Jove
Visualize
Contáctanos

Videos de Conceptos Relacionados

Cofactors and Coenzymes01:24

Cofactors and Coenzymes

Enzymes are proteins made of amino acids. The functional group of each constituent amino acid catalyzes a wide variety of chemical reactions via ionic interactions or acid-base reactions. However, amino acids cannot catalyze oxidation-reduction and group transfer reactions and need to be aided by non-protein components called cofactors. Cofactors are also referred to as the chemical teeth of an enzyme.
Cofactors can be metallic ions or organic molecules called coenzymes. These types of helper...
Cofactors and Coenzymes01:27

Cofactors and Coenzymes

Enzymes require additional components for proper function. There are two such classes of molecules: cofactors and coenzymes. Cofactors are metallic ions and coenzymes are non-protein organic molecules. Both of these types of helper molecule can be tightly bound to the enzyme or bound only when the substrate binds.
Cofactors and Coenzymes01:27

Cofactors and Coenzymes

Enzymes require additional components for proper function. There are two such classes of molecules: cofactors and coenzymes. Cofactors are metallic ions and coenzymes are non-protein organic molecules. Both of these types of helper molecule can be tightly bound to the enzyme or bound only when the substrate binds.
Reduction of Alkenes: Asymmetric Catalytic Hydrogenation02:17

Reduction of Alkenes: Asymmetric Catalytic Hydrogenation

Catalytic hydrogenation of alkenes is a transition-metal catalyzed reduction of the double bond using molecular hydrogen to give alkanes. The mode of hydrogen addition follows syn stereochemistry.
The metal catalyst used can be either heterogeneous or homogeneous. When hydrogenation of an alkene generates a chiral center, a pair of enantiomeric products is expected to form. However, an enantiomeric excess of one of the products can be facilitated using an enantioselective reaction or an...
Heterogeneous Catalysis01:22

Heterogeneous Catalysis

Heterogeneous catalysis involves a catalyst in a different phase from the reactants. It is a process where the catalyst and the reactants are in distinct phases, typically solid and gas or liquid.Most heterogeneous catalysts are metals, metal oxides, or acids. The list includes transition metals like iron (Fe), cobalt (Co), nickel (Ni), palladium (Pd), platinum (Pt), chromium (Cr), manganese (Mn), tungsten (W), silver (Ag), and copper (Cu). These metals possess partially vacant d orbitals that...
Introduction to Mechanisms of Enzyme Catalysis01:13

Introduction to Mechanisms of Enzyme Catalysis

For many years, scientists thought that enzyme-substrate binding took place in a simple "lock-and-key" fashion. This model stated that the enzyme and substrate fit together perfectly in one instantaneous step. However, current research supports a more refined view scientists call induced fit. The induced-fit model expands upon the lock-and-key model by describing a more dynamic interaction between enzyme and substrate. As the enzyme and substrate come together, their interaction causes a mild...

También podría leer

Artículos Relacionados

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

Ordenar por
Same author

Escaping the Iron Law of Electrochemical CO<b><sub>2</sub></b> Reduction Using Pd<sub>12</sub>L<sub>24</sub> Cages as Artificial 2nd Coordination Spheres.

Inorganic chemistry·2026
Same author

Cooperative Dinuclear Activation of a Formate Intermediate in the Hydrogenation of CO<sub>2</sub> to Methanol.

Molecules (Basel, Switzerland)·2026
Same author

Photo-Driven CO<sub>2</sub> Reduction With a Heterogenized Re Catalyst in the Metal-Organic Framework PCN-777: Effects of Catalyst Loading and Anchoring Strategy on Catalysis.

ChemSusChem·2026
Same author

Reduced-Symmetry Homoleptic Pd<sub>2</sub>L<sub>4</sub> Cages Stabilized by Noncovalent π-Interactions.

Chemistry (Weinheim an der Bergstrasse, Germany)·2025
Same author

Polyoxometalate-Directed Assembly of Robust Coordination Cages: Overcoming Kinetic Inertness and Conformational Mismatch.

Angewandte Chemie (International ed. in English)·2025
Same author

Precious Metal-Free Artificial Leaf for Photosynthesis of Hydrogen Peroxide from Water.

ChemSusChem·2025
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: May 28, 2026

Development of Heterogeneous Enantioselective Catalysts using Chiral Metal-Organic Frameworks (MOFs)
08:25

Development of Heterogeneous Enantioselective Catalysts using Chiral Metal-Organic Frameworks (MOFs)

Published on: January 17, 2020

La catálisis enantioselectiva controlada por el "cofactor"

Paweł Dydio1, Christophe Rubay, Tendai Gadzikwa

  • 1Van't Hoff Institute for Molecular Sciences, University of Amsterdam, Amsterdam, The Netherlands.

Journal of the American Chemical Society
|October 4, 2011
PubMed
Resumen
Este resumen es generado por máquina.

Un nuevo complejo de rodio achiral se vuelve quiral al unirse a pequeños huéspedes, lo que permite la catálisis asimétrica. Las mejores moléculas invitadas produjeron catalizadores de hidrogenación con hasta un 99% de enantioselectividad.

Más Videos Relacionados

Versatile CO2 Transformations into Complex Products: A One-pot Two-step Strategy
07:36

Versatile CO2 Transformations into Complex Products: A One-pot Two-step Strategy

Published on: November 9, 2019

Sequence-specific Labeling of Nucleic Acids and Proteins with Methyltransferases and Cofactor Analogues
12:07

Sequence-specific Labeling of Nucleic Acids and Proteins with Methyltransferases and Cofactor Analogues

Published on: November 22, 2014

Videos de Experimentos Relacionados

Last Updated: May 28, 2026

Development of Heterogeneous Enantioselective Catalysts using Chiral Metal-Organic Frameworks (MOFs)
08:25

Development of Heterogeneous Enantioselective Catalysts using Chiral Metal-Organic Frameworks (MOFs)

Published on: January 17, 2020

Versatile CO2 Transformations into Complex Products: A One-pot Two-step Strategy
07:36

Versatile CO2 Transformations into Complex Products: A One-pot Two-step Strategy

Published on: November 9, 2019

Sequence-specific Labeling of Nucleic Acids and Proteins with Methyltransferases and Cofactor Analogues
12:07

Sequence-specific Labeling of Nucleic Acids and Proteins with Methyltransferases and Cofactor Analogues

Published on: November 22, 2014

Área de la Ciencia:

  • Química organometálica Química orgánica de los metales.
  • Catalización asimétrica por catálisis asimétrica.
  • Química supramolecular de las moléculas.

Sus antecedentes:

  • Los catalizadores achirales suelen carecer de enantioselectividad en las reacciones químicas.
  • Los catalizadores quirales son esenciales para la síntesis de compuestos enantioméricamente puros.
  • Diseñar catalizadores que puedan adaptar su quiralidad es un desafío significativo.

Objetivo del estudio:

  • Desarrollar un complejo de rodio achiral capaz de catálisis asimétrica.
  • Investigar el uso de invitados de aniones quirales (cofactores) para inducir la quiralidad.
  • Para optimizar la selección de cofactores de alta enantioselectividad en las reacciones de hidrogenación.

Principales métodos:

  • Síntesis de un complejo de bisfosfina rodio achiral con un sitio de unión al huésped.
  • Selección de una biblioteca de invitados de aniones quirales (cofactores).
  • Evaluación de los catalizadores quirales resultantes en reacciones asimétricas de hidrogenación.

Principales resultados:

  • El complejo de rodio reconoció y unió con éxito cofactores quirales, convirtiéndose en quirales.
  • Los catalizadores de hidrogenación formados utilizando los mejores cofactores lograron una alta enantioselectividad (hasta el 99% ee).
  • Un experimento de competencia demostró que el cofactor óptimo dominaba la catálisis incluso en una mezcla.

Conclusiones:

  • Un complejo de rodio achiral puede convertirse en quiral a través de la unión del huésped, lo que permite la catálisis asimétrica.
  • La selección de cofactores quirales apropiados es fundamental para lograr una alta enantioselectividad.
  • Este sistema ofrece un enfoque versátil para el desarrollo de catalizadores de hidrogenación asimétricos sintonizables.