| |
| |
| |
| Names | |
|---|---|
| Preferred IUPAC name
But-2-ynedinitrile | |
| Identifiers | |
3D model (JSmol) |
|
| ChemSpider |
|
PubChem CID |
|
CompTox Dashboard (EPA) |
|
| |
| |
| 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 |
+500.4 kJ/mol |
| Related compounds | |
Related compounds |
Carbon suboxide Cyanogen |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
Dicyanoacetylene, also called carbon subnitrideorbut-2-ynedinitrile (IUPAC), is a compound of carbon and nitrogen with chemical formula C4N2. It has a linear molecular structure, N≡C−C≡C−C≡N (often abbreviated as NC4N), 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]
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 a reaction between a dihaloacetylene and a cyanide salt:[citation needed]
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.
Solid dicyanoacetylene has been detected in the atmosphere of Titanbyinfrared 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[update], 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]
