4.8 Article

Russian-Doll-Like Molecular Cubes

Journal

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 143, Issue 6, Pages 2537-2544

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/jacs.0c11703

Keywords

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Funding

  1. National Natural Science Foundation of China [22001047, 21971257]
  2. Science and Technology Research Project of Guangzhou, China [202002010007]
  3. Hunan Science and Technology Plan Project, China [2019TP1001]

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This study synthesized two large double-shell supramolecular cages by self-assembly, providing a new approach for simulating complex virus capsids and exploring potential applications in functional recognition, delivery, and detection of various guest molecules.
Nanosized cage-within-cage compounds represent a synergistic molecular self-assembling form of three-dimensional architecture that has received particular research focus. Building multilayered ultralarge cages to simulate complicated virus capsids is believed to be a tough synthetic challenge. Here, we synthesize two large double-shell supramolecular cages by facile self-assembly of presynthesized metal-organic hexatopic terpyridine ligands with metal ions. Differing from the mixture of prisms formed from the inner tritopic ligand, the redesigned metal-organic hexatopic ligands bearing high geometric constraints that led to the exclusive formation of discrete double-shell structures. These two unique nested cages are composed of inner cubes (5.1 nm) and outer huge truncated cubes (12.0 and 13.2 nm) with six large bowl-shape subcages distributed on six faces. The results with molecular weights of 75 232 and 77 667 Da were among the largest synthetic cage-in-cage supramolecules reported to date. The composition, size and shape were unambiguously characterized by a combination of H-1 NMR, DOSY, ESI-MS, TWIM-MS, TEM, AFM, and SAXS. This work provides an interesting model for functional recognition, delivery, and detection of various guest molecules in the field of supramolecular materials.

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