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High performance organic field effect transistor devices based on intrinsically scalable materials are of great significance in wearable electronics. In this work, an exclusive approach is reported to rationale the carrier mobility and stretchability of the conjugate polymers (CPs) by modifying the symmetry of the side chains species. Semiconductor CPs with symmetrical alkyl side chains (P(C-C)), symmetrical siloxane side chains (P(Si-Si)), and asymmetrical silicon-carbon side chains (P(C-Si)) are synthesized to investigate the influence of these side chains on the carrier mobility and mechanical behavior. The result shows that silicon-carbon asymmetric side chains can modulate the aggregation degree of polymer chains with a coherence length of 134 Å and maintain the mobility at 0.90 cm 2 V -1 s -1 . P(C-Si) exhibits superior tensile properties that even elongation up to 100% the value of mobility retains a majority properties. The main reason is that the lowest coherence length of P(C-Si) polymer leads to an increased proportion of amorphous zones in its polymer film, which efficiently dissipates mechanical stresses. This study provides an efficient strategy for the design and synthesis of the CPs with high carrier transport properties-mechanical stability., (© 2021 Wiley-VCH GmbH.)

Three isoindigo-based conjugated polymers modified with linear hybrid siloxane-based side chains were synthesized (PIID-Cm-Si7, m = 5–7). All polymers showed good solubilities in halogenated hydrocarbons, aromatic hydrocarbons, ethers, alkanes, and esters. The polymer films of PIID-C5-Si7, PIID-C6-Si7, and PIID-C7-Si7 achieved mobilities of 0.32, 0.82, and 1.58 cm2 V−1 s−1, respectively. [ABSTRACT FROM AUTHOR]