スクエア酸

外観

白色～うすい黄褐色、結晶性粉末～粉末

解説

スクエア酸,白色の固体．分解点300 ℃ 以上．ヒドロキシ基がイオン解離して生じるモノアニオンやジアニオンは，二つのカルボニル基の電子求引効果と共鳴による負電荷の酸素原子上への分散のため安定化される．これにより，スクエア酸は通常の有機酸に比べて非常に酸性度が高い．pK1 1.7，pK1 3.2．アニリンやピロール誘導体などと反応して，中心に四員環骨格をもつ色素化合物(squaryliun dyes)を分子内塩の形で形成する．また，Cu，FeⅢなどの比色定量試薬として用いられる．
森北出版「化学辞典（第2版）

製造

スクエア酸,四角酸ともいう．ジクロロジフルオロエテンの二量化，脱ハロゲン化，加水分解などを経て合成される．

化学的特性

Squaric acid (3,4-dihydroxycyclobut-3-ene-1,2-dione), also known as quadratic acid, has the fascinating structure, and is a vinylogous carboxylic acid. The parent compound is a white,crystalline powder which melts at~300℃. It is highly acidic (pKa 1.5 for the first proton and 3.4 for the second) due to resonance stabilization of the anion and exhibits IR resonances indicative of strong hydrogen bonding [2326cm-1 (OH),1818 cm-1 (C=O), and 1639cm-1 (C=C)].The UV absorption spectrum suggests that the acid is essentially completely ionized. Squaric acid is freely soluble in water but has poor solubility in many organic solvents.Solutions give an intense purple color with iron(III) chloride, and are also known to decolorize bromine water, cerium(IV) nitrate, and permanganate solutions.As the carbonyl groups are similar to those of carboxylic acids rather than those of ketones, squaric acid does not react in the phenylhydrazine test.The squarate dianion is thought to be completely symmetrical (unlike squaric acid itself), with all C-C and C-O bond lengths being, respectively, identical, as the negative charges are equally distributed between allthe oxygen atoms.The IR spectrum of dipotassium squarate (dipotassium 3,4-dioxocy-clobut-1-ene-1,2-diolate) differs greatly from that of squaric acid, with the loss of the car-bonyl (C=O) and alkene(C=C) absorptions seen in the protonated form, and supportsthe proposed symmetrical structure.

使用

Squaric acid used as intermediate for squaraine dyes and heterocycles. Squaric acid is an immunotherapy used to treat common warts. This treatment is non-toxic, and easy to use. The treatment activated your immune system to combat the warts and therefore it may cause an allergic reaction , similar to poison oak. This reaction can be managed with a topical cortisone cream. Blistering and lightening of the skin may occur, but rarely.
Squaric acid derivatives – synthetic targets for ring expansion reactions

定義

ChEBI: A carbon oxoacid that consists of 1,2-diketocyclobut-3-ene bearing two enolic hydroxy substituents at positions 3 and 4.

一般的な説明

3,4-dihydroxy-3-cyclobutene-1,2 dione, commonly known as squaric acid, is widely used in bioorganic and medicinal chemistry. It is an inhibitor of glyoxylase, semiqauric acid, pyruvate dehrogenase, and transketolase. It is used as a replacement for phosphate in a peptide-based ligand for an SH₂ domain. Its derivatives are high-affinity ligands for excitatory amino acid receptors. These derivatives are also used as dyes for fluorescence detection of small biological molecules.

生物学的応用

squaric acid is widely used in bioorganic and medicinal chemistry. It is an inhibitor of glyoxylase, semiqauric acid, pyruvate dehrogenase, and transketolase. It is used as a replacement for phosphate in a peptide-based ligand for an SH2 domain. Its derivatives are high-affinity ligands for excitatory amino acid receptors. These derivatives are also used as dyes for fluorescence detection of small biological molecules.
squaric acid can be used:
In fluorescence detection in immunoassays, hybridization assays, enzymatic reactions, and other analytical procedures.
To form diffraction quality crystals.
To synthesize a squarate dianion, which is used as a building block to create uncharged polymeric networks. These ordered structures are used in catalysis, nonlinear optics, electrical conductivity, molecular recognition, and molecular sieves.

純化方法

Purify squaric acid by recrystallisation from H2O — this is quite simple because the acid is ~ 7% soluble in boiling H2O and only 2% at room temperature. It is not soluble in Me2CO or Et2O; hence it can be rinsed with these solvents and dried in air or a vacuum. It is not hygroscopic and gives an intense purple colour with FeCl3. It has IR max at 1820 (C=O) and 1640 (C=C) cm-1, and UV max at 269.5nm ( 37K M-1cm -1). [Cohn et al. J Am Chem Soc 81 3480 1959, Park et al. J Am Chem Soc 84 2919 1962] See also pKa values of 0.59 ±0.09 and 3.48 ±0.023 [Scwartz & Howard J Phys Chem 74 4374 1970]. [Schmidt & Reid Synthesis 869 1978, Beilstein 8 IV 2701.]