Abstract
Heterocyclic [8]circulenes are an important class of polycyclic aromatic hydrocarbon molecules because of their unique structural properties and promising applications. However, the synthesis of heterocyclic [8]circulenes is still limited and thus is an important synthetic challenge. Here we describe the first example of a π-extended diaza[8]circulene surrounded by and fused with six hexagons and two pentagons, which was successfully synthesized only by a combined in-solution and on-surface synthetic strategy. State-of-the-art scanning tunneling microscopy with a CO-functionalized tip and density functional theory calculations revealed its planar conformation and unique electronic structure.
Original language | English |
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Pages (from-to) | 11363-11369 |
Number of pages | 7 |
Journal | Journal of the American Chemical Society |
Volume | 142 |
Issue number | 26 |
DOIs | |
Publication status | Published - Jul 1 2020 |
Externally published | Yes |
Bibliographical note
Publisher Copyright:Copyright © 2020 American Chemical Society.
ASJC Scopus Subject Areas
- Catalysis
- General Chemistry
- Biochemistry
- Colloid and Surface Chemistry