TY - JOUR
T1 - Low-Temperature Direct Arylation Polymerization for the Sustainable Synthesis of a Library of Low-Defect Donor-Acceptor Conjugated Polymers via Pd/Ag Dual-Catalysis
AU - Kim, Hwangseok
AU - Yoo, Hyeonjin
AU - Kim, Hongsik
AU - Park, Jun Mo
AU - Lee, Byoung Hoon
AU - Choi, Tae Lim
N1 - Publisher Copyright:
© 2025 American Chemical Society.
PY - 2025/4/9
Y1 - 2025/4/9
N2 - Donor-acceptor alternating conjugated polymers (D-A CPs) are one of the best materials for high-performance organic electronic devices, owing to their low bandgap and high charge carrier mobility. However, most of the D-A CPs are synthesized by less sustainable polymerization methods. To address this issue, direct arylation polymerization (DArP), eliminating the need for transmetalating agents, was developed over the past two decades. Nevertheless, C-H activation during DArP still requires significantly harsh reaction conditions, limiting the precision and applicability of CPs. In this report, we demonstrate a versatile and sustainable Pd/Ag dual-catalytic DArP conducted at low or even room temperatures, thereby yielding low-defect D-A CPs. Initially, electron-deficient acceptor substrates with various electronic properties and pKa underwent successful concerted-metalation-deprotonation (CMD) via Ag catalysis with mild conditions and highly chemoselective Pd-catalyzed C-C coupling. This synergistic dual-catalysis allowed for the library synthesis of D-A and A-A CPs from acceptor C-H monomers and aryl halide monomers at low temperatures (25-70 °C) in sustainable solvents such as p-cymene. Interestingly, the D-A CPs obtained via Pd/Ag DArP displayed higher structural regularity and crystallinity, eventually outperforming those prepared by conventional synthetic methods in device performances of ambipolar organic field-effect transistors (μe up to 0.80 cm2 V-1 s-1) and complementary metal-oxide semiconductor inverters (gain up to 102).
AB - Donor-acceptor alternating conjugated polymers (D-A CPs) are one of the best materials for high-performance organic electronic devices, owing to their low bandgap and high charge carrier mobility. However, most of the D-A CPs are synthesized by less sustainable polymerization methods. To address this issue, direct arylation polymerization (DArP), eliminating the need for transmetalating agents, was developed over the past two decades. Nevertheless, C-H activation during DArP still requires significantly harsh reaction conditions, limiting the precision and applicability of CPs. In this report, we demonstrate a versatile and sustainable Pd/Ag dual-catalytic DArP conducted at low or even room temperatures, thereby yielding low-defect D-A CPs. Initially, electron-deficient acceptor substrates with various electronic properties and pKa underwent successful concerted-metalation-deprotonation (CMD) via Ag catalysis with mild conditions and highly chemoselective Pd-catalyzed C-C coupling. This synergistic dual-catalysis allowed for the library synthesis of D-A and A-A CPs from acceptor C-H monomers and aryl halide monomers at low temperatures (25-70 °C) in sustainable solvents such as p-cymene. Interestingly, the D-A CPs obtained via Pd/Ag DArP displayed higher structural regularity and crystallinity, eventually outperforming those prepared by conventional synthetic methods in device performances of ambipolar organic field-effect transistors (μe up to 0.80 cm2 V-1 s-1) and complementary metal-oxide semiconductor inverters (gain up to 102).
UR - http://www.scopus.com/inward/record.url?scp=105002392784&partnerID=8YFLogxK
U2 - 10.1021/jacs.4c16831
DO - 10.1021/jacs.4c16831
M3 - Article
C2 - 40163371
AN - SCOPUS:105002392784
SN - 0002-7863
VL - 147
SP - 11886
EP - 11895
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 14
ER -