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

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

Radical Chain-Growth Polymerization: Mechanism

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 the...
Anionic Chain-Growth Polymerization: Mechanism01:04

Anionic Chain-Growth Polymerization: Mechanism

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 acceptor.
Cationic Chain-Growth Polymerization: Mechanism00:57

Cationic Chain-Growth Polymerization: Mechanism

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 generated carbocation,...
Step-Growth Polymerization: Overview01:03

Step-Growth Polymerization: Overview

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

Molecular Weight of Step-Growth Polymers

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...

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

Antibody-based regimens targeting PD-1/PD-L1 and VEGF/VEGFR in advanced or metastatic NSCLC: a meta-analysis of RCTs.

Frontiers in immunology·2026
Same author

Ultrafast and high-precision 3D printing <i>via</i> type-I-initiated xanthate-mediated RAFT polymerization.

Chemical science·2026
Same author

Thermodynamic Limits to Molecular Doping in Conjugated Polymers: A Perspective on Phase Behavior and Miscibility.

Advanced materials (Deerfield Beach, Fla.)·2026
Same author

Recyclable Graft Polymer Enabled by RAFT Step-Growth Polymerization and Deconstruction.

Chemistry (Weinheim an der Bergstrasse, Germany)·2026
Same author

Deep-learning-based sub-meter urban construction-site mapping reveals China's dual-track urban renewal.

National science review·2026
Same author

Instability of prevailing small molecule acceptors in organic solar cells toward water/nucleophiles.

Science advances·2026

相关实验视频

Updated: May 12, 2026

Microwave-assisted Functionalization of Poly(ethylene glycol) and On-resin Peptides for Use in Chain Polymerizations and Hydrogel Formation
15:33

Microwave-assisted Functionalization of Poly(ethylene glycol) and On-resin Peptides for Use in Chain Polymerizations and Hydrogel Formation

Published on: October 30, 2013

通过"穿透"进行RAFT阶段增长聚合.

Wenjie Mao1, Jiajia Li1, Xiaofeng Pan1

  • 1State and Local Joint Engineering Laboratory for Novel Functional Polymeric Materials, Jiangsu Key Laboratory of Advanced Functional Polymer Design and Application, Department of Polymer Science and Engineering, College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou 215123, China.

ACS polymers Au
|February 9, 2026
PubMed
概括
此摘要是机器生成的。

研究人员开发了可降解的移植聚合物,使用可逆添加-碎片化链转移 (RAFT) 阶段增长聚合. 这种多功能方法允许可调节的侧链和双刺激响应骨干用于先进的功能材料.

关键词:
在RAFT的聚合物化过程中,苏米 (SUMI) 是一个数字.可降解的聚合物可降解性聚合物通过接种通过接种.一步增长的聚合聚合.

更多相关视频

Grafting Multiwalled Carbon Nanotubes with Polystyrene to Enable Self-Assembly and Anisotropic Patchiness
11:09

Grafting Multiwalled Carbon Nanotubes with Polystyrene to Enable Self-Assembly and Anisotropic Patchiness

Published on: April 1, 2018

3D Printing and In Situ Surface Modification via Type I Photoinitiated Reversible Addition-Fragmentation Chain Transfer Polymerization
07:28

3D Printing and In Situ Surface Modification via Type I Photoinitiated Reversible Addition-Fragmentation Chain Transfer Polymerization

Published on: February 18, 2022

相关实验视频

Last Updated: May 12, 2026

Microwave-assisted Functionalization of Poly(ethylene glycol) and On-resin Peptides for Use in Chain Polymerizations and Hydrogel Formation
15:33

Microwave-assisted Functionalization of Poly(ethylene glycol) and On-resin Peptides for Use in Chain Polymerizations and Hydrogel Formation

Published on: October 30, 2013

Grafting Multiwalled Carbon Nanotubes with Polystyrene to Enable Self-Assembly and Anisotropic Patchiness
11:09

Grafting Multiwalled Carbon Nanotubes with Polystyrene to Enable Self-Assembly and Anisotropic Patchiness

Published on: April 1, 2018

3D Printing and In Situ Surface Modification via Type I Photoinitiated Reversible Addition-Fragmentation Chain Transfer Polymerization
07:28

3D Printing and In Situ Surface Modification via Type I Photoinitiated Reversible Addition-Fragmentation Chain Transfer Polymerization

Published on: February 18, 2022

科学领域:

  • 聚合物化学 聚合物化学
  • 材料科学 材料科学 材料科学
  • 生物材料是一种生物材料.

背景情况:

  • 具有可降解骨干和可调节侧链的移植聚合物对于先进的功能材料至关重要.
  • 应用包括生物医学系统和刺激响应材料.

研究的目的:

  • 开发一种用于合成可降解移植聚合物的多功能战略.
  • 为了实现对侧链长度,质性和骨干可降解性的精确控制.
  • 为了实现聚合后修改,以加强对聚合物架构的控制.

主要方法:

  • 利用可逆的添加碎片化链转移 (RAFT) 阶段增长聚合.
  • 采用了双功能的聚甲基烯酸盐 (PMA) 宏观体和一个双功能的乙烯基单体.
  • 纳入一个小分子RAFT剂作为一个共同体,以减轻固体障碍.

主要成果:

  • 合成的移植共聚合物具有可定制的侧链长度和可调节的风湿学特性.
  • 在聚合物骨干中通过酸和酸链接 (氨解和水解) 实现了双刺激响应的降解性.
  • 使用嵌入式RAFT功能进行架构控制,证明了聚合后链扩展.

结论:

  • 介绍了一个模块化和强大的平台,用于工程可降解的移植聚合物.
  • 开发的聚合物提供可编程架构和多功能性.
  • 适用于药物输送和智能材料中的应用.