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Tasnim, Tarannum ; Shafiei, Negin ; Laminack, Katelyn , et al. ChemRxiv,2024. DOI: 10.26434/chemrxiv-2024-jncx1
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Abstract: While charge-transfer complexes involving halogen-bonding interactions have emerged as an alternative strategy for the photogeneration of carbon radicals, examples using (fluoro)alkyl bromides are limited. This report describes adual catalytic approach for radical generation from α-bromodifluoroesters and amides under visible light irradiation. Mechanistic studies suggest that the reaction proceeds through in-situ bromide displacement using a catalytic iodide salt, generat_x005f_x0002_ing a C–I bond that can be engaged by our halogen-bonding photocatalysis platform.
Purchased from AmBeed: 621-23-8 ; 88-58-4 ; 635-90-5 ; 354-08-5
CAS No. : | 635-90-5 | MDL No. : | MFCD00005343 |
Formula : | C10H9N | Boiling Point : | No data available |
Linear Structure Formula : | - | InChI Key : | GEZGAZKEOUKLBR-UHFFFAOYSA-N |
M.W : | 143.19 | Pubchem ID : | 12480 |
Synonyms : |
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Chemical Name : | 1-Phenyl-1H-pyrrole |
Signal Word: | Warning | Class: | |
Precautionary Statements: | P261-P305+P351+P338 | UN#: | |
Hazard Statements: | H315-H319-H335 | Packing Group: | |
GHS Pictogram: |
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