Surface-fluorinated TiO 2 was prepared with the help of anhydrous hydrogen fluoride (AHF) via vaporphase fluorination at 473 K for 2 h and characterized by XRD, SEM, UV-visible diffuse reflectance, Raman, XPS, and ATR-FTIR, respectively. XRD and UV-visible diffuse reflectance show that fluorination does not change the bulk crystal structure and optical absorption of TiO 2 under the abovementioned preparation condition. However, the photoinduced hydrophilicity, photocatalytic H 2 evolution, and organic contaminant decomposition are greatly improved by the insertion of fluorine. XPS, ATR-FTIR, and Raman measurements of TiO 2 and surface-fluorinated TiO 2 reveal that fluorination remarkably increases the adsorption of polar molecules, including water and some organics, which is mainly attributed to the enhancement of surface acidity, and the formation of the surface hydroxyl radicals, which is beneficial for both photocatalytic oxidation reaction and hydrophilicity. Therefore, as expected, H 2 evolution from water, aldehyde decomposition, and methylene blue degradation increase, and water contact angle decreases, on the surface-fluorinated TiO 2 under UV light irradiation.

No abstract

No abstract

No vinyl ether by‐products are formed in the palladium(0)‐complex catalyzed hydroalkoxylation of hexafluoropropene (see scheme). Saturated hydrofluoroethers are selectively synthesized with alcohols or phenols under neutral conditions in the presence of [Pd(PPh3)4]/dppb. dppb=1,4‐bis(diphenylphosphanyl)butane.