Dichlorine monoxide

Dichlorine monoxide
Structure of dichlorine monoxide: Cl-O bond length is 170.0 pm, bond angle is 110.9°.
Space-filling model of dichlorine monoxide
Names
Other names
Oxygen dichloride
Dichlorine oxide
Chlorine(I) oxide
Hypochlorous oxide
Hypochlorous anhydride
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
ECHA InfoCard 100.029.312
Properties
Cl2O
Molar mass 86.9054 g/mol
Appearance brownish-yellow gas
Melting point −120.6 °C (−185.1 °F; 152.6 K)
Boiling point 2.0 °C (35.6 °F; 275.1 K)
very soluble, hydrolyses 143 g Cl2O per 100 g water
Solubility in other solvents soluble in CCl4
Structure
0.78 ± 0.08 D
Thermochemistry
265.9 J K−1 mol−1
+80.3 kJ mol−1
Hazards
Safety data sheet [1]
NFPA 704
Flammability code 4: Will rapidly or completely vaporize at normal atmospheric pressure and temperature, or is readily dispersed in air and will burn readily. Flash point below 23 °C (73 °F). E.g., propane Health code 3: Short exposure could cause serious temporary or residual injury. E.g., chlorine gas Reactivity code 3: Capable of detonation or explosive decomposition but requires a strong initiating source, must be heated under confinement before initiation, reacts explosively with water, or will detonate if severely shocked. E.g., fluorine Special hazards (white): no codeNFPA 704 four-colored diamond
4
3
3
Related compounds
Other cations
 Nitrous oxide, dibromine monoxide, water
Related compounds
 Oxygen difluoride, chlorine dioxide
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references

Dichlorine monoxide, is an inorganic compound with the molecular formula Cl2O. It was first synthesised in 1834 by Antoine Jérôme Balard, who along with Gay-Lussac also determined its composition. In older literature it is often referred to as chlorine monoxide,[2] which can be a source of confusion as that name now refers to the neutral species ClO.

At room temperature it exists as a brownish-yellow gas which is soluble in both water and organic solvents. Chemically, it is a member of the chlorine oxide family of compounds, as well as being the anhydride of hypochlorous acid. It is a strong oxidiser and chlorinating agent.

Preparation

The earliest method of synthesis was to treat mercury(II) oxide with chlorine gas.[2] However this method is expensive, as well as highly dangerous due to the risk of mercury poisoning.

2 Cl2 + HgO → HgCl2 + Cl2O

A safer and more convenient method of production is the reaction of chlorine gas with hydrated sodium carbonate, at 20-30°C.

2 Cl2 + 2 Na2CO3 + H2O → Cl2O + 2 NaHCO3 + 2 NaCl
2 Cl2 + 2 NaHCO3 → Cl2O + 2 CO2 + 2 NaCl + H2O

This reaction can be performed in the absence of water but requires heating to 150-250°C; as dichlorine monoxide is unstable at these temperatures[3] it must therefore be continuously removed to prevent thermal decomposition.

2 Cl2 + Na2CO3 → Cl2O + CO2 + 2 NaCl


Structure

The structure of dichlorine monoxide is similar to that of water and hypochlorous acid, with the molecule adopting a bent molecular geometry due to the lone pairs on the oxygen; resulting in C2V molecular symmetry. The bond angle is slightly larger than normal, likely due to steric repulsion between the bulky chlorine atoms.

In the solid state, it crystallises in the tetrahedral space group I41/amd, making it isostructural to the high pressure form of water, ice VIII.[4]

Reactions

Dichlorine monoxide is highly soluble in water,[5] where it exists in an equilibrium with HOCl. The rate of hydrolysis is slow enough to allow the extraction of Cl2O with organic solvents such as CCl4,[2] but the equilibrium constant ultimately favours the formation of hypochlorous acid.[6]

2 HOCl ⇌ Cl2O + H2O K (0 °C) = 3.55x10−3 dm3/mol

Despite this, it has been suggested that dichlorine monoxide may be the active species in the reactions of HOCl with olefins and aromatic compounds,[7][8] as well as in the chlorination of drinking water.[9]

With inorganic compounds

Dichlorine monoxide reacts with metal halides, with the loss of Cl2, to form unusual oxyhalides.[10][11][2]

VOCl3 + Cl2O → VO2Cl + 2 Cl2
TiCl4 + Cl2O → TiOCI2 + 2 Cl2
SbCI5 + 2 CI2O → SbO2CI + 4 Cl2

Similar reactions have also been observed with certain inorganic halides.[12][13]

AsCI3 + 2 CI2O → AsO2CI + 3 Cl2
NOCl + Cl2O → NO2Cl + Cl2

With organic compounds

Dichlorine monoxide is an effective chlorinating agent. It can be used for either the side-chain or ring chlorination of deactivated aromatic substrates.[14] For activated aromatics such as phenols and aryl-ethers it primarily reacts to give ring halogenated products.[15] It has been suggested that dichlorine monoxide may be the active species in the reactions of HOCl with olefins and aromatic compounds.[7][8]

Photochemistry

Dichlorine monoxide undergoes photodissociation, eventually forming O2 and Cl2. The process is primarily radical based, with flash photolysis showing radical hypochlorite (ClO·) to be a key intermediate.[16]

2 Cl2O → 2 Cl2 + O2

Explosive properties

Dichlorine monoxide is explosive, although there is a lack of modern research into this behaviour. Room temperature mixtures with oxygen could not be detonated by an electric spark until they contained at least 23.5% Cl2O.[17] which is an exceedingly high minimum explosive limit. There are conflicting reports of it exploding on exposure to strong light.[18][19] Heating above 120°C, or a rapid rate of heating at lower temperatures also apparently lead to explosions.[2] Liquid dichlorine monoxide has been reported to be shock-sensitive.[20]

References

  1. ↑ "CHLORINE MONOXIDE". CAMEO Chemicals. National Oceanic and Atmospheric Administration. Retrieved 12 May 2015.
  2. 1 2 3 4 5 Renard, J. J.; Bolker, H. I. (1 August 1976). "The chemistry of chlorine monoxide (dichlorine monoxide)". Chemical Reviews. 76 (4): 487–508. doi:10.1021/cr60302a004.
  3. ↑ Hinshelwood, Cyril Norman; Prichard, Charles Ross (1923). "CCCXIII.—A homogeneous gas reaction. The thermal decomposition of chlorine monoxide. Part I". Journal of the Chemical Society, Transactions. 123: 2730. doi:10.1039/CT9232302730.
  4. ↑ Minkwitz, R.; Bröchler, R.; Borrmann, H. (1 January 1998). "Tieftemperatur-Kristallstruktur von Dichlormonoxid, Cl2O". Zeitschrift für Kristallographie. 213 (4): 237–239. doi:10.1524/zkri.1998.213.4.237.
  5. ↑ Davis, D. S. (1942). "Nomograph for the Solubility of Chlorine Monoxide in Water". Industrial & Engineering Chemistry. 34 (5): 624–624. doi:10.1021/ie50389a021.
  6. ↑ Aylett, founded by A.F. Holleman ; continued by Egon Wiberg ; translated by Mary Eagleson, William Brewer ; revised by Bernhard J. (2001). Inorganic chemistry (1st English ed., [edited] by Nils Wiberg. ed.). San Diego, Calif. : Berlin: Academic Press, W. de Gruyter. p. 442. ISBN 9780123526519.
  7. 1 2 Swain, C. Gardner; Crist, DeLanson R. (1 May 1972). "Mechanisms of chlorination by hypochlorous acid. The last of chlorinium ion, Cl+". Journal of the American Chemical Society. 94 (9): 3195–3200. doi:10.1021/ja00764a050.
  8. 1 2 Sivey, John D.; McCullough, Corey E.; Roberts, A. Lynn (1 May 2010). "Chlorine Monoxide (Cl2O) and Molecular Chlorine (Cl2) as Active Chlorinating Agents in Reaction of Dimethenamid with Aqueous Free Chlorine". Environmental Science & Technology. 44 (9): 3357–3362. doi:10.1021/es9038903.
  9. ↑ Powell, Steven C. (1 May 2010). "The active species in drinking water chlorination: the case for Cl2O". Environmental Science & Technology. 44 (9): 3203–3203. doi:10.1021/es100800t.
  10. ↑ Oppermann, H. (1967). "Untersuchungen an Vanadinoxidchloriden und Vanadinchloriden. I. Gleichgewichte mit VOCl3, VO2Cl und VOCl2". Zeitschrift für anorganische und allgemeine Chemie. 351 (3-4): 113–126. doi:10.1002/zaac.19673510302.
  11. ↑ Dehnicke, Kurt (1961). "Titan(IV)-Oxidchlorid TiOCl2". Zeitschrift für anorganische und allgemeine Chemie. 309 (5-6): 266–275. doi:10.1002/zaac.19613090505.
  12. ↑ Dehnicke, Kurt (1 December 1964). "Über die Oxidchloride PO2Cl, AsO2Cl und SbO2Cl". Chemische Berichte. 97 (12): 3358–3362. doi:10.1002/cber.19640971215.
  13. ↑ Martin, H. (1 January 1966). "Kinetic Relationships between Reactions in the Gas Phase and in Solution". Angewandte Chemie International Edition in English. 5 (1): 78–84. doi:10.1002/anie.196600781.
  14. ↑ Marsh, F. D.; Farnham, W. B.; Sam, D. J.; Smart, B. E. (1 August 1982). "Dichlorine monoxide: a powerful and selective chlorinating reagent". Journal of the American Chemical Society. 104 (17): 4680–4682. doi:10.1021/ja00381a032.
  15. ↑ Sivey, John D.; Roberts, A. Lynn (21 February 2012). "Assessing the Reactivity of Free Chlorine Constituents Cl2, Cl2O, and HOCl Toward Aromatic Ethers". Environmental Science & Technology. 46 (4): 2141–2147. doi:10.1021/es203094z.
  16. ↑ Basco, N.; Dogra, S. K. (22 June 1971). "Reactions of Halogen Oxides Studied by Flash Photolysis. II. The Flash Photolysis of Chlorine Monoxide and of the ClO Free Radical". Proceedings of the Royal Society A: Mathematical, Physical and Engineering Sciences. 323 (1554): 401–415. doi:10.1098/rspa.1971.0112.
  17. ↑ Cady, George H.; Brown, Robert E. (September 1945). "Minimum Explosive Concentration of Chlorine Monoxide Diluted with Oxygen". Journal of the American Chemical Society. 67 (9): 1614–1615. doi:10.1021/ja01225a501.
  18. ↑ Iredale, T.; Edwards, T. G. (April 1937). "Photoreaction of Chlorine Monoxide and Hydrogen". Journal of the American Chemical Society. 59 (4): 761–761. doi:10.1021/ja01283a504.
  19. ↑ Wallace, Janet I.; Goodeve, C. F. (1 January 1931). "The heats of dissociation of chlorine monoxide and chlorine dioxide". Transactions of the Faraday Society. 27: 648. doi:10.1039/TF9312700648.
  20. ↑ Pilipovich, Donald.; Lindahl, C. B.; Schack, Carl J.; Wilson, R. D.; Christe, Karl O. (1972). "Chlorine trifluoride oxide. I. Preparation and properties". Inorganic Chemistry. 11 (9): 2189–2192. ISSN 0020-1669. doi:10.1021/ic50115a040.
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