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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...
2.0K
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
Characteristics and Nomenclature of Copolymers01:24

Characteristics and Nomenclature of Copolymers

2.5K
Copolymers are the products obtained from the polymerization of multiple monomer species. So, in a polymer chain itself, there can be multiple repeating units that come from different monomers. The process of synthesizing a polymer from different monomer species is called copolymerization. When two monomers are involved, the polymer is known as a bipolymer. Polymers with three and four monomers are termed terpolymers and quaterpolymers, respectively. Figure 1 depicts the copolymerization of...
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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...
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Olefin Metathesis Polymerization: Ring-Opening Metathesis Polymerization (ROMP)01:16

Olefin Metathesis Polymerization: Ring-Opening Metathesis Polymerization (ROMP)

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Ring-opening metathesis polymerization or ROMP involves strained cycloalkenes as starting materials. The mechanism of ROMP proceeds by reacting cycloalkene with Grubbs catalyst to give metallacyclobutane intermediate which undergoes a ring-opening reaction to form new carbene. The new carbene reacts with another molecule of cycloalkene. Repetition of these steps leads to the formation of an unsaturated open-chain polymer product. All these steps are reversible, however, relieving the ring...
2.5K

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Application of a Coupling Agent to Improve the Dielectric Properties of Polymer-Based Nanocomposites
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在溶液中的受限驱动聚合物中堵塞交叉车.

Setarehalsadat Changizrezaei1, Mikko Karttunen1,2, Colin Denniston1

  • 1Department of Physics and Astronomy, The University of Western Ontario, London, Canada. schangiz@uwo.ca.

Soft matter
|October 30, 2024
PubMed
概括

拉蒂斯-博尔兹曼分子动力学模拟揭示了聚合物压缩行为. 在高速速度下,受限聚合物表现出伪双态共存,有密集区域和非密集区域.

科学领域:

  • 软物质物理学 软物质物理学
  • 聚合物物理 聚合物物理
  • 计算生物物理学的计算生物物理学

背景情况:

  • 封闭聚合物表现出独特的行为,与散装系统不同.
  • 对材料科学和纳米技术来说,了解在外力作用下聚合物变形至关重要.

研究的目的:

  • 为了研究由球形合体驱动的封闭聚合物的压缩动力学.
  • 分析单体相互作用和合体速度对聚合物变形和相位行为的影响.

主要方法:

  • 采用了拉蒂斯-博尔茨曼分子动力学 (LBMD) 模拟.
  • 模拟涉及一个被困在流体中的聚合物,被一个大球推动.
  • 对于单体相互作用,Lennard-Jones潜在的排斥和吸引都被使用了.

主要成果:

  • 在低速度下,不管发生什么相互作用,聚合物仍然处于非密度状态.
  • 在临界速度 (v*) 以上,聚合物的后部转换为高密度状态,平均平方单体位移 (MSD) 较低.
  • 聚合物前面保持高MSD的非密度状态,表明伪二态共存.

结论:

  • 合体速度是诱导密度过渡在受限聚合物中的关键因素.

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  • 观察到的假二态共存突出显示了受限制和外力作用下复杂的聚合物动态.
  • 对聚合物折叠事件的进一步调查为动态过程提供了洞察力.