Small molecule activation by multimetallic uranium complexes supported by siloxide ligands

被引:27
|
作者
Barluzzi, Luciano [1 ]
Falcone, Marta [1 ]
Mazzanti, Marinella [1 ]
机构
[1] Ecole Polytech Fed Lausanne, Inst Sci & Ingn Chim 1, CH-1015 Lausanne, Switzerland
基金
瑞士国家科学基金会;
关键词
ELECTRON-TRANSFER REACTIONS; CHALCOGEN-ATOM-TRANSFER; CARBON-DIOXIDE ACTIVATION; MULTIPLE BOND FORMATION; E-U E; MAGNETIC COMMUNICATION; TRIVALENT URANIUM; CRYSTAL-STRUCTURES; NITROUS-OXIDE; NITRIDE;
D O I
10.1039/c9cc05605j
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The synthesis and reactivity of uranium compounds supported by the tris-tert-butoxysiloxide ligand is surveyed. The multiple binding modes of the tert-butoxysiloxide ligand have proven very well suited to stabilize highly reactive homo- and heteropolymetallic complexes of uranium that have shown an unusual high reactivity towards small molecules such as CO2, CS2, chalcogens and azides. Moreover, these ligands have allowed the isolation of dinuclear nitride and oxide bridged complexes of uranium in various oxidation states. The ability of the tris-tert-butoxysiloxide ligands to trap alkali ions in these nitride or oxide complexes leads to unprecedented ligand based and metal based reduction and functionalization of N-2, CO, CO2 and H-2.
引用
收藏
页码:13031 / 13047
页数:17
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