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相关概念视频

Cationic Chain-Growth Polymerization: Mechanism00:57

Cationic Chain-Growth Polymerization: Mechanism

2.8K
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...
2.8K
Anionic Chain-Growth Polymerization: Mechanism01:04

Anionic Chain-Growth Polymerization: Mechanism

2.4K
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...
2.4K
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
Polymer Classification: Architecture01:14

Polymer Classification: Architecture

3.7K
Polymers are classified as linear or branched on the basis of their chain architecture. The polymer chains in linear polymers have a long chain-like structure with minimal to no branching at all. Even if a polymer features large substituent groups on the monomer, which appear as branches to the skeleton, it is not considered a branched polymer. A branched polymer contains secondary polymer chains that arise from the main polymer chain. The branching occurs when the polymer growth shifts from...
3.7K
Molecular Weight of Step-Growth Polymers01:08

Molecular Weight of Step-Growth Polymers

2.7K
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...
2.7K
Step-Growth Polymerization: Overview01:03

Step-Growth Polymerization: Overview

4.3K
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...
4.3K

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Self-assembling Morphologies Obtained from Helical Polycarbodiimide Copolymers and Their Triazole Derivatives
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Self-assembling Morphologies Obtained from Helical Polycarbodiimide Copolymers and Their Triazole Derivatives

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中性聚合物的桥梁诱导聚合:动力学和形态学.

Hitesh Garg1,2, Satyavani Vemparala1,2

  • 1The Institute of Mathematical Sciences, C.I.T. Campus, Taramani, Chennai 600113, India. vani@imsc.res.in.

Soft matter
|September 19, 2025
PubMed
概括

吸引人的群众桥梁聚合物链,导致聚合. 刚性和柔性聚合物的这种聚合门与单链崩有关,形态取决于聚合物的灵活性和挤压尺寸.

科学领域:

  • 聚合物物理 聚合物物理
  • 软物质物理学 软物质物理学
  • 计算化学计算化学

背景情况:

  • 吸引人的群众可以通过充当桥梁剂来影响聚合物链的行为.
  • 了解聚合物聚合对于材料科学和生物系统至关重要.
  • 聚合物的灵活性和拥挤性质之间的相互作用决定了聚合.

研究的目的:

  • 用分子动力学模拟来研究由有吸引力的群体诱导的聚合物聚合.
  • 探讨聚合物刚度 (刚性与柔性) 对聚合行为的影响.
  • 阐明单链崩和多链聚合之间的关系.

主要方法:

  • 用分子动力学模拟来建模聚合物链和crowders.
  • 系统密度,拥挤尺寸和聚合物灵活性被系统地变化.
  • 分析的重点是关键的吸引力强度,聚合值,以及由此产生的形态.

主要成果:

  • 具有吸引力的聚合物通过桥梁相互作用诱导聚合物聚合.
  • 聚合的关键吸引力在刚性棒和柔性聚合物之间有所不同.
  • 聚合值与单个柔性链的线圈-球体过渡有关.
  • 随着系统密度的增加和人群规模的增加,聚合量会减少.

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Controlling the Size, Shape and Stability of Supramolecular Polymers in Water
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Facile Synthesis of Worm-like Micelles by Visible Light Mediated Dispersion Polymerization Using Photoredox Catalyst
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Self-assembling Morphologies Obtained from Helical Polycarbodiimide Copolymers and Their Triazole Derivatives
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Controlling the Size, Shape and Stability of Supramolecular Polymers in Water
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Controlling the Size, Shape and Stability of Supramolecular Polymers in Water

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Facile Synthesis of Worm-like Micelles by Visible Light Mediated Dispersion Polymerization Using Photoredox Catalyst
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Facile Synthesis of Worm-like Micelles by Visible Light Mediated Dispersion Polymerization Using Photoredox Catalyst

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  • 形态学取决于灵活性:棒形成捆绑,灵活的聚合物形成集群.
  • 结论:

    • 通过有吸引力的拥挤介导的桥梁相互作用是聚合物聚合的关键.
    • 聚合物刚性,挤压尺寸和系统密度协同控制聚合动态和形态.
    • 单链崩和多链聚合现象之间存在着根本的联系.