N,N′-Bis(2-cyclohexylethyl)naphtho[2,3-b:6,7-b′] dithiophene diimides: Effects of substituents

Masahiro Nakano, Daisuke Hashizume, Kazuo Takimiya

Research output: Contribution to journalArticlepeer-review

7 Citations (Scopus)

Abstract

Naphtho[2,3-b:6,7-b′]dithiophene-4,5,9,10-tetracarboxylic diimide (NDTI) is a promising electron-deficient building block for n-type organic conductors, and the performance of NDTI-based field-effect transistors (FETs) is largely dependent on the substituents that alter the supramolecular organization in the solid state and, in turn, the intermolecular orbital overlap. For this reason, the rational selection of substituent on imide nitrogen atoms and/or thiophene α-positions is the key to developing superior n-type organic semiconductors. We here report new NDTI derivatives having N-(2-cyclohexylethyl) groups. Despite their one-dimensional packing structures in the solid state regardless of the presence or absence of chlorine groups at the thiophene α-positions, their FETs show promising performance with electron mobilities higher than 0.1 cm2. V-1.s-1 under ambient conditions. We also discuss how the cyclohexylethyl groups affect the packing structure in comparison with analogous n-octyl derivatives having the same number of carbon atoms.

Original languageEnglish
Article number981
JournalMolecules
Volume21
Issue number8
DOIs
Publication statusPublished - 2016 Aug
Externally publishedYes

Keywords

  • Application of naphthalene diimide
  • Crystal structure
  • Organic field-effect transistor
  • Organic synthesis
  • Supramolecular chemistry

ASJC Scopus subject areas

  • Analytical Chemistry
  • Chemistry (miscellaneous)
  • Molecular Medicine
  • Pharmaceutical Science
  • Drug Discovery
  • Physical and Theoretical Chemistry
  • Organic Chemistry

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