Affiliation:
1. Institute of Inorganic Chemistry and Institute for Sustainable Chemistry & Catalysis with Boron (ICB) Julius-Maximilians-Universität Würzburg Am Hubland 97074 Würzburg Germany
Abstract
AbstractDespite the great success of the concept of doping organic compounds with BN units to access new materials with tailored properties, its use in polymer chemistry has only been realized quite recently. Herein, we present a comprehensive study of oligo‐ and poly(arylene iminoborane)s comprising a backbone of phenylene or thiophene moieties, as well as combinations thereof, linked via B=N units. The novel polymers can be regarded as BN analogues of poly(p‐phenylene vinylene) (PPV) or poly(thiophene vinylene) (PTV) or their copolymers. Our modular synthetic approach allowed us to prepare four polymers and 12 monodisperse oligomers with modulated electronic properties. Alternating electron‐releasing diaminoarylene and electron‐accepting diborylarylene building blocks gave rise to a pronounced donor‐acceptor character. Effective π‐conjugation over the arylene iminoborane backbone is evidenced by systematic bathochromic shifts of the low‐energy UV‐vis absorption maximum with increasing chain length, which is furthermore supported by crystallographic and computational investigations. Furthermore, all compounds investigated show emission of visible light in the solid state and aggregation‐induced emission (AIE) behavior, due to the presence of partially flexible linear B=N linkages in the backbone.
Funder
Deutsche Forschungsgemeinschaft
Subject
General Chemistry,Catalysis,Organic Chemistry
Cited by
6 articles.
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