Enhanced optical nonlinearities in push-pull organic systems with polyenic-mesoionic ring mixed bridges
Autor(a) principal: | |
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Data de Publicação: | 2008 |
Outros Autores: | |
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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Journal of the Brazilian Chemical Society (Online) |
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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 |
_version_ |
1750318169363316736 |