Synergistic photoredox and nickel catalytic cross-coupling systems have attracted great attention as a promising methodology for the production of aryl C–N bonds under mild conditions. They are also an extreme challe...Synergistic photoredox and nickel catalytic cross-coupling systems have attracted great attention as a promising methodology for the production of aryl C–N bonds under mild conditions. They are also an extreme challenge because they are dramatically affected by the extremely widespread photoinduced electron transfer (PET) from the organic photoredox catalysts to the Ni^(Ⅱ). By regulating the geometry configuration of ligands to compulsively generate the twisting of the conjugation between the dye-based ligands and the Ni^(Ⅱ)-carboxylate nodes in the metal–organic frameworks (MOFs), herein, we report a new heterogeneous approach to directly overcome this inherent challenge. The rigid plane structure of phenoxazine as compared to triphenylamine promotes the twisted Ni^(Ⅱ)-phenoxazine conjunction in the metal–organic frameworks and guarantees the diode-like photoelectron flow characteristics, which successfully execute the reversed-directional ground-state electronic conductivity, where the unwanted photoinduced electron transfer processes from the phenoxazine-moieties to the Ni^(Ⅱ) sites are potentially avoided. This synergistic photoredox and nickel catalytic approach, which offers control over the direction of the electron transfer, provides a mild concise C–N cross-coupling strategy utilizing a Ni^(Ⅱ) catalyst along with a photocatalyst that operates at room temperature under visible light and is extendable to aryl bromide and aryl chloride systems.展开更多
基金supported by the National Natural Science Foundation of China(grant numbers 22171034,21890381 and 21820102001).
文摘Synergistic photoredox and nickel catalytic cross-coupling systems have attracted great attention as a promising methodology for the production of aryl C–N bonds under mild conditions. They are also an extreme challenge because they are dramatically affected by the extremely widespread photoinduced electron transfer (PET) from the organic photoredox catalysts to the Ni^(Ⅱ). By regulating the geometry configuration of ligands to compulsively generate the twisting of the conjugation between the dye-based ligands and the Ni^(Ⅱ)-carboxylate nodes in the metal–organic frameworks (MOFs), herein, we report a new heterogeneous approach to directly overcome this inherent challenge. The rigid plane structure of phenoxazine as compared to triphenylamine promotes the twisted Ni^(Ⅱ)-phenoxazine conjunction in the metal–organic frameworks and guarantees the diode-like photoelectron flow characteristics, which successfully execute the reversed-directional ground-state electronic conductivity, where the unwanted photoinduced electron transfer processes from the phenoxazine-moieties to the Ni^(Ⅱ) sites are potentially avoided. This synergistic photoredox and nickel catalytic approach, which offers control over the direction of the electron transfer, provides a mild concise C–N cross-coupling strategy utilizing a Ni^(Ⅱ) catalyst along with a photocatalyst that operates at room temperature under visible light and is extendable to aryl bromide and aryl chloride systems.
