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Palladium(0) Deposited on PAMAM Dendrimers as a Catalyst for C–C Cross Coupling Reactions

PAMAM dendrimers of generations G2–G3 as well as a partially substituted derivative of generation G4 and a low-molecular-weight tricyclic ligand 4 were used to bind Pd(0) nanoparticles. The obtained adducts were tested as catalysts for C–C cross-coupling reactions, such as the Suzuki-Miyaura, Hiyama...

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Autores principales: Borkowski, Tomasz, Subik, Paweł, Trzeciak, Anna M., Wołowiec, Stanisław
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6259269/
https://www.ncbi.nlm.nih.gov/pubmed/21221061
http://dx.doi.org/10.3390/molecules16010427
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author Borkowski, Tomasz
Subik, Paweł
Trzeciak, Anna M.
Wołowiec, Stanisław
author_facet Borkowski, Tomasz
Subik, Paweł
Trzeciak, Anna M.
Wołowiec, Stanisław
author_sort Borkowski, Tomasz
collection PubMed
description PAMAM dendrimers of generations G2–G3 as well as a partially substituted derivative of generation G4 and a low-molecular-weight tricyclic ligand 4 were used to bind Pd(0) nanoparticles. The obtained adducts were tested as catalysts for C–C cross-coupling reactions, such as the Suzuki-Miyaura, Hiyama, Heck and Sonogashira reaction. The highest yields of the coupling product, diphenylacetylene, were obtained with all the catalysts studied in the Sonogashira coupling performed in ethanol with K(2)CO(3) as base. Very good results, 85–100%, were also found in the Suzuki-Miyaura cross-coupling, while the efficiency of the Hiyama coupling appeared lower, with 38–52% of 2-Methylbiphenyl formed. In all reactions, the G2–Pd(0) catalyst, containing an unmodified dendrimer, afforded the highest yields of the cross-coupling products.
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spelling pubmed-62592692018-12-07 Palladium(0) Deposited on PAMAM Dendrimers as a Catalyst for C–C Cross Coupling Reactions Borkowski, Tomasz Subik, Paweł Trzeciak, Anna M. Wołowiec, Stanisław Molecules Article PAMAM dendrimers of generations G2–G3 as well as a partially substituted derivative of generation G4 and a low-molecular-weight tricyclic ligand 4 were used to bind Pd(0) nanoparticles. The obtained adducts were tested as catalysts for C–C cross-coupling reactions, such as the Suzuki-Miyaura, Hiyama, Heck and Sonogashira reaction. The highest yields of the coupling product, diphenylacetylene, were obtained with all the catalysts studied in the Sonogashira coupling performed in ethanol with K(2)CO(3) as base. Very good results, 85–100%, were also found in the Suzuki-Miyaura cross-coupling, while the efficiency of the Hiyama coupling appeared lower, with 38–52% of 2-Methylbiphenyl formed. In all reactions, the G2–Pd(0) catalyst, containing an unmodified dendrimer, afforded the highest yields of the cross-coupling products. MDPI 2011-01-10 /pmc/articles/PMC6259269/ /pubmed/21221061 http://dx.doi.org/10.3390/molecules16010427 Text en © 2011 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Article
Borkowski, Tomasz
Subik, Paweł
Trzeciak, Anna M.
Wołowiec, Stanisław
Palladium(0) Deposited on PAMAM Dendrimers as a Catalyst for C–C Cross Coupling Reactions
title Palladium(0) Deposited on PAMAM Dendrimers as a Catalyst for C–C Cross Coupling Reactions
title_full Palladium(0) Deposited on PAMAM Dendrimers as a Catalyst for C–C Cross Coupling Reactions
title_fullStr Palladium(0) Deposited on PAMAM Dendrimers as a Catalyst for C–C Cross Coupling Reactions
title_full_unstemmed Palladium(0) Deposited on PAMAM Dendrimers as a Catalyst for C–C Cross Coupling Reactions
title_short Palladium(0) Deposited on PAMAM Dendrimers as a Catalyst for C–C Cross Coupling Reactions
title_sort palladium(0) deposited on pamam dendrimers as a catalyst for c–c cross coupling reactions
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6259269/
https://www.ncbi.nlm.nih.gov/pubmed/21221061
http://dx.doi.org/10.3390/molecules16010427
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