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

Radical Chain-Growth Polymerization: Mechanism01:09

Radical Chain-Growth Polymerization: Mechanism

2.5K
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...
2.5K
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
Preparation of Diols and Pinacol Rearrangement01:57

Preparation of Diols and Pinacol Rearrangement

3.3K
Compounds bearing two hydroxyl groups are known as diols. When the hydroxyl groups are located on adjacent carbon atoms, the diols are called vicinal diols or glycols. Under acidic conditions, vicinal diols undergo a specific reaction called pinacol rearrangement.
The reaction begins with transferring a proton from the acid catalyst to one of the hydroxyl groups, producing an oxonium ion.
3.3K
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
Loss of Carboxy Group as CO2: Decarboxylation of Malonic Acid Derivatives01:35

Loss of Carboxy Group as CO2: Decarboxylation of Malonic Acid Derivatives

1.9K
Just like β-keto acids—which upon thermal decarboxylation form ketones—β-dicarboxylic acids undergo decarboxylation to generate monocarboxylic acids with the liberation of carbon dioxide.
1.9K
Step-Growth Polymerization: Overview01:03

Step-Growth Polymerization: Overview

3.4K
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...
3.4K

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

Anomer-Selective Vorbrüggen Reaction for the Catalytic Synthesis of C<sub>2</sub>-Deoxynucleoside Analogues.

Journal of the American Chemical Society·2026
Same author

Latent Catalysis as a Platform for Accessing Diverse Material Properties in Vat Photopolymerization 3D Printing.

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

Polyolefin blends with co-continuous architectures enabled by dynamic covalent crosslinking.

Science advances·2026
Same author

Implications of Solvent Vapor Annealing on Crystallinity and Orientation of Covalent Organic Framework Thin Films.

ACS omega·2026
Same author

Cobalt-Catalyzed Syntheses of Acrylamides and Succindiamides from Alkynes and Amines Promoted by Light.

Journal of the American Chemical Society·2026
Same author

Fluoroolefin-vinyl ether copolymer ionic fluorogels for PFAS remediation from water.

Polymer chemistry·2026
Same journal

Customizing Ionic Micelles by Dynamic Coassembly of Sequence-Defined Peptoid Block Copolymers.

Macromolecules·2026
Same journal

Investigating Polyethylene Solubility for Solvent-Based Recycling: Experiments and SAFT‑γ Mie Predictions.

Macromolecules·2026
Same journal

Molecular Dynamics Simulations of the Structural and Thermodynamic Properties of Poly(<i>l</i>‑lactic acid) in the Presence of Water.

Macromolecules·2026
Same journal

From Solvent-Mediated Micellization to Packing in a Face-Centered Cubic Structure of Poloxamers.

Macromolecules·2026
Same journal

Nonlocal Effect of Percolated Particle Networks on Viscoelasticity of Polymer-Filler Nanocomposites: A Mesoscale Simulation Study.

Macromolecules·2026
Same journal

Helicity of a confined bottlebrush ring polymer.

Macromolecules·2026
查看所有相关文章

相关实验视频

Updated: Jun 11, 2025

Fabricating Superhydrophobic Polymeric Materials for Biomedical Applications
09:22

Fabricating Superhydrophobic Polymeric Materials for Biomedical Applications

Published on: August 28, 2015

19.1K

修改通过C-H功能化降解的聚甲.

Victoria J Barber1, Meredith A Borden1, Jill W Alty1

  • 1Department of Chemistry, The University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599, United States.

Macromolecules
|October 7, 2024
PubMed
概括
此摘要是机器生成的。

研究人员修改了可生物降解的聚合物 (caprolactone) 来制造新的可降解聚合物. 功能化减缓了降解,为可持续塑料和医疗用途提供了控制聚合物分解的新方法.

更多相关视频

Designed for Molecular Recycling: A Lignin-Derived Semi-aromatic Biobased Polymer
10:22

Designed for Molecular Recycling: A Lignin-Derived Semi-aromatic Biobased Polymer

Published on: November 30, 2020

3.4K
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

相关实验视频

Last Updated: Jun 11, 2025

Fabricating Superhydrophobic Polymeric Materials for Biomedical Applications
09:22

Fabricating Superhydrophobic Polymeric Materials for Biomedical Applications

Published on: August 28, 2015

19.1K
Designed for Molecular Recycling: A Lignin-Derived Semi-aromatic Biobased Polymer
10:22

Designed for Molecular Recycling: A Lignin-Derived Semi-aromatic Biobased Polymer

Published on: November 30, 2020

3.4K
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

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
  • 生物材料工程 生物材料工程

背景情况:

  • 在可持续塑料和医疗植入物中对可降解聚合物的需求日益增加.
  • 需要更好地了解和控制聚合物降解速率.
  • 聚烯是一种广泛使用的可生物降解聚烯.

研究的目的:

  • 调查C-H化对聚烯酸的特性和降解的影响.
  • 探索调节可生物降解聚合物的降解方法.
  • 了解聚合物结构和降解动力学之间的关系.

主要方法:

  • 聚甲的C-H光化).
  • 材料属性的表征 (结晶性,疏水性).
  • 使用小分子替代物的动力学研究来分析降解率.

主要成果:

  • 聚乙烯的化改变了材料特性,降低了结晶性和疏水性.
  • 尽管水性降低了,但相比于非功能化聚合物,化聚 ((caprolactone) 的降解速度较慢.
  • 动力学研究表明,与基相邻的功能化会减缓水解.

结论:

  • 化是一种可行的方法来修改可生物降解的聚合物,如聚烯.
  • 聚合物功能化可以显著影响降解速率,提供一种控制手段.
  • 分子结构和散装材料特性之间的相互作用对于预测和调节聚合物降解至关重要.