Squaric acid

Squaric acid, also called quadratic acid because its four carbon atoms approximately form a square, is a dibasic organic acid with the chemical formula C4O2(OH)2.[3]

Squaric acid[1]
Structural formula (carbon atoms omitted)
Ball-and-stick-model
Names
IUPAC name
3,4-Dihydroxycyclobut-3-ene-1,2-dione
Other names
Quadratic acid
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.018.875
UNII
Properties
C4H2O4
Molar mass 114.056 g·mol−1
Appearance white crystalline powder
Melting point > 300 °C (572 °F; 573 K)
Acidity (pKa) 1.5, 3.4
Hazards
R-phrases (outdated) R36/37/38 R43
S-phrases (outdated) S26 S36
Flash point 190 °C (374 °F; 463 K)[2]
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Y verify (what is YN ?)
Infobox references

The conjugate base of squaric acid is the hydrogensquarate anion C
4HO−
4; and the conjugate base of the hydrogensquarate anion is the divalent squarate anion C
4O2−
4. This is one of the oxocarbon anions, which consist only of carbon and oxygen.

Squaric acid is a reagent for chemical synthesis, used for instance to make photosensitive squaraine dyes and inhibitors of protein tyrosine phosphatases.

Chemical properties

Squaric acid is a white crystalline powder.[4] The onset of thermal decomposition depends on the different thermodynamic conditions such as heating rates.

The structure of squaric acid is not a perfect square, as the carbon–carbon bond lengths are not quite equal. The high acidity with pKa = 1.5 for the first proton and pKa = 3.4 for the second is attributable to resonance stabilization of the anion.[5] Because the negative charges are equally distributed between each oxygen atom, the dianion of squaric acid is completely symmetrical (unlike squaric acid itself) with all C−C bond lengths identical and all C−O bond lengths identical.

Squaric acid dianion resonance forms
Ball-and-stick model of the squarate ion

Derivatives

Many of the reactions of squaric acid involve the OH groups. The molecule behaves as a strong dicarboxylic acid. It is stronger acid than typical carboxylic acids.[6]

C4O2(OH)2 → [C4O3(OH)]− + H+ pK = 1.5
[C4O3(OH)]− → [C4O4]2- + H+ pK = 3.5

The OH groups are labile in squaric acid. It forms a dichloride with thionyl chloride:

C4O2(OH)2 + 2 SOCl2 → C4O2Cl2 + 2 HCl + 2 SO2

The chlorides are good leaving groups, reminiscent of acid chlorides. They are displaced by diverse nucleophiles. In this way dithiosquarate can be prepared.[7]

The bis(methylether) is prepared by alkylation with trimethyl orthoformate.[8]

Squaramides are prepared by displacement of alkoxy or chloride groups from C4O2X2 (X = OR, Cl).[7][9]

One or both of the oxygen (=O) groups in the squarate anion can be replaced by dicyanomethylene =C(CN)2. The resulting anions, such as 1,2-bis(dicyanomethylene)squarate and 1,3-bis(dicyanomethylene)squarate, retain the aromatic character of squarate and have been called pseudo-oxocarbon anions.

Photolysis of squaric acid in a solid argon matrix at 10 K (−263 °C) affords acetylenediol.[10]

Coordination complexes

Squarate dianion behaves similarly to oxalate, forming mono- and polynuclear complexes with hard metal ions. Cobalt(II) squarate hydrate Co(C4O4)(H2O)2 (yellow, cubic) can be prepared by autoclaving cobalt(II) hydroxide and squaric acid in water at 200 °C. The water is bound to the cobalt atom, and the crystal structure consists of a cubic arrangement of hollow cells, whose walls are either six squarate anions (leaving a 7 Å wide void) or several water molecules (leaving a 5 Å void).[11]

Cobalt(II) squarate dihydroxide Co3(OH)2(C4O4)2·3H2O (brown) is obtained together with the previous compound. It has a columnar structure including channels filled with water molecules; these can be removed and replaced without destroying the crystal structure. The chains are ferromagnetic; they are coupled antiferromagnetically in the hydrated form, ferromagnetically in the anhydrous form.[11]

Copper(II) squarate monomeric and dimeric mixed-ligand complexes were synthesized and characterized.[12] Infrared, electronic and Q-Band EPR spectra as well as magnetic susceptibilities are reported.

The same method yields iron(II) squarate dihydroxide Fe2(OH)2(C4O4) (light brown).[11]

Syntheses

The original synthesis started with the ethanolysis of perfluorocyclobutene to give 1,2-diethoxy-3,3,4,4-tetrafluoro-1-cyclobutene. Hydrolysis gives the squaric acid.[13][3]

Although impractical, squarate and related anions such deltate C
3O2−
3 and acetylenediolate C
2O2−
2 are obtainable by reductive coupling of carbon monoxide using organouranium complexes.[14][15]

Medical uses

Medically, SADBE or squaric acid dibutyl ester or dibutyl squarate derives from a squaric acid.[16] is used for the treatment of warts.[17] Squaric acid dibutyl ester is also used for treating alopecia areata or alopecia totalis (autoimmune hair loss) through topical immunotherapy involving the production of an allergic rash.[18] Squaric acid dibutylester is currently undergoing trials for use in treating herpes labialis (cold sores).[19]

Diethylsquarate was utilized in the synthesis of Perzinfotel.

See also

References
  1. 3,4-Dihydroxy-3-cyclobutene-1,2-dione. Sigma-Aldrich
  2. 3,4-Dihydroxy-3-cyclobutene-1,2-dione, 98+%. Alfa Aesar
  3. Robert West (1980). "History of the Oxocarbons". In Robert West (ed.). Oxocarbons. Academic Press. pp. 1–14. doi:10.1016/B978-0-12-744580-9.50005-1. ISBN 9780127445809.
  4. Lee, K.-S.; Kweon, J. J.; Oh, I.-H.; Lee, C. E. (2012). "Polymorphic phase transition and thermal stability in squaric acid (H
    2    C
    4    O
    4    )". J. Phys. Chem. Solids. 73 (7): 890–895. doi:10.1016/j.jpcs.2012.02.013.
  5. West, Robert; Powell, David L. (1963). "New Aromatic Anions. III. Molecular Orbital Calculations on Oxygenated Anions". J. Am. Chem. Soc. 85 (17): 2577–2579. doi:10.1021/ja00900a010.
  6. "Acidity Tables for Heteroatom Organic Acids and Carbon Acids".
  7. Arthur H. Schmidt (1980). "Reaktionen von Quadratsäure und Quadratsäure-Derivaten". Synthesis. 1980 (12): 961. doi:10.1055/s-1980-29291.
  8. Liu, Hui; Tomooka, Craig S.; Xu, Simon L.; et al. (1999). "Dimethyl Squarate and ITS Conversion to 3-Ethenyl-4-Methoxycyclobutene-1,2-Dione and 2-Butyl-6-Ethenyl-5-Methoxy-1,4-Benzoquinone". Organic Syntheses. 76: 189. doi:10.15227/orgsyn.076.0189.
  9. Ian Storer, R.; Aciro, Caroline; Jones, Lyn H. (2011). "Squaramides: Physical Properties, Synthesis and Applications". Chem. Soc. Rev. 40 (5): 2330–2346. doi:10.1039/c0cs00200c. PMID 21399835.
  10. Maier, Günther; Rohr, Christine (1995). "Ethynediol: Photochemical generation and matrix-spectroscopic identification". Liebigs Annalen. 1996 (3): 307–309. doi:10.1002/jlac.199619960303.
  11. Hitoshi, Kumagai; Hideo, Sobukawa; Mohamedally, Kurmoo (2008). "Hydrothermal syntheses, structures and magnetic properties of coordination frameworks of divalent transition metals". Journal of Materials Science. 43 (7): 2123–2130. Bibcode:2008JMatS..43.2123K. doi:10.1007/s10853-007-2033-8. S2CID 95205908.
  12. Reinprecht, J. T.; Miller, J. G.; Vogel, G. C.; et al. (1979). "Synthesis and Characterization of Copper(II) Squarate Complexes". Inorg. Chem., 19, 927-931
  13. Park, J. D.; Cohen, S. & Lacher, J. R. (1962). "Hydrolysis Reactions of Halogenated Cyclobutene Ethers: Synthesis of Diketocyclobutenediol". J. Am. Chem. Soc. 84 (15): 2919–2922. doi:10.1021/ja00874a015.
  14. Frey, Alistair S.; Cloke, F. Geoffrey N.; Hitchcock, Peter B. (2008). "Mechanistic Studies on the Reductive Cyclooligomerisation of CO by U(III) Mixed Sandwich Complexes; the Molecular Structure of [(U(η-C8H6{Si′Pr3-1,4}2)(η-Cp*)]2(μ-η1:η1-C2O2)". Journal of the American Chemical Society. 130 (42): 13816–13817. doi:10.1021/ja8059792. PMID 18817397.
  15. Summerscales, Owen T.; Frey, Alistair S. P.; Cloke, F. Geoffrey N.; Hitchcock, Peter B. (2009). "Reductive disproportionation of carbon dioxide to carbonate and squarate products using a mixed-sandwich U(III) complex". Chemical Communications (2): 198–200. doi:10.1039/b815576c. PMID 19099067.
  16. "Squaric acid dibutyl ester".
  17. "Warts". Wilmington Dermatology Center. Retrieved 2011-10-23.
  18. Holzer, A. M.; Kaplan, L. L.; Levis, W. R. (2006). "Haptens as drugs: contact allergens are powerful topical immunomodulators". J. Drugs Dermatol. 5 (5): 410–416. PMID 16703776.
  19. http://clinicaltrials.gov/show/NCT01971385
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