Chloryl

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Chloryl
Structural formula
Space-filling model of crystal structure
Preferred IUPAC name

Chloryl

Systematic name

Dioxo-λ5-chloranylium

Identifiers
CAS number 25052-55-5
ChemSpider 19127824 YesY
Jmol-3D images {{#if:O=[Cl+]=O|Image 1
Except where noted otherwise, data are given for materials in their standard state (at 25 °C (77 °F), 100 kPa)
Infobox references

In chemistry, chloryl refers to the red-colored cation having the chemical formula ClO+
2. It is a polyatomic ion, structurally identical to chlorite and having the same chemical formula but with chlorine in the +5 oxidation state rather than +3. In chloryl, the two oxygen atoms oxidize the central chlorine atom, forming one double covalent bond each, and another element or ion oxidizes the chlorine further, leaving the chlorine with one electron pair. (In chlorite, one oxygen atom forms a double covalent bond with the central chlorine atom, and another oxygen atom forms a single bond with the chlorine atom and an ionic bond, or, more rarely, another single covalent bond). Chloryl is isoelectronic with sulfur dioxide.[1] Chloryl compounds, such as FClO
2 and [ClO2][RuF6], are all highly reactive, and react violently with water and most organic compounds.[2][3]

Structure

The ClO+
2 cation is isoelectronic with SO
2,[1] 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.[4]

The red color of ClO+
2 is caused by electron transitions into an antibonding orbital. The analogous transition in SO
2 is not in the visible spectrum, so 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.[1]

Compounds

Thermal ellipsoid 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 (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 cloryl cation.

The second category features red-colored compounds that are highly reactive. These include chloryl fluorosulfate, ClO
2SO
3F, and dichloryl trisulfate, (ClO
2)
2(S
3O
10). These chloryl compounds form red solutions in fluorosulfuric acid, and do contain a red-colored ClO+
2 cation which dissociates in solution. In the solid state, the Raman and infrared spectra indicate strong interactions with the counterion.[1][2] Not all chloryl compounds in the solid state are necessarily ionic. The reaction products of FClO
2 with BF
3 and PF
5 are assumed to be molecular adducts rather than true salts.[1][5]

One notable chloryl compound is dichlorine hexoxide, which exists as an ionic compound more accurately described as chloryl perchlorate, [ClO
2]+
[ClO
4]−
.[6] It is a red fuming liquid under standard conditions.

Chloryl compounds are best prepared by the reaction of FClO
2 with a strong Lewis acid. For example:[5]

FClO
2 + AsF
5 → [ClO2][AsF6]

Other synthesis routes are also possible, including:[5]

5 ClO
2 + 3 AsF
5 → 2 [ClO2][AsF6] + AsF
3O + 4 Cl
2
Cl
2O
4 + 2 SbF
5 → [ClO2][SbF6] + SbF
3O + 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:[5]

[ClO2][PtF6] + FNO
2 → [NO2][PtF6] + FClO
2

References

  1. ↑ 1.0 1.1 1.2 1.3 1.4 H. A. Carter; W. M. Johnson; F. Aubke (1969). "Chloryl compounds. Part II. Chloryl hexafluoroarsenate and chloryl fluoride". Canadian Journal of Chemistry 47 (24): 4619–4625. 
  2. ↑ 2.0 2.1 Christe, K. O.; Schack, C. J.; Pilipovich, D.; Sawodny, W. (1969). "Chloryl cation, ClO+
    2    ". Inorganic Chemistry 8 (11): 2489–2494. doi:10.1021/ic50081a050.     
  3. ↑ Bougon, R.; Cicha, W. V.; Lance, M.; Meublat, L.; Nierlich, M.; Vigner, J. (1991). "Preparation characterization and crystal structure of chloryl hexafluororuthenate(1-). Crystal structure of [ClF
    2    ]+
    [RuF
    6    ]−
    ". Inorganic Chemistry 30 (1): 102–109. doi:10.1021/ic00001a019.     
  4. ↑ David L. Cooper (2001). "Spin-coupled description of the chemical bonding to hypercoordinate chlorine". Theoretical Chemistry Accounts 105 (4-5): 323–327. doi:10.1007/PL00013292. 
  5. ↑ 5.0 5.1 5.2 5.3 K. O. Christe; C. J. Schack (1976). Harry Julius Emeléus, A. G. Sharpe, ed. Chlorine Oxyfluorides. Advances in inorganic chemistry and radiochemistry, Volume 18. Academic Press. pp. 356–358. ISBN 0-12-023618-4. 
  6. ↑ Tobias, K. M.; Jansen, M. (1986). "Crystal Structure of Cl
    2    O
    6    ". Angewandte Chemie International Edition in English 25 (11): 993–994. doi:10.1002/anie.198609931.     
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