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Updated: Aug 9, 2025

Functionalized Spirocyclic Heterocycle Synthesis and Cytotoxicity Assay
Published on: February 9, 2021
Challenging the Limitations of Tetranitro Biimidazole through Introducing a gem-Dinitromethyl Scaffold
Shangbiao Feng1,2, Baoseng Zhang1, Chunwang Luo1
1School of Environmental and Safety Engineering, North University of China, Taiyuan 030051, China.
Abstract:
A gem-dinitromethyl group was successfully introduced into the TNBI·2H2O structure (TNBI: 4,4',5,5'-tetranitro-2,2'-bi-1H-imidazole) to obtain 1-(dinitromethyl)-4,4',5,5'-tetranitro-1H,1'H-2,2'-biimidazole (DNM-TNBI). Benefiting from the transformation of an N-H proton into a gem-dinitromethyl group, the current limitations of TNBI were well solved. More importantly, DNM-TNBI has high density (1.92 g·cm-3, 298 K), good oxygen balance (15.3%), and excellent detonation properties (Dv = 9102 m·s-1, P = 37.6 GPa), suggesting that it has great potential as an oxidizer or a high-performance energetic material.
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