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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...

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Detalles Bibliográficos
Autores principales: Xu, Junwen, Ou, Junjie, Chen, Lianfang, Zhang, Haiyang, Ma, Shujuan, Ye, Mingliang
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/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.
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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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