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“Activated Borane”: A Porous Borane Cluster Polymer as an Efficient Lewis Acid-Based Catalyst
[Image: see text] Borane cluster-based porous covalent networks, named activated borane (ActB), were prepared by cothermolysis of decaborane(14) (nido-B(10)H(14)) and selected hydrocarbons (toluene, ActB-Tol; cyclohexane, ActB-cyHx; and n-hexane, ActB-nHx) under anaerobic conditions. These amorphous...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10660343/ https://www.ncbi.nlm.nih.gov/pubmed/38026813 http://dx.doi.org/10.1021/acscatal.3c04011 |
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author | Lamač, Martin Urbán, Béla Horáček, Michal Bůžek, Daniel Leonová, Lucie Stýskalík, Aleš Vykydalová, Anna Škoch, Karel Kloda, Matouš Mahun, Andrii Kobera, Libor Lang, Kamil Londesborough, Michael G. S. Demel, Jan |
author_facet | Lamač, Martin Urbán, Béla Horáček, Michal Bůžek, Daniel Leonová, Lucie Stýskalík, Aleš Vykydalová, Anna Škoch, Karel Kloda, Matouš Mahun, Andrii Kobera, Libor Lang, Kamil Londesborough, Michael G. S. Demel, Jan |
author_sort | Lamač, Martin |
collection | PubMed |
description | [Image: see text] Borane cluster-based porous covalent networks, named activated borane (ActB), were prepared by cothermolysis of decaborane(14) (nido-B(10)H(14)) and selected hydrocarbons (toluene, ActB-Tol; cyclohexane, ActB-cyHx; and n-hexane, ActB-nHx) under anaerobic conditions. These amorphous solid powders exhibit different textural and Lewis acid (LA) properties that vary depending on the nature of the constituent organic linker. For ActB-Tol, its LA strength even approaches that of the commonly used molecular LA, B(C(6)F(5))(3). Most notably, ActBs can act as heterogeneous LA catalysts in hydrosilylation/deoxygenation reactions with various carbonyl substrates as well as in the gas-phase dehydration of ethanol. These studies reveal the potential of ActBs in catalytic applications, showing (a) the possibility for tuning catalytic reaction outcomes (selectivity) in hydrosilylation/deoxygenation reactions by changing the material’s composition and (b) the very high activity toward ethanol dehydration that exceeds the commonly used γ-Al(2)O(3) by achieving a stable conversion of ∼93% with a selectivity for ethylene production of ∼78% during a 17 h continuous period on stream at 240 °C. |
format | Online Article Text |
id | pubmed-10660343 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-106603432023-11-21 “Activated Borane”: A Porous Borane Cluster Polymer as an Efficient Lewis Acid-Based Catalyst Lamač, Martin Urbán, Béla Horáček, Michal Bůžek, Daniel Leonová, Lucie Stýskalík, Aleš Vykydalová, Anna Škoch, Karel Kloda, Matouš Mahun, Andrii Kobera, Libor Lang, Kamil Londesborough, Michael G. S. Demel, Jan ACS Catal [Image: see text] Borane cluster-based porous covalent networks, named activated borane (ActB), were prepared by cothermolysis of decaborane(14) (nido-B(10)H(14)) and selected hydrocarbons (toluene, ActB-Tol; cyclohexane, ActB-cyHx; and n-hexane, ActB-nHx) under anaerobic conditions. These amorphous solid powders exhibit different textural and Lewis acid (LA) properties that vary depending on the nature of the constituent organic linker. For ActB-Tol, its LA strength even approaches that of the commonly used molecular LA, B(C(6)F(5))(3). Most notably, ActBs can act as heterogeneous LA catalysts in hydrosilylation/deoxygenation reactions with various carbonyl substrates as well as in the gas-phase dehydration of ethanol. These studies reveal the potential of ActBs in catalytic applications, showing (a) the possibility for tuning catalytic reaction outcomes (selectivity) in hydrosilylation/deoxygenation reactions by changing the material’s composition and (b) the very high activity toward ethanol dehydration that exceeds the commonly used γ-Al(2)O(3) by achieving a stable conversion of ∼93% with a selectivity for ethylene production of ∼78% during a 17 h continuous period on stream at 240 °C. American Chemical Society 2023-10-30 /pmc/articles/PMC10660343/ /pubmed/38026813 http://dx.doi.org/10.1021/acscatal.3c04011 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Lamač, Martin Urbán, Béla Horáček, Michal Bůžek, Daniel Leonová, Lucie Stýskalík, Aleš Vykydalová, Anna Škoch, Karel Kloda, Matouš Mahun, Andrii Kobera, Libor Lang, Kamil Londesborough, Michael G. S. Demel, Jan “Activated Borane”: A Porous Borane Cluster Polymer as an Efficient Lewis Acid-Based Catalyst |
title | “Activated Borane”: A Porous Borane
Cluster Polymer as an Efficient Lewis Acid-Based Catalyst |
title_full | “Activated Borane”: A Porous Borane
Cluster Polymer as an Efficient Lewis Acid-Based Catalyst |
title_fullStr | “Activated Borane”: A Porous Borane
Cluster Polymer as an Efficient Lewis Acid-Based Catalyst |
title_full_unstemmed | “Activated Borane”: A Porous Borane
Cluster Polymer as an Efficient Lewis Acid-Based Catalyst |
title_short | “Activated Borane”: A Porous Borane
Cluster Polymer as an Efficient Lewis Acid-Based Catalyst |
title_sort | “activated borane”: a porous borane
cluster polymer as an efficient lewis acid-based catalyst |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10660343/ https://www.ncbi.nlm.nih.gov/pubmed/38026813 http://dx.doi.org/10.1021/acscatal.3c04011 |
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