Synthesis of 4, 8‐Dinitraminodifurazano[3, 4‐b, e]pyrazine Derived Nitrogen‐Rich Salts as Potential Energetic Materials. Issue 2 (16th January 2018)
- Record Type:
- Journal Article
- Title:
- Synthesis of 4, 8‐Dinitraminodifurazano[3, 4‐b, e]pyrazine Derived Nitrogen‐Rich Salts as Potential Energetic Materials. Issue 2 (16th January 2018)
- Main Title:
- Synthesis of 4, 8‐Dinitraminodifurazano[3, 4‐b, e]pyrazine Derived Nitrogen‐Rich Salts as Potential Energetic Materials
- Authors:
- Li, Wei
Tian, Junjun
Qi, Xiujuan
Wang, Kangcai
Jin, Yunhe
Wang, Binshen
Zhang, Qinghua - Abstract:
- Abstract: A series of new energetic compounds based on 4, 8‐dinitraminodifurazano[3, 4‐ b, e ]pyrazine were synthesised and fully characterized by NMR and IR spectroscopy, and elemental analysis. The structures of compounds 3‐a, 3‐c, 3‐f, and 3‐g were determined by single‐crystal X‐ray diffraction analysis. The physicochemical and energetic properties of these energetic compounds including density, thermal stability, and energetic performance (e. g., detonation velocities and detonation pressures) were investigated. The combination of nitrogen‐rich 4, 8‐dihydrodifurazano[3, 4‐ b, e ]pyrazine framework with highly energetic nitramino moieties endowed these as‐synthesised compounds with excellent detonation performance. Among these as‐synthesised compounds, five energetic salts (3‐a, 3‐b, 3‐c, 3‐f, and 3‐g ) exhibited satisfactory calculated detonation velocities (8921–9413 m s ‐1 ), which were superior to cyclo‐1, 3, 5‐trimethylene‐2, 4, 6‐trinitamine (RDX) (8878 m s ‐1 ). Notably, compound 3‐f exhibits an excellent calculated detonation velocity of 9166 m s ‐1 and also acceptable impact and friction sensitivities (IS=8 J, FS=108 N). The prominent detonation performance with moderate sensitivities indicates that compound 3‐f has the potential to compete with traditional high explosives. Abstract : A series of nitramino energetic salts based on 4, 8‐dinitraminodifurazano[3, 4‐ b, e ]pyrazine (DFP ) was synthesized, which exhibited the excellent detonation performanceAbstract: A series of new energetic compounds based on 4, 8‐dinitraminodifurazano[3, 4‐ b, e ]pyrazine were synthesised and fully characterized by NMR and IR spectroscopy, and elemental analysis. The structures of compounds 3‐a, 3‐c, 3‐f, and 3‐g were determined by single‐crystal X‐ray diffraction analysis. The physicochemical and energetic properties of these energetic compounds including density, thermal stability, and energetic performance (e. g., detonation velocities and detonation pressures) were investigated. The combination of nitrogen‐rich 4, 8‐dihydrodifurazano[3, 4‐ b, e ]pyrazine framework with highly energetic nitramino moieties endowed these as‐synthesised compounds with excellent detonation performance. Among these as‐synthesised compounds, five energetic salts (3‐a, 3‐b, 3‐c, 3‐f, and 3‐g ) exhibited satisfactory calculated detonation velocities (8921–9413 m s ‐1 ), which were superior to cyclo‐1, 3, 5‐trimethylene‐2, 4, 6‐trinitamine (RDX) (8878 m s ‐1 ). Notably, compound 3‐f exhibits an excellent calculated detonation velocity of 9166 m s ‐1 and also acceptable impact and friction sensitivities (IS=8 J, FS=108 N). The prominent detonation performance with moderate sensitivities indicates that compound 3‐f has the potential to compete with traditional high explosives. Abstract : A series of nitramino energetic salts based on 4, 8‐dinitraminodifurazano[3, 4‐ b, e ]pyrazine (DFP ) was synthesized, which exhibited the excellent detonation performance coupled with moderate sensitivities. … (more)
- Is Part Of:
- ChemistrySelect. Volume 3:Issue 2(2018)
- Journal:
- ChemistrySelect
- Issue:
- Volume 3:Issue 2(2018)
- Issue Display:
- Volume 3, Issue 2 (2018)
- Year:
- 2018
- Volume:
- 3
- Issue:
- 2
- Issue Sort Value:
- 2018-0003-0002-0000
- Page Start:
- 849
- Page End:
- 854
- Publication Date:
- 2018-01-16
- Subjects:
- detonation performance -- 4, 8-dihydrodifurazano[3, 4-b, e]pyrazine -- high-energy-density materials -- sensitivity -- synthesis
Chemistry -- Periodicals
540.5 - Journal URLs:
- http://onlinelibrary.wiley.com/ ↗
http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)2365-6549 ↗ - DOI:
- 10.1002/slct.201702678 ↗
- Languages:
- English
- ISSNs:
- 2365-6549
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3172.241000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 14532.xml