A series of asymmetric monoimidazolium dihydroboronium-based ionic liquids （ILs） were synthesized from amine-boranes. All the resulting ILs were fully characterized by 1H and 13C NMR, IR spectroscopy, elemental analysis or high resolution mass spectrum. Compared with the symmetric bisimidazolium dihydroboronium-based ILs, these new ILs exhibited improved properties with shorter ignition delay times （IDs）, higher densities, and lower phase transition temperature showing the promising application potential as green propellants. A series of asymmetric monoimidazolium dihydroboronium-based ionic liquids （ILs） were synthesized from amine-boranes. All the resulting ILs were fully characterized by 1H and 13C NMR, IR spectroscopy, elemental anal- ysis or high resolution mass spectrum. Compared with the symmetric bisimidazolium dihydroboronium-based ILs, these new ILs exhibited improved properties with shorter ignition delay times （IDs）, higher densities, and lower phase transition temperature showing the promising application potential as green propellants.
A series of 3-nitro-5-nitroimino-1,2,4-oxadiazole-based energetic salts were synthesized from 3-nitro-5-nitroimino-1,2,4-oxadiazole anion and nitrogen-rich cations. They were fully characterized by IR,elemental analysis and NMR spectroscopy. The structure of triaminoguanidinium salt（1-e） was confirmed by single crystal X-ray diffraction. All salts showed good thermal stability with decomposed temperature ranging from 155 8C to 258 8C, and positive heats of formation from 226.0 k J/mol to554.1 k J/mol. Thus, the theoretic detonation pressure was predicted from 28.70 GPa to 37.60 GPa and velocities from 8526 m/s to 9354 m/s. Among them, guanidinium salt（1-c） exhibited both high decomposition temperature（258 8C） and detonation velocity（9319 m/s）.
