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相关概念视频

Olefin Metathesis Polymerization: Acyclic Diene Metathesis (ADMET)00:53

Olefin Metathesis Polymerization: Acyclic Diene Metathesis (ADMET)

Acyclic diene metathesis polymerization or ADMET polymerization involves cross-metathesis of terminal dienes, such as 1,8-nonadiene, to give linear unsaturated polymer and ethylene. As ADMET is a reversible process, the formed ethylene gas must be removed from the reaction mixture to complete the polymerization process.
Similar to cross-metathesis, ADMET also involves the formation of metallacyclobutane intermediate by [2+2] cycloaddition of one of the double bonds of a terminal diene with...
Cycloaddition Reactions: MO Requirements for Thermal Activation01:16

Cycloaddition Reactions: MO Requirements for Thermal Activation

Thermal cycloadditions are reactions where the source of activation energy needed to initiate the reaction is provided in the form of heat. A typical example of a thermally-allowed cycloaddition is the Diels–Alder reaction, which is a [4 + 2] cycloaddition. In contrast, a [2 + 2] cycloaddition is thermally forbidden.
Radical Reactivity: Intramolecular vs Intermolecular01:33

Radical Reactivity: Intramolecular vs Intermolecular

Radical reactions can occur either intermolecularly or intramolecularly. In an intermolecular radical reaction, a nucleophilic radical adds to an electrophilic alkene or vice versa. In such reactions, the radical and generally the alkene, which is also called the radical trap, are two different molecules. Additionally, for such intermolecular reactions to occur, the radical trap must be active, present in an excess concentration, and the radical starting material must have a weak carbon–halogen...
Pericyclic Reactions: Introduction01:17

Pericyclic Reactions: Introduction

Pericyclic reactions are organic reactions that occur via a concerted mechanism without generating any intermediates. The reactions proceed through the movement of electrons in a closed loop to form a cyclic transition state, where rearrangement of the σ and π bonds yields specific products.
Pericyclic reactions can be classified into three categories: electrocyclic reactions, cycloaddition reactions, and sigmatropic rearrangements. Electrocyclic reactions and sigmatropic rearrangements are...
Cycloaddition Reactions: MO Requirements for Photochemical Activation01:12

Cycloaddition Reactions: MO Requirements for Photochemical Activation

Some cycloaddition reactions are activated by heat, while others are initiated by light. For example, a [2 + 2] cycloaddition between two ethylene molecules occurs only in the presence of light. It is photochemically allowed but thermally forbidden.
Predicting Reaction Outcomes02:24

Predicting Reaction Outcomes

Kinetics describes the rate and path by which a reaction occurs. In contrast, thermodynamics deals with state functions and describes the properties, behavior, and components of a system. It is not concerned with the path taken by the process and cannot address the rate at which a reaction occurs. Although it does provide information about what can happen during a reaction process, it does not describe the detailed steps of what appears on an atomic or a molecular level. On the other hand,...

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Utilization of Stop-flow Micro-tubing Reactors for the Development of Organic Transformations
13:09

Utilization of Stop-flow Micro-tubing Reactors for the Development of Organic Transformations

Published on: January 4, 2018

有效的动力宏循环化.

Wen Feng1, Kazuhiro Yamato, Liuqing Yang

  • 1College of Chemistry, Key Laboratory for Radiation Physics and Technology of Ministry of Education, and Institute of Nuclear Science and Technology, Sichuan University, Chengdu, 610064, Sichuan, China.

Journal of the American Chemical Society
|February 5, 2009
PubMed
概括
此摘要是机器生成的。

研究人员实现了大型芳香性橄胺宏循环的高效合成. 前体折叠和固体效应解释了这些动态宏循环反应的高产量,产生了大,形状持久的结构.

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A Microwave-Assisted Direct Heteroarylation of Ketones Using Transition Metal Catalysis
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A Microwave-Assisted Direct Heteroarylation of Ketones Using Transition Metal Catalysis

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Last Updated: Jun 25, 2026

Utilization of Stop-flow Micro-tubing Reactors for the Development of Organic Transformations
13:09

Utilization of Stop-flow Micro-tubing Reactors for the Development of Organic Transformations

Published on: January 4, 2018

Anionic Polymerization of an Amphiphilic Copolymer for Preparation of Block Copolymer Micelles Stabilized by &#960;-&#960; Stacking Interactions
10:53

Anionic Polymerization of an Amphiphilic Copolymer for Preparation of Block Copolymer Micelles Stabilized by π-π Stacking Interactions

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A Microwave-Assisted Direct Heteroarylation of Ketones Using Transition Metal Catalysis
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A Microwave-Assisted Direct Heteroarylation of Ketones Using Transition Metal Catalysis

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科学领域:

  • 超分子化学 超分子化学
  • 有机合成 有机合成
  • 材料科学 材料科学 材料科学

背景情况:

  • 动力学控制的宏循环化反应通常产生较差的结果.
  • 脊柱硬化胺基可以采用明确的形状.
  • 之前的研究表明,橄胺形成了新月形状.

研究的目的:

  • 为了研究芳香性橄胺宏循环的高效形成.
  • 了解出乎意料的高收益率背后的机制.
  • 合成具有显著内部空洞的大型宏观循环.

主要方法:

  • 合成具有六个甲基链接残留物的芳香性橄胺宏循环.
  • 运动模拟和试验合的奥利戈胺基前体.
  • 一个阶段的多组分宏循环化反应,使用元二胺和对二酸化物.

主要成果:

  • 在高产量中形成的宏循环,偏离动力模拟.
  • 确定了前体折叠和远程绝缘效应是关键因素.
  • 大型宏循环 (70-90个成员环) 的空腔长度高达2.9纳米被有效合成 (>80%的产量).

结论:

  • 这项研究介绍了一种罕见的,高效的动态宏循环化系统.
  • 前体构成和固体效应对于高效的宏循环形成至关重要.
  • 这种方法产生了大,形状持久的宏循环,具有潜在的应用.