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Terthiophene Functionalized Conjugated Triarm Polymers Containing Poly(fluorene-2,7-vinylene) Arms Having Different Cores—Synthesis and Their Unique Optical Properties

[Image: see text] Optical properties of three types of terthiophene (3T) functionalized conjugated triarm (star-shaped) polymers consisting of poly(9,9-di-n-octyl-fluorene-2,7-vinylene) (PFV) arms and different [2,4,6-tri(biphenyl)benzene (TBP), 1,3,5-tri(benzyl)benzene (TBB), and triphenylamine (TP...

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Autores principales: Nomura, Kotohiro, Miwata, Tomohiro, Shinozuka, Takuya, Morita, Munetsugu, Geerts, Yves H., Fujiki, Michiya, Asano, Motoko S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2018
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6641954/
https://www.ncbi.nlm.nih.gov/pubmed/31458719
http://dx.doi.org/10.1021/acsomega.8b00676
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author Nomura, Kotohiro
Miwata, Tomohiro
Shinozuka, Takuya
Morita, Munetsugu
Geerts, Yves H.
Fujiki, Michiya
Asano, Motoko S.
author_facet Nomura, Kotohiro
Miwata, Tomohiro
Shinozuka, Takuya
Morita, Munetsugu
Geerts, Yves H.
Fujiki, Michiya
Asano, Motoko S.
author_sort Nomura, Kotohiro
collection PubMed
description [Image: see text] Optical properties of three types of terthiophene (3T) functionalized conjugated triarm (star-shaped) polymers consisting of poly(9,9-di-n-octyl-fluorene-2,7-vinylene) (PFV) arms and different [2,4,6-tri(biphenyl)benzene (TBP), 1,3,5-tri(benzyl)benzene (TBB), and triphenylamine (TPA)] cores, prepared by combined olefin metathesis with Wittig coupling, have been studied. Relative intensities [increases in the higher vibronic bands, (0, 1) fluorescence (FL)] of the fully conjugated TPA-core polymers, TPA(PFV-3T)(3), in the fluorescence (FL) spectra in tetrahydrofuran (toluene) solution were higher than those in the other triarm polymers, TBP(PFV-3T)(3), TBB(PFV-3T)(3), whereas no significant differences were observed in their UV–vis spectra; notable temperature dependences were not observed in the UV–vis and FL spectra (at −5, 25, and 55 °C). Remarkable differences were not observed in the spectra in these polymer thin films, whereas λ(max) values red-shifted due to the formation of J-type aggregates. The observation for the time-resolved study well corresponds to results for the steady-state fluorescence measurements. The observed unique emission by the star-shaped (triarm) polymer containing the TPA core would be assumed to be due to a difference in nature of the core (higher coplanarity) compared to that of the others.
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spelling pubmed-66419542019-08-27 Terthiophene Functionalized Conjugated Triarm Polymers Containing Poly(fluorene-2,7-vinylene) Arms Having Different Cores—Synthesis and Their Unique Optical Properties Nomura, Kotohiro Miwata, Tomohiro Shinozuka, Takuya Morita, Munetsugu Geerts, Yves H. Fujiki, Michiya Asano, Motoko S. ACS Omega [Image: see text] Optical properties of three types of terthiophene (3T) functionalized conjugated triarm (star-shaped) polymers consisting of poly(9,9-di-n-octyl-fluorene-2,7-vinylene) (PFV) arms and different [2,4,6-tri(biphenyl)benzene (TBP), 1,3,5-tri(benzyl)benzene (TBB), and triphenylamine (TPA)] cores, prepared by combined olefin metathesis with Wittig coupling, have been studied. Relative intensities [increases in the higher vibronic bands, (0, 1) fluorescence (FL)] of the fully conjugated TPA-core polymers, TPA(PFV-3T)(3), in the fluorescence (FL) spectra in tetrahydrofuran (toluene) solution were higher than those in the other triarm polymers, TBP(PFV-3T)(3), TBB(PFV-3T)(3), whereas no significant differences were observed in their UV–vis spectra; notable temperature dependences were not observed in the UV–vis and FL spectra (at −5, 25, and 55 °C). Remarkable differences were not observed in the spectra in these polymer thin films, whereas λ(max) values red-shifted due to the formation of J-type aggregates. The observation for the time-resolved study well corresponds to results for the steady-state fluorescence measurements. The observed unique emission by the star-shaped (triarm) polymer containing the TPA core would be assumed to be due to a difference in nature of the core (higher coplanarity) compared to that of the others. American Chemical Society 2018-05-09 /pmc/articles/PMC6641954/ /pubmed/31458719 http://dx.doi.org/10.1021/acsomega.8b00676 Text en Copyright © 2018 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle Nomura, Kotohiro
Miwata, Tomohiro
Shinozuka, Takuya
Morita, Munetsugu
Geerts, Yves H.
Fujiki, Michiya
Asano, Motoko S.
Terthiophene Functionalized Conjugated Triarm Polymers Containing Poly(fluorene-2,7-vinylene) Arms Having Different Cores—Synthesis and Their Unique Optical Properties
title Terthiophene Functionalized Conjugated Triarm Polymers Containing Poly(fluorene-2,7-vinylene) Arms Having Different Cores—Synthesis and Their Unique Optical Properties
title_full Terthiophene Functionalized Conjugated Triarm Polymers Containing Poly(fluorene-2,7-vinylene) Arms Having Different Cores—Synthesis and Their Unique Optical Properties
title_fullStr Terthiophene Functionalized Conjugated Triarm Polymers Containing Poly(fluorene-2,7-vinylene) Arms Having Different Cores—Synthesis and Their Unique Optical Properties
title_full_unstemmed Terthiophene Functionalized Conjugated Triarm Polymers Containing Poly(fluorene-2,7-vinylene) Arms Having Different Cores—Synthesis and Their Unique Optical Properties
title_short Terthiophene Functionalized Conjugated Triarm Polymers Containing Poly(fluorene-2,7-vinylene) Arms Having Different Cores—Synthesis and Their Unique Optical Properties
title_sort terthiophene functionalized conjugated triarm polymers containing poly(fluorene-2,7-vinylene) arms having different cores—synthesis and their unique optical properties
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6641954/
https://www.ncbi.nlm.nih.gov/pubmed/31458719
http://dx.doi.org/10.1021/acsomega.8b00676
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