Intramolecular Locked Dithioalkylbithiophene-Based Semiconductors for High-Performance Organic Field-Effect Transistors

Abstract

New 3,3-dithioalkyl-2,2-bithiophene (SBT)-based small molecular and polymeric semiconductors are synthesized by end-capping or copolymerization with dithienothiophen-2-yl units. Single-crystal, molecular orbital computations, and optical/electrochemical data indicate that the SBT core is completely planar, likely via S(alkyl)S(thiophene) intramolecular locks. Therefore, compared to semiconductors based on the conventional 3,3-dialkyl-2,2-bithiophene, the resulting SBT systems are planar (torsional angle <1 degrees) and highly -conjugated. Charge transport is investigated for solution-sheared films in field-effect transistors demonstrating that SBT can enable good semiconducting materials with hole mobilities ranging from approximate to 0.03 to 1.7 cm(2) V-1 s(-1). Transport difference within this family is rationalized by film morphology, as accessed by grazing incidence X-ray diffraction experiments.