Affiliation:
1. Current address: Institute of Organic Chemistry II and Advanced Materials Ulm University Albert-Einstein-Allee 11 89081 Ulm Germany
2. Institute of Organic Chemistry University of Freiburg Albertstraße 21 79104 Freiburg Germany
3. Cluster of Excellence livMatS @ FIT - Freiburg Center for Interactive Materials and Bioinspired Technologies University of Freiburg Georges-Köhler-Allee 105 79110 Freiburg Germany
Abstract
AbstractWith their bent π‐systems, cyclic conjugation and inherent cavities, conjugated nanohoops are attractive for organic electronics applications. For ease of processing and morphological stability, an incorporation into polymers is desirable, but to date was hampered with few exceptions by synthetic difficulties. We herein present a unique strategy for the synthesis of conjugated nanohoop polymers using a dibenzo[a,e]pentalene (DBP) as central connector. We demonstrate this versatility by synthesizing three electronically diverse copolymers with dithienyldiketo(pyrrolopyrrol), fluorene and carbazole comonomers, and report the first donor‐acceptor nanohoop polymer. Optoelectronic investigations reveal the prevalence of cyclic or linear conjugation, depending on the comonomer unit, and ambipolar electrochemical properties through the antiaromatic character of the DBP units. As the first report on using conjugated nanohoops for charge storage as positive electrode materials, we show a significant improvement in battery performance in a nanohoop‐containing polymer compared to an equivalent nanohoop‐free reference polymer. We believe this study will pave the way for the synthesis of a diverse range of nanohoop polymers and further stimulate their exploration for charge storage in batteries.
Funder
Deutsche Forschungsgemeinschaft
Cited by
1 articles.
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