Abstract

The photoswitching behavior of new double cationic azobenzene derivatives AZOpyr and AZOimid were studied by in situ irradiation in the cavity of the 1H-NMR spectrometer. The setup of the experiments allowed us to easily collect and, at real-time, valuable spectral information to quantify the concentration of photoisomers without deconvolution of the data. With this information, the equilibrium constant and thermodynamics parameters of the photoinduced equilibrium at photostationary state were possible to determine. At the same time, this type of experiment also allowed us to obtain precise structural information (i.e., chemical shift, integration, and constant coupling of each isomer) based on the pattern of the signals of 1H-NMR spectra of the photoswitches. The same irradiation system was utilized to study the fatigue of the cationic AZOpyr and AZOimid in several solvents, finding that these probes are photostable in methanol, dimethyl sulfoxide, and propyl ammonium formate.