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Dendritic structured palladium complexes: magnetically retrievable, highly efficient heterogeneous nanocatalyst for Suzuki and Heck cross-coupling reactions

Safoora Sheikh, Mohammad Ali Nasseri, Mohammad Chahkandi, Oliver Reiser, Ali Allahresani

2022RSC Advances21 citationsDOIOpen Access PDF

Abstract

is reported for catalytic C-C cross-coupling reactions of challenging substrates. Mainly, a great variety of aryl chlorides can be used as substrates for Suzuki-Miyaura and Mizoroki-Heck reactions under mild reaction conditions (60-90 °C) and low catalyst loading (<1 mol% Pd) in aqueous media. The presence of numerous polar groups in the polymer matrix increases the solubility of the catalyst in water, thus facilitating its operation in aqueous environments. The immobilization of the catalyst on the surface of a magnetic platform allows its effective recovery and reuse without significant loss of catalytic activity for at least six cycles with total leaching of <1% palladium metal, meeting the requirements for acceptable metal residues in the pharmaceutical industry.

Topics & Concepts

PalladiumHeck reactionSuzuki reactionChemistryCoupling (piping)Combinatorial chemistryPolymer chemistryOrganic chemistryCatalysisMaterials scienceMetallurgyCatalytic Cross-Coupling ReactionsCatalytic C–H Functionalization MethodsMulticomponent Synthesis of Heterocycles
Dendritic structured palladium complexes: magnetically retrievable, highly efficient heterogeneous nanocatalyst for Suzuki and Heck cross-coupling reactions | Litcius