Cyclopropane, 1,1,2-trimethyl-

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Phase change 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: Thermodynamics Research Center, NIST Boulder Laboratories, Chris Muzny director

Quantity Value Units Method Reference Comment
Tboil326. ± 3.KAVGN/AAverage of 10 values; Individual data points
Quantity Value Units Method Reference Comment
Tfus134.9 ± 0.1KAVGN/AAverage of 8 values; Individual data points

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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.

Data compiled as indicated in comments:
LL - Sharon G. Lias and Joel F. Liebman
LBLHLM - Sharon G. Lias, John E. Bartmess, Joel F. Liebman, John L. Holmes, Rhoda D. Levin, and W. Gary Mallard

View reactions leading to C6H12+ (ion structure unspecified)

Ionization energy determinations

IE (eV) Method Reference Comment
8.90 ± 0.05EIHolmes and Lossing, 1991LL
8.90EILaderoute and Harrison, 1985LBLHLM

Appearance energy determinations

Ion AE (eV) Other Products MethodReferenceComment
C5H9+9.86CH3EILaderoute and Harrison, 1985LBLHLM

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.

Holmes and Lossing, 1991
Holmes, J.L.; Lossing, F.P., Ionization energies of homologous organic compounds and correlation with molecular size, Org. Mass Spectrom., 1991, 26, 537. [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]


Notes

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