Synthesis of purine-based ionic liquids and their applications

Detalhes bibliográficos
Autor(a) principal: Carreira, Ana R. F.
Data de Publicação: 2021
Outros Autores: Veloso, Telma, Schaeffer, Nicolas, Pereira, Joana L., Ventura, Sónia P. M., Rizzi, Cécile, Plénet, Juliette Sirieix, Passos, Helena, Coutinho, João A. P.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10773/33197
Resumo: Bio-based ionic liquids (ILs) are being increasingly sought after, as they are more sustainable and eco-friendly. Purines are the most widely distributed, naturally occurring N-heterocycles, but their low water-solubility limits their application. In this work, four purines (theobromine, theophylline, xanthine, and uric acid) were combined with the cation tetrabutylammonium to synthesize bio-based ILs. The physico-chemical properties of the purine-based ILs were characterized, including their melting and decomposition temperatures and water-solubility. The ecotoxicity against the microalgae Raphidocelis subcapitata was also determined. The ILs show good thermal stability (>457 K) and an aqueous solubility enhancement ranging from 53- to 870-fold, in comparison to their respective purine percursors, unlocking new prospects for their application where aqueous solutions are demanded. The ecotoxicity of these ILs seems to be dominated by the cation, and it is similar to chloride-based IL, emphasizing that the use of natural anions does not necessarily translate to more benign ILs. The application of the novel ILs in the formation of aqueous biphasic systems (ABS), and as solubility enhancers, was also evaluated. The ILs were able to form ABS with sodium sulfate and tripotassium citrate salts. The development of thermoresponsive ABS, using sodium sulfate as a salting-out agent, was accomplished, with the ILs having different thermosensitivities. In addition, the purine-based ILs acted as solubility enhancers of ferulic acid in aqueous solution.
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spelling Synthesis of purine-based ionic liquids and their applicationsSynthesisEcotoxicitySolubilityLiquid–liquid equilibriumThermoresponsive systemsBio-based ionic liquids (ILs) are being increasingly sought after, as they are more sustainable and eco-friendly. Purines are the most widely distributed, naturally occurring N-heterocycles, but their low water-solubility limits their application. In this work, four purines (theobromine, theophylline, xanthine, and uric acid) were combined with the cation tetrabutylammonium to synthesize bio-based ILs. The physico-chemical properties of the purine-based ILs were characterized, including their melting and decomposition temperatures and water-solubility. The ecotoxicity against the microalgae Raphidocelis subcapitata was also determined. The ILs show good thermal stability (>457 K) and an aqueous solubility enhancement ranging from 53- to 870-fold, in comparison to their respective purine percursors, unlocking new prospects for their application where aqueous solutions are demanded. The ecotoxicity of these ILs seems to be dominated by the cation, and it is similar to chloride-based IL, emphasizing that the use of natural anions does not necessarily translate to more benign ILs. The application of the novel ILs in the formation of aqueous biphasic systems (ABS), and as solubility enhancers, was also evaluated. The ILs were able to form ABS with sodium sulfate and tripotassium citrate salts. The development of thermoresponsive ABS, using sodium sulfate as a salting-out agent, was accomplished, with the ILs having different thermosensitivities. In addition, the purine-based ILs acted as solubility enhancers of ferulic acid in aqueous solution.MDPI2022-02-15T19:40:19Z2021-11-02T00:00:00Z2021-11-02info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10773/33197eng10.3390/molecules26226958Carreira, Ana R. F.Veloso, TelmaSchaeffer, NicolasPereira, Joana L.Ventura, Sónia P. M.Rizzi, CécilePlénet, Juliette SirieixPassos, HelenaCoutinho, João A. P.info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2024-02-22T12:03:43Zoai:ria.ua.pt:10773/33197Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-20T03:04:36.923095Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Synthesis of purine-based ionic liquids and their applications
title Synthesis of purine-based ionic liquids and their applications
spellingShingle Synthesis of purine-based ionic liquids and their applications
Carreira, Ana R. F.
Synthesis
Ecotoxicity
Solubility
Liquid–liquid equilibrium
Thermoresponsive systems
title_short Synthesis of purine-based ionic liquids and their applications
title_full Synthesis of purine-based ionic liquids and their applications
title_fullStr Synthesis of purine-based ionic liquids and their applications
title_full_unstemmed Synthesis of purine-based ionic liquids and their applications
title_sort Synthesis of purine-based ionic liquids and their applications
author Carreira, Ana R. F.
author_facet Carreira, Ana R. F.
Veloso, Telma
Schaeffer, Nicolas
Pereira, Joana L.
Ventura, Sónia P. M.
Rizzi, Cécile
Plénet, Juliette Sirieix
Passos, Helena
Coutinho, João A. P.
author_role author
author2 Veloso, Telma
Schaeffer, Nicolas
Pereira, Joana L.
Ventura, Sónia P. M.
Rizzi, Cécile
Plénet, Juliette Sirieix
Passos, Helena
Coutinho, João A. P.
author2_role author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Carreira, Ana R. F.
Veloso, Telma
Schaeffer, Nicolas
Pereira, Joana L.
Ventura, Sónia P. M.
Rizzi, Cécile
Plénet, Juliette Sirieix
Passos, Helena
Coutinho, João A. P.
dc.subject.por.fl_str_mv Synthesis
Ecotoxicity
Solubility
Liquid–liquid equilibrium
Thermoresponsive systems
topic Synthesis
Ecotoxicity
Solubility
Liquid–liquid equilibrium
Thermoresponsive systems
description Bio-based ionic liquids (ILs) are being increasingly sought after, as they are more sustainable and eco-friendly. Purines are the most widely distributed, naturally occurring N-heterocycles, but their low water-solubility limits their application. In this work, four purines (theobromine, theophylline, xanthine, and uric acid) were combined with the cation tetrabutylammonium to synthesize bio-based ILs. The physico-chemical properties of the purine-based ILs were characterized, including their melting and decomposition temperatures and water-solubility. The ecotoxicity against the microalgae Raphidocelis subcapitata was also determined. The ILs show good thermal stability (>457 K) and an aqueous solubility enhancement ranging from 53- to 870-fold, in comparison to their respective purine percursors, unlocking new prospects for their application where aqueous solutions are demanded. The ecotoxicity of these ILs seems to be dominated by the cation, and it is similar to chloride-based IL, emphasizing that the use of natural anions does not necessarily translate to more benign ILs. The application of the novel ILs in the formation of aqueous biphasic systems (ABS), and as solubility enhancers, was also evaluated. The ILs were able to form ABS with sodium sulfate and tripotassium citrate salts. The development of thermoresponsive ABS, using sodium sulfate as a salting-out agent, was accomplished, with the ILs having different thermosensitivities. In addition, the purine-based ILs acted as solubility enhancers of ferulic acid in aqueous solution.
publishDate 2021
dc.date.none.fl_str_mv 2021-11-02T00:00:00Z
2021-11-02
2022-02-15T19:40:19Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
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dc.identifier.uri.fl_str_mv http://hdl.handle.net/10773/33197
url http://hdl.handle.net/10773/33197
dc.language.iso.fl_str_mv eng
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dc.relation.none.fl_str_mv 10.3390/molecules26226958
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