Synthesis and Properties of Azahomocorannulenyl Cations and Radicals

Yosuke Hamamoto, Kotaro Ochiai, Yongxin Li, Enrico Tapavicza, Shingo Ito*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

6 Citations (Scopus)

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 languageEnglish
Article numbere202319022
JournalAngewandte Chemie - International Edition
Volume63
Issue number7
DOIs
Publication statusPublished - Feb 12 2024
Externally publishedYes

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

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