Photophysical properties of push-pull monocationic D-π-A thiophene based derivatives: Fluorosolvatochromism and pH studies.

Photophysical properties of two thiophene salts of the form D-π-A are studied in several solvents and at various pH values of the aqueous solution. The studied compounds embrace methoxy group as electron donating moiety at one end and cationic amidine group with and without fluorine atom at the ortho position of the amidine group as the electron withdrawing group at the other end of the molecules and separated by thiophene ring. The two thiophene derivatives are 4-(5-(4-methoxyphenyl)thiophen-2-yl)benzamidine hydrochloride salt (MOTB) and 2-fluoro-4-(5-(4-methoxyphenyl) thiophen-2-yl)benzamidine hydrochloride salt (FMOTB). The observed changes in the fluorescence emission spectra with the nature of the solvent were found to be much more pronounced than the corresponding absorption spectra which signify an emission from the intramolecular charge transfer state. The higher bathochromic shift in the fluorescence emission spectra than the absorption spectra indicates that the excited state dipole moment is larger than that of the ground state. It has also been observed that the presence of the fluorine atom in the electron withdrawing part does not show any changes in the absorption spectra while a clear bathochromic shift is observed in the fluorescence emission spectra indicating an enhanced strength of the electron withdrawing ability in case of FMOTB. Effect of pH was also studied and pK values were evaluated. The observed photophysical properties were correlated to the normalized solvent polarity parameter (E) when solvents are classified to protic and aprotic solvents. This designates the importance of hydrogen bonding interactions. We have also applied a couple of linear solvation energy relationships for better understanding of the exact contribution of each solvent parameter on each photophysical property. We have found that both Catalán's and Laurence's treatments show that the photophysical properties are mainly controlled by the solvent's non-specific interactions. However, these models were not sufficient to interpret the observed data without the inclusion of the participation of the specific interactions.