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Metal-Ligand Bonds02:51

Metal-Ligand Bonds

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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...
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Structural Isomerism02:34

Structural Isomerism

19.2K
Isomerism in Complexes
Isomers are different chemical species that have the same chemical formula. Structural isomerism of coordination compounds can be divided into two subcategories, the linkage isomers and coordination-sphere isomers.
Linkage isomers occur when the coordination compound contains a ligand that can bind to the transition metal center through two different atoms. For example, the CN− ligand can bind through the carbon atom or through the nitrogen atom. Similarly, SCN− can...
19.2K
Complexation Equilibria: The Chelate Effect01:19

Complexation Equilibria: The Chelate Effect

518
In complexation reactions, metal atoms or cations interact with ligands to form donor-acceptor adducts called metal complexes. Ligands that bind through one donor site are monodentate, ligands with two donor sites are bidentate, and those with more than two donor sites are polydentate ligands. For example, ethylene diamine is a bidentate ligand that binds through two nitrogen donor atoms, forming a five-membered ring. EDTA is a polydentate ligand that binds through four oxygen and two nitrogen...
518
Stereoisomerism02:52

Stereoisomerism

11.9K
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...
11.9K
Colors and Magnetism03:02

Colors and Magnetism

11.7K
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...
11.7K
Valence Bond Theory02:42

Valence Bond Theory

8.6K
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...
8.6K

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Updated: Jul 7, 2025

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

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聚合物控制的的反应性 (II) 前体:抗铁磁合的 (III) -氧化与 (II) -氧化形式.

Debasish Samanta1, Pinaki Saha1, Suvendu Maity1

  • 1Department of Chemistry, Ramakrishna Mission Residential College, Narendrapur, Kolkata 700103, India.

Inorganic chemistry
|December 23, 2023
PubMed
概括

鲁复合体表现出基于它们的配体的不同反应性. 一种前体促进甲氧化脱甲基化,另一种促进C-H激活,导致多样化的键形成和独特的以为中心的反应.

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

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Synthesis and Evaluation of a Ruthenium-based Mitochondrial Calcium Uptake Inhibitor
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Synthesis and Evaluation of a Ruthenium-based Mitochondrial Calcium Uptake Inhibitor

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相关实验视频

Last Updated: Jul 7, 2025

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

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

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Synthesis and Evaluation of a Ruthenium-based Mitochondrial Calcium Uptake Inhibitor
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Synthesis and Evaluation of a Ruthenium-based Mitochondrial Calcium Uptake Inhibitor

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科学领域:

  • 有机金属化学 有机金属化学
  • 协调化学 协调化学
  • 催化剂是一种催化剂.

背景情况:

  • 复合物是有机合成中的多功能催化剂.
  • 了解对反应性的联体效应对于设计新的转换至关重要.

研究的目的:

  • 为了研究两种 (II) 前体与三氧化亚利氨基衍生物的不同反应性.
  • 探索氧化物种的后续反应及其对键形成的影响.

主要方法:

  • (II/III) 复合物的合成和表征.
  • 单晶X射线晶体学. 单晶X射线晶体学.
  • 电子偏磁共振 (EPR) 光谱学.电子偏磁共振 (EPR) 光谱学.
  • 密度函数理论 (DFT) 的计算.

主要成果:

  • [Ru(PPh3) 3Cl2]前体产生甲氧脱甲基化和一个[Phenolato-RuIII-Phenolato]单位.
  • [Ru(PPh3) 3 ((CO) ((H) Cl]前体导致C-H激活和一个[Phenolato-RuII-Aryl]单位.
  • 氧化类型具有多种反应性,包括PPh3氧化,二元化,C-C合和H抽象,形成独特的以为中心的产品.

结论:

  • 基环境显著决定了复合体中的反应路径和产品形成.
  • 该研究强调了介导的新型键形成反应,包括Ru-Ru键形成和C-C合.
  • 这些发现提供了对控制的反应性和催化潜力的电子和结构因素的见解.