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Step-Growth Polymerization: Overview01:03

Step-Growth Polymerization: Overview

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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...
4.5K
Molecular Weight of Step-Growth Polymers01:08

Molecular Weight of Step-Growth Polymers

2.9K
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...
2.9K
Radical Chain-Growth Polymerization: Overview01:10

Radical Chain-Growth Polymerization: Overview

3.6K
Chain-growth or addition polymerization is successive addition reactions of monomers with a polymer chain. In radical chain-growth polymerization, the reaction proceeds via a free-radical intermediate. The free radical is formed from radical initiators, which spontaneously generate free radicals by homolytic fission. Organic peroxides (such as dibenzoyl peroxide, as shown in Figure 1) or azo compounds are popular radical initiators. A low concentration ratio of radical initiator to monomer is...
3.6K
Anionic Chain-Growth Polymerization: Mechanism01:04

Anionic Chain-Growth Polymerization: Mechanism

2.6K
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...
2.6K
Anionic Chain-Growth Polymerization: Overview01:20

Anionic Chain-Growth Polymerization: Overview

2.7K
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,...
2.7K
Radical Chain-Growth Polymerization: Mechanism01:09

Radical Chain-Growth Polymerization: Mechanism

3.6K
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 species into...
3.6K

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相关实验视频

Updated: Feb 20, 2026

Synthesis of Cyclic Polymers and Characterization of Their Diffusive Motion in the Melt State at the Single Molecule Level
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Synthesis of Cyclic Polymers and Characterization of Their Diffusive Motion in the Melt State at the Single Molecule Level

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单聚合物生长动态

Chunming Liu1, Kaori Kubo1, Endian Wang2

  • 1Department of Chemistry and Chemical Biology, Cornell University, Ithaca, NY 14583, USA.

Science (New York, N.Y.)
|October 21, 2017
PubMed
概括
此摘要是机器生成的。

科学家使用磁针实时观察聚合物生长, 这些步骤与单体纠有关,影响聚合率和聚合物多样性.

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科学领域:

  • 聚合物化学
  • 生物物理
  • 材料科学

背景情况:

  • 链增长聚合是基本的,但单个分子层面的实时动态不太清楚.
  • 了解聚合物生长机制对于设计具有特定性质的新材料至关重要.

研究的目的:

  • 可视化和分析单聚合物链增长的实时动态.
  • 在环开放转化聚合过程中研究链延长的分子机制.

主要方法:

  • 使用磁以实时应用受控力和跟踪单聚合物延伸.
  • 使用分子动力学模拟来模拟和理解观察到的聚合现象.

主要成果:

  • 观察到,在环开放转化聚合过程中,聚合物扩展以离散的"等待和跳跃"步骤发生,而不是连续发生.
  • 确定了由新加入的单体形成和解脱的结构纠是这些步骤的原因.
  • 证明纠配置影响聚合率和聚合物长度的异质性.

结论:

  • 单聚合物可视化显示了聚合物的非连续增长动态.
  • 单体的形状纠是聚合动力学和聚合物长度分布的关键决定因素.