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相关概念视频

Lewis Acids and Bases02:33

Lewis Acids and Bases

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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...
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Lewis Acids and Bases02:16

Lewis Acids and Bases

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This lesson delves into Lewis acids and bases in the context of the octet rule for electron-deficient compounds. Here, the concept is discussed, emphasizing the group 13 elements like boron or aluminium. Since group 13 elements possess three valence electrons, they form trivalent compounds with a sextet of electrons and a vacant orbital for the central atom. Consequently, these electron-deficient compounds accept electrons from other species to complete their octet in a chemical reaction. They...
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Bronsted-Lowry Acids and Bases02:58

Bronsted-Lowry Acids and Bases

103.3K
The acid-base reaction class has been studied for quite some time. In 1680, Robert Boyle reported traits of acid solutions that included their ability to dissolve many substances, to change the colors of certain natural dyes, and to lose these traits after coming in contact with alkali (base) solutions. In the eighteenth century, it was recognized that acids have a sour taste, react with limestone to liberate a gaseous substance (now known to be CO2), and interact with alkalis to form neutral...
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Brønsted-Lowry Acids and Bases02:16

Brønsted-Lowry Acids and Bases

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In 1923, the Brønsted–Lowry definition of acids and bases was proposed by Johannes Brønsted and Thomas Lowry. According to this theory, a Brønsted acid is defined as a species that donates a proton in a chemical reaction and gets converted to its conjugate base. A Brønsted base is defined as a species that accepts a proton in a chemical reaction and gets converted into its conjugate acid. These transfers of protons are caused by the displacement of electrons in these reactions, which is...
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Water: A Bronsted-Lowry Acid and Base02:30

Water: A Bronsted-Lowry Acid and Base

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The reaction between a Brønsted-Lowry acid and water is called acid ionization. For example, when hydrogen fluoride dissolves in water and ionizes, protons are transferred from hydrogen fluoride molecules to water molecules, yielding hydronium ions and fluoride ions:
57.6K
Formation of Complex Ions03:45

Formation of Complex Ions

25.7K
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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Updated: Jan 16, 2026

Characterizing Lewis Pairs Using Titration Coupled with In Situ Infrared Spectroscopy
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电场与易斯酸性中断并逆向回到易斯基函数.

Lopita Swain1, Esha Paul1, Karthik Gopakumar1

  • 1Department of Chemistry, National Institute of Technology, Rourkela, Odisha, 769008, India.

Chemistry, an Asian journal
|September 26, 2025
PubMed
概括
此摘要是机器生成的。

外部电场 (EF) 显著影响化学反应,改变电子转移. 这些场可以催化或抑制反应,并观察到特定的最大抑制点 (ERP).

关键词:
密度函数理论计算密度函数理论计算外部电场催化剂 外部电场催化剂易斯酸催化剂的作用奥克萨·迪尔斯-阿尔德反应

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科学领域:

  • 计算化学是一种计算化学.
  • 化学反应性 化学反应性
  • 量子化学是一种量子化学.

背景情况:

  • 外部电场 (EF) 通过改变电子转移来影响化学反应.
  • 易斯酸 (LA) 催化反应对外部干扰很敏感.

研究的目的:

  • 研究EFs对环二烯 (Cp) 和甲 (HCHO) 之间的Oxa Diels-Alder (ODA) 反应的影响.
  • 分析EF如何调节反应通路和催化活性.

主要方法:

  • 使用密度函数理论 (DFT) 的计算.
  • 该研究研究了Oxa Diels-Alder反应机制在不同的EF下.

主要成果:

  • 发现EFs可以作为反应催化剂或抑制剂,具体取决于它们的方向.
  • 确定了一个电静电阻点 (ERP),代表最大抑制.
  • 较强的EF可以将催化从易斯酸 (LA) 转换为易斯基 (LB) 途径 (正常电子需求到反向电子需求).

结论:

  • 在化学反应中,EFs充当了多功能反应性调节器.
  • EF可以在LA和LB控制的路径之间切换反应机制.
  • 该研究提供了对使用外部场的电子转移和反应性控制的见解.