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  2. Organofluorine chemistry - Wikipedia

    en.wikipedia.org/wiki/Organofluorine_chemistry

    Some important organofluorine compounds. A: fluoromethane B: isoflurane C: a CFC D: an HFC E: triflic acid F: Teflon G: PFOS H: fluorouracil I: fluoxetine Organofluorine chemistry describes the chemistry of organofluorine compounds, organic compounds that contain a carbon–fluorine bond.

  3. 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 ...

  4. Category:Fluorocarbons - Wikipedia

    en.wikipedia.org/wiki/Category:Fluorocarbons

    Main page; Contents; Current events; Random article; About Wikipedia; Contact us

  5. File:The Periodic Table of the Elements in Pictures.pdf

    en.wikipedia.org/wiki/File:The_Periodic_Table_of...

    English: This pictorial periodic table is colorful, boring, and packed with information. In addition to the element's name, symbol, and atomic number, each element box has a drawing of one of the element's main human uses or natural occurrences.

  6. List of gases - Wikipedia

    en.wikipedia.org/wiki/List_of_gases

    This list is sorted by boiling point of gases in ascending order, but can be sorted on different values. "sub" and "triple" refer to the sublimation point and the triple point, which are given in the case of a substance that sublimes at 1 atm; "dec" refers to decomposition. "~" means approximately. Blue type items have an article available by ...

  7. Tetrafluoroethylene - Wikipedia

    en.wikipedia.org/wiki/Tetrafluoroethylene

    A convenient, safe method for generating TFE is the pyrolysis of the sodium salt of pentafluoropropionic acid: [6]. C 2 F 5 CO 2 Na → C 2 F 4 + CO 2 + NaF. The depolymerization reaction – vacuum pyrolysis of PTFE at 650–700 °C (1,200–1,290 °F) in a quartz vessel – is a traditional laboratory synthesis of TFE.

  8. Hydrofluorocarbon - Wikipedia

    en.wikipedia.org/wiki/Hydrofluorocarbon

    Fluorocarbons with few C–F bonds behave similarly to the parent hydrocarbons, but their reactivity can be altered significantly.For example, both uracil and 5-fluorouracil are colourless, high-melting crystalline solids, but the latter is a potent anti-cancer drug.

  9. Hydrofluoroolefin - Wikipedia

    en.wikipedia.org/wiki/Hydrofluoroolefin

    Chemical structure of 1,3,3,3-tetrafluoropropene (HFO-1234ze). Hydrofluoroolefins (HFOs) are unsaturated organic compounds composed of hydrogen, fluorine and carbon.These organofluorine compounds are of interest as refrigerants.