A straightforward protocol using readily available aromatic amines,N,N,N',N'-tetramethyl-p-phenylenediamine or N,N,N',N'-tetramethylbenzidine,as photocatalysts was developed for theefficient hydrodehal...A straightforward protocol using readily available aromatic amines,N,N,N',N'-tetramethyl-p-phenylenediamine or N,N,N',N'-tetramethylbenzidine,as photocatalysts was developed for theefficient hydrodehalogenation of organic halides,such as 4'-bromoacetophenone,polyfluoroarenes,cholorobenzene,and 2,2',4,4'-tetrabromodiphenyl ether(a resistant and persistent organic pollu-tant).The strongly reducing singlet excited states of the amines enabled diffusion-controlled disso-ciative electron transfer to effectively cleave carbon-halogen bonds,followed by radical hydrogena-tion.Diisopropylethylamine served as the terminal electron/proton donor and regenerated theamine sensitizers.展开更多
Hierarchical Si C nanowire-supported Pd nanoparticles showed high photocatalytic activity for the C–X(X = Br, I) borylation of aryl halides at 30 °C. The Si C/Pd Mott-Schottky contact enhances the rapid transfer...Hierarchical Si C nanowire-supported Pd nanoparticles showed high photocatalytic activity for the C–X(X = Br, I) borylation of aryl halides at 30 °C. The Si C/Pd Mott-Schottky contact enhances the rapid transfer of the photogenerated electrons from Si C to the Pd nanoparticles. As a result, the concentrated energetic electrons in the Pd nanoparticles can facilitate the cleavage of C–I or C–Br bonds, which normally requires high-temperature thermal processes. We show that the present Pd/Si C photocatalyst is capable of catalyzing the transformation of a large variety of aryl halides to their corresponding boronate esters under visible light irradiation, with excellent yields.展开更多
文摘A straightforward protocol using readily available aromatic amines,N,N,N',N'-tetramethyl-p-phenylenediamine or N,N,N',N'-tetramethylbenzidine,as photocatalysts was developed for theefficient hydrodehalogenation of organic halides,such as 4'-bromoacetophenone,polyfluoroarenes,cholorobenzene,and 2,2',4,4'-tetrabromodiphenyl ether(a resistant and persistent organic pollu-tant).The strongly reducing singlet excited states of the amines enabled diffusion-controlled disso-ciative electron transfer to effectively cleave carbon-halogen bonds,followed by radical hydrogena-tion.Diisopropylethylamine served as the terminal electron/proton donor and regenerated theamine sensitizers.
基金supported by the National Natural Science Foudation of China(21473232,21673271,U1710112)
文摘Hierarchical Si C nanowire-supported Pd nanoparticles showed high photocatalytic activity for the C–X(X = Br, I) borylation of aryl halides at 30 °C. The Si C/Pd Mott-Schottky contact enhances the rapid transfer of the photogenerated electrons from Si C to the Pd nanoparticles. As a result, the concentrated energetic electrons in the Pd nanoparticles can facilitate the cleavage of C–I or C–Br bonds, which normally requires high-temperature thermal processes. We show that the present Pd/Si C photocatalyst is capable of catalyzing the transformation of a large variety of aryl halides to their corresponding boronate esters under visible light irradiation, with excellent yields.
