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  2. Biological aspects of fluorine - Wikipedia

    en.wikipedia.org/wiki/Biological_aspects_of_fluorine

    In the body, PFCs bind to proteins such as serum albumin. Their tissue distribution in humans is unknown, but studies in rats suggest it is present mostly in the liver, kidney, and blood. They are not metabolized by the body but are excreted by the kidneys. Dwell time in the body varies greatly by species.

  3. Fluorine - Wikipedia

    en.wikipedia.org/wiki/Fluorine

    Fluorine is a chemical element; it has symbol F and atomic number 9. It is the lightest halogen [note 1] and exists at standard conditions as pale yellow diatomic gas. Fluorine is extremely reactive as it reacts with all other elements except for the light inert gases. It is highly toxic.

  4. Fluoride - Wikipedia

    en.wikipedia.org/wiki/Fluoride

    Fluorine, in the form of fluoride, is considered to be a micronutrient for human health, necessary to prevent dental cavities, and to promote healthy bone growth. [28] The tea plant (Camellia sinensis L.) is a known accumulator of fluorine compounds, released upon forming infusions such as the common beverage. The fluorine compounds decompose ...

  5. Fluorine compounds - Wikipedia

    en.wikipedia.org/wiki/Fluorine_compounds

    The fluorinefluorine 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]

  6. 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 ...

  7. Fluorodeoxyglucose (18F) - Wikipedia

    en.wikipedia.org/wiki/Fluorodeoxyglucose_(18F)

    The fluorine in [18 F]FDG decays radioactively via beta-decay to 18 O −. After picking up a proton H + from a hydronium ion in its aqueous environment, the molecule becomes glucose-6-phosphate labeled with harmless nonradioactive "heavy oxygen" in the hydroxyl at the C-2 position. The new presence of a 2-hydroxyl now allows it to be ...

  8. Carbon–fluorine bond - Wikipedia

    en.wikipedia.org/wiki/Carbon–fluorine_bond

    The high electronegativity of fluorine (4.0 for fluorine vs. 2.5 for carbon) gives the carbon–fluorine bond a significant polarity or dipole moment. The electron density is concentrated around the fluorine, leaving the carbon relatively electron poor. This introduces ionic character to the bond through partial charges (C δ+ —F δ−). The ...

  9. 1,2-Difluoroethane - Wikipedia

    en.wikipedia.org/wiki/1,2-Difluoroethane

    This increases the risk of inhalation. 1,2-difluoroethane is toxic to humans through several mechanisms. First, because it has a high density, it can displace oxygen in the lungs causing suffocation. In addition, inhaled fluorocarbons causes the myocardium to become more sensitive to catecholamines, which results in deadly cardiac arrhythmias.