Bis-salophen palladium complex immobilized on Fe3O4@SiO2 nanoparticles as a highly active and durable phosphine-free catalyst for Heck and copper-free Sonogashira coupling reactions-Reference-Cited by-同舟云学术

Bis-salophen palladium complex immobilized on Fe3O4@SiO2 nanoparticles as a highly active and durable phosphine-free catalyst for Heck and copper-free Sonogashira coupling reactions

Published:2019 Issue:9 Volume:48 Page:3132-3145
ISSN:1477-9226
Container-title:Dalton Transactions
language:en
Short-container-title:Dalton Trans.

Author:

Sardarian Ali Reza¹²³⁴⁵,Kazemnejadi Milad¹²³⁴⁵,Esmaeilpour Mohsen¹²³⁴⁵

Affiliation:

1. Department of Chemistry

2. College of Sciences

3. Shiraz University

4. Shiraz 71946 84795

5. Iran

Abstract

A new Fe₃O₄@SiO₂ superparamagnetic nanoparticles functionalized by a bis-salophen Schiff base Pd(ii)-complex and used as efficient catalyst for Heck and Sonogashira reactions in aqueous media.

Funder

Iran National Science Foundation

Publisher

Royal Society of Chemistry (RSC)

Subject

Inorganic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2019/DT/C9DT00060G

Reference74 articles.

1. Palladium complexes containing multidentate phenoxy–pyridyl–amidate ligands: Highly efficient catalyst for Heck coupling of deactivated aryl halides

2. Improved Procedures for the Palladium-Catalyzed Coupling of Terminal Alkynes with Aryl Bromides (Sonogashira Coupling)

3. Heck Reactions in the Presence of P(t-Bu)3: Expanded Scope and Milder Reaction Conditions for the Coupling of Aryl Chlorides