Supramolecular interaction between a hydrophilic coumarin dye and macrocyclic hosts: spectroscopic and calorimetric study.

The photophysics of a hydrophilic molecule, 7-(diethylamino)-coumarin-3-carboxylic acid (7-DCCA), was studied in the presence of two macrocycles, (2-hydroxypropyl)-γ-cyclodextrin and cucurbit[7]uril. We have used steady-state absorption, fluorescence, and time-resolved fluorescence emission spectroscopy; Fourier transform infrared (FTIR) spectroscopy; (1)H NMR spectroscopy; and isothermal titration calorimetry (ITC) to confirm the supramolecular host-guest complex formation. The spectral properties of 7-DCCA were modulated in the presence of both macrocycles. It was assigned that 7-DCCA forms a 1:2 complex with (2-hydroxypropyl)-γ-cyclodextrin and cucurbit[7]uril. The large modulation of the emission properties of 7-DCCA in the presence of the macrocycles indicates the formation of supramolecular complexes. A significant shift in the bond vibration frequencies in the FTIR studies showed encapsulation of the dyes in the hydrophobic cavity of the macrocycles. This is further substantiated by the (1)H NMR studies, in which the upfield and downfield shifts of the protons were observed in both the aliphatic and aromatic region in the presence of macrocycles. The time-resolved anisotropy measurements further reinforce the conception of host-guest supramolecular complex formation because, in both cases, the rotational relaxation time increases significantly compared to that in water. A deeper understanding between the differences in interaction of an anionic molecule with cucurbit[7]uril and (2-hydroxypropyl)-γ-cyclodextrin will be achieved through this work. From the ITC measurement, we have formulated the forces due to complex formation.