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Molecular Weight of Step-Growth Polymers01:08

Molecular Weight of Step-Growth Polymers

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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...
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Polymer Classification: Architecture01:14

Polymer Classification: Architecture

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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...
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Step-Growth Polymerization: Overview01:03

Step-Growth Polymerization: Overview

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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...
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Polymer Classification: Stereospecificity01:26

Polymer Classification: Stereospecificity

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

Radical Chain-Growth Polymerization: Chain Branching

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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...
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Relaxation of Skeletal Muscles

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The period of muscle contraction primarily influences the duration of stimulation at the neuromuscular junction (NMJ), the presence of free calcium ions in the sarcoplasm, and the availability of energy or ATP to support contractions.
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DNA Nanotubes as a Versatile Tool to Study Semiflexible Polymers
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测序定义的聚合物的细分放松.

Karin J Bichler1, Bruno Jakobi1, Gerald J Schneider1,2

  • 1Department of Chemistry, Louisiana State University, Baton Rouge, LA 70803, United States of America.

Journal of physics. Condensed matter : an Institute of Physics journal
|December 2, 2023
PubMed
概括

该研究使用介电光谱学研究了测序定义的聚合物P(CnEG4). 结果显示,聚合物动态受分子量和C单元长度的影响,影响细分放松和玻璃过渡温度.

科学领域:

  • 聚合物科学 聚合物科学
  • 材料科学 材料科学 材料科学
  • 物理化学 物理化学

背景情况:

  • 了解聚合物动态对于设计具有特定性质的材料至关重要.
  • 序列定义的聚合物可以精确控制聚合物架构和行为.
  • 介电光谱是一种强大的工具,用于探测聚合物放松动态.

研究的目的:

  • 为了研究序列定义的聚合物的动态行为 P(CnEG4).
  • 了解分子量和C单元长度对聚合物放松的影响.
  • 为了将细分放松与玻璃过渡温度相关联.

主要方法:

  • 介电光谱学被用来研究动态行为.
  • 细分和二次放松过程的分析.
  • 确定放松时间和玻璃过渡温度.

主要成果:

  • 观察到一个细分放松和一个二次放松.
  • 细分放松时间取决于低温时的分子量,但在高温时这种效应会减弱.
  • 增加C单元的长度加快了细分放松,并降低了玻璃过渡温度.

结论:

关键词:
介电光谱学是一种介电光谱学.细分放松放松的部分.测序定义的聚合物.

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  • 聚合物P(CnEG4) 的动态行为对分子量和序列长度敏感.
  • 随着C单元长度的增加,加速的细分松会导致更低的玻璃过渡温度.
  • 这些发现提供了对测序定义的聚合物的结构性质关系的见解.