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相关概念视频

Cationic Chain-Growth Polymerization: Mechanism00:57

Cationic Chain-Growth Polymerization: Mechanism

2.3K
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...
2.3K
Anionic Chain-Growth Polymerization: Overview01:20

Anionic Chain-Growth Polymerization: Overview

2.1K
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,...
2.1K
Anionic Chain-Growth Polymerization: Mechanism01:04

Anionic Chain-Growth Polymerization: Mechanism

2.0K
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...
2.0K
Radical Chain-Growth Polymerization: Mechanism01:09

Radical Chain-Growth Polymerization: Mechanism

2.5K
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...
2.5K
Olefin Metathesis Polymerization: Overview01:13

Olefin Metathesis Polymerization: Overview

2.1K
Recently, the development of olefin metathesis polymerization advanced the field of polymer synthesis. Simply put, the reorganization of substituents on their double bonds between two olefins in the presence of a catalyst is known as the olefin metathesis reaction. The use of metathesis reaction for polymer synthesis is called olefin metathesis polymerization.
Ruthenium-based Grubbs catalyst is the most commonly used catalyst for olefin metathesis polymerization. Grubbs catalyst consists...
2.1K
Free-Radical Chain Reaction and Polymerization of Alkenes02:35

Free-Radical Chain Reaction and Polymerization of Alkenes

7.8K
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.
7.8K

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相关实验视频

Updated: Jun 23, 2025

Reductive Electropolymerization of a Vinyl-containing Poly-pyridyl Complex on Glassy Carbon and Fluorine-doped Tin Oxide Electrodes
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Reductive Electropolymerization of a Vinyl-containing Poly-pyridyl Complex on Glassy Carbon and Fluorine-doped Tin Oxide Electrodes

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关于乙烯基乙的阴离子聚合的最近发展.

Sourav Singha1, Swagata Pan1, Syamal S Tallury2

  • 1Polymer Research Centre and Centre for Advanced Functional Materials, Department of Chemical Sciences, Indian Institute of Science Education and Research Kolkata, Mohanpur 741246, Nadia, West Bengal, India.

ACS polymers Au
|June 17, 2024
PubMed
概括

性聚合的近期进展包括性可逆添加-碎片化链转移 (RAFT) 聚合,使得室温的室外反应成为可能. 这些方法具有成本效益和环境效益,具有刺激响应控制和改善的聚合物立体规律性.

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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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Last Updated: Jun 23, 2025

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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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Depolymerizable Olefinic Polymers Based on Fused-Ring Cyclooctene Monomers
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科学领域:

  • 聚合物化学 聚合物化学
  • 有机化学 有机化学

背景情况:

  • 传统的阴离子聚合需要惰性大气和低温.
  • 最近的创新已经克服了这些局限性,提供了更容易获得的方法.

研究的目的:

  • 审查最近在阴离子聚合过程中的发展.
  • 要突出新的技术,如阴离子可逆添加-碎片化链转移 (RAFT) 聚合.
  • 讨论催化剂系统和外部刺激控制方面的进展.

主要方法:

  • 审查最近关于阴离子聚合技术的文献.
  • 分析在户外和室温条件下运行的方法.
  • 探索刺激反应性聚合和催化剂修饰的研究.

主要成果:

  • 电离式RAFT聚合物的发展.
  • 新的技术允许在室温下在室外聚合.
  • 外部刺激 (热量,光,化学物质,电能) 允许控制的聚合.
  • 在单个容器中组合聚合方法.
  • 催化剂的修改导致高立体规律性聚合物.

结论:

  • 阴离子聚合已经发展出新的,多功能和可控的方法.
  • 这些进步提供了具有成本效益和环保的替代品.
  • 未来的前景包括进一步控制和更广泛的应用.