Chemistry:Mercury(I) chloride

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Mercury(I) chloride
Mercury Chloride.jpg
Calomel-2D.png
Calomel-xtal-3D-vdW.png
Names
IUPAC name
Dimercury dichloride
Other names
Mercury(I) chloride
Mercurous chloride
Calomel
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
EC Number
  • 233-307-5
25976
RTECS number
  • OV8750000
UNII
UN number 3077
Properties
Hg2Cl2
Molar mass 472.09 g/mol
Appearance White solid
Density 7.150 g/cm3
Melting point 383 °C (721 °F; 656 K) (sublimes)
0.2 mg/100 mL
1.43×10−18[1]
Solubility insoluble in ethanol, ether
−26.0·10−6 cm3/mol
1.973
Structure
tetragonal
Thermochemistry
196 J·mol−1·K−1[2]
−265 kJ·mol−1[2]
Hazards
Safety data sheet ICSC 0984
GHS pictograms GHS07: HarmfulGHS09: Environmental hazard
GHS Signal word Warning
H302, H315, H319, H335, H410
P261, P264, P270, P271, P273, P280, P301+312, P302+352, P304+340, P305+351+338, P312, P321, P330, P332+313, P337+313, P362, P391, P403+233, P405, P501
NFPA 704 (fire diamond)
Flammability code 0: Will not burn. E.g. waterHealth code 3: Short exposure could cause serious temporary or residual injury. E.g. chlorine gasReactivity code 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogenSpecial hazards (white): no codeNFPA 704 four-colored diamond
0
3
0
Flash point Non-flammable
Lethal dose or concentration (LD, LC):
210 mg/kg (rat, oral)[3]
Related compounds
Other anions
 Mercury(I) fluoride
Mercury(I) bromide
Mercury(I) iodide
Related compounds
 Mercury(II) chloride
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

Mercury(I) chloride is the chemical compound with the formula Hg2Cl2. Also known as the mineral calomel[4] (a rare mineral) or mercurous chloride, this dense white or yellowish-white, odorless solid is the principal example of a mercury(I) compound. It is a component of reference electrodes in electrochemistry.[5][6]

History

The name calomel is thought to come from the Greek καλός "beautiful", and μέλας "black"; or καλός and μέλι "honey" from its sweet taste.[4] The "black" name (somewhat surprising for a white compound) is probably due to its characteristic disproportionation reaction with ammonia, which gives a spectacular black coloration due to the finely dispersed metallic mercury formed. It is also referred to as the mineral horn quicksilver or horn mercury.[4]

Calomel was taken internally and used as a laxative,[4] for example to treat George III in 1801, and disinfectant, as well as in the treatment of syphilis, until the early 20th century. Until fairly recently,[when?] it was also used as a horticultural fungicide, most notably as a root dip to help prevent the occurrence of clubroot amongst crops of the family Brassicaceae.[7]

Mercury became a popular remedy for a variety of physical and mental ailments during the age of "heroic medicine". It was prescribed by doctors in America throughout the 18th century, and during the revolution, to make patients regurgitate and release their body from "impurities". Benjamin Rush was a well-known advocate of mercury in medicine and used calomel to treat sufferers of yellow fever during its outbreak in Philadelphia in 1793. Calomel was given to patients as a purgative or cathartic until they began to salivate and was often administered to patients in such great quantities that their hair and teeth fell out.[8]

Yellow fever was also treated with calomel.[9]

Lewis and Clark brought calomel on their expedition. Researchers used that same mercury, found deep in latrine pits, to retrace the locations of their respective locations and campsites.[10]

Properties

Mercury is unique among the group 12 metals for its ability to form the M–M bond so readily. Hg2Cl2 is a linear molecule. The mineral calomel crystallizes in the tetragonal system, with space group I4/m 2/m 2/m. The unit cell of the crystal structure is shown below:

Ball-and-stick model of calomel's unit cell Ball-and-stick model of the distorted octahedral coordination of mercury in calomel
unit cell distorted octahedral coordination of Hg

The Hg–Hg bond length of 253 pm (Hg–Hg in the metal is 300 pm) and the Hg–Cl bond length in the linear Hg2Cl2 unit is 243 pm.[11] The overall coordination of each Hg atom is octahedral as, in addition to the two nearest neighbours, there are four other Cl atoms at 321 pm. Longer mercury polycations exist.

Preparation and reactions

Mercurous chloride forms by the reaction of elemental mercury and mercuric chloride:

Hg + HgCl2 → Hg2Cl2

It can be prepared via metathesis reaction involving aqueous mercury(I) nitrate using various chloride sources including NaCl or HCl.

2 HCl + Hg2(NO3)2 → Hg2Cl2 + 2 HNO3

Ammonia causes Hg2Cl2 to disproportionate:

Hg2Cl2 + 2 NH3 → Hg + Hg(NH2)Cl + NH4Cl

Calomel electrode

Main page: Physics:Saturated calomel electrode

Mercurous chloride is employed extensively in electrochemistry, taking advantage of the ease of its oxidation and reduction reactions. The calomel electrode is a reference electrode, especially in older publications. Over the past 50 years, it has been superseded by the silver/silver chloride (Ag/AgCl) electrode. Although the mercury electrodes have been widely abandoned due to the dangerous nature of mercury, many chemists believe they are still more accurate and are not dangerous as long as they are handled properly. The differences in experimental potentials vary little from literature values. Other electrodes can vary by 70 to 100 millivolts.[citation needed]

Photochemistry

Mercurous chloride decomposes into mercury(II) chloride and elemental mercury upon exposure to UV light.

Hg2Cl2 → HgCl2 + Hg

The formation of Hg can be used to calculate the number of photons in the light beam, by the technique of actinometry.

By utilizing a light reaction in the presence of mercury(II) chloride and ammonium oxalate, mercury(I) chloride, ammonium chloride and carbon dioxide are produced.

2 HgCl2 + (NH4)2C2O4 Light→ Hg2Cl2(s) + 2 [NH+4][Cl−] + 2 CO2

This particular reaction was discovered by J. M. Eder (hence the name Eder reaction) in 1880 and reinvestigated by W. E. Rosevaere in 1929.[12]

Related mercury(I) compounds

Mercury(I) bromide, Hg2Br2, is light yellow, whereas mercury(I) iodide, Hg2I2, is greenish in colour. Both are poorly soluble. Mercury(I) fluoride is unstable in the absence of a strong acid.

Safety considerations

Main page: Medicine:Mercury poisoning

Mercurous chloride is toxic, although due to its low solubility in water it is generally less dangerous than its mercuric chloride counterpart. It was used in medicine as a diuretic and purgative (laxative) in the United States from the late 1700s through the 1860s. Calomel was also a common ingredient in teething powders in Britain up until 1954, causing widespread mercury poisoning in the form of pink disease, which at the time had a mortality rate of 1 in 10.[13] These medicinal uses were later discontinued when the compound's toxicity was discovered.

It has also found uses in cosmetics as soaps and skin lightening creams, but these preparations are now illegal to manufacture or import in many countries including the US, Canada, Japan and the European Union.[14] A study of workers involved in the production of these preparations showed that the sodium salt of 2,3-dimercapto-1-propanesulfonic acid (DMPS) was effective in lowering the body burden of mercury and in decreasing the urinary mercury concentration to normal levels.[15]

References

  1. ↑ John Rumble (June 18, 2018) (in English). CRC Handbook of Chemistry and Physics (99 ed.). CRC Press. pp. 5–188. ISBN 978-1138561632. 
  2. ↑ 2.0 2.1 Zumdahl, Steven S. (2009). Chemical Principles 6th Ed.. Houghton Mifflin Company. p. A22. ISBN 978-0-618-94690-7. 
  3. ↑ "Mercury compounds [except (organo) alkyls (as Hg)"]. Immediately Dangerous to Life and Health Concentrations (IDLH). National Institute for Occupational Safety and Health (NIOSH). https://www.cdc.gov/niosh/idlh/7439976.html. 
  4. ↑ 4.0 4.1 4.2 4.3 Chisholm, Hugh, ed (1911). "Calomel". Encyclopædia Britannica (11th ed.). Cambridge University Press. 
  5. ↑ Housecroft, C. E.; Sharpe, A. G. (2004). Inorganic Chemistry (2nd ed.). Prentice Hall. pp. 696–697. ISBN 978-0-13-039913-7. 
  6. ↑ Skoog, Douglas A.; Holler, F. James; Nieman, Timothy A. (1998). Principles of Instrumental Analysis (5th ed.). Saunders College Pub.. pp. 253–271. ISBN 978-0-03-002078-0. 
  7. ↑ Buczacki, S., Pests, Diseases and Disorders of Garden Plants, Collins, 1998, pp 449-50. ISBN:0-00-220063-5
  8. ↑ Koehler, Christopher S. W. (January 2001). "Heavy Metal Medicine". Today's Chemist at Work 10 (1): 61–65. ISSN 1062-094X. http://pubs.acs.org/subscribe/journals/tcaw/10/i01/html/01chemch.html. Retrieved 2009-02-02. 
  9. ↑ Johnston, Elizabeth Lichtenstein (1901). Recollections of a Georgia Loyalist...written in 1836. New York: Mansfield & Company. p. 82. https://archive.org/details/recollectionsag00johngoog.  pp. 82-83.
  10. ↑ Inglis-Arkell, Esther. "Archaeologists Tracked Lewis and Clark by Following Their Trail of Laxatives" (in en-US). io9. https://io9.gizmodo.com/archaeologists-tracked-lewis-and-clark-by-following-the-1727887223?commerce_insets_disclosure=on. 
  11. ↑ Wells A.F. (1984) Structural Inorganic Chemistry 5th edition Oxford Science Publications ISBN:0-19-855370-6
  12. ↑ Roseveare, W. E. (1930). "The X-Ray Photochemical Reaction between Potassium Oxalate and Mercuric Chloride". J. Am. Chem. Soc. 52 (7): 2612–2619. doi:10.1021/ja01370a005. 
  13. ↑ Sneader, Walter (2005). Drug Discovery: A History. John Wiley and Sons. pp. 45–46. ISBN 978-0-471-89980-8. https://books.google.com/books?id=mYQxRY9umjcC&pg=PA46. Retrieved 2009-02-02. 
  14. ↑ "Commission Directive 86/199/EEC, OJ L 149, p. 38 of 3.6.1986". http://eur-lex.europa.eu/LexUriServ/LexUriServ.do?uri=CONSLEG:1976L0768:20080424:en:PDF. 
  15. ↑ D. Gonzalez-Ramirez; M. Zuniga-Charles; A. Narro-Juarez; Y. Molina-Recio; K. M. Hurlbut; R. C. Dart; H. V. Aposhian (1 October 1998). "DMPS (2,3-Dimercaptopropane-1-sulfonate, Dimaval) Decreases the Body Burden of Mercury in Humans Exposed to Mercurous Chloride" (free full text). The Journal of Pharmacology and Experimental Therapeutics 287 (1): 8–12. PMID 9765315. http://jpet.aspetjournals.org/cgi/content/abstract/287/1/8. 

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