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DC Field | Value | Language |
---|---|---|
dc.contributor.author | Sarkar, Debayan | en_US |
dc.date.accessioned | 2024-06-28T11:37:30Z | - |
dc.date.available | 2024-06-28T11:37:30Z | - |
dc.date.issued | 2024 | - |
dc.identifier.citation | Bishi, S., Kar, M., Mandal, T. K., & Sarkar, D. (2024). G-C3N4 catalysed sustainable synthesis of (hetero)aryl acids and regioselective α-bromo ketones in one pot under visible light catalysis. Catalysis Science and Technology. Scopus. https://doi.org/10.1039/d4cy00029c | en_US |
dc.identifier.issn | 2044-4753 | - |
dc.identifier.other | EID(2-s2.0-85190260908) | - |
dc.identifier.uri | https://doi.org/10.1039/d4cy00029c | - |
dc.identifier.uri | https://dspace.iiti.ac.in/handle/123456789/13719 | - |
dc.description.abstract | Heterogeneous metal-free 2D semiconductor g-C3N4 with outstanding electronic characteristics is an emerging alternative redox catalyst to conventional thermochemical catalysts, where it functions as a high-performance photocatalyst towards a sustainable synthesis of high-value organic molecules. Herein, we reported the excellent activity of g-C3N4 toward the selective oxidation of (hetero)aryl methyl halides to (hetero)aryl carboxylic acids under sunlight with oxygen molecules in air as a benign oxidant. To ensure maximum atom efficiency, the generated by-product HBr can be reutilized for the synthesis of α-bromo ketones with zero effluent discharge, signifying an eco-friendly process. g-C3N4 features a remarkable enhancement in performance for the selective photocatalytic oxidation of (hetero)aryl methyl halide with subsequent generation of α-bromo ketones in one pot with an excellent isolated yield of 90-97%. © 2024 The Royal Society of Chemistry. | en_US |
dc.language.iso | en | en_US |
dc.publisher | Royal Society of Chemistry | en_US |
dc.source | Catalysis Science and Technology | en_US |
dc.title | g-C3N4 catalysed sustainable synthesis of (hetero)aryl acids and regioselective α-bromo ketones in one pot under visible light catalysis | en_US |
dc.type | Journal Article | en_US |
Appears in Collections: | Department of Chemistry |
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