Palladium nanoparticles supported on SiO 2 by chemical vapor deposition (CVD) technique as efficient catalyst for Suzuki-Miyaura coupling of aryl bromides and iodides: Selective coupling of halophenols

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Abstract

Nanoparticles of palladium were supported on SiO 2 by chemical vapor deposition technique. The obtained Pd nanocatalyst was characterized by various techniques. This catalyst was found to be very efficient for the selective cross-coupling of hydroxyl-substituted aryl iodides and bromide with arylboronic acids in water at room temperature to produce the corresponding hydroxyl-substituted biaryls. Coupling of phenylboronic acid with aryl iodides and bromides carrying substituents other than hydroxy group was also performed efficiently in refluxing ethanol. Copyright © 2012 John Wiley & Sons, Ltd. Palladium nanoparticles supported on SiO 2 as an efficient heterogeneous catalyst was prepared by CVD technique and applied in Suzuki coupling reaction mild conditions. The Suzuki reaction of halophenols was conducted at room temperature in the presence of this catalyst. Copyright © 2012 John Wiley & Sons, Ltd.

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Iranpoor, N., Firouzabadi, H., Safavi, A., Motevalli, S., & Doroodmand, M. M. (2012). Palladium nanoparticles supported on SiO 2 by chemical vapor deposition (CVD) technique as efficient catalyst for Suzuki-Miyaura coupling of aryl bromides and iodides: Selective coupling of halophenols. Applied Organometallic Chemistry, 26(8), 417–424. https://doi.org/10.1002/aoc.2868

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