Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5390618 | Chemical Physics Letters | 2006 | 6 Pages |
Abstract
Phototherapy of neonatal jaundice involves Z-E-isomerisation around an exocyclic double bond in bilirubin. Our results of a CASSCF study on dipyrrinone, a bilirubin model, show a conical intersection between the ground and first excited singlet states associated with the Z-E-isomerisation. The conical intersection, located ca. 50Â kJ/mol below the Franck-Condon-point, together with the S1 minimum, ca. 50Â kJ/mol below the conical intersection, are able to explain the available time-resolved spectroscopic data (the very short lifetime of the initially excited state and transient 'dark state' intermediate) as well as bilirubin's very low fluorescence quantum yield and the medium-efficient photoisomerisation reaction.
Related Topics
Physical Sciences and Engineering
Chemistry
Physical and Theoretical Chemistry
Authors
Burkhard Zietz, Fredrik Blomgren,