Toward larger cyclo-9,10-anthryleneparaphenylenes
Nanohoops of different sizes can be generated from various aromatic building blocks. By a cross-coupling strategy of an anthracene-based kinked precursor and 9,10-diborylated anthracene, nanohoops based on diphenylanthracene units were synthesized and isolated up to the nonamer with 36 para-connecte...
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| Hauptverfasser: | , , , |
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| Dokumenttyp: | Article (Journal) |
| Sprache: | Englisch |
| Veröffentlicht: |
27 March 2026
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| In: |
Chemistry - a European journal
Year: 2026, Pages: 1-13 |
| ISSN: | 1521-3765 |
| DOI: | 10.1002/chem.70878 |
| Online-Zugang: | Verlag, kostenfrei, Volltext: https://doi.org/10.1002/chem.70878 Verlag, kostenfrei, Volltext: https://onlinelibrary.wiley.com/doi/abs/10.1002/chem.70878 
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| Verfasserangaben: | Moritz P. Schuldt, Frank Rominger, Sven M. Elbert, Michael Mastalerz |
| Zusammenfassung: | Nanohoops of different sizes can be generated from various aromatic building blocks. By a cross-coupling strategy of an anthracene-based kinked precursor and 9,10-diborylated anthracene, nanohoops based on diphenylanthracene units were synthesized and isolated up to the nonamer with 36 para-connected aromatic rings. Their three-dimensional structures were investigated by X-ray diffraction, and their reactivity against oxygen was studied. The trimeric macrocycle was rearomatized to the corresponding cyclo-9,10-anthryleneparaphenylene (CAPP) in solution, which turned out to be prone to oxidation. |
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| Beschreibung: | Gesehen am 22.04.2026 |
| Beschreibung: | Online Resource |
| ISSN: | 1521-3765 |
| DOI: | 10.1002/chem.70878 |