Synthesis and Electron Accepting Properties of Two Di(benz[f]indenone)-Fused Tetraazaanthracene Isomers

We designed and synthesized a novel di­(benz­[f]­indenone)-fused tetraazaanthracene derivative and isolated its two isomers, 1a and 1s, having anti and syn configurations, respectively. Their structure and that of the condensation reaction intermediates, anti-2a and syn-2s, were fully characterized using one- and two-dimensional nuclear magnetic resonance spectroscopy and single-crystal X-ray diffraction. The optical and electronic properties of 1a and 1s were investigated using ultraviolet–visible absorption and fluorescence spectroscopies, cyclic voltammetry, and time-dependent density functional theory calculations. The presence of the carbonyl and ethynyltris­(isopropyl)­silane groups endows the di­(benzoindenone)-fused azaacene derivatives with a strong electron accepting character. With an electron affinity of approximately −3.7 eV, the two isomers represent attractive electron-deficient molecular systems for the generation of n-channel semiconducting materials. Organic field effect transistors of 1a and 1s showed electron transport, and organic solar cells gave a proof of concept of the potential of the two compounds as electron acceptor materials when they are paired with an electron donor polymer.