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

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
Conjugate Addition of Enolates: Michael Addition01:08

Conjugate Addition of Enolates: Michael Addition

2.4K
The attack of a nucleophile at the β carbon of an α,β-unsaturated carbonyl compound is called conjugate addition. Conjugate addition reactions of active methylene compounds, such as β-diketones, β-keto esters, β-keto nitriles, and α-nitro ketones, are called Michael addition reactions.
2.4K
Cyclohexenones via Michael Addition and Aldol Condensation: The Robinson Annulation01:27

Cyclohexenones via Michael Addition and Aldol Condensation: The Robinson Annulation

2.1K
Robinson annulation is a base-catalyzed reaction for the synthesis of 2-cyclohexenone derivatives from 1,3-dicarbonyl donors (such as cyclic diketones, β-ketoesters, or β-diketones) and α,β-unsaturated carbonyl acceptors. Named after Sir Robert Robinson, who discovered it, this reaction yields a six-membered ring with three new C–C bonds (two σ bonds and one π bond).
2.1K
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
Radical Chain-Growth Polymerization: Overview01:10

Radical Chain-Growth Polymerization: Overview

2.3K
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...
2.3K

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

Pillararene-Catalyzed Kemp Elimination: High Efficiency through Orthogonal Self-Sorting Binding and Ion Modulation.

The Journal of organic chemistry·2026
Same author

Thiyl radical reversible-deactivation polymerization <i>via</i> degenerative transfer with vinyl sulfides.

Chemical science·2025
Same author

A Galactose-Functionalized Pyrrolopyrrole <i>Aza</i>-BODIPY for Highly Efficient Detection of Eight Aliphatic and Aromatic Biogenic Amines: Monitoring Food Freshness and Bioimaging.

Biosensors·2025
Same author

Chiral Perturbation Strategies for Circularly Polarized Thermally Activated Delayed-Fluorescence Small Molecules: Progress in the Application of Organic Light-Emitting Diodes.

Nanomaterials (Basel, Switzerland)·2025
Same author

Pyrrolopyrrole Cyanine <i>J-</i>Aggregates with Amplified Superoxide Radical Generation, GSH Depletion, and Photothermal Action for Hypoxic Cancer Phototherapy.

ACS applied materials & interfaces·2025
Same author

Advances in Chiral Macrocycles: Molecular Design and Applications.

Chemistry (Weinheim an der Bergstrasse, Germany)·2024

相关实验视频

Updated: May 22, 2025

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

3.2K

阿扎-迈克尔添加-碎片化环开放聚合

Dan Huang1,2, Zhen Zhu2, Derong Cao1

  • 1School of Chemistry and Chemical Engineering, State Key Laboratory of Luminescent Materials and Devices, South China University of Technology, Guangzhou 510640, China.

Journal of the American Chemical Society
|May 20, 2025
PubMed
概括
此摘要是机器生成的。

这项研究引入了一种新的环开聚合方法,该方法在环境条件下打破循环单体中的C ((sp3) -N键. 这种新方法产生了具有可控性质和意想不到的cis-stereoselectivity的功能性多氨酸.

更多相关视频

3D Printing and In Situ Surface Modification via Type I Photoinitiated Reversible Addition-Fragmentation Chain Transfer Polymerization
07:28

3D Printing and In Situ Surface Modification via Type I Photoinitiated Reversible Addition-Fragmentation Chain Transfer Polymerization

Published on: February 18, 2022

3.4K
Controlled Photoredox Ring-Opening Polymerization of O-Carboxyanhydrides Mediated by Ni/Zn Complexes
05:48

Controlled Photoredox Ring-Opening Polymerization of O-Carboxyanhydrides Mediated by Ni/Zn Complexes

Published on: November 21, 2017

8.0K

相关实验视频

Last Updated: May 22, 2025

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

3.2K
3D Printing and In Situ Surface Modification via Type I Photoinitiated Reversible Addition-Fragmentation Chain Transfer Polymerization
07:28

3D Printing and In Situ Surface Modification via Type I Photoinitiated Reversible Addition-Fragmentation Chain Transfer Polymerization

Published on: February 18, 2022

3.4K
Controlled Photoredox Ring-Opening Polymerization of O-Carboxyanhydrides Mediated by Ni/Zn Complexes
05:48

Controlled Photoredox Ring-Opening Polymerization of O-Carboxyanhydrides Mediated by Ni/Zn Complexes

Published on: November 21, 2017

8.0K

科学领域:

  • 聚合物化学
  • 有机合成
  • 材料科学

背景情况:

  • 在无应力循环单体中裂解碳- (C ((sp3) -N) 键,以进行环开聚合 (ROP) 是一个重大挑战.
  • 现有的方法通常需要严苛的条件或仅限于应力单体.

研究的目的:

  • 开发一种新的策略,用于在较少应力循环单体中裂解C ((sp3) -N键.
  • 为了实现受控的环开放聚合,产生功能性聚胺.
  • 研究聚合的立体化学结果和机制.

主要方法:

  • 连锁增长聚合机制的级联aza-Michael/逆aza-Michael反应的整合
  • 在环境条件下使用压力较小的循环单体.
  • 密度函数理论 (DFT) 计算以阐明立体选择性.

主要成果:

  • 在未受压力循环单体中成功切割C ((sp3) -N键.
  • 合成含有肉的聚氨酸,其分子量可控,分散度较小.
  • 在聚合过程中显示出意想不到的cis-stereoselectivity.
  • 证明了优异的聚合控制,包括与转换和高链端忠实度的线性分子量增加.
  • 通过序列控制的聚合物共聚和合成显示的多功能应用.

结论:

  • 开发的协议提供了一个新的C-N键裂解策略,用于环开放聚合.
  • 这种方法为具有主链功能的聚合物提供了一个简单的合成途径.
  • 这些发现为设计和合成先进的聚合物架构开辟了新的途径.