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Straightforward Immobilization of Phosphonic Acids and Phosphoric Acid Esters on Mesoporous Silica and Their Application in an Asymmetric Aldol Reaction
The combined benefits of moisture-stable phosphonic acids and mesoporous silica materials (SBA-15 and MCM-41) as large-surface-area solid supports offer new opportunities for several applications, such as catalysis or drug delivery. We present a comprehensive study of a straightforward synthesis met...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6409583/ https://www.ncbi.nlm.nih.gov/pubmed/30759838 http://dx.doi.org/10.3390/nano9020249 |
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author | Weinberger, Christian Heckel, Tatjana Schnippering, Patrick Schmitz, Markus Guo, Anpeng Keil, Waldemar Marsmann, Heinrich C. Schmidt, Claudia Tiemann, Michael Wilhelm, René |
author_facet | Weinberger, Christian Heckel, Tatjana Schnippering, Patrick Schmitz, Markus Guo, Anpeng Keil, Waldemar Marsmann, Heinrich C. Schmidt, Claudia Tiemann, Michael Wilhelm, René |
author_sort | Weinberger, Christian |
collection | PubMed |
description | The combined benefits of moisture-stable phosphonic acids and mesoporous silica materials (SBA-15 and MCM-41) as large-surface-area solid supports offer new opportunities for several applications, such as catalysis or drug delivery. We present a comprehensive study of a straightforward synthesis method via direct immobilization of several phosphonic acids and phosphoric acid esters on various mesoporous silicas in a Dean–Stark apparatus with toluene as the solvent. Due to the utilization of azeotropic distillation, there was no need to dry phosphonic acids, phosphoric acid esters, solvents, or silicas prior to synthesis. In addition to modeling phosphonic acids, immobilization of the important biomolecule adenosine monophosphate (AMP) on the porous supports was also investigated. Due to the high surface area of the mesoporous silicas, a possible catalytic application based on immobilization of an organocatalyst for an asymmetric aldol reaction is discussed. |
format | Online Article Text |
id | pubmed-6409583 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-64095832019-03-11 Straightforward Immobilization of Phosphonic Acids and Phosphoric Acid Esters on Mesoporous Silica and Their Application in an Asymmetric Aldol Reaction Weinberger, Christian Heckel, Tatjana Schnippering, Patrick Schmitz, Markus Guo, Anpeng Keil, Waldemar Marsmann, Heinrich C. Schmidt, Claudia Tiemann, Michael Wilhelm, René Nanomaterials (Basel) Article The combined benefits of moisture-stable phosphonic acids and mesoporous silica materials (SBA-15 and MCM-41) as large-surface-area solid supports offer new opportunities for several applications, such as catalysis or drug delivery. We present a comprehensive study of a straightforward synthesis method via direct immobilization of several phosphonic acids and phosphoric acid esters on various mesoporous silicas in a Dean–Stark apparatus with toluene as the solvent. Due to the utilization of azeotropic distillation, there was no need to dry phosphonic acids, phosphoric acid esters, solvents, or silicas prior to synthesis. In addition to modeling phosphonic acids, immobilization of the important biomolecule adenosine monophosphate (AMP) on the porous supports was also investigated. Due to the high surface area of the mesoporous silicas, a possible catalytic application based on immobilization of an organocatalyst for an asymmetric aldol reaction is discussed. MDPI 2019-02-12 /pmc/articles/PMC6409583/ /pubmed/30759838 http://dx.doi.org/10.3390/nano9020249 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Weinberger, Christian Heckel, Tatjana Schnippering, Patrick Schmitz, Markus Guo, Anpeng Keil, Waldemar Marsmann, Heinrich C. Schmidt, Claudia Tiemann, Michael Wilhelm, René Straightforward Immobilization of Phosphonic Acids and Phosphoric Acid Esters on Mesoporous Silica and Their Application in an Asymmetric Aldol Reaction |
title | Straightforward Immobilization of Phosphonic Acids and Phosphoric Acid Esters on Mesoporous Silica and Their Application in an Asymmetric Aldol Reaction |
title_full | Straightforward Immobilization of Phosphonic Acids and Phosphoric Acid Esters on Mesoporous Silica and Their Application in an Asymmetric Aldol Reaction |
title_fullStr | Straightforward Immobilization of Phosphonic Acids and Phosphoric Acid Esters on Mesoporous Silica and Their Application in an Asymmetric Aldol Reaction |
title_full_unstemmed | Straightforward Immobilization of Phosphonic Acids and Phosphoric Acid Esters on Mesoporous Silica and Their Application in an Asymmetric Aldol Reaction |
title_short | Straightforward Immobilization of Phosphonic Acids and Phosphoric Acid Esters on Mesoporous Silica and Their Application in an Asymmetric Aldol Reaction |
title_sort | straightforward immobilization of phosphonic acids and phosphoric acid esters on mesoporous silica and their application in an asymmetric aldol reaction |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6409583/ https://www.ncbi.nlm.nih.gov/pubmed/30759838 http://dx.doi.org/10.3390/nano9020249 |
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