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Step-Growth Polymerization: Overview01:03

Step-Growth Polymerization: Overview

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

Molecular Weight of Step-Growth Polymers

2.9K
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...
2.9K
Radical Chain-Growth Polymerization: Overview01:10

Radical Chain-Growth Polymerization: Overview

3.6K
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...
3.6K
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
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
Radical Chain-Growth Polymerization: Mechanism01:09

Radical Chain-Growth Polymerization: Mechanism

3.6K
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 species into...
3.6K

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Updated: Feb 20, 2026

Synthesis of Cyclic Polymers and Characterization of Their Diffusive Motion in the Melt State at the Single Molecule Level
06:55

Synthesis of Cyclic Polymers and Characterization of Their Diffusive Motion in the Melt State at the Single Molecule Level

Published on: September 26, 2016

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シングルポリマーの成長の動態

Chunming Liu1, Kaori Kubo1, Endian Wang2

  • 1Department of Chemistry and Chemical Biology, Cornell University, Ithaca, NY 14583, USA.

Science (New York, N.Y.)
|October 21, 2017
PubMed
まとめ
この要約は機械生成です。

科学者たちは 磁気ピンチを使って リアルタイムでポリマーの成長を観察し 鎖の延長中に 明確な待ち跳びのステップを明らかにしました これらのステップはモノメアの絡み合いに関連し,ポリメリゼーション率とポリマーの多様性に影響を与えます.

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High-resolution Imaging and Analysis of Individual Astral Microtubule Dynamics in Budding Yeast

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関連する実験動画

Last Updated: Feb 20, 2026

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科学分野:

  • ポリマー化学
  • バイオ物理学
  • 材料科学

背景:

  • 鎖成長ポリメリゼーションは基本的ですが,単一分子レベルでそのリアルタイムダイナミクスは十分に理解されていません.
  • ポリマーの成長メカニズムを理解することは,特定の性質を持つ新しい材料の設計に不可欠です.

研究 の 目的:

  • 単一ポリマー鎖の成長のリアルタイムダイナミクスを視覚化して分析する.
  • リング開きメタテシスのポリメリゼーションにおける鎖の延長の基礎となる分子機構を調査する.

主な方法:

  • 制御された力を適用し,単一のポリマー拡張をリアルタイムで追跡するために磁気ピンチを使用しました.
  • 観察されたポリメリゼーション現象をモデル化し理解するために分子動力学シミュレーションを使用した.

主要な成果:

  • リング開きメタテシスのポリメリゼーション中のポリマー拡張は,連続的にではなく,離散的な"待機とジャンプ"ステップで起こることが観察されました.
  • これらのステップの原因として,新たに組み込まれたモノマーから構成の絡み合いの形成と解き放たれを特定した.
  • 絡み合いの構成がポリマー化率とポリマー長さの異質性に影響することを実証した.

結論:

  • 単一ポリマーの可視化では,ポリメリゼーションにおける不連続の成長ダイナミクスを明らかにする.
  • モノメアの適合性絡み合いは,ポリマー化運動とポリマー長さの分布を決定する重要な要因である.