Size Selective Corona Interactions from Self‐Assembled Rosette and Single‐Walled Carbon Nanotubes

Abstract Nanoparticle corona phases, especially those surrounding anisotropic particles, are central to determining their catalytic, molecular recognition, and interfacial properties. It remains a longstanding challenge to chemically synthesize and control such phases at the nanoparticle surface. In this work, the supramolecular chemistry of rosette nanotubes (RNTs), well‐defined hierarchically self‐assembled nanostructures formed from heteroaromatic bicyclic bases, is used to create molecularly precise and continuous corona phases on single‐walled carbon nanotubes (SWCNTs). These RNT–SWCNT (RS) complexes exhibit the lowest solvent‐exposed surface area (147.8 ± 60 m⁻¹) measured to date due to its regular structure. Through Raman spectroscopy, molecular‐scale control of the free volume is also observed between the two annular structures and the effects of confined water. SWCNT photoluminescence (PL) within the RNT is also modulated considerably as a function of their diameter and chirality, especially for the (11, 1) species, where a PL increase compared to other species can be attributed to their chiral angle and the RNT's inward facing electron densities. In summary, RNT chemistry is extended to the problem of chemically defining both the exterior and interior corona interfaces of an encapsulated particle, thereby opening the door to precision control of core–shell nanoparticle interfaces.