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The Excited-State Decay of 1-Methyl-2(1H)-pyrimidinone is an Activated Process

✍ Scribed by Gerald Ryseck; Thomas Schmierer; Karin Haiser; Dr. Wolfgang Schreier; Prof. Dr. Wolfgang Zinth; Prof. Dr. Peter Gilch


Publisher
John Wiley and Sons
Year
2011
Tongue
English
Weight
598 KB
Volume
12
Category
Article
ISSN
1439-4235

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✦ Synopsis


Abstract

The photophysics of 1‐methyl‐2(1__H__)‐pyrimidinone (1MP) dissolved in water is investigated by steady‐state and time‐resolved fluorescence, UV/Vis absorption, and IR spectroscopy. In the experiments, excitation light is tuned to the lowest‐energy absorption band of 1MP peaking at 302 nm. At room temperature (291 K) its fluorescence lifetime amounts to 450 ps. With increasing temperature this lifetime decreases and equals 160 ps at 338 K. Internal conversion (IC) repopulating the ground state and intersystem crossing (ISC) to a triplet state are the dominant decay channels of the excited singlet state. At room temperature both channels contribute equally to the decay, that is, the quantum yields of IC and ISC are both approximately 0.5. The temperature dependence of UV/Vis transient absorption signals shows that the activation energy of the IC process (2140 cm^−1^) is higher than that of the ISC process (640 cm^−1^).


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