About: Synthesis, electrochemical, and optical properties of new fluorescent substituted thieno[3,2-b][1]benzothiophenes     Goto   Sponge   NotDistinct   Permalink

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  • The synthesis, electrochemical and optical properties of three fluorescent substituted thieno[3,2-b][1]benzothiophenes (TBT) derivatives, including 3-methoxythieno[3,2-b][1]benzothiophene (3-MeO-TBT), 2,3-dimethylthieno[3,2-b][1]benzothiophene (2,3-diMe-TBT), and 6-methoxythieno[3,2-b][1]benzothiophene-2-carboxylate (6-MeO-TBT-2-COOMe), were investigated. T0he oxidation potential values varied between 1.40 and 1.20 V/SCE according to the electronic substituent effect, and electropolymerization attempts, performed in 0.1 M LiClO4 acetonitrile solution, led to the formation of very thin films of poly(3-MeO-TBT) and poly(2,3-di-Me-TBT). Electronic absorption spectra, fluorescence excitation and emission spectra, fluorescence quantum yields (ΦF) , lifetimes (τF), and other photophysical parameters of the three new TBT derivatives were measured in DMSO solutions at room temperature. For the methyl-and methoxy-substituted TBT derivatives, the fluorescence emission peak were slightly red shifted re
  • The synthesis, electrochemical and optical properties of three fluorescent substituted thieno[3,2-b][1]benzothiophenes (TBT) derivatives, including 3-methoxythieno[3,2-b][1]benzothiophene (3-MeO-TBT), 2,3-dimethylthieno[3,2-b][1]benzothiophene (2,3-diMe-TBT), and 6-methoxythieno[3,2-b][1]benzothiophene-2-carboxylate (6-MeO-TBT-2-COOMe), were investigated. T0he oxidation potential values varied between 1.40 and 1.20 V/SCE according to the electronic substituent effect, and electropolymerization attempts, performed in 0.1 M LiClO4 acetonitrile solution, led to the formation of very thin films of poly(3-MeO-TBT) and poly(2,3-di-Me-TBT). Electronic absorption spectra, fluorescence excitation and emission spectra, fluorescence quantum yields (ΦF) , lifetimes (τF), and other photophysical parameters of the three new TBT derivatives were measured in DMSO solutions at room temperature. For the methyl-and methoxy-substituted TBT derivatives, the fluorescence emission peak were slightly red shifted re (en)
Title
  • Synthesis, electrochemical, and optical properties of new fluorescent substituted thieno[3,2-b][1]benzothiophenes
  • Synthesis, electrochemical, and optical properties of new fluorescent substituted thieno[3,2-b][1]benzothiophenes (en)
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  • Synthesis, electrochemical, and optical properties of new fluorescent substituted thieno[3,2-b][1]benzothiophenes
  • Synthesis, electrochemical, and optical properties of new fluorescent substituted thieno[3,2-b][1]benzothiophenes (en)
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  • RIV/60461373:22310/10:00023678!RIV11-MSM-22310___
http://linked.open...avai/riv/aktivita
http://linked.open...avai/riv/aktivity
  • Z(MSM6046137301)
http://linked.open...iv/cisloPeriodika
  • 5
http://linked.open...vai/riv/dodaniDat
http://linked.open...aciTvurceVysledku
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  • 291511
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  • RIV/60461373:22310/10:00023678
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  • thienobenzothiophene; synthesis; electrochemistry; optical properties (en)
http://linked.open.../riv/klicoveSlovo
http://linked.open...odStatuVydavatele
  • US - Spojené státy americké
http://linked.open...ontrolniKodProRIV
  • [950E78AE27E4]
http://linked.open...i/riv/nazevZdroje
  • Journal of Fluorescence
http://linked.open...in/vavai/riv/obor
http://linked.open...ichTvurcuVysledku
http://linked.open...cetTvurcuVysledku
http://linked.open...UplatneniVysledku
http://linked.open...v/svazekPeriodika
  • 20
http://linked.open...iv/tvurceVysledku
  • Svoboda, Jiří
  • Kozmík, Václav
  • Aaron, Jean-Jacques
  • Brochon, Jean-Claude
  • Lo, Cheikh
  • Na, Li
http://linked.open...ain/vavai/riv/wos
  • 000281716500009
http://linked.open...n/vavai/riv/zamer
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  • 1053-0509
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  • 22310
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