C₅H₉⁺ (structure unspecified)

• Formula: C₅H₉⁺
• Molecular weight: 69.1244
• Information on this page:
  • Gas phase ion energetics data
  • References
  • Notes
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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.

Reactions leading to C₅H₉⁺ (ion structure unspecified)

References

Go To: Top, 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.

Tomer, Turk, et al., 1972
Tomer, K.B.; Turk, J.; Shapiro, R.H., Anchimeric assistance in electron-impact reactions: Homoallylic systems, Org. Mass Spectrom., 1972, 6, 235. [all data]

Sergeev, Akopyan, et al., 1973
Sergeev, Yu.L.; Akopyan, M.E.; Vilesov, F.I.; Chizhov, Yu.V., Photoionization processes in gaseous cyclohexane, and chloro- and bromocyclohexane, High Energy Chem., 1973, 7, 369, In original 418. [all data]

Lossing and Traeger, 1975
Lossing, F.P.; Traeger, J.C., Free radicals by mass spectrometry XLVI. Heats of formation of C₅H₇ and C₅H₉ radicals and cations., J. Am. Chem. Soc., 1975, 19, 9. [all data]

Lossing and Traeger, 1975, 2
Lossing, F.P.; Traeger, J.C., Stabilization in cyclopentadienyl, cyclopentenyl, and cyclopentyl cations, J. Am. Chem. Soc., 1975, 97, 1579. [all data]

Puttemans, 1974
Puttemans, J.P., Ionisation de cycloalcanes (C₅ a C₁₂) en spectroscopie photoelectronique et par impact electronique, Ing. Chim. (Brussels), 1974, 56, 64. [all data]

Laderoute and Harrison, 1985
Laderoute, K.R.; Harrison, A.G., Cyclopropane intermediates in the rearrangement and fragmentation of olefinic molecular ions, Org. Mass Spectrom., 1985, 20, 624. [all data]

Lossing and Holmes, 1984
Lossing, F.P.; Holmes, J.L., Stabilization energy and ion size in carbocations in the gas phase, J. Am. Chem. Soc., 1984, 106, 6917. [all data]

Pottie, Harrison, et al., 1961
Pottie, R.F.; Harrison, A.G.; Lossing, F.P., Free radicals by mass spectrometry. XXIV. Ionization potentials of cycloalkyl free radicals and cycloalkanes, J. Am. Chem. Soc., 1961, 83, 3204. [all data]

Herzschuh and Sicker, 1981
Herzschuh, R.; Sicker, A., Stereochemische einflusse auf die ionisations- und auftrittsenergien cis/trans-isomerer dimethylcycloalkane, Z. Chem., 1981, 21, 409. [all data]

Natalis, 1964
Natalis, P., Etude du comportement d'isomeres geometriques sous l'impact electronique. V. Comparaison des donnees obtenues, par differentes methodes, pour les 1,2-dimethylcyclohexanes cis et trans, Bull. Soc. Chim. Belges, 1964, 73, 961. [all data]

Fedorova, Denisov, et al., 1973
Fedorova, M.S.; Denisov, Y.V.; Poptapov, V.K., Mass-spectrometric study of the photoionisation processes of tricyclo[5,2,1,0^2,6] decane and its alkyl derivatives, Russ. J. Phys. Chem., 1973, 47, 1498. [all data]

Natalis and Franklin, 1966
Natalis, P.; Franklin, J.L., Etude du comportement d'isomeres geometriques sous l'impact electronique. VI. Les cis- et trans-1,2-di-terbutyl-ethylenes, Bull. Soc. Chim. Belges, 1966, 75, 328. [all data]

Notes

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• Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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