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Free-Radical Chain Reaction and Polymerization of Alkenes02:35

Free-Radical Chain Reaction and Polymerization of Alkenes

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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.
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Radical Chain-Growth Polymerization: Mechanism01:09

Radical Chain-Growth Polymerization: Mechanism

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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...
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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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Olefin Metathesis Polymerization: Overview01:13

Olefin Metathesis Polymerization: Overview

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Recently, the development of olefin metathesis polymerization advanced the field of polymer synthesis. Simply put, the reorganization of substituents on their double bonds between two olefins in the presence of a catalyst is known as the olefin metathesis reaction. The use of metathesis reaction for polymer synthesis is called olefin metathesis polymerization.
Ruthenium-based Grubbs catalyst is the most commonly used catalyst for olefin metathesis polymerization. Grubbs catalyst consists...
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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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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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通过RAFT交换机的聚合物功能化.

Owen Reid Courtney1, Samantha Marie Clouthier1, Sébastien Perrier2,3

  • 1Department of Chemistry, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina 27599-3290, United States.

ACS macro letters
|September 14, 2023
PubMed
概括
此摘要是机器生成的。

本研究介绍了一种简单的方法,用于聚合物终端组功能化,使用可逆添加碎片化链转移 (RAFT) 聚合. 这种技术有效地引入了多个多样化的功能组,简化了聚合物修饰和分析.

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科学领域:

  • 聚合物化学 聚合物化学
  • 宏观分子科学 宏观分子科学

背景情况:

  • 精确控制聚合物架构和功能对于先进的材料应用至关重要.
  • 聚合物终端组修改的传统方法可能是复杂的,范围有限的.

研究的目的:

  • 开发一种简单而通用的方法,用于聚合物的终端组功能化.
  • 展示如何同时引入多种多样化的功能.
  • 建立一种替代分析方法来确定功能化程度.

主要方法:

  • 使用可逆添加碎片化链转移 (RAFT) 聚合的交换过程.
  • 采用RAFT链传递剂 (CTA) 进行聚合物终端组的修改.
  • 分析反应上游剂以量化功能化程度.

主要成果:

  • 成功实现了线性聚合物和接种共聚合物的终端组功能化.
  • 已证明具有很高的功能组耐受性,使其能够引入广泛的功能.
  • 展示了多个功能组的同时安装.
  • 验证了反应超剂的使用,作为确定功能化程度的可靠方法.

结论:

  • 开发的基于RAFT的交换过程为聚合物终端组功能化提供了一种简单,高效和多用途的方法.
  • 这种方法促进了多样化和多重功能的引入,扩大了聚合物设计的可能性.
  • 超分析为量化聚合物功能化提供了一个实用的替代方案.