Sodium telluride


Sodium telluride
Sodium telluride
Identifiers
CAS number 12034-41-2
Properties
Molecular formula Na2Te
Molar mass 173.58 g/mol
Appearance white powder,
hygroscopic
Density 2.90 g/cm3, solid
Melting point

953°C

Solubility in water very soluble
Hazards
EU classification not listed
NFPA 704
NFPA 704.svg
0
2
1
 YesY telluride (verify) (what is: YesY/N?)
Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa)
Infobox references

Sodium telluride is the chemical compound with the formula Na2Te. This salt is the conjugate base of the thermally unstable acid hydrogen telluride, but it is usually prepared by reduction of tellurium with sodium. Na2Te is a challenging material to handle because it is very sensitive to air. Air oxidizes it initially to polytellurides, which have the formula Na2Tex (x > 1), and ultimately Te metal. Samples of Na2Te, which are colourless when absolutely pure, generally appear purple or gray due to the effects of air oxidation.

Synthesis, structure, and solution properties

The synthesis is typically conducted using ammonia as the solvent.

Na2Te, like many related compounds with the formula M2X, adopts the antifluorite structure. Thus, in solid Na2Te each Te2− ion is surrounded by eight Na+ ions and each Na+ ion is surrounded by four Te2− ions.[1]

Simple salts of the type M2X, where X is a monoatomic anion, are not typically soluble in any solvent because they have a high lattice energy. Upon addition of water - even moist air - or treatment with alcohols, Te2− protonates:

Na2Te + H2O → NaHTe + NaOH

Because of this reaction, many processes attributed to Na2Te may involve NaHTe (CAS # 65312-92-7), which is more soluble and formed readily.

Applications in organic chemistry

Na2Te finds use in organic synthesis, both as a reagent for reductions and as a source of Te in the synthesis of organotellurium compounds.[2] Aryl halides are substituted to diaryl tellurides, as illustrated by the synthesis of dinaphthyltelluride:

Na2Te + 2 C10H7I → (C10H7)2Te + 2 NaI

Na2Te reacts with 1,3-diynes to give the corresponding tellurophene, which are structurally analogous to thiophenes:

Na2Te + RC≡C-C≡CR + 2 H2O → TeC4R2H2 + 2 NaOH

As a reducing agent, Na2Te converts nitro groups to amines and will cleave certain C-X bonds.[2]

References

  1. ^ Wells, A.F. (1984) Structural Inorganic Chemistry, Oxford: Clarendon Press. ISBN 0-19-855370-6.
  2. ^ a b ”Sodium Telluride” Dittmer, D. C. in Encyclopedia of Reagents for Organic Synthesis © 2001. DOI: 10.1002/047084289X.rs103.



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