| Names | |
|---|---|
|  IUPAC name  Silver(I) azide  | |
| Other names  Argentous azide  | |
| Identifiers | |
3D model (JSmol)  | |
| ChemSpider | |
| ECHA InfoCard | 100.034.173 | 
 PubChem CID  | |
| UNII | |
 CompTox Dashboard (EPA)  | |
  | |
  | |
| Properties | |
| AgN3 | |
| Molar mass | 149.888 g/mol | 
| Appearance | colorless crystals | 
| Density | 4.42 g/cm3 | 
| Melting point | 250 °C (482 °F; 523 K) explosive | 
| Boiling point | decomposes | 
| Solubility in other solvents | 2.0×10−8 g/L | 
| Structure | |
| Orthorhombic oI16 [1] | |
| Ibam, No 72 | |
| Hazards | |
| Occupational safety and health (OHS/OSH): | |
Main hazards  | Very toxic, explosive | 
| NFPA 704 (fire diamond) | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).  | |
Silver azide is the chemical compound with the formula AgN3. It is a silver(I) salt of hydrazoic acid. It forms colorless crystals. Like most azides, it is a primary explosive.
Silver azide can be prepared by treating an aqueous solution of silver nitrate with sodium azide. [2] The silver azide precipitates as a white solid, leaving sodium nitrate in solution.
X-ray crystallography shows that AgN3 is a coordination polymer with square planar Ag+ coordinated by four azide ligands. Correspondingly, each end of each azide ligand is connected to a pair of Ag+ centers. The structure consists of two-dimensional AgN3 layers stacked one on top of the other, with weaker Ag–N bonds between layers. The coordination of Ag+ can alternatively be described as highly distorted 4 + 2 octahedral, the two more distant nitrogen atoms being part of the layers above and below. [3]
|   |   |   |   | 
| Part of a layer | Layer stacking | 4 + 2 coordination of Ag+ | 2 + 1 coordination of N in N−3 | 
In its most characteristic reaction, the solid decomposes explosively, releasing nitrogen gas:
The first step in this decomposition is the production of free electrons and azide radicals; thus the reaction rate is increased by the addition of semiconducting oxides. [4] Pure silver azide explodes at 340 °C, but the presence of impurities lowers this down to 270 °C. [5] This reaction has a lower activation energy and initial delay than the corresponding decomposition of lead azide. [6]
AgN3, like most heavy metal azides, is a dangerous primary explosive. Decomposition can be triggered by exposure to ultraviolet light or by impact. [2] Ceric ammonium nitrate [NH4]2[Ce(NO3)6] is used as an oxidising agent to destroy AgN3 in spills. [5]
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