通常在催化交叉合反应中应用的双酸N-的氧化活性和潜力
Gregory A Dawson1, Maria C Seith1, Michelle C Neary2
1Department of Chemistry, New York University, 100 Washington Square East, New York, NY, 10003, USA.
Angewandte Chemie (International ed. in English)
|September 12, 2024
概括
催化剂中的正方形平面几何学允许氧化还原活性双酸N-连接体稳定基物种. 这项研究阐明了联体电子对催化活性和交叉合反应稳定性的影响.
科学领域:
- 有机金属化学 有机金属化学
- 催化剂是一种催化剂.
- 计算化学计算化学
背景情况:
- 双酸N-连接体对于催化交叉合反应至关重要.
- 之前的假设表明,生物佐林配体缺乏氧化还原活性.
研究的目的:
- 为了研究复合体中的生物佐林和伊米达佐林配体的氧化还原活性.
- 了解连接体电子特性和协调几何学如何影响催化活性和稳定性.
主要方法:
- 有机金属研究研究.
- 频谱学分析的分析.
- 计算建模计算建模
- 对连接体和复合物的循环电压测量 (CV) 分析.
主要成果:
- 方形平面几何学可以实现连接体的氧化还原活性,稳定基物种.
- 复合转移了还原潜力,并减少了连接体之间的氧化还原潜力差异.
- 连接物特性影响化物解离和化激活中的反应性.
结论:
- 连接体电子效应和协调几何学显著影响金属制剂的稳定性和氧化还原潜力.
- 量化连接物特性为控制催化交叉合反应提供了基准.
相关概念视频
Metal-Ligand Bonds
20.6K
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...
20.6K
Ladder Diagrams: Redox Equilibria
443
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+...
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+...
443
Redox Equilibria: Overview
544
A reduction-oxidation reaction is commonly called a redox reaction. In a redox reaction, electrons are transferred from one species to another rather than being shared between or among atoms. The reducing agent or reductant is the species that loses electrons and gets oxidized in the process. The species that gains electrons and gets reduced in the process is the oxidizing agent or oxidant. Redox reactions are represented as two separate equations called half-reactions, where one equation...
544
Complexation Equilibria: The Chelate Effect
479
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...
479
Oxidation-Reduction Reactions
64.5K
Oxidation–Reduction Reactions
64.5K
Complexometric Titration: Ligands
926
Different monodentate and polydentate ligands are used as complexing agents in complexometric titration reactions. The formation of complexes by mono- and bidentate ligands involves two or more intermediate steps, limiting their use as complexing agents. In comparison, polydentate ligands can form complexes with metal ions in a single-step process, facilitating sharper end points. This means polydentate ligands, such as amino carboxylic acid derivatives, are most commonly employed in...
926
![Mizoroki-Heck Cross-coupling Reactions Catalyzed by Dichloro{bis[1,1',1''-phosphinetriyltripiperidine]}palladium Under Mild Reaction Conditions](/_next/image?url=https%3A%2F%2Fcloudfront.jove.com%2FCDNSource%2Fteasers%2F51444.jpg&w=3840&q=50)

