Advancements in conjugated donor-acceptor (D-A) polymers with superior semiconducting performance and reliability are pivotal to the evolution of flexible electronics. However, the development of electron-accepting building blocks has lagged far behind that of electron-donating ones, hindering the progression of ambipolar and n-type semiconductor polymers-especially ambipolar types-and thereby limiting the construction of logic circuits and p-n heterojunctions. In this study, we introduce a new electron-accepting building block, 2Ar'Ar2DPP, meticulously engineered for semiconducting polymers tailored to flexible electronics applications. Synthesized through the modification of conventional diketopyrrolopyrrole (DPP), 2Ar'Ar2DPP─including 2TPh2DPP and 3T2DPP─incorporates structural innovations, merging a single DPP unit with two aromatic groups into a configuration featuring two DPP units and three aromatic groups. This modification enhances the electron-accepting ability and modulates intra- and intermolecular D-A interactions. 2TPh2DPP and 3T2DPP were investigated to explore their structure-property relationships. Specifically, 3T2DPP demonstrates improved backbone planarity, extended π-conjugation, and more efficient intramolecular D-A interactions. These features result in significantly lower LUMO levels and narrower band gaps compared to those of conventionally utilized thiophene-flanked DPP and even its dimer. Moreover, the change in the molecular structural symmetry of 3T2DPP induces a relatively large dipole moment, thereby enhancing intermolecular interactions. Consequently, polymers derived from 2Ar'Ar2DPP exhibit ambipolar semiconducting performance in flexible organic field-effect transistors, achieving hole and electron mobilities of up to 6.0 and 2.1 cm² V^-1 s^-1, respectively, with good bending resistance. These preliminary results indicate that 2Ar'Ar2DPP holds significant promise for the future design of conjugated materials for flexible electronics.

Bolun Huang

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