Chloryl
{{Short description|Ion}}
{{Chembox
| ImageFile1 = Chloryl-cation-2D-A.png
| ImageSize1 = 150px
| ImageAlt1 = Structural formula
| ImageCaption1 =
| ImageFile2 = Chloryl-cation-from-xtal-2008-CM-3D-SF.png
| ImageSize2 = 150px
| ImageAlt2 = Space-filling model of crystal structure
| ImageCaption2 =
| IUPACName = Dioxo-λ3-chloranium
| OtherNames = {{ubl|Chlorylium|Dioxochloronium(V)}}
| Section1 = {{Chembox Identifiers
| CASNo = 25052-55-5
| ChEBI = 29418
| ChemSpiderID = 19127824
| Gmelin = 100601
| SMILES = O=[Cl+]=O
| InChI = 1S/ClO2/c2-1-3/q+1
| InChIKey = UVQYMEMTCMFUIN-UHFFFAOYSA-N}}
}}
In chemistry, chloryl refers to a triatomic cation with chemical formula {{chem|ClO|2|+}}. This species has the same general structure as chlorite ({{chem|ClO|2|−}}) but it is electronically different, with chlorine having a +5 oxidation state (rather than the +3 of chlorite). This makes it a rare example of a positively charged oxychloride. Chloryl compounds, such as Chloryl fluoride and [ClO2][RuF6], are all highly reactive and react violently with water and most organic compounds.{{Cite journal | first4 = W. | last4 = Sawodny | journal = Inorganic Chemistry | volume = 8| pages = 2489–2494 | issue = 11 | first3 = D. | last3 = Pilipovich| year = 1969 | title = Chloryl cation, {{chem|ClO|2|+}} | last1 = Christe | first1 = K. O. | first2 = C. J. | last2 = Schack | doi = 10.1021/ic50081a050}}{{Cite journal | last6 = Vigner | first5 = M. | last5 = Nierlich | first6 = J. | journal = Inorganic Chemistry| pages = 102–109| issue = 1 | volume = 30 | first4 = L. | last4 = Meublat | last1 = Bougon| year = 1991 | title = Preparation characterization and crystal structure of chloryl hexafluororuthenate(1-). Crystal structure of {{chem|[ClF|2|]|+|[RuF|6|]|-}} | first1 = R. | last2 = Cicha | first3 = M. | last3 = Lance | first2 = W. V. | doi = 10.1021/ic00001a019}}
Structure
The {{chem|ClO|2|+}} cation is isoelectronic with Sulfur dioxide,{{cite journal|last1=Carter|first1=H. A.|last2=Johnson|first2=W. M.|last3=Aubke|first3=F.|title=Chloryl compounds. Part II. Chloryl hexafluoroarsenate and chloryl fluoride|journal=Canadian Journal of Chemistry|date=15 December 1969|volume=47|issue=24|pages=4619–4625|doi=10.1139/v69-763}} and has a bent structure with a bond angle close to 120°. The Cl–O bond is of bond order 1.5, with its Lewis structure consisting of a double bond and a dative bond which does not utilize d-orbitals.{{cite journal
| title = Spin-coupled description of the chemical bonding to hypercoordinate chlorine
| author = David L. Cooper
| journal = Theoretical Chemistry Accounts
| year = 2001
| volume = 105
| issue = 4–5
| pages = 323–327
| doi = 10.1007/PL00013292
| s2cid = 96226065
}}
The red color of {{chem|ClO|2|+}} is caused by electron transitions into an antibonding orbital. The analogous transition in {{chem|SO|2}} is not in the visible spectrum, so {{chem|SO|2}} is colorless. The strength of interaction with the counterion affects the energy of this antibonding orbital; thus, in colorless chloryl compounds, strong interactions with the counterion, corresponding with the higher covalent character of the bonding, shift the transition energy out of the visible spectrum.
Compounds
File:Chloryl-hexafluoroantimonate-xtal-2008-Cl-coordination-CM-3D-ellipsoids.png model of the coordination environment of chlorine in chloryl hexafluoroantimonate, [ClO2][SbF6], showing F–Cl interactions.]]
There are two categories of chloryl compounds. The first category is colorless, and includes chloryl fluoride ({{chem|FClO|2}}). These are moderately reactive. Although named as an ionic "chloryl" compound, chloryl fluoride is more a covalent compound than an ionic compound of fluoride and chloryl cation.
The second category features red-colored compounds that are highly reactive. These include chloryl fluorosulfate, {{chem|ClO|2|SO|3|F}}, and dichloryl trisulfate, {{chem|(ClO|2|)|2|(S|3|O|10|)}}. These chloryl compounds form red solutions in fluorosulfuric acid, and do contain a red-colored {{chem|ClO|2|+}} cation which dissociates in solution. In the solid state, the Raman and infrared spectra indicate strong interactions with the counterion. Not all chloryl compounds in the solid state are necessarily ionic. The reaction products of {{chem|FClO|2}} with boron trifluoride and phosphorus pentafluoride are assumed to be molecular adducts rather than true salts.{{cite book
| author = K. O. Christe
| author2 = C. J. Schack
| title = Chlorine Oxyfluorides
| series = Advances in inorganic chemistry and radiochemistry, Volume 18
| editor = Harry Julius Emeléus, A. G. Sharpe
| pages = 356–358
| publisher = Academic Press
| year = 1976
| isbn = 0-12-023618-4
| url = https://books.google.com/books?id=EWlBFTxYth4C&q=chloryl+cation&pg=PA319
}}
One notable chloryl compound is dichlorine hexoxide, which exists as an ionic compound more accurately described as chloryl perchlorate, {{chem|[ClO|2|]|+|[ClO|4|]|-}}.{{Cite journal | journal = Angewandte Chemie International Edition in English | volume = 25 | issue = 11| pages = 993–994 | first2 = M. | last2 = Jansen | title = Crystal Structure of {{chem|Cl|2|O|6}}| year = 1986 | last1 = Tobias | first1 = K. M. | doi = 10.1002/anie.198609931}} It is a red fuming liquid under standard conditions.
Chloryl compounds are best prepared by the reaction of {{chem|FClO|2}} with a strong Lewis acid. For example:
:{{chem|FClO|2}} + {{chem|AsF|5}} → [ClO2][AsF6]
Other synthesis routes are also possible, including:
:5 {{chem|ClO|2}} + 3 {{chem|AsF|5}} → 2 [ClO2][AsF6] + {{chem|AsF|3|O}} + 4 {{chem|Cl|2}}
:{{chem|Cl|2|O|6}} + 2 {{chem|SbF|5}} → [ClO2][SbF6] + {{chem|SbF|3|O}} + {{chem|FClO|3}}
Metathesis reactions may be carried out with strong Lewis bases. For example, the reaction of the hexafluoroplatinate salt with nitryl fluoride yields the nitronium salt:
:[ClO2][PtF6] + {{chem|FNO|2}} → [NO2][PtF6] + {{chem|FClO|2}}
References
{{Reflist}}