Single-Molecule-Magnet Behavior in Mononuclear Homoleptic Tetrahedral Uranium(III) Complexes

被引:31
|
作者
Pereira, Laura C. J. [1 ]
Camp, Clement [2 ,3 ]
Coutinho, Joana T. [1 ]
Chatelain, Lucile [2 ,3 ,4 ]
Maldivi, Pascale [2 ,3 ]
Almeida, Manuel [1 ]
Mazzanti, Marinella [4 ]
机构
[1] Univ Lisboa CFMCUL, Inst Super Tecn, C2TN, P-2695066 Bobadela Lrs, Portugal
[2] Univ Grenoble Alpes, INAC SCIB, RICC, F-38000 Grenoble, France
[3] CEA, INAC SCIB, F-38000 Grenoble, France
[4] Ecole Polytech Fed Lausanne, Inst Sci & Ingn Chim, CH-1015 Lausanne, Switzerland
关键词
LANTHANIDE COMPLEXES; RELAXATION; CHEMISTRY; ANISOTROPY; LIGANDS;
D O I
10.1021/ic501520c
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The magnetic properties of the two uranium coordination compounds, [K(18c6)][U(OSi-((OBu)-Bu-t)(3))(4)] and [K(18c6)][U(N(SiMe3)(2))(4)], both presenting the U-III ion in similar pseudotetrahedral coordination environments but with different O- or N-donor ligands, have been measured. The static magnetic susceptibility measurements and density functional theory studies suggest the presence of different ligand fields in the two compounds. Alternating-current susceptibility studies conducted at frequencies ranging from 95 to 9995 Hz and at temperatures in the 1.7-10 K range revealed for both compounds slow magnetic relaxation already at zero static magnetic field with similar energy barriers U similar to 24 K.
引用
收藏
页码:11809 / 11811
页数:3
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