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相关概念视频

Olefin Metathesis Polymerization: Ring-Opening Metathesis Polymerization (ROMP)01:16

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

2.5K
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...
2.5K
Olefin Metathesis Polymerization: Overview01:13

Olefin Metathesis Polymerization: Overview

2.0K
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...
2.0K
Radical Chain-Growth Polymerization: Mechanism01:09

Radical Chain-Growth Polymerization: Mechanism

2.3K
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...
2.3K
Cationic Chain-Growth Polymerization: Mechanism00:57

Cationic Chain-Growth Polymerization: Mechanism

2.2K
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...
2.2K
Radical Chain-Growth Polymerization: Overview01:10

Radical Chain-Growth Polymerization: Overview

2.2K
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...
2.2K
Base-Catalyzed Ring-Opening of Epoxides02:26

Base-Catalyzed Ring-Opening of Epoxides

8.1K
Due to their highly strained structures, epoxides can readily undergo ring-opening reactions through nucleophilic substitution, either in the presence of an acid or a base. The nucleophilic substitution reactions in the presence of acid are called acid-catalyzed ring-opening reactions, and nucleophilic substitution reactions in the presence of a base are called base-catalyzed ring-opening reactions. Epoxides undergo base-catalyzed ring-opening reactions in the presence of a strong nucleophile...
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相关实验视频

Updated: May 9, 2025

Synthesis of Terpolymers at Mild Temperatures Using Dynamic Sulfur Bonds in PolyS-Divinylbenzene
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在含硫环开放式共聚合和聚合中进行序列控制.

Bhargav R Manjunatha1, Cesare Gallizioli1, Christoph Fornacon-Wood1

  • 1Universität Bayreuth: Universitat Bayreuth, Makromolekulare Chemie, GERMANY.

Angewandte Chemie (International ed. in English)
|May 5, 2025
PubMed
概括

新的方法可以精确合成含硫聚合物,提供可降解性和可回收性等增强性质. 这通过控制硫化学,为新材料和新应用打开了大门.

关键词:
含硫聚合物的聚合物.聚合催化剂的聚合.环开放聚合的聚合方式

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Depolymerizable Olefinic Polymers Based on Fused-Ring Cyclooctene Monomers
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Controlled Photoredox Ring-Opening Polymerization of O-Carboxyanhydrides Mediated by Ni/Zn Complexes
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Controlled Photoredox Ring-Opening Polymerization of O-Carboxyanhydrides Mediated by Ni/Zn Complexes
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科学领域:

  • 聚合物化学 聚合物化学
  • 材料科学 材料科学 材料科学
  • 有机合成 有机合成

背景情况:

  • 含硫的聚合物提供了超越商品塑料的独特材料特性.
  • 目前这些聚合物的合成方法发展不足,难以控制.
  • 在共聚合过程中对硫中心进行重组是一个重要的合成挑战.

研究的目的:

  • 审查含硫聚合物的选择性合成的最新进展.
  • 为获得量身定制的含硫共聚合物和聚合物结构提供路线图.
  • 突出这些聚合物在新兴应用中的潜力.

主要方法:

  • 对控制聚合中硫中心反应的最新方法的审查.
  • 对抑制或利用硫中心重组的技术进行分析.
  • 探索开环共聚化策略的研究.

主要成果:

  • 新兴的方法允许精确控制含硫聚合物结构.
  • 这些聚合物表现出更好的可降解性,化学可循环利用性和结晶性.
  • 新的单体原料通过受控的硫化学变得可用.

结论:

  • 现在可以精确合成含硫聚合物.
  • 这些先进的聚合物与基于氧的类似物相比,具有优越的性能.
  • 控制的硫化学是解锁新材料应用的关键.