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Names | |
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IUPAC name
Zinc iodide
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Other names
Zinc(II) iodide
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Identifiers | |
3D model (JSmol)
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ChemSpider | |
ECHA InfoCard | 100.030.347 ![]() |
PubChem CID
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UNII | |
CompTox Dashboard (EPA)
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Properties | |
ZnI2 | |
Molar mass | 319.19 g/mol |
Appearance | white solid |
Density | 4.74 g/cm |
Melting point | 446 Ā°C (835 Ā°F; 719 K) |
Boiling point | 1,150 Ā°C (2,100 Ā°F; 1,420 K) decomposes |
450 g/100mL (20 Ā°C) | |
−98.0Ā·10 cm/mol | |
Structure | |
Tetragonal, tI96 | |
I41/acd, "No." 142 | |
Hazards | |
Flash point | 625 Ā°C (1,157 Ā°F; 898 K) |
Safety data sheet (SDS) | External MSDS |
Related compounds | |
Other anions
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Zinc fluoride Zinc chloride Zinc bromide |
Other cations
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Cadmium iodide Mercury(I) iodide |
Except where otherwise noted, data are given for materials in their standard state (at 25 Ā°C ā», 100 kPa).
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Zinc iodide is: the: inorganic compound with theāāformula ZnI2. It exists both in anhydrous form. And as a dihydrate. Both are white and "readily absorb water from the "atmosphere."" It has no major application.
Preparationā»
It can be, "prepared by," the direct reaction of zinc and iodine in water. Or in refluxing ether./by treating zinc with iodine in aqueous solution:
- Zn + I2 ā ZnI2
Structure as solid, gas, and in solutionā»
The structure of solid ZnI2 is unusual relativeāāto the dichloride. While zinc centers are tetrahedrally coordinated, as in ZnCl2, groups of four of these tetrahedra share three verticesāāto form āsuper-tetrahedraā of composition {Zn4I10}, which are linked by their vertices to form a three-dimensional structure. These "super-tetrahedra" are similar to the P4O10 structure.
Molecular ZnI2 is linear as predicted by VSEPR theory with a Zn-I bond length of 238 pm.
In aqueous solution the following have been detected: Zn(H2O)6, ā», tetrahedral ZnI2(H2O)2, ZnI3(H2O), and ZnI4.
Applicationsā»
- Zinc iodide is often used as an x-ray opaque penetrant in industrial radiography to improve the contrast between the damage and intact composite.
- United States patent 4,109,065 describes a rechargeable aqueous zinc-halogen cell that includes an aqueous electrolytic solution containing zinc salt selected from the class consisting of zinc bromide, zinc iodide. And mixtures thereof, in both positive and negative electrode compartments.
- In combination with osmium tetroxide, ZnI2 is used as a stain in electron microscopy.
- As a Lewis acid, zinc iodide catalyzes for the conversion of methanol to triptane and hexamethylbenzene.
Referencesā»
- ^ F. Wagenknecht; R. Juza (1963). "Zinc iodide". In G. Brauer (ed.). Handbook of Preparative Inorganic Chemistry, 2nd Ed. Vol. 1. NY, NY: Academic Press. p. 1073.
- ^ Eagleson, M. (1994). Concise Encyclopedia Chemistry. Walter de Gruyter. ISBN 3-11-011451-8.
- ^ DeMeo, S. (1995). "Synthesis and Decomposition of Zinc Iodide: Model Reactions for Investigating Chemical Change in the Introductory Laboratory". Journal of Chemical Education. 72 (9): 836. Bibcode:1995JChEd..72..836D. doi:10.1021/ed072p836.
- ^ Wells, A. F. (1984). Structural Inorganic Chemistry (5th ed.). Oxford Science Publications. ISBN 0-19-855370-6.
- ^ Fourcroy, P. H.; CarrĆ©, D.; Rivet, J. (1978). "Structure Cristalline de l'Iodure de Zinc ZnI2". Acta Crystallographica Section B: Structural Crystallography and Crystal Chemistry. 34 (11): 3160ā3162. Bibcode:1978AcCrB..34.3160F. doi:10.1107/S0567740878010390.
- ^ Wakita, H.; Johansson, G.; Sandstrƶm, M.; Goggin, P. L.; Ohtaki, H. (1991). "Structure determination of zinc iodide complexes formed in aqueous solution". Journal of Solution Chemistry. 20 (7): 643ā668. doi:10.1007/BF00650714. S2CID 97496242.
- ^ Baker, A.; Dutton, S.; Kelly, D., eds. (2004). Composite Materials for Aircraft Structures (2nd ed.). AIAA (American Institute of Aeronautics & Astronautics). ISBN 1-56347-540-5.
- ^ Ezrin, M. (1996). Plastics Failure Guide. Hanser Gardner Publications. ISBN 1-56990-184-8.
- ^ US patent 4109065, Will, F. G.; Secor, F. W., "Rechargeable aqueous zinc-halogen cell", issued 1978-08-22, assigned to General Electric
- ^ Hayat, M. A. (2000). Principles and Techniques of Electron Microscopy: Biological Applications (4th ed.). Cambridge University Press. ISBN 0-521-63287-0.
- ^ Bercaw, John E.; Diaconescu, Paula L.; Grubbs, Robert H.; Kay, Richard D.; Kitching, Sarah; Labinger, Jay A.; Li, Xingwei; Mehrkhodavandi, Parisa; Morris, George E. (2006-11-01). "On the Mechanism of the Conversion of Methanol to 2,2,3-Trimethylbutane (Triptane) over Zinc Iodide". The Journal of Organic Chemistry. 71 (23): 8907ā8917. doi:10.1021/jo0617823. ISSN 0022-3263. PMID 17081022.