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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
Ladder Diagrams: Redox Equilibria01:30

Ladder Diagrams: Redox Equilibria

446
Ladder diagrams are useful tools for understanding redox equilibrium reactions, especially the effects of concentration changes on the electrochemical potential of the reaction. The vertical axis in the redox ladder diagrams represents the electrochemical potential, E. The area of predominance is demarcated using the Nernst equation.
Consider the Fe3+/Fe2+ half-reaction, which has a standard-state potential of +0.771 V. At potentials more positive than +0.771 V, Fe3+ predominates, whereas Fe2+...
446
π Electron Effects on Chemical Shift: Aromatic and Antiaromatic Compounds01:14

π Electron Effects on Chemical Shift: Aromatic and Antiaromatic Compounds

1.2K
In aromatic compounds, such as benzene, the circulation of (4n + 2) π-electrons sets up a diamagnetic or diatropic ring current around the perimeter of the molecule. This current induces a magnetic field that opposes the external field inside the ring and reinforces it on the outside. The protons in benzene are deshielded and exhibit high chemical shifts in the range 6.5–8.5 ppm. The shielding effect at the center of the ring is evident in complex aromatic molecules, such as...
1.2K
Thermal and Photochemical Electrocyclic Reactions: Overview01:26

Thermal and Photochemical Electrocyclic Reactions: Overview

2.3K
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.
2.3K
The Bohr Model02:18

The Bohr Model

52.2K
Following the work of Ernest Rutherford and his colleagues in the early twentieth century, the picture of atoms consisting of tiny dense nuclei surrounded by lighter and even tinier electrons continually moving about the nucleus was well established. This picture was called the planetary model since it pictured the atom as a miniature “solar system” with the electrons orbiting the nucleus like planets orbiting the sun. The simplest atom is hydrogen, consisting of a single proton as...
52.2K
Voltammetry: Factors Affecting Measurements01:21

Voltammetry: Factors Affecting Measurements

149
A current produced due to the redox reactions of the analyte at the working and auxiliary electrodes is called a faradaic current. The reaction can be divided into two types. The current generated due to the reduction of the analyte is called cathodic current, and it carries a positive charge. In contrast, the current produced by analyte oxidation is known as an anodic current, and it has a negative charge. The applied potential at the working electrode determines the faradaic current flow, and...
149

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相关实验视频

Updated: Jun 20, 2025

Isotopic Effect in Double Proton Transfer Process of Porphycene Investigated by Enhanced QM/MM Method
05:51

Isotopic Effect in Double Proton Transfer Process of Porphycene Investigated by Enhanced QM/MM Method

Published on: July 19, 2019

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伪约翰-泰勒效应打破了双电子氧电还原中的pH依赖性.

Baokai Xia1, Jiale Du1, Ming Li1

  • 1Key Laboratory for Soft Chemistry and Functional Materials (Ministry of Education), School of Chemistry and Chemical Engineering, School of Energy and Power Engineering, Nanjing University of Science and Technology, Nanjing, 210094, China.

Advanced materials (Deerfield Beach, Fla.)
|July 20, 2024
PubMed
概括

这项研究引入了一种抗pH的催化剂,用于将氧气电还原为过氧化 (H2O2). 利用伪约翰-泰勒效应,TiOxFy材料在广泛的pH范围内保持高效率,使成本有效的H2O2生产成为可能.

关键词:
氧降解反应是氧降解反应.过氧化是一种过氧化.它们的pH值.伪约翰·泰勒效应

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科学领域:

  • 电化学 电化学 电化学
  • 材料科学 材料科学 材料科学
  • 催化剂是一种催化剂.

背景情况:

  • 小分子化因不同质子捐赠环境而依赖于pH值.
  • 两电子氧气电还原到过氧化 (H2O2) 是一个可持续的过程.
  • 开发适应pH的催化剂对于保持一致的电化学性能至关重要.

研究的目的:

  • 为了展示一种抗pH的氧气电还原系统.
  • 调查伪约翰-泰勒效应在催化剂稳定性中的作用.
  • 为了实现高效和成本效益的过氧化生产.

主要方法:

  • 运行拉曼光谱分析催化剂行为.
  • 当地环境分析,以了解接口现象.
  • 密度函数理论 (DFT) 模拟以阐明反应机制.
  • 用于生产成本评估的技术经济分析.

主要成果:

  • 开发了一种新的TiOxFy催化剂,通过伪约翰-泰勒效应表现出pH电阻.
  • 催化剂在pH1到13之间表现出最小的活性衰变 (3.2%),不同于常见的催化剂 (78.6%衰变).
  • 实现了高法拉第效率 (93.4-96.4%) 和H2O2产率 (高达614毫克厘米-2小时-1).
  • 最低的H2O2生产成本被发现为0.37美元/公斤-1.1美元.

结论:

  • TiOxFy中的伪约翰-泰勒效应有效调节局部pH值和中间吸附/脱附.
  • 这项工作为稳定的电化学过程提供了伪约翰-泰勒效应的新应用.
  • 开发的系统为经济的过氧化合成在各种pH条件下提供了一个有希望的途径.