Effect of the graft ratio on the properties of polythiophene-g-poly(ethylene glycol)

Graft copolymers formed by anchoring poly(ethylene glycol) (PEG) chains to conjugated polythiophene have been prepared by copolymerizing two compounds: unsubstituted -terthiophene (Th-3) and a thiophene-derived macromonomer having an -terthiophene conjugated sequence and one Th-3 bearing a PEG chain...

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Autores: Maione, Silvana, Fabregat Jové, Georgina|||0000-0001-8967-9950, Valle Mendoza, Luis Javier del|||0000-0001-9916-1741, Bendrea, Anca Dana, Cianga, Luminita, Cianga, Ioan, Estrany Coda, Francesc|||0000-0002-2696-1489, Alemán Llansó, Carlos|||0000-0003-4462-6075
Tipo de recurso: artículo
Fecha de publicación:2015
País:España
Institución:Universitat Politècnica de Catalunya (UPC)
Repositorio:UPCommons. Portal del coneixement obert de la UPC
Idioma:inglés
OAI Identifier:oai:upcommons.upc.edu:2117/26387
Acceso en línea:https://hdl.handle.net/2117/26387
https://dx.doi.org/10.1002/polb.23617
Access Level:acceso abierto
Palabra clave:Polyethers
Conducting polymers
bioactive platforms
biocompatibility
bottle-brush polymers
cell proliferation
conducting polymers
conjugated polymers
grafted copolymers
molecular brushes
polyethers
POLY(ETHYLENE GLYCOL)
POLYMER BRUSHES
IV COLLAGEN
POLYTHIOPHENE
COPOLYMERS
CHAINS
FABRICATION
SCAFFOLDS
SURFACES
ATRP
Polímers conductors
Polimerització
Àrees temàtiques de la UPC::Enginyeria química
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oai_identifier_str oai:upcommons.upc.edu:2117/26387
network_acronym_str ES
network_name_str España
repository_id_str
spelling Effect of the graft ratio on the properties of polythiophene-g-poly(ethylene glycol)Maione, SilvanaFabregat Jové, Georgina|||0000-0001-8967-9950Valle Mendoza, Luis Javier del|||0000-0001-9916-1741Bendrea, Anca DanaCianga, LuminitaCianga, IoanEstrany Coda, Francesc|||0000-0002-2696-1489Alemán Llansó, Carlos|||0000-0003-4462-6075PolyethersConducting polymersbioactive platformsbiocompatibilitybottle-brush polymerscell proliferationconducting polymersconjugated polymersgrafted copolymersmolecular brushespolyethersPOLY(ETHYLENE GLYCOL)POLYMER BRUSHESIV COLLAGENPOLYTHIOPHENECOPOLYMERSCHAINSFABRICATIONSCAFFOLDSSURFACESATRPPolímers conductorsPolimeritzacióÀrees temàtiques de la UPC::Enginyeria químicaGraft copolymers formed by anchoring poly(ethylene glycol) (PEG) chains to conjugated polythiophene have been prepared by copolymerizing two compounds: unsubstituted -terthiophene (Th-3) and a thiophene-derived macromonomer having an -terthiophene conjugated sequence and one Th-3 bearing a PEG chain with molecular weight of 2000 as substitute at the 3-position of the central heterocycle (Th-3-PEG(2000)). The grafting ratio of the resulting copolymers (PTh3*-g-PEG), which were obtained using 75:25 and 50:50 Th-3-PEG(2000):Th-3 weight ratios, is significantly smaller than that of copolymers derived from polymerization of macromonomers consisting of a -pentathiophene sequence in which the central ring bears a PEG chain of M-w = 2000 (PTh5-g-PEG). The electroactivity and electrochemical stability of PTh3*-g-PEG is not only higher than that of PTh5-g-PEG but also higher than that of PTh3, the latter presenting a very compact structure that makes difficult the access and escape of dopant ions into the polymeric matrix during the redox processes. Furthermore, the optical -(*) lowest transition energy of PTh3*-g-PEG is lower than that of both PTh5-g-PEG and PTh3. These properties, combined with suitable wettability and roughness, result in an excellent behavior as bioactive platform of PTh3*-g-PEG copolymers, which are more biocompatible, in terms of cellular adhesion and proliferation, and electro-compatible than PTh5-g-PEG. (c) 2014 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2015, 53, 239-252Peer Reviewed20152015-02-1520152015-02-17journal articlehttp://purl.org/coar/resource_type/c_6501AMhttp://purl.org/coar/version/c_ab4af688f83e57aainfo:eu-repo/semantics/articleapplication/pdfhttps://hdl.handle.net/2117/26387https://dx.doi.org/10.1002/polb.23617reponame:UPCommons. Portal del coneixement obert de la UPCinstname:Universitat Politècnica de Catalunya (UPC)Inglésengopen accesshttp://purl.org/coar/access_right/c_abf2Attribution-NonCommercial-NoDerivs 3.0 Spainhttp://creativecommons.org/licenses/by-nc-nd/3.0/es/info:eu-repo/semantics/openAccessoai:upcommons.upc.edu:2117/263872026-05-27T15:37:01Z
dc.title.none.fl_str_mv Effect of the graft ratio on the properties of polythiophene-g-poly(ethylene glycol)
title Effect of the graft ratio on the properties of polythiophene-g-poly(ethylene glycol)
spellingShingle Effect of the graft ratio on the properties of polythiophene-g-poly(ethylene glycol)
Maione, Silvana
Polyethers
Conducting polymers
bioactive platforms
biocompatibility
bottle-brush polymers
cell proliferation
conducting polymers
conjugated polymers
grafted copolymers
molecular brushes
polyethers
POLY(ETHYLENE GLYCOL)
POLYMER BRUSHES
IV COLLAGEN
POLYTHIOPHENE
COPOLYMERS
CHAINS
FABRICATION
SCAFFOLDS
SURFACES
ATRP
Polímers conductors
Polimerització
Àrees temàtiques de la UPC::Enginyeria química
title_short Effect of the graft ratio on the properties of polythiophene-g-poly(ethylene glycol)
title_full Effect of the graft ratio on the properties of polythiophene-g-poly(ethylene glycol)
title_fullStr Effect of the graft ratio on the properties of polythiophene-g-poly(ethylene glycol)
title_full_unstemmed Effect of the graft ratio on the properties of polythiophene-g-poly(ethylene glycol)
title_sort Effect of the graft ratio on the properties of polythiophene-g-poly(ethylene glycol)
dc.creator.none.fl_str_mv Maione, Silvana
Fabregat Jové, Georgina|||0000-0001-8967-9950
Valle Mendoza, Luis Javier del|||0000-0001-9916-1741
Bendrea, Anca Dana
Cianga, Luminita
Cianga, Ioan
Estrany Coda, Francesc|||0000-0002-2696-1489
Alemán Llansó, Carlos|||0000-0003-4462-6075
author Maione, Silvana
author_facet Maione, Silvana
Fabregat Jové, Georgina|||0000-0001-8967-9950
Valle Mendoza, Luis Javier del|||0000-0001-9916-1741
Bendrea, Anca Dana
Cianga, Luminita
Cianga, Ioan
Estrany Coda, Francesc|||0000-0002-2696-1489
Alemán Llansó, Carlos|||0000-0003-4462-6075
author_role author
author2 Fabregat Jové, Georgina|||0000-0001-8967-9950
Valle Mendoza, Luis Javier del|||0000-0001-9916-1741
Bendrea, Anca Dana
Cianga, Luminita
Cianga, Ioan
Estrany Coda, Francesc|||0000-0002-2696-1489
Alemán Llansó, Carlos|||0000-0003-4462-6075
author2_role author
author
author
author
author
author
author
dc.subject.none.fl_str_mv Polyethers
Conducting polymers
bioactive platforms
biocompatibility
bottle-brush polymers
cell proliferation
conducting polymers
conjugated polymers
grafted copolymers
molecular brushes
polyethers
POLY(ETHYLENE GLYCOL)
POLYMER BRUSHES
IV COLLAGEN
POLYTHIOPHENE
COPOLYMERS
CHAINS
FABRICATION
SCAFFOLDS
SURFACES
ATRP
Polímers conductors
Polimerització
Àrees temàtiques de la UPC::Enginyeria química
topic Polyethers
Conducting polymers
bioactive platforms
biocompatibility
bottle-brush polymers
cell proliferation
conducting polymers
conjugated polymers
grafted copolymers
molecular brushes
polyethers
POLY(ETHYLENE GLYCOL)
POLYMER BRUSHES
IV COLLAGEN
POLYTHIOPHENE
COPOLYMERS
CHAINS
FABRICATION
SCAFFOLDS
SURFACES
ATRP
Polímers conductors
Polimerització
Àrees temàtiques de la UPC::Enginyeria química
description Graft copolymers formed by anchoring poly(ethylene glycol) (PEG) chains to conjugated polythiophene have been prepared by copolymerizing two compounds: unsubstituted -terthiophene (Th-3) and a thiophene-derived macromonomer having an -terthiophene conjugated sequence and one Th-3 bearing a PEG chain with molecular weight of 2000 as substitute at the 3-position of the central heterocycle (Th-3-PEG(2000)). The grafting ratio of the resulting copolymers (PTh3*-g-PEG), which were obtained using 75:25 and 50:50 Th-3-PEG(2000):Th-3 weight ratios, is significantly smaller than that of copolymers derived from polymerization of macromonomers consisting of a -pentathiophene sequence in which the central ring bears a PEG chain of M-w = 2000 (PTh5-g-PEG). The electroactivity and electrochemical stability of PTh3*-g-PEG is not only higher than that of PTh5-g-PEG but also higher than that of PTh3, the latter presenting a very compact structure that makes difficult the access and escape of dopant ions into the polymeric matrix during the redox processes. Furthermore, the optical -(*) lowest transition energy of PTh3*-g-PEG is lower than that of both PTh5-g-PEG and PTh3. These properties, combined with suitable wettability and roughness, result in an excellent behavior as bioactive platform of PTh3*-g-PEG copolymers, which are more biocompatible, in terms of cellular adhesion and proliferation, and electro-compatible than PTh5-g-PEG. (c) 2014 Wiley Periodicals, Inc. J. Polym. Sci., Part B: Polym. Phys. 2015, 53, 239-252
publishDate 2015
dc.date.none.fl_str_mv 2015
2015-02-15
2015
2015-02-17
dc.type.none.fl_str_mv journal article
http://purl.org/coar/resource_type/c_6501
AM
http://purl.org/coar/version/c_ab4af688f83e57aa
dc.type.openaire.fl_str_mv info:eu-repo/semantics/article
format article
dc.identifier.none.fl_str_mv https://hdl.handle.net/2117/26387
https://dx.doi.org/10.1002/polb.23617
url https://hdl.handle.net/2117/26387
https://dx.doi.org/10.1002/polb.23617
dc.language.none.fl_str_mv Inglés
eng
language_invalid_str_mv Inglés
language eng
dc.rights.none.fl_str_mv open access
http://purl.org/coar/access_right/c_abf2
Attribution-NonCommercial-NoDerivs 3.0 Spain
http://creativecommons.org/licenses/by-nc-nd/3.0/es/
dc.rights.openaire.fl_str_mv info:eu-repo/semantics/openAccess
rights_invalid_str_mv open access
http://purl.org/coar/access_right/c_abf2
Attribution-NonCommercial-NoDerivs 3.0 Spain
http://creativecommons.org/licenses/by-nc-nd/3.0/es/
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.source.none.fl_str_mv reponame:UPCommons. Portal del coneixement obert de la UPC
instname:Universitat Politècnica de Catalunya (UPC)
instname_str Universitat Politècnica de Catalunya (UPC)
reponame_str UPCommons. Portal del coneixement obert de la UPC
collection UPCommons. Portal del coneixement obert de la UPC
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