Affiliation:
1. Institute of Inorganic Chemistry and Institute for Sustainable Chemistry and Catalysis with Boron (ICB) Julius‐Maximilians‐Universität Würzburg Am Hubland 97074 Würzburg Germany
Abstract
AbstractAn unprecedented poly(thiophene iminoborane)—a boron–nitrogen analogue of the well‐established conjugated organic polymer poly(thiophene vinylene)—is presented. The polymer synthesis is achieved by selective Si/B exchange polycondensation of a 2,5‐diborylthiophene with a 2,5‐diaminothiophene derivative. For the latter, a facile synthetic strategy is devised, which makes this versatile, strongly electron‐releasing building block easily accessible. The novel polymer and a series of monodisperse thiophene iminoborane oligomers reveal systematic bathochromic shifts in their absorption with increasing chain length, and thus extended π‐conjugation over the BN units along the backbone, which is further supported by TD‐DFT calculations.
Funder
Deutsche Forschungsgemeinschaft
Deutsche Bundesstiftung Umwelt
Subject
Materials Chemistry,Polymers and Plastics,Organic Chemistry
Cited by
3 articles.
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