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Zirconium(IV) iodide

From Wikipedia, the free encyclopedia
Zirconium(IV) iodide
Names
Other names
zirconium tetraiodide
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard100.034.332Edit this at Wikidata
EC Number
  • 237-780-9
UNII
  • InChI=1S/4HI.Zr/h4*1H;/q;;;;+4/p-4 checkY
    Key: XLMQAUWIRARSJG-UHFFFAOYSA-J checkY
  • InChI=1/4HI.Zr/h4*1H;/q;;;;+4/p-4
    Key: XLMQAUWIRARSJG-XBHQNQODAZ
  • [Zr+4].[I-].[I-].[I-].[I-]
Properties
ZrI4
Molar mass598.842 g/mol
Appearanceorange-yellow crystalline
hygroscopic
Density4.914 g/cm3
Melting point499[1] °C (930 °F; 772 K)
(triple point)
Boiling point431 °C (808 °F; 704 K) (sublimes)
Structure
Monoclinic,mP30
P2/c, No. 13
Hazards
GHS labelling:
GHS05: Corrosive
Danger
H314
P260,P264,P280,P301+P330+P331,P303+P361+P353,P304+P340,P305+P351+P338,P310,P321,P363,P405,P501
NFPA 704 (fire diamond)
Related compounds
Otheranions
Zirconium(IV) fluoride
Zirconium(IV) chloride
Zirconium(IV) bromide
Othercations
Titanium tetraiodide
Hafnium tetraiodide
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)
Chemical compound

Zirconium(IV) iodide is thechemical compound with the formulaZrI4. It is the most readily available iodide of zirconium. It is an orange-coloured solid that degrades in the presence of water. The compound was once prominent as an intermediate in the purification of zirconium metal.

Structure

[edit]

Like most binary metal halides, zirconium(IV) iodide adopts a polymeric structure. As characterized byX-ray crystallography, the compound consists of octahedral Zr(IV) centers interconnected by four doubly bridging iodide ligands. The Zr-I distances of 2.692 (terminal) and 3.030 Å[2][3]

Synthesis and reactions

[edit]

This compound can be prepared by heating zirconium metal and an excess of iodine.[1] The solid is purified by sublimation (400 °C, 10-4 mm Hg).[4]

2 I2 + Zr → ZrI4

Pyrolysis of zirconium(IV) iodide gas by contact with a hot wire was the first industrial process for the commercial production of pure ductile metallic zirconium. Thiscrystal bar process was developed byAnton Eduard van Arkel andJan Hendrik de Boer in 1925.[5]

Heating the tetraiodide with zirconium metal giveszirconium triiodide:[4]

3 ZrI4 + 4 Zr → 7 ZrI3

References

[edit]
  1. ^abEberly, K. C. (1963). "Zirconium(IV) Iodide".Inorganic Syntheses. Vol. 7. pp. 52–54.doi:10.1002/9780470132388.ch13.ISBN 978-0-470-13238-8.{{cite book}}:ISBN / Date incompatibility (help).
  2. ^Krebs, B.; Henkel, G.; Dartmann, M. (1979). "Kristallstruktur von Zirkoniumtetrajodid ZrI4: ein neuer AB4-Strukturtyp".Acta Crystallogr.B35 (2): 274-278.doi:10.1107/S0567740879003344.
  3. ^Troyanov, S. I. (1986). "Crystal Structure of γ-ZrI4".Kristallografiya.31: 446-449.
  4. ^abGuthrie, Dennis H.; Corbett, John D. (1981). "Synthesis and Structure of an Infinite-Chain Form of ZrI2 (α)".Journal of Solid State Chemistry.37 (2):256–263.doi:10.1016/0022-4596(81)90092-X.
  5. ^van Arkel, A. E.; de Boer, J. H. (1925). "Darstellung von reinem Titanium-, Zirkonium-, Hafnium- und Thoriummetall".Zeitschrift für anorganische und allgemeine Chemie (in German).148 (1):345–350.doi:10.1002/zaac.19251480133.
Zr(II)
Zr(III)
Zr(IV)
Acids and complexes
Organozirconium(IV)
Salts and covalent derivatives of theiodide ion
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