Chemistry:Acetylenedicarboxylic acid
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| Names | |
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| Preferred IUPAC name
But-2-ynedioic acid | |
| Other names
2-Butynedioic acid
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| Identifiers | |
3D model (JSmol)
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| 3DMet | |
| 878357 | |
| ChEBI | |
| ChemSpider | |
| EC Number |
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| 26624 | |
| KEGG | |
PubChem CID
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| UNII | |
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| Properties | |
| H 2C 4O 4 | |
| Molar mass | 114.056 g·mol−1 |
| Appearance | Crystalline solid |
| Melting point | 175 to 176 °C (347 to 349 °F; 448 to 449 K) (decomposes)[2] 180–187 °C (decomposes)[1] |
| Conjugate base | Hydrogen acetylenedicarboxylate (chemical formula HC 4O− 4) |
| Hazards | |
| GHS pictograms |   
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| GHS Signal word | Danger |
| H301, H314, H315, H319, H335 | |
| P260, P261, P264, P270, P271, P280, P301+310, P301+330+331, P302+352, P303+361+353, P304+340, P305+351+338, P310, P312, P321, P330, P332+313, P337+313, P362, P363, P403+233, P405, P501 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
 verify (what is   ?)
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| Infobox references | |
Acetylenedicarboxylic acid or butynedioic acid is an organic compound (a dicarboxylic acid) with the formula H
2C
4O
4 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 C
4O2−
4, which consists only of carbon and oxygen, making it an oxocarbon anion. Partial ionization yields the monovalent hydrogen acetylenedicarboxylate anion HC
4O−
4.
The acid was first described in 1877 by Polish chemist Ernest Bandrowski.[2][3][4] 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.[2]
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).[5]
Anions and salts
Hydrogen acetylenedicarboxylate (often abbreviated as Hadc or HADC) is a monovalent anion of acetylenedicarboxylic acid with the formula HC
4O−
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 NaHC
4O
4 · 2H2O and CsHC
4O
4 · 2H2O, nearly coplanar in the guanidinium salt [C(NH
2)
3]+
[HC
4O
4]−
, but off by 60° or more in other salts such as anhydrous KHC
4O
4.[6]
Potassium hydrogen acetylenedicarboxylate is a potassium salt of HADC with chemical formula KHC
4O
4 or K+
HC
4O−
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.[7][8]
Acetylenedicarboxylate (often abbreviated as ADC or adc) is a divalent anion with formula C
4O2−
4 or [O
2C–C≡C–CO
2]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 C
2O2−
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+[C
4O
4]2− · (C
5H
4N)
2]
n.[9][10] Thallium(I) acetylenedicarboxylate (Tl
2C
4O
4) decomposes at 195 °C, leaving a residue of pyrophoric thallium powder.[11]
See also
References
- ↑ 1.0 1.1 "Acetylenedicarboxylic acid". Sigma-Aldrich. https://www.sigmaaldrich.com/catalog/product/aldrich/a15207.
- ↑ 2.0 2.1 2.2 Abbott, T. W.; Arnold, R. T.; Thompson, R. B.. "Acetylenedicarboxylic acid". Organic Syntheses. http://www.orgsyn.org/demo.aspx?prep=cv2p0010.; Collective Volume, 2, pp. 10
- ↑ Bandrowski, E. (1877). "Ueber Acetylendicarbonsäure". Berichte der Deutschen Chemischen Gesellschaft 10: 838–842. doi:10.1002/cber.187701001231. https://zenodo.org/record/1425134.
- ↑ E. Bandrowski (1879). "Weitere Beiträge zur Kenntniss der Acetylendicarbonsäure". Berichte der Deutschen Chemischen Gesellschaft 12 (2): 2212–2216. doi:10.1002/cber.187901202261. https://zenodo.org/record/1425196.
- ↑ Daglar, Ozgun; Çakmakçı, Emrah; Hizal, Gurkan; Tunca, Umit; Durmaz, Hakan (2020-05-05). "Extremely fast synthesis of polythioether based phase change materials (PCMs) for thermal energy storage" (in en). European Polymer Journal 130: 109681. doi:10.1016/j.eurpolymj.2020.109681. ISSN 0014-3057. http://www.sciencedirect.com/science/article/pii/S0014305720307163.
- ↑ Leban, I; Rupnik, A (1992). "Structure of guanidinium hydrogen acetylenedicarboxylate, CH6N+3·C4HO4−". Acta Crystallographica Section C 48 (5): 821. doi:10.1107/S010827019101154X.
- ↑ Leban, Ivan; Golič, Ljubo; Speakman, J. Clare (1973). "Crystal structures of the acid salts of some dibasic acids. Part VII. An X-ray study of potassium hydrogen acetylenedicarboxylate: The α-form". J. Chem. Soc., Perkin Trans. 2 (6): 703–705. doi:10.1039/P29730000703.
- ↑ Miyakubo, Keisuke (1994). Nuclear magnetic resonance studies of dynamical structure of one-dimensional hydrogen-bonded system in the acid salts of some dicarboxylic acids (PDF) (Ph.D.). Osaka University.
- ↑ Li, Ming-xing; Shao, Min; Dai, Hui; An, Bao-li; Lu, Wen-cong; Zhu, Yu; Du, Chen-xia (2005). "Synthesis and Crystal Structure of a Novel Copper(II) Complex with Acetylenedicarboxylate and 2,2′-Bipyridine". Chinese Chemical Letters 16 (10): 1405–1408.
- ↑ Shao, Min; Li, Ming-xing; Dai, Hui; Lu, Wen-cong; An, Bao-li (2007). "Polynuclear complexes incorporating Cu(II) and Mn(II) centers bridged by acetylenedicarboxylate: Structure, thermal stability and magnetism". Journal of Molecular Structure 829 (1–3): 155–160. doi:10.1016/j.molstruc.2006.06.021.
- ↑ Ahlers, Ruth; Ruschewitz, Uwe (2009). "Non-centrosymmetric coordination polymers based on thallium and acetylenedicarboxylate". Solid State Sciences 11 (6): 1058–1064. doi:10.1016/j.solidstatesciences.2009.03.008. http://bib-pubdb1.desy.de/record/91913.
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