Organomercury



Organomercury refers to the group of Merbromin ("Mercurichrome").

The toxicity of organomercury compounds presents both dangers and benefits. Dimethylmercury in particular, is notoriously toxic, but has found use as an antiseptic.

Synthesis

Organomercury compounds are generated by many methods, including the direct reaction of hydrocarbons and mercury(II) salts. In this regard, organomercury chemistry more closely resembles organopalladium chemistry and contrasts with organocadmium compounds.

Mercuration of aromatic rings

Electron-rich arenes undergo direct "mercuration" upon treatment with Hg(O2CCH3)2. The one acetate group that remains on mercury can be displaced by chloride:[1]

C6H5OH + Hg(O2CCH3)2 → C6H4(OH)-2-HgO2CCH3 + CH3CO2H
C6H4(OH)-2-HgO2CCH3 + NaCl → C6H4(OH)-2-HgCl + NaO2CCH3

Addition to alkenes

The Hg2+ center binds to alkenes, inducing the addition of methanol gives an α--mercuri ester:[2]

Hg(O2CCH3)2 + CH2=CHCO2CH3 → CH3OCH2CH(HgO2CCH3)CO2CH3

The resulting Hg-C bond can be cleaved with alkyl bromide:

CH3OCH2CH(HgO2CCH3)CO2CH3 + Br2 → CH3OCH2CHBrCO2CH3 + BrHgO2CCH3

Reaction of Hg(II) compounds with carbanion equivalents

A general synthetic route to organomercury compounds entails alkylation with boils at 57 °C at 16 torr. The compound is slightly soluble in ethanol and soluble in ether.

Similarly, diphenylmercury (m.p. 121-123 °C) can be prepared by reaction of mercury chloride and phenylmagnesium bromide. A related preparation entails formation of phenyl sodium in the presence of mercury(II) salts. [4]

Other methods

Hg(II) can be alkylated by treatment with diazonium salts in the presence of copper metal. In this way 2-chloromercuri-naphthalene has been prepared.[5]

Phenyl(trichloromethyl)mercury compounds can be prepared by generating dichlorocarbene in the presence of phenylmercuric chloride. A convenient carbene source is sodium trichloroacetate.[6] This compound on heating releases dichlorocarbene:

C6H5HgCCl3 → C6H5HgCl + CCl2

Reactions

Organomercury compounds are versatile synthetic intermediates due to the well controlled conditions that they undergo cleavage of the Hg-C bonds. Diphenylmercury is a source of the phenyl radical in certain syntheses. Treatment with aluminium gives triphenyl aluminium:

Ph2Hg + 2 Al → (AlPh3)2 + 3 Hg

As indicated above, organomercury compounds react with halogens to give the corresponding organic halide.

Applications

Due to its toxicity and low nucleophilicity, organomercury compounds find limited use. The Wolfenstein-Boters reaction.

See also

CH He
CLi CBe CB CC CN CO CF Ne
CNa CMg CAl CSi CP CS CCl Ar
CK CCa CSc CTi CV CCr CMn CFe CCo CNi CCu CZn CGa CGe CAs CSe CBr Kr
CRb CSr CY CZr CNb CMo CTc CRu CRh CPd CAg CCd CIn CSn CSb CTe CI Xe
CCs CBa CHf CTa CW CRe COs CIr CPt CAu CHg CTl CPb CBi CPo CAt Rn
Fr Ra Rf Db Sg Bh Hs Mt Ds Rg Uub Uut Uuq Uup Uuh Uus Uuo
↓
La Ce Pr Nd Pm Sm Eu Gd Tb Dy Ho Er Tm Yb Lu
Ac Th Pa CU Np Pu Am Cm Bk Cf Es Fm Md No Lr


carbon
Core organic chemistry many uses in chemistry.
Academic research, but no widespread use Bond unknown / not assessed.

References

  1. ^ Whitmore, F. C.; Hanson, E. R. (1941). "o-Chloromercuriphenol". Org. Synth.; Coll. Vol. 1: 161. 
  2. ^ Carter, H. E.; West, H. D. (1955 prep = cv3p0774). "dl-Serine". Org. Synth.; Coll. Vol. 3: 774. 
  3. ^ Synthetic Methods of Organometallic and Inorganic Chemistry Volume 5, Copper, Silver, Gold, Zinc, Cadmium, and Mercury W.A. Herrmann Ed. ISBN 3-13-103061-5
  4. ^ Calvery, H. O. (1941). "Diphenylmercury". Org. Synth.; Coll. Vol. 1: 228. 
  5. ^ Nesmajanow, A. N. (1943). "β-Naphthylmercuric Chloride". Org. Synth.; Coll. Vol. 2: 432. 
  6. ^ Logan, T. J. (1973). "Phenyl(trichloromethyl)mercury". Org. Synth.; Coll. Vol. 5: 969. 
 
This article is licensed under the GNU Free Documentation License. It uses material from the Wikipedia article "Organomercury". A list of authors is available in Wikipedia.