Madhuri Mukhopadhyay

Spectral Signatures of Intramolecular Charge Transfer Process in β-Enaminones: A Combined Experimental and Theoretical Analysis

In this paper, we present spectroscopic signatures of intramolecular charge transfer (ICT) and effects of solvent on the ICT process in 3-(phenylamino)-2-cyclohexen-1-one (PACO), a member of the well-known molecular family, the beta-enaminones. The dual fluorescence in the steady state emission spectra of the molecule in polar solvents indicates the occurrence of ICT, which is further supported by time-resolved studies, using time correlated single photon counting technique with picosecond resolution. To understand the nature of the charge transfer, pH dependent studies of the probe in water were performed, where a quenching of fluorescence was observed even in the presence of very low concentrations of acids. Solvent induced fluorescence quenching was observed in ethanol and methanol. The ICT process was also investigated by quantum chemical calculations. To understand the role of solvents in the ICT process, we have theoretically studied the macroscopic and microscopic solvation of the probe in water. The absorption spectra of the molecule in the gas phase as well as in water were simulated using time dependent density functional theory with cc-pVTZ basis set and self-consistent reaction field theory that models macroscopic solvation. The possibility of microscopic solvation in water was probed theoretically and the formation of 1:3 molecular clusters by PACO with water molecules has been confirmed. Our findings could have a bearing on pH sensing applications of the probe.

Nanopools Governing Proton Transfer in Diametrical Ways in the Ground and Excited State

We present here the effects of geometrically constrained environments on the proton transfer reaction of 4-methyl 2,6-diformyl phenol (MFOH) both in the ground and excited states by employing steady-state and time-resolved fluorescence spectroscopy having picosecond and femtosecond resolutions. The nanometer-sized water pools formed in the ternary microemulsion of n-heptane-aerosol OT-water promote reprotonation of the probe. As we go on increasing the water content up to a certain value in the ground state whereas deprotonation is favored in the excited state. The emission intensity has a complex behavior as the water content is changed in the system. The lower fluidity of confined water within the reverse micelle with respect to the normal bulk water alters the related dynamics of the H-bonded network. These observations are rationalized on the basis of altered ionic water activity in the confined surroundings, i.e., on dielectric constant, ionic mobility, pH, and the favorable orientation of dipoles in the medium. Our observations might be helpful to infer about the characteristics of nanoreactors, which often mimic many biological hydrophilic pockets.

Effect of Surfactant-Perturbed Nanocaging on the Ground and Excited State Proton Transfer Reaction

The effect of mixed cyclodextrin-surfactant systems on the ground and excited state proton transfer reactions of 4-methyl-2,6-diformylphenol (MFOH) in aqueous solution has been investigated by steady state and time-resolved fluorescence spectroscopy. It has been found that micellar media perturbs the solvation of MFOH and facilitates nanocaging. In the presence of micelle, MFOH preferentially resides in the interfacial region. Depending on the local pH due to compartmentalization of reaction media, normal or anionic form of MFOH dominates. Encapsulation of the probe within the cyclodextrin nanocavity enhances the shorter lifetime component of MFOH unexpectedly, which has been explained on the basis of reduced solvation and reduced dipolar effect due to confinement.