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

Atomic Nuclei: Types of Nuclear Relaxation01:28

Atomic Nuclei: Types of Nuclear Relaxation

1.1K
Nuclear relaxation restores the equilibrium population imbalance and can occur via spin–lattice or spin–spin mechanisms, which are first-order exponential decay processes.
In spin–lattice or longitudinal relaxation, the excited spins exchange energy with the surrounding lattice as they return to the lower energy level. Among several mechanisms that contribute to spin–lattice relaxation, magnetic dipolar interactions are significant. Here, the excited nucleus transfers...
1.1K
Olefin Metathesis Polymerization: Ring-Opening Metathesis Polymerization (ROMP)01:16

Olefin Metathesis Polymerization: Ring-Opening Metathesis Polymerization (ROMP)

3.3K
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...
3.3K
Polymer Classification: Crystallinity01:21

Polymer Classification: Crystallinity

4.1K
Unlike ionic or small covalent molecules, polymers do not form crystalline solids due to the diffusion limitations of their long-chain structures. However, polymers contain microscopic crystalline domains separated by amorphous domains.
Crystalline domains are the regions where polymer chains are aligned in an orderly manner and held together in proximity by intermolecular forces. For example, chains in the crystalline domains of polyethylene and nylon are bound together by van der Waals...
4.1K
Polymer Classification: Stereospecificity01:26

Polymer Classification: Stereospecificity

3.4K
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...
3.4K
Molecular Weight of Step-Growth Polymers01:08

Molecular Weight of Step-Growth Polymers

2.9K
Step growth polymerization involves bi or multifunctional monomers. Bifunctional monomers react to form linear step growth polymers, whereas multifunctional monomers react to form non-linear or branched polymers.
As the step-growth polymerization involves step-wise condensation of monomers, the molecular weight also builds up eventually. Consequently, high molecular weight polymers are obtained at the late stages of the polymerization, where 99% of monomers have been consumed.
The extent of the...
2.9K
Step-Growth Polymerization: Overview01:03

Step-Growth Polymerization: Overview

4.5K
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...
4.5K

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

Modeling the flow-driven disassembly and extensional rheology of end-linking telechelic polymers.

The Journal of chemical physics·2026
Same author

Experimental-data-driven thermal conductivity prediction and inverse composition design for alloys.

RSC advances·2026
Same author

Elongational flow response of compressible polymer melts.

The Journal of chemical physics·2026
Same author

Learning Latent Representations to Bridge Coarse-Grained and Atomistic Resolutions in Polymer Simulations.

Journal of chemical theory and computation·2026
Same author

Shape elasticity in colloidal bent-core liquid crystals.

Soft matter·2026
Same author

From Coils to Rods: Structure and Dynamics of Polyelectrolytes in Water.

ACS macro letters·2026

相关实验视频

Updated: Mar 6, 2026

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

8.5K

在环聚合物融中,中间时间亚扩散和应力松.

Baicheng Mei1,2, Gary S Grest3, Thomas C O'Connor4

  • 1Department of Materials Science and Engineering, University of Illinois, Urbana, Illinois 61801, USA.

The Journal of chemical physics
|March 4, 2026
PubMed
概括

大规模模拟显示,环融动态取决于宏分子,而不是线性链纠. 一个交叉的聚合度 (ND) 成功地组织了动态缩放指数和扩散常数.

更多相关视频

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

4.0K
Controlled Synthesis and Fluorescence Tracking of Highly Uniform PolyN-isopropylacrylamide Microgels
11:34

Controlled Synthesis and Fluorescence Tracking of Highly Uniform PolyN-isopropylacrylamide Microgels

Published on: September 8, 2016

10.8K

相关实验视频

Last Updated: Mar 6, 2026

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

8.5K
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

4.0K
Controlled Synthesis and Fluorescence Tracking of Highly Uniform PolyN-isopropylacrylamide Microgels
11:34

Controlled Synthesis and Fluorescence Tracking of Highly Uniform PolyN-isopropylacrylamide Microgels

Published on: September 8, 2016

10.8K

科学领域:

  • 聚合物物理 聚合物物理
  • 软物质物理学 软物质物理学
  • 计算生物物理学的计算生物物理学

背景情况:

  • 非连锁环融化的动力学对于软材料和细胞生物物理学至关重要.
  • 了解它们的缓慢动态是聚合物科学的关键挑战.

研究的目的:

  • 研究单体和质量中心 (CM) 平均方位位移 (MSD) 和模拟环融体中的应力放松.
  • 分析动态减速使用亚扩散分数时间缩放指数.
  • 探索聚合度和刚度对动态的影响.

主要方法:

  • 模拟模拟环融模型的大规模分子动力学.
  • 对单体和CMMSD以及应力放松功能的分析.
  • 通过分数时间缩放指数来描述动态减速.

主要成果:

  • 动力学不是通过线性链纠 (N/Ne) 组织的.
  • 基于宏分子的交叉聚合度 (ND) 成功地崩了动态缩放指数,并组织了长期的CM自我扩散.
  • 不同的属性表现出不同的指数,具有一个或两个线性变异与log的线性变异模式.
  • 在高N或度的CM-MSD和应力放松指数的交叉表明动态解和激活运输.

结论:

  • 通过ND量化的大分子化,是比N/Ne更有效的措施来组织环融动态.
  • 在高N或度下观察到一种新的动态解和过渡到激活运输.
  • 结果表明潜在的分子间集体对压力的贡献,类似于软体物质.