Article ID Journal Published Year Pages File Type
5375911 Chemical Physics 2008 11 Pages PDF
Abstract
Pigment Yellow 101 (P.Y.101) is a fluorescent yellow pigment which exhibits a surprisingly rich photochemistry of several competing reaction pathways as revealed by recent time-resolved femtosecond experiments. Our elaborate quantum chemical investigations employing density functional theory (DFT) and time-dependent DFT (TDDFT) show that the observed fluorescence competes with excited state intramolecular proton transfer and trans-cis isomerization processes. Moreover, the experimentally observed spectral features of the complicated excited state dynamics can be assigned to stable trans-diol, trans-keto and cis-diol, cis-keto isomers on the ground and excited state surfaces. Still, due to its molecular size P.Y.101 poses a challenge to electronic structure theory and many problems occur in particular with respect to the excited state calculations. Thus, P.Y.101 serves also as an educative example for which TDDFT yields a reasonable vertical electronic spectrum, but fails in the prediction of excited state structures, when standard GGA or hybrid functionals with low fractions of Hartree-Fock exchange are employed. This failure is attributed to the charge-transfer failure of TDDFT.
Related Topics
Physical Sciences and Engineering Chemistry Physical and Theoretical Chemistry
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