The reaction mechanism of palladium-catalyzed visible light-driven carboxylation of aryl halides and triflates with a photoredox catalyst was examined in detail. Experimental and theoretical studies indicated that the active species for photoredox-catalyzed reduction was cationic ArPd(II)+ species to generate nucleophilic ArPd(I) or its further reduced ArPd(0)− species, which reacted with CO2 to give carboxylic acids. Hydrodehalogenated compounds, main byproducts in this carboxylation, were thought to be generated by protonation of these reduced species.
Toriumi, N.; Shimomaki, K.; Caner, J.; Murata, K.; Martin, R.; Iwasawa, N.
Bull. Chem. Soc. Jpn. 2021, 94, (7), 1846-1853
DOI:
10.1246/bcsj.20210151
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