Prospects and Applications of Palladium Nanoparticles in the Cross‐coupling of (hetero)aryl Halides and Related Analogues

• Main Authors: Jude I. Ayogu, Efeturi A. Onoabedje
• Format: Article
• Language: English
• Published: Wiley-VCH 2021-04-01
• Series: ChemistryOpen
• Subjects: nanoparticles; cross-coupling reactions; Suzuki-Miyaura cross-coupling; Heck reaction; supported catalysts
• Online Access: https://doi.org/10.1002/open.202000309

Abstract Discovering efficient methods for the formation of carbon‐carbon bonds is a central ongoing theme in organic synthesis. Cross‐coupling reactions catalysed by metal nanoparticles are attractive alternatives to the traditional use of metal counterparts due to the catalytic tunability, selectivity, recyclability and reusability of the nanoparticles. The ongoing search for sustainable processes demands that reusable and environmentally benign catalysts are used. While the advantages of nanoparticles catalysts over bulk catalysts cannot be overemphasised, the problem of sintering, agglomeration and leaching are drawbacks to their full industrial applications. Hence, efforts are being made towards advancing the efficiency of the catalytic nanoparticle systems over the years. This review presents the progress, the challenges and the prospects of palladium nanoparticle with focus on Heck, Suzuki, Hiyama and Sonogashira cross‐coupling reactions involving (hetero) aryl halides and the analogues.