Abstract
Cycloheptatrienyl (tropyl) molecules are representative non-alternant hydrocarbons that offer interesting chemistry because of their unique structures and properties. However, there have been a limited number of polycyclic aromatic tropyl cations and radicals reported in the literature. Herein, we report the synthesis of a series of azahomocorannulene derivatives, where the key reactions are a 1,3-dipolar cycloaddition of polycyclic aromatic azomethine ylides with dibenzotropone and a subsequent palladium-catalyzed cyclization. X-ray diffraction analysis revealed that the obtained azahomocorannulenyl cation and radical adopt planar structures and exhibit unique packing structures. Their electronic and optical properties were investigated experimentally and theoretically to reveal their aromatic character.
Original language | English |
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Article number | e202319022 |
Journal | Angewandte Chemie - International Edition |
Volume | 63 |
Issue number | 7 |
DOIs | |
Publication status | Published - Feb 12 2024 |
Externally published | Yes |
Bibliographical note
Publisher Copyright:© 2023 Wiley-VCH GmbH.
ASJC Scopus Subject Areas
- Catalysis
- General Chemistry
Keywords
- 1,3-Dipolar Cycloaddition
- Azahomocorannulene
- Polycyclic Aromatic Molecules
- Tropyl Radicals
- Tropylium