4.6 Article

Synthesis and Optoelectronic Characterization of Perylene Diimide-Quinoline Based Small Molecules

Journal

MOLECULES
Volume 24, Issue 23, Pages -

Publisher

MDPI
DOI: 10.3390/molecules24234406

Keywords

functional perylene; Suzuki reaction; non fullerene acceptors; electrochemical and optical properties

Funding

  1. General Secretariat for Research and Technology (GSRT)
  2. Hellenic Foundation for Research and Innovation (HFRI) [2358]

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Perylene diimide (PDI) is one of the most studied functional dyes due to their structural versatility and fine tuning of the materials properties. Core substituted PDIs are prominent n-type semiconductor materials that could be used as non-fullerene acceptors in organic photovoltaics. Herein, we develop versatile organic building blocks based on PDI by decorating the PDI core with quinoline groups. Styryl and hydroxy phenyl mono and difunctionalized molecules were prepared using mono-nitro and dibromo bay substituted PDIs by Suzuki coupling with the respective boronic acid derivatives. A novel methodology using nitro-PDI under Suzuki coupling conditions as an electrophile partner was successfully tested. Furthermore, the PDI derivatives were used for the synthesis of soluble, electron accepting small molecules combining PDI with weak electron withdrawing quinoline derivatives. The new molecules presented wide absorbance in the visible spectrum from 450 to almost 700 nm while their LUMO levels and their energy levels are in the range of -3.8 to -4.2 eV.

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