An efficient method to synthesize TNAD by the nitration of 1,4,5,8-tetraazabicyclo-[4,4,0]-decane with N2O5 and acidic ionic liquids
English
An efficient method to synthesize TNAD by the nitration of 1,4,5,8-tetraazabicyclo-[4,4,0]-decane with N2O5 and acidic ionic liquids
-
Key words:
- 1,4,5,8-Tetraazabicyclo-[4,4,0]-decane
- / N2O5
- / Inert solvent
- / Acidic ionic liquids
- / TNAD
-
-
-
[1] R.L. Willer, Synthesis and characterization of high energy compounds TNAD, Chin. J. Explos. Propell. 8 (1983) 65-69.[1] R.L. Willer, Synthesis and characterization of high energy compounds TNAD, Chin. J. Explos. Propell. 8 (1983) 65-69.
-
[2] Q.L. Yan, X.J. Li, Y. Wang, W.H. Zhang, F.Q. Zhao, Combustion mechanism of double-base propellant containing nitrogen heterocyclic nitroamines: the effect of heat and mass transfer to the burning characteristics, Combust. Flame 156 (2009) 633-641.[2] Q.L. Yan, X.J. Li, Y. Wang, W.H. Zhang, F.Q. Zhao, Combustion mechanism of double-base propellant containing nitrogen heterocyclic nitroamines: the effect of heat and mass transfer to the burning characteristics, Combust. Flame 156 (2009) 633-641.
-
[3] L. Qiu, W.H. Zhu, J.J. Xiao, Molecule dynamics simulations of trans-1,4,5,8-tetranitro-1,4,5,8-tetraazadecalin-based polymer-bonded explosives, J. Phys. Chem. B. 111 (2006) 1559-1566.[3] L. Qiu, W.H. Zhu, J.J. Xiao, Molecule dynamics simulations of trans-1,4,5,8-tetranitro-1,4,5,8-tetraazadecalin-based polymer-bonded explosives, J. Phys. Chem. B. 111 (2006) 1559-1566.
-
[4] Q.L. Yan, X.J. Li, L.Y. Zhang, Compatibility study of trans-1,4,5,8-tetranitro-1,4,5,8-tetraazadecalin(TNAD) with some energetic components and inert materials, J. Hazard. Mater. 160 (2008) 529-534.[4] Q.L. Yan, X.J. Li, L.Y. Zhang, Compatibility study of trans-1,4,5,8-tetranitro-1,4,5,8-tetraazadecalin(TNAD) with some energetic components and inert materials, J. Hazard. Mater. 160 (2008) 529-534.
-
[5] S. Zeman, Z. Friedl, A new approach to the application of molecular surface electrostatic potential in the study of detonation, Propell. Explos. Pyrot. 37 (2012) 609-613.[5] S. Zeman, Z. Friedl, A new approach to the application of molecular surface electrostatic potential in the study of detonation, Propell. Explos. Pyrot. 37 (2012) 609-613.
-
[6] Y.Y. Wei, M. Lu, C.X. Lü, Z. Li, Study on synthetic technology of TNAD, in: Theory and Practice of Energetic Materials, Beijing University of Science and Technology, Beijing, 1996.[6] Y.Y. Wei, M. Lu, C.X. Lü, Z. Li, Study on synthetic technology of TNAD, in: Theory and Practice of Energetic Materials, Beijing University of Science and Technology, Beijing, 1996.
-
[7] C. Cai, C.X. Lü, Nitrolysis with nitrogen pentoxide for synthesis of 1,4,5,8-teranitro-1,4,5,8-tetraazabicyclo-[4,4,0]-decalin, Chin. J. Explos. Propell. 28 (2005) 50-51.[7] C. Cai, C.X. Lü, Nitrolysis with nitrogen pentoxide for synthesis of 1,4,5,8-teranitro-1,4,5,8-tetraazabicyclo-[4,4,0]-decalin, Chin. J. Explos. Propell. 28 (2005) 50-51.
-
[8] M. Lu, C.X. Lü, The improvement of technology for synthesising 1 4,6,9-tetranitro-1,4,6,9-tetraazabicyclo-[4,4,0]-decane, J. Nanjing Univ. Sci. Technol. 21 (1997) 110-113.[8] M. Lu, C.X. Lü, The improvement of technology for synthesising 1 4,6,9-tetranitro-1,4,6,9-tetraazabicyclo-[4,4,0]-decane, J. Nanjing Univ. Sci. Technol. 21 (1997) 110-113.
-
[9] R.W. Millar, S.P. Philbin, Novel syntheses of nitramines and nitrate esters by nitrodesilylation reactions using dinitrogen pentoxide(N2O5), Tetrahedron 53 (1997) 4371-4386.[9] R.W. Millar, S.P. Philbin, Novel syntheses of nitramines and nitrate esters by nitrodesilylation reactions using dinitrogen pentoxide(N2O5), Tetrahedron 53 (1997) 4371-4386.
-
[10] M.B. Talawar, R. Sivabalan, B.G. Polke, et al., Establishment of process technology for the manufacture of dinitrogen pentoxide and its utility for the synthesis of most powerful explosive of today-CL-20, J. Hazard. Mater. 124 (2005) 153-164.[10] M.B. Talawar, R. Sivabalan, B.G. Polke, et al., Establishment of process technology for the manufacture of dinitrogen pentoxide and its utility for the synthesis of most powerful explosive of today-CL-20, J. Hazard. Mater. 124 (2005) 153-164.
-
[11] H.Z. Zhi, J. Luo, J.A. Feng, C.X. Lü, An efficient method to synthesize HMX by nitrolysis of DPT with N2O5 and a novel ionic liquid, Chin. Chem. Lett. 20 (2009) 379-382.[11] H.Z. Zhi, J. Luo, J.A. Feng, C.X. Lü, An efficient method to synthesize HMX by nitrolysis of DPT with N2O5 and a novel ionic liquid, Chin. Chem. Lett. 20 (2009) 379-382.
-
[12] G.B. Cheng, X.F. Qi, C.X. Lü, Synthesis of RDX catalyzed by Bronsted acidic ionic liquids, J. Energy Mater. 28 (2010) 35-44.[12] G.B. Cheng, X.F. Qi, C.X. Lü, Synthesis of RDX catalyzed by Bronsted acidic ionic liquids, J. Energy Mater. 28 (2010) 35-44.
-
[13] N.L. Lancaster, V. Llopis-Mester, Aromatic nitrations in ionic liquids: the importance of cation choice, Chem. Commun. 22 (2003) 2812-2813.[13] N.L. Lancaster, V. Llopis-Mester, Aromatic nitrations in ionic liquids: the importance of cation choice, Chem. Commun. 22 (2003) 2812-2813.
-
[14] M.J. Earle, S.P. Katdare, K.R. Seddon, Paradigm confirmed: the first use of ionic liquids to dramatically influence the outcome of chemical reactions, Org. Lett. 6 (2004) 707-710.[14] M.J. Earle, S.P. Katdare, K.R. Seddon, Paradigm confirmed: the first use of ionic liquids to dramatically influence the outcome of chemical reactions, Org. Lett. 6 (2004) 707-710.
-
[15] K. Smith, S.F. Liu, G.A. EL-Hiti, Regioselective mononitration of simple aromatic compounds under mild conditions in ionic liquids, Ind. Eng. Chem. Res. 44 (2005) 8611-8615.[15] K. Smith, S.F. Liu, G.A. EL-Hiti, Regioselective mononitration of simple aromatic compounds under mild conditions in ionic liquids, Ind. Eng. Chem. Res. 44 (2005) 8611-8615.
-
[16] K.K. Laali, J.V. Gettwert, Electrophilic nitration of aromatics in ionic liquid solvents, J. Org. Chem. 66 (2001) 35-40.[16] K.K. Laali, J.V. Gettwert, Electrophilic nitration of aromatics in ionic liquid solvents, J. Org. Chem. 66 (2001) 35-40.
-
[17] K. Qiao, C. Yokoyama, Nitration of aromatic compounds with nitric acid catalyzed by ionic liquids, Chem. Lett. 33 (2004) 808-810.[17] K. Qiao, C. Yokoyama, Nitration of aromatic compounds with nitric acid catalyzed by ionic liquids, Chem. Lett. 33 (2004) 808-810.
-
[18] R.R. Bak, A.J. Smallridge, A fast and mild method for the nitration of aromatic rings, Tetrahedron Lett. 42 (2001) 6767-6769.[18] R.R. Bak, A.J. Smallridge, A fast and mild method for the nitration of aromatic rings, Tetrahedron Lett. 42 (2001) 6767-6769.
-
[19] X.F. Qi, G.B. Cheng, C.X. Lü, Nitration of toluene with nitric acid in the presence of acidic ionic liquid, Chin. J. Energy Mater. 16 (2008) 398-400.[19] X.F. Qi, G.B. Cheng, C.X. Lü, Nitration of toluene with nitric acid in the presence of acidic ionic liquid, Chin. J. Energy Mater. 16 (2008) 398-400.
-
[20] G.B. Cheng, D.S. Qian, C.X. Lü, Nitration of simple aromatics with NO2 under air atmosphere in the presence of novel Bronsted acidic ionic liquids, Synth. Comm. 38 (2008) 537-545.[20] G.B. Cheng, D.S. Qian, C.X. Lü, Nitration of simple aromatics with NO2 under air atmosphere in the presence of novel Bronsted acidic ionic liquids, Synth. Comm. 38 (2008) 537-545.
-
[21] M.G. Kuba, R. Prins, G.D. Pirngruber, Gas-phase nitration of toluene with zeolite beta, Appl. Catal. A 333 (2007) 78-89.[21] M.G. Kuba, R. Prins, G.D. Pirngruber, Gas-phase nitration of toluene with zeolite beta, Appl. Catal. A 333 (2007) 78-89.
-
[22] B. Barletta, E. Bolzacchini, S. Meinardi, M. Orlandi, B. Rindone, The NO3 radicalmediated liquid phase nitration of phenols with nitrogen dioxide, Environ. Sci. Technol. 34 (2000) 2224-2230.[22] B. Barletta, E. Bolzacchini, S. Meinardi, M. Orlandi, B. Rindone, The NO3 radicalmediated liquid phase nitration of phenols with nitrogen dioxide, Environ. Sci. Technol. 34 (2000) 2224-2230.
-
-
扫一扫看文章
计量
- PDF下载量: 0
- 文章访问数: 1417
- HTML全文浏览量: 34

下载: