Photoresponsive Binding Dynamics in High-Affinity Cucurbit[8]uril-Dithienylethene Host-Guest Complexes

Detalhes bibliográficos
Autor(a) principal: Colaço, Miriam
Data de Publicação: 2021
Outros Autores: Máximo, Patrícia, Jorge Parola, A., Basílio, Nuno
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10362/127174
Resumo: This work was supported by the Associate Laboratory for Green Chemistry-LAQV which is financed by national funds from FCT/MCTES (UIDB/50006/2020 and UIDP/50006/2020). FCT/MCTES is also acknowledged for supporting the National Portuguese NMR Network (ROTEIRO/0031/2013-PINFRA/22161/2016, cofinanced by FEDER through COMPETE 2020, POCI, PORL, and FCT through PIDDAC) and for the grants PTDC/QUI-COL/32351/2017, PTDC/QUI-QFI/30951/2017 and CEECIND/00466/2017.
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spelling Photoresponsive Binding Dynamics in High-Affinity Cucurbit[8]uril-Dithienylethene Host-Guest Complexesdiarylethenesinclusion complexeskineticsphotochemistrysupramolecular chemistryCatalysisOrganic ChemistryThis work was supported by the Associate Laboratory for Green Chemistry-LAQV which is financed by national funds from FCT/MCTES (UIDB/50006/2020 and UIDP/50006/2020). FCT/MCTES is also acknowledged for supporting the National Portuguese NMR Network (ROTEIRO/0031/2013-PINFRA/22161/2016, cofinanced by FEDER through COMPETE 2020, POCI, PORL, and FCT through PIDDAC) and for the grants PTDC/QUI-COL/32351/2017, PTDC/QUI-QFI/30951/2017 and CEECIND/00466/2017.The use of external stimuli to control the binding kinetics in supramolecular systems is of critical importance for the development of advanced molecular machines and devices. In this work, a study focused on the kinetics of a water-soluble host-guest system based on cucurbit[8]uril and two dithienylethene (DTE) photoswitches is reported. It is shown that for the DTE guest comprising two anionic sulfonate side arms appended to pyridinium moieties, the formation/dissociation of the pseudorotaxane structures is slowed down by more than 100000-fold with respect to its bipyridinium analogue. The decrease in ingression rate leads to the emergence of a competitive metastable product with the open DTE isomer that has an important influence in the overall binding kinetics. Moreover, the host-guest dissociation kinetics is demonstrated to be approximately 100-fold slower for the closed DTE isomer (t1/2=107 h vs. t1/2=1.2 h for the open isomer) allowing control over the dissociation rate with light.DQ - Departamento de QuímicaLAQV@REQUIMTERUNColaço, MiriamMáximo, PatríciaJorge Parola, A.Basílio, Nuno2022-07-03T00:31:04Z2021-07-022021-07-02T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10362/127174eng0947-6539PURE: 32211938https://doi.org/10.1002/chem.202100974info: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:RCAAP2024-03-11T05:07:14Zoai:run.unl.pt:10362/127174Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-20T03:46:03.469826Repositório 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 Photoresponsive Binding Dynamics in High-Affinity Cucurbit[8]uril-Dithienylethene Host-Guest Complexes
title Photoresponsive Binding Dynamics in High-Affinity Cucurbit[8]uril-Dithienylethene Host-Guest Complexes
spellingShingle Photoresponsive Binding Dynamics in High-Affinity Cucurbit[8]uril-Dithienylethene Host-Guest Complexes
Colaço, Miriam
diarylethenes
inclusion complexes
kinetics
photochemistry
supramolecular chemistry
Catalysis
Organic Chemistry
title_short Photoresponsive Binding Dynamics in High-Affinity Cucurbit[8]uril-Dithienylethene Host-Guest Complexes
title_full Photoresponsive Binding Dynamics in High-Affinity Cucurbit[8]uril-Dithienylethene Host-Guest Complexes
title_fullStr Photoresponsive Binding Dynamics in High-Affinity Cucurbit[8]uril-Dithienylethene Host-Guest Complexes
title_full_unstemmed Photoresponsive Binding Dynamics in High-Affinity Cucurbit[8]uril-Dithienylethene Host-Guest Complexes
title_sort Photoresponsive Binding Dynamics in High-Affinity Cucurbit[8]uril-Dithienylethene Host-Guest Complexes
author Colaço, Miriam
author_facet Colaço, Miriam
Máximo, Patrícia
Jorge Parola, A.
Basílio, Nuno
author_role author
author2 Máximo, Patrícia
Jorge Parola, A.
Basílio, Nuno
author2_role author
author
author
dc.contributor.none.fl_str_mv DQ - Departamento de Química
LAQV@REQUIMTE
RUN
dc.contributor.author.fl_str_mv Colaço, Miriam
Máximo, Patrícia
Jorge Parola, A.
Basílio, Nuno
dc.subject.por.fl_str_mv diarylethenes
inclusion complexes
kinetics
photochemistry
supramolecular chemistry
Catalysis
Organic Chemistry
topic diarylethenes
inclusion complexes
kinetics
photochemistry
supramolecular chemistry
Catalysis
Organic Chemistry
description This work was supported by the Associate Laboratory for Green Chemistry-LAQV which is financed by national funds from FCT/MCTES (UIDB/50006/2020 and UIDP/50006/2020). FCT/MCTES is also acknowledged for supporting the National Portuguese NMR Network (ROTEIRO/0031/2013-PINFRA/22161/2016, cofinanced by FEDER through COMPETE 2020, POCI, PORL, and FCT through PIDDAC) and for the grants PTDC/QUI-COL/32351/2017, PTDC/QUI-QFI/30951/2017 and CEECIND/00466/2017.
publishDate 2021
dc.date.none.fl_str_mv 2021-07-02
2021-07-02T00:00:00Z
2022-07-03T00:31:04Z
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/10362/127174
url http://hdl.handle.net/10362/127174
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 0947-6539
PURE: 32211938
https://doi.org/10.1002/chem.202100974
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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
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