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ethylmercury(1+)
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ethylmercury(1+)

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Also known as [HgEt](+), ETHYL MERCURY ION

Ethylmercury (sometimes ethyl mercury) is a cation composed of an organic CH3CH2— species (an ethyl group) bound to a mercury(II) centre, making it a type of organometallic cation, and giving it a chemical formula C2H5Hg+. The main source of ethylmercury is thiomersal.

Wikidata facts

Mass
231.01
Show 3 more facts
canonical SMILES
CC[Hg+]
chemical formula
C₂H₅Hg⁺
Commons category
Ethylmercury
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Encyclopedic overview

7 sections
Contents
  • Synthesis and structure
  • Toxicity
  • Public health concerns
  • See also
  • References and notes
  • Further reading
  • External links

Ethylmercury (sometimes ethyl mercury) is a cation composed of an organic CH3CH2— species (an ethyl group) bound to a mercury(II) centre, making it a type of organometallic cation, and giving it a chemical formula C2H5Hg+. The main source of ethylmercury is thiomersal.

==Synthesis and structure== thumb|left|Structures of two main types of complexes derived from "ethylmercury". X− = anion, L = neutral Lewis base. Ethylmercury (C2H5Hg+) is a substituent of compounds: it occurs as a component of compounds of the formula C2H5HgX where X = chloride, thiolate, or another organic group. Most famously X = the mercaptide group of thiosalicylic acid as in thiomersal. In the body, ethylmercury is most commonly encountered as derivatives with a thiolate attached to the mercury. In these compounds, Hg(II) has a linear or sometimes trigonal coordination geometry. Given the comparable electronegativities of mercury and carbon, the mercury-carbon bond is described as covalent.

Excerpted from Wikipedia’s “ethylmercury(1+)” article, available under the CC BY-SA 4.0 licence.

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