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相关概念视频

Radical Chain-Growth Polymerization: Overview01:10

Radical Chain-Growth Polymerization: Overview

2.3K
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...
2.3K
Step-Growth Polymerization: Overview01:03

Step-Growth Polymerization: Overview

3.3K
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...
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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
Cationic Chain-Growth Polymerization: Mechanism00:57

Cationic Chain-Growth Polymerization: Mechanism

2.2K
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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基于自燃聚乙烯的反向块序列用于定制终端组和自组装行为.

Ji Woo Kim1, Tae-Il Kang2, Eunpyo Choi3

  • 1School of Polymer Science and Engineering, Chonnam National University, 77 Yongbong-ro, Buk-gu, Gwangju 61186, Korea.

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概括

这项研究引入了用于控制聚合物结构和降解的自燃聚乙烯 (PBE) 两性分子. 这些功能性表面活性剂使可调节组装,降解和药物输送应用成为可能.

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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
  • 超分子化学 超分子化学

背景情况:

  • 开发具有可控降解的先进聚合物材料对于药物输送和纳米技术等应用至关重要.
  • 自焚聚合物提供独特的降解途径,由外部刺激触发.
  • 设计具有可调节自组装和降解特性的两性聚合物仍然是一个挑战.

研究的目的:

  • 报告一个模块化设计的自燃聚乙 (PBE) 两性.
  • 为了实现对聚合物链结构,终端组放置和降解行为的精确控制.
  • 为了证明使用这些新型两动物来控制货物释放的潜力.

主要方法:

  • 模块化自燃聚乙烯 (PBE) 两性生物的合成,具有不同的块序列和末端组.
  • 研究受结构变异和碳酸盐含量影响的细胞形成和形态.
  • 评估水性环境中的微粒降解及其与常规表面活性剂的转化.
  • 展示小分子货物装载和按需释放的混合微粒.

主要成果:

  • 实现了用于自燃PBE两体的模块化设计,从而能够精确控制结构和降解.
  • 区块序列和末端组的调整允许在外部刺激下有效地进行头到尾的脱聚合.
  • 观察到带有表面显示的末端群体和可调整形态的微粒形成.
  • 形成了可降解的微粒,能够用表面活性剂转化为球形结构,并促进受控的货物释放.

结论:

  • 开发的PBE两类提供了一个多功能平台,用于创建功能性,刺激响应的表面活性剂.
  • 这种设计使可调节的自组装,降解和可控释放功能成为可能.
  • 模块化方法为设计各种应用的先进聚合物材料提供了强大的工具.