Article ID Journal Published Year Pages File Type
1313903 Journal of Fluorine Chemistry 2012 11 Pages PDF
Abstract

The advantageous impact of a pentafluorosulfanyl substituent on the properties of furazan-containing energetic materials was demonstrated by the synthesis and study of the energetic properties of ten new compounds. The thermal stability of these compounds was evaluated by DSC and TGA, whereas densities, heats of formation, pressures of detonation and speeds of detonation were obtained computationally. On the basis of these data, it was concluded that the combination of the SF5 substituent with the furazan ring led to materials of higher density and predicted detonation properties than other known furazans or SF5-containing materials. In addition, the synthetic studies provided insight regarding the electron-withdrawing nature of the furazan ring, in particular its effect on the basicity and nucleophilic reactivity of amino furazans.

Graphical abstractTen new SF5-containing furazan materials have been synthesized and their energetic properties examined.Figure optionsDownload full-size imageDownload as PowerPoint slideHighlights► Pentafluorosulfanylacetic acid is a useful building block for preparation of new furazan energetic materials. ► SF5-substituted furazans have densities greater than materials containing either moiety alone. ► SF5-substituted furazans have enhanced energetic properties when compared to materials containing either moiety alone. ► The low nucleophilicity of aminofurazans makes synthesis of derivatives challenging.

Related Topics
Physical Sciences and Engineering Chemistry Inorganic Chemistry
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