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関連する概念動画

Olefin Metathesis Polymerization: Acyclic Diene Metathesis (ADMET)00:53

Olefin Metathesis Polymerization: Acyclic Diene Metathesis (ADMET)

2.3K
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...
2.3K
Ziegler–Natta Chain-Growth Polymerization: Overview01:17

Ziegler–Natta Chain-Growth Polymerization: Overview

4.2K
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...
4.2K
Anionic Chain-Growth Polymerization: Overview01:20

Anionic Chain-Growth Polymerization: Overview

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

Step-Growth Polymerization: Overview

4.6K
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...
4.6K
Anionic Chain-Growth Polymerization: Mechanism01:04

Anionic Chain-Growth Polymerization: Mechanism

2.6K
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...
2.6K
Free-Radical Chain Reaction and Polymerization of Alkenes02:35

Free-Radical Chain Reaction and Polymerization of Alkenes

10.2K
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.
10.2K

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関連する実験動画

Updated: Mar 17, 2026

Atom Transfer Radical Polymerization of Functionalized Vinyl Monomers Using Perylene as a Visible Light Photocatalyst
06:49

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

Published on: April 22, 2016

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直接 (ヘテロ) アリレーション ポリメリゼーション:トレンドと展望

Thomas Bura1, J Terence Blaskovits1, Mario Leclerc1

  • 1Department of Chemistry, Université Laval , Quebec City, QC, Canada G1V 0A6.

Journal of the American Chemical Society
|July 28, 2016
PubMed
まとめ

直接アリレーションポリメリゼーションは,高品質の結合ポリマーを作成するための効率的で原子経済的な方法を提供します. このアプローチは合成を簡素化し 副産物を減らし ポリマー科学を前進させます

科学分野:

  • 材料科学
  • ポリマー化学

背景:

  • 結合ポリマーは金属と合成ポリマーの性質を組み合わせ,独特の電気的,光学的,機械的な特性を提供します.
  • 結合ポリマーの現在の合成方法は複雑で,重要な副産物を生成する可能性があります.

研究 の 目的:

  • 結合ポリマーを合成するための直接 (ヘテロ) アリレーションポリメリゼーションの進歩をレビューする.
  • 高分子量で欠陥のないポリマーを生産するための効率的で適応可能な反応条件を強調する.

主な方法:

  • (ヘテロ) アリルハライドと (ヘテロ) アリルハライドの間の炭素-炭素結合の形成を含む直接 (ヘテロ) アリルポリメリゼーション.
  • 一般的な適用性と高品質のポリマーのために反応条件の最適化.

主要な成果:

  • 直接アリレーションを用いた高分子量,欠陥のない結合ポリマーの製造に成功した.
  • ブロミンチオフェン単位などの課題を特定し,解決策を提案する.

結論:

  • 直接アリレーションポリメリゼーションは,従来のクロスカップリング方法の汎用的で原子経済的な代替手段です.
  • この方法は,結合ポリマーの合成とアプリケーションの将来に重要な希望を持っています.

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Ethylene Polymerizations Using Parallel Pressure Reactors and a Kinetic Analysis of Chain Transfer Polymerization
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Ethylene Polymerizations Using Parallel Pressure Reactors and a Kinetic Analysis of Chain Transfer Polymerization

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Depolymerizable Olefinic Polymers Based on Fused-Ring Cyclooctene Monomers
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Depolymerizable Olefinic Polymers Based on Fused-Ring Cyclooctene Monomers

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関連する実験動画

Last Updated: Mar 17, 2026

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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Ethylene Polymerizations Using Parallel Pressure Reactors and a Kinetic Analysis of Chain Transfer Polymerization
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Ethylene Polymerizations Using Parallel Pressure Reactors and a Kinetic Analysis of Chain Transfer Polymerization

Published on: November 27, 2015

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Depolymerizable Olefinic Polymers Based on Fused-Ring Cyclooctene Monomers
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Depolymerizable Olefinic Polymers Based on Fused-Ring Cyclooctene Monomers

Published on: December 16, 2022

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