通过可见光光催化剂导航未激活的功能化
Guang-Mei Cao1, Si-Shun Yan2, Lei Song1
1College of Carbon Neutrality Future Technology, Sichuan University, Chengdu 610065, P. R. China. lsong@scu.edu.cn.
Chemical Society reviews
|June 19, 2025
概括
可见光光催化使未被激活的基直接功能化,有效地创建复杂的分子. 本综述涵盖了这个快速发展的化学领域的关键反应,机制和未来的机会.
科学领域:
- 有机化学 有机化学
- 光催化作用的光催化
- 合成化学 合成化学
背景情况:
- 未激活基的直接功能化对于合成复杂分子至关重要.
- 光催化剂在这个领域取得了显著的进步,使得新的转变成为可能.
- 可见光光催化剂提供了一种可持续和高效的方法.
研究的目的:
- 提供对未激活基的可见光光催化功能的全面概述.
- 要突出关键的反应,机械的见解,和合成的实用性.
- 讨论该领域最近的进展,挑战和未来的机会.
主要方法:
- 对的可见光光催化功能的文献综述.
- 分析机械路径,包括水功能化和功能丧失.
- 强调涉及功能化基保留的转化.
主要成果:
- 详细概述了用于基功能化的各种光催化反应.
- 对水功能化,功能化和保留反应的机械洞察力.
- 展示这些方法在复杂分子构造中的合成实用性.
结论:
- 可见光光催化是一种强大的策略,用于未激活的基功能化.
- 取得了重大进展,但在扩大范围和效率方面仍然存在挑战.
- 未来的机遇在于开发新的催化剂,反应和应用.
相关概念视频
Reduction of Alkenes: Catalytic Hydrogenation
12.6K
Alkenes undergo reduction by the addition of molecular hydrogen to give alkanes. Because the process generally occurs in the presence of a transition-metal catalyst, the reaction is called catalytic hydrogenation.
Metals like palladium, platinum, and nickel are commonly used in their solid forms — fine powder on an inert surface. As these catalysts remain insoluble in the reaction mixture, they are referred to as heterogeneous catalysts.
The hydrogenation process takes place on the...
Metals like palladium, platinum, and nickel are commonly used in their solid forms — fine powder on an inert surface. As these catalysts remain insoluble in the reaction mixture, they are referred to as heterogeneous catalysts.
The hydrogenation process takes place on the...
12.6K
Cycloaddition Reactions: MO Requirements for Photochemical Activation
2.2K
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.
2.2K
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
Reduction of Alkynes to cis-Alkenes: Catalytic Hydrogenation
8.2K
Introduction
Like alkenes, alkynes can be reduced to alkanes in the presence of transition metal catalysts such as Pt, Pd, or Ni. The reaction involves two sequential syn additions of hydrogen via a cis-alkene intermediate.
Like alkenes, alkynes can be reduced to alkanes in the presence of transition metal catalysts such as Pt, Pd, or Ni. The reaction involves two sequential syn additions of hydrogen via a cis-alkene intermediate.
8.2K
Reduction of Alkenes: Asymmetric Catalytic Hydrogenation
3.4K
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...
3.4K
Alkynes to Aldehydes and Ketones: Hydroboration-Oxidation
19.0K
Introduction
One of the convenient methods for the preparation of aldehydes and ketones is via hydration of alkynes. Hydroboration-oxidation of alkynes is an indirect hydration reaction in which an alkyne is treated with borane followed by oxidation with alkaline peroxide to form an enol that rapidly converts into an aldehyde or a ketone. Terminal alkynes form aldehydes, whereas internal alkynes give ketones as the final product.
One of the convenient methods for the preparation of aldehydes and ketones is via hydration of alkynes. Hydroboration-oxidation of alkynes is an indirect hydration reaction in which an alkyne is treated with borane followed by oxidation with alkaline peroxide to form an enol that rapidly converts into an aldehyde or a ketone. Terminal alkynes form aldehydes, whereas internal alkynes give ketones as the final product.
19.0K

![[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)
