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相关概念视频

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

Radical Chain-Growth Polymerization: Overview

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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
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
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...
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Cationic Chain-Growth Polymerization: Mechanism00:57

Cationic Chain-Growth Polymerization: Mechanism

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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
Radical Chain-Growth Polymerization: Mechanism01:09

Radical Chain-Growth Polymerization: Mechanism

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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...
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相关实验视频

Updated: Jan 14, 2026

Fabricating Degradable Thermoresponsive Hydrogels on Multiple Length Scales via Reactive Extrusion, Microfluidics, Self-assembly, and Electrospinning
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酸催化动态聚合物的可逆按需激活,用于梯度驱动的重塑

David Reisinger1, Laura Wimberger2, Roman Korotkov1

  • 1Polymer Competence Center Leoben GmbH, 8700 Leoben, Austria.

Journal of the American Chemical Society
|October 20, 2025
PubMed
概括

这项研究引入了一种用于精确控制动态共价适应网络 (CAN) 的新型光酸. 这一突破使得光感应的重塑和复杂的微观结构的创建具有可调的机械特性.

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科学领域:

  • 材料科学
  • 聚合物化学
  • 摄影化学

背景情况:

  • 协价适应性网络 (CAN) 提供可回收性和稳定性,但缺乏动态和静态状态之间的急剧过渡.
  • 现有的CAN在实现对网络动态的精确控制方面存在局限性,限制了它们的应用.

研究的目的:

  • 开发一种光酸,用于在烯光聚合物中对动态键交换进行时空控制.
  • 通过可见光实现动态和静态聚合物网络状态之间的精确可逆切换.

主要方法:

  • 在乙烯光聚合物中引入光酸.
  • 使用可见光触发螺旋异体化和酸催化转化以进行网络重新排列.
  • 使用应力放松实验来评估机械性能变化.
  • 产生光酸梯度用于微米级控制.
  • 应用多光子激光写作来制造微观结构.

主要成果:

  • 通过米洛胺光酸对动态键交换进行精确和可逆的时空控制.
  • 在动态和静态网络状态之间实现了急剧的过渡,导致机械性质的显著差异.
  • 成功生成了微米级的活性光酸梯度.
  • 开发了一种无形重塑方法,
  • 使用多光子激光写作制造多种微观结构.

结论:

  • 开发的梅洛酸光系统为CAN动力学提供了前所未有的控制.
  • 这种技术为光控制微力学和先进材料制造开辟了新的途径.
  • 该系统的快速异构和耐疲劳性是其在动态材料应用中的潜力的关键.