Rubidium azide

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Rubidium azide
File:Rubidium azide.svg
File:RbN3.png
Names
IUPAC name
Rubidium(1+);azide
Other names
Rubidium azide
Identifiers
3D model (JSmol)
ChemSpider
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  • [N-]=[N+]=[N-].[Rb+]
Properties
RbN3
Molar mass 127.49 g⋅mol−1
Appearance Colorless needles[1]
Density 2.79 g⋅cm−3[1][2]
Melting point 317–321 °C (603–610 °F; 590–594 K)[2][4]
Boiling point Decomposes
  • 107.1 g/100 g (16 °C)
  • 114.1 g/100 g (17 °C)[3]
Solubility 0.182 g/100 g (16 °C, ethanol)[3]
Thermochemistry
−0.1 kcal⋅mol−1[2]
Hazards
NFPA 704 (fire diamond)

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Related compounds
Other anions
Rubidium nitrate
Other cations
Lithium azide
Sodium azide
Potassium azide
Silver azide
Ammonium azide
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Rubidium azide is an inorganic compound with the formula RbN3. It is the rubidium salt of the hydrazoic acid HN3. Like most azides, it is explosive.[4]

Preparation

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Rubidium azide can be created by the reaction between rubidium sulfate and barium azide which results in formation of easily separated insoluble barium sulfate:[3]

Rb2SO4 + Ba(N3)2 → 2 RbN3 + BaSO4

In at least one study, rubidium azide was produced by the reaction between butyl nitrite, hydrazine monohydrate, and rubidium hydroxide in the presence of ethanol:

C4H9ONO + N2H4·H2O + RbOH → RbN3 + C4H9OH + 3 H2O

This formula is typically used to synthesize potassium azide from caustic potash.[5]

Rubidium azide has been investigated for possible use in alkali vapor cells, which are components of atomic clocks, atomic magnetometers and atomic gyroscopes. Azides are desirable starting materials because they decompose into rubidium metal and nitrogen gas when exposed to UV light. According to one publication:

Among the different techniques used to fill microfabricated alkali vapor cell [sic], UV decomposition of rubidium azide (RbN3) into metallic Rb and nitrogen in Al2O3 coated cells is a very promising approach for low-cost wafer-level fabrication.[6]

Structure

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At room temperature, rubidium azide has the same structure as potassium hydrogen fluoride; a distorted caesium chloride structure. At 315 °C and 1 atm, rubidium azide will transition to the normal caesium chloride structure. The II/I transition temperature of rubidium azide is within 2 °C of its melting point.[4]

Rubidium azide has a high pressure structure transition, which occurs at about 4.8 kilobars of pressure at 0 °C. The transition boundary of the II/III transition can be defined by the relationship P=4.82+0.0240t, where P is the pressure in kilobars and t is the temperature in degrees Celsius.[4]

Reactions

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As with all azides, it will decompose and release nitrogen gas when heated or severely shocked:

2 RbN3 → 2 Rb + 3 N2

Discharge rubidium azide in nitrogen gas will produce rubidium nitride.[7]

Hazards

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At 4.1 kilobars of pressure and about 460 °C, rubidium azide will explosively decompose.[4] Under normal circumstances, it explodes at 395 °C.[2] It also decomposes upon exposure to ultraviolet light.[6]

Rubidium azide is very sensitive to mechanical shock, with an impact sensitivity comparable to that of TNT.[8]

Like all azides, rubidium azide is toxic.

References

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