Tetrazene

Source: Wikipedia, the free encyclopedia.
Not to be confused with Tetrazine, Tetracene, or Tetrazene explosive.
Tetrazene
Names
IUPAC name
(2E)-2-Tetraazene
Other names
(2E)-2-Tetraazen; Tetraaz-1-ene
Identifiers
3D model (
JSmol
)
ChemSpider
  • InChI=1S/H4N4/c1-3-4-2/h(H2,1,4)(H2,2,3); checkY
    Key: MAZKAODOCXYDCM-UHFFFAOYSA-N checkY
  • N/N=N/N
Properties
H4N4
Molar mass 60.060 g·mol−1
Related compounds
Related binary azanes
 Ammonia
Hydrazine
Triazane
Related compounds
Diazene
Triazene
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)

Tetrazene is a

trimethylsilyl.[1] Isomeric with tetrazine is ammonium azide
.

priming compositions
.

Properties

Tetrazene has eleven

standard heat of formation at 301.3 kJ/mol. The eleven isomers can be arranged into three groups: straight-chain tetrazenes, four-membered cyclotetrazane, and three-membered cyclotriazanes. Each straight-chain tetrazene isomer possesses one N=N double bond and two N-N single bonds.[2] Tautomerizations do occur between the isomers. The ionic compound ammonium azide
is also a constitutional isomer of tetrazene.

Organometallic derivatives

A variety of coordination complexes are known for R2N42- (R = methyl, benzyl).[3]

References

  1. ISBN 978-0-08-037941-8
    .
  2. ^
    doi:10.1016/j.theochem.2006.12.009
    .
  3. PMID 29620870
    .


Stub icon

This article about chemical compounds is a stub. You can help Wikipedia by expanding it.

Retrieved from "https://en.wikipedia.org/w/index.php?title=Tetrazene&oldid=1200791503"