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Study of Pd-based catalysts within red algae-derived polysaccharide supports in a Suzuki cross-coupling reaction

Simple palladium complexes were heterogenized into red algae derived polysaccharide supports, and the effects of polysaccharide, catalyst and solvent types on the performances in a Suzuki cross-coupling reaction were tested. It was found that using palladium salts with sodium triphenylphosphine tris...

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Autores principales: Wolfson, Adi, Biton, Shira, Levy-Ontman, Oshrat
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9089795/
https://www.ncbi.nlm.nih.gov/pubmed/35558602
http://dx.doi.org/10.1039/c8ra08408d
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author Wolfson, Adi
Biton, Shira
Levy-Ontman, Oshrat
author_facet Wolfson, Adi
Biton, Shira
Levy-Ontman, Oshrat
author_sort Wolfson, Adi
collection PubMed
description Simple palladium complexes were heterogenized into red algae derived polysaccharide supports, and the effects of polysaccharide, catalyst and solvent types on the performances in a Suzuki cross-coupling reaction were tested. It was found that using palladium salts with sodium triphenylphosphine trisulfonate (TPPTS) as a ligand supported on ι-carrageenans and ethanol as the solvent yielded the best systems. Moreover, the conversion rates of these heterogeneous systems were higher than their homogeneous analogues, and they were easily recycled five times. SEM-EDS analysis of Pd(OAc)(2)(TPPTS)(2) that was immobilized on ι-carrageenan support was also performed, demonstrating that the system has a porous structure composed of Pd complex that was embedded within the ι-carrageenan. In addition, both ι-Pd(OAc)(2)(TPPTS)(2) and ι-Pd(OAc)(2) systems, were composed of nanoparticles, as proven by TEM analysis.
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spelling pubmed-90897952022-05-11 Study of Pd-based catalysts within red algae-derived polysaccharide supports in a Suzuki cross-coupling reaction Wolfson, Adi Biton, Shira Levy-Ontman, Oshrat RSC Adv Chemistry Simple palladium complexes were heterogenized into red algae derived polysaccharide supports, and the effects of polysaccharide, catalyst and solvent types on the performances in a Suzuki cross-coupling reaction were tested. It was found that using palladium salts with sodium triphenylphosphine trisulfonate (TPPTS) as a ligand supported on ι-carrageenans and ethanol as the solvent yielded the best systems. Moreover, the conversion rates of these heterogeneous systems were higher than their homogeneous analogues, and they were easily recycled five times. SEM-EDS analysis of Pd(OAc)(2)(TPPTS)(2) that was immobilized on ι-carrageenan support was also performed, demonstrating that the system has a porous structure composed of Pd complex that was embedded within the ι-carrageenan. In addition, both ι-Pd(OAc)(2)(TPPTS)(2) and ι-Pd(OAc)(2) systems, were composed of nanoparticles, as proven by TEM analysis. The Royal Society of Chemistry 2018-11-12 /pmc/articles/PMC9089795/ /pubmed/35558602 http://dx.doi.org/10.1039/c8ra08408d Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/
spellingShingle Chemistry
Wolfson, Adi
Biton, Shira
Levy-Ontman, Oshrat
Study of Pd-based catalysts within red algae-derived polysaccharide supports in a Suzuki cross-coupling reaction
title Study of Pd-based catalysts within red algae-derived polysaccharide supports in a Suzuki cross-coupling reaction
title_full Study of Pd-based catalysts within red algae-derived polysaccharide supports in a Suzuki cross-coupling reaction
title_fullStr Study of Pd-based catalysts within red algae-derived polysaccharide supports in a Suzuki cross-coupling reaction
title_full_unstemmed Study of Pd-based catalysts within red algae-derived polysaccharide supports in a Suzuki cross-coupling reaction
title_short Study of Pd-based catalysts within red algae-derived polysaccharide supports in a Suzuki cross-coupling reaction
title_sort study of pd-based catalysts within red algae-derived polysaccharide supports in a suzuki cross-coupling reaction
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9089795/
https://www.ncbi.nlm.nih.gov/pubmed/35558602
http://dx.doi.org/10.1039/c8ra08408d
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