Issue 53, 2014

Design and synthesis of a new phosphinite-functionalized clay composite for the stabilization of palladium nanoparticles. Application as a recoverable catalyst for C–C bond formation reactions

Abstract

A new clay composite carrying phosphinite-functionalized ionic liquid moieties (CCPIL) has been designed and synthesized. Palladium nanoparticles were uniformly ligated by CCPIL. After characterization, this composite has been applied as a heterogeneous catalyst for the Suzuki–Miyaura reaction of aryl halides with phenylboronic acid on water in the presence of NaOH as the base. These nanoparticles have also been applied for copper-free Sonogashira–Hagihara reaction in TBAB and Mizoroki–Heck reaction under solvent-free conditions. The catalyst was also found to be stable towards moisture and air and its catalytic activity remained almost unchanged after exposure to air for three months.

Graphical abstract: Design and synthesis of a new phosphinite-functionalized clay composite for the stabilization of palladium nanoparticles. Application as a recoverable catalyst for C–C bond formation reactions

Supplementary files

Article information

Article type
Paper
Submitted
22 Apr 2014
Accepted
21 May 2014
First published
21 May 2014

RSC Adv., 2014,4, 27674-27682

Author version available

Design and synthesis of a new phosphinite-functionalized clay composite for the stabilization of palladium nanoparticles. Application as a recoverable catalyst for C–C bond formation reactions

H. Firouzabadi, N. Iranpoor, A. Ghaderi, M. Gholinejad, S. Rahimi and S. Jokar, RSC Adv., 2014, 4, 27674 DOI: 10.1039/C4RA03645J

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