A molecular redox switch via iron translocation in a bicompartmental ligand

被引:28
作者
Belle, C
Pierre, JL
Saint-Aman, E
机构
[1] Univ Grenoble 1, Lab Chim Biomimet, LEDSS, CNRS UMR 5616, F-38041 Grenoble 9, France
[2] Univ Grenoble 1, Lab Electrochim Organ & Photochim Redox, LEOPR, CNRS UMR 5630, F-38041 Grenoble, France
关键词
D O I
10.1039/a805958f
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Mononuclear complexes of an unsymmetrical bicompartmental ligand containing an iron ion that can occupy either the 'soft nitrogen box' or the 'hard oxygen box' have been synthesized. When the ferric iron is electrochemically reduced or when the ferrous iron is electrochemically oxidized, it hops from one binding site to the other. The process is reversible. During the switching process, the iron ion remains bound to the bridging phenolate ligand and the iron translocation may be regarded as a 'pendular motion'.
引用
收藏
页码:1399 / 1402
页数:4
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