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  2. Carbon tetrafluoride - Wikipedia

    en.wikipedia.org/wiki/Carbon_tetrafluoride

    Tetrafluoromethane is the product when any carbon compound, including carbon itself, is burned in an atmosphere of fluorine. With hydrocarbons, hydrogen fluoride is a coproduct. It was first reported in 1926. [7] It can also be prepared by the fluorination of carbon dioxide, carbon monoxide or phosgene with sulfur tetrafluoride.

  3. Tetrafluoride - Wikipedia

    en.wikipedia.org/wiki/Tetrafluoride

    A tetrafluoride is a chemical compound with four fluorines in its formula. ... tetrafluoride, CfF 4; Carbon ... may form compounds containing the term tetrafluoride ...

  4. Monofluoride - Wikipedia

    en.wikipedia.org/wiki/Monofluoride

    Because the fluoride anion is highly basic, many alkali metal fluorides form bifluorides with the formula MHF 2. Sodium and potassium bifluorides are significant to the chemical industry. [2] Among other monofluorides, only silver(I) [3] and thallium(I) [4] fluorides are well-characterized. Both are very soluble, unlike the other halides of ...

  5. Fluorine compounds - Wikipedia

    en.wikipedia.org/wiki/Fluorine_compounds

    Manganese tetrafluoride is an unstable solid that decomposes even at room temperature. [62] Only one of the two allotropes, α-MnF 4, is understood. In this compound, manganese forms –MnF 6 – octahedra which share bridging fluorines to make –Mn 4 F 20 – rings which are then further connected three dimensionally. [63]

  6. Carbon–fluorine bond - Wikipedia

    en.wikipedia.org/wiki/Carbon–fluorine_bond

    The carbon–fluorine bond is a polar covalent bond between carbon and fluorine that is a component of all organofluorine compounds. It is one of the strongest single bonds in chemistry (after the B–F single bond, Si–F single bond, and H–F single bond), and relatively short, due to its partial ionic character.

  7. Organofluorine chemistry - Wikipedia

    en.wikipedia.org/wiki/Organofluorine_chemistry

    This is significantly stronger than the bonds of carbon with other halogens (an average bond energy of e.g. C-Cl bond is around 320 kJ/mol [1]) and is one of the reasons why fluoroorganic compounds have high thermal and chemical stability. The carbon–fluorine bond is relatively short (around 1.4 Å [1]).

  8. Tetrafluoroethylene - Wikipedia

    en.wikipedia.org/wiki/Tetrafluoroethylene

    Tetrafluoroethylene (TFE) is a fluorocarbon with the chemical formula C 2 F 4. It is the simplest perfluorinated alkene. This gaseous species is used primarily in the industrial preparation of fluoropolymers. It was first reported as "dicarbon tetrafluoride" in 1890. [2]

  9. 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 ...