4.6 Article

Synthesis and photophysical properties of novel multisubstituted benzene and naphthalene derivatives with high 2D-π-conjugation

Journal

OPTICAL MATERIALS
Volume 47, Issue -, Pages 118-128

Publisher

ELSEVIER
DOI: 10.1016/j.optmat.2015.07.011

Keywords

Photoluminescence; Electrochemistry; 2D-pi-conjugated derivatives; [2+1+2+1] cycloaddition; Blue light emitters

Funding

  1. NCN [DEC-011/01/B/ST5/06309]
  2. NCBiR [PBS2/A5/40/2014]
  3. Forszt project
  4. European Social
  5. DoktoRIS project

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A new small molecule, with D-A-D framework was prepared in good yield by using a [2+1+2+1] cycloaddition followed by the [4+2] Diels-Alders reaction. Additionally, tetra-substituted naphthalene derivatives were also prepared from in situ generated benzyne (using 2-trimethylsilylphenyl triflate and cesium fluoride). All of this compounds exhibit strong 2D-pi-conjugation. The influence of this type of interactions on photophysical properties with the aid of DFT calculations was examined. The preliminary tests of application possibility of synthesized compounds in devices for optoelectronics were carried out as well. (C) 2015 Published by Elsevier B.V.

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