光催化
光化学
氧化还原
催化作用
化学
可见光谱
电子转移
氧气
亚胺
业务
超氧化物
材料科学
光电子学
有机化学
作者
Huimin Hao,Ji‐Long Shi,Hui Fang Xu,Xia Li,Xianjun Lang
标识
DOI:10.1016/j.apcatb.2019.01.037
摘要
TiO2 is the most established semiconductor photocatalyst. The prominence of TiO2 is becoming increasingly obvious because its interfacial redox reactions have implication on a wide range processes such as energy conversion and environmental remediation. Herein, we exploited the surface complex created by the interaction between organic molecules with binding sites and accommodating surface of TiO2 for visible light-driven selective aerobic oxidation reactions. A novel surface complex formed between N-hydroxyphthalimide (NHPI) and TiO2 was discovered. The NHPI-TiO2 complex turned out to be an outstanding visible light photocatalyst and was successfully used in the selective oxidation of amines into imines with atmosphere O2 under blue LED irradiation. The stability of the NHPI-TiO2 complex was preserved by 3 mol% of (2,2,6,6-tetramethylpiperidin-1-yl)oxyl (TEMPO) acting as a cooperative catalyst. Moreover, selectivities for the imine products were also promoted by TEMPO. Superoxide anion radical (O2−) were evidenced to be the primary reactive oxygen species (ROS) to execute the oxidative conversions. This work suggests that TiO2 surface complexes can be robust photocatalysts for visible light-driven selective aerobic reactions, provided that an appropriate cooperative redox catalyst exists to channel the photocatalytic electron transfer.
科研通智能强力驱动
Strongly Powered by AbleSci AI