Synthesis of trisilasupersumanene shows strong binding to fullerenes, indicating novel assembly structures.
A silicon-doped nanographenic bowl, trisilasupersumanene 1, was synthesized via a 3-fold palladium-catalyzed sila-annulation from the hexachlorinated trifluorenocoronene. Incorporating silole rings into the aromatic framework leads to new reduction waves in cyclic voltammetry and low-lying LUMO levels. The bowl 1 exhibits high binding affinity to fullerenes C60 and C70, forming supramolecular complexes 1⊃C60 and (1)2⊃C70 with unique packing arrangements. Notably, (1)2⊃C70 features a rare clam-like structure in the crystal, entirely different from its binding behavior in solution.
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Yang et al. (2025) studied this question.
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