在 [Fe(qsal-5-Brq) 2]+ 复合体中旋转交叉,复合体中含有基诺林替代的Qsal连接体
Feng-Li Chen1, Yu-Chen Sun1, Xin-Li Liu1
1State Key Laboratory of Coordination Chemistry, Collaborative Innovation Center of Advanced Microstructures, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing 210023, China.
Inorganic chemistry
|May 2, 2024
概括
这项研究报告了新的铁(III) 旋转交叉 (SCO) 综合体,使用氨酸替代的连接体. 溶解显著改变了SCO的特性,突出了新型SCO材料的潜力.
科学领域:
- 协调化学 协调化学
- 材料科学 材料科学 材料科学
- 超分子化学 超分子化学
背景情况:
- 旋转交叉 (SCO) 材料对分子开关和传感器有兴趣.
- 铁 (III) 复合体提供可调节的SCO特性.
- 干设计对于控制SCO行为至关重要.
研究的目的:
- 为了合成和表征新的铁 (III) 复合物,用氨酸替代的Qsal配体.
- 调查结构和磁性特性,包括SCO行为.
- 探讨溶解对上海合作组织特征的影响.
主要方法:
- 合成四种铁 (III) 复合物,其中含有氨酸替代的Qsal配体 (Hqsal-5-Brq).
- 使用X射线衍射进行结构性表征.
- 磁感应度测量用于研究旋转交叉过渡.
- 对SCO属性的溶解效应的研究.
主要成果:
- 准备和表征了四个Fe (III) 复合体.
- 综合体1和2 (P1̅) 呈现出突然的歇斯底里性SCO.
- 化合物3和4仍然处于高旋转状态.
- 溶解导致上海合作组织的行为发生了变化,包括逐步和两步过渡.
结论:
- 这项研究成功地开发了Fe (III) -SCO复合物,使用了用诺林替代的Hqsal配体.
- 结构特征如1D链和超分子相互作用影响SCO.
- 溶解是调整SCO特性的一个关键因素,表明了先进材料的潜力.
更多相关视频
相关概念视频
Valence Bond Theory
8.5K
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...
8.5K
Colors and Magnetism
11.6K
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...
11.6K
Spin–Spin Coupling: One-Bond Coupling
957
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,...
957
Spin–Spin Coupling: Three-Bond Coupling (Vicinal Coupling)
1.1K
Vicinal or three-bond coupling is commonly observed between protons attached to adjacent carbons. Here, nuclear spin information is primarily transferred via electron spin interactions between adjacent C‑H bond orbitals. This generally favors the antiparallel arrangement of spins, so 3J values are usually positive.
The extent of coupling depends on the C‑C bond length, the two H‑C‑C angles, any electron-withdrawing substituents, and the dihedral angle between the...
The extent of coupling depends on the C‑C bond length, the two H‑C‑C angles, any electron-withdrawing substituents, and the dihedral angle between the...
1.1K
Metal-Ligand Bonds
20.7K
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...
20.7K
Spin–Spin Coupling: Two-Bond Coupling (Geminal Coupling)
1.0K
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...
1.0K


