Synthesis and Characterization of Self-Assembled Nanoscopic Metallarectangles Capable of Binding Fullerenes with Size-Selective Responses

Two
new metallarectangles, 4 and 5, were
obtained from the self-assembly of areneruthenium-based molecular
clips 2 and 3 with a new dipyridyl donor
ligand 1 containing a diamide core and ethynyl spacers.
The metallarectangles were characterized by multinuclear NMR, electrospray
ionization mass spectrometry, and UV–vis spectroscopy,
and the molecular structure of 4 was unambiguously determined
by single-crystal X-ray diffraction analysis. Because of the presence
of an extended π-electron aromatic surface, the tetracene-containing
molecular rectangle 5 was capable of binding C60 and C70 fullerenes as quantified by UV–vis, emission,
and 1H NMR experiments, providing an example
of a supramolecular host capable of recognizing large guest molecules.