TY - JOUR
T1 - Low-Defect, High Molecular Weight Indacenodithiophene (IDT) Polymers Via a C-H Activation
T2 - Evaluation of a Simpler and Greener Approach to Organic Electronic Materials
AU - Ponder, James F.
AU - Chen, Hu
AU - Luci, Alexander M.T.
AU - Moro, Stefania
AU - Turano, Marco
AU - Hobson, Archie L.
AU - Collier, Graham S.
AU - Perdigão, Luís M.A.
AU - Moser, Maximilian
AU - Zhang, Weimin
AU - Costantini, Giovanni
AU - Reynolds, John R.
AU - McCulloch, Iain
N1 - Publisher Copyright:
© 2021 American Chemical Society.
PY - 2021/10/4
Y1 - 2021/10/4
N2 - The development, optimization, and assessment of new methods for the preparation of conjugated materials is key to the continued progress of organic electronics. Direct C-H activation methods have emerged and developed over the last 10 years to become an invaluable synthetic tool for the preparation of conjugated polymers for both redox-active and solid-state applications. Here, we evaluate direct (hetero)arylation polymerization (DHAP) methods for the synthesis of indaceno[1,2-b:5,6-b′]dithiophene-based polymers. We demonstrate, using a range of techniques, including direct visualization of individual polymer chains via high-resolution scanning tunneling microscopy, that DHAP can produce polymers with a high degree of regularity and purity that subsequently perform in organic thin-film transistors comparably to those made by other cross-coupling polymerizations that require increased synthetic complexity. Ultimately, this work results in an improved atom economy by reducing the number of synthetic steps to access high-performance molecular and polymeric materials.
AB - The development, optimization, and assessment of new methods for the preparation of conjugated materials is key to the continued progress of organic electronics. Direct C-H activation methods have emerged and developed over the last 10 years to become an invaluable synthetic tool for the preparation of conjugated polymers for both redox-active and solid-state applications. Here, we evaluate direct (hetero)arylation polymerization (DHAP) methods for the synthesis of indaceno[1,2-b:5,6-b′]dithiophene-based polymers. We demonstrate, using a range of techniques, including direct visualization of individual polymer chains via high-resolution scanning tunneling microscopy, that DHAP can produce polymers with a high degree of regularity and purity that subsequently perform in organic thin-film transistors comparably to those made by other cross-coupling polymerizations that require increased synthetic complexity. Ultimately, this work results in an improved atom economy by reducing the number of synthetic steps to access high-performance molecular and polymeric materials.
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U2 - 10.1021/acsmaterialslett.1c00478
DO - 10.1021/acsmaterialslett.1c00478
M3 - Article
AN - SCOPUS:85116187315
SN - 2639-4979
VL - 3
SP - 1503
EP - 1512
JO - ACS Materials Letters
JF - ACS Materials Letters
IS - 10
ER -