Subcomponent Self-Assembly and Guest-Binding Properties of Face-Capped Fe4L48+ Capsules

被引：150

作者：

Bilbeisi, Rana A. ^{[1
]}

Clegg, Jack K. ^{[1
]}

Elgrishi, Noemie ^{[1
]}

de Hatten, Xavier ^{[1
]}

Devillard, Marc ^{[1
]}

Breiner, Boris ^{[1
]}

Mal, Prasenjit ^{[1
]}

Nitschke, Jonathan R. ^{[1
]}

机构：

[1] Univ Cambridge, Dept Chem, Cambridge CB2 1EW, England

来源：

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY | 2012年 / 134卷 / 11期

基金：

英国工程与自然科学研究理事会;

关键词：

NUMBER INCOMMENSURATE CLUSTER; DYNAMIC COVALENT CHEMISTRY; COORDINATION CAGES; DIELS-ALDER; HOST-GUEST; RECOGNITION; COMPLEXES; TETRAHEDRON; HELICATE; BEHAVIOR;

D O I：

10.1021/ja2092272

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

A general method for preparing Fe4L4 face-capped tetrahedral cages through subcomponent self-assembly was developed and has been demonstrated using four different C-3-symmetric triamines, 2-formylpyridine, and iron(II). Three of the triamines were shown also to form Fe2L3 helicates when the appropriate stoichiometry of subcomponents was used. Two of the cages were observed to have nearly identical Fe-Fe distances in the solid state, which enabled their ligands to be coincorporated into a collection of mixed cages. Only one of the cages combined a sufficiently large cavity with the sufficiently small pores required for guest binding, taking up a wide variety of guest species in size- and shape-selective fashion.

引用

页码：5110 / 5119

页数：10

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