A simple, quick and novel protocol for biaryl synthesis using LiCl-promoted in situ-generated Pd nanoparticles

被引:3
|
作者
Phukan, Parmita [1 ]
Boruah, Preeti Rekha [1 ]
Gehlot, Praveen Singh [2 ]
Kumar, Arvind [2 ]
Sarma, Diganta [1 ]
机构
[1] Dibrugarh Univ, Dept Chem, Dibrugarh 786004, Assam, India
[2] CSIR, AcSIR, Cent Salt & Marine Chem Res Inst, GB Marg, Bhavnagar 364002, Gujarat, India
关键词
green chemistry; LiCl; nanoparticles; palladium chloride; Suzuki-Miyaura reaction; DIELS-ALDER REACTION; SHAPE-CONTROLLED SYNTHESIS; CROSS-COUPLING REACTIONS; PALLADIUM NANOPARTICLES; HIGHLY EFFICIENT; FACILE SYNTHESIS; HECK REACTIONS; SUZUKI; CARBON; OXIDATION;
D O I
10.1002/aoc.4009
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
This paper describes a simple and a very quick protocol for biaryl synthesis using the Suzuki-Miyaura cross-coupling reaction. A quintessential role of salting-out agent LiCl was observed in the Suzuki-Miyaura cross-coupling reaction that enhanced the reduction rate of Pd (II) to a considerable extent, resulting in the formation of nanosized palladium in a few seconds. The isolated Pd nanoparticles were characterized with X-ray diffraction, dynamic light scattering, TGA, transmission electron microscopy and scanning electron microscopy-dispersive X-ray spectroscopy. The Suzuki-Miyaura cross-coupling reaction proceeded very well with the in situ-generated Pd nanocatalysts furnishing the desired biaryl adducts with excellent yields.
引用
收藏
页数:7
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