Lorenzo A. Mariano, Vu Ha Anh Nguyen, Valerio Briganti, Alessandro Lunghi
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引用次数: 0
摘要
磁各向异性会减缓磁弛豫,在永磁体的设计中发挥着重要作用。特别是 Co(II)的配位化合物,在存在流配位环境时会表现出很大的磁各向异性,并已被用作单分子磁体原型。然而,人们只对钴的广阔化学空间进行了有限的取样,这可能掩盖了实现大磁各向异性的其他化学途径。在此,我们对钴(II)的化学空间进行了计算高通量探索,以寻找新的单分子磁体。我们自动组装了大约 15000 个新型 Co(II)配合物,并使用多参考ab initio 方法对它们进行了全面表征。对这些结果的分析表明,具有破纪录磁各向异性的化合物也可以通过四配位或更高配位实现,超越了双配位线性配合物的既定范例。
Charting new regions of Cobalt's chemical space with maximally large magnetic anisotropy: A computational high-throughput study
Magnetic anisotropy slows down magnetic relaxation and plays a prominent role
in the design of permanent magnets. Coordination compounds of Co(II) in
particular exhibit large magnetic anisotropy in the presence of
low-coordination environments and have been used as single-molecule magnet
prototypes. However, only a limited sampling of Cobalt's vast chemical space
has been performed, potentially obscuring alternative chemical routes toward
large magnetic anisotropy. Here we perform a computational high-throughput
exploration of Co(II)'s chemical space in search of new single-molecule
magnets. We automatically assemble a diverse set of about 15000 novel complexes
of Co(II) and fully characterize them with multi-reference ab initio methods.
More than 100 compounds exhibit magnetic anisotropy comparable to or larger
than leading known compounds. The analysis of these results shows that
compounds with record-breaking magnetic anisotropy can also be achieved with
coordination four or higher, going beyond the established paradigm of
two-coordinated linear complexes.