Synthesis, Stable Radical Anion and Energy Storage Performance of Pentacene Tetraimides

Abstract Imide functionalization has been widely proved to be an effective approach to enrich optoelectronic properties of polycyclic aromatic hydrocarbons (PAHs). However, appending multiple imide groups onto linear acenes is still a synthetic challenge. Herein, we demonstrate that by taking advantage of a “breaking and mending” strategy, a linear pentacene tetraimides (PeTI) was synthesized through a three‐step sequence started from the naphthalene diimides (NDI). Compared with the parent pentacene, PeTI shows a deeper‐lying lowest unoccupied molecular orbital (LUMO) energy level, narrower band gap and better stability. The redox behavior of PeTI was firstly evaluated by generating a stable radical anion specie with the assistance of cobaltocene (CoCp 2 ), and the structure of the electron transfer (ET) complex was confirmed by the X‐ray crystallography. Moreover, due to the presence of multiple redox‐active sites, we are able to show that the state‐of‐the‐art energy storage performance of the dealkylated PeTI (designated as PeTCTI) in organic potassium ion batteries (OPIBs) as an anode. Our results shed light on the application of multiple imides functionalized linear acenes, and the reported synthetic strategy provides an effective way to get access to longer nanoribbon imides with fascinating electronic properties.