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  2. N-tert-Butylbenzenesulfinimidoyl chloride - Wikipedia

    en.wikipedia.org/wiki/N-Tert-butylbenzenesulfini...

    N-tert-Butylbenzenesulfinimidoyl chloride is a useful oxidant for organic synthesis reactions. [1] It is a good electrophile, and the sulfimide S=N bond can be attacked by nucleophiles, such as alkoxides, enolates, and amide ions.

  3. Lithium bis(trifluoromethanesulfonyl)imide - Wikipedia

    en.wikipedia.org/wiki/Lithium_bis(trifluorome...

    This page was last edited on 25 January 2025, at 20:59 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.

  4. Lithium tetrafluoroborate - Wikipedia

    en.wikipedia.org/wiki/Lithium_tetrafluoroborate

    It is a white crystalline powder. It has been extensively tested for use in commercial secondary batteries, an application that exploits its high solubility in nonpolar solvents. [ 2 ]

  5. Triphenylmethyl hexafluorophosphate - Wikipedia

    en.wikipedia.org/wiki/Triphenylmethyl_hexafluoro...

    Triphenylmethyl hexafluorophosphate (also triphenylcarbenium hexafluorophosphate, trityl hexafluorophosphate, or tritylium hexafluorophosphate) is an organic salt with the formula [(C 6 H 5) 3 C] + [PF 6] −, consisting of the triphenylcarbenium cation [(C 6 H 5) 3 C] + and the hexafluorophosphate anion [PF 6] −.

  6. Silver tetrafluoroborate - Wikipedia

    en.wikipedia.org/wiki/Silver_tetrafluoroborate

    Silver tetrafluoroborate can be prepared by several methods. A simple route entails dissolving silver carbonate in aqueous [[tetrafluoroboric acid. [3] It can also be produced by treating silver(I) fluoride with boron trifluoride in nitromethane solution.

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