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首页> 外文期刊>Chemical science >In-depth investigation of large axial magnetic anisotropy in monometallic 3d complexes using frequency domain magnetic resonance and ab?initio methods: a study of trigonal bipyramidal Co(ii)
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In-depth investigation of large axial magnetic anisotropy in monometallic 3d complexes using frequency domain magnetic resonance and ab?initio methods: a study of trigonal bipyramidal Co(ii)

机译:利用频域磁共振和绝对方法深入研究单金属3d配合物中的大轴向磁各向异性:三角双锥体Co(ii)的研究

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The magnetic properties of 3d monometallic complexes can be tuned through geometric control, owing to their synthetic accessibility and relative structural simplicity. Monodentate ligands offer great potential for fine-tuning the coordination environment to engineer both the axial and rhombic zero-field splitting (ZFS) parameters. In [CoCl _(3) (DABCO)(HDABCO)] ( 1 ), the trigonal bipyramidal Co( II ) centre has two bulky axial ligands and three equatorial chloride ligands. An in-depth experimental and theoretical study of 1 reveals a large easy-plane magnetic anisotropy (+ve D ) with a negligible rhombic zero-field splitting ( E ) due to the strict axial symmetry imposed by the C _(3) symmetric ligand and trigonal space group. The large easy-plane magnetic anisotropy ( D = +44.5 cm ~(?1) ) is directly deduced using high-field EPR and frequency-domain magnetic resonance (FDMR) studies. Ab initio calculations reveal a large positive contribution to the D term arising from ground state/excited state mixing of the ~(4) E′′ states at ~4085 cm ~(?1) and a minor contribution from the spin–flip transition as well. The nature of the slow relaxation in 1 is elucidated through analysis of the rates of relaxation of magnetisation, taking into account Raman and direct spin–lattice relaxation processes and Quantum Tunnelling of the Magnetisation (QTM). The terms relating to the direct process and QTM were found based on the fit of the field-dependence of τ at 2 K. Subsequently, these were used as fixed parameters in the fit of the temperature-dependence of τ to obtain the Raman terms. This experimental–theoretical investigation provides further insight into the power of FDMR and ab initio methods for the thorough investigation of magnetic anisotropy. Thus, these results contribute to design criteria for high magnetic anisotropy systems.
机译:由于3d单金属配合物的合成可及性和相对的结构简单性,可以通过几何控制来调节其磁性。单齿配体为微调配位环境提供了巨大潜力,可用于设计轴向和菱形零场分裂(ZFS)参数。在[CoCl_(3)(DABCO)(HDABCO)](1)中,三角双锥体Co(II)中心具有两个庞大的轴向配体和三个赤道氯化物配体。对1的深入实验和理论研究表明,由于C _(3)对称配体施加了严格的轴向对称性,因此大的易平面磁各向异性(+ ve D)具有可忽略的菱形零场分裂(E)和三角空间群。使用高场EPR和频域磁共振(FDMR)研究直接推导出大的易平面磁各向异性(D = +44.5 cm〜(?1))。从头算计算表明,在〜4085 cm〜(?1)处〜(4)E''状态的基态/激发态混合对D项有很大的正贡献,而自旋-翻转跃迁的贡献很小。好。通过分析磁化的弛豫速率,并考虑了拉曼和直接自旋-晶格弛豫过程以及磁化的量子隧穿(QTM),可以阐明1中缓慢弛豫的性质。基于τ在2 K时的场相关性的拟合来找到与直接过程和QTM有关的项。随后,将它们用作τ的温度相关性的拟合中的固定参数以获得拉曼项。这一实验理论研究为深入研究FD各向异性和从头开始方法提供了更深入的了解。因此,这些结果有助于高磁各向异性系统的设计标准。

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