Keywords
decomposition temperature
difluoroamino group
difluoroamino(dinitro)methyl group
energetic alkyl esters
impact sensitivity.
nitro alcohols
Abstract
Difluoroamination and esterification reactions were utilized for the preparation of NF2-analogs of 2,2,2-trinitroethyl 4,4,4-trinitrobutanoate with replacing one or two nitro groups. Difluoroamino products possess promising properties as ingredients of metallized energetic materials.
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