Diphenylchlorarsine

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Diphenylchlorarsine
Identifiers
Abbreviations Ph2AsCl
CAS number 712-48-1 YesY
PubChem 12836
ChemSpider 12306 YesY
Jmol-3D images {{#if:Cl[As](C1=CC=CC=C1)C2=CC=CC=C2Cl[As](c1ccccc1)c2ccccc2|Image 1
Image 2
Properties
Molecular formula C12H10AsCl
Molar mass 264.59 g mol−1
Density 1.55 g/cm3
Melting point 40–42 °C
 YesY (verify) (what is: YesY/N?)
Except where noted otherwise, data are given for materials in their standard state (at 25 °C (77 °F), 100 kPa)
Infobox references

Diphenylchloroarsine (DA) is the organoarsenic compound with the formula (C6H5)2AsCl. It is a low-melting solid. It is highly toxic and was once used in chemical warfare. It is also an intermediate in the preparation of other organoarsenic compounds. The molecule consists of a pyramidal As(III) center attached to two phenyl rings and one chloride.

Preparation and structure

It was first produced in 1878 by Michaelis and La Coste. It is prepared by the reduction of diphenylarsonic acid with sulfur dioxide. An idealized equation is shown:[1]

Ph2AsO2H + SO2 + HCl → Ph2AsCl + H2O + SO3

The structure consists of pyramidal As centre. The As-Cl distance is 2.26 A and the Cl-As-C and C-As-C angles are 96 and 105°, respectively.[2]

Uses

It is a useful reagent for the preparation of other diphenylarsenic compounds, e.g. by reactions with Grignard reagents:

RMgBr + (C6H5)2AsCl → (C6H5)2AsR + MgBrCl
(R = alkyl, aryl)

Safety

Diphenylchlorarsine is known to cause sneezing, coughing, headache, salivation, and vomiting. China and Japan are negotiating remediation of stocks of a variety of organoarsenic weapons stored in northeastern China including chlorodiphenylarsine.[3]

Chemical warfare

Diphenylchlorarsine was used as a chemical weapon on the Western front during the trench warfare of World War I.[4] It belongs to the class of chemicals classified as vomiting agents. Other such agents are diphenylcyanoarsine (DC) and diphenylaminechlorarsine (DM, adamsite).[5] Diphenylchlorarsine could penetrate the gas masks of the time and irritated violently forcing removal of the protecting device. The Germans called it "Maskenbrecher", "mask breaker", together with other substances with similar effect: Adamsite, diphenylarsincyanide, diphenylaminarsincyanide.[citation needed]

References

  1. Blicke, F. F.; Smith, F. D. (1929). "Action of Aromatic Grignard Reagents on Arsenic Trioxide". Journal of the American Chemical Society 51 (5): 1558–1565. doi:10.1021/ja01380a038. 
  2. Trotter, J. (1962). "Stereochemistry of Arsenic. IV. Chlorodiphenylarsine". Canadian Journal of Chemistry 40 (8): 1590–1593. doi:10.1139/v62-241. 
  3. "Abandoned Chemical Weapons (ACW) in China". 02/06/2004. 
  4. Gilbert, M. (1995). The First World War—A Complete History. HarperCollins. ISBN 0805047344. 
  5. Holstege, C. P.; Boyle, J. S. (2008-11-26). "CBRNE - Vomiting Agents - Dm, Da, Dc". Medscape. 
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