TY - JOUR
T1 - Synthesis, characterization and performance of difurazanopyrazine derivatives
AU - Liu, Ning
AU - Lian, Peng
AU - Lai, Wei Peng
AU - Li, Hui
AU - Wang, Bo Zhou
PY - 2014/8/25
Y1 - 2014/8/25
N2 - Six difurazanopyrazine derivatives (I~VI) were synthesized using 4H, 8H-difurazano[3, 4-b:3', 4'-e]pyrazine(DFP) as starting material, via salification, substitution, addition, nitration, chlorination and azidation reaction, and their structures were characterized by IR, NMR, and elemental analysis. Using compound II, IV, VI with nitrofurazan, ntriateester, azide group as typical one, the thermal performances were studied by differential scanning calorimetry(DSC) and thermogravimetric(TG), and the physical and chemical properties were calculated by Gaussian 09, and the detonation performance by VLW. Results show that the three compounds have good thermal stability with thermal decomposition temperature of 318.3, 197.5℃, and 250.5℃, respectively. The density, detonation velocity and detonation pressure of compound IV are 2.0 g·cm-3, 9067 m·s-1 and 43 GPa, respectively. Compared with HMX, compound IV exhibits similar detonation velocity, higher density and detonation pressure.
AB - Six difurazanopyrazine derivatives (I~VI) were synthesized using 4H, 8H-difurazano[3, 4-b:3', 4'-e]pyrazine(DFP) as starting material, via salification, substitution, addition, nitration, chlorination and azidation reaction, and their structures were characterized by IR, NMR, and elemental analysis. Using compound II, IV, VI with nitrofurazan, ntriateester, azide group as typical one, the thermal performances were studied by differential scanning calorimetry(DSC) and thermogravimetric(TG), and the physical and chemical properties were calculated by Gaussian 09, and the detonation performance by VLW. Results show that the three compounds have good thermal stability with thermal decomposition temperature of 318.3, 197.5℃, and 250.5℃, respectively. The density, detonation velocity and detonation pressure of compound IV are 2.0 g·cm-3, 9067 m·s-1 and 43 GPa, respectively. Compared with HMX, compound IV exhibits similar detonation velocity, higher density and detonation pressure.
KW - Characterization
KW - Difurazanopyrazine derivatives
KW - Organic chemistry
KW - Performance
KW - Synthesis
UR - http://www.scopus.com/inward/record.url?scp=84906952036&partnerID=8YFLogxK
U2 - 10.3969/j.issn.1006-9941.2014.04.009
DO - 10.3969/j.issn.1006-9941.2014.04.009
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AN - SCOPUS:84906952036
SN - 1006-9941
VL - 22
SP - 473
EP - 477
JO - Hanneng Cailiao/Chinese Journal of Energetic Materials
JF - Hanneng Cailiao/Chinese Journal of Energetic Materials
IS - 4
ER -