naphthalen-6-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
Δr1633. ± 17.kJ/molG+TSReed, Hare, et al., 2000gas phase
Quantity Value Units Method Reference Comment
Δr1600. ± 17.kJ/molIMRBReed, Hare, et al., 2000gas phase

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
1.26 ± 0.17IMRBReed, Hare, et al., 2000EA between F5-nitrobenze and SO2
1.344 ± 0.087CIDCReed, Hare, et al., 2000 

Protonation reactions

C10H6- + Hydrogen cation = Naphth-2-yl

By formula: C10H6- + H+ = C10H7

Quantity Value Units Method Reference Comment
Δr1633. ± 17.kJ/molG+TSReed, Hare, et al., 2000gas phase
Quantity Value Units Method Reference Comment
Δr1600. ± 17.kJ/molIMRBReed, Hare, et al., 2000gas phase

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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