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Probing the Axial Distortion Effect on the Magnetic Anisotropy of Octahedral Co(II) Complexes

机译:抑制八面体CO(II)复合物磁各向异性的轴向畸变效应

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摘要

Three mononuclear octahedral Co(II) complexes are reported, [Co(py)(4)(SCN)(2)] (1), [Co(py)(4)(Cl)(2)]center dot H2O (2), and [Co(py)(4)(Br)(2)] (3), that exhibit different distortions with compression (1) or elongation (2 and 3) of the axial positions. Easy plane magnetic anisotropy was confirmed by magnetic, HFEPR, and computational studies for all complexes. Further analyses indicate that both the sign and magnitude of zero-field splitting parameters experience a significant change (D >= +/- 150 cm(-1)) by tuning of the axial and equatorial ligand field strength. Slow magnetic relaxation is observed for all compounds which is dominated by the Raman process involving both acoustic and optical phonons.
机译:报道了三种单核八面体CO(II)复合物,[CO(PY)(4)(4)(SCN)(2)](1),[CO(PY)(4)(CL)(2)]中心点H2O(2 )和[Co(py)(4)(4)(2)(2)](3),其具有轴向位置的压缩(1)或伸长率(2和3)的不同扭曲。 通过磁,HFEPR和所有复合物的计算研究确认易于平面磁各向异性。 进一步分析表明零场分割参数的符号和幅度均通过调谐轴向和赤道配体场强度来经历显着的变化(D> = +/-150cm(-1))。 对于由涉及声学和光学声子的拉曼工艺支配的所有化合物观察到缓慢的磁性弛豫。

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