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相关概念视频

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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Radical Chain-Growth Polymerization: Overview01:10

Radical Chain-Growth Polymerization: Overview

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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...
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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: Architecture01:14

Polymer Classification: Architecture

2.7K
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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Fixing Double-strand Breaks02:04

Fixing Double-strand Breaks

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The double-stranded structure of DNA has two major advantages. First, it serves as a safe repository of genetic information where one strand serves as the back-up in case the other strand is damaged. Second, the double-helical structure can be wrapped around proteins called histones to form nucleosomes, which can then be tightly wound to form chromosomes. This way, DNA chains up to 2 inches long can be contained within microscopic structures in a cell. A double-stranded break not only damages...
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Phosphodiester Linkages01:01

Phosphodiester Linkages

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Overview
Phosphodiester bond forms when a phosphoric acid molecule (H3PO4) links with two hydroxyl groups (–OH) of two other molecules, forming two ester bonds. Two water molecules are released in this process. The phosphodiester bond is commonly found in nucleic acids (DNA and RNA) and plays a critical role in their structure and function.
Phosphodiester Bonds Link Nucleotides Together
DNA and RNA are polynucleotides or long chains of nucleotides that are linked together. A nucleotide is...
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Updated: Jun 16, 2025

Stretching Short Sequences of DNA with Constant Force Axial Optical Tweezers
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Stretching Short Sequences of DNA with Constant Force Axial Optical Tweezers

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拉伸多态灵活的链条和循环.

Geunho Noh1, Panayotis Benetatos1

  • 1Department of Physics, <a href="https://ror.org/040c17130">Kyungpook National University</a>, Daegu 41566, Republic of Korea.

Physical review. E
|August 20, 2024
PubMed
概括
此摘要是机器生成的。

这项研究模拟了可逆聚合物循环,就像DNA中的循环一样,揭示了独特的弹性和相变. 与简单链相比,多状态循环和拉链表现出不同的行为.

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科学领域:

  • 聚合物物理 聚合物物理
  • 生物物理学的生物物理.
  • 统计力学就是统计力学.

背景情况:

  • 聚合物循环结构在DNA循环和变性等生物过程中是至关重要的.
  • 循环形成改变了聚合物链的弹性特性,由于变化.
  • 可逆循环形成引入了复杂的多态形态行为.

研究的目的:

  • 模拟和分析多态可逆聚合物循环的机械和热力学特性.
  • 为了研究循环和拉链高斯链模型中的力-延伸关系.
  • 为了探索由交替循环和拉链段组成的高斯式项链的相位行为.

主要方法:

  • 开发用于循环和拉链高斯链的理论模型.
  • 在固定延伸 (Helmholtz) 和固定力 (Gibbs) 集群中计算力-延伸关系.
  • 一个高斯式项链模型的力-温度相位图的构造.

主要成果:

  • 与单一链相比,多状态系统具有明显的拉伸弹性和集体不等价性.
  • 这些模型揭示了由可逆循环和拉链形成产生的独特行为.
  • 在高斯式项链中,从循环状态到混合状态的强力诱导相位过渡被确定.

结论:

  • 可逆多态聚合物循环表现出复杂的弹性和集体依赖性质.
  • 理论模型提供了关于生物聚合物在强力作用下的行为的见解.
  • 这些发现表明,聚合物系统中可能存在由力控制的形状变化.