Enhanced optical nonlinearities in push-pull organic systems with polyenic-mesoionic ring mixed bridges

Detalhes bibliográficos
Autor(a) principal: Machado,Ana Elizabete de A.
Data de Publicação: 2008
Outros Autores: Gama,Alfredo Arnóbio de S. da
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=S0103-50532008000700022
Resumo: Large values of the static first(β) and second(γ) hyperpolarizabilities were obtained for donor-acceptor molecules having mixed bridges with mesoionic rings inserted between polyenic moieties. The magnitudes of β and γ were calculated at the AM1/TDHF semiempirical level. Donor(D)/acceptor(A) pairs of different strengths were used to test the potential of the new model bridges. The largest value was obtained by linking thedicyanomethylene(A) and phenylamine(D) at the opposite ends of mixed bridges.Unlike D/A molecules traditionally reported in the literature, the phenylamine was linked to the bridge by the nitrogen heteroatom. The effect of the nature and size of the bridge in the magnitude of the hyperpolarizabilities was investigated. The push-pull systems with the extended bridges, containing two mesoionic rings and polyenic moieties, present the larger magnitudes values of β and γ.The results show that the combination of the selectedbridges and D/Apairs can be responsible for very large hyperpolarizabilities.
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spelling Enhanced optical nonlinearities in push-pull organic systems with polyenic-mesoionic ring mixed bridgesβ and γ hyperpolarizabilitiespolyenic/mesoionic bridgesdonor-bridge-acceptor organic systemsAM1/TDHF methodologyLarge values of the static first(β) and second(γ) hyperpolarizabilities were obtained for donor-acceptor molecules having mixed bridges with mesoionic rings inserted between polyenic moieties. The magnitudes of β and γ were calculated at the AM1/TDHF semiempirical level. Donor(D)/acceptor(A) pairs of different strengths were used to test the potential of the new model bridges. The largest value was obtained by linking thedicyanomethylene(A) and phenylamine(D) at the opposite ends of mixed bridges.Unlike D/A molecules traditionally reported in the literature, the phenylamine was linked to the bridge by the nitrogen heteroatom. The effect of the nature and size of the bridge in the magnitude of the hyperpolarizabilities was investigated. The push-pull systems with the extended bridges, containing two mesoionic rings and polyenic moieties, present the larger magnitudes values of β and γ.The results show that the combination of the selectedbridges and D/Apairs can be responsible for very large hyperpolarizabilities.Sociedade Brasileira de Química2008-01-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532008000700022Journal of the Brazilian Chemical Society v.19 n.7 2008reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.1590/S0103-50532008000700022info:eu-repo/semantics/openAccessMachado,Ana Elizabete de A.Gama,Alfredo Arnóbio de S. daeng2017-05-05T00:00:00Zoai:scielo:S0103-50532008000700022Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2017-05-05T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false
dc.title.none.fl_str_mv Enhanced optical nonlinearities in push-pull organic systems with polyenic-mesoionic ring mixed bridges
title Enhanced optical nonlinearities in push-pull organic systems with polyenic-mesoionic ring mixed bridges
spellingShingle Enhanced optical nonlinearities in push-pull organic systems with polyenic-mesoionic ring mixed bridges
Machado,Ana Elizabete de A.
β and γ hyperpolarizabilities
polyenic/mesoionic bridges
donor-bridge-acceptor organic systems
AM1/TDHF methodology
title_short Enhanced optical nonlinearities in push-pull organic systems with polyenic-mesoionic ring mixed bridges
title_full Enhanced optical nonlinearities in push-pull organic systems with polyenic-mesoionic ring mixed bridges
title_fullStr Enhanced optical nonlinearities in push-pull organic systems with polyenic-mesoionic ring mixed bridges
title_full_unstemmed Enhanced optical nonlinearities in push-pull organic systems with polyenic-mesoionic ring mixed bridges
title_sort Enhanced optical nonlinearities in push-pull organic systems with polyenic-mesoionic ring mixed bridges
author Machado,Ana Elizabete de A.
author_facet Machado,Ana Elizabete de A.
Gama,Alfredo Arnóbio de S. da
author_role author
author2 Gama,Alfredo Arnóbio de S. da
author2_role author
dc.contributor.author.fl_str_mv Machado,Ana Elizabete de A.
Gama,Alfredo Arnóbio de S. da
dc.subject.por.fl_str_mv β and γ hyperpolarizabilities
polyenic/mesoionic bridges
donor-bridge-acceptor organic systems
AM1/TDHF methodology
topic β and γ hyperpolarizabilities
polyenic/mesoionic bridges
donor-bridge-acceptor organic systems
AM1/TDHF methodology
description Large values of the static first(β) and second(γ) hyperpolarizabilities were obtained for donor-acceptor molecules having mixed bridges with mesoionic rings inserted between polyenic moieties. The magnitudes of β and γ were calculated at the AM1/TDHF semiempirical level. Donor(D)/acceptor(A) pairs of different strengths were used to test the potential of the new model bridges. The largest value was obtained by linking thedicyanomethylene(A) and phenylamine(D) at the opposite ends of mixed bridges.Unlike D/A molecules traditionally reported in the literature, the phenylamine was linked to the bridge by the nitrogen heteroatom. The effect of the nature and size of the bridge in the magnitude of the hyperpolarizabilities was investigated. The push-pull systems with the extended bridges, containing two mesoionic rings and polyenic moieties, present the larger magnitudes values of β and γ.The results show that the combination of the selectedbridges and D/Apairs can be responsible for very large hyperpolarizabilities.
publishDate 2008
dc.date.none.fl_str_mv 2008-01-01
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=S0103-50532008000700022
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532008000700022
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S0103-50532008000700022
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.19 n.7 2008
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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