使用可见光进行光电氧催化,用于合成提桑衍生物
Wen Liao1, Jing Hou2, Hongding Tang2
1Department of Polymer Materials, School of Materials Science and Engineering, Tongji University, Shanghai 201804, P. R. China.
Organic letters
|August 16, 2023
概括
一种新的可见光促进的方法合成了没有过渡金属的桑衍生物. 这种高效的C-C键形成策略可用于光启动器和药品.
科学领域:
- 有机化学 有机化学
- 摄影化学的使用.
- 催化剂是一种催化剂.
背景情况:
- 硫桑衍生物 (TXs) 在各种应用中至关重要,包括光启动器和药品.
- 现有的合成方法通常需要过渡金属或恶劣的条件,限制其范围和可持续性.
- 开发高效的,无金属的合成路径用于TX具有显著的兴趣.
研究的目的:
- 开发一种新的,不含过渡金属的光反氧催化策略,用于合成桑衍生物.
- 研究可见光促进的分子内循环的机制.
- 为了证明开发的方法的可扩展性和适用性,以生产有价值的TXs衍生品.
主要方法:
- 使用可见光辐射来促进反应.
- 使用了一种没有过渡金属的光氧催化方法.
- 进行了机理学研究和密度函数理论 (DFT) 计算,以阐明反应途径.
主要成果:
- 实现了桑衍生物的高效和区域选择性合成.
- 反应通过分子内循环进行,涉及原子转移,C-C键形成和氧化脱.
- 该方法表现出卓越的反应性,并成功扩展到克级.
结论:
- 已经建立了一个新的和可持续的可见光促进的,没有过渡金属的桑衍生物合成策略.
- 机械学的见解提供了对光氧催化分子内循环的更深入的理解.
- 可扩展性和广泛适用性突出显示了这种方法在工业合成光发起剂和药物的潜力.
相关概念视频
Photochemical Electrocyclic Reactions: Stereochemistry
1.9K
The absorption of UV–visible light by conjugated systems causes the promotion of an electron from the ground state to the excited state. Consequently, photochemical electrocyclic reactions proceed via the excited-state HOMO rather than the ground-state HOMO. Since the ground- and excited-state HOMOs have different symmetries, the stereochemical outcome of electrocyclic reactions depends on the mode of activation; i.e., thermal or photochemical.
Selection Rules: Photochemical Activation
Selection Rules: Photochemical Activation
1.9K
Cycloaddition Reactions: MO Requirements for Photochemical Activation
2.1K
Some cycloaddition reactions are activated by heat, while others are initiated by light. For example, a [2 + 2] cycloaddition between two ethylene molecules occurs only in the presence of light. It is photochemically allowed but thermally forbidden.
2.1K
The Z-Scheme of Electron Transport in Photosynthesis
10.2K
The light reactions of photosynthesis assume a linear flow of electrons from water to NADP+. During this process, light energy drives the splitting of water molecules to produce oxygen. However, oxidation of water molecules is a thermodynamically unfavorable reaction and requires a strong oxidizing agent. This is accomplished by the first product of light reactions: oxidized P680 (or P680+), the most powerful oxidizing agent known in biology. The oxidized P680 that acquires an electron from the...
10.2K
Redox Reactions
55.8K
Oxidation-reduction or redox reactions involve the transfer of electrons from one molecule or atom to another. When an atom gains an electron, another atom must lose an electron, meaning oxidation and reduction must occur together. Since the redox occurs in pairs, the atom that gets oxidized is also called the reducing agent or reductant, and the atom that is reduced is also called the oxidizing agent or oxidant. A straightforward way to remember the definitions of oxidation and reduction is...
55.8K
Oxidation of Alkenes: Syn Dihydroxylation with Osmium Tetraoxide
10.4K
Alkenes are converted to 1,2-diols or glycols through a process called dihydroxylation. It involves the addition of two hydroxyl groups across the double bond with two different stereochemical approaches, namely anti and syn. Dihydroxylation using osmium tetroxide progresses with syn stereochemistry.
10.4K
Thermal and Photochemical Electrocyclic Reactions: Overview
2.4K
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.
2.4K
![[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)
![Cercosporin-Photocatalyzed [4+1]- and [4+2]-Annulations of Azoalkenes Under Mild Conditions](/_next/image?url=https%3A%2F%2Fcloudfront.jove.com%2FCDNSource%2Fteasers%2F60786.jpg&w=3840&q=50)
