Jove
Visualize
Contáctanos

Videos de Conceptos Relacionados

Radical Formation: Overview01:03

Radical Formation: Overview

2.1K
A bond can be broken either by heterolytic bond cleavage to form ions or homolytic bond cleavage to yield radicals. A fishhook arrow is used to represent the motion of a single electron in homolytic bond cleavage. There are two main sources from which radicals can be formed:
Radicals from spin-paired molecules:
Radicals can be obtained from spin-paired molecules either by homolysis or electron transfer. While two radicals are formed in the former, an electron is added in the...
2.1K
Radical Reactivity: Overview01:11

Radical Reactivity: Overview

2.1K
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...
2.1K
Radical Formation: Addition00:47

Radical Formation: Addition

1.7K
Radicals can be formed by adding a radical to a spin-paired molecule. This is typically observed with unsaturated species, where the addition of a radical across the π bond leads to the production of a new radical by dissolving the π bond. For example, the addition of a Br radical to an alkene yields a carbon-centered radical.
Similar to charge conservation in chemical reactions, spin conservation is implicit for radical reactions. Accordingly, the product formed must possess an...
1.7K
Radical Reactivity: Intramolecular vs Intermolecular01:33

Radical Reactivity: Intramolecular vs Intermolecular

1.8K
Radical reactions can occur either intermolecularly or intramolecularly. In an intermolecular radical reaction, a nucleophilic radical adds to an electrophilic alkene or vice versa. In such reactions, the radical and generally the alkene, which is also called the radical trap, are two different molecules. Additionally, for such intermolecular reactions to occur, the radical trap must be active, present in an excess concentration, and the radical starting material must have a weak...
1.8K
Radical Formation: Homolysis00:54

Radical Formation: Homolysis

3.6K
A bond is formed between two atoms by sharing two electrons. When this bond is broken by supplying sufficient energy, either two electrons can be taken up by one atom forming ions by the cleavage called heterolysis, or the two electrons are shared by two atoms, with one each creating radicals by the cleavage called homolysis.
3.6K
Radical Formation: Abstraction00:47

Radical Formation: Abstraction

3.5K
The electron of an atom can be abstracted from a compound by a relatively unstable radical to generate a new radical of relatively greater stability. For example, an initiator which forms radicals by homolysis can abstract a suitable species like a hydrogen atom or a halogen atom from a compound to generate a new radical. This ability of radicals to propagate by abstraction is a crucial feature of radical chain reactions.
Even though homolysis produces radicals, it is different from radical...
3.5K

También podría leer

Artículos Relacionados

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

Ordenar por
Same author

Amplified chiroptic response in a multi-helical penta-perylene structure.

Chemical science·2026
Same author

Designing effective single-molecule electromagnets with radially π-conjugated carbon structures.

Nature communications·2026
Same author

Scanning Tunneling Microscope-Based Break-Junction TechniqueA Tutorial.

ACS physical chemistry Au·2026
Same author

A Computationally Efficient and Accurate Method for Predicting Conductance of Single-Molecule Junctions.

Nano letters·2026
Same author

Dual activation of MC3R and MC4R drives weight loss and reduces food intake in male primates with obesity.

Nature communications·2026
Same author

Strong Coupling in Orthogonal Nanographenes.

Chemistry (Weinheim an der Bergstrasse, Germany)·2026
Same journal

Linker Engineering toward NIR-II Metal-Organic Framework with Maximal Emission beyond 1000 nm for Inflammatory Bowel Disease Imaging.

Journal of the American Chemical Society·2026
Same journal

Observing Kinetic Selectivity in Anthracene Photodimerization through Selective Quenching by Excited States of Proximate Rare Earth Cations.

Journal of the American Chemical Society·2026
Same journal

Sequence-Dependent Folding of Recognition-Encoded Melamine Oligomers.

Journal of the American Chemical Society·2026
Same journal

Large Thermo- and Mechanosalient Actuation via Cooperative Twist Elasticity-Induced Packing Motif Conversion.

Journal of the American Chemical Society·2026
Same journal

Discovery and Biosynthesis of Lanthipeptides Featuring an Azepinoindole Scaffold by Radical <i>S</i>-Adenosylmethionine Enzyme-Catalyzed C-C Bond Formation.

Journal of the American Chemical Society·2026
Same journal

Enantiopurity-Controlled Magnetism in a Two-Dimensional Organic-Inorganic Material.

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

Video Experimental Relacionado

Updated: Jul 19, 2025

Single-Molecule F&#246;rster Resonance Energy Transfer Methods for Real-Time Investigation of the Holliday Junction Resolution by GEN1
11:27

Single-Molecule Förster Resonance Energy Transfer Methods for Real-Time Investigation of the Holliday Junction Resolution by GEN1

Published on: September 18, 2019

9.5K

Conexiones radicales de una sola molécula

Liang Li1, Claudia R Prindle1, Wanzhuo Shi1

  • 1Department of Chemistry, Columbia University, New York, New York 10027, United States.

Journal of the American Chemical Society
|August 9, 2023
PubMed
Resumen
Este resumen es generado por máquina.

Los radicales estables ofrecen propiedades electrónicas únicas para dispositivos moleculares y espíntrónica. Esta perspectiva describe los principios de diseño para crear radicales estables y comprender su comportamiento en las uniones moleculares.

Más Videos Relacionados

All-electronic Nanosecond-resolved Scanning Tunneling Microscopy: Facilitating the Investigation of Single Dopant Charge Dynamics
11:33

All-electronic Nanosecond-resolved Scanning Tunneling Microscopy: Facilitating the Investigation of Single Dopant Charge Dynamics

Published on: January 19, 2018

9.7K
Combining Single-molecule Manipulation and Imaging for the Study of Protein-DNA Interactions
14:43

Combining Single-molecule Manipulation and Imaging for the Study of Protein-DNA Interactions

Published on: August 27, 2014

11.6K

Videos de Experimentos Relacionados

Last Updated: Jul 19, 2025

Single-Molecule F&#246;rster Resonance Energy Transfer Methods for Real-Time Investigation of the Holliday Junction Resolution by GEN1
11:27

Single-Molecule Förster Resonance Energy Transfer Methods for Real-Time Investigation of the Holliday Junction Resolution by GEN1

Published on: September 18, 2019

9.5K
All-electronic Nanosecond-resolved Scanning Tunneling Microscopy: Facilitating the Investigation of Single Dopant Charge Dynamics
11:33

All-electronic Nanosecond-resolved Scanning Tunneling Microscopy: Facilitating the Investigation of Single Dopant Charge Dynamics

Published on: January 19, 2018

9.7K
Combining Single-molecule Manipulation and Imaging for the Study of Protein-DNA Interactions
14:43

Combining Single-molecule Manipulation and Imaging for the Study of Protein-DNA Interactions

Published on: August 27, 2014

11.6K

Área de la Ciencia:

  • La electrónica molecular
  • Espintrónica orgánica
  • Ciencias de los materiales

Sus antecedentes:

  • Los radicales poseen estructuras electrónicas de caparazón abierto únicas, lo que los hace prometedores para dispositivos electrónicos.
  • Las aplicaciones incluyen conducción eléctrica y conmutación en circuitos moleculares y espintrónica molecular.
  • Existen desafíos en la síntesis de radicales estables y la caracterización de sus propiedades dentro de las uniones moleculares.

Objetivo del estudio:

  • Proporcionar principios de diseño para la síntesis de radicales estables adecuados para las uniones moleculares.
  • Ofrecer conocimientos actuales sobre las propiedades electrónicas de los radicales en dispositivos de una sola molécula.
  • Fomentar la investigación y el desarrollo de sistemas moleculares basados en radicales.

Principales métodos:

  • Revisión de las propiedades químicas y físicas de los sistemas radicales establecidos.
  • Análisis de los principios de diseño para la síntesis radical.
  • Exploración del comportamiento radical en las uniones moleculares y dispositivos de una sola molécula.

Principales resultados:

  • Los sistemas radicales establecidos muestran potencial para la electrónica molecular y la espintrónica.
  • Los principios de diseño pueden guiar la creación de radicales estables para aplicaciones específicas.
  • Comprender las propiedades radicales en las uniones moleculares es crucial para el desarrollo de dispositivos.

Conclusiones:

  • Los radicales estables son componentes clave para el avance de la electrónica molecular y la espintrónica.
  • Una mayor investigación sobre la síntesis y las propiedades de los radicales acelerará el desarrollo de nuevos dispositivos moleculares.
  • Esta perspectiva sirve como guía para los investigadores en el campo de los sistemas moleculares basados en radicales.