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  2. Chloryl fluoride - Wikipedia

    en.wikipedia.org/wiki/Chloryl_fluoride

    ClO 2 F was first reported by Schmitz and Schumacher in 1942, who prepared it by the fluorination of ClO 2. [2] The compound is more conveniently prepared by reaction of sodium chlorate and chlorine trifluoride [3] and purified by vacuum fractionation, i.e. selectively condensing this species separately from other products. This species is a ...

  3. Organofluorine chemistry - Wikipedia

    en.wikipedia.org/wiki/Organofluorine_chemistry

    The structure of organofluorine compounds can be distinctive. As shown below, perfluorinated aliphatic compounds tend to segregate from hydrocarbons. This "like dissolves like effect" is related to the usefulness of fluorous phases and the use of PFOA in processing of fluoropolymers. In contrast to the aliphatic derivatives, perfluoroaromatic ...

  4. Fluorine compounds - Wikipedia

    en.wikipedia.org/wiki/Fluorine_compounds

    Several elements show their highest oxidation state only in a few compounds, one of which is the fluoride; and some elements' highest known oxidation state is seen exclusively in a fluoride. For groups 1–5, 13–16 (except nitrogen), the highest oxidation states of oxides and fluorides are always equal. Differences are only seen in chromium ...

  5. Biological aspects of fluorine - Wikipedia

    en.wikipedia.org/wiki/Biological_aspects_of_fluorine

    They are not metabolized by the body but are excreted by the kidneys. Dwell time in the body varies greatly by species. Rodents have half-lives of days, while in humans they remain for years. Many animals show sex differences in the ability to rid the body of PFAAs, but without a clear pattern. Gender differences of half lives vary by animal ...

  6. Free-radical halogenation - Wikipedia

    en.wikipedia.org/wiki/Free-radical_halogenation

    Radical fluorination with the pure element is difficult to control and highly exothermic; care must be taken to prevent an explosion or a runaway reaction. With chlorine the reaction is moderate to fast; with bromine, slow and requires intense UV irradiation; and with iodine, it is practically nonexistent and thermodynamically unfavored.

  7. Chlorine - Wikipedia

    en.wikipedia.org/wiki/Chlorine

    As another difference, chlorine has a significant chemistry in positive oxidation states while fluorine does not. Chlorination often leads to higher oxidation states than bromination or iodination but lower oxidation states than fluorination. Chlorine tends to react with compounds including M–M, M–H, or M–C bonds to form M–Cl bonds. [40]

  8. Interhalogen - Wikipedia

    en.wikipedia.org/wiki/Interhalogen

    It has the same molecular shape as chlorine trifluoride. Iodine trifluoride (IF 3) is a yellow solid that decomposes above −28 °C. It can be synthesised from the elements, but care must be taken to avoid the formation of IF 5. F 2 attacks I 2 to yield IF 3 at −45 °C in CCl 3 F. Alternatively, at low temperatures, the fluorination reaction

  9. Chlorine trifluoride - Wikipedia

    en.wikipedia.org/wiki/Chlorine_trifluoride

    Chlorine trifluoride is an interhalogen compound with the formula ClF 3. It is a colorless, poisonous, corrosive, and extremely reactive gas that condenses to a pale-greenish yellow liquid, the form in which it is most often sold (pressurized at room temperature). It is famous for its extreme oxidation properties.