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Di(1H-tetrazol-5-yl)methane as Neutral Ligand in Energetic Transition Metal Complexes.
Freis, Manuel; Klapötke, Thomas M; Stierstorfer, Jörg; Szimhardt, Norbert.
Afiliação
  • Freis M; Energetic Materials Research, Department of Chemistry, University of Munich (LMU) , Butenandtstr. 5-13, D-81377, Munich, Germany.
  • Klapötke TM; Energetic Materials Research, Department of Chemistry, University of Munich (LMU) , Butenandtstr. 5-13, D-81377, Munich, Germany.
  • Stierstorfer J; Energetic Materials Research, Department of Chemistry, University of Munich (LMU) , Butenandtstr. 5-13, D-81377, Munich, Germany.
  • Szimhardt N; Energetic Materials Research, Department of Chemistry, University of Munich (LMU) , Butenandtstr. 5-13, D-81377, Munich, Germany.
Inorg Chem ; 56(14): 7936-7947, 2017 Jul 17.
Article em En | MEDLINE | ID: mdl-28653835
ABSTRACT
The synthesis of di(1H-tetrazol-5-yl)methane (1, 5-DTM), starting from commercially available sodium azide and malononitrile, is described. This tetrazole was characterized and investigated for use as a neutral nitrogen-rich ligand in various energetic transition metal complexes ([CuCl2(5-DTM)2]·2H2O (2), [Co(H2O)2(5-DTM)2]Cl2 (3), [Ni(H2O)2(5-DTM)2]Cl2 (4), [Co(H2O)2(5-DTM)2](NO3)2 (6), [Ni(H2O)2(5-DTM)2](NO3)2 (7), [Zn(H2O)2(5-DTM)2](NO3)2 (8), {[Cu3(SO4)2(5-DTM-H)2(H2O)4(5-DTM)2]·2H2O}∞ (9), [Cu(H2O)2(5-DTM)2](NO3)2 (11), [Cu(NO3)2(5-DTM)2]·2H2O (12), [Cu(NO3)2(5-DTM)2] (13), [Cu(H2O)2(5-DTM)2](ClO4)2 (14), and [Cu(ClO4)2(5-DTM)2] (15). Obtained coordination compounds were characterized using single crystal X-ray diffraction (except for 7 and 13), IR spectroscopy, elemental analysis, and differential thermal analysis. The sensitivities to external stimuli (impact, friction, electrostatic discharge) were determined. Complexes 12 and 13 were tested for their ignitability by laser irradiation.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2017 Tipo de documento: Article