Difference between revisions of "Iodine pentoxide"

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|  ChemSpiderID = 140179
 
|  ChemSpiderID = 140179
 
|  InChI = InChI=1S/I2O5/c3-1(4)7-2(5)6
 
|  InChI = InChI=1S/I2O5/c3-1(4)7-2(5)6
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|  StdInChI=
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|  InChIKey =
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|  StdInChIKey =
 
   }}
 
   }}
 
| Section2 = {{Chembox Properties
 
| Section2 = {{Chembox Properties
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   }}
 
   }}
 
| Section3 = {{Chembox Structure
 
| Section3 = {{Chembox Structure
|  Reference = <ref>{{citation | title = Iodine Oxide. Part III. The Crystal Structure of I<sub>2</sub>O<sub>5</sub> | last1 = Selte | first1 = Kari | last2 = Kjekshus | first2 = Arne | journal = Acta Chem. Scand. | year = 1970 | volume = 24 | issue = 6 | pages = 1912–24 | doi = 10.3891/acta.chem.scand.24-1912}}.</ref>
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|  Reference = <ref name="Struct">{{citation | title = Iodine Oxide. Part III. The Crystal Structure of I<sub>2</sub>O<sub>5</sub> | last1 = Selte | first1 = Kari | last2 = Kjekshus | first2 = Arne | journal = Acta Chem. Scand. | year = 1970 | volume = 24 | issue = 6 | pages = 1912–24 | doi = 10.3891/acta.chem.scand.24-1912}}.</ref>
|  SpaceGroup = P2<sub>1</sub>/''c''
+
|  SpaceGroup = P2<sub>1</sub>/''c'' (No. 14)
 
|  Coordination = distorted square-pyramidal (I)
 
|  Coordination = distorted square-pyramidal (I)
 
|  LattConst_a = 1103.6(3) pm
 
|  LattConst_a = 1103.6(3) pm
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|  LattConst_c = 813.5(2) pm
 
|  LattConst_c = 813.5(2) pm
 
|  LattConst_beta = 107.18(2)
 
|  LattConst_beta = 107.18(2)
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  }}
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| Section4 = {{Chembox Thermochemistry
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|  Reference = <ref name="G&E">{{Greenwood&Earnshaw1st|pages=997–99}}.</ref>
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|  DeltaHf = −158.1 kJ mol<sup>−1</sup>
 
   }}
 
   }}
 
| Section7 = {{Chembox Hazards
 
| Section7 = {{Chembox Hazards
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|  Reference = <ref>{{GHS class NZ|id=15707|accessdate=2010-09-10}}.</ref>
 
|  ExternalMSDS =  
 
|  ExternalMSDS =  
 
|  EUIndex = not listed
 
|  EUIndex = not listed
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|  GHSPictograms = {{GHS03|Ox. Sol. 2}}{{GHS05|Skin Corr. 1B, Eye Dam. 1}}
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|  GHSSignalWord = DANGER
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|  HPhrases = {{H-phrases|272|314|318}}
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|  PPhrases = {{P-phrases|210|220|221|260|264|280| 301+330+331|303+361+353|363|304+340|310|321|305+351+338|370+378|405|501}}
 
|  FlashPt = non-flammable
 
|  FlashPt = non-flammable
 
   }}
 
   }}
 
| Section8 = {{Chembox Related
 
| Section8 = {{Chembox Related
|  OtherCpds = [[Iodic acid]]
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|  OtherCpds = [[Anhydro-iodic acid]]<br/>[[Iodic acid]]
 
   }}
 
   }}
 
}}
 
}}
'''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">{{Greenwood&Earnshaw1st|pages=997–99}}.</ref> It is a white solid that is very [[hygroscopic]]. It is formed by direct reaction of the elements in a glow discharge, but is most conveniently prepared by dehydrating [[iodic acid]] at 200&nbsp;°C. Above 300&nbsp;°C, it decomposes to the elements.<ref name="G&E"/>
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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 "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&nbsp;°C. Above 300&nbsp;°C, it decomposes to the elements.<ref name="G&E"/>
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==Structure==
  
 
==Notes and references==
 
==Notes and references==

Latest revision as of 18:16, 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 [12029-98-0]
EC number 234-740-2
ChemSpider 140179
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 (No. 14)
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 ΔfHo298 −158.1 kJ mol−1
Hazards[4]
EU index number not listed
GHS pictograms Ox. Sol. 2Skin Corr. 1B, Eye Dam. 1
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

  1. Commercial "I2O5" is said to be essentially anhydro-iodic acid, HI3O8 or HIO3·I2O5.[3]

References

  1. 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.
  2. 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. 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.
  4. 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

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