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1 September 2005 Photoreaction of Skin-sensitizing Trimethyl Psoralen with Lipid Membrane Models
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Abstract

The concerted photoreaction between trimethyl psoralen (TMP) and isomeric model compounds of oleic acid methyl ester (OAME) and eadilic acid methyl ester (EAME) are explored using density functional theory. The S1 surfaces all reveal large barriers (25–31 kcal/mol) to reach the decay channels, whereas the S2 surfaces differ considerably between the furan and pyrone side adducts. For the pyrone side adducts, a small barrier to reach the intersection between the S1 and S2 states is found, followed by a small second barrier on the S1 surface to the low-lying decay channel. For the furan-side adducts, no such intersection between S1 and S2 is seen, which thus prevents these products from being formed in high yields. The photoinduced cycloaddition is more favorable between OAME and the pyrone side double bond of TMP than for any of the other systems, which agrees with the experimental findings that this is formed in the highest yield. The computed UV absorption spectra of TMP and the TMP(pyrone)-OAME cycloadduct agree well with the experimental spectra.

Xiao Yi Li and Leif A. Eriksson "Photoreaction of Skin-sensitizing Trimethyl Psoralen with Lipid Membrane Models," Photochemistry and Photobiology 81(5), 1153-1160, (1 September 2005). https://doi.org/10.1562/2005-03-21-RA-467
Received: 21 March 2005; Accepted: 1 May 2005; Published: 1 September 2005
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