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Search for "D–π–A structure" in Full Text gives 2 result(s) in Beilstein Journal of Organic Chemistry.

Post-synthesis from Lewis acid–base interaction: an alternative way to generate light and harvest triplet excitons

  • Hengjia Liu and
  • Guohua Xie

Beilstein J. Org. Chem. 2022, 18, 825–836, doi:10.3762/bjoc.18.83

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  • 7 in Figure 5), which consisted of the twisted A–π–DπA structure with N-(4-aminophenyl)carbazole (CzPA) as electron donor unit, pyridine as electron acceptor unit, and 9,9-dioctylfluorene (F) as π-conjugated linker [32]. Compound 7 showed remarkable dual-fluorescence properties when mixed with a
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Published 12 Jul 2022

Synthesis, photophysical and electrochemical properties of pyridine, pyrazine and triazine-based (D–π–)2A fluorescent dyes

  • Keiichi Imato,
  • Toshiaki Enoki,
  • Koji Uenaka and
  • Yousuke Ooyama

Beilstein J. Org. Chem. 2019, 15, 1712–1721, doi:10.3762/bjoc.15.167

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  • lowering of the LUMO energy level are dependent on the electron-withdrawing ability of the azine ring, which increases in the order of OUY-2 < OUK-2 < OUJ-2. Keywords: DπA structure; fluorescent dyes; pyrazine; pyridine; triazine; Introduction Donor–π-conjugated–acceptor (D–π–A) dyes are constructed of
  • . Thus, the D–π–A dyes exhibit intense photoabsorption and fluorescence emission properties based on the intramolecular charge transfer (ICT) excitation from the D moiety to the A moiety [1][2][3][4]. Moreover, the DπA structure possesses considerable structural characteristics: the increase in the
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Published 22 Jul 2019
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