了解金属皇冠单分子磁铁中的自旋结构,使用磁性康普顿散射
Aniruddha Deb1, Thaddeus T Boron, Masayoshi Itou
1Department of Chemistry, University of Michigan , Ann Arbor, Michigan 48109, United States.
Journal of the American Chemical Society
|March 15, 2014
概括
磁性康普顿散射揭示了混合3d-4f金属冠中的旋转对齐. 兰化物4f旋转与3d旋转保持一致,而Dy2Mn4对其磁矩有显著的轨道贡献.
科学领域:
- 材料科学 材料科学 材料科学
- 固态物理 固态物理
- 无机化学 无机化学
背景情况:
- 3d-4f混合金属冠以单分子磁性行为而闻名.
- 了解旋转和轨道贡献对于设计分子磁铁至关重要.
研究的目的:
- 描述Gd2Mn4,Dy2Mn4和Y2Mn4金属冠中的自旋结构和轨道相互作用.
- 直接确定单旋对磁矩的贡献.
- 为了将分子设计与磁性相关联.
主要方法:
- 磁性康普顿散射探测旋转结构和轨道相互作用.
- SQUID磁力测量仪用于测量总磁矩.
- 分析单旋和总磁矩的关系.
主要成果:
- 在Gd2Mn4和Dy2Mn4中的兰化物4f旋转与Mn3d旋转平行.
- 在Y2Mn4.4中,有旋转转移到O2p轨道的证据.
- Gd2Mn4和Y2Mn4的轨道贡献很小,而Dy2Mn4的轨道对其磁矩有很大的贡献.
结论:
- 磁性康普顿散射提供了对金属冠的自旋贡献的直接洞察.
- 分子设计显著影响轨道对磁性质的贡献.
- 这项研究阐明了3d-4f系统中自旋和轨道磁力之间的相互作用.
更多相关视频
09:00Experimental Methods for Spin- and Angle-Resolved Photoemission Spectroscopy Combined with Polarization-Variable Laser
Published on: June 28, 2018
9.3K
09:06Visualizing Uniaxial-strain Manipulation of Antiferromagnetic Domains in Fe1+YTe Using a Spin-polarized Scanning Tunneling Microscope
Published on: March 24, 2019
6.6K
相关概念视频
NMR Spectroscopy: Spin–Spin Coupling
3.4K
The spin state of an NMR-active nucleus can have a slight effect on its immediate electronic environment. This effect propagates through the intervening bonds and affects the electronic environments of NMR-active nuclei up to three bonds away; occasionally, even farther. This phenomenon is called spin–spin coupling or J-coupling. Coupling interactions are mutual and result in small changes in the absorption frequencies of both nuclei involved. While nuclei of the same element are involved...
3.4K
Valence Bond Theory
8.9K
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...
8.9K
Colors and Magnetism
12.1K
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...
12.1K
Spin–Spin Coupling: One-Bond Coupling
1.2K
Coupling interactions are strongest between NMR-active nuclei bonded to each other, where spin information can be transmitted directly through the pair of bonding electrons. While nuclei polarize their electrons to the opposite spins, the bonding electron pair has opposite spins. Configurations with antiparallel nuclear spins are expected to be lower in energy. When coupling makes antiparallel states more favorable, J is considered to have a positive value. The one-bond coupling constant, 1J,...
1.2K
Atomic Nuclei: Nuclear Spin State Overview
1.9K
NMR-active nuclei have energy levels called 'spin states' that are associated with the orientations of their nuclear magnetic moments. In the absence of a magnetic field, the nuclear magnetic moments are randomly oriented, and the spin states are degenerate. When an external magnetic field is applied, the spin states have only 2 + 1 orientations available to them. A proton with = ½ has two available orientations. Similarly, for a quadrupolar nucleus with a nuclear spin value of one, the...
1.9K
Spin–Spin Coupling Constant: Overview
1.2K
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...
1.2K
