Pinwheel-like Curved Aromatics from the Cyclotrimerization of Strained Alkyne Cycloparaphenylenes

Carbon nanomaterials composed of curved aromatics, such as carbon nanotubes, are difficult to selectively synthesize and modify precisely. Smaller molecular fragments of curved nanomaterials, such as cycloparaphenylenes, benefit from the precision of bottom-up synthesis, however, efforts to expand the curved molecular framework into even larger structures often rely on restrictive early stage synthetic strategies or difficult to control polymerizations. In this work we report a high yielding, strain-promoted, late-stage modification of a series of [n + 1]CPPs. We show that the conversion of these [n + 1]CPPs into soluble, pinwheel-like multipore carbon nanostructures is achievable via a straightforward and efficient 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. We also demonstrate the strain-enhanced nature of the reaction under the optimized conditions, showing that strained internal-alkyne [n + 1]CPPs efficiently undergo complete conversion whereas unstrained diphenylacetylene remains completely unreacted. We anticipate that this work will have broader impacts on the study of reactivity in strained-alkyne-containing hydrocarbons, and that access to this new molecular architecture will inspire new research and applications in materials science and related fields.