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相关概念视频

Formation of Complex Ions03:45

Formation of Complex Ions

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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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Lewis Acids and Bases02:33

Lewis Acids and Bases

44.4K
In 1923, G. N. Lewis proposed a generalized definition of acid-base behavior in which acids and bases are identified by their ability to accept or to donate a pair of electrons and form a coordinate covalent bond.
A coordinate covalent bond (or dative bond) occurs when one of the atoms in the bond provides both bonding electrons. For example, a coordinate covalent bond occurs when a water molecule combines with a hydrogen ion to form a hydronium ion. A coordinate covalent bond also results when...
44.4K
Ionic Bonding and Electron Transfer02:48

Ionic Bonding and Electron Transfer

41.9K
Ions are atoms or molecules bearing an electrical charge. A cation (a positive ion) forms when a neutral atom loses one or more electrons from its valence shell, and an anion (a negative ion) forms when a neutral atom gains one or more electrons in its valence shell. Compounds composed of ions are called ionic compounds (or salts), and their constituent ions are held together by ionic bonds: electrostatic forces of attraction between oppositely charged cations and anions. 
41.9K
Complexation Equilibria: Overview01:23

Complexation Equilibria: Overview

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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...
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Common Ion Effect03:24

Common Ion Effect

42.0K
Compared with pure water, the solubility of an ionic compound is less in aqueous solutions containing a common ion (one also produced by dissolution of the ionic compound). This is an example of a phenomenon known as the common ion effect, which is a consequence of the law of mass action that may be explained using Le Châtelier’s principle. Consider the dissolution of silver iodide:
42.0K
Ionic Strength: Effects on Chemical Equilibria01:19

Ionic Strength: Effects on Chemical Equilibria

1.6K
The addition of an inert ionic compound increases the solubility of a sparingly soluble salt. For example, adding potassium nitrate to a saturated solution of calcium sulfate significantly enhances the solubility of calcium sulfate. Le Châtelier's principle cannot predict this shift in the equilibrium. Instead, this could be explained in terms of changes in the effective concentration of the ions in solution in the presence of added inert salt.
In this solution, the primary...
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In Situ Lithiated Reference Electrode: Four Electrode Design for In-operando Impedance Spectroscopy
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单独的诱导效应不能解释路易斯导体形成和电极接口的解离

Sevan Menachekanian1, Matthew J Voegtle1, Robert E Warburton2

  • 1Department of Chemistry, University of Southern California, Los Angeles, California 90089, United States.

Journal of the American Chemical Society
|March 2, 2023
PubMed
概括
此摘要是机器生成的。

研究人员在电极表面创建了一个易斯酸添加物. 由于离子效应,-键在负电位上分裂,这对于理解电催化和电吸收至关重要.

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科学领域:

  • 表面化学
  • 电化学
  • 材料科学

背景情况:

  • 在电化接口上理解易斯键是电催化和电吸收的关键.
  • 接口的复杂性往往阻碍了对这些纽带的系统研究.
  • 需要一个模型系统来探测界面的易斯酸相互作用.

研究的目的:

  • 在电极表面创建和研究一个主要组的易斯酸添加物.
  • 在不同的电极电位下调查这个引电的行为.
  • 阐明电气化接口中的易斯键裂变机制.

主要方法:

  • 在电极上使用mercaptopyridine (Lewis基) 和三化物 (BF3,Lewis酸) 形成易斯酸.
  • 电化学测量以研究不同电位的添加物稳定性和裂变.
  • 使用Li+BF4-电解质进行可逆性研究.

主要成果:

  • 在电极表面上形成了稳定的易斯键 (N-B).
  • 在大约 -0.3 V 的负电位下,N-B 键分裂,而无电流时则是 Ag/AgCl.
  • 当从Li+BF4电解质提供BF3时,裂变是完全可逆的.
  • 电感应和界面离子效应都会影响N-B键.

结论:

  • 介面离子结构和平衡, 不仅仅是电感应, 驱动易斯键裂变在负电位.
  • 这项工作为界面的易斯酸相互作用提供了基本的见解.
  • 这些发现对于电催化和电吸收系统的设计具有重要意义.