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相关概念视频

Free-Radical Chain Reaction and Polymerization of Alkenes02:35

Free-Radical Chain Reaction and Polymerization of Alkenes

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The conversion of alkenes to macromolecules called polymers is a reaction of high commercial importance. The structure of the polymer is defined by a repeating unit, while the terminal groups are considered insignificant. The average degree of polymerization represents the number of repeating units in the polymer molecule and is denoted by the subscript n.
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Olefin Metathesis Polymerization: Acyclic Diene Metathesis (ADMET)00:53

Olefin Metathesis Polymerization: Acyclic Diene Metathesis (ADMET)

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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...
2.0K
Cycloaddition Reactions: MO Requirements for Photochemical Activation01:12

Cycloaddition Reactions: MO Requirements for Photochemical Activation

2.2K
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.
2.2K
Olefin Metathesis Polymerization: Overview01:13

Olefin Metathesis Polymerization: Overview

2.3K
Recently, the development of olefin metathesis polymerization advanced the field of polymer synthesis. Simply put, the reorganization of substituents on their double bonds between two olefins in the presence of a catalyst is known as the olefin metathesis reaction. The use of metathesis reaction for polymer synthesis is called olefin metathesis polymerization.
Ruthenium-based Grubbs catalyst is the most commonly used catalyst for olefin metathesis polymerization. Grubbs catalyst consists...
2.3K
Radical Chain-Growth Polymerization: Chain Branching01:17

Radical Chain-Growth Polymerization: Chain Branching

2.0K
The skeletal structure of polymers synthesized via radical polymerization is always branched. For example, the polymerization of ethylene by radical polymerization results in a low-density grade of polyethylene with a heavily branched skeletal structure. Here, the radical site abstracts hydrogen from the growing chain, and the radical site shifts from the end (a primary carbon center) to anywhere within the growing chain (a secondary carbon center). Consequently, the part of the chain from the...
2.0K
Anionic Chain-Growth Polymerization: Mechanism01:04

Anionic Chain-Growth Polymerization: Mechanism

2.1K
The mechanism for anionic chain-growth polymerization involves initiation, propagation, and termination steps. In the initiation step, a nucleophilic anion, such as butyl lithium, initiates the polymerization process by attacking the π bond of the vinylic monomer. As a result, a carbanion, stabilized by the electron‐withdrawing group, is generated. The resulting carbanion acts as a Michael donor in the propagation step and attacks the second vinylic monomer, which acts as a Michael...
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相关实验视频

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Ethylene Polymerizations Using Parallel Pressure Reactors and a Kinetic Analysis of Chain Transfer Polymerization
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Ethylene Polymerizations Using Parallel Pressure Reactors and a Kinetic Analysis of Chain Transfer Polymerization

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通过乙烯插入对表面乙烯聚合物的可视化

Weijun Guo1,2, Junqing Yin3, Zhen Xu2

  • 1SynCat@Beijing, Synfuels China Technology Co., Ltd., Beijing 101407, China.

Science (New York, N.Y.)
|March 10, 2022
PubMed
概括

这项研究使用扫描道显微镜可视化乙烯聚合. 它揭示了碳化铁表面的自我启动机制,证实了分子层面的乙烯插入途径.

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A Simple and Efficient Protocol for the Catalytic Insertion Polymerization of Functional Norbornenes
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A Simple and Efficient Protocol for the Catalytic Insertion Polymerization of Functional Norbornenes

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科学领域:

  • 催化剂
  • 聚合物化学
  • 表面科学

背景情况:

  • 催化乙烯聚合是制造聚乙烯的化学工业的基石.
  • 广泛接受的Cosse-Arlman机制描述了通过乙烯插入金属-碳键的链增长.
  • 这种机制的实验性,分子水平的证实一直缺乏.

研究的目的:

  • 为乙烯聚合机制提供直接,微观和时空实验证据.
  • 在分子水平上可视化乙烯聚合的过程.
  • 在特定的催化表面上阐明乙烯聚合的启动和传播步骤.

主要方法:

  • 使用扫描道显微镜 (STM) 在现场可视化乙烯聚合.
  • 使用碳化铁单晶表面作为催化剂.
  • 对聚合中间体和链生长动态的观察.

主要成果:

  • 观察到乙烯聚合发生在碳化物域边界的特定三角铁位点.
  • 确定了一种新的自我启动途径,涉及表面固的乙烯中间体.
  • 随后将乙烯插入到该中间体中,证实了链的生长.

结论:

  • 直接的实验证据证实了分子水平上的乙烯聚合途径.
  • 这些发现证实并完善了Cossee-Arlman机制的理解.
  • 这项研究强调了特定表面位点和中间体在催化聚合中的作用.