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探究轴向畸变对八面体Co(II)配合物磁各向异性的影响。

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

作者信息

Deng Yi-Fei, Singh Mukesh Kumar, Gan Dexuan, Xiao Tongtong, Wang Yinuo, Liu Shihao, Wang Zhenxing, Ouyang Zhongwen, Zhang Yuan-Zhu, Dunbar Kim R

机构信息

Department of Chemistry, Southern University of Science and Technology, Shenzhen 518055, China.

Department of Chemistry, Texas A & M University, College Station, Texas 77842, United States.

出版信息

Inorg Chem. 2020 Jun 1;59(11):7622-7630. doi: 10.1021/acs.inorgchem.0c00531. Epub 2020 May 11.

Abstract

Three mononuclear octahedral Co(II) complexes are reported, [Co(py)(SCN)] (), [Co(py)(Cl)]·HO (), and [Co(py)(Br)] (), that exhibit different distortions with compression () or elongation ( and ) of the axial positions. Easy plane magnetic anisotropy was confirmed by magnetic, HF-EPR, and computational studies for all complexes. Further analyses indicate that both the sign and magnitude of zero-field splitting parameters experience a significant change ( ≥ ±150 cm) 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.

摘要

报道了三种单核八面体Co(II)配合物,[Co(py)(SCN)] ()、[Co(py)(Cl)]·H₂O ()和[Co(py)(Br)] (),它们在轴向位置呈现出不同的畸变,有的是压缩(),有的是伸长(和)。通过对所有配合物的磁性、高频电子顺磁共振和计算研究证实了易平面磁各向异性。进一步分析表明,通过调整轴向和赤道配体场强度,零场分裂参数的符号和大小都经历了显著变化(≥±150 cm⁻¹)。观察到所有化合物都有缓慢的磁弛豫现象,这主要由涉及声子和光学声子的拉曼过程主导。

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