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相关概念视频

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

Anionic Chain-Growth Polymerization: Mechanism

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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...
2.2K
Step-Growth Polymerization: Overview01:03

Step-Growth Polymerization: Overview

3.9K
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...
3.9K
Radical Chain-Growth Polymerization: Mechanism01:09

Radical Chain-Growth Polymerization: Mechanism

3.0K
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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Radical Chain-Growth Polymerization: Overview01:10

Radical Chain-Growth Polymerization: Overview

2.8K
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...
2.8K
Anionic Chain-Growth Polymerization: Overview01:20

Anionic Chain-Growth Polymerization: Overview

2.3K
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,...
2.3K

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Synthesis of Cyclic Polymers and Characterization of Their Diffusive Motion in the Melt State at the Single Molecule Level
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动态微溶液中的定向超分子聚合:线性移动的聚合物的末端冲击单体

Shota Matoba1, Chisako Kanzaki1, Kae Yamashita1

  • 1Department of Biomolecular Chemistry, Graduate School of Life and Environmental Sciences, Kyoto Prefectural University, Shimogamo, Sakyo-ku, Kyoto 606-8522, Japan.

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|June 1, 2021
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概括

研究人员开发了一种使用烯二氧化物 (PBI) 单体的定向超分子聚合方法. 微流通道中的剪切力选择性地激活生长的聚合物的一端,从而实现受控的生长和阻断共聚合物合成.

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科学领域:

  • 超分子化学
  • 材料科学
  • 聚合物化学

背景情况:

  • 定向连锁反应在自然界中很常见,但在人工自组装中具有挑战性.
  • 现有的人工一维自组装系统缺乏受控的定向增长.

研究的目的:

  • 开发一种使用二胺 (PBI) 衍生物的定向超分子聚合系统.
  • 研究剪切力在控制聚合物生长和实现块共聚合物的作用.

主要方法:

  • 在微流通道系统中使用乙烯衍生物 (PBI) 作为单体.
  • 在不同流速和剪切应力下研究核化和生长动态.
  • 使用现场光光谱和线性二极化来监测聚合.
  • 将该策略应用于二块共聚物形成的双单体系统.

主要成果:

  • 通过剪切力诱导PBI单体的自发核形成.
  • 剪切应力在定向聚合物的一端选择性地加速了聚合物生长.
  • 定向增长占主导地位,而不是自由单体核.
  • 通过聚合物末端的选择性反应成功合成了双块共聚物,形成了分子异质连接.

结论:

  • 单个聚合物端的摩擦诱导激活可以实现定向超分子聚合.
  • 这种策略广泛适用于定向超分子块共聚化.
  • 允许在聚合物中精确形成分子异质连接.