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Thiophene, tetrahydro-, 1,1-dioxide

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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:
LBLHLM - Sharon G. Lias, John E. Bartmess, Joel F. Liebman, John L. Holmes, Rhoda D. Levin, and W. Gary Mallard
LLK - Sharon G. Lias, Rhoda D. Levin, and Sherif A. Kafafi

Ionization energy determinations

IE (eV) Method Reference Comment
9.8PEAitken, Gosney, et al., 1984LBLHLM
9.91 ± 0.07PIEvlasheva, Puchkova, et al., 1975LLK
10.75PEAitken, Gosney, et al., 1984Vertical value; LBLHLM
10.24PEMuller, Schweig, et al., 1974Vertical value; LLK

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.

Aitken, Gosney, et al., 1984
Aitken, R.A.; Gosney, I.; Farries, H.; Palmer, M.H.; Simpson, I.; Cadogan, J.I.G.; Tinley, E.J., Chemical repercussions of orbital interactions through bond and through space. The reactivity of the double bond in unsaturated cyclic sulphones towards aziridine formation and epoxidation, Tetrahedron, 1984, 40, 2487. [all data]

Evlasheva, Puchkova, et al., 1975
Evlasheva, T.I.; Puchkova, V.V.; Potapov, V.K.; Gur'yanova, E.N., Ionisation potentials and electron-donating properties of sulphones, Russ. J. Phys. Chem., 1975, 49, 453. [all data]

Muller, Schweig, et al., 1974
Muller, C.; Schweig, A.; Mock, W.L., Through-conjugation through the sulfone group in 2,5-di-tert- butylthiophene 1,1-dioxide, J. Am. Chem. Soc., 1974, 96, 280. [all data]


Notes

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