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Curved aromatic hydrocarbons often display better solubility and more desirable electronic properties in comparison to their flat counterparts. Macrocyclic curved aromatics possess these traits as well as shape-persistent pores ideal for host-guest interactions. A quintessential macrocyclic curved aromatic molecule is the cycloparaphenylene, or [n]CPP. Our group has developed a new class of these carbon nanohoops, called [n+1]CPPs, that incorporate a strained alkyne (“+1”) into the carbon backbone. We have previously shown the [n+1]CPPs to be a promising new class of strain-promoted azide-alkyne cycloaddition click reagents. Herein, we show that the [n+1]CPPs can also be converted into pinwheel-like multi-pore large molecules via a straightforward and high yielding metal-mediated alkyne cyclotrimerization reaction. We provide insight into suitable metals for this transformation, the photophysics of these trimeric molecules, as well as their strain profiles and crystal packing. 

Polycatechol nanohoop ligands are readily synthesized from fluorinated precursors and metalated, opening the door to new carbon nanohoop-based metal–organic materials.