Abstract:It was found that lignin β‐O‐4 ketone models could undergo smoothly the hydrogenolysis via light‐induced water‐donating transfer hydrogenation, which provides an example of using inexpensive and eco‐friendly water as the H‐transfer reagent to enable hydrogenolysis of lignin β‐O‐4 ketone models under catalyst‐free condition. Preliminary mechanistic investigations suggest that the mechanistic pathway involves the formation of acetophenone radicals.
“…Numerous studies have been carried out to transform lignin into low-weight molecules for fuels or chemicals using various methods, such as photolysis, pyrolysis, enzymatic methods and chemical catalysis. 5–8 However, none of these efforts have yet produced lignin valorization methods that are commercially feasible. To date, metallic catalysts have commonly been used at relatively high temperatures and pressures in homogeneous and heterogeneous catalytic studies for lignin conversion.…”
Lignin is the largest renewable source of aromatic compounds, creating an opportunity for chemical industry as a feedstock provided that the deconstruction and upgrading methods become economically feasible. Lignin valorization...
“…Numerous studies have been carried out to transform lignin into low-weight molecules for fuels or chemicals using various methods, such as photolysis, pyrolysis, enzymatic methods and chemical catalysis. 5–8 However, none of these efforts have yet produced lignin valorization methods that are commercially feasible. To date, metallic catalysts have commonly been used at relatively high temperatures and pressures in homogeneous and heterogeneous catalytic studies for lignin conversion.…”
Lignin is the largest renewable source of aromatic compounds, creating an opportunity for chemical industry as a feedstock provided that the deconstruction and upgrading methods become economically feasible. Lignin valorization...
We report a ligand‐to‐metal charge‐transfer (LMCT) process that used ferric (III) chloride as efficient chlorination reagent to mediate the vicinal dichlorination of alkenes. Under 420 nm LED light, the easily available and safe ferric (III) chloride could facilitate various alkenes to transform as 1,2‐dichloride compounds with good to excellent yields (19 examples). The strategy showed a more economic protocol than CuCl2, and provided a significant reference for the light‐Induced dichlorination in industrial catalysis.
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