Pd-PEPPSI complexes based on 1,2,4-triazol-3-ylidene ligands as efficient catalysts in the Suzuki—Miyaura reaction
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DOI: 10.1007/s11172-018-2040-8
Abstract: The palladium complexes of the Pd-PEPPSI type with N-heterocyclic carbenes of the 1,2,4-triazole series were synthesized in 76—99% yields by the reactions of PdCl2 with 1,4-di- alkyl-1,2,4-triazolium salts in pyridine in the presence of KBr… read more here.
Keywords: peppsi complexes; based triazol; complexes based; suzuki miyaura ... See more keywords
Mechanically Robust Hybrid Gel Beads Loaded with “Naked” Palladium Nanoparticles as Efficient, Reusable, and Sustainable Catalysts for the Suzuki–Miyaura Reaction
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DOI: 10.1021/acssuschemeng.2c05484
Abstract: The increase in demand for Pd and its low abundance pose a significant threat to its future availability, rendering research into more sustainable Pd-based technologies essential. Herein, we report Pd scavenging mechanically robust hybrid gel… read more here.
Keywords: gel beads; suzuki miyaura; robust hybrid; mechanically robust ... See more keywords
Poly(o-aminothiophenol)-stabilized Pd nanoparticles as efficient heterogenous catalysts for Suzuki cross-coupling reactions
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DOI: 10.1039/c7ra09947a
Abstract: Poly(o-aminothiophenol) (PATP)-stabilized Pd nanoparticles with Pd nanoparticles embedded in a polymer matrix have been obtained through a facile one-step route by mixing o-aminothiophenol monomer and Pd(NO3)2 in an acidic aqueous solution without additional template or… read more here.
Keywords: stabilized nanoparticles; poly aminothiophenol; suzuki cross; coupling reactions ... See more keywords