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

Polymer Classification: Architecture01:14

Polymer Classification: Architecture

2.6K
Polymers are classified as linear or branched on the basis of their chain architecture. The polymer chains in linear polymers have a long chain-like structure with minimal to no branching at all. Even if a polymer features large substituent groups on the monomer, which appear as branches to the skeleton, it is not considered a branched polymer. A branched polymer contains secondary polymer chains that arise from the main polymer chain. The branching occurs when the polymer growth shifts from...
2.6K
Anionic Chain-Growth Polymerization: Overview01:20

Anionic Chain-Growth Polymerization: Overview

2.0K
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,...
2.0K
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
Polymer Classification: Stereospecificity01:26

Polymer Classification: Stereospecificity

2.4K
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...
2.4K
Radical Chain-Growth Polymerization: Chain Branching01:17

Radical Chain-Growth Polymerization: Chain Branching

1.9K
The skeletal structure of polymers synthesized via radical polymerization is always branched. For example, the polymerization of ethylene by radical polymerization results in a low-density grade of polyethylene with a heavily branched skeletal structure. Here, the radical site abstracts hydrogen from the growing chain, and the radical site shifts from the end (a primary carbon center) to anywhere within the growing chain (a secondary carbon center). Consequently, the part of the chain from the...
1.9K
Chair Conformation of Cyclohexane02:02

Chair Conformation of Cyclohexane

14.2K
The chair conformation is the most stable form of cyclohexane due to the absence of angle and torsional strain. The absence of angle strain is a result of cyclohexane’s bond angle being very close to the ideal tetrahedral bond angle of 109.5° in its chair conformer. Similarly, the torsional strain is also absent owing to the perfectly staggered arrangement of bonds.
The hydrogen atoms linked to carbons are arranged in two different axial and equatorial orientations to achieve this...
14.2K

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

Corrigendum to "HSF1, in association with MORC2, downregulates ArgBP2 via the PRC2 family in gastric cancer cells" [Biochim. Biophys. Acta. Mol. Basis. Dis. 2018 Apr;1864(4 Pt A):1104-1114/PMID: 29339121].

Biochimica et biophysica acta. Molecular basis of disease·2024
Same author

Marine sulfated glycans inhibit the interaction of heparin with S-protein of SARS-CoV-2 Omicron XBB variant.

Glycoconjugate journal·2024
Same author

Formation of brominated and nitrated byproducts during unactivated peroxymonosulfate oxidation of phenol.

Journal of hazardous materials·2024
Same author

MAMLCDA: A Meta-Learning Model for Predicting circRNA-Disease Association Based on MAML Combined With CNN.

IEEE journal of biomedical and health informatics·2024
Same author

Editorial: Heparan sulfate-binding proteins in health and disease.

Frontiers in molecular biosciences·2024
Same author

The heat shock factor 20-HSF4-cellulose synthase A2 module regulates heat stress tolerance in maize.

The Plant cell·2024
Same journal

Fundamentals, Measurement and Regulation of the Conductance of Single Molecule Junctions.

Angewandte Chemie (International ed. in English)·2026
Same journal

Quantitative Photoswitching of Spin States in o-Fluoroazobenzene-Loaded Metal-Organic Frameworks.

Angewandte Chemie (International ed. in English)·2026
Same journal

Cobalt Nanoparticles Confined in Defective Carbon Matrices for Robust Intermittent CO<sub>2</sub> Methanation.

Angewandte Chemie (International ed. in English)·2026
Same journal

Copper(II/III) Redox Couple Enables C─H Methylation via a Radical Mechanism Analogous to SAM Enzymes.

Angewandte Chemie (International ed. in English)·2026
Same journal

Ring Strain Engineering of Cyclic Ethers for High-Performance Sodium Metal Batteries.

Angewandte Chemie (International ed. in English)·2026
Same journal

Bond Length as a Unified Descriptor for Stable Iodine Battery.

Angewandte Chemie (International ed. in English)·2026
查看所有相关文章

相关实验视频

Updated: May 22, 2025

DNA Nanotubes as a Versatile Tool to Study Semiflexible Polymers
08:00

DNA Nanotubes as a Versatile Tool to Study Semiflexible Polymers

Published on: October 25, 2017

6.8K

I-B型主链聚罗他素网络

Wenbin Wang1, Ruixue Bai1, Chunyu Wang1

  • 1Shanghai Jiao Tong University, School of Chemistry and Chemical Engineering, Shanghai, CHINA.

Angewandte Chemie (International ed. in English)
|May 20, 2025
PubMed
概括
此摘要是机器生成的。

研究人员开发了一种新方法来制造先进的I-B型主链聚罗塔克桑 (PRs). 这些新型的聚甲网络 (PRNs) 显示出显著增强的机械性能和自我恢复能力.

关键词:
机械互锁的聚合物 * 主链聚酸盐 * 主客化学 * 内部分子运动 * 机械适应性

更多相关视频

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 Programmable Main-chain Liquid-crystalline Elastomers Using a Two-stage Thiol-acrylate Reaction
11:17

Synthesis of Programmable Main-chain Liquid-crystalline Elastomers Using a Two-stage Thiol-acrylate Reaction

Published on: January 19, 2016

21.5K

相关实验视频

Last Updated: May 22, 2025

DNA Nanotubes as a Versatile Tool to Study Semiflexible Polymers
08:00

DNA Nanotubes as a Versatile Tool to Study Semiflexible Polymers

Published on: October 25, 2017

6.8K
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 Programmable Main-chain Liquid-crystalline Elastomers Using a Two-stage Thiol-acrylate Reaction
11:17

Synthesis of Programmable Main-chain Liquid-crystalline Elastomers Using a Two-stage Thiol-acrylate Reaction

Published on: January 19, 2016

21.5K

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
  • 超分子化学 超分子化学

背景情况:

  • 对机械互锁材料来说,聚乙烯 (PRs) 提供了特殊的灵活性.
  • I-B型主链PR,具有多个集成的轮子和堵塞器,难以合成和未经探索.
  • 开发新的合成路线对于释放它们的潜力至关重要.

研究的目的:

  • 为I-B型主链聚洛他桑 (PRs) 引入一种简单的合成策略.
  • 构建第一个I-B型主链聚甲网络 (PRN).
  • 调查新型PRN的机械性能和自我恢复能力.

主要方法:

  • 采用"主机-客户端识别,然后点击聚合"策略进行PR合成.
  • 合成了I-B型主链PRs,随后形成了聚甲网络 (PRN).
  • 其特点是PRN的机械性能 (骨折应变,性,抗穿孔性) 和自我恢复.

主要成果:

  • 成功合成了I-B型主链PR和第一个PRN.
  • 与对照组相比,PRN在骨折应变,性和穿孔抵抗方面表现出超过27倍的增强.
  • 由于有限的机械键移动,PRN表现出显著的自我恢复能力.

结论:

  • 为I-B型主链PR网络综合制定了一种新且简单的策略.
  • 类型I-B主链PR显著提高材料性能,特别是机械强度和自我恢复.
  • 这项研究为开发先进的动态聚合物材料提供了宝贵的见解.