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Facile Synthesis of Bis-pentafluoroarylated Anthracene Derivatives for N-type Organic-Field-Effect Transistor Applications.

Ryota SatoTakeshi YasudaTakanobu HirotoTakaki KanbaraJunpei Kuwabara
Published in: Chemistry (Weinheim an der Bergstrasse, Germany) (2023)
Diphenylanthracene (DPA) and its derivatives are promising semiconducting materials for p-type organic-field-effect transistors (OFETs). In this study, to develop n-type semiconducting materials with an anthracene core, pentafluorobenzene was introduced into anthracene by C-H direct arylation, enabling the synthesis of various bis(pentafluorophenyl)anthracene (DPA-F) derivatives. The high reactivity of the pentafluorobenzene C-H bond allows direct arylation for synthesizing DPA-F derivatives in a single step. The introduction of strong electron-withdrawing pentafluorophenyl groups provides the anthracene derivatives with n-type semiconducting properties, in contrast to the p-type properties of the parent DPAs. Among the synthesized compounds, 2,6-bis(pentafluorophenyl)anthracene shows a high electron mobility of 0.12±0.02 cm 2 /Vs and an on/off ratio>10 6 in OFETs. The high crystallinity results in the smooth electron transport. This study provides a facile synthetic method for n-type semiconducting materials and insights into the molecular design of the positional effects of aromatic substituents on anthracene.
Keyphrases
  • amino acid
  • single molecule
  • electron transfer
  • electron microscopy