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Valence Bond Theory02:42

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
Thermal and Photochemical Electrocyclic Reactions: Overview01:26

Thermal and Photochemical Electrocyclic Reactions: Overview

2.3K
Electrocyclic reactions are reversible reactions. They involve an intramolecular cyclization or ring-opening of a conjugated polyene. Shown below are two examples of electrocyclic reactions. In the first reaction, the formation of the cyclic product is favored. In contrast, in the second reaction, ring-opening is favored due to the high ring strain associated with cyclobutene formation.
2.3K
Coordination Number and Geometry02:57

Coordination Number and Geometry

15.8K
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.
15.8K
Crystal Field Theory - Tetrahedral and Square Planar Complexes02:46

Crystal Field Theory - Tetrahedral and Square Planar Complexes

42.5K
Tetrahedral Complexes
Crystal field theory (CFT) is applicable to molecules in geometries other than octahedral. In octahedral complexes, the lobes of the dx2−y2 and dz2 orbitals point directly at the ligands. For tetrahedral complexes, the d orbitals remain in place, but with only four ligands located between the axes. None of the orbitals points directly at the tetrahedral ligands. However, the dx2−y2 and dz2 orbitals (along the Cartesian axes) overlap with the ligands less than the dxy,...
42.5K
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
Aromatic Hydrocarbon Cations: Structural Overview01:18

Aromatic Hydrocarbon Cations: Structural Overview

2.8K
Cycloheptatriene is a neutral monocyclic unsaturated hydrocarbon that consists of an odd number of carbon atoms and an intervening sp3 carbon in the ring. The three double bonds in the ring correspond to 6 π electrons, which is a Huckel number, and therefore satisfies the criteria of 4n + 2 π electrons. However, the intervening sp3 carbon disrupts the continuous overlap of p orbitals. As a result, cycloheptatriene is not aromatic.
Removing one hydrogen from the intervening CH2 group...
2.8K

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Updated: Jul 1, 2025

Amide Coupling Reaction for the Synthesis of Bispyridine-based Ligands and Their Complexation to Platinum as Dinuclear Anticancer Agents
07:20

Amide Coupling Reaction for the Synthesis of Bispyridine-based Ligands and Their Complexation to Platinum as Dinuclear Anticancer Agents

Published on: May 28, 2014

14.0K

NIR-II来自循环金属化二核Pt (III) 复合物的排放.

Irene Melendo1, Sara Fuertes1, Antonio Martín1

  • 1Instituto de Síntesis Química y Catálisis Homogénea (ISQCH), CSIC-Universidad de Zaragoza, Pedro Cerbuna 12, 50009 Zaragoza, Spain.

Inorganic chemistry
|March 8, 2024
PubMed
概括

新的 (II) 二核复合物被合成并氧化成 (III) 衍生物. 这些二白金(III) 复合体表现出可调节的近红外辐射,受到轴联体和温度的影响.

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The Synthesis, Characterization and Reactivity of a Series of Ruthenium N-triphosPh Complexes
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Catalytic Reactions at Amine-Stabilized and Ligand-Free Platinum Nanoparticles Supported on Titania During Hydrogenation of Alkenes and Aldehydes
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相关实验视频

Last Updated: Jul 1, 2025

Amide Coupling Reaction for the Synthesis of Bispyridine-based Ligands and Their Complexation to Platinum as Dinuclear Anticancer Agents
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Catalytic Reactions at Amine-Stabilized and Ligand-Free Platinum Nanoparticles Supported on Titania During Hydrogenation of Alkenes and Aldehydes
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科学领域:

  • 协调化学 协调化学
  • 有机金属化学 有机金属化学
  • 材料科学 材料科学 材料科学

背景情况:

  • 双核复合物由于其独特的电子和光物理特性而引起人们的兴趣.
  • 了解金属与金属的相互作用和连接体的影响对于设计新型功能材料至关重要.

研究的目的:

  • 为了合成和表征新的半灯塔Pt (II) 双核复合体.
  • 研究这些复合物的氧化到二 (((III) 衍生物.
  • 探索由此产生的Pt (II) 和Pt (III) 系统的光物理性质,特别是近红外辐射.

主要方法:

  • 合成半灯Pt(II) 双核复合物与特定的配体 (1-纳夫二-1-H-pyrazole和mercaptopyrimidines).
  • 在各种条件下 (空气,阳光,黑暗) 使用光环形的氧化反应.
  • 单晶X射线衍射用于结构阐明.
  • 光谱分析 (吸收和发射) 和密度函数理论 (DFT) 的计算.

主要成果:

  • 选择性合成单个异构体的Pt(II) 双核复合体与短的Pt-Pt距离.
  • 氧化二 (((III) 衍生物与 Pt-Pt 键的形成,受轴联体的影响.
  • 可调节的低能吸收和广泛的近红外 (NIR) 辐射 (985-1070nm在RT) 的观测,取决于轴联体和温度.

结论:

  • 合成的双核复合体Pt (II) 和Pt (III) 显示出可控制的光物理性质.
  • 轴联体在调整电子结构和排放特征方面发挥着重要作用.
  • 这些发现为潜在的光电子应用提供了对复合物的结构性质关系的见解.