Cyclooctyne


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

2Hydrogen + Cyclooctyne = Cyclooctane

By formula: 2H2 + C8H12 = C8H16

Quantity Value Units Method Reference Comment
Δr-291. ± 0.8kJ/molChydRoth, Hopf, et al., 1994liquid phase; solvent: Isooctane
Δr-289.kJ/molChydTurner, Jarrett, et al., 1973liquid phase; solvent: Acetic acid

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 C8H12+ (ion structure unspecified)

Ionization energy determinations

IE (eV) Method Reference Comment
8.9PEBieri, Heilbronner, et al., 1974 
9.10PESchmidt, Schweig, et al., 1974Vertical value

References

Go To: Top, Reaction thermochemistry data, Gas phase ion energetics data, Notes

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

Roth, Hopf, et al., 1994
Roth, W.R.; Hopf, H.; Horn, C., Propargyl-Stabilisierungsenergie, Chem. Ber., 1994, 127, 1781-1795. [all data]

Turner, Jarrett, et al., 1973
Turner, R.B.; Jarrett, A.D.; Goebel, P.; Mallon, B.J., Heats of hydrogenation. 9. Cyclic acetylenes and some miscellaneous olefins, J. Am. Chem. Soc., 1973, 95, 790-792. [all data]

Bieri, Heilbronner, et al., 1974
Bieri, G.; Heilbronner, E.; Kloster-Jensen, E.; Schmelzer, A.; Wirz, J., Electronic states of 1,5-cyclooctadiyne radical cation and of related systems: the electronic structure of cis-bent carbon-carbon triple bonds, Helv. Chim. Acta, 1974, 57, 1265. [all data]

Schmidt, Schweig, et al., 1974
Schmidt, H.; Schweig, A.; Krebs, A., Splitting of the degenerate acetylenic πMOs; a probe for ring strain, Tetrahedron Lett., 1974, 16, 1471. [all data]


Notes

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