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首页> 外文期刊>Chemistry: A European journal >From-Core and From-End Direct CH Arylations: A Step-Saving New Synthetic Route to Thieno[3,4-c]pyrrole-4,6-dione (TPD)-Incorporated D---A--D Functional Oligoaryls
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From-Core and From-End Direct CH Arylations: A Step-Saving New Synthetic Route to Thieno[3,4-c]pyrrole-4,6-dione (TPD)-Incorporated D---A--D Functional Oligoaryls

机译:从核心和从末端直接CH芳基化:一步步节省的新方法合成Thieno [3,4-c]吡咯-4,6-dione(TPD)掺入D--A--D功能性低聚芳基

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摘要

In contrast to the traditional multistep synthesis, herein an efficient and fewer-steps new synthetic strategy is demonstrated for the facile preparation of organic-electronically important D--A--D-type oligoaryls through sequential direct CH arylations. This methodology has shown that the synthesis of thieno[3,4-c]pyrrole-4,6-dione (TPD)- or furano[3,4-c]pyrrole-4,6-dione (FPD)-centred target molecules could be accessed step-economically either from the core structure (acceptor) or from the end structure (donor), which supplied a more flexible and succinct new synthetic alternative to the preparation of the -functional small-molecule semiconducting materials. In addition, optical and electrochemical properties of the synthesized oligoaryls were examined.
机译:与传统的多步合成相反,本文证明了一种有效且少步的新合成策略,可通过连续的直接CH芳基化轻松制备有机电子重要的D-A-D型低聚芳基。该方法学表明以噻吩并[3,4-c]吡咯-4,6-二酮(TPD)-或呋喃并[3,4-c]吡咯-4,6-dione(FPD)为中心的靶分子的合成可以从核心结构(受体)或末端结构(供体)经济地进行步入,这为制备功能性小分子半导体材料提供了更灵活,简洁的新合成替代品。另外,检查了合成的低聚芳基的光学和电化学性质。

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