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Germanium disulfide

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(Redirected fromGermanium(IV) sulfide)
Germanium disulfide
Ball and stick model of crystalline germanium sulfide.
Ball and stick model of crystalline germanium sulfide.
Names
Systematic IUPAC name
Germanium(IV) sulfide[1]
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard100.031.537Edit this at Wikidata
EC Number
  • 234-705-1
  • InChI=1S/GeS2/c2-1-3 checkY
    Key: YIZVROFXIVWAAZ-UHFFFAOYSA-N checkY
  • InChI=1/GeS2/c2-1-3
    Key: YIZVROFXIVWAAZ-UHFFFAOYAU
  • S=[Ge]=S
Properties
GeS2
Molar mass136.75 g·mol−1
AppearanceWhite, translucent crystals
Density2.94 g cm−3
Melting point840 °C (1,540 °F; 1,110 K)
Boiling point1,530 °C (2,790 °F; 1,800 K)
0.45 g/100 mL
Solubilitysoluble in liquidammonia
−53.3·10−6 cm3/mol
Structure
monoclinic,mP36
Pc, No. 7
tetrahedral at Ge, bent at S
Thermochemistry
50 J /(mol K)
−150.06 kJ/mol
Related compounds
Related compounds
Carbon disulfide

Germanium dioxide
Germanium diselenide
Germanium monosulfide
Lead disulfide
Silicon sulfide
Tin disulfide

Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
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Chemical compound

Germanium disulfide orGermanium(IV) sulfide is theinorganic compound with the formulaGeS2. It is a white high-meltingcrystalline solid.[1][2] The compound is a 3-dimensional polymer,[3][4] in contrast tosilicon disulfide, which is a one-dimensional polymer. The Ge-S distance is 2.19 Å.[3]

Isolation, production, reactions

[edit]

Germanium disulfide was first found in samples ofargyrodite. The fact that germanium sulfide does not dissolve in aqueous acid facilitated its isolation.[5]

Germanium disulfide is produced by treating a solution ofgermanium tetrachloride in a concentratedhydrochloric acid solution withhydrogen sulfide. It precipitates as a white solid.[6]

It is insoluble in water, it dissolves in aqueous solutions ofsodium sulfide owing to the formation of thiogermanates:

GeS2 + Na2S → Na2GeS3

Natural occurrence

[edit]

Natural GeS2 is restricted to fumaroles of some burning coal-mining waste heaps.[7]

References

[edit]
  1. ^abJohnson, O. H. (1952). "Germanium and its Inorganic Compounds".Chemical Reviews.51 (3):431–469.doi:10.1021/cr60160a002.
  2. ^Golubkov, A. V.; Dubrovskii, G. B.; Shelykh, A. I. (1998). "Preparation and properties of GeS2 single crystals".Semiconductors.32 (7):734–735.Bibcode:1998Semic..32..734G.doi:10.1134/1.1187494.S2CID 101832592.
  3. ^abZachariasen, W. H. (1936). "The Crystal Structure of Germanium Disulphide".Journal of Chemical Physics.4 (9):618–619.Bibcode:1936JChPh...4..618Z.doi:10.1063/1.1749915.
  4. ^Kulikova, L. F.; Lityagina, L. M.; Zibrov, I. P.; Dyuzheva, T. I.; Nikolaev, N. A.; Brazhkin, V. V. (2014). "High-pressure, high-temperature study of GeS2 and GeSe2".Inorg. Mater.50 (8):768–774.doi:10.1134/S002016851408010X.S2CID 98354736.
  5. ^Winkler, C. (1886)."Mittheilungen über das Germanium".Journal für Praktische Chemie.34 (1):177–229.doi:10.1002/prac.18860340122.
  6. ^P. W. Schenk (1963). "Germanium Disulfide". In G. Brauer (ed.).Handbook of Preparative Inorganic Chemistry, 2nd Ed. Vol. 2pages=723-724. NY,NY: Academic Press.
  7. ^"Unnamed (Ge Sulphide)".
Ge(II)
Ge(IV)
Sulfides(S2−)


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