An ultrastable olefin-linked covalent organic framework for photocatalytic decarboxylative alkylations under highly acidic conditions

Author(s):  
Miao Tian ◽  
Yichun Wang ◽  
Xiubin Bu ◽  
Yichen Wang ◽  
Xiaobo Yang

The application of two-dimensional covalent organic frameworks (2D-COFs) as photoredox catalysts offers a sustainable alternative for visible-light-driven organic transformations. However, under highly complicated organic reaction conditions, maintaining their basic structure...

2017 ◽  
Vol 5 (44) ◽  
pp. 22933-22938 ◽  
Author(s):  
Yongfeng Zhi ◽  
Ziping Li ◽  
Xiao Feng ◽  
Hong Xia ◽  
Yumin Zhang ◽  
...  

A robust two-dimensional covalent organic framework (COF-JLU5), which exhibits excellent heterogeneous photocatalytic performances for oxidative C–H functionalizations under visible-light irradiation using O2as a green oxygen source, is reported.


2021 ◽  
Author(s):  
Luqiu Li ◽  
Dongguang Yin ◽  
Xiandi Guo

Covalent organic frameworks (COFs) representing an emerging class of porous crystalline material have shown promising visible-light-driven hydrogen evolution activity. However, they have a high recombination ratio of charge carriers and...


Synthesis ◽  
2019 ◽  
Vol 51 (16) ◽  
pp. 3021-3054 ◽  
Author(s):  
Yi Wei ◽  
Quan-Quan Zhou ◽  
Fen Tan ◽  
Liang-Qiu Lu ◽  
Wen-Jing Xiao

Visible-light-driven organic photochemical reactions have attracted substantial attention from the synthetic community. Typically, catalytic quantities of photosensitizers, such as transition metal complexes, organic dyes, or inorganic semiconductors, are necessary to absorb visible light and trigger subsequent organic transformations. Recently, in contrast to these photocatalytic processes, a variety of photocatalyst-free organic photochemical transformations have been exploited for the efficient formation of carbon–carbon and carbon–heteroatom bonds. In addition to not requiring additional photocatalysts, they employ low-energy visible light irradiation, have mild reaction conditions, and enable broad substrate diversity and functional group tolerance. This review will focus on a summary of representative work in this field in terms of different photoexcitation modes.1 Introduction2 Visible Light Photoexcitation of a Single Substrate3 Visible Light Photoexcitation of Reaction Intermediates4 Visible Light Photoexcitation of EDA Complexes between Substrates5 Visible Light Photoexcitation of EDA Complexes between Substrates and Reaction Intermediates6 Visible Light Photoexcitation of Products7 Conclusion and Outlook


Molecules ◽  
2021 ◽  
Vol 26 (3) ◽  
pp. 556
Author(s):  
Bonwoo Koo ◽  
Haneul Yoo ◽  
Ho Jeong Choi ◽  
Min Kim ◽  
Cheoljae Kim ◽  
...  

The expanding scope of chemical reactions applied to nucleic acids has diversified the design of nucleic acid-based technologies that are essential to medicinal chemistry and chemical biology. Among chemical reactions, visible light photochemical reaction is considered a promising tool that can be used for the manipulations of nucleic acids owing to its advantages, such as mild reaction conditions and ease of the reaction process. Of late, inspired by the development of visible light-absorbing molecules and photocatalysts, visible light-driven photochemical reactions have been used to conduct various molecular manipulations, such as the cleavage or ligation of nucleic acids and other molecules as well as the synthesis of functional molecules. In this review, we describe the recent developments (from 2010) in visible light photochemical reactions involving nucleic acids and their applications in the design of nucleic acid-based technologies including DNA photocleaving, DNA photoligation, nucleic acid sensors, the release of functional molecules, and DNA-encoded libraries.


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