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相关概念视频

Ziegler–Natta Chain-Growth Polymerization: Overview01:17

Ziegler–Natta Chain-Growth Polymerization: Overview

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Ziegler–Natta polymerization is another form of addition or chain‐growth polymerization used for synthesizing linear polymers over branched polymers. The catalyst used for polymerization is the Ziegler–Natta catalyst, named after Karl Ziegler and Giulio Natta, who developed it in 1953. This catalyst is an organometallic complex of titanium tetrachloride and triethyl aluminum, with the active form of the catalyst being an alkyl titanium compound. Using the Ziegler–Natta...
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Step-Growth Polymerization: Overview01:03

Step-Growth Polymerization: Overview

3.6K
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...
3.6K
Radical Chain-Growth Polymerization: Overview01:10

Radical Chain-Growth Polymerization: Overview

2.7K
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...
2.7K
Cationic Chain-Growth Polymerization: Mechanism00:57

Cationic Chain-Growth Polymerization: Mechanism

2.1K
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...
2.1K
Molecular Weight of Step-Growth Polymers01:08

Molecular Weight of Step-Growth Polymers

2.1K
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...
2.1K
Anionic Chain-Growth Polymerization: Mechanism01:04

Anionic Chain-Growth Polymerization: Mechanism

1.7K
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...
1.7K

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相关实验视频

Updated: May 3, 2026

Synthesis of Cyclic Polymers and Characterization of Their Diffusive Motion in the Melt State at the Single Molecule Level
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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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单晶线性聚合物通过可见光触发的高化学定量聚合.

Letian Dou1, Yonghao Zheng, Xiaoqin Shen

  • 1California NanoSystems Institute, University of California, Santa Barbara, CA 93106, USA.

Science (New York, N.Y.)
|January 18, 2014
PubMed
概括

研究人员开发了一种可见光触发的聚合法,以制造大,高质量的聚合物单晶体. 这种可逆的过程允许研究单个聚合物链,克服了聚合物科学中的一个关键挑战.

科学领域:

  • 聚合物科学 聚合物科学
  • 材料化学 材料化学
  • 晶体学 晶体学是指结晶学.

背景情况:

  • 制备大尺寸,高质量的聚合物单晶在聚合物科学中是一个重大挑战.
  • 现有的方法往往在可扩展性和控制晶体完美的问题上扎.

研究的目的:

  • 为了展示一种新的可见光触发的高化学聚合反应.
  • 为了获得宏观大小,高质量的聚合物单晶.
  • 调查聚合过程的可逆性,并研究单个聚合物链.

主要方法:

  • 使用一种结合染料分子进行可见光触发的拓化学聚合.
  • 研究了单晶,缩溶液和半晶薄膜中的聚合.
  • 采用热解来研究脱聚合过程和机械剥落来分离单个聚合物纤维.

主要成果:

  • 成功获得了宏观大小,高质量的聚合物单晶.
  • 证明聚合不仅在单晶中有效,而且在缩溶液和薄膜中也有效.
  • 通过热解证实了聚合-脱聚合过程的可逆性.
  • 通过机械剥皮,使单个长长的聚合物链能够被隔离和研究.

结论:

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Atom Transfer Radical Polymerization of Functionalized Vinyl Monomers Using Perylene as a Visible Light Photocatalyst
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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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Atom Transfer Radical Polymerization of Functionalized Vinyl Monomers Using Perylene as a Visible Light Photocatalyst
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Atom Transfer Radical Polymerization of Functionalized Vinyl Monomers Using Perylene as a Visible Light Photocatalyst

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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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  • 一种可见光触发的聚合法提供了一条可行的途径,以宏观的聚合物单晶.
  • 这种聚合物的可逆性为动态聚合物材料开辟了可能性.
  • 能够分离单个聚合物链的能力促进了对聚合物链属性的基础研究.