Szakács, Zoltán and Bojtár, Márton and Drahos, László and Hessz, Dóra and Kállay, Mihály and Vidóczy, Tamás and Bitter, István and Kubinyi, Miklós (2016) The kinetics and mechanism of photooxygenation of 4’-diethylamino-3-hydroxyflavone. PHOTOCHEMICAL & PHOTOBIOLOGICAL SCIENCES, 15. pp. 219-227. ISSN 1474-905X
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Abstract
The photolysis reactions of 4’-diethylamino-3-hydroxyflavone (D), a versatile fluorescent probe showing excited-state intramolecular proton transfer (ESIPT), and the magnesium chelate of D (MgD2+) have been studied in acetonitrile solution. Upon UV irradiation both species were oxidized into O-4-diethylaminobenzoyl salicylic acid, differently from the photoreaction of the parent compound 3-hydroxyflavone (3HF) which was described to undergo rearrangement to 3-hydroxy-3-phenyl-indan-1,2-dione. The photooxygenation of the Mg2+ complex was found to be significantly faster than the reaction of the pure dye. As the kinetic analysis of the absorption spectra of samples under irradiation showed, the rate coefficients for the oxygenations of the excited state dye and complex have close values, kox(D*) = 2.4 × 107 min−1, kox(MgD2+*) = 3.9 × 107 min−1; the difference arises from the higher photooxygenation quantum yield of the complex, Φ(MgD2+) = 2.3 × 10−3, than the respective value for the pure dye, Φ(D) = 1.5 × 10−4. The potential energy surface of the photooxygenation of D was calculated assuming a reaction path in which the phototautomer formed from D via ESIPT, reacts in its triplet state with triplet molecular oxygen O2, a mechanism similar to that suggested for the photoreaction of the parent 3HF. The moderate values for the transition state energies confirmed the plausibility of the hypothetical mechanism.
Item Type: | Article |
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Subjects: | Q Science / természettudomány > QD Chemistry / kémia > QD02 Physical chemistry / fizikai kémia |
Depositing User: | Dóra Hessz |
Date Deposited: | 10 Jun 2016 12:08 |
Last Modified: | 10 Jun 2016 12:08 |
URI: | http://real.mtak.hu/id/eprint/36240 |
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