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相关概念视频

Radical Chain-Growth Polymerization: Overview01:10

Radical Chain-Growth Polymerization: Overview

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...
Radical Chain-Growth Polymerization: Mechanism01:09

Radical Chain-Growth Polymerization: Mechanism

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 species into the...
Radical Chain-Growth Polymerization: Chain Branching01:17

Radical Chain-Growth Polymerization: Chain Branching

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...
Anionic Chain-Growth Polymerization: Overview01:20

Anionic Chain-Growth Polymerization: Overview

The polymerization process that involves carbanion as an intermediate is called anionic polymerization. It is also a type of addition or chain-growth polymerization. Anionic polymerization gets initiated by a strong nucleophile such as an organolithium or a Grignard reagent. The most commonly used initiator for anionic polymerization is butyl lithium. Monomers involved in anionic polymerization must possess a vinyl group bonded to one or two electron-withdrawing groups. For instance,...
Anionic Chain-Growth Polymerization: Mechanism01:04

Anionic Chain-Growth Polymerization: Mechanism

The mechanism for anionic chain-growth polymerization involves initiation, propagation, and termination steps. In the initiation step, a nucleophilic anion, such as butyl lithium, initiates the polymerization process by attacking the π bond of the vinylic monomer. As a result, a carbanion, stabilized by the electron‐withdrawing group, is generated. The resulting carbanion acts as a Michael donor in the propagation step and attacks the second vinylic monomer, which acts as a Michael acceptor.
Ziegler–Natta Chain-Growth Polymerization: Overview01:17

Ziegler–Natta Chain-Growth Polymerization: Overview

Ziegler–Natta polymerization is another form of addition or chain‐growth polymerization used for synthesizing linear polymers over branched polymers. The catalyst used for polymerization is the Ziegler–Natta catalyst, named after Karl Ziegler and Giulio Natta, who developed it in 1953. This catalyst is an organometallic complex of titanium tetrachloride and triethyl aluminum, with the active form of the catalyst being an alkyl titanium compound. Using the Ziegler–Natta catalyst, high molecular...

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Synthesis of Information-bearing Peptoids and their Sequence-directed Dynamic Covalent Self-assembly
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循环聚合物的"无尽"路线.

Christopher W Bielawski1, Diego Benitez, Robert H Grubbs

  • 1Arnold and Mabel Beckman Laboratories of Chemical Synthesis, Division of Chemistry and Chemical Engineering, California Institute of Technology, Pasadena, CA 91125, USA.

Science (New York, N.Y.)
|September 21, 2002
PubMed
概括
此摘要是机器生成的。

一种新的聚合法通过将链末连接到金属复合物来创建循环聚合物. 这种方法简化了纯循环聚合物的生产,克服了传统方法的局限性.

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科学领域:

  • 聚合物化学 聚合物化学
  • 宏分子科学 宏分子科学
  • 有机合成 有机合成

背景情况:

  • 循环聚合物的传统宏循环化策略通常需要线性聚合物前体和高稀释条件.
  • 这些传统方法存在重大缺点,阻碍了大量纯循环材料的高效生产.
  • 对新型宏分子支架的需求日益增加,以满足商业聚合物新兴应用的需求.

研究的目的:

  • 开发一种新的合成路径,用于生产循环聚合物.
  • 克服与传统的宏循环化技术相关的局限性.
  • 为先进的聚合物应用提供方便访问独特的宏分子结构.

主要方法:

  • 开发了一种新的聚合过程,在这种过程中,不断增长的聚合物链末端仍然与金属复合体协调.
  • 这种in-situ循环化策略可以避免需要预先形成的线性前体.
  • 该方法消除了通常用于宏循环的高稀释条件的要求.

主要成果:

  • 开发的合成路径成功生产了循环聚合物.
  • 这种方法有效地消除了生产大量纯循环材料的障碍.
  • 合成了循环聚乙烯,与它们的线性对应物相比,它们表现出明显的物理特性.

结论:

  • 已经建立了一种新的,高效的合成循环聚合物的方法.
  • 这一策略促进了纯循环聚合物的生产,提供了独特的宏分子支架.
  • 合成的循环聚合物表现出独特的特性,表明了新的商业应用的潜力.