Ferrocene-Based Tetradentate Schiff Bases as Supporting Ligands in Uranium Chemistry

被引:36
|
作者
Camp, Clement [1 ,2 ]
Chatelain, Lucile [1 ,2 ,3 ]
Mougel, Victor [1 ,2 ]
Pecaut, Jacques [1 ,2 ]
Mazzanti, Marinella [3 ]
机构
[1] Univ Grenoble Alpes, INAC LCIB, RICC, F-38000 Grenoble, France
[2] CEA Grenoble, INAC LCIB, F-38000 Grenoble, France
[3] Ecole Polytech Fed Lausanne, Inst Sci & Ingn Chim, CH-1015 Lausanne, Switzerland
关键词
SINGLE-MOLECULE-MAGNET; MULTIELECTRON REDOX CHEMISTRY; RING-OPENING POLYMERIZATION; CATION-CATION INTERACTIONS; PENTAVALENT-URANYL; DIAMIDE LIGANDS; METAL-COMPLEXES; ACTIVATION; REACTIVITY; NITRIDE;
D O I
10.1021/acs.inorgchem.5b00467
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Uranyl(VI), uranyl(V), and uranium(IV) complexes supported by ferrocene-based tetradentate Schiff-base ligands were synthesized, and their solid-state and solution structures were determined. The redox properties of all complexes were investigated by cyclic voltammetry. The bulky salfen-Bu-t(2) allows the preparation of a stable uranyl(V) complex, while a stable U(IV) bis-ligand complex is obtained from the salt metathesis reaction between [UI4(OEt2)(2)] and K(2)salfen. The reduction of the [U(salfen)(2)] complex leads to an unprecedented intramolecular reductive coupling of the Schiff-base ligand resulting in a C-C bond between the two ferrocene-bound imino groups.
引用
收藏
页码:5774 / 5783
页数:10
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