“…A low yield (46 %) of the coupling product was observed with homogeneous Pd(OAc) 2 (Table 1, (Table 1, entry 3), whereas, as described by Jeffery and David, [15] the presence of soluble ammonium salts (7.0 mol % NBu 4 Cl) increased the yield (65 %, Table 1, entry 5). The coupling reaction carried out with soaked Pd 2 occurred in 79 % yield, thus confirming that polyionic gels provide a particularly appropriate environment for organometallic catalysis.…”
A highly polar micro‐environment, which is suitable for efficient metal scavenging and heterogeneous catalyst preparation, is provided by polyionic gel beads 1 (see scheme). These heterogeneous media enable easy product isolation and catalyst recycling. As an example, a Pd‐soaked ionic gel 2 is shown to transform into a highly efficient and recyclable catalyst 3 in the Suzuki cross‐coupling reaction.
“…A low yield (46 %) of the coupling product was observed with homogeneous Pd(OAc) 2 (Table 1, (Table 1, entry 3), whereas, as described by Jeffery and David, [15] the presence of soluble ammonium salts (7.0 mol % NBu 4 Cl) increased the yield (65 %, Table 1, entry 5). The coupling reaction carried out with soaked Pd 2 occurred in 79 % yield, thus confirming that polyionic gels provide a particularly appropriate environment for organometallic catalysis.…”
A highly polar micro‐environment, which is suitable for efficient metal scavenging and heterogeneous catalyst preparation, is provided by polyionic gel beads 1 (see scheme). These heterogeneous media enable easy product isolation and catalyst recycling. As an example, a Pd‐soaked ionic gel 2 is shown to transform into a highly efficient and recyclable catalyst 3 in the Suzuki cross‐coupling reaction.
“…Recent reports showed that the palladium nanoparticles acted as active catalysts for C-C coupling reactions [11][12][13][14]. The Pd(0) nanoparticles can be formed under reducing agents or sonochemical reactions.…”
“…So, we replaced styrene by 2,3-dihydrofuran 11 and performed the reaction in similar conditions as those previously described. …”
Section: Catalyst Recycling In the Heck Reactionmentioning
confidence: 99%
“…ILs are of special interest due to their specific properties: they present good chemical and thermal stability, low vapour pressure, wide liquid range, good solubility for a wide range of organic and inorganic reagents and they allow the facile separation of the products and recycling of the ILs containing the catalysts. 8,9 In addition to this, the use of ILs in the Heck reaction has opened new insights and perspectives: 10 (i) ILs containing imidazolium cations stabilize ligandfree precursors of catalysts (free of η 2 donor ligands such as phosphines), consequently catalysts like palladium acetate proved to be efficient even at low concentrations and have been widely used; 8,11,12 (ii) When performed in ILs, the reaction rate was significantly increased. [13][14][15] In certain cases, this enabled the regioselectivity of the products obtained to be controlled; 16 (iii)…”
Palladate salts from imidazolium and pyridinium ionic liquids (ILs) were used as catalysts in Heck reaction. When compared to traditional precatalysts, they demonstrated to be more efficient catalysts. These results are attributed to the presence of nanoparticles (NPs) which served as a reservoir of palladium species. Indeed the use of palladate salts from ILs, that produce no byproducts, provide better control of the formation and surface composition of the NPs leading to a constant recyclability.
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