4.7 Article

Aryl-bisalkynyl bridged perylene diimides dimers: Efficient synthesis, properties and improved electron mobilities

Journal

DYES AND PIGMENTS
Volume 144, Issue -, Pages 184-189

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.dyepig.2017.05.030

Keywords

Perylene diimides; Bisalkynyl compound; Organic functional dyes; Efficient synthesis; High electron mobility

Funding

  1. National Natural Science Foundation of China [21376038, 21421005, 21406027, 21576040]
  2. National Basic Research Program of China [2013CB733702]
  3. Dalian Agency for Science and Technology [2015R040]
  4. Fundamental Research Funds for the Central Universities [DUT16RC(4)02]

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A series of aryl-bisalkynyl bridged perylene diimides derivatives were efficiently synthesized through the Sonogashira-type coupling reaction, and their photophysical, electrochemical and electron-transporting properties were investigated in detail. With the introduction of aryl-bisallcynyl groups, their absorption spectra exhibit extra strong absorption in the short wavelength region and therefore realizing broad wavelength range from 300 to 700 nm, which can overcome the weakness of narrow half: peak width of N,N'-bis(1-ethylpropyl)perylene-3,4,9,10-tetracarboxylic acid bisimides (PDI). The lowest unoccupied molecular orbital (LUMO) levels (about -4.00 eV) are lower than that of the prototype PDI, which make them potential for excellent electron-transporting materials. As a result, the improved electron mobilities of 10(-4) cm(2) s(-1), which is three orders of magnitude higher than that of PDI, were obtained in space charge limited current (SCLC) devices. (C) 2017 Published by Elsevier Ltd.

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