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相关概念视频

Valence Bond Theory02:42

Valence Bond Theory

11.4K
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...
11.4K
Colors and Magnetism03:02

Colors and Magnetism

14.3K
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...
14.3K
Atomic Nuclei: Nuclear Spin State Overview01:03

Atomic Nuclei: Nuclear Spin State Overview

2.1K
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...
2.1K
Spin–Spin Coupling: Two-Bond Coupling (Geminal Coupling)01:20

Spin–Spin Coupling: Two-Bond Coupling (Geminal Coupling)

1.8K
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...
1.8K
Stereoisomerism02:52

Stereoisomerism

14.2K
Isomerism in Complexes
Isomers are different chemical species that have the same chemical formula.
Transition metal complexes often exist as geometric isomers, in which the same atoms are connected through the same types of bonds but with differences in their orientation in space. Coordination complexes with two different ligands in the cis and trans positions from a ligand of interest form isomers. For example, the octahedral [Co(NH3)4Cl2]+ ion has two isomers (Figure 1) In the cis...
14.2K
Spin–Spin Coupling Constant: Overview01:08

Spin–Spin Coupling Constant: Overview

1.6K
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...
1.6K

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Determination of the Photoisomerization Quantum Yield of a Hydrazone Photoswitch
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在超分子螺旋体中切换刺激-响应的自旋状态,弥合固溶液-固溶液双稳定性.

Debopam Sarkar1, Sounak Ghosh1, Pradip Kumar Mondal2

  • 1Solid State and Structural Chemistry Unit, Indian Institute of Science, Bangalore 560012, Karnataka, India.

Inorganic chemistry
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概括

研究人员开发了新的铁螺旋飞机,可以在固体和溶液阶段的自旋状态之间切换. 这一突破为创造超越晶体状态的可处理,可切换的分子设备提供了潜力.

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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:

  • 设计固体和溶液阶段的双可变分子系统是具有挑战性的.
  • 旋转交叉系统在晶体中得到了很好的研究,但溶液相切换是罕见的.
  • 可加工和功能性材料需要在不同阶段的两性稳定性.

研究的目的:

  • 报告一种新的金属超分子螺旋体家族,在固体和溶液阶段具有双稳定性.
  • 为了研究这些螺旋飞机的旋转状态切换行为.
  • 探索这些系统对功能性材料的潜力.

主要方法:

  • 合成单晶X射线衍射用于结构特征.
  • 固态磁性测量以确认旋转状态切换.
  • 溶液相变温度埃文斯1HNMR光谱用于研究自旋动力学.

主要成果:

  • 一个新的[Fe2L3]螺旋体家族被合成和特征化.
  • 两架直升机 (M1和M2) 在固体和溶液阶段都展示了温度依赖的自旋状态切换.
  • 核磁共振研究揭示了溶液中的动态自旋状态平衡,提供了分子水平的见解.

结论:

  • [Fe2L3]螺旋体代表了一种新型的溶液可访问的可比系统.
  • 这些发现使可切换分子装置的开发能够超越晶体状态.
  • 旋转状态切换对超分子环境和晶体溶剂分子敏感.