Jove
Visualize
联系我们
JoVE
x logofacebook logolinkedin logoyoutube logo
关于 JoVE
概览领导团队博客JoVE 帮助中心
作者
出版流程编辑委员会范围与政策同行评审常见问题投稿
图书馆员
用户评价订阅访问资源图书馆顾问委员会常见问题
研究
JoVE JournalMethods CollectionsJoVE Encyclopedia of Experiments存档
教育
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab Manual教师资源中心教师网站
使用条款与条件
隐私政策
政策

相关概念视频

Colors and Magnetism03:02

Colors and Magnetism

13.9K
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...
13.9K
Valence Bond Theory02:42

Valence Bond Theory

11.1K
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...
11.1K
Properties of Transition Metals02:58

Properties of Transition Metals

29.4K
Transition metals are defined as those elements that have partially filled d orbitals. As shown in Figure 1, the d-block elements in groups 3–12 are transition elements. The f-block elements, also called inner transition metals (the lanthanides and actinides), also meet this criterion because the d orbital is partially occupied before the f orbitals.
29.4K
Coordination Number and Geometry02:57

Coordination Number and Geometry

18.8K
For transition metal complexes, the coordination number determines the geometry around the central metal ion. Table 1 compares coordination numbers to molecular geometry. The most common structures of the complexes in coordination compounds are octahedral, tetrahedral, and square planar.
18.8K
Metal-Ligand Bonds02:51

Metal-Ligand Bonds

23.8K
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...
23.8K
Crystal Field Theory - Octahedral Complexes02:58

Crystal Field Theory - Octahedral Complexes

30.4K
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...
30.4K

您也可能阅读

相关文章

通过共同作者、期刊和引用图与本文相关的文章。

排序
Same author

Kinetic Approach for Assessing Absolute Hydrogen Potential (pH<sub>abs</sub>) across Diverse Solvents.

The journal of physical chemistry. A·2026
Same author

Relationship between Transition-Metal Hydride Bond Lengths and Stretching Wavenumbers.

Inorganic chemistry·2024
Same author

Mechanochemical Synthesis of Chromium(III) Complexes Containing Bidentate PN and Tridentate P-NH-P and P-NH-P' Ligands.

ACS omega·2024
Same author

Reactivity umpolung (reversal) of ligands in transition metal complexes.

Chemical Society reviews·2024
Same author

<i>Trans</i> Ligand Determines the Stability of Paramagnetic Manganese(II) Hydrides of the Type <i>trans</i>-[MnH(L)(dmpe)<sub>2</sub>]<sup>+</sup> Where L is PMe<sub>3</sub>, C<sub>2</sub>H<sub>4</sub>, or CO.

Inorganic chemistry·2023
Same author

Density Functional Theory Study on the Selective Reductive Amination of Aldehydes and Ketones over Their Reductions to Alcohols Using Sodium Triacetoxyborohydride.

ACS omega·2022
Same journal

Synthetic Porous Carbons for High-Energy, High-Power Supercapacitors.

Chemical reviews·2026
Same journal

Navigating Misfolded Terrain: ER-Associated Degradation of Membrane Proteins.

Chemical reviews·2026
Same journal

Ink Design for Printing Perovskite Solar Cells and Modules.

Chemical reviews·2026
Same journal

Advanced Single-Atom Catalysts for Thermal-Catalytic C1 Chemistry.

Chemical reviews·2026
Same journal

Copper-Dependent Polysaccharide Monooxygenases: Mechanism and Function.

Chemical reviews·2026
Same journal

To Biotic or Abiotic: Biohybrid Systems for Artificial Photosynthesis.

Chemical reviews·2026
查看所有相关文章

相关实验视频

Updated: Jan 8, 2026

Line Shape Analysis of Dynamic NMR Spectra for Characterizing Coordination Sphere Rearrangements at a Chiral Rhenium Polyhydride Complex
10:52

Line Shape Analysis of Dynamic NMR Spectra for Characterizing Coordination Sphere Rearrangements at a Chiral Rhenium Polyhydride Complex

Published on: July 27, 2022

3.2K

超磁性过渡金属化物复合物

Adi Fishkin1, Robert H Morris1

  • 1Department of Chemistry, University of Toronto, 80 Saint George St., Toronto, Ontario M5S3H6, Canada.

Chemical reviews
|December 22, 2025
PubMed
概括
此摘要是机器生成的。

偏磁性化物复合物 (PHC) 呈现的金属化物键比二磁性类似物弱. 它们的多样性反应性和在地球上丰富的金属中的普遍性突出显示了它们对可持续催化物的潜力.

更多相关视频

Author Spotlight: Magnetometric Characterization of Intermediates in the Solid-State Electrochemistry of Redox-Active Metal-Organic Frameworks
06:53

Author Spotlight: Magnetometric Characterization of Intermediates in the Solid-State Electrochemistry of Redox-Active Metal-Organic Frameworks

Published on: June 9, 2023

2.6K
The Synthesis, Characterization and Reactivity of a Series of Ruthenium N-triphosPh Complexes
10:51

The Synthesis, Characterization and Reactivity of a Series of Ruthenium N-triphosPh Complexes

Published on: April 10, 2015

12.6K

相关实验视频

Last Updated: Jan 8, 2026

Line Shape Analysis of Dynamic NMR Spectra for Characterizing Coordination Sphere Rearrangements at a Chiral Rhenium Polyhydride Complex
10:52

Line Shape Analysis of Dynamic NMR Spectra for Characterizing Coordination Sphere Rearrangements at a Chiral Rhenium Polyhydride Complex

Published on: July 27, 2022

3.2K
Author Spotlight: Magnetometric Characterization of Intermediates in the Solid-State Electrochemistry of Redox-Active Metal-Organic Frameworks
06:53

Author Spotlight: Magnetometric Characterization of Intermediates in the Solid-State Electrochemistry of Redox-Active Metal-Organic Frameworks

Published on: June 9, 2023

2.6K
The Synthesis, Characterization and Reactivity of a Series of Ruthenium N-triphosPh Complexes
10:51

The Synthesis, Characterization and Reactivity of a Series of Ruthenium N-triphosPh Complexes

Published on: April 10, 2015

12.6K

科学领域:

  • 无机化学 无机化学
  • 有机金属化学 有机金属化学
  • 催化剂是一种催化剂.

背景情况:

  • 偏磁化物复合物 (PHC) 对于理解化学反应至关重要.
  • 描述这些复杂物为结合和反应性提供了洞察力.

研究的目的:

  • 为了对PHC的结构,结合,能量,制备,表征和反应进行分类.
  • 揭示PHC特性及其催化应用的趋势.

主要方法:

  • 终端和桥梁化物的结晶学表征.
  • 实验和理论键能量的表化.
  • 磁力测量和电子磁共振 (EPR) 研究.
  • 对高精度合常数和NMR数据的分析.

主要成果:

  • 与类似联体的PHC与二磁性化物相比显示较弱的M-H键.
  • 桥接化物通常由于反铁磁合而表现出降低的磁矩.
  • 观察到广泛的超细合常量,受粘合轨道和费米接触期的影响.
  • 十种化合物显示在偏磁状态下存在化物1H NMR共振.
  • 详细介绍了涉及疑似PHC的40多个同质催化过程.

结论:

  • PHC显示独特的结合和反应模式.
  • 它们在地球上丰富的金属中普遍存在,这使得它们对于可持续的催化非常重要.
  • 对PHC的特性和应用的进一步研究是有必要的.