TY - JOUR
T1 - Twin states and conical intersections in linear polyenes
AU - Fuß, W.
AU - Haas, Y.
AU - Zilberg, S.
PY - 2000/9/15
Y1 - 2000/9/15
N2 - We suggest for linear conjugated polyenes a twin state model which represents the ground state (S0) and first excited state (S1) as a superposition of mainly two mesomeric structures, the fully spin-paired one and a diradical. This model rationalizes why the bond-length alternation, which is pronounced in S0, more or less disappears in S1 and why the bond-alternation vibration (highest frequency C=C stretch) is raised in S1 and depressed in S0. The similarity to the Peierls effect and Kohn anomaly in one-dimensional metals is emphasized. Moreover, the conical intersection between S2 and S1 is qualitatively predicted, and invoking in addition, some spectroscopic and other observations and the phase-change rule, that between S1 and S0 can also be predicted. Compared with the consideration of densities of states and matrix elements, these intersections more satisfactorily explain the S2/S1 and S1/S0 internal conversions and their dependence on chain length, substituents, solvent and temperature and is furthermore consistent with photochemistry. This also includes an exponential gap rule for the internal-conversion rates, which is derived from a proposed dependence of the energy at the intersection on the S1-S0 energy gap. (C) 2000 Elsevier Science B.V.
AB - We suggest for linear conjugated polyenes a twin state model which represents the ground state (S0) and first excited state (S1) as a superposition of mainly two mesomeric structures, the fully spin-paired one and a diradical. This model rationalizes why the bond-length alternation, which is pronounced in S0, more or less disappears in S1 and why the bond-alternation vibration (highest frequency C=C stretch) is raised in S1 and depressed in S0. The similarity to the Peierls effect and Kohn anomaly in one-dimensional metals is emphasized. Moreover, the conical intersection between S2 and S1 is qualitatively predicted, and invoking in addition, some spectroscopic and other observations and the phase-change rule, that between S1 and S0 can also be predicted. Compared with the consideration of densities of states and matrix elements, these intersections more satisfactorily explain the S2/S1 and S1/S0 internal conversions and their dependence on chain length, substituents, solvent and temperature and is furthermore consistent with photochemistry. This also includes an exponential gap rule for the internal-conversion rates, which is derived from a proposed dependence of the energy at the intersection on the S1-S0 energy gap. (C) 2000 Elsevier Science B.V.
UR - http://www.scopus.com/inward/record.url?scp=0034666265&partnerID=8YFLogxK
U2 - 10.1016/S0301-0104(00)00200-7
DO - 10.1016/S0301-0104(00)00200-7
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AN - SCOPUS:0034666265
SN - 0301-0104
VL - 259
SP - 273
EP - 295
JO - Chemical Physics
JF - Chemical Physics
IS - 2-3
ER -