替代剂对的联体为中心的电催化演变的替代作用(III) corroles
Qing-Hua Yu1, Yu-Fei Li2, Xu-You Cao1
1School of Chemistry and Chemical Engineering, Guangdong Provincial Key Laboratory of Fuel Cell Technology, South China University of Technology, Guangzhou 510641, P.R. China. chhyliu@scut.edu.cn.
Dalton transactions (Cambridge, England : 2003)
|February 20, 2025
概括
带有电子提取组的抗角质催化剂显示了对电催化演变的增强性能. 这些修改后的催化剂具有可调节的特性,可以在各种介质中提高活性.
科学领域:
- 无机化学 无机化学
- 材料科学 材料科学 材料科学
- 电化学 电化学 电化学
背景情况:
- 科罗尔是具有潜在催化应用的宏循环配体.
- 电催化进化是可持续能源的关键过程.
研究的目的:
- 为了合成和评估反 (III) 三烯作为进化的电催化剂.
- 调查五甲替代剂对催化活性的影响.
主要方法:
- 合成具有不同五二基组的反 (III) 三基环.
- 在有机和水溶液中的催化演变的电化学评估.
主要成果:
- 带有五甲替代剂的抗环表现出显著的电催化演化反应 (HER) 活性.
- 替代剂的电子吸收特性增加与增强的HER活性相关.
结论:
- 抗 (III) 三烯基环是进化过程中的有效电催化剂.
- 通过电子提取组调整角质连接体的电子性质,可以提高催化性能.
更多相关视频
相关概念视频
Complexation Equilibria: The Chelate Effect
420
In complexation reactions, metal atoms or cations interact with ligands to form donor-acceptor adducts called metal complexes. Ligands that bind through one donor site are monodentate, ligands with two donor sites are bidentate, and those with more than two donor sites are polydentate ligands. For example, ethylene diamine is a bidentate ligand that binds through two nitrogen donor atoms, forming a five-membered ring. EDTA is a polydentate ligand that binds through four oxygen and two nitrogen...
420
Reduction of Alkenes: Asymmetric Catalytic Hydrogenation
3.2K
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...
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...
3.2K
Regioselectivity of Electrophilic Additions-Peroxide Effect
8.4K
In the presence of organic peroxides, the addition of hydrogen bromide to an alkene yields the isomer that is not predicted by Markovnikov’s rule. For example, the addition of hydrogen bromide to 2-methylpropene in the presence of peroxides gives 1-bromo-2-methylpropane. This addition reaction proceeds via a free radical mechanism, which reverses the regioselectivity. The free radical reaction mechanism involves three stages: initiation, propagation, and termination.
8.4K
Metal-Ligand Bonds
20.5K
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...
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...
20.5K
Electrophilic Aromatic Substitution: Sulfonation of Benzene
5.7K
Sulfonation of benzene is a reaction wherein benzene is treated with fuming sulfuric acid at room temperature to produce benzenesulfonic acid. Fuming sulfuric acid is a mixture of sulfur trioxide and concentrated sulfuric acid.
5.7K
Directing and Steric Effects in Disubstituted Benzene Derivatives
2.9K
When disubstituted benzenes undergo electrophilic substitution, the product distribution depends on the directing effect of both substituents. When the directing effects of both substituents reinforce each other, a single product is obtained. For example, bromination of p-nitrotoluene occurs ortho to the methyl group and meta to the nitro group, which is the same position, resulting in a single product. However, if the directing effects of the two groups oppose each other, the...
2.9K


