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Synthesis, catalytic activity, and leaching studies of a heterogeneous Pd-catalyst including an immobilized bis(oxazoline) ligand

The synthesis and characterization of a novel catalytic system including Pd(OAc)(2) attached to a bis(oxazoline) (=BOX) ligand that is covalently bonded to 3-mercaptopropyl-functionalized silica gel is presented. The catalyst was tested for Suzuki–Miyaura reactions of different aryl halides with phe...

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Detalles Bibliográficos
Autores principales: Gruber-Woelfler, H., Radaschitz, P.F., Feenstra, P.W., Haas, W., Khinast, J.G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3405295/
https://www.ncbi.nlm.nih.gov/pubmed/22875995
http://dx.doi.org/10.1016/j.jcat.2011.10.013
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author Gruber-Woelfler, H.
Radaschitz, P.F.
Feenstra, P.W.
Haas, W.
Khinast, J.G.
author_facet Gruber-Woelfler, H.
Radaschitz, P.F.
Feenstra, P.W.
Haas, W.
Khinast, J.G.
author_sort Gruber-Woelfler, H.
collection PubMed
description The synthesis and characterization of a novel catalytic system including Pd(OAc)(2) attached to a bis(oxazoline) (=BOX) ligand that is covalently bonded to 3-mercaptopropyl-functionalized silica gel is presented. The catalyst was tested for Suzuki–Miyaura reactions of different aryl halides with phenylboronic acid. The heterogeneity of the catalytic system was investigated using different approaches, indicating that there is virtually no Pd leaching into the reaction solution under the applied reaction conditions. Furthermore, our results show that the catalytic system can be reused multiple times without significant loss of stability or structure.
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spelling pubmed-34052952012-08-06 Synthesis, catalytic activity, and leaching studies of a heterogeneous Pd-catalyst including an immobilized bis(oxazoline) ligand Gruber-Woelfler, H. Radaschitz, P.F. Feenstra, P.W. Haas, W. Khinast, J.G. J Catal Article The synthesis and characterization of a novel catalytic system including Pd(OAc)(2) attached to a bis(oxazoline) (=BOX) ligand that is covalently bonded to 3-mercaptopropyl-functionalized silica gel is presented. The catalyst was tested for Suzuki–Miyaura reactions of different aryl halides with phenylboronic acid. The heterogeneity of the catalytic system was investigated using different approaches, indicating that there is virtually no Pd leaching into the reaction solution under the applied reaction conditions. Furthermore, our results show that the catalytic system can be reused multiple times without significant loss of stability or structure. Elsevier 2012-02 /pmc/articles/PMC3405295/ /pubmed/22875995 http://dx.doi.org/10.1016/j.jcat.2011.10.013 Text en © 2012 Elsevier Inc. https://creativecommons.org/licenses/by-nc-nd/3.0/Open Access under CC BY-NC-ND 3.0 (https://creativecommons.org/licenses/by-nc-nd/3.0/) license
spellingShingle Article
Gruber-Woelfler, H.
Radaschitz, P.F.
Feenstra, P.W.
Haas, W.
Khinast, J.G.
Synthesis, catalytic activity, and leaching studies of a heterogeneous Pd-catalyst including an immobilized bis(oxazoline) ligand
title Synthesis, catalytic activity, and leaching studies of a heterogeneous Pd-catalyst including an immobilized bis(oxazoline) ligand
title_full Synthesis, catalytic activity, and leaching studies of a heterogeneous Pd-catalyst including an immobilized bis(oxazoline) ligand
title_fullStr Synthesis, catalytic activity, and leaching studies of a heterogeneous Pd-catalyst including an immobilized bis(oxazoline) ligand
title_full_unstemmed Synthesis, catalytic activity, and leaching studies of a heterogeneous Pd-catalyst including an immobilized bis(oxazoline) ligand
title_short Synthesis, catalytic activity, and leaching studies of a heterogeneous Pd-catalyst including an immobilized bis(oxazoline) ligand
title_sort synthesis, catalytic activity, and leaching studies of a heterogeneous pd-catalyst including an immobilized bis(oxazoline) ligand
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3405295/
https://www.ncbi.nlm.nih.gov/pubmed/22875995
http://dx.doi.org/10.1016/j.jcat.2011.10.013
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