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相关概念视频

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
Cationic Chain-Growth Polymerization: Mechanism00:57

Cationic Chain-Growth Polymerization: Mechanism

2.3K
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
Step-Growth Polymerization: Overview01:03

Step-Growth Polymerization: Overview

3.5K
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...
3.5K
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
Olefin Metathesis Polymerization: Acyclic Diene Metathesis (ADMET)00:53

Olefin Metathesis Polymerization: Acyclic Diene Metathesis (ADMET)

1.9K
Acyclic diene metathesis polymerization or ADMET polymerization involves cross-metathesis of terminal dienes, such as 1,8-nonadiene, to give linear unsaturated polymer and ethylene. As ADMET is a reversible process, the formed ethylene gas must be removed from the reaction mixture to complete the polymerization process.
Similar to cross-metathesis, ADMET also involves the formation of metallacyclobutane intermediate by [2+2] cycloaddition of one of the double bonds of a terminal diene with...
1.9K
Free-Radical Chain Reaction and Polymerization of Alkenes02:35

Free-Radical Chain Reaction and Polymerization of Alkenes

7.8K
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.
7.8K

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Atom Transfer Radical Polymerization of Functionalized Vinyl Monomers Using Perylene as a Visible Light Photocatalyst
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通过悬浮组激活进行甲烯酸聚合物的散装解聚合

Rhys W Hughes1, Megan E Lott1, Isabella S Zastrow1

  • 1George & Josephine Butler Polymer Research Laboratory, Department of Chemistry, Center for Macromolecular Science & Engineering, University of Florida, Gainesville, Florida 32611, United States.

Journal of the American Chemical Society
|February 21, 2024
PubMed
概括

这项研究引入了一种通过结合特定单体的高效解聚甲酸 (PMMA) 的方法. 这种工艺使得即使是超高分子量PMMA,也能达到95%以上的转化为甲基甲酸盐 (MMA),从而实现可持续的聚合物材料开发.

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Microwave-assisted Functionalization of Polyethylene glycol and On-resin Peptides for Use in Chain Polymerizations and Hydrogel Formation
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科学领域:

  • 聚合物化学
  • 可持续材料科学
  • 化学工程

背景情况:

  • 传统的基聚聚合聚甲酸 (PMMA) 在高效脱聚化方面存在挑战.
  • 现有的脱聚合方法通常与高分子量聚合物扎或需要催化剂.
  • 越来越需要可持续的方法来回收和重复使用PMMA等聚合物材料.

研究的目的:

  • 开发一种有效的,无催化剂的PMMA共聚物的脱聚合方法.
  • 研究功能化PMMA的脱聚合,包括超高分子量变体和网络.
  • 展示创建可持续聚甲酸材料的潜力.

主要方法:

  • 通过常规的基聚聚合物合成含有低mol%的胺单体的PMMA共聚物.
  • 合成的PMMA共聚物的无催化剂散装解聚.
  • 由此产生的副产品的脱聚合效率和分子量.
  • 将该方法扩展到聚合甲酸网络.

主要成果:

  • 从功能化PMMA转化为甲基甲酸盐 (MMA) 达到>95%.
  • 证明了超高分子量PMMA (10^6-10^7g/mol) 的近量脱聚合.
  • 与链末启动的方法相比,生产的聚合物副产品分子重量明显较低.
  • 展示了聚合甲酸网络的高解聚合程度.

结论:

  • 开发的方法提供了有效和可持续的PMMA脱聚合方法.
  • 这种技术即使对高分子量聚合物和网络具有挑战性也是有效的.
  • 这种方法对推进可持续的聚合物科学和应用具有重大前景.