Synthesizing Interlocked Molecules Dynamically

被引:53
作者
Haussmann, Philip C. [1 ,2 ]
Stoddart, J. Fraser [1 ,2 ,3 ]
机构
[1] Univ Calif Los Angeles, Calif NanoSyst Inst, Los Angeles, CA 90095 USA
[2] Univ Calif Los Angeles, Dept Chem, Los Angeles, CA 90095 USA
[3] Northwestern Univ, Dept Chem, Evanston, IL 60208 USA
关键词
self-assembly; dynamic covalent chemistry; templated synthesis; rotaxanes; catenanes; TEMPLATE-DIRECTED SYNTHESIS; OLEFIN-METATHESIS CATALYSTS; CROWN-ETHER COMPLEXES; SUPRAMOLECULAR CHEMISTRY; COMBINATORIAL CHEMISTRY; BIOLOGICAL PRINCIPLES; EFFICIENT SYNTHESIS; SELF-ORGANIZATION; RATIONAL DESIGN; RING;
D O I
10.1002/tcr.20173
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
As the complexity of mechanically interlocked molecular architectures increases, it is important to understand the underlying principles, such as molecular recognition and self-assembly processes, that govern the practice of template-directed synthesis necessary to create these particular compounds. In this review, we explain the importance of dynamic processes in the synthesis of mechanically interlocked compounds. We show how many different dynamic covalent bonds have been used in the synthesis of rotaxanes, catenanes, and other higher-order mechanically interlocked compounds, with the goal of revealing the state of the art in dynamic covalent chemistry. (C) 2009 The Japan Chemical Journal Forum and Wiley Periodicals, Inc. Chem Rec 9: 136-154; 2009: Published online in Wiley InterScience (www.interscience.wiley.com) DOI 10.1002/tcr.20173
引用
收藏
页码:136 / 154
页数:19
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