Improved Charge Transport In Fused-Ring Bridged Hemi-Isoindigo-Based Small Molecules By Incorporating A Thiophene Unit For Solution-Processed Organic Field-Effect Transistors

Two acceptor-donor-acceptor small molecules based on a fused ring indacenodithieno[3,2-b]thiophene (IDTT) as a donor, and hemi-isoindigo units, methyleneoxindole (IDTT-MI) and thienylmethyleneoxindole (IDTT-T-MI) as acceptors were synthesized and characterized for application in solution-processed organic field-effect transistors. The incorporation of a thiophene bridge which extended the conjugation of the backbone maintained highly co-planar structures, and also endowed the small molecule with ordered crystalline structures and interconnected morphology. Consequently, IDTT-T-MI-based organic field-effect transistors exhibited a highest hole mobility of 0.80 cm(2) V-1 s(-1), which was the highest mobility for solution-processed hemi-isoindigo-based organic semiconductor materials.