Tricarbon
| Tricarbon | |
|---|---|
 | |
| Other names Triatomic carbon[citation needed] | |
| Identifiers | |
| CAS number | 12075-35-3  |
| PubChem | 6432003 |
| ChemSpider | 4937270 |
| Jmol-3D images | {{#if:[C]=C=[C]|Image 1 |
| |
| |
| Properties | |
| Molecular formula | C3 |
| Molar mass | 36.03 g mol−1 |
| Thermochemistry | |
| Std enthalpy of formation ΔfH |
820.06 kJ mol−1 |
| Standard molar entropy S |
237.27 J K−1 mol−1 |
| Related compounds | |
| Related alkanylidenes | Diatomic carbon |
| Except where noted otherwise, data are given for materials in their standard state (at 25 °C (77 °F), 100 kPa) | |
| Infobox references | |
Tricarbon (systematically named 1λ2,3λ2-propadiene and μ-carbidodicarbon) is an inorganic compound with the chemical formula C
2(μ-C) (also written [C(μ-C)C] or C
3). It is a colourless gas that only persists in dilution or solution as an adduct. It is one of the simplest unsaturated carbenes.
It is a small carbon cluster first spectroscopically observed in the beginning 20th century in the tail of a comet by William Huggins and subsequently identified in stellar atmospheres. Tricarbon can be found in interstellar space and can be produced in the laboratory by a process called laser ablation. Small carbon clusters like tricarbon and dicarbon are regarded as soot precursors and are implicated in the formation of certain industrial diamonds and in the formation of fullerenes. The ground state molecular geometry of tricarbon has been identified as linear via its characteristic symmetric and antisymmetric stretching and bending vibrational modes and bears bond lengths of 129 to 130 picometer corresponding to those of alkenes. The ionization potential is determined experimentally at 11 to 13.5 electron-volts.[1] In contrast to the linear tricarbon molecule the C3+ cation is bent.
C3 has also been identified as a transient species in various combustion reactions.[citation needed]
The generation of C3 was investigated by Professor Emeritus Philip S. Skell of Pennsylvania State University in the 1960s.[citation needed]
Nomenclature
The systematic names 1λ2,3λ2-propadiene, and μ-carbidodicarbon, valid IUPAC names, are constructed according to the substitutive and additive nomenclatures, respectively.
In appropriate contexts, tricarbon can be viewed as propadiene with four hydrogen atoms removed, or as propane with eight electrons removed; and as such, propadienediylidene or propanetetraylidene, respectively, may be used as a context-specific systematic names, according to substitutive nomenclature. By default, these names pay no regard to the radicality of the tricarbon molecule. In even more specific context, these can also name the non-radical singlet state, whereas the diradical state is named propadienediylylidene, or propanediyldiylidene, and the tetraradical state is named propedienetetrayl or propanetetraylylidene.
See also
- Hydrocarbons
- Alkenes
- List of molecules in interstellar space
- Cyclopropatriene
References
- ↑ Nicolas, Christophe; et al. (2006). "Vacuum Ultraviolet Photoionization of C3". J. Am. Chem. Soc. 128 (1): 220–226. doi:10.1021/ja055430. PMID 16390150.
Further reading
- Gaydon, Alfred G.; Wolfhard, Hans G. (1979). Flames: their structure, radiation and temperature (4. ed., rev. ed.). London: Chapman and Hall. ISBN 0-412-15390-4.
- Hinkle, Kenneth W.; Keady, John J.; Bernath, Peter F. (1988). "Detection of C3 in the Circumstellar Shell of IRC+10216". Science 241 (4871): 1319–1322. Bibcode:1988Sci...241.1319H. doi:10.1126/science.241.4871.1319. PMID 17828935.
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