Issue 20, 2016

Recyclable glucose-derived palladium(0) nanoparticles as in situ-formed catalysts for cross-coupling reactions in aqueous media

Abstract

In situ-generated, glucose-derived palladium(0) nanoparticles were shown to be convenient and effective catalysts for aqueous Mizoroki–Heck, Sonogashira and Suzuki–Miyaura cross-coupling reactions. The addition of only 4–10 mol% glucose to the reaction mixture lead to a significant increase in yield of the desired products in comparison to processes that omitted the renewable sugar. Interestingly, the Mizoroki–Heck reaction was observed to proceed in good yield even as the reaction reached acidic pH levels. Extensive analysis of the size and morphology of the in situ-formed palladium nanoparticles using advanced analytical techniques showed that the zero valent metal was surrounded by hydrophilic hydroxyl groups. The increased aqueous phase affinity afforded by these groups allowed for facile recycling of the catalyst.

Graphical abstract: Recyclable glucose-derived palladium(0) nanoparticles as in situ-formed catalysts for cross-coupling reactions in aqueous media

Supplementary files

Article information

Article type
Paper
Submitted
02 Dec 2015
Accepted
29 Jan 2016
First published
08 Feb 2016

RSC Adv., 2016,6, 16115-16121

Author version available

Recyclable glucose-derived palladium(0) nanoparticles as in situ-formed catalysts for cross-coupling reactions in aqueous media

J. E. Camp, J. J. Dunsford, O. S. G. Dacosta, R. K. Blundell, J. Adams, J. Britton, R. J. Smith, T. W. Bousfield and M. W. Fay, RSC Adv., 2016, 6, 16115 DOI: 10.1039/C5RA25712C

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