A Low-Valent Iron Imido Heterocubane Cluster: Reversible Electron Transfer and Catalysis of Selective C-C Couplings

被引:11
作者
Lichtenberg, Crispin [1 ]
Garcia Rubio, Ines [1 ]
Viciu, Liliana [1 ]
Adelhardt, Mario [2 ]
Meyer, Karsten [2 ]
Jeschke, Gunnar [1 ]
Gruetzmacher, Hansjoerg [1 ]
机构
[1] ETH, Dept Chem & Appl Biosci, CH-8093 Zurich, Switzerland
[2] Univ Erlangen Nurnberg, Dept Chem & Pharm, Erlangen Nurnberg FAU, D-91058 Erlangen, Germany
关键词
C-C coupling; cluster compounds; heterocubanes; homogeneous catalysis; low-valent iron; MULTIPLE OXIDATION-STATES; SYNTHETIC ANALOGS; ACTIVE-SITES; FE PROTEIN; SERIES N; REDUCTION; CORE; COMPLEXES; ENVIRONMENTS; NITROGENASE;
D O I
10.1002/anie.201505668
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Enzymes and cofactors with iron-sulfur heterocubane core structures, [Fe4S4], are often found in nature as electron transfer reagents in fundamental catalytic transformations. An artificial heterocubane with a [Fe4N4] core is reported that can reversibly store up to four electrons at very negative potentials. The neutral [Fe4N4] and the singly reduced low-valent [Fe4N4](-) heterocubanes were isolated and fully characterized. The low-valent species bears one unpaired electron, which is localized predominantly at one iron center in the electronic ground state but fluctuates with increasing temperatures. The electrons stored or released by the [Fe4N4]/[Fe4N4](-) redox couple can be used in reductive or oxidative CC couplings and even allow catalytic one-pot reactions, which show a remarkably enhanced selectivity in the presence of the [Fe4N4] heterocubanes.
引用
收藏
页码:13012 / 13017
页数:6
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