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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. Organofluorine chemistry - Wikipedia

    en.wikipedia.org/wiki/Organofluorine_chemistry

    Introducing the carbon–fluorine bond to organic compounds is the major challenge for medicinal chemists using organofluorine chemistry, as the carbon–fluorine bond increases the probability of having a successful drug by about a factor of ten. [30] Over half of agricultural chemicals contain C-F bonds. A common example is trifluralin. [31]

  5. 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 ...

  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. 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 ...

  8. Hydrogen fluoride - Wikipedia

    en.wikipedia.org/wiki/Hydrogen_fluoride

    Due to strong and extensive hydrogen bonding, it boils near room temperature, a much higher temperature than other hydrogen halides. Hydrogen fluoride is an extremely dangerous gas, forming corrosive and penetrating hydrofluoric acid upon contact with moisture. The gas can also cause blindness by rapid destruction of the corneas.

  9. Fluorinated gases - Wikipedia

    en.wikipedia.org/wiki/Fluorinated_gases

    The F-gas Regulation adopts an approach based on containment and recovery of F-gases as well as imposing obligations on reporting, training and labeling on those using F-gases. On 26 September 2011, the Commission issued a report on the application, effects and adequacy of the Regulation, drawing from the results of an analytical study it ...