Progress in the synthesis and exploitation of catenanes since the Millennium

被引:190
作者
Evans, Nicholas H. [1 ]
Beer, Paul D. [2 ]
机构
[1] Univ Lancaster, Dept Chem, Lancaster LA1 4YB, England
[2] Univ Oxford, Dept Chem, Inorgan Chem Lab, Oxford OX1 3QR, England
基金
英国工程与自然科学研究理事会; 欧洲研究理事会;
关键词
MOLECULAR TREFOIL KNOT; RING-CLOSING METATHESIS; ASSEMBLED MULTICOMPONENT CATENANES; DYNAMIC COMBINATORIAL SYNTHESIS; DONOR/PI-ACCEPTOR INTERACTIONS; CHLORIDE ANION RECOGNITION; METAL-ORGANIC FRAMEWORKS; HIGH-YIELD SYNTHESIS; TEMPLATE SYNTHESIS; FUNCTIONALIZED CATENANE;
D O I
10.1039/c4cs00029c
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Catenanes - molecules consisting of interlocked macrocyclic rings - have been prepared by templation strategies for some thirty years. The utilization of Cu-vertical bar cation, aromatic donor-acceptor interactions and hydrogen bonding assisted self-assembly strategies has led to the construction of numerous examples of these aesthetically pleasing species. This review seeks to discuss key developments in the synthesis and functional application of catenanes that have occurred since the Millennium. The much expanded range of metal cation templates; the genesis and growth of anion templation, as well as the use of alternative supramolecular interactions (halogen bonding and radical templation) and thermodynamically controlled reactions to synthesize catenanes are detailed. The class of catenanes that may be described as "molecular machines'' are then highlighted and to conclude, attempts to fabricate catenanes onto surfaces and into metal organic frameworks (MOFs) are discussed.
引用
收藏
页码:4658 / 4683
页数:26
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