4.6 Article

Synthesis, photophysics and electrochemistry of novel, nitrogen-containing heterocyclic derivatives

Journal

NEW JOURNAL OF CHEMISTRY
Volume 37, Issue 7, Pages 1982-1988

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c3nj00078h

Keywords

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Funding

  1. SWIFT [POKL.08.02.01-24-005/10]
  2. European Community

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A series of new pi-conjugated donor (thienyl - T) and acceptor (A) oligomers were prepared by Stille coupling reaction. The T-A oligomers consisting of thiophene/bithiophene as donors and 1,2,4-triazine as an acceptor were prepared to investigate their photophysical and electrochemical properties. These compounds were spectroscopically confirmed to be highly conjugated. These UV-vis data show that the number and position of the thiophene considerably affect the width of the HOMO-LUMO gap and the rigidity of the conjugated system. Compounds A2TA, A3TA, A4TA show photoluminescence in a range 466-543 nm.

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