2013
DOI: 10.1002/anie.201209708
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Generation of a Dynamic System of Three‐Dimensional Tetrahedral Polycatenanes

Abstract: Seven of the best: A dynamic combinatorial library of polycatenated tetrahedra was prepared by complexation between a dynamic Fe4L6 tetrahedral cage, constructed from ligands containing an electron‐deficient naphthalenediimide core, and an electron‐rich aromatic crown ether, 1,5‐dinaphtho[38]crown‐10. The highest order species in the library is the tetrahedral [7]catenane.Permissions: WILEY-VCH

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Cited by 125 publications
(48 citation statements)
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“…64 [7]catenane structure with the naphthalene diimide units threading through the macrocycles (Fig 14). 66 Interestingly, when a smaller tetrahedral cage was prepared, steric constraints prevented saturation of the naphthalene diimide sites, with evidence of only two macrocycles being incorporated into the assembly. …”
Section: Metal-ligand Bonds Within the Mim Frameworkmentioning
confidence: 99%
“…64 [7]catenane structure with the naphthalene diimide units threading through the macrocycles (Fig 14). 66 Interestingly, when a smaller tetrahedral cage was prepared, steric constraints prevented saturation of the naphthalene diimide sites, with evidence of only two macrocycles being incorporated into the assembly. …”
Section: Metal-ligand Bonds Within the Mim Frameworkmentioning
confidence: 99%
“…For the complex S 2 , the 1 H NMR spectrum exhibited broad resonance peaks presumably owing to the low tumbling motion on the NMR time scale for the large supramolecular architecture. [18] Three characteristic singlets corresponding to tpy H 3′,5′ protons were observed at 8.89, 8.78, and 8.60 ppm with downfield shifts, along with the upfield shifts of tpy H 6,6″ protons compared to L 2 and T . Additionally, the methylene and methoxy protons at 4.44 and 3.88 ppm also exhibited down-field shifts, agreeing with the expected structure.…”
mentioning
confidence: 99%
“…1 H NMR spectrum of S 5 displayed a complex and broad resonance in the aromatic region, which was attributed to the conformational heterogeneity of the giant supramolecular structure. [18] Nevertheless, there were two diagnostic triplets at 4.46 and 4.25 ppm (methylene groups) and two sharp singlets at 3.86 and 3.92 ppm (methoxy groups) in the non-aromatic region, suggesting the formation of the expected discrete structure (Figure S59). The ESI mass spectrum of S 6 (Figure 3a) showed eleven distinct peaks with continuous charge states (from 13 + to 23 +) confirming the molecular composition of 6 L 6 units, 3 T units, 36 Cd 2+ ions, and 72 PF 6 − units.…”
mentioning
confidence: 99%
“…Given that this stoichiometry exceeds the degree of catenation previously observed for N 6 (Fig. 4), we infer that the third crown ether is not likely to be catenated 16,24…”
Section: Resultsmentioning
confidence: 51%