Chemistry:Octacene
From HandWiki
Octacene is an organic compound and a polycyclic aromatic hydrocarbon and the eighth member of the acene or polyacene family of linear fused benzene rings.[1][2][3] Its сhemical formula is C
34H
20.
Synthesis
In 2010, the Bettinger group reported a photochemical synthesis of octacene and nonacene, utilizing a cryogenic matrix-isolation technique to stabilize these highly reactive acenes. This approach requires precursors containing a double α-diketone bridge to enable the formation of octacene and nonacene.[4]
References
- ↑ "Octacene" (in en). NIST. https://webbook.nist.gov/cgi/formula?ID=C258333.
- ↑ Siegel, Jay S.; Wu, Yao-Ting (13 November 2014) (in en). Polyarenes I. Springer. p. 21. ISBN 978-3-662-43379-9. https://books.google.com/books?id=5jBgBQAAQBAJ&dq=octacene&pg=PA21. Retrieved 24 July 2025.
- ↑ Zeitter, Nico; Hippchen, Nikolai; Baur, Philipp; Unterreiner, Tamara V.; Rominger, Frank; Freudenberg, Jan; Bunz, Uwe H. F. (February 2024). "Pentacene to Octacene: The Limit of Fourfold TIPS-Ethynylation" (in en). Organic Materials 06 (1): 12–17. doi:10.1055/a-2241-0243. ISSN 2625-1825. https://www.thieme-connect.com/products/ejournals/abstract/10.1055/a-2241-0243. Retrieved 25 July 2025.
- ↑ Lerena, Laura; Zuzak, Rafal; Godlewski, Szymon; Echavarren, Antonio M. (2024). "The Journey for the Synthesis of Large Acenes" (in en). Chemistry – A European Journal 30 (57). doi:10.1002/chem.202402122. ISSN 1521-3765. PMID 39077888. Bibcode: 2024ChEuJ..30E2122L. https://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/chem.202402122. Retrieved 24 July 2025.
