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• W2029366137 abstract "The photochemical cis/trans isomerization of urocanic acid (UCA, (E)-3-(1′H-imidazol-4′-yl)propenoic acid) was investigated using complete active space SCF (CASSCF) ab initio calculations. The singlet ground state and the triplet and the singlet manifolds of the lowest-lying π→π* (HOMO→LUMO) excitation of the neutral and the anionic UCA were calculated using the 6-31G* and the 6-31+G* basis sets, respectively. The torsional barrier of the double bond of the propenoic acid moiety in UCA is observed to be considerably lower in the T1 and S1 excited states of the neutral UCA and in the T1 but not in the S1 excited state of the anionic UCA, as compared to the S0 state of the respective protonation form. The cis-isomer of both the neutral and the anionic UCA is lower in energy than the trans-isomer in the S0, T1, and S1 states. This energy difference is larger in the excited states than in the ground state, probably due to strengthening of the intramolecular hydrogen bond of cis-UCA as the molecule is excited. The results of the calculations, interpreted in terms of the idea that UCA is deprotonated upon electronic excitation, led to construction of a new model for the photoisomerization mechanisms of UCA. According to this model, the trans-to-cis isomerization proceeds via both the triplet and the singlet manifolds in the deprotonated form of UCA. This isomerization may occur in the S0 state of the neutral UCA as well. The cis-to-trans isomerization is suggested to proceed only in the S0 state of the neutral UCA. ©1999 John Wiley & Sons, Inc. Int J Quant Chem 72: 25–37, 1999" @default.
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• W2029366137 date "1999-01-01" @default.
• W2029366137 modified "2023-10-06" @default.
• W2029366137 title "A CASSCF study on the lowest ???* excitation of urocanic acid" @default.
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• W2029366137 doi "https://doi.org/10.1002/(sici)1097-461x(1999)72:1<25::aid-qua3>3.0.co;2-z" @default.
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