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Ammonium selenide

From Wikipedia, the free encyclopedia
Ammonium selenide[1]
Names
Other names
  • Dimmonium selenide
Identifiers
3D model (JSmol)
  • InChI=1S/2H3N.Se/h2*1H3;/q;;-2/p+2
    Key: JISUIHCFTLLJLJ-UHFFFAOYSA-P
  • [NH4+].[NH4+].[Se-2]
Properties
(NH4)2Se
Molar mass 115.05 g/mol
Appearance White solid
Reacts
Solubility Soluble in sodium hydroxide[2]
Structure
Orthorhombic
Related compounds
Other anions
Ammonium sulfide
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Ammonium selenide is a chemical compound with the symbol (NH4)2Se. It is claimed to be a white solid and there is little to no spectroscopic evidence on this compound.[1][2]

Preparation

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It was first claimed to be prepared in 1898 by reacting concentrated ammonia and hydrogen selenide gas.[1] However, this has been disproved in 1926 as it was shown that ammonium selenide was unstable in water. Instead, ammonium selenide was produced by the reaction of anhydrous ammonia and hydrogen selenide gas(made from the reaction of iron(II) selenide and hydrochloric acid). However, there is no X-ray crystallography on this compound.[2]

Reactions

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Ammonium selenide reacts with water and various acids. For example, it reacts with nitric acid to form selenous acid.[3] It also reacts with various metals, such as calcium, to produce their respective selenides.[4]

References

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  1. ^ a b c Victor Lenher; Edgar F. Smith (1898). "Ammonium Selenide". Journal of the American Chemical Society. 20 (4). ACS Publications: 277–278. doi:10.1021/ja02066a007. Retrieved 15 March 2021.
  2. ^ a b c Wendehorst, Erwin (1926). "Über das Ammoniumselenid". Zeitschrift für anorganische und allgemeine Chemie (in German). 153 (1): 263–268. doi:10.1002/zaac.19261530124.
  3. ^ Wendehorst 1926, p. 268: "Salz- und Schwefelsäure bewirken augenblicklichen Zerfall; Salpetersäure und andere Oxydationsmittel oxydieren weiter zu H2SeO3 bzw. H2SeO4." [Hydrochloric and sulfuric acids effect instantaneous decomposition; nitric acid and other oxidizers oxidize further to H2SeO3 or resp. H2SeO4.]
  4. ^ T. Petze; J. Kohle (1977). "Über die Darstellung von CaSe, SrSe, BaSe und EuSe durch Reaktion der Metalle mit Selenwasserstoff in flüssigem Ammoniak". Zeitschrift für anorganische und allgemeine Chemie (in German). 437 (1): 193–196. doi:10.1002/zaac.19774370127.