超分子化学
亚胺
化学
共价键
齿合度
链烷
结晶学
离子
动态共价化学
锌
立体化学
分子
有机化学
晶体结构
催化作用
作者
Kelly S. Chichak,Stuart Cantrill,Anthony R. Pease,Sheng‐Hsien Chiu,Gareth W. V. Cave,Jerry L. Atwood,J. Fraser Stoddart
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2004-05-27
卷期号:304 (5675): 1308-1312
被引量:805
标识
DOI:10.1126/science.1096914
摘要
The realization of the Borromean link in a wholly synthetic molecular form is reported. The self-assembly of this link, which is topologically achiral, from 18 components by the template-directed formation of 12 imine and 30 dative bonds, associated with the coordination of three interlocked macrocycles, each tetranucleating and decadentate overall, to a total of six zinc(II) ions, is near quantitative. Three macrocycles present diagonally in pairs, six exo -bidentate bipyridyl and six endo -diiminopyridyl ligands to the six zinc(II) ions. The use, in concert, of coordination, supramolecular, and dynamic covalent chemistry allowed the highly efficient construction, by multiple cooperative self-assembly processes, of a nanoscale dodecacation with an approximate diameter of 2.5 nanometers and an inner chamber of volume 250 Å 3 , lined with 12 oxygen atoms.
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