The interface engineering of CeO2/CoO with different spatial orientations modifies the electronic band structure, thereby stabilizing photogenerated charge carriers in the conduction band and improving photocatalytic SMC reaction under visible light.
For the first time, an ionic liquid-mediated nickel-catalysed mild yet efficient protocol has been developed for biaryl synthesis via Suzuki–Miyaura cross coupling (SMC) reactions.
A highly efficient catalytic system for the Suzuki–Miyaura reaction of deactivated and hindered aryl chlorides using trace amounts of commercial catalysts was reported.
PIII-doped heterosumanenes are synthesized to show diverse coordination patterns with transition metals. The coordination complexes with Pd2+ have been proved to be promising catalysts for the Suzuki–Miyaura coupling reaction of aryl chlorides.
Herein, we report a commercially available natural saponin acting as a surfactant and serving as a micellar catalyst, enabling Suzuki–Miyaura cross-coupling effectively with highly challenging heteroaromatic substrates in water at room temperature.