Chemistry:Dicyanoacetylene
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| Names | |
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| Preferred IUPAC name
But-2-ynedinitrile | |
| Identifiers | |
3D model (JSmol)
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| ChemSpider | |
PubChem CID
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| Properties | |
| C4N2 | |
| Molar mass | 76.058 g·mol−1 |
| Density | 0.907 g/cm3 |
| Melting point | 20.5 °C (68.9 °F; 293.6 K) |
| Boiling point | 76.5 °C (169.7 °F; 349.6 K) |
| Thermochemistry | |
Std enthalpy of
formation (ΔfH⦵298) |
+500.4 kJ/mol |
| Related compounds | |
Related compounds
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Carbon suboxide Cyanogen |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
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| Infobox references | |
Dicyanoacetylene, also called carbon subnitride or but-2-ynedinitrile (IUPAC), is a compound of carbon and nitrogen with chemical formula C
4N
2. It has a linear molecular structure, N≡C–C≡C–C≡N (often abbreviated as NC
4N), with alternating triple and single covalent bonds. It can be viewed as acetylene with the two hydrogen atoms replaced by cyanide groups.
At room temperature, dicyanoacetylene is a clear liquid. Because of its high endothermic heat of formation, it can explode to carbon powder and nitrogen gas, and it burns in oxygen with a bright blue-white flame at a temperature of 5,260 K (4,990 °C; 9,010 °F), the hottest flame in oxygen; burned in ozone at high pressure the flame temperature exceeds 6,000 K (5,730 °C; 10,340 °F).[1]
Synthesis
Dicyanoacetylene can be prepared by passing nitrogen gas over a sample of graphite heated to temperatures between 2673 and 3000 K.[2] It may also be synthesized via an SN2 reaction between a dihaloacetylene and a cyanide salt:
[math]\ce{ C2X2 + 2 R-CN -> C4N2 + 2 RX }[/math]
As a reagent in organic chemistry
Dicyanoacetylene is a powerful dienophile because the cyanide groups are electron-withdrawing, so it is a useful reagent for Diels-Alder reactions with unreactive dienes. It even adds to the aromatic compound durene (1,2,4,5-tetramethylbenzene) to form a substituted bicyclooctatriene.[3] Only the most reactive of dienophiles can attack such aromatic compounds.
In outer space
Solid dicyanoacetylene has been detected in the atmosphere of Titan by infrared spectroscopy.[4] As the seasons change on Titan, the compound condenses and evaporates in a cycle, which allows scientists on Earth to study Titanian meteorology.
(As of 2006), the detection of dicyanoacetylene in the interstellar medium has been impossible, because its symmetry means it has no rotational microwave spectrum. However, similar asymmetric molecules like cyanoacetylene have been observed, and its presence in those environments is therefore suspected.[5]
See also
- Cyanogen, N≡C−C≡N
- Diacetylene, H−C≡C−C≡C−H
- Cyanopolyynes
References
- ↑ Kirshenbaum, A. D.; Grosse, A. V. (1956). "The Combustion of Carbon Subnitride, C4N2, and a Chemical Method for the Production of Continuous Temperatures in the Range of 5000–6000K". Journal of the American Chemical Society 78 (9): 2020. doi:10.1021/ja01590a075.
- ↑ Ciganek, E.; Krespan, C. G. (1968). "Syntheses of Dicyanoacetylene". The Journal of Organic Chemistry 33 (2): 541–544. doi:10.1021/jo01266a014.
- ↑ Weis, C. D. (1963). "Reactions of Dicyanoacetylene". Journal of Organic Chemistry 28 (1): 74–78. doi:10.1021/jo01036a015.
- ↑ Samuelson, R. E.; Mayo, L. A.; Knuckles, M. A.; Khanna, R. J. (1997). "C4N2 Ice in Titan's North Polar Stratosphere". Planetary and Space Science 45 (8): 941–948. doi:10.1016/S0032-0633(97)00088-3. Bibcode: 1997P&SS...45..941S.
- ↑ Kołos, R. (2002). "Exotic Isomers of Dicyanoacetylene: A Density Functional Theory and ab initio Study". Journal of Chemical Physics 117 (5): 2063–2067. doi:10.1063/1.1489992. Bibcode: 2002JChPh.117.2063K. https://zenodo.org/record/1000211.
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