naphthalen-3-yl-2-ide anion


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: John E. Bartmess

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Individual Reactions

C10H6- + Hydrogen cation = Naphth-2-yl

By formula: C10H6- + H+ = C10H7

Quantity Value Units Method Reference Comment
Δr377.0 ± 3.1kcal/molG+TSReed, Hare, et al., 2000gas phase; Between tBuOD and 1-pentyne
Quantity Value Units Method Reference Comment
Δr369.3 ± 3.0kcal/molIMRBReed, Hare, et al., 2000gas phase; Between tBuOD and 1-pentyne

Gas phase ion energetics data

Go To: Top, Reaction thermochemistry data, References, Notes

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
0.60 ± 0.11IMRBReed, Hare, et al., 2000Between F5-pyridine and CS2

Protonation reactions

C10H6- + Hydrogen cation = Naphth-2-yl

By formula: C10H6- + H+ = C10H7

Quantity Value Units Method Reference Comment
Δr377.0 ± 3.1kcal/molG+TSReed, Hare, et al., 2000gas phase; Between tBuOD and 1-pentyne
Quantity Value Units Method Reference Comment
Δr369.3 ± 3.0kcal/molIMRBReed, Hare, et al., 2000gas phase; Between tBuOD and 1-pentyne

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.

Reed, Hare, et al., 2000
Reed, D.R.; Hare, M.; Kass, S.R., Formation of gas-phase dianions and distonic ions as a general method for the synthesis of protected reactive intermediates. Energetics of 2,3-and 2,6-dehydronaphthalene, J. Am. Chem. Soc., 2000, 122, 43, 10689-10696, https://doi.org/10.1021/ja002351j . [all data]


Notes

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