超分子化学
化学
笼子
分子
结晶学
三吡啶
壳体(结构)
小角X射线散射
配体(生物化学)
水溶液中的金属离子
纳米技术
金属
材料科学
光学
散射
有机化学
物理
数学
受体
生物化学
复合材料
组合数学
作者
Die Liu,Kaixiu Li,Mingzhao Chen,Tingting Zhang,Zhengguang Li,Jun Yin,Lipeng He,Jun Wang,Panchao Yin,Yi‐Tsu Chan,Pingshan Wang
摘要
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 1H 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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