Coupled Nanomechanical Motions: Metal-Ion-Effected, pH-Modulated, Simultaneous Extension/Contraction Motions of Double-Domain Helical/Linear Molecular Strands

被引:36
作者
Stadler, Adrian-Mihail [1 ,2 ]
Lehn, Jean-Marie P. [1 ]
机构
[1] Univ Strasbourg, Inst Sci & Ingn Supramol, Lab Chim Supramol, F-67000 Strasbourg, France
[2] KIT, Inst Nanotechnol INT, D-76344 Eggenstein Leopoldshafen, Germany
关键词
TERMINAL HYDROXYMETHYL GROUPS; UNIDIRECTIONAL ROTARY MOTION; PYRIMIDINE-HYDRAZONE LIGAND; DYNAMIC CHEMICAL-DEVICES; EFFICIENT ACCESS; COORDINATION; GENERATION; HELICITY; CHEMISTRY; CHANNELS;
D O I
10.1021/ja408752m
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A new class of shape-enforced synthetic polyheterocyclic molecular strands, containing both a helical and a linear domain, has been designed and synthesized. On reaction with Pb(II), under the effect of cation binding to the coordination subunits, the helical section unfolds into a linear shape in the complex and the linear domain folds into a helical ligand wrapped around the bound cations. Such double-domain ligand strands are thus able to undergo a combined unfolding-folding interconversion on binding and release of metal cations. These changes can be modulated through coupling to a competing ligand that reversibly binds and releases metal cations, when respectively unprotonated and protonated, on effecting alternate pH changes. The resulting process thus performs nanomechanical extension/contraction molecular motions of a linear motor type, which is fueled by acid-base neutralization.
引用
收藏
页码:3400 / 3409
页数:10
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