Ultrafast deactivation of bilirubin: dark intermediates and two-photon isomerization.
Phys Chem Chem Phys
; 18(10): 7148-55, 2016 Mar 14.
Article
em En
| MEDLINE
| ID: mdl-26887629
ABSTRACT
Bilirubin is a neurotoxic product responsible for neonatal jaundice, which is generally treated by phototherapy. The photoreaction involves ultrafast internal conversion via an elusive intermediate and Z-E isomerization with minor yield (less than 3% in solution). The structure of the intermediate remains unclear. Here, the combination of UV-vis and mid-IR ultrafast transient absorption spectroscopy reports a comprehensive picture of the mechanism and provides essential structural information about the intermediate species. Thus, spectral dynamics during the earliest ps unveils a wavepacket travelling from the Franck-Condon region to the crossing point with a dark state. The latter shows a tighter molecular skeleton than the ground state and decays with 15 ps time constant. Remarkably, the relative contribution of a non-decaying component increases linearly with pump energy, suggesting that Z-E isomerization could also be triggered by two-photon excitation. Implications for the photochemistry of protein-bound open tetrapyrroles are discussed.
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1
Base de dados:
MEDLINE
Assunto principal:
Bilirrubina
Idioma:
En
Ano de publicação:
2016
Tipo de documento:
Article