U-Co bond: Reduction of [U(TsXy)(Cl)(thf)] [1; TsXy=HC(SiMe2NAr)3; Ar=3,5-Me2C6H3] with KC8in toluene afforded the new arene-bridged diuranium complex 2, whereas reduction of 1 in aliphatic hydrocarbons resulted in C-N bond activation and formation of an imido-aryl complex, which exhibits an unusual ferromagnetic interaction between the two uranium centers. The synthetic utility of 2 was demonstrated by the first synthesis of a U-Co complex, [U(TsXy)Co(CO)3(PPh3)] (3). Copyright © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim

Patel, D., Moro, F., Mcmaster, J., Lewis, W., Blake, A., Liddle, S. (2011). A formal high oxidation state inverse-sandwich diuranium complex: A new route to f-block-metal bonds. ANGEWANDTE CHEMIE. INTERNATIONAL EDITION, 50(44), 10388-10392 [10.1002/anie.201104110].

A formal high oxidation state inverse-sandwich diuranium complex: A new route to f-block-metal bonds

Moro, Fabrizio;
2011

Abstract

U-Co bond: Reduction of [U(TsXy)(Cl)(thf)] [1; TsXy=HC(SiMe2NAr)3; Ar=3,5-Me2C6H3] with KC8in toluene afforded the new arene-bridged diuranium complex 2, whereas reduction of 1 in aliphatic hydrocarbons resulted in C-N bond activation and formation of an imido-aryl complex, which exhibits an unusual ferromagnetic interaction between the two uranium centers. The synthetic utility of 2 was demonstrated by the first synthesis of a U-Co complex, [U(TsXy)Co(CO)3(PPh3)] (3). Copyright © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim
Articolo in rivista - Articolo scientifico
arenes; density functional theory; metal-metal bonds; redox reactivity; uranium; Catalysis; Chemistry (all)
English
2011
50
44
10388
10392
none
Patel, D., Moro, F., Mcmaster, J., Lewis, W., Blake, A., Liddle, S. (2011). A formal high oxidation state inverse-sandwich diuranium complex: A new route to f-block-metal bonds. ANGEWANDTE CHEMIE. INTERNATIONAL EDITION, 50(44), 10388-10392 [10.1002/anie.201104110].
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10281/210651
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