Tellurium tetraazide

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Tellurium tetraazide
Names
IUPAC name
Tellurium(IV) tetraazide
Other names
Tellurium tetraazide
Identifiers
3D model (JSmol)
PubChem CID
  • InChI=1S/N12Te/c1-5-9-13(10-6-2,11-7-3)12-8-4
    Key: UGNSLJQACMUEMZ-UHFFFAOYSA-N
  • [N-]=[N+]=N\[Te](\N=[N+]=[N-])(\N=[N+]=[N-])\N=[N+]=[N-]
Properties
Te(N3)4
Molar mass 295.7 g/mol
AppearanceYellow solid
Related compounds
Related compounds
[Te(N3)3][SbF6];
[Me4N][Te(N3)5]
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Tellurium tetraazide is an inorganic chemical compound with the formula Te(N3)4. It is a highly sensitive explosive and takes the form of a yellow solid. It has been prepared directly as a precipitate of the reaction between tellurium tetrafluoride and trimethylsilyl azide. [1]

Related Research Articles

<span class="mw-page-title-main">Tellurium</span> Chemical element, symbol Te and atomic number 52

Tellurium is a chemical element with the symbol Te and atomic number 52. It is a brittle, mildly toxic, rare, silver-white metalloid. Tellurium is chemically related to selenium and sulfur, all three of which are chalcogens. It is occasionally found in its native form as elemental crystals. Tellurium is far more common in the Universe as a whole than on Earth. Its extreme rarity in the Earth's crust, comparable to that of platinum, is due partly to its formation of a volatile hydride that caused tellurium to be lost to space as a gas during the hot nebular formation of Earth.

In chemistry, azide is a linear, polyatomic anion with the formula N−3 and structure N=N+=N. It is the conjugate base of hydrazoic acid HN3. Organic azides are organic compounds with the formula RN3, containing the azide functional group. The dominant application of azides is as a propellant in air bags.

<span class="mw-page-title-main">Sodium azide</span> Chemical compound

Sodium azide is an inorganic compound with the formula NaN3. This colorless salt is the gas-forming component in some car airbag systems. It is used for the preparation of other azide compounds. It is an ionic substance, is highly soluble in water, and is very acutely poisonous.

<span class="mw-page-title-main">Silver azide</span> Chemical compound

Silver azide is the chemical compound with the formula AgN3. It is a silver(I) salt of hydrazoic acid. It forms a colorless crystals. Like most azides, it is a primary explosive.

<span class="mw-page-title-main">Thallium azide</span> Chemical compound

Thallium azide, TlN3, is a yellow-brown crystalline solid poorly soluble in water. Although it is not nearly as sensitive to shock or friction as lead azide, it can easily be detonated by a flame or spark. It can be stored safely dry in a closed non-metallic container.

<span class="mw-page-title-main">Copper(II) azide</span> Chemical compound

Copper(II) azide is a medium density explosive with the molecular formula Cu(N3)2.

<span class="mw-page-title-main">Ammonium azide</span> Chemical compound

Ammonium azide is the chemical compound with the formula [NH4]N3, being the salt of ammonia and hydrazoic acid. Like other inorganic azides, this colourless crystalline salt is a powerful explosive, although it has a remarkably low sensitivity. [NH4]N3 is physiologically active and inhalation of small amounts causes headaches and palpitations. It was first obtained by Theodor Curtius in 1890, along with other azides.

<span class="mw-page-title-main">Potassium azide</span> Chemical compound

Potassium azide is the inorganic compound having the formula KN3. It is a white, water-soluble salt. It is used as a reagent in the laboratory.

<span class="mw-page-title-main">Lithium azide</span> Chemical compound

Lithium azide is the lithium salt of hydrazoic acid. It is an unstable and toxic compound that decomposes into lithium and nitrogen when heated.

Barium azide is an inorganic azide with the formula Ba(N3)2. It is a barium salt of hydrazoic acid. Like most azides, it is explosive. It is less sensitive to mechanical shock than lead azide.

<span class="mw-page-title-main">Chlorine azide</span> Chemical compound

Chlorine azide is an inorganic compound that was discovered in 1908 by Friedrich Raschig. Concentrated ClN3 is notoriously unstable and may spontaneously detonate at any temperature.

<span class="mw-page-title-main">Bromine azide</span> Chemical compound

Bromine azide is an explosive inorganic compound with the formula BrN3. It has been described as a crystal or a red liquid at room temperature. It is extremely sensitive to small variations in temperature and pressure, with explosions occurring at Δp ≥ 0.05 Torr and also upon crystallization, thus extreme caution must be observed when working with this chemical.

<span class="mw-page-title-main">Fluorine azide</span> Chemical compound

Fluorine azide or triazadienyl fluoride is a yellow green gas composed of nitrogen and fluorine with formula FN3. Its properties resemble those of ClN3, BrN3, and IN3. The bond between the fluorine atom and the nitrogen is very weak, leading to this substance being very unstable and prone to explosion. Calculations show the F–N–N angle to be around 102° with a straight line of 3 nitrogen atoms.

Tellurium nitride describes chemical compounds of Te containing N3−. Efforts have been made toward the binary nitrides but the results are inconclusive and it appears that such materials are unstable. Still unconfirmed is Te4N4, which would be an analogue of tetraselenium tetranitride (Se4N4) and tetrasulfur tetranitride (S4N4). It has long been known that ammonia reacts with tellurium tetrachloride, which is similar to the method of synthesis of S4N4. The reaction of TeCl4 with a THF solution of N(SiMe3)3 gives a well-defined tellurium nitride [Te6N8(TeCl2)4(THF)4].

<span class="mw-page-title-main">Rubidium azide</span> Chemical compound

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.

<span class="mw-page-title-main">Zinc azide</span> Chemical compound

Zinc azideZn(N3)2 is an inorganic compound composed of zinc cations (Zn2+) and azide anions (N−3). It is a white, explosive solid that can be prepared by the protonolysis of diethylzinc with hydrazoic acid:

<span class="mw-page-title-main">Caesium azide</span> Chemical compound

Caesium azide or cesium azide is an inorganic compound of caesium and nitrogen. It is a salt of azide with the formula CsN3.

<span class="mw-page-title-main">Transition metal azide complex</span>

Transition metal azide complexes are coordination complexes containing one or more azide (N3) ligands.

Homoleptic azido compounds are chemical compounds in which the only anion or ligand is the azide group, -N3. The breadth of homoleptic azide compounds spans nearly the entire periodic table. With rare exceptions azido compounds are highly shock sensitive and need to be handled with the upmost caution. Binary azide compounds can take on several different structures including discrete compounds, or one- two, and three-dimensional nets, leading some to dub them as "polyazides". Reactivity studies of azide compounds are relatively limited due to how sensitive they can be. The sensitivity of these compounds tends to be correlated with the amount of ionic or covalent character the azide-element bond has, with ionic character being far more stable than covalent character. Therefore, compounds such as silver or sodium azide – which have strong ionic character – tend to possess more synthetic utility than their covalent counterparts. A few other notable exceptions include polymeric networks which possess unique magnetic properties, group 13 azides which unlike most other azides decompose to nitride compounds (important materials for semiconductors), other limited uses as synthetic reagents for the transfer for azide groups, or interest in high energy density materials.

References

  1. Klapötke, Thomas M.; Krumm, Burkhard; Mayer, Peter; Schwab, Ingo (8 December 2003). "Binary Tellurium(IV) Azides: Te(N3)4 and [Te(N3)5]". Angewandte Chemie. 42 (47): 5843–5846. doi:10.1002/anie.200352656 . Retrieved 3 November 2023.