articleJournal of the American Chemical SocietyFeb 1, 2007Closed access

Facile Synthesis of Highly π-Extended Heteroarenes, Dinaphtho[2,3- b :2‘,3‘- f ]chalcogenopheno[3,2- b ]chalcogenophenes, and Their Application to Field-Effect Transistors

Hiroshima University

PubMed
Indexed incrossrefpubmed

Abstract

A facile three-step synthetic procedure for highly π-extended heteroarenes, dinaphtho[2,3-b:2‘,3‘-f]thieno[3,2-b]thiophene (DNTT) and dinaphtho[2,3-b:2‘,3‘-f]selenopheno[3,2-b]selenophene (DNSS), was established. Solution UV−vis spectra and electrochemistry indicated that they have relatively low-lying HOMO levels and large HOMO−LUMO energy gaps. OFET devices fabricated with evaporated thin-films of DNTT and DNSS showed excellent FET characteristics in air, and the highest field-effect mobility of DNTT- and DNSS-based OFETs is 2.9 and 1.9 cm2 V-1 s-1, respectively.

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884
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53.51
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Authors

2

Topics & keywords

Keywords
  • Chemistry
  • Thiophene
  • Organic field-effect transistor
  • HOMO/LUMO
  • Electrochemistry
  • Field-effect transistor
  • Stereochemistry
  • Transistor
UN Sustainable Development Goals
  • Affordable and clean energy
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