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Hydrogen telluride

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Hydrogen telluride
Structural diagram of the hydrogen telluride molecule
Structural diagram of the hydrogen telluride molecule
Space-filling model of the hydrogen telluride molecule
Space-filling model of the hydrogen telluride molecule
Names
IUPAC name
hydrogen telluride
Other names
hydrotelluric acid
tellane
tellurium hydride
Identifiers
ECHA InfoCard 100.029.073 Edit this at Wikidata
Properties
H2Te
Molar mass 129.6158 g mol−1
Appearance colourless gas
Density 3.310 g/cm3, gas
2.57 g/cm3 (-20 °C, liquid)
Melting point −49 °C (224 K) ( [1]
Boiling point −2.2 °C (271.8 K)(unstable above -2 °C)
0.70 g/100 mL
Acidity (pKa) 2.6
Structure
bent
Thermochemistry
0.7684 kJ/g
Hazards
Occupational safety and health (OHS/OSH):
Main hazards
toxic
Related compounds
Other anions
H2O
H2S
H2Se
H2Po
Other cations
Na2Te
Ag2Te
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Hydrogen telluride (tellurane) is the inorganic compound with the formula H2Te. The simplest hydride of tellurium, it is rarely encountered because of it decomposes rapidly to the constituent elements. However, the gas can exist at very low concentrations long enough to be readily detected by the odour of rotting garlic or rotting leeks. Most compounds with Te-H bonds (tellurols) are unstable with respect to loss of H2. H2Te is chemically and structurally similar to hydrogen selenide, both are acidic. The H-Te-H angle is about 90°. Volatile tellurium compounds often have unpleasant odours, reminiscent of decayed leeks or garlic.[2]

Synthesis

H2Te is prepared by the acidification of salts of Te2−, such as Al2Te3 and Na2Te.[3] Na2Te can be generated by the reaction of Na and Te in anhydrous ammonia. The intermediate in the acidification, HTe
, is a stable anion. Sodium hydrogen telluride, NaHTe, can be made by reducing tellurium with NaBH
4
.[3]

Preparation

Tellurium hydrides is usually prepared in the laboratory by hydrolysis of the telluride derivatives of electropositive metals.[4] Typical is the hydrolysis of aluminum telluride:

Al2Te3 + 6 H2O → 2 Al(OH)3 + 3 H2Te

Magnesium and alkali metal tellurides can also be hydrolyzed. Usually these procedures require acid since the H2Te is rather acidic. Electrolytic methods have been developed.[5]

Properties

H
2
Te
is an endothermic compound, unstable in air and easily oxidised to water and elemental tellurium:[6]

2 H
2
Te
+ O
2
→ 2 H
2
O
+ 2 Te

It is almost as acidic as phosphoric acid (Ka = 8.1×10−3), having a Ka value of about 2.3×10−3.[6] It reacts with many metals to form tellurides.[7]

See also

References

  1. ^ Lide, David R., ed. (2006). CRC Handbook of Chemistry and Physics (87th ed.). Boca Raton, FL: CRC Press. ISBN 0-8493-0487-3.
  2. ^ Greenwood, N. N.; & Earnshaw, A. (1997). Chemistry of the Elements (2nd Edn.), Oxford:Butterworth-Heinemann. ISBN 0-7506-3365-4.
  3. ^ a b Nicola Petragnani; Hélio A. Stefani (2007). Tellurium in organic synthesis. Best synthetic methods (2nd ed.). Academic Press. p. 6. ISBN 0-08-045310-4.
  4. ^ Shriver, Atkins. Inorganic Chemistry, Fifth Edition. W. H. Freeman and Company, New York, 2010; pp 407.
  5. ^ F. Fehér, "Hydrogen Telluride" in Handbook of Preparative Inorganic Chemistry, 2nd Ed. Edited by G. Brauer, Academic Press, 1963, NY. Vol. 1. pp. 438.
  6. ^ a b Egon Wiberg; Arnold Frederick Holleman (2001). Nils Wiberg (ed.). Inorganic chemistry. Academic Press. p. 589. ISBN 0-12-352651-5. {{cite book}}: Unknown parameter |other= ignored (|others= suggested) (help)
  7. ^ Henry Enfield Roscoe; Carl Schorlemmer (1878). A treatise on chemistry. Vol. 1. Appleton. pp. 367–368.