Equilibrium and thermodynamic studies of chromic overcrowded fluorenylidene-acridanes with modified fluorene moieties

Chromic materials, an important class of stimuli-responsive materials, have aroused extensive attention in recent years. Normally, their color is based on changes in morphology. Few examples of chromic material based on conformational isomerization, such as in overcrowded alkenes, have been reported previously. Furthemore, experimental thermodynamic studies of overcrowded bistricyclic aromatic enes have not been carried out to our knowledge. Here, we show that N-phenyl-substituted fluorenylidene-acridanes, with a properly modified fluorene moiety, performs chromisms originating from conformational changes. Thermodynamic studies determine equilibrium constants, changes in enthalpy, entropy, and free energy in solution, enabling in-depth understanding of the equilibrium behavior of overcrowded alkenes and providing useful information for designing functional chromic compounds. Single-crystal X-ray diffraction analysis of fluorenylidene-acridanes in this work clearly shows well-tuned charge transfer from the acridane to the fluorene moiety. Various chromic behaviors such as mechanochromism, thermochromism, solvatochromism, vapochromism, and proton-induced chromism also support understanding of conformational isomerism. Bicyclic aromatic olefins are promising chromic materials but the equilibrium between their folded and twisted conformers is not well understood. Here, a combination of experimental and computational methods allows measurement of the equilibrium constants and thermodynamic parameters, offering insight into their chromic behaviour.