Difference between revisions of "Iodine pentoxide"
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− | '''Iodine pentoxide''', I<sub>2</sub>O<sub>5</sub>, is the most stable of the [[oxide]]s of [[iodine]]: it was first prepared in 1813 by (independently) [[Joseph-Louis Gay-Lussac|Gay-Lussac]] and [[Humphrey Davy|Davy]].<ref name="G&E"/> It is a white solid that is very [[hygroscopic]].{{#tag:ref|Commercial | + | '''Iodine pentoxide''', I<sub>2</sub>O<sub>5</sub>, is the most stable of the [[oxide]]s of [[iodine]]: it was first prepared in 1813 by (independently) [[Joseph-Louis Gay-Lussac|Gay-Lussac]] and [[Humphrey Davy|Davy]].<ref name="G&E"/> It is a white solid that is very [[hygroscopic]].{{#tag:ref|Commercial "I<sub>2</sub>O<sub>5</sub>" is said to be essentially [[anhydro-iodic acid]], HI<sub>3</sub>O<sub>8</sub> or HIO<sub>3</sub>·I<sub>2</sub>O<sub>5</sub>.<ref name="G&E"/>|group=Note}} It is formed by direct reaction of the elements in a glow discharge, but is most conveniently prepared by dehydrating [[iodic acid]] at 200 °C. Above 300 °C, it decomposes to the elements.<ref name="G&E"/> |
==Structure== | ==Structure== |
Revision as of 14:29, 10 September 2010
Iodine pentoxide | |
---|---|
IUPAC name | diiodine pentaoxide |
Other names | iodic anhydride |
Identifiers | |
InChI | InChI=InChI=1S/I2O5/c3-1(4)7-2(5)6 |
CAS number | [ | ]
EC number | |
ChemSpider | |
Properties[1] | |
Chemical formula | I2O5 |
Molar mass | 333.81 g mol−1 |
Appearance | white solid |
Density | 4.799 g cm−3 |
Melting point |
300 °C decomp |
Solubility in water | reacts |
Structure[2] | |
Space group | P21/c |
Lattice constant | a = 1103.6(3) pm, b = 506.3(1) pm, c = 813.5(2) pm, α = 90°, β = 107.18(2)°, γ = 90° |
Coordination geometry | distorted square-pyramidal (I) |
Thermochemistry[3] | |
Std enthalpy of formation ΔfH |
−158.1 kJ mol−1 |
Hazards[4] | |
EU index number | not listed |
GHS pictograms | |
GHS signal word | DANGER |
GHS hazard statements | H272, H314, H318 |
GHS precautionary statements | P210, P220, P221, P260, P264, P280, P301+330+331, P303+361+353, P363, P304+340, P310, P321, P305+351+338, P370+378 |
Flash point | non-flammable |
Related compounds | |
Other compounds | Anhydro-iodic acid Iodic acid |
Except where noted otherwise, data are given for materials in their standard state (at 25 °C, 100 kPa) |
Iodine pentoxide, I2O5, is the most stable of the oxides of iodine: it was first prepared in 1813 by (independently) Gay-Lussac and Davy.[3] It is a white solid that is very hygroscopic.[Note 1] It is formed by direct reaction of the elements in a glow discharge, but is most conveniently prepared by dehydrating iodic acid at 200 °C. Above 300 °C, it decomposes to the elements.[3]
Structure
Notes and references
Notes
- ↑ Commercial "I2O5" is said to be essentially anhydro-iodic acid, HI3O8 or HIO3·I2O5.[3]
References
- ↑ CRC Handbook of Chemistry and Physics, 62nd ed.; Weast, Robert C., Ed.; CRC Press: Boca Raton, FL, 1981; p B-107. ISBN 0-8493-0462-8.
- ↑ Selte, Kari; Kjekshus, Arne Iodine Oxide. Part III. The Crystal Structure of I2O5. Acta Chem. Scand. 1970, 24 (6), 1912–24. DOI: 10.3891/acta.chem.scand.24-1912.
- ↑ 3.0 3.1 3.2 3.3 Greenwood, Norman N.; Earnshaw, A. Chemistry of the Elements; Pergamon: Oxford, 1984; pp 997–99. ISBN 0-08-022057-6.
- ↑ HSNO Chemical Classification Information Database, <http://www.ermanz.govt.nz/Chemicals/ChemicalDisplay.aspx?SubstanceID=15707> (accessed 10 September 2010), New Zealand Environmental Risk Management Authority.
External links
See also the corresponding article on Wikipedia. |
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