A series of metallo-supramolecular ring-in-ring structures was generated by assembling Cd(II) ions and the multivalent terpyridine ligands (L(1-3)) composed of one 60°-bent and two 120°-bent bis(terpyridine)s with varying alkyl linker lengths. The mechanistic study for the self-assembly process excluded an entropically templated pathway and showed that the intramolecularly complexed species is the key intermediate leading to ring-in-ring formation. The next-generation superstructure, a spiderweb, was produced in quantitative yield using the elongated decakis(terpyridine) ligand (L(5)).

Three unsymmetrical, 60°-bended bisterpyridine ligands with varying phenylene spacer lengths have been synthesized via the Suzuki-Miyaura coupling reactions. Their self-assembly processes were found to be strongly dependent on the ligand geometry. Upon complexation with Zn(II) ions, only 2,4''-di(4'-terpyridinyl)-1,1':4',1''-terphenyl underwent self-selection to give a trinuclear metallomacrocycle with perfect heteroleptic connectivity and the other two afforded a mixture of constitutional isomers. The metallosupramolecular assemblies were characterized by NMR spectroscopy, electrospray mass spectrometry (ESI MS), and single-crystal X-ray diffraction. In particular, the identification of isomeric architecture was accomplished using tandem mass spectrometry (MS(2)) coupled with traveling wave ion mobility mass spectrometry (TWIM MS).

Two hexanuclear metalloprisms possessing three dibenzo[24]crown-8 units were generated in quantitative yields by complexation of the predesigned tetratopic 2,2':6',2''-terpyridine ligand (T) with Cd and Zn ions, respectively. The prismatic hosts were subsequently self-assembled with the trifunctional guest molecule (TriG) containing dibenzylammonium ions to afford the corresponding metallo-supramolecular pseudo-suit[3]anes. It was serendipitously found that the host-guest inclusion rates could be modulated by the subtle dynamic difference in metal-ligand frameworks, finally leading to a selective encapsulation event in the presence of both metallo-suits.

Metal-ligand coordination and host-guest recognition are introduced into the hybrid system in order to prepare supramolecular gels, which can be responsive to multiple external stimuli such as metal ions, competitive guest/host molecules, and oxidants. To this end, the triangular terpyridine-based metallocycles functionalized with 1-adamantyl and ferrocenyl groups are constructed through self-assembly, and further used as supramolecular cross-linkers for gelation of β-CD-containing copolymers. Their gelation and stimuli-response tests are discussed, and an application of the metallotriangles for serving as supramolecular glue is demonstrated through a series of adhesion experiments. This approach enables facile access to construction of multifunctional metallosupramolecules as well as functional hybrid materials.

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