Benzoquinonetetracarboxylic acid

Benzoquinonetetracarboxylic acid
Names
IUPAC name
3,6-dioxocyclohexa-1,4-diene-1,2,4,5-tetracarboxylic acid
Identifiers
ChemSpider 310781 N
Jmol interactive 3D Image
PubChem 350050
Properties
C10H4O10
Molar mass 284.14 g/mol
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

In chemistry, 1,4-benzoquinonetetracarboxylic acid is an organic compound with formula C
10
H
4
O
10
, or (C6O2)(-(CO)OH)4, which can be viewed as deriving from para-benzoquinone C
6
H
4
O
2
through replacement of the four hydrogen atoms by carboxyl functional groups -(CO)OH.

By removal of four protons, the acid is expected to yield the anion C
10
O4−
10
, benzoquinonetetracarboxylate, which is one of the oxocarbon anions (consisting solely of oxygen and carbon. By loss of 1 through 3 protons it forms the anions C
10
H
3
O
10
, C
10
H
2
O2−
10
, and C
10
H
1
O3−
10
, called respectively trihydrogen-, dihydrogen-, and hydrogenbenzoquinonetetracarboxylate. The same names are used for the corresponding esters.

Removal of two water molecules gives the compound benzoquinonetetracarboxylic dianhydride, C
10
O
8
, one of the oxides of carbon.[1]

The acid can be obtained by from durene (1,2,4,5-tetramethylbenzene) via dinitropyromellitic and diaminopyromellitic acids.[2][3][4]

See also

References

  1. P. R. Hammond (1963), 1,4-Benzoquinone Tetracarboxylic Acid Dianhydride, C10O8: A Strong Acceptor. Science, Vol. 142. no. 3591, p. 502 doi:10.1126/science.142.3591.502
  2. B. I. Zapadinskii, B. I. Liogon'kii, and A. A. Berlin (1973), Syntheses of Tetracarboxylic Acids. Russian Chemical Reviews, volume 42 issue 11, page 939. Online version accessed on 2010-01-03.
  3. J. U. Nef (1887), Annalen, volume 237, page 19. Cited by Zapadinskii et al.
  4. J. U. Nef (1890), Annalen, volume 258, page 282. Cited by Zapadinskii et al.
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