From Surf Wiki (app.surf) — the open knowledge base
Circulene
Class of chemical
Class of chemical
A circulene is a macrocyclic arene in which a central polygon is surrounded and fused by benzenoids. Nomenclature within this class of molecules is based on the number of benzene rings surrounding the core, which is equivalent to the size of the central polygon. Examples which have been synthesized include [5]circulene (corannulene), [6]circulene (coronene), [7]circulene, and [12]circulene (kekulene) These compounds belong to a larger class of geodesic polyarenes. Whereas [5]circulene is bowl-shaped and [6]circulene is planar, [7]circulene has a unique saddle-shaped structure (compare to cones and partial cones in calixarenes). The helicenes are a conceptually related class of structures in which the array of benzene rings form an open helix rather than a closed ring.
Quadrannulene ([4]circulene)
The simple [4]circulene compound itself has not been synthesized, but a derivative, tetrabenzo[4]circulene, also called quadrannulene, has.
[8]Circulenes
The isolation of the [8]circulene derivative 2,5,6,9,10,13,14-octamethyl-3,4,7,8,11,12,15,16-octa(4-tolyl)[8]circulene has been reported. Tetrabenzo[8]circulene (TB8C), a functionally stable form of the parent molecule [8]circulene has also been reported.
Heterocyclic circulenes
A heterocyclic circulene is one in which the fused rings around the periphery are not simple hydrocarbons, but instead contain at least one other element. Sulflower is a stable heterocyclic octacirculene based on thiophene.
Gallery
Image:Corannulene.svg|Corannulene ([5]circulene) Image:Coronene 200.svg|Coronene ([6]circulene) Image:-7-circulene.svg|[7]circulene Image:Kekulene.svg|Kekulene ([12]circulene)
References
References
- (1972). "Heterocirculenes a new class of polycyclic aromatic hydrocarbons". Tetrahedron Letters.
- (1983). "Synthesis and characterization of [7]circulene". Journal of the American Chemical Society.
- (1988). "Synthesis and molecular structure of [7]circulene". Journal of the American Chemical Society.
- (1996). "Convenient New Synthesis of [7]Circulene". Angew. Chem. Int. Ed. Engl..
- ''Extended systems of closed helicene. Synthesis and characterization of [7] and [7.7]-circulene'' Koji Yamamoto Pure Appl. Chem., Vol. 65, No. 1, pp. 157-163, '''1993'''. [http://www.iupac.org/publications/pac/1993/pdf/6501x0157.pdf Online article]
- (2010). "Quadrannulene: A Nonclassical Fullerene Fragment". Angew. Chem. Int. Ed..
- (2013). "Synthesis, Structural Analysis, and Properties of [8]Circulenes". Angew. Chem. Int. Ed..
- (24 February 2014). "Synthesis and Structural Data of Tetrabenzo[8]circulene". Chem. Eur. J..
- (2013). "Tetrabenzo[8]circulene: Aromatic Saddles from Negatively Curved Graphene". J. Am. Chem. Soc..
- (2 December 2016). "General Method for the Synthesis of Functionalized Tetrabenzo[8]circulenes". The Journal of Organic Chemistry.
This article was imported from Wikipedia and is available under the Creative Commons Attribution-ShareAlike 4.0 License. Content has been adapted to SurfDoc format. Original contributors can be found on the article history page.
Ask Mako anything about Circulene — get instant answers, deeper analysis, and related topics.
Research with MakoFree with your Surf account
Create a free account to save articles, ask Mako questions, and organize your research.
Sign up freeThis content may have been generated or modified by AI. CloudSurf Software LLC is not responsible for the accuracy, completeness, or reliability of AI-generated content. Always verify important information from primary sources.
Report