2,4-Dinitrophenyl and Pentaerythrityltrinitrate as Explosophoric Units in the Synthesis of New Energetic Materials
M. Romero, J. Cortes Morales, Eduardo González‐Zamora, A. Gutiérrez-Carillo
Abstract
M. Romero, J. Cortes Morales, Eduardo González‐Zamora, A. Gutiérrez-Carillo
Abstract
Three novel energetic compounds were prepared from the common precursor 1-fluoro-2,4-dinitrobenzene by using nucleophilic aromatic substitution as a key step with pentaerythritol, pentaerythritoltrinitrate, or glycidol. The thermal stability of 3-(2,4-dinitrophenoxy)-2,2-bis[(nitrooxy)methyl]propyl nitrate was assessed by differential scanning calorimetry and its X-ray structure was determined. In light of the success in using 2,4-dinitroanisole as an additive in explosive formulations, some of the analogous compounds prepared in the present study may be considered as suitable materials for diverse composite energetic material formulations.
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Three novel energetic compounds were prepared from the common precursor 1-fluoro-2,4-dinitrobenzene by using nucleophilic aromatic substitution as a key step with pentaerythritol, pentaerythritoltrinitrate, or glycidol. The thermal stability of 3-(2,4-dinitrophenoxy)-2,2-bis[(nitrooxy)methyl]propyl nitrate was assessed by differential scanning calorimetry and its X-ray structure was determined. In light of the success in using 2,4-dinitroanisole as an additive in explosive formulations, some of the analogous compounds prepared in the present study may be considered as suitable materials for diverse composite energetic material formulations.
Key concepts: Chemistry, Glycidol, Nucleophilic aromatic substitution, Energetic material, Pentaerythritol, Thermal stability, Differential scanning calorimetry, Explosive material