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过渡金属离子对一族具有五角双锥型Ln(III)离子的空气稳定型3d-4f离子对化合物中单分子磁体性质的影响。

Effect of the Transition Metal Ions on the Single-Molecule Magnet Properties in a Family of Air-Stable 3d-4f Ion-Pair Compounds with Pentagonal Bipyramidal Ln(III) Ions.

作者信息

Li Shan, Xiong Jin, Yuan Qiong, Zhu Wen-Hua, Gong Hui-Wen, Wang Fei, Feng Chuan-Qi, Wang Shi-Quan, Sun Hao-Ling, Gao Song

机构信息

Collaborative Innovation Center for Advanced Organic Chemical Materials Co-constructed by the Province and Ministry, Ministry of Education Key Laboratory for the Synthesis and Application of Organic Functional Molecules, Hubei University, Wuhan 430062, P. R. China.

Beijing National Laboratory for Molecular Sciences, State Key Laboratory of Rare Earth Materials Chemistry and Applications, College of Chemistry and Molecular Engineering, Peking University, No. 5 Yiheyuan Road, Beijing 100871, P. R. China.

出版信息

Inorg Chem. 2021 Dec 20;60(24):18990-19000. doi: 10.1021/acs.inorgchem.1c02828. Epub 2021 Dec 1.

Abstract

Single-molecule magnets (SMMs) are expected to be promising candidates for the applications of high-density information storage materials and quantum information processing. Lanthanide SMMs have attracted considerable interest in recent years due to their excellent performance. It has always been interesting but not straightforward to study the relaxation and blocking mechanisms by embedding 3d ions into 4f SMMs. Here we report a family of air-stable 3d-4f ion-pair compounds, YFe (), DyCr (), DyFe (), DyCo (), and DyYFe (), composed of pentagonal bipyramidal () Ln cations and transition metallocyanate anions. The ion-pair nature makes the dipole-dipole interactions almost the only component of the magnetic interactions that can be clarified and analytically resolved under proper approximation. Therefore, this family provides an intuitive opportunity to investigate the effects of 3d-4f and 4f-4f magnetic interactions on the behavior of site-resolved 4f SMMs. Dynamic magnetic measurements of under a 4 kOe external field reveal slow magnetic relaxation originating from the isolated [Fe] ( = /) ions. Under zero dc field, compounds show similar magnetic relaxation processes coming from the separated pentagonal bipyramidal () Dy ions with high Orbach barriers of 592(5), 596(4), 595(3), and 606(4) K, respectively. Comparatively, both compounds and exhibit two distinct relaxation processes, respectively from the [Fe] and Dy [ = 596(4) K for and 610(7) K for ] ions, under a 4 kOe dc field. The dipolar interactions between the neighboring TM (TM = transition metal, Cr or [Fe]) and Dy ions were revealed to have little effect on the thermal relaxation in compounds , , and , or the coexistence of the two separate relaxation processes in compounds and under a 4 kOe dc field, but they significantly affect the quantum tunneling of magnetization and the magnetic hysteresis behavior of and at low temperatures compared to those of .

摘要

单分子磁体(SMMs)有望成为高密度信息存储材料和量子信息处理应用的有前途的候选者。近年来,镧系单分子磁体因其优异的性能而备受关注。将3d离子嵌入4f单分子磁体中来研究其弛豫和阻塞机制一直很有趣,但并非易事。在此,我们报道了一系列空气稳定的3d-4f离子对化合物,YFe()、DyCr()、DyFe()、DyCo()和DyYFe(),它们由五角双锥()Ln阳离子和过渡金属氰酸盐阴离子组成。离子对性质使得偶极-偶极相互作用几乎成为在适当近似下可被阐明和解析的磁相互作用的唯一组成部分。因此,该系列化合物为研究3d-4f和4f-4f磁相互作用对位点分辨的4f单分子磁体行为的影响提供了直观的机会。在4 kOe外场下对进行的动态磁测量揭示了源自孤立的[Fe](= /)离子的缓慢磁弛豫。在零直流场下,化合物显示出类似的磁弛豫过程,分别来自分离的五角双锥()Dy离子,其具有592(5)、596(4)、595(3)和606(4) K的高奥巴赫势垒。相比之下,在4 kOe直流场下,化合物和分别表现出两种不同的弛豫过程,分别来自[Fe]离子和Dy离子(对于为596(4) K,对于为610(7) K)。结果表明,相邻的TM(TM = 过渡金属,Cr或[Fe])和Dy离子之间的偶极相互作用对化合物、和中的热弛豫几乎没有影响,或者在4 kOe直流场下对化合物和中两个独立弛豫过程的共存几乎没有影响,但与相比,它们在低温下显著影响和的磁化量子隧穿和磁滞行为。

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