Issue 38, 2023

Buckybowl and its chiral hybrids featuring eight-membered rings and helicene units

Abstract

Here we report the synthesis of a novel buckybowl (7) with a high bowl-to-bowl inversion barrier (ΔG = 38 kcal mol−1), which renders the rate of inversion slow enough at room temperature to establish two chiral polycyclic aromatic hydrocarbons (PAHs). By strategic fusion of eight-membered rings to the rim of 7, the chiral hybrids 8 and 9 are synthesized and display helicity and positive and negative curvature, allowing the enantiomers to be configurationally stable and their chiroptical properties are thoroughly examined. Computational and experimental studies reveal the enantiomerization mechanisms for the chiral hybrids and demonstrate that the eight-membered ring strongly affects the conformational stability. Because of its static and doubly curved conformation, 9 shows a high binding affinity towards C60. The OFET performance of 7–9 could be tuned and the hybrids show ambipolar characteristics. Notably, the 9·C60 cocrystal exhibits well-balanced ambipolar performance with electron and hole mobilities of up to 0.19 and 0.11 cm2 V−1 s−1, respectively. This is the first demonstration of a chiral curved PAH and its complex with C60 for organic devices. Our work presents new insight into buckybowl-based design of PAHs with configurational stability and intriguing optoelectronic properties.

Graphical abstract: Buckybowl and its chiral hybrids featuring eight-membered rings and helicene units

Supplementary files

Article information

Article type
Edge Article
Submitted
06 Feb 2023
Accepted
07 Mar 2023
First published
14 Mar 2023
This article is Open Access

All publication charges for this article have been paid for by the Royal Society of Chemistry
Creative Commons BY-NC license

Chem. Sci., 2023,14, 10420-10428

Buckybowl and its chiral hybrids featuring eight-membered rings and helicene units

Y. Duan, M. Chen, H. Hayashi, H. Yamada, X. Liu and L. Zhang, Chem. Sci., 2023, 14, 10420 DOI: 10.1039/D3SC00658A

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