Aryl- and heteroaryl units are present in a wide variety of natural products, pharmaceuticals, and functional materials. The method for reduction of aryl halides with ubiquitous distribution is highly sought after for late-stage construction of various aromatic compounds. The visible-light-driven reduction of aryl halides to aryl radicals by electron transfer provides an efficient, simple, and environmentally friendly method for the construction of aromatic compounds. This review summarizes the recent progress in the generation of aryl radicals by visible-light-driven reduction of aryl halides with metal complexes, organic compounds, semiconductors as catalysts, and alkali-assisted reaction system. The ability and mechanism of reduction of aromatic halides in various visible light induced systems are summarized, intending to illustrate a comprehensive introduction of this research topic to the readers.
P-n junction BiOBr/ZnO composites were prepared by a facile solvothermal process with double Br sources of CTAB and KBr. The samples were characterized by XRD, XPS, SEM, TEM, HRTEM, DRS, BET and PL. The BiOBr/ZnO composites exhibited much higher photocatalytic activity than single BiOBr and ZnO for the degradation of phenol under simulated sunlight irradiation. The enhanced photocatalytic activity of BiOBr/ZnO composites could be mainly ascribed to the high-efficiency separation of photogenerated electron-hole pairs through BiOBr/ZnO p-n junction. The reaction mechanism for the removal of phenol was also discussed. Hole and ·OH were the main reactive species. Moreover, the influence of disparate ratios of double Br sources to BiOBr/ZnO composites was also investigated. The results indicated that the BiOBr/ZnO composites prepared by double Br sources showed better photocatalytic activities than the sample prepared by single Br source.
Glycine‐functionalized reduced graphene oxide (GRGO) was prepared through the reaction of glycine and chlorine‐functionalized reduced graphene oxide. The product was characterized by SEM, HRTEM, IR, Raman, and XPS. The nitrogen content (8.28%) was high in product, peak at 285.8 eV was assigned to the C–N bond, which implied that the chlorine residues in raw material were substituted by amine group of glycine. The intensity ratio of D and G peak was about 1.5, which also implied that more saturated carbon atoms were present in the product. Results of SEM, IR, and XPS confirmed that glycine molecules were attached to graphene sheets. Compared with reduced graphene oxide (61.5 mg/g) and active carbon (45.2 mg/g), GRGO had a good adsorption capacity (98.9 mg/g) for methylene blue. The adsorption process was fitted to three kinetic models and three adsorption isotherm models. The adsorption process complied with pseudo‐second order kinetic model and Langmuir model.
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