What is it about?
this project is about Suzuki–Miyaura and Heck–Mizoroki cross-coupling reactions in mild conditions.
Featured Image
Why is it important?
In spite of a great deal of heterogeneous catalytic systems suggested for Suzuki–Miyaura and Heck–Mizoroki cross-coupling reactions to date, furnishing such a reactions in aqueous and also mild conditions is still an essential requirement, especially for more challenging partners due to the performance of side reactions in Suzuki–Miyaura crosscoupling reactions and inherent difculty of Heck–Mizoroki cross-coupling reactions under mild conditions
Perspectives
In this paper, we have synthesized a novel thiophene methanimine-palladium Schiff base complex anchored on decorated γ-Fe2O3 with 2-aminoethyl dihydrogen phosphate (γ-Fe2O3/AEPH2-TC-Pd) as a highly efcient magnetically separable nanocatalyst (Scheme 1). We hoped to conduct these coupling reactions upon mild and aqueous media by means of the existence of nitrogen and sulfur containing ligand in the catalyst structure, which can strongly stabilized the palladium species.
Roya Jahanshahi
Ferdowsi University of Mashhad
Read the Original
This page is a summary of: Thiophene Methanimine–Palladium Schiff Base Complex Anchored on Magnetic Nanoparticles: A Novel, Highly Efficient and Recoverable Nanocatalyst for Cross-Coupling Reactions in Mild and Aqueous Media, Catalysis Letters, August 2017, Springer Science + Business Media,
DOI: 10.1007/s10562-017-2170-x.
You can read the full text:
Contributors
The following have contributed to this page
