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相关概念视频

Reduction of Alkynes to cis-Alkenes: Catalytic Hydrogenation02:24

Reduction of Alkynes to cis-Alkenes: Catalytic Hydrogenation

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Introduction
Like alkenes, alkynes can be reduced to alkanes in the presence of transition metal catalysts such as Pt, Pd, or Ni. The reaction involves two sequential syn additions of hydrogen via a cis-alkene intermediate.
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Electron Behavior00:54

Electron Behavior

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Overview
Electrons are negatively charged subatomic particles that are attracted to an orbit around the positively-charged nucleus of an atom. They reside in locations that are associated with energy levels called shells and are further organized into sub-shells and orbitals within each shell.
Electrons Orbit the Nucleus
Electrons are found in specific locations outside of the nucleus. The shell in which an electron resides indicates the general energy level of the electron: those closer to the...
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Reduction of Alkenes: Catalytic Hydrogenation02:13

Reduction of Alkenes: Catalytic Hydrogenation

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Alkenes undergo reduction by the addition of molecular hydrogen to give alkanes. Because the process generally occurs in the presence of a transition-metal catalyst, the reaction is called catalytic hydrogenation.
Metals like palladium, platinum, and nickel are commonly used in their solid forms — fine powder on an inert surface. As these catalysts remain insoluble in the reaction mixture, they are referred to as heterogeneous catalysts.
The hydrogenation process takes place on the...
12.9K
Reduction of Alkenes: Asymmetric Catalytic Hydrogenation02:17

Reduction of Alkenes: Asymmetric Catalytic Hydrogenation

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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...
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Reduction of Benzene to Cyclohexane: Catalytic Hydrogenation01:28

Reduction of Benzene to Cyclohexane: Catalytic Hydrogenation

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Unlike the easy catalytic hydrogenation of an alkene double bond, hydrogenation of a benzene double bond under similar reaction conditions does not take place easily. For example, in the reduction of stilbene, the benzene ring remains unaffected while the alkene bond gets reduced. Hydrogenation of an alkene double bond is exothermic and a favorable process. In contrast, to hydrogenate the first unsaturated bond of benzene, an energy input is needed; that is, the process is endothermic. This is...
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Radical Formation: Homolysis00:54

Radical Formation: Homolysis

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A bond is formed between two atoms by sharing two electrons. When this bond is broken by supplying sufficient energy, either two electrons can be taken up by one atom forming ions by the cleavage called heterolysis, or the two electrons are shared by two atoms, with one each creating radicals by the cleavage called homolysis.
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在单分子结合中以电子催化脱

Hongliang Chen1,2,3, Feng Jiang4, Chen Hu5

  • 1Department of Chemistry, Northwestern University, 2145 Sheridan Road, Evanston, Illinois 60208, United States.

Journal of the American Chemical Society
|May 27, 2021
PubMed
概括

电子可以在单个分子中意外触发化学反应, 改变它们的电性质. 这项研究揭示了电子催化驱动分子结的乙转化,影响电导度的测量.

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科学领域:

  • 分子电子
  • 表面科学
  • 催化剂

背景情况:

  • 通过单个分子传输电子是分子电子学的一个关键领域.
  • 电子可以作为激素反应的催化剂,这种因素在导电性研究中经常被忽视.
  • 意想不到的电子介导反应可以影响单分子结合的测量.

研究的目的:

  • 研究分子导电性的反直觉结构-属性关系.
  • 展示和理解单分子结合中的电子催化.
  • 探索电子催化乙转化机制.

主要方法:

  • 单分子连接的制造和特征.
  • 电化学组合实验.
  • 理论计算 (例如密度函数理论).

主要成果:

  • 具有和双乙烯骨干的分子与具有合双乙烯骨干的分子具有相似的导电性.
  • 在单分子结点中观察到乙转化.
  • 发现电子触发了氧化还原过程,电场促进了脱.

结论:

  • 电子催化在解释单分子导电率数据方面起着至关重要的作用.
  • 通过电子催化脱在结处发生乙转化.
  • 这项工作为单个分子水平的电催化生产机制提供了洞察力.