Electrochemical synthesis of the copolymer poly(2-methoxy-5-bromo-p-phenylenevinylene)/(2,5-dicyano-p-phenylenevinylene) (MB-PPV/DCN-PPV): tuning properties

Detalhes bibliográficos
Autor(a) principal: Klider,Karine C. C. W. S.
Data de Publicação: 2014
Outros Autores: Santos,Fábio S., Péres,Laura O., Wohnrath,Karen, Garcia,Jarem R.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Journal of the Brazilian Chemical Society (Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532014000300021
Resumo: The present work describes an electrochemical method to produce the copolymer poly(2-methoxy-5-bromo-p-phenylenevinylene)/(2,5-dicyano-p-phenylenevinylene) (cop-MB-PPV/DCN-PPV). This copolymer was proposed due to its D-A characteristic produced by the presence of the electron-donating methoxy moiety and the electron-withdrawing dicyano moiety. The copolymer was electrochemically synthetized by cathodic reduction of the convenient starting materials dissolved in a DMF/LiClO4 using a mercury pool acting as working electrode. The copolymer was characterized by infrared (IR), UV-Vis and fluorescence (FL) spectroscopy and cyclic voltammetry (CV). All the results were compared to the MB-PPV homopolymer. The analysis of electrochemical measurements and IR indicated that the cop-MB-PPV/DCN-PPV was obtained through the formation of blocks containing DCN-PPV units linked by blocks containing MB-PPV units. The electronic structure, performed by CV, UV-Vis and FL showed that the conduction band is more stabilized in the copolymer than in homopolymer. Furthermore, the FL spectra indicated that the light emission of the cop-MB-PPV/DCN-PPV in chloroform solution occurs by means of excimer formation.
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spelling Electrochemical synthesis of the copolymer poly(2-methoxy-5-bromo-p-phenylenevinylene)/(2,5-dicyano-p-phenylenevinylene) (MB-PPV/DCN-PPV): tuning propertiesPPV-like copolymerdonor-acceptor structurepolymeric solar cellelectrochemical polymerizationThe present work describes an electrochemical method to produce the copolymer poly(2-methoxy-5-bromo-p-phenylenevinylene)/(2,5-dicyano-p-phenylenevinylene) (cop-MB-PPV/DCN-PPV). This copolymer was proposed due to its D-A characteristic produced by the presence of the electron-donating methoxy moiety and the electron-withdrawing dicyano moiety. The copolymer was electrochemically synthetized by cathodic reduction of the convenient starting materials dissolved in a DMF/LiClO4 using a mercury pool acting as working electrode. The copolymer was characterized by infrared (IR), UV-Vis and fluorescence (FL) spectroscopy and cyclic voltammetry (CV). All the results were compared to the MB-PPV homopolymer. The analysis of electrochemical measurements and IR indicated that the cop-MB-PPV/DCN-PPV was obtained through the formation of blocks containing DCN-PPV units linked by blocks containing MB-PPV units. The electronic structure, performed by CV, UV-Vis and FL showed that the conduction band is more stabilized in the copolymer than in homopolymer. Furthermore, the FL spectra indicated that the light emission of the cop-MB-PPV/DCN-PPV in chloroform solution occurs by means of excimer formation.Sociedade Brasileira de Química2014-03-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532014000300021Journal of the Brazilian Chemical Society v.25 n.3 2014reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.5935/0103-5053.20140033info:eu-repo/semantics/openAccessKlider,Karine C. C. W. S.Santos,Fábio S.Péres,Laura O.Wohnrath,KarenGarcia,Jarem R.eng2014-03-19T00:00:00Zoai:scielo:S0103-50532014000300021Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2014-03-19T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false
dc.title.none.fl_str_mv Electrochemical synthesis of the copolymer poly(2-methoxy-5-bromo-p-phenylenevinylene)/(2,5-dicyano-p-phenylenevinylene) (MB-PPV/DCN-PPV): tuning properties
title Electrochemical synthesis of the copolymer poly(2-methoxy-5-bromo-p-phenylenevinylene)/(2,5-dicyano-p-phenylenevinylene) (MB-PPV/DCN-PPV): tuning properties
spellingShingle Electrochemical synthesis of the copolymer poly(2-methoxy-5-bromo-p-phenylenevinylene)/(2,5-dicyano-p-phenylenevinylene) (MB-PPV/DCN-PPV): tuning properties
Klider,Karine C. C. W. S.
PPV-like copolymer
donor-acceptor structure
polymeric solar cell
electrochemical polymerization
title_short Electrochemical synthesis of the copolymer poly(2-methoxy-5-bromo-p-phenylenevinylene)/(2,5-dicyano-p-phenylenevinylene) (MB-PPV/DCN-PPV): tuning properties
title_full Electrochemical synthesis of the copolymer poly(2-methoxy-5-bromo-p-phenylenevinylene)/(2,5-dicyano-p-phenylenevinylene) (MB-PPV/DCN-PPV): tuning properties
title_fullStr Electrochemical synthesis of the copolymer poly(2-methoxy-5-bromo-p-phenylenevinylene)/(2,5-dicyano-p-phenylenevinylene) (MB-PPV/DCN-PPV): tuning properties
title_full_unstemmed Electrochemical synthesis of the copolymer poly(2-methoxy-5-bromo-p-phenylenevinylene)/(2,5-dicyano-p-phenylenevinylene) (MB-PPV/DCN-PPV): tuning properties
title_sort Electrochemical synthesis of the copolymer poly(2-methoxy-5-bromo-p-phenylenevinylene)/(2,5-dicyano-p-phenylenevinylene) (MB-PPV/DCN-PPV): tuning properties
author Klider,Karine C. C. W. S.
author_facet Klider,Karine C. C. W. S.
Santos,Fábio S.
Péres,Laura O.
Wohnrath,Karen
Garcia,Jarem R.
author_role author
author2 Santos,Fábio S.
Péres,Laura O.
Wohnrath,Karen
Garcia,Jarem R.
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Klider,Karine C. C. W. S.
Santos,Fábio S.
Péres,Laura O.
Wohnrath,Karen
Garcia,Jarem R.
dc.subject.por.fl_str_mv PPV-like copolymer
donor-acceptor structure
polymeric solar cell
electrochemical polymerization
topic PPV-like copolymer
donor-acceptor structure
polymeric solar cell
electrochemical polymerization
description The present work describes an electrochemical method to produce the copolymer poly(2-methoxy-5-bromo-p-phenylenevinylene)/(2,5-dicyano-p-phenylenevinylene) (cop-MB-PPV/DCN-PPV). This copolymer was proposed due to its D-A characteristic produced by the presence of the electron-donating methoxy moiety and the electron-withdrawing dicyano moiety. The copolymer was electrochemically synthetized by cathodic reduction of the convenient starting materials dissolved in a DMF/LiClO4 using a mercury pool acting as working electrode. The copolymer was characterized by infrared (IR), UV-Vis and fluorescence (FL) spectroscopy and cyclic voltammetry (CV). All the results were compared to the MB-PPV homopolymer. The analysis of electrochemical measurements and IR indicated that the cop-MB-PPV/DCN-PPV was obtained through the formation of blocks containing DCN-PPV units linked by blocks containing MB-PPV units. The electronic structure, performed by CV, UV-Vis and FL showed that the conduction band is more stabilized in the copolymer than in homopolymer. Furthermore, the FL spectra indicated that the light emission of the cop-MB-PPV/DCN-PPV in chloroform solution occurs by means of excimer formation.
publishDate 2014
dc.date.none.fl_str_mv 2014-03-01
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=S0103-50532014000300021
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532014000300021
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.5935/0103-5053.20140033
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 Sociedade Brasileira de Química
publisher.none.fl_str_mv Sociedade Brasileira de Química
dc.source.none.fl_str_mv Journal of the Brazilian Chemical Society v.25 n.3 2014
reponame:Journal of the Brazilian Chemical Society (Online)
instname:Sociedade Brasileira de Química (SBQ)
instacron:SBQ
instname_str Sociedade Brasileira de Química (SBQ)
instacron_str SBQ
institution SBQ
reponame_str Journal of the Brazilian Chemical Society (Online)
collection Journal of the Brazilian Chemical Society (Online)
repository.name.fl_str_mv Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)
repository.mail.fl_str_mv ||office@jbcs.sbq.org.br
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