| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 67810 | Journal of Molecular Catalysis A: Chemical | 2007 | 5 Pages |
The MCM-41-supported sulfur palladium(0) complex has been synthesized from 3-(2-cyanoethylsulfanyl)propyltriethoxysilane via immobilization on MCM-41, followed by reacting with palladium chloride, and then the reduction with hydrazine hydrate. The complex has been characterized by powder X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS) and it is a highly active catalyst for the heterogeneous Suzuki reaction affording a variety of biaryls in high to excellent isolated yields. Our system not only solves the basic problems of catalyst separation and recovery but also avoids the use of phosphine ligands.
Graphical abstractThe MCM-41-supported sulfur palladium(0) complex has been synthesized from 3-(2-cyanoethylsulfanyl)propyltriethoxysilane via immobilization on MCM-41, followed by reacting with palladium chloride, and then the reduction with hydrazine hydrate. This complex is a highly active catalyst for the heterogeneous Suzuki reaction affording a variety of biaryls in high to excellent yields. Figure optionsDownload full-size imageDownload as PowerPoint slide
