Solubilization of Poly{1,4-phenylene-[9,9-bis(4-phenoxy-butylsulfonate)] fluorene-2,7-diyl} in Water by Nonionic Amphiphiles

Detalhes bibliográficos
Autor(a) principal: Burrows, Hugh D.
Data de Publicação: 2009
Outros Autores: Tapia, María J., Fonseca, Sofia M., Pradhan, Swapna, Scherf, Ullrich, Silva, Cláudia L., Pais, Alberto A. C. C., Valente, Artur J. M., Schillén, Karin, Alfredsson, Viveka, Carnerup, Anna M., Tomsic, Matija, Jamnik, Andrej
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)
Texto Completo: https://hdl.handle.net/10316/10263
https://doi.org/10.1021/la8042044
Resumo: In the presence of the nonionic alkyloxyethylene surfactant n-dodecylpentaoxyethylene glycol ether (C12E5), the anionic conjugated polyelectrolyte (CPE) poly{1,4-phenylene-[9,9-bis(4-phenoxy-butylsulfonate)]fluorene-2,7-diyl} (PBS-PFP) dissolves in water, leading to a blue shift in fluorescence and dramatic increases in fluorescence quantum yields above the surfactant critical micelle concentration (cmc). No significant changes were seen with a poly(ethylene oxide) of similar size to the surfactant headgroup, confirming that specific surfactant−polyelectrolyte interactions are important. From UV−visible and fluorescence spectroscopy, dynamic light scattering (DLS), small-angle X-ray scattering (SAXS), cryogenic transmission electron microscopy (cryo-TEM), and electrical conductivity, together with our published NMR and small-angle neutron scattering (SANS) results, we provide a coherent model for this behavior in terms of breakup of PBS-PFP clusters through polymer−surfactant association leading to cylindrical aggregates containing isolated polymer chains. This is supported by molecular dynamics simulations, which indicate stable polymer−surfactant structures and also provide indications of the tendency of C12E5 to break up polymer clusters to form these mixed polymer−surfactant aggregates. Radial electron density profiles of the cylindrical cross section obtained from SAXS results reveal the internal structure of such inhomogeneous species. DLS and cryo-TEM results show that at higher surfactant concentrations the micelles start to grow, possibly partially due to formation of long, threadlike species. Other alkyloxyethylene surfactants, together with poly(propylene glycol) and hydrophobically modified poly(ethylene glycol), also solubilize this polymer in water, and it is suggested that this results from a balance between electrostatic (or ion-dipole), hydrophilic, and hydrophobic interactions. There is a small, but significant, dependence of the emission maximum on the local environment.
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spelling Solubilization of Poly{1,4-phenylene-[9,9-bis(4-phenoxy-butylsulfonate)] fluorene-2,7-diyl} in Water by Nonionic AmphiphilesIn the presence of the nonionic alkyloxyethylene surfactant n-dodecylpentaoxyethylene glycol ether (C12E5), the anionic conjugated polyelectrolyte (CPE) poly{1,4-phenylene-[9,9-bis(4-phenoxy-butylsulfonate)]fluorene-2,7-diyl} (PBS-PFP) dissolves in water, leading to a blue shift in fluorescence and dramatic increases in fluorescence quantum yields above the surfactant critical micelle concentration (cmc). No significant changes were seen with a poly(ethylene oxide) of similar size to the surfactant headgroup, confirming that specific surfactant−polyelectrolyte interactions are important. From UV−visible and fluorescence spectroscopy, dynamic light scattering (DLS), small-angle X-ray scattering (SAXS), cryogenic transmission electron microscopy (cryo-TEM), and electrical conductivity, together with our published NMR and small-angle neutron scattering (SANS) results, we provide a coherent model for this behavior in terms of breakup of PBS-PFP clusters through polymer−surfactant association leading to cylindrical aggregates containing isolated polymer chains. This is supported by molecular dynamics simulations, which indicate stable polymer−surfactant structures and also provide indications of the tendency of C12E5 to break up polymer clusters to form these mixed polymer−surfactant aggregates. Radial electron density profiles of the cylindrical cross section obtained from SAXS results reveal the internal structure of such inhomogeneous species. DLS and cryo-TEM results show that at higher surfactant concentrations the micelles start to grow, possibly partially due to formation of long, threadlike species. Other alkyloxyethylene surfactants, together with poly(propylene glycol) and hydrophobically modified poly(ethylene glycol), also solubilize this polymer in water, and it is suggested that this results from a balance between electrostatic (or ion-dipole), hydrophilic, and hydrophobic interactions. There is a small, but significant, dependence of the emission maximum on the local environment.American Chemical Society2009-05-19info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttps://hdl.handle.net/10316/10263https://hdl.handle.net/10316/10263https://doi.org/10.1021/la8042044engLangmuir. 25:10 (2009) 5545-55560743-7463Burrows, Hugh D.Tapia, María J.Fonseca, Sofia M.Pradhan, SwapnaScherf, UllrichSilva, Cláudia L.Pais, Alberto A. C. C.Valente, Artur J. M.Schillén, KarinAlfredsson, VivekaCarnerup, Anna M.Tomsic, MatijaJamnik, Andrejinfo:eu-repo/semantics/openAccessreponame:Repositórios Científicos de Acesso Aberto de Portugal (RCAAP)instname:FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiainstacron:RCAAP2021-10-26T08:04:00Zoai:estudogeral.uc.pt:10316/10263Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireinfo@rcaap.ptopendoar:https://opendoar.ac.uk/repository/71602025-05-29T05:23:28.653599Repositórios Científicos de Acesso Aberto de Portugal (RCAAP) - FCCN, serviços digitais da FCT – Fundação para a Ciência e a Tecnologiafalse
dc.title.none.fl_str_mv Solubilization of Poly{1,4-phenylene-[9,9-bis(4-phenoxy-butylsulfonate)] fluorene-2,7-diyl} in Water by Nonionic Amphiphiles
title Solubilization of Poly{1,4-phenylene-[9,9-bis(4-phenoxy-butylsulfonate)] fluorene-2,7-diyl} in Water by Nonionic Amphiphiles
spellingShingle Solubilization of Poly{1,4-phenylene-[9,9-bis(4-phenoxy-butylsulfonate)] fluorene-2,7-diyl} in Water by Nonionic Amphiphiles
Burrows, Hugh D.
title_short Solubilization of Poly{1,4-phenylene-[9,9-bis(4-phenoxy-butylsulfonate)] fluorene-2,7-diyl} in Water by Nonionic Amphiphiles
title_full Solubilization of Poly{1,4-phenylene-[9,9-bis(4-phenoxy-butylsulfonate)] fluorene-2,7-diyl} in Water by Nonionic Amphiphiles
title_fullStr Solubilization of Poly{1,4-phenylene-[9,9-bis(4-phenoxy-butylsulfonate)] fluorene-2,7-diyl} in Water by Nonionic Amphiphiles
title_full_unstemmed Solubilization of Poly{1,4-phenylene-[9,9-bis(4-phenoxy-butylsulfonate)] fluorene-2,7-diyl} in Water by Nonionic Amphiphiles
title_sort Solubilization of Poly{1,4-phenylene-[9,9-bis(4-phenoxy-butylsulfonate)] fluorene-2,7-diyl} in Water by Nonionic Amphiphiles
author Burrows, Hugh D.
author_facet Burrows, Hugh D.
Tapia, María J.
Fonseca, Sofia M.
Pradhan, Swapna
Scherf, Ullrich
Silva, Cláudia L.
Pais, Alberto A. C. C.
Valente, Artur J. M.
Schillén, Karin
Alfredsson, Viveka
Carnerup, Anna M.
Tomsic, Matija
Jamnik, Andrej
author_role author
author2 Tapia, María J.
Fonseca, Sofia M.
Pradhan, Swapna
Scherf, Ullrich
Silva, Cláudia L.
Pais, Alberto A. C. C.
Valente, Artur J. M.
Schillén, Karin
Alfredsson, Viveka
Carnerup, Anna M.
Tomsic, Matija
Jamnik, Andrej
author2_role author
author
author
author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Burrows, Hugh D.
Tapia, María J.
Fonseca, Sofia M.
Pradhan, Swapna
Scherf, Ullrich
Silva, Cláudia L.
Pais, Alberto A. C. C.
Valente, Artur J. M.
Schillén, Karin
Alfredsson, Viveka
Carnerup, Anna M.
Tomsic, Matija
Jamnik, Andrej
description In the presence of the nonionic alkyloxyethylene surfactant n-dodecylpentaoxyethylene glycol ether (C12E5), the anionic conjugated polyelectrolyte (CPE) poly{1,4-phenylene-[9,9-bis(4-phenoxy-butylsulfonate)]fluorene-2,7-diyl} (PBS-PFP) dissolves in water, leading to a blue shift in fluorescence and dramatic increases in fluorescence quantum yields above the surfactant critical micelle concentration (cmc). No significant changes were seen with a poly(ethylene oxide) of similar size to the surfactant headgroup, confirming that specific surfactant−polyelectrolyte interactions are important. From UV−visible and fluorescence spectroscopy, dynamic light scattering (DLS), small-angle X-ray scattering (SAXS), cryogenic transmission electron microscopy (cryo-TEM), and electrical conductivity, together with our published NMR and small-angle neutron scattering (SANS) results, we provide a coherent model for this behavior in terms of breakup of PBS-PFP clusters through polymer−surfactant association leading to cylindrical aggregates containing isolated polymer chains. This is supported by molecular dynamics simulations, which indicate stable polymer−surfactant structures and also provide indications of the tendency of C12E5 to break up polymer clusters to form these mixed polymer−surfactant aggregates. Radial electron density profiles of the cylindrical cross section obtained from SAXS results reveal the internal structure of such inhomogeneous species. DLS and cryo-TEM results show that at higher surfactant concentrations the micelles start to grow, possibly partially due to formation of long, threadlike species. Other alkyloxyethylene surfactants, together with poly(propylene glycol) and hydrophobically modified poly(ethylene glycol), also solubilize this polymer in water, and it is suggested that this results from a balance between electrostatic (or ion-dipole), hydrophilic, and hydrophobic interactions. There is a small, but significant, dependence of the emission maximum on the local environment.
publishDate 2009
dc.date.none.fl_str_mv 2009-05-19
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 https://hdl.handle.net/10316/10263
https://hdl.handle.net/10316/10263
https://doi.org/10.1021/la8042044
url https://hdl.handle.net/10316/10263
https://doi.org/10.1021/la8042044
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Langmuir. 25:10 (2009) 5545-5556
0743-7463
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dc.publisher.none.fl_str_mv American Chemical Society
publisher.none.fl_str_mv American Chemical Society
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