Photo- and Electro-Driven Molecular Switching System of Aryl-Bridged Photochromic Radical Complexes.

Abstract

Fast photochromic molecules have received much interest in the potential application as a real-time switching trigger in material and biological chemistry. Pentaarylbiimidazole (PABI) and phenoxyl-imidazolyl radical complex (PIC) are one of the fast photochromic molecules based on imidazolyl radicals. Because the photochromic reaction of these fast photochromic molecules proceeds from the optically forbidden S1 state, it is difficult to estimate the excitation energy to induce the photochromic reactions by spectroscopic techniques. In this study, we performed the electrochemical measurements for PABI and PIC to investigate the electronic properties and to determine the S0-S1 transition energies. In addition, we also revealed that the electrochemical reduction of PABI and PIC generates the radical anion which spontaneously shows the C-N bond breaking reaction to produce the radical species. The initial photochromic dimer is reproduced by the reversible oxidation of the anion species. This characteristic photochromic and electrochromic properties can be applicable to the photowritable electrochromic devices with high spatial resolution.