Multicomponent reactions (MCRs), as a powerful one-pot combinatorial synthesis tool, have been recently applied to the synthesis of covalent organic frameworks (COFs). Compared with the thermally driven MCRs, the photocatalytic MCR-based COF synthesis has not yet been investigated. Herein, we first report the construction of COFs by a photocatalytic multicomponent reaction. Upon visible-light irradiation, a series of COFs with excellent crystallinity, stability, and permanent porosity are successfully synthesized via photoredox-catalyzed multicomponent Petasis reaction under ambient conditions. Additionally, the obtained exhibits excellent photoactivity and recyclability for the visible-light-driven oxidative hydroxylation of arylboronic acids. The concept of photocatalytic multicomponent polymerization not only enriches the methodology for COF synthesis but also opens a new avenue for the construction of COFs that might not be possible with the existing synthetic methods based on thermally driven MCRs.
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Front Chem
December 2024
Biomolécules: Conception, Isolement et Synthèse (BioCIS), UMR CNRS 8076, Université Paris-Saclay, Orsay, France.
Platform chemicals obtained from biomass will play an important role in chemical industry. Already existing compounds or not yet established chemicals are produced from this renewable feedstock. Using photochemical reactions as sustainable method for the conversion of matter furthermore permits to develop processes that are interesting from the ecological and economical point of view.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
December 2024
Hubei University, School of Materials Science and Engineering, 368, Youyi Street, 430062, Wuhan, CHINA.
Polynuclear Au(I) cluster photocatalysts, known for their high activity and stability, hold substantial potential in organic synthetic chemistry. This study synthesized two Au(I) supramolecular cluster catalysts with different nuclearities: a tetranuclear cluster, C1 ([(dppmAu2)2L1]•PF6-), and a hexadecanuclear cluster, C2 [(dppmAu2)6(Au4)(L1)4]•4PF6-, through a multicomponent stepwise self-assembly approach. Both cluster structures feature aurophilicity interaction motifs that endow them with exceptional photocatalytic performance, exhibiting optical band gaps of 2.
View Article and Find Full Text PDFEnviron Sci Pollut Res Int
December 2024
Department of Organic Chemistry, Faculty of Chemistry, Alzahra University, Tehran, Iran.
The efficient utilization of light and the prolonged lifetime of photo-induced charge carriers are essential elements that contribute to superior photocatalytic activity. Yolk-shell nanostructures with porous shells and mobile cores offer significant structural advantages in achieving these goals. However, designing yolk-shell multicomponent nanocomposites with diverse architectures remains a persistent challenge.
View Article and Find Full Text PDFOrg Lett
December 2024
State Key Laboratory of Green Pesticide, Engineering Research Center of Photoenergy Utilization for Pollution Control and Carbon Reduction, College of Chemistry, Central China Normal University, Wuhan, 430070, China.
A multicomponent heterogeneous semiconductor photocatalytic sulfinylsulfonylation of alkenes with alkyl iodides and SO was displayed under mild metal-free conditions by using boron carbonitride (BCN) as the alternative photocatalyst. This approach has resulted in the production of a wide range of structurally diverse sultine products in moderate to high yields, using readily available starting materials including alkyl iodides and olefins with broad functional group tolerance. The method is also suitable for the late-stage functionalization of complex bioactive molecules.
View Article and Find Full Text PDFOrg Biomol Chem
November 2024
Department of Nuclear Medicine, Jeonbuk National University Medical School and Hospital, Jeonju, 54907, Republic of Korea.
Alkyl sulfones are found in numerous valuable organic molecules. Here, we describe a promising approach for the one-pot synthesis of alkyl sulfones under visible light. Aryl diazo salts were allowed to react with styrene derivatives and sodium metabisulfite in the presence of thiophenol as a hydrogen atom transfer reagent and rhodamine B as a photocatalyst to yield alkyl sulfones.
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