Difluorodioxirane

Add links
Source: Wikipedia, the free encyclopedia.
Difluorodioxirane
Names
IUPAC name
3,3-difluorodioxirane
Other names
  • DFDO
  • Difluordioxiran
  • Dioxirane, 3,3-difluoro-
  • Dioxirane, difluoro-
Identifiers
3D model (
JSmol
)
ChemSpider
  • InChI=1S/CF2O2/c2-1(3)4-5-1
    Key: QDWGHBBFJKJQRE-UHFFFAOYSA-N
  • FC1(F)OO1
Properties
CF2O2
Molar mass 82.006 g/mol
Density 1.7±0.1 g/cm3
Boiling point -129.6±35.0 °C at 760 mmHg
Vapor pressure 86623.3±0.2 mmHg
Hazards
Flash point -121.8±21.8 °C
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Difluorodioxirane (CF2O2) is a rare, stable member of the dioxirane family, known for a single oxygen-oxygen bond (O-O). Unlike most dioxiranes that decompose quickly, difluorodioxirane is surprisingly stable at room temperature, making it potentially useful for further research and applications.

Synthesis

Difluorodioxirane was first synthesised by Russo and DesMarteau in 1993 by treating fluorocarbonyl hypofluorite (FCOOF) with X2 (= F2, Cl2 or ClF) over pelletized CsF in a flow system.[3]

It also likely exists as a possible intermediate in reactions involving other fluorine-containing compounds.[4][5]

Properties

Unlike most dioxiranes that decompose quickly, difluorodioxirane is surprisingly stable at room temperature[6] due to the stabilising interacton of two fluorine atoms with the ring. This effect makes the O-O bond less reactive and more stable compared to other dioxiranes. The central F–C–F angle is 109°, approximately a tetrahedral angle.[7]

Difluorodioxirane is known for its ability to perform regiospecific and stereoselective oxidations. This makes it a valuable tool in organic synthesis for precise manipulation of molecules.[8]

Despite its increased stability, difluorodioxirane can still act as an oxidizing agent, transferring oxygen to other molecules. it often leads to cleaner and more predictable reaction outcomes due to its controlled reactivity.

Uses

Difluorodioxirane itself has not yet found widespread applications due to its recent discovery. However, its unique stability and reactivity similar to other dioxiranes suggest potential uses in several areas:

  • Organic synthesis: Due to its oxidizing properties, difluorodioxirane could be a valuable reagent in organic reactions, particularly for controlled oxidation processes. Researchers are exploring its potential applications in epoxidation (adding oxygen atoms to create epoxide rings), hydroxylation (adding hydroxyl groups -OH), and other oxidation reactions.
  • Development of new catalysts: The stability and reactivity profile of difluorodioxirane make it a promising candidate for the development of new and more efficient catalysts for various organic transformations.

See also

References

  1. ^ "CAS Common Chemistry". CAS Common Chemistry. 2024-04-09. Retrieved 2024-04-09.
  2. ^ "Difluorodioxirane". ChemSpider. 2022-07-21. Retrieved 2024-04-09.
  3. ISSN 0570-0833
    .
  4. PMID 38518697
    .
  5. ISSN 0020-1669
    .
  6. ISSN 0570-0833
    .
  7. ISSN 0002-7863
    .
  8. ISSN 0002-7863
    .
Retrieved from "https://en.wikipedia.org/w/index.php?title=Difluorodioxirane&oldid=1226595080"