A novel synthesis method for nitrogen-rich energetic frameworks containing bistetrazoles: assembling an advanced high-energy density material with high nitrogen content and good oxygen balance

The synthesis of bistetrazole via a one-step process including substitution-cyclisation-cracking reaction has been reported for the first time. The combination of a nitrogen-rich energetic framework and a high oxygen detonation group perfectly fulfills the target of maintaining a high level of nitro...

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Veröffentlicht in:Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2024-11, Vol.12 (43), p.29638-29644
Hauptverfasser: Yu, Xuezhi, Tang, Jie, Lei, Caijin, Xue, Chungui, Yang, Hongwei, Xiao, Chuan, Cheng, Guangbin
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Sprache:eng
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Zusammenfassung:The synthesis of bistetrazole via a one-step process including substitution-cyclisation-cracking reaction has been reported for the first time. The combination of a nitrogen-rich energetic framework and a high oxygen detonation group perfectly fulfills the target of maintaining a high level of nitrogen content and good oxygen balance while avoiding the safety risks. H 2 TT , with 81.5% nitrogen content, demonstrates a very high heat of formation (Δ H f = 5.54 kJ g −1 ) and superior detonation velocity ( D = 8932 m s −1 ) to RDX ( D = 8795 m s −1 ). After the introduction of dinitromethyl high oxygen groups, the target compound BDNTT has an oxygen balance of −11.6% and a high crystal density up to 1.914 g cm −3 , and exhibited superior detonation performance ( D = 9633 m s −1 , P = 41.4 GPa) to HMX ( D = 9144 m s −1 , P = 39.3 GPa). At the same time, the nitrogen content and oxygen balance of the BDNTT reached a decent level of 54.1% and −11.6%, respectively. Future researchers can use this study as experience to design advanced high-energy density materials. Target compound BDNTT exhibits excellent detonation performance and indicates the potential as a novel type of high-energy density material (HEDM).
ISSN:2050-7488
2050-7496
DOI:10.1039/d4ta05721j