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相关概念视频

Cationic Chain-Growth Polymerization: Mechanism00:57

Cationic Chain-Growth Polymerization: Mechanism

2.4K
The cationic polymerization mechanism consists of three steps: initiation, propagation, and termination. In the initiation step of the polymerization process, the π bond of a monomer gets protonated by the Lewis acid catalyst, which is formed from boron trifluoride and water. The protonation of the π bond generates a carbocation stabilized by the electron‐donating group. In the propagation step, the π bond of the second monomer acts as a nucleophile and attacks the...
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Anionic Chain-Growth Polymerization: Mechanism01:04

Anionic Chain-Growth Polymerization: Mechanism

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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...
2.1K
Radical Chain-Growth Polymerization: Mechanism01:09

Radical Chain-Growth Polymerization: Mechanism

2.8K
The radical chain-growth polymerization mechanism consists of three steps: initiation, propagation, and termination of polymerization. The polymerization initiates when a free radical generated from the radical initiator adds to the unsaturated bond in the monomer. The unpaired electron of the free radical and one π electron in the unsaturated bond creates a σ bond between the free radical and the monomer. As a result, the other π electron in the unsaturated bond converts this...
2.8K
Step-Growth Polymerization: Overview01:03

Step-Growth Polymerization: Overview

3.6K
Step-growth or condensation polymerization is a stepwise reaction of bi or multifunctional monomers to form long-chain polymers. As all the monomers are reactive, most of the monomers are consumed at the early stages of the reaction to form small chains of reactive oligomers, which then combine to form long polymer chains in the late stages. Hence, the reaction has to proceed for a long time to achieve high molecular weight polymers.
Many natural and synthetic polymers are produced by...
3.6K
Molecular Weight of Step-Growth Polymers01:08

Molecular Weight of Step-Growth Polymers

2.3K
Step growth polymerization involves bi or multifunctional monomers. Bifunctional monomers react to form linear step growth polymers, whereas multifunctional monomers react to form non-linear or branched polymers.
As the step-growth polymerization involves step-wise condensation of monomers, the molecular weight also builds up eventually. Consequently, high molecular weight polymers are obtained at the late stages of the polymerization, where 99% of monomers have been consumed.
The extent of the...
2.3K
Anionic Chain-Growth Polymerization: Overview01:20

Anionic Chain-Growth Polymerization: Overview

2.2K
The polymerization process that involves carbanion as an intermediate is called anionic polymerization. It is also a type of addition or chain-growth polymerization. Anionic polymerization gets initiated by a strong nucleophile such as an organolithium or a Grignard reagent. The most commonly used initiator for anionic polymerization is butyl lithium. Monomers involved in anionic polymerization must possess a vinyl group bonded to one or two electron-withdrawing groups. For instance,...
2.2K

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大分子驱动的超分子聚合由拥挤效应诱导.

Joost J B V D Tol1, Magda M J Dekker1, Ádám Müller1

  • 1Macromolecular and Organic Chemistry Group, Department of Chemical Engineering and Chemistry, Institute for Complex Molecular Systems, Eindhoven University of Technology, P.O. Box 513, Eindhoven, 5600 MB, The Netherlands.

Angewandte Chemie (International ed. in English)
|July 8, 2025
PubMed
概括

在有机溶剂中的宏分子拥挤指导了超分子聚合和组装. 这项研究探讨了群众如何控制聚合物形成,并在合成系统中创建新的凝结,对齐的结构.

关键词:
拥挤的人群拥挤.大分子分子是巨分子.扣留 扣留 扣留 扣留 扣留在超分子聚合过程中.

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科学领域:

  • 超分子化学 超分子化学
  • 聚合物科学 聚合物科学
  • 软物质物理学 软物质物理学

背景情况:

  • 大分子拥挤在生物系统中对于调节动态过程至关重要.
  • 它对有机介质中合成超分子聚合物的影响在很大程度上尚未被探索.

研究的目的:

  • 系统地研究由宏分子聚合物排斥的体积效应对有机介质中超分子聚合物的影响.
  • 通过宏分子拥挤来探索超分子组装的可调性.

主要方法:

  • 利用各种光盘超分子单体进行序列组装成聚合物和更高阶聚合物 (HOA).
  • 在不同度,大小和极性下研究了超分子组件的相位图.
  • 测试了不同的单体,宏分子和溶剂,以确定一般适用性.

主要成果:

  • 研究人员发现,宏分子聚合物对有机介质中聚合物和HOA的形成至关重要.
  • 超分子组装相位图显示了强烈的依赖于聚合物度,大小和极性,从而可以控制聚合.
  • 高缩度诱导过渡到相隔状态,在干燥样本中形成大,凝结和对齐的组件.

结论:

  • 大分子拥挤是指导在合成有机环境中的超分子聚合的多功能工具.
  • 这项研究提供了对拥挤系统中的组装过程的基本见解.
  • 开辟了在水系统之外应用宏分子拥挤原理的新途径.