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Germanium(II) iodide

From Wikipedia, the free encyclopedia
Germanium(II) iodide
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard100.033.620Edit this at Wikidata
EC Number
  • 236-998-1
  • InChI=1S/GeI2/c2-1-3
    Key: IAGYEMVJHPEPGE-UHFFFAOYSA-N
  • I[Ge]I
Properties
GeI2
Molar mass326.439 g·mol−1
Appearanceyellow solid[1]
Density5.37 g·cm−3 (25 °C)[2]
Melting point428 °C[3]
Boiling point550 °C (decomposes)[3]
Structure
P3m1 (No. 164)[4]
Related compounds
Otheranions
germanium(II) fluoride
germanium(II) chloride
germanium(II) bromide
Othercations
tin(II) iodide
lead(II) iodide
Related compounds
germanium(IV) iodide
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
Chemical compound

Germanium(II) iodide is aniodide ofgermanium, with the chemical formula of GeI2.

Preparation

[edit]

Germanium(II) iodide can be produced by reactinggermanium(IV) iodide withhydriodic acid andhypophosphorous acid andwater:[1]

GeI4 + H2O + H3PO2 → GeI2 + H3PO3 + 2 HI

It can also be formed by the reaction ofgermanium monosulfide orgermanium monoxide andhydrogen iodide.[1]

GeO + 2 HI → GeI2 + H2O
GeS + 2 HI → GeI2 + H2S}

It can also be produced from the direct reaction of germanium and iodine at 200 – 400 °C:[1]

Ge + I2 → GeI2

Germanium(II) iodide can also be formed from the decomposition of HGeI3, which can be prepared by reacting HGeCl3 with hydroiodic acid:[5]

HGeCl3 + 3 HI → HGeI3 + HCl
HGeI3 → GeI2 + HI

Properties

[edit]

Germanium(II) iodide is a yellow crystal that slowly hydrolyzes into germanium(II) hydroxide in the presence of moisture. It is insoluble inhydrocarbons and slightly soluble inchloroform andcarbon tetrachloride. It has acadmium iodide structure withlattice parameters a = 413 pm and c = 679 pm.[1] It disproportionates to germanium and germanium tetraiodide at 550 °C.[6]

Applications

[edit]

Germanium(II) iodide can react withcarbene to form stable compounds.[2] It is also used in the electronics industry to produce germanium layersepitaxially throughdisproportionation reactions.[7]

References

[edit]
  1. ^abcdeGeorg Brauer (Hrsg.), unter Mitarbeit vonMarianne Baudler u. a.:Handbuch der Präparativen Anorganischen Chemie. 3., umgearbeitete Auflage. Band I, Ferdinand Enke, Stuttgart 1975, ISBN 3-432-02328-6, S. 727.
  2. ^abSigma-Aldrich Co.,product no. {{{id}}}.
  3. ^abWilliam M. Haynes (2012),CRC Handbook of Chemistry and Physics, 93rd Edition, CRC Press, pp. 4–65,ISBN 978-143988049-4
  4. ^Jean d’Ans, Ellen Lax, Roger Blachnik (1998),Taschenbuch für Chemiker und Physiker, Springer DE, p. 472,ISBN 364258842-5{{citation}}: CS1 maint: multiple names: authors list (link)
  5. ^Wolfgang Kirmse (2013),Carbene Chemistry 2e, Elsevier, p. 540,ISBN 978-032316145-9
  6. ^Holleman, Arnold Frederik; Wiberg, Egon (2001), Wiberg, Nils (ed.),Inorganic Chemistry, translated by Eagleson, Mary; Brewer, William, San Diego/Berlin: Academic Press/De Gruyter, p. 959,ISBN 0-12-352651-5
  7. ^A.G. Milnes (1972),Heterojunctions and Metal Semiconductor Junctions, Elsevier, p. 104,ISBN 032314136-6
Ge(II)
Ge(IV)
Salts and covalent derivatives of theiodide ion
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