Jove
Visualize
Contáctanos
JoVE
x logofacebook logolinkedin logoyoutube logo
ACERCA DE JoVE
Visión GeneralLiderazgoBlogCentro de Ayuda JoVE
AUTORES
Proceso de PublicaciónConsejo EditorialAlcance y PolíticasRevisión por ParesPreguntas FrecuentesEnviar
BIBLIOTECARIOS
TestimoniosSuscripcionesAccesoRecursosConsejo Asesor de BibliotecasPreguntas Frecuentes
INVESTIGACIÓN
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchivo
EDUCACIÓN
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualCentro de Recursos para ProfesoresSitio de Profesores
Términos y Condiciones de Uso
Política de Privacidad
Políticas

Videos de Conceptos Relacionados

Cationic Chain-Growth Polymerization: Mechanism00:57

Cationic Chain-Growth Polymerization: Mechanism

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 generated carbocation,...
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...
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.
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,...
Olefin Metathesis Polymerization: Overview01:13

Olefin Metathesis Polymerization: Overview

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...
Step-Growth Polymerization: Overview01:03

Step-Growth Polymerization: Overview

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...

También podría leer

Artículos Relacionados

Artículos vinculados a este trabajo por autores compartidos, revista y gráfico de citas.

Ordenar por
Same author

Visualizing Interfacial Charge Trapping in a Heterostructure of a Monolayer Metal-Organic Framework on a van der Waals Substrate.

Journal of the American Chemical Society·2026
Same author

Kondo Chains of Organic Radicals on Metallic Surfaces: A Model System of Heavy Fermion Quantum Criticality.

Journal of the American Chemical Society·2025
Same author

Kondo Resonance of a Carbon-Centered Radical in a Single-Molecule Junction.

Journal of the American Chemical Society·2025
Same author

Variable π-d orbital hybridization in 2D transition metal-organic frameworks.

Nanoscale·2025
Same author

A Mixed-Valence and Mixed-Spin Two-Dimensional Ferromagnetic Metal-Organic Coordination Framework.

ACS nano·2025
Same author

Single-Molecule Resolved Conformational and Orbital Symmetry Breaking in Tetraphenylethylene-Based Macrocycles.

Journal of the American Chemical Society·2024
Same journal

Radical Cascades on Seawater Microdroplets Drive Atmospheric Mercury Oxidation.

Journal of the American Chemical Society·2026
Same journal

Superior Selective and Fast NH<sub>3</sub> Adsorption of Soft Porous MOF/Ionic Liquid Composites with Ordering Phase Transitions.

Journal of the American Chemical Society·2026
Same journal

Systematic Catalyst Variation for Improved Stereoselective Epoxide Polymerization: Subtle Modifications Resulting in Superior Efficiency.

Journal of the American Chemical Society·2026
Same journal

Deciphering the Halide Chemistry of Cl<sup>-</sup> and Br<sup>-</sup> in Enhancing Kinetics of Mg Plating/Stripping.

Journal of the American Chemical Society·2026
Same journal

Electrosynthesis of C<sub>6</sub> Chemicals by Propylene Oxidative Coupling on Au Surface.

Journal of the American Chemical Society·2026
Same journal

Statistical AI Enables Precise Screening of Multielement Catalysts.

Journal of the American Chemical Society·2026
Ver todos los artículos relacionados

Video Experimental Relacionado

Updated: May 14, 2026

Synthesis and Characterization of Self-Assembled Metal-Organic Framework Monolayers Using Polymer-Coated Particles
06:48

Synthesis and Characterization of Self-Assembled Metal-Organic Framework Monolayers Using Polymer-Coated Particles

Published on: June 14, 2024

Polymerización de dirección en superficie con plantilla dirigida a metal.

Tao Lin1, Xue Song Shang, Jinne Adisoejoso

  • 1Department of Physics, The Hong Kong University of Science and Technology, Clear Water Bay, Hong Kong, China.

Journal of the American Chemical Society
|February 23, 2013
PubMed
Resumen
Este resumen es generado por máquina.

Las plantillas dirigidas al metal permiten una polimerización controlada en la superficie, lo que produce estructuras de porfirina macromoleculares uniformes. Este avance en la síntesis de abajo hacia arriba ofrece macromoléculas ordenadas y de tamaño específico en las superficies.

Más Videos Relacionados

Using Polystyrene-block-poly(acrylic acid)-coated Metal Nanoparticles as Monomers for Their Homo- and Co-polymerization
09:02

Using Polystyrene-block-poly(acrylic acid)-coated Metal Nanoparticles as Monomers for Their Homo- and Co-polymerization

Published on: July 9, 2015

3D Printing and In Situ Surface Modification via Type I Photoinitiated Reversible Addition-Fragmentation Chain Transfer Polymerization
07:28

3D Printing and In Situ Surface Modification via Type I Photoinitiated Reversible Addition-Fragmentation Chain Transfer Polymerization

Published on: February 18, 2022

Videos de Experimentos Relacionados

Last Updated: May 14, 2026

Synthesis and Characterization of Self-Assembled Metal-Organic Framework Monolayers Using Polymer-Coated Particles
06:48

Synthesis and Characterization of Self-Assembled Metal-Organic Framework Monolayers Using Polymer-Coated Particles

Published on: June 14, 2024

Using Polystyrene-block-poly(acrylic acid)-coated Metal Nanoparticles as Monomers for Their Homo- and Co-polymerization
09:02

Using Polystyrene-block-poly(acrylic acid)-coated Metal Nanoparticles as Monomers for Their Homo- and Co-polymerization

Published on: July 9, 2015

3D Printing and In Situ Surface Modification via Type I Photoinitiated Reversible Addition-Fragmentation Chain Transfer Polymerization
07:28

3D Printing and In Situ Surface Modification via Type I Photoinitiated Reversible Addition-Fragmentation Chain Transfer Polymerization

Published on: February 18, 2022

Área de la Ciencia:

  • Ciencia de los materiales Ciencia de los materiales.
  • Química de las superficies.
  • Química supramolecular de las moléculas.

Sus antecedentes:

  • La polimerización en superficie es un método de abajo hacia arriba para crear estructuras macromoleculares.
  • Los métodos actuales a menudo resultan en amplias distribuciones de tamaño y adsorción desordenada.

Objetivo del estudio:

  • Desarrollar una estrategia para la polimerización controlada en la superficie utilizando plantillas dirigidas hacia el metal.
  • Para sintetizar estructuras macromoleculares de porfirina con distribución de tamaño estrecho y alto orden.

Principales métodos:

  • Utilizó un precursor bifuncional con grupos finales de piridil y bromo.
  • Empleó una estrategia de plantilla lineal basada en la coordinación piridil-Cu-piridil en una superficie Au111.
  • Investigó la polimerización utilizando microscopía de túnel de barrido y simulaciones cinéticas de Monte Carlo.

Principales resultados:

  • Se logró el acoplamiento controlado de Ullmann de monómeros a través de la plantilla dirigida por metal.
  • Estructuras de porfirina macromoleculares sintetizadas con una distribución de tamaño estrecho.
  • Demostró el papel del cobre en la catalización de la formación de enlaces C-C, el control del tamaño y la organización de las estructuras.

Conclusiones:

  • La plantilla dirigida por metal ofrece un control preciso sobre la polimerización en la superficie.
  • Este método permite la síntesis de porfirinas macromoleculares altamente ordenadas y específicas de tamaño.
  • El enfoque avanza en la fabricación de abajo hacia arriba de arquitecturas macromoleculares funcionales.