A novel magnetic nanoparticle-supported oxime palladacycle catalyst was successfully prepared and characterized. The magnetically recoverable catalyst was evaluated in the room temperature Suzuki–Miyaura cross-coupling reaction of aryl iodides and bromides in aqueous media. The catalyst was shown to be highly active under phosphine-free and low Pd loading (0.3 mol%) conditions. The catalyst could be easily separated from the reaction mixture using an external magnet and reused for six consecutive runs without significant loss of activity.The authors are grateful to Institute for Advanced Studies in Basic Sciences (IASBS) Research Council and Iran National Science Foundation (INSF-Grant number of 93020713) for support of this work
WOS: 000414155500013In any catalysis system, regeneration of the used catalyst is of great importanc...
A reliable method for encapsulation of palladium nanoparticles (6–8 nm particles) in halloysite (Pd@...
In this project, the aim was to carry out the Suzuki reaction using a new and unique catalyst with a...
A novel magnetic nanoparticle-supported oxime palladacycle catalyst was successfully prepared and ch...
In this work, a new magnetic composite comprising starch, imidazolium and triazol groups is used as ...
Abstract: In this work, Pd nanoparticles (Pd-NPs) were decorated on modified magnetic nanoparticles ...
Palladium supported magnetic nanoparticle (Pd@Fe3O4/AMOCAA) was easily prepared in the presence of S...
International audiencePhosphonated polyethylenimine grafted on iron oxide nanoparticles was used as ...
A magnetic nanoparticle (MNP)-supported di(2-pyridyl)methanol palladium dichloride complex was prepa...
Palladacycles are highly efficient precatalysts in cross-coupling reactions whose immobilization on ...
A novel catalytic system based on palladium nanoparticles (Pd-NPs) immobilized onto the surface of g...
The development of new solid supports for palladium has received a lot of interest lately. These cat...
The development of new solid supports for palladium has received a lot of interest lately. These cat...
Carbon-carbon cross-coupling reactions are among the most important synthetic tools for the preparat...
We here report the preparation of supported palladium nanoparticles (NPs) stabilized by pendant phos...
WOS: 000414155500013In any catalysis system, regeneration of the used catalyst is of great importanc...
A reliable method for encapsulation of palladium nanoparticles (6–8 nm particles) in halloysite (Pd@...
In this project, the aim was to carry out the Suzuki reaction using a new and unique catalyst with a...
A novel magnetic nanoparticle-supported oxime palladacycle catalyst was successfully prepared and ch...
In this work, a new magnetic composite comprising starch, imidazolium and triazol groups is used as ...
Abstract: In this work, Pd nanoparticles (Pd-NPs) were decorated on modified magnetic nanoparticles ...
Palladium supported magnetic nanoparticle (Pd@Fe3O4/AMOCAA) was easily prepared in the presence of S...
International audiencePhosphonated polyethylenimine grafted on iron oxide nanoparticles was used as ...
A magnetic nanoparticle (MNP)-supported di(2-pyridyl)methanol palladium dichloride complex was prepa...
Palladacycles are highly efficient precatalysts in cross-coupling reactions whose immobilization on ...
A novel catalytic system based on palladium nanoparticles (Pd-NPs) immobilized onto the surface of g...
The development of new solid supports for palladium has received a lot of interest lately. These cat...
The development of new solid supports for palladium has received a lot of interest lately. These cat...
Carbon-carbon cross-coupling reactions are among the most important synthetic tools for the preparat...
We here report the preparation of supported palladium nanoparticles (NPs) stabilized by pendant phos...
WOS: 000414155500013In any catalysis system, regeneration of the used catalyst is of great importanc...
A reliable method for encapsulation of palladium nanoparticles (6–8 nm particles) in halloysite (Pd@...
In this project, the aim was to carry out the Suzuki reaction using a new and unique catalyst with a...