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Design, synthesis and evaluation of redox, second order nonlinear optical properties and theoretical DFT studies of novel bithiophene azo dyes functionalized with thiadiazole acceptor groups

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Resumo:Two series of novel thermally stable second-order nonlinear optical (NLO) heterocyclic azo dyes 4-5 have been designed and synthesized. The two series of compounds were based on different combinations of acceptor groups (thiadiazole or arylthiadiazole electron-deficient heterocycles) linked to bithiophene which acts at the same time as a donor group and as a pi-conjugated bridge. The solvatochromic behavior of azo dyes 4-5 was investigated in several solvents of different polarity, while their thermal stability was evaluated using thermogravimetric analysis. Optimized ground-state molecular geometries and an estimation of the lowest energy single electron vertical excitation energies in DMF solutions were obtained using density functional theory (DFT). Their redox properties were studied by cyclic voltammetry, while hyper-Rayleigh scattering (HRS) was employed to evaluate their second-order nonlinear optical properties. The measured molecular first hyperpolarizabilities and the observed electrochemical behavior showed variations for the different acceptor systems used (thiadiazole or arylthiadiazole) and were also sensitive to the electronic acceptor strength of the substituents (R) linked to thiadiazole or arylthiadiazole heterocycles. Donor-acceptor arylthiadiazole-bithienyl diazenes exhibit the most promising thermal (Td = 237-305 ºC) and solvatochromic (beta = 1117-2503 cm-1) properties and second order nonlinear optical response (136-226 x 10-30 esu).
Autores principais:Castro, M. Cidália R.
Outros Autores:Schellenberg, Peter Michael; Belsley, M.; Fonseca, A. Maurício C.; Fernandes, Sara S. M.; Raposo, M. Manuela M.
Assunto:Heterocyclic azo dyes Bithiophene Thiadiazole Auxiliary donor/acceptor heterocycles Solvatochromic probes Redox properties Hyper-Rayleigh scattering (HRS) Density functional theory (DFT) Thermal stability Nonlinear optical (NLO) materials Synthesis Thermogravimetric analysis (TGA)
Ano:2012
País:Portugal
Tipo de documento:artigo
Tipo de acesso:acesso aberto
Instituição associada:Universidade do Minho
Idioma:inglês
Origem:RepositóriUM - Universidade do Minho
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author Castro, M. Cidália R.
author2 Schellenberg, Peter Michael
Belsley, M.
Fonseca, A. Maurício C.
Fernandes, Sara S. M.
Raposo, M. Manuela M.
author2_role author
author
author
author
author
author_facet Castro, M. Cidália R.
Schellenberg, Peter Michael
Belsley, M.
Fonseca, A. Maurício C.
Fernandes, Sara S. M.
Raposo, M. Manuela M.
author_role author
contributor_name_str_mv RepositóriUM - Universidade do Minho
country_str PT
creators_json_txt [{\"Person.name\":\"Castro, M. Cidália R.\"},{\"Person.name\":\"Schellenberg, Peter Michael\"},{\"Person.name\":\"Belsley, M.\"},{\"Person.name\":\"Fonseca, A. Maurício C.\"},{\"Person.name\":\"Fernandes, Sara S. M.\"},{\"Person.name\":\"Raposo, M. Manuela M.\"}]
datacite.contributors.contributor.contributorName.fl_str_mv RepositóriUM - Universidade do Minho
datacite.creators.creator.creatorName.fl_str_mv Castro, M. Cidália R.
Schellenberg, Peter Michael
Belsley, M.
Fonseca, A. Maurício C.
Fernandes, Sara S. M.
Raposo, M. Manuela M.
datacite.date.Accepted.fl_str_mv 2012-01-01T00:00:00Z
datacite.date.available.fl_str_mv 2012-12-20T16:36:26Z
datacite.date.embargoed.fl_str_mv 2012-12-20T16:36:26Z
datacite.rights.fl_str_mv http://purl.org/coar/access_right/c_abf2
datacite.subjects.subject.fl_str_mv Heterocyclic azo dyes
Bithiophene
Thiadiazole
Auxiliary donor/acceptor heterocycles
Solvatochromic probes
Redox properties
Hyper-Rayleigh scattering (HRS)
Density functional theory (DFT)
Thermal stability
Nonlinear optical (NLO) materials
Synthesis
Thermogravimetric analysis (TGA)
datacite.titles.title.fl_str_mv Design, synthesis and evaluation of redox, second order nonlinear optical properties and theoretical DFT studies of novel bithiophene azo dyes functionalized with thiadiazole acceptor groups
dc.contributor.none.fl_str_mv RepositóriUM - Universidade do Minho
dc.creator.none.fl_str_mv Castro, M. Cidália R.
Schellenberg, Peter Michael
Belsley, M.
Fonseca, A. Maurício C.
Fernandes, Sara S. M.
Raposo, M. Manuela M.
dc.date.Accepted.fl_str_mv 2012-01-01T00:00:00Z
dc.date.available.fl_str_mv 2012-12-20T16:36:26Z
dc.date.embargoed.fl_str_mv 2012-12-20T16:36:26Z
dc.format.none.fl_str_mv application/pdf
application/pdf
dc.identifier.none.fl_str_mv https://hdl.handle.net/1822/21925
dc.language.none.fl_str_mv eng
dc.publisher.none.fl_str_mv Elsevier
dc.rights.none.fl_str_mv http://purl.org/coar/access_right/c_abf2
dc.subject.none.fl_str_mv Heterocyclic azo dyes
Bithiophene
Thiadiazole
Auxiliary donor/acceptor heterocycles
Solvatochromic probes
Redox properties
Hyper-Rayleigh scattering (HRS)
Density functional theory (DFT)
Thermal stability
Nonlinear optical (NLO) materials
Synthesis
Thermogravimetric analysis (TGA)
dc.title.fl_str_mv Design, synthesis and evaluation of redox, second order nonlinear optical properties and theoretical DFT studies of novel bithiophene azo dyes functionalized with thiadiazole acceptor groups
dc.type.none.fl_str_mv http://purl.org/coar/resource_type/c_6501
description Two series of novel thermally stable second-order nonlinear optical (NLO) heterocyclic azo dyes 4-5 have been designed and synthesized. The two series of compounds were based on different combinations of acceptor groups (thiadiazole or arylthiadiazole electron-deficient heterocycles) linked to bithiophene which acts at the same time as a donor group and as a pi-conjugated bridge. The solvatochromic behavior of azo dyes 4-5 was investigated in several solvents of different polarity, while their thermal stability was evaluated using thermogravimetric analysis. Optimized ground-state molecular geometries and an estimation of the lowest energy single electron vertical excitation energies in DMF solutions were obtained using density functional theory (DFT). Their redox properties were studied by cyclic voltammetry, while hyper-Rayleigh scattering (HRS) was employed to evaluate their second-order nonlinear optical properties. The measured molecular first hyperpolarizabilities and the observed electrochemical behavior showed variations for the different acceptor systems used (thiadiazole or arylthiadiazole) and were also sensitive to the electronic acceptor strength of the substituents (R) linked to thiadiazole or arylthiadiazole heterocycles. Donor-acceptor arylthiadiazole-bithienyl diazenes exhibit the most promising thermal (Td = 237-305 ºC) and solvatochromic (beta = 1117-2503 cm-1) properties and second order nonlinear optical response (136-226 x 10-30 esu).
dirty 0
eu_rights_str_mv openAccess
format article
fulltext.url.fl_str_mv https://repositorium.uminho.pt/bitstreams/ab974c16-3507-4135-b80a-b71ebe6e7c8f/download
id rum_87ea033cb774f162815452ea46bd82a3
identifier.url.fl_str_mv https://hdl.handle.net/1822/21925
instacron_str repositorium
institution Universidade do Minho
instname_str Universidade do Minho
language eng
network_acronym_str rum
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oai_identifier_str oai:repositorium.uminho.pt:1822/21925
organization_str_mv urn:organizationAcronym:repositorium
person_str_mv Castro, M. Cidália R.
Schellenberg, Peter Michael
Belsley, M.
Fonseca, A. Maurício C.
Fernandes, Sara S. M.
Raposo, M. Manuela M.
publishDate 2012
publisher.none.fl_str_mv Elsevier
reponame_str RepositóriUM - Universidade do Minho
repository_id_str urn:repositoryAcronym:rum
service_str_mv urn:repositoryAcronym:rum
spelling engElsevierporTwo series of novel thermally stable second-order nonlinear optical (NLO) heterocyclic azo dyes 4-5 have been designed and synthesized. The two series of compounds were based on different combinations of acceptor groups (thiadiazole or arylthiadiazole electron-deficient heterocycles) linked to bithiophene which acts at the same time as a donor group and as a pi-conjugated bridge. The solvatochromic behavior of azo dyes 4-5 was investigated in several solvents of different polarity, while their thermal stability was evaluated using thermogravimetric analysis. Optimized ground-state molecular geometries and an estimation of the lowest energy single electron vertical excitation energies in DMF solutions were obtained using density functional theory (DFT). Their redox properties were studied by cyclic voltammetry, while hyper-Rayleigh scattering (HRS) was employed to evaluate their second-order nonlinear optical properties. The measured molecular first hyperpolarizabilities and the observed electrochemical behavior showed variations for the different acceptor systems used (thiadiazole or arylthiadiazole) and were also sensitive to the electronic acceptor strength of the substituents (R) linked to thiadiazole or arylthiadiazole heterocycles. Donor-acceptor arylthiadiazole-bithienyl diazenes exhibit the most promising thermal (Td = 237-305 ºC) and solvatochromic (beta = 1117-2503 cm-1) properties and second order nonlinear optical response (136-226 x 10-30 esu).application/pdfapplication/pdfporDesign, synthesis and evaluation of redox, second order nonlinear optical properties and theoretical DFT studies of novel bithiophene azo dyes functionalized with thiadiazole acceptor groupsCastro, M. Cidália R.Schellenberg, Peter MichaelBelsley, M.Fonseca, A. Maurício C.Fernandes, Sara S. M.Raposo, M. Manuela M.HostingInstitutionOrganizationalRepositóriUM - Universidade do Minhoe-mailmailto:repositorium@usdb.uminho.ptrepositorium@usdb.uminho.ptISSNIsPartOf0143-7208DOIIsPartOf10.1016/j.dyepig.2012.05.0142012-12-20T16:36:26Z201220122012-01-01T00:00:00ZHandlehttps://hdl.handle.net/1822/21925http://purl.org/coar/access_right/c_abf2open accessHeterocyclic azo dyesBithiopheneThiadiazoleAuxiliary donor/acceptor heterocyclesSolvatochromic probesRedox propertiesHyper-Rayleigh scattering (HRS)Density functional theory (DFT)Thermal stabilityNonlinear optical (NLO) materialsSynthesisThermogravimetric analysis (TGA)747486 bytes759228 bytesliteraturehttp://purl.org/coar/resource_type/c_6501journal articlehttp://purl.org/coar/access_right/c_abf2application/pdffulltexthttps://repositorium.uminho.pt/bitstreams/ab974c16-3507-4135-b80a-b71ebe6e7c8f/downloadhttp://purl.org/coar/access_right/c_abf2application/pdffulltexthttps://repositorium.uminho.pt/bitstreams/77fe85a8-6d56-4853-966b-b26cfe2c50d9/download
spellingShingle Design, synthesis and evaluation of redox, second order nonlinear optical properties and theoretical DFT studies of novel bithiophene azo dyes functionalized with thiadiazole acceptor groups
Castro, M. Cidália R.
Heterocyclic azo dyes
Bithiophene
Thiadiazole
Auxiliary donor/acceptor heterocycles
Solvatochromic probes
Redox properties
Hyper-Rayleigh scattering (HRS)
Density functional theory (DFT)
Thermal stability
Nonlinear optical (NLO) materials
Synthesis
Thermogravimetric analysis (TGA)
status SINGLETON
subject.fl_str_mv Heterocyclic azo dyes
Bithiophene
Thiadiazole
Auxiliary donor/acceptor heterocycles
Solvatochromic probes
Redox properties
Hyper-Rayleigh scattering (HRS)
Density functional theory (DFT)
Thermal stability
Nonlinear optical (NLO) materials
Synthesis
Thermogravimetric analysis (TGA)
title Design, synthesis and evaluation of redox, second order nonlinear optical properties and theoretical DFT studies of novel bithiophene azo dyes functionalized with thiadiazole acceptor groups
title_full Design, synthesis and evaluation of redox, second order nonlinear optical properties and theoretical DFT studies of novel bithiophene azo dyes functionalized with thiadiazole acceptor groups
title_fullStr Design, synthesis and evaluation of redox, second order nonlinear optical properties and theoretical DFT studies of novel bithiophene azo dyes functionalized with thiadiazole acceptor groups
title_full_unstemmed Design, synthesis and evaluation of redox, second order nonlinear optical properties and theoretical DFT studies of novel bithiophene azo dyes functionalized with thiadiazole acceptor groups
title_short Design, synthesis and evaluation of redox, second order nonlinear optical properties and theoretical DFT studies of novel bithiophene azo dyes functionalized with thiadiazole acceptor groups
title_sort Design, synthesis and evaluation of redox, second order nonlinear optical properties and theoretical DFT studies of novel bithiophene azo dyes functionalized with thiadiazole acceptor groups
topic Heterocyclic azo dyes
Bithiophene
Thiadiazole
Auxiliary donor/acceptor heterocycles
Solvatochromic probes
Redox properties
Hyper-Rayleigh scattering (HRS)
Density functional theory (DFT)
Thermal stability
Nonlinear optical (NLO) materials
Synthesis
Thermogravimetric analysis (TGA)
topic_facet Heterocyclic azo dyes
Bithiophene
Thiadiazole
Auxiliary donor/acceptor heterocycles
Solvatochromic probes
Redox properties
Hyper-Rayleigh scattering (HRS)
Density functional theory (DFT)
Thermal stability
Nonlinear optical (NLO) materials
Synthesis
Thermogravimetric analysis (TGA)
url https://hdl.handle.net/1822/21925
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