Pd/Halloysite as a Novel, Efficient and Reusable Heterogeneous Nanocatalyst for the Synthesis of p-Phenylenevinylene Oligomers

被引:6
作者
Molano, William A. [1 ]
Cardenas, Juan C. [1 ]
Sierra, Cesar A. [1 ]
Carriazo, Jose G. [2 ]
Ochoa-Puentes, Cristian [1 ]
机构
[1] Univ Nacl Colombia, Dept Quim, Grp Invest Macromol & Sintesis Organ Sostenible, Sede Bogota, Carrera 45 26-85, Bogota 5997, Colombia
[2] Univ Nacl Colombia, Dept Quim, ESCA, Sede Bogota, Carrera 45 26-85, Bogota 5997, Colombia
关键词
Halloysite; Heck reaction; nanocatalyst; palladium; p-phenylenevinylene oligomers; CROSS-COUPLING REACTIONS; C-H FUNCTIONALIZATION; WITTIG-HECK REACTION; LIGAND-FREE SUZUKI; ONE-POT SYNTHESIS; PALLADIUM NANOPARTICLES; OPTICAL-PROPERTIES; POLY(P-PHENYLENEVINYLENE) DERIVATIVES; CATALYTIC APPLICATION; HALLOYSITE NANOTUBES;
D O I
10.1002/slct.201800344
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The potential applications of poly(p-phenylene vinylene) derivatives and its oligomers in organic electronics have attracted great interest in recent years. In this study, a novel palladium supported on halloysite heterogeneous catalyst (Pd/HNTs) was prepared, characterized and its catalytic activity for obtaining p-phenylenevinylene oligomers was investigated in the Heck coupling of styrene and 2,5-diiodo-1,4-dimethoxybenzene using conventional and environmentally benign solvents. Thus, in the presence of 0.75 mol% catalyst, the product was obtained in 76% yield using ethanol as solvent. To evaluate the versatility of the Pd/HNTs catalyst, the synthesis of a series of p-phenylenevinylene oligomers and divinylbenzene derivatives was performed obtaining yields between 58 and 93%. In addition, the catalyst could be recovered and reused for four reaction cycles without significant loss of its catalytic activity. Finally, the photophysical characterization of the synthesized molecules was performed.
引用
收藏
页码:4430 / 4438
页数:9
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