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Metal-Ligand Bonds02:51

Metal-Ligand Bonds

22.9K
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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Extraction: Advanced Methods00:56

Extraction: Advanced Methods

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Metal ions can be separated from one another by complexation with organic ligands–the chelating agent– to form uncharged chelates. Here, the chelating agent must contain hydrophobic groups and behave as a weak acid, losing a proton to bind with the metal. Since most organic ligands used in this process are insoluble or undergo oxidation in the aqueous phase, the chelating agent is initially added to the organic phase and extracted into the aqueous phase. The metal-ligand complex is...
839
Properties of Organometallic Compounds01:23

Properties of Organometallic Compounds

1.4K
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.
1.4K
Formation of Complex Ions03:45

Formation of Complex Ions

24.9K
A type of Lewis acid-base chemistry involves the formation of a complex ion (or a coordination complex) comprising a central atom, typically a transition metal cation, surrounded by ions or molecules called ligands. These ligands can be neutral molecules like H2O or NH3, or ions such as CN− or OH−. Often, the ligands act as Lewis bases, donating a pair of electrons to the central atom. These types of Lewis acid-base reactions are examples of a broad subdiscipline called coordination...
24.9K
Complexation Equilibria: The Chelate Effect01:19

Complexation Equilibria: The Chelate Effect

894
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...
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Interfacial Electrochemical Methods: Overview01:06

Interfacial Electrochemical Methods: Overview

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Interfacial electrochemical methods focus on the phenomena occurring at the boundary between an electrode and a solution, as opposed to bulk methods that concentrate on the solution's overall properties. These interfacial methods are classified as either static or dynamic based on the presence of a nonzero current in the electrochemical cell and the consistency of analyte concentrations. Static methods, such as potentiometry, measure the cell's potential without any significant current...
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Author Spotlight: Magnetometric Characterization of Intermediates in the Solid-State Electrochemistry of Redox-Active Metal-Organic Frameworks
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使用金属有机框架的中间结合控制提高了电化学CO2的减少

Dae-Hyun Nam1, Osama Shekhah2, Geonhui Lee1

  • 1Department of Electrical and Computer Engineering, University of Toronto, 10 King's College Road, Toronto, Ontario M5S 3G4, Canada.

Journal of the American Chemical Society
|December 15, 2020
PubMed
概括

金属有机框架 (MOF) 控制电化学二氧化碳减排中的中间结合,增强二氧化碳的选择性. 这种网状化学方法优化了银纳米粒子催化,以实现高效的二氧化碳转化.

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科学领域:

  • 材料科学
  • 电化学
  • 催化剂

背景情况:

  • 控制中间结合对于调整电化学二氧化碳减排 (CO2RR) 的产品选择性和活性至关重要.
  • 金属有机框架 (MOF) 提供了一个封装金属催化剂和调整其本地环境的平台.

研究的目的:

  • 在MOF中利用网状化学来控制封装金属催化剂的CO2RR中间结合.
  • 通过优化孔隙开放度和易斯酸度等MOF属性来增强CO2RR电催化.

主要方法:

  • 在面中心立方MOF中有机链接器和金属节点的系统变化.
  • 在MOF中封装银 (Ag) 纳米粒子.
  • 在反应条件下进行操作式X射线吸收光谱 (XAS) 和现场拉曼光谱.

主要成果:

  • 在CO2RR的操作条件下,MOF表现出稳定性.
  • 调整MOF特性优化了Ag纳米粒子上的*CO结合模式.
  • 与二酸链接剂相比,使用二二酸链接剂的二氧化碳选择性从74%提高到94%.

结论:

  • 网状化学提供了一个有效的策略来设计增强CO2RR的MOF.
  • 用MOF封装的催化剂可以精确控制中间结合,从而提高CO选择性.
  • 这项工作提出了使用MOF的CO2RR新材料设计方法.