What a difference a methyl group makes-probing choline-urea molecular interactions through urea structure modification
Autor(a) principal: | |
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Data de Publicação: | 2018 |
Outros Autores: | , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
Texto Completo: | http://hdl.handle.net/10198/20084 |
Resumo: | There is a lack of fundamental knowledge on deep eutectic solvents, even for the most extensively studied mixtures, such as the mixture of cholinium chloride and urea, which prevents a judicious choice of components to prepare new solvents. The objective of this work is to study and understand the fundamental interactions between cholinium chloride and urea that lead to the experimentally observed melting temperature depression. To do so, the structure of urea was strategically and progressively modified, in order to block certain interaction centres, and the solid–liquid equilibrium data of each new binary system was experimentally measured. Using this approach, it was concluded that the most important interaction between cholinium chloride and urea occurs through hydrogen bonding between the chloride anion and the amine groups. Any blockage of these groups severely hampers the melting point depression effect. Raman spectroscopy and DFT calculations were utilized to study in more detail this hydrogen bonding and its nuances. |
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What a difference a methyl group makes-probing choline-urea molecular interactions through urea structure modificationThere is a lack of fundamental knowledge on deep eutectic solvents, even for the most extensively studied mixtures, such as the mixture of cholinium chloride and urea, which prevents a judicious choice of components to prepare new solvents. The objective of this work is to study and understand the fundamental interactions between cholinium chloride and urea that lead to the experimentally observed melting temperature depression. To do so, the structure of urea was strategically and progressively modified, in order to block certain interaction centres, and the solid–liquid equilibrium data of each new binary system was experimentally measured. Using this approach, it was concluded that the most important interaction between cholinium chloride and urea occurs through hydrogen bonding between the chloride anion and the amine groups. Any blockage of these groups severely hampers the melting point depression effect. Raman spectroscopy and DFT calculations were utilized to study in more detail this hydrogen bonding and its nuances.This work was developed in the scope of the project CICECO – Aveiro Institute of Materials, POCI-01-0145-FEDER-007679 (Ref. FCT UID/CTM/50011/2019) and Associate Laboratory LSRELCM, POCI-01-0145-FEDER-006984 (Ref. FCT UID/EQU/50020/2019), and project MultiBiorefinery (POCI-01-0145-FEDER-016403), all financed by national funds through the FCT/ MCTES (PIDDAC) and when appropriate co-financed by FEDER under the PT2020 Partnership Agreement. M. A. R. M. acknowledges financial support from NORTE-01-0145-FEDER-000006 – funded by NORTE2020 through PT2020 and ERDF. L. P. S. acknowledges FCT for her PhD grant (SFRH/BD/135976/2018). C. F. A. acknowledges FCT for her PhD grant (SFRH/BD/129040/2017). M. M. N. and M. M. F. acknowledge FCT for their researcher contracts (IF/01468/2015 and IF/00894/2015 respectively) under the program IF 2015.Biblioteca Digital do IPBSilva, Liliana P.Araújo, CatarinaAbranches, Dinis O.Melle-Franco, ManuelMartins, Mónia A.R.Nolasco, Mariela M.Ribeiro-Claro, Paulo J.A.Pinho, SimãoCoutinho, João A.P.2018-01-19T10:00:00Z20192019-01-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10198/20084engSilva, Liliana P.; Araújo, Catarina F.; Abranches, Dinis O.; Melle-Franco, Manuel; Martins, Mónia A.R.; Nolasco, Mariela M.; Ribeiro-Claro, Paulo J.A.; Pinho, Simão P.; Coutinho, João A.P. (2019). What a difference a methyl group makes-probing choline-urea molecular interactions through urea structure modification. Physical Chemistry Chemical Physics. ISSN 1463-9076. 21, p. 18278-182891463-907610.1039/c9cp03552dinfo: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:RCAAP2023-11-21T10:45:54Zoai:bibliotecadigital.ipb.pt:10198/20084Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T23:10:52.822867Repositório 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 |
What a difference a methyl group makes-probing choline-urea molecular interactions through urea structure modification |
title |
What a difference a methyl group makes-probing choline-urea molecular interactions through urea structure modification |
spellingShingle |
What a difference a methyl group makes-probing choline-urea molecular interactions through urea structure modification Silva, Liliana P. |
title_short |
What a difference a methyl group makes-probing choline-urea molecular interactions through urea structure modification |
title_full |
What a difference a methyl group makes-probing choline-urea molecular interactions through urea structure modification |
title_fullStr |
What a difference a methyl group makes-probing choline-urea molecular interactions through urea structure modification |
title_full_unstemmed |
What a difference a methyl group makes-probing choline-urea molecular interactions through urea structure modification |
title_sort |
What a difference a methyl group makes-probing choline-urea molecular interactions through urea structure modification |
author |
Silva, Liliana P. |
author_facet |
Silva, Liliana P. Araújo, Catarina Abranches, Dinis O. Melle-Franco, Manuel Martins, Mónia A.R. Nolasco, Mariela M. Ribeiro-Claro, Paulo J.A. Pinho, Simão Coutinho, João A.P. |
author_role |
author |
author2 |
Araújo, Catarina Abranches, Dinis O. Melle-Franco, Manuel Martins, Mónia A.R. Nolasco, Mariela M. Ribeiro-Claro, Paulo J.A. Pinho, Simão Coutinho, João A.P. |
author2_role |
author author author author author author author author |
dc.contributor.none.fl_str_mv |
Biblioteca Digital do IPB |
dc.contributor.author.fl_str_mv |
Silva, Liliana P. Araújo, Catarina Abranches, Dinis O. Melle-Franco, Manuel Martins, Mónia A.R. Nolasco, Mariela M. Ribeiro-Claro, Paulo J.A. Pinho, Simão Coutinho, João A.P. |
description |
There is a lack of fundamental knowledge on deep eutectic solvents, even for the most extensively studied mixtures, such as the mixture of cholinium chloride and urea, which prevents a judicious choice of components to prepare new solvents. The objective of this work is to study and understand the fundamental interactions between cholinium chloride and urea that lead to the experimentally observed melting temperature depression. To do so, the structure of urea was strategically and progressively modified, in order to block certain interaction centres, and the solid–liquid equilibrium data of each new binary system was experimentally measured. Using this approach, it was concluded that the most important interaction between cholinium chloride and urea occurs through hydrogen bonding between the chloride anion and the amine groups. Any blockage of these groups severely hampers the melting point depression effect. Raman spectroscopy and DFT calculations were utilized to study in more detail this hydrogen bonding and its nuances. |
publishDate |
2018 |
dc.date.none.fl_str_mv |
2018-01-19T10:00:00Z 2019 2019-01-01T00:00:00Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://hdl.handle.net/10198/20084 |
url |
http://hdl.handle.net/10198/20084 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Silva, Liliana P.; Araújo, Catarina F.; Abranches, Dinis O.; Melle-Franco, Manuel; Martins, Mónia A.R.; Nolasco, Mariela M.; Ribeiro-Claro, Paulo J.A.; Pinho, Simão P.; Coutinho, João A.P. (2019). What a difference a methyl group makes-probing choline-urea molecular interactions through urea structure modification. Physical Chemistry Chemical Physics. ISSN 1463-9076. 21, p. 18278-18289 1463-9076 10.1039/c9cp03552d |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
application/pdf |
dc.source.none.fl_str_mv |
reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação instacron:RCAAP |
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Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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RCAAP |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
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Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
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