Palladium catalyst coordinated in knitting N-heterocyclic carbene porous polymers for efficient Suzuki–Miyaura coupling reactions. Issue 3 (1st December 2014)

• Record Type: Journal Article
• Authors: Xu, Shujun; Song, Kunpeng; Li, Tao; Tan, Bien
• Is Part Of: Journal of materials chemistry. Volume 3:Issue 3(2015)
• Page Start: 1272
• Page End: 1278
• Publication Date: 2014-12-01
• Subjects: Materials -- Research -- Periodicals; Chemistry, Analytic -- Periodicals; Environmental sciences -- Research -- Periodicals; 543.0284
• DOI: 10.1039/c4ta05265j
• Languages: English
• ISSNs: 2050-7488

Abstract

Abstract : Microporous polymers were synthesised using external cross-linked N -heterocyclic carbene and benzene. These materials can serve as ligands to bind metal ions and demonstrated high catalytic activity for efficient Suzuki–Miyaura coupling reactions. Abstract : Three N -heterocyclic carbenes (NHCs) were successfully integrated into the skeleton of hyper-crosslinked polymers (HCPs) via an external cross-linking reaction. The structure and composition of the solid catalyst was characterized by SEM, N2 sorption, FT-IR, XPS and CP/MAS NMR. Depending on the nature of the NHCs, the Brunauer–Emmett–Teller (BET) surface area of HCPs could be tuned and a BET surface area as high as 1229 m 2 g −1 was achieved. The Poly-NHC-2–Pd 2+ catalyst afforded rapid conversion for the Suzuki–Miyaura cross-coupling reactions of various aryl halides and arylboronic acids even at a Pd loading of 0.057 mmol% in aqueous media. In particular, because of the substantial porosity and individual pore structure toward the entrapped Pd species, Poly-NHC-2–Pd 2+ showed outstanding stability and recyclability, which could be reused at least 5 times without significant loss of activity. The developed microporous catalyst combined with the NHC-functionalize is one of the most efficient heterogeneous systems for Suzuki–Miyaura cross-coupling reactions of aryl halides.