Bicyclopropenyl
| |
| |
| Names | |
|---|---|
| Preferred IUPAC name
[1,1′-Bi(cyclopropane)]-1,1′-diene | |
| Other names
1,1′-Bi(cycloprop-2-en-1-yl)
3,3'-Bicyclopropenyl | |
| Identifiers | |
3D model (JSmol)
|
|
| ChemSpider | |
PubChem CID
|
|
CompTox Dashboard (EPA)
|
|
| |
| |
| Properties | |
| C6H6 | |
| Molar mass | 78.1 g/mol |
| Melting point | −75 °C; −103 °F; 198 K |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
| |
Bicyclopropenyl (bicycloprop-2-enyl, C6H6) is an organic compound and one of several valence isomers of benzene. The molecule can be described as two coupled cyclopropene units. The positions of the alkene groups can vary and therefore two other isomers are known: bicycloprop-1,2-enyl and bicyclopropen-1-yl.
The synthesis of all three isomers was reported in 1989 By Billups and Haley.[1][2] The 3,3 isomer was formed in two steps by reaction of 1,4-bis(trimethylsilyl)buta-1,3-diene with methyllithium and dichloromethane, introducing two cyclopropane rings into the molecule. The bis(2-chloro-3-(trimethylsilyl)cyclopropan-1-yl) formed is reacted with TBAF. In this latter reaction fluoride couples to the trimethylsilyl group, in the process forming the double bond and forcing the chlorine atom to leave as chloride. In presence of silver ions bicycloprop-2-enyl rearranges to Dewar benzene. The compound can also be trapped by cyclopentadiene. Above -10 °C it decomposes with polymerization.
An X-ray crystal structure has been reported.[3] The bond length for the central bond is short by 1.503 Ångström (150.3 pm).
The other two isomers are increasingly unstable. Bicycloprop-1-enyl can only be detected in trapping experiments.
| Properties benzene valence isomers | ||
|---|---|---|
| Compound | Calc. Heat of formation[4][5] | Calc. Heat of formation [4][5] |
| 0 K (KJ/mole) | 298 K (KJ/mole) | |
| Benzene | 100.5 | 82.0 |
| Dewar benzene | 415.5 | 397.1 |
| Benzvalene | 397.5 | 378.1 |
| Prismane | 567.2 | 547.0 |
| Bicycloprop-2-enyl | 593.6 | 578.8 |
Derivatives can be much more stable, for example perfluorohexamethylbicyclopropenyl that must be heated to 360 °C to be as unstable.[6]
References
[edit]- ^ Billups, W. E.; Haley, M. M. (1989). "Bicycloprop-2-enyl (C6H6)". Angewandte Chemie International Edition in English. 28 (12): 1711. doi:10.1002/anie.198917111.
- ^ Billups, W. E.; Haley, M. M.; Boese, R.; Bläser, D. (1994). "Synthesis of the bicyclopropenyls". Tetrahedron. 50 (36): 10693–10700. doi:10.1016/S0040-4020(01)89261-9.
- ^ Boese, R.; Blaeser, D.; Gleiter, R.; Pfeifer, K. H.; Billups, W. E.; Haley, M. M. (1993). "Structure and photoelectron spectrum of 3,3'-bicyclopropenyl". Journal of the American Chemical Society. 115 (2): 743. doi:10.1021/ja00055a052.
- ^ a b Cheung, Y. (1998). "Ab initio calculations of the heats of formation for (CH)6 isomers". Journal of Molecular Structure: THEOCHEM. 454: 17–20. doi:10.1016/S0166-1280(98)00189-4.
- ^ a b G2 level, isodesmic bond separation scheme
- ^ Billups, W. E.; M. Haley, Michael; Boese, Roland; Bläser, Dieter (1994-01-01). "Synthesis of the bicyclopropenyls". Tetrahedron. The International Journal for the Rapid Publication of Critical. 50 (36): 10693–10700. doi:10.1016/S0040-4020(01)89261-9.
Text is available under the CC BY-SA 4.0 license; additional terms may apply.
Images, videos and audio are available under their respective licenses.
