2,3-Dihydrothiophene 1,1-dioxide

• Formula: C₄H₆O₂S
• Molecular weight: 118.154
• IUPAC Standard InChI: InChI=1S/C4H6O2S/c5-7(6)3-1-2-4-7/h1,3H,2,4H2 Copy

  
• IUPAC Standard InChIKey: DYGJDTCGUUMUBL-UHFFFAOYSA-N Copy
• CAS Registry Number: 1192-16-1
• Chemical structure:
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• Other names: Thiophene, 2,3-dihydro-, 1,1-dioxide; Sulfol-2-ene; α-Sulfolene; 2-Sulfolene
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• Information on this page:
  • Gas phase ion energetics data
  • References
  • Notes
• Other data available:
  • Gas phase thermochemistry data
  • Condensed phase thermochemistry data
  • Phase change data
  • Reaction thermochemistry data
  • Mass spectrum (electron ionization)
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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 by: Sharon G. Lias, John E. Bartmess, Joel F. Liebman, John L. Holmes, Rhoda D. Levin, and W. Gary Mallard

Ionization energy determinations

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]

Kuhn, Klessinger, et al., 1987
Kuhn, H.J.; Klessinger, M.; Ruscic, B.; Klasinc, L., On the empirical correlation schemes for ionization energies in ring compounds, Int. J. Mass Spectrom. Ion Phys., 1987, 43, 147. [all data]

Notes

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• Data from NIST Standard Reference Database 69: NIST Chemistry WebBook
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