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  2. Carbon tetrafluoride - Wikipedia

    en.wikipedia.org/wiki/Carbon_tetrafluoride

    Tetrafluoromethane, also known as carbon tetrafluoride or R-14, is the simplest perfluorocarbon (C F 4).As its IUPAC name indicates, tetrafluoromethane is the perfluorinated counterpart to the hydrocarbon methane.

  3. 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.

  4. Fluorocarbon - Wikipedia

    en.wikipedia.org/wiki/Fluorocarbon

    As a result, fluorocarbons have low intermolecular attractive forces and are lipophobic in addition to being hydrophobic and non-polar. Reflecting the weak intermolecular forces these compounds exhibit low viscosities when compared to liquids of similar boiling points, low surface tension and low heats of vaporization.

  5. Chemical polarity - Wikipedia

    en.wikipedia.org/wiki/Chemical_polarity

    When comparing a polar and nonpolar molecule with similar molar masses, the polar molecule in general has a higher boiling point, because the dipole–dipole interaction between polar molecules results in stronger intermolecular attractions. One common form of polar interaction is the hydrogen bond, which is also

  6. 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]

  7. Carbonyl fluoride - Wikipedia

    en.wikipedia.org/wiki/Carbonyl_fluoride

    Carbonyl fluoride is usually produced as a decomposition product of fluorinated hydrocarbons in the thermal decomposition thereof, for example from trifluoromethanol or tetrafluoromethane in the presence of water:

  8. Fluorous chemistry - Wikipedia

    en.wikipedia.org/wiki/Fluorous_chemistry

    Fluorous chemistry involves the use of perfluorinated compounds or perfluorinated substituents to facilitate recovery of a catalyst or reaction product. Perfluorinated groups impart unique physical properties including high solubility in perfluorinated solvents.

  9. Carbon tetrachloride - Wikipedia

    en.wikipedia.org/wiki/Carbon_tetrachloride

    Because of this symmetric geometry, CCl 4 is non-polar. Methane gas has the same structure, making carbon tetrachloride a halomethane. As a solvent, it is well suited to dissolving other non-polar compounds such as fats and oils. It can also dissolve iodine.