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Triazidotrinitro benzene: 1,3,5-(N-3)(3)-2,4,6-(NO2)(3)C-6
Author(s): Adam D, Karaghiosoff K, Klapotke TM, Holl G, Kaiser M
Source: PROPELLANTS EXPLOSIVES PYROTECHNICS    Volume: 27    Issue: 1    Pages: 7-11    Published: MAR 2002  
Times Cited: 9     References: 30     
Abstract: Triazidotrinitro benzene. 1,3,5-(N-3)(3)-2,4,6-(NO2)(3)C-6 (1) was synthesized by nitration of triazidodinitro benzene, 1,3,5-(N-3)(3)-2,4-(NO2)(2)C6H with either a mixture of fuming nitric and concentrated sulfuric acid (HNO3/H2SO4) or with N2O5. Crystals were obtained by the slow evaporation of an acetone/acetic acid mixture at room temperature over a period of 2 weeks and characterized by single crystal X-ray diffraction: monoclinic, P 2(t)/ c (no. 14), a = 0.54256(4), b = 1.8552(1), c = 1.2129(1) nm, beta = 94.91 (1), V = 1.2163(2) nm(3), Z = 4, Q = 1.836 g(.)cm(-3), R-all=0.069. Triazidotrinitro benzene has a remarkably high density (1.84g. cm(-3)). The standard heat of formation of compound I was computed at B3LYP/6-31G(d,p) level of theory to be DeltaHdegrees(f)= 765.8 kJ(.)mol(-1) which translates to 2278.0 kJ(.)kg(-1). The expected detonation properties of compound I were calculated using the semi-empirical equations suggested by Kamlet and Jacobs: detonation pressure, P = 18.4 GPa and detonation velocity, D 8100 m(.)s(-1).
Document Type: Article
Language: English
Reprint Address: Klapotke, TM (reprint author), Univ Munich, Dept Chem, Marchioninistr 15, D-81377 Munich, Germany
Addresses:
1. Univ Munich, Dept Chem, D-81377 Munich, Germany
2. Swisttal Heinmertsheim, Bundeswehr Res Inst Mat Fuels & Lubricants, D-53913 Swisttal, Germany
Publisher: WILEY-V C H VERLAG GMBH, PO BOX 10 11 61, D-69451 WEINHEIM, GERMANY
Subject Category: Chemistry, Applied; Engineering, Chemical
IDS Number: 532PH
ISSN: 0721-3115
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