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相关概念视频

Cationic Chain-Growth Polymerization: Mechanism00:57

Cationic Chain-Growth Polymerization: Mechanism

2.4K
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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Anionic Chain-Growth Polymerization: Mechanism01:04

Anionic Chain-Growth Polymerization: Mechanism

2.1K
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...
2.1K
Polymer Classification: Stereospecificity01:26

Polymer Classification: Stereospecificity

2.5K
Polymerization generates chiral centers along the entire backbone of a polymer chain. Accordingly, the stereochemistry of the substituent group has a significant effect on polymer properties. Polymers formed from monosubstituted alkene monomers feature chiral carbons at every alternate position in the polymer backbone. Relative to the predominant orientation of substituents at the adjacent chiral carbons, the polymer can exist in three different configurations: isotactic, syndiotactic, and...
2.5K
Anionic Chain-Growth Polymerization: Overview01:20

Anionic Chain-Growth Polymerization: Overview

2.1K
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,...
2.1K
Ziegler–Natta Chain-Growth Polymerization: Overview01:17

Ziegler–Natta Chain-Growth Polymerization: Overview

3.4K
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...
3.4K
Polymers02:34

Polymers

36.4K
The word polymer is derived from the Greek words “poly” which means “many” and “mer” which means “parts”. Polymers are long chains of molecules composed of repeating units of smaller molecules, known as monomers. They either occur naturally, such as DNA and proteins, or can be constructed synthetically, like plastics. They have varied structural characteristics, such as linear chains, branched chains, or complex networks, that contribute to the...
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相关实验视频

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

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通过控制非生物聚合物中的阴离子切换动态来定制聚合物

Thi V Tran1, Eryn Lee1, Yennie H Nguyen1

  • 1Department of Chemistry, University of Houston, 4800 Calhoun Road, Houston, Texas 77004, United States.

Journal of the American Chemical Society
|September 7, 2022
PubMed
概括

研究人员使用金属催化剂和二次金属子开发了一种控制非生物聚合的新策略. 这种方法可以精确调节聚合物链的生长,克服乙烯聚合过程中快速链终结的局限性.

科学领域:

  • 聚合物化学
  • 有机金属化学

背景情况:

  • 由于链条的快速终结, 控制非生物的聚合是很有挑战性的.
  • 现有的方法在终止发生之前难以应用外部触发器.

研究的目的:

  • 开发一种用于调节非生物聚合物的新策略.
  • 利用金属催化剂和二次金属离子之间的化学平衡来控制聚合.

主要方法:

  • 用不同的替代剂合成两个基基-聚乙烯糖变体 (Ni1和Ni2).
  • 在各种盐 (Li+,Na+,Cs+) 的存在下使用这些复合物的乙烯聚合研究.
  • 对聚合模式 (非切换与动态切换) 的溶剂极性影响 (托/乙烯混合物) 的研究.
  • 使用NMR光谱分析反应产物以阐明机制.

主要成果:

  • 链的增长对电子效应敏感,而终结则取决于固态和电子因素.
  • 调整溶剂极性可以控制非切换或动态切换的聚合模式.
  • 用Ni1/Li+/Na+生产双模聚乙烯,其分数取决于阴离子比率.
  • 使用Ni2/Cs+实现了具有受控分子量和低分散性的单模聚乙烯.

结论:

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Controlling the Size, Shape and Stability of Supramolecular Polymers in Water

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Methionine Functionalized Biocompatible Block Copolymers for Targeted Plasmid DNA Delivery

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  • 开发的策略通过利用金属催化剂-平衡来有效调节非生物聚合物.
  • 通过快速的阳离子交换促进的动态切换机制得到实验证据的支持.
  • 这种方法可以精确控制聚合物特性,如分子量和分散性.