| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1308871 | Inorganica Chimica Acta | 2011 | 6 Pages |
A convenient procedure is described for the synthesis of symmetrical biaryls via Ullmann coupling reaction catalyzed by palladium nanoparticles stabilized in a polymer matrix. A wide range of aryl halide substrates is transformed into corresponding symmetrical biaryls at a mild reaction condition. Living nature of the nanocatalysts is revealed by in situ recycling methodology and transmission electron microscopy (TEM). Calculation based on density functional theory (DFT) was performed to have better insight on mechanistic cycle and the result was supported by experimental evidence. Preliminary investigation also reveals that these PdNPs act as efficient catalyst in Heck and copper free Sonogashira reactions.
Graphical abstractA wide range of aryl halide substrates is transformed into corresponding symmetrical biaryls at a mild reaction condition using palladium nanoparticles stabilized in a polymer matrix. Living nature of the nanocatalysts is revealed by in situ recycling methodology and transmission electron microscopy (TEM).Figure optionsDownload full-size imageDownload as PowerPoint slideResearch highlights► Polyethyleneimine stabilizes palladium nanoparticles thermally. ► The Ullmann coupling occurs at mild reaction condition. ► The palladium nanoparticles stay live for consecutive catalytic cycles. ► Density functional theory helps to understand the mechanism of Ullmann coupling.
