4.5 Article

Preparation and characterization of Pd (II) based on 2,5-pyridinedicar-boxylic acid as novel recyclable metal-organic frameworks for Suzuki-Miyaura reaction

Journal

JOURNAL OF ORGANOMETALLIC CHEMISTRY
Volume 1001, Issue -, Pages -

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.jorganchem.2023.122889

Keywords

Suzuki-Miyaura reaction; MOF; Catalyst; 2,5-pyridinedicarboxylic acid; [Pd/PDCA]n

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A novel recyclable metal-organic framework catalyst was synthesized and applied in the Suzuki-Miyaura reaction, achieving high yields of biaryl derivatives. The catalyst exhibited excellent catalytic efficiency and reusability.
A novel recyclable metal-organic framework (MOF) based on Pd(II) and 2,5-Pyridinedicarboxylic acid ([Pd/ PDCA]n) was synthesized and characterized by different methods such as FT-IR, XRD, SEM, EDX, TGA and ICPAES analysis. The [Pd/PDCA]n catalyst was used as a heterogeneous catalyst in the Suzuki-Miyaura reaction on to prepare biaryl derivatives from aryl halides (1 mmol) with arylboronic acids (1.5 mmol) and 0.1 g of K2CO3 in DMF (10 mL) solvent conditions at 110 degrees C in about 15 min with a 96 % yield and reusable MOF for the efficient preparation of biaryl derivatives through Suzuki-Miyaura reaction in an eco-friendly system. The catalyst displayed excellent yields and catalytic efficiency compared to other catalysts, and it was found to be recoverable and reusable without losing its activity after several cycles. This study presents a new approach for the sustainable preparation of biaryl derivatives using a reusable catalyst. The structure of the synthesized products was confirmed by NMR analysis and melting point.

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