Interplay of Interactions Governing the Dynamic Conversions of Acyclic and Macrocyclic Helicates

被引:34
作者
Campbell, Victoria E. [3 ]
de Hatten, Xavier [1 ,2 ]
Delsuc, Nicolas [1 ,2 ]
Kauffmann, Brice [1 ,2 ]
Huc, Ivan [1 ,2 ]
Nitschke, Jonathan R. [3 ]
机构
[1] Univ Bordeaux, CNRS, UMR5248, Inst Europeen Chim & Biol, F-33607 Pessac, France
[2] Univ Bordeaux, CNRS, UMS3033, Inst Europeen Chim & Biol, F-33607 Pessac, France
[3] Univ Cambridge, Dept Chem, Cambridge CB2 1EW, England
关键词
dynamic covalent chemistry; macrocyclization; self-assembly; substitution; systems chemistry; SYSTEMS CHEMISTRY; CHEMICAL-SYSTEMS; COMPLEXES; COVALENT; LIGAND;
D O I
10.1002/chem.200900693
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A rigid, helical macrocycle that contains two copper(I) ions has been synthesized through subcomponent self-assembly. Although it does not obey the "rule of coordinative saturation", this macrocycle could be prepared through subcomponent substitution starting from a tri(copper(I)) helicate, in a reaction in which copper(I) was ejected. The macrocycle was observed to readily participate in a sequence of transformations between helical structures mediated by the electronic effects of substituents, entropic effects, the conformational preferences of organic building blocks, and the coordinative preferences of the metal ion. The thermodynamic parameters governing the interconversion of an "open" helicate and the "closed" macrocycle were determined through van 't Hoff analysis, allowing quantification of the entropic driving force for macrocyclization.
引用
收藏
页码:6138 / 6142
页数:5
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