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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,...

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Autores principales: Latos, Piotr, Culkin, Alice, Barteczko, Natalia, Boncel, Sławomir, Jurczyk, Sebastian, Brown, Lucy C., Nockemann, Peter, Chrobok, Anna, Swadźba-Kwaśny, Małgorzata
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2018
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.
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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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