Is the origin of green fluorescence in unsymmetrical four-ring bent-core liquid crystals single or double proton transfer?

The origin of green fluorescence in unsymmetrical four-ring bent-core liquid crystals (BCLCs) is not understood clearly. There is no analysis of the photo-physical properties, in particular, excited state dynamical behaviour of these molecules. Because of the availability of two proton transfer sites in these systems, there is no clear explanation of the involvement of single or double proton transfer reactions in the origin of large Stokes shifted green fluorescence band. Therefore, we employ the femtosecond transient absorption spectroscopy technique to recognize the formation of transient species in the excited state and its associated dynamics in the Femto-picosecond time domain. In order to validate the experimental photo-physical properties, the time-dependent density functional theory (TDDFT) calculations have performed. Our results indicate that the four-ring bent-core system is an excellent example of exhibiting two proton transfer reactions in a sequential process. Further, these two proton transfer sites are not coupled electronically to each other; therefore, monoketo and diketo tautomer exhibit very close absorption and emission positions. The large Stokes shifted green emission in these systems is mainly contributed by monoketo tautomer (MK-C*). The linking ester functional group of both sites plays a significant role in controlling the rate of proton transfer reactions. A good correlation observed between theoretical and experimental results.