二吸附于一个dysprosocenium单分子磁铁
Sophie C Corner1, Gemma K Gransbury1, Iñigo J Vitorica-Yrezabal1
1Department of Chemistry, The University of Manchester, Oxford Road, Manchester M13 9PL, U.K.
Inorganic chemistry
|February 15, 2024
概括
将烯与复合物的协调通过增强旋声放松来降低磁性歇斯底里温度. 然而,磁化逆转的有效障碍仍然很高,显示了单分子磁体应用的潜力.
科学领域:
- 材料科学 材料科学 材料科学
- 量子化学 是一个量子化学.
- 纳米技术 纳米技术
背景情况:
- 具有强大的轴性晶场的复合体显示出作为单分子磁铁 (SMM) 的承诺,用于高密度数据存储.
- 最近的dysprosocenium离子 ([Dy(CpR) 2]+) 在液温度以上呈现磁性歇斯底里.
- 通过最大限度地减少旋声放松,减少横向连接体场对于提高SMM性能至关重要.
研究的目的:
- 为了研究赤道二协调对dysprosocenium离子体的磁性特性的影响.
- 了解引入的横向场如何影响SMM中的磁放松机制和歇斯底里.
- 评估磁化逆转对能量障碍的影响.
主要方法:
- 与赤道二联体 (PhX,o-C6H4F2) 合成二复合体.
- 磁性表征包括歇斯底里测量.
- 分析磁放松动态,包括奥巴赫和拉曼过程.
- 结构和电子效应的计算分析.
主要成果:
- 与母电离子相比,halobenzenes的赤道协调降低了磁性歇斯底里温度.
- 观察到一声声 (奥巴赫) 和两声声 (拉曼) 放松机制的效率增加.
- 确定了一种音声瓶效应,在低温下导致不同的放松率.
- 磁化逆转的有效障碍仍然很高 (>1000厘米-1),与父复合体相比仅略有降低.
结论:
- 在dysprosocenium复合体中,赤道二协调增强了通过旋声子相互作用的磁性放松,降低了歇斯底里温度.
- 尽管降低了hysteresis,但由于高有效的能源障碍,SMM的性能仍然很有希望.
- 这些发现提供了对先进的SMM的合理设计策略的见解.
更多相关视频
06:53Author Spotlight: Magnetometric Characterization of Intermediates in the Solid-State Electrochemistry of Redox-Active Metal-Organic Frameworks
Published on: June 9, 2023
2.0K
08:50High-Speed Magnetic Tweezers for Nanomechanical Measurements on Force-Sensitive Elements
Published on: May 12, 2023
2.1K
相关概念视频
Colors and Magnetism
11.7K
Color in Coordination Complexes
When atoms or molecules absorb light at the proper frequency, their electrons are excited to higher-energy orbitals. For many main group atoms and molecules, the absorbed photons are in the ultraviolet range of the electromagnetic spectrum, which cannot be detected by the human eye. For coordination compounds, the energy difference between the d orbitals often allows photons in the visible range to be absorbed and emitted, which is seen as colors by the human...
When atoms or molecules absorb light at the proper frequency, their electrons are excited to higher-energy orbitals. For many main group atoms and molecules, the absorbed photons are in the ultraviolet range of the electromagnetic spectrum, which cannot be detected by the human eye. For coordination compounds, the energy difference between the d orbitals often allows photons in the visible range to be absorbed and emitted, which is seen as colors by the human...
11.7K
Valence Bond Theory
8.6K
Coordination compounds and complexes exhibit different colors, geometries, and magnetic behavior, depending on the metal atom/ion and ligands from which they are composed. In an attempt to explain the bonding and structure of coordination complexes, Linus Pauling proposed the valence bond theory, or VBT, using the concepts of hybridization and the overlapping of the atomic orbitals. According to VBT, the central metal atom or ion (Lewis acid) hybridizes to provide empty orbitals of suitable...
8.6K
Structure of Benzene: Molecular Orbital Model
9.1K
According to the molecular orbital (MO) model, benzene has a planar structure with a regular hexagon of six sp2 hybridized carbons. As shown in Figure 1, each carbon is bonded to three other atoms with C–C–C and H–C–C bond angles of 120°. The C–H bond length is 109 pm, and the C–C bond length is 139 pm which is midway between the single bond length of sp3 hybridized carbons (154 pm) and sp2 hybridized carbons (133 pm).
9.1K
Spin–Spin Coupling Constant: Overview
923
In bromoethane, the three methyl protons are coupled to the two methylene protons that are three bonds away. In accordance with the n+1 rule, the signal from the methyl protons is split into three peaks with 1:2:1 relative intensities. The methylene protons appear as a quartet, with the relative intensities of 1:3:3:1.
Qualitatively, any spin plus-half nucleus polarizes the spins of its electrons to the minus-half state. Consequently, the paired electron in the hydrogen–carbon bond must...
Qualitatively, any spin plus-half nucleus polarizes the spins of its electrons to the minus-half state. Consequently, the paired electron in the hydrogen–carbon bond must...
923
π Electron Effects on Chemical Shift: Overview
1.1K
An applied magnetic field causes loosely bound π-electrons in organic molecules to circulate, producing a local or induced diamagnetic field over a large spatial volume. As the molecules tumble in solution, the field generated by π-electrons in spherical substituents results in a zero net field. However, the net field generated by π-electrons in non-spherical substituents is not zero. The effect of this induced field depends on the orientation of the molecule with respect to B0,...
1.1K
NMR Spectroscopy of Benzene Derivatives
8.2K
Simple unsubstituted benzene has six aromatic protons, all chemically equivalent. Therefore, benzene exhibits only a singlet peak at δ 7.3 ppm in the 1H NMR spectrum. The observed shift is far downfield because the aromatic ring current strongly deshields the protons. Any substitution on the benzene ring makes the aromatic protons nonequivalent, and the protons split each other. The peak is, therefore, no longer a singlet and the splitting pattern and their associated coupling...
8.2K
