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Development of effective potassium acetate extractant

Carboxylates are commonly used in the food and pharmaceutical industry and due to their extensive use, carboxylates present a significant environmental burden. In this context, valine based, heteroditopic receptor 1 was prepared and its ability to bind simultaneously potassium cation and acetate ani...

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Autores principales: Zakrzewski, Maciej, Załubiniak, Dominika, Piątek, Piotr
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8695828/
https://www.ncbi.nlm.nih.gov/pubmed/35423584
http://dx.doi.org/10.1039/d1ra00859e
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author Zakrzewski, Maciej
Załubiniak, Dominika
Piątek, Piotr
author_facet Zakrzewski, Maciej
Załubiniak, Dominika
Piątek, Piotr
author_sort Zakrzewski, Maciej
collection PubMed
description Carboxylates are commonly used in the food and pharmaceutical industry and due to their extensive use, carboxylates present a significant environmental burden. In this context, valine based, heteroditopic receptor 1 was prepared and its ability to bind simultaneously potassium cation and acetate anion in water containing CH(3)CN solutions was demonstrated. Under liquid–liquid extraction conditions the receptor 1 was capable of extracting hydrophilic AcOK salt from aqueous solution and was proved to be nearly ten times more effective than the equimolar mixture of monotopic receptors. Furthermore, compound 1 could extract one of the most popular nonsteroidal anti-inflammatory drugs, ibuprofen (IbuOK), from relatively dilute aqueous solutions.
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spelling pubmed-86958282022-04-13 Development of effective potassium acetate extractant Zakrzewski, Maciej Załubiniak, Dominika Piątek, Piotr RSC Adv Chemistry Carboxylates are commonly used in the food and pharmaceutical industry and due to their extensive use, carboxylates present a significant environmental burden. In this context, valine based, heteroditopic receptor 1 was prepared and its ability to bind simultaneously potassium cation and acetate anion in water containing CH(3)CN solutions was demonstrated. Under liquid–liquid extraction conditions the receptor 1 was capable of extracting hydrophilic AcOK salt from aqueous solution and was proved to be nearly ten times more effective than the equimolar mixture of monotopic receptors. Furthermore, compound 1 could extract one of the most popular nonsteroidal anti-inflammatory drugs, ibuprofen (IbuOK), from relatively dilute aqueous solutions. The Royal Society of Chemistry 2021-03-16 /pmc/articles/PMC8695828/ /pubmed/35423584 http://dx.doi.org/10.1039/d1ra00859e Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Zakrzewski, Maciej
Załubiniak, Dominika
Piątek, Piotr
Development of effective potassium acetate extractant
title Development of effective potassium acetate extractant
title_full Development of effective potassium acetate extractant
title_fullStr Development of effective potassium acetate extractant
title_full_unstemmed Development of effective potassium acetate extractant
title_short Development of effective potassium acetate extractant
title_sort development of effective potassium acetate extractant
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8695828/
https://www.ncbi.nlm.nih.gov/pubmed/35423584
http://dx.doi.org/10.1039/d1ra00859e
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