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Formation of Complex Ions03:45

Formation of Complex Ions

18.8K
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...
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Complexation Equilibria: Overview01:23

Complexation Equilibria: Overview

1.6K
Complexation reactions take place when dative or coordinate covalent bonds form between metal ions and ligands. The compounds formed in these reactions are called coordination compounds. The number of bonds formed between the metal ion and the ligands is called its coordination number. Generally, most metal ions in an aqueous solution are solvated by water molecules and thus exist as aqua complexes.
The equilibrium constant of the complexation reaction is represented as the formation constant...
1.6K
Complexation Equilibria: The Chelate Effect01:19

Complexation Equilibria: The Chelate Effect

1.7K
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...
1.7K
Precipitation and Co-precipitation01:17

Precipitation and Co-precipitation

4.8K
Precipitation and coprecipitation methods can be used to separate a mixture of ions in a solution. In qualitative inorganic analysis, ions that form sparingly soluble precipitates with the same reagent are separated based on the differences in solubility products. For example, consider the separation of Cu(II) and Fe(II) ions by precipitation as insoluble sulfides. First, copper(II) sulfide is precipitated by the addition of acidic H2S, where the dissociation of H2S is suppressed. Adding H2S...
4.8K
Electrodeposition01:08

Electrodeposition

2.7K
Electrodeposition is a technique used to separate an analyte from interferents by electrochemical processes. Here, the analyte is a metal ion that can be deposited on an electrode immersed in the sample solution. The electrochemical setup consists of an anode and a cathode. When an electric current is applied to the setup, oxidation occurs at the anode. At the cathode, which consists of a large metal surface, metal ions undergo reduction and deposit onto the surface.
Electrodeposition can...
2.7K
Extraction: Advanced Methods00:56

Extraction: Advanced Methods

1.3K
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...
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相关实验视频

Updated: May 2, 2026

Synthesis and Performance Characterizations of Transition Metal Single Atom Catalyst for Electrochemical CO2 Reduction
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Synthesis and Performance Characterizations of Transition Metal Single Atom Catalyst for Electrochemical CO2 Reduction

Published on: April 10, 2018

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过多的变化*CO中介结构和Cu在酸性电化学反应中的产品选择性

Suhwan Yoo1,2, Sejin Park1, Jihoon Son3

  • 1Department of Chemistry, Seoul National University, Seoul 08826, Republic of Korea.

Journal of the American Chemical Society
|April 2, 2025
PubMed
概括
此摘要是机器生成的。

过多的像Cs+可以通过改变铜上的CO吸附来阻碍电化学二氧化碳减排 (CO2RR),从而有利于的演变而不是C2+产品. 聚合物结合剂可以恢复CO2RR性能.

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Accumulation and Analysis of Cuprous Ions in a Copper Sulfate Plating Solution
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Accumulation and Analysis of Cuprous Ions in a Copper Sulfate Plating Solution

Published on: March 20, 2019

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Ion Mobility-Mass Spectrometry Techniques for Determining the Structure and Mechanisms of Metal Ion Recognition and Redox Activity of Metal Binding Oligopeptides
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Ion Mobility-Mass Spectrometry Techniques for Determining the Structure and Mechanisms of Metal Ion Recognition and Redox Activity of Metal Binding Oligopeptides

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相关实验视频

Last Updated: May 2, 2026

Synthesis and Performance Characterizations of Transition Metal Single Atom Catalyst for Electrochemical CO2 Reduction
10:57

Synthesis and Performance Characterizations of Transition Metal Single Atom Catalyst for Electrochemical CO2 Reduction

Published on: April 10, 2018

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Accumulation and Analysis of Cuprous Ions in a Copper Sulfate Plating Solution
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Accumulation and Analysis of Cuprous Ions in a Copper Sulfate Plating Solution

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Ion Mobility-Mass Spectrometry Techniques for Determining the Structure and Mechanisms of Metal Ion Recognition and Redox Activity of Metal Binding Oligopeptides
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Ion Mobility-Mass Spectrometry Techniques for Determining the Structure and Mechanisms of Metal Ion Recognition and Redox Activity of Metal Binding Oligopeptides

Published on: September 7, 2019

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科学领域:

  • 电化学
  • 表面科学
  • 催化剂

背景情况:

  • 电化学二氧化碳减排 (CO2RR) 对可持续化学至关重要.
  • 已知阴离子度会影响酸性介质中的CO2RR选择性.

研究的目的:

  • 调查过多的阴离子如何影响CO吸附配置和CO2RR产物分布.
  • 阐明二氧化碳排放率选择性变化背后的机制.

主要方法:

  • 操作减弱的全反射面增强红外吸收光谱 (ATR-SEIRAS) 来监测CO吸收.
  • 密度函数理论 (DFT) 模拟以了解-CO 相互作用.
  • 用不同度和聚合物结合物的电化学实验.

主要成果:

  • 增加Cs+度将CO吸附从顶部转移到Cu表面的桥梁配置.
  • 高Cs+度促进演变反应 (HER) 并抑制C-C合.
  • 在Cu表面的聚合物粘合剂通过防止阳离子干扰来恢复CO2RR的选择性.

结论:

  • 阴离子度显著影响CO吸附中间体和CO2RR通路.
  • 通过 Cs+ 稳定 CO 桥阻碍了 C-C 合,有利于 HER.
  • 用聚合物结合剂对催化剂表面进行修改提供了一种减轻有害阴离子效应和增强CO2RR的策略.