Luminescent halogen-substituted 2-(N-arylimino)pyrrolyl boron complexes: the internal heavy-atom effect

Detalhes bibliográficos
Autor(a) principal: Rodrigues, Ana I.
Data de Publicação: 2020
Outros Autores: Krishnamoorthy, Paramasivam, Gomes, Clara S. B., Carmona, Nicolas, Di Paolo, Roberto E., Pander, Piotr, Pina, João, Melo, J. Sérgio Seixas de, Dias, Fernando B., Calhorda, Maria José, Maçanita, António L., Morgado, Jorge, Gomes, Pedro T.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10316/90796
https://doi.org/10.1039/D0DT01845G
Resumo: A group of new boron complexes [BPh2{κ2N,N′-NC4H3-2-C(H)[double bond, length as m-dash]N-C6H4X}] (X = 4-Cl 4c, 4-Br 4d, 4-I 4e, 3-Br 4f, 2-Br 4g, 2-I 4h) containing different halogens as substituents in the N-aryl ring have been synthesized and characterized in terms of their molecular properties. Their photophysical characteristics have been thoroughly studied in order to understand whether these complexes exhibit an internal heavy-atom effect. Phosphorescence emission was found for some of the synthesized halogen-substituted boron molecules, particularly for 4g and 4h. DFT and TDDFT calculations showed that the lower energy absorption band resulted from the HOMO to LUMO (π–π*) transition, except for 2-I 4h, where the HOMO−1 to LUMO transition was also involved. The strong participation of iodine orbitals in HOMO−1 is reflected in the calculated absorption spectra of the iodine derivatives, especially 2-I 4h, when spin–orbit coupling (SOC) was included. Organic light-emitting diodes (OLEDs) based on these complexes, in the neat form or dispersed in a matrix, were also fabricated and tested. The devices based on films prepared by thermal vacuum deposition showed the best performance. When neat complexes were used, a maximum luminance (Lmax) of 1812 cd m−2 was obtained, with a maximum external quantum efficiency (EQEmax) of 0.15%. An EQEmax of ca. 1% along with a maximum luminance of 494 cd m−2 were obtained for a device fabricated by co-deposition of the boron complex and a host compound (1,3-bis(N-carbazolyl)benzene, mCP).
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spelling Luminescent halogen-substituted 2-(N-arylimino)pyrrolyl boron complexes: the internal heavy-atom effectA group of new boron complexes [BPh2{κ2N,N′-NC4H3-2-C(H)[double bond, length as m-dash]N-C6H4X}] (X = 4-Cl 4c, 4-Br 4d, 4-I 4e, 3-Br 4f, 2-Br 4g, 2-I 4h) containing different halogens as substituents in the N-aryl ring have been synthesized and characterized in terms of their molecular properties. Their photophysical characteristics have been thoroughly studied in order to understand whether these complexes exhibit an internal heavy-atom effect. Phosphorescence emission was found for some of the synthesized halogen-substituted boron molecules, particularly for 4g and 4h. DFT and TDDFT calculations showed that the lower energy absorption band resulted from the HOMO to LUMO (π–π*) transition, except for 2-I 4h, where the HOMO−1 to LUMO transition was also involved. The strong participation of iodine orbitals in HOMO−1 is reflected in the calculated absorption spectra of the iodine derivatives, especially 2-I 4h, when spin–orbit coupling (SOC) was included. Organic light-emitting diodes (OLEDs) based on these complexes, in the neat form or dispersed in a matrix, were also fabricated and tested. The devices based on films prepared by thermal vacuum deposition showed the best performance. When neat complexes were used, a maximum luminance (Lmax) of 1812 cd m−2 was obtained, with a maximum external quantum efficiency (EQEmax) of 0.15%. An EQEmax of ca. 1% along with a maximum luminance of 494 cd m−2 were obtained for a device fabricated by co-deposition of the boron complex and a host compound (1,3-bis(N-carbazolyl)benzene, mCP).Royal Society of Chemistry2020info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://hdl.handle.net/10316/90796http://hdl.handle.net/10316/90796https://doi.org/10.1039/D0DT01845Geng1477-92261477-9234https://pubs.rsc.org/en/content/articlelanding/2020/DT/D0DT01845G#!divAbstractRodrigues, Ana I.Krishnamoorthy, ParamasivamGomes, Clara S. B.Carmona, NicolasDi Paolo, Roberto E.Pander, PiotrPina, JoãoMelo, J. Sérgio Seixas deDias, Fernando B.Calhorda, Maria JoséMaçanita, António L.Morgado, JorgeGomes, Pedro T.info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2022-05-25T05:38:10Zoai:estudogeral.uc.pt:10316/90796Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T21:10:49.519122Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv Luminescent halogen-substituted 2-(N-arylimino)pyrrolyl boron complexes: the internal heavy-atom effect
title Luminescent halogen-substituted 2-(N-arylimino)pyrrolyl boron complexes: the internal heavy-atom effect
spellingShingle Luminescent halogen-substituted 2-(N-arylimino)pyrrolyl boron complexes: the internal heavy-atom effect
Rodrigues, Ana I.
title_short Luminescent halogen-substituted 2-(N-arylimino)pyrrolyl boron complexes: the internal heavy-atom effect
title_full Luminescent halogen-substituted 2-(N-arylimino)pyrrolyl boron complexes: the internal heavy-atom effect
title_fullStr Luminescent halogen-substituted 2-(N-arylimino)pyrrolyl boron complexes: the internal heavy-atom effect
title_full_unstemmed Luminescent halogen-substituted 2-(N-arylimino)pyrrolyl boron complexes: the internal heavy-atom effect
title_sort Luminescent halogen-substituted 2-(N-arylimino)pyrrolyl boron complexes: the internal heavy-atom effect
author Rodrigues, Ana I.
author_facet Rodrigues, Ana I.
Krishnamoorthy, Paramasivam
Gomes, Clara S. B.
Carmona, Nicolas
Di Paolo, Roberto E.
Pander, Piotr
Pina, João
Melo, J. Sérgio Seixas de
Dias, Fernando B.
Calhorda, Maria José
Maçanita, António L.
Morgado, Jorge
Gomes, Pedro T.
author_role author
author2 Krishnamoorthy, Paramasivam
Gomes, Clara S. B.
Carmona, Nicolas
Di Paolo, Roberto E.
Pander, Piotr
Pina, João
Melo, J. Sérgio Seixas de
Dias, Fernando B.
Calhorda, Maria José
Maçanita, António L.
Morgado, Jorge
Gomes, Pedro T.
author2_role author
author
author
author
author
author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Rodrigues, Ana I.
Krishnamoorthy, Paramasivam
Gomes, Clara S. B.
Carmona, Nicolas
Di Paolo, Roberto E.
Pander, Piotr
Pina, João
Melo, J. Sérgio Seixas de
Dias, Fernando B.
Calhorda, Maria José
Maçanita, António L.
Morgado, Jorge
Gomes, Pedro T.
description A group of new boron complexes [BPh2{κ2N,N′-NC4H3-2-C(H)[double bond, length as m-dash]N-C6H4X}] (X = 4-Cl 4c, 4-Br 4d, 4-I 4e, 3-Br 4f, 2-Br 4g, 2-I 4h) containing different halogens as substituents in the N-aryl ring have been synthesized and characterized in terms of their molecular properties. Their photophysical characteristics have been thoroughly studied in order to understand whether these complexes exhibit an internal heavy-atom effect. Phosphorescence emission was found for some of the synthesized halogen-substituted boron molecules, particularly for 4g and 4h. DFT and TDDFT calculations showed that the lower energy absorption band resulted from the HOMO to LUMO (π–π*) transition, except for 2-I 4h, where the HOMO−1 to LUMO transition was also involved. The strong participation of iodine orbitals in HOMO−1 is reflected in the calculated absorption spectra of the iodine derivatives, especially 2-I 4h, when spin–orbit coupling (SOC) was included. Organic light-emitting diodes (OLEDs) based on these complexes, in the neat form or dispersed in a matrix, were also fabricated and tested. The devices based on films prepared by thermal vacuum deposition showed the best performance. When neat complexes were used, a maximum luminance (Lmax) of 1812 cd m−2 was obtained, with a maximum external quantum efficiency (EQEmax) of 0.15%. An EQEmax of ca. 1% along with a maximum luminance of 494 cd m−2 were obtained for a device fabricated by co-deposition of the boron complex and a host compound (1,3-bis(N-carbazolyl)benzene, mCP).
publishDate 2020
dc.date.none.fl_str_mv 2020
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/10316/90796
http://hdl.handle.net/10316/90796
https://doi.org/10.1039/D0DT01845G
url http://hdl.handle.net/10316/90796
https://doi.org/10.1039/D0DT01845G
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 1477-9226
1477-9234
https://pubs.rsc.org/en/content/articlelanding/2020/DT/D0DT01845G#!divAbstract
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.publisher.none.fl_str_mv Royal Society of Chemistry
publisher.none.fl_str_mv Royal Society of Chemistry
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
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instacron:RCAAP
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reponame_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
collection Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
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