Tetraoxygen difluoride

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Tetraoxygen difluoride
Tetraoxygen difluoride.svg
Names
Other names
Difluorotetraoxidane
Identifiers
3D model (JSmol)
  • InChI=1S/F2O4/c1-3-5-6-4-2
    Key: GFNATQMVAVFBGQ-UHFFFAOYSA-N
  • FOOOOF
Properties
O4F2
Molar mass 101.993 g·mol−1
Appearancered-brown solid (at < −191 °C)
Melting point −191 °C (−311.8 °F; 82.1 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Tetraoxygen difluoride is an inorganic chemical compound of oxygen, belonging to the family of oxygen fluorides. It consists of two O2F units bound together with a weak O-O bond, and is the dimer of the O2F radical. [1]

Contents

Preparation

Tetraoxygen difluoride can be prepared in two steps. In the first step, a photochemically generated fluorine atom reacts with oxygen to form the dioxygen fluoride radical. [1]

This radical subsequently undergoes dimerization, entering an equilibrium with tetraoxygen difluoride at temperatures under −175 °C: [1]

At the same time, the dioxygen fluoride radicals decompose into dioxygen difluoride and oxygen gas, which shifts the above equilibrium with O4F2 to the left. [2]

Properties

Tetraoxygen difluoride is dark red-brown as a solid and has a melting point around −191 °C. [1]

It is a strong fluorinating and oxidizing agent, even stronger than dioxygen difluoride, so that it can, for example, oxidize Ag(II) to Ag(III) or Au(III) to Au(V). This process creates the corresponding anions AgF-
4
and AuF-
6
. With non-noble substances this oxidation can lead to explosions even at low temperatures. As an example, elemental sulfur reacts explosively to form sulfur hexafluoride even at −180 °C. [1]

Similar to [O2F] or O2F2, tetraoxygen difluoride tends to form salts with the dioxygenyl cation O+
2
when it reacts with fluoride acceptors such as boron trifluoride (BF3). In the case of BF3, this leads to the formation of O2+•BF4: [1]

O4F2 + 2BF3 -> 2O2+BF4

Similarly, for arsenic pentafluoride it reacts to create O2+AsF6. [1]

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<span class="mw-page-title-main">Chemical reaction</span> Process that results in the interconversion of chemical species

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<span class="mw-page-title-main">Stoichiometry</span> Calculation of relative weights of reactants and products in chemical reactions

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2
, and one of the most stable xenon compounds. Like most covalent inorganic fluorides it is moisture-sensitive. It decomposes on contact with water vapor, but is otherwise stable in storage. Xenon difluoride is a dense, colourless crystalline solid.

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Krypton difluoride, KrF2 is a chemical compound of krypton and fluorine. It was the first compound of krypton discovered. It is a volatile, colourless solid at room temperature. The structure of the KrF2 molecule is linear, with Kr−F distances of 188.9 pm. It reacts with strong Lewis acids to form salts of the KrF+ and Kr
2
F+
3
cations.

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The dioxygenyl(or dioxyl) ion, O+
2
, is a rarely-encountered oxycation in which both oxygen atoms have a formal oxidation state of +1/2. It is formally derived from oxygen by the removal of an electron:

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A hexafluoride is a chemical compound with the general formula QXnF6, QXnF6m−, or QXnF6m+. Many molecules fit this formula. An important hexafluoride is hexafluorosilicic acid (H2SiF6), which is a byproduct of the mining of phosphate rock. In the nuclear industry, uranium hexafluoride (UF6) is an important intermediate in the purification of this element.

<span class="mw-page-title-main">Disulfur difluoride</span> Chemical compound

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2
) groups. This large family of compounds can be divided into ionic and covalent peroxide. The first class mostly contains the peroxides of the alkali and alkaline earth metals whereas the covalent peroxides are represented by such compounds as hydrogen peroxide and peroxymonosulfuric acid (H2SO5). In contrast to the purely ionic character of alkali metal peroxides, peroxides of transition metals have a more covalent character.

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References

  1. 1 2 3 4 5 6 7 Holleman, Arnold F. (2017). Anorganische Chemie: Band 1, Grundlagen und Hauptgruppenelemente (in German). Vol. 1. Egon Wiberg, Nils Wiberg (103rd ed.). Berlin. ISBN   978-3-11-026932-1. OCLC   968134975.{{cite book}}: CS1 maint: location missing publisher (link)
  2. "Sauerstoff-Fluoride". roempp.thieme.de. Retrieved 2021-10-14.