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  2. Fluorine - Wikipedia

    en.wikipedia.org/wiki/Fluorine

    [21] [22] Conversely, bonds to other atoms are very strong because of fluorine's high electronegativity. Unreactive substances like powdered steel, glass fragments, and asbestos fibers react quickly with cold fluorine gas; wood and water spontaneously combust under a fluorine jet. [5] [23]

  3. Fluorine compounds - Wikipedia

    en.wikipedia.org/wiki/Fluorine_compounds

    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] The covalent radius of fluorine of about 71 picometers found in F 2 molecules is significantly larger than that in other compounds because of this weak ...

  4. Fluorocarbon - Wikipedia

    en.wikipedia.org/wiki/Fluorocarbon

    Perfluoroalkanes are very stable because of the strength of the carbon–fluorine bond, one of the strongest in organic chemistry. [4] Its strength is a result of the electronegativity of fluorine imparting partial ionic character through partial charges on the carbon and fluorine atoms, which shorten and strengthen the bond (compared to carbon-hydrogen bonds) through favorable covalent ...

  5. Diatomic molecule - Wikipedia

    en.wikipedia.org/wiki/Diatomic_molecule

    All diatomic molecules are linear and characterized by a single parameter which is the bond length or distance between the two atoms. Diatomic nitrogen has a triple bond, diatomic oxygen has a double bond, and diatomic hydrogen, fluorine, chlorine, iodine, and bromine all have single bonds. [6]

  6. Fluoride - Wikipedia

    en.wikipedia.org/wiki/Fluoride

    Fluoride (/ ˈ f l ʊər aɪ d, ˈ f l ɔːr-/) [3] is an inorganic, monatomic anion of fluorine, with the chemical formula F − (also written [F] −), whose salts are typically white or colorless.

  7. Carbon–fluorine bond - Wikipedia

    en.wikipedia.org/wiki/Carbon–fluorine_bond

    Carbon–fluorine bonds can have a bond dissociation energy (BDE) of up to 130 kcal/mol. [2] The BDE (strength of the bond) of C–F is higher than other carbon–halogen and carbon–hydrogen bonds. For example, the BDEs of the C–X bond within a CH 3 –X molecule is 115, 104.9, 83.7, 72.1, and 57.6 kcal/mol for X = fluorine, hydrogen ...

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  9. Uranium hexafluoride - Wikipedia

    en.wikipedia.org/wiki/Uranium_hexafluoride

    UF 6 reacts with water, releasing hydrofluoric acid. The compound reacts with aluminium, forming a surface layer of AlF 3 that resists any further reaction from the compound. Uranium hexafluoride is a mild oxidant. [10] It is a Lewis acid as evidenced by its binding to form heptafluorouranate(VI), [UF 7] −. [11]