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相关概念视频

Valence Bond Theory02:42

Valence Bond Theory

8.8K
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...
8.8K
Structural Isomerism02:34

Structural Isomerism

19.5K
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...
19.5K
Complexation Equilibria: The Chelate Effect01:19

Complexation Equilibria: The Chelate Effect

564
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...
564
Metal-Ligand Bonds02:51

Metal-Ligand Bonds

21.1K
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...
21.1K
Properties of Transition Metals02:58

Properties of Transition Metals

26.4K
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.
26.4K
Properties of Organometallic Compounds01:23

Properties of Organometallic Compounds

1.1K
Organometallic compounds are compounds that contain a carbon–metal bond. Carbon belongs to an organyl group like alkyl, aryl, allyl, or benzyl groups. The metal can be from Group I or Group II of the periodic table, a transition metal, or a semimetal.
1.1K

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相关实验视频

Updated: Jul 24, 2025

Accessing Valuable Ligand Supports for Transition Metals: A Modified, Intermediate Scale Preparation of 1,2,3,4,5-Pentamethylcyclopentadiene
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Accessing Valuable Ligand Supports for Transition Metals: A Modified, Intermediate Scale Preparation of 1,2,3,4,5-Pentamethylcyclopentadiene

Published on: March 20, 2017

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混合价值四金属链.

M Pilar Del Río1, B Eva Villarroya1, José A López1

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

Chemistry (Weinheim an der Bergstrasse, Germany)
|July 4, 2023
PubMed
概括

这项研究引入了具有分数氧化状态的新型四金属链,使电子移位成为可能. 这些金属链表现出可调节的吸收光谱,为新材料提供了潜力.

关键词:
紫外线对紫外线的看法和的价值观 和的价值观金属金属债券 金属金属债券金属链条 - 金属链条有混合价值的混合价值.

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Synthesis of Hypervalent Iodonium Alkynyl Triflates for the Application of Generating Cyanocarbenes
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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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Accessing Valuable Ligand Supports for Transition Metals: A Modified, Intermediate Scale Preparation of 1,2,3,4,5-Pentamethylcyclopentadiene
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Accessing Valuable Ligand Supports for Transition Metals: A Modified, Intermediate Scale Preparation of 1,2,3,4,5-Pentamethylcyclopentadiene

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Synthesis of Hypervalent Iodonium Alkynyl Triflates for the Application of Generating Cyanocarbenes
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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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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:

  • 双核单位 ([Ir2(μ-OPy) 2(CO) [4]) 是关键的组成部分.
  • 连接这些单元形成四金属链.

研究的目的:

  • 为了合成和表征中性和二性四金属链.
  • 研究这些新型复合体的电子特性和结构特征.
  • 探索终端连接体对金属链的影响.

主要方法:

  • 中性[X-{Ir2}-{Ir2}-X]和二性[L-{Ir2}-{Ir2}-L]2+复合物的合成.
  • 频谱分析 (UV-Vis吸收) 用于确定电子属性.
  • 结构性表征,以了解金属对金属的键长度和连接体效应.

主要成果:

  • 复合体具有 +1.5 的分数平均氧化状态,具有电子移位.
  • 轴联体对金属-金属键长度的影响很小,但该链会影响Ir-L/X键.
  • 在溶液中观察到围绕Ir-Ir键的自由旋转,在化物复合物中具有低能量过渡状态.
  • 在438-504 nm的吸收波段可以通过终端连接体调节.

结论:

  • 成功合成和表征了新的四金属链.
  • 证明了电子移位和可调节的光学特性.
  • 突出了金属链和终端连接体的显著结构和电子影响.