4.6 Article

Exchange-Biasing in a Dinuclear Dysprosium(III) Single-Molecule Magnet with a Large Energy Barrier for Magnetisation Reversal

期刊

CHEMISTRY-A EUROPEAN JOURNAL
卷 26, 期 30, 页码 6773-6777

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/chem.202000719

关键词

dinuclear compounds; dysprosium; exchange interactions; hysteresis loop; single-molecule magnets

资金

  1. NSFC [21871219, 21773130, 21620102002]
  2. Joint Fund of the Natural Science Foundation of Zhejiang Province [LQY18B010001]
  3. Joint Fund of the Natural Science Foundation of Qingshan Lake [LQY18B010001]
  4. Key Laboratory Construction Program of Xi'an Municipal Bureau of Science and Technology [201805056ZD7CG40]
  5. China Postdoctoral Science Foundation [2017M623150]
  6. Shaanxi Postdoctoral Science Foundation [2017BSHTDZZ08]
  7. China Scholarship Council
  8. University of Manchester
  9. Royal Society
  10. EPSRC [EP/R011079/1]
  11. European Research Council [ERC-2017-ADG-786734]

向作者/读者索取更多资源

A dichlorido-bridged dinuclear dysprosium(III) single-molecule magnet [Dy2L2(mu-Cl)(2)(thf)(2)] has been made by using a diamine-bis(phenolate) ligand, H2L. Magnetic studies show an energy barrier for magnetisation reversal (U-eff) around 1000 K. An exchange-biasing effect is clearly seen in magnetic hysteresis with steps up to 3 K. Ab initio calculations exclude the possibility of a pure dipolar origin of this effect leading to the conclusion that super-exchange through the chloride bridging ligands is important.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

Article Chemistry, Multidisciplinary

Switching the coordination geometry to enhance erbium(III) single-molecule magnets

Qian-Cheng Luo, Ning Ge, Yuan-Qi Zhai, Tengbo Wang, Lin Sun, Qi Sun, Fanni Li, Zhendong Fu, Yan-Zhen Zheng

Summary: Two erbium(III) complexes, [ErCl(OArAd)3][Na(THF)6] (1) and Er(OArAd)3 (2), were prepared using a hard base ligand with large steric hindrance. The change in coordination geometry around the Er(III) site from distorted tetrahedral to flat trigonal pyramid geometry in different solvent environments enhanced the single-molecule magnet (SMM) behavior, with a field-induced effective energy barrier (Ueff) of 43(1) cm -1 for the latter. The study demonstrates the importance of a strong equatorial ligand field and high local symmetry in suppressing quantum tunneling of the magnetization (QTM) to achieve high-performance erbium(III)-based SMMs.

CHINESE CHEMICAL LETTERS (2023)

Article Chemistry, Multidisciplinary

Closely Related Organometallic Er(III) Single-Molecule Magnets with Sizably Different Relaxation Times of Quantum Tunneling of Magnetization

Tianjiao Xue, You-Song Ding, Daniel Reta, Qi-Wei Chen, Xiaofei Zhu, Zhiping Zheng

Summary: In this study, three new single-molecule magnets (SMMs) were reported for potential applications in information storage and quantum processing. These SMMs demonstrated similar magnetic properties but distinct quantum tunnelling of magnetization (QTM) relaxation times, suggesting the influence of nonmagnetic components and crystal environment on the behavior of SMMs.

CRYSTAL GROWTH & DESIGN (2023)

Article Chemistry, Inorganic & Nuclear

Inelastic Neutron Scattering Measurement of the Ground State Tunneling Gap in Tb and Ho Analogues of a Dy Field-Induced Single-Molecule Magnet

Alessandro Soncini, Richard A. Mole, Colette Boskovic, Aiden M. Atkin, Marcus J. Giansiracusa, Simone Calvello, Elodie Rousset, Robert W. Gable, Wasinee Phonsri, Keith S. Murray, James K. Howard

Summary: Recent advances in single-molecule magnet research have focused on the interpretation of inelastic neutron scattering data for rare earth-containing SMMs. This study presents the synthesis of rare earth complexes and their magnetic and INS studies, supported by ab initio calculations. The static magnetic properties and crystal field excitations of the compounds were investigated, and the INS spectra and magnetic behavior were interpreted using ab initio calculations and high-resolution INS measurements.

INORGANIC CHEMISTRY (2023)

Article Chemistry, Multidisciplinary

Two-dimensional semiconducting Cu(i)/Sb(iii) bimetallic hybrid iodides with a double perovskite structure and photocurrent response

Qian-Wen Li, Le-Yu Bi, Mohamed Saber Lassoued, Qian-Cheng Luo, Rong Yan, Xin-Kai Ding, Gao-Yang Gou, Yan-Zhen Zheng

Summary: In this study, stable lead-free hybrid halide double perovskites incorporating copper and antimony were successfully synthesized. These two-dimensional perovskites exhibited small band gaps, high solubility in organic solvents, and could form smooth and uniform thin films. Furthermore, they showed excellent photoelectric responses and high moisture and thermal stabilities, suggesting their potential for optoelectronic applications.

NANOSCALE (2023)

Article Engineering, Chemical

Control of pore structure by the solvent effect for efficient ethane/ethylene separation

Shao-Min Wang, Hao-Ran Liu, Su-Tao Zheng, Hao-Ling Lan, Qing-Yuan Yang, Yan-Zhen Zheng

Summary: This study successfully designed and synthesized ethane-selective adsorbents for ethylene purification using crystal engineering strategy. Among them, Co-9-ina exhibited the highest C2H6/C2H4 selectivity and adsorption capacity. Theoretical calculations and experimental results demonstrated that pyridine rings have stronger van der Waals interactions with ethane.

SEPARATION AND PURIFICATION TECHNOLOGY (2023)

Article Engineering, Chemical

The molecular nature of the eliminating azeotropy of dimethyl carbonate-ethanol system by ionic liquid entrainer

Yan-Zhen Zheng, Yu-Xin Jiang, Yu Zhou, Yu-Cang Zhang

Summary: The microstructural features of dimethyl carbonate (DMC)-ethanol azeotrope mixtures were studied using FTIR and DFT. It was found that different IL concentrations can break the DMC-ethanol interaction complex, leading to the separation of the azeotrope. The strength and nature of hydrogen bonds between DMC/IL and ethanol were also evaluated.

SEPARATION AND PURIFICATION TECHNOLOGY (2023)

Article Chemistry, Inorganic & Nuclear

A bis(silyldiamido) dysprosium single-molecule magnet

Tian Han, You-Song Ding

Summary: A complex with a dysprosium ion coordinated by two bulky chelating silyldiamide ligands was synthesized and characterized. The coordination geometry allowed slow magnetic relaxation up to 42 K, making it the first silyldiamido dysprosium single-molecule magnet.

INORGANIC CHEMISTRY FRONTIERS (2023)

Article Chemistry, Inorganic & Nuclear

Zero-Field Splitting in Cyclic Molecular Magnet {Cr8Y8}: A High-Frequency ESR Study

Zhendong Fu, Zhong-Wen Ouyang, Qian-Cheng Luo, Yan-Zhen Zheng, Wei Tong, Huanpeng Bu, Hanjie Guo, Jin-Kui Zhao

Summary: In this study, the magnetism of Cr8Y8 was investigated using high-frequency electron spin resonance (HF-ESR) method. It was confirmed that Cr8Y8 has an S = 12 ground state and a zero-field splitting (ZFS) due to axial magnetic anisotropy. The validity of the macrospin model was also demonstrated. This research contributes to a deeper understanding of the magnetism of Cr8Y8 and highlights the importance of the HF-ESR method in determining ZFS parameters with very small magnitude.

MAGNETOCHEMISTRY (2023)

Article Chemistry, Multidisciplinary

Determinative Effect of Axial Linearity on Single-Molecule Magnet Performance in Dinuclear Dysprosium Complexes

Tian Han, You-Song Ding, Marcus J. Giansiracusa, Nicholas F. Chilton, Richard E. P. Winpenny, Yan-Zhen Zheng

Summary: Two dichloride-bridged dinuclear dysprosium(III) complexes based on salen ligands, [Dy(L-1)(mu-Cl)(thf)](2) and [Dy-2(L-2)(2)(mu-Cl)(2)(thf)(2)], were reported. Complex 2 showed clear slow relaxation of the magnetization due to the two short Dy-O-(PhO) bonds with an angle of approximately 143 degrees, while complex 1 exhibited slower relaxation due to an angle of around 90 degrees. The structural difference in the relative angles of the two O-(PhO)-Dy-O-(PhO) vectors in these complexes resulted in significant differences in their dipolar ground states, leading to open magnetic hysteresis in complex 3 and not in complex 2.

CHEMISTRY-A EUROPEAN JOURNAL (2023)

Article Chemistry, Inorganic & Nuclear

Electron Paramagnetic Resonance Spectra of Pentagonal Bipyramidal Gadolinium Complexes

Jonatan B. Petersen, You-Song Ding, Sandeep Gupta, Aditya Borah, Eric J. L. McInnes, Yan-Zhen Zheng, Ramaswamy Murugavel, Richard E. P. Winpenny

Summary: In this study, the zero-field splitting (ZFS) of Gd3+ pentagonal bipyramidal complexes was investigated to understand the mechanisms of ground state splitting. The results showed that the ZFS is dominated by the B20 term, which is inversely proportional to the donor strength of the axial ligands. Additionally, the magnitude of B20 was found to be inversely proportional to the thermal barrier for the reversal of the magnetic moment of the corresponding isostructural Dy3+ complexes.

INORGANIC CHEMISTRY (2023)

Article Chemistry, Inorganic & Nuclear

Synergy of Magnetic Anisotropy and Ferromagnetic Interaction Triggering a Dimeric Cr(II) Zero-Field Single-Molecule Magnet

Yuzhu Li, Zhaopeng Zeng, Yan Guo, Xingman Liu, Yi-Quan Zhang, Zhongwen Ouyang, Zhenxing Wang, Xiangyu Liu, Yan-Zhen Zheng

Summary: A novel CrII-dimeric complex has been constructed using a bulky silyl-amide ligand. The crystal structure analysis reveals a binuclear motif with two equivalent tetra-coordinate CrII centers displaying quasi-square planar geometry. Magnetic studies and theoretical calculations indicate the presence of slow dynamic magnetic relaxation and a non-negligible ferromagnetic coupling in the dimeric Cr-Cr units.

INORGANIC CHEMISTRY (2023)

Article Chemistry, Multidisciplinary

Determination of molecular hydration in solution via changes in magnetic anisotropy

Marcus J. Giansiracusa, Michele Vonci, Yasmin L. Whyatt, Carys Williams, Kevin Mason, David Parker, Eric J. L. McInnes, Nicholas F. Chilton

Summary: EPR spectroscopy is used to show that a t-butyl-pyridyl-functionalised Er-III DOTA derivative coordinates water, while its methylphosphinate analogue does not.

CHEMICAL COMMUNICATIONS (2023)

Article Chemistry, Multidisciplinary

Direct observation of magnetoelastic coupling in a molecular spin qubit: new insights from crystal field neutron scattering data

Maja A. Dunstan, Marcus J. Giansiracusa, Michele Vonci, Simone Calvello, Dehong Yu, Alessandro Soncini, Colette Boskovic, Richard A. Mole

Summary: In this study, we show for the first time that magnetic relaxation times and mechanisms can be directly observed as crystal field peak broadening in inelastic neutron scattering (INS) spectra. By measuring both crystal field excitations and phonon density of states, we are able to determine the magnetoelastic coupling between the lower energy crystal field states and phonons. This information is crucial for the advancement of single-molecule magnets (SMMs) and has previously only been obtained in external magnetic fields. Additionally, we find a relaxation rate of quantum-tunnelling of magnetisation consistent with previous EPR spectroscopy data.

CHEMICAL SCIENCE (2023)

Article Chemistry, Multidisciplinary

Assembly of MnIII ions into di-, tetra-, deca-nuclear coordination complexes, zero- to three-dimensional molecular frameworks: molecular spin flop to and short-range bulk magnetic spin flop ordering

Jayasree Kumar, Ibtesham Tarannum, Yan-Zhen Zheng, Saurabh Kumar Singh, Kartik Chandra Mondal

Summary: This study investigates the influence of various ligands on the structures and reactions of coordination compounds with Mn(III) ions. The resulting complexes exhibit different nuclearities and magnetic properties.

CRYSTENGCOMM (2023)

Article Chemistry, Inorganic & Nuclear

A 3D lead chloride hybrid exhibits self-trapped emission and exceptional stability

Mohamed Saber Lassoued, Qian-Cheng Luo, Yan-Zhen Zheng

Summary: A new 3D lead chloride hybrid, (H2MPP)2Pb5Cl14, has been isolated, which exhibits broadband emission with a large Stokes shift and a high color rendering index (CRI), mainly attributed to the self-trapped exciton mechanism (STE). It also shows higher stability under moisture, UV light and heat.

INORGANIC CHEMISTRY FRONTIERS (2023)

暂无数据