Nesting Well-Defined Pt Nanoparticles within a Hierarchically Porous Polymer as a Heterogeneous Suzuki–Miyaura Catalyst
A hierarchically porous polymer (HPP) consisting of micropores (∼1 nm) within a 3D continuous mesoporous wall (∼15 nm) was used to support well-defined Pt nanoparticles (2 nm in diameter) as a heterogeneous catalyst for the Suzuki–Miyaura cross-coupling reaction in the liquid phase. The ligand-cappe...
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creator | Kim, Soobin Varga, Gábor Seo, Myungeun Sápi, András Rácz, Viktória Gómez-Pérez, Juan F Sebők, Dániel Lee, Jeonghyeon Kukovecz, Ákos Kónya, Zoltán |
description | A hierarchically porous polymer (HPP) consisting of micropores (∼1 nm) within a 3D continuous mesoporous wall (∼15 nm) was used to support well-defined Pt nanoparticles (2 nm in diameter) as a heterogeneous catalyst for the Suzuki–Miyaura cross-coupling reaction in the liquid phase. The ligand-capped nanoparticles were loaded into the polymer and treated with plasma to expose the active surface. The dual porosity was essential: the block polymer-templated mesopores provided the reactants facile access to the nanoparticle center, which was firmly immobilized by the microporous surface. Compared to inorganic mesoporous silica supports, which are intrinsically susceptible to basic hydrolysis, the Pt-HPP featured higher activity for all halide leaving groups, even in green solvents, as well as excellent recyclability. Only 5% decrease in activity was observed after 10 cycles. Pt-HPP was one of the most active heterogeneous catalysts for aryl chloride substrates compared to literature Pt or Pd examples. |
doi_str_mv | 10.1021/acsanm.1c00396 |
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The ligand-capped nanoparticles were loaded into the polymer and treated with plasma to expose the active surface. The dual porosity was essential: the block polymer-templated mesopores provided the reactants facile access to the nanoparticle center, which was firmly immobilized by the microporous surface. Compared to inorganic mesoporous silica supports, which are intrinsically susceptible to basic hydrolysis, the Pt-HPP featured higher activity for all halide leaving groups, even in green solvents, as well as excellent recyclability. Only 5% decrease in activity was observed after 10 cycles. Pt-HPP was one of the most active heterogeneous catalysts for aryl chloride substrates compared to literature Pt or Pd examples.</description><identifier>ISSN: 2574-0970</identifier><identifier>EISSN: 2574-0970</identifier><identifier>DOI: 10.1021/acsanm.1c00396</identifier><language>eng</language><publisher>American Chemical Society</publisher><ispartof>ACS applied nano materials, 2021-04, Vol.4 (4), p.4070-4076</ispartof><rights>2021 The Authors. 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Nano Mater</addtitle><description>A hierarchically porous polymer (HPP) consisting of micropores (∼1 nm) within a 3D continuous mesoporous wall (∼15 nm) was used to support well-defined Pt nanoparticles (2 nm in diameter) as a heterogeneous catalyst for the Suzuki–Miyaura cross-coupling reaction in the liquid phase. The ligand-capped nanoparticles were loaded into the polymer and treated with plasma to expose the active surface. The dual porosity was essential: the block polymer-templated mesopores provided the reactants facile access to the nanoparticle center, which was firmly immobilized by the microporous surface. Compared to inorganic mesoporous silica supports, which are intrinsically susceptible to basic hydrolysis, the Pt-HPP featured higher activity for all halide leaving groups, even in green solvents, as well as excellent recyclability. Only 5% decrease in activity was observed after 10 cycles. 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Nano Mater</addtitle><date>2021-04-23</date><risdate>2021</risdate><volume>4</volume><issue>4</issue><spage>4070</spage><epage>4076</epage><pages>4070-4076</pages><issn>2574-0970</issn><eissn>2574-0970</eissn><abstract>A hierarchically porous polymer (HPP) consisting of micropores (∼1 nm) within a 3D continuous mesoporous wall (∼15 nm) was used to support well-defined Pt nanoparticles (2 nm in diameter) as a heterogeneous catalyst for the Suzuki–Miyaura cross-coupling reaction in the liquid phase. The ligand-capped nanoparticles were loaded into the polymer and treated with plasma to expose the active surface. The dual porosity was essential: the block polymer-templated mesopores provided the reactants facile access to the nanoparticle center, which was firmly immobilized by the microporous surface. Compared to inorganic mesoporous silica supports, which are intrinsically susceptible to basic hydrolysis, the Pt-HPP featured higher activity for all halide leaving groups, even in green solvents, as well as excellent recyclability. Only 5% decrease in activity was observed after 10 cycles. Pt-HPP was one of the most active heterogeneous catalysts for aryl chloride substrates compared to literature Pt or Pd examples.</abstract><pub>American Chemical Society</pub><doi>10.1021/acsanm.1c00396</doi><tpages>7</tpages><orcidid>https://orcid.org/0000-0002-2736-2015</orcidid><orcidid>https://orcid.org/0000-0002-9406-8596</orcidid><orcidid>https://orcid.org/0000-0001-5624-1063</orcidid><orcidid>https://orcid.org/0000-0002-7131-1629</orcidid><orcidid>https://orcid.org/0000-0003-0716-9557</orcidid><orcidid>https://orcid.org/0000-0002-5218-3502</orcidid><orcidid>https://orcid.org/0000-0001-6557-0731</orcidid><oa>free_for_read</oa></addata></record> |
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title | Nesting Well-Defined Pt Nanoparticles within a Hierarchically Porous Polymer as a Heterogeneous Suzuki–Miyaura Catalyst |
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