The synthesis of π-extended pyrenes keeps attracting considerable attention. In particular, frameworks containing nonbenzenoid rings might display intriguing properties. Here, we report a practical synthetic pathway to access a new buckybowl (1), which is composed of four five-membered rings externally fused to a pyrene core. The buckybowl 1 exhibits antiaromaticity involving 22 π-electrons, a rapid bowl-to-bowl interconversion, and a small band gap. Furthermore, this buckybowl could be subjected to Scholl cyclodehydrogenation to prepare the doubly curved nanocarbons (2 and 2), which exist as two diastereomers, as demonstrated by X-ray crystal structure determination. Variable temperature H NMR measurements reveal that 2 can isomerize into 2 under thermal conditions, with an activation free energy of 27.1 kcal mol. Both the enantiomers of 2 can be separated by chiral HPLC and their chiroptical properties are thoroughly examined. In addition, the nanocarbon 2 with two gulf architectures facilitates host-guest chemistry with a variety of guests, including PDI, TDI, C and C.
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| http://dx.doi.org/10.1039/d4sc03460k | DOI Listing |
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