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  2. Fluorine compounds - Wikipedia

    en.wikipedia.org/wiki/Fluorine_compounds

    Fluorine's chemistry is dominated by its strong tendency to gain an electron. It is the most electronegative element and elemental fluorine is a strong oxidant. The removal of an electron from a fluorine atom requires so much energy that no known reagents are known to oxidize fluorine to any positive oxidation state. [20]

  3. Electrophilic aromatic directing groups - Wikipedia

    en.wikipedia.org/wiki/Electrophilic_aromatic...

    Due to a stronger resonance effect and inductive effect than the heavier halogens, fluorine is anomalous. The partial rate factor of electrophilic aromatic substitution on fluorobenzene is often larger than one at the para position, making it an activating group. [ 11 ]

  4. Fluoride - Wikipedia

    en.wikipedia.org/wiki/Fluoride

    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 into products including fluoride ions. Fluoride is the most bioavailable form of fluorine, and as such, tea is potentially a vehicle for fluoride dosing. [29]

  5. Tetrafluoroborate - Wikipedia

    en.wikipedia.org/wiki/Tetrafluoroborate

    4 serves as a fluorine source to deliver an equivalent of fluoride. [2] The Balz–Schiemann reaction for the synthesis of aryl fluorides is the best known example of such a reaction. [3] Ether and halopyridine adducts of HBF 4 have been reported to be effective reagents for the hydrofluorination of alkynes. [4]

  6. Tetrakis (3,5-bis (trifluoromethyl)phenyl)borate - Wikipedia

    en.wikipedia.org/wiki/Tetrakis(3,5-bis(trifluoro...

    The [BAr F 4] − anion with four fluorinated aryl groups distributed tetrahedrally about a central boron atom. Tetrakis[3,5-bis(trifluoromethyl)phenyl]borate is an anion with chemical formula [{3,5-(CF 3) 2 C 6 H 3} 4 B] −, which is commonly abbreviated as [BAr F 4] −, indicating the presence of fluorinated aryl (Ar F) groups.

  7. Radical fluorination - Wikipedia

    en.wikipedia.org/wiki/Radical_fluorination

    The O–F bond of hypofluorites is relatively weak. For trifluoromethyl hypofluorite (CF 3 OF), it has been estimated to be 43.5 kcal/mol (182 kJ/mol). [9] The ability of trifluoromethyl hypofluorite to transfer fluorine to alkyl radicals is notably demonstrated by reacting independently generated ethyl radicals from ethene and tritium in the presence of CF 3 OF. [10]

  8. Fluoroanion - Wikipedia

    en.wikipedia.org/wiki/Fluoroanion

    In chemistry, a fluoroanion or fluorometallate anion is a polyatomic anion that contains one or more fluorine atoms. The ions and salts form from them are also known as complex fluorides. They can occur in salts, or in solution, but seldom as pure acids. Fluoroanions often contain elements in higher oxidation states. They mostly can be ...

  9. Tetrafluoroberyllate - Wikipedia

    en.wikipedia.org/wiki/Tetrafluoroberyllate

    The Be–F bond length is between 145 and 153 pm.The beryllium is sp 3 hybridized, leading to a longer bond than in BeF 2, where beryllium is sp hybridized. [11] In trifluoroberyllates, there are actually BeF 4 tetrahedra arranged in a triangle, so that three fluorine atoms are shared on two tetrahedra each, resulting in a formula of Be 3 F 9.