Conjugated Polymers from Direct Arylation Polycondensation of 3,4-Difluorothiophene-Substituted Aryls: Synthesis and Properties.

3,4-Difluorothiophene-substituted aryls, i.e., 1,4-bis(3,4-difluorothiophen-2-yl)-benzene (Ph-2FTh), 1,4-bis(3,4-difluorothiophen-2-yl)-2,5-difluorobenzene (2FPh-2FTh) and 4,7-bis(3,4-difluorothiophen-2-yl)-2,1,3-benzothiadiazole (BTz-2FTh), are synthesized as C-H monomers for the synthesis of conjugated polymers (CPs) via direct arylation polycondensation (DArP) with diketopyrrolopyrrole (DPP) and isoindigo (IID) derivatives as C-Br monomers. The Gibbs free energies of activation for direct arylation (ΔG 298K , kcal mol -1 ) for α-C-H bonds of thiophene moieties as calculated by density functional theory (DFT) are 14.3, 16.5 and 16.4 kcal mol -1 for Ph-2FTh, 2FPh-2FTh and BTz-2FTh, respectively, meaning that inserting an electron-deficient unit in 3,3',4,4'-tetrafluoro-2,2'-bithiophene (4FBT, ΔG 298K : 14.6 kcal mol -1 ) may cause a reactivity decrease of the C-H monomers. Photophysical and semiconducting properties of the resulting six CPs (i.e., DPP-Ph, DPP-2FPh, DPP-BTz, 2FIID-Ph, 2FIID-2FPh and 2FIID-BTz) are characterized in detail. DPP-based CPs showed ambipolar transport properties while IID-based ones exhibited n-type behaviour owing to the deeper frontier molecular orbital energy levels of IID-based CPs. With source/drain electrodes modified with polyethylenimine ethoxylated, n-channel organic thin-film transistors with maximum electron mobility of 0.40, 0.54, 0.29, 0.05, 0.16 and 0.01 cm 2 V -1 s -1 for DPP-Ph, DPP-2FPh, DPP-BTz, 2FIID-Ph, 2FIID-2FPh and 2FIID-BTz, respectively, were fabricated. DPP-2FPh exhibits the best device performance due to the good film morphology and the highest intermolecular packing order. This article is protected by copyright. All rights reserved.