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Perfluoroaryl iodides

Reactions of CgHjCHjBr (X = Cl, Br) with Hg metal proceed on UV irradiation . Perfluoroaryl iodides can undergo thermal reactions with Hg e.g., C5F5I and Hg at 300°C for 30 h provide (CgF5)2Hg (75 % yield) and Hglj ... [Pg.327]

Polymer-bound phenyliodine difluoride, which also has been used as a reagent to add fluorine to alkenes, can be prepared by the addition of xenon difluoride to the polymer [134, 135 136] Methyl iodide is converted to trifluoro methyliodine difluoride by treatment with fluorine at -110 C [137] Perfluoro-alkyliodine tetrafluorides could be synthesized from the perfluoroalkyliodine difluorides and fluorine [138] or chlorine trifluoride [139] Perfluoroalkyl [140] and perfluoroaryl [141] iodides are oxidized to the corresponding iodine difluorides by chlorine trifluoride. [Pg.48]

Castro et al. 44) found that the order of reactivity of various halides in coupling reactions with ethynylcopper compounds in DMF is ArSX, ArX > RCOX ArCHaX, RCH=CHCH2X, ArCOCHaX > RCH= CHX, Alkyl-X. A somewhat different order is observed for the reactivity of some organic halides towards perhaloarylcopper reagents in THF (97, 147) Allyl Aryl > Alkyl and perfluoroaryl, perfluoro-vinyl > aryl > perfluoroalkyl. Acid halides were also far more reactive than aryl iodides in ethereal solvents 146). The ease of halide displacement is I > Br > Cl. [Pg.262]

Ullmann coupling reactions of perfluoroaryl ttnd -heteioaiyl iodides and bromides with copper proceed readily. ... [Pg.566]


See other pages where Perfluoroaryl iodides is mentioned: [Pg.95]    [Pg.95]    [Pg.80]    [Pg.570]    [Pg.570]    [Pg.83]   
See also in sourсe #XX -- [ Pg.675 ]

See also in sourсe #XX -- [ Pg.675 ]

See also in sourсe #XX -- [ Pg.675 ]




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Perfluoroaryl

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