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.