6533b82dfe1ef96bd1291e91

RESEARCH PRODUCT

Multi-layered, covalently supported ionic liquid phase (mlc-SILP) as highly cross-linked support for recyclable palladium catalysts for the suzuki reaction in aqueous medium

Renato NotoFrancesco GiacaloneValeria La ParolaLeonarda F. LiottaCarmela AprileMichelangelo GruttadauriaAnna Maria Pia Salvo

subject

catalyst recyclingInorganic chemistryAzobisisobutyronitrilechemistry.chemical_elementGeneral ChemistrySettore CHIM/06 - Chimica OrganicaMesoporous silicapalladiumCatalysisBiphenyl compoundchemistry.chemical_compoundSuzuki reactionchemistryIonic liquidMagic angle spinningPalladiumionic liquid

description

The reaction between an excess of 1,4-bis(3-vinylimidazolium-1-yl) bromide and a mercaptopropyl-modified amorphous silica gel or ordered mesoporous silica SBA-15 in the presence of azobisisobutyronitrile (AIBN) afforded new materials, which have a high loading of imidazolium moieties. These materials, which contain a highly cross-linked polymeric network, have been denoted as multi-layered, covalently supported ionic liquid phase (mlc-SILP) and have been used as support for palladium catalysts containing a high loading of the metal (10 wt%). Such materials were characterized by several techniques (13C magic angle spinning nuclear magnetic resonance, the Brunauer–Emmett–Teller technique, small-angle X-ray scattering, X-ray diffraction, X-ray photoelectron spectroscopy, and transmission electron microscopy). The presence of a homogeneous distribution of palladium nanoparticles was established. The palladium catalysts displayed good activity allowing the synthesis of several biphenyl compounds in high yields working with only 0.1 mol% of palladium loading at mild temperatures (room temperature or 50 °C) in ethanol/water. Reactions carried out on a 10-mmol scale required only 10 mg of catalysts. Good recyclability was observed.

10.1002/adsc.201100186https://researchportal.unamur.be/en/publications/06d8e8e1-3e96-41a2-8573-8087e3f282d7