Abstract
The effect of microsolvation on excited-state proton transfer (ESPT) reaction of 3-hydroxyflavone (3HF) and its inclusion complex with gamma-cyclodextrin (gamma-CD) was studied using computational approaches. From molecular dynamics simulations, two possible inclusion complexes formed by the chromone ring (C-ring, Form I) and the phenyl ring (P-ring, Form II) of 3HF insertion to gamma-CD were observed. Form II is likely more stable because of lower fluctuation of 3HF inside the hydrophobic cavity and lower water accessibility to the encapsulated 3HF. Next, the conformation analysis of these models in the ground (S-0) and the first excited (S-1) states was carried out by density functional theory (DFT) and time-dependent DFT (TD-DFT) calculations, respectively, to reveal the photophysical properties of 3HF influenced by the gamma-CD. The results show that the intermolecular hydrogen bonding (interHB) between 3HF and gamma-CD, and intramolecular hydrogen bonding (intraHB) within 3HF are strengthened in the S-1 state confirmed by the shorter interHB and intraHB distances and the red-shift of O-H vibrational modes involving in the ESPT process. The simulated absorption and emission spectra are in good agreement with the experimental data. Significantly, in the S-1 state, the keto form of 3HF is stabilized by gamma-CD, explaining the increased quantum yield of keto emission of 3HF when complexing with gamma-CD in the experiment. In the other word, ESPT of 3HF is more favorable in the gamma-CD hydrophobic cavity than in aqueous solution.
