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Olefin Metathesis Polymerization: Overview01:13

Olefin Metathesis Polymerization: Overview

Recently, the development of olefin metathesis polymerization advanced the field of polymer synthesis. Simply put, the reorganization of substituents on their double bonds between two olefins in the presence of a catalyst is known as the olefin metathesis reaction. The use of metathesis reaction for polymer synthesis is called olefin metathesis polymerization.
Ruthenium-based Grubbs catalyst is the most commonly used catalyst for olefin metathesis polymerization. Grubbs catalyst consists of a...
Olefin Metathesis Polymerization: Ring-Opening Metathesis Polymerization (ROMP)01:16

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

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

Olefin Metathesis Polymerization: Acyclic Diene Metathesis (ADMET)

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

Cationic Chain-Growth Polymerization: Mechanism

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 generated carbocation,...
Radical Chain-Growth Polymerization: Mechanism01:09

Radical Chain-Growth Polymerization: Mechanism

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 the...
Ziegler–Natta Chain-Growth Polymerization: Overview01:17

Ziegler–Natta Chain-Growth Polymerization: Overview

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 catalyst, high molecular...

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Updated: Jun 25, 2026

Depolymerizable Olefinic Polymers Based on Fused-Ring Cyclooctene Monomers
08:12

Depolymerizable Olefinic Polymers Based on Fused-Ring Cyclooctene Monomers

Published on: December 16, 2022

环膨胀元解聚合:取决于催化剂的聚合配置文件.

Yan Xia1, Andrew J Boydston, Yefeng Yao

  • 1Arnold and Mabel Beckman Laboratory of Chemical Synthesis, Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, California 91125, USA.

Journal of the American Chemical Society
|February 10, 2009
PubMed
概括

使用循环催化剂的环膨胀元解聚合 (REMP) 显示了基于长度的明显的聚合物生长机制. 催化剂长度决定了聚合是否类似于链增长或阶段增长,从而影响了分子重量演变.

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Photogeneration of N-Heterocyclic Carbenes: Application in Photoinduced Ring-Opening Metathesis Polymerization
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Photogeneration of N-Heterocyclic Carbenes: Application in Photoinduced Ring-Opening Metathesis Polymerization

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Particles without a Box: Brush-first Synthesis of Photodegradable PEG Star Polymers under Ambient Conditions
06:56

Particles without a Box: Brush-first Synthesis of Photodegradable PEG Star Polymers under Ambient Conditions

Published on: October 10, 2013

相关实验视频

Last Updated: Jun 25, 2026

Depolymerizable Olefinic Polymers Based on Fused-Ring Cyclooctene Monomers
08:12

Depolymerizable Olefinic Polymers Based on Fused-Ring Cyclooctene Monomers

Published on: December 16, 2022

Photogeneration of N-Heterocyclic Carbenes: Application in Photoinduced Ring-Opening Metathesis Polymerization
12:19

Photogeneration of N-Heterocyclic Carbenes: Application in Photoinduced Ring-Opening Metathesis Polymerization

Published on: November 29, 2018

Particles without a Box: Brush-first Synthesis of Photodegradable PEG Star Polymers under Ambient Conditions
06:56

Particles without a Box: Brush-first Synthesis of Photodegradable PEG Star Polymers under Ambient Conditions

Published on: October 10, 2013

科学领域:

  • 聚合物化学 聚合物化学
  • 有机金属化学 有机金属化学
  • 材料科学 材料科学 材料科学

背景情况:

  • 环膨胀元解聚合 (REMP) 是合成循环聚合物的通用方法.
  • 最近出现了循环催化剂,为REMP提供了新的可能性.
  • 了解催化剂架构对聚合机制的影响对于控制聚合物特性至关重要.

研究的目的:

  • 通过循环Ru催化剂调解REMP的详细聚合机制的研究.
  • 探索催化剂架构,特别是长,如何影响分子重量演变和聚合物拓.
  • 在REMP中阐明对最终聚合物分子重量的热力学控制.

主要方法:

  • 循环Ru催化剂的合成和表征,具有不同的长 (五碳与六碳).
  • 在各种反应条件下对聚合物的详细动力学研究.
  • 使用像ICP-MS.这样的技术分析聚合物分子量演变.
  • 聚合物链末端和拓的表征使用融化状态魔力角旋转 (13)C NMR光谱学.

主要成果:

  • 观察到两种不同的分子重量进化:链式增长与六碳和阶段式增长与五碳.
  • 五碳结合催化剂显示准备释放,与传播竞争,导致逐步增长行为.
  • 最终的聚合物分子重量是热力学控制的,达到大环尺寸 (60-120 kDa) 独立于催化剂结构.
  • 六碳结合催化剂在循环聚合物中体现了缓慢的结合,而五碳结合催化剂的结合是最小的.

结论:

  • 催化剂带的长度显著决定了REMP的机制,影响了分子重量增长.
  • 热力学平衡控制REMP过程中循环聚合物的最终分子量.
  • 无论催化剂结构如何,REMP都能生产具有最小链末的循环聚合物,这突显了该过程的效率.