Jove
Visualize
联系我们
JoVE
x logofacebook logolinkedin logoyoutube logo
关于 JoVE
概览领导团队博客JoVE 帮助中心
作者
出版流程编辑委员会范围与政策同行评审常见问题投稿
图书馆员
用户评价订阅访问资源图书馆顾问委员会常见问题
研究
JoVE JournalMethods CollectionsJoVE Encyclopedia of Experiments存档
教育
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab Manual教师资源中心教师网站
使用条款与条件
隐私政策
政策

相关概念视频

Radical Chain-Growth Polymerization: Overview01:10

Radical Chain-Growth Polymerization: Overview

2.7K
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...
2.7K
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...
2.4K
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
Free-Radical Chain Reaction and Polymerization of Alkenes02:35

Free-Radical Chain Reaction and Polymerization of Alkenes

8.3K
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.
8.3K
Step-Growth Polymerization: Overview01:03

Step-Growth Polymerization: Overview

3.7K
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...
3.7K
Ziegler–Natta Chain-Growth Polymerization: Overview01:17

Ziegler–Natta Chain-Growth Polymerization: Overview

3.5K
Ziegler–Natta polymerization is another form of addition or chain‐growth polymerization used for synthesizing linear polymers over branched polymers. The catalyst used for polymerization is the Ziegler–Natta catalyst, named after Karl Ziegler and Giulio Natta, who developed it in 1953. This catalyst is an organometallic complex of titanium tetrachloride and triethyl aluminum, with the active form of the catalyst being an alkyl titanium compound. Using the Ziegler–Natta...
3.5K

您也可能阅读

相关文章

通过共同作者、期刊和引用图与本文相关的文章。

排序
Same author

Chain Length Dependence of Chemically Controlled Reactions in Polymerization.

Journal of the American Chemical Society·2026
Same author

Photocatalytic Depolymerization of Commercial Polymethacrylates via a Solvent-Independent Pathway.

Journal of the American Chemical Society·2026
Same author

Beyond the Chemical Recycling of Polymethacrylates: Depolymerization of Polymethacrylamides.

Chimia·2026
Same author

Dithioketal Polymers Via Radical Polymerization of γ-Dithiobutyrolactone.

Angewandte Chemie (International ed. in English)·2026
Same author

Direct Polymer-on-Polymer Grafting of Polyolefins under Visible Light.

Journal of the American Chemical Society·2026
Same author

Enzyme-Activated Dual-Locked Probes for Detecting Nitroreductase and Carboxylesterase.

Chemical & biomedical imaging·2026

相关实验视频

Updated: Oct 2, 2025

Depolymerizable Olefinic Polymers Based on Fused-Ring Cyclooctene Monomers
08:12

Depolymerizable Olefinic Polymers Based on Fused-Ring Cyclooctene Monomers

Published on: December 16, 2022

3.4K

反向RAFT聚合:通过无催化剂去聚合方法产生近量化单体

Hyun Suk Wang1, Nghia P Truong1, Zhipeng Pei2

  • 1Laboratory of Polymeric Materials, Department of Materials, ETH Zurich, Vladimir-Prelog-Weg 5, Zurich 8093, Switzerland.

Journal of the American Chemical Society
|February 25, 2022
PubMed
概括

研究人员开发了一种无催化剂的方法来去聚合聚甲酸盐,再生单体. 这种可逆基聚合的突破使得聚合物重建或新凝的形成成为可能,从而推进了聚合物科学的应用.

更多相关视频

Controlled Photoredox Ring-Opening Polymerization of O-Carboxyanhydrides Mediated by Ni/Zn Complexes
05:48

Controlled Photoredox Ring-Opening Polymerization of O-Carboxyanhydrides Mediated by Ni/Zn Complexes

Published on: November 21, 2017

8.2K
Synthesis of Monodisperse Cylindrical Nanoparticles via Crystallization-driven Self-assembly of Biodegradable Block Copolymers
11:42

Synthesis of Monodisperse Cylindrical Nanoparticles via Crystallization-driven Self-assembly of Biodegradable Block Copolymers

Published on: June 20, 2019

7.9K

相关实验视频

Last Updated: Oct 2, 2025

Depolymerizable Olefinic Polymers Based on Fused-Ring Cyclooctene Monomers
08:12

Depolymerizable Olefinic Polymers Based on Fused-Ring Cyclooctene Monomers

Published on: December 16, 2022

3.4K
Controlled Photoredox Ring-Opening Polymerization of O-Carboxyanhydrides Mediated by Ni/Zn Complexes
05:48

Controlled Photoredox Ring-Opening Polymerization of O-Carboxyanhydrides Mediated by Ni/Zn Complexes

Published on: November 21, 2017

8.2K
Synthesis of Monodisperse Cylindrical Nanoparticles via Crystallization-driven Self-assembly of Biodegradable Block Copolymers
11:42

Synthesis of Monodisperse Cylindrical Nanoparticles via Crystallization-driven Self-assembly of Biodegradable Block Copolymers

Published on: June 20, 2019

7.9K

科学领域:

  • 聚合物化学
  • 材料科学
  • 有机化学

背景情况:

  • 对聚合物研究和应用来说,逆转受控基聚合和再生单体至关重要.
  • 实现高效且无催化剂的聚甲烯酸脱聚化是一个重大挑战.

研究的目的:

  • 报告各种聚合甲酸盐的新型,高效且无催化剂的脱聚合方法.
  • 证明脱聚合产品在聚合物重建和新材料合成中的有用性.

主要方法:

  • 使用可逆添加碎片链转移 (RAFT) 聚合来合成具有高终端群忠实性的聚合甲酸盐.
  • 应用的热条件 (120 °C) 产生链末激素,启动快速去聚合 ("解脱") 过程.
  • 研究了线性,体积大,交叉连接和功能性聚合甲酸盐的脱聚合,包括聚甲酸盐和聚乙烯基醇甲甲酸盐.

主要成果:

  • 实现了各种聚合甲酸盐的近量化 (高达92%) 脱聚合.
  • 从去聚合产品中成功重建线性聚合物.
  • 从脱聚合材料制造出新型不溶性凝,这些凝也能够进行脱聚合.

结论:

  • 开发的脱聚合方法显著扩大了通过受控激素聚合合成的聚合物的能力.
  • 这项研究突破了聚合物脱聚合的极限,
  • 这些发现使得聚合物回收,合成和先进材料开发的新应用成为可能.