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

Characteristics and Nomenclature of Copolymers01:24

Characteristics and Nomenclature of Copolymers

2.5K
Copolymers are the products obtained from the polymerization of multiple monomer species. So, in a polymer chain itself, there can be multiple repeating units that come from different monomers. The process of synthesizing a polymer from different monomer species is called copolymerization. When two monomers are involved, the polymer is known as a bipolymer. Polymers with three and four monomers are termed terpolymers and quaterpolymers, respectively. Figure 1 depicts the copolymerization of...
2.5K
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
Radical Chain-Growth Polymerization: Overview01:10

Radical Chain-Growth Polymerization: Overview

2.4K
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...
2.4K
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
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
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

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

Linear Amphiphilic P(BzMA-co-DMAEMA) Statistical Copolymers: Synthesis via RAFT Polymerization and Formation of Nanoassemblies in Aqueous Media.

Polymers·2026
Same author

Ex Vivo Characterization and In Vivo Nasal Delivery of Ropinirole-Loaded PEO-b-PCL/Tween 80/β-Cyclodextrin Systems in C57BL/6J Mice.

Molecules (Basel, Switzerland)·2026
Same author

Effect of Ion Specificity on the Interfacial Behavior of Amphiphilic Hyperbranched Copolymer H-P(OEGMA-<i>co</i>-LMA).

The journal of physical chemistry. B·2026
Same author

Self-Assembled (Nano)Structures of Human Serum Albumin with Thermoresponsive Chitosan-<i>g</i>-PNIPAM Graft Copolymer.

Polymers·2026
Same author

Synthesis of Comb-like and Coil-Comb Polystyrene-Polyglycidol Copolymers via Click Chemistry: Self-Assembly and Biological Evaluation.

Polymers·2026
Same author

Amylopectin Copolymers Grafted with RAFT-Obtained Synthetic Polymers: Synthesis and Aqueous Solution Behavior.

Biomacromolecules·2026
Same journal

RETRACTED: Alshabanah et al. Elastic Nanofibrous Membranes for Medical and Personal Protection Applications: Manufacturing, Anti-COVID-19, and Anti-Colistin Resistant Bacteria Evaluation. <i>Polymers</i> 2021, <i>13</i>, 3987.

Polymers·2026
Same journal

Correction: Kang et al. Energy-Saving Electrospinning with a Concentric Teflon-Core Rod Spinneret to Create Medicated Nanofibers. <i>Polymers</i> 2020, <i>12</i>, 2421.

Polymers·2026
Same journal

Influence of Self-Adhesive Resin Composite Deep Marginal Elevation on the Sealing Ability of CAD/CAM Lithium Disilicate Glass-Ceramic Inlays: An In Vitro Study.

Polymers·2026
Same journal

Modulating Exciton Dynamics Through Fluorescent Side Group Incorporation in Benzodithiophene-Benzotriazole-Isoindigo Terpolymers.

Polymers·2026
Same journal

PLA/PBSA Biocomposites Reinforced with Tangerine Tree-Derived Agro-Industrial Waste for Rigid Packaging: Effect of Extraction Treatment on Morphology and Thermo-Mechanical Performance.

Polymers·2026
Same journal

Synergistic Coatings Based on Chitosan and <i>Eugenia caryophyllata</i> Essential Oil to Improve Postharvest Quality of <i>Capsicum chinense</i>.

Polymers·2026
查看所有相关文章

相关实验视频

Updated: Jun 25, 2025

Facile and Efficient Preparation of Tri-component Fluorescent Glycopolymers via RAFT-controlled Polymerization
10:54

Facile and Efficient Preparation of Tri-component Fluorescent Glycopolymers via RAFT-controlled Polymerization

Published on: June 19, 2015

9.7K

通过RAFT聚合的四组件统计共聚合物.

Dimitrios Vagenas1, Stergios Pispas1

  • 1Theoretical and Physical Chemistry Institute, National Hellenic Research Foundation, 48 Vassileos Constantinou Avenue, 11635 Athens, Greece.

Polymers
|May 25, 2024
PubMed
概括
此摘要是机器生成的。

研究人员开发了新的甲基酸共聚合物来模仿蛋白质的行为. 这些合成聚合物在生物流体中表现出自我组装和稳定性,提供了潜在的生物材料应用.

关键词:
在RAFT的聚合物化过程中,两性共聚物是两性共聚物.生物灵感聚合物是生物灵感聚合物.多元组件聚合物的聚合物.聚电解质的电解质是多电解质的蛋白质是一种蛋白质.响应性共聚合物 响应性共聚合物统计共聚合物 统计共聚合物

更多相关视频

Synthesis of Monodisperse Cylindrical Nanoparticles via Crystallization-driven Self-assembly of Biodegradable Block Copolymers
11:42

Synthesis of Monodisperse Cylindrical Nanoparticles via Crystallization-driven Self-assembly of Biodegradable Block Copolymers

Published on: June 20, 2019

7.8K
Facile Synthesis of Worm-like Micelles by Visible Light Mediated Dispersion Polymerization Using Photoredox Catalyst
07:39

Facile Synthesis of Worm-like Micelles by Visible Light Mediated Dispersion Polymerization Using Photoredox Catalyst

Published on: June 8, 2016

9.5K

相关实验视频

Last Updated: Jun 25, 2025

Facile and Efficient Preparation of Tri-component Fluorescent Glycopolymers via RAFT-controlled Polymerization
10:54

Facile and Efficient Preparation of Tri-component Fluorescent Glycopolymers via RAFT-controlled Polymerization

Published on: June 19, 2015

9.7K
Synthesis of Monodisperse Cylindrical Nanoparticles via Crystallization-driven Self-assembly of Biodegradable Block Copolymers
11:42

Synthesis of Monodisperse Cylindrical Nanoparticles via Crystallization-driven Self-assembly of Biodegradable Block Copolymers

Published on: June 20, 2019

7.8K
Facile Synthesis of Worm-like Micelles by Visible Light Mediated Dispersion Polymerization Using Photoredox Catalyst
07:39

Facile Synthesis of Worm-like Micelles by Visible Light Mediated Dispersion Polymerization Using Photoredox Catalyst

Published on: June 8, 2016

9.5K

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
  • 生物材料是一种生物材料.

背景情况:

  • 蛋白质在生物系统中起着至关重要的作用,但需要合成替代品.
  • 开发模仿蛋白质行为的合成大分子是一个重大挑战.

研究的目的:

  • 为了合成和描述新的多元组件,基于甲基酸盐的统计共聚物.
  • 研究这些共聚合物在水溶液中的自我组装行为和合体稳定性.
  • 评估它们作为蛋白质模仿者的潜力以及它们在生物流体环境中的生物相容性.

主要方法:

  • 可逆添加碎片化链转移 (RAFT) 聚合用于合成线性和超分支四聚合物.
  • 使用1H-NMR和ATR-FTIR光谱学进行表征.
  • 使用动态光散射 (DLS),电泳光散射 (ELS) 和光谱学 (FS) 的行为研究.

主要成果:

  • 成功合成了具有受控分子架构的统计四聚合物.
  • 在水溶液中表现出自我组装行为和聚合物形成.
  • 在胎儿牛血清/酸盐缓冲盐水 (FBS/PBS) 溶液中表现出合稳定性和生物相容性.

结论:

  • 合成的甲基酸基四聚合物显示出作为蛋白质模仿剂的前景.
  • 大分子拓学影响自我组装和溶液的行为.
  • 这些共聚合物具有潜在生物材料应用的有利特性.