Implications of remote water molecules on the electron transfer coupled processes at a nonporphyrinic Mn(III)-hydroxido complex

被引:17
|
作者
El Ghachtouli, Sanae [1 ,2 ]
Lassalle-Kaiser, Benedikt [2 ,3 ]
Dorlet, Pierre [4 ]
Guillot, Regis [2 ]
Anxolabehere-Mallart, Elodie [1 ]
Costentin, Cyrille [1 ]
Aukauloo, Ally [2 ,5 ]
机构
[1] Univ Paris Diderot, Electrochim Mol Lab, UMR CNRS P7 7591, F-75205 Paris 13, France
[2] Univ Paris 11, ICMMO, UMR 8182, F-91405 Orsay, France
[3] Univ Calif Berkeley, Lawrence Berkeley Lab, Phys Biosci Div, Berkeley, CA 94720 USA
[4] CNRS, URA 2096, Lab Stress Oxydant & Detoxicat, F-91191 Gif Sur Yvette, France
[5] CEA, IBiTec S, SM SB2, F-91191 Gif Sur Yvette, France
关键词
PHOTOSYSTEM-II; MONONUCLEAR; ACTIVATION; OXIDATION; DESIGN; MANGANESE(III); CHEMISTRY; DINUCLEAR; DIOXYGEN; OXYGEN;
D O I
10.1039/c1ee01078f
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Electrochemical studies of a new Mn(III)(OH) complex clearly evidence that the presence of outer spheres water molecules is essential for the reversibility of Mn-III/II and Mn-IV/III redox processes. In the Mn-III/II case we found an isotope effect for D2O and (OH2)-O-18 allowing us to propose a mechanism for H2O/HO- ligand exchange coupled electron transfer activation of Mn-OH2
引用
收藏
页码:2041 / 2044
页数:4
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