Jove
Visualize
联系我们
JoVE
x logofacebook logolinkedin logoyoutube logo
关于 JoVE
概览领导团队博客JoVE 帮助中心
作者
出版流程编辑委员会范围与政策同行评审常见问题投稿
图书馆员
用户评价订阅访问资源图书馆顾问委员会常见问题
研究
JoVE JournalMethods CollectionsJoVE Encyclopedia of Experiments存档
教育
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab Manual教师资源中心教师网站
使用条款与条件
隐私政策
政策

相关概念视频

Cationic Chain-Growth Polymerization: Mechanism00:57

Cationic Chain-Growth Polymerization: Mechanism

2.3K
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...
2.3K
Anionic Chain-Growth Polymerization: Mechanism01:04

Anionic Chain-Growth Polymerization: Mechanism

2.0K
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...
2.0K
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
Polymers02:34

Polymers

35.7K
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...
35.7K
Olefin Metathesis Polymerization: Acyclic Diene Metathesis (ADMET)00:53

Olefin Metathesis Polymerization: Acyclic Diene Metathesis (ADMET)

1.9K
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...
1.9K
Ziegler–Natta Chain-Growth Polymerization: Overview01:17

Ziegler–Natta Chain-Growth Polymerization: Overview

3.3K
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...
3.3K

您也可能阅读

相关文章

通过共同作者、期刊和引用图与本文相关的文章。

排序
Same author

Quantum transduction from electron spin state to a signaling state in a wild-type LOV photoreceptor.

bioRxiv : the preprint server for biology·2026
Same author

Vinyl Ether Maleic Anhydride Copolymers: Efficient and Reusable Sorbents for Removing Heavy Metals from Water.

ACS macro letters·2026
Same author

Photoresponsive Polymers for Debonding-on-Demand Pressure-Sensitive Adhesives.

ACS applied materials & interfaces·2026
Same author

Tuning Mechanical and Self-Healing Properties Using Multivalent Crosslinking.

Macromolecules·2026
Same author

Molecular Springs in Dynamic Covalent Polymer Networks.

Macromolecules·2026
Same author

Redefining the Limits: Atom Transfer Radical Polymerization of Vinyl Ketone Monomers under Light.

ACS macro letters·2026

相关实验视频

Updated: Jun 25, 2025

Self-assembling Morphologies Obtained from Helical Polycarbodiimide Copolymers and Their Triazole Derivatives
09:22

Self-assembling Morphologies Obtained from Helical Polycarbodiimide Copolymers and Their Triazole Derivatives

Published on: February 7, 2017

7.8K

通过碳胺驱动组装的过渡性共价聚合物.

Nirob K Saha1, William S Salvia1, Dominik Konkolewicz1

  • 1Department of Chemistry and Biochemistry, Miami University, 651 E High St, Oxford, OH, 45056, United States.

Angewandte Chemie (International ed. in English)
|May 21, 2024
PubMed
概括
此摘要是机器生成的。

研究人员使用EDC从二碳酸制成新型过渡共价聚合物. 这些聚合物提供可调节的寿命和受控的组装/拆卸,推进非平衡聚合系统.

关键词:
无化物无水化物碳二氧化物二氧化物化学燃料 化学燃料 化学燃料没有平衡的组件组合.聚合聚合的过程中.

更多相关视频

Synthesis of Information-bearing Peptoids and their Sequence-directed Dynamic Covalent Self-assembly
09:34

Synthesis of Information-bearing Peptoids and their Sequence-directed Dynamic Covalent Self-assembly

Published on: February 6, 2020

7.2K
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

7.9K

相关实验视频

Last Updated: Jun 25, 2025

Self-assembling Morphologies Obtained from Helical Polycarbodiimide Copolymers and Their Triazole Derivatives
09:22

Self-assembling Morphologies Obtained from Helical Polycarbodiimide Copolymers and Their Triazole Derivatives

Published on: February 7, 2017

7.8K
Synthesis of Information-bearing Peptoids and their Sequence-directed Dynamic Covalent Self-assembly
09:34

Synthesis of Information-bearing Peptoids and their Sequence-directed Dynamic Covalent Self-assembly

Published on: February 6, 2020

7.2K
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

7.9K

科学领域:

  • 聚合物化学 聚合物化学
  • 超分子化学 超分子化学
  • 材料科学 材料科学 材料科学

背景情况:

  • 生物化学系统在动力控制下利用失衡的聚合物.
  • 由化学燃料驱动的非生物超分子聚合物得到了很好的研究.
  • 具有暂时共价键的聚合物尚未得到充分研究,但为更强的暂时结构和可调节的动力学提供了潜力.

研究的目的:

  • 研究从简单的水性二糖酸中衍生的过渡性共价聚合物的形成和特性.
  • 探索这些聚合物在不平衡聚合系统中的潜力.
  • 为了证明对聚合物组装和拆卸动力学的控制.

主要方法:

  • 使用碳二胺EDC的水性二氧化酸的聚合.
  • 聚合物分子重量的表征和分解动力学.
  • 系统地研究影响聚合物性质的因素 (溶剂极性,试剂度,温度,单体结构).

主要成果:

  • 成功生成了分子重量超过15,000的过渡性共价聚合物 (无水化物).
  • 在几个小时到几周内证明了聚合物分解,具有可调节的拆卸动力学.
  • 通过单体设计和反应条件,确定了对组装和拆卸动力学的显著控制.

结论:

  • 简单的水性二碳酸和EDC可以形成过渡的共价聚合物 (无水化物).
  • 这些聚合物表现出可控制的寿命和动力学,补充了现有的超分子系统.
  • 这些发现突出了在不平衡聚合过程中微调动力控制的潜力.