People | Locations | Statistics |
---|---|---|
Naji, M. |
| |
Motta, Antonella |
| |
Aletan, Dirar |
| |
Mohamed, Tarek |
| |
Ertürk, Emre |
| |
Taccardi, Nicola |
| |
Kononenko, Denys |
| |
Petrov, R. H. | Madrid |
|
Alshaaer, Mazen | Brussels |
|
Bih, L. |
| |
Casati, R. |
| |
Muller, Hermance |
| |
Kočí, Jan | Prague |
|
Šuljagić, Marija |
| |
Kalteremidou, Kalliopi-Artemi | Brussels |
|
Azam, Siraj |
| |
Ospanova, Alyiya |
| |
Blanpain, Bart |
| |
Ali, M. A. |
| |
Popa, V. |
| |
Rančić, M. |
| |
Ollier, Nadège |
| |
Azevedo, Nuno Monteiro |
| |
Landes, Michael |
| |
Rignanese, Gian-Marco |
|
Branco, Paula Sério
in Cooperation with on an Cooperation-Score of 37%
Topics
Publications (4/4 displayed)
- 2019N-Heterocyclic Olefin Catalysis for the Ring Opening of Cyclic Amidine Compounds: A Pathway to the Synthesis of ϵ-Caprolactam- and γ-Lactam-Derived Aminescitations
- 2015Design of oligoaziridine-PEG coatings for efficient nanogold cellular biotaggingcitations
- 2013Nano-magnetite (Fe3O4) as a support for recyclable catalysts in the development of sustainable methodologiescitations
- 2013First application of core-shell Ag@Ni magnetic nanocatalyst for transfer hydrogenation reactions of aromatic nitro and carbonyl compoundscitations
Places of action
Organizations | Location | People |
---|
article
First application of core-shell Ag@Ni magnetic nanocatalyst for transfer hydrogenation reactions of aromatic nitro and carbonyl compounds
Abstract
A magnetically separable core-shell Ag@Ni nanocatalyst was prepared by a simple one-pot synthetic route using oleylamine both as solvent and reducing agent and triphenylphosphine as surfactant. The synthesized nanoparticles were characterized by several techniques such as X-ray diffraction pattern (XRD), high resolution transmission electron microscopy (HR-TEM), selected area electron diffraction (SAED) pattern, and energy dispersive X-ray spectroscopy (EDS). The core-shell Ag@Ni nanocatalyst was found to have very excellent activity for the transfer hydrogenation reactions of aromatic nitro and carbonyl compounds under mild conditions using isopropyl alcohol as hydrogen donor. Excellent chemoselectivity and regioselectivity for the nitro group reduction was demonstrated.