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 C(60). The OFET performance of 7-9 could be tuned and the hybrids show ambipolar characteristics. Notably, the 9·C(60) cocrystal exhibits well-balanced ambipolar performance with electron and hole mobilities of up to 0.19 and 0.11 cm(2) V(-1) s(-1), respectively. This is the first demonstration of a chiral curved PAH and its complex with C(60) for organic devices. Our work presents new insight into buckybowl-based design of PAHs with configurational stability and intriguing optoelectronic properties.