A self-assembled ML truncated square and its application as a container for fullerenes.

An unprecedented bisthianthrene dipyridyl ligand was designed and synthesized for coordination driven self-assembly. The combination of this conformationally dynamic linker with a 90° convergent metal corner exclusively afforded a novel ML truncated square-like metallamacrocycle. The single crystal X-ray structure reveals a belt-shaped geometry with a cavity diameter of 13.7 Å. The breathable cavity and electron-rich thianthreno panels enable the highly efficient binding of the fullerenes C ( = 5.1 × 10 M) and C ( = 3.7 × 10 M). The encapsulation of C is fully confirmed by NMR, mass spectroscopy and single crystal X-ray diffraction analyses. The cyclic voltammograms further reveal that the truncated square is redox active. The strong binding affinity, adaptive complexation, and redox activity of the thianthrene-incorporated metallamacrocycle provide new insights into the design of supramolecular hosts.