Issue 13, 2014

Cross-coupling reaction between arylboronic acids and carboranyl iodides catalyzed by graphene oxide (GO)-supported Pd(0) recyclable nanoparticles for the synthesis of carboranylaryl ketones

Abstract

Well-dispersed palladium(0) nanoparticles with small and narrow size distributions were synthesized conveniently on a graphene oxide (GO) surface. The GO-supported nano-Pd0 was found to be a highly efficient and recyclable catalyst for the carbonylative cross-coupling reaction between arylboronic acids and aryl and carboranyl iodides, respectively. Benzophenone and a series of carboranylaryl ketones, 1-R-2-[C([double bond, length as m-dash]O)Ar]-1,2-C2B10H10 (R = H, Me, Ph; Ar = C6H5, C6H4-4-OMe and C6H4-4-F), were synthesized and fully characterized. The catalyst was recyclable at least three times with sustained activity.

Graphical abstract: Cross-coupling reaction between arylboronic acids and carboranyl iodides catalyzed by graphene oxide (GO)-supported Pd(0) recyclable nanoparticles for the synthesis of carboranylaryl ketones

  • This article is part of the themed collection: Carboranes

Supplementary files

Article information

Article type
Paper
Submitted
19 Sep 2013
Accepted
18 Oct 2013
First published
24 Oct 2013

Dalton Trans., 2014,43, 5014-5020

Cross-coupling reaction between arylboronic acids and carboranyl iodides catalyzed by graphene oxide (GO)-supported Pd(0) recyclable nanoparticles for the synthesis of carboranylaryl ketones

A. O. Biying, V. R. Vangala, C. S. Chen, L. P. Stubs, N. S. Hosmane and Z. Yinghuai, Dalton Trans., 2014, 43, 5014 DOI: 10.1039/C3DT52560K

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