Squaric acid

Squaric acid is a white crystalline powder. 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 pKa1 = 1.5 for the first proton and pKa2 = 3.4 for the second is attributable to resonance stabilization of the anion: 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. ==Derivatives==

Many of the reactions of squaric acid involve the OH groups. The molecule behaves similarly to a strong dicarboxylic acid. It is stronger acid than typical carboxylic acids. :, pKa1 = 1.5 :, pKa2 = 3.5 The OH groups are labile, and squaric acid forms a dichloride with thionyl chloride: : The chlorides leave easily, reminiscent of acid chlorides. They are displaced by diverse nucleophiles. In this way dithiosquarate can be prepared. The bis(methylether) is prepared by alkylation with trimethyl orthoformate. Dibutyl squarate is used for the treatment of warts and for alopecia areata. Diethyl squarate has been used as an intermediate in the synthesis of perzinfotel. Squaramides are prepared by displacement of alkoxy or chloride groups from (X = OR, Cl). Likewise, reaction with arenes gives photosensitive squaraine dyes. Other derivatives inhibit of protein tyrosine phosphatases. One or both of the oxygen (=O) groups in the squarate anion can be replaced by dicyanomethylene . 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 affords acetylenediol. Coordination complexes The squarate dianion behaves similarly to oxalate, forming mono- and polynuclear complexes with hard metal ions. Cobalt(II) squarate hydrate (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). Cobalt(II) squarate dihydroxide (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. Infrared, electronic and Q-Band EPR spectra as well as magnetic susceptibilities are reported. The same method yields iron(II) squarate dihydroxide (light brown). == Synthesis ==

The original synthesis started with the ethanolysis of hexafluorocyclobutene to give 1,2-diethoxy-3,3,4,4-tetrafluoro-1-cyclobutene. Hydrolysis gives squaric acid. == See also ==