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Reduction of Alkenes: Catalytic Hydrogenation02:13

Reduction of Alkenes: Catalytic Hydrogenation

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Alkenes undergo reduction by the addition of molecular hydrogen to give alkanes. Because the process generally occurs in the presence of a transition-metal catalyst, the reaction is called catalytic hydrogenation.
Metals like palladium, platinum, and nickel are commonly used in their solid forms — fine powder on an inert surface. As these catalysts remain insoluble in the reaction mixture, they are referred to as heterogeneous catalysts.
The hydrogenation process takes place on the...
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Reduction of Benzene to Cyclohexane: Catalytic Hydrogenation01:28

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Unlike the easy catalytic hydrogenation of an alkene double bond, hydrogenation of a benzene double bond under similar reaction conditions does not take place easily. For example, in the reduction of stilbene, the benzene ring remains unaffected while the alkene bond gets reduced. Hydrogenation of an alkene double bond is exothermic and a favorable process. In contrast, to hydrogenate the first unsaturated bond of benzene, an energy input is needed; that is, the process is endothermic. This is...
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Reduction of Alkenes: Asymmetric Catalytic Hydrogenation02:17

Reduction of Alkenes: Asymmetric Catalytic Hydrogenation

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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...
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Reduction of Alkynes to cis-Alkenes: Catalytic Hydrogenation02:24

Reduction of Alkynes to cis-Alkenes: Catalytic Hydrogenation

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Introduction
Like alkenes, alkynes can be reduced to alkanes in the presence of transition metal catalysts such as Pt, Pd, or Ni. The reaction involves two sequential syn additions of hydrogen via a cis-alkene intermediate.
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Ligand Binding and Linkage00:49

Ligand Binding and Linkage

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Allosteric proteins have more than one ligand binding site; the binding of a ligand to any of these sites influences the binding of ligands to the other sites. When a protein is allosteric, its binding sites are called coupled or linked.  In the case of enzymes, the site that binds to the substrate is known as the active site and the other site is known as the regulatory site. When a ligand binds to the regulatory site, this leads to conformational changes in the protein that can influence...
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Metal-Ligand Bonds02:51

Metal-Ligand Bonds

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The hemoglobin in the blood, the chlorophyll in green plants, vitamin B-12, and the catalyst used in the manufacture of polyethylene all contain coordination compounds. Ions of the metals, especially the transition metals, are likely to form complexes.
In these complexes, transition metals form coordinate covalent bonds, a kind of Lewis acid-base interaction in which both of the electrons in the bond are contributed by a donor (Lewis base) to an electron acceptor (Lewis acid). The Lewis acid in...
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  1. Home
  2. Convertir Los Nanocúmulos De Au En Activos Catalíticos Para La Reducción De Co2 Impulsada Por La Luz Visible A Través De Ligandos Puentes
  1. Home
  2. Convertir Los Nanocúmulos De Au En Activos Catalíticos Para La Reducción De Co2 Impulsada Por La Luz Visible A Través De Ligandos Puentes

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Convertir los nanocúmulos de Au en activos catalíticos para la reducción de CO2 impulsada por la luz visible a través

Xiaofeng Cui1,2, Jin Wang1, Bing Liu3

  • 1Hefei National Laboratory for Physical Sciences at the Microscale, iChEM (Collaborative Innovation Center of Chemistry for Energy Materials), School of Chemistry and Materials Science, and National Synchrotron Radiation Laboratory , University of Science and Technology of China , Hefei , Anhui 230026 , P. R. China.

Journal of the American Chemical Society
|November 9, 2018

Ver abstracta en PubMed

Resumen
Este resumen es generado por máquina.

Este estudio mejora los nanocúmulos de oro (Au NC) para la reducción de dióxido de carbono (CO2) impulsada por el sol mediante el injerto de cationes metálicos. Esta estrategia crea sitios catalíticos activos, mejorando la fotocatálisis de luz visible para la conversión de CO2.

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Área de la Ciencia:

  • Ciencias de los materiales
  • Fotocatálisis
  • Nanotecnología

Sus antecedentes:

  • Los materiales fotocatalíticos de luz visible son cruciales para la conversión de CO2 impulsada por la energía solar.
  • Los nanocúmulos de oro (Au NC) pueden cosechar la luz visible, pero carecen de sitios catalíticos para la reducción de CO2.

Objetivo del estudio:

  • Desarrollar Au NC catalíticamente activos para la reducción de CO2 con luz visible.
  • Diseñar la superficie de las Au NC para mejorar el rendimiento fotocatalítico.

Principales métodos:

  • Injerto de cationes metálicos (Fe2+, Co2+, Ni2+, Cu2+) en Au NC utilizando la l-cisteína como ligando puente.
  • Investigando la transferencia de electrones facilitada por el enlace metal- azufre.
  • Encapsulación de Au NC con marcos metálico-orgánicos para mejorar la fotoestabilidad.

Principales resultados:

  • Los cationes metálicos injertados actúan como sitios catalíticos para la reducción de CO2 al recibir electrones fotoinducidos.
  • El ajuste de cationes metálicos permite el control de la eficiencia de transferencia de electrones y la activación de CO2.
  • La encapsulación con marcos metálico-orgánicos mejora significativamente la fotostabilidad del catalizador basado en Au NC.

Conclusiones:

  • Una estrategia novedosa transforma efectivamente los Au NC en fotocatalizadores activos para la reducción de CO2.
  • La ingeniería de superficie de grupos metálicos ofrece una ruta prometedora para el diseño de fotocatalizadores avanzados.
  • Este trabajo avanza en las tecnologías de conversión de CO2 impulsadas por la energía solar.