Jove
Visualize
Contáctanos

Videos de Conceptos Relacionados

Photochemical Electrocyclic Reactions: Stereochemistry01:26

Photochemical Electrocyclic Reactions: Stereochemistry

The absorption of UV–visible light by conjugated systems causes the promotion of an electron from the ground state to the excited state. Consequently, photochemical electrocyclic reactions proceed via the excited-state HOMO rather than the ground-state HOMO. Since the ground- and excited-state HOMOs have different symmetries, the stereochemical outcome of electrocyclic reactions depends on the mode of activation; i.e., thermal or photochemical.
Selection Rules: Photochemical Activation
Thermal and Photochemical Electrocyclic Reactions: Overview01:26

Thermal and Photochemical Electrocyclic Reactions: Overview

Electrocyclic reactions are reversible reactions. They involve an intramolecular cyclization or ring-opening of a conjugated polyene. Shown below are two examples of electrocyclic reactions. In the first reaction, the formation of the cyclic product is favored. In contrast, in the second reaction, ring-opening is favored due to the high ring strain associated with cyclobutene formation.
Crystal Field Theory - Tetrahedral and Square Planar Complexes02:46

Crystal Field Theory - Tetrahedral and Square Planar Complexes

Tetrahedral Complexes
Crystal field theory (CFT) is applicable to molecules in geometries other than octahedral. In octahedral complexes, the lobes of the dx2−y2 and dz2 orbitals point directly at the ligands. For tetrahedral complexes, the d orbitals remain in place, but with only four ligands located between the axes. None of the orbitals points directly at the tetrahedral ligands. However, the dx2−y2 and dz2 orbitals (along the Cartesian axes) overlap with the ligands less than the dxy,...
Electron Transport Chain: Complex III and IV01:43

Electron Transport Chain: Complex III and IV

During the electron transport chain, electrons from NADH and FADH2 are first transferred to complexes I and II, respectively. These two complexes then transfer the electrons to ubiquinol, which carries them further to complex III. Complex III passes the electrons across the intermembrane space to Cyt c, which carries them further to complex IV. Complex IV donates electrons to oxygen and reduces it to water. As electrons pass through complexes I, III, and IV, the energy released aids the pumping...
Thermal Electrocyclic Reactions: Stereochemistry01:17

Thermal Electrocyclic Reactions: Stereochemistry

The stereochemistry of electrocyclic reactions is strongly influenced by the orbital symmetry of the polyene HOMO. Under thermal conditions, the reaction proceeds via the ground-state HOMO.
Selection Rules: Thermal Activation
Conjugated systems containing an even number of π-electron pairs undergo a conrotatory ring closure. For example, thermal electrocyclization of (2E,4E)-2,4-hexadiene, a conjugated diene containing two π-electron pairs, gives trans-3,4-dimethylcyclobutene.
Deactivation Processes: Jablonski Diagram01:25

Deactivation Processes: Jablonski Diagram

Luminescence, the emission of light by a substance that has absorbed energy, is a process that involves the interaction of molecules with light. The energy-level diagram, or Jablonski diagram, is a graphical representation of these interactions, illustrating the various states and transitions a molecule can undergo. In a typical Jablonski diagram, the lowest horizontal line represents the ground-state energy of the molecule, which is usually a singlet state. This state represents the energies...

También podría leer

Artículos Relacionados

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

Ordenar por
Same author

Dihydromyricetin Ameliorates Myocardial Ischemia-Reperfusion Injury by Modulating CKLF1-Mediated Cardiomyocyte Pyroptosis.

Phytotherapy research : PTR·2026
Same author

The role of fat-free mass index in evaluating protein-energy wasting in maintenance hemodialysis patients: a multicenter cross-sectional study.

Frontiers in nutrition·2026
Same author

OGFOD1: a critical mediator of chemoresistance in acute myeloid leukemia.

Frontiers in pharmacology·2026
Same author

Comparison of the effects of different types of nasointestinal tube placement techniques for ICU patients: a Bayesian network meta-analysis.

BMC anesthesiology·2026
Same author

TRPC6 mediates goblet cell differentiation in COPD.

Respiratory research·2026
Same author

Development of an Efficient Murine Tissue Expansion Model for Skin Regeneration Research.

Journal of visualized experiments : JoVE·2026
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: Jun 17, 2026

BEST: Barcode Enabled Sequencing of Tetrads
12:59

BEST: Barcode Enabled Sequencing of Tetrads

Published on: May 1, 2014

Transferencia bidireccional de electrones en las tetradas moleculares.

Andrew C Benniston1, Anthony Harriman, Peiyi Li

  • 1Molecular Photonics Laboratory, School of Chemistry, Bedson Building, Newcastle University, Newcastle upon Tyne NE1 7RU, United Kingdom.

Journal of the American Chemical Society
|December 17, 2009
PubMed
Resumen

La excitación selectiva de dos colores de las tetradas moleculares dirige la transferencia de electrones a lo largo del eje molecular. Este control da como resultado una diferencia significativa de 40.000 veces en las vidas del estado de carga separada.

Más Videos Relacionados

Single-Molecule Förster 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

Determination of Tripartite Interaction between Two Monomers of a MADS-box Transcription Factor and a Calcium Sensor Protein by BiFC-FRET-FLIM Assay
14:34

Determination of Tripartite Interaction between Two Monomers of a MADS-box Transcription Factor and a Calcium Sensor Protein by BiFC-FRET-FLIM Assay

Published on: December 25, 2021

Videos de Experimentos Relacionados

Last Updated: Jun 17, 2026

BEST: Barcode Enabled Sequencing of Tetrads
12:59

BEST: Barcode Enabled Sequencing of Tetrads

Published on: May 1, 2014

Single-Molecule Förster 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

Determination of Tripartite Interaction between Two Monomers of a MADS-box Transcription Factor and a Calcium Sensor Protein by BiFC-FRET-FLIM Assay
14:34

Determination of Tripartite Interaction between Two Monomers of a MADS-box Transcription Factor and a Calcium Sensor Protein by BiFC-FRET-FLIM Assay

Published on: December 25, 2021

Área de la Ciencia:

  • La fotoquímica es la fotoquímica.
  • La biofísica molecular es la biofísica molecular.
  • Dinámica de transferencia de electrones Dinámica de transferencia de electrones

Sus antecedentes:

  • Las tetradas moleculares son sistemas complejos capaces de complejos procesos de transferencia de electrones.
  • El control de la direccionalidad de la transferencia de electrones es crucial para el diseño de dispositivos moleculares avanzados.

Objetivo del estudio:

  • Para investigar el efecto de la excitación cromófora selectiva en la direccionalidad de la transferencia de electrones en una tetradia molecular.
  • Para cuantificar el impacto de la longitud de onda de excitación en la vida útil de los estados de carga separada.

Principales métodos:

  • Utilizando excitación láser de dos colores para dirigirse selectivamente cromóforos específicos dentro de la tetrad molecular.
  • Empleando técnicas espectroscópicas de resolución temporal para monitorear y medir la vida útil de los estados de carga separada.

Principales resultados:

  • Se demostró que la dirección de la transferencia de electrones está dictada por el cromóforo iluminado.
  • Se observó una notable disparidad de 40.000 veces en las vidas de los estados de carga separada basados en la excitación.
  • Estableció un control preciso sobre el flujo de electrones dentro del sistema molecular.

Conclusiones:

  • La excitación selectiva proporciona una poderosa herramienta para dirigir la transferencia de electrones en sistemas moleculares.
  • La disparidad de vida observada pone de relieve el potencial de las aplicaciones de conmutación y almacenamiento de energía ultrarrápidas.
  • Este trabajo avanza en la comprensión fundamental de la dinámica de separación de cargas en arquitecturas moleculares complejas.