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  2. Perchloryl fluoride - Wikipedia

    en.wikipedia.org/wiki/Perchloryl_fluoride

    Perchloryl fluoride is produced primarily by the fluorination of perchlorates. The initial syntheses in the early 1950s used fluorine gas or fluorides and anodic oxidation as the fluorinating agents, but these give explosive gaseous mixtures. [8] A common fluorinator in modern syntheses is antimony pentafluoride: [3]: 372–373 ClO − 4 + 3 HF ...

  3. Fluorine compounds - Wikipedia

    en.wikipedia.org/wiki/Fluorine_compounds

    The fluorine–fluorine bond of the difluorine molecule is relatively weak when compared to the bonds of heavier dihalogen molecules. The bond energy is significantly weaker than those of Cl 2 or Br 2 molecules and similar to the easily cleaved oxygen–oxygen bonds of peroxides or nitrogen–nitrogen bonds of hydrazines. [8]

  4. Organofluorine chemistry - Wikipedia

    en.wikipedia.org/wiki/Organofluorine_chemistry

    Organofluorine compounds are prepared by numerous routes, depending on the degree and regiochemistry of fluorination sought and the nature of the precursors. The direct fluorination of hydrocarbons with F 2, often diluted with N 2, is useful for highly fluorinated compounds: R 3 CH + F 2 → R 3 CF + HF

  5. Fluorine - Wikipedia

    en.wikipedia.org/wiki/Fluorine

    It also has a high electron affinity, second only to chlorine, [17] and tends to capture an electron to become isoelectronic with the noble gas neon; [3] it has the highest electronegativity of any reactive element. [18] Fluorine atoms have a small covalent radius of around 60 picometers, similar to those of its period neighbors oxygen and neon.

  6. Chloryl fluoride - Wikipedia

    en.wikipedia.org/wiki/Chloryl_fluoride

    ClO 2 F was first reported by Schmitz and Schumacher in 1942, who prepared it by the fluorination of ClO 2. [2] The compound is more conveniently prepared by reaction of sodium chlorate and chlorine trifluoride [3] and purified by vacuum fractionation, i.e. selectively condensing this species separately from other products. This species is a ...

  7. Halogenation - Wikipedia

    en.wikipedia.org/wiki/Halogenation

    Commonly, fluorination reagents are employed instead of F 2. Such reagents include cobalt trifluoride, chlorine trifluoride, and iodine pentafluoride. [4] The method electrochemical fluorination is used commercially for the production of perfluorinated compounds. It generates small amounts of elemental fluorine in situ from hydrogen fluoride ...

  8. Chlorofluorocarbon - Wikipedia

    en.wikipedia.org/wiki/Chlorofluorocarbon

    The rest of the unaccounted carbon bonds are occupied by chlorine atoms. The value of this equation is always a three figure number. An easy example is that of CFC-12, which gives: 90+12=102 -> 1 carbon, 0 hydrogens, 2 fluorine atoms, and hence 2 chlorine atoms resulting in CCl 2 F 2. The main advantage of this method of deducing the molecular ...

  9. Chlorine trifluoride - Wikipedia

    en.wikipedia.org/wiki/Chlorine_trifluoride

    Chlorine trifluoride is an interhalogen compound with the formula ClF 3. It is a colorless, poisonous, corrosive, and extremely reactive gas that condenses to a pale-greenish yellow liquid, the form in which it is most often sold (pressurized at room temperature). It is famous for its extreme oxidation properties.