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相关概念视频

Step-Growth Polymerization: Overview01:03

Step-Growth Polymerization: Overview

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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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Polymers02:34

Polymers

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The word polymer is derived from the Greek words “poly” which means “many” and “mer” which means “parts”. Polymers are long chains of molecules composed of repeating units of smaller molecules, known as monomers. They either occur naturally, such as DNA and proteins, or can be constructed synthetically, like plastics. They have varied structural characteristics, such as linear chains, branched chains, or complex networks, that contribute to the...
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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...
2.3K
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...
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Molecular Weight of Step-Growth Polymers01:08

Molecular Weight of Step-Growth Polymers

2.2K
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...
2.2K
Free-Radical Chain Reaction and Polymerization of Alkenes02:35

Free-Radical Chain Reaction and Polymerization of Alkenes

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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.
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Self-assembling Morphologies Obtained from Helical Polycarbodiimide Copolymers and Their Triazole Derivatives
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在聚合与自组合的合平衡下,聚合/脱聚化诱导的自组合

Jiyun Nam1, Changsu Yoo1, Myungeun Seo1,2

  • 1Department of Chemistry, Korea Advanced Institute of Science and Technology (KAIST), Daejeon 34141, Republic of Korea.

Journal of the American Chemical Society
|May 8, 2024
PubMed
概括
此摘要是机器生成的。

通过可逆聚合和脱聚合的聚合物链的动态控制,可以使块共聚物以温度触发自组装成可调节的软材料.

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科学领域:

  • 聚合物化学
  • 材料科学
  • 超分子化学

背景情况:

  • 脱聚化提供了一种可持续的途径,使聚合物分解为单体.
  • 可逆聚合和脱聚合可以通过温度控制.
  • 块共聚物的自组对于创建纳米结构至关重要.

研究的目的:

  • 通过可逆聚合/脱聚合来证明对块共聚物的自组合的动态控制.
  • 研究纳米物体中的温度诱导的可逆形态转变.
  • 探索这些动态系统作为软材料的潜力.

主要方法:

  • 使用从聚乙烯氧化物开始的 δ-瓦莱洛的环开聚合.
  • 使用温度循环诱导聚合/脱聚合/再聚合.
  • 在选择性溶剂中研究了块共聚物纳米物体的形态过渡.

主要成果:

  • 通过温度波动实现了对块共聚物的自组合的可逆控制.
  • 通过调节包装参数,证明可逆形态转换 (例如,杆-球-杆,纤维-杆-纤维).
  • 观察到溶剂选择性在较低温度下增强脱聚合,这是由于效应.

结论:

  • 聚合/脱聚化诱导自组装 (PDISA) 为动态纳米物体形成提供了一种新的方法.
  • 在块共聚物中成功实现了对温度的响应性形态变化.
  • 这些动态软材料具有适用于可调节的宏观性质 (如粘度) 的潜力.