化学
铁磁性
磁各向异性
伊辛模型
五角双锥分子几何
结晶学
咪唑酯
凝聚态物理
协调球
磁化
晶体结构
无机化学
磁场
物理
量子力学
作者
Fatima El‐Khatib,Benjamin Cahier,M. López-Jordà,Régis Guillot,Éric Rivière,Hala Hafez,Zeinab Saad,Jean‐Jacques Girerd,Nathalie Guihéry,Talal Mallah
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2017-08-23
卷期号:56 (17): 10655-10663
被引量:12
标识
DOI:10.1021/acs.inorgchem.7b01609
摘要
The preparation of a binuclear Ni(II) complex with a pentacoordinate environment using a cryptand organic ligand and the imidazolate bridge is reported. The coordination sphere is close to trigonal bipyramidal (tbp) for one Ni(II) and to square pyramidal (spy) for the other. The use of the imidazolate bridge that undergoes π-π stacking with two benzene rings of the chelating ligand induces steric hindrance that stabilizes the pentacoordinate environment. Magnetic measurements together with theoretical studies of the spin states energy levels allow fitting the data and reveal a large Ising-type anisotropy and a weak anti-ferromagnetic exchange coupling between the metal ions. The magnitude and the nature of the magnetic anisotropy and the difference in anisotropy between the two metal ions are rationalized using wave-function-based calculations. We show that a slight distortion of the coordination sphere of Ni(II) from spy to tbp leads to an Ising-type anisotropy. Broken-symmetry density functional calculations rationalize the weak anti-ferromagnetic exchange coupling through the imidazolate bridge.
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