Understanding the differences in photochemical properties of substituted aminopyrimidines (original) (raw)
2011, Theoretical Chemistry Accounts
The luminescent patterns of several members of the aminopyrimidine family are very different, showing not fluorescence at all, only a fluorescence band, normal or anomalous, or dual fluorescence, depending on the substituents and on the environment (gas phase vs. polar solvents). In this work, we study the lowest excited states of several members of this family that exhibit different fluorescence patterns to try to explain their photochemistry and to understand the effect of the substituents and the environment. We have found that several excited states (local excited (LE), charge transfer (CT) and n N-p* states) have minima on the lowest excited potential energy surface (S 1), being their relative energy the determinant factor of the luminescent behavior. If the more stable S 1 minima are of n N-p* character, a non-radiative deexcitation channel is the most efficient and the system shows no fluorescence. If the CT and/or LE states are the most stable, the non-radiative deactivation channel is not accessible and the system fluoresces. The relative energies of the CT and LE minima (affected by substituents and by the presence of a polar solvent) and the different magnitude of the oscillator strength for the radiative transition to the ground state determine which emission is more efficient, giving place to normal, anomalous or dual fluorescence. The study has been carried out by CASSCF/CASPT2 computations, including the solvent effect by means of the PCM model. Keywords Photochemistry Á Intramolecular charge transfer Á Fluorescence Á Aminopyrimidines Á Ab initio calculations Published as part of the special issue celebrating theoretical and computational chemistry in Spain.
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