photocatalytic chemistry

Visible-light organophotocatalysis serves as a sustainable synthetic tool to construct molecular skeletons under mild conditions. Metal-free organic photocatalysts feature low cost, good biocompatibility and adjustable redox properties, avoiding expensive transition-metal catalysts. Nevertheless, narrow substrate adaptability and insufficient stereocontrol remain major challenges. This project aims to develop new visible-light-driven radical transformations mediated by organic photocatalysts. Commercially available photocatalysts will be screened, and key parameters including solvent, catalyst loading and additives will be optimized. Target reactions focus on radical cyclization and selective C–C bond formation. After establishing optimal conditions, the substrate scope and functional group compatibility will be examined. Control experiments together with spectroscopic studies will be conducted to reveal the catalytic mechanism. Products will be characterized by NMR and HRMS, and stereoselectivity will be analysed via chiral HPLC. This work expects to provide practical, environmentally friendly synthetic protocols for complex organic molecules.

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Publication Details

Journal
California Digital Library
Published
2026-07-30
DOI
https://doi.org/10.48321/d1b7512d2e
Primary Topic
Radical Photochemical Reactions
Type
article
Field-Weighted Citation Impact
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article

photocatalytic chemistry

Yuxin Cheng
California Digital Library
Radical Photochemical Reactions
article

photocatalytic chemistry

Yuxin Cheng
article en

Abstract

Visible-light organophotocatalysis serves as a sustainable synthetic tool to construct molecular skeletons under mild conditions. Metal-free organic photocatalysts feature low cost, good biocompatibility and adjustable redox properties, avoiding expensive transition-metal catalysts. Nevertheless, narrow substrate adaptability and insufficient stereocontrol remain major challenges. This project aims to develop new visible-light-driven radical transformations mediated by organic photocatalysts. Commercially available photocatalysts will be screened, and key parameters including solvent, catalyst loading and additives will be optimized. Target reactions focus on radical cyclization and selective C–C bond formation. After establishing optimal conditions, the substrate scope and functional group compatibility will be examined. Control experiments together with spectroscopic studies will be conducted to reveal the catalytic mechanism. Products will be characterized by NMR and HRMS, and stereoselectivity will be analysed via chiral HPLC. This work expects to provide practical, environmentally friendly synthetic protocols for complex organic molecules.

California Digital Library
Chinese University of Hong Kong (HK)
Openalex Percentile: Top 17%
Radical Photochemical Reactions
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