Rational classification of a series of aromatic donor–acceptor systems within the twisting intramolecular charge transfer model, a time-dependent density-functional theory investigation.

The goal of this paper is to rationalize the fluorescence activity, experimentally observed for 21 molecules of the same family as the 4-(N,N-dimethyl)anilines, based on their potential energy surfaces calculated within the twisting intramolecular charge transfer model. A classification in four groups is proposed according to the sign of two parameters, ΔE[sup gap], characterizing the energy difference between the vertical locally and charge transfer excited states, and ΔE[sup 1S] (or ΔE[sup 1S] for pretwisted systems), representing the energy gain of the charge transfer excited state with a perpendicular conformation compared to the first vertical excited state. In this study, the time-dependent density-functional theory has been used to calculate the potential energy surfaces of the ground and excited states along the twisting angle. Computed excitation energies and optimized ground state geometries have been obtained with both B3LYP and MPW1PW91 functionals using a 6-311+G(2d,p), and a 6-31G(d) basis set, respectively. From this study, it follows that ΔE[sup gap] and ΔE[sup 1S] are the main parameters necessary to understand the fluorescence activity of these molecules. The fact that the same fluorescence activity is observed for the members of each group (or subcategory for the particular case of group II), reveals the underlying twisting mechanism as a common process for all the investigated molecules, which explains their experimental dual and nondual emission. © 2003 American Institute of Physics. [ABSTRACT FROM AUTHOR]