Distinction of trans–cis photoisomers with comparable optical properties in multiple-state photochromic systems – examining a molecule with three azobenzenes via in situ irradiation NMR spectroscopy

N shifts reveals that the configuration of one sidechain has an influence on the chemical shifts of both the other sidechains. Interconversion kinetics upon irradiation with ultraviolet (UV) light as well as molar fractions in photostationary states (PSS) were examined. Analysis of thermal fading of the different photoisomers into the ground state shows that thermal relaxation rates of all three azobenzene moieties behave as if they were independent of each other.