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  2. Electrophilic fluorination - Wikipedia

    en.wikipedia.org/wiki/Electrophilic_fluorination

    The mechanism of electrophilic fluorination remains controversial. At issue is whether the reaction proceeds via an S N 2 or single-electron transfer (SET) process. In support of the S N 2 mechanism, aryl Grignard reagents and aryllithiums give similar yields of fluorobenzene in combination with N-fluoro-o-benzenedisulfonimide (NFOBS), even though the tendencies of these reagents to ...

  3. Selectfluor - Wikipedia

    en.wikipedia.org/wiki/Selectfluor

    Electrophilic fluorinating reagents could in principle operate by electron transfer pathways or an S N 2 attack at fluorine. This distinction has not been decided. [2] By using a charge-spin separated probe, [3] it was possible to show that the electrophilic fluorination of stilbenes with Selectfluor proceeds through an SET/fluorine atom transfer mechanism.

  4. Organofluorine chemistry - Wikipedia

    en.wikipedia.org/wiki/Organofluorine_chemistry

    Organofluorine chemistry describes the chemistry of organofluorine compounds, organic compounds that contain a carbon–fluorine bond. Organofluorine compounds find diverse applications ranging from oil and water repellents to pharmaceuticals , refrigerants, and reagents in catalysis .

  5. Electrochemical fluorination - Wikipedia

    en.wikipedia.org/wiki/Electrochemical_fluorination

    Electrochemical fluorination (ECF), or electrofluorination, is a foundational organofluorine chemistry method for the preparation of fluorocarbon-based organofluorine compounds. [1] The general approach represents an application of electrosynthesis .

  6. Perfluorobutanesulfonyl fluoride - Wikipedia

    en.wikipedia.org/wiki/Perfluorobutanesulfonyl...

    As mentioned above, aryl and alkenyl nonaflates are useful as electrophiles in palladium catalyzed cross coupling reactions. Their reactivity generally mirrors that of the more commonly encountered triflate electrophiles, but nonaflates tend to be less prone to hydrolysis to ketones (in the case of alkenyl sulfonates) and phenols (in the case of aryl sulfonates).

  7. Quenching (fluorescence) - Wikipedia

    en.wikipedia.org/wiki/Quenching_(fluorescence)

    Typically quinine fluoresces blue, which is visible in the right sample. The left sample contains chloride ions which quench quinine's fluorescence, so the left sample does not fluoresce visibly (the violet light is just scattered laser light). In chemistry, quenching refers to any process which decreases the fluorescent intensity of a given ...

  8. Substitution reaction - Wikipedia

    en.wikipedia.org/wiki/Substitution_reaction

    Substitution reactions in organic chemistry are classified either as electrophilic or nucleophilic depending upon the reagent involved, whether a reactive intermediate involved in the reaction is a carbocation, a carbanion or a free radical, and whether the substrate is aliphatic or aromatic. Detailed understanding of a reaction type helps to ...

  9. Electrophile - Wikipedia

    en.wikipedia.org/wiki/Electrophile

    The electrophilic Br-Br molecule interacts with electron-rich alkene molecule to form a π-complex 1. Forming of a three-membered bromonium ion The alkene is working as an electron donor and bromine as an electrophile. The three-membered bromonium ion 2 consisted of two carbon atoms and a bromine atom forms with a release of Br −.

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