Nonadiabatic Coupling Dictates the Site-Specific Excited-State Decay Pathways of Fluorophenols.

Abstract

In this paper, a combined photophysical and electronic structure theory study demonstrating a remarkable site-specific fluorine substitution effect on the excited-state dynamics of monofluorophenols has been presented. The S₁ ← S₀ electronic origin band of phenol is shifted to a longer wavelength for para substitution, but to shorter wavelengths for ortho and meta substitutions. The observed sequence of excitation wavelengths of 2-fluorophenol (2FP) < 3-fluorophenol (3FP) < phenol < 4-fluorophenol (4FP) is consistent with the transition energies predicted by TDDFT/CAMB3LYP/6-311++G(d,p) and CASSCF(8,8)/Dunning cc-pVDZ theoretical methods. The most notable contrast of excited-state dynamics is revealed in the different features of the fluorescence spectra; the fluorescence yield of 4FP is almost 6 times larger compared to that of 3FP and the spectral bandwidth of 2FP is nearly 1.5 times larger than that of 4FP. Electronic structure calculation predicts a low-energy S₁/S₀ conical intersection (CI) near the ¹ππ* minimum with respect to the prefulvenic vibronic mode of the aromatic ring, and the energetic location of this CI is altered with the substitution site of the fluorine atom. The predicted energy barrier to this prefulvenic CI is smallest for 3FP but largest for 4FP, leading to a facilitated nonradiative electronic relaxation of the former (3FP), and emission occurs with a much diminished fluorescence intensity.