Cu Anchored Carbon Nitride (Cu/CN) Catalyzes Selective Oxidation of Thiol by Controlling Reactive Oxygen Species Generation
Source abstract
Abstract
High Resolution Image Download MS PowerPoint Slide Production of H 2 O 2 using heterogeneous semiconductor photocatalysts has emerged as an ecofriendly and practical approach across various applications, ranging from environmental detoxification to fuel cells and chemical synthesis. Extensive efforts have been devoted to engineering semiconductors to enhance their catalytic capabilities for H 2 O 2 production. However, in chemical synthesis, the utilization of the potent oxidant H 2 O 2 can present challenges in selectively oxidizing organic compounds. In this study, we introduce copper atoms into carbon nitride (Cu/CN), facilitating the generation of hydroperoxyl radicals (·OOH) as primary reactive oxidants and offering reaction conditions entirely devoid of H 2 O 2 via the Fenton reaction. Cu/CN demonstrates selective oxidation of thiols to disulfides, in contrast to other current heterogeneous photocatalysts that yield undesired overoxidized side products, such as thiosulfinate and thiosulfonate. Cu/CN’s controllable capacity for specific ROS generation, broad substrate scopes, and recyclability empower greener and highly selective photooxidation of organic compounds.
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Research context
OpenAlex topics: Sulfur-Based Synthesis Techniques · Chemical Synthesis and Reactions · Oxidative Organic Chemistry Reactions
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
Department of Chemical and Biological Engineering, and Institute of Chemical Processes, Seoul National University, Seoul 08826, Republic of Korea
Missile Research Institute, Agency for Defense Development, Daejeon 34186, Republic of Korea
Department of Chemistry, Korea Military Academy, Seoul 01805, Republic of Korea
Center for Nanoparticle Research, Institute for Basic Science, Seoul 08826, Republic of Korea
Funding
National Research Foundation of Korea · Institute for Basic Science
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