Luminescent halogen-substituted 2-(N-arylimino)pyrrolyl boron complexes: the internal heavy-atom effect
Autor(a) principal: | |
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Data de Publicação: | 2020 |
Outros Autores: | , , , , , , , , , , , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
DOI: | 10.1039/D0DT01845G |
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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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 Luminescent halogen-substituted 2-(N-arylimino)pyrrolyl boron complexes: the internal heavy-atom effect Rodrigues, Ana I. 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 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 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. 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. 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) instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação instacron:RCAAP |
instname_str |
Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
instacron_str |
RCAAP |
institution |
RCAAP |
reponame_str |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
collection |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) |
repository.name.fl_str_mv |
Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação |
repository.mail.fl_str_mv |
|
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1822183347314491392 |
dc.identifier.doi.none.fl_str_mv |
10.1039/D0DT01845G |