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Tetrahydroxy-1,4-benzoquinone


Tetrahydroxy-1,4-benzoquinone, also called tetrahydroxy-p-benzoquinone, tetrahydroxybenzoquinone, or tetrahydroxyquinone (THBQ, THQ), is an organic compound with formula . Its molecular structure consists of a cyclohexadiene ring with four hydroxyl groups and two ketone groups in opposite (para) positions.

The compound gives a light red solution in water,

The compound can be synthesized from glyoxal or from myo-inositol, a natural compound widely present in plants. THBQ forms an adduct with 4,4′-bipyridine in a 2:3 ratio.

Salts of THBQ

Like most phenols, THBQ is acidic and easily loses the four hydrogen ions from the hydroxyl groups, yielding anions such as and .

The calcium salt is the dark purple pigment produced from inositol by Chromohalobacter beijerinckii in the fermentation of salt beans, already noted by T. Hof in 1935.

The dark purple and insoluble dipotassium salt was prepared by Preisler and Berger in 1942, by oxidizing inositol with nitric acid and reacting the result with potassium carbonate in the presence of oxygen. Reaction of this salt with hydrochloric acid produces THBQ in good yield.

The black tetrapotassium salt was prepared by West and Niu in 1962, by reacting THBQ with potassium methoxide in methanol. The salt is diamagnetic and the infrared spectrum suggests that the C–C and C–O distances are all equal, with the ring slightly distorted in the "chair" conformation. Partial oxidation of affords a green, strongly paramagnetic solid, conjectured to be , and complete oxidation yields potassium rhodizonate .

The greenish-black sodium salt was described by Fatiadi and Sanger in 1962.

The dark-violet lithium salt has been proposed as an electrode material for batteries as it can be oxidized to the rhodizonate and reduced to the hexahydroxybenzene salt . In the absence of oxygen, is stable to about 450 °C and then decomposes leaving a residue of lithium carbonate. Indeed, the rhodizonate appears to disproportionate at about 400 °C into and cyclohexanehexone that promptly decomposes into carbon monoxide, carbon dioxide, and carbon. forms a hydrate that loses its water at about 250 °C.

References

References

  1. "[[The Merck Index]]".
  2. Klug, H. P.. (1965). "The crystal structure of tetrahydroxy-''p''-benzoquinone". Acta Crystallographica.
  3. Miller, M. W.. (1961). "Microbial Metabolites". McGraw-Hill.
  4. (1962). "Tetrahydroxyquinone".
  5. (2001). "Interpenetrating supramolecular lattices in 4,4′-bipyridine-2,3,5,6-tetrahydroxy-1,4-benzoquinone (3/2)". Acta Crystallographica Section C.
  6. (1935). "Recueil des travaux botaniques néerlandais". F.E. Macdonald; Dutch Botanical Society.
  7. (September 2019). "On the pigment of ''Pseudomonas beijerinckii'' Hof (''Chromohalobacter beijerinckii'')". Enzymologia.
  8. Elvehjem, C. A.. (June 1947). "Vitamins and Hormones—Advances in Research and Applications". American Journal of Public Health and the Nation's Health.
  9. (1954). "Industrial Fermentations}}{{page needed".
  10. (1942). "Preparation of tetrahydroxyquinone and rhodizonic acid salts from the product of the oxidation of inositol with nitric acid". Journal of the American Chemical Society.
  11. (1962). "Symmetrical Resonance Stabilized Anions, C''n''O{{su". Journal of the American Chemical Society.
  12. (2009). "Lithium salt of tetrahydroxybenzoquinone: toward the development of a sustainable Li-ion battery". Journal of the American Chemical Society.
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