cyclobutanone enolate anion


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: John E. Bartmess

Electron affinity of neutral species

EAneutral (eV) Method Reference Comment
1.8010 ± 0.0080LPDBrinkman, Berger, et al., 1993 
1.843 ± 0.065PDZimmerman, Jackson, et al., 1978 

Protonation reactions

C4H5O- + Hydrogen cation = Cyclobutanone

By formula: C4H5O- + H+ = C4H6O

Quantity Value Units Method Reference Comment
Δr367.1 ± 4.1kcal/molG+TSBrickhouse and Squires, 1988gas phase; Between Me2C=NOH, EtCHO
Quantity Value Units Method Reference Comment
Δr359.0 ± 4.0kcal/molIMRBBrickhouse and Squires, 1988gas phase; Between Me2C=NOH, EtCHO

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.

Brinkman, Berger, et al., 1993
Brinkman, E.A.; Berger, S.; Marks, J.; Brauman, J.I., Molecular Rotation and the Observation of Dipole-Bound States of Anions, J. Chem. Phys., 1993, 99, 10, 7586, https://doi.org/10.1063/1.465688 . [all data]

Zimmerman, Jackson, et al., 1978
Zimmerman, A.H.; Jackson, R.L.; Janousek, B.K.; Brauman, J.J., Electron photodetachment from cyclic enolate anions in the gas phase: Electron affinities of cyclic enolate radicals, J. Am. Chem. Soc., 1978, 100, 4674. [all data]

Brickhouse and Squires, 1988
Brickhouse, M.D.; Squires, R.R., Gas Phase Bronsted vs. Lewis Acid-Base Reactions of 6,6-Dimethylfulvene. A Sensitive Probe of the Electronic Structures of Organic Anions, J. Am. Chem. Soc., 1988, 110, 9, 2706, https://doi.org/10.1021/ja00217a002 . [all data]


Notes

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