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- W2496322605 abstract "The acid-base chemistry of difluoramine, HNF2, and its methyl derivative is being studied to establish the existence of difluorammonium compounds and to obtain new oxidizers containing difluoramino groups. The protic acids, hydrogen chloride and trifluoroacetic acid, do not form compounds with difluoramine in the condensed state; methyldifluoramine, however, may form a weak complex with hydrogen chloride. Trimethylaluminum, a strong Lewis acid, reacts with difluoramine liberating methane. The postulated intermediate, has not yet been isolated. Although trimethylgallium and difluoramine do not form a compound at low temperatures, methane is slowly evolved. Both difluoramine and methyldifluoramine form 1:1 adducts with sulfur trioxide. NMR analysis of the difluoramine adduct indicates that the proton and fluorine atoms are no longer adjacent, possibly indicating that it is difluoramidosulfamic acid." @default.
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- W2496322605 date "1966-01-01" @default.
- W2496322605 modified "2023-10-18" @default.
- W2496322605 title "Reactions of Difluoramine with Lewis Acids" @default.
- W2496322605 doi "https://doi.org/10.1021/ba-1966-0054.ch014" @default.
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