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1,3-Cyclopentadiene, 5,5-dimethyl-


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:
LBLHLM - S.G. Lias, J.E. Bartmess, J.F. Liebman, J.L. Holmes, R.D. Levin, and W.G. Mallard
RDSH - H.M. Rosenstock, K. Draxl, B.W. Steiner, and J.T. Herron

View reactions leading to C7H10+ (ion structure unspecified)

Ionization energy determinations

IE (eV)MethodReferenceComment
8.2PEGuimon, Pfister-Guillouzo, et al., 1985LBLHLM
8.22 ± 0.05EIMeyer and Harrison, 1964RDSH
8.45PEGuimon, Pfister-Guillouzo, et al., 1985Vertical value; LBLHLM

Appearance energy determinations

IonAE (eV)Other ProductsMethodReferenceComment
C6H7+10.75CH3EIHarrison, Haynes, et al., 1965RDSH

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.

Guimon, Pfister-Guillouzo, et al., 1985
Guimon, C.; Pfister-Guillouzo, G.; Dubac, J.; Laporterie, A.; Manuel, G.; Iloughmane, H., Electronic structure of Group 14 («eta»4-metallole)tricarbonyliron complexes, Organometallics, 1985, 4, 636. [all data]

Meyer and Harrison, 1964
Meyer, F.; Harrison, A.G., Ionization potentials of methyl-substituted benzenes and cyclopentadienes, Can. J. Chem., 1964, 42, 2256. [all data]

Harrison, Haynes, et al., 1965
Harrison, A.G.; Haynes, P.; McLean, S.; Meyer, F., The mass spectra of methyl-substituted cyclopentadienes, J. Am. Chem. Soc., 1965, 87, 5099. [all data]


Notes

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