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Inductive Effects on Chemical Shift: Overview01:27

Inductive Effects on Chemical Shift: Overview

1.1K
The protons in unsubstituted alkanes are strongly shielded with chemical shifts below 1.8 ppm. Methine, methylene, and methyl protons appear at approximately 1.7, 1.2 and 0.7 ppm, while the proton signal from methane appears at 0.23 ppm. An electronegative substituent, such as chlorine, withdraws the electron density from the protons, increasing their chemical shift. Progressive substitution of the hydrogens in methane by chlorine shifts the proton signals increasingly downfield, to 3.05 ppm in...
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π Electron Effects on Chemical Shift: Overview01:27

π Electron Effects on Chemical Shift: Overview

1.1K
An applied magnetic field causes loosely bound π-electrons in organic molecules to circulate, producing a local or induced diamagnetic field over a large spatial volume. As the molecules tumble in solution, the field generated by π-electrons in spherical substituents results in a zero net field. However, the net field generated by π-electrons in non-spherical substituents is not zero. The effect of this induced field depends on the orientation of the molecule with respect to B0,...
1.1K
Induced-fit Model01:13

Induced-fit Model

80.9K
Most chemical reactions in cells require enzymes—biological catalysts that speed up the reaction without being consumed or permanently changed. They reduce the activation energy needed to convert the reactants into products. Enzymes are proteins, that usually work by binding to a substrate—a reactant molecule that they act upon.
Enzymes exhibit substrate specificity, meaning that they can only bind to certain substrates. This is mainly determined by the shape and chemical...
80.9K
Crystal Field Theory - Octahedral Complexes02:58

Crystal Field Theory - Octahedral Complexes

26.6K
Crystal Field Theory
To explain the observed behavior of transition metal complexes (such as colors), a model involving electrostatic interactions between the electrons from the ligands and the electrons in the unhybridized d orbitals of the central metal atom has been developed. This electrostatic model is crystal field theory (CFT). It helps to understand, interpret, and predict the colors, magnetic behavior, and some structures of coordination compounds of transition metals.
CFT focuses on...
26.6K
Induced Electric Dipoles01:28

Induced Electric Dipoles

4.2K
A permanent electric dipole orients itself along an external electric field. This rotation can be quantified by defining the potential energy because the external torque does work in rotating it. Then, the potential energy is minimum at the parallel configuration and maximum at the antiparallel configuration. While the former is a stable equilibrium, the latter is an unstable equilibrium.
Since the absolute value of potential energy holds no physical meaning, its zero value can be chosen as per...
4.2K
Ligand Binding and Linkage00:49

Ligand Binding and Linkage

4.8K
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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Video Experimental Relacionado

Updated: Jul 9, 2025

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

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Efecto inductivo en sitios de un solo átomo

Chang-Xin Zhao1, Xinyan Liu2, Jia-Ning Liu1

  • 1Beijing Key Laboratory of Green Chemical Reaction Engineering and Technology, Department of Chemical Engineering, Tsinghua University, Beijing 100084, China.

Journal of the American Chemical Society
|December 6, 2023
PubMed
Resumen
Este resumen es generado por máquina.

Los investigadores encontraron que la reducción de la distancia entre los dopajes heteroatómicos y los sitios de un solo átomo aumenta la actividad electrocatalítica para la reacción de reducción de oxígeno (ORR). Este descubrimiento optimiza los catalizadores para aplicaciones como las baterías de zinc-aire.

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Quantitative Atomic-Site Analysis of Functional Dopants/Point Defects in Crystalline Materials by Electron-Channeling-Enhanced Microanalysis
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Synthesis and Performance Characterizations of Transition Metal Single Atom Catalyst for Electrochemical CO2 Reduction
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Synthesis and Performance Characterizations of Transition Metal Single Atom Catalyst for Electrochemical CO2 Reduction

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Videos de Experimentos Relacionados

Last Updated: Jul 9, 2025

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

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Quantitative Atomic-Site Analysis of Functional Dopants/Point Defects in Crystalline Materials by Electron-Channeling-Enhanced Microanalysis
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Quantitative Atomic-Site Analysis of Functional Dopants/Point Defects in Crystalline Materials by Electron-Channeling-Enhanced Microanalysis

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Synthesis and Performance Characterizations of Transition Metal Single Atom Catalyst for Electrochemical CO2 Reduction
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Synthesis and Performance Characterizations of Transition Metal Single Atom Catalyst for Electrochemical CO2 Reduction

Published on: April 10, 2018

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Área de la Ciencia:

  • Ciencias de los materiales
  • La electroquímica
  • Catálisis

Sus antecedentes:

  • Los catalizadores monoatómicos (SAC) ofrecen una alta actividad electrocatalítica.
  • El dopaje heteroatómico puede mejorar aún más el rendimiento de SAC.
  • La influencia precisa de las posiciones de dopaje en la actividad no se comprende completamente.

Objetivo del estudio:

  • Investigar la relación entre las posiciones de dopaje heteroatómico y la actividad electrocatalítica.
  • Para aclarar el efecto inductivo de los sitios de un solo átomo.
  • Desarrollar una estrategia de síntesis para optimizar las SAC para la reacción de reducción de oxígeno (ORR).

Principales métodos:

  • Propuso una estrategia de síntesis utilizando la modificación del ligando para controlar la distancia entre los dopantes y los sitios de un solo átomo.
  • Sitio de un solo átomo de Fe-N3P1 fabricado.
  • Actividad electrocatalítica evaluada para el ORR.

Principales resultados:

  • Demostró que la reducción de la brecha espacial entre los heteroátomos dopados y los sitios de un solo átomo mejora la actividad ORR.
  • Se logró un rendimiento electrocatalítico optimizado con el Fe-N3P1 SAC sintetizado con precisión.
  • El nuevo catalizador muestra una notable actividad ORR.

Conclusiones:

  • El efecto inductivo de los sitios de un solo átomo es crucial para la actividad ORR.
  • El control preciso de la distancia del sitio de un solo átomo de dopante es clave para optimizar los SAC.
  • El SAC Fe-N3P1 desarrollado muestra un potencial significativo para dispositivos de almacenamiento y conversión de energía como las baterías de zinc-aire y las pilas de combustible.