通过线性自由能量关系揭示铜催化基键形成的机械模式
Guo-Xiong Xu1, Ji-Ren Liu1, Zeng Gao2
1Center of Chemistry for Frontier Technologies, Department of Chemistry, State Key Laboratory of Clean Energy Utilization, Zhejiang University, Hangzhou, China.
Nature communications
|December 23, 2025
概括
这项研究引入了线性自由能量关系 (LFER) 来预测铜催化基反应中的机制. 这为设计新的碳-碳键构成提供了定量指南.
科学领域:
- 有机化学 有机化学
- 催化剂是一种催化剂.
- 反应机制 反应机制
背景情况:
- 铜催化基反应得到了广泛的研究,但在机理上是复杂的.
- 区分减少消除,外层激素替代和离子对机制是具有挑战性的.
研究的目的:
- 揭示铜催化基转换中C-C键形成的线性自由能量关系 (LFER).
- 开发一个准确的LFER模型来预测激素键形成机制.
主要方法:
- 已建立的LFER尺度用于连接体,基因和核友.
- 应用了LFER模型来分析132,300个潜在的铜催化基转化.
主要成果:
- 成功地描述了大量反应中C-C键形成的机制.
- 开发了一个基于LFER的预测模型,用于机械洞察.
结论:
- 该研究为铜催化中的未来C-C键设计提供了详细的机制指南.
- 通过对激进债券形成偏好进行系统的,定量性的洞察,促进了机械学的理解.
相关概念视频
Radical Reactivity: Overview
2.6K
Radicals, the highly reactive species, gain stability by undergoing three different reactions. The first reaction involves a radical-radical coupling, in which a radical combines with another radical, forming a spin‐paired molecule. The second reaction is between a radical and a spin‐paired molecule, generating a new radical and a new spin‐paired molecule. The third reaction is radical decomposition in a unimolecular reaction, forming a new radical and a spin‐paired...
2.6K
Radical Formation: Overview
2.6K
A bond can be broken either by heterolytic bond cleavage to form ions or homolytic bond cleavage to yield radicals. A fishhook arrow is used to represent the motion of a single electron in homolytic bond cleavage. There are two main sources from which radicals can be formed:
Radicals from spin-paired molecules:
Radicals can be obtained from spin-paired molecules either by homolysis or electron transfer. While two radicals are formed in the former, an electron is added in the...
Radicals from spin-paired molecules:
Radicals can be obtained from spin-paired molecules either by homolysis or electron transfer. While two radicals are formed in the former, an electron is added in the...
2.6K
Radical Formation: Addition
2.1K
Radicals can be formed by adding a radical to a spin-paired molecule. This is typically observed with unsaturated species, where the addition of a radical across the π bond leads to the production of a new radical by dissolving the π bond. For example, the addition of a Br radical to an alkene yields a carbon-centered radical.
Similar to charge conservation in chemical reactions, spin conservation is implicit for radical reactions. Accordingly, the product formed must possess an...
Similar to charge conservation in chemical reactions, spin conservation is implicit for radical reactions. Accordingly, the product formed must possess an...
2.1K
Radical Formation: Homolysis
4.2K
A bond is formed between two atoms by sharing two electrons. When this bond is broken by supplying sufficient energy, either two electrons can be taken up by one atom forming ions by the cleavage called heterolysis, or the two electrons are shared by two atoms, with one each creating radicals by the cleavage called homolysis.
4.2K
Radical Reactivity: Intramolecular vs Intermolecular
2.1K
Radical reactions can occur either intermolecularly or intramolecularly. In an intermolecular radical reaction, a nucleophilic radical adds to an electrophilic alkene or vice versa. In such reactions, the radical and generally the alkene, which is also called the radical trap, are two different molecules. Additionally, for such intermolecular reactions to occur, the radical trap must be active, present in an excess concentration, and the radical starting material must have a weak...
2.1K
Radical Reactivity: Nucleophilic Radicals
2.6K
Radicals adjacent to electron-donating groups are called nucleophilic radicals. These radicals readily react with electrophilic alkenes. The SOMO–LUMO interactions are the driving force for the reaction, where the high-energy SOMO of the electron-rich, nucleophilic radicals interacts with the low-energy LUMO of the electron-deficient, electrophilic alkenes. Such SOMO–LUMO interactions are the basis of reactive radical traps, affecting the selectivity in radical reactions. For...
2.6K
![[DPEPhosbcpCu]PF6: A General and Broadly Applicable Copper-Based Photoredox Catalyst](/_next/image?url=https%3A%2F%2Fcloudfront.jove.com%2FCDNSource%2Fteasers%2F59739.jpg&w=3840&q=50)

