Homogeneous heterogeneous catalysis in CuO-nanoparticle-catalyzed C-C coupling reactions
Copper based nanocatalysts have recently emerged as attractive catalysts for a diversity of bond formations, such as C-C, C-N, C-O, C-S, and C-Se. However, the identification of truly heterogeneous versus homogeneous catalytic conditions remains an ongoing challenge within the field. Herein, we repo...
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Published in | Green chemistry : an international journal and green chemistry resource : GC Vol. 21; no. 19; pp. 5284 - 529 |
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Main Authors | , , , , , , |
Format | Journal Article |
Published |
30.09.2019
|
Online Access | Get full text |
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Summary: | Copper based nanocatalysts have recently emerged as attractive catalysts for a diversity of bond formations, such as C-C, C-N, C-O, C-S, and C-Se. However, the identification of truly heterogeneous
versus
homogeneous catalytic conditions remains an ongoing challenge within the field. Herein, we report that in cuprous oxide (Cu
2
O) nanoparticle-mediated C-C homo-coupling and cross-coupling reactions, the presence of a base facilitates the copper complex mediated homogeneous catalytic pathway. Whereas in the absence of a base, the reaction can proceed heterogeneously on the surface of Cu
2
O nanoparticles. We distinguished the homogenous
versus
heterogeneous pathways using a combination of reactor study, ultraviolet-visible extinction spectroscopy, electrospray ionization mass spectrometry, flame atomic absorption spectroscopy, transmission electron microscopy, and density-functional theory calculations. Our findings indicate that Cu
2
O nanoparticles can catalyze C-C coupling reactions under lingandless and base-free conditions
via
a truly heterogeneous pathway paving the way for the development of highly efficient, robust and sustainable processes.
Copper based nanocatalysts have recently emerged as attractive catalysts for a diversity of bond formations, such as C-C, C-N, C-O, C-S, and C-Se. |
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Bibliography: | 10.1039/c9gc01930h Electronic supplementary information (ESI) available. See DOI |
ISSN: | 1463-9262 1463-9270 |
DOI: | 10.1039/c9gc01930h |