4.8 Article

Synthesis, Physical Properties, and Field-Effect Mobility of Isomerically Pure syn-/anti-Anthradithiophene Derivatives

Journal

ORGANIC LETTERS
Volume 14, Issue 16, Pages 4062-4065

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/ol301626u

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Funding

  1. Japan Regional Innovation Strategy Program by the Excellence (creating international research hub for advanced organic electronics) of Japan Science and Technology Agency (JST)
  2. Ministry of Education, Culture, Sports, Science and Technology, Japan

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Isomerically pure syn-/anti-isomers of 2,8-dimethylanthradithiophene (DMADT) were synthesized in five steps and characterized using thermogravimetry, X-ray single crystal analysis, UV-vis absorption, and electrochemical measurements. The physical properties in solution were slightly different for each isomer, whereby the more obvious differences were observed in the solid state. A field-effect transistor using the anti-isomer showed a much higher performance than that using the syn-isomer.

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