1,1,3,3-tetrafluoroacetone

• Formula: C₃H₂F₄O
• Molecular weight: 130.0410
• IUPAC Standard InChI: InChI=1S/C3H2F4O/c4-2(5)1(8)3(6)7/h2-3H Copy

  
• IUPAC Standard InChIKey: QAPXLUZMMFIIBI-UHFFFAOYSA-N Copy
• CAS Registry Number: 360-52-1
• Chemical structure:
  This structure is also available as a 2d Mol file or as a computed 3d SD file
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• Species with the same structure:
  • 1,1,3,3-tetrafluoroacetone
• Other names: 2-Propanone, 1,1,3,3-tetrafluoro-
• Information on this page:
  • Reaction thermochemistry data
  • References
  • Notes
• Other data available:
  • Gas phase ion energetics data
  • Ion clustering data
  • UV/Visible spectrum
• Data at other public NIST sites:
  • Gas Phase Kinetics Database
• Options:
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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 as indicated in comments:
B - John E. Bartmess
M - Michael M. Meot-Ner (Mautner) and Sharon G. Lias

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Individual Reactions

C₃HF₄O^- +  =

By formula: C₃HF₄O^- + H⁺ = C₃H₂F₄O

 +  = ( • )

By formula: Cl^- + C₃H₂F₄O = (Cl^- • C₃H₂F₄O)

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.

Farid and McMahon, 1980
Farid, R.; McMahon, T.B., The gas phase acidities of fluorinated acetones. An ICR investigation of the role of fluorine substituents in the stabilization of planar carbanions, Can. J. Chem., 1980, 58, 2307. [all data]

Larson and McMahon, 1984
Larson, J.W.; McMahon, T.B., Fluoride and chloride affinities of main group oxides, fluorides, oxofluorides, and alkyls. Quantitative scales of lewis acidities from ion cyclotron resonance halide-exchange equilibria, J. Phys. Chem., 1984, 88, 1083. [all data]

Notes

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• Symbols used in this document:
  

  ΔrG°	Free energy of reaction at standard conditions
  ΔrH°	Enthalpy of reaction at standard conditions

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