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[1]Green synthesis of diketopyrrolopyrrole- and thiazolothiazole-based conjugated polymers via schiff-base condensation and cyclization for field-effect transistors:ACS Appl. Electron. Mater.,2026,8):953-960.
[2]Synthesis, structures and air-stable n-type organic field-effect transistor (OFET) properties of functionalized-phenanthrene conjugated asymmetric n-heteroacenes:Chem. Eur. J.,2025,31):e20240.
[3]Green synthesis of high-performance conjugated polymers through optimizing fused-ring structures and molecular weights for organic field-effect transistors:ACS Appl. Mater. Interfaces,2025,17):31183-31191.
[4]Donor-Acceptor Covalent-Organic Frameworks Based on Phthalimide as an Electron-Deficient Unit for Efficient Visible-Light Catalytic Hydrogen Evolution, ACS Applied Materials and Interfaces, 2023,15(16),20310 - 20316
[5]Incorporation of sequence aza-substitution and thiophene bridge in linear conjugated polymers toward highly efficient photo-catalytic hydrogen evolution, Macromolecular Rapid Communications, 2022, 43, 2100872.
[6]Aza-substitution on naphthalene diimide-based conjugated polymers for n-type bottom gate/top contact polymer transistors under ambient conditions, Journal of Materials Chemistry C, 2021, 9, 633-639.
[7]Diaza-substituted conjugated polymers based on naphthalene diimide for n-type fielde-ffect transistors, Dyes and Pigments, 2021, 194, 109660.
[8]Taming charge transport and mechanical properties of conjugated polymers with linear siloxane side chains, Macromolecules, 2021, 54, 5440-5450.
[9]Intrinsically stretchable n-type polymer semiconductor through side chain engineering, Macromolecules, 2021, 54, 8849-8859.
[10]One-step synthesis of an acceptor–donor–acceptor small molecule based on indacenodithieno[3, 2-b]thiophene and benzothiadiazole units for high-performance solution-processed organic field-effect transistors, Journal of Materials Chemistry C, 2020, 8, 14180-14185.
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