Unexpectedly flexible graphene nanoribbons with a polyacene ladder skeleton

Detalhes bibliográficos
Autor(a) principal: Unruh, Marvin T.
Data de Publicação: 2021
Outros Autores: Scherf, Ullrich, Bahmann, Hilke, Rodrigues, Ana Clara B., Cunha, Carla, Melo, J. Sérgio Seixas de, Schedlbauer, Jakob, Lupton, John M.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10316/96944
https://doi.org/10.1039/D1TC02302K
Resumo: A new conjugated ladder polymer with a polyacene skeleton was synthesized in a Aldol-type condensation protocol between benzylic and aryl-ketone side groups of suitably functionalized single-stranded precursor polymers. The photophysical behavior of the new conjugated polyacene ladder polymer PAL comprising a polyacene skeleton has been investigated by steady-state and time-resolved photoluminescence spectroscopy in solvents of different viscosity and polarity, and by single-molecule spectroscopy (SMS). From the time-resolved photoluminescence experiments it is concluded that the excited state deactivation mainly results from energy transfer processes without significant conformational relaxation. When solutions in solvent mixtures of a good (THF) and a non-solvent (water) are studied, pronounced differences are seen between PAL and the well-known poly(para-phenylene) ladder polymer MeLPPP. Single molecule spectroscopy (SMS) reveals a remarkable heterogeneity in molecular shape, very much unlike MeLPPP, as determined by the polarization anisotropy and various photophysical properties. Several molecular models of PAL are characterized with density functional theory supporting this observation. We demonstrate that the PL lifetime, peak position, spectral width and vibronic intensity correlate with each other, implying that the polymer behaves as an intramolecular J-aggregate. Compared to MeLPPP, intramolecular energy transfer is not particularly efficient because of the high degree of disorder, which is also seen in the modest degree of photon antibunching and the pronounced temporal dynamics thereof due to the slow singlet-singlet annihilation.
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spelling Unexpectedly flexible graphene nanoribbons with a polyacene ladder skeletonA new conjugated ladder polymer with a polyacene skeleton was synthesized in a Aldol-type condensation protocol between benzylic and aryl-ketone side groups of suitably functionalized single-stranded precursor polymers. The photophysical behavior of the new conjugated polyacene ladder polymer PAL comprising a polyacene skeleton has been investigated by steady-state and time-resolved photoluminescence spectroscopy in solvents of different viscosity and polarity, and by single-molecule spectroscopy (SMS). From the time-resolved photoluminescence experiments it is concluded that the excited state deactivation mainly results from energy transfer processes without significant conformational relaxation. When solutions in solvent mixtures of a good (THF) and a non-solvent (water) are studied, pronounced differences are seen between PAL and the well-known poly(para-phenylene) ladder polymer MeLPPP. Single molecule spectroscopy (SMS) reveals a remarkable heterogeneity in molecular shape, very much unlike MeLPPP, as determined by the polarization anisotropy and various photophysical properties. Several molecular models of PAL are characterized with density functional theory supporting this observation. We demonstrate that the PL lifetime, peak position, spectral width and vibronic intensity correlate with each other, implying that the polymer behaves as an intramolecular J-aggregate. Compared to MeLPPP, intramolecular energy transfer is not particularly efficient because of the high degree of disorder, which is also seen in the modest degree of photon antibunching and the pronounced temporal dynamics thereof due to the slow singlet-singlet annihilation.Royal Society of Chemistry2021-07-15info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articlehttp://hdl.handle.net/10316/96944http://hdl.handle.net/10316/96944https://doi.org/10.1039/D1TC02302Keng2050-75262050-7534Unruh, Marvin T.Scherf, UllrichBahmann, HilkeRodrigues, Ana Clara B.Cunha, CarlaMelo, J. Sérgio Seixas deSchedlbauer, JakobLupton, John M.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:RCAAP2022-05-25T06:36:04Zoai:estudogeral.uc.pt:10316/96944Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T21:15:06.005120Repositório 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 Unexpectedly flexible graphene nanoribbons with a polyacene ladder skeleton
title Unexpectedly flexible graphene nanoribbons with a polyacene ladder skeleton
spellingShingle Unexpectedly flexible graphene nanoribbons with a polyacene ladder skeleton
Unruh, Marvin T.
title_short Unexpectedly flexible graphene nanoribbons with a polyacene ladder skeleton
title_full Unexpectedly flexible graphene nanoribbons with a polyacene ladder skeleton
title_fullStr Unexpectedly flexible graphene nanoribbons with a polyacene ladder skeleton
title_full_unstemmed Unexpectedly flexible graphene nanoribbons with a polyacene ladder skeleton
title_sort Unexpectedly flexible graphene nanoribbons with a polyacene ladder skeleton
author Unruh, Marvin T.
author_facet Unruh, Marvin T.
Scherf, Ullrich
Bahmann, Hilke
Rodrigues, Ana Clara B.
Cunha, Carla
Melo, J. Sérgio Seixas de
Schedlbauer, Jakob
Lupton, John M.
author_role author
author2 Scherf, Ullrich
Bahmann, Hilke
Rodrigues, Ana Clara B.
Cunha, Carla
Melo, J. Sérgio Seixas de
Schedlbauer, Jakob
Lupton, John M.
author2_role author
author
author
author
author
author
author
dc.contributor.author.fl_str_mv Unruh, Marvin T.
Scherf, Ullrich
Bahmann, Hilke
Rodrigues, Ana Clara B.
Cunha, Carla
Melo, J. Sérgio Seixas de
Schedlbauer, Jakob
Lupton, John M.
description A new conjugated ladder polymer with a polyacene skeleton was synthesized in a Aldol-type condensation protocol between benzylic and aryl-ketone side groups of suitably functionalized single-stranded precursor polymers. The photophysical behavior of the new conjugated polyacene ladder polymer PAL comprising a polyacene skeleton has been investigated by steady-state and time-resolved photoluminescence spectroscopy in solvents of different viscosity and polarity, and by single-molecule spectroscopy (SMS). From the time-resolved photoluminescence experiments it is concluded that the excited state deactivation mainly results from energy transfer processes without significant conformational relaxation. When solutions in solvent mixtures of a good (THF) and a non-solvent (water) are studied, pronounced differences are seen between PAL and the well-known poly(para-phenylene) ladder polymer MeLPPP. Single molecule spectroscopy (SMS) reveals a remarkable heterogeneity in molecular shape, very much unlike MeLPPP, as determined by the polarization anisotropy and various photophysical properties. Several molecular models of PAL are characterized with density functional theory supporting this observation. We demonstrate that the PL lifetime, peak position, spectral width and vibronic intensity correlate with each other, implying that the polymer behaves as an intramolecular J-aggregate. Compared to MeLPPP, intramolecular energy transfer is not particularly efficient because of the high degree of disorder, which is also seen in the modest degree of photon antibunching and the pronounced temporal dynamics thereof due to the slow singlet-singlet annihilation.
publishDate 2021
dc.date.none.fl_str_mv 2021-07-15
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/10316/96944
http://hdl.handle.net/10316/96944
https://doi.org/10.1039/D1TC02302K
url http://hdl.handle.net/10316/96944
https://doi.org/10.1039/D1TC02302K
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 2050-7526
2050-7534
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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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