Magnetostructural relations from a combined ab initio and ligand field analysis for the nonintuitive zero-field splitting in Mn(III) complexes

被引:54
作者
Maurice, Remi [1 ,2 ]
de Graaf, Coen [2 ,3 ]
Guihery, Nathalie [1 ]
机构
[1] Univ Toulouse 3, IRSAMC, Lab Chim & Phys Quant, UMR 5626, F-31062 Toulouse 4, France
[2] Univ Rovira & Virgili, Dept Quim Fis & Inorgan, Tarragona 43007, Spain
[3] ICREA, Barcelona 08010, Spain
关键词
TRANSITION-METAL-COMPLEXES; HIGH-SPIN; PARAMAGNETIC-RESONANCE; MAGNETIC-ANISOTROPY; ELECTRONIC-STRUCTURE; MOLECULES; EPR;
D O I
10.1063/1.3480014
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The zero-field splitting (ZFS) of a model monometallic Mn(III) complex is theoretically studied as function of a systematic symmetry lowering. First, we treat the octahedral case for which the standard S.D.S model Hamiltonian cannot be applied due to a zero-field splitting in the absence of anisotropy induced by the spin-orbit coupling between the two spatial components of the E-5(g) state at second-order of perturbation. Next, the symmetry is lowered to D-4h and D-2h and the anisotropic spin Hamiltonian is extracted using effective Hamiltonian theory. A simple relation is derived between the ratio E/vertical bar D vertical bar and the applied rhombic and axial distortions. Moreover, it is shown that close to O-h symmetry, the orbital mixing due to spin-orbit coupling can be accurately described with Stevens fourth-order operators. The calculated tendencies are interpreted within a refined Racah plus ligand field model and it is shown that the ZFS parameters in Mn(III) complexes follow special rules that are nonintuitive compared to other d(n) configurations. Finally, some angular distortions are applied to study their effect on the anisotropy. (C) 2010 American Institute of Physics. [doi: 10.1063/1.3480014]
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页数:12
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