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RESEARCH PRODUCT
Evidences of release and catch mechanism in the Heck reaction catalyzed by palladium immobilized on highly cross-linked-supported imidazolium salts
Giacomo StrappavecciaLucia Anna BivonaLucia Anna BivonaLuigi VaccaroCinzia PaviaChiara PetrucciCarmela AprileFrancesco GiacaloneAnna Maria Pia SalvoMichelangelo Gruttadauriasubject
Suzuki reactionchemistry.chemical_elementIonic liquidHeterogeneous catalysisCatalysisCatalysisMetalchemistry.chemical_compoundHeterogeneous catalysiCC cross-couplingHeck reactionSuzuki reactionHeck reactionPolymer chemistryOrganic chemistryPhysical and Theoretical ChemistryHeterogeneous catalysisChemistryProcess Chemistry and TechnologyArylSettore CHIM/06 - Chimica OrganicaIonic liquidsvisual_artIonic liquidvisual_art.visual_art_mediumPalladiumdescription
Abstract Palladium (10 wt%) on a highly cross-linked imidazolium-based material was used as catalyst in 0.1 mol% in the Heck reaction between several alkenes and aryl iodides. Products were obtained from good to high yields. Deeper investigations showed a release of Pd species in solution and their capture by the imidazolium-based support. When a sixfold amount of support was employed the re-captured Pd species (0.5–0.6 wt%) were not anymore catalytically active. This result represents a new interesting aspect of this work since the highly cross-linked imidazolium-based material can act also as Pd scavenger avoiding the release of the metal in solution. Important differences between Heck and Suzuki reactions have been evidenced when the reactions were carried out in the presence of the scavenging support.
| year | journal | country | edition | language |
|---|---|---|---|---|
| 2014-06-01 | Journal of Molecular Catalysis A: Chemical |