TY - JOUR
T1 - Fused electron deficient semiconducting polymers for air stable electron transport
AU - Onwubiko, Ada
AU - Yue, Wan
AU - Jellett, Cameron
AU - Xiao, Mingfei
AU - Chen, Hung Yang
AU - Ravva, Mahesh Kumar
AU - Hanifi, David A.
AU - Knall, Astrid Caroline
AU - Purushothaman, Balaji
AU - Nikolka, Mark
AU - Flores, Jean Charles
AU - Salleo, Alberto
AU - Bredas, Jean Luc
AU - Sirringhaus, Henning
AU - Hayoz, Pascal
AU - McCulloch, Iain
N1 - Publisher Copyright:
© The Author(s) 2018.
PY - 2018/12/1
Y1 - 2018/12/1
N2 - Conventional semiconducting polymer synthesis typically involves transition metal-mediated coupling reactions that link aromatic units with single bonds along the backbone. Rotation around these bonds contributes to conformational and energetic disorder and therefore potentially limits charge delocalisation, whereas the use of transition metals presents difficulties for sustainability and application in biological environments. Here we show that a simple aldol condensation reaction can prepare polymers where double bonds lock-in a rigid backbone conformation, thus eliminating free rotation along the conjugated backbone. This polymerisation route requires neither organometallic monomers nor transition metal catalysts and offers a reliable design strategy to facilitate delocalisation of frontier molecular orbitals, elimination of energetic disorder arising from rotational torsion and allowing closer interchain electronic coupling. These characteristics are desirable for high charge carrier mobilities. Our polymers with a high electron affinity display long wavelength NIR absorption with air stable electron transport in solution processed organic thin film transistors.
AB - Conventional semiconducting polymer synthesis typically involves transition metal-mediated coupling reactions that link aromatic units with single bonds along the backbone. Rotation around these bonds contributes to conformational and energetic disorder and therefore potentially limits charge delocalisation, whereas the use of transition metals presents difficulties for sustainability and application in biological environments. Here we show that a simple aldol condensation reaction can prepare polymers where double bonds lock-in a rigid backbone conformation, thus eliminating free rotation along the conjugated backbone. This polymerisation route requires neither organometallic monomers nor transition metal catalysts and offers a reliable design strategy to facilitate delocalisation of frontier molecular orbitals, elimination of energetic disorder arising from rotational torsion and allowing closer interchain electronic coupling. These characteristics are desirable for high charge carrier mobilities. Our polymers with a high electron affinity display long wavelength NIR absorption with air stable electron transport in solution processed organic thin film transistors.
UR - http://www.scopus.com/inward/record.url?scp=85041358401&partnerID=8YFLogxK
U2 - 10.1038/s41467-018-02852-6
DO - 10.1038/s41467-018-02852-6
M3 - Article
C2 - 29379022
AN - SCOPUS:85041358401
SN - 2041-1723
VL - 9
JO - Nature Communications
JF - Nature Communications
IS - 1
M1 - 416
ER -