Quinone

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"Quinones" redirects here. For other uses, see Quiñones. Not to be confused with quinine.

A quinone is a class of organic compounds that are formally "derived from aromatic compounds [such as benzene or naphthalene] by conversion of an even number of –CH= groups into –C(=O)– groups with any necessary rearrangement of double bonds," resulting in "a fully conjugated cyclic dione structure."[1] The class includes some heterocyclic compounds.

The prototypical member of the class is 1,4-benzoquinone or cyclohexadienedione, often called simply quinone (thus the name of the class). Other important examples are 1,2-benzoquinone (ortho-quinone), 1,4-naphthoquinone and 9,10-anthraquinone.

Properties[edit]

Quinones are oxidized derivatives of aromatic compounds and are often readily made from reactive aromatic compounds with electron-donating substituents such as phenols and catechols, which increase the nucleophilicity of the ring and contributes to the large redox potential needed to break aromaticity. (Quinones are conjugated but not aromatic). Quinones are electrophilic Michael acceptors stabilised by conjugation. Depending on the quinone and the site of reduction, reduction can either rearomatise the compound or break the conjugation. Conjugate addition nearly always breaks the conjugation.

The term quinone is also used more generally for a large class of compounds formally derived from aromatic quinones through replacement of some hydrogen atoms by other atoms or radicals.

Occurrence and uses[edit]

Production of hydrogen peroxide[edit]

A large scale industrial application of quinones is for the production of hydrogen peroxide. 2-Alkylanthraquinones are hydrogenated to the corresponding hydroquinones (quinizarins), which then transfer H
2
to oxygen:

dihydroanthraquinone + O
2
→ anthraquinone + H
2
O
2

In this way, several billion kilograms of H
2
O
2
are produced annually.[2]

Biochemistry[edit]

Derivatives of quinones are common constituents of biologically relevant molecules. Some serve as electron acceptors in electron transport chains such as those in photosynthesis (plastoquinone, phylloquinone), and aerobic respiration (ubiquinone). Phylloquinone is also known as Vitamin K1 as it is used by animals to help form certain proteins, which are involved in blood coagulation, bone formation, and other processes.

A natural example of the oxidation of hydroquinone to quinone is in the spray of bombardier beetles; hydroquinone is reacted with hydrogen peroxide to produce a fiery blast of steam, a strong deterrent in the animal world.

Medicinal[edit]

Natural or synthetic quinones show a biological or pharmacological activity, and some of them show antitumoral activity. They embody some claims in herbal medicine. These applications include purgative (sennosdes), antimicrobacterial (rhein- and saprorthoquinone), anti-tumor (emodin and jugone), inhibition of PGE2 biosynthesis (arnebinone and arnebifuranone) and anti-cardiovascular disease (tanshinone).[3]

Dyes[edit]

Many natural and artificial coloring substances (dyes and pigments) are quinone derivatives. They are second only to azo dyes in importance as dyestuffs, with particular emphasis on blue colors. Alizarin (1,2-dihydroxy-9,10-anthraquinone), extracted from the madder plant, was the first natural dye to be synthesized from coal tar.

Reagents in organic chemistry[edit]

Benzoquinone is used in organic chemistry as an oxidizing agent. Stronger quinone oxidising agents exist; for instance: chloranil and 2,3-dichloro-5,6-dicyano-1,4-benzoquinone (also known as DDQ).[4]

Battery charge carrier[edit]

In 2013 researchers announced the use of 9,10-anthraquinone-2,7-disulphonic acid (AQDS; a quinone found naturally in rhubarb) as a charge carrier in metal-free flow batteries. Each of the carbon-based molecules holds two units of electrical charge, compared with one unit in conventional batteries, implying that a battery could store twice as much energy in a given volume.[5]AQDS undergoes rapid, reversible two-electron/two-proton reduction on a glassy carbon electrode in sulphuric acid. An aqueous flow battery with inexpensive carbon electrodes, combining the quinone/hydroquinone couple with the Br
2
/Br
redox couple, yields a peak galvanic power density exceeding 0.6 W cm−2 at 1.3 A cm−2. Cycling showed >99 per cent storage capacity retention per cycle. The organic anthraquinone species can be synthesized from inexpensive commodity chemicals. This organic approach permits tuning of the reduction potential and solubility by adding functional groups. Adding two hydroxy groups to AQDS increases the open circuit potential of the cell by 11%.[6]

Nomenclature[edit]

Quinones are commonly named with a prefix that indicates the parent aromatic hydrocarbon ("benzo-" for benzene, "naphtho-" for naphthalene, "anthra-" for anthracene, etc.) and the "-quinone" suffix. Infix multipliers "-di-", "-tri-", "-tetra-" (etc.) are used when there are 4, 6, 8 (etc.) carbonyls. The position of the carbonyl groups can be indicated before the prefix (as in "1,4,5,8-naphthodiquinone") or after it ("anthra-1,4-quinone").

See also[edit]

References[edit]

  1. ^ IUPAC, Compendium of Chemical Terminology, 2nd ed. (the "Gold Book") (1997). Online corrected version:  (1995) "Quinones".
  2. ^ Gustaaf Goor, Jürgen Glenneberg, Sylvia Jacobi “Hydrogen Peroxide” in Ullmann's Encyclopedia of Industrial Chemistry 2007, Wiley-VCH, Weinheim. doi: 10.1002/14356007.a13_443.pub2.
  3. ^ Liu H., "Extraction and Isolation of Compounds from Herbal Medicines" in 'Traditional Herbal Medicine Research Methods', ed by Willow JH Liu 2011 John Wiley and Sons, Inc.
  4. ^ March, Jerry (1985), Advanced Organic Chemistry: Reactions, Mechanisms, and Structure (3rd ed.), New York: Wiley, ISBN 0-471-85472-7 
  5. ^ "From Harvard, a Cheaper Storage Battery". New York Times. January 8, 2014. Retrieved January 10, 2014. 
  6. ^ Huskinson, B.; Marshak, M. P.; Suh, C.; Er, S. L.; Gerhardt, M. R.; Galvin, C. J.; Chen, X.; Aspuru-Guzik, A. N.; Gordon, R. G.; Aziz, M. J. (2014). "A metal-free organic–inorganic aqueous flow battery". Nature 505 (7482): 195–198. doi:10.1038/nature12909. PMID 24402280.  edit

External links[edit]