Magnetic anisotropy of two cyclic hexanuclear Fe(III) clusters entrapping alkaline ions

被引:90
作者
Waldmann, O [1 ]
Schülein, J
Koch, A
Müller, P
Bernt, I
Saalfrank, RW
Andres, HP
Güdel, HU
Allenspach, P
机构
[1] Univ Erlangen Nurnberg, Inst Phys 3, D-91058 Erlangen, Germany
[2] Univ Erlangen Nurnberg, Inst Organ Chem, D-91058 Erlangen, Germany
[3] Univ Bern, Dept Chem & Biochem, CH-3000 Bern 9, Switzerland
[4] Swiss Fed Inst Technol, Lab Neutronenstreuung, CH-5232 Villigen, Switzerland
[5] PSI, CH-5232 Villigen, Switzerland
关键词
D O I
10.1021/ic9906510
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The magnetic anisotropy of the two cyclic hexanuclear Fe(III) clusters [Li subset of Fe(6)L(6)]Cl . 6CHCl(3) and [Na subset of Fe(6)L(6)]Cl . 6CHCl(3), L = N(CH(2)CH(2)O)(3), was investigated. Based on a spin Hamiltonian formalism, the magnetic anisotropy was calculated exactly to first order, i.e., in the strong exchange limit, using Bloch's perturbational approach and irreducible tensor operator techniques. Experimentally, the magnetic anisotropy was investigated by magnetic susceptibility and high-field torque magnetometry of single crystals as well as inelastic neutron scattering. It is demonstrated that torque magnetometry provides a valuable tool for the study of magnetic anisotropy in spin cluster complexes. The experimental data could be accurately reproduced by;he calculations, and the different methods yield consistent values for the coupling constants and zero-field-splitting parameters. Both the anisotropy and the exchange interaction parameter are found to increase with increasing Fe-O-Fe angle.
引用
收藏
页码:5879 / 5886
页数:8
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