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Water-Tolerant Trifloaluminate Ionic Liquids: New and Unique Lewis Acidic Catalysts for the Synthesis of Chromane
The first example of triflometallate ionic liquids, named in analogy to chlorometallate ionic liquids, is reported. Trifloaluminate ionic liquids, synthesized from 1-alkyl-3-methylimidazolium triflates and aluminum triflate, were characterized by multinuclear NMR spectroscopy and FT-IR spectroscopy,...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6240586/ https://www.ncbi.nlm.nih.gov/pubmed/30483493 http://dx.doi.org/10.3389/fchem.2018.00535 |
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author | Latos, Piotr Culkin, Alice Barteczko, Natalia Boncel, Sławomir Jurczyk, Sebastian Brown, Lucy C. Nockemann, Peter Chrobok, Anna Swadźba-Kwaśny, Małgorzata |
author_facet | Latos, Piotr Culkin, Alice Barteczko, Natalia Boncel, Sławomir Jurczyk, Sebastian Brown, Lucy C. Nockemann, Peter Chrobok, Anna Swadźba-Kwaśny, Małgorzata |
author_sort | Latos, Piotr |
collection | PubMed |
description | The first example of triflometallate ionic liquids, named in analogy to chlorometallate ionic liquids, is reported. Trifloaluminate ionic liquids, synthesized from 1-alkyl-3-methylimidazolium triflates and aluminum triflate, were characterized by multinuclear NMR spectroscopy and FT-IR spectroscopy, revealing the existence of oligonuclear, multiply-charged trifloaluminate anions, with multiple bridging triflate modes. Acceptor numbers were determined to quantify their Lewis acidity, rendering trifloaluminate ionic liquids as medium-strength Lewis acids (AN = ca. 65). Used as acidic catalysts in the cycloaddition of 2,4-dimethylphenol and isoprene (molar ratio 2:1) to prepare chromane, trifloaluminate systems outperformed literature systems, showing high activity (conversions 94–99%, selectivities 80–89%) and at low loadings (0.2 mol%) at 35°C. Using these new systems as supported ionic liquid phase (SILP) on multi-walled carbon nanotubes (ionic liquid loading 16 wt%) delivered a recyclable catalytic system, with activity enhanced with respect to the homogenous regime. |
format | Online Article Text |
id | pubmed-6240586 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-62405862018-11-27 Water-Tolerant Trifloaluminate Ionic Liquids: New and Unique Lewis Acidic Catalysts for the Synthesis of Chromane Latos, Piotr Culkin, Alice Barteczko, Natalia Boncel, Sławomir Jurczyk, Sebastian Brown, Lucy C. Nockemann, Peter Chrobok, Anna Swadźba-Kwaśny, Małgorzata Front Chem Chemistry The first example of triflometallate ionic liquids, named in analogy to chlorometallate ionic liquids, is reported. Trifloaluminate ionic liquids, synthesized from 1-alkyl-3-methylimidazolium triflates and aluminum triflate, were characterized by multinuclear NMR spectroscopy and FT-IR spectroscopy, revealing the existence of oligonuclear, multiply-charged trifloaluminate anions, with multiple bridging triflate modes. Acceptor numbers were determined to quantify their Lewis acidity, rendering trifloaluminate ionic liquids as medium-strength Lewis acids (AN = ca. 65). Used as acidic catalysts in the cycloaddition of 2,4-dimethylphenol and isoprene (molar ratio 2:1) to prepare chromane, trifloaluminate systems outperformed literature systems, showing high activity (conversions 94–99%, selectivities 80–89%) and at low loadings (0.2 mol%) at 35°C. Using these new systems as supported ionic liquid phase (SILP) on multi-walled carbon nanotubes (ionic liquid loading 16 wt%) delivered a recyclable catalytic system, with activity enhanced with respect to the homogenous regime. Frontiers Media S.A. 2018-11-12 /pmc/articles/PMC6240586/ /pubmed/30483493 http://dx.doi.org/10.3389/fchem.2018.00535 Text en Copyright © 2018 Latos, Culkin, Barteczko, Boncel, Jurczyk, Brown, Nockemann, Chrobok and Swadźba-Kwaśny. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Chemistry Latos, Piotr Culkin, Alice Barteczko, Natalia Boncel, Sławomir Jurczyk, Sebastian Brown, Lucy C. Nockemann, Peter Chrobok, Anna Swadźba-Kwaśny, Małgorzata Water-Tolerant Trifloaluminate Ionic Liquids: New and Unique Lewis Acidic Catalysts for the Synthesis of Chromane |
title | Water-Tolerant Trifloaluminate Ionic Liquids: New and Unique Lewis Acidic Catalysts for the Synthesis of Chromane |
title_full | Water-Tolerant Trifloaluminate Ionic Liquids: New and Unique Lewis Acidic Catalysts for the Synthesis of Chromane |
title_fullStr | Water-Tolerant Trifloaluminate Ionic Liquids: New and Unique Lewis Acidic Catalysts for the Synthesis of Chromane |
title_full_unstemmed | Water-Tolerant Trifloaluminate Ionic Liquids: New and Unique Lewis Acidic Catalysts for the Synthesis of Chromane |
title_short | Water-Tolerant Trifloaluminate Ionic Liquids: New and Unique Lewis Acidic Catalysts for the Synthesis of Chromane |
title_sort | water-tolerant trifloaluminate ionic liquids: new and unique lewis acidic catalysts for the synthesis of chromane |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6240586/ https://www.ncbi.nlm.nih.gov/pubmed/30483493 http://dx.doi.org/10.3389/fchem.2018.00535 |
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