A new molecular switch: redox-driven translocation mechanism of the copper cation

被引:51
作者
Kalny, D
Elhabiri, M
Moav, T
Vaskevich, A
Rubinstein, I
Shanzer, A
Albrecht-Gary, AM
机构
[1] Univ Strasbourg, CNRS, Lab Phys Chim Bioinorgan, UMR 7509, F-67000 Strasbourg, France
[2] Weizmann Inst Sci, Dept Organ Chem, IL-76100 Rehovot, Israel
[3] Weizmann Inst Sci, Dept Mat & Interfaces, IL-76100 Rehovot, Israel
关键词
D O I
10.1039/b204145f
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
We report the synthesis of a novel molecular switch based on a double-stranded ditopic ligand which operates through the Cu-II/Cu-I couple; the mononuclear cuprous and cupric complexes were characterised by absorption spectrophotometry; reversible motion of the copper ion between the two binding sites is driven by an auxiliary oxidation and reduction reaction; the rate-limiting steps of this translocation process were determined as well as the corresponding kinetic parameters.
引用
收藏
页码:1426 / 1427
页数:2
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