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Cationic Chain-Growth Polymerization: Mechanism00:57

Cationic Chain-Growth Polymerization: Mechanism

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The cationic polymerization mechanism consists of three steps: initiation, propagation, and termination. In the initiation step of the polymerization process, the π bond of a monomer gets protonated by the Lewis acid catalyst, which is formed from boron trifluoride and water. The protonation of the π bond generates a carbocation stabilized by the electron‐donating group. In the propagation step, the π bond of the second monomer acts as a nucleophile and attacks the...
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Types of Step-Growth Polymers: Polyesters01:20

Types of Step-Growth Polymers: Polyesters

2.5K
The introduction of polyesters has brought major development to the textile industry. The wrinkle-free behavior of polyester blends has eliminated the need for starching and ironing clothes.
Polyesters are commonly prepared from terephthalic acid and ethylene glycol; the crude product is known as poly(ethylene terephthalate) or PET. However, polyesters are synthesized industrially by transesterification of dimethyl terephthalate with ethylene glycol at 150 °C. The two reactants and the polymer...
2.5K
Polymers02:34

Polymers

40.1K
The word polymer is derived from the Greek words “poly” which means “many” and “mer” which means “parts”. Polymers are long chains of molecules composed of repeating units of smaller molecules, known as monomers. They either occur naturally, such as DNA and proteins, or can be constructed synthetically, like plastics. They have varied structural characteristics, such as linear chains, branched chains, or complex networks, that contribute to the...
40.1K
Anionic Chain-Growth Polymerization: Mechanism01:04

Anionic Chain-Growth Polymerization: Mechanism

2.3K
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...
2.3K
Anionic Chain-Growth Polymerization: Overview01:20

Anionic Chain-Growth Polymerization: Overview

2.4K
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,...
2.4K
Olefin Metathesis Polymerization: Overview01:13

Olefin Metathesis Polymerization: Overview

2.4K
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 of a...
2.4K

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Video Experimental Relacionado

Updated: Dec 25, 2025

Constructing Thioether/Vinyl Sulfide-tethered Helical Peptides Via Photo-induced Thiol-ene/yne Hydrothiolation
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Constructing Thioether/Vinyl Sulfide-tethered Helical Peptides Via Photo-induced Thiol-ene/yne Hydrothiolation

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Redes de tiol-ene de macrómeros de poliuretano definidos por secuencia

Emily A Hoff1, Guilhem X De Hoe2, Christopher M Mulvaney1

  • 1Robert Frederick Smith School of Chemical & Biomolecular Engineering, Cornell University, 120 Olin Hall, Ithaca, New York 14835, United States.

Journal of the American Chemical Society
|March 24, 2020
PubMed
Resumen
Este resumen es generado por máquina.

Los investigadores desarrollaron un método escalable para crear polímeros definidos por secuencia utilizando monómeros basados en vainilina. Este avance permite la síntesis a escala de gramos y revela propiedades dependientes de la secuencia en redes entrelazadas.

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Área de la Ciencia:

  • Química de los polímeros
  • Ciencias de los materiales
  • Síntesis orgánica

Sus antecedentes:

  • Las limitaciones de escalabilidad dificultan las aplicaciones de polímeros definidos por secuencia en plásticos, fibras y compuestos.
  • La influencia de la secuencia de monómeros en las propiedades de las redes entrelazadas es en gran medida desconocida.

Objetivo del estudio:

  • Desarrollar una ruta sintética escalable para producir cantidades de gramos de materiales definidos por secuencia.
  • Investigar el impacto de la secuencia de monómeros en las propiedades de las redes de polímeros reticulados.

Principales métodos:

  • Se utilizaron monómeros de bajo costo y funcionales basados en la vanilina para la síntesis.
  • Se utiliza la aminación reductora secuencial y la carbación para ensamblar oligómeros de poliuretano.
  • Se logra la síntesis a escala de gramos minimizando la purificación cromatográfica y evitando soportes sólidos/líquidos.

Principales resultados:

  • Se han sintetizado con éxito tres oligómeros de poliuretano definidos por secuencia con secuencias de monómeros controladas con precisión.
  • Se ha demostrado la producción a escala de gramos de oligómeros definidos por secuencia.
  • Se observó que la secuencia de monómeros influye en la topología de la red y en los módulos de goma en materiales reticulados.

Conclusiones:

  • Presenta una estrategia sintética escalable para termofijos definidos por secuencia.
  • Destaca el impacto significativo de la secuencia de monómeros en las propiedades del material.
  • Abre nuevas vías para el diseño de materiales poliméricos avanzados con características personalizadas.