通过低坐标金属中心之间的直接轨道相互作用在M4 (M = Ni,Cu) 集群中的强电子和磁合
Khetpakorn Chakarawet, Mihail Atanasov1,2, Jonathan Marbey3
1Max-Planck Institut für Kohlenforschung, Mülheim an der Ruhr D-45470, Germany.
Journal of the American Chemical Society
|October 28, 2020
概括
这项研究探讨了四核过渡金属集群与直接的金属轨道重叠,揭示了独特的电子和磁性特性,如大型自旋基态和和铜化合物的缓慢磁性放松.
科学领域:
- 无机化学
- 材料科学
- 磁化学
背景情况:
- 具有低坐标金属中心的四核过渡金属集群因其独特的电子和磁性特性而引起兴趣.
- 直接的金属-金属轨道重叠是影响这些星团行为的一个关键特征.
- 了解这些相互作用对于设计新的磁性材料至关重要.
研究的目的:
- 研究四核过渡金属集群化合物M4 ((NPtBu3) 4) 和[M4 ((NPtBu3) 4) ][B ((C6F5) 4) 的电子和磁性特性 (M = Ni,Cu).
- 阐明结合相互作用及其对磁性行为的影响.
- 探索这些系统中缓慢磁放松的潜力.
主要方法:
- 四核和铜集群化合物的合成和表征.
- 进行X射线衍射,电化学,磁性和光谱分析.
- 相关的电子结构计算.
主要成果:
- 直接的轨道重叠导致大自旋基态和非局部化,自旋相关的电子在集群中.
- 在集群中观察到的铁磁基态和移动电子磁性.
- 阴离子团具有显著的磁性异构和零场缓慢的磁性放松.
- 铜团通过拉曼过程显示缓慢的磁放松.
结论:
- 在低坐标的金属集群中,金属与金属的直接轨道相互作用会产生独特的电子和磁性.
- 这些集群是分子磁力和旋转应用的有希望的候选者.
- 这些发现突出了通过集群设计的磁性行为的可调性.
更多相关视频
相关概念视频
Valence Bond Theory
10.4K
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...
10.4K
¹H NMR: Long-Range Coupling
2.3K
The coupling interactions of nuclei across four or more bonds are usually weak, with J values less than 1 Hz. While these are usually not observed in spectra, the presence of multiple bonds along the coupling pathway can result in observable long-range coupling.
In alkenes, spin information is communicated via σ–π overlap, as seen in allylic (four-bond) and homoallylic (five-bond) couplings. These coupling interactions are stronger when the σ bond is parallel to the alkene...
In alkenes, spin information is communicated via σ–π overlap, as seen in allylic (four-bond) and homoallylic (five-bond) couplings. These coupling interactions are stronger when the σ bond is parallel to the alkene...
2.3K
Colors and Magnetism
13.2K
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...
13.2K
Crystal Field Theory - Octahedral Complexes
29.5K
Crystal Field Theory
To explain the observed behavior of transition metal complexes (such as colors), a model involving electrostatic interactions between the electrons from the ligands and the electrons in the unhybridized d orbitals of the central metal atom has been developed. This electrostatic model is crystal field theory (CFT). It helps to understand, interpret, and predict the colors, magnetic behavior, and some structures of coordination compounds of transition metals.
CFT focuses on...
To explain the observed behavior of transition metal complexes (such as colors), a model involving electrostatic interactions between the electrons from the ligands and the electrons in the unhybridized d orbitals of the central metal atom has been developed. This electrostatic model is crystal field theory (CFT). It helps to understand, interpret, and predict the colors, magnetic behavior, and some structures of coordination compounds of transition metals.
CFT focuses on...
29.5K
Spin–Spin Coupling: Two-Bond Coupling (Geminal Coupling)
1.4K
Two NMR-active nuclei bonded to a central atom can be involved in geminal or two-bond coupling. Geminal coupling is commonly seen between diastereotopic protons in chiral molecules and unsymmetrical alkenes, among others.
The central atom need not be NMR-active because its electrons are affected by the electron polarization of the spin-active atoms. However, spin information is transmitted less effectively than in one-bond coupling, and 2J values are usually weaker than 1J values. The energy of...
The central atom need not be NMR-active because its electrons are affected by the electron polarization of the spin-active atoms. However, spin information is transmitted less effectively than in one-bond coupling, and 2J values are usually weaker than 1J values. The energy of...
1.4K
Metal-Ligand Bonds
23.1K
The hemoglobin in the blood, the chlorophyll in green plants, vitamin B-12, and the catalyst used in the manufacture of polyethylene all contain coordination compounds. Ions of the metals, especially the transition metals, are likely to form complexes.
In these complexes, transition metals form coordinate covalent bonds, a kind of Lewis acid-base interaction in which both of the electrons in the bond are contributed by a donor (Lewis base) to an electron acceptor (Lewis acid). The Lewis acid in...
In these complexes, transition metals form coordinate covalent bonds, a kind of Lewis acid-base interaction in which both of the electrons in the bond are contributed by a donor (Lewis base) to an electron acceptor (Lewis acid). The Lewis acid in...
23.1K


![The Synthesis of [Sn10SiSiMe334]2- Using a Metastable SnI Halide Solution Synthesized via a Co-condensation Technique](/_next/image?url=https%3A%2F%2Fcloudfront.jove.com%2FCDNSource%2Fteasers%2F54498.jpg&w=3840&q=50)