Multicomponent Metallo-Supramolecular Nanocapsules Assembled from Calix[4]resorcinarene-Based Terpyridine Ligands

• Published in: Journal of the American Chemical Society Vol. 142; no. 15; pp. 7134 - 7144
• Main Authors: He, Lipeng, Wang, Shi-Cheng, Lin, Lin-Ting, Cai, Jhen-Yu, Li, Lijie, Tu, Tsung-Han, Chan, Yi-Tsu
• Format: Journal Article
• Language: English
• Published: WASHINGTON American Chemical Society 15.04.2020; Amer Chemical Soc
• Subjects: Chemistry; Chemistry, Multidisciplinary; Physical Sciences; Science & Technology; MOBILITY-MASS-SPECTROMETRY; DESIGN; CAVITAND; CONSTRUCTION; COMPLEXES; SIERPINSKI TRIANGLES; CRYSTALS; COORDINATION; GUEST ENCAPSULATION; RESORCINARENE CAPSULE
• ISSN: 0002-7863; 1520-5126
• DOI: 10.1021/jacs.0c01482

Tetrafunctionalized calix[4]­resorcinarene cavitands commonly serve as supramolecular scaffolds for construction of coordination-driven self-assembled capsules. However, due to the calix-like shape, the structural diversity of assemblies is mostly restricted to dimeric and hexameric capsules. Previously, we reported a spontaneous heteroleptic complexation strategy based on a pair of self-recognizable terpyridine-based ligands and CdII ions. Building on this complementary ligand pairing system, herein three types of nanocapsules, including a dimeric capsule, a Sierpiński triangular prism, and a cubic star, could be readily obtained through dynamic complexation reactions between a tetratopic cavitand-based ligand and various multitopic counterparts in the presence of CdII ions. The dimeric capsular assemblies display the spacer-length-dependent self-sorting behavior in a four-component system. Moreover, the precise multicomponent self-assembly of a Sierpiński triangular prism and a cubic star possessing three and six cavitand-based motifs, respectively, demonstrates that such self-assembly methodology is able to efficiently enhance architectural complexity for calix[4]­resorcinarene-containing metallo-supramolecules.