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相关概念视频

Radical Reactivity: Steric Effects01:10

Radical Reactivity: Steric Effects

1.9K
The presence of electron-donating, electron-withdrawing, or conjugating groups adjacent to a radical center, imparts electronic stabilization to the radicals. Examples of such electronically-stabilized radicals are triphenylmethyl, tetramethylpiperidine‐N‐oxide, and 2,2‐diphenyl‐1‐picrylhydrazyl. These radicals are remarkably stable and are known as persistent radicals. Some of the persistent radicals can even be isolated and purified.
Along with electronic...
1.9K
Radical Chain-Growth Polymerization: Mechanism01:09

Radical Chain-Growth Polymerization: Mechanism

2.4K
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...
2.4K
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
Radical Chain-Growth Polymerization: Overview01:10

Radical Chain-Growth Polymerization: Overview

2.3K
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...
2.3K
Radical Reactivity: Overview01:11

Radical Reactivity: Overview

2.0K
Radicals, the highly reactive species, gain stability by undergoing three different reactions. The first reaction involves a radical-radical coupling, in which a radical combines with another radical, forming a spin‐paired molecule. The second reaction is between a radical and a spin‐paired molecule, generating a new radical and a new spin‐paired molecule. The third reaction is radical decomposition in a unimolecular reaction, forming a new radical and a spin‐paired...
2.0K
Free-Radical Chain Reaction and Polymerization of Alkenes02:35

Free-Radical Chain Reaction and Polymerization of Alkenes

7.6K
The conversion of alkenes to macromolecules called polymers is a reaction of high commercial importance. The structure of the polymer is defined by a repeating unit, while the terminal groups are considered insignificant. The average degree of polymerization represents the number of repeating units in the polymer molecule and is denoted by the subscript n.
7.6K

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相关实验视频

Updated: May 13, 2025

Isolating Free Carbenes, their Mixed Dimers and Organic Radicals
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Isolating Free Carbenes, their Mixed Dimers and Organic Radicals

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稳定的二根基衍生的结合基聚合物.

Lingli Zhao1, Hao Liu1, Wenhao Li2

  • 1Hunan University, College of Chemistry and Chemical Engineering,, CHINA.

Angewandte Chemie (International ed. in English)
|May 12, 2025
PubMed
概括
此摘要是机器生成的。

研究人员开发了稳定的结合基聚合物 (RPs),具有非局部化的旋转. 这些材料表现出独特的电子和自旋特性,显示了光电子和量子应用的前景.

关键词:
结合基聚合物 * π-磁化 * 半导体性质 * 量子连贯性质 * 结构-性质关系

更多相关视频

Atom Transfer Radical Polymerization of Functionalized Vinyl Monomers Using Perylene as a Visible Light Photocatalyst
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Atom Transfer Radical Polymerization of Functionalized Vinyl Monomers Using Perylene as a Visible Light Photocatalyst

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Depolymerizable Olefinic Polymers Based on Fused-Ring Cyclooctene Monomers
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Depolymerizable Olefinic Polymers Based on Fused-Ring Cyclooctene Monomers

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相关实验视频

Last Updated: May 13, 2025

Isolating Free Carbenes, their Mixed Dimers and Organic Radicals
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Isolating Free Carbenes, their Mixed Dimers and Organic Radicals

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Atom Transfer Radical Polymerization of Functionalized Vinyl Monomers Using Perylene as a Visible Light Photocatalyst
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Atom Transfer Radical Polymerization of Functionalized Vinyl Monomers Using Perylene as a Visible Light Photocatalyst

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Depolymerizable Olefinic Polymers Based on Fused-Ring Cyclooctene Monomers
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Depolymerizable Olefinic Polymers Based on Fused-Ring Cyclooctene Monomers

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科学领域:

  • 材料科学 材料科学 材料科学
  • 聚合物化学 聚合物化学
  • 量子计算是一种量子计算.

背景情况:

  • 结合基聚合物 (RPs) 对于与自旋相关的冷凝物质物理学和量子应用至关重要.
  • 在合成具有非局部自旋特性的稳定RP方面存在挑战.

研究的目的:

  • 开发一种简单的方法来合成稳定的结合基聚合物.
  • 调查这些新型RP的电子和自旋特性.

主要方法:

  • 通过化二基单体和双化DPP单元的共聚化合成了两种环境稳定结合的RP (RPH和RPC).
  • 描述了RP的旋转移位,电子特性 (近红外吸收,氧化还原行为) 和π-偏磁性.

主要成果:

  • 在RP中实现了有利的旋转移位,其中S=1/2的地面状态.
  • 观察到强烈的近红外吸收 (>1000 nm) 和多阶段的两极性氧化还原特性.
  • 在RPH薄膜中证明了优异的双极载体传输 (移动性高达0.41/0.38cm2V-1s-1) 和显著的室温量子连贯时间 (T1 = 1.88μs,T2 = 218ns).

结论:

  • 引入了一种简单的方法来构建稳定的联RP.
  • 突出了RP的集成电子和自旋特性,用于光电子和量子信息操纵.