The Excited‐State N−H Tautomerization Rate in Free‐Base Corroles

Abstract

AbstractCorrole is a tetrapyrrolic dye with a structure that resembles porphyrin, apart from a single missing carbon. The absence of this carbon results in the re‐arrangement of the double bonds within the macrocycle, and the presence of three pyrrolic protons in the central cavity in its free‐base form. These protons lead to the existence of two distinct tautomeric structures that exist in a dynamic equilibrium. Although the ground‐state energies of the tautomers are similar, the excited states show a significant difference in energy which unbalances the equilibrium between the tautomers and results in rapid excited‐state tautomerization, favouring one tautomeric species over the other. Although the excited‐state tautomerization process has been known for a long time, very few studies have been performed on it, leaving many key aspects of the process poorly understood. Herein we show how ultrafast photoluminescence can be used to experimentally determine the rates of excited‐state tautomerization and activation energies of three free‐base corrole derivatives thus allowing us to completely describe the excited‐state dynamics of the unusual excited state of free‐base corrole and opening the door to the development of new materials that can exploit its unique characteristics.