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相关概念视频

Anionic Chain-Growth Polymerization: Overview01:20

Anionic Chain-Growth Polymerization: Overview

2.6K
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,...
2.6K
Anionic Chain-Growth Polymerization: Mechanism01:04

Anionic Chain-Growth Polymerization: Mechanism

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

Radical Chain-Growth Polymerization: Overview

3.2K
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...
3.2K
Radical Chain-Growth Polymerization: Mechanism01:09

Radical Chain-Growth Polymerization: Mechanism

3.4K
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...
3.4K
Free-Radical Chain Reaction and Polymerization of Alkenes02:35

Free-Radical Chain Reaction and Polymerization of Alkenes

9.4K
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.
9.4K
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

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Updated: Jan 22, 2026

Anionic Polymerization of an Amphiphilic Copolymer for Preparation of Block Copolymer Micelles Stabilized by &#960;-&#960; Stacking Interactions
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Anionic Polymerization of an Amphiphilic Copolymer for Preparation of Block Copolymer Micelles Stabilized by π-π Stacking Interactions

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通过连续的光降解来进行连续的激素-阳离子聚合.

Hong Zhao1, Yi Liu1, Jin-Xiang Ai2

  • 1Key Laboratory of Green Chemistry & Technology of Ministry of Education, College of Chemistry, Sichuan University, Chengdu, 610064, P.R. China.

Angewandte Chemie (International ed. in English)
|January 21, 2026
PubMed
概括
此摘要是机器生成的。

这项研究引入了一种使用光还原的新型序列激素-离子聚合法. 这种方法避免了危险的试剂,扩大了单体选择和聚合物科学中的应用.

关键词:
阳离子聚合的多聚化.摄影化学的使用.聚合方式的聚合.极端聚合方式的多聚化.

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Atom Transfer Radical Polymerization of Functionalized Vinyl Monomers Using Perylene as a Visible Light Photocatalyst
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Free Radicals in Chemical Biology: from Chemical Behavior to Biomarker Development
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Atom Transfer Radical Polymerization of Functionalized Vinyl Monomers Using Perylene as a Visible Light Photocatalyst
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Atom Transfer Radical Polymerization of Functionalized Vinyl Monomers Using Perylene as a Visible Light Photocatalyst

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Free Radicals in Chemical Biology: from Chemical Behavior to Biomarker Development
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Free Radicals in Chemical Biology: from Chemical Behavior to Biomarker Development

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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

背景情况:

  • 聚合物的特性取决于结构,推动了聚合方法的创新.
  • 现有的激素和离子聚合技术具有局限性,包括危险的试剂和能源密集型工艺.

研究的目的:

  • 开发一种新的序列激素-离子聚合法.
  • 消除在离子聚合过程中对危险的基试剂的依赖.
  • 扩大可用于阴离子聚合的单体的范围.

主要方法:

  • 在现场通过光还原产生碳基和碳离子.
  • 序列激素-阳离子链生长机制.
  • 照片诱导的连续单电子转移减少.

主要成果:

  • 成功演示了一种连续的激素-阳离子 (共) 聚合.
  • 消除了对的需求以及相关的安全和能源问题.
  • 克服了具有不同电子性质的共聚合单体的局限性.
  • 通过功能化的大规模合成和火山化展示了实际应用.

结论:

  • 开发的光诱导序列激素-离子聚合法为传统方法提供了更安全,更通用的替代方案.
  • 这一战略扩大了阳离子聚合的范围,使新型聚合物和材料的合成成为可能.
  • 该方法对学术研究和工业聚合物生产都有很大的潜力.