Palladium catalyst supported on PEGylated imidazolium based phosphinite ionic liquid-modified magnetic silica core-shell nanoparticles: a worthy and highly water-dispersible catalyst for organic reactions in water

被引:47
|
作者
Bahadorikhalili, Saeed [1 ]
Ma'mani, Leila [2 ]
Mahdavi, Hossein [1 ]
Shafiee, Abbas [3 ,4 ]
机构
[1] Univ Tehran, Coll Sci, Dept Chem, Tehran, Iran
[2] Shahid Beheshti Univ Med Sci, Dept Tissue Engn, Sch Adv Technol Med, Tehran, Iran
[3] Univ Med Sci, Dept Med Chem, Fac Pharm, Tehran 14176, Iran
[4] Univ Med Sci, Pharmaceut Sci Res Ctr, Tehran 14176, Iran
来源
RSC ADVANCES | 2015年 / 5卷 / 87期
基金
美国国家科学基金会;
关键词
CROSS-COUPLING REACTIONS; HECK REACTION; HETEROGENEOUS CATALYST; RECYCLABLE CATALYSTS; 4-NITROPHENOL REDUCTION; PD NANOPARTICLES; SUZUKI REACTION; ARYL CHLORIDES; AQUEOUS-MEDIUM; EFFICIENT;
D O I
10.1039/c5ra12747e
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A highly water-dispersible palladium nanocatalyst was fabricated by the immobilization of Pd onto the surface of PEGylated imidazolium based phosphinite ionic liquid functionalized gamma-Fe2O3@SiO2 core-shell nanoparticles. This nanocatalyst (denoted as [Pd@PEGylated ImIL-OPPh2-gamma-Fe2O3@SiO2]) was assessed as a promising Pd catalyst in different organic reactions including Mizoroki-Heck and Sonogashira coupling reactions of aryl halides and the reduction reaction of 4-nitrophenol (4-NP) to 4-aminophenol (4AP). From the application point of view, this nanocatalyst showed high thermal versatility, stability, recoverability, and compatibility in aqueous media. The catalyst recovery test revealed that its performance and catalytic activity stayed indefectible during several sequential runs. The loading level of Pd in the [Pd@PEGylated ImIL-OPPh2-gamma-Fe2O3@SiO2] catalyst was 0.087 mmol g(-1). Pivotal properties including high robustness, efficiency and turnover frequency (TOF), mild reaction conditions, utilization of water as a green solvent, simple product work-up, and facile catalyst recovery make this catalyst favourable from the environmental and economic points of view.
引用
收藏
页码:71297 / 71305
页数:9
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