Issue 4, 2015

Room temperature Suzuki coupling of aryl iodides, bromides, and chlorides using a heterogeneous carbon nanotube-palladium nanohybrid catalyst

Abstract

Palladium nanoparticles were immobilized on multi-walled carbon nanotubes by a layer-by-layer approach, resulting in a well-defined assembly. The nanohybrid was found effective in promoting Suzuki cross couplings of various halogenated aromatics, including chlorinated ones, with arylboronic acids under sustainable conditions. The heterogeneous catalyst could also easily be recovered from the reaction mixture and reused with no loss of activity over several cycles.

Graphical abstract: Room temperature Suzuki coupling of aryl iodides, bromides, and chlorides using a heterogeneous carbon nanotube-palladium nanohybrid catalyst

Supplementary files

Article information

Article type
Paper
Submitted
16 Dec 2014
Accepted
29 Jan 2015
First published
29 Jan 2015
This article is Open Access
Creative Commons BY license

Catal. Sci. Technol., 2015,5, 2388-2392

Room temperature Suzuki coupling of aryl iodides, bromides, and chlorides using a heterogeneous carbon nanotube-palladium nanohybrid catalyst

D. V. Jawale, E. Gravel, C. Boudet, N. Shah, V. Geertsen, H. Li, I. N. N. Namboothiri and E. Doris, Catal. Sci. Technol., 2015, 5, 2388 DOI: 10.1039/C4CY01680G

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