| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1321382 | Journal of Organometallic Chemistry | 2014 | 6 Pages |
•We describe microwave assisted halloysite external surface functionalization.•HNT surface was modified with ionic liquids.•The obtained material was employed as support for Pd nanoparticles.•It was tested as catalyst in the Suzuki reaction.
Microwave assisted halloysite (HNT) external surface functionalization with ionic liquids is described. HNTs modification was achieved in two steps: a) grafting of 3-mercaptopropyl trimethoxysilane on the external surface of HNT by a microwave irradiation; b) anchorage of vinylimidazolium ionic liquids by a thiol-ene reaction. MW irradiation allowed us to obtain high loading onto the HNT surface compared to those obtained through conventional synthesis. Fourier transform infrared spectroscopy and thermogravimetric analysis confirmed that the grafting has occurred only on the external surface of HNT. Turbidimetric and dynamic light scattering analyses showed that the introduction of ionic liquid on the HNT surface involves the formation of aggregates. One of these materials has been used as support for Palladium particles and tested, as catalyst, in the Suzuki reaction between phenylboronic acid and some aryl halide to give the corresponding biaryl in high yield. A catalytic efficiency higher than conventionally used support was achieved.
Graphical abstractA new catalytic system based on modified halloysite nanotubes was employed in the Suzuki reactions under microwave irradiation. The halloysite was functionalized, by microwave irradiation, in two steps: a) grafting of 3-mercaptopropyl trimethoxysilane on the external surface of HNT; b) anchorage of vinylimidazolium ionic liquids by a thiol-ene reaction.Figure optionsDownload full-size imageDownload as PowerPoint slide
