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Assessment of Cardiac Function and Energetics in Isolated Mouse Hearts Using 31P NMR Spectroscopy
Published on: August 31, 2010
Versatile functionalization of 3,5-diamino-4-nitropyrazole for promising insensitive energetic compounds
Yongxing Tang1, Jinchao Ma1, Gregory H Imler2
1Department of Chemistry, University of Idaho, Moscow, Idaho, 83844-2343 USA. jshreeve@uidaho.edu and Nanjing University of Science and Technology, Nanjing, Jiangsu, 210094 China.
Abstract:
Variation of functional groups offers an efficient approach for tuning properties of materials such as thermal stability, and detonation performance while improving sensitivities to mechanical stimuli. Now versatile functionalization of 3,5-diamino-4-nitropyrazole involving the introduction of a tetrazole ring, or a guanyl group, or ring expansion is described. All of the compounds were fully characterized and some of them (2, 9 and 13) were verified by single crystal X-ray diffraction. Based on their good thermal stabilities and high detonation performance as well as insensitive properties, they are potentially insensitive energetic compounds.
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