:Xenon trioxide
{{chembox
| Verifiedfields = changed
| Watchedfields = changed
| verifiedrevid = 476998178
| Name = Xenon trioxide
| ImageFile = Xenon-trioxide-2D.png
| ImageClass = skin-invert-image
| ImageSize = 180px
| ImageName = Structural formula, showing lone pair
| ImageFile1 = Xenon-trioxide-3D-vdW.png
| ImageClass1 = bg-transparent
| ImageSize1 = 160px
| ImageName1 = Space-filling model
| IUPACName = Xenon trioxide
Xenon(VI) oxide
| OtherNames = Xenic anhydride
| Section1 = {{Chembox Identifiers
| InChI = 1/O3Xe/c1-4(2)3
| InChIKey = ZWAWYSBJNBVQHP-UHFFFAOYAR
| SMILES = O=Xe(=O)=O
| StdInChI_Ref = {{stdinchicite|correct|chemspider}}
| StdInChI = 1S/O3Xe/c1-4(2)3
| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}}
| StdInChIKey = ZWAWYSBJNBVQHP-UHFFFAOYSA-N
| CASNo_Ref = {{cascite|correct|CAS}}
| CASNo = 13776-58-4
| UNII_Ref = {{fdacite|correct|FDA}}
| UNII = IM8XMX5O5Q
| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}
| ChemSpiderID =21106493
}}
| Section2 = {{Chembox Properties
| Formula = XeO3
| MolarMass = 179.288 g/mol
| Appearance = colourless crystalline solid
| Density = 4.55 g/cm3, solid
| Solubility = Soluble (with reaction)
| MeltingPtC = 25
| MeltingPt_notes = Violent decomposition
| pKa =
}}
| Section3 = {{Chembox Structure
| MolShape = trigonal pyramidal (C3v)
}}
| Section4 = {{Chembox Thermochemistry
| DeltaHf = 402 kJ·mol−1{{cite book| author = Zumdahl, Steven S.|title =Chemical Principles 6th Ed.| publisher = Houghton Mifflin Company| year = 2009| isbn = 978-0-618-94690-7|page=A23}}
| Entropy =
}}
| Section7 = {{Chembox Hazards
| NFPA-H = 4 | NFPA-R=4 | NFPA-F=0 | NFPA-S = OX}}
| Section8 = {{Chembox Related
| OtherCompounds = Xenon tetroxide
Xenic acid
}}
}}
Xenon trioxide is an unstable compound of xenon in its +6 oxidation state. It is a very powerful oxidizing agent, and liberates oxygen from water slowly, accelerated by exposure to sunlight. It is dangerously explosive upon contact with organic materials. When it detonates, it releases xenon and oxygen gas.
Chemistry
Synthesis of xenon trioxide is by aqueous hydrolysis of {{chem|XeF|6|link=Xenon hexafluoride}}:
:{{chem|XeF|6}} + 3 {{chem|H|2|O}} → {{chem|XeO|3}} + 6 HF
The resulting xenon trioxide crystals are a strong oxidising agent and can oxidise most substances that are at all oxidisable. However, it is slow-acting and this reduces its usefulness.{{cite book | title = Chemistry of the Elements | author1 = Greenwood, N. | author2 = Earnshaw, A. | publisher = Butterworth-Heinemann | year = 1997 | location = Oxford }}
Above 25 °C, xenon trioxide is very prone to violent explosion:
:2 XeO3 → 2 Xe + 3 O2 {{pad|5em}}(ΔHf = −403 kJ/mol)
When it dissolves in water, an acidic solution of xenic acid is formed:
:XeO3(aq) + H2O → H2XeO4 {{eqm}} H+ + {{chem|HXeO|4|-}}
This solution is stable at room temperature and lacks the explosive properties of xenon trioxide. It oxidises carboxylic acids quantitatively to carbon dioxide and water.{{cite journal | journal = Talanta |date=July 1966 | volume = 13 | issue = 7 | pages = 945–949 | title = Titrimetric determination of some organic acids by xenon trioxide oxidation | author1 = Jaselskis B. | author2 = Krueger R. H. | pmid = 18959958 | doi = 10.1016/0039-9140(66)80192-3 }}
Alternatively, 15-crown-5 coordinates to xenon trioxide to give a complex stable at room-temperature against mechanical shock.{{cite journal|doi=10.1002/anie.201806640|journal=Angewandte Chemie|title=A stable crown ether complex with a noble-gas compound|first1=Katherine Mary|last1=Marczenko|first2=Hélène Paule Anne|last2=Mercier|first3=Gary J.|last3=Schrobilgen|publisher=Wiley-VCH}}
Alternatively, it dissolves in alkaline solutions to form xenates. The {{chem|HXeO|4|-}} anion is the predominant species in xenate solutions.{{Cite journal| last1 = Peterson | first1 = J. L.| last2 = Claassen | first2 = H. H.| last3 = Appelman | first3 = E. H.| title = Vibrational spectra and structures of xenate(VI) and perxenate(VIII) ions in aqueous solution| journal = Inorganic Chemistry | volume = 9| issue = 3| pages = 619–621 | date=March 1970 | doi = 10.1021/ic50085a037}} These are not stable and begin to disproportionate into perxenates (+8 oxidation state) and xenon and oxygen gas.{{cite book
| title = Main group chemistry
| url = https://archive.org/details/maingroupchemist00hend_891
| url-access = limited
| author = W. Henderson
| location = Great Britain
| publisher = Royal Society of Chemistry
| year = 2000
| isbn = 0-85404-617-8
| pages = [https://archive.org/details/maingroupchemist00hend_891/page/n161 152]–153
}} Solid perxenates containing {{chem|XeO|6|4-}} have been isolated by reacting {{chem|XeO|3|}} with an aqueous solution of hydroxides. Xenon trioxide reacts with inorganic fluorides such as KF, RbF, or CsF to form stable solids of the form {{chem|MXeO|3|F}}.{{cite book
| title = Inorganic chemistry
| author1 = Egon Wiberg
| author2 = Nils Wiberg
| author3 = Arnold Frederick Holleman
| publisher = Academic Press
| year = 2001
| isbn = 0-12-352651-5
| page = 399
}}
Physical properties
Hydrolysis of xenon hexafluoride or xenon tetrafluoride yields a solution from which colorless XeO3 crystals can be obtained by evaporation.{{cite book | series = Advances in Inorganic Chemistry, Volume 46 | title = Recent Advances in Noble-gas Chemistry | author1 = John H. Holloway | author2 = Eric G. Hope | editor = A. G. Sykes | publisher = Academic Press | year = 1998 | isbn = 0-12-023646-X | page = 65 }} The crystals are stable for days in dry air, but readily absorb water from humid air to form a concentrated solution. The crystal structure is orthorhombic with a = 6.163 Å, b = 8.115 Å, c = 5.234 Å, and 4 molecules per unit cell. The density is 4.55 g/cm3.{{Cite journal | doi = 10.1021/ja00889a037 | year = 1963 | last1 = Templeton | first1 = D. H. | title = Crystal and Molecular Structure of Xenon Trioxide | last2 = Zalkin | first2 = A. | last3 = Forrester | first3 = J. D. | last4 = Williamson | first4 = S. M. | journal = Journal of the American Chemical Society | volume = 85 | issue = 6| pages = 817 | url = https://escholarship.org/uc/item/4d31b0pf | url-access = subscription }}
class="wikitable" style="margin:1em auto; text-align:center;"
| 200px | 200px | 180px |
ball-and-stick model of part of the crystal structure of XeO3 | space-filling model | coordination geometry of XeO3 |
Safety
XeO3 should be handled with great caution. Samples have detonated when undisturbed at room temperature. Dry crystals react explosively with cellulose.{{Cite journal | doi = 10.1126/science.139.3554.506 | title = Xenon Hydroxide: an Experimental Hazard | year = 1963 | last1 = Bartlett | first1 = N. | last2 = Rao | first2 = P. R. | journal = Science | volume = 139 | issue = 3554| pages = 506 | pmid = 17843880|bibcode = 1963Sci...139..506B }}
References
{{reflist}}
External links
- [http://www.webelements.com/webelements/compounds/text/Xe/O3Xe1-13776584.html Webelements periodic table: page on Xenon(VI) oxide]
{{Xenon compounds}}
{{Noble gas compounds}}
{{Oxides}}