Synthesis and thermal behavior of new liquid crystals arylaldoxime esters

Detalhes bibliográficos
Autor(a) principal: Tavares,Aline
Data de Publicação: 2012
Outros Autores: Arruda,Bárbara C., Boes,Elvis S., Stefani,Valter, Stassen,Hubert K., Campo,Leandra F., Bechtold,Ivan H., Merlo,Aloir A.
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=S0103-50532012000500013
Resumo: We report the synthesis of a series of liquid-crystalline materials based on arylaldoxime esters and the characterization of these materials by ¹H, 13C NMR, ATR/FT-IR spectroscopy and elemental analysis. The chemical stability and liquid-crystalline as well as photophysical properties of the compounds are described being dependent on the heating/cooling cycles. The changes in chemical stability and the liquid crystals properties of arylaldoxime esters were observed during these thermal cycles by IR analysis. All samples underwent a thermal degradation yielding the corresponding nitriles and carboxylic acid as evidenced by IR and ¹H NMR spectra. Due to the decomposition process, information about the mesomorphic behaviour is lost. The UV-Vis absorption spectra in solution display three absorption bands between 230 and 340 nm. The fluorescence spectra exhibit a broad and structureless emission band located at 430 nm. Ab initio calculations were performed to obtain information on the molecular structure and properties of the title compounds.
id SBQ-2_8dd5df3d9c27ffa3e89f6584a700ca4c
oai_identifier_str oai:scielo:S0103-50532012000500013
network_acronym_str SBQ-2
network_name_str Journal of the Brazilian Chemical Society (Online)
repository_id_str
spelling Synthesis and thermal behavior of new liquid crystals arylaldoxime estersarylaldoxime estersliquid crystalsinfra-red analysisisoxazolinesWe report the synthesis of a series of liquid-crystalline materials based on arylaldoxime esters and the characterization of these materials by ¹H, 13C NMR, ATR/FT-IR spectroscopy and elemental analysis. The chemical stability and liquid-crystalline as well as photophysical properties of the compounds are described being dependent on the heating/cooling cycles. The changes in chemical stability and the liquid crystals properties of arylaldoxime esters were observed during these thermal cycles by IR analysis. All samples underwent a thermal degradation yielding the corresponding nitriles and carboxylic acid as evidenced by IR and ¹H NMR spectra. Due to the decomposition process, information about the mesomorphic behaviour is lost. The UV-Vis absorption spectra in solution display three absorption bands between 230 and 340 nm. The fluorescence spectra exhibit a broad and structureless emission band located at 430 nm. Ab initio calculations were performed to obtain information on the molecular structure and properties of the title compounds.Sociedade Brasileira de Química2012-05-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532012000500013Journal of the Brazilian Chemical Society v.23 n.5 2012reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.1590/S0103-50532012000500013info:eu-repo/semantics/openAccessTavares,AlineArruda,Bárbara C.Boes,Elvis S.Stefani,ValterStassen,Hubert K.Campo,Leandra F.Bechtold,Ivan H.Merlo,Aloir A.eng2012-06-01T00:00:00Zoai:scielo:S0103-50532012000500013Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2012-06-01T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false
dc.title.none.fl_str_mv Synthesis and thermal behavior of new liquid crystals arylaldoxime esters
title Synthesis and thermal behavior of new liquid crystals arylaldoxime esters
spellingShingle Synthesis and thermal behavior of new liquid crystals arylaldoxime esters
Tavares,Aline
arylaldoxime esters
liquid crystals
infra-red analysis
isoxazolines
title_short Synthesis and thermal behavior of new liquid crystals arylaldoxime esters
title_full Synthesis and thermal behavior of new liquid crystals arylaldoxime esters
title_fullStr Synthesis and thermal behavior of new liquid crystals arylaldoxime esters
title_full_unstemmed Synthesis and thermal behavior of new liquid crystals arylaldoxime esters
title_sort Synthesis and thermal behavior of new liquid crystals arylaldoxime esters
author Tavares,Aline
author_facet Tavares,Aline
Arruda,Bárbara C.
Boes,Elvis S.
Stefani,Valter
Stassen,Hubert K.
Campo,Leandra F.
Bechtold,Ivan H.
Merlo,Aloir A.
author_role author
author2 Arruda,Bárbara C.
Boes,Elvis S.
Stefani,Valter
Stassen,Hubert K.
Campo,Leandra F.
Bechtold,Ivan H.
Merlo,Aloir A.
author2_role author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Tavares,Aline
Arruda,Bárbara C.
Boes,Elvis S.
Stefani,Valter
Stassen,Hubert K.
Campo,Leandra F.
Bechtold,Ivan H.
Merlo,Aloir A.
dc.subject.por.fl_str_mv arylaldoxime esters
liquid crystals
infra-red analysis
isoxazolines
topic arylaldoxime esters
liquid crystals
infra-red analysis
isoxazolines
description We report the synthesis of a series of liquid-crystalline materials based on arylaldoxime esters and the characterization of these materials by ¹H, 13C NMR, ATR/FT-IR spectroscopy and elemental analysis. The chemical stability and liquid-crystalline as well as photophysical properties of the compounds are described being dependent on the heating/cooling cycles. The changes in chemical stability and the liquid crystals properties of arylaldoxime esters were observed during these thermal cycles by IR analysis. All samples underwent a thermal degradation yielding the corresponding nitriles and carboxylic acid as evidenced by IR and ¹H NMR spectra. Due to the decomposition process, information about the mesomorphic behaviour is lost. The UV-Vis absorption spectra in solution display three absorption bands between 230 and 340 nm. The fluorescence spectra exhibit a broad and structureless emission band located at 430 nm. Ab initio calculations were performed to obtain information on the molecular structure and properties of the title compounds.
publishDate 2012
dc.date.none.fl_str_mv 2012-05-01
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=S0103-50532012000500013
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532012000500013
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S0103-50532012000500013
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.23 n.5 2012
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_ 1750318173469540352