2(1H)-Pyridinethione, 1-methyl-


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: Hussein Y. Afeefy, Joel F. Liebman, and Stephen E. Stein

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Individual Reactions

2(1H)-Pyridinethione, 1-methyl- = Pyridine, 2-(methylthio)-

By formula: C6H7NS = C6H7NS

Quantity Value Units Method Reference Comment
Δr-2.6 ± 1.3kcal/molEqkBeak and Lee, 1969liquid phase; solvent: CDCl3; NMR

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: Sharon G. Lias, Rhoda D. Levin, and Sherif A. Kafafi

Ionization energy determinations

IE (eV) Method Reference Comment
7.84 ± 0.02EIGronneberg and Undheim, 1972 
7.69 ± 0.03PECook, El-Abbady, et al., 1977Vertical value

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.

Beak and Lee, 1969
Beak, P.; Lee, J.T., Jr., Equilibration studies. 2-Methylthiopyridine-N-methyl-2-thiopyridone, J. Org. Chem., 1969, 34, 2125-2128. [all data]

Gronneberg and Undheim, 1972
Gronneberg, T.; Undheim, K., Mass spectrometry of onium compounds. XI: ionization potentials of hydroxy and mercapto pyridines, Org. Mass Spectrom., 1972, 6, 823. [all data]

Cook, El-Abbady, et al., 1977
Cook, M.J.; El-Abbady, S.; Katritzky, A.R.; Guimon, C.; Pfister-Guillouzo, G., Photoelectron spectra of hydroxy- and mercapto-pyridines and models of fixed structure, J. Chem. Soc. Perkin Trans. 2, 1977, 1652. [all data]


Notes

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