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相关概念视频

Cationic Chain-Growth Polymerization: Mechanism00:57

Cationic Chain-Growth Polymerization: Mechanism

2.8K
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...
2.8K
Anionic Chain-Growth Polymerization: Mechanism01:04

Anionic Chain-Growth Polymerization: Mechanism

2.4K
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...
2.4K
Radical Chain-Growth Polymerization: Mechanism01:09

Radical Chain-Growth Polymerization: Mechanism

3.3K
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...
3.3K
Radical Chain-Growth Polymerization: Chain Branching01:17

Radical Chain-Growth Polymerization: Chain Branching

2.4K
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...
2.4K
Anionic Chain-Growth Polymerization: Overview01:20

Anionic Chain-Growth Polymerization: Overview

2.5K
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,...
2.5K
Radical Chain-Growth Polymerization: Overview01:10

Radical Chain-Growth Polymerization: Overview

3.1K
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...
3.1K

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相关实验视频

Updated: Jan 10, 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

Published on: September 26, 2016

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链末端激发聚合物合作运动.

Quanyin Xu1, Zhenghao Wu2, Katelyn Randazzo3

  • 1School of Chemistry and Chemical Engineering, State Key Laboratory of Bio-Based Fiber Materials, Key Laboratory of Surface and Interface Science of Polymer Materials of Zhejiang Province, Zhejiang Sci-Tech University, Hangzhou 310018, China.

Science advances
|November 26, 2025
PubMed
概括

聚合物链末端显著影响玻璃过渡温度 (Tg) 和动态脆弱性 (m). 较短的聚合物链具有更多的链末,由于放松速度更快,因此显示出较低的Tg和m,简化了聚合物玻璃形成机制.

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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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相关实验视频

Last Updated: Jan 10, 2026

Synthesis of Cyclic Polymers and Characterization of Their Diffusive Motion in the Melt State at the Single Molecule Level
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Ethylene Polymerizations Using Parallel Pressure Reactors and a Kinetic Analysis of Chain Transfer Polymerization
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科学领域:

  • 聚合物科学 聚合物科学
  • 材料科学 材料科学 材料科学
  • 软冷凝物质物理学 软冷凝物质物理学

背景情况:

  • 聚合物表现出独特的玻璃形成特性,受到链接连接的影响.
  • 像玻璃过渡温度 (Tg) 和动态脆弱性 (m) 这样的关键性质随着聚合物链的长度而变化.

研究的目的:

  • 为了阐明聚合物玻璃形成中的链长度依赖行为.
  • 揭示链末和玻璃性质 (Tg,m) 之间的相关性.

主要方法:

  • 在合作重组区域内分析链条末端的数量.
  • 相关性研究将链条末端连接到Tg和m.
  • 引入一个刚性指数来对最终组角色进行分类.

主要成果:

  • 在链末度和聚合物玻璃性质之间发现了强烈的相关性.
  • 快速放松的链端减少了结构重组的合作性要求.
  • 减少链条长度导致Tg和m的降低.

结论:

  • 聚合物链末端通过促进合作运动,在玻璃形成中发挥着至关重要的作用.
  • 提出了聚合物玻璃形成的统一机制,考虑了链末端效应,长度和拓.
  • 这些发现对化学,软凝聚物质和材料科学有广泛的影响.