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Contents

   



(Top)
 


1 Hypofluorites  





2 See also  





3 References  














Hypofluorous acid






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From Wikipedia, the free encyclopedia
 


Hypofluorous acid

Hypofluorous acid

Gas-phase structure

Hypofluorous acid
  Hydrogen, H
  Oxygen, O
  Fluorine, F

Names

IUPAC name

Hypofluorous acid

Other names
  • Fluoranol
  • Fluoric(-I) acid
  • Hydrogen hypofluorite
  • Hydrogen fluorate(-I)
  • Hydrogen monofluoroxygenate(0)
  • Hydroxyl fluoride
  • Identifiers

    CAS Number

    3D model (JSmol)

    ChemSpider

    PubChem CID

    CompTox Dashboard (EPA)

    • InChI=1S/FHO/c1-2/h2H ☒N

      Key: AQYSYJUIMQTRMV-UHFFFAOYSA-N ☒N

  • InChI=1/FHO/c1-2/h2H

    Key: AQYSYJUIMQTRMV-UHFFFAOYAN

    • OF

    Properties

    Chemical formula

    HOF

    Molar mass

    36.0057 g/mol

    Appearance

    pale yellow liquid above −117 °C
    white solid below −117 °C

    Melting point

    −117 °C (−179 °F; 156 K)

    Boiling point

    decomposes at 0 °C (32 °F; 273 K)[citation needed]

    Structure

    Point group

    Cs

    Hazards

    Occupational safety and health (OHS/OSH):

    Main hazards

    Explosive, strong oxidizer, corrosive

    NFPA 704 (fire diamond)

    NFPA 704 four-colored diamondHealth 4: Very short exposure could cause death or major residual injury. E.g. VX gasFlammability 0: Will not burn. E.g. waterInstability 4: Readily capable of detonation or explosive decomposition at normal temperatures and pressures. E.g. nitroglycerinSpecial hazard OX: Oxidizer. E.g. potassium perchlorate
    4
    0
    4

    Related compounds

    Other cations

    Lithium hypofluorite

    Related compounds

  • Hypobromous acid
  • Hypoiodous acid
  • Hydroxylamine
  • Methanol
  • Trifluoromethanol
  • Trifluoromethyl hypofluorite
  • Oxygen difluoride
  • Nitroxyl
  • Hydrogen cyanide
  • Formaldehyde
  • Formyl fluoride
  • Carbonyl fluoride
  • Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

    ☒N verify (what is checkY☒N ?)

    Infobox references

    Hypofluorous acid, chemical formula HOF, is the only known oxyacid of fluorine and the only known oxoacid in which the main atom gains electrons from oxygen to create a negative oxidation state. The oxidation state of the oxygen in this acid (and in the hypofluorite ion OF and in its salts called hypofluorites) is 0, while its valence is 2. It is also the only hypohalous acid that can be isolated as a solid. HOF is an intermediate in the oxidationofwaterbyfluorine, which produces hydrogen fluoride, oxygen difluoride, hydrogen peroxide, ozone and oxygen. HOF is explosive at room temperature, forming HF and O2:[1]

    2 HOF → 2 HF + O2

    This reaction is catalyzed by water.[2]

    It was isolated in the pure form by passing F2 gas over ice at −40 °C, rapidly collecting the HOF gas away from the ice, and condensing it:[2]

    F2 + H2O → HOF + HF

    The compound has been characterized in the solid phase by X-ray crystallography[1] as a bent molecule with an angle of 101°. The O–F and O–H bond lengths are 144.2 and 96.4 picometres, respectively. The solid framework consists of chains with O–H···O linkages. The structure has also been analyzed in the gas phase, a state in which the H–O–F bond angle is slightly narrower (97.2°).

    Thiophene chemists commonly call a solution of hypofluorous acid in acetonitrile (generated in situ by passing gaseous fluorine through water in acetonitrile) Rozen's reagent.[3]

    Hypofluorites[edit]

    Hypofluorites are formally derivatives of OF, which is the conjugate base of hypofluorous acid. One example is trifluoromethyl hypofluorite (CF3OF), which is a trifluoromethyl ester of hypofluorous acid. The conjugate base is known in salts such as lithium hypofluorite.

    See also[edit]

    References[edit]

    1. ^ a b W. Poll; G. Pawelke; D. Mootz; E. H. Appelman (1988). "The Crystal Structure of Hypofluorous Acid : Chain Formation by O-H · · · O Hydrogen Bonds". Angew. Chem. Int. Ed. Engl. 27 (3): 392–3. doi:10.1002/anie.198803921.
  • ^ a b Appelman, Evan H. (1973-04-01). "Nonexistent compounds. Two case histories". Accounts of Chemical Research. 6 (4): 113–117. doi:10.1021/ar50064a001. ISSN 0001-4842.
  • ^ For Rozen's original popularizations, see: For subsequent use, see, e.g.
    • Singh, Raman; Kaur, Rajneesh; Gupta, Tarang; Kulbir, Kulbir; Singh, Kuldeep (2019). "Applications of Rozen's Reagent in Oxygen-Transfer and C-H Activation Reactions". Synthesis. 51 (2): 371–383. doi:10.1055/s-0037-1609638. S2CID 104572566.
    • Dell, Emma J.; Campos, Luis M. (2012). "The preparation of thiophene-S,S-dioxides and their role in organic electronics". J. Mater. Chem. 22 (26): 12945–12952. doi:10.1039/C2JM31220D.
  • H3AsO4
  • HArF
  • HAt
  • HSO3F
  • H[BF4]
  • HBr
  • HBrO
  • HBrO2
  • HBrO3
  • HBrO4
  • HCl
  • HClO
  • HClO2
  • HClO3
  • HClO4
  • HCN
  • HCNO
  • H2CrO4/H2Cr2O7
  • H2CO3
  • H2CS3
  • HF
  • HFO
  • HI
  • HIO
  • HIO2
  • HIO3
  • HIO4
  • HMnO4
  • H2MnO4
  • H2MoO4
  • HNC
  • NaHCO3
  • HNCO
  • HNO
  • HNO2
  • HNO3
  • H2N2O2
  • HNO5S
  • H3NSO3
  • H2O
  • H2O2
  • H2O3
  • H2O4
  • H2O5
  • H3PO2
  • H3PO3
  • H3PO4
  • H4P2O7
  • H5P3O10
  • H2[PtCl6]
  • H2S
  • H2S2
  • H2Se
  • H2SeO3
  • H2SeO4
  • H4SiO4
  • H2[SiF6]
  • HSCN
  • HNCS
  • H2SO3
  • H2SO4
  • H2SO5
  • H2S2O3
  • H3O
  • H2S2O6
  • H2S2O7
  • H2S2O8
  • CF3SO3H
  • H2Te
  • H2TeO3
  • H6TeO6
  • H4TiO4
  • H2Po
  • H[Co(CO)4]

  • Retrieved from "https://en.wikipedia.org/w/index.php?title=Hypofluorous_acid&oldid=1206735760"

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    This page was last edited on 13 February 2024, at 00:21 (UTC).

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