Electrosynthesis and optical characterization of poly(p-phenylene), polypyrrole and poly(p-phenylene)-polypyrrole films
Autor(a) principal: | |
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Data de Publicação: | 2014 |
Outros Autores: | , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Materials research (São Carlos. Online) |
Texto Completo: | http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-14392014000200007 |
Resumo: | Poly(p-phenylene) (PPP), polypyrrole (PPY), and poly(p-phenylene-pyrrole) (PPP-PPY) films were electrochemically synthesized in acetronitrile by cyclic voltammetry. For comparison purposes, the films were characterized by cyclic voltammetry in a monomer-free solution, and their optical responses were also obtained in the UV-VIS range of energy after varying the applied potentials. The absorbance spectra of the PPP-PPY film exhibited bands typically seen in the spectra of the homopolymers, PPP and PPY films, but better defined, intense, and related to reversible color transitions. Although it was not possible to confirm by using infrared and Raman spectroscopy that a copolymer was in fact obtained, the presence of both monomers, pyrrole and biphenyl, in the polymerization medium turned easier the process of film formation, yielding darker, more uniform, and rougher films as it was verified by photographic images and AFM (atomic force microscopy) images. |
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Electrosynthesis and optical characterization of poly(p-phenylene), polypyrrole and poly(p-phenylene)-polypyrrole filmspolyphenylenepolypyrroleconducting polymersPoly(p-phenylene) (PPP), polypyrrole (PPY), and poly(p-phenylene-pyrrole) (PPP-PPY) films were electrochemically synthesized in acetronitrile by cyclic voltammetry. For comparison purposes, the films were characterized by cyclic voltammetry in a monomer-free solution, and their optical responses were also obtained in the UV-VIS range of energy after varying the applied potentials. The absorbance spectra of the PPP-PPY film exhibited bands typically seen in the spectra of the homopolymers, PPP and PPY films, but better defined, intense, and related to reversible color transitions. Although it was not possible to confirm by using infrared and Raman spectroscopy that a copolymer was in fact obtained, the presence of both monomers, pyrrole and biphenyl, in the polymerization medium turned easier the process of film formation, yielding darker, more uniform, and rougher films as it was verified by photographic images and AFM (atomic force microscopy) images.ABM, ABC, ABPol2014-04-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-14392014000200007Materials Research v.17 n.2 2014reponame:Materials research (São Carlos. Online)instname:Universidade Federal de São Carlos (UFSCAR)instacron:ABM ABC ABPOL10.1590/S1516-14392014005000008info:eu-repo/semantics/openAccessSoares,Juliana CoatriniFoschini,MaurícioEiras,CarlaSanches,Edgar AparecidoGonçalves,Déboraeng2014-05-06T00:00:00Zoai:scielo:S1516-14392014000200007Revistahttp://www.scielo.br/mrPUBhttps://old.scielo.br/oai/scielo-oai.phpdedz@power.ufscar.br1980-53731516-1439opendoar:2014-05-06T00:00Materials research (São Carlos. Online) - Universidade Federal de São Carlos (UFSCAR)false |
dc.title.none.fl_str_mv |
Electrosynthesis and optical characterization of poly(p-phenylene), polypyrrole and poly(p-phenylene)-polypyrrole films |
title |
Electrosynthesis and optical characterization of poly(p-phenylene), polypyrrole and poly(p-phenylene)-polypyrrole films |
spellingShingle |
Electrosynthesis and optical characterization of poly(p-phenylene), polypyrrole and poly(p-phenylene)-polypyrrole films Soares,Juliana Coatrini polyphenylene polypyrrole conducting polymers |
title_short |
Electrosynthesis and optical characterization of poly(p-phenylene), polypyrrole and poly(p-phenylene)-polypyrrole films |
title_full |
Electrosynthesis and optical characterization of poly(p-phenylene), polypyrrole and poly(p-phenylene)-polypyrrole films |
title_fullStr |
Electrosynthesis and optical characterization of poly(p-phenylene), polypyrrole and poly(p-phenylene)-polypyrrole films |
title_full_unstemmed |
Electrosynthesis and optical characterization of poly(p-phenylene), polypyrrole and poly(p-phenylene)-polypyrrole films |
title_sort |
Electrosynthesis and optical characterization of poly(p-phenylene), polypyrrole and poly(p-phenylene)-polypyrrole films |
author |
Soares,Juliana Coatrini |
author_facet |
Soares,Juliana Coatrini Foschini,Maurício Eiras,Carla Sanches,Edgar Aparecido Gonçalves,Débora |
author_role |
author |
author2 |
Foschini,Maurício Eiras,Carla Sanches,Edgar Aparecido Gonçalves,Débora |
author2_role |
author author author author |
dc.contributor.author.fl_str_mv |
Soares,Juliana Coatrini Foschini,Maurício Eiras,Carla Sanches,Edgar Aparecido Gonçalves,Débora |
dc.subject.por.fl_str_mv |
polyphenylene polypyrrole conducting polymers |
topic |
polyphenylene polypyrrole conducting polymers |
description |
Poly(p-phenylene) (PPP), polypyrrole (PPY), and poly(p-phenylene-pyrrole) (PPP-PPY) films were electrochemically synthesized in acetronitrile by cyclic voltammetry. For comparison purposes, the films were characterized by cyclic voltammetry in a monomer-free solution, and their optical responses were also obtained in the UV-VIS range of energy after varying the applied potentials. The absorbance spectra of the PPP-PPY film exhibited bands typically seen in the spectra of the homopolymers, PPP and PPY films, but better defined, intense, and related to reversible color transitions. Although it was not possible to confirm by using infrared and Raman spectroscopy that a copolymer was in fact obtained, the presence of both monomers, pyrrole and biphenyl, in the polymerization medium turned easier the process of film formation, yielding darker, more uniform, and rougher films as it was verified by photographic images and AFM (atomic force microscopy) images. |
publishDate |
2014 |
dc.date.none.fl_str_mv |
2014-04-01 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-14392014000200007 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-14392014000200007 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.1590/S1516-14392014005000008 |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess |
eu_rights_str_mv |
openAccess |
dc.format.none.fl_str_mv |
text/html |
dc.publisher.none.fl_str_mv |
ABM, ABC, ABPol |
publisher.none.fl_str_mv |
ABM, ABC, ABPol |
dc.source.none.fl_str_mv |
Materials Research v.17 n.2 2014 reponame:Materials research (São Carlos. Online) instname:Universidade Federal de São Carlos (UFSCAR) instacron:ABM ABC ABPOL |
instname_str |
Universidade Federal de São Carlos (UFSCAR) |
instacron_str |
ABM ABC ABPOL |
institution |
ABM ABC ABPOL |
reponame_str |
Materials research (São Carlos. Online) |
collection |
Materials research (São Carlos. Online) |
repository.name.fl_str_mv |
Materials research (São Carlos. Online) - Universidade Federal de São Carlos (UFSCAR) |
repository.mail.fl_str_mv |
dedz@power.ufscar.br |
_version_ |
1754212664641323008 |