Abstract
We introduce a class of supramolecular precursors, termed 'folda-bonders', which utilize macrocycles to fold and precisely align reactive groups, effectively acting as bonding facilitators. This design enables highly efficient, selective, and mild 'click-like' reactions, making them particularly well-suited for the modular synthesis of complex structures. In this study, we highlight the versatility of folda-bonders in the one-pot aqueous synthesis of chiral ring-in-ring complexes exhibiting torsion-induced circularly polarized luminescence (CPL). Cucurbit[8]uril macrocycles facilitate the pseudostatic pre-folding of bis(4-phenyl pyridinium) derivatives, which act as folda-bonders, enabling efficient, purification-free covalent cyclization mediated by an axially chiral fragment. The single-crystal structure, obtained directly from the product solution, confirms the formation of a chiral ring-in-ring configuration. The macrocycle-imparted rigidity, combined with the tunable flexibility of alkyl linkers, drives the emergence of distinct chiroptical properties in the ring-in-ring complexes. Remarkably, torsion within the strained shorter alkyl linker is responsible for generating CPL, whereas longer linkers retain chirality, as evidenced by CD signals, but do not exhibit CPL. These findings demonstrate the potential of integrating noncovalent and covalent strategies to design sophisticated molecular architectures with tailored functional properties.