecht, et al., 1988gas phase

References

Go To: Top, Gas phase thermochemistry data, Condensed phase thermochemistry data, Reaction thermochemistry data, Notes

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

Roth, Biermann, et al., 1978
Roth, W.R.; Biermann, M.; Dekker, H.; Jochems, R.; Mosselman, C.; Hermann, H., Energy profile of the o-quinodimethane-benzocyclobutene equilibrium, Chem. Ber., 1978, 111, 3892-3903. [all data]

Roth and Scholz, 1981
Roth, W.R.; Scholz, B.P., Energy profile of the o-quinodimethane = benzocyclobutene equilibrium. Part 2., Chem. Ber., 1981, 114, 3741-3750. [all data]

Oth, Olsen, et al., 1977
Oth, J.F.M.; Olsen, H.; Synder, J.P., Energetics of heteroextrusion reactions. N2 vs. N2O, J. Am. Chem. Soc., 1977, 99, 8505-8507. [all data]

Turner, Goebel, et al., 1968
Turner, R.B.; Goebel, P.; Mallon, B.J.; Doering, W.E.; Coburn, J.F., Jr.; Pomerantz, M., Heats of hydrogenation. VIII. Compounds with three- and four-membered rings, J. Am. Chem. Soc., 1968, 90, 4315-4322. [all data]

Roth, Ebbrecht, et al., 1988
Roth, W.R.; Ebbrecht, T.; Beitat, A., o-Quinodimethane-benzocyclobutene equilibrium: oxygen trapping technique, Chem. Ber., 1988, 121, 1357-1358. [all data]


Notes

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