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基于氮杂蒽的电活性材料:制备、结构、电化学、光谱学及应用——综述

Azaacenes Based Electroactive Materials: Preparation, Structure, Electrochemistry, Spectroscopy and Applications-A Critical Review.

作者信息

Kotwica Kamil, Wielgus Ireneusz, Proń Adam

机构信息

Institute of Physical Chemistry, Polish Academy of Sciences, Kasprzaka 44/52, 01-224 Warszawa, Poland.

Faculty of Chemistry, Warsaw University of Technology, Noakowskiego 3, 00-664 Warszawa, Poland.

出版信息

Materials (Basel). 2021 Sep 8;14(18):5155. doi: 10.3390/ma14185155.

Abstract

This short critical review is devoted to the synthesis and functionalization of various types of azaacenes, organic semiconducting compounds which can be considered as promising materials for the fabrication of n-channel or ambipolar field effect transistors (FETs), components of active layers in light emitting diodes (LEDs), components of organic memory devices and others. Emphasis is put on the diversity of azaacenes preparation methods and the possibility of tuning their redox and spectroscopic properties by changing the C/N ratio, modifying the nitrogen atoms distribution mode, functionalization with electroaccepting or electrodonating groups and changing their molecular shape. Processability, structural features and degradation pathways of these compounds are also discussed. A unique feature of this review concerns the listed redox potentials of all discussed compounds which were normalized vs. Fc/Fc. This required, in frequent cases, recalculation of the originally reported data in which these potentials were determined against different types of reference electrodes. The same applied to all reported electron affinities (EAs). EA values calculated using different methods were recalculated by applying the method of Sworakowski and co-workers (Org. Electron. 2016, 33, 300-310) to yield, for the first time, a set of normalized data, which could be directly compared.

摘要

这篇简短的批判性综述致力于各类氮杂蒽的合成与功能化,氮杂蒽是一类有机半导体化合物,可被视为制造n沟道或双极性场效应晶体管(FET)、发光二极管(LED)有源层组件、有机存储器件组件等的有前景的材料。重点在于氮杂蒽制备方法的多样性,以及通过改变C/N比、改变氮原子分布模式、用电受体或给电子基团进行功能化以及改变其分子形状来调节其氧化还原和光谱性质的可能性。还讨论了这些化合物的可加工性、结构特征和降解途径。本综述的一个独特之处在于列出了所有讨论化合物相对于Fc/Fc归一化的氧化还原电位。这在很多情况下需要重新计算最初报道的数据,其中这些电位是相对于不同类型的参比电极测定的。这同样适用于所有报道的电子亲和能(EA)。使用不同方法计算的EA值通过应用Sworakowski及其同事的方法(《有机电子学》,2016年,33卷,300 - 310页)进行重新计算,首次得到了一组可直接比较的归一化数据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4887/8472324/eddd175e2ef2/materials-14-05155-g001.jpg

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