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氢氧化物桥联的五配位镝单分子磁体,在仅含镧系元素的二聚体中展现出创纪录的磁化热弛豫势垒。

Hydroxide-bridged five-coordinate Dy single-molecule magnet exhibiting the record thermal relaxation barrier of magnetization among lanthanide-only dimers.

作者信息

Xiong Jin, Ding Hai-Yan, Meng Yin-Shan, Gao Chen, Zhang Xue-Jing, Meng Zhao-Sha, Zhang Yi-Quan, Shi Wei, Wang Bing-Wu, Gao Song

机构信息

Beijing National Laboratory of Molecular Science , College of Chemistry and Molecular Engineering , State Key Laboratory of Rare Earth Materials Chemistry and Applications , Peking University , Beijing , 100871 , P. R. China . Email:

Jiangsu Key Laboratory for NSLSCS , School of Physical Science and Technology , Nanjing Normal University , Nanjing 210023 , P. R. China.

出版信息

Chem Sci. 2017 Feb 1;8(2):1288-1294. doi: 10.1039/c6sc03621j. Epub 2016 Oct 30.

Abstract

A hydroxide-bridged centrosymmetric Dy dimer with each Dy being five-coordinated has been synthesized using bulky hindered phenolate ligands. Magnetic studies revealed that this compound exhibits a slow magnetic relaxation of a single-ion origin together with a step-like magnetic hysteresis of the magnetic coupled cluster. The thermal relaxation barrier of magnetization is 721 K in the absence of a static magnetic field, while the intramolecular magnetic interaction is very large among reported 4f-only dimers. CASSCF calculations with a larger active space were performed to understand the electronic structure of the compound. The thermal relaxation regime and the quantum tunneling regime are well separated, representing a good model to study the relaxation mechanism of SMMs with intramolecular Dy-Dy magnetic interactions.

摘要

使用庞大的受阻酚盐配体合成了一种具有中心对称的氢氧化物桥联Dy二聚体,每个Dy为五配位。磁性研究表明,该化合物表现出单离子起源的缓慢磁弛豫以及磁耦合簇的阶梯状磁滞现象。在没有静磁场的情况下,磁化的热弛豫势垒为721 K,而在已报道的仅含4f的二聚体中,分子内磁相互作用非常大。进行了具有更大活性空间的CASSCF计算以了解该化合物的电子结构。热弛豫区和量子隧穿区得到了很好的分离,是研究具有分子内Dy-Dy磁相互作用的单分子磁体弛豫机制的良好模型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1f6e/5359878/dcb09e0cc596/c6sc03621j-f1.jpg

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