Beilstein Journal of Organic Chemistry (Feb 2017)

Synthesis and optical properties of new 5'-aryl-substituted 2,5-bis(3-decyl-2,2'-bithiophen-5-yl)-1,3,4-oxadiazoles

  • Anastasia S. Kostyuchenko,
  • Tatyana Yu. Zheleznova,
  • Anton J. Stasyuk,
  • Aleksandra Kurowska,
  • Wojciech Domagala,
  • Adam Pron,
  • Alexander S. Fisyuk

DOI
https://doi.org/10.3762/bjoc.13.34
Journal volume & issue
Vol. 13, no. 1
pp. 313 – 322

Abstract

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New photoluminescent donor–acceptor–donor (DAD) molecules, namely 5'-aryl-substituted 2,5-bis(3-decyl-2,2'-bithiophen-5-yl)-1,3,4-oxadiazoles were prepared by palladium-catalyzed coupling from readily available compounds such as ethyl 3-decyl-2,2'-bithiophene-5-carboxylate and aryl halides. The obtained compounds feature increasing bathochromic shifts in their emission spectra with increasing aryl-substituent size yielding blue to bluish-green emissions. At the same time, their absorption spectra are almost independent from the identity of the terminal substituent with λmax values ranging from 395 to 405 nm. The observed trends are perfectly predicted by quantum chemical DFT/TDDFT calculations carried out for these new molecules.

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