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Free-Radical Chain Reaction and Polymerization of Alkenes02:35

Free-Radical Chain Reaction and Polymerization of Alkenes

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.
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 Reactivity: Overview01:11

Radical Reactivity: Overview

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 molecule. These three...
Radical Reactivity: Electrophilic Radicals01:02

Radical Reactivity: Electrophilic Radicals

Radicals adjacent to electron‐withdrawing groups are called electrophilic radicals. These radicals readily react with nucleophilic alkenes. For example, the malonate radical, in which the radical center is flanked by two electron‐withdrawing groups, reacts readily with butyl vinyl ether, which consists of an electron‐donating oxygen substituent. The reaction between electrophilic malonate radical and nucleophilic vinyl ether is favored because the radical has a low‐energy SOMO, which interacts...
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...

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Updated: Jun 3, 2026

Atom Transfer Radical Polymerization of Functionalized Vinyl Monomers Using Perylene as a Visible Light Photocatalyst
06:49

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

Published on: April 22, 2016

La polimerización radical por transferencia atómica mediada electroquímicamente mediante transferencia atómica.

Andrew J D Magenau1, Nicholas C Strandwitz, Armando Gennaro

  • 1Center for Macromolecular Engineering, Department of Chemistry, Carnegie Mellon University, 4400 Fifth Avenue, Pittsburgh, PA 15213, USA.

Science (New York, N.Y.)
|April 2, 2011
PubMed
Resumen

El potencial electroquímico controla de manera reversible la polimerización radical de transferencia atómica mediante el uso de un catalizador de cobre. Este método permite la sintonización en tiempo real de la cinética de polimerización y la síntesis de polímeros vivos con un alto control.

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Área de la Ciencia:

  • Química de Polímeros La Química de Polímeros es la química de los polímeros.
  • La electroquímica es electroquímica.
  • La catálisis es la catálisis.

Sus antecedentes:

  • La polimerización radical por transferencia atómica (ATRP) ofrece un control preciso de las propiedades del polímero.
  • Los métodos ATRP existentes a menudo requieren condiciones específicas y el manejo del catalizador.
  • El desarrollo de sistemas ATRP sintonizables externamente es crucial para la síntesis avanzada de polímeros.

Objetivo del estudio:

  • Para demostrar el control electroquímico sobre el ATRP.
  • Para lograr la modulación en tiempo real de la cinética de polimerización.
  • Para permitir la polimerización viva utilizando un catalizador activado electroquímicamente.

Principales métodos:

  • Utilizando un catalizador de cobre (Cu ((II) / Ligand) activado por una reducción de un electrón a través del potencial electroquímico aplicado.
  • Modulación de las tasas de polimerización mediante el ajuste de la magnitud del potencial aplicado.
  • Empleando potenciales intermitentes de varios pasos para iniciar y controlar la polimerización.

Principales resultados:

  • La activación reversible del catalizador de cobre por el potencial electroquímico.
  • Ajustabilidad en tiempo real de la cinética de polimerización a través de la modulación de potencial.
  • Polimerización viva exitosa con pesos moleculares controlados y distribuciones estrechas en bajas concentraciones de catalizador (50 ppm).

Conclusiones:

  • El control electroquímico proporciona un nuevo método externo para la gestión de ATRP.
  • Este enfoque ofrece una manipulación precisa y en tiempo real de los procesos de polimerización.
  • El método desarrollado es eficiente, ya que permite la síntesis controlada de polímeros con un mínimo de catalizadores.