Anthocyanin color stabilization by host‐guest complexation with p‐sulfonatocalix[n]arenes
Autor(a) principal: | |
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Data de Publicação: | 2021 |
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/10362/124894 |
Resumo: | Funding Information: Funding: This research was supported by the Associated Laboratory for Sustainable Chemistry, Clean Processes and Technologies LAQV through national funds from UIDB/50006/2020. FCT/MCTES is also acknowledged for supporting the National Portuguese NMR Network (ROTEIRO/0031/2013‐PINFRA/22161/2016, co‐financed by FEDER through COMPETE 2020, POCI, PORL, and FCT through PIDDAC) and for the grant PTDC/QUI‐COL/32351/2017. J.M. is grateful for the doctoral grant awarded by CONACYT (MEX/Ref. 288188). N.B. acknowledges FCT for the contract CEECIND/00466/2017. |
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7160 |
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Anthocyanin color stabilization by host‐guest complexation with p‐sulfonatocalix[n]arenesAnthocyaninsColor stabilityHost‐guest systemsP‐Sulfonatocalix[n]arenesAnalytical ChemistryChemistry (miscellaneous)Molecular MedicinePharmaceutical ScienceDrug DiscoveryPhysical and Theoretical ChemistryOrganic ChemistryFunding Information: Funding: This research was supported by the Associated Laboratory for Sustainable Chemistry, Clean Processes and Technologies LAQV through national funds from UIDB/50006/2020. FCT/MCTES is also acknowledged for supporting the National Portuguese NMR Network (ROTEIRO/0031/2013‐PINFRA/22161/2016, co‐financed by FEDER through COMPETE 2020, POCI, PORL, and FCT through PIDDAC) and for the grant PTDC/QUI‐COL/32351/2017. J.M. is grateful for the doctoral grant awarded by CONACYT (MEX/Ref. 288188). N.B. acknowledges FCT for the contract CEECIND/00466/2017.Flavylium‐based compounds in their acidic and cationic form bring color to aqueous solutions, while under slightly acidic or neutral conditions they commonly bring discoloration. Selective host‐guest complexation between water‐soluble p‐sulfonatocalix[n]arenes (SCn) macrocycles and the flavylium cationic species can increase the stability of the colored form, expanding its domain over the pH scale. The association constants between SCn and the cationic (acid) and neutral basic forms of flavylium‐based compounds were determined through UV‐Vis host‐guest titrations at different pH values. The affinity of the hosts for synthetic chromophore was found to be higher than for a natural anthocyanin (Oenin). The higher affinity of SC4 for the synthetic flavylium was confirmed by1H NMR showing a preferential interaction of the flavylium phenyl ring with the host cavity. In contrast with its synthetic counterpart, the flavylium substitution pattern in the anthocyanin seems to limit the inclusion of the guest in the host’s binding pocket. In this case, the higher affinity was observed for the octamer (SC8) likely due to its larger cavity and higher number of negatively charged sulfonate groups.LAQV@REQUIMTEDQ - Departamento de QuímicaRUNMendoza, JohanCruz, Luisde Freitas, VictorPina, FernandoBasílio, Nuno2021-09-21T02:07:57Z2021-09-042021-09-04T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10362/124894eng1420-3049PURE: 33823005https://doi.org/10.3390/molecules26175389info: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:RCAAP2024-05-22T17:56:14Zoai:run.unl.pt:10362/124894Portal AgregadorONGhttps://www.rcaap.pt/oai/openairemluisa.alvim@gmail.comopendoar:71602024-05-22T17:56:14Repositório 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 |
Anthocyanin color stabilization by host‐guest complexation with p‐sulfonatocalix[n]arenes |
title |
Anthocyanin color stabilization by host‐guest complexation with p‐sulfonatocalix[n]arenes |
spellingShingle |
Anthocyanin color stabilization by host‐guest complexation with p‐sulfonatocalix[n]arenes Mendoza, Johan Anthocyanins Color stability Host‐guest systems P‐Sulfonatocalix[n]arenes Analytical Chemistry Chemistry (miscellaneous) Molecular Medicine Pharmaceutical Science Drug Discovery Physical and Theoretical Chemistry Organic Chemistry |
title_short |
Anthocyanin color stabilization by host‐guest complexation with p‐sulfonatocalix[n]arenes |
title_full |
Anthocyanin color stabilization by host‐guest complexation with p‐sulfonatocalix[n]arenes |
title_fullStr |
Anthocyanin color stabilization by host‐guest complexation with p‐sulfonatocalix[n]arenes |
title_full_unstemmed |
Anthocyanin color stabilization by host‐guest complexation with p‐sulfonatocalix[n]arenes |
title_sort |
Anthocyanin color stabilization by host‐guest complexation with p‐sulfonatocalix[n]arenes |
author |
Mendoza, Johan |
author_facet |
Mendoza, Johan Cruz, Luis de Freitas, Victor Pina, Fernando Basílio, Nuno |
author_role |
author |
author2 |
Cruz, Luis de Freitas, Victor Pina, Fernando Basílio, Nuno |
author2_role |
author author author author |
dc.contributor.none.fl_str_mv |
LAQV@REQUIMTE DQ - Departamento de Química RUN |
dc.contributor.author.fl_str_mv |
Mendoza, Johan Cruz, Luis de Freitas, Victor Pina, Fernando Basílio, Nuno |
dc.subject.por.fl_str_mv |
Anthocyanins Color stability Host‐guest systems P‐Sulfonatocalix[n]arenes Analytical Chemistry Chemistry (miscellaneous) Molecular Medicine Pharmaceutical Science Drug Discovery Physical and Theoretical Chemistry Organic Chemistry |
topic |
Anthocyanins Color stability Host‐guest systems P‐Sulfonatocalix[n]arenes Analytical Chemistry Chemistry (miscellaneous) Molecular Medicine Pharmaceutical Science Drug Discovery Physical and Theoretical Chemistry Organic Chemistry |
description |
Funding Information: Funding: This research was supported by the Associated Laboratory for Sustainable Chemistry, Clean Processes and Technologies LAQV through national funds from UIDB/50006/2020. FCT/MCTES is also acknowledged for supporting the National Portuguese NMR Network (ROTEIRO/0031/2013‐PINFRA/22161/2016, co‐financed by FEDER through COMPETE 2020, POCI, PORL, and FCT through PIDDAC) and for the grant PTDC/QUI‐COL/32351/2017. J.M. is grateful for the doctoral grant awarded by CONACYT (MEX/Ref. 288188). N.B. acknowledges FCT for the contract CEECIND/00466/2017. |
publishDate |
2021 |
dc.date.none.fl_str_mv |
2021-09-21T02:07:57Z 2021-09-04 2021-09-04T00:00:00Z |
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/10362/124894 |
url |
http://hdl.handle.net/10362/124894 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
1420-3049 PURE: 33823005 https://doi.org/10.3390/molecules26175389 |
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 |
instname_str |
Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
instacron_str |
RCAAP |
institution |
RCAAP |
reponame_str |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
collection |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
repository.name.fl_str_mv |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
repository.mail.fl_str_mv |
mluisa.alvim@gmail.com |
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1817545822509727744 |