Sheldrick G M. SHELXL-97, Program for the Refining of Crystal Structure[M]. University of Gttingen, Germany, 1997.
[2]
Chavez D E, Hiskey M A, Gilardi R D. 3,3-Azobis(6-amino-1,2,4,5-tetrazine): a novel high-nitrogen energetic material[J]. Angew Chem Int Ed, 2000, 39: 1791-1793.
[3]
Kerth J, Lbbecke S. Synthesis and characterization of 3,3-azobis(6-amino-1,2,4,5-tetrazine) DAAT-a new promising nitrogen-rich compound[J]. Propellants Explos Pyrotech, 2002, 27: 111-118.
[4]
Neutz J, Grosshardt O, Schaufele S, et al. Synthesis, characterization and thermal behaviour of guanidinium-5-aminotetrazolate (GA)-a new nitrogen-rich compound[J]. Propellants Explos Pyrotech, 2003, 28: 181-188.
[5]
Ciezak J A, Trevino S F. The inelastic neutron scattering spectra of a-3-amino-5-nitro-1,2,4-2H-triazole: experiment and DFT calculations[J]. Chem Phys Lett, 2005, 403: 329-333.
[6]
Levchik S V, Balabanovich A I, Ivashkevich O A, et al. The thermal decomposition of aminotetrazoles. II. 1-Methyl-5-aminotetrazole and 1,5-diaminotetrazole[J]. Thermochim Acta, 1993, 225: 53-65.
[7]
Lesnikovich A I, Ivashkevich O A, Levchik S V, et al. Thermal decomposition of aminotetrazoles[J]. Thermochim Acta, 2002, 388: 233-251.
[8]
Audebert P, Sadki S, Miomandre F, et al. New functionalized tetrazines: synthesis, electrochemical and spectroscopic properties[J]. New J Chem, 2004, 28: 387-392.
[9]
Hu W X, Rao G W, Sun Y Q. Synthesis and antitumor activity of s-tetrazine derivatives[J]. Bioorganic & Medicinal Chemistry Letters, 2004, 14: 1177-1181.
[10]
Saikia A, Sivabalan R, Polke B G, et al. Synthesis and characterization of 3,6-bis(1H-1,2,3,4-tetrazol-5-ylamino)-1,2,4,5-tetrazine (BTATz): Novel high-nitrogen content insensitive high energy material[J]. Journal of Hazardous Materials, 2009, 170: 306-313.
[11]
Shawali A S, Elsheikh S M. Annelated[1,2,4,5]tetrazines[J]. J Heterocycl Chem, 2001, 38: 541-559.
[12]
Sheldrick G M. SHELXS-97, Program for the Solution of Crystal Structure[M]. University of Gttingen, Germany, 1997.
