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Theoretical study on the excited states of psoralen compounds bonded to a thymine residue
Author(s) -
Nakata A.,
Baba T.,
Takahashi H.,
Nakai H.
Publication year - 2003
Publication title -
journal of computational chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.907
H-Index - 188
eISSN - 1096-987X
pISSN - 0192-8651
DOI - 10.1002/jcc.10380
Subject(s) - excited state , pyrone , psoralen , thymine , photochemistry , chemistry , furocoumarins , furan , singlet state , excitation , density functional theory , ultraviolet , computational chemistry , atomic physics , materials science , stereochemistry , organic chemistry , optoelectronics , physics , dna , biochemistry , quantum mechanics
Time‐dependent density functional theory calculations have been performed for the excited states of psoralen, 5‐methoxypsoralen, and 8‐methoxypsoralen in systems and furan and pyrone monoadducts bonded to a thymine residue. The theoretical assignments to ultraviolet (UV) absorption spectra of isolated systems have been performed. The present calculations have clarified that the excitation energies of the first singlet excited (S 1 ) state of monoadducts are blue‐shifted compared with the isolated systems. It is shown that, in particular, the S 1 excitation energy of the pyrone monoadduct is significantly blue‐shifted and, therefore, the pyrone monoadduct is not excited by UV‐A light (300–400 nm), which is used in the photochemotherapy. © 2003 Wiley Periodicals, Inc. J Comput Chem 25: 179–188, 2004