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相关概念视频

Cationic Chain-Growth Polymerization: Mechanism00:57

Cationic Chain-Growth Polymerization: Mechanism

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

Radical Chain-Growth Polymerization: Mechanism

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

Free-Radical Chain Reaction and Polymerization of Alkenes

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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.
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Anionic Chain-Growth Polymerization: Mechanism01:04

Anionic Chain-Growth Polymerization: Mechanism

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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...
2.4K
Step-Growth Polymerization: Overview01:03

Step-Growth Polymerization: Overview

4.3K
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...
4.3K
Ziegler–Natta Chain-Growth Polymerization: Overview01:17

Ziegler–Natta Chain-Growth Polymerization: Overview

3.9K
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...
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Updated: Jan 11, 2026

Controlled Photoredox Ring-Opening Polymerization of O-Carboxyanhydrides Mediated by Ni/Zn Complexes
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由催化拉塞米化驱动的立体融合聚合物

Zheng-Fei Liu1, Yu-Tao Wang1, Ye Liu1

  • 1State Key Laboratory of Fine Chemicals, Frontiers Science Center for Smart Materials, Dalian University of Technology, Dalian 116024, China.

Journal of the American Chemical Society
|November 13, 2025
PubMed
概括
此摘要是机器生成的。

动态动态分辨率聚合 (DKRP) 克服了传统方法的50%的产量限制. 这种新方法通过快速的种族化实现了从种族混合物中100%的纯聚合物的产量.

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Ethylene Polymerizations Using Parallel Pressure Reactors and a Kinetic Analysis of Chain Transfer Polymerization
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科学领域:

  • 聚合物化学
  • 有机合成
  • 催化剂

背景情况:

  • 动态分辨率聚合 (KRP) 合成了反纯聚合物,但仅限于50%的理论产量.
  • 随着转换率接近50%的变化,立体规律性会降低.

研究的目的:

  • 为了克服KRP的产量限制.
  • 开发一种高达100%产量的聚合物合成方法.

主要方法:

  • 采用快速种族化来实现动态动态分辨率聚合 (DKRP).
  • 使用一个直角的催化系统:一个易斯酸对 (tris{perfluorophenyl) 和N,N-dimethylbutylamine) 和一个合催化剂 ((R) -SalBinamAl).
  • 将DKRP方法应用于血清β-propiothiolactones.

主要成果:

  • 达到了100%的转化和96%的 (R) -enantiomer过剩.
  • 通过催化种族化驱动的立体融合环开放聚合过程.
  • 克服了传统动态分辨率所固有的50%的产量限制.

结论:

  • DKRP使得从racemic单体中精确合成enantiopure聚合物,其理论产量高达100%.
  • 这项研究提供了催化种族化驱动的立体融合环开放聚合的第一个例子.