Triafulvalene
Triafulvalene or cyclopropenylidenecyclopropene is a fulvalene hydrocarbon with chemical formula C6H4, composed of two linked cyclopropene rings. Triafulvalene has never been isolated,[1] since it can decompose via an isodesmic reaction.[2] However, this molecule is of theoretical significance for theoretical organic chemists,[3] and its structure, stability, and spectral properties are well-studied.[4]
Names | |
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Other names
[1,1'-Bi(cyclopropylidene)]-2,2'-diene 1,1'-Bi(cycloprop-2-en-1-ylidene) | |
Identifiers | |
3D model (JSmol) |
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Properties | |
C6H4 | |
Molar mass | 76.098 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
Infobox references | |
See also
References
- Carey, Francis A.; Richard J. Sundberg (2007). Advanced Organic Chemistry: Part A: Structure and Mechanisms. Springer Science & Business Media. pp. 755–787. ISBN 0-387448-99-3.
- Neuenschwander, Markus (1986), "Synthetic and NMR spectroscopic investigations of fulvenes and fulvalenes" (PDF), Pure Appl. Chem., 58 (1): 55–66, doi:10.1351/pac198658010055
- Scott, Anthony P.; Agranat, Israel; Biedermann, P. Ulrich; Riggs, Noel V.; Radom, Leo (1997). "Fulvalenes, Fulvenes, and Related Molecules: An ab Initio Study". The Journal of Organic Chemistry. 62 (7): 2026–2038. doi:10.1021/jo962407l. ISSN 0022-3263.
- "Time Dependent Density Functional Study on the Electronic Spectra of Some Derivatives of Triafulvalene" (PDF). Canadian Chemical Transactions: 438–445. 2016-01-06. doi:10.13179/canchemtrans.2015.03.04.0241.
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