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| Content Provider | Royal Society of Chemistry (RSC) |
|---|---|
| Author | Previtali, Carlos Mario Churio, María Sandra Conde, Federico Rubén |
| Copyright Year | 2007 |
| Abstract | Characterization of the excited states of the mycosporine-like amino acid palythine (λmax = 320 nm) in aqueous solutions was achieved experimentally. The low value for the photodegradation quantum yield, (1.2 ± 0.2) × 10−5, confirms that palythine is highly photostable in air saturated-aqueous solutions. Laser flash photolysis of acetone in the presence of palythine allowed for the observation of a transient spectrum which is consistent with the triplet–triplet absorption of palythine. Kinetic treatment of the transient signals yields a lifetime of the triplet state of ca. 9 µs and a triplet energy around 330 kJ mol−1. The photoacoustic calorimetry results are consistent with non-radiative decay as the major fate of excited palythine. A comparison of the photodegradation quantum yields and photophysical properties of palythine with those previously determined for the other mycosporine-like amino acids, shinorine and porphyra-334, suggests that geometrical isomerization around the CN bond may contribute to the rapid deactivation of this group of molecules. |
| Starting Page | 669 |
| Ending Page | 674 |
| Page Count | 6 |
| File Format | HTM / HTML PDF |
| ISSN | 1474905X |
| Volume Number | 6 |
| Issue Number | 6 |
| Journal | Photochemical & Photobiological Sciences |
| DOI | 10.1039/b618314j |
| Language | English |
| Publisher | Royal Society of Chemistry |
| Access Restriction | Subscribed |
| Subject Keyword | Photodegradation Carboxylic acid Isomerization Covalent bond Calorimetry Mycosporine-like amino acid Flash photolysis Quantum tunnelling Acetone |
| Content Type | Text |
| Resource Type | Article |
| Subject | Physical and Theoretical Chemistry |
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