Revisiting butafulvene formation by thermal dimerization of fluorene-based dialkynes: effects of aromatic substituents
Butafulvenes, together with pentafulvenes and [3]radialenes, form a series of constitutional benzene isomers in which aromaticity changes significantly and can be strongly substituent dependent. Butafulvene, as a member of this series, is frequently proposed to be antiaromatic. Based on butafulvenes...
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| Hauptverfasser: | , , , |
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| Dokumenttyp: | Article (Journal) |
| Sprache: | Englisch |
| Veröffentlicht: |
January 2, 2025
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| In: |
Chemistry - a European journal
Year: 2025, Jahrgang: 31, Heft: 1, Pages: 1-9 |
| ISSN: | 1521-3765 |
| DOI: | 10.1002/chem.202403049 |
| Online-Zugang: | Verlag, kostenfrei, Volltext: https://doi.org/10.1002/chem.202403049 Verlag, kostenfrei, Volltext: https://onlinelibrary.wiley.com/doi/abs/10.1002/chem.202403049 
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| Verfasserangaben: | Moritz P. Schuldt, Tatjana Maximenko, Frank Rominger, and Michael Mastalerz |
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| 245 | 1 | 0 | |a Revisiting butafulvene formation by thermal dimerization of fluorene-based dialkynes |b effects of aromatic substituents |c Moritz P. Schuldt, Tatjana Maximenko, Frank Rominger, and Michael Mastalerz |
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| 520 | |a Butafulvenes, together with pentafulvenes and [3]radialenes, form a series of constitutional benzene isomers in which aromaticity changes significantly and can be strongly substituent dependent. Butafulvene, as a member of this series, is frequently proposed to be antiaromatic. Based on butafulvenes Hopf, Zimmerman and coworkers first time described, derivatives thereof were synthesized and the effects of substituents on both the stability of the intermediate isobenzenes and on their optoelectronic and (anti)aromatic properties are discussed. | ||
| 650 | 4 | |a Antiaromaticity | |
| 650 | 4 | |a Butafulvene | |
| 650 | 4 | |a DFT Calculations | |
| 650 | 4 | |a Fluorene | |
| 650 | 4 | |a Isobenzenes | |
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