Electrolytic methods have been developed.2
H2Te can also be prepared by hydrolysis of the telluride derivatives of electropositive metals.3 The typical hydrolysis is that of aluminium telluride:
Other salts of Te2− such as MgTe and sodium telluride can also be used. Na2Te can be made by the reaction of Na and Te in anhydrous ammonia.4 The intermediate in the hydrolysis, HTe−, can be isolated as salts as well. NaHTe can be made by reducing tellurium with NaBH4.5
Hydrogen telluride cannot be efficiently prepared from its constituent elements, in contrast to H2Se.6
H2Te is an endothermic compound, degrading to the elements at room temperature:
Light accelerates the decomposition. It is unstable in air, being oxidized to water and elemental tellurium:7
It is almost as acidic as phosphoric acid (Ka = 8.1×10−3), having a Ka value of about 2.3×10−3.8 It reacts with many metals to form tellurides.9
Greenwood, N. N.; & Earnshaw, A. (1997). Chemistry of the Elements (2nd Edn.), Oxford:Butterworth-Heinemann. ISBN 0-7506-3365-4. /wiki/ISBN_(identifier) ↩
F. Fehér, "Hydrogen Telluride" in Handbook of Preparative Inorganic Chemistry, 2nd Ed. Edited by G. Brauer, Academic Press, 1963, NY. Vol. 1. pp. 438. ↩
Shriver, Atkins. Inorganic Chemistry, Fifth Edition. W. H. Freeman and Company, New York, 2010; pp 407. ↩
Nicola Petragnani; Hélio A. Stefani (2007). Tellurium in organic synthesis. Best synthetic methods (2nd ed.). Academic Press. p. 6. ISBN 978-0-08-045310-1. 978-0-08-045310-1 ↩
Egon Wiberg; Arnold Frederick Holleman (2001). Nils Wiberg (ed.). Inorganic chemistry. Translated by Mary Eagleson. Academic Press. p. 589. ISBN 0-12-352651-5. 0-12-352651-5 ↩
Henry Enfield Roscoe; Carl Schorlemmer (1878). A treatise on chemistry. Vol. 1. Appleton. pp. 367–368. ↩