Tuning Emitting Color of Electroluminescent Devices Containing Tris(2-acyl-1,3-indandionate)aluminum(III) Complexes as Emitting Layers
Autor(a) principal: | |
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Data de Publicação: | 2019 |
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=S0103-50532019000801647 |
Resumo: | In this study, a novel type of tris(2-acyl-1,3-indandione)-aluminum(III) coordination compounds of the general formula [Al(acind)3]H2O, where 2-acyl-1,3-indandione (acind), 2-acetyl-1,3-indandione (aind), 2-benzoyl-1,3-indandione (bind), and 4-methyl-2-benzoyl-1,3-indandione (mbind), were synthesized and characterized by elemental analysis (CHN), Fourier transform infrared (FTIR) and nuclear magnetic resonance (1H NMR) spectroscopies, thermal analysis (TG/DTG and DTA), and optical absorption spectroscopy in the UV-Vis region. These compounds present remarkably high green luminescence in powder and in thin-film forms. However, when these compounds are applied in glass/ITO/β-NPB/spiro-2CBP/[Al(acind)3]/Al and glass/ITO/β-NPB/[Al(acind)3]/LiF/Al electroluminescent devices, where spiro-2CBP is 2,7-bis(carbazol-9-yl)-9,9-spirobifluorene and β-NPB is N,N’-bis(naphthalen-2-yl)-N,N’-bis(phenyl)-benzidine, the emission color tuned from green to red, reflecting a change from the direct charge recombination in the emitting layer of the [Al(acind)3] complexes to an exciplex-based emission in which [Al(acind)3] complexes and spiro 2-CBP acted as acceptor and donor, respectively. These results suggest that [Al(acind)3] complexes have potential applications as molecular light converter materials for fabricating new electroluminescent devices. |
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Tuning Emitting Color of Electroluminescent Devices Containing Tris(2-acyl-1,3-indandionate)aluminum(III) Complexes as Emitting Layerstris(2-acyl-1,3-indandionate)aluminum(III)OLEDred and green light emittingtuning emitting colorselectroluminescenceIn this study, a novel type of tris(2-acyl-1,3-indandione)-aluminum(III) coordination compounds of the general formula [Al(acind)3]H2O, where 2-acyl-1,3-indandione (acind), 2-acetyl-1,3-indandione (aind), 2-benzoyl-1,3-indandione (bind), and 4-methyl-2-benzoyl-1,3-indandione (mbind), were synthesized and characterized by elemental analysis (CHN), Fourier transform infrared (FTIR) and nuclear magnetic resonance (1H NMR) spectroscopies, thermal analysis (TG/DTG and DTA), and optical absorption spectroscopy in the UV-Vis region. These compounds present remarkably high green luminescence in powder and in thin-film forms. However, when these compounds are applied in glass/ITO/β-NPB/spiro-2CBP/[Al(acind)3]/Al and glass/ITO/β-NPB/[Al(acind)3]/LiF/Al electroluminescent devices, where spiro-2CBP is 2,7-bis(carbazol-9-yl)-9,9-spirobifluorene and β-NPB is N,N’-bis(naphthalen-2-yl)-N,N’-bis(phenyl)-benzidine, the emission color tuned from green to red, reflecting a change from the direct charge recombination in the emitting layer of the [Al(acind)3] complexes to an exciplex-based emission in which [Al(acind)3] complexes and spiro 2-CBP acted as acceptor and donor, respectively. These results suggest that [Al(acind)3] complexes have potential applications as molecular light converter materials for fabricating new electroluminescent devices.Sociedade Brasileira de Química2019-08-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532019000801647Journal of the Brazilian Chemical Society v.30 n.8 2019reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.21577/0103-5053.20190064info:eu-repo/semantics/openAccessCosta,Israel F.Moura,Jandeilson L.Aderne,Rian E.Avila,Harold C.Cremona,MarcoBrito,Hermi F.Felinto,Maria Cláudia F. C.Faustino,Wagner M.Teotonio,Ercules E. S.eng2019-08-08T00:00:00Zoai:scielo:S0103-50532019000801647Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2019-08-08T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false |
dc.title.none.fl_str_mv |
Tuning Emitting Color of Electroluminescent Devices Containing Tris(2-acyl-1,3-indandionate)aluminum(III) Complexes as Emitting Layers |
title |
Tuning Emitting Color of Electroluminescent Devices Containing Tris(2-acyl-1,3-indandionate)aluminum(III) Complexes as Emitting Layers |
spellingShingle |
Tuning Emitting Color of Electroluminescent Devices Containing Tris(2-acyl-1,3-indandionate)aluminum(III) Complexes as Emitting Layers Costa,Israel F. tris(2-acyl-1,3-indandionate)aluminum(III) OLED red and green light emitting tuning emitting colors electroluminescence |
title_short |
Tuning Emitting Color of Electroluminescent Devices Containing Tris(2-acyl-1,3-indandionate)aluminum(III) Complexes as Emitting Layers |
title_full |
Tuning Emitting Color of Electroluminescent Devices Containing Tris(2-acyl-1,3-indandionate)aluminum(III) Complexes as Emitting Layers |
title_fullStr |
Tuning Emitting Color of Electroluminescent Devices Containing Tris(2-acyl-1,3-indandionate)aluminum(III) Complexes as Emitting Layers |
title_full_unstemmed |
Tuning Emitting Color of Electroluminescent Devices Containing Tris(2-acyl-1,3-indandionate)aluminum(III) Complexes as Emitting Layers |
title_sort |
Tuning Emitting Color of Electroluminescent Devices Containing Tris(2-acyl-1,3-indandionate)aluminum(III) Complexes as Emitting Layers |
author |
Costa,Israel F. |
author_facet |
Costa,Israel F. Moura,Jandeilson L. Aderne,Rian E. Avila,Harold C. Cremona,Marco Brito,Hermi F. Felinto,Maria Cláudia F. C. Faustino,Wagner M. Teotonio,Ercules E. S. |
author_role |
author |
author2 |
Moura,Jandeilson L. Aderne,Rian E. Avila,Harold C. Cremona,Marco Brito,Hermi F. Felinto,Maria Cláudia F. C. Faustino,Wagner M. Teotonio,Ercules E. S. |
author2_role |
author author author author author author author author |
dc.contributor.author.fl_str_mv |
Costa,Israel F. Moura,Jandeilson L. Aderne,Rian E. Avila,Harold C. Cremona,Marco Brito,Hermi F. Felinto,Maria Cláudia F. C. Faustino,Wagner M. Teotonio,Ercules E. S. |
dc.subject.por.fl_str_mv |
tris(2-acyl-1,3-indandionate)aluminum(III) OLED red and green light emitting tuning emitting colors electroluminescence |
topic |
tris(2-acyl-1,3-indandionate)aluminum(III) OLED red and green light emitting tuning emitting colors electroluminescence |
description |
In this study, a novel type of tris(2-acyl-1,3-indandione)-aluminum(III) coordination compounds of the general formula [Al(acind)3]H2O, where 2-acyl-1,3-indandione (acind), 2-acetyl-1,3-indandione (aind), 2-benzoyl-1,3-indandione (bind), and 4-methyl-2-benzoyl-1,3-indandione (mbind), were synthesized and characterized by elemental analysis (CHN), Fourier transform infrared (FTIR) and nuclear magnetic resonance (1H NMR) spectroscopies, thermal analysis (TG/DTG and DTA), and optical absorption spectroscopy in the UV-Vis region. These compounds present remarkably high green luminescence in powder and in thin-film forms. However, when these compounds are applied in glass/ITO/β-NPB/spiro-2CBP/[Al(acind)3]/Al and glass/ITO/β-NPB/[Al(acind)3]/LiF/Al electroluminescent devices, where spiro-2CBP is 2,7-bis(carbazol-9-yl)-9,9-spirobifluorene and β-NPB is N,N’-bis(naphthalen-2-yl)-N,N’-bis(phenyl)-benzidine, the emission color tuned from green to red, reflecting a change from the direct charge recombination in the emitting layer of the [Al(acind)3] complexes to an exciplex-based emission in which [Al(acind)3] complexes and spiro 2-CBP acted as acceptor and donor, respectively. These results suggest that [Al(acind)3] complexes have potential applications as molecular light converter materials for fabricating new electroluminescent devices. |
publishDate |
2019 |
dc.date.none.fl_str_mv |
2019-08-01 |
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=S0103-50532019000801647 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532019000801647 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.21577/0103-5053.20190064 |
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.30 n.8 2019 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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1750318182086737920 |