TY - JOUR
T1 - Synthesis, crystal structure, thermal decomposition and sensitivity properties of (AIM)(HTNR) and (AIM)(PA)
AU - Tang, Zhan
AU - Yang, Li
AU - Qiao, Xiao Jing
AU - Wu, Bi Dong
AU - Zhang, Tong Lai
AU - Zhou, Zun Ning
AU - Yu, Kai Bei
PY - 2012/1/25
Y1 - 2012/1/25
N2 - Two new energetic compounds (AIM)(HTNR) and (AIM)(PA)(AIM=2-azidoimidazole, TNR=2,4,6-trini- troresorcinol, PA=picric acid) have been prepared by AIM(2-azidoimidazolium) and TNR(2,4,6-trinitroresorcinol) or PA(picric acid) and characterized by elemental analysis and FTIR spectrum. Their crystal structures were determined by X-ray single-crystal diffraction analysis. The obtained results show that (AIM)(HTNR) crystal belongs to monoclinic, P2 1/c space group, a=1.1306(2) nm, b=0.70305(14) nm, c=1.7398(4) nm, β=106.91°, V=1.3231(5) nm 3, D c=1.778g/cm 3, Z=4, R 1=0.0524, wR 2[I >2σ(I)]=0.1067 and S=1.092 and (AIM)(PA) crystal belongs to monoclinic P21/c space group, a=0.80303(16) nm, b=0.81395(16) nm, c=2.0471(4) nm, β=93.93(3)°, V=1.3349(5) nm 3, D c=1.683 3g/cm, Z=4, R 1=0.0784, wR 2[I >2σ(I)]=0.1814 and S=1.098. Both the compounds have electrostatic attraction and hydrogen bonds, which contribute to making the constructions more stable. The decomposition of the two compounds was studied via differential scanning calorimetry(DSC) and thermogravimetry-derivative thermogravimetry(TG-DTG) techniques at a heating rate of 10°C/min, and the results show that both the compounds underwent one intensive exothermic decomposition stage. Sensitivity tests reveal that the title compounds were insensitive to friction and im- pact and sensitive to flame and could be applied in potential pyrotechnics.
AB - Two new energetic compounds (AIM)(HTNR) and (AIM)(PA)(AIM=2-azidoimidazole, TNR=2,4,6-trini- troresorcinol, PA=picric acid) have been prepared by AIM(2-azidoimidazolium) and TNR(2,4,6-trinitroresorcinol) or PA(picric acid) and characterized by elemental analysis and FTIR spectrum. Their crystal structures were determined by X-ray single-crystal diffraction analysis. The obtained results show that (AIM)(HTNR) crystal belongs to monoclinic, P2 1/c space group, a=1.1306(2) nm, b=0.70305(14) nm, c=1.7398(4) nm, β=106.91°, V=1.3231(5) nm 3, D c=1.778g/cm 3, Z=4, R 1=0.0524, wR 2[I >2σ(I)]=0.1067 and S=1.092 and (AIM)(PA) crystal belongs to monoclinic P21/c space group, a=0.80303(16) nm, b=0.81395(16) nm, c=2.0471(4) nm, β=93.93(3)°, V=1.3349(5) nm 3, D c=1.683 3g/cm, Z=4, R 1=0.0784, wR 2[I >2σ(I)]=0.1814 and S=1.098. Both the compounds have electrostatic attraction and hydrogen bonds, which contribute to making the constructions more stable. The decomposition of the two compounds was studied via differential scanning calorimetry(DSC) and thermogravimetry-derivative thermogravimetry(TG-DTG) techniques at a heating rate of 10°C/min, and the results show that both the compounds underwent one intensive exothermic decomposition stage. Sensitivity tests reveal that the title compounds were insensitive to friction and im- pact and sensitive to flame and could be applied in potential pyrotechnics.
KW - 2,4,6-trinitroresorcinol
KW - 2-azidoimidazolium
KW - Crystal structure
KW - Picric acid
KW - Thermal decomposition Article ID 1005-9040(2012)-01-004-05
UR - http://www.scopus.com/inward/record.url?scp=84859299156&partnerID=8YFLogxK
M3 - Article
AN - SCOPUS:84859299156
SN - 1005-9040
VL - 28
SP - 4
EP - 8
JO - Chemical Research in Chinese Universities
JF - Chemical Research in Chinese Universities
IS - 1
ER -