@article {6768, title = {Brazilwood Reds: The (Photo)Chemistry of Brazilin and Brazilein}, journal = {Journal of Physical Chemistry A}, volume = {117}, year = {2013}, note = {

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Rondao, Raquel Sergio Seixas de Melo, J. Pina, Joao Melo, Maria J. Vitorino, Tatiana Jorge Parola, A.
POCI [PTDC/QUI-QUI/099388/2008]; FCT [SFRH/BD/38882/2007]; FEDER/COMPETE; T.V. a BI grant [PTDC/EAT-EAT/104930/2008]; REQUIMTE [PEst-C/EQB/LA0006/2011]; CQC [PEst-C/QUI/UI0313/2011]
We are grateful to POCI (project PTDC/QUI-QUI/099388/2008), FCT and FEDER/COMPETE for further funding. RR acknowledges FCT for a Ph.D. grant (SFRH/BD/38882/2007), and T.V. a BI grant under Project PTDC/EAT-EAT/104930/2008. Finally, we thank REQUIMTE supporting project PEst-C/EQB/LA0006/2011 and CQC supporting project PEst-C/QUI/UI0313/2011.
Amer chemical soc
Washington

}, month = {2013}, pages = {10650-10660}, abstract = {

The ground and excited state (in the singlet state, S-1) acid-base equilibria, together with the photophysical properties of the two main constituents of brazilwood, brazilin and brazilein, have been investigated in aqueous solutions in the pH range: -1 \< pH \< 10. Brazilin is the colorless reduced form of brazilein where three ground and three excited state species (BredHn, with n = 2-4 representing the protonated hydroxyl groups) are observed with two corresponding acidity constants: pK(a1) = 6.6 and pK(a2) = 9.4 (pK(a1)(*) = 4.7 and pK(a2)(*) = 9.9, obtained from the Forster cycle). In the case of brazilein, three ground species (pK(a1) = 6.5 and pK(a2) = 9.5) and four excited state species were identified (again from the Forster cycle: pK(a1)(*) = 3.9 and pK(a2)(*) = 9.8). The colorless species (brazilin) presents a high fluorescence quantum yield (phi(F) = 0.33) and competitive radiative channel (k(F) = 1.3 x 10(9) s(-1)) over radiationless processes (k(NR) = 2.6 x 10(9) s(-1)). In contrast to this behavior, brazilein displays a phi(F) value 2 orders of magnitude lower and a dominance of the radiationless decay pathways, which is suggested to be linked to an excited state proton transfer leading to a quinoidal-like structure. This is further supported by time-resolved data (obtained in a ps time domain). The overall data indicates that brazilin is more prone to degradation than brazilein, mainly due to the high efficiency of the racliationless decay channel (likely through internal conversion), which confers a stabilizing inherent characteristic to the latter. In the case of brazilein, the efficiency of the radiationless channel is linked to an excited state intramolecular proton transfer resulting from an excited state equilibrium involving neutral and zwitterionic tautomeric species of this compound. Furthermore, a theoretical study has been performed with the determination of the optimized ground-state and excited molecular geometries for the two compounds together with the prediction of the lowest vertical one-electron excitation energy and the relevant molecular orbital contours and charge densities changes using density functional theory calculations. These were found to corroborate differences in acidity in the ground and excited states.

}, isbn = {1089-5639}, url = {://WOS:000326126100010}, author = {Rondao, R. and de Melo, JSS and Pina, J and Melo, MJ and Vitorino, T. and A. J. Parola} }