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相关概念视频

Complexation Equilibria: The Chelate Effect01:19

Complexation Equilibria: The Chelate Effect

1.1K
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...
1.1K
Reduction of Alkenes: Asymmetric Catalytic Hydrogenation02:17

Reduction of Alkenes: Asymmetric Catalytic Hydrogenation

3.8K
Catalytic hydrogenation of alkenes is a transition-metal catalyzed reduction of the double bond using molecular hydrogen to give alkanes. The mode of hydrogen addition follows syn stereochemistry.
The metal catalyst used can be either heterogeneous or homogeneous. When hydrogenation of an alkene generates a chiral center, a pair of enantiomeric products is expected to form. However, an enantiomeric excess of one of the products can be facilitated using an enantioselective reaction or an...
3.8K
Metal-Ligand Bonds02:51

Metal-Ligand Bonds

23.6K
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...
23.6K
Catalysis02:50

Catalysis

29.9K
The presence of a catalyst affects the rate of a chemical reaction. A catalyst is a substance that can increase the reaction rate without being consumed during the process. A basic comprehension of a catalysts’ role during chemical reactions can be understood from the concept of reaction mechanisms and energy diagrams.
29.9K
Halogenation of Alkenes02:46

Halogenation of Alkenes

18.2K
Halogenation is the addition of chlorine or bromine across the double bond in an alkene to yield a vicinal dihalide. The reaction occurs in the presence of inert and non-nucleophilic solvents, such as methylene chloride, chloroform, or carbon tetrachloride.
Consider the bromination of cyclopentene. Molecular bromine is polarized in the proximity of the π electrons of cyclopentene. An electrophilic bromine atom adds across the double bond, forming a cyclic bromonium ion intermediate.
18.2K
Introduction to Electrophilic Addition Reactions of Alkenes02:24

Introduction to Electrophilic Addition Reactions of Alkenes

10.0K
The double bond in a simple, unconjugated alkene is a region of high electron density that can act as a weak base or a nucleophile. The filled π orbital (HOMO) of the double bond can interact with the empty LUMO of an electrophile. A bonding interaction occurs when the electrophile attacks between the two carbons; the electrophile then accepts a pair of electrons from the π bond and undergoes addition across the double bond, yielding a single product.
Addition and elimination...
10.0K

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相关实验视频

Updated: Dec 30, 2025

Combining Solid-state and Solution-based Techniques: Synthesis and Reactivity of ChalcogenidoplumbatesII or IV
10:42

Combining Solid-state and Solution-based Techniques: Synthesis and Reactivity of ChalcogenidoplumbatesII or IV

Published on: December 29, 2016

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双素-素结合催化剂 双素结合催化剂

Wei Wang1, Haofu Zhu1, Lei Feng1

  • 1School of Chemistry and Chemical Engineering , Shandong University , Jinan 250100 , China.

Journal of the American Chemical Society
|January 22, 2020
PubMed
概括

自然的自然的自然的自然.

科学领域:

  • 有机化学 有机化学
  • 超分子化学 超分子化学
  • 催化剂是一种催化剂.

背景情况:

  • 非共价S··O结合会影响蛋白质结构.
  • 在化学反应中利用弱非共价力是一项挑战.
  • 传统的Rauhut-Currier反应需要强大的易斯基.

研究的目的:

  • 开发一种双素-素结合催化策略.
  • 为了使Rauhut-Currier类型的反应使用新的催化相互作用.
  • 在化学合成中实现区域选择性和更广泛的基质范围.

主要方法:

  • 设计了一种双素-素结合催化策略.
  • 在捐赠者,enone和酒精之间采用了同时的Se·O结合相互作用.
  • 实施了一种连续的双Se·O结合催化方法.

主要成果:

  • 双素-素结合策略成功促进了Rauhut-Currier类型的反应.
  • 这种方法使得用不那么有反应性和传统上无法接触到的基质进行反应.
  • 区域选择性是通过区分基组通过素结合来实现的.

结论:

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Preparation of SNS CobaltII Pincer Model Complexes of Liver Alcohol Dehydrogenase
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Preparation of SNS CobaltII Pincer Model Complexes of Liver Alcohol Dehydrogenase

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  • 双素-素结合为有机合成提供了一种新的催化方法.
  • 这种策略克服了Rauhut-Currier反应的传统方法的局限性.
  • 该方法通过使用弱相互作用来证明对反应性和选择性的精确控制.