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Hydrazinium azide

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Hydrazinium azide
Names
IUPAC name
Hydrazinium azide
Identifiers
3D model (JSmol)
  • InChI=1S/N3.H4N2/c1-3-2;1-2/h;1-2H2/q-1;/p+1
    Key: UZXHZRFWCCZBDW-UHFFFAOYSA-O
  • N[NH3+].[N-]=[N+]=[N-]
Properties
H5N5
Molar mass 75.075 g·mol−1
Appearance White solid
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Hydrazinium azide or hydrazine azide is a chemical compound with formula H
5
N
5
or [N
2
H+
5
]
[N
3
]
. It is a salt of the hydrazinium cation N
2
H+
5
and the azide anion N
3
. It can be seen as a derivative of hydrazine N
2
H
4
and hydrazoic acid HN
3
. It is an unstable solid.

The compound is of scientific interest because of its high nitrogen content (93% nitrogen by weight) and explosive properties.[1]

Structure

[edit]

The solid undergoes structural phase transition to a different crystalline arrangement at a pressure of 13 GPa.[2]

Chemistry

[edit]

Hydrazinium azide decomposes explosively into hydrazine, ammonia, and nitrogen gas:[3]

12 N
5
H
5
→ 3 N
2
H
4
+ 16 NH
3
+ 19 N
2

Crystallization with an equimolar amount hydrazine yields the solid hydrazinium azide hydrazinate, [N
2
H+
5
]
[N
3
]
·[N
2
H
4
]
, or N
7
H
9
, as monoclinic crystals. This compound is less hygroscopic and less volatile than pure hydrazinium azide. It decomposes explosively into nitrogen, hydrogen, and ammonia.[4]

At pressure of 40 GPa, hydrazinium azide decomposes yielding a linear nitrogen allotrope N
8
or N≡+NN−N=N−N+N≡N, that decomposes to ε-N2 below 25 GPa.[2]

Reaction of hydrazinium azide with sulfuric acid gives quantitative yields of pure hydrazinediium sulfate and hydrazoic acid:[5]

[N
2
H+
5
][N
3
] + H2SO4 → [N
2
H2+
6
][SO2−
4
] + HN3

See also

[edit]

References

[edit]
  1. ^ Chiglien, G.; Etienne, J.; Jaulmes, S.; Laruelle, P. (15 September 1974). "Structure cristalline de l'azoture d'hydrazinium, N5H5". Acta Crystallographica Section B. 30 (9): 2229–2233. doi:10.1107/S0567740874006790.
  2. ^ a b Duwal, Sakun; Ryu, Young-Jay; Kim, Minseob; Yoo, Choong-Shik; Bang, Sora; Kim, Kyungtae; Hur, Nam Hwi (7 April 2018). "Transformation of hydrazinium azide to molecular N8 at 40 GPa". The Journal of Chemical Physics. 148 (13): 134310. Bibcode:2018JChPh.148m4310D. doi:10.1063/1.5021976. OSTI 1432864. PMID 29626901.
  3. ^ G. B. Manelis (2003). Thermal decomposition and combustion of explosives and propellants. CRC Press. p. 235. ISBN 0-415-29984-5.
  4. ^ Hammerl, Anton; Klapötke, Thomas M.; Piotrowski, Holger; Holl, Gerhard; Kaiser, Manfred (2001). "Synthesis and Characterization of Hydrazinium Azide Hydrazinate". Propellants, Explosives, Pyrotechnics. 26 (4): 161–164. doi:10.1002/1521-4087(200110)26:4<161::AID-PREP161>3.0.CO;2-O.
  5. ^ Klapötke, T.; Peter S. White; Inis C. Tornieporth-Oetting (1996). "Reaction of hydrazinium azide with sulfuric acid: the X-ray structure of [N
    2
    H
    6
    ][SO
    4
    ]
    ". Polyhedron. 15 (15): 2579–2582. doi:10.1016/0277-5387(95)00527-7.