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Palladium catalyst imbedded in polymers of intrinsic microporosity for the Suzuki–Miyaura coupling reaction
Polymers of intrinsic microporosity (PIMs) are porous polymers with rigid ladder-type chain structures. Synthesizing these polymers usually involves the step polymerization of two types of monomer, namely, active fluorine-substituted aromatic ring monomers and phenolic monomers. Herein, we report a...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9087636/ https://www.ncbi.nlm.nih.gov/pubmed/35547052 http://dx.doi.org/10.1039/c8ra06214e |
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author | Xu, Junwen Ou, Junjie Chen, Lianfang Zhang, Haiyang Ma, Shujuan Ye, Mingliang |
author_facet | Xu, Junwen Ou, Junjie Chen, Lianfang Zhang, Haiyang Ma, Shujuan Ye, Mingliang |
author_sort | Xu, Junwen |
collection | PubMed |
description | Polymers of intrinsic microporosity (PIMs) are porous polymers with rigid ladder-type chain structures. Synthesizing these polymers usually involves the step polymerization of two types of monomer, namely, active fluorine-substituted aromatic ring monomers and phenolic monomers. Herein, we report a new PIMs preparation method using self-synthesized fluorinated monomers and common monomer 5,5′,6,6′-tetrahydroxy-3,3,3′,3′-tetramethyl spirobisindane. The fluorinated monomers were synthesized through the imidization of tetrafluorophthalic anhydride and aromatic diamines. The resulting PIMs served as a support for palladium, with the formed catalyst showing potential for application in the Suzuki–Miyaura coupling reaction. |
format | Online Article Text |
id | pubmed-9087636 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-90876362022-05-10 Palladium catalyst imbedded in polymers of intrinsic microporosity for the Suzuki–Miyaura coupling reaction Xu, Junwen Ou, Junjie Chen, Lianfang Zhang, Haiyang Ma, Shujuan Ye, Mingliang RSC Adv Chemistry Polymers of intrinsic microporosity (PIMs) are porous polymers with rigid ladder-type chain structures. Synthesizing these polymers usually involves the step polymerization of two types of monomer, namely, active fluorine-substituted aromatic ring monomers and phenolic monomers. Herein, we report a new PIMs preparation method using self-synthesized fluorinated monomers and common monomer 5,5′,6,6′-tetrahydroxy-3,3,3′,3′-tetramethyl spirobisindane. The fluorinated monomers were synthesized through the imidization of tetrafluorophthalic anhydride and aromatic diamines. The resulting PIMs served as a support for palladium, with the formed catalyst showing potential for application in the Suzuki–Miyaura coupling reaction. The Royal Society of Chemistry 2018-10-16 /pmc/articles/PMC9087636/ /pubmed/35547052 http://dx.doi.org/10.1039/c8ra06214e Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by/3.0/ |
spellingShingle | Chemistry Xu, Junwen Ou, Junjie Chen, Lianfang Zhang, Haiyang Ma, Shujuan Ye, Mingliang Palladium catalyst imbedded in polymers of intrinsic microporosity for the Suzuki–Miyaura coupling reaction |
title | Palladium catalyst imbedded in polymers of intrinsic microporosity for the Suzuki–Miyaura coupling reaction |
title_full | Palladium catalyst imbedded in polymers of intrinsic microporosity for the Suzuki–Miyaura coupling reaction |
title_fullStr | Palladium catalyst imbedded in polymers of intrinsic microporosity for the Suzuki–Miyaura coupling reaction |
title_full_unstemmed | Palladium catalyst imbedded in polymers of intrinsic microporosity for the Suzuki–Miyaura coupling reaction |
title_short | Palladium catalyst imbedded in polymers of intrinsic microporosity for the Suzuki–Miyaura coupling reaction |
title_sort | palladium catalyst imbedded in polymers of intrinsic microporosity for the suzuki–miyaura coupling reaction |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9087636/ https://www.ncbi.nlm.nih.gov/pubmed/35547052 http://dx.doi.org/10.1039/c8ra06214e |
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