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 inGreen chemistry : an international journal and green chemistry resource : GC Vol. 21; no. 19; pp. 5284 - 529
Main Authors Addanki Tirumala, Ravi Teja, Dadgar, Andishaeh, Mohammadparast, Farshid, Ramakrishnan, Sundaram Bhardwaj, Mou, Tong, Wang, Bin, Andiappan, Marimuthu
Format Journal Article
Published 30.09.2019
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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.
Bibliography:10.1039/c9gc01930h
Electronic supplementary information (ESI) available. See DOI
ISSN:1463-9262
1463-9270
DOI:10.1039/c9gc01930h