Nucleophilic Catalyzed Structural Binary Cleavage of a Fused [5,5]-Bicyclic Compound
Ajay Kumar Chinnam1, Richard J Staples2, Jean'ne M Shreeve1
1Department of Chemistry, University of Idaho, Moscow, Idaho 83844-2343 United States.
Abstract:
Structural binary cleavage of 3,7-diamino-2,6-dinitro-1H,5H-pyrazolo-[1,2-a]pyrazole-1,5-dione 3, under nucleophilic conditions, leads to the formation of a monocyclic pyrazole unit of 5-amino-4-nitro-1,2-dihydro-3H-pyrazol-3-one, 4. Additionally, various salts of the pyrazole ring were synthesized and fully characterized. Detonation properties and mechanical sensitivities of 4 and other new compounds are remarkably improved compared to 3. This simple and efficient strategy is highly desirable for future studies on the development of insensitive and high performing materials.
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