π扩展和n掺杂的荧光蒽

IF 3.6 2区 化学 Q1 CHEMISTRY, ORGANIC
Franziska Spruner von Mertz, Jonas Polkaehn, Alexander Villinger, Peter Ehlers, Peter Langer
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引用次数: 0

摘要

合成了新型π扩展和n掺杂的荧光蒽,并对其进行了深入的研究。这八个未取代的化合物是在以CH活化为最后一个关键反应步骤的多步合成中得到的。这些结构在荧光蒽支架上的π膨胀位置和吡啶氮原子的位置不同。这有助于深入研究荧光蒽结构的这种变化对其整体性质的影响。因此,研究了这些多芳杂环的光学和电化学性质,并进行了DFT/TD-DFT和NICS计算。本文对b型和l型、j型扩展型和n型掺杂型荧光蒽进行了深入的研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

π-Expanded and N-Doped Fluoranthenes

π-Expanded and N-Doped Fluoranthenes
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.
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来源期刊
Journal of Organic Chemistry
Journal of Organic Chemistry 化学-有机化学
CiteScore
6.20
自引率
11.10%
发文量
1467
审稿时长
2 months
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.
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