Franziska Spruner von Mertz, Jonas Polkaehn, Alexander Villinger, Peter Ehlers, Peter Langer
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Novel π-expanded and N-doped fluoranthenes were synthesized and thoroughly investigated. These eight unsubstituted compounds are obtained in a multistep synthesis with CH activation as the last key reaction step. The structures vary in their position of π-expansion on the fluoranthene scaffold and the location of the pyridinic nitrogen atom. This facilitates an in-depth investigation of the impact of such alterations in the fluoranthene structure on their overall properties. Accordingly, optical and electrochemical properties of these polyaromatic heterocycles were investigated, and DFT/TD-DFT and NICS calculations were performed. This paper entails a thorough study on b- and l,j-expanded and N-doped fluoranthenes.
期刊介绍:
Journal of Organic Chemistry welcomes original contributions of fundamental research in all branches of the theory and practice of organic chemistry. In selecting manuscripts for publication, the editors place emphasis on the quality and novelty of the work, as well as the breadth of interest to the organic chemistry community.