4.8 Article

Core-Fluorinated Naphthalene Diimides: Synthesis, Characterization, and Application in n-Type Organic Field-Effect Transistors

Journal

ORGANIC LETTERS
Volume 18, Issue 3, Pages 456-459

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.orglett.5b03489

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Funding

  1. DFG Priority Program [SPP 1355]
  2. BASF SE

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A series of difluoro- and tetrafluoro-substituted naphthalene diimides (NDIs) were synthesized by halogen exchange reactions of corresponding bromo-NDIs with CsF in dioxane. Two strong electron acceptor molecules 6 and 8 with low-lying LUMO energy levels of -4.27 and -4.54 eV were obtained, starting from tetrafluoro-NDI. Organic field-effect transistors (OFETs) based on these fluorinated NDIs were fabricated by vapor deposition, exhibiting n-channel field-effect character under ambient conditions with the highest mobility of 0.1 cm(2) V-1 s(-1).

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