1,3,5-Cycloheptatriene-7-(2,4,6-cycloheptatrien-1-ylidene)-

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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

6Hydrogen + 1,3,5-Cycloheptatriene-7-(2,4,6-cycloheptatrien-1-ylidene)- = Cycloheptane, cycloheptylidene-

By formula: 6H2 + C14H12 = C14H24

Quantity Value Units Method Reference Comment
Δr-547.14 ± 0.54kJ/molChydTurner, Meador, et al., 1957solid phase; solvent: Diethylcarbitol

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: Sharon G. Lias, Rhoda D. Levin, and Sherif A. Kafafi

View reactions leading to C14H12+ (ion structure unspecified)

Ionization energy determinations

IE (eV) Method Reference
7.0 ± 0.1EIKlots, Compton, et al., 1974

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.

Turner, Meador, et al., 1957
Turner, R.B.; Meador, W.R.; Doering, W.E.; Knox, L.H.; Mayer, J.R.; Wiley, D.W., Heats of hydrogenation. III. Hydrogenation of cycllooctatetraene and of some seven-membered non-benzenoid aromatic compounds, J. Am. Chem. Soc., 1957, 79, 4127-4133. [all data]

Klots, Compton, et al., 1974
Klots, C.E.; Compton, R.N.; Raaen, V.F., Electronic and ionic properties of of molecular TTF and TCMQ, J. Chem. Phys., 1974, 60, 1177. [all data]


Notes

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