Issue 28, 2010

A new functionalized mesoporous matrix supported Pd(ii)-Schiff base complex: an efficient catalyst for the Suzuki–Miyaura coupling reaction

Abstract

A new Pd(II) bounded 2D-hexagonally ordered functionalized MCM-41 type material (IV) has been synthesized. Functionalization was carried out by the anchoring of 3-aminopropyltriethoxysilane in the MCM-41 type mesoporous material, followed by grafting with 2,6-diacetylpyridine (DAP) to give a N3-type Schiff base chelating attachment for the Pd(II) species. Fourier transform infrared (FTIR), powder X-ray diffraction (PXRD) and high resolution transmission electron microscopy (HRTEM) studies have been used to characterize the material. Material IV behaves as a highly active catalyst towards Suzuki–Miyaura cross-coupling reaction for the synthesis of biaryl organics. In addition, IV acts as a true heterogeneous catalyst in coupling reaction. It was found that this catalyst is highly efficient and recyclable towards Suzuki–Miyaura reaction with high turn over frequencies. X-Ray photoelectron spectroscopic (XPS) analysis was employed to understand the oxidation state of the palladium atom in the catalyst (IV) and its loading in the material.

Graphical abstract: A new functionalized mesoporous matrix supported Pd(ii)-Schiff base complex: an efficient catalyst for the Suzuki–Miyaura coupling reaction

Supplementary files

Article information

Article type
Paper
Submitted
15 Feb 2010
Accepted
07 May 2010
First published
07 Jun 2010

Dalton Trans., 2010,39, 6395-6402

A new functionalized mesoporous matrix supported Pd(II)-Schiff base complex: an efficient catalyst for the Suzuki–Miyaura coupling reaction

K. Dhara, K. Sarkar, D. Srimani, S. K. Saha, P. Chattopadhyay and A. Bhaumik, Dalton Trans., 2010, 39, 6395 DOI: 10.1039/C003142A

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