• Source: Acetylenedicarboxylic acid

Acetylenedicarboxylic acid or butynedioic acid is an organic compound (a dicarboxylic acid) with the formula H2C4O4 or HO−C(=O)−C≡C−C(=O)−OH. It is a crystalline solid that is soluble in diethyl ether.
The removal of two protons yields the acetylenedicarboxylate dianion C4O2−4, which consists only of carbon and oxygen, making it an oxocarbon anion. Partial ionization yields the monovalent hydrogen acetylenedicarboxylate anion HC4O−4.
The acid was first described in 1877 by Polish chemist Ernest Bandrowski. It can be obtained by treating α,β-dibromosuccinic acid with potassium hydroxide KOH in methanol or ethanol. The reaction yields potassium bromide and potassium acetylenedicarboxylate. The salts are separated and the latter is treated with sulfuric acid.
Acetylenedicarboxylic acid is used in the synthesis of dimethyl acetylenedicarboxylate, an important laboratory reagent. The acid is commonly traded as a laboratory chemical. It can also be reacted with sulfur tetrafluoride to produce hexafluoro-2-butyne, a powerful dienophile for use in Diels-Alder reactions.
Fatty alcohol esters of acetylenedicarboxylic acid can be used for the preparation of phase change materials (PCM).




Anions and salts


Hydrogen acetylenedicarboxylate (often abbreviated as Hadc or HADC) is a monovalent anion of acetylenedicarboxylic acid with the formula HC4O−4 or HO−C(=O)−C≡C−CO−2. The anion can be derived from acetylenedicarboxylic acid by removal of a single proton or from the acetylenedicarboxylate dianion by addition of a proton. The name is also used for any salt of this anion. Salts of this anion are of interest in crystallography because they contain unusually short and strong hydrogen bonds. In many crystalline salts (with the exception of the lithium one), the HADC units form linear chains connected by strong hydrogen bonds. Each carboxylate group is usually planar; but the two groups may lie in different planes due to rotation about the carbon–carbon bonds. They are coplanar in the hydrated salts NaHC4O4·2H2O and CsHC4O4·2H2O, nearly coplanar in the guanidinium salt [C(NH2)3]+[HC4O4]−, but off by 60° or more in other salts such as anhydrous KHC4O4.
Potassium hydrogen acetylenedicarboxylate is a potassium salt of HADC with chemical formula KHC4O4 or K+HC4O−4, often abbreviated as KHadc. It is often called potassium hydrogen acetylenedicarboxylate or monopotassium acetylenedicarboxylate. The salt can be obtained from acetylenedicarboxylic acid and is a common laboratory starting material for the synthesis of other derivatives of that acid. In the crystalline form, the hydrogen acetylenedicarboxylate anions are joined into linear chains by uncommonly short hydrogen bonds.

Acetylenedicarboxylate (often abbreviated as ADC or adc) is a divalent anion with formula C4O2−4 or [O2C−C≡C−CO2]2−; or any salt or ester thereof. The anion can be derived from acetylenedicarboxylic acid by the loss of two protons. It is one of several oxocarbon anions which, like carbonate CO2−3 and oxalate C2O2−4, consist solely of carbon and oxygen. The ADC anion can aсt as a ligand in organometallic complexes, such as the blue polymeric complex with copper(II) and 2,2′-bipyridine, [Cu2+[C4O4]2−·(C5H4N)2]n. Thallium(I) acetylenedicarboxylate (Tl2C4O4) decomposes at 195 °C, leaving a residue of pyrophoric thallium powder.




See also


Acetylenedicarboxylate decarboxylase
Oxalic acid
Acetylenediol




References

Kata Kunci Pencarian:

• Acetylenedicarboxylic acid
• List of carboxylic acids
• Dimethyl acetylenedicarboxylate
• Lindlar catalyst
• Dicarboxylic acid
• Succimer
• Propiolic acid
• Ernest Tytus Bandrowski
• 1,4-Butynediol
• 2-Butyne