Triazane is an inorganic compound with the chemical formula NH
2
NHNH
2
or N
3
H
5
.[2] Triazane is the third simplest acyclic azane after ammonia and hydrazine. It can be synthesized from hydrazine but is unstable and cannot be isolated in the free base form, only as salt forms such as triazanium sulfate. Attempts to convert triazanium salts to the free base release only diazene and ammonia. [3] Triazane was first synthesized as a ligand of the silver complex ion: tris(μ2-triazane-κ2N1,N3)disilver(2+). Triazane has also been synthesized in electron-irradiated ammonia ices and detected as a stable gas-phase product after sublimation.[4]

Triazane
Triazane.svg
Names
Systematic IUPAC name
Triazane[1]
Identifiers
3D model (JSmol)
ChemSpider
  • InChI=1S/H5N3/c1-3-2/h3H,1-2H2
    Key: PYHOFAHZHOBVGV-UHFFFAOYSA-N
  • NNN
Properties
N
3
H
5
Molar mass 47.0598 g·mol−1
Related compounds
Other anions
Triphosphane
Related Binary azanes
ammonia
diazane
Related compounds
Diazene
Triazene
Tetrazene
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references

Compounds containing the triazane skeletonEdit

Several compounds containing the triazane skeleton are known, including 1-methyl-1-nitrosohydrazine, produced from the solventless reaction of methylhydrazine and an alkyl nitrite:

CN
2
H
6
+ RNO
2
CN
3
H
5
O
+ ROH

1-Methyl-1-nitrosohydrazine is a colorless solid, sensitive to impact, but not to friction. It melts at 45°C and decomposes at 121°C.

ReferencesEdit

  1. ^ "triazane - PubChem Public Chemical Database". The PubChem Project. USA: National Center for Biotechnology Information.
  2. ^ IUPAC Goldbook
  3. ^ Wiberg, Holleman & Wiberg. Inorganic Chemistry. p 627. ISBN 9780123526519
  4. ^ Forstel, Maksyutenko, Jones, Sun, Chen, Chang, & Kaiser. "Detection of the Elusive Triazane Molecule ([N
    3
    H
    5
    ]
    ) in the Gas Phase", ChemPhysChem, 2015, 16, 3139.

External linksEdit