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Nickel–palladium bimetallic nanoparticles supported on multi-walled carbon nanotubes; versatile catalyst for Sonogashira cross-coupling reactions

We have developed an efficient method to generate highly active nickel–palladium bimetallic nanoparticles supported on multi-walled carbon nanotubes (Ni–Pd/MWCNTs) by dry mixing of the nickel and palladium salts utilizing the mechanical energy of a ball-mill. These nanoparticles were successfully em...

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Autores principales: Wilson, Katherine A., Picinich, Lacey A., Siamaki, Ali R.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9996231/
https://www.ncbi.nlm.nih.gov/pubmed/36909771
http://dx.doi.org/10.1039/d3ra00027c
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author Wilson, Katherine A.
Picinich, Lacey A.
Siamaki, Ali R.
author_facet Wilson, Katherine A.
Picinich, Lacey A.
Siamaki, Ali R.
author_sort Wilson, Katherine A.
collection PubMed
description We have developed an efficient method to generate highly active nickel–palladium bimetallic nanoparticles supported on multi-walled carbon nanotubes (Ni–Pd/MWCNTs) by dry mixing of the nickel and palladium salts utilizing the mechanical energy of a ball-mill. These nanoparticles were successfully employed in Sonogashira cross-coupling reactions with a wide array of functionalized aryl halides and terminal alkynes under ligand and copper free conditions using a Monowave 50 heating reactor. Notably, the concentration of palladium can be lowered to a minimum amount of 0.81% and replaced by more abundant and less expensive nickel nanoparticles while effectively catalyzing the reaction. The remarkable reactivity of the Ni–Pd/MWCNTs catalyst toward Sonogashira cross-coupling reactions is attributed to the high degree of the dispersion of Ni–Pd nanoparticles with small particle size of 5–10 nm due to an efficient grinding method. The catalyst was easily removed from the reaction mixture by centrifugation and reused several times with minimal loss of catalytic activity. Furthermore, the concentration of catalyst in Sonogashira reactions can be reduced to a minimum amount of 0.01 mol% while still providing a high conversion of the Sonogashira product with a remarkable turnover number (TON) of 7200 and turnover frequency (TOF) of 21 600 h(−1). The catalyst was fully characterized by a variety of spectroscopic techniques including X-ray diffraction (XRD), transmission electron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS).
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spelling pubmed-99962312023-03-10 Nickel–palladium bimetallic nanoparticles supported on multi-walled carbon nanotubes; versatile catalyst for Sonogashira cross-coupling reactions Wilson, Katherine A. Picinich, Lacey A. Siamaki, Ali R. RSC Adv Chemistry We have developed an efficient method to generate highly active nickel–palladium bimetallic nanoparticles supported on multi-walled carbon nanotubes (Ni–Pd/MWCNTs) by dry mixing of the nickel and palladium salts utilizing the mechanical energy of a ball-mill. These nanoparticles were successfully employed in Sonogashira cross-coupling reactions with a wide array of functionalized aryl halides and terminal alkynes under ligand and copper free conditions using a Monowave 50 heating reactor. Notably, the concentration of palladium can be lowered to a minimum amount of 0.81% and replaced by more abundant and less expensive nickel nanoparticles while effectively catalyzing the reaction. The remarkable reactivity of the Ni–Pd/MWCNTs catalyst toward Sonogashira cross-coupling reactions is attributed to the high degree of the dispersion of Ni–Pd nanoparticles with small particle size of 5–10 nm due to an efficient grinding method. The catalyst was easily removed from the reaction mixture by centrifugation and reused several times with minimal loss of catalytic activity. Furthermore, the concentration of catalyst in Sonogashira reactions can be reduced to a minimum amount of 0.01 mol% while still providing a high conversion of the Sonogashira product with a remarkable turnover number (TON) of 7200 and turnover frequency (TOF) of 21 600 h(−1). The catalyst was fully characterized by a variety of spectroscopic techniques including X-ray diffraction (XRD), transmission electron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS). The Royal Society of Chemistry 2023-03-09 /pmc/articles/PMC9996231/ /pubmed/36909771 http://dx.doi.org/10.1039/d3ra00027c Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Wilson, Katherine A.
Picinich, Lacey A.
Siamaki, Ali R.
Nickel–palladium bimetallic nanoparticles supported on multi-walled carbon nanotubes; versatile catalyst for Sonogashira cross-coupling reactions
title Nickel–palladium bimetallic nanoparticles supported on multi-walled carbon nanotubes; versatile catalyst for Sonogashira cross-coupling reactions
title_full Nickel–palladium bimetallic nanoparticles supported on multi-walled carbon nanotubes; versatile catalyst for Sonogashira cross-coupling reactions
title_fullStr Nickel–palladium bimetallic nanoparticles supported on multi-walled carbon nanotubes; versatile catalyst for Sonogashira cross-coupling reactions
title_full_unstemmed Nickel–palladium bimetallic nanoparticles supported on multi-walled carbon nanotubes; versatile catalyst for Sonogashira cross-coupling reactions
title_short Nickel–palladium bimetallic nanoparticles supported on multi-walled carbon nanotubes; versatile catalyst for Sonogashira cross-coupling reactions
title_sort nickel–palladium bimetallic nanoparticles supported on multi-walled carbon nanotubes; versatile catalyst for sonogashira cross-coupling reactions
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9996231/
https://www.ncbi.nlm.nih.gov/pubmed/36909771
http://dx.doi.org/10.1039/d3ra00027c
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AT picinichlaceya nickelpalladiumbimetallicnanoparticlessupportedonmultiwalledcarbonnanotubesversatilecatalystforsonogashiracrosscouplingreactions
AT siamakialir nickelpalladiumbimetallicnanoparticlessupportedonmultiwalledcarbonnanotubesversatilecatalystforsonogashiracrosscouplingreactions